US1972092A - Cellulose derivative composition - Google Patents
Cellulose derivative composition Download PDFInfo
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- US1972092A US1972092A US646298A US64629832A US1972092A US 1972092 A US1972092 A US 1972092A US 646298 A US646298 A US 646298A US 64629832 A US64629832 A US 64629832A US 1972092 A US1972092 A US 1972092A
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- 239000000203 mixture Substances 0.000 title description 37
- 229920002678 cellulose Polymers 0.000 title description 26
- 239000001913 cellulose Substances 0.000 title description 26
- 150000002148 esters Chemical class 0.000 description 30
- 239000002253 acid Substances 0.000 description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 9
- -1 n-decyl Chemical group 0.000 description 9
- 239000000020 Nitrocellulose Substances 0.000 description 7
- 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 description 7
- 229920001220 nitrocellulos Polymers 0.000 description 7
- 239000004014 plasticizer Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 240000008548 Shorea javanica Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000002843 carboxylic acid group Chemical group 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 229960001777 castor oil Drugs 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- PUFGCEQWYLJYNJ-UHFFFAOYSA-N didodecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCC PUFGCEQWYLJYNJ-UHFFFAOYSA-N 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 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
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PGIBJVOPLXHHGS-UHFFFAOYSA-N Di-n-decyl phthalate Chemical compound CCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCC PGIBJVOPLXHHGS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001279 adipic acids Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 150000003022 phthalic acids Chemical class 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- RLPSARLYTKXVSE-UHFFFAOYSA-N 1-(1,3-thiazol-5-yl)ethanamine Chemical compound CC(N)C1=CN=CS1 RLPSARLYTKXVSE-UHFFFAOYSA-N 0.000 description 1
- BAZVBVCLLGYUFS-UHFFFAOYSA-N 1-o-butyl 2-o-dodecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC BAZVBVCLLGYUFS-UHFFFAOYSA-N 0.000 description 1
- ULIJUDULYQTGKI-UHFFFAOYSA-N 6-decoxy-6-oxohexanoic acid Chemical compound CCCCCCCCCCOC(=O)CCCCC(O)=O ULIJUDULYQTGKI-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
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- HCQHIEGYGGJLJU-UHFFFAOYSA-N didecyl hexanedioate Chemical compound CCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCC HCQHIEGYGGJLJU-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- MZYHMUONCNKCHE-UHFFFAOYSA-N naphthalene-1,2,3,4-tetracarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(C(O)=O)C(C(O)=O)=C21 MZYHMUONCNKCHE-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000005336 safety glass Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- UYERRXOXXRNFHC-UHFFFAOYSA-N tridodecyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCC)CC(=O)OCCCCCCCCCCCC UYERRXOXXRNFHC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
Definitions
- This invention relates to cellulose derivative compositions, and more particularly, to such compositions including as plasticizers therefor organic polycarboxylic acid esters containing an esterified higher alkyl group.
- An object of the present invention is to provide cellulose derivative compositions of improved water resistance.
- a further object is to provide cellulose derivative compositions which are substantially permanently flexible, and having im- 115 proved durability.
- esters 20 of organic polycarboxylic acids at least one acid hydrogen atom of which has beenreplaced by'a normal saturated aliphatic radical containing from -15 carbon atoms, inclusive, as a plasticizer for the cellulose derivative.
- the invention contemplates within its'tscope the use of esters of any of the organic polycarboxylic acids, whether belonging to the aromatic or aliphatic series.
- One or more of the carboxylic hydrogen atoms is replaced by a normal saturated 80 aliphatic radical containing from 10-15 carbon atoms corresponding to the following listof alcoholsz n-decyl CmHziOH n-undecyl C11H23OH lauryL, CHHZBOH. n-tridecyl C13H27OH myristyl C14H29OH, n-pentadecyl C15H31OH.
- the esters may. contain only one of the" above listed alkyl groups and may contain a free car boxylic' acid group.
- an ester containing one normal saturated aliphatic group having 10-15 carbon atoms may have another carboxylic acid group esterified with any other alcohol.
- the invention includes the use of neutral esters of organic polycarboxylic' acids in which all of the carboxylic acid groups are esterified, such esters containingone or more
- the invention also includes the use of fled to yield the esters included within the present invention'may contain two or more carboxylic acid groups.
- organic acids are named as typical of those which may be used: orthophthalic, terephthalic, oxalic, succinic, adipic, ,maleic, fumaric, tartaric, malic, citric, quinolinic, vtrimesic, .pyromellitic, naphthalic, naphthalene tetracarboxylic, tricarballylic, hexahydrophthalic, hydroxy phthalic, uvitic, tetrachlorophthalic, sebacic, itaconic, and pimelic.
- esters are preferably made by bringing together the desired alcohols and acids (or where theanhydride of the polycarboxylic acid is available it may be used in lieu'of the acid) and then heating the mixture, preferably attemperatures above 100 C. so that the water produced by the esterification will boil oil and thus permit the reaction to go to completion.
- the removal of this water may be assisted'by adding to the esterification mixture a carrier liquid, such as benzene or toluene, which will distill out with the water at a temperature below 100 C., in which case the esterification may becarried on at a lower temperature than would otherwise be used.
- An inert gas, such as carbon dioxide may be continua ously passedthrough the reacting mixture to accomplislrthe same purpose, namely, to facilitate the removal of water.
- Example 1 r Parts Cellulose nitrate 100 Dilauryl phthalate 35
- Example 2 Parts Cellulose nitrate Dilauryl phthalateul 20 Tricresyl phosphate 15
- Example 3 I 7 Parts Cellulose acetate 100 Dilauryl phthalate 30 3
- Example 4 Parts Cellulose acetate 100 Dilauryl phthalate 20 Triacetin; 15
- Example 5 Parts Cellulose nitrate 100 Lauryl butyl phthalate 35
- Example 6 Parts Cellulose nitrate 100 Cyclohexyl decyl phthalate 35
- LACQUER COMPOSITIONS Example 7 v Parts Cellulose nitrate 12 Damar -1 3 Lauryl butyl adipate 4 Castor oil 2.6 Solvent 166.5
- Example 8 Parts Benzyl cellulose 4 D'ilauryl succinate 1 Hexyl caproate 1 Solvent 24
- Example 9 Parts Benzyl cellulose 4 Damarn 1 Didecyl adipate 1 Solvent r 24
- Example 10 Parts Cellulose nitrate 12.0 Damar 3.0 'Dilauryl 'adipate 4.0 Pigment 16.3 Castor oil 2.6 Solvent 161.6
- Example 11 Parts Cellulose nitrate 12 Damar 3 Didecyl phthalate 4 Castor -oil 2.6 Solvent -11. 166.5
- pigments may be included in these compositions.
- Thecellulose derivative compositions containing the esters described above may be used either as lacquersor as molding compositions, as shown in the above examples, or as dopes for use in the preparation of coated fabrics. In the case of the lacquers and the dopes, they may be applied by spraying, brushing; flowing, spreading under adoctor knife, or by other suitablemethodsof ap- 'plication. When used as molding compositions thin films which fin'd'use' as "strengthening layers They also can be pressed.
- the cellulose derivative compositions which may include esters or ethers, are characterized by the fact that they are exceptionally resistant to water, since the plasticizers used in these compositions areall esters of higher aliphatic alcohols having substantial Water resistance.
- the compositions are exceptionally durable and substantially permanently flexible, due to the use of the herein described esters as plasticizers. These esters have higher molecular weights than the commonly used plasticizers and, consequently, have higher boiling points and lower vapor pressures, properties which insure substantially permanent retention of the plasticizer in the cellulose derivative composition, and hence a flexible and durable product.
- the esters are satisfactorily compatible with cellulose derivatives and give compositions of exceptionally favorable properties.
- a composition of matter comprising a cellulose derivative and an ester of an organicpolycarboxylic acid, at least one acid hydrogen atom of, which has been replaced by the radical of a normal primary monohydric aliphatic alcohol.
- a composition of matter comprising a cellulose derivative and an neutral. ester of an organic polycarboxylic acid, at least one acid hydrogen atom of which has been replaced by the radical of a normal primary monohydric aliphatic alcohol containing from 10-15 carbon. atoms, inclusive..
- composition of matter comprising a cellulose derivative and an ester of. an organic polycarboxylic acid, eachof the acid hydrogen atoms.
- a composition. of matter comprising a cellulose derivative and an'ester of an organic dicarboxylic acid, at, least one acid. hydrogen atom oi which has been replaced by the radical of a. normal primary monohydric aliphatic alcohol j containing from 10-15 carbon atoms, inclusive.
- a compositionof. matter comprising a cellu-' lose derivative and a neutral ester. of. an' organic dicarbox-ylic acid,.at least one. acidhydrogen atom of which". hasbeen replaced by the. radical'oii' a normal. primary monohydric. aliphatic alcohol containing from.10-15 carbon. atoms, inclusive. l
- a composition of matter comprising. a cellulose derivative and an ester of an organic di'c'ar-, boxylic acid, each of the acid hydrogen atoms of which have been replaced by theradi'cal of a normal primary monohydric aliphatic alcohol containing from 10-15carbon atoms, inclusive.
- composition of matter comprising a cellu-' lose derivative and an ester of aphthalic acid
- composition of matter comprising a cellu monohydric aliphatic alcohol containing from 10-15 carbon atoms, inclusive.
- composition of matter comprising a cellulose derivative and an ester of a phthalic acid
- composition of matter comprising a cellulose derivative and a normal primary decyl phthalate.
- composition of matter comprising a cellulose derivative and di-normal primary decyl phthalate.
- a composition of matter comprising a cellulose derivative and an ester of adipic acid, at least one acid hydrogen atom of which has been replaced by the radical of a normal primary monohydric aliphatic alcohol containing from 10-15 carbon atoms, inclusive.
- composition of matter comprising a cellulose derivative and di-normal primary decyl adipate.
- composition of matter comprising a cellulose derivative and normal primary decyl cyclohexyl phthalate.
- a composition of matter comprising a cellulose derivativeand an ester of an organic dicarboxylic acid of the group consisting of phthalic and adipic acids, at least one acid hydrogen of which has been replaced by a normal primary, decyl radical.
- a composition of matter comprising a cellulose derivative and an ester of an organic dicarboxylic acid of the group consisting of phthalic and adipic acids, at least one acid hydrogen of which has been replaced by the radical of a normal primary monohydric alcohol containing from ten to fifteen carbon atoms, inclusive.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Patented Sept. 4,
PATENT OFFICE CELLULO SE DERIVATIVE COMPOSITION George De Witt Graves and Walter Eastby Lawson, Wflmington, Del., assignors to E. I. du Pont deNemourst Company, Wilmington, Del., a corporation of Delaware No Drawing. Application December 8, 1932,,
Serial No. 646,298
16 Claims.
This inventionrelates to cellulose derivative compositions, and more particularly, to such compositions including as plasticizers therefor organic polycarboxylic acid esters containing an esterified higher alkyl group. This application is a continuation in part of Graves and Lawson United States application'Serial No. 543,387, filed June 10, 1931, entitled Cellulose derivative compositions.
An object of the present invention is to provide cellulose derivative compositions of improved water resistance. A further object is to provide cellulose derivative compositions which are substantially permanently flexible, and having im- 115 proved durability. Other objects will be apparent from the description of the invention hereinafter given.
The above objects are accomplished according to the present invention by the use of esters 20 of organic polycarboxylic acids, at least one acid hydrogen atom of which has beenreplaced by'a normal saturated aliphatic radical containing from -15 carbon atoms, inclusive, as a plasticizer for the cellulose derivative. I
The invention contemplates within its'tscope the use of esters of any of the organic polycarboxylic acids, whether belonging to the aromatic or aliphatic series. One or more of the carboxylic hydrogen atoms is replaced by a normal saturated 80 aliphatic radical containing from 10-15 carbon atoms corresponding to the following listof alcoholsz n-decyl CmHziOH n-undecyl C11H23OH lauryL, CHHZBOH. n-tridecyl C13H27OH myristyl C14H29OH, n-pentadecyl C15H31OH.
The esters may. contain only one of the" above listed alkyl groups and may contain a free car boxylic' acid group. Alternatively, an ester containing one normal saturated aliphatic group having 10-15 carbon atoms, may have another carboxylic acid group esterified with any other alcohol. esters of polycarboxylic acids in which more than one acid hydrogen is replaced with a normal saturated aliphatic group having from 10-15 carbon.
atoms. Accordingly, the inventionincludes the use of neutral esters of organic polycarboxylic' acids in which all of the carboxylic acid groups are esterified, such esters containingone or more The invention also includes the use of fled to yield the esters included within the present invention'may contain two or more carboxylic acid groups. The following organic acids are named as typical of those which may be used: orthophthalic, terephthalic, oxalic, succinic, adipic, ,maleic, fumaric, tartaric, malic, citric, quinolinic, vtrimesic, .pyromellitic, naphthalic, naphthalene tetracarboxylic, tricarballylic, hexahydrophthalic, hydroxy phthalic, uvitic, tetrachlorophthalic, sebacic, itaconic, and pimelic.
These esters are preferably made by bringing together the desired alcohols and acids (or where theanhydride of the polycarboxylic acid is available it may be used in lieu'of the acid) and then heating the mixture, preferably attemperatures above 100 C. so that the water produced by the esterification will boil oil and thus permit the reaction to go to completion. The removal of this water may be assisted'by adding to the esterification mixture a carrier liquid, such as benzene or toluene, which will distill out with the water at a temperature below 100 C., in which case the esterification may becarried on at a lower temperature than would otherwise be used. An inert gas, such as carbon dioxide, may be continua ously passedthrough the reacting mixture to accomplislrthe same purpose, namely, to facilitate the removal of water.
The following examples are given to illustrate typical molding and lacquer cellulose derivative compositions employing the above described esters as plasticizers for the cellulose derivative:--
MOLDING COMPOSITIONS Example 1 r Parts Cellulose nitrate 100 Dilauryl phthalate 35 Example 2 Parts Cellulose nitrate Dilauryl phthalateul 20 Tricresyl phosphate 15 Example 3 I 7 Parts Cellulose acetate 100 Dilauryl phthalate 30 3 Example 4 Parts Cellulose acetate 100 Dilauryl phthalate 20 Triacetin; 15
Example 5 Parts Cellulose nitrate 100 Lauryl butyl phthalate 35 Example 6 Parts Cellulose nitrate 100 Cyclohexyl decyl phthalate 35 LACQUER COMPOSITIONS Example 7 v Parts Cellulose nitrate 12 Damar -1 3 Lauryl butyl adipate 4 Castor oil 2.6 Solvent 166.5
Example 8 Parts Benzyl cellulose 4 D'ilauryl succinate 1 Hexyl caproate 1 Solvent 24 Example 9 Parts Benzyl cellulose 4 Damarn 1 Didecyl adipate 1 Solvent r 24 Example 10 Parts Cellulose nitrate 12.0 Damar 3.0 'Dilauryl 'adipate 4.0 Pigment 16.3 Castor oil 2.6 Solvent 161.6
Example 11 Parts Cellulose nitrate 12 Damar 3 Didecyl phthalate 4 Castor -oil 2.6 Solvent -11. 166.5
polybasic acid or phenol-formaldehyde resins,
pigments, and the like, may be included in these compositions.
Not only dicarboxylic acid esters may beused,
as shown in the above compositions, but also tri- 'carboxylic, or higher polycarboxylic acid esters may be used, such as trilauryl citrate. Thecellulose derivative compositions containing the esters described above may be used either as lacquersor as molding compositions, as shown in the above examples, or as dopes for use in the preparation of coated fabrics. In the case of the lacquers and the dopes, they may be applied by spraying, brushing; flowing, spreading under adoctor knife, or by other suitablemethodsof ap- 'plication. When used as molding compositions thin films which fin'd'use' as "strengthening layers They also can be pressed.
for safety glass and in other applications where materials of this sort are regularly used.
The cellulose derivative compositions, which may include esters or ethers, are characterized by the fact that they are exceptionally resistant to water, since the plasticizers used in these compositions areall esters of higher aliphatic alcohols having substantial Water resistance. The compositions are exceptionally durable and substantially permanently flexible, due to the use of the herein described esters as plasticizers. These esters have higher molecular weights than the commonly used plasticizers and, consequently, have higher boiling points and lower vapor pressures, properties which insure substantially permanent retention of the plasticizer in the cellulose derivative composition, and hence a flexible and durable product. The esters are satisfactorily compatible with cellulose derivatives and give compositions of exceptionally favorable properties.
As many apparently widely different embodiments of this invention may be made without de-T parting from the spirit and scope thereof, it is to be understood that we do not limit ourselves to the specific embodiments thereof except as defined in the appended claims.
We claim;
1. A composition of matter comprising a cellulose derivative and an ester of an organicpolycarboxylic acid, at least one acid hydrogen atom of, which has been replaced by the radical of a normal primary monohydric aliphatic alcohol.
containing from 10-15 carbon atoms, inclusivelf 2. A composition of matter comprising a cellulose derivative and an neutral. ester of an organic polycarboxylic acid, at least one acid hydrogen atom of which has been replaced by the radical of a normal primary monohydric aliphatic alcohol containing from 10-15 carbon. atoms, inclusive..
3.,Acomposition of matter comprising a cellulose derivative and an ester of. an organic polycarboxylic acid, eachof the acid hydrogen atoms.
of whichv have beenreplaced by the radical of a normal primary monohydric aliphatic alcohol containing from. 10-15 carbon atoms, inclusive.
4. A composition. of matter comprising a cellulose derivative and an'ester of an organic dicarboxylic acid, at, least one acid. hydrogen atom oi which has been replaced by the radical of a. normal primary monohydric aliphatic alcohol j containing from 10-15 carbon atoms, inclusive.
5. A compositionof. matter comprisinga cellu-' lose derivative and a neutral ester. of. an' organic dicarbox-ylic acid,.at least one. acidhydrogen atom of which". hasbeen replaced by the. radical'oii' a normal. primary monohydric. aliphatic alcohol containing from.10-15 carbon. atoms, inclusive. l
6. A composition of matter comprising. a cellulose derivative and an ester of an organic di'c'ar-, boxylic acid, each of the acid hydrogen atoms of which have been replaced by theradi'cal of a normal primary monohydric aliphatic alcohol containing from 10-15carbon atoms, inclusive.
7'. A composition of matter comprising a cellu-' lose derivative and an ester of aphthalic acid,".at
least one acid'hydrogen atom of which has been I lose derivative and a neutral'ester offa phthalic acid; atleast one acid hydrogen atom of which has been replaced by the radical of 'anormalprimary 8. A composition of matter comprising a cellu monohydric aliphatic alcohol containing from 10-15 carbon atoms, inclusive.
9. A composition of matter comprising a cellulose derivative and an ester of a phthalic acid,
each of the acid hydrogen atoms of which have been replaced by the radical of a normal primary monohydric aliphatic alcohol containing from 10-15 carbon atoms, inclusive.
10. A composition of matter comprising a cellulose derivative and a normal primary decyl phthalate.
11. A composition of matter comprising a cellulose derivative and di-normal primary decyl phthalate.
12. A composition of matter comprising a cellulose derivative and an ester of adipic acid, at least one acid hydrogen atom of which has been replaced by the radical of a normal primary monohydric aliphatic alcohol containing from 10-15 carbon atoms, inclusive.
13. A composition of matter comprising a cellulose derivative and di-normal primary decyl adipate.
14. A composition of matter comprising a cellulose derivative and normal primary decyl cyclohexyl phthalate.
15. A composition of matter comprising a cellulose derivativeand an ester of an organic dicarboxylic acid of the group consisting of phthalic and adipic acids, at least one acid hydrogen of which has been replaced by a normal primary, decyl radical.
16. A composition of matter comprising a cellulose derivative and an ester of an organic dicarboxylic acid of the group consisting of phthalic and adipic acids, at least one acid hydrogen of which has been replaced by the radical of a normal primary monohydric alcohol containing from ten to fifteen carbon atoms, inclusive.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US646298A US1972092A (en) | 1932-12-08 | 1932-12-08 | Cellulose derivative composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US646298A US1972092A (en) | 1932-12-08 | 1932-12-08 | Cellulose derivative composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1972092A true US1972092A (en) | 1934-09-04 |
Family
ID=24592512
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US646298A Expired - Lifetime US1972092A (en) | 1932-12-08 | 1932-12-08 | Cellulose derivative composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1972092A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2420381A (en) * | 1943-02-23 | 1947-05-13 | Emery Industries Inc | Plasticized zein composition |
| US2460574A (en) * | 1945-04-05 | 1949-02-01 | Goodrich Co B F | Vinyl chloride polymers plasticized with dialkyl chlorophthalates |
| US2510915A (en) * | 1946-05-18 | 1950-06-06 | Hercules Powder Co Ltd | Hydrogenated condensate of 10-hendecenoic acid and maleic anhydride and esters thereof |
-
1932
- 1932-12-08 US US646298A patent/US1972092A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2420381A (en) * | 1943-02-23 | 1947-05-13 | Emery Industries Inc | Plasticized zein composition |
| US2460574A (en) * | 1945-04-05 | 1949-02-01 | Goodrich Co B F | Vinyl chloride polymers plasticized with dialkyl chlorophthalates |
| US2510915A (en) * | 1946-05-18 | 1950-06-06 | Hercules Powder Co Ltd | Hydrogenated condensate of 10-hendecenoic acid and maleic anhydride and esters thereof |
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