US2227495A - Method for producing delustered rayon - Google Patents
Method for producing delustered rayon Download PDFInfo
- Publication number
- US2227495A US2227495A US267453A US26745339A US2227495A US 2227495 A US2227495 A US 2227495A US 267453 A US267453 A US 267453A US 26745339 A US26745339 A US 26745339A US 2227495 A US2227495 A US 2227495A
- Authority
- US
- United States
- Prior art keywords
- viscose
- rayon
- ether
- terpene
- delusterant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920000297 Rayon Polymers 0.000 title description 81
- 239000002964 rayon Substances 0.000 title description 32
- 238000004519 manufacturing process Methods 0.000 title description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 75
- 235000007586 terpenes Nutrition 0.000 description 31
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- 239000002932 luster Substances 0.000 description 28
- 239000000203 mixture Substances 0.000 description 26
- 150000003505 terpenes Chemical class 0.000 description 24
- 238000000034 method Methods 0.000 description 19
- 238000009987 spinning Methods 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000002480 mineral oil Substances 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- 235000010446 mineral oil Nutrition 0.000 description 12
- 239000000049 pigment Substances 0.000 description 12
- -1 terpene compound Chemical class 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000010665 pine oil Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 241000779819 Syncarpia glomulifera Species 0.000 description 4
- 238000004061 bleaching Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000001739 pinus spp. Substances 0.000 description 4
- 229940036248 turpentine Drugs 0.000 description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 238000005054 agglomeration Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 150000002170 ethers Chemical class 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
- 238000002156 mixing Methods 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 229960004418 trolamine Drugs 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- 229930006727 (-)-endo-fenchol Natural products 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- GQVMHMFBVWSSPF-SOYUKNQTSA-N (4E,6E)-2,6-dimethylocta-2,4,6-triene Chemical compound C\C=C(/C)\C=C\C=C(C)C GQVMHMFBVWSSPF-SOYUKNQTSA-N 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- KUKRLSJNTMLPPK-UHFFFAOYSA-N 4,7,7-trimethylbicyclo[2.2.1]hept-2-ene Chemical group C1CC2(C)C=CC1C2(C)C KUKRLSJNTMLPPK-UHFFFAOYSA-N 0.000 description 1
- GLVKGYRREXOCIB-UHFFFAOYSA-N Bornylene Natural products CC1CCC(C(C)(C)C)C=C1 GLVKGYRREXOCIB-UHFFFAOYSA-N 0.000 description 1
- IAIHUHQCLTYTSF-MRTMQBJTSA-N Fenchyl alcohol Chemical compound C1C[C@]2(C)[C@H](O)C(C)(C)[C@H]1C2 IAIHUHQCLTYTSF-MRTMQBJTSA-N 0.000 description 1
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 229940088601 alpha-terpineol Drugs 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 229930006739 camphene Natural products 0.000 description 1
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
- GQVMHMFBVWSSPF-UHFFFAOYSA-N cis-alloocimene Natural products CC=C(C)C=CC=C(C)C GQVMHMFBVWSSPF-UHFFFAOYSA-N 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- IAIHUHQCLTYTSF-UHFFFAOYSA-N fenchyl alcohol Natural products C1CC2(C)C(O)C(C)(C)C1C2 IAIHUHQCLTYTSF-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000005404 monopole Effects 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000010494 opalescence Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical group O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229930004725 sesquiterpene Natural products 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 229930006978 terpinene Natural products 0.000 description 1
- 150000003507 terpinene derivatives Chemical class 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- IHPKGUQCSIINRJ-UHFFFAOYSA-N β-ocimene Natural products CC(C)=CCC=C(C)C=C IHPKGUQCSIINRJ-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
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
Definitions
- This invention relates to a method of producing rayon and more particularly it relates to an improved method of producing rayon having a low luster.
- Rayon having a subdued luster may be made by several methods.
- a pigment usually titanium dioxide, is incorporated in the spinning solution. This method is fairly effective in producing yarns of reduced luster, but 10 for yarns of very low luster, the quantity of pigment required is such that the yarn is weakened appreciably and the solution has an abrasive action on the spinning orifice.
- yarns delustered by pigments regain their luster upon being dyed to a dark color since the pigment has little efiect upon the smoothness of the filament surface.
- an immiscible liquid is dispersed in the spinning solution, and the rayon is spun and finished in substantially the usual manner.
- This method of delustering depends for its efiect on the roughness produced in the surface of the filament and is thus effective on dark or light yarns.
- Refined mineral oil may be used as the delusterant.
- dispersions in viscose are unstable; the particles agglomerate and produce breaks or weak spots in the filament. For this reason, it is very diflicult to produce low denier filaments from Viscose containing mineral oil as the delustering agent. Pine oil, which forms more stable dispersions in viscose, may be used to overcome this disadvantage.
- pine oil delusters only partially to a pearly opalescence rather than to a completely dull state and furthermore it has a persistent residual odor which is difficult to remove.
- Mineral and pine oil both impart a slightly yellowish cast to rayon in which they are used as delusterants.
- the terpene ether utilized in the delusterant composition in the improved method of this invention is characterized by containing an ether linkage connecting a terpenic group with a second group. It may be prepared by the etherification of the hydroxyl group of a terpene alcohol with another alcohol, or it may be prepared by the direct addition of an alcohol at a double bond of an unsaturated terpenic group of a terpene compound.
- the alcohol used as an etherifying agent may be, for example, methyl, ethyl, propyl, butyl, amyl, beta-chloroethyl, chloropropyl, isopropyl, isobutyl, secondary butyl, furiuryl, tetrahydrofurfuryl, benzyl alcohol, the monomethyl or monoethyl ether of ethylene glycol or of diethylene glycol, and so forth.
- the alcohol may be dihydric, for example, ethylene glycol, diethylene glycol, propylene glycol, etc., which allows two terpenic groups to form ether linkages to the alcoholic group, if this is desired.
- the terpene alcohol used to prepare the terpene ether may be any terpene alcohol having a reactive hydroxyl group, such as, for example, alpha-terpineol, borneol, fenchyl alcohol, etc. Crude cuts rich in such terpene alcohols or mixtures thereof, pine oil for example, may likewise be etherified.
- the unsaturated terpene compounds used to prepare the terpene ether by the addition of an alcohol at a double bond may be, for example pinene in alpha or beta form, dipentene, terpinene terpinolene, camphene, bornylene, myrcene, allo-ocimene, sesqui terpenes, polyterpenes, etc.
- Crude mixtures, i. e. terpene cuts such as turpentine, for example, may be used and in general it is not essential that the resulting crude other be highly purified for use in the method according to this invention.
- the ether formed by the addition of methyl alcohol to pinene may be made by reacting methyl alcohol with turpen time.
- the ether of a terpene or terpene compound and an alcohol is termed herein and in the claims, for convenience, a terpene ether.
- one or more terpene ethers is introduced into the viscose prior to the spinning thereof.
- the terpene ether may be dispersed directly in the viscose or it may be added to the sodium hydroxide, water, and cellulose xanthate mixture used to make the viscose.
- the substance may first be emulsified in Water and the emulsion then mixed with the viscose or its ingredients.
- emulsifying agents such as, for example, sodium oleate, sulphonated vegetable oils, Turkey red oil, Monopole oil, synthetic wetting agents, etc., may be used to aid in preparing such an emulsion.
- the dispersed particles of the delusterant composition are very small in size, say below 5 or 6 microns.
- the quantity of delusterant substance added depends upon the degree of luster desired for the rayon. Luster decreases as the quantity of delusterant substance is increased.
- the quantity of terpene ether or ethers utilized as delusterant may be varied from about 0.05% by weight to about 5% by Weight of the viscose solution.
- the viscose After the delusterant substance is dispersed in the viscose, the viscose is spun and the thread produced therefrom is finished in the usual manner.
- the dispersion of a terpene ether in viscose is quite stable so that the viscose may stand for a considerable time, say up to 60 or more hours, without spinning difficulties being encountered due to agglomerations of the dispersed particles.
- the finishing operations 1. e. Washing, desulphurizing, bleaching, drying, etc, remove substantially all or a part of the delusterant substance.
- the quantity remaining in the rayon depends of course upon the conditions employed in the finishing operations and also depends somewhat upon the volatility of the particular substance used.
- Residual delusterant is, in the method according to this invention, usually harmless since the substances utilized are very mild in odor and tend only to add weight and to soften the handle of the rayon slightly.
- the employment of terpene ethers derived from the lower aliphatic alcohols, methyl alcohol, for example, is preferable. These ethers are substantially completely removed in the normal course of finishing the rayon.
- the delusterant substances used in the practice of this invention are an aid in the washing and desulphurizing treatments since they improve penetration of the treating liquors.
- the delusterant composition may comprise a mixture of one of the above mentioned terpene ethers and a refined mineral oil such as Nujol or other light colored or colorless liquid petroleum fraction of low volatility, the ether in quantity from about 5% to 100% of the mixture, preferably in quantity from about 10% to about 40% by weight of the mixture.
- the delusterant composition will be added to the viscose in such amount that the said mixture will constitute from about 0.05% to about 5% by weight of the viscose, according to the effect desired.
- the mixture may be dispersed directly in the viscose or, if desired. it may first be emulsified in water or dilute alkali with the aid of an emulsifying agent, for example, sulphonated castor oil, and the emulsion mixed into the viscose to form a uniform dispersion. The viscose is then spun and the thread finished as usual.
- the terpene ether admixed with the mineral oil prevents the spinning difiiculties due to agglomeration of the mineral oil particles usually encountered with mineral oil.
- the delusterant composition used in the practice of this invention may also comprise a terpene ether and an inert solid delustering agent such as a pigment.
- the delustering composition may comprise a mixture of the terpene ether and titanium dioxide. Tin oxide, barium sulphate, antimony oxide, etc. may be used.
- the ether has delustering properties in itself and in addition aids in dispersing the pigment and further has the important advantage of preventing agglomeration of the pigment particles.
- the pigment is utilized with greater efficiency and less is required; weakening of the filament and plugging of the spinnerettes due to pigment agglomerates are avoided.
- titanium dioxide may, for example, be triturated in a ball mill with one of the hereinabove mentioned ethers, using relatively small quantities of the latter, for example, to the extent of about to about 25% by weight of the mixture.
- the mixture may then be further dispersed in a dilute sodium hydroxide solution in the ball mill.
- the dispersion is then in convenient form for addition to a viscose solution.
- a larger proportion of the terpene ether may be used, in which case the pigment may be dispersed in the ether and then pasted or dispersed further in water, or preferably in a dilute sodium hydroxide solution and added to the viscose.
- the delusterant composition in the method according to this invention is a convenient vehicle, for incorporation in the viscose solution of substances aifecting the handle of the rayon spun therefrom.
- softeners such as the esterification products of triethanolamine, castor oil fatty acids or other fatty acids may conveniently be added to the delusterant composition.
- Example 1 To a spinning charge of 1700 parts by weight of viscose solution made in the usual manner and containing 6.55% sodium hydroxide and cellulose xanthate equivalent to about 7% cellulose, was added 8.5 parts by weight of the ether of pinene and methyl alcohol made by reacting methyl alcohol with wood turpentine, whereby the methyl alcohol adds at a double bond of the pinene.
- the ether was added slowly in a fine stream to the viscose while agitating with a lightin mixer, and the agitation continued, incorporation and addition requiring about minutes.
- the average size of the dispersed particles or droplets of the ether was 4 microns, measured immediately after mixing and again 24 hours later.
- a fixing bath was prepared by dissolving 160 parts of 85% sulphuric acid and 320 parts of sodium sulphate in 520 parts of water, all parts being by weight. Thirty gallons of coagulant were prepared for each spinnerette. The coagulant was circulated at a rate of about 1 to 1.5 liters per minutes, filtering to remove suspended sulphur. The viscose containing the dispersed additive terpene ether was spun by extrusion into the fixing bath in the usual manner, a 40 filament 100 denier yarn being formed.
- the yarn was skeined and washed free of acid by a series of water washes at 40-50 C. It was desulphurized in a circulating bath of 2% sodium sulphide at 50 C., about 15 minutes being required. The yarn was then washed free of alkali by a series of washes with Water at 40-50 C., followed by a cold wash at 25 C. The yarn was bleached for minutes at 25 C. in a bath containing 118 cc. of bleach solution for each 10 liters of bleaching bath, the bleach solution having been prepared by chlorinating a 2% sodium hydroxide solution to the phenolphthalein flash point. The bleaching bath was carefully kept slightly alkaline.
- the yarn was washed free of bleach by a series of water washes at 25 C. It was then steeped for 10-15 minutes in a, 0.5% hydrochloric acid solution at 25 C. and washed free of acid by several water washes at 50-60 C. It was then hydroextracted, whizzed, and conditioned at relative humidity and F.
- the yarn produced in this example had an appearance slightly lower in luster than commercial semi-dull yarn, and was characterized by a pleasing whiteness.
- Example 2 The procedure of Example 1 was followed except that a quantity of delusterant 2.5% by weight of the viscose was added and dispersed therein.
- the delusterant consisted of a mixture of 90% of the terpene ether used in Example 1 and 10% of the esterification product of triethanolamine and castor oil fatty acids.
- the viscose containing the dispersed delusterant was spun into a 40 filament denier yarn and the yarn finished as in Example 1.
- the yarn .'had a degree of luster about midway between commercial semi-dull and dull yarn, the latter being completely without luster.
- the yarn was soft in handle and had a pleasing whiteness.
- Example 3 A delusterant composition was made by forming an emulsion of 79% of the ether of pinene and methyl alcohol prepared by reacting methyl alcohol with wood turpentine, 7.9% sodium oleate, and 13.1% water. This emulsion was mixed into viscose. A 40 filament 90 denier yarn was then spun from the viscose and the yarn finished as in Example 1.
- Example 4 The ether of pinene and methyl alcohol was dispersed in viscose in the manner of Example 1 except that a quantity 5% of the weight of the viscose was added. The viscose was spun into a i0 filament denier yarn and the yarn finished as in Example 1.
- Example 5 A delusterant composition was prepared by mixing nine parts by weight of the additive ether of pinene and ethylene glycol, prepared by reacting the latter with wood turpentine, with one part by weight of the esterification product of tri ethanolamine and caster oil fatty acids. This delusterant was dispersed in viscose in the manner of Example 1, adding a quantity 2.5% by weight of the viscose. The viscose was then spun to a 40' filament 89 denier yarn and the yarn finished as in Example 1.
- a yarn of soft handle having a degree of luster somewhat lower than commercial semi-dull yarn and having a pleasing whiteness was obtained.
- Example 6 A delusterant composition was prepared by mixing seven parts by weight of the refined mineral oil known as Nujol with three parts of the additive ether of pinene and methyl alcohol. This delusterant was dispersed in the manner of Example 1, adding a quantity 05% of the Weight of the viscose. The viscose was spun into a 40 filament S5 denier yarn and the yarn finished as in Example 1. It is of interest to note that the delusterant readily dispersed to particle size such that all particles were below 6 microns and that twenty-four hours later the particle size was unchanged.
- the yarns produced in the foregoing examples were characterized by a pleasing whiteness, in some cases a dead whiteness, as compared with the o-palescence produced when rayon is delustered with either pine oil or mineral oil as in previous methods. They retain their dullness when dyed to dark shades. Low denier yarns of reduced luster are readily produced as the dispersed delusterant does not agglomerate in the viscose. Furthermore, the yarns produced in accordance with this invention are odorless.
- viscose containing a dispersed terpene ether retains its spinnability toa high degree, that is, low denier filaments are readily spun therefrom.
- dispersed mineral oil in viscose makes for very poor spinnability and that the use of a terpene ether with the mineral oil greatly improves the spinnability.
- using the terpene ether as the sole delusterant makes for superior spinnability even when compared to the use of oils such as pine oil. Finer filaments of delustered rayon may thus be spun than was heretofore possible.
- a viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether as a delustering agent is provided.
- a viscose spinning solution for the manufacture of rayon of low luster containing an additive ether of pinene and an alcohol as a delustering agent.
- a viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene as a delustering agent.
- a viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether and an additional delustering agent is provided.
- a viscose spinning solution for the manufac ture of rayon of low luster containing a terpene ether and a refined mineral oil as delustering agents.
- a viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether and a pigment as delustering agents.
- a viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene and a refined mineral oil as delustering agents.
- a viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene and a pigment as delustering agents.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
Description
Patented Jan. 7, 1941 UNITED STATES METHOD FOR PRODUCING DELUS'IERED RAYON Walter E. Gloor, Milltown, N. -J.. assignor to Hercules Powder Company, Wilmington, Del, a corporation of Delaware No Drawing. Application April 12, 1939,
. Serial No. 267,453
8 Claims.
This invention relates to a method of producing rayon and more particularly it relates to an improved method of producing rayon having a low luster.
Rayon having a subdued luster may be made by several methods. In one method, a pigment, usually titanium dioxide, is incorporated in the spinning solution. This method is fairly effective in producing yarns of reduced luster, but 10 for yarns of very low luster, the quantity of pigment required is such that the yarn is weakened appreciably and the solution has an abrasive action on the spinning orifice. In addition, as is well known, yarns delustered by pigments regain their luster upon being dyed to a dark color since the pigment has little efiect upon the smoothness of the filament surface.
In another method, an immiscible liquid is dispersed in the spinning solution, and the rayon is spun and finished in substantially the usual manner. This method of delustering depends for its efiect on the roughness produced in the surface of the filament and is thus effective on dark or light yarns. Refined mineral oil may be used as the delusterant. However, dispersions in viscose are unstable; the particles agglomerate and produce breaks or weak spots in the filament. For this reason, it is very diflicult to produce low denier filaments from Viscose containing mineral oil as the delustering agent. Pine oil, which forms more stable dispersions in viscose, may be used to overcome this disadvantage. However, pine oil delusters only partially to a pearly opalescence rather than to a completely dull state and furthermore it has a persistent residual odor which is difficult to remove. Mineral and pine oil both impart a slightly yellowish cast to rayon in which they are used as delusterants.
It is an object of this invention to provide a method of producing rayon of reduced or low luster or rayon which is without luster in a simple and expedient manner, without, at the same time, unduly weakening the rayon or imparting undesired odor.
It is a further object to provide a method of producing odorless rayon which is substantially without luster or of reduced luster whether the rayon is white or dyed a dark color or black and still further to produce such rayon in a type having low denier filaments.
It is a still further object to provide a method of producing rayon of reduced luster characterized by a pleasing whiteness.
These objects are accomplished according to this invention, byv spinning rayon from a viscose solution containing a dispersed delusterant composition comprising a terpene ether. The viscose is coagulated and the rayon finished in the usual manner.
The terpene ether utilized in the delusterant composition in the improved method of this invention is characterized by containing an ether linkage connecting a terpenic group with a second group. It may be prepared by the etherification of the hydroxyl group of a terpene alcohol with another alcohol, or it may be prepared by the direct addition of an alcohol at a double bond of an unsaturated terpenic group of a terpene compound. The alcohol used as an etherifying agent may be, for example, methyl, ethyl, propyl, butyl, amyl, beta-chloroethyl, chloropropyl, isopropyl, isobutyl, secondary butyl, furiuryl, tetrahydrofurfuryl, benzyl alcohol, the monomethyl or monoethyl ether of ethylene glycol or of diethylene glycol, and so forth. The alcohol may be dihydric, for example, ethylene glycol, diethylene glycol, propylene glycol, etc., which allows two terpenic groups to form ether linkages to the alcoholic group, if this is desired.
The terpene alcohol used to prepare the terpene ether may be any terpene alcohol having a reactive hydroxyl group, such as, for example, alpha-terpineol, borneol, fenchyl alcohol, etc. Crude cuts rich in such terpene alcohols or mixtures thereof, pine oil for example, may likewise be etherified.
The unsaturated terpene compounds used to prepare the terpene ether by the addition of an alcohol at a double bond may be, for example pinene in alpha or beta form, dipentene, terpinene terpinolene, camphene, bornylene, myrcene, allo-ocimene, sesqui terpenes, polyterpenes, etc. Crude mixtures, i. e. terpene cuts such as turpentine, for example, may be used and in general it is not essential that the resulting crude other be highly purified for use in the method according to this invention. For example, the ether formed by the addition of methyl alcohol to pinene may be made by reacting methyl alcohol with turpen time. The ether of a terpene or terpene compound and an alcohol is termed herein and in the claims, for convenience, a terpene ether.
In producing rayon characterized by reduced luster in accordance with this invention, one or more terpene ethers is introduced into the viscose prior to the spinning thereof. The terpene ether may be dispersed directly in the viscose or it may be added to the sodium hydroxide, water, and cellulose xanthate mixture used to make the viscose. If desired, the substance may first be emulsified in Water and the emulsion then mixed with the viscose or its ingredients. If desired, emulsifying agents such as, for example, sodium oleate, sulphonated vegetable oils, Turkey red oil, Monopole oil, synthetic wetting agents, etc., may be used to aid in preparing such an emulsion. Preferably, the dispersed particles of the delusterant composition are very small in size, say below 5 or 6 microns.
The quantity of delusterant substance added depends upon the degree of luster desired for the rayon. Luster decreases as the quantity of delusterant substance is increased. The quantity of terpene ether or ethers utilized as delusterant may be varied from about 0.05% by weight to about 5% by Weight of the viscose solution.
After the delusterant substance is dispersed in the viscose, the viscose is spun and the thread produced therefrom is finished in the usual manner. The dispersion of a terpene ether in viscose is quite stable so that the viscose may stand for a considerable time, say up to 60 or more hours, without spinning difficulties being encountered due to agglomerations of the dispersed particles.
The finishing operations, 1. e. Washing, desulphurizing, bleaching, drying, etc, remove substantially all or a part of the delusterant substance. The quantity remaining in the rayon depends of course upon the conditions employed in the finishing operations and also depends somewhat upon the volatility of the particular substance used. Residual delusterant is, in the method according to this invention, usually harmless since the substances utilized are very mild in odor and tend only to add weight and to soften the handle of the rayon slightly. In general, the employment of terpene ethers derived from the lower aliphatic alcohols, methyl alcohol, for example, is preferable. These ethers are substantially completely removed in the normal course of finishing the rayon. The delusterant substances used in the practice of this invention are an aid in the washing and desulphurizing treatments since they improve penetration of the treating liquors.
In the method according to this invention, there may alternatively be spun a viscose solution containing a dispersed delusterant composition comprising terpene ether and an additional delustering agent. For example, the delusterant composition may comprise a mixture of one of the above mentioned terpene ethers and a refined mineral oil such as Nujol or other light colored or colorless liquid petroleum fraction of low volatility, the ether in quantity from about 5% to 100% of the mixture, preferably in quantity from about 10% to about 40% by weight of the mixture. The delusterant composition will be added to the viscose in such amount that the said mixture will constitute from about 0.05% to about 5% by weight of the viscose, according to the effect desired. The mixture may be dispersed directly in the viscose or, if desired. it may first be emulsified in water or dilute alkali with the aid of an emulsifying agent, for example, sulphonated castor oil, and the emulsion mixed into the viscose to form a uniform dispersion. The viscose is then spun and the thread finished as usual. The terpene ether admixed with the mineral oil prevents the spinning difiiculties due to agglomeration of the mineral oil particles usually encountered with mineral oil.
The delusterant composition used in the practice of this invention may also comprise a terpene ether and an inert solid delustering agent such as a pigment. For example, the delustering composition may comprise a mixture of the terpene ether and titanium dioxide. Tin oxide, barium sulphate, antimony oxide, etc. may be used. In such a mixture, the ether has delustering properties in itself and in addition aids in dispersing the pigment and further has the important advantage of preventing agglomeration of the pigment particles. As a result, the pigment is utilized with greater efficiency and less is required; weakening of the filament and plugging of the spinnerettes due to pigment agglomerates are avoided.
In practicing this modification of this invention, titanium dioxide may, for example, be triturated in a ball mill with one of the hereinabove mentioned ethers, using relatively small quantities of the latter, for example, to the extent of about to about 25% by weight of the mixture. The mixture may then be further dispersed in a dilute sodium hydroxide solution in the ball mill. The dispersion is then in convenient form for addition to a viscose solution. A larger proportion of the terpene ether may be used, in which case the pigment may be dispersed in the ether and then pasted or dispersed further in water, or preferably in a dilute sodium hydroxide solution and added to the viscose.
The delusterant composition in the method according to this invention is a convenient vehicle, for incorporation in the viscose solution of substances aifecting the handle of the rayon spun therefrom. For example, softeners such as the esterification products of triethanolamine, castor oil fatty acids or other fatty acids may conveniently be added to the delusterant composition.
The examples following further illustrate the method in accordance with this invention by specific embodiments thereof:
Example 1 To a spinning charge of 1700 parts by weight of viscose solution made in the usual manner and containing 6.55% sodium hydroxide and cellulose xanthate equivalent to about 7% cellulose, was added 8.5 parts by weight of the ether of pinene and methyl alcohol made by reacting methyl alcohol with wood turpentine, whereby the methyl alcohol adds at a double bond of the pinene. The ether was added slowly in a fine stream to the viscose while agitating with a lightin mixer, and the agitation continued, incorporation and addition requiring about minutes. The average size of the dispersed particles or droplets of the ether was 4 microns, measured immediately after mixing and again 24 hours later.
A fixing bath was prepared by dissolving 160 parts of 85% sulphuric acid and 320 parts of sodium sulphate in 520 parts of water, all parts being by weight. Thirty gallons of coagulant were prepared for each spinnerette. The coagulant was circulated at a rate of about 1 to 1.5 liters per minutes, filtering to remove suspended sulphur. The viscose containing the dispersed additive terpene ether was spun by extrusion into the fixing bath in the usual manner, a 40 filament 100 denier yarn being formed.
The yarn was skeined and washed free of acid by a series of water washes at 40-50 C. It was desulphurized in a circulating bath of 2% sodium sulphide at 50 C., about 15 minutes being required. The yarn was then washed free of alkali by a series of washes with Water at 40-50 C., followed by a cold wash at 25 C. The yarn was bleached for minutes at 25 C. in a bath containing 118 cc. of bleach solution for each 10 liters of bleaching bath, the bleach solution having been prepared by chlorinating a 2% sodium hydroxide solution to the phenolphthalein flash point. The bleaching bath was carefully kept slightly alkaline. After bleaching, the yarn was washed free of bleach by a series of water washes at 25 C. It was then steeped for 10-15 minutes in a, 0.5% hydrochloric acid solution at 25 C. and washed free of acid by several water washes at 50-60 C. It was then hydroextracted, whizzed, and conditioned at relative humidity and F.
The yarn produced in this example had an appearance slightly lower in luster than commercial semi-dull yarn, and was characterized by a pleasing whiteness.
Example 2 The procedure of Example 1 was followed except that a quantity of delusterant 2.5% by weight of the viscose was added and dispersed therein. In addition, the delusterant consisted of a mixture of 90% of the terpene ether used in Example 1 and 10% of the esterification product of triethanolamine and castor oil fatty acids.
The viscose containing the dispersed delusterant was spun into a 40 filament denier yarn and the yarn finished as in Example 1. The yarn .'had a degree of luster about midway between commercial semi-dull and dull yarn, the latter being completely without luster. The yarn was soft in handle and had a pleasing whiteness.
Example 3 A delusterant composition was made by forming an emulsion of 79% of the ether of pinene and methyl alcohol prepared by reacting methyl alcohol with wood turpentine, 7.9% sodium oleate, and 13.1% water. This emulsion was mixed into viscose. A 40 filament 90 denier yarn was then spun from the viscose and the yarn finished as in Example 1.
A yarn of very low luster and pleasing whiteness was obtained.
Example 4 The ether of pinene and methyl alcohol was dispersed in viscose in the manner of Example 1 except that a quantity 5% of the weight of the viscose was added. The viscose was spun into a i0 filament denier yarn and the yarn finished as in Example 1.
A dead white yarn, substantially lusterless, was obtained.
Example 5 A delusterant composition was prepared by mixing nine parts by weight of the additive ether of pinene and ethylene glycol, prepared by reacting the latter with wood turpentine, with one part by weight of the esterification product of tri ethanolamine and caster oil fatty acids. This delusterant was dispersed in viscose in the manner of Example 1, adding a quantity 2.5% by weight of the viscose. The viscose was then spun to a 40' filament 89 denier yarn and the yarn finished as in Example 1.
A yarn of soft handle having a degree of luster somewhat lower than commercial semi-dull yarn and having a pleasing whiteness was obtained.
Example 6 A delusterant composition was prepared by mixing seven parts by weight of the refined mineral oil known as Nujol with three parts of the additive ether of pinene and methyl alcohol. This delusterant was dispersed in the manner of Example 1, adding a quantity 05% of the Weight of the viscose. The viscose was spun into a 40 filament S5 denier yarn and the yarn finished as in Example 1. It is of interest to note that the delusterant readily dispersed to particle size such that all particles were below 6 microns and that twenty-four hours later the particle size was unchanged.
A yarn of pleasing white appearance having a luster slightly less than commercial semi-dull yarn was obtained.
The yarns produced in the foregoing examples were characterized by a pleasing whiteness, in some cases a dead whiteness, as compared with the o-palescence produced when rayon is delustered with either pine oil or mineral oil as in previous methods. They retain their dullness when dyed to dark shades. Low denier yarns of reduced luster are readily produced as the dispersed delusterant does not agglomerate in the viscose. Furthermore, the yarns produced in accordance with this invention are odorless.
In the method in accordance with this invention there is the further advantage that viscose containing a dispersed terpene ether retains its spinnability toa high degree, that is, low denier filaments are readily spun therefrom. It has been hereinbefore mentioned that dispersed mineral oil in viscose makes for very poor spinnability and that the use of a terpene ether with the mineral oil greatly improves the spinnability. However, using the terpene ether as the sole delusterant makes for superior spinnability even when compared to the use of oils such as pine oil. Finer filaments of delustered rayon may thus be spun than was heretofore possible.
It will be understood that the details and examples hereinbefore set forth are illustrative only, and that the invention as broadly described and claimed is in no way limited thereby.
What I claim and desire to protect by Letters Patent is:
l. A viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether as a delustering agent.
2. A viscose spinning solution for the manufacture of rayon of low luster containing an additive ether of pinene and an alcohol as a delustering agent.
3. A viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene as a delustering agent.
l. A viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether and an additional delustering agent.
5. A viscose spinning solution for the manufac ture of rayon of low luster containing a terpene ether and a refined mineral oil as delustering agents.
6. A viscose spinning solution for the manufacture of rayon of low luster containing a terpene ether and a pigment as delustering agents.
'7. A viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene and a refined mineral oil as delustering agents.
8. A viscose spinning solution for the manufacture of rayon of low luster containing the additive methyl ether of pinene and a pigment as delustering agents.
WALTER E. GLOOR.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US267453A US2227495A (en) | 1939-04-12 | 1939-04-12 | Method for producing delustered rayon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US267453A US2227495A (en) | 1939-04-12 | 1939-04-12 | Method for producing delustered rayon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2227495A true US2227495A (en) | 1941-01-07 |
Family
ID=23018835
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US267453A Expired - Lifetime US2227495A (en) | 1939-04-12 | 1939-04-12 | Method for producing delustered rayon |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2227495A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2440094A (en) * | 1943-07-12 | 1948-04-20 | Ind Rayon Corp | Spinning solution and a process of making it |
-
1939
- 1939-04-12 US US267453A patent/US2227495A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2440094A (en) * | 1943-07-12 | 1948-04-20 | Ind Rayon Corp | Spinning solution and a process of making it |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2227495A (en) | Method for producing delustered rayon | |
| US2052558A (en) | Production and treatment of artificial materials | |
| US2334358A (en) | Artificial cellulosic filament delustered with titanium salt | |
| GB884143A (en) | Improvements in or relating to x-ray detectable thread | |
| US2030738A (en) | Cellulosic spinning solutions containing aliphatic silicon compounds | |
| US2950207A (en) | Production of filaments having improved whiteness | |
| US2071024A (en) | Cellulosic structures and method of preparing same | |
| US2284839A (en) | Cellulose spinning solution and filament produced therefrom | |
| US3565652A (en) | Method of coloring viscose | |
| US2099441A (en) | Cellulosic product and method for preparing same | |
| US2128604A (en) | Manufacture of artificial silk | |
| US2077699A (en) | Cellulosic structures | |
| US2099455A (en) | Cellulosic article of manufacture and method for preparing same | |
| US1999182A (en) | Artificial filament | |
| US2249175A (en) | Preparation of solutions of heatripened cellulose xanthate | |
| US2000671A (en) | Artificial silk filament | |
| US2030737A (en) | Cellulosic spinning solutions containing aromatic silicon derivatives | |
| US2012232A (en) | Composition of matter and process of producing same | |
| US2107668A (en) | Method of producing artificial silk | |
| US2039303A (en) | Manufacture of artificial materials | |
| US2234626A (en) | Manufacture of viscose solutions | |
| US2080002A (en) | Reenforced rubber article | |
| US2077700A (en) | Artificial silk having subdued luster | |
| US2022411A (en) | Manufacture of artificial filaments, threads, films, fabrics, and the like | |
| US2066385A (en) | Manufacture of artificial silk |