[0001] The present invention relates to a novel composite material based on cellulosic fibres
and chitosan. More particularly, the present invention relates to a composite material
basically formed of cellulose fibres and chitosan and which is biodegradable, for
example, in the soil. The invention also relates to a method for the preparation of
such a composite material.
[0002] The composite material of the invention is useful in a wide variety of applications,
mainly but not limited to a sheet form used, for example, as a wrapping sheet for
foods, a sheet material for agricultural use, temporary pots for growing young garden
trees and seedlings, goods for hydroponics and the like. The services expected for
the sheet materials in the above-mentioned applications are mostly of a temporary
nature, so that it is desirable that the sheet material can be spontaneously decomposed
after use or at the end of the service season without leaving any decomposition products
which may cause environmental pollution problems.
[0003] Most of the sheet materials for the above-mentioned applications currently in use
are made from a film of a plastic material, such as polyvinyl chloride and polyethylene,
or a cellulose fibre-based sheet, i.e. paper, coated with a synthetic resin such as
a polyethylene, or a melamine resin with the object of enhancing the mechanical strength
of the base sheet. The synthetic polymer-based constituents in the conventional sheet
materials are not biodegradable, so that a serious problem is sometimes caused by
the waste materials after use left in the environment without being properly disposed
causing environmental pollution. In consideration of this problem, a photodegradable
polymer has been proposed by incorporating a photosensitizer into a certain synthetic
polymer. Such a photodegradable polymer is still not free from the problem of environmental
pollution because the decomposition product thereof
per se is a potential pollutant of the environment when the amount thereof is relatively
large. Moreover, the photodegradable polymer cannot be decomposed when the waste thereof
is out of reach of light, for example in the soil.
[0004] Cellulosic materials, including lignocellulose, pectocellulose and bacteria cellulose,
are natural products produced by plants and fungi which are readily available. Cellulosic
materials are of course absolutely free from the problem of environmental pollution
of the soil by waste thereof as is typically evidenced by the fact that cellulosic
materials constitute an important constituent of composts. Accordingly, a cellulose-based
sheet material is required having a sufficiently high mechanical strength not only
in the dry but also in the wet state which is also biodegradable and thus causes no
environmental or soil pollution.
[0005] We have now developed a novel sheet material based on cellulose fibres having a sufficiently
high mechanical strengths together with boidegradability to meet the above described
requirements for sheet materials for temporary use.
[0006] Accordingly, the present invention provides a composite material which comprises:
(a) cellulose fibres shaped in the form of a sheet; (b) chitosan in an amount in the
range of from 1% to 99% by weight based on the amount of cellulose fibres; and (c)
a higher fatty acid in an amount in the range of from 0.05% to 1.0% by weight based
on the amount of the cellulose fibres.
[0007] It is preferred that the higher fatty acid as a treatment agent of the sheet material
of the cellulose fibres impregnated with chitosan has at least 12 carbon atoms per
molecule and that the amount thereof is in the range of from 0.05% to 1% by weight
based on the weight of the cellulose fibres.
[0008] The cellulose fibre and chitosan-based composite sheet material of the invention
can be prepared by first forming sheets of the cellulose fibres in a process similar
to paper making and then soaking the sheet of cellulose fibres with an aqueous solution
of a chitosan salt, followed by drying. Alternatively, the composite sheet material
can be prepared by forming sheets from an aqueous slurry of cellulose fibres containing
chitosan in the form of a salt. The composite sheet comprising a higher fatty acid
can be prepared by soaking the composite sheet of cellulose fibres and chitosan with
a solution of the higher fatty acid followed by drying.
[0009] As is described above, the basic constituents of the inventive composite material
are cellulose fibres and chitosan which impregnates a sheet of the cellulose fibres
in a limited amount. The cellulose fibres can be obtained from various sources including,
mostly, wood and is avilable in the form of chemical pulp, mechanical pulp and the
like.
[0010] Chitosan is a deacetylation product of chitin which is a nitrogen-containing polymeric
commpound occurring in large quantities in nature and is a principal constituent of
the shells of insects, lobsters, crabs and the like as well as a constituent of certain
microorganisms. Chitosan may have different degrees of deacetylation depending on
the conditions of the deacetylation treatment of chitin. Chitosan, as such, is insoluble
in water but can be solubilized when chitosan is converted into the form of a salt
with, for example, acetate ions or chlorine ions. The so-called chitinous substances
include chitin and chitosans in general. Since chitinous substances belong to a class
of natural products, various species of microorganisms are known to decompose the
chitinous substances. This fact is evidenced by the tests undertaken by the inventors
who collected samples of soils from a number of cultivated lands all over the territory
of Japan to test the biodegradability of chitosan therein to find microorganisms capable
of decomposing chitosan having a relatively high degree of deacetylation.
[0011] Chitosan has previously been used industrially as a flocculating agent in the technology
of waste water disposal. In recent years, investigations have been undertaken for
the development of a chitinous substance as a bioadaptable material. Further, an attempt
has been made to improve the surface strength of paper with chitosan (see, for example,
British Patent No. 458,813 and "Proceedings of the 2nd International Conference of
Chitin and Chitosan¨, 1982). No prior art is known, however, of a composite material
composed of cellulose fibres and chitosan, in particular, surface-treated with a higher
fatty acid.
[0012] Needless to say, cellulose fibres in a sheet-like form and chitosan shaped in a sheet,
when alone, cannot retain their strength or form in a hydrous soil. Namely, a sheet
of cellulose fibres rapidly disintegrates into discrete fibres in a wet condition
and a sheet of chitosan is converted into a gel-like material. It is a discovery that,
when cellulose fibres and chitosan form a composite, the composite material can retain
its shape and mechanical strength even in a hydrous soil for a length of time and
thereafter gradually be decomposed by the microorganisms living in the soil. A composite
material composed of cellulose fibres and chitosan alone is water-absorptive, but
the composite can be provided with water repellency when it is treated with a higher
fatty acid so that the stability of the composite material in the wet condition can
be further increased without unduly affecting biodegradability.
[0013] The treatment of a composite sheet of cellulose fibres and chitosan with a higher
fatty acid is performed by bringing the composite sheet into contact with a solution
of the fatty acid in a concentration of from 0.1 to 0.5% by weight in a suitable organic
solvent, followed by drying. The amount of the higher fatty acid impregnating the
composite sheet is in the rage of from 0.05% to 1% by weight or, preferably, in the
range of from 0.1% to 0.6% by weight based on the amount of the cellulose fibres.
The content of the higher fatty acid has some influence on the biodegradability of
the composite sheet in soil. The organic solvent to dissolve the higher fatty acid
is not limited, provided that it is inert to chitosan. Methyl alcohol is an example
of a suitable organic solvent though not limited thereto. The higher fatty acid is
selected from those insoluble in water and should have at least 12 carbon atoms per
molecule. Stearic and palmitic acids are preferred in respect of the water repellency
imparted to the composite sheets treated therewith.
[0014] The composite sheet of cellulose fibres and chitosan can be prepared in several different
ways as described below. First, cellulose fibres are shaped into the form of a sheet
by a method similar to paper making and then the sheet of cellulose fibres is coated
or soaked with an aqueous solution of chitosan acidified with acetic or hydrochloric
acid. Secondly, cellulose fibres are first treated with an aqueous solution of chitosan
and the thus chitosan-treated cellulose fibres are shaped into a sheet-like form.
Thirdly, cellulose fibres are slurried in an aqueous medium containing chitosan and
sheet-making is performed from this slurry.
[0015] It is important that the average molecular weight and degree of deacetylation of
chitosan, as well as the compounding amount thereof with the cellulose fibres, should
be selected appropriately in order to control adequately the mechanical properties
of the composite material and the biodegradability thereof. For example, the chitosan
should have a degree of deacetylation of at least 40% in order to have an adequate
sheet-forming power. Further, the chitosan should preferably have an average molecular
weight in the range from 2,000 to 500,000. Presumabley, a type of chemical bond is
formed between the surface of the cellulose fibres and chitosan so that the composite
sheet having biodegradability is imparted with a high mechanical strength whilst still
retaining its water-absorptivity. The treatment with a higher fatty acid forms a water-repellent
film on the surface of the composite sheet so as to decrease the water-absorptivity
of the sheet.
[0016] The following Examples are given to illustrate the composite material of the invention
and the method for the preparation thereof in more detail although the scope of the
invention is not limited thereby in any way. The water absorption in % by weight of
composite sheets prepared in Example 4 and treated with a higher fatty acid as a function
of the number of carbon atoms per molecule of the fatty acid when the sheet was dipped
in water overnight is shown in the single Figure of the drawings.
Example 1
[0017] A sheet of paper having a basis weight of 50 g/m² and made from a mechnaical pulp
was soaked with an aqueous solution of chitosan having an average molecular weight
of about 50,000 and a degree of deacetylation of about 99% acidified with acetic acid
in different concentrations followed by drying at 105 °C. The contents of chitosan
in the thus prepared composite sheets were 1 to 50% by weight based on the cellulose
fibres of the paper. The composite sheets were each soaked with 0.1% by weight solution
of stearic acid in methyl alcohol followed by drying. The amount of stearic acid picked
up by the composite sheet was 0.12% by weight based on the cellulose fibres. These
composite sheets were subjected to the determination of the breaking length both in
a dry and in a wet condition to give the results shown in Table 1 which also incudes
the data obtained by omitting addition of chitosan. Further, the sheets were buried
in a soil of a cultivated land containing 60% by weight of water at 25 °C in a depth
of 2 to 8 cm from the surface and kept there over months to evaluate the biodegradability
for which a measure was given by the number of months taken until the breaking length
of the sheet in a wet condition had been decreased to 0.5 km or less.

[0018] The results in Table 1 show that the sheet of cellulose fibres can be imparted with
an increased strength even in a wet condition by composite-making with chitosan in
an amount of 1% by weight or larger. In addition, the biodegradability of the composite
sheet is controllable by the amount of chitosan compounded with the cellulose fibres.
Example 2.
[0019] Several stearic acid-treated composite sheets of cellulose fibres and chitosan were
prepared in substantially the same manner as in Example 1 except that several chitosans
having different average molecular weights were used and the compounding amount of
the chitosan was always 3% by weight based on the cellulose fibres in the form of
a sheet of paper prepared from a mechanical pulp. The composite sheets were subjected
to the evaluation test of the biodegradability in the same manner as in Example 1
to give the results shown in Table 2.
Table 2
| Molecular weight of chitosan, x 10³ |
2 |
50 |
200 |
500 |
| Months for decomposition |
0-1 |
3-6 |
4-8 |
6-12 |
[0020] The results in Table 2 show that the molecular weight of chitosan had an influence
on the biodegradability of the composite sheets and the length of time taken for biodegradation
of the composite sheet was longer when the chitosan had a larger average molecular
weight. The biodegradability of the composite sheet was little influenced by the treatment
with stearic acid.
Example 3.
[0021] Several composite sheets of cellulose fibres and chitosan, each having a basis weight
of about 50 g/m², were prepared by sheet-making from an aqueous slurry of fine cellulose
fibres after thorough beating with admixture of an aqueous solution of chitosan having
a varied degree of deacetylation of 40 to 100% acidified with acetic acid followed
by neutralization. The amount of chitosan added to the slurry was 2% by weight based
on the amount of the cellulose fibres in the slurry. It was found that pick-up of
the chitosan added to the slurry by the sheet after sheet making was substantially
complete. The composite sheets were subjected to the treatment with stearic acid in
the same manner as in Example 1. The breaking lengths in wet of these composite sheets
are shown in Table 3 below, from which it is understood that chitosan should desirably
have a degree of deacetylation of at least 40% in order to exhibit a practical reinforcing
effect on the sheet of cellulose fibres although the use of chitosan having a degree
of deacetylation lower than 40% was not ineffective in increasing the wet strength
of the sheet as compared with a similar sheet prepared without addition of chitosan
which had a wet strength of 0.3 km.
Table 3
| Degree of deacetylation, % |
32 |
40 |
51 |
65 |
84 |
92 |
99 |
| Breaking length, wet, km |
0.9 |
1.9 |
2.0 |
2.0 |
2.2 |
2.3 |
2.4 |
Example 4.
[0022] Several composite sheets of cellulose fibres and chitosan were prepared in the same
manner as in Example 1 and subjected to a treatment with a higher fatty acid also
in the same manner as in Example 1 excepting the use of various higher fatty acids
having 6 to 18 carbon atoms in a molecule dissolved in methyl alcohol each in a concentration
of 0.5% by weight. The composite sheets thus prepared contained 0.59% by weight of
the higher fatty acid based on the cellulose fibres. The amounts of water in % by
weight absorbed by these composite sheets kept overnight in water are shown graphically
in the figure of the accompanying drawing as a function of the number of carbon atoms
in a molecule of the fatty acids. As is shown by the graph, the amount of water absorption
was very significantly decreased when the fatty acid was lauric acid or a higher one.
[0023] Further, the composite sheets of cellulose fibres and chitosan were treated with
a methyl alcohol solution of stearic acid in varied concentrations of 0.1 to 1 .0%
by weight and the amount of water absorption of the thus treated sheets was determined
to find that the degree of hydrophobicity imparted to the composite sheet remained
unchanged when the concentration of the stearic acid solution was increased over
0.5% by weight despite the rapid increase of the amount of stearic acid picked up
by the composite sheets. This fact led to a conclusion that the treatment with a higher
fatty acid should be performed by using a solution of the fatty acid in a concentration
not exceeding 0.5% by weight.
1. A composite material which comprises:
(a) cellulose fibres shaped in the form of a sheet;
(b) chitosan in an amount in the range of from 1% to 99% by weight based on the amount
of cellulose fibres; and
(c) a higher fatty acid in an amount in the range of from 0.05% to 1.0% by weight
based on the amount of the cellulose fibres.
2. A composite material as claimed in Claim 1 wherein the chitosan has a degree of
deacetylation of at least 40%.
3. A composite material as claimed in Claim 1 or Claim 2 wherein the chitosan has
an average molecular weight in the range of from 2,000 to 500,000.
4. A composite material as claimed in any one of the preceding claims wherein the
higher fatty acid is a saturated aliphatic carboxylic acid containing from 12 to 18
carbon atoms.
5. A method for the preparation of a composite material as calimed in Claim 1 which
comprises the steps of:
(1) preparing a sheet composed of cellulose fibres impregnated with chitosan;
(2) soaking the sheet with a solution of a higher fatty acid in an organic solvent;
and
(3) drying the thus soaked sheet.
6. A method as claimed in Claim 5 wherein the solution of the higher fatty acid has
a concentration in the range of from 0.1% to 0.5% by weight of the fatty acid.
7. A method as claimed in Claim 5 or Claim 6 wherein the organic solvent is methyl
alcohol.
8. A method as claimed in any one of Claims 5 to 7 wherein the sheet composed of cellulose
fibres impregnated with chitosan is prepared by soaking a sheet of cellulose fibres
with an acidic solution of chitosan and drying the sheet.
9. A method as claimed in any one of Claims 5 to 8 wherein the amount of chitosan
impregnating the sheet of cellulose fibres is in the range of from 1% to 99% by weight
based on the amount of cellulose fibres.
10. A method as claimed in any one of Claims 5 to 9 wherein the chitosan has an average
molecular weight in the range of from 2,000 to 500,000.