US1710078A - Cellulose-nitrate plastic - Google Patents
Cellulose-nitrate plastic Download PDFInfo
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- US1710078A US1710078A US477931A US47793121A US1710078A US 1710078 A US1710078 A US 1710078A US 477931 A US477931 A US 477931A US 47793121 A US47793121 A US 47793121A US 1710078 A US1710078 A US 1710078A
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- Prior art keywords
- solvent
- softener
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- pyroxylin
- cellulose
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- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 title description 29
- 229920001220 nitrocellulos Polymers 0.000 title description 28
- 239000000020 Nitrocellulose Substances 0.000 title description 16
- 239000004033 plastic Substances 0.000 title description 3
- 229920003023 plastic Polymers 0.000 title description 3
- 239000002904 solvent Substances 0.000 description 50
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 20
- 229940079938 nitrocellulose Drugs 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 229960002380 dibutyl phthalate Drugs 0.000 description 10
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 230000007935 neutral effect Effects 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 239000004264 Petrolatum Substances 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 239000002649 leather substitute Substances 0.000 description 6
- 229940066842 petrolatum Drugs 0.000 description 6
- 235000019271 petrolatum Nutrition 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- YZBOVSFWWNVKRJ-UHFFFAOYSA-N Monobutylphthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(O)=O YZBOVSFWWNVKRJ-UHFFFAOYSA-N 0.000 description 4
- 238000004049 embossing Methods 0.000 description 4
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- IPKKHRVROFYTEK-UHFFFAOYSA-N dipentyl phthalate Chemical compound CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCC IPKKHRVROFYTEK-UHFFFAOYSA-N 0.000 description 2
- 229940067592 ethyl palmitate Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- QDSSWFSXBZSFQO-UHFFFAOYSA-N 2-amino-6-ethyl-1h-pyrimidin-4-one Chemical compound CCC1=CC(=O)N=C(N)N1 QDSSWFSXBZSFQO-UHFFFAOYSA-N 0.000 description 1
- JEABIFHLYSDNRJ-UHFFFAOYSA-N 2-o-butyl 1-o-ethyl benzene-1,2-dicarboxylate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC JEABIFHLYSDNRJ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- -1 ethyl palmitate Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000005908 glyceryl ester group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/16—Esters of inorganic acids
- C08L1/18—Cellulose nitrate, i.e. nitrocellulose
Definitions
- This invention pertains to cellulose nitrate compositions containing a composite softener, and relates particularly to the manufacture of artificial leather of which films or layers of pyroxylin constitute an essential art.
- One object of my invention is to improve on modifiers or softeners for films or other cellulose nitrate plastics.
- Another object of my invention is to provide cellulose nitrate compositions which can be used as a coating on woven fabrics to produce artificial leather or fabrikoid having great durability and pliability.
- softener I mean a material of such low volatility that said material will remain for a long period as a constitutent of the pyroxylin coating or-film of which it originally formed a part. I have found it convenient to divide the softeners for cellu-' lose nitrate into two main classes, viz, solvent softeners and non-solvent softeners.
- solvent softeners as their name implies, have a substantial solvent action on cellulose nitrate, whereas the nonsolvent sof teners are practically devoid of any such action.
- solvent action of the solvent softeners is an action which is effective at ordinary temperatures, that is, temperatures between 10 and 0., with the result that the pliability of a cellulose nitrate film contain ing said softener is substantially increased at ordinary atmospheric temperatures.
- These solvent softeners which form one element'of 35 my invention, may be described as active solvents to distinguish them from the so-called latent solvents.
- the softener commonly used at the present time in artificial leather is castor oil, a nonsolvent for cellulose nitrate.
- Various other vegetable oils, all non-solvent softeners, have also been suggested for this purpose.
- esters of higher aliphatic acids For the non-solvent softener, I have found it advantageous to use a member of a class of substances which may be generically designated esters of higher aliphatic acids.
- this class of substances there may be cited certain vegetable oils such as castor oil,- blowncottonseed oil, and preferably the oils with a low iodine number such as blown or unblown cocoanut oil, all of these oils being composed chiefly of glyceryl esters of higher aliphatic acids; and there may also be cited the synthetic esters such as ethyl palmitate, the glycol esters of the fatty acids .the relatively non-volatile aromatic esters, as
- triphenyl phosphate ortho-, meta-, or para-tricresyl phoshate, and orthometaor para-cresyl esters of cocoanut oil acids and (2) esters of aromatic acids such as neutral phthalic acid esters of alcohols having from 2 to 6 carbon atoms, benzyl benzoate and amyl cinnamate.
- Suitable phthalic esters are ethyl butyl phthalate, dibutyl phthalate and diamyl phthalate.
- a solvent softener other than an aromatic ester there may be cited xylene-sub phon-methylamid. 1 a
- the ratio of solvent softener to non-solvent softener used in practising my invention may vary within wide limits, depending not only upon the conditions to which the film or artificial leather is to be subjected, but also upon the particular substances employed as softeners. In any case, sufficient non-solvent softener is incorporated in the composition to mask or overcome the stickiness caused by the solvent softener.
- the ratio of pyroxylin to total softener will ordinarily be between 1 to 0.75 and 1 to 2.0.
- a solvent softener which I have found to be especially valuable as an element of a composite softener is di-(normal) butyl phthalate. This substance may be produced in the following way:
- phthalic anhydride Three parts by weight of phthalic anhydride are added to 3 parts of normal butyl alcohol (B. P. 115-117. C.) and the mixture heated to 117 C. for eight hours. This completes the first reaction with the formation of mono-butyl phthalate which remains dissolved in the excess alcohol. Three percent by weight ofdry hydrogen chloride is dissolved in the mixture, which is heated to 117 for eight hours. The second reaction is accompanied by the separation of a layer of water. This is separated and the heating continued for an additional eight hours. The resulting liquid product is first washed with water to remove the hydrochloric acid; then with strong sodium carbonate to remove the monobutyl phthalate and any free .phthalic acid; and finally with water several times until neutral.
- the di-butyl hthalate is purified from alcohol and dried y passing a current of air through the liquid heated to 160 C.
- the product is a liquid, odorless, slightly yellow in color and may be obtained water white by distilling under diminished pressure.
- the yield is 83.6% of the theoretical. Boiling point under 29 mm. pressure is 210 C.
- Tricresyl phosphate Q parts Ethyl palmitate 15 parts Liquid petrolatum 10 parts Pyroxy 100 parts Excellent results may be obtained with a mixture containing 40 to 50 parts of dibutyl phthalate and from about 60 to 50 parts of cocoanut oil plus liquid petrolatum, for each 100 parts of pyroxylin.
- the mixtures covered by the above examples are dissolved in a suitable solvent, such as a mixture ofequal parts of ethyl acetate and benzone, and theresulting solution is then applied to a fabric and the solvent'allowed to I evaporate.
- a suitable solvent such as a mixture ofequal parts of ethyl acetate and benzone
- ' iszto act as a lubricant to preveht the surface film of pyroxylin from sticking to the embossing roll during the embossing operation.
- I pr ferably use the solvent softener alone in the base coats of the artificialleather goods a d the combination of solvent and non-solvent softener in the upper (i. e. exterior) coat or coats only.
- the non-solvent softener in the exterior coat will prevent adhesion of the pyroxylin surface to the embossing roll, while the large proportion of solvent softener in the base coats will render the coated fabric exceedingly pliable.
- Another advantage of a mixture of a solvent softener with a non-solvent softener is that the tendency toward exudation displayed by a non-solvent softener is very much reduced by the presence of the solvent softener.
- a solvent softener is practically non-exuding, so that the ratio of non-solvent softener to solvent softener will be determined in some cases by the requirements to be met in regard to avoiding exudation,
- a pyroxylin'coated fabric suitable for embossing may be prepared, for example, by applying two base coats in which the softener is composed of dibutyl phthalate, the ratio of pyroxylin to softener being 10 to 8 and then applying two additional coats having a composition such as that set forth in any one of the above examples numbered I to VI.
- liquid petrolatum is used in conjunction with another non-solvent softener; the main reason for this is as follows: In attempting to use liquid petrolatum'alone as a lubricant it was soon found that enough of this lubricant could not be added to give the necessary absence of stickiness without causing precipitation of the pyroxylin. I then discovered that this difficulty could be overcome by adding a non-volatile neutral ester of phthalic acid,
- a product comprising cellulose nitrate, a non-volatile neutral butyl ester of .phthalic acid, and a non-solvent softener.
- a product comprising cellulose nitrate, dibutyl phthalate, and a non-solvent softener.
- a product comprising cellulose nitrate
- a product comprising cellulosenitrate, a non-volatile neutral ester of phthalic acid, and a non-solvent softener comprising an ester of a higher aliphatic acid.
- a product comprising cellulose nitrate, from about 5 to 10 parts of a non-volatile neutral butyl ester of hthalic acid, and about and a non-solvent softener comprising an 100 parts of a non-so vent softener comprisester of a higher ali hatic acid and a noning an ester of a higher aliphatic acid. volatile oily paraflin ydrocarbon.
- a product comprising cellulose nitrate 9.
- a product comprising cellulose nitrate, In testimony whereof I afiix my si ature. 10 a non-volatile neutral ester of phthalic acid, GEORGE L. SCHWA TZ.
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Description
Patented Apr. 23, 1929.
UNITED STATES PATENT OFFICE.-
GEORGE L. SCHWARTZ, OF WILMINGTON, DELAWARE, ASSIGNOR TO E. I. DU FONT DE NEMOURS & COMPANY, OF WILMINGTON, DELAWARE, A CORPORATION OF DELA- WARE.
CELLULOSE-NITRATE PLASTIC.
N Drawing.
This invention pertains to cellulose nitrate compositions containing a composite softener, and relates particularly to the manufacture of artificial leather of which films or layers of pyroxylin constitute an essential art.
One object of my invention is to improve on modifiers or softeners for films or other cellulose nitrate plastics.
Another object of my invention is to provide cellulose nitrate compositions which can be used as a coating on woven fabrics to produce artificial leather or fabrikoid having great durability and pliability.
By the term softener I mean a material of such low volatility that said material will remain for a long period as a constitutent of the pyroxylin coating or-film of which it originally formed a part. I have found it convenient to divide the softeners for cellu-' lose nitrate into two main classes, viz, solvent softeners and non-solvent softeners.
The solvent softeners, as their name implies, have a substantial solvent action on cellulose nitrate, whereas the nonsolvent sof teners are practically devoid of any such action. This. solvent action of the solvent softeners is an action which is effective at ordinary temperatures, that is, temperatures between 10 and 0., with the result that the pliability of a cellulose nitrate film contain ing said softener is substantially increased at ordinary atmospheric temperatures. These solvent softeners, which form one element'of 35 my invention, may be described as active solvents to distinguish them from the so-called latent solvents.
The softener commonly used at the present time in artificial leather is castor oil, a nonsolvent for cellulose nitrate. Various other vegetable oils, all non-solvent softeners, have also been suggested for this purpose. Solvent softeners in general ten-d to impart greater flexibility to pyroxylin films than do non-solvent softeners, but the difliculty encountered in using them is that they render the film so sticky that it cannot be satisfactorily embossed. 7
I have now discovered that the objectionable stickiness caused by the solvent softener may be overcome, and at the same time a substantial increase in pliability obtained, by using the solvent softener in combination with a non-solvent softener.
Application filed June 16, 1921,
For the non-solvent softener, I have found it advantageous to use a member of a class of substances which may be generically designated esters of higher aliphatic acids. As
examples of this class of substances there may be cited certain vegetable oils such as castor oil,- blowncottonseed oil, and preferably the oils with a low iodine number such as blown or unblown cocoanut oil, all of these oils being composed chiefly of glyceryl esters of higher aliphatic acids; and there may also be cited the synthetic esters such as ethyl palmitate, the glycol esters of the fatty acids .the relatively non-volatile aromatic esters, as
for example, (1) triphenyl phosphate ortho-, meta-, or para-tricresyl phoshate, and orthometaor para-cresyl esters of cocoanut oil acids, and (2) esters of aromatic acids such as neutral phthalic acid esters of alcohols having from 2 to 6 carbon atoms, benzyl benzoate and amyl cinnamate. Suitable phthalic esters are ethyl butyl phthalate, dibutyl phthalate and diamyl phthalate. As an instance of a solvent softener other than an aromatic ester there may be cited xylene-sub phon-methylamid. 1 a
The ratio of solvent softener to non-solvent softener used in practising my invention may vary within wide limits, depending not only upon the conditions to which the film or artificial leather is to be subjected, but also upon the particular substances employed as softeners. In any case, sufficient non-solvent softener is incorporated in the composition to mask or overcome the stickiness caused by the solvent softener.
The ratio of pyroxylin to total softener will ordinarily be between 1 to 0.75 and 1 to 2.0.
A solvent softener which I have found to be especially valuable as an element of a composite softener is di-(normal) butyl phthalate. This substance may be produced in the following way:
Three parts by weight of phthalic anhydride are added to 3 parts of normal butyl alcohol (B. P. 115-117. C.) and the mixture heated to 117 C. for eight hours. This completes the first reaction with the formation of mono-butyl phthalate which remains dissolved in the excess alcohol. Three percent by weight ofdry hydrogen chloride is dissolved in the mixture, which is heated to 117 for eight hours. The second reaction is accompanied by the separation of a layer of water. This is separated and the heating continued for an additional eight hours. The resulting liquid product is first washed with water to remove the hydrochloric acid; then with strong sodium carbonate to remove the monobutyl phthalate and any free .phthalic acid; and finally with water several times until neutral. The di-butyl hthalate is purified from alcohol and dried y passing a current of air through the liquid heated to 160 C. The product is a liquid, odorless, slightly yellow in color and may be obtained water white by distilling under diminished pressure. The yield is 83.6% of the theoretical. Boiling point under 29 mm. pressure is 210 C.
A few of the specific softener compositions which may be used in accordance with my invention may be tabulated follows:
I. Castor oil 100 parts Di(normal) butyl phthalate 5 to 10parts Pyroxylin parts II. Blown cottonseed oil 100 parts Dibutyl phthalate 6 parts Pyroxylin -4 53 parts III. IV. V. Dibutyl phthalate: 80. 60 45 parts Ethyl palmjtate 25 parts Liquid petrolatum; 20 15 15 parts Cocoanut oil 40 parts Pyroxylln 100 -100 100 parts VI. Tricresyl phosphate Q parts Ethyl palmitate 15 parts Liquid petrolatum 10 parts Pyroxy 100 parts Excellent results may be obtained with a mixture containing 40 to 50 parts of dibutyl phthalate and from about 60 to 50 parts of cocoanut oil plus liquid petrolatum, for each 100 parts of pyroxylin. As will be evident from the above exam ples, the smaller the ratio of solvent, to nonsolvent, softener, the greater is the ratio of total ,softener to pyroxylin./
As will be understood bythose' skilled in the art of making artificial leather, the mixtures covered by the above examples are dissolved in a suitable solvent, such as a mixture ofequal parts of ethyl acetate and benzone, and theresulting solution is then applied to a fabric and the solvent'allowed to I evaporate.
As has been indicated above, the chief function of the non-solvent softener, when a relatively large amount of solvent softener is used,
' iszto act as a lubricant to preveht the surface film of pyroxylin from sticking to the embossing roll during the embossing operation.
In order to obtain the maximum pliability through the use of a solvent softener, I pr ferably use the solvent softener alone in the base coats of the artificialleather goods a d the combination of solvent and non-solvent softener in the upper (i. e. exterior) coat or coats only. The non-solvent softener in the exterior coat will prevent adhesion of the pyroxylin surface to the embossing roll, while the large proportion of solvent softener in the base coats will render the coated fabric exceedingly pliable.
Another advantage of a mixture of a solvent softener with a non-solvent softener is that the tendency toward exudation displayed by a non-solvent softener is very much reduced by the presence of the solvent softener. A solvent softener is practically non-exuding, so that the ratio of non-solvent softener to solvent softener will be determined in some cases by the requirements to be met in regard to avoiding exudation,
A pyroxylin'coated fabric suitable for embossing may be prepared, for example, by applying two base coats in which the softener is composed of dibutyl phthalate, the ratio of pyroxylin to softener being 10 to 8 and then applying two additional coats having a composition such as that set forth in any one of the above examples numbered I to VI.
It will be noted that in Examples III to VI, the liquid petrolatum is used in conjunction with another non-solvent softener; the main reason for this is as follows: In attempting to use liquid petrolatum'alone as a lubricant it was soon found that enough of this lubricant could not be added to give the necessary absence of stickiness without causing precipitation of the pyroxylin. I then discovered that this difficulty could be overcome by adding a non-volatile neutral ester of phthalic acid,
and a non-solvent softener.
'2. A product comprising cellulose nitrate, a non-volatile neutral butyl ester of .phthalic acid, and a non-solvent softener.
3. A product comprising cellulose nitrate, dibutyl phthalate, and a non-solvent softener.
4. A product comprising cellulose nitrate,
di-(normal) butyl phthalate, and a non-solvent softener. v
5. A product comprising cellulosenitrate, a non-volatile neutral ester of phthalic acid, and a non-solvent softener comprising an ester of a higher aliphatic acid.
6. A product comprising cellulose nitrate, from about 5 to 10 parts of a non-volatile neutral butyl ester of hthalic acid, and about and a non-solvent softener comprising an 100 parts of a non-so vent softener comprisester of a higher ali hatic acid and a noning an ester of a higher aliphatic acid. volatile oily paraflin ydrocarbon.
7. A product comprising cellulose nitrate, 9. A product comprising cellulose nitrate,
6 a solvent softener, and a non-solvent softener from 40 to 50 parts of dibutyl phthalate, and 10 comprising an ester of a higher aliphatic acid from 6" to 50 parts of a non-solvent softener and a non-volatile oily saturated hydrocarcomprisin an ester ofahigher aliphatic acid bon. plus liqui petrolatum.
8. A product comprising cellulose nitrate, In testimony whereof I afiix my si ature. 10 a non-volatile neutral ester of phthalic acid, GEORGE L. SCHWA TZ.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US477931A US1710078A (en) | 1921-06-16 | 1921-06-16 | Cellulose-nitrate plastic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US477931A US1710078A (en) | 1921-06-16 | 1921-06-16 | Cellulose-nitrate plastic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1710078A true US1710078A (en) | 1929-04-23 |
Family
ID=23897904
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US477931A Expired - Lifetime US1710078A (en) | 1921-06-16 | 1921-06-16 | Cellulose-nitrate plastic |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1710078A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2481687A (en) * | 1946-03-30 | 1949-09-13 | Eastman Kodak Co | Hot melt coating composition |
-
1921
- 1921-06-16 US US477931A patent/US1710078A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2481687A (en) * | 1946-03-30 | 1949-09-13 | Eastman Kodak Co | Hot melt coating composition |
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