US2037013A - Manufacture or treatment of products or articles having a basis of cellulose derivatives - Google Patents
Manufacture or treatment of products or articles having a basis of cellulose derivatives Download PDFInfo
- Publication number
- US2037013A US2037013A US676338A US67633833A US2037013A US 2037013 A US2037013 A US 2037013A US 676338 A US676338 A US 676338A US 67633833 A US67633833 A US 67633833A US 2037013 A US2037013 A US 2037013A
- Authority
- US
- United States
- Prior art keywords
- cellulose
- filaments
- oxanones
- oxanone
- treatment
- 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
- 229920002678 cellulose Polymers 0.000 title description 35
- 239000001913 cellulose Substances 0.000 title description 28
- 238000011282 treatment Methods 0.000 title description 22
- 238000004519 manufacturing process Methods 0.000 title description 17
- 150000003528 tetrahydropyranones Chemical class 0.000 description 33
- 239000000463 material Substances 0.000 description 29
- 235000010980 cellulose Nutrition 0.000 description 28
- 238000000034 method Methods 0.000 description 27
- 239000002904 solvent Substances 0.000 description 22
- 239000004744 fabric Substances 0.000 description 21
- 239000000047 product Substances 0.000 description 18
- 229920002301 cellulose acetate Polymers 0.000 description 17
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 14
- 150000002170 ethers Chemical class 0.000 description 12
- 230000001112 coagulating effect Effects 0.000 description 9
- 238000009987 spinning Methods 0.000 description 7
- 229920003086 cellulose ether Polymers 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 5
- 238000002166 wet spinning Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- -1 dichlorethylene, trichlorethylene, chloroform Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- 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 2
- 230000032683 aging Effects 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 150000003456 sulfonamides Chemical class 0.000 description 2
- 150000003899 tartaric acid esters Chemical class 0.000 description 2
- 239000002562 thickening agent 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 101100114416 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) con-10 gene Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-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
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000012237 artificial material Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- VOBHVQRBBHSZAZ-UHFFFAOYSA-N bis(3-methylbutyl) 2,3-dihydroxybutanedioate Chemical compound CC(C)CCOC(=O)C(O)C(O)C(=O)OCCC(C)C VOBHVQRBBHSZAZ-UHFFFAOYSA-N 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 150000001733 carboxylic acid esters Chemical group 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- PCYQQSKDZQTOQG-NXEZZACHSA-N dibutyl (2r,3r)-2,3-dihydroxybutanedioate Chemical group CCCCOC(=O)[C@H](O)[C@@H](O)C(=O)OCCCC PCYQQSKDZQTOQG-NXEZZACHSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 235000004879 dioscorea Nutrition 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical compound O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 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
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000008096 xylene Substances 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1545—Six-membered rings
Definitions
- This invention relates to the manufacture or treatment of products or articles made of or containing cellulose derivatives.
- the invention is based on the discovery that certain'cyclic compounds have a solvent or softening action upon cellulose derivatives and may be applied very widely in the arts in processes and products in which a solvent or softening action upon cellulose derivatives is desired.
- the cyclic compounds of the present invention are compounds containing a ring which consists of a keto group, an ether oxygen atom and four methylene or substituted methylene groups. These compounds will for convenience be termed oxanones.
- the simplest compound of the senes is tetra-hydropyrone I /CHr-CH2 o co GET-CH2 which will be hereinafter termed IA-oxanone.
- the invention contemplates processes and products utilizing the solvent or softening (including plasticizing) properties of'these compounds for cellulose deriva tives.
- 1.4-oxanone possesses very high solvent power for acetone-soluble cellulose acetate and -for other esters and ethers of cellulose including nitrocellulose. Substitution of the hydrogen atoms of the methylene groups in 1.4-oxanone tends to decrease somewhat the solvent power of the product except where the substituent groups themselves confer solvent or softening properties.
- alkylated, aralkylated or arylated 1.41-oxanones have in general less solvent power for acetone-soluble cellulose acetate than has the parent 1.4-oxanone.
- 1.4-oxanone substituted in the methylene groups by polar groups, for instance carboxylic ester groups has again high solvent power for cellulose acetate.
- the present invention relates therefore to processes in which the solvent or softening power of the oxanones is employed in the production and treatment of artificial filaments, ribbons, films and the like comprising cellulose esters or ethers,
- the oxanones may be employed in media for the cotaining high concentrations 0 1, 1932, applicaal No. 676,338.
- the oxanones may be employed in media for the cotaining high concentrations 0 1, 1932, applicaal No. 676,338.
- the oxanones may be employed in processes for stretching, shrinking, improving the pliability, tenacity, or extension ofartificial filaments and the like, as well as in sizing, dyeing, printing, discharging, loading, mordanting, delustring and relustring artificial materials con- 10 taining esters or ethers of cellulose.
- the oxanones may be employed in coagulating baths for the'wet spinning of cellulose derivatives, whether or not oxanones are present in the spinning solutions, and it is of 15 particular advantage for many purposes to employ relatively high concentrations of the oxanones in the coagulating baths.
- the filaments or other products may be treated in subsequent treatment baths containing oxanones.
- softening agents or plasticizers of the-present invention 5 are also highly valuable for the treatment of already formed articles made of or containing cellulose derivatives, for example filaments, yarns, threads,'ribbons, films, fabrics and the like. Such treatments may have various objects.
- woven fabrics to slip or of warp or circular knitted fabrics to split or ladder may be diminished or eliminated by treatment with the oxanones of the present invention in the manner described in U. S. application Serial No. 152,516 filed 3rd December, 1926.
- the solvents may be used to improve the pliability or extension of filaments, threads and the like made of or containing cellulose derivatives, and in particular to improve the knotting properties of comparatively thick filaments orartificial horsehair.
- Such treatment with the oxanones is preferably effected without tension or only under alight tension so that the materials are able to shrink.
- Shrinking of the filaments, yarns and the like either to imv -treatment baths con- 25 i other products of cellulose acetate or other cellulose derivatives.
- the filaments or other products during or subsequent to softening with the oxanones or mixtures containing the same are subjected to a stretching treatment.
- the softening of the filaments or other products may be effected by treatment with the oxanones or solutions thereof, or the oxanones may be incorporated in the materials by incorporating them in the spinning solution and spinningundersuchconditions that theproportion of oxanone requisite to produce the desired degree of softening is retained in the filaments.
- the required proportion may be incorporated in the spinning solution and the latter spun by dry spinning methods.
- the stretching treatment of the softened filaments or other products may be applied in a single operation and preferably gradually, or may be applied in a number of stages, preferably without intermediate elimination of the solvent as described in U. S. application Serial No. 402,785.
- sizes may be made up containing the oxanones so as to effect a lubrication pf the yarns or other materials, particularly for facilitating textile operations, such as winding, winding and twisting, beaming and the like.
- Such sizes may be made up with or without suitable thickening agents, such as polymerized vinyl compounds, or oxidized linseed oil or other drying oils.
- the oxanones are also of considerable value in processes for altering or modifying the optical characteristics of filaments, fabrics and the like containing cellulose esters or ethers, for example in relation to colour or lustre, and are of particular value .in processes involving the absorption of various liquid or solid materials by filaments, yarns, threads, fabrics and the like containing the cellulose esters or ethers. For example, such products may be treated with the oxanones during or before a treatment adapted to dye, print,
- the oxanones of the present invention may be utilized to reluster fabrics or other materials containing cellulose acetate or other esters or ethers of cellulose which have been delustered by the action of moist steam or of hot aqueous media, and reference is made in this connection to U. S. Patent No. 1,808,098.
- Such relustering may be uniformly applied over the whole fabric or material, or may be local so as to produce an effect fabric.
- the oxanone may forinstance be printed with the aid of a suitable thickening agent on the delustered fabric and the whole dried to reluster the fabric in the printed portions.
- Dyestuffs, pigments, discharges or other effect materials may be included in the oxanone printing paste.
- the oxanones of the present invention may be employed as such, particularly where they are liquids and their solvent power has been reduced by suitable substituent groups, as for instance alkyl groups.
- suitable substituent groups as for instance alkyl groups.
- the oxanones may, of course, be mixed with other solvents, or, where their solvent power is too great, they may be mixed with suitable diluents.
- the oxanones may be employed in conjunction with other solvents and/or dilu- 'ents, for example acetone, methyl acetone, methyl olefine glycols, for instance the monomethyl and ethyl ethers of ethylene and propylene glycol and ethylene glycol mono-acetate and methyl glycol mono-acetate, methylene chloride, ethylene chloride, dichlorethylene, trichlorethylene, chloroform, methyl, ethyl or other alcohols, benzene, toluene, xylene or other aromatic, aliphatic or cyclo aliphatic hydrocarbons, and ethers, for instance iso-propyl ether.
- glycols for instance the monomethyl and ethyl ethers of ethylene and propylene glycol and ethylene glycol mono-acetate and methyl glycol mono-acetate
- methylene chloride ethylene chloride, dichlorethylene, trichlorethylene, chloroform,
- the oxanones may be employed in conjunction with relatively high boiling solvents or plasticizers which may themselves be oxanones, as for example 2.6- dimethyl-1.4-oxanone-3.fi-dicarboxylic acid dibutyl or di-iso-amyl ester, or may be other high boiling solvents or plasticizers, for example triacetin, diethyl phthalate, dibutyl phthalate, sulphonamides, for example alkylated xylene sulphonamides, sulphonanilides, tartrates, for instance dibutyl or di-iso-amyl tartrate, or diphenylol propane, triphenyl phosphate, tricresyl phosphate (the latter two preferably in conjunction with sulphonamides, tartrates or other highly compatible plasticizers), or other phenolic plasticizers.
- solvents or plasticizers which may themselves be oxanones, as for example 2.6- dimethyl
- the oxanones may be employed in conjunction with medium boiling solvents such as ethyl lactate, diacetone alcohol and tetrachlorethane.
- medium boiling solvents such as ethyl lactate, diacetone alcohol and tetrachlorethane.
- mixtures of any of the above solvents, diluents and plasticizers may be employed inconjunction with the oxanones for the purposes of the present invention.
- a 25% solution of cellulose acetate in'acetone is extruded through spinning nozzles into a coagulating bath consisting of a 30-40% aqueous, alcoholic, or aqueous-alcoholic solution of 1.4- oxanone.
- the soft filaments after emergence from the coagulating bath are carried through a guide to a rotating roller having a peripheral speed of 50-70 metres per minute.
- the filaments may be drawn down to very fine deniers.
- the excess oxanone is removed, as for example by washing it with a more dilute solution of oxanone, for instance a -15% solution, and the filaments are finally dried.
- the spinning solution may contain 10% on the weight of the cellulose acetate of lA-oxanone.
- Example 2 Filaments or yarns of cellulose, acetate in hank or other suitable form are soaked for about 2 minutes in a bath consisting of 30-40% aqueous,
- oxanone and are thereafter stretched to the desired degree, for example by more than 100% of A fabric consisting of cellulose acetate yarns cient time to cause the oxanone to evaporate and is then washed with warm water, soaped for a few minutes at 50 C. in a solution containing 2 grams of soap perv litre and finally rinsed.
- a fabric consisting of cellulose acetate yarns cient time to cause the oxanone to evaporate and is then washed with warm water, soaped for a few minutes at 50 C. in a solution containing 2 grams of soap perv litre and finally rinsed.
- the printing paste includes a dyestufi
- yarns, films and the like comprising extruding a solution containing an organic derivative of cellulose into a coagulating bath containing an oxanone.
- I yarns, films and the like comprising extruding a solution containing cellulose acetate into a coagulating bath containing a high proportion of an oxanone.
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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)
- Artificial Filaments (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
This compoun Patented Apr. 14, 1936 I UNITED STATES MANUFACTURE OR TREATMENT OF PROD- UCTS OR ARTICLES CELLULOSE DERIVA HAVING A BASIS OF TIVES Henry Dreyfus, London, England No Drawing. Original application July Divided and this Serial No. 620,545. tion June 1'7, 1933, Seri Britain July 30, 1931 16 Claims.
This invention relates to the manufacture or treatment of products or articles made of or containing cellulose derivatives.
This application is a division of my application Serial No. 620,545 filed 1st July 1932.
The invention is based on the discovery that certain'cyclic compounds have a solvent or softening action upon cellulose derivatives and may be applied very widely in the arts in processes and products in which a solvent or softening action upon cellulose derivatives is desired. The cyclic compounds of the present invention are compounds containing a ring which consists of a keto group, an ether oxygen atom and four methylene or substituted methylene groups. These compounds will for convenience be termed oxanones. The simplest compound of the senes is tetra-hydropyrone I /CHr-CH2 o co GET-CH2 which will be hereinafter termed IA-oxanone.
d with its substitution derivatives constitute the most important solvents and softening agents of the present invention.
As previously indicated the invention contemplates processes and products utilizing the solvent or softening (including plasticizing) properties of'these compounds for cellulose deriva tives. 1.4-oxanone possesses very high solvent power for acetone-soluble cellulose acetate and -for other esters and ethers of cellulose including nitrocellulose. Substitution of the hydrogen atoms of the methylene groups in 1.4-oxanone tends to decrease somewhat the solvent power of the product except where the substituent groups themselves confer solvent or softening properties. Thus, for instance, alkylated, aralkylated or arylated 1.41-oxanones have in general less solvent power for acetone-soluble cellulose acetate than has the parent 1.4-oxanone. On the other hand 1.4-oxanone substituted in the methylene groups by polar groups, for instance carboxylic ester groups, has again high solvent power for cellulose acetate.
The present invention relates therefore to processes in which the solvent or softening power of the oxanones is employed in the production and treatment of artificial filaments, ribbons, films and the like comprising cellulose esters or ethers,
. and comprises quite broadly the treatment of the materials at any stage during or subsequent .to their formation. Thus, for example, the oxanones may be employed in media for the cotaining high concentrations 0 1, 1932, applicaal No. 676,338. In Great agulation of products spun by wet spinning processes from spinning solutions containing cellulose esters or ethers, or may be employed in subsequent treatment baths for such products. Again, the oxanones may be employed in processes for stretching, shrinking, improving the pliability, tenacity, or extension ofartificial filaments and the like, as well as in sizing, dyeing, printing, discharging, loading, mordanting, delustring and relustring artificial materials con- 10 taining esters or ethers of cellulose. I
As stated above, the oxanones may be employed in coagulating baths for the'wet spinning of cellulose derivatives, whether or not oxanones are present in the spinning solutions, and it is of 15 particular advantage for many purposes to employ relatively high concentrations of the oxanones in the coagulating baths. Moreover, after a wet spinning operation in which the oxanone is included in the spinning solution or in '20 the coagulating bath, or in which no oxanone is used at all, the filaments or other products may be treated in subsequent treatment baths containing oxanones. Wet spinning processes in which coagulating or after i solvents are employed are described in U. S. Patent No. 1,467,493 and U. S. applications Serial Nos. 402,785 filed 26th October, 1929, and 418,414 filed 3rd January, 1930. 30
In addition to being of value in the production of artificial filaments and other products containing cellulose esters and ethers by wet spinning processes as described above the solvents, softening agents or plasticizers of the-present invention 5 are also highly valuable for the treatment of already formed articles made of or containing cellulose derivatives, for example filaments, yarns, threads,'ribbons, films, fabrics and the like. Such treatments may have various objects. For ex- 40 ample the tendency of woven fabrics to slip or of warp or circular knitted fabrics to split or ladder may be diminished or eliminated by treatment with the oxanones of the present invention in the manner described in U. S. application Serial No. 152,516 filed 3rd December, 1926. The solvents may be used to improve the pliability or extension of filaments, threads and the like made of or containing cellulose derivatives, and in particular to improve the knotting properties of comparatively thick filaments orartificial horsehair. Such treatment with the oxanones is preferably effected without tension or only under alight tension so that the materials are able to shrink. Shrinking of the filaments, yarns and the like either to imv -treatment baths con- 25 i other products of cellulose acetate or other cellulose derivatives. In such an application the filaments or other products during or subsequent to softening with the oxanones or mixtures containing the same are subjected to a stretching treatment. The softening of the filaments or other products may be effected by treatment with the oxanones or solutions thereof, or the oxanones may be incorporated in the materials by incorporating them in the spinning solution and spinningundersuchconditions that theproportion of oxanone requisite to produce the desired degree of softening is retained in the filaments. Thus the required proportion may be incorporated in the spinning solution and the latter spun by dry spinning methods. The stretching treatment of the softened filaments or other products may be applied in a single operation and preferably gradually, or may be applied in a number of stages, preferably without intermediate elimination of the solvent as described in U. S. application Serial No. 402,785. From the point of view of producing regularity of stretch and'also for reasons of economy it is particularly advantageous to stretch the filaments or other products while they are in warp formation by applying the stretching force to the warp as a whole. Such a process is described in U. S. application Serial No. 602,844 filed 2nd April, 1932.
For the treatment of filaments, yarns and the like of cellulose derivatives, sizes may be made up containing the oxanones so as to effect a lubrication pf the yarns or other materials, particularly for facilitating textile operations, such as winding, winding and twisting, beaming and the like. Such sizes may be made up with or without suitable thickening agents, such as polymerized vinyl compounds, or oxidized linseed oil or other drying oils.
The oxanones are also of considerable value in processes for altering or modifying the optical characteristics of filaments, fabrics and the like containing cellulose esters or ethers, for example in relation to colour or lustre, and are of particular value .in processes involving the absorption of various liquid or solid materials by filaments, yarns, threads, fabrics and the like containing the cellulose esters or ethers. For example, such products may be treated with the oxanones during or before a treatment adapted to dye, print,
esses,'the acid wool and directcotton dyestuffs,
certainvat dyestuffs, pigments (white or coloured,)
for example titanium oxide, and certain discharges, for example the formaldehyde sulphoxylate discharges. Furthermore in printing and similar operations, it is customary to apply a steaming or ageing treatment to fix the dyestuff or other agent in the material. By incorporating the oxanones in the printing pastes or similar compositions the materials may be simply dried under such conditions as to volatilize the oxanone in order to effect fixation without having recourse to steaming or ageing. 1.4-oxanone and its lower homologues are particularly useful for this purpose. Again in the treatment of yarns, fabrics, etc. the oxanones of the present invention may be utilized to reluster fabrics or other materials containing cellulose acetate or other esters or ethers of cellulose which have been delustered by the action of moist steam or of hot aqueous media, and reference is made in this connection to U. S. Patent No. 1,808,098. Such relustering may be uniformly applied over the whole fabric or material, or may be local so as to produce an effect fabric. The oxanone may forinstance be printed with the aid of a suitable thickening agent on the delustered fabric and the whole dried to reluster the fabric in the printed portions. Dyestuffs, pigments, discharges or other effect materials may be included in the oxanone printing paste.
In the above applications of the oxanones of the present invention to products made of or containing cellulose acetate or other cellulose esters or ethers, the oxanones may be employed as such, particularly where they are liquids and their solvent power has been reduced by suitable substituent groups, as for instance alkyl groups. The oxanones may, of course, be mixed with other solvents, or, where their solvent power is too great, they may be mixed with suitable diluents. Thus, for example the oxanones may be employed in conjunction with other solvents and/or dilu- 'ents, for example acetone, methyl acetone, methyl olefine glycols, for instance the monomethyl and ethyl ethers of ethylene and propylene glycol and ethylene glycol mono-acetate and methyl glycol mono-acetate, methylene chloride, ethylene chloride, dichlorethylene, trichlorethylene, chloroform, methyl, ethyl or other alcohols, benzene, toluene, xylene or other aromatic, aliphatic or cyclo aliphatic hydrocarbons, and ethers, for instance iso-propyl ether. Furthermore, the oxanones may be employed in conjunction with relatively high boiling solvents or plasticizers which may themselves be oxanones, as for example 2.6- dimethyl-1.4-oxanone-3.fi-dicarboxylic acid dibutyl or di-iso-amyl ester, or may be other high boiling solvents or plasticizers, for example triacetin, diethyl phthalate, dibutyl phthalate, sulphonamides, for example alkylated xylene sulphonamides, sulphonanilides, tartrates, for instance dibutyl or di-iso-amyl tartrate, or diphenylol propane, triphenyl phosphate, tricresyl phosphate (the latter two preferably in conjunction with sulphonamides, tartrates or other highly compatible plasticizers), or other phenolic plasticizers. Again, the oxanones may be employed in conjunction with medium boiling solvents such as ethyl lactate, diacetone alcohol and tetrachlorethane. Moreover, mixtures of any of the above solvents, diluents and plasticizers may be employed inconjunction with the oxanones for the purposes of the present invention.
e As previously mentioned 1.4-oxanone itself is and either delustered or of a normal lustre is printed with the following printing paste:-
Grams Dyestuff or pigment 10-35 Diethylene glycol 60-75 Water 160 l.4=oxanone 200-500 Gum arable (1:1) 400-600 CoHa-?H CHCOH5 CuHr-CH CH CH-CuHg and CHFCHK C CH: OHs-C H. CHr-C C-CH8 The invention is particularly important in relation to the treatment of artificial silk, ribbons, films, fabrics and the like of cellulose acetate, but it may also be applied in the treatment of similar products of cellulose nitrate and also of cellulose formate, cellulose propionate, cellulose butyrate, cellulose nltro-acetate (of low nitrogen content) and other organic esters of cellulose or mixed esters, and. also ethyl or benzyl celluloses or other cellulose, ethers or mixed ethers or mixed ether-esters.
The following examples serve to illustrate the invention but are not-to be considered as limiting it in any way:-
- Example 1 A 25% solution of cellulose acetate in'acetone is extruded through spinning nozzles into a coagulating bath consisting of a 30-40% aqueous, alcoholic, or aqueous-alcoholic solution of 1.4- oxanone. The soft filaments after emergence from the coagulating bath are carried through a guide to a rotating roller having a peripheral speed of 50-70 metres per minute. The filaments may be drawn down to very fine deniers, After leaving the feed roller the excess oxanone is removed, as for example by washing it with a more dilute solution of oxanone, for instance a -15% solution, and the filaments are finally dried. In this example the spinning solution may contain 10% on the weight of the cellulose acetate of lA-oxanone.
Example 2 Filaments or yarns of cellulose, acetate in hank or other suitable form are soaked for about 2 minutes in a bath consisting of 30-40% aqueous,
' alcoholic, or aqueous-alcoholic solution of 1.4-
oxanone and are thereafter stretched to the desired degree, for example by more than 100% of A fabric consisting of cellulose acetate yarns cient time to cause the oxanone to evaporate and is then washed with warm water, soaped for a few minutes at 50 C. in a solution containing 2 grams of soap perv litre and finally rinsed. Where a delustered fabric has been used and the printing paste includes a dyestufi, the lustre of the printed areas is restored.
What I claim and desire to secure by Letters Patent is:-
1. In a process for the manufacture of filaments, yarns, threads, films, fabrics, and other. materials comprising organic derivatives of cellulose, the step of treating the materials with oxano nes.
2. In a process for the manufacture of filaments, yarns, threads, films, fabrics, and other materials comprising cellulose acetate, the step of treating the materials with oxanones.
3. In a process for the manufacture of filaments, yams, threads, films, fabrics, and other materials comprising cellulose acetate, the step of treating the materials with 1.4-oxanone.
4. Process for the manufacture of filaments,
yarns, films and the like, comprising extruding a solution containing an organic derivative of cellulose into a coagulating bath containing an oxanone.
5. Process for the manufacture of filaments, yarns, films and the like, comprising extruding a solution containing cellulose acetate into a coagulating bath containing 1.4-oxanone.
6. Process for the manufacture of filaments,
I yarns, films and the like, comprising extruding a solution containing cellulose acetate into a coagulating bath containing a high proportion of an oxanone.
'7. In a process for the manufacture of filaments, yarns, films or other products comprising organic derivatives of cellulose, the step of treating the materials after their formation with oxanones.
8. In a process for the manufacture of filaments, yarns, threads,'films, fabrics, or other materials comprising organic derivatives of cellulose, the step of softening the materials with the aid of oxanones,
9. Process for the manufacture of filaments, threads, yarns, andthe like comprising organic derivatives of cellulose, comprising softening the materials with the aid of an oxanone and subjecting them to a stretching treatment.
10. Process for the manufacture of filaments, threads, yarns, and the like comprising organic derivatives of cellulose, comprising softening a number of filaments, threads, yarns, and the like in warp formation with the aid of an oxa-' none and subjecting them to a stretching operation.
11. Process for the manufacture of filaments, threads, yarns, and the like comprising cellulose acetate, comprising softening the materials with the aid of 1.4-oxanone and subjecting them to a stretching operation.
12; Process for the manufacture of filaments, threads, yarns, and the like comprising organic derivatives of cellulose, comprising softening the materials with the aid of an ing the materials to shrink.
oxanone and allow- 13. In processes for colouring filaments, yarns,
threads, films, fabrics and othermaterials comprising organic derivatives of cellulose, the step of treating the materials with media comprising oxanones.
- 14. In processes for colouring filaments, yarns, threads, films, fabrics and other materials comprising cellulose acetate, the step of treating the materials with media comprising 1.4-oxanone.
15. In processes for modifying the lustre of filaments, yarns, threads, films, fabrics and other materials comprising organic derivatives of cellulose, the step of treating the materials with media comprising oxanones.
16, In processes for modifying the lustre of filaments, yarns, threads, films, fabrics and other materials comprising cellulose acetate, the step of treating the materials with media comprising l.4-oxanone.
HENRY DREYFUS. 20
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US676338A US2037013A (en) | 1932-07-01 | 1933-06-17 | Manufacture or treatment of products or articles having a basis of cellulose derivatives |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US620545A US2037010A (en) | 1931-07-30 | 1932-07-01 | Cellulose derivative composition |
| US676338A US2037013A (en) | 1932-07-01 | 1933-06-17 | Manufacture or treatment of products or articles having a basis of cellulose derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2037013A true US2037013A (en) | 1936-04-14 |
Family
ID=27088734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US676338A Expired - Lifetime US2037013A (en) | 1932-07-01 | 1933-06-17 | Manufacture or treatment of products or articles having a basis of cellulose derivatives |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2037013A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2436059A (en) * | 1943-03-04 | 1948-02-17 | Eastman Kodak Co | Discharge printing of colored cellulose acetate fabrics with the aid of an intermediate thiocyanate treatment |
-
1933
- 1933-06-17 US US676338A patent/US2037013A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2436059A (en) * | 1943-03-04 | 1948-02-17 | Eastman Kodak Co | Discharge printing of colored cellulose acetate fabrics with the aid of an intermediate thiocyanate treatment |
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