JP3482275B2 - Resin composition - Google Patents

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to synthetic resins such as polyvinyl chloride resin, polyurethane resin, polyacrylic resin, polyamide resin, polyester resin, polyamino acid resin, polyolefin resin, and epoxy resin, and polyvalent alginic acid. The present invention relates to a resin composition containing a metal salt. More specifically, the present invention relates to a resin composition having good moisture breathability, that is, having a high hygroscopic property and a quick moisture releasing property, and is preferably used for packaging materials, clothing materials, synthetic leather and the like.

[0002]

2. Description of the Related Art Polyvinyl chloride resin, polyurethane resin, polyacrylic resin, polyamide resin, polyester resin, polyamino acid resin, polyolefin resin,
BACKGROUND ART Synthetic resins such as epoxy resins are used as films in various applications such as packaging materials, clothes, and covering materials.

However, these resins are generally highly hydrophobic and not highly water-breathing. Here, water respiration is
It is a physical property related to hygroscopicity and moisture desorption of a resin, and refers to the ability to take in a large amount of water into the resin rapidly under high humidity conditions and to rapidly release water under low humidity conditions.

Since the above-mentioned synthetic resin has a low moisture respiration property, it cannot follow the changes in the humidity of the outside world, causing a disadvantage that moisture condensation occurs on the resin surface. Since these resins are often used as films for packaging materials, clothing materials, coating materials and the like, the drawback that condensation is likely to occur is fatal, and improvement thereof is strongly desired.

Further, these synthetic resins are often used as synthetic leather. Here, synthetic leather is woven cloth,
A natural leather-like surface layer composed of a polymeric material on a support such as knitted cloth, paper, or non-woven fabric, most of which is a modified polyamide on the surface of polyvinyl chloride, polyamide, or polyurethane microporous material. It is a material that is finished in a leather pattern by adding a finishing layer such as polyurethane, polyacrylic acid derivative, and polyamino acid blend. The performance of synthetic leather has improved in recent years, and although it is not inferior to natural leather in terms of appearance and performance, recently, the sensitivity and demands of consumers have also increased, and a moist texture closer to natural leather has been obtained. Improvement is desired.

In order to enhance such a peculiar texture of leather, a method of mixing collagen with resin (Japanese Patent Laid-Open No. 61-1 / 1986)
63850, JP-A-5-279967) and a method using an esterified protein (JP-A-6-988).
No. 5) is disclosed. However, the synthetic leathers produced by these methods have insufficient moisture breathability, and therefore, in the present situation, they are not satisfactory in terms of moist texture.

[0007]

SUMMARY OF THE INVENTION It is an object of the present invention to provide a resin composition having excellent moisture respiration properties, which is suitable for obtaining a film which is less likely to cause dew condensation and a synthetic leather having a moist texture. To do.

[0008]

In order to solve the above problems, the present invention has the following constitution. That is, the resin composition of the present invention is characterized by containing 0.01 to 100 parts by weight of a polyvalent metal salt of alginic acid with respect to 100 parts by weight of a synthetic resin.

As the synthetic resin, polyvinyl chloride,
One or a mixture of two or more selected from polyurethane resins, polyacrylic acid resins, polyamide resins, polyester resins, polyamino acid resins, polyolefin resins and epoxy resins can be mentioned.

The polyvalent metal salt of alginic acid is selected from calcium alginate, zinc alginate, magnesium alginate and barium alginate.
Seed or a mixture of two or more species. The polyvalent metal salt of alginic acid is preferably a granular material having an average particle size of 0.1 to 100 μm.

The resin composition of the present invention comprises the above-mentioned synthetic resin 10
Further, 0.001 to 50 parts by weight of a cell forming agent may be contained with respect to 0 part by weight. The resin composition of the present invention can be produced by adding and mixing 0.01 to 100 parts by weight of a polyvalent metal salt of alginic acid to 100 parts by weight of a molten or dissolved synthetic resin.

The packaging or clothing film and the synthetic leather of the present invention use the above resin composition. The resin composition used for the synthetic leather is a polyvalent metal of alginic acid based on 100 parts by weight of at least one synthetic resin selected from polyvinyl chloride resin, polyurethane resin, polyamide resin, polyester resin and polyamino acid resin. Examples thereof include a resin composition containing 0.01 to 100 parts by weight of a salt and 0.001 to 50 parts by weight of a bubble forming agent.

[0013]

BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described below. (1) Synthetic Resin The synthetic resin used in the present invention is not particularly limited and may be either a thermoplastic resin or a thermosetting resin, but is preferably polyvinyl chloride resin, polyurethane resin, polyacrylic resin, polyamide. At least one resin selected from the group consisting of resins, polyester resins, polyamino acid resins, polyolefin resins and epoxy resins can be mentioned.

As the polyvinyl chloride resin, in addition to vinyl chloride homopolymers, for example, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinylidene chloride copolymers, vinyl chloride-ethylene copolymers, ethylene-vinyl acetate are used. Also included are vinyl chloride copolymers such as copolymers obtained by graft-polymerizing vinyl chloride on the copolymer.

Polyurethane resin includes polyisocyanate (compound having two or more isocyanate groups (-NCO) in one molecule) and polyol (active hydrogen group (-) in one molecule).
It is a resin synthesized from a compound having two or more OH and —NH ₂ ). Examples of the polyisocyanate include tolylene diisocyanate, diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanate, tolidine diisocyanate, naphthalene diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, hydrogenated xylylene diisocyanate and dicyclohexylmethane diisocyanate. Further, as the polyol, polypropylene glycol and its modified product, polytetramethylene glycol and its modified product, polymer polyol (acrylonitrile / styrene radical-polymerized in polypropylene glycol), polyether polyamine, condensed polyester polyol, lactone system Polyester polyol, polycarbonate polyol, polybutadiene polyol, acrylic polyol,
Partially saponified ethylene-vinyl acetate copolymers, phenolic polyols, phosphorus-containing polyols, halogen-containing polyols and the like can be mentioned.

Polyamide resin is a resin synthesized by polycondensation of dicarboxylic acid and diamine, polycondensation of ω-aminocarboxylic acid, ring-opening polymerization of lactam composed of ω-aminocarboxylic acid, and the like. Polycondensation product of tetramethylenediamine and adipate (nylon 46), Ring-opening polymerization product of ε-caprolactam or ε-aminocaproic acid (nylon 6), Polycondensation product of hexamethylenediamine and adipate (nylon 66), Polycondensate of hexamethylenediamine and sebacate (nylon 610), Polycondensate of hexamethylenediamine and dodecanedioate (nylon 61)
2), a ring-opening polymer of ω-aminoundecanoic acid (nylon 11), a ring-opening polymer of ω-laurolactam or ω-aminododecanoic acid (nylon 12), and the like.

The polyester resin is a resin obtained by a polycondensation reaction between a dibasic acid or a dibasic acid ester and a dihydric alcohol and having an ester bond in the main chain. Dibasic acids include phthalic anhydride, isophthalic acid, terephthalic acid, succinic acid, succinic anhydride, adipic acid, azelaic acid, sebacic acid, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, tetrabromophthalic anhydride, tetrachloro Examples thereof include phthalic anhydride, het anhydride, endomethylenetetrahydrophthalic anhydride, maleic anhydride, fumaric acid and itaconic acid, and examples of dibasic acid esters include dimethyl terephthalate and dimethyl naphthalenedicarboxylate. As the dihydric alcohol, ethylene glycol, propylene glycol, 1,3-butylene glycol, 1,6-hexanediol, diethylene glycol, dipropylene glycol, neopentyl glycol, triethylene glycol, hydrogenated bisphenol A, bisphenol dihydroxypropyl ether, 1,4-butanediol, cyclohexane dimethanol, etc. are mentioned.

The polyacrylic acid resin is a resin mainly composed of a polymer of acrylic acid, methacrylic acid and a derivative thereof, and includes polymers such as methyl acrylate, ethyl acrylate, methyl methacrylate and acrylonitrile, and vinyl acetate. Also included are copolymers with vinyl chloride, styrene and the like.

The polyamino acid resin is a polymer obtained by polycondensing α-amino acids through peptide bonds. As the polyolefin resin, ethylene, propylene,
Olefin such as butene, butadiene, isoprene,
Examples thereof include homopolymers of diolefins such as pentadiene and copolymers composed of any combination thereof. Specifically, low density polyethylene, high density polyethylene, polypropylene, ethylene-propylene copolymer, polybutadiene, polyisoprene, etc. Is mentioned.

The epoxy resin is a polyfunctional epoxy compound and a polyvalent amine curing agent such as diethylenetriamine or diaminodiphenylmethane or bisphenol A.
A resin obtained by a polymerization reaction with a polyhydric phenol compound or a polyhydric alcohol compound such as, for example, bisphenol A type epoxy resin obtained from epichlorohydrin and bisphenol A, epichlorohydrin and a cycloaliphatic derivative such as cyclopentadiene Obtained cycloaliphatic epoxy resin, glycidyl amine type epoxy resin obtained from epichlorohydrin and hydantoin, epoxy resin obtained from polyvalent epoxy compound and polyvalent amine compound, obtained from polyvalent epoxy compound and polyvalent alcohol compound The epoxy resin etc. which are mentioned are mentioned.

These synthetic resins may be used as a mixture of two or more kinds in any combination.

(2) Polyvalent metal salt of alginic acid Alginic acid is one of polysaccharides, and is mannuronic acid and its isomer, glucuronic acid (C ₅ H ₉ O ₅ .COO).
It is a dehydrated polymer of H). Alginic acid is usually obtained by treating a sodium carbonate extract of dried seaweed with hydrochloric acid. The polyvalent metal salt of alginic acid of the present invention has a structure in which alginic acid is crosslinked with a polyvalent metal ion, and unlike alginic acid, it is insoluble in water. Further, the polyvalent metal salt of alginic acid may have a gel state simply by cross-linking with a polyvalent metal ion, but in the present invention, a granular material, preferably an average particle diameter measured by a laser light scattering method is It is desirable to prepare and use the particles (beads) of about 0.1 to 100 μm.

Such a polyvalent metal salt of alginic acid can be prepared, for example, by preparing an aqueous solution of a monovalent metal salt of alginic acid and an alkali metal such as sodium or potassium into fine particles by a spray drying method, an emulsion method or the like, and then adding the polyvalent metal salt. It can be obtained by immersing in an aqueous solution containing ions. In addition, an aqueous solution of the monovalent metal salt of alginic acid or one obtained by treating it with an acid is stirred in an aqueous solution having polyvalent metal ions, and then the insoluble matter is separated, dried and pulverized to obtain a granular material. Good.

Here, as the polyvalent metal salt, calcium, zinc, beryllium, magnesium, barium, cadmium, mercury, strontium, radium, lead, copper,
Examples thereof include metal salts with iron, aluminum, cobalt, nickel, chromium, manganese and the like. Among them, calcium alginate, zinc alginate, magnesium alginate and barium alginate are preferable, and calcium alginate is particularly preferable.

Calcium alginate is characterized by excellent breathability in water, and even when it absorbs moisture, there is almost no difference in shape and size. FIG. 1 shows the results of measuring the water respiration of calcium alginate beads. This is because the sample pre-dried in an atmosphere of 20% relative humidity was placed in an atmosphere of 95% relative humidity, the weight change was recorded, and when equilibrium was reached (the sample was placed in an atmosphere of 95% relative humidity). 100 hours after the start), the sample was moved again to a relative humidity atmosphere of 20%, and the change in weight was recorded. It can be seen that the calcium alginate beads have a higher water respiration property than silica gel, zeolite, or microcrystalline cellulose that is usually used as a granular filler.

2 and 3 show the particle size distribution of calcium alginate beads and cellulose fine particles (trade name AC powder, manufactured by Nisshinbo Industries Inc.) in the air and in water using a laser particle sizer for laser light scattering. It is the result measured by the method. It can be seen that the particle size of the calcium alginate beads is 35 μm in air and 38 μm in water, which is not much different from the value in air even in water (FIG. 2). On the other hand, regarding the cellulose fine particles, the average particle diameter in air is 40 μm,
The average particle size in water is 60 μm (FIG. 3).

As described above, the polyvalent metal salt of alginic acid of the present invention has both high water breathability and excellent dimensional stability when absorbing moisture, and by using this as a resin improving agent, dew condensation hardly occurs. A resin composition suitable for a film useful as a packaging material, a synthetic leather having a moist texture and texture, and the like can be obtained.

The amount of polyvalent metal alginate used in the present invention is 0.01 with respect to 100 parts by weight of the resin composition.
To 100 parts by weight, preferably 0.1 to 50 parts by weight, and more preferably 2 to 10 parts by weight. If the amount of the polyvalent metal salt of alginic acid is less than this range, there is no effect of adding the compound, and if it is more than this range, the physical properties inherent to the resin are impaired, which is not preferable.

(3) Cell-Forming Agent In the present invention, the surface layer may be made finer to improve the texture of the resin surface. In that case, a suitable cell-forming agent is added to the resin composition. Preferably.

As a method for making the surface layer finely porous,
Examples of commonly used methods include a wet method using a poor solvent or a dry method by heating, but the method is not particularly limited as long as the surface layer can be made finely porous. Listed below are the cell-forming agents used in the main methods of making microporous.

In the dry method by heating, a foaming agent is used. Such foaming agents include sodium bicarbonate, ammonium bicarbonate, ammonium carbonate, ammonium nitrite, sodium borohydride, azodicarbonamide,
Azobisformamide, azobisisobutyronitrile,
Barium azodicarboxylate, N, N'-dinitrosopentamethylenetetramine, N, N'-dinitroso-N, N
′ -Dimethylterephthalamide, benzenesulfonyl hydrazide, p-toluenesulfonyl hydrazide, p, p
′ -Oxybisbenzenesulfonyl hydrazide, p-toluenesulfonyl semicarbazide, 5-phenyl-1
H-tetrazole and the like can be mentioned. Of these, sodium bicarbonate, azodicarbonamide, azobisformamide, and N, N'-dinitrosopentamethylenetetramine are preferable.

In the wet method using a poor solvent, the solvent in the solution used also serves as a bubble forming agent. As the solvent used, water, fluorocarbons, chlorine compounds, petroleum hydrocarbons, esters, ketones, ethers,
Examples thereof include alcohols.

Among them, chlorine compounds include chloroform, carbon tetrachloride and dichlorobenzene; petroleum hydrocarbons include benzene, toluene, xylene, pyridine, hexane and petroleum ether; and esters include:
Ethyl acetate, methyl acetate; acetone as ketones;
Examples of ethers include diethyl ether; examples of alcohols include methanol, ethanol, propanol, butanol and the like. Of these, water, chloroform or dichlorobenzene is preferable.

Further, a deliquescent substance can be used as a bubble forming agent. That is, when a deliquescent substance is added to the resin and then washed with water, the deliquescent substance is eluted into water and the surface layer becomes finely porous. Examples of deliquescent substances include calcium chloride, sodium hydroxide,
Examples thereof include ferric chloride, potassium hydroxide, lithium hydroxide, etc., but calcium chloride is preferable.

The bubble forming agent is usually the synthetic resin 100 described above.
It is used in the range of 0.001 to 50 parts by weight with respect to parts by weight. If the amount of the bubble forming agent is less than 0.001 part by weight, the effect of addition is not obtained. Further, if it is used in an amount of more than 50 parts by weight, the resin strength becomes too low, which is not preferable.

(4) Other Additives The resin composition of the present invention further comprises known substances generally added to synthetic resins, that is, an antioxidant and a heat-resisting agent, in order to impart desired characteristics according to the purpose. Stabilizers, stabilizers such as UV absorbers, antistatic agents, flame retardants, lubricants, plasticizers and crystallization accelerators, crystal nucleating agents, antibacterial agents, and other inorganic or organic fillers for reinforcement, etc. It is also possible to mix. Further, it is of course possible to mix other synthetic resins than the above synthetic resins exemplified as the synthetic resin used in the present invention.

(5) Production of Resin Composition of the Present Invention The resin composition of the present invention is obtained by mixing a polyvalent metal salt of alginic acid with a synthetic resin in a dissolved state or a molten state under heating conditions. That is, in the mixing method in a dissolved state, to a synthetic resin or a monomer or prepolymer thereof dissolved in a predetermined solvent, a predetermined amount of powdered particles of a polyvalent metal alginate salt is added, and a mixer, a roll mill, a ball mill, or an atomizer. It is common to employ a method of kneading with a rotary kneader such as a lighter or sand grinder.

As for the melt mixing method under heating conditions, powders of alginic acid polyvalent metal salt are blended together with other components in predetermined amounts, and a Henschel type mixer, a V blender, a tumbler type mixer or the like is used. After premixing with a generally known mixer, this mixture is mixed with a single-screw kneader, a meshing direction rotating type, a non-meshing direction rotating type, a meshing direction rotating type, a non-meshing direction rotating type, etc. Biaxial kneader, calendar,
Melt kneading is generally performed by a continuous melt kneading method such as paste coating or a batch type melt kneading method such as roll or Banbury. The heating conditions at the time of melt kneading are not particularly limited, but usually 80 to 3
The temperature is 50 ° C, preferably 100 to 250 ° C.

There are no particular restrictions on the timing of addition of the polyvalent metal salt of alginic acid, and it may be added at any point during the method for producing the resin composition. For example, it may be added at the stage of a monomer or a prepolymer and used as it is for the polymerization.

(6) Molding of the resin composition of the present invention The resin composition of the present invention can be made into various molded articles according to a usual method for molding synthetic resins. Preferably, a film-like molded product such as a packaging material, a covering material, a clothing material, a non-woven material, a fibrous material for woven or knitted fabric, or a laminate obtained by coating or laminating on the surface of paper, non-woven fabric or the like. Used as a part of the body. The molded product of the resin composition of the present invention is excellent in moisture breathability, less likely to cause dew condensation, etc., and has high dimensional stability with little dimensional change due to changes in ambient humidity.

The molding method of the resin composition of the present invention is not particularly limited, and can be processed according to each purpose. For example, the molding method includes injection molding, extrusion molding, compression molding, sheet molding, lamination molding, hollow molding, vacuum molding, transfer molding, blow molding, calendar processing, casting processing, paste coating method, powder molding and the like. You can

The resin composition of the present invention can be preferably used as a material for synthetic leather. In the case of synthetic leather, on a support such as woven cloth, knitted cloth, paper, and non-woven fabric, a layer made of the resin composition of the present invention whose surface is made finely porous using the above-mentioned cell-forming agent or the like is applied or Laminated by a method such as laminating to form a natural leather-like surface layer. As the synthetic resin used for the surface layer of such synthetic leather,
Polyvinyl chloride, polyamide or polyurethane are preferred. Further, it is preferable that a finish layer of modified polyamide, polyurethane, polyacrylic acid derivative, polyamino acid blend, or the like is provided on the surface of these fine porous layers to give a leather pattern finish. The synthetic leather thus obtained is excellent in moisture breathability and has a moisturized and peculiar texture.

[0043]

EXAMPLES The present invention will be further described below with reference to examples. The evaluation method of water respiration in the following examples is as follows.

[Test Method for Moisture Respiration] From the sheet-like materials obtained in the following examples, 20 mm × 20 mm × 1 mm
The test piece was cut out and left overnight in an atmosphere of 20% relative humidity as an experimental sample. This experimental sample was left in an atmosphere of 95% relative humidity for 100 hours to measure the water absorption amount (95% RH) with respect to its own weight. Furthermore, after leaving the experimental sample in an atmosphere of 95% relative humidity for 100 hours, 2
The sample was allowed to stand in an atmosphere of 0% relative humidity for 100 hours to measure the water release content (20% RH) with respect to its own weight.

<Examples 1 to 3: Example of application to polyvinyl chloride resin> (1) Production of calcium alginate 700 kg of sodium alginate obtained from dried seaweed
The sodium alginate aqueous solution prepared by dissolving 10 times the amount of water in a cylinder was heated to 230 ° C. using a spray dryer (Niro, Mobilminor atomizer).
After spray-drying to form fine particles, the solution was brought into contact with a 20% calcium chloride aqueous solution to undergo ionic cross-linking to obtain 500 g of water-insoluble and spherical (average particle size 23 μm) calcium alginate beads (dry weight conversion). . What was spray-dried was used below as calcium alginate.

(2) Production of polyvinyl chloride resin sheet 100 parts by weight of polyvinyl chloride resin (PVC; average degree of polymerization = 1020) as a synthetic resin, 50 parts by weight of DOP (di-2-ethylhexyl phthalate) as a plasticizer, 1.5 parts by weight of azodicarbonamide as a cell-forming agent (foaming agent),
The amount of calcium alginate prepared above was added to the composition consisting of 3 parts by weight of Ba—Zn composite stabilizer (mixture of fatty acid salt of Ba and Zn and epoxy compound).

A paste-like product obtained by thoroughly kneading the above-mentioned compound at room temperature was preheated (130 ° C.) with a heating press.
After heating for 30 minutes), heat at 220 ℃ for 1 minute, 150
A sheet of mm × 150 mm × 1 mm was formed. A 20 mm × 20 mm × 1 mm test piece was cut out from the obtained sheet and used as a sample to evaluate water respiration. The evaluation results are shown in Table 1.

<Comparative Examples 1 and 2> The same operations and evaluations as in Examples 1 to 3 were carried out except that calcium alginate was not added (Comparative Example 1). Further, the same operations and evaluations as in Examples 1 to 3 were carried out except that collagen (collagen particles for synthetic leather having an average particle size of 7 μm) was added instead of calcium alginate in the amount shown in Table 1 (Comparative Example 2). . The evaluation results are shown in Table 1.

<Examples 4 to 6: Application example to polyurethane resin> Polyether polyol (average molecular weight = 300)
0) 100 parts by weight, 40 parts by weight of diphenylmethane diisocyanate (pure MDI), 3 parts by weight of water, 0.2 parts by weight of tertiary amine, 0.2 parts by weight of stannous octylate as a stabilizer, The amounts of calcium alginate produced in Examples 1 to 3 were blended as shown in Table 1. Premixed with a hot press (1
After that, it was heated at 180 ° C. for 15 minutes to form a sheet of 150 mm × 150 mm × 1 mm. 20 mm from the obtained polyurethane (PU) sheet
A test piece of × 20 mm × 1 mm was cut out and used as a sample to evaluate water respiration. The evaluation results are shown in Table 1.

<Comparative Examples 3 to 4> Similar to Comparative Examples 1 and 2, one without calcium alginate (Comparative Example 3) and one with collagen added in place of calcium alginate (Comparative Example) The same operations and evaluations as in Examples 4 to 6 were carried out except that the procedure (4) was replaced. Table 1 shows the evaluation results
Shown in.

<Examples 7 to 8: Example of application to polyolefin resin> 100 parts by weight of powdery low density polyethylene (LPDE; average degree of polymerization = 1300, average particle size = about 40 µm) was used as a viscosity reducing agent. 0.5 parts by weight of an aliphatic monocarboxylic acid condensate (trade name: Tirabazole H-40: manufactured by Taiyo Kagaku Co., Ltd.) and the amount of calcium alginate produced in Examples 1 to 3 shown in Table 1 were added. 1
The melt-kneaded product at 40 ° C was extruded from a T-die at 180 ° C using an extruder (manufactured by Toshiba Machine Co., Ltd.). A film having a width of 50 mm and a thickness of 100 μm was obtained, and a test piece of 20 mm × 20 mm was cut out from the film to give a sample, and the moisture respiration was evaluated in the same manner as in Examples 1 to 3. The evaluation results are shown in Table 2.

<Comparative Examples 5 to 6> In the same manner as in Comparative Examples 1 and 2, except that calcium alginate was not added (Comparative Example 5) and collagen was added instead of calcium alginate (Comparative Example 6). Operated and evaluated in the same manner as in Examples 7 to 8. The evaluation results are shown in Table 2.

<Examples 9 to 10: Application example to polyamino acid resin> Polyamino acid resin (PAA; average degree of polymerization = 20)
00) dimethylformamide solution (solid content 10%)
The amount of calcium alginate produced in Examples 1 to 3 was added to the above. The above formulations were mixed well and then cast on a glass plate. From this, 20mm
A test piece of × 20 mm × 1 mm was cut out and used as a sample to evaluate water respiration. The evaluation results are shown in Table 1.

Comparative Examples 7 to 8 Same as Examples 9 to 10 except that calcium alginate was not added (Comparative Example 7) and collagen was added instead of calcium alginate (Comparative Example 8). Was operated and evaluated.
The evaluation results are shown in Table 1.

<Examples 11 to 12: Application example to polyacrylic acid type resin> 100 parts by weight of a powder of polyacrylonitrile resin (PAN; average molecular weight 50000) was dissolved in 1000 parts by weight of dimethylformamide. The above-mentioned calcium alginate in the amount shown in Table 1 was added to this solution, stirred, and uniformly kneaded.

This solution was cast on a Teflon plate using a doctor knife coater. 8 hours at 60 ° C, then 8
It was dried under reduced pressure at 0 ° C. for 8 hours to obtain a film having a thickness of 130 μm. This was cut into 20 mm × 20 mm to prepare a sample, and the water respiration property was evaluated. The evaluation results are shown in Table 1.

<Comparative Examples 9 to 10> Examples 11 to 12 except that calcium alginate was not added (Comparative Example 9) and collagen was added instead of calcium alginate (Comparative Example 10). The same operation and evaluation were performed. The evaluation results are shown in Table 1.

<Examples 13 to 14: Application example to polyacrylic acid type resin> 30 g of an acrylic resin varnish (PA; trade name Hitaloid 1206, manufactured by Hitachi Chemical Co., Ltd.) having a solid content concentration of 50% was added with 10 g of ethyl acetate, It was mixed with 10 g of methyl isobutyl ketone, 10 g of isopropyl alcohol, 5 g of butyl cellosolve, 30 g of toluene, and 5 g of dioctyl phthalate. The calcium alginate was added to this mixed solution in an amount shown in Table 1 and mixed uniformly.

This solution was cast on a copper plate using a doctor knife coater and dried at 60 ° C. Coating thickness is 1
It was 00 μm. The film attached to the copper plate is cut together with the copper plate to obtain a 20 mm x 20 mm cutting plate, which is used as a sample.
Water respiration was evaluated. The evaluation results are shown in Table 1.

<Comparative Examples 11 to 12> Calcium alginate not added (Comparative Example 11) and collagen added in place of calcium alginate (Comparative Example 12)
The same operation as in Examples 13 to 14 except that
An evaluation was made. The evaluation results are shown in Table 1.

<Examples 15 to 16: Epoxy resin (E
Example of application to X)> 92 parts by weight of polyvalent epoxy compound (polyethylene glycol diglycidyl ether, n = 9, 262 WPE: trade name Denacol EX-830, manufactured by Nagase Kasei Co., Ltd.), and triethylenetetramine 8 as a curing agent Parts by weight were mixed. The calcium alginate was added to this mixed solution in the amount shown in Table 1. This solution was cast on a Teflon plate using a knife coater. This was heat-treated at 120 ° C. for 3 hours. The coating thickness is 100
was μm. The obtained film was peeled from the Teflon plate and cut into a size of 20 mm × 20 mm, which was used as a sample to evaluate water respiration. The evaluation results are shown in Table 1.

<Comparative Examples 13 to 14> Calcium alginate not added (Comparative Example 13) and collagen added in place of calcium alginate (Comparative Example 14)
The same operation as in Examples 15 to 16 except that
An evaluation was made. The evaluation results are shown in Table 1.

[0063]

[Table 1]

(Note 1) PVC: Polyvinyl chloride resin PU: Polyurethane resin LDPE: Low density polyethylene resin PAA: Polyamino acid resin PAN: Polyacrylonitrile resin PA: Acrylic resin EX: Epoxy resin (Note 2) Amount of improvement agent added PVC: Addition amount based on 100 parts by weight of PVC resin PU: Addition amount based on 100 parts by weight of polyol / MDI mixture LDPE: Addition amount based on 100 parts by weight of PAA: Addition amount based on 100 parts by weight of PAA PAN: Addition amount based on 100 parts by weight of PA PA: PA 100 parts by weight Addition amount to parts EX: Addition amount to 100 parts by weight of polyvalent epoxy compound / curing agent mixture

[0065]

EFFECT OF THE INVENTION The resin composition of the present invention has a high hygroscopic property under high humidity conditions and a good moisture releasing property under low humidity conditions.
Since it has an excellent water breathability, it is less likely to cause dew condensation when it is used as a film such as a packaging material, and exhibits good dimensional stability against changes in humidity. Further, due to its excellent moisture respiration property, it is useful as a material for synthetic leather because it gives a moist texture unique to leather when synthetic leather is used.

[Brief description of drawings]

FIG. 1 is a diagram showing a change in water content of each compounding agent with respect to a change in humidity for comparing the water respiration of calcium alginate of the present invention with silica gel, zeolite, and microcrystalline cellulose.

FIG. 2 is a graph showing changes in average particle diameter with respect to changes in humidity for examining the dimensional stability of calcium alginate of the present invention.

FIG. 3 is a diagram showing a change in average particle diameter of cellulose fine particles with respect to a change in humidity, for comparing the dimensional stability of calcium alginate of the present invention and cellulose fine particles (AC powder; manufactured by Nisshinbo Co., Ltd.).

[Explanation of symbols]

1 ... Curve showing water content of calcium alginate beads 2 ... Curve showing water content of silica gel 3 ... Curve showing water content of zeolite 4 ... Water content of microcrystalline cellulose Shown curve 5 ... Particle size distribution curve of calcium alginate beads measured in air 6 ... Particle size distribution curve of calcium alginate beads measured in water 7 ... Particle size distribution curve 8 of cellulose fine particles measured in air 8. ..Particle size distribution curve of cellulose fine particles measured in water

Front page continued (72) Inventor Hironobu Minami, Takaramachi Ichibansan No.3 Taiyo-Chemical Company, Yokkaichi, Mie Prefectural Research Institute (72) Inventor, Katsuyasu Nakata Takaramachi Ichiban No.3 Taiyo-Chemical Company, Yokkaichi, Mie (56) References JP-A-4-348165 (JP, A) JP-A-3-74445 (JP, A) (58) Fields investigated (Int.Cl. ⁷ , DB name) C08L 1/00 -101/16

Claims (8)

(57) [Claims] 1. A resin composition comprising 0.01 to 100 parts by weight of a polyvalent metal salt of alginic acid based on 100 parts by weight of a synthetic resin , wherein the polyvalent metal salt of alginic acid is
A resin composition which is a powder or granular material having a uniform particle size of 0.1 to 100 μm . 2. The synthetic resin is at least one selected from the group consisting of polyvinyl chloride, polyurethane resin, polyacrylic acid resin, polyamide resin, polyester resin, polyamino acid resin, polyolefin resin and epoxy resin. The resin composition according to claim 1. 3. The polyvalent metal salt of alginic acid is at least one selected from calcium alginate, zinc alginate, magnesium alginate and barium alginate.
The resin composition according to claim 1, which is a seed. 4. The resin composition according to claim 1, further comprising 0.001 to 50 parts by weight of a cell-forming agent with respect to 100 parts by weight of the synthetic resin. 5. The production of the resin composition according to claim 1, wherein 0.01 to 100 parts by weight of a polyvalent metal salt of alginic acid is added and mixed to 100 parts by weight of the molten or dissolved synthetic resin. Method. 6. A film for packaging or clothing using the resin composition according to claim 1. 7. Synthetic leather using the resin composition according to claim 1. 8. At least one synthetic resin 10 selected from polyvinyl chloride resin, polyurethane resin, polyamide resin, polyester resin, and polyamino acid resin.
With respect to 0 part by weight, a polyvalent metal salt of alginic acid 0.01 to
The synthetic leather according to claim 7, wherein a resin composition containing 100 parts by weight and 0.001 to 50 parts by weight of a cell forming agent is used.