rexresearch.com
Luigi CASSAR, et al.
Photocatalytic Cement
http://www.physorg.com/news67012896.html
May 16th, 2006
New
Kind
of Cement Absorbs Pollution
An Italian company has begun marketing a cement that
is capable of absorbing pollution from vehicles.
style="font-weight: bold; font-style: italic;" class="box-ads">
Italcementi, which spent 10 years developing its TX Active, said
the building material is capable of reducing urban pollution by
more than 40 percent, the Italian news agency ANSA reported
Tuesday.
Tests on a road near Milan showed TX Active cut the level of
nitrogen dioxide and carbon monoxide by as much as 65 percent.
It functions via a chemical process called photocatalysis, whereby
sunlight triggers a chemical reaction when titanium dioxide on the
surface of the cement comes into contact with pollutants in the
air. TX Active works most effectively in bright sunlight.
Italcementi said test results have been verified by independent
bodies like the National Research Council.
TX Active cement has already been used on a number of buildings,
including Air France's new headquarters at Paris' Charles de
Gaulle Airport, Rome's Dives in Misericordia church and Bordeaux's
Hotel de Police.
Euroscan -- Columnist ( November 8, 2006 )
A Concrete Step Toward Cleaner Air
by
Bruno
Giussani
Visitors to the Venice Biennale
can check out the smog-eating cement that Italian inventors
claim will help cities clean themselves
Venice hardly counts among the most-polluted places in the world.
There are no cars traveling its narrow streets, and all traffic is
either by foot or by boat. So despite the crowded walkways and
canals, the air in Venice is far cleaner than that of, say, Milan,
Italy's economic capital, which recent figures indicate has some
of the worst air quality in Europe.
Even so, visitors to the Italian Pavilion of the architecture
exhibition in the Venice Biennale, which will remain open until
Nov. 19, will get a breath of fresh air. That's because parts of
the concrete walls and grounds have been built with cement
containing an active agent that, in presence of light, breaks air
pollutants such as carbon monoxide, nitrogen oxide, benzene, and
others through a natural chemical process called photocatalysis.
The demonstration is a reminder that smart innovation applies also
to mundane products and can offer unexpected solutions even for
complex problems such as air pollution. The technology, called TX
Active, has been under development for almost 10 years in the labs
of Italcementi, the world's fifth-biggest cement producer, and is
starting to be applied commercially to buildings and streets in
Italy, France, Belgium, and elsewhere.
Painting the Town
The results so far are astonishing: A street in the town of
Segrate, near Milan, with an average traffic of 1,000 cars per
hour, has been repaved with the compound, "and we have measured a
reduction in nitric oxides of around 60%," says Italcementi's
spokesperson Alberto Ghisalberti. In a test over an 8,000 square
meter (or approximately 2 acres) industrial area paved with active
blocks near Bergamo, Italcementi's hometown, the reduction was
measured at 45%.
In large cities such as Milan, with persistent pollution problems
caused by car emissions, smoke from heating systems, and
industrial activities, both the company and outside experts
estimate that covering 15% of all visible urban surfaces (painting
the walls, repaving the roads) with products containing TX Active
could abate pollution by up to 50%, depending on the specific
atmospheric conditions.
Of course, this approach isn't meant to replace efforts to curb
pollution, but it can significantly magnify their effects. Here's
how it works: The active principle—basically a blend of titanium
dioxide that acts as photocatalyzer — can be incorporated in
cement, mortar, paints, and plaster.
The Big Bite
In the presence of natural or artificial light (this applies also
indoors) the photocatalyzer significantly speeds up the natural
oxidation processes that cause the decomposition of pollutants,
transforming them into less harmful compounds such as water,
nitrates, or carbon dioxide.
"These aren't necessarily 'clean', but from an environmental
standpoint they're much more tolerable," says Rossano Amadelli of
the Italian National Research Council (CNR), the scientists who
led the laboratory testing of the TX Active materials.
The patented pollution-reduction technology — which in Italy is
becoming known as "cemento mangiasmog" or "smog-eating cement" —
comes at a premium, of course, but the extra cost is limited by
the fact that the active principle only needs to be used on the
surface.
Keeping It Clean
"To transform the facade of a five-story building into a
photocatalytic surface would add only 100 or so euros ($120) to
the cost of a traditional paint or plaster," Ghisalberti
estimates. Paving a street or a sidewalk is a different story, but
still not extreme: Photocatalytic blocks cost about one-third more
than usual paving, which is still far less than the long-term cost
of doing nothing about air pollution.
It turns out that the photocatalyzing cement has another
advantage, one that has great appeal to star architects such as
Richard Meier. TX Active not only hastens the decomposition of
organic and inorganic pollutants, it also prevents their build-up
on surfaces, helping to preserve a building's pristine appearance
over time.
The spectacular design of Meier's Dives in Misericordia Church in
Rome, includes three concrete self-bearing white sails, topping
out at 26 meters. One of Meier's material requirements was that
the whiteness of the sails be durable. That has been achieved
through the application of the active principle, which basically
"self-cleans" the surfaces.
The same system has been applied to the new Air France
headquarters inside the Charles de Gaulle airport in Paris, a
place with high concentrations of hydrocarbons and where, needless
to say, a standard white facade would not remain white for long.
Giussani is a Swiss writer, tech entrepreneur, conference host,
and the author of Roam: Making Sense of the Wireless Internet. He
blogs at www.LunchOverIP.com.
TX Active® : Presentation of the
first active solution to the problem of pollution
“The commitment to sustainable
development, which is a feature of the operations of the
Italcementi Group, does not end with our industrial management
policies. This duty, together with the progress linked to the
development of our ‘Innovation Project’, has led us to open up
a new horizon for Italcementi. Alongside the production of
cement which is of increasingly high performance from a
structural viewpoint, we are entering a new sector: that of
special cement products aimed at providing a genuine
industrialized solution to the problem of pollution in
cities”.
Carlo Pesenti,
Italcementi Group CEO, presented the launch of the industrial
scale production and marketing of photocatalytic products
manufactured with the TX Active principle, the fruits of the
Italcementi Group research laboratory. It is an important,
proactive industrial solution which will make a significant
impact in the fight against smog.
“We have backed research and innovation since, for a group
such as ours, it ensures our development and the ability to be
competitive on a global scale; in addition, it is often
stressed that innovation is essential for the country’s
development, and today I am delighted to underline the fact
that this outcome is the result of Italian research.
Moreover,” Pesenti added, “we believe that the
mission of a major industrial group also includes meeting the
need to improve the quality of life for all of us. With this
product we feel we can provide a proactive solution for at
least one of those problems which are seen everyday in the air
quality of our cities. Thus we offer the public sector and
other principals the possibility of opting for structured,
long-lasting and targeted solutions as part of their programs
to fight pollution”.
In a large city such as Milan, researchers have calculated – on
the basis of test results – that covering 15% of visible urban
surfaces with products containing TX Active® would enable a
reduction in pollution of approximately 50%.
TX Active is
a photocatalytic principle for cement products which can reduce
organic and inorganic pollutants that are present in the air.
Its effectiveness has been thoroughly tested and thus certified
by important independent research centers (CNR, ARPA,
IspraResearchCenter). Its formulation is the result of 10 years
of research, tests and applications carried out by CTG (Centro
Tecnico di Gruppo, a company in the Italcementi Group)
which has led to the final formulation of the active principle.
Italcementi will make this material available to the whole
construction sector which will thus be able to offer products
with high quality standards under the “TX Active®” brand.
US6824826
Use of photocatalytic
preparations of colloidal titanium dioxide for preserving
the original appearance of cementitious, stone, or marble
products
Inventor: Luigi CASSAR, et
al.
Applicant: ITALCEMENTI SPA [IT]
Abstract -- Use of
photocatalytic preparations of colloidal titanium dioxide
optionally doped with a metal chosen from groups I-VA, and the
lanthanide and actinide series of the periodic table, for
preserving the original appearance of cementitious, stone, and
marble products.
Current U.S. Class: 427/258 ; 106/286.1;
106/286.4; 106/286.5; 106/286.8; 106/287.18; 106/287.19; 427/256;
427/269; 427/279; 427/283; 427/287; 427/294; 427/350; 427/372.2
Current International Class: C04B 41/65
(20060101); C04B 41/60 (20060101); C04B 41/45 (20060101); C01G
23/047 (20060101); C01G 23/053 (20060101); C01G 23/00 (20060101);
C04B 41/50 (20060101); B05D 001/36 ()
FIELD OF THE INVENTION
The present invention refers to the use of colloidal
photocatalytic preparations of titanium, dioxide (TiO.sub.2) for
maintaining the original appearance of cementitious, stone, or
marble products.
PRIOR ART
The conservation of architectural assets depends to a considerable
extent on the environment in which they are located. The problem
of the preservation of such assets assumes important dimensions if
it is considered that the action of atmospheric agents has become
increasingly aggressive over time.
The conservation of architectural structures, buildings and
artefacts subject to outdoor exposure has to do with forces that
act in an important way on the surface is of the constructions or
in the layers immediately below the surface and that regard the
depositing of organic and inorganic materials which usually adhere
to the aforesaid organic substrate, and the action of acid rain.
One of the main problems of architectural cementitious, stone, or
marble products therefore regards the constant maintenance over
time of their original appearance, which is undermined by the
natural process of ageing due to the influence of atmospheric
agents.
The need is therefore particularly felt for economical systems of
intervention which enable conservation of the aesthetic
characteristics of the surface of constructions made of
cementitious, stone, or marble material.
With the aim of protecting such artefacts, various techniques are
resorted to, the most common of which consist in applying
water-repellent products, such as silicone solutions that are
stable in alkaline environments and are stable to light and
weather. Unfortunately, the progressive increase in the pollutants
present in a typical metropolitan environment, perhaps also on
account of their frequently acidic nature, has markedly limited
the duration of this type of protection, with consequent aesthetic
degradation of the artefact.
In order to overcome this new problem, various solutions have been
proposed. For example, the patent IT 1286492 (in the name of the
present applicant) illustrates a hydraulic binder for cementitious
compositions which comprises in its mass a titanium-dioxide based
photocatalyst that is able to oxidize, and hence neutralize, the
polluting substances present in the environment. This type of
solution is certainly valid as regards the protection of the
surface of the artefact from any possible deterioration caused,
for example, by wind abrasion, but clearly it implies the use of
enormous amounts of photocatalyst as compared to those actually
needed. In fact, the photocatalyst is present not only on the
surface of the artefact or in the immediately underlying layers,
i.e., in the areas where its presence proves useful, but in the
entire cementitious mass, which, for the most part, will never
come into contact with external agents.
Alternative solutions have also been proposed (see, for example,
the European patent, application No. EP 0 885 857 in the name of
the present applicant) which regard cementitious levelling
plasters containing various polymeric additives and photocatalysts
that are able to oxidize the polluting substances present in the
environment, but these cementitious-based formulations are white,
and cannot be used, for instance, on marble or stone materials
without consequently modifying their aesthetic characteristics.
The use of anatase, which is one of the tetragonal crystalline
forms of titanium dioxide, as photocatalyst for the oxidation of
organic pollutants has been known for some time, also in the form
of colloidal preparations.
The patent EP 784034 (in the name of Matsushita Electric Works)
describes substrates obtained by depositing titanium dioxide on
the surface of a substrate by deposition of a solution containing
ammonium titanium fluoride, followed by calcining. The patent EP
614682 (in the name of Fuji Electric) illustrates a titanium-based
or titanium/activated carbon-based photocatalyst fixed on a
fluororesin to obtain sheets or panels to be applied externally on
buildings for removing low concentrations of NO.sub.x.
The incorporation of metal ions (doping agents) in these
preparations alters the photocatalytic activity of titanium
dioxide to a substantial extent. The most important parameters are
the type of ion, the concentration of the dopants, and the thermal
treatment useful for the formation of the photocatalyst.
Brezova V. et al., J. Photochem. Photobiol. A: Chem., 109, (1997),
177-183, analyze the influence of various metal ions and their
concentrations in a particular application of titanium dioxide as
photocatalyst, namely, in the oxidation of phenol. In particular,
preparations of colloidal titanium dioxide are described, in which
the titanium dioxide is doped with various metals at 5% atom/atom,
following a procedure whereby colloidal titanium dioxide is first
prepared, and next the salt of the doping metal is mixed under
heating. Among the various metal ions tested, cerium is reported
to reduce the photocatalytic activity of the colloidal titanium
dioxide. In the publication, as in other previous publications on
this subject, no mention is made of the use of the said
photocatalytic products on cementitious materials.
The patent EP 633964 (in the name of Fujisawa, Hashimoto, and
Ishihara Sangyo Kaisha) describes a TiO.sub.2 based photocatalyst
preferably doped with V, Fe, Cu. Co, Ni, Zn, Ru, Rh, Pd. Ag, Pt,
or Au, and fixed on a fluorinated polymer for adhesion to the
substrate. This photocatalyst is useful for purifying air, but
also water, from various undesired substances.
SUMMARY OF THE INVENTION
It has' now been surprisingly found that colourless colloidal
preparations of titanium dioxide, or of one of its precursors,
possibly doped with elements chosen from groups I-VA, and the
lanthanide and actinide series of the periodic table, or mixtures
thereof, preferably magnesium, cerium, niobium or lanthanium, wh n
applied on the surface of cementitious, stone, or marble products,
are able to preserve the original appearance of the surface,
without altering the characteristics of the cementitious, stone,
or marble material.
The solution devised thus regards a system for treating
cementitious, stone, or marble surfaces by using titanium
dioxide-based colourless colloidal suspensions, the titanium
dioxide being possibly doped with elements chosen from groups
I-VA, and the lanthanide and actinide series of the periodic
table.
DETAILED DESCRIPTION OF THE
INVENTION
The present invention refers to the use of colourless colloidal
preparations of titanium dioxide or one of its precursors, for the
conservation of the original appearance of cementitious, stone,
and marble products, by means of application of said preparations
on the given surface.
The colloidal preparations of titanium dioxide or one of its
precursors useful for the purposes of the present invention may
contain a metal ion chosen from groups I-VA, and the lanthanide or
actinide series of the periodic table, and preferably comprising
lithium, beryllium, magnesium, scandium, yttrium, lanthanium,
cerium, niobium, vanadium, zirconium, and mixtures thereof. More
preferably, the colloidal preparations of titanium dioxide or one
of its precursors according to the present invention are doped
with ions selected from the group consisting of magnesium, cerium,
niobium, and lanthanium.
The amount of doping agent, i.e., of metal ion present in the
preparations useful for the purposes of the present invention,
ranges from 0.1 to 5% (percentage expressed as metal-ion atoms
with respect to the atoms of titanium), preferably from 0.1 to 1%.
Preferably, the titanium dioxide present in the preparations
according to the invention is prevalently in the form of anatase;
i.e., the particles of photocatalyst have an anatase structure at
least for 75%.
As precursor of titanium dioxide useful for the purposes of the
present invention is meant any product that is able to produce
titanium dioxide prevalently in the form of anatase, possibly with
appropriate types of thermal treatment. For example, TiCl.sub.4,
TiOSO.sub.4, titanium alkoxide (for instance, titanium
isopropoxide) can be effectively used as precursors for the
purposes of the present invention.
By polluting substances that are oxidized by the photocatalysts of
the present invention are meant the organic substances that may be
present in the environment as a result of motor-vehicle exhaust or
industrial emissions, such as benzene, aromatic volatile
compounds, pesticides, phenols, and benzofluorides, without
excluding inorganic compounds, such as nitrogen oxides (NO.sub.x)
which can be oxidized to yield nitrates.
By cementitious artefact is meant any product in the hardened
state deriving from a cementitious composition or cementitious
mixture, by cementitious composition or cementitious mixture being
meant any composition in which the binder is mixed with water and
possibly with aggregates of various grain size. The cementitious
compositions thus include both cementitious pastes, i.e., pastes
consisting of binder and water (devoid of aggregates), and
conglomerates, i.e., mixtures of water, cement and aggregates.
The aggregates or inert substances may be coarse aggregates, such
as crushed stones or gravel, or fine aggregates, such as sand, and
are classified according to UNI 8520 Standards. Examples of
conglomerates are mortars (mixtures of binder, water, and fine
aggregate) and concretes (mixtures of water, binder, fine
aggregate, and coarse aggregate). Among the cementitious products
preferred according to the present invention are cited the
so-called "architectural concretes", i.e., in situ castings with
non-treated surfaces (plane or shaped) or treated surfaces (for
example, sanded).
By marble or stone products are meant the marbles proper, i.e.
crystallized metamorphic limestones, "calcetiri", cipollinos,
limestone, dolomites, polishable limestone breccias, onyx marbles,
serpentines, and ophicalcites; granites proper, i.e., intrusive
magmatic rocks consisting of quartz, sodium and potassium
feldspars, and micas, other intrusive magmatic rocks (diorites,
gabbros, etc.), and the corresponding porphyritic-structured
effusive magmatic rocks, metamorphic rocks, such as "gnelsa" and
"serizi"; travertine and the so-called commercial stone, such as
sandstone, tuff, quartzites, mica schists, slates, basalts, etc.
Titanium dioxide in colloidal form is prepared using sol-gel
techniques so as to have particles of a size of between 10 and 200
.ANG., preferably between 50 and 100 .ANG..
In contrast with what is reported in the prior art, hydrolysis of
the titanium dioxide takes: place directly in the presence of the
salt of the doping element by co-precipitation or mixing. In fact
the preparation of two distinct colloidal suspensions, one
containing the titanium dioxide and the other the salt of the
doping metal, which are subsequently mixed together, is described
in the prior art.
The colloidal suspension is then treated so as to obtain a
colloidal film over the material that is to be preserved, a
necessary step for assessing the photocatalytic action of titanium
dioxide in the presence of the various types of pollutants.
In particular, the colloid in aqueous suspension may be sprayed or
applied using a brush directly on the product in small successive
amounts until the desired thickness is reached.
UV and visible-light measurements using diffused-reflectance
spectroscopy reveal the minimum quantity suitable for guaranteeing
maximum light absorption by the TiO.sub.2.
As an alternative, the colloidal suspension can be vacuum-dried in
order to obtain a titanium-dioxide powder which can be preserved
for an unlimited period and re-suspended in water, maintaining its
colloidal properties.
When applied on the surface of cementitious, stone, or marble
products, the colloidal preparations according to the present
invention effectively protect the product from alterations due to
organic pollutants, and in general from atmospheric agents, by
causing their photo-oxidation.
Generally, when inorganic pollutants do not find an organic
substrate to adhere to, they encounter greater difficulties in
depositing on the surface of the product
As compared to the methods of the prior art, the application of
the preparations in question guarantees a form of protection of
the above-mentioned products that is long-lasting by using amounts
of material, namely titanium dioxide or one of its precursors,
that are considerably smaller than those required by the methods
described previously.
In particular, the effectiveness of the titanium dioxide according
to the present invention, possibly doped with metal ions belonging
to groups I-VA, and the lanthanide or actinide series of the
periodic table, as compared to the use of other formulations of
titanium dioxide, considerably accelerates photo-oxidation of
polluting agents, as illustrated in the assays described later
(Examples 9, 10 and 11).
Particularly surprising is the fact that the colloidal titanium
dioxide prepared according to the present invention reveals
excellent adhesion to the cementitious, marble or stone material
to be protected.
This was verified by subjecting specimens of cementitious and
marble material treated with the titanium-dioxide colloidal
suspension to leaching in water under stirring (Examples 7 and 8).
It is to be noted that the colloid according to the present
invention finds in cementitious, marble or stone materials an
optimal substrate for the photocatalytic action envisaged, whilst
for other materials, such as glass, adhesion of the colloid is
possible only via a type or thermal treatment which is
particularly burdensome, at approximately 5 000.degree. C., in the
presence of an organic crosslinking agent.
The activity of the colloidal preparation has moreover proved
effective after various cycles of fouling with coloured organic
substrates and subsequent cleaning of the specimens treated, thus
demonstrating the effect of the photocatalyst over time. Examples
of implementation of the present invention will now be described.
In these examples, the percentage of dopant is to be understood
calculated as metal-ion atoms with respect to the titanium atoms.
EXAMPLE 1
Preparation of Colloidal Titanium
Dioxide
The preparation in question is based on the controlled hydrolysis
of the titanium-dioxide precursor. The typical preparation
involves the addition of titanium isopropoxide to a solution 0.1 M
of HNO.sub.3 to obtain 0.565 mol. of titanium dioxide per liter.
In particular, in a 1-liter beaker containing water (750 ml) and
HNO.sub.3 at a 65% concentration (5.2 ml), titanium isopropoxide
(125 ml) was added slowly under vigorous stirring. The resulting
solution was heated up to 80.degree. C. for 8-12 hours,
maintaining vigorous stirring. In this way, the isopropanol that
had formed was evaporated. The volume of the reaction mixture was
kept at 200 ml by adding water.
EXAMPLE 2
Preparation of Colloidal Titanium
Dioxide Doped With Cerium
Using cerium (Ill) nitrate hexahydrate (0.0277 g) to be dissolved
in the hydrolysis water (150 ml), and titanium isopropoxide (25
ml), and following the procedure described in Example 1, the
product in question, containing 0.1% Ce.sup.3+, was obtained.
EXAMPLE 3
Preparation of Colloidal Titanium
Dioxide Doped With Niobium
Using niobium (V) pentachloride (0.0223 g) to be dissolved in
acetone (10 ml), and titanium isopropoxide (25 ml), and following
the procedure described in Example 1, the product in question,
containing 0.1% Nb.sup.5+, was obtained.
EXAMPLE 4
Preparation of Colloidal Titanium
Dioxide Doped With Magnesium
Using magnesium (II) chloride hexahydrate (0.0213 g) to be
dissolved in the hydrolysis water (150 ml), and titanium
isopropoxide (25 ml), and following the procedure described in
Example 1, the product in question, containing 0.1% Mg.sup.2+, was
obtained.
EXAMPLE 5
Preparation of Colloidal Titanium
Dioxide Doped With Lanthanium
Using lanthanium (III) nitrate hexahydrate (0.037 g) to be
dissolved in the hydrolysis water (150 ml), and titanium
isopropoxide (25 ml), and following the procedure described in
Example 1, the product in question, containing 0.1% La.sup.3+, was
obtained.
EXAMPLE 6
Preparation of Colloidal Films on
Glass Substrates
The colloid (10 ml) prepared as described in Examples 1-5 was put
in a hermetically sealed glass container so as to hinder complete
evaporation of the water and at the same time favour the regular
growth of the particles from an average size of 50 .ANG. to a
maximum size of 100/200 .ANG., and was then heated up to
200-220.degree. C. overnight. The precipitated colloid was
re-suspended by mechanical stirring and vacuum heat-concentrated
until a concentration of 150 g/l was obtained. Next, Carbowax 2000
(300 mg) was added, and the dispersion underwent stirring for 8
hours until total dissolution of the Carbowax was achieved and a
homogeneous suspension was obtained.
The resulting product was spread on glass substrates and set to
dry in a muffle oven at 500.degree. C. for 30 minutes. The film
was characterized by means of diffused-reflectance spectroscopy.
Without the use of the Carbowax crosslinking agent it is
impossible to get the colloid to adhere to a glass substrate.
EXAMPLE 7
Preparation of Colloidal Films on
Cementitious-Mortar Substrates
The colloid (10 ml) prepared as described in Examples 1-5 was put
in a hermetically sealed glass container so as to hinder complete
evaporation of the water and at the same time favour the regular
growth of the particles from an average size of 50 .ANG. to a
maximum size of 100/200 .ANG., and was then heated up to
200-220.degree. C. overnight.
Specimens of cementitious mortar (disks sized 25.times.8.times.2.5
cm) were prepared using white cement Italbianco Italcementi 52.5
R.
After the preparation, the specimens were cured for 1 day in
moulds in an environment at 20.degree. C. and relative humidity
(RH)>90%. After ejection, the specimens were kept for a further
7 days at 20.degree. C. and RH.apprxeq.160%.
The aqueous suspension was brush-applied on the said specimens of
cementitious mortar.
The colloid was brush-applied in small successive amounts until
the typical spectrum observed in diffused-reflectance spectroscopy
was obtained. Leaching tests ware carried out in water for 48
hours, under stirring, and these tests confirmed the adhesion of
the colloid. Each test specimen was then observed in
diffracted-reflectance spectroscopy. In all, the equivalent in
weight of approximately 1 g/m.sup.2 was applied on each test
specimen.
EXAMPLE 8
Preparation of Colloidal Films on
Marble Substrates
The colloid (10 ml) prepared as described in Examples 1-5 was put
in a hermetically sealed glass container so as to hinder complete
evaporation of the water and at the same time favour the regular
growth of the particles from an average size of 50 .ANG. to a
maximum size of 100/200 .ANG., and was then heated up to
200-220.degree. C. overnight.
The colloidal suspension was vacuum-dried so as to obtain a
titanium-dioxide powder, which was re-suspended in water (45 g/l)
and brush-applied on a specimen of white Carrara marble
(dimensions, 3.times.3.times.3 cm). Leaching tests were carried
out in water for 48 hours, under stirring, and these tests
confirmed the adhesion of the colloid. Each test specimen was then
observed in diffracted-reflectance spectroscopy. An amount of
titanium dioxide corresponding in weight to approximately 1
g/m.sup.2 was evaluated.
EXAMPLE 9
Degradation of 4-Chlorophenol
4-chlorophenol 10 mM (3 ml) was put in an irradiation cell, in
which each time were suspended the specimens prepared according to
Example 7 with the colloids prepared according to Examples 14 and
containing the catalysts according to the invention, and, as a
standard specimen for comparison, a specimen prepared in a similar
way using Degussa titanium dioxide, which, to the knowledge of the
present applicant, is the most active photo-oxidation catalyst
present on the market. The cell was closed under oxygen, and the
degradation of the 4-chlorophenol was monitored by
spectrophotometry, measuring the degradation times (in hours). The
results are given in FIG. 1 below.
FIG. 1
Coll. TiO.sub.2 +Mg
Coll. TiO.sub.2 +Nb
Coll. TiO.sub.2 +Ce
Coll. TiO.sub.2 Degussa TiO.sub.2
Degradation time (hours)
As may be seen in FIG. 1, the specimens containing the dopant ions
yield a time of degradation of the pollutant lower both with
respect to the test specimen containing colloidal titanium dioxide
and with respect to the standard specimen containing Degussa
titanium dioxide.
EXAMPLE 10
Degradation of Naphthionic Acid
Following basically the procedure described in Example 9, but
performing the decomposition of naphthionic add 0.026 mM (3 ml) in
water, an evaluation was made of the behaviour of the specimen
prepared according to Example 7, using the titanium-dioxide
colloid doped with lanthanium according to classic methods and
prepared as described in Example 5. For comparison, two
non-colloidal standard specimens of Degussa titanium dioxide were
evaluated, one as such, and the other doped with lanthanium
according to classic methods. The results are given in FIG. 2
below.
FIG. 2
Coll. TiO.sub.2 +La
Coll. TiO.sub.2 Degussa TiO.sub.2 +La 1% Degussa TiO.sub.2
Degradation time (minutes)
As may be seen in FIG. 2, the degradation time for the colloidal
titanium dioxide is lower than for the Degussa titanium dioxide,
both in the case of the specimen containing the dopant ion and in
the case of the specimen not containing the dopant ion.
EXAMPLE 11
Degradation of
3-4-Dihydroxycinnamic Acid
Following basically the procedure described in Example 9, and
using 34 dihydroxycinnamic acid 0.26 mM (3 ml) in water, the
following were evaluated: a) behaviour of the specimen prepared
according to Example 7, using the titanium-dioxide colloid doped
with niobium prepared as described in Example 3; b) behaviour of
the specimen prepared according to Example 7, using the
titanium-dioxide colloid doped with magnesium prepared as
described in Example 4; and c) behaviour of the specimen of
colloidal titanium dioxide prepared according to Example 8 on a
marble test specimen.
For comparison, a standard specimen of Degussa non-colloidal
titanium dioxide was evaluated. The results are illustrated in
FIG. 3.
FIG. 3
Coll. TiO.sub.2 +Mg
Coll. TiO.sub.2 +Nb Coll. TiO.sub.2 on marble
Coll. TiO.sub.2 on mortar Degussa TiO.sub.2
Decolorizing time (minutes)
As may be seen in FIG. 3, the decolorizing times (oxidation of the
pollutant) of the photocatalysts according to the present
invention are in all cases shorter than for the Degussa titanium
dioxide in the non-colloidal form.
EXAMPLE 12
Degradation of Alcoholic Extract
of Tobacco
Following basically the procedure described in Example 9, and
using alcoholic extract of tobacco on cement matrices, the
following were evaluated: a) behaviour of the specimen prepared
according to Example 7, using the titanium-dioxide colloid
described in Example 1; b) behaviour of the specimen prepared
according to Example 7, using the titanium-dioxide colloid doped
with cerium prepared as described in Example 2; and c) behaviour
of the specimen prepared according to Example 7, using the
titanium-dioxide colloid doped with magnesium as described in
Example 4.
The alcoholic extract of tobacco was added in an amount such as to
produce a drop in transmittance from 75 to 40, read at 450 nm.
For comparison, Degussa titanium dioxide standard specimens, one
at 10% and one at 0.1%, were evaluated. The results are
illustrated in FIG. 4.
FIG. 4
Coll. TiO.sub.2 +Mg
Coll. TiO.sub.2 +Ce
Coll. TiO.sub.2 +Nb
Coll. TiO.sub.2 Degussa TiO.sub.2, 10% Degussa TiO.sub.2, 0.1%
Degradation time (hours)
As may be seen in FIG. 4, the times of degradation of the
pollutant for the photocatalysts according to the present
invention are in all cases shorter than for the Degussa titanium
dioxide in the non-colloidal form.