rexresearch
Charles
F. ECKART, et al.
Mulch Paper
http://blog.modernmechanix.com/papering-the-world-to-make-crops-grow/2/#mmGal
Papering the World to Make Crops Grow
STRIPS of paper, three feet wide and less than one thirty-second
of an inch in thickness, have increased the production of
pineapples in the Hawaiian Islands by more than forty per cent.
Laid in a field of sun-grown Sumatra tobacco, in Florida, the
same kind of paper increased production more than fifty per
cent. Papering fields of tomatoes in California raised their
yield by some sixty per cent, while strawberries, their roots so
protected, produced forty per cent more berries than the same
varieties planted in a neighboring and un-papered field.
For fifteen months or more, prior to 1923, experiments in the
papering of pineapple fields in Hawaii were carried on with
uniformly the same results. This year, more than 4,250 miles of
paper were laid, at a cost of approximately $250,000, on the
pineapple plantations of Hawaii. The result is an increase of
from twenty-five to sixty per cent in the production of the
pineapple plants, an average of at least forty per cent; the
elimination of weeding, which costs on the average $45 per acre;
the conservation of moisture; the prevention of baking of the
soil, and the removal of the necessity for cultivation
throughout the crop life of the pineapple, which is about five
years.
The device is the discovery of C. F. Eckart, the Burbank of the
Hawaiian Islands. It consists of the laying of a mulch paper,
made of asphalt-treated felt, not dissimilar to a thin roofing
paper, in rows across the field. In this paper, six inches from
each edge, and, therefore, twenty-four inches apart in the
center, holes are punched with a trowel, and the pineapple
cuttings, “ratoons,” are set in these holes. As the paper is
laid, the earth is turned up over, the edges, to hold it flat
and to prevent it from blowing away. The plants are set
“staggering” in adjacent lines, so that while the rows along the
paper are even, those across the field are not.
The same method used in the planting -of the pineapples is
adopted in the setting out of tobacco, tomato, cabbage or other
plants. Experiments are now being conducted on the use of the
paper with grapes, and with flowering plants, in short, with all
crops which have a high value per acre. It also has been applied
with success to sugar cane in the Hawaiian Islands. Not only
does it increase the amount of production of each plant, but it
increases the size of the fruits or vegetables or the number and
size of the leaves.
The paper virtually puts every plant root into a forcing
hothouse. The roots are kept shaded, heat is retained as is also
moisture, the combination necessary to the greatest root and
plant growth, and weeds, being unable to pierce the paper
covering, cannot grow. The use of the paper, by this combination
of retained heat and moisture, has extended the area in which
pineapples can be produced profitably to higher altitudes and
colder temperatures in the Hawaiian Islands than ever before. In
Florida, the increase in individual fields of sun-grown tobacco
has reached as high as seventy-one per cent, but this is above
the average. In the culture of tomatoes, the increase in yield
ranged from twenty-one per cent to 168 per cent, under widely
varying conditions.
Surface evaporation from the area covered with the paper is so
greatly reduced that it is virtually negligible, the moisture
being conserved entirely for the use of the plant. This
reduction of surface evaporation to a minimum eliminates the
undesirable and often disastrous caking and cracking of the
soil. Heat loss by evaporation of surface moisture also is
prevented, producing and maintaining additional warmth in the
soil. The paper receives the direct impact of the raindrops and
so prevents the soil from packing. Some of the papers used are
perforated with many small holes, so as to allow moisture from
rain, dew, and fogs to seep slowly through, increasing the
moisture so stored in the soil beneath the paper.
The paper is applied by hand, with men carrying the rolls on
steel rods, and other men following behind with hoes to cover
the edges with a binder of earth; by machine layers, drawn by
horses, with special devices for the turning in of the binder of
earth ; and, on level fields, by double machines, laying two
rows at a time, drawn by a tractor. These machines also lay
their own earth binder.
CA215027
Method of Enhancing the Growth of Plants

http://aenews.wsu.edu/Oct03AENews/Oct03AENews.htm
Searching for Alternatives to Plastic Mulch
Dr.
Carol Miles, Lydia Garth, Madhu Sonde, and Martin Nicholson,
WSU Vancouver Research and Extension Unit
[
PDF ]
Conclusions
The purpose of this study was to determine if there are suitable
alternatives to plastic mulch with respect to weed control and
crop production in the Pacific Northwest. In this study we found
that there were no differences in the quality or durability of
the alternative mulch treatments or in the quality and yield of
the vegetable crop. The oil had no effect on the longevity or
qualities of the paper mulch. The paper mulches proved as high
in quality as the plastic mulch and Garden Bio-Film. In adjacent
observation plots, paper was laid in the field and then oils
were applied. There was no difference in quality of the mulch
whether oil was applied before or after laying the mulch in the
field. In an additional adjacent observation plot, paper with no
oil was laid in the field and overhead irrigation was applied
throughout the summer. There was no difference in the quality of
the mulch whether irrigation was applied through drip or
overhead irrigation.
In 2004 we intend to continue investigating alternatives to
plastic mulch. We will test different weights of paper and again
test Garden Bio-Film mulch. We will also evaluate the response
of several types of vegetable crops (warmer temperature vs.
cooler temperature) to the different mulches.
Dr. Carol Miles and her co-authors Lydia Garth, Madhu Sonde, and
Martin Nicholson conducted their mulch alternatives study at the
WSU Vancouver Research and Extension Unit,
http://agsyst.wsu.edu. Miles, Sonde, and Nicholson can be
reached at (360) 576-6030 or via Miles' email address:
milesc@wsu.edu. Lydia Garth is a senior at Columbia River High
School in Vancouver. She participated in this study as part of
her senior science project.
SOURCES OF
MULCH
Paper
Newark Paperboard Products
620 11th Ave, Longview, WA 98632
(360) 423- 3420
Attn: Jim McDaniel, General Manager
Garden Bio-Film
Biogroup USA, Inc.
107 Regents PI. Ponte Vedra Beach, FL 32802
(904) 280-5094; Fax: (904) 543-8113; http://www.biogroupusa.com
http://www.ars.usda.gov/is/pr/2001/010312.htm
Paper
Mulch Coated with Vegetable Oil Offers Biodegradable
Alternative to Plastic
by Linda
McGraw
[ PDF ]

March 12, 2001
Paper is gaining over plastic in mulches used to grow commercial
fruits and vegetables as well as the home-grown varieties,
according to Agricultural Research Service (ARS) studies in
Peoria, Ill. A main reason for this trend is that
vegetable-oil-coated paper mulch may be a less costly
alternative to plastic mulches, which are expensive to remove.
Brown paper coated with vegetable oils like soybean and linseed
oil can protect the crop from weeds and insects and is
completely biodegradable, according to ARS chemist Randal L.
Shogren at the National Center for Agricultural Utilization
Research (NCAUR) in Peoria, Ill. That gives paper a big
advantage over plastic mulches that cost about $240 an acre. Soy
oil costs around 15 cents a pound, so growers and home gardeners
can expect a reasonable cost for paper mulches made with
vegetable oil.
Shogren coated plain brown kraft paper--used to make grocery
store bags--with several types of vegetable oils, including
soybean, linseed and a chemically-modified soybean oil plus a
catalyst. The vegetable-oil-coated paper withstood wind and rain
long enough for the crop to grow, but then began degrading in
the soil.
In trials, Shogren found that kraft paper treated with a
combination of epoxidized soybean oil and citric acid held up
for 13 weeks compared to untreated kraft paper, which was 50
percent degraded in 2-1/2 weeks. A U.S. patent on the technology
has been approved. Field trials in Live Oak, Fla., in
cooperation with the University of Florida (Gainesville) are in
progress. Currently, field trials are being planned with an
industry partner.
Shogren presented information on the paper mulches at the 6th
International Conference on Frontiers of Polymers and Advanced
Materials in Recife, Brazil, March 5-9.
ARS is the chief scientific research agency of the U.S.
Department of Agriculture.
Scientific contact: Randal L. Shogren, ARS National Center for
Agricultural Utilization Research, Peoria, Ill., phone (309)
681-6354, fax (309) 681-6691, shogrerl@ncaur.usda.gov.
US6312826
Paper coated with polymerized vegetable oils for use as
biodegradable mulch
[ PDF ]
Inventor(s): SHOGREN RANDAL L
Abstract
-- Biodegradable, agricultural mulches are prepared by coating
paper with a cross-linked drying oil or a cross-linked,
functionally modified drying oil. These mulches are inexpensive
to produce, and are also water-resistant, mechanically stable
and highly effective as weed barriers. The reactivities of
various drying oils permit the development of a broad spectrum
of coating systems and coating properties. In one embodiment of
the invention, it is contemplated to complete cross-linking of
coated paper in the field through either oxidative or
photoinitiated processes.
BACKGROUND
OF THE INVENTION
1. Field of the Invention
Polyethylene films are used extensively in agriculture as
greenhouse covers, forage covers and agricultural mulch.
Worldwide yearly consumption for polyethylene mulch film alone
is currently over 1 billion pounds (M. H. Jensen, presentation
at 27th National Agricultural Plastics Congress, 1998). Plastic
mulches and row covers help retain soil moisture, increase soil
temperature, inhibit weed growth, reduce insect damage and
thereby increase yields (D. F. Anderson, M. A. Garisto, J. C.
Bourrut, M. W. Schonbeck, R. Jaye, A. Wurzberger and R.
DeGregorio, J. Sustain. Agric. 7, 39-61, 1995; J. W. Courter,
University of Illinois Cooperative Extension Service Circular
No. 1009, Champaign, Ill., 1969; D. E. Hill, L. Hankin and G. R.
Stephens, Connecticut Agric. Exp. Sta. Bull. No. 805, New Haven,
Conn., 1982). Most mulches are used for vegetable and fruit
production due to their relatively high value. Disposal or
recycling of polyethylene films, however, has become a daunting
problem. Agricultural mulch, in particular, is very difficult to
recycle due to contamination with dirt and debris as well as
loss in mechanical properties from UV catalyzed oxidation. Many
landfills reject mulch film because of pesticide residues and
thus it must be treated as hazardous waste (B. Hofstetter, New
Farm 13, 56-57, 1991). A biodegradable mulch would have the dual
advantages of avoiding costs of removal and disposal as well as
contributing humus to the soil.
This invention relates to a biodegradable, water resistant,
agricultural mulch that is produced from paper and a
cross-linked drying oil.
2.
Description of the Prior Art
Several different types of degradable mulch have been considered
including polyethylene film containing prooxidants (W. J.
Maddever and G. M. Chapman, Proceedings of the Soc. Plast. Eng.
47th Ann. Tech. Conf., 1352-1355, 1989), starch-polyvinyl (PVOH)
alcohol films (F. H. Otey, A. M. Mark, C. L. Mehltretter and C.
R. Russell, Ind. Eng. Chem. Prod. Res. Develop. 13, 90-92,
1974), biodegradable polyester films (J. M. Mayer and D. L.
Kaplan, Trends in Polym. Sci. 2, 227-235, 1994) and coated paper
or fiber mats (J. Vandenberg and J. Tiessen, Hortscience 7,
464-465. 1972 and A. Bastiaansen, A. Hanzen, D. DeWit and H.
Tournois, PCT Int. Pat. Appl. WO9609355, 1996). Although
polyethylene films will disintegrate, resulting fragments may
require decades to completely biodegrade, and toxicity of
degradation products is largely unknown (A. C. Albertsson and S.
Karlsson, J. Appl. Polym. Sci. 35, 1289-1302, 1988). Starch-PVOH
films have rather poor resistance to water and thus would not be
expected to maintain their integrity during rain. Progress is
being made on laminating starch-PVOH films with different types
of water-resistant, biodegradable polyesters (J. W. Lawton, in
Cereals, Novel Uses and Processes, Plenum Press, New York, 1997,
p. 43-47). Although biodegradable polyesters such as polylactic
acid, polycaprolactone and polybutylene succinate have excellent
mechanical properties (J. M. Mayer and D. L. Kaplan, Trends in
Polym. Sci. 2, 227-235, 1994), their cost ($2-8/lb.) is much
higher than for polyethylene ($0.4/lb. resin, $1-2/lb. film) (D.
F. Anderson, M. A. Garisto, J. C. Bourrut, M. W. Schonbeck, R.
Jaye, A. Wurzberger and R. DeGregorio, J. Sustain. Agric. 7,
39-61, 1995 and Anonymous, Plastics Technol., May, 1998, p. 87).
Uncoated paper, although inexpensive ($0.28/lb. for kraft paper)
(Anonymous, North American Pulp and Paper Yearbook, Resource
Information Systems, Charlottesville, Va., 1996, 95), degrades
too rapidly to protect most crops adequately (D. F. Anderson, M.
A. Garisto, J. C. Bourrut, M. W. Schonbeck, R. Jaye, A.
Wurzberger and R. DeGregorio, J. Sustain. Agric. 7, 39-61,
1995).
Various types of coatings for paper have been developed to slow
degradation and improve wet strength. Rivise (C. W. Rivise,
Paper Trade J. 89, 55-57, 1929), Hutchins (A. E. Hutchins, Minn.
Agr. Expt. Sta. Bull. No. 298, 1933) and Flint (L. H. Flint,
U.S. Dept. of Agric. Tech. Bull. No. 75, 1928), have reviewed
some of the early work on the use of paper mulches. In 1870, the
first U.S. patent pertaining to utilization of paper as a mulch
described the use of tarred paper to exclude insects from roots
(S. Brunson, U.S. Pat. No. 104,418, 1870). By the 1920's,
chiefly through the work of Eckart in Hawaii on sugar cane and
pineapple, the dramatic advantages of tar or asphalt coated
paper for improving yields of fruits and vegetable became
apparent. Paper impregnated with paraffin wax (V. Z. Tzelik,
Russ. Pat. 28,223, 1930) and animal or vegetable oils ( W. A.
Hall, Brit. Pat. 370,482, 1931) were also claimed for mulch use.
With the advent of synthetic polymers in the 1940's and 1950's,
polyethylene largely displaced paper in mulching applications,
likely due to its low cost and excellent strength and
flexibility.
Recently, however, there has been a resurgence in research and
practical interest in coated paper mulches, probably due to
concerns about disposal of polyethylene as well as the desire of
organic farmers to have a natural, totally degradable mulch.
Most of the coatings considered have been synthetic polymers
such as polyethylene (J. W. Courter, University of Illinois
Cooperative Extension Service Circular No. 1009, Champaign,
Ill., 1969 and J. Vandenberg and J. Tiessen, Hortscience 7,
464-465, 1972), or various polymer latexes (G. E. Shanley and M.
J. Lubar, Brit UK Pat. Appl. GB2158058, 1985; R. E. Weber and M.
L. Delucia, Eur. Pat. Appl. EP454104, 1991; C. Desmarais, Can.
Pat. Appl. CA2092963, 1994; R. F. Lippoldt and W. W. Woods, U.S.
Pat. No. 3,427,194, 1969 and J. S. Vandemark and R. T. Seith,
U.S. Pat. No. 3,939,606, 1976). Non-woven mats of cellulosic
fibers and polyesters have also been considered (R. A.
Clendinning, J. E. Potts and W. D. Niegisch, U.S. Pat. No.
3,850,863, 1976 and S. H. Monroe, J. A. Goettmann and G. A.
Funk, U.S. Pat. No. 5,532,298, 1996). Anderson et al (D. F.
Anderson, M. A. Garisto, J. C. Bourrut, M. W. Schonbeck, R.
Jaye, A. Wurzberger and R. DeGregorio, J. Sustain. Agric. 7,
39-61, 1995) recently showed that the rate of loss of tensile
strength of paper in soil can be slowed slightly by soaking it
in soybean oil. Zhang et al (L. Zhang, H. Liu, L. Zheng, J.
Zhang, Y. Du and H. Feng, Ind. Eng. Chem. Res. 35, 4682-4685,
1996) found that coating a regenerated cellulose film with a
thin layer of tung oil followed by polymerization slowed weight
loss in soil (half life increased from 30 to 37 days).
SUMMARY
We have now discovered that paper treated with a coating
comprising a cross-linked drying oil or cross-linked,
functionally modified drying oil exhibits many of the desired
properties of a biodegradable, water-resistant agricultural
mulch needed for present day applications. The reactivities of
the various drying oils permit the development of a broad
spectrum of coating systems and coating properties. For example,
partial or complete cross-linking of the drying oil-coated paper
may occur in the field through either oxidative or
photoinitiated processes.
In accordance with this discovery, it is an object of the
invention to provide novel compositions of matter comprising a
paper substrate coated, and/or impregnated, with a treatment
comprising a polymerized drying oil.
Another object of the invention is to provide an inexpensive,
biodegradable agricultural mulch that is water-resistant,
mechanically stable and highly effective as a weed barrier.
It is also an object of the invention to develop a system for
tailoring the production scheme and functional properties of an
agricultural mulch to a particular end use application.
Other objects and advantages of the invention will be readily
apparent from the ensuing description.
DETAILED
DESCRIPTION OF THE INVENTION
The basic substrate for use in this invention is paper. The term
"paper" is in its broadest sense refers to any sheet or
continuous web of intermeshed fibrous material. Typically, these
sheets or webs are formed by depositing fibers of vegetable,
mineral, animal or synthetic origin from a fluid suspension into
a thin layer, and thereafter removing the fluid and drying the
resulting sheet or web. For purposes of the invention, the fiber
should be predominantly biodegradable, and is therefore
preferably derived from a cellulosic raw material, such as wood
pulp, kenaf, rag, straw, bagasse, recycled paper, etc. The paper
may also be treated with additives and coatings conventionally
used in the paper-making industry, provided that these
treatments do not interfere with the cross-linked drying oil
treatments of this invention. It is also contemplated that paper
pulp can be treated with the coating materials described, below,
and the treated pulp can then be pressed under conditions of
heat and pressure into a mat. For purposes of economy and
performance, a preferred paper for use herein is conventional
kraft paper.
The biodegradable paper coatings of the invention are defined in
reference to Formula I: ##STR1## ##STR2##
wherein the exact arrangement of CH2, R@1, R@2 and CH groups
relative to one another depends on the type of fatty acid and on
the rearrangement after radical activation or conjugation.
The actual coating that is applied to the paper sheet is: (1) a
polymer having the structure of Formula I; (2) a combination of
(a) a drying oil that will polymerize to yield a polymer having
the structure of Formula I in a polymerization reaction and (b)
a catalyst to promote said polymerization reaction; or (3) a
combination of (a) a functionally modified drying oil that will
polymerize to yield a polymer having the structure of Formula I
in a polymerization reaction and (b) a catalyst to promote said
polymerization reaction.
The drying oils contemplated herein include plant, animal,
synthetic and semi-synthetic glycerides, particularly
triglycerides, that can be transformed into hard, resinous
materials (see Encyclopedia of Polymer Science and Technology,
ed. H. F. Monk et al., John Wiley & Sons, 1966, pp.
216-234). The expression "drying oils" is generic to both drying
oils, which dry (harden) at normal atmospheric conditions, and
semidrying oils, which must be baked at elevated temperatures in
order to harden. Unless otherwise indicated, "drying oil" will
be used herein in its broadest sense to refer to both types of
drying oil. The unsaturated fatty acids of a drying or
semidrying oil comprise double bonds that are readily available
for entering into oxidative or other reactions involved in the
drying process. Common sources of drying oils include castor
oil, fish oils, linseed oil, oiticica oil, safflower oil,
soybean oil, sunflower oil, and tung oil. Of course the oils
that contain the higher levels of polyunsaturated fatty acids,
such as soybean oil, linseed oil and safflower oil are the most
reactive in terms of having available sites for cross-linking.
The drying oils may be polymerized (i.e. cross-linked) through a
variety of mechanisms, linkages, and cross-linkers. For
instance, the cross-linking may be "intra", that is, between
fatty acid ester chains on the same triglyceride; or it may be
"inter", that is, between a fatty acid ester chain of one
triglyceride and a fatty acid ester chain on another
triglyceride. The cross-linking, whether intra or inter, may be
directly from one methylene group to another, or may involve a
linker, such as that resulting from reaction of an epoxidized
oil with a curing agent, such as a polyol, a polybasic acid, an
amine, a polyamine, a polythiol, or a polyphenol. Specific
exemplary reagents for this purpose include:
polyols: ethylene glycol, glycerol, sorbitol, propylene glycol,
and oligomers thereof; as well as hydroxylated oils such as
castor oil
polybasic acids: succinic acid, adipic acid, butane
tetracarboxylic acid, citric acid, succinic anhydride,
octenylsuccinic anhydride, and phthalic anhydride;
amines: octylamine, and ethylamine;
polyamines: ethylene diamine and triethylene tetramine;
polyphenols: phenol-formaldehyde resin
A preferred curing agent is citric acid, because of its rapid
rate of reaction with epoxidized oil at relatively low
temperatures. Another approach to cross-linking is to react the
drying oil with maleic anhydride and then react the maleated oil
with a polyol. Also contemplated herein are cross-linked alkyds
having a structure in accordance with Formula I wherein
z.gtoreq.1. Alkyds would typically be produced by reacting a
polyol with a polybasic acid and free fatty acids.
In one preferred embodiment of the invention, the drying oil is
simply reacted with oxygen to form hydroperoxides which
decompose to form various free radicals in the presence of a
drying catalyst; particularly, metal ion catalysts, such as
cobalt, manganese, copper, chromium, iron and calcium. The
radicals then combine to form carbon-oxygen or carbon-carbon
cross-links.
In another preferred embodiment, the drying oil is first either
partially or completely epoxidized. The resultant oxirane rings
are then available for photoinitiated cross-linking. Optionally,
the epoxidized oil and a catalyst can be coated on the paper,
and the cross-linking would then take place when the paper is
exposed to sunlight in the field. Alternatively, the epoxidized
oil may be reacted with a curing agent to modify the drying oil
by addition of a linker as described above. When acidic
catalysts such as quaternary ammonium halides are used as
catalysts in the latter reaction, the primary reaction product
is a polyester containing a secondary hydroxyl group .beta. to
the carboxyl carbon. Other catalysts for effecting
polymerization across the oxirane ring are well established in
the art.
Partial polymerization is easily controlled by regulating the
temperature of reaction. For example, the reaction can be
stopped by rapidly lowering the temperature of the mixture, as
in ice water, prior to applying the partially polymerized oil
onto the paper. The reaction is then easily completed at a later
time, such as by passing the treated paper through an oven, or
the like. Partially reacted epoxidized oils are available for
photoinitiated cross-linking through the remaining oxirane
rings. For the partially epoxidized oils, oxidative
cross-linking can be promoted between remaining sites of
unsaturation and reactive functional groups introduced by the
curing agent. As indicated above, both the photoinitiated
cross-linking and the oxidative cross-linking of the coated
paper can be completed in the field.
The drying oil or modified drying oil is applied to the paper by
any conventional means such as by spraying, wiping, or by
passing the paper through a bath. The catalyst can be blended
with the oil or applied to the paper as a separate stage. In
order to interrupt or completely delay cross-linking until the
coated paper is put into use, the sheet can be simply wound into
a roll in order to exclude both oxygen and/or light needed to
initiate the remaining cross-linking reaction. Of course it is
understood that the viscosity of the drying oil applied to the
paper can be controlled by partial cross-linking or by partial
polymerization prior to applying the oil to the paper. As
discussed further below, this approach may be desirable when
control over impregnation into the paper is needed.
The nature of the coating treatment on the paper is a function
of a number of variables including the porosity of the paper,
the initial viscosity of the treatment material, the mode and
application rate of the treatment material, the contact period
of the paper and treatment before the drying oil becomes
completely cross-linked, the temperature during the contact
period and the like. For example, the more porous the paper and
the more fluid the treatment material, the more of the treatment
material that will become absorbed by the paper. Likewise, the
longer the period of contact between the paper and the drying
oil before completing the cross-linking, the more the drying oil
will tend to impregnate the paper. Conversely, by increasing the
density of the paper or the viscosity of the treatment material,
or by shortening the period of contact before completing the
cross-linking, the amount of material absorbed by the paper can
be reduced. It is envisioned that the extent of penetration of
the treatment into the paper can be controlled over a broad
continuum; but that typically some of the material will be
absorbed, and some of the material will ultimately reside as a
coating over the one or more of the surfaces of the paper. For
purposes of this invention, the terms "treatment" and "coating"
as used herein include material that may actually be absorbed
into (i.e. penetrate or impregnate) the fibrous structure of the
paper. Additionally, it is to be understood that the treatment
may be applied to one or both surfaces (i.e. sides) of the paper
sheet, and that the treatment may comprise non-cross-linked
drying oil, or drying oil in various stages of cross-linking.
The polymerization reactions contemplated for use herein and
described above are all well known. Accordingly, determination
of the appropriate conditions (e.g. time, temperature, and
catalyst) for conducting a particular reaction would be well
within the skill of the person in the art. Likewise, tailoring
these conditions to achieve a particular result in the coating
step would be within the skill of the ordinary artisan. For most
applications, the coating weight would be in the range of about
10-300% (7-200 g/m@2) of the paper for a given area. Usually,
the level of coating will be in the range of 25-100% (15-65
g/m@2), with the preferred amount being in the range of 40-80%
(25-55 g/m@2).
A variety of additives may be included in the coating treatment.
For example, the optional addition of a darkening or opacifying
agent such as carbon black, charcoal or dark organic dye to the
polymerized oil or the paper are commonly used in plastic
mulches to screen out the sun and thus make it more difficult
for plants to grow underneath. Also, pigments of other colors
may be added to help regulate the soil temperature or control
the growth response of the cultivated plants. Of course,
fertilizers, pesticides, fungicides, biocontrol agents,
biodegradation enhancers and the like may optionally be added to
the coating.
The coated paper products of this invention have utility as
agricultural mulches for all the same applications for sheeted
mulches as known in the art. That is, they can be rolled out in
orchards, gardens, fields, and potted plants for the purposes of
retaining soil moisture, increasing soil temperature, inhibiting
weed growth, and reducing insect damage. At the end of the
growing season, or whenever the benefit of the mulch is no
longer needed, the mulch is simply cultivated into the soil and
allowed to biodegrade. It is apparent from the data in Example 5
that coating with vegetable oil resins extends the useful life
of paper mulches to a length of time close to that required for
many crops (about 10 weeks).
The treated paper of this invention is characterized by at least
comparable, and in some cases, significantly improved,
mechanical and functional properties as compared to untreated
paper or to paper treated with the same amount (comparable add
on) of nonpolymerized oil. For instance, as shown in the
Examples below, treated kraft paper exhibits at least a two-fold
increase in elongation to break vs. untreated paper. In a soil
burial test, treated samples exhibit at least two-fold, and in
some cases several-fold, increase in the half life over
untreated paper. As a barrier to plants, tests described in the
Examples show that the treated paper reduces penetration by
plants up to 80% after 84 days as compared to the untreated
control.
EXAMPLES
Materials used in the ensuing examples were as follows:
Brown kraft paper having a weight of 66 g/m@2. Raw linseed oil
was obtained from Alnoroil Co., Valley Stream, N.Y. and had an
iodine value of >177 and a saponification value of 189-195.
Cobalt octoate solution (6% Co in mineral spirits) was obtained
from Pfaltz & Bauer. Epoxidized soybean oil was Paraplex
G-62 from C. P. Hall Co., Bedford Park, Ill. and had about 7%
oxirane oxygen. Citric acid and tetrabutylammonium bromide were
reagent grade and were purchased from Aldrich Chem. Co. Citric
acid was ground with a mortar and pestle and passed through an
80 mesh screen prior to use.
Abbreviations for coating treatments used in the examples are as
follows:
<t
LO = linsead oil
SO = soybean oil
ESO = epoxidized soybean oil
CA = citric acid
TBABr = tetrabutylammonium bromide
Examples 1-5 relate to the first year trials and Example 6
relates to the second year trials. Legends for FIGS. 1-10 are as
follows: uncoated kraft paper (.tangle-soliddn.), uncatalyzed LO
coated paper (.largecircle.), catalyzed LO coated paper
(.circle-solid.), ESO/CA coated paper (.tangle-solidup.),
ESO/CA/TBABr coated paper at 147% add-on (.box-solid.),
ESO/CA/TBABr coated paper at 51% add-on (.quadrature.),
uncatalyzed SO at 56.4% add-on (.Arrow-up bold.), catalyzed SO
at 71.8% add-on (.diamond-solid.), uncatalyzed SO at 38.6%
add-on ({character pullout}), catalyzed SO at 25% add-on
({character pullout})
Example 1
Preparation of Paper Coated with Polymerized Linseed Oil
Linseed oil (LO, 120 g) and cobalt octoate solution (0.40 g)
were magnetically stirred for 10 min. then the mixture was
applied to pieces of kraft paper (50.8.times.91.4 cm) using a
paint brush. The oil penetrated quickly into the paper due to
its low viscosity. The coated paper was hung from a rope and
allowed to "dry" overnight. Coating weight was approximately 45
g/m@2.
Fourier Transform Infrared Spectroscopy (FTIR)
Samples of paper coated with polymerized linseed oil (LO coated
paper) were prepared for FTIR analysis were pulverized in liquid
nitrogen using a Wig-L-Bug Amalgamator, mixed with KBr and
pressed into pellets. Spectra were obtained using a Nicolet
Impact 410 spectrometer. For LO coated paper, no absorbance
corresponding to C--H stretching adjacent to carbon-carbon
double bonds of LO (3010 cm@-1, data not shown) was seen,
indicating that most of the double bonds reacted.
Example 2
Preparation of Epoxidized Soybean Oil-Based Polyesters
Epoxidized soybean oil (ESO, 349 g, 1.5 mole epoxy), citric acid
(CA, 99 g, 1.5 mole carboxyl) and tetrabutylammonium bromide
(TBABr, 3.2 g) were first partially polymerized by heating in a
3 l beaker equipped with an air stirrer and hot plate. After the
temperature of the mixture reached 110 DEG C. (about 10 min.),
the beaker was placed into a bucket of ice to stop the reaction.
Pre-polymerization was conducted in order to better disperse the
CA in the ESO. The partially polymerized ESO resin was then
spread onto paper sheets using glass rods. The ESO resin
penetrated only part way into the paper due to its high
viscosity. Polymerization was completed by placing the coated
paper onto steel sheets covered with teflon/aluminum foil
(Bytac, Norton Performance Plastics, Akron, Ohio) and heating in
an oven at 165 DEG C. for 3 min. A similar experiment was
conducted without the TBABr catalyst to evaluate possible
effects of TBABr on biodegradation rates, described in Example
3, below.
FTIR
Analysis
The ESO/CA coated paper was analyzed by FTIR as described above
in Example 1 for LO coated paper. The absorbances corresponding
to citric acid carboxyl carbonyl stretch (1701 cm@-1) and
epoxide ring vibration (822 cm@-1) disappeared, indicating that
essentially all ESO and CA reacted. Interestingly, the reaction
seems to occur with or without the TBABr catalyst.
Example 3
Testing for Biodegradation in Soil
Coated papers as well as uncoated paper were cut into
5.08.times.10.16 cm pieces, weighed and sewn into nylon mesh
bags having openings about 3 mm in size. Three replicates of
each sample for each of 4 time points were then buried under 6
in. of soil in a field plot [National Center for Agricultural
Utilization Research (NCAUR), Peoria, Ill.] starting on June 30.
During summer weeks in which there was no rain, the plot was
sprinkled with about 1.3 cm. of water. Samples were removed from
the ground at 14, 42, 84 and 140 days. After removal, samples
were brushed lightly, gently rinsed with deionized water,
equilibrated for 7 days at 23 DEG C. and 50% relative humidity,
weighed and tested for tensile properties (see below). Average
outdoor temperatures were about 21 DEG C. over the first 3
months of the experiment and then declined gradually to 0 DEG C.
over the next 2 months. Rainfall was very light the first six
weeks (<2 cm/week) and then increased.
The results are shown in FIG. 1. The higher initial (at 0 time)
weight/area values of the coated papers reflect the added weight
of the coating. Rates of weight loss during soil burial as a
percentage of initial weight, were most rapid in uncoated paper,
followed by LO coated paper and finally ESO/CA coated paper.
Rates of decrease in weight and strength were similar for ESO/CA
and ESO/CA/TBABr coated papers, suggesting that TBABr does not
significantly impede biodegradation. Close examination of the
buried samples show that uncoated paper had torn or
disintegrated into small pieces by 6 weeks while the coated
papers remained whole. After 12 weeks, LO coated paper has also
disintegrated while the ESO/CA coated paper has begun to tear.
There were no significant changes in the measured thicknesses
with time up to 6 weeks so losses in weight were due to
decreases in density and focal losses in area. Specimens were
examined with a JEOL JSM 6400V scanning electron microscope. The
resulting SEM photographs (not shown) revealed that, by 6 weeks,
fungal cells and hyphae have extensively colonized the surface
and interior of uncoated paper. Fibrillar breakage and
defibrillation are evident. Fungal growth was also widespread on
the surface of LO coated paper at 6 weeks but there was little
penetration to the interior. The LO coating covers and fills the
spaces between cellulose fibrils, so less surface area is
available for microorganism growth. In contrast, the surface of
ESO/CA coated paper showed only focal areas of microbial
colonization after 6 weeks, suggesting that the ESO based resin
may be more resistant to biodegradation than LO. It is somewhat
surprising that LO coated paper appears to degrade faster than
ESO/CA coated paper considering that the double bonds in LO are
polymerized to single C--C or C--O bonds. The latter are
normally thought to be more resistant to biodegradation than the
ester linkages found in ESO/CA. However, the greater thickness
of the ESO/CA coated paper or the greater ratio of resin to
paper may also influence biodegradation rates.
It is apparent from FTIR spectra of coated papers after exposure
to soil for 12 weeks (data not shown) that for LO coated paper,
absorbances from the LO component (2929 and 2856 cm@-1 from C--H
stretching and 1741 cm@-1 from C=0 stretching) are greatly
diminished relative to the cellulosic component (1163, 1059,
1034 cm@-1 from C--O stretching). The ESO/CA coated paper
likewise showed a smaller preferential loss of the oil
component. These data suggest that the polymerized oil coatings
protect the cellulosic fibers from premature microbial attack by
acting as a sacrificial barrier.
Example 4
Weed Growth Inhibition
Three pieces of each of the coated papers and control (uncoated
paper) 50.8.times.91.4 cm in size were placed onto rototilled
ground in the NCAUR field plot. The outer edges (about 10 cm) of
the samples were buried in the dirt to keep the samples
stationary. The number of weeds protruding through openings in
the samples were recorded over time (FIG. 2).
These data show that weed growth is most rapid for uncoated
paper followed by LO coated paper then ESO/CA coated paper. This
is consistent with the degradation data in Example 3. By 6
weeks, the uncoated paper had several tears or holes and weed
growth through the paper began. Most of the uncoated paper on
top of the soil disappeared (biodegraded and/or blown away) by 9
weeks. Loss of strength of uncoated paper during rain may also
have contributed to its disintegration. In contrast, the coated
papers remain mostly intact, albeit with some cracks and holes,
up to 14 weeks.
Example 5
Tensile Testing and Elongation to Break Evaluation
Dog-bone type V tensile bars (4-5 for each sample) were cut and
tested according to ASTM D638-91 using an Instron model 4201
Universal Testing Machine. Crosshead speed was 20 mm/min and
gage length was 25.4 mm. Both tensile strength and elongation to
break were evaluated in the Instron.
FIG. 3 shows that the initial tensile strength of LO coated
paper (82 MPa) is slightly higher than for uncoated paper (68
MPa). Since the LO penetrated into the paper (the overall
thickness was 85 .mu.m for both LO coated paper and uncoated
paper), overall strength per unit area is higher for LO coated
paper since the polymerized oil replaces air. Likewise, tensile
strengths of the ESO/CA and ESO/CA/TBABr coated papers (45 MPa)
are lower than the uncoated paper because much of the weaker
resin did not penetrate the paper (thickness 180 .mu.m). Rates
of decrease in tensile strength with time decreased in the order
uncoated paper>LO coated paper>ESO/CA coated paper (FIG.
3).
As shown in FIG. 4, elongations to break of coated and uncoated
paper were 3.+-.1% at 0 time. Interestingly, elongation values
for coated papers increased to 7.+-.1% after 2 weeks of soil
exposure while those for uncoated paper remained unchanged. The
reason for this is unknown, but could result from a decrease in
fiber cohesion from rain or starch binder degradation, such that
more of the load is transferred to the flexible resin.
Example 6
Kraft paper samples were coated with polymerized linseed oil as
described in Example 1 and with epoxidized soybean oil-based
polyesters as described in Example 2. Physical and functional
properties of these coated samples were tested as described in
Examples 3-5 as compared to kraft paper coated with
uncross-linked soybean oil, linseed oil and paraffin wax. The
uncross-linked soybean oil at the 39% add on level and the
cross-linked soybean oil at the 25% add on level were applied to
the paper with a paint sprayer. Tensile strength and elongation
to break were determined by the previously-described procedures
for both wet and dry samples. The results presented in Tables I
A and I B show that the cross-linked coatings of the invention
contribute significantly to the tensile strength and elongation
to break of the wetted papers. The kinetic data for weight loss
during soil burial are reported in Table II and in FIGS. 5-8.
These data demonstrate a significant effect of the cross-linked
coatings in the prolongation of the paper half life. Data
regarding the effectiveness of the coated papers as plant
barriers are shown in FIGS. 9 and 10.
TABLE I A
Dry and Wet Tensile Strengths of Kraft Paper Coated with Native
and Polymerized Oils
TABLE I B
Dry and Wet Elongations to Break of Kraft Paper Coated with
Native and Polymerized Oils
TABLE II
Kinetic Data for Weight Loss during Soil Burial of Kraft Paper
Coated with Native and Polymerized Oils
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