Stuff & Stuff Blog March 2022

    Alexander RABINOVICH, et al. --    Plasmatron Fuel Reformer
    Science & Mechanics ( February 1970 )
    http://connection.ebscohost.com/c/articles/2639544/plasmatron-device-can-cut-car-nox
    Professional Engineering;12/08/99, Vol. 12 Issue 22, p50 ( December 1999 )
    Plasmatron device can cut car NOx
         by Diinah Greek
ABSTRACT -- Offers a look at the plasmatron device developed by Alexander Rabinovich and colleagues in the plasma technology division at the Massachusetts Institute of Technology. Ability to cut emissions of pollutants such as nitrogen oxides; Mechanism; Testing; Features.

http://worldwidescience.org/topicpages/p/plasmatron+fuel+reformer.html
Plasmatron-catalyst system
A plasmatron-catalyst system. The system generates hydrogen-rich gas and comprises a plasmatron and at least one catalyst for receiving an output from the plasmatron to produce hydrogen-rich gas. In a preferred embodiment, the plasmatron receives as an input air, fuel and water/steam for use in the reforming process. The system increases the hydrogen yield and decreases the amount of carbon monoxide.

HYDROGEN GENERATION FROM PLASMATRON REFORMERS : A PROMISING TECHNOLOGY FOR NOX ADSORBER REGENERATION AND OTHER AUTOMOTIVE APPLICATIONS
Plasmatron reformers are being developed at MIT and ArvinMeritor [1]. In these reformers a special low power electrical discharge is used to promote partial oxidation conversion of hydrocarbon fuels into hydrogen and CO. The partial oxidation reaction of this very fuel rich mixture is difficult to initiate. The plasmatron provides continuous enhanced volume initiation. To minimize electrode erosion and electrical power requirements, a low current, high voltage discharge with wide area electrodes is used. The reformers operate at or slightly above atmospheric pressure. Plasmatron reformers provide the advantages of rapid startup and transient response; efficient conversion of the fuel to hydrogen rich gas; compact size; relaxation or elimination of reformer catalyst requirements; and capability to process difficult to reform fuels, such as diesel and bio-oils. These advantages facilitate use of onboard hydrogen-generation technology for diesel exhaust after-treatment. Plasma-enhanced reformer technology can provide substantial conversion even without the use of a catalyst. Recent progress includes a substantial decrease in electrical power consumption (to about 200 W), increased flow rate (above 1 g/s of diesel fuel corresponding to approximately 40 kW of chemical energy), soot suppression and improvements in other operational features.. Plasmatron reformer technology has been evaluated for regeneration of NOx adsorber after-treatment systems. At ArvinMeritor tests were performed on a dual-leg NOx adsorber system using a Cummins 8.3L diesel engine both in a test cell and on a vehicle. A NOx adsorber system was tested using the plasmatron reformer as a regenerator and without the reformer i.e., with straight diesel fuel based regeneration as the baseline case. The plasmatron reformer was shown to improve NOx regeneration significantly compared to the baseline diesel case. The net result of these initial tests was a significant decrease in fuel penalty, roughly 50% at moderate adsorber temperatures. This fuel penalty improvement is accompanied by a dramatic drop in slipped hydrocarbon emissions, which decreased by 90% or more. Significant advantages are demonstrated across a wide range of engine conditions and temperatures. The study also indicated the potential to regenerate NOx adsorbers at low temperatures where diesel fuel based regeneration is not effective, such as those typical of idle conditions. Two vehicles, a bus and a light duty truck, have been equipped for plasmatron reformer NOx adsorber regeneration tests...

Onboard Plasmatron Hydrogen Production for Improved Vehicles
A plasmatron fuel reformer has been developed for onboard hydrogen generation for vehicular applications. These applications include hydrogen addition to spark-ignition internal combustion engines, NOx trap and diesel particulate filter (DPF) regeneration, and emissions reduction from spark ignition internal combustion engines First, a thermal plasmatron fuel reformer was developed. This plasmatron used an electric arc with relatively high power to reform fuels such as gasoline, diesel and biofuels at an oxygen to carbon ratio close to 1. The draw back of this device was that it has a high electric consumption and limited electrode lifetime due to the high temperature electric arc. A second generation plasmatron fuel reformer was developed. It used a low-current high-voltage electric discharge with a completely new electrode continuation. This design uses two cylindrical electrodes with a rotating discharge that produced low temperature volumetric cold plasma., The lifetime of the electrodes was no longer an issue and the device was tested on several fuels such as gasoline, diesel, and biofuels at different flow rates and different oxygen to carbon ratios. Hydrogen concentration and yields were measured for both the thermal and non-thermal plasmatron reformers for homogeneous (non-catalytic) and catalytic reforming of several fuels. The technology was licensed to an industrial auto part supplier (ArvinMeritor) and is being implemented for some of the applications listed above. The Plasmatron reformer has been successfully tested on a bus for NOx trap regeneration. The successful development of the plasmatron reformer and its implementation in commercial applications including transportation will bring several benefits to the nation. These benefits include the reduction of NOx emissions, improving engine efficiency and reducing the nation's oil consumption. The objective of this program has been to develop attractive applications of plasmatron fuel reformer technology for onboard applications in internal combustion engine vehicles using diesel, gasoline and biofuels. This included the reduction of NOx and particulate matter emissions from diesel engines using plasmatron reformer generated hydrogen-rich gas, conversion of ethanol and bio-oils into hydrogen rich gas, and the development of new concepts for the use of plasmatron fuel reformers for enablement of HCCI engines.

PATENTS
Alexander RABINOVICH : Plasmatron Fuel Reformer
LOW POWER COMPACT PLASMA FUEL CONVERTER WO0114702
    Plasmatron-internal combustion engine system US5425332
    Plasmatron-internal combustion engine system   US5437250
    Apparatus and Method for NOx Reduction US2007289291
    Rapid response plasma fuel converter systems US5887554
    Integrated plasmatron-turbine system for the production and utilization of hydrogen-rich gas US5852927
    Homogeneous charge compression ignition control utilizing plasmatron fuel converter technology    US2004099226
    PLASMATRON FUEL CONVERTER HAVING DECOUPLED AIR FLOW CONTROL    WO2004094795
    WIDE DYNAMIC RANGE MULTISTAGE PLASMATRON REFORMER SYSTEM    WO2005094335
    HYDROGEN AND CARBON MONOXIDE ENHANCED KNOCK RESISTANCE IN SPARK IGNITION GASOLINE ENGINES    WO2004111417

    Zhaohui ZHONG , et al.
    Graphene Infrared Lens
    http://www.dailymail.co.uk/sciencetech/article-2584617/The-contact-lens-infrared-vision.html
    19 March 2014
    The contact lens that could let you see in the dark: Researchers reveal graphene 'supervision' sensor
    By Mark Prigg
    Researchers have unveiled plans for a smart contact lens that could give its wearer infrared 'night vision'.
    The team say that by sandwiching graphene inside the lens they can build a sensor capable of capturing every from visible light to infrared.
    They have already built a prototype smaller than a fingernail, and experts say it could one day be built into lenses for soldiers and others who need to see in the dark...
    Zhaohui Zhong at the University of Michigan say their layered approach can lead to ultrathin sensors...
    It takes advantage of graphene's 'supersensor' properties.
    The material shows a very strong effect when it’s struck by photons (light energy).
    It turns into what is known as a 'hot carrier' - an effect that can be measured, processed, and turned into an image.

    US2012225296    UNIFORM MULTILAYER GRAPHENE BY CHEMICAL VAPOR DEPOSITION
    Inventor(s):     ZHONG ZHAOHUI et al

    Glassesoff Vision Training App
    http://www.dailymail.co.uk/sciencetech/article-2583746/The-app-let-throw-away-reading-glasses.html
    18 March 2014
    Could the 'eye training' app really let you throw away your reading glasses?
    By Mark Prigg
    A new app that claims to be able to improve people's eyesight by 'training' them with a series of exercises has become a hit.
    Called GlassesOff, it uses a series of patterns to create 15 minutes exercises for users.
    If done three times a week, its makers say it could mean they no longer need reading glasses after three months.
    The app uses a series of games, puzzles and tests to improve a user's eyesight - if they can play for 15 minutes three times a week for three months.

    HOW IT WORKS
    GlassesOff uses a completely different approach that is exclusively aimed at teaching the visual system of the brain to better use its potential.
    This allows the brain to compensate for blurred information captured by the eyes as we age.
    The foundation for this technology is provided by the brain's ability to adapt, the app makers say.
    The app uses patterns designed to strengthen connections within circuits relevant to a task, such as recognizing letters when reading.
    'Traditionally, near distance reading improvement solutions were limited to optical corrections such as glasses, contact lenses and refractive surgery,' said said Nimrod Madar, CEO of GlassesOff.
         'However, human vision performance is in fact limited by two factors: the quality of an image captured by the eye and the image processing capability of the brain as it interprets such images.
    'Our solution is designed to improve reading by enhancing the image processing function of the visual cortex, demonstrating the amazing potential of the human brain...

    http://www.glassesoff.com/
    http://uripolat.files.wordpress.com/2012/06/srep00278.pdf
    http://uripolat.files.wordpress.com/2011/05/2004-polat-pnas-amblyopia.pdf
    http://uripolat.files.wordpress.com/2012/06/2009-practical_pl.pdf
    http://uripolat.files.wordpress.com/2012/06/sterkin_yehezkel_polat_vr_2012.pdf
    http://www.glassesoff.com/wp-content/uploads/2013/05/ARVO_2013.pdf
    http://www.glassesoff.com/wp-content/uploads/2013/05/ARVO_2012.pdf
    http://www.glassesoff.com/wp-content/uploads/2013/05/AAO_2012.pdf
    http://uripolat.files.wordpress.com/2011/05/2009-experreviews1.pdf

Alberto PERBELLINI / Carlo VENTURA:   Epigenetic Reprograming
Nonstem adult cells can be epigenetically reprogrammed backward to a state where they can become neural, cardiac, skeletal, muscle or insulin-producing cells:

Use of retinoic esters of hyaluronic acid for the differentiation of totipotent stem cells -- US2006216820
The present the invention relates to a new use of retinoic of hyaluronic acid, that exhibit pre-differentiating activity on totipotent stem cells. The invention also relates to a process to differentiate said stem cells and to select molecules capable of modulating the pro-differentiating activity of those esters.

Attila ALPEREN --    POWER EXTRACTION FROM PRESSURE
PESWiki.coM Pure Energy Systems NewS    September 18, 2013
http://TurXotorDemo.com
2013 : TurXotor Demo
    On October 24-27, the Turkish government will be holding a four-day Turkish Innovation Fair in Istanbul featuring the best Turkish technologies of the year, and that two of the Alperen Group technologies will be among the three on display.
    On September 7, Attila Alperen told me that his Alperen™ Group's TurXotor® motor is poised to be among the top three featured at the event. He said that the Turkish government wants to create a large electric car industry in Turkey around this invention that will enable electric vehicles to never have to be plugged in, and to be able to operate with only a few batteries on board, because the power source is onboard, pulling energy from the environment somehow -- harnessing the wheelwork of nature, as Tesla coined it.
    TurXotor® is a motor that works as a generator at the same time -- the only system like this in the world, as far as Mr. Alperen is aware. So the TurXotor® motor powers the wheels of the electric vehicle -- and produces electricity at the same time, both to replenish the source battery and provide extra for the other electrical needs of the vehicle such as lights, radio, heat, windows, etc.
    The Alperen™ Group doesn't describe their technology as a "free energy" technology. They shy away from words like "overunity" as well. They depict it as merely an efficient regeneration of the used technology. But obviously, if they are propelling a vehicle down the road, they have to be harvesting energy from somewhere beside the battery, if they don't have to ever recharge the battery from an external source.
    Attila said this will solve two problems presently associated with electric cars: range, and battery costs. The range will become unlimited, and the battery costs will be significantly reduced, because the vehicle will only need enough to serve as a buffer for acceleration input and deceleration harvesting of regenerative braking. They won't be needed for storage for duration travel. You'll be able to travel as far as you want without ever stopping for fuel or to recharge your batteries.
    This will be the first time the TurXotor® will be publicly demonstrated. The event will enable interested parties worldwide to see the technology demonstrated as well as discuss licensing manufacturing of the technology. Normally, Attila is not very accommodating for people to come and see the technology demonstrated, so this will be a rare opportunity.
    Attila said that at the event, the TurXotor® motor-generator will be demonstrated in isolation, showing its attributes of torque, electricity generation, and efficiency. It will also be open to inspection, not concealed in a "black box" of any kind.
    Though such a technology has a myriad of applications, at present, the only application that is being licensed is for manufacturing the motor to fit electric vehicles, or trains, or ships.

    WO2013048352
    METHOD OF POWER EXTRACTION FROM PRESSURE
    The method of invention consists of the extraction and utilization of potential energy as usable energy contained in pressurized liquid, air, and gas which is transferred via transfer lines such as pipes without losing the pressure values of inlet and outlet of the system.

    Basinçtan güç ekstraksiyon (açiga çikartma) yöntemi.    TR201109533
    Yüksek verimli türbin.    TR201107424

David CRAIK : Conotoxin Analgesic
http://www.smh.com.au/national/chronic-pain-relief-scientists-trial-nonaddictive-drug-from-snail-venom-20140317-34y5l.html
March 18, 2014
Chronic pain relief: Scientists trial non-addictive drug from snail venom
Lucy Carroll
Venom used to paralyse their prey: The carnivorous tropical marine cone snail.
A new drug extracted from snail venom could provide a breakthrough in treating severe chronic pain without the risk of addiction and dangerous side effects, researchers have found...

PATENTS
Novel nucleic acid molecules    AU2006200422
Cyclised conotoxin peptides    AU6070599
A novel molecule    AU784222
CYCLISED ALPHA-CONOTOXIN PEPTIDES    US8354372
TYROSINE-RICH CONOPEPTIDES    US2010093620
Cyclised alpha-conotoxin peptides    CN101448516
CYCLISED CONOTOXIN PEPTIDES    ES2308847
CYSTINE KNOT MOLECULES    US2011244564
J-SUPERFAMILY CONOTOXIN PEPTIDES    US2011064668
NOVEL NUCLEIC ACID MOLECULES    AT482975

Brajendra SHARMA, et al.":    Plastic to Diesel Fuel ( See also : ZADGAONKAR ... CHERRY ... CORTRIGHT ... ITO .. McNAMARA )
http://news.illinois.edu/news/14/0212bags_oil_BrajendraKumarSharma.html
http://www.sciencedaily.com/releases/2014/02/140212132853.htm
February 12, 2014
Plastic shopping bags make a fine diesel fuel
    Used plastic shopping bags can be converted into petroleum products that serve a multitude of purposes.
by Diana Yates

..."You can get only 50 to 55 percent fuel from the distillation of petroleum crude oil," Sharma said. "But since this plastic is made from petroleum in the first place, we can recover almost 80 percent fuel from it through distillation."
    Previous studies have used pyrolysis to convert plastic bags into crude oil. Sharma's team took the research further, however, by fractionating the crude oil into different petroleum products and testing the diesel fractions to see if they complied with national standards for ultra-low-sulfur diesel and biodiesel fuels.
    "A mixture of two distillate fractions, providing an equivalent of U.S. diesel #2, met all of the specifications" required of other diesel fuels in use today -- after addition of an antioxidant, Sharma said.
    "This diesel mixture had an equivalent energy content, a higher cetane number (a measure of the combustion quality of diesel requiring compression ignition) and better lubricity than ultra-low-sulfur diesel," he said...

Fuel Processing Technology, 2014; 122: 79
DOI: 10.1016/j.fuproc.2014.01.019
Brajendra K. Sharma, Bryan R. Moser, Karl E. Vermillion, Kenneth M. Doll, Nandakishore Rajagopalan : Production, characterization and fuel properties of alternative diesel fuel from pyrolysis of waste plastic grocery bags.
    http://www.sciencedirect.com/science/article/pii/S0378382014000290?via=ihub
    Fuel Processing Technology -- Volume 122, June 2014, Pages 79–90
    http://dx.doi.org/10.1016/j.fuproc.2014.01.019
    Production, characterization and fuel properties of alternative diesel fuel from pyrolysis of waste plastic grocery bags ?
    Brajendra K. Sharmaa, Bryan R. Moserb, Karl E. Vermillionb, Kenneth M. Dollb, Nandakishore Rajagopalana
    Abstract
    Pyrolysis of HDPE waste grocery bags followed by distillation resulted in a liquid hydrocarbon mixture with average structure consisting of saturated aliphatic paraffinic hydrogens (96.8%), aliphatic olefinic hydrogens (2.6%) and aromatic hydrogens (0.6%) that corresponded to the boiling range of conventional petroleum diesel fuel (#1 diesel 190–290 °C and #2 diesel 290–340 °C)...

    3. Results and discussion
    3.1. Preparation and chemical composition of pyrolyzed plastics
    The pyrolysis temperature range of 420–440 °C was chosen based on previous studies [34]. These temperatures resulted in decomposition reactions of HDPE to provide hydrocarbons of different chain lengths. Pyrolysis of waste plastic grocery bags at temperatures of 420–440 °C provided 74% yield of liquid product referred to as PCO, as shown in Fig. 1. Although not determined in the present paper, literature data suggested gaseous product obtained from pyrolysis of PE consisted primarily of ethane and ethene (C2, 52%) and C4 (32%) compounds [34]. The higher solid residue yield (17%) is likely due to the inorganic content and/or char content and/or unconverted HDPE. As the pyrolysis of PE has higher activation energy (280–320 kJ/mol) compared to polypropylene (190–220 kJ/mol), therefore, increasing the pyrolysis temperature to certain extent could result in increased amounts of the liquid fraction [34]. Also, this residue may have been the fraction boiling above 420 °C (analogous to the higher boiling vacuum gas oil fraction, VGO from petroleum distillation). Further thermal cracking of this product could have been achieved by increasing pyrolysis temperature and/or time, which we speculate would have resulted in higher yields of the desired PCO fraction. This residue along with the VGO fraction from PCO have potential to be used as lubricant basestocks, which upon further refining such as dewaxing/wax isomerization may yield API Group II/III lubricant base oils...

Zhe Liu, et al.     ---     ZL-105 vs Cancer
http://www2.warwick.ac.uk/newsandevents/pressreleases/new_drug_raises/
New drug raises potential for cancer treatment revolution
A revolution in cancer treatment could soon be underway following a breakthrough that may lead to a dramatic improvement in cancer survival rates.
A new study at the University of Warwick, published today in the journal Angewandte Chemie International Edition, has developed a new drug that can manipulate the body’s natural signalling and energy systems, allowing the body to attack and shut down cancerous cells.
Called ZL105, the drug is a compound based on the precious metal iridium. The study has found ZL105 could potentially replace currently used anticancer drugs, which become less effective over time, cause a wide-range of side-effects and damage healthy cells as well as cancerous...
“In contrast, the new iridium-based drug is specifically designed not to attack DNA, but to have a novel mechanism of action, meaning that it could not only dramatically slow down and halt cancer growth, but also significantly reduce the side effects suffered by patients” argues Professor Sadler.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201311161/abstract;jsessionid=487D95E3B88B65F3288F6BC1F5D4638E.f01t03
Angewandte Chemie International Edition, Vol. 53 Issue 13
DOI: 10.1002/anie.201311161
The Potent Oxidant Anticancer Activity of Organoiridium Catalysts
Dr. Zhe Liu, et al
Abstract
Platinum complexes are the most widely used anticancer drugs; however, new generations of agents are needed. The organoiridium(III) complex [(?5-Cpxbiph)Ir(phpy)(Cl)] (1-Cl), which contains p-bonded biphenyltetramethylcyclopentadienyl (Cpxbiph) and C^N-chelated phenylpyridine (phpy) ligands, undergoes rapid hydrolysis of the chlorido ligand. In contrast, the pyridine complex [(?5-Cpxbiph)Ir(phpy)(py)]+ (1-py) aquates slowly, and is more potent (in nanomolar amounts) than both 1-Cl and cisplatin towards a wide range of cancer cells. The pyridine ligand protects 1-py from rapid reaction with intracellular glutathione. The high potency of 1-py correlates with its ability to increase substantially the level of reactive oxygen species (ROS) in cancer cells. The unprecedented ability of these iridium complexes to generate H2O2 by catalytic hydride transfer from the coenzyme NADH to oxygen is demonstrated. Such organoiridium complexes are promising as a new generation of anticancer drugs for effective oxidant therapy.

NOVEL IRIDIUM/RHODIUM ANTI-CANCER COMPOUNDS   US2013065864    Inventor: HABTEMARIAM ABRAHA/LIU
Osmium (ii) arene azo anti-cancer complexes    CN103108880

Gots Ebola ? Got Cobalt Hexammine ?
realclearscience.com april 21, 2014
Possible Cure for Ebola Virus Infection?
by Alex B. Berezow
    ...In the journal Nature, scientists -- who conducted much of their work in the secretive, high-containment biological laboratory maintained by USAMRIID at Fort Detrick, Maryland -- have reported the discovery of a small molecule that rescues rodents and monkeys from various hemorrhagic fevers. Even more, the drug exhibited activity against a wide range of viruses.
    The molecule, named BCX4430... can be accidentally used by the virus when it is trying to grow inside of our cells. For the virus, this is a fatal mistake. BCX4430 blocks further growth and reproduction...
The most compelling experiment the research team ran involved the infection of cynomolgus macaque monkeys with deadly Marburg virus. Macaques were given twice daily doses of BCX4430 for 14 days beginning 1 hour, 24 hours, or 48 hours post-infection. (See graph. There were six monkeys in each treatment group.)
As shown above, all of the monkeys that did not receive BCX4430 (labeled "vehicle") died by day 12. However, every monkey (except for one) that received a dose of BCX4430 survived, even if the initial dose came 48 hours after infection. In total, 17 out of 18 treated monkeys lived...
Amazingly, in vitro experiments showed that BCX4430 could potentially work against a wide range of viruses, including SARS, MERS, influenza, dengue, and measles.

http://www.nature.com/nature/journal/vaop/ncurrent/full/nature13027.html
Nature 508: 402-405 (2014).
doi:10.1038/nature13027
Protection against filovirus diseases by a novel broad-spectrum nucleoside analogue BCX4430
Travis K. Warren,    et al.
Filoviruses are emerging pathogens and causative agents of viral haemorrhagic fever. Case fatality rates of filovirus disease outbreaks are among the highest reported for any human pathogen, exceeding 90% (ref. 1). Licensed therapeutic or vaccine products are not available to treat filovirus diseases. Candidate therapeutics previously shown to be efficacious in non-human primate disease models are based on virus-specific designs and have limited broad-spectrum antiviral potential. Here we show that BCX4430, a novel synthetic adenosine analogue, inhibits infection of distinct filoviruses in human cells. Biochemical, reporter-based and primer-extension assays indicate that BCX4430 inhibits viral RNA polymerase function, acting as a non-obligate RNA chain terminator. Post-exposure intramuscular administration of BCX4430 protects against Ebola virus and Marburg virus disease in rodent models. Most importantly, BCX4430 completely protects cynomolgus macaques from Marburg virus infection when administered as late as 48 hours after infection. In addition, BCX4430 exhibits broad-spectrum antiviral activity against numerous viruses, including bunyaviruses, arenaviruses, paramyxoviruses, coronaviruses and flaviviruses. This is the first report, to our knowledge, of non-human primate protection from filovirus disease by a synthetic drug-like small molecule. We provide additional pharmacological characterizations supporting the potential development of BCX4430 as a countermeasure against human filovirus diseases and other viral diseases representing major public health threats.

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SALZMANN, Michael : New Water
newwatersources.org
    Water is still being created by geological forces. That water, usually in a potable form, comes to the earth's surface in thousands of places, some well known like Jericho and Bahrain where it has provided drinking water for thousands of people for thousands of years. It pours into deep mines all over the world. Hundreds of houses on the rocky shores of Maine get their fresh water from wells drilled into the shoreline granite. Copenhagen gets all its water from a few wells. In Northern Europe, water that can be tapped by wells that do not depend on aquifers is called "ground water". The hallmark of new, or primary, water springs and wells is that they provide water at constant temperature and flow.
    But this world-wide source of "new water" has been ignored by geologists and laymen in most countries including the United States. They were taught that all potable water comes from the "hydrological cycle" which merely recycles water already on the surface of our earth.
    Michael H. Salzman, an engineer and administrator, researched, wrote and published a book providing detailed information on "new water". As published in 1960, it can be read and/or downloaded from this website. It is not readily available in libraries.
    Mike was a long time friend. He handed me one of his last copies in 1970 and asked me to see if I could get some recognition for it. He told me some wealthy people wanting to get approval for funds to build an aqueduct to bring water from the Colorado River to southern California (they succeeded) had bought up and burned all the copies they could find. They also tried (and failed) to have him fired as Director of the Los Angeles Housing Authority.
    Today, there is renewed interest in "new water". Two companies are working on projects to bring potable "new water" to areas where surface and ordinary well water are contaminated or nearly exhausted. Including wells for primary water drilled in Australia, Southern California and elsewhere, it appears more than 1,000 such wells have been drilled in recent years.
    Free online PDF : New Water for a Thirsty World by Michael Salzman ( 1960 ) Contents ... Forward by Aldous Huxley and Preface ... Table of Contents ... Chapter l - Introduction ... Chapter 2 - What is Water? ... Chapter 3 - New Water ... Chapter 4 - The Modern Sience of Hydrology and its Limitations ... Chapter 5 - The Dynamic Earth, part I ... Chapter 6 - The Dynamic Earth, part II ... Chapter 7 - Man's Challenge ... Chapter 8 - References, Index & About the Author

https://www.youtube.com/watch?v=WDxk5g6jXQ8
Cryptoviewing : A Stark Prediction Of Future Events

https://www.investmentwatchblog.com/antibodies-derived-from-natural-covid-infection-are-more-abundant-and-at-least-10x-more-potent-than-immunity-generated-by-vaccination-alone/
Antibodies derived from natural COVID infection are more abundant and at least 10x more potent than immunity generated by vaccination alone

http://www.womensystems.com/2022/03/study-reportedly-proves-pfizers-covid.html
Study Reportedly Proves Pfizer’s Covid Vaccine Hits Liver and Converts to DNA in 6 Hours

https://www.bitchute.com/video/FP8ZtEaliS2g/
Clif's explanation of Russia's takedown of biowarfare labs in Ukraine, presumably assisted by alliance intel:

https://www.bitchute.com/video/IvXrbUPLydK7/
Patterns of deployment of toxic batches
Paardekooper's analysis, re-posted on many channels. Among its implications are that this test was part of the preparation for another much bigger bio-weapon attack. Hence the urgency of shutting down the biowar agent production facilities in Ukraine.

https://www.youtube.com/watch?v=MjxlvduyJyc
Pfizer Vaccine Becomes DNA in Liver Cells. (In-vitro Swedish Study)

https://www.youtube.com/watch?v=iQOibpIDx-4
The Physics of UFOs: Eric Weinstein + Hal Puthoff

https://igorchudov.substack.com/p/worst-fears-realized-pfizer-mrna?utm_source=url
Worst Fears Realized: Pfizer mRNA Transcribes into DNA -- mRNA Vaccines Actually are "Gene Therapy", Study Shows
A new study is out: Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line.
...What the article shows is that in vitro, using a human liver cell line, Pfizer mRNA vaccine uses a natural reverse transcriptase enzyme called LINE-1, and the genetic code of the vaccine is reverse transcribed into the DNA.
It also explains that vaccine mRNA actually does travel to the liver as one of the preferred sites (the other sites, as we heard, are ovaries and more)....
Cancer Code
Considering that Sars-Cov-2 “spike protein” has cancer code from Moderna 2017’ patent 9,587,003, it is imperative to find out the implications of this reverse transcription, and whether the vaccinated now have any undesirable genetic code embedded into their DNA.
Of particular interest is whether this mRNA-induced reverse transcription affects the “germ line”, such as eggs and sperm cells, and whether it also affects the fetus of pregnant mothers...

https://dailyexpose.uk/2022/02/24/graphene-is-being-transmitted-from-vaccinated/
Graphene Is Being Transmitted from the “Vaccinated” to Vaccine-Free People
In his latest set of slides of blood samples taken from both “vaccinated” and unvaccinated people, Dr. Philippe van Welbergen demonstrated that the graphene being injected into people is organising and growing into larger fibres and structures, gaining magnetic properties or an electrical charge and the fibres are showing indications of more complex structures with striations....

Best o' Stuff & Stuff -- Links from past issues

    Thorsten LUDWIG : Hans Coler / Stromzeuger & Magnetstromapparat
    http://vimeo.com/72048742
    Thorsten Ludwig - Der Coler Stromerzeuger (Clip)
    Space energy exists , as scientists give - but to harness it is not yet . Stubbornly holding in the free-energy scene rumored that space power converter only therefore are not yet on the market , because powerful interests prevent this. The " Coler - power generator " seems to confirm this suspicion. Invented in the 1920s by the German researcher Hans Coler supplied the device , according to respected scientists actually have more energy than it consumed . But the outbreak of World War II stopped the development. After the war, the British Coler brought to their island , and soon after the inventor died. Dr. Thorsten Ludwig and Andreas Manthey of the German Association for Space Energy ( dvr - raumenergie.de ) felt decades later on an intelligence report , based on which they ventured to a replica of the legendary Coler - generator. The preliminary result they presented at the Free Energy Congress in Königstein.
The complete article is shown here:
bit.ly/ExoMagazin4-2013

http://www.thorstenludwig.de/aboutme.htm
Dr. Thorsten Ludwig
Tuning Coler Magnetic Current Apparatus With Magnetoacoustic Resonance


    Instant Ice Age
    http://www.youtube.com/watch?v=gf0JlHuX8ZY
An Ice Age caused by the sudden dimming of the electric plasma Sun may well occur within 30 years ( 50 at most ). We are not prepared : billions will die of starvation and cold. Got Electroculture ?

    http://www.ice-age-ahead-iaa.ca/45/index.html
    [ Rolf A. F. Witzsche ]
    "Below a minimal plasma-density threshold, the primer fields collapse, the Sun becomes inactive. 70% less solar energy is being radiated. The Ice Age begins. The transition may be as short as a day."..


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    DIAZ, Illac : "Liter of Light" Solar Lightbulb
    http://aliteroflight.org
    http://www.gizmag.com/pop-bottles-provide-light/19829/
    Social project uses pop bottles to provide indoor lighting for the poor

...The Solar Bottle Bulb, as it is called, was originally designed by students from the Massachusetts Institute of Technology (MIT). Its construction and installation is simple. A clear one-liter pop bottle is filled with water, chlorine is added, then the bottle is squeezed part way through a hole in a piece of corrugated tin. A corresponding hole is cut in the tin roof of a house, the tin-and-bottle is secured over the hole so that the bottom of the bottle hangs down through the ceiling/roof, then caulking is applied to prevent rain from getting in.

    When sunlight hits the roof and the top of the bottle, its rays are carried down through the water and dispersed into the interior of the home, giving off about as much light as a 55-watt bulb. Given that many of these homes lack windows, they might otherwise be nearly pitch black inside...

    YouTube Videos :

    http://www.youtube.com/watch?v=cQCHvO2H0_0
    http://www.youtube.com/watch?v=i5YQ4t5apPM

        HOW TO BUILD A SOLAR BOTTLE BULB

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    TAGHIAN, Tollo, et al. : High-Frequency Accelerated Wound Healing
    http://www.uc.edu/news/NR.aspx?id=19331
    2/3/2014
    UC Research Tests Range of Electrical Frequencies that Help Heal Chronic Wounds
     M.B. Reilly

    Hard-to-heal wounds, like diabetic ulcers, fester because of insufficient blood supply at the wound site. However, the application of an electrical stimulus can promote the growth of blood vessels, and new UC research examines the best stimulus parameters (such as frequency and magnitude) for successful therapy.
    And externally applied low-amplitude electric fields have been shown to help hard-to-heal chronic wounds, like those associated with diabetes, where there is insufficient blood supply and drug treatments are not effective. The externally applied electric field manipulates the body’s naturally occurring electricity, such that the new vessels are formed, and blood supply to the wound is increased.
    University of Cincinnati physics and biomedical engineering researchers recently tested for the most-effective magnitude and frequency when applying an external low-amplitude electric field to vascular cells, which are key to healing chronic wounds. Physics doctoral student Toloo Taghian will present the results at the March 3-7 American Physical Society meeting in Denver. The title of her presentation is “Co-Regulation of Cell Behavior by Electromagnetic Stimulus and Extracellular Environment.”
    The team discovered that high-frequency electrical stimulus, similar to that generated by cell phones and Wi-Fi networks, increased the growth of blood vessel networks by as much as 50 percent, while low-frequency electrical stimulus did not produce such an effect. As part of their work, the UC team has developed a specialized antenna to apply the electrical signals to a localized wound, and that design is now the subject of a provisional patent.

    HOW HIGH-FREQUENCY ELECTRICITY AFFECTS VASCULAR CELL GROWTH
    The high-frequency electrical stimulus is able to change the ionic environment surrounding the endothelial cells, which form the lining of blood vessels. Inside the cells, this stimulus can create links with proteins (proteins have existing charges that react with the applied electrical field) to activate pathway signals leading to growth in the capillary network. The high-frequency electrical stimulus also causes cells to produce chemicals called “growth factors” that help sustain growing vascular networks.
    Said Taghian, “Electrical stimulation activates the pathway for angiogenesis (formation of new blood vessels), and the vascular network growth is enhanced. We can expect that, as a result, wound closure would be enhanced, leading to a faster healing.”
    The potential for electrical-based treatment of wounds is far reaching. Given the targeted, localized nature of such wound treatment, the application of electrical stimulus could replace or reduce the need for drug-based treatments which affect the entire body and may carry side effects. Importantly, such therapy could be applied using a hand-held device without the need to remove the wound dressing.
    The stimulus frequency used by the team was as high as 7.5 billion cycles per second (Gigahertz, or GHz), and as low as 60 cycles per second (Hertz, or Hz), which is the same frequency used in 120V power outlets in the United States. The vascular tissue cells were exposed to the electrical fields for one hour per day for seven days, and the rate of wound healing was observed for 24 hours after each treatment.

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    MACLEAN, Michelle, et al. : Photoinactivation of Bacteria
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2663198/
    Appl Environ Microbiol. Apr 2009; 75(7): 1932–1937.
    Inactivation of Bacterial Pathogens following Exposure to Light from a 405-Nanometer Light-Emitting Diode Array
    Michelle Maclean,* Scott J. MacGregor, John G. Anderson, and Gerry Woolsey
    Abstract
    This study demonstrates the susceptibility of a variety of medically important bacteria to inactivation by 405-nm light from an array of light-emitting diodes (LEDs), without the application of exogenous photosensitizer molecules. Selected bacterial pathogens, all commonly associated with hospital-acquired infections, were exposed to the 405-nm LED array, and the results show that both gram-positive and gram-negative species were successfully inactivated, with the general trend showing gram-positive species to be more susceptible than gram-negative bacteria. Detailed investigation of the bactericidal effect of the blue-light treatment on Staphylococcus aureus suspensions, for a range of different population densities, demonstrated that 405-nm LED array illumination can cause complete inactivation at high population densities: inactivation levels corresponding to a 9-log10 reduction were achieved. The results, which show the inactivation of a wide range of medically important bacteria including methicillin-resistant Staphylococcus aureus, demonstrate that, with further development, narrow-spectrum 405-nm visible-light illumination from an LED source has the potential to provide a novel decontamination method with a wide range of potential applications.

    Inactivation of microorganisms using methods involving exposure to light is an area of increasing research interest in part because of the intractable problem of microbial antibiotic resistance. Ultraviolet (UV) light is well established as a light inactivation treatment, inducing effects ranging from DNA damage, primarily as a result of UV absorption by DNA at wavelengths of 240 nm to 280 nm (3), to sublethal damage of DNA repair systems caused by near-UV light (24). The use of UV light, however, has limitations due to its detrimental effects on skin tissue and components of the eye (28). On the other hand, visible-light inactivation, which traditionally requires the addition of photosensitizing molecules and is termed photodynamic inactivation (PDI), has been developed as a treatment for cancer and other medical ailments (11). The rapidly increasing problem of microbial antibiotic resistance has ignited research interest into the use of PDI as an alternative antimicrobial treatment. Numerous in vitro PDI studies have been made involving microbial inactivation, with successful results for bacteria, fungi, yeasts, viruses, and parasites (29, 7, 12, 2, 5). Furthermore, recent work has shown that photosensitization of bacterial cells is independent of the antibiotic resistance spectrum (17).

    The focus of the present study, however, concerns the photoinactivation of bacterial cells without the involvement of an applied photosensitizer. Previous studies have shown that exposure to visible light, more specifically, blue-light wavelengths, causes inactivation of certain bacterial species, including Propionobacterium acnes, Helicobacter pylori, and some oral pigmented bacteria (1, 8, 22). This inactivation mechanism, known to be oxygen dependent (6), is thought to be a result of the photoexcitation of naturally occurring endogenous porphyrins, which act as endogenous photosensitizers within the bacterial cells. This porphyrin excitation leads to energy transfer and, ultimately, the production of highly cytotoxic, oxygen-derived species, most notably, singlet oxygen (11, 26).

    Previous work has demonstrated that Staphylococcus aureus can be photodynamically inactivated using 400- to 420-nm visible-light, with maximum visible-light inactivation at 405 nm (13, 9, 10, 14), through an oxygen-dependent process (15). This inactivation of S. aureus is thought to be the result of a porphyrin-mediated process similar to that demonstrated with P. acnes. A previous study by Maclean et al. (14) utilized a broad-spectrum xenon white-light source combined with a range of optical filters to identify the sensitivity of S. aureus to wavelengths of light within the visible region. The present study investigates specifically the use of 405-nm light as the inactivating wavelength and also extends the scope of previous studies by producing new information on the sensitivities of a range of bacterial pathogens to the bactericidal effects of 405-nm light.

    The inactivating light used in the present study was generated from 405-nm light-emitting diodes (LEDs). Investigations were carried out on the use of the 405-nm light from the LED array source for the inactivation of methicillin-resistant S. aureus (MRSA) and a range of other important nosocomial bacterial pathogens—both gram-positive and gram-negative types—in the absence of any chemical pretreatment. The results are discussed with regard to the possible cellular mechanisms involved in this light-based inactivation and to the potential use of this method for environmental decontamination applications in both clinical and nonclinical environments....

    MATERIALS AND METHODS
    LED light source.
    High-intensity 405-nm light was achieved with the LEDs in the form of a close-packed rectangular array of 99 individual LEDs in an 11 by 9 matrix. The light of these 405-nm LEDs is generated in the active region of an InGaN/GaN semiconductor junction. These arrays (OD-405-99-070) are produced by OptoDiode Corp (CA). The emission spectrum of the 405-nm LED array is shown in Fig. ?Fig.1.1. It can be seen that the center wavelength for maximum emission is close to 405 nm, and the bandwidth is ~10 nm at full-width half-maximum. The LED array was bonded to a heat sink and fan to minimize the temperature of the semiconductor junction. The junction temperature was maintained at around 30°C, well below the specified maximum operating temperature of 100°C. This arrangement also ensured that the heat produced by the complete light system was low and had no effect on the test samples exposed to the 405-nm light. The arrangement was mounted in a polyvinyl chloride housing designed to fit on top of a 12-well microplate (without lid), with the LED array positioned directly above a single sample well. The LED array was powered by a direct current supply with the output controllable in the range 0 to 3 A and 0 to 15 V. For all experiments the current was set to 0.5 ± 0.05 A at a voltage of 11.2 ± 0.1 V...

    RESULTS
    Results for the inactivation of a selection of gram-positive and gram-negative bacterial samples, each with an initial population density 105 CFU/ml, are shown in Fig. ?Fig.22 and Fig. ?Fig.3,3, respectively. The control trend lines in both Fig. ?Fig.22 and Fig. ?Fig.33 are averages of the data from all the experiments and demonstrate that the unexposed populations show no significant change throughout the duration of the experiments. In the conventional manner for expression of inactivation data, log10(N/N0) is plotted as a function of exposure time, where N0 and N are the bacterial populations in CFU/ml prior to and following inactivation, respectively. When exposed to 405-nm light, the different gram-positive bacteria behaved in a similar manner, with the exception of Enterococcus faecalis. For the Staphylococcus, Streptococcus, and Clostridium strains, the highest levels of inactivation were recorded, with an approximately 5-log10 reduction in CFU counts observed following exposure between 60 and 90 min to 405-nm light with an irradiance of 10 mW/cm2. Exposure of E. faecalis suspensions, however, to the same irradiance of 10 mW/cm2 for up to 120 min resulted in negligible inactivation. Nevertheless, as shown in Fig. ?Fig.3,3, longer exposure times did result in some inactivation of E. faecalis. Significant inactivation, compared to the nonexposed E. faecalis control sample, was demonstrated for a 240-min exposure period, and a 2.6-log10 reduction was recorded following exposure for 360 min...
    Significant inactivation of the gram-negative bacteria (Fig. ?(Fig.3)3) was seen following exposure to 405-nm light with an irradiance of 10 mW/cm2. In general, for a given reduction in population, the gram-negative species required longer exposure times than the gram-positive species. For example, a 180-min exposure was required to achieve a 4.2-log10 reduction with Acinetobacter baumannii, and 300-min exposure was required to achieve a 3.1-log10 reduction with Escherichia coli.

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    http://keelynet.wordpress.com/2010/11/20/violet-light-technology-combats-hospital-infections/
    November 20, 2010
    Violet Light Technology Combats Hospital Infections

    A pioneering lighting system that can kill hospital superbugs — including MRSA and C. difficile — has been developed by researchers at the University of Strathclyde in Glasgow, Scotland. The technology decontaminates the air and exposed surfaces by bathing them in a narrow spectrum of visible-light wavelengths, known as HINS-light.

    Professor Anderson said: “The technology kills pathogens but is harmless to patients and staff, which means for the first time, hospitals can continuously disinfect wards and isolation rooms.

    “The system works by using a narrow spectrum of visible-light wavelengths to excite molecules contained within bacteria. This in turn produces highly reactive chemical species that are lethal to bacteria such as meticillin-resistant Staphylococcus aureus, or MRSA, and Clostridium difficile, known as C.diff.”...

    US2008305004
    INACTIVATION OF GRAM-POSITIVE BACTERIA

    A method for inactivating medically important Gram-positive bacteria including Methicillin-resistant Staphylococcus aureus (MRSA), Coagulase-Negative Staphylococcus (CONS), Streptococcus, Enterococcus and Clostridium species, comprising exposure to visible light, and in particular light within the wavelength range 400-500 nm

    SUMMARY OF THE INVENTION
    [0011] Exposing these bacteria to blue light, or white light containing blue light, has been found to stimulate an inactivation process. An advantage of using light in the visible-wavelength region is that there is no detrimental effect on human or animal health. Consequently, the method can be used for an extensive range of applications, such as air disinfection, contact-surface and materials disinfection and, most noteworthy, wound protection and tissue disinfection.

    WAVELENGTH DOSE J/cm<2> /log
    ORGANISM RANGE (J/cm<2> ) reduction
    S. aureus 4135   >400 nm (100% intensity) 630 126
    S. aureus 4135 >400 nm (75% intensity) 729 145.8
    S. aureus 4135 >400 nm (50% intensity) 648 144
    S. aureus 4135 <500 nm 189.6 37.92
    S. aureus 4135 400-500 nm 290.8 58.2
    MRSA 15975 >400 nm 1260 252
    MRSA 16a >400 nm 945 189
    S. epidermidis >400 nm 840 168
    NCTC 7944
    Strep. pyogenes >400 nm 1440 288
    NCTC 8198
    E. faecalis >400 nm 2880 1440

    [0043] The use of 400-500 nm, in particular 400-450 nm, wavelengths of visible light (blue light) has proved to be an effective means of inactivation of Staphylococcus strains, including MRSA, as well as CONS, Streptococcus, Enterococcus and Clostridium, with increased inhibition rates in the 400-420 nm range and in particular, around 405 nm. This demonstrates that a light source (continuous source, flashlamp, laser etc.) with output at wavelengths in these regions could potentially be used in clinical environments for the reduction in levels of methicillin-resistant Staphylococcus aureus, and other medically important Gram-positive species, present in the air and on contact surfaces and materials, and most importantly, could be used for wound protection and tissue treatment. The exact parameters required would depend on the bacterial strain, the wavelength of the light being used and the light intensity. These can be readily determined experimentally.

    DMSO / Vitamin C vs Cancer
    wakingtimes.com
    August 22, 2013
    The Magic Duo for Cancer Treatment That Frightens The FDA and Conventional Medicine
    Dave Mihalovic
    Use of DMSO (Dimethyl sulfoxide) in medicine dates back decades. It was predominantly used as a topical anagesic, anti-inflammatory and antioxidant. Today, we know that DMSO can treat a variety of disorders including arthritis, mental illness, emphysema, and even cancer. While this is now considered a superb cancer treatment, orthodox medicine is not interested in discussing its benefits. If DMSO were to be implemented and used in cancer treatment, the “true cure rate” for orthodox medicine would rise from 3% to above 90%! Here’s why...

    DMSO – Vitamin C Treatment

    Vitamin C is so simlar to glucose, that cells, and especially cancer cells, consume vitamin C the same way they would consume glucose.

    Cancer cells are anaerobic obligates, which means they depend upon glucose as their primary source of metabolic fuel. Cancer cells employ transport mechanisms called glucose transporters to actively pull in glucose.

    In the vast majority of animals, vitamin C is synthesized from glucose in only four metabolic steps. Hence, the molecular shape of vitamin C is remarkably similar to glucose. Cancer cells will actively transport vitamin C into themselves, possibly because they mistake it for glucose. Another plausible explanation is that they are using the vitamin C as an antioxidant. Regardless, the vitamin C accumulates in cancer cells.

    If large amounts of vitamin C are presented to cancer cells, large amounts will be absorbed. In these unusually large concentrations, the antioxidant vitamin C will start behaving as a pro-oxidant as it interacts with intracellular copper and iron. This chemical interaction produces small amounts of hydrogen peroxide.

    Because cancer cells are relatively low in an intracellular anti-oxidant enzyme called catalase, the high dose vitamin C induction of peroxide will continue to build up until it eventually lyses the cancer cell from the inside out! This effectively makes high dose IVC a non-toxic chemotherapeutic agent that can be given in conjunction with conventional cancer treatments. Based on the work of several vitamin C pioneers before him, Dr. Riordan was able to prove that vitamin C was selectively toxic to cancer cells if given intravenously. This research was recently reproduced and published by Dr. Mark Levine at the National Institutes of Health.

    As feared by many oncologists, small doses may actually help the cancer cells because small amounts of vitamin C may help the cancer cells arm themselves against the free-radical induced damage caused by chemotherapy and radiation. Only markedly higher doses of vitamin C willselectively build up as peroxide in the cancer cells to the point of acting in a manner similar to chemotherapy. These tumor-toxic dosages can only be obtained by intravenous administration.

    Over a span of 15 years of vitamin C research, Dr. Riordan’s RECNAC (cancer spelled backwards) research team generated 20 published papers on vitamin C and cancer. RECNAC even inspired its second cancer research institute, known as RECNAC II, at the University of Puerto Rico. This group recently published an excellent paper in Integrative Cancer Therapies, titled “Orthomolecular Oncology Review: Ascorbic Acid and Cancer 25 Years Later.” RECNAC data has shown that vitamin C is toxic to tumor cells without sacrificing the performance of chemotherapy.

    Intravenous vitamin C also does more than just kill cancer cells. It boosts immunity. It can stimulate collagen formation to help the body wall off the tumor. It inhibits hyaluronidase, an enzyme that tumors use to metastasize and invade other organs throughout the body. It induces apoptosis to help program cancer cells into dying early. It corrects the almost universal scurvy in cancer patients. Cancer patients are tired, listless, bruise easily, and have a poor appetite. They don’t sleep well and have a low threshold for pain. This adds up to a very classic picture of scurvy that generally goes unrecognized by their conventional physicians.

    Because cancer cells consume 15 times more glucose than normal cells, under the right conditions, cancer cells should consume 15 times more vitamin C than a normal cell. While normal cells benefit from vitamin C, the microbes inside of the cancer cells may be killed by vitamin C. It is microbes which are inside of the cancer cells which cause cancer and which force a cancer cell to remain cancerous.

    It should be mentioned that two-time Nobel Prize winner Linus Pauling, and an associate, Dr. Ewan Cameron, M.D., were able to extend the lives of cancer patients more than 10-fold using only 10 grams of vitamin C a day by I.V.

    This protocol will modify the Pauling/Cameron protocol four different ways:
    1) It will include DMSO in the evening dose to help Vitamin C target cancer cells and get inside of cancer cells,
    2) It includes a very, very low glucose diet so that the cancer cells will feast on Vitamin C instead of glucose,
    3) It includes 15% or less potassium ascorbate, which has a special affinity for cancer cells,
    4) It will include as little sodium ascorbate (or other sodium forms of Vitamin C) as possible because these types of Vitamin C do not get inside of cancer cells very well.

    Regarding the use of potassium ascorbate, a foundation in Italy has proven that potassium ascorbate can be used to cure cancer (WARNING:no more than 15% of the Vitmain C you take should be a potassium version!!). See: Pantellini Foundation (Italy)

    WARNING: Do NOT use potassium ascorbate or any other form of potassium as your primary source of Vitamin C!!! If you use potassium ascorbate work with the vendor of this product to insure you are taking safe doses relative to non-potassium forms of Vitamin C!!! If your vendor does not make a recommendation, then use 15% as the maximum portion of Vitamin C that is a potassium form!!

    The second thing this treatment uses is DMSO. DMSO is used to “open” the ports on the cancer cells to assist getting vitamin C inside the cancer cells. DMSO is very well known to target cancer cells and open their ports. To better understand this concept see this article.
    In summary, there are three things that help get the vitamin C inside the cancer cells:
    1) Cancer cells consume 15 times more glucose than normal cells and cancer cells cannot tell the difference between glucose and vitamin C.
    2) The use of potassium ascorbate as a part of the Vitamin C protocol.
    3) The use of DMSO.
    A fourth unique thing about this protocol is the “cancer diet.” The cancer diet for this treatment focuses on a LOW GLUCOSE cancer diet. In this way, the cancer cells have less glucose to interfere with their consumption of vitamin C!

    Possible Swelling and Inflammation

    There are two possible results when large amounts of vitamin C get inside of a cancer cell. First, the vitamin C can kill the microbe(s) inside the cancer cell and the cell will safely revert into a normal cell; or second, the vitamin C can kill the cancer cell itself.

    While the first of these two options will not cause any swelling or inflammation, the second option may cause swelling and inflammation.

    For this reason, anyone on this protocol who would be put at risk by swelling and/or inflammation (e.g. in a tumor), should carefully and slowly build-up to the theraputic dose of vitamin C, watching carefully for any potential swelling or inflammation.

    Details of the Treatment

    Many people have difficulties working with DMSO. In some cases, when taken transdermally (through the skin) there is a skin rash which is simply too severe to continue the treatment. When you get your bottle of DMSO put one drop on your skin, spread it around a little bit and see if you have an allergic reaction (i.e. severe rash). If not, an hour later put 10 drops on your skin and spread it thin.

    If you do have a reaction, you may still be able to take the DMSO orally (added to 4 ounces of water). But if you cannot take the DMSO orally, and you have a skin reaction to the DMSO, you will have to abandon this treatment.

    If you want to know more about DMSO, see this website:

    http://www.dmso.org/articles/information/muir.htm

    The Importance of the DMSO

    This treatment uses DMSO (in the evening) and vitamin C (twice a day). The theory of this treatment is that the DMSO will be used first (in the evening dose), either taken orally (with water) or transdermally (through the skin). In about 10 minutes the DMSO will have targeted the cancer cells and will start “opening up” their ports.

    In the evening dose, about ten minutes after taking the DMSO, the vitamin C will be taken with water. When the vitamin C gets to the cancer cells the cells natural affinity for consuming vitamin C (because the cancer cells “think” the vitamin C is glucose) should be enhanced by the fact that the cancer cells have been “opened up” by DMSO.

    The theory is that the DMSO will allow a larger concentration of vitamin C to get inside the cancer cells than would normally occur.

    As already mentioned, once vitamin C can get inside of a cancer cell the cell may revert into a normal cell or it may be killed. If enough cancer cells are killed, some swelling may occur.

    The Vitamin C To Be Used **VERY Important**

    There are several different types of vitamin C. The most common type of vitmain C is ascorbic acid, which is not bound to a mineral. This type of vitamin C is largely useless until it has bound to minerals already in the body.
    The ideal vitamin C product will have both ascorbic acid, no more than 15% potassium ascorbate or potassium carbonate and other forms of mineral ascorbates or carbonates or other forms of Vitamin C.

    Since sodium is generally found outside of cells and potassium is generally found inside of cells, to get vitamin C inside of cells it is best to use a potassium ascorbate. However, for safety reasons, most of the Vitamin C cannot be a potassium version of Vitamin C (talk to your vendor). If you can avoid sodium ascorbate and use some other non-potassium form of Vitamin C (e.g. ascorbic acid) use it.

    Some buffered vitamin C products have ascorbic acid and several different kinds of mineral ascorbates or carbonates (e.g. zinc carbonate). This is good, but it may be necessary to add some potassium ascorbate to get the percentage of potassium up to 15% (or whatever maximum your potassium vendor tells you). Include as little sodium ascorbate as possible.

    The DMSO and Vitamin C Protocol

    This treatment will be taken twice a day.

    The morning dose will only include Vitamin C. Remember to take VERY LITTLE glucose during this treatment!!

    The evening treatment will include two phases.

    In the evening, Phase One will be 1 TEAspoon of DMSO, taken orally or transdermally or some combination thereof.

    Phase Two of the evening dose should follow Phase One by 10 minutes and will consist of 5 grams of vitamin C taken orally in water.

    The Morning Dose – Vitamin C Only

    The morning dose, which should be taken about twelve hours before the evening dose, should contain 5 grams of vitamin C. Fifteen percent or less (or whatever your potassium vendor tells you) should be a form of potassium carbonate (or some other potassium version of Vitamin C). The other eighty-five percent should contain zero potassium Vitamin C and as little sodium Vitamin C as possible.

    The Evening Dose (DMSO and Vitamin C): Phase One: Taking the DMSO

    The DMSO used in this protocol should be at least 99% pure DMSO mixed with 30% water. In other words, you should buy “70/30? DMSO, which means 70% pure DMSO and 30% water. Some DMSO vendors sellDMSO Gel or DMSO Liquid.

    The amount of DMSO taken during this treatment is so low that normally it can be taken orally if it is mixed with 4 ounces of water. However, if for any reason the DMSO cannot be taken orally it can be spread over the skin (such as the arms, legs or stomach) and taken transdermally (through the skin).

    The DMSO should be put in a glass of water before taking it orally. The glass of water should have at least 4 ounces of water in it!

    The Evening Dose:

    1a DMSO Orally) If you are taking the DMSO orally, put 4 ounces of a quality bottled water in a glass. Then put ONE TEAspoon of DMSO in the water. Drink the water (and thus the DMSO).

    Because the DMSO may cause stomach irritation, you may want to build up to the theraputic dose of DMSO. For example, you might use the following build-up:
    Day 1 – Evening) Use 1/4 TEAspoon of DMSO in 4 ounces of water,
    Day 2 – Evening) Use 1/2 TEAspoon of DMSO in 4 ounces of water,
    Day 3 – Evening) Use 3/4 TEAspoon of DMSO in 4 ounces of water,
    Day 4 – Evening) Use 1 TEAspoon of DMSO in 4 ounces of water,
    Day 5 – Evening) Continue using the 1 TEAspoon of DMSO in 4 ounces of water.

    1b – DMSO Transdermally) If you are taking the DMSO transdermally (through the skin), put ONE TEAspoon of DMSO on your arms, legs or stomach (as close to the cancer as possible). Spread the DMSO very thin (i.e. over a wide area of skin). Ten minutes after spreading the DMSO on the skin, and AFTER the DMSO has penetrated the skin (and the skin is dry), you can put a skin cream on where you rubbed the DMSO to prevent a rash.

    The Evening Dose: Phase Two: Taking the Vitamin C

    The evening dose, which should be taken about ten minutes after taking the DMSO, should contain 5 grams of vitamin C. Fifteen percent or less (or whatever your potassium vendor tells you) should be a form of potassium carbonate (or some other potassium version of Vitamin C). The other eighty-five percent should contain no potassium Vitamin C and as little sodium Vitamin C as possible. (Of course, the vitamin C may be pre-mixed).

    Here is one highly recommended potassium vitamin C vendor (Fifteen percent or LESS of the Vitamin C should be a potassium version unless your vendor of potassium ascorbate tells you differently):
    Excellent Buffered Vitamin C Product

    One rounded teaspoon contains 4 grams of absorbic acid and 700 mg of potassium ascorbate. It also has zero mg of sodium (which is ideal). The ideal product will have potassium ascorbate without sodium ascorbate, but with other forms of Vitamin C.

    As with all vitamin C products, keep this product out of the reach of children! It can be very dangerous if very high doses are taken.

    If you have a type of cancer which could lead to a dangerous situation if swelling and inflammation resulted from this treatment, SLOWLY build up the dose of Vitamin C.

    For example, you might use the following build-up (for both morning and evening):
    Day 1) Use 1/4 TEAspoon of vitamin C, in 6 ounces of water
    Day 2) Use 1/2 TEAspoon of vitamin C, in 6 ounces of water
    Day 3) Use 3/4 TEAspoon of vitamin C, in 6 ounces of water
    Day 4) Use 1 level TEAspoon of vitamin C, in 6 ounces of water
    Day 5) Start the full treatment at full doses

    If you experience any potentially dangerous swelling or inflammation during any of the days, DISCONTINUE THIS TREATMENT.

    Ohoo Algae Gel
    http://www.dailymail.co.uk/sciencetech/article-2590695/The-end-water-bottle-Edible-algae-balloon-cut-plastic-waste.html
    27 March 2014
    End of the water bottle? Edible algae 'balloon' could cut plastic waste
    To solve the rising number of plastic bottles filling up landfills around the world, a trio of designers has created an alternative - a container made from an edible algae balloon.
    Called Ooho, the spheres can be produced in different sizes, hygienically protect the liquid inside, and cost just 2 cents (less than a penny) each.
    The design was recently crowned one of 12 winners of the second annual Lexus Design Award and is due to go on sale in Boston later this year.

    HOW IS THE OOHO MADE?
    The Ooho sphere has a double gelatinous membrane.
    It is made using a mixture of sodium alginate, taken from brown algae, and calcium chloride.
    The spheres are created using gelification - a technique used in cooking to turn liquids into gel by adding an edible gelling agent...
    The double membrane hygienically protects the liquid inside and can be expanded for different sized Oohos, pictured. The inventors experimented with various spherification techniques, using different ingredients and proportions, before settling on the Ooho final 'recipe'

    JI, David, et al. : Cellulose Supercapacitor
    http://phys.org/news/2014-04-trees-high-tech-cellulose-energy-storage.html#jCp
    Apr 07, 2014
    Trees go high-tech: Process turns cellulose into energy storage devices

    Based on a fundamental chemical discovery by scientists at Oregon State University, it appears that trees may soon play a major role in making high-tech energy storage devices.

    OSU chemists have found that cellulose – the most abundant organic polymer on Earth and a key component of trees – can be heated in a furnace in the presence of ammonia, and turned into the building blocks for supercapacitors...

    The new approach just discovered at Oregon State can produce nitrogen-doped, nanoporous carbon membranes – the electrodes of a supercapacitor – at low cost, quickly, in an environmentally benign process. The only byproduct is methane, which could be used immediately as a fuel or for other purposes.

    "The ease, speed and potential of this process is really exciting," said Xiulei (David) Ji, an assistant professor of chemistry in the OSU College of Science, and lead author on a study announcing the discovery in Nano Letters, a journal of the American Chemical Society. The research was funded by OSU.

    "For the first time we've proven that you can react cellulose with ammonia and create these N-doped nanoporous carbon membranes," Ji said. "It's surprising that such a basic reaction was not reported before. Not only are there industrial applications, but this opens a whole new scientific area, studying reducing gas agents for carbon activation.
    "We're going to take cheap wood and turn it into a valuable high-tech product," he said.
    These carbon membranes at the nano-scale are extraordinarily thin – a single gram of them can have a surface area of nearly 2,000 square meters. That's part of what makes them useful in supercapacitors. And the new process used to do this is a single-step reaction that's fast and inexpensive. It starts with something about as simple as a cellulose filter paper – conceptually similar to the disposable paper filter in a coffee maker...

http://pubs.acs.org/doi/abs/10.1021/nl500859p
Pyrolysis of Cellulose under Ammonia Leads to Nitrogen-Doped Nanoporous Carbon Generated through Methane Formation,
Wei Luo, et al.
Nano Lett., 2014, 14 (4), pp 2225–2229
Abstract
Here, we present a simple one-step fabrication methodology for nitrogen-doped (N-doped) nanoporous carbon membranes via annealing cellulose filter paper under NH3. We found that nitrogen doping (up to 10.3 at %) occurs during cellulose pyrolysis under NH3 at as low as 550 °C. At 700 °C or above, N-doped carbon further reacts with NH3, resulting in a large surface area (up to 1973.3 m2/g). We discovered that the doped nitrogen, in fact, plays an important role in the reaction, leading to carbon gasification. CH4 was experimentally detected by mass spectrometry as a product in the reaction between N-doped carbon and NH3. When compared to conventional activated carbon (1533.6 m2/g), the N-doped nanoporous carbon (1326.5 m2/g) exhibits more than double the unit area capacitance (90 vs 41 mF/m2).

http://www.theverge.com/2014/5/28/5757952/tooth-regrowth-through-laser-therapy-is-possible-researchers-say
Lasers can help damaged teeth grow back, researchers say

http://opencircuitdesign.com/
Open Circuit Design -- bright ideas. . . no strings attached
The Open Circuit Design website is the repository for the suite of open-source EDA (Electronic Design Automation) tools including Magic, IRSIM, Netgen, PCB, and XCircuit. These tools are all provided for free under the GNU Public License (GPL) or similar open-source license.

Zhifeng REN : Mg-Ag-Sb Thermoelectrics
http://www.toolsforgreenliving.com/2014/05/high-efficiency-thermoelectric-material.html
Magnesium-Silver-Antimony Thermoelectrics

    "This new material is better than the traditional material, Bismuth telluride, and can be used for waste heat conversion into electricity much more efficiently," said Zhifeng Ren, M.D. Anderson Chair professor of physics at UH and the lead author of a paper describing the discovery, published online by Nano Energy.
    University of Houston physicists have discovered a new thermoelectric material offering high performance at temperatures ranging from room temperature up to 300 degrees Celsius, or about 573 degrees Fahrenheit.
    "This new material is better than the traditional material, Bismuth telluride, and can be used for waste heat conversion into electricity much more efficiently," said Zhifeng Ren, M.D. Anderson Chair professor of physics at UH and the lead author of a paper describing the discovery, published online by Nano Energy.
    Ren, who is also principal investigator at the Texas Center for Superconductivity at UH, said the work could be important for clean energy research and commercialization at temperatures of about 300 degrees Celsius.
    Bismuth telluride has been the standard thermoelectric material since the 1950s and is used primarily for cooling, although it can also be used at temperatures up to 250 C, or 482 F, for power generation, with limited efficiency.
    For this discovery, Ren and other members of his lab used a combination of magnesium, silver and antimony to generate electricity from heat using the thermoelectric principle. They added a small amount of nickel, after which Ren said the compound worked even better.
    The work was done in collaboration with researchers from the UH Department of Chemistry and the Massachusetts Institute of Technology. Huaizhou Zhao and Jiehe Sui, a member of Ren's lab whose home institute is the Harbin Institute of Technology in China, were primary contributors; Zhao is now a research scientist at the Institute of Physics with the Chinese Academy of Sciences.
    The material works well up to 300 C, Ren said; work to improve its efficiency is ongoing.
    The potential for capturing heat - from power plants, industrial smokestacks and even vehicle tailpipes - and converting it into electricity is huge, allowing heat that is currently wasted to be used to generate power. Ren said temperatures there can range from 200 C to 1,000 C, and until now, there hasn't been a thermoelectric material capable of working once conditions get beyond the lower levels of heat. Much of the demand ranges from 250 C to 300 C, he said.
    Ren long has worked in thermoelectrics, among other scientific fields. His research group published an article in the journal Science in 2008 establishing that the efficiency - the technical term is the "figure of merit" - of Bismuth telluride could be increased as much as 20 percent by changing how it is processed. At the time, Ren was at Boston College.
    And his lab last summer published a paper in the Proceedings of the National Academy of Sciences establishing tin telluride with the addition of the chemical element indium as a material capable of converting waste heat to electricity. But tin telluride works best at temperatures higher than about 300 C, or about 573 F, making it important to continue looking for another material that works at lower temperatures.
    Ren's group isn't the first to study the new material, which has not been named but is referred to in the Nano Energy paper as simply MgAgSb-based materials, using the chemical names for the elements used to create it. The paper cites work done in 2012 by M.J. Kirkham, et al; that work used magnesium, silver and antimony in equal parts, Ren said, but resulted in impurities and poor conducting properties.
    He said his lab found that using slightly less silver and antimony, and mixing the elements separately - putting magnesium and silver first in the ball milling process, adding the antimony after several hours - eliminated the impurities and significantly improved the thermoelectric properties.
    "We had much different qualities," he said. "Better, with no impurities, and smaller grain size, along with much better thermoelectric properties."

METHODS OF FABRICATING THERMOELECTRIC ELEMENTS     WO2014058988 // US2014102498
ELECTRODE MATERIALS AND CONFIGURATIONS FOR THERMOELECTRIC DEVICES WO2014011247 //   US2013247953
Thermoelectric Materials and Methods for Synthesis Thereof    US2013256609
Half-heusler alloys with enhanced figure of merit and methods of making   US2012326097 (A1) KR20140040072 (A) JP2014508395
US2013234375    Methods of Synthesizing Thermoelectric Materials
US2013175484    Half-Heusler Alloys with Enhanced Figure of Merit and Methods of Making
Thermoelectric system and method of operating same   US2012160290
WO2012138979 THERMOELECTRIC MATERIALS AND METHODS FOR SYNTHESIS THEREOF
SOLAR THERMOELECTRIC CONVERSION US8168879

    LIPOSOMAL VITAMIN C

    How to Make Liposomal Vitamin C At Home
    Have you ever wished you could get the many health benefits of high-dose intravenous (IV) vitamin C at home, at low cost? Discover a cheap and simple way to multiply the effectiveness of oral Vitamin C. One gram of this simple megavitamin C can do the work of up to 8 grams of pure vitamin C by intravenous injection! Wellness expert Arthur Doerksen shows you how to make it in your kitchen in less than 10 minutes. The iSonic P4810 ultrasonic unit is recommended. Check Amazon.
    Amount to Take: Start with one ounce a day, increase if needed.
    IMPORTANT UPDATE - Remember to soak the lecithin granules for 3 - 4 hours before blending with the Vitamin C. With liquid lecithin, use 50% less, no soaking required.

    ES2105973 --    Liposomal composition for cellular regeneration of the skin.
    Liposomal composition for cellular regeneration of the skin, consisting of a suspension of liposomes with a size of 75 to 300 mm which encapsulate each of the active principles glycolic acid, vitamin C and vitamin E. The composition comprises: Content of active principle Liposomal glycolic acid 5.0-30.0% 0.100-0.600% Liposomal vitamin C 5.0-30.0% 0.250-1.500% Liposomal vitamin E 0.0025-0.0100% Excipient made up to 100 ml

    http://www.anti-agingresearchcenter.org/bio-technology/liposomal-encapsulated-vitamin-c.html
    The Life, Health Implications of LET Vitamin C
    Cardiologist, Thomas Levy, MD JD, a frequent Vitamin C lecturer and the author of two books on the subject theorizes in his book, Curing the Incurable, that it is likely the human body was not intended to get all its ascorbate (Vitamin C) from dietary sources. He presents eight evidences for this theory:
    The need for ascorbate (Vitamin C) in the human body for basic maintenance of basic structure and function is essential and fluctuates greatly based on health status and environmental conditions.
    Even in IV doses exceeding 200 grams per day, no toxicity for ascorbate has ever been documented.
    Human livers have all the ingredients necessary to synthesize ascorbate except one — the enzyme L-Gulonolactone oxidase (GLO).
    Humans have the gene required to produce GLO but it is defective in the vast majority of the population.
    Some humans apparently synthesize ascorbate as not all individuals deprived of dietary ascorbate develop scurvy.
    Most mammals, reptiles, and amphibians do synthesize ascorbate. Some of the larger mammals produce upwards of 100 grams daily.
    Intravenous doses of ascorbate have shown powerful antioxidant, anti-toxin and anti-pathogenic properties in humans. (Dr. Levy cites many cases of this including Fred Klenner’s use of ascorbate to cure 60 out of 60 cases of polio in the late 1940s.)
    The uptake of ascorbate by the intestines is very inefficient.
    Since Liposomal Encapsulation Technology can deliver virtually 100% of a nutrient directly to the bloodstream, it promises to eliminate the huge loss of bioavailability when dose sizes of actively   transported nutrients are increased. This bio-availability chart was developed from a study done by J.L. Groff, S.S. Gropper, and S.M. Hunt which was published in the book Advanced Nutrition and Human Metabolism, West Publishing Co., 1995, pages 222-237.
Concerning the inefficiency of the body’s uptake of Vitamin C, studies show that the body has an increasing resistance to traditional forms of oral Vitamin C — tablets, powders, capsules — as dose size increases.
    J.L. Groff (1995 - see chart at left) demonstrated that less than 2 grams of a 12 gram oral dose of Vitamin C actually gets to the bloodstream. Based on that study, 2 grams of liposomal encapsulated Vitamin C has the bio-availability equal to 24-500 mg tablets of the nutrient.

http://nerdtrek.com/self-powered-laser-pistol-revolutionizes-warfare/
Victor I. Klimov - "Energy From The Vacuum" - Verification
Self-Powered Laser Pistol Revolutionizes Warfare
    "Five years ago, Dr. Victor Klimov at Los Alamos National Laboratory produced a permanent solution to the world’s energy crisis. This work is printed in leading physics journals of the world and was validated by two US National Labs: LANL and NREL. It is scientific fact so look it up before you disrespect in the comments below.
    Nanocrystalline power is what we’re talking about here folks. The solution to the world’s energy crisis lies in tiny nanoycrystalline solar cells which can absorb the light of a specific wave length in such a way that one photon input to a solar cell can energize more than one output electron. When the output electron absorbs a photon, it disappears for a short amount of time into the quantum field. Once in the virtual state, the electron can borrow energy from the vacuum and then appears in our reality. After this the highly excited electron (with all its excess energy taken freely from the active virtual state vacuum) can energize up to 7 output electrons.
    This leads to a theoretical coefficient of performance (COP) of up to 700%. A COP = 200% can be easily achieved and it has been, as have been higher values. The experiment has also been replicated successfully and validated by the National Renewable Energy Laboratory in Golden Colorado. [Herb Brody, "Solar Power - Seriously Souped Up." New Scientist, May 27, 2006, p 45].
    Note that at about COP = 3.0, one could conceivably add clamped positive feedback of one of those output electrons back to the “dive back into the seething virtual state vacuum” input, replacing the original electron input, and the unit would be “self-powering” (powered by energy from the vacuum) while putting out the other two electrons as output.
    Or by using some of the output current in a standard photon radiation-producing process, one could have the positive feedback input changed to a radiation photon, to replace the initial solar input entirely.
    In this fashion, once “jump started” by some source of solar radiation, the resulting “solar panel” system would become totally self-powering, taking all its input and output energy directly from the seething active virtual state vacuum itself.
    Indeed, if many of these tiny nano-crystals are packed together, their output furnishes their own input photons and thus the assemblage becomes “self-powering”. An assemblage about the size of your thumb is sufficient to power a large electric automobile.
    It appears that Klimov’s team and its work is being used presently to develop super-powerful but exceptionally small ultra laser weapons that will revolutionize modern warfare. E.g., a powerful, self-powered Klimov laser weapon the size of a bazooka and carried by one infantryman can in principle be developed that can destroy large buildings, destroy hostile tanks and vehicles easily, destroy ships and boats and trains, shoot down hostile aircraft, and — with a small sensor apparatus added — detect and shoot down incoming hostile field artillery rounds.
    Such a weapon is self-powering, and so it “never runs out of bullets”. No ammunition resupply is needed.
    It appears that the long-desired super-powerful laser pistol is also being developed for U.S. Internal Security civilian guard forces, also as an application of Klimov’s work. Such a pistol will be able to disable or even kill a targeted human or a group of them at a mile and a half. And it will be self-powering."

    KLIMOV's PATENTS
    Thick-shell nanocrystal quantum dots -- US7935419
    HYBRID PHOTOVOLTAICS BASED ON SEMICONDUCTOR NANOCRYSTALS AND AMORPHOUS SILICON -- US2010236614
    Mixed semiconductor nanocrystal compositions -- US7888855
    Nanocrystal structures -- US2009253224
    Single-exciton nanocrystal laser -- US2009116524
    CARRIER MULTIPLICATION IN QUANTUM-CONFINED SEMICONDUCTOR MATERIALS -- WO2006110919
    MULTIFUNCTIONAL NANOCRYSTALS-- WO2006060355
    NON-CONTACT PUMPING OF LIGHT EMITTERS VIA NON-RADIATIVE ENERGY TRANSFER -- WO2005117124
    COLLOIDAL QUANTUM DOT LIGHT EMITTING DIODES -- WO2005094271
    NANOCRYSTAL/SOL-GEL NANOCOMPOSITES -- WO2005047573
    NANOCRYSTAL/SOL-GEL NANOCOMPOSITES -- WO2005049711
    Semiconductor nanocrystal quantum dots and metallic nanocrystals as UV blockers and colorants for suncreens and/or sunless tanning compositions -- US2005265935
    Optical amplifiers and lasers -- US6819692
    Activation of molecular catalysts using semiconductor quantum dots -- US8029652
    Optical limiting materials -- US5741442
    Nanocrystal/photonic crystal composites -- US2007063208
    Femtosecond chirp-free transient absorption method and apparatus -- US6191861

    Nano-Iron Oxide Suture
http://onlinelibrary.wiley.com/enhanced/doi/10.1002/anie.201401043/
    Organ Repair, Hemostasis, and In Vivo Bonding of Medical Devices by Aqueous Solutions of Nanoparticles
Anne Meddahi-Pellé, et al
    Abstract
    Sutures are traumatic to soft connective tissues, such as liver or lungs. Polymer tissue adhesives require complex in vivo control of polymerization or cross-linking reactions and currently suffer from being toxic, weak, or inefficient within the wet conditions of the body. Herein, we demonstrate using Stöber silica or iron oxide nanoparticles that nanobridging, that is, adhesion by aqueous nanoparticle solutions, can be used in vivo in rats to achieve rapid and strong closure and healing of deep wounds in skin and liver. Nanoparticles were also used to fix polymer membranes to tissues even in the presence of blood flow, such as occurring after liver resection, yielding permanent hemostasis within a minute. Furthermore, medical devices and tissue engineering constructs were fixed to organs such as a beating heart. The simplicity, rapidity, and robustness of nanobridging bode well for clinical applications, surgery, and regenerative medicine.

    NANO-IRON OXIDE PATENTS
    Method for synthesizing supramolecular materials -- US8536281
    CN103531323    Preparation method for magnetic liquid without surfactants
    CN103288140 Method for simply regulating ferroferric oxide nanoparticle morphology
    USUS8445025 Hybrid Superparamagnetic Iron Oxide Nanoparticles and Polyethylenimine as a Magnetocomplex for Gene Transfection
    Preparation method of chitosan hydrogel containing magnetic nanoparticle   CN102766267
    CN102515283    Preparation method of magnetic iron oxide nanoparticle capable of stably dispersing in water
    KR101141716 LARGE-SCALE MANUFACTURING METHOD OF HIGH-SURFACE AREA IRON OXIDE NANOPARTICLES
    JP2012036489    METHOD FOR MANUFACTURING METAL NANOPARTICLE POWDER, AND METAL NANOPARTICLE POWDER
   IRON/IRON OXIDE NANOPARTICLE AND USE THEREOF US2011104073
    Method for manufacturing iron oxide nanorod    TWI344940
    Preparation method of iron oxide nanorod    CN102134102

    Carlo GIANSANTI : Copper Head Shield
    http://www.carlocopper.com/

Copper Mask
    When the lung receive this energy that we inhale through the copper mask they get reinforced and through the immune system starts clearing them of any bacteria:swine ,or bird flu,malaria, t,b, or any other type of bacteria*.As this energy reaches the capillaries of the lang and starts flowing though the vascular system,energies the veins leading to the heart ,so cleaning them of any cholesterol formation and at the same time reinforcing the muscles of the heart*,
    As it travels through the rest of the body, clears all the vascular system to the smallest capillaries,reinforces all the muscles of the organs of the body, liver, kidneys,prostate,etc.etc. and during this reconstructive process eliminates any type of cancer formation in our system.
    Anybody who has problem with the HIV infection will notice that their immune system will either suppress this symptoms or maybe eliminate the infection all together*.
    I tried to contact some 9/11 organizations related to the problem of breathing caused by the fall of the Twin Towers to the people involved in the rescued or simply staying or living in the area of the tragedy,but was not able to contact anybody, so I decided to write in this web page, and try to prove me wrong.
    In the last 8 years of research I have helped dozens of people with respiratory problems,to the most problematic and sever ashma problems and 100% of them had the problem eliminated, I tried it with people with sever paralesys and a few days improving in their movements, try it ,you will feel like a miracle.

http://www.youtube.com/watch?v=kkDAEa6AQck
Carlo Giansanti Copper Invention / American Inventor - Carlo Giansanti

US6266824 Head shield
    An electromagnetic shielding apparatus for covering and protecting the head of a user from EMF radiation which may be worn by itself or discretely beneath other head gear. A head covering is fabricated from a conductive, non-magnetizable material such as copper, bronze, brass or the like which may be drawn and shaped into a web or mesh material. The resulting shield is lightweight, air permeable and supple enough to be worn beneath other head gear.

Ieuan THOMAS -- Zero-Fuel / Cold Heat Engine
http://www.energyfromthevacuum.com/Disc19ColdHeatCanada/index19.html
http://www.energyfromthevacuum.com/Disc31ZeroFuelMotor/4DISCSILVERBUGCOLLECTION.html

In 1971, William Doyle Sr., Project Financier, asked Ieuan Thomas to hand write an explanation of his Fuelless Self-Powering Negative Electricity Generator Systems for the new Canadian Chief of Defense Staff in Ottawa, and to also write a “self-analysis” explaining Ieuan's commercial motivations and ambitions for the technology.//
According to Willian Doyle Jr., this final design of the Zero Fuel Engine System was basically an upgraded design modification and adaptation of Vicktor Schaubergers' Repulsine Vacuum Motor which had been brought to Toronto by Vicktor Schauberger, under Operation Paperclip Project Silverbug. This project was ongoing by Order of two U.S. Presidents (both Truman and Eisenhower) circa 1944-1961 in both the U.S. at Wright Patterson AFB in Ohio, in Texas, and in Canada at AVRO aka the A. V. Roe Aircraft Company, where the Lancaster Bombers were built during WWII.

http://www.alternative-energy-news.info/cutting-aviation-emissions-with-bottletop-technology/
    June 1st, 2009
    Cutting Aviation Emissions with ‘Bottletop Technolgy’

    Most of the time we ignore simple solutions dismissing them as too simplistic. But often we can achieve immeasurable amount of success with simple and practical solutions. We might think about the shape of wings and speed of airplanes but we don’t give much thought to an airplane’s wings in terms of reducing fuel and carbon emissions by making changes to those wings. But someone was looking at airplane’s wings and thinking of clean and green energy. If we make tiny holes in plane’s wing they can reduce airline fuel intake by up to 40 per cent. A team of British scientists are relying upon the same principle that applies when you blow across the top of a bottle to make a sound.

Don ESTES, et al. : Psiometrics
http://www.psiometrics.com/
P.E.A.K. ALEMBIC   ( PERMEATION OF ENERGES, ALLASSO AND KTISIS ENERGIES )

    An alembic is a distilling device that is used by alchemists to purify, separate and transform the elements. The P.E.A.K. Alembic ™ is a phase modulated, quadrature transform device that differs from a distiller in the following manner:

    1. A distiller uses an electrical circuit to heat water. The Alembic utilizes a proprietary Algorithm of Transformation™ and a perfected sound (Great Diesis Wave™) to cavitate water. In a distiller the water expands and boils. In the alembic it implodes.

    2. In the distiller, a positive and negative are shorted on a metal plate that heats up and boils the water. In the Alembic, two 24K gold waveguides are separated by the water, which must become the conduit of its own transformation by choosing to resolve the differential between the real and imaginary phases of the perfected universal white sound. A distiller operates with a positive and negative circuit. The Alembic utilizes two positives.

    3. In a distiller, the water molecules go over together as steam. In the Alembic, the molecules are disassembled, rearranged and reassembled into vapourized molecular bonds that hold the memory of the experience of transformation.

    4. Water from a distiller is dead water. Water from the Alembic is not only alive, but indeed ressurected with the resources required for transformation...acknowledging the need for change - active pursuit - releasing resistance - removing unwholesomeness - gathering dedicated support and taking the step to the next highest level.

    5. Distilled water is not totally pure. Water from the Alembic exceeds the capability of any known test to find impurities. Purity is the essence of holiness and, as such, the resultant distillate stands as a standard of reference for perfection, perserverance, faith, and growth...moving to the next highest level of order.

http://www.harmonicresolution.com/AlembicSanctuary%20LowRes.mov
http://www.harmonicresolution.com/PEAKAlembic2.mov

... Or Do, Do, Please !!!