US3114592A - Process for the production of elements made of hydrated cellulose - Google Patents
Process for the production of elements made of hydrated cellulose Download PDFInfo
- Publication number
- US3114592A US3114592A US123116A US12311661A US3114592A US 3114592 A US3114592 A US 3114592A US 123116 A US123116 A US 123116A US 12311661 A US12311661 A US 12311661A US 3114592 A US3114592 A US 3114592A
- Authority
- US
- United States
- Prior art keywords
- viscose
- production
- oxide
- hydrated cellulose
- dimethyl
- 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 claims description 14
- 239000001913 cellulose Substances 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 229920000297 Rayon Polymers 0.000 claims description 46
- 238000001556 precipitation Methods 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 description 12
- 238000009987 spinning Methods 0.000 description 11
- -1 dimethyl lauryl Chemical group 0.000 description 10
- 239000000654 additive Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- QDTCBEZXBDUOCR-UHFFFAOYSA-N n,n-dibutylbutan-1-amine oxide Chemical compound CCCC[N+]([O-])(CCCC)CCCC QDTCBEZXBDUOCR-UHFFFAOYSA-N 0.000 description 2
- WYFCAMVESRXVCT-UHFFFAOYSA-N n,n-diethyloctan-1-amine oxide Chemical compound CCCCCCCC[N+]([O-])(CC)CC WYFCAMVESRXVCT-UHFFFAOYSA-N 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LKQUDAOAMBKKQW-UHFFFAOYSA-N N,N-dimethylaniline N-oxide Chemical compound CN(C)(=O)C1=CC=CC=C1 LKQUDAOAMBKKQW-UHFFFAOYSA-N 0.000 description 1
- NIPCVVZKBBTPHG-UHFFFAOYSA-N N-(2-methoxyethyl)-N-methyldodecan-1-amine oxide Chemical compound COCC[N+](CCCCCCCCCCCC)(C)[O-] NIPCVVZKBBTPHG-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- UHLPJISGHUJKKM-UHFFFAOYSA-N n,n-di(propan-2-yl)propan-2-amine oxide Chemical compound CC(C)[N+]([O-])(C(C)C)C(C)C UHLPJISGHUJKKM-UHFFFAOYSA-N 0.000 description 1
- WOSXILICBSSMRZ-UHFFFAOYSA-N n,n-dimethylbutan-1-amine oxide Chemical compound CCCC[N+](C)(C)[O-] WOSXILICBSSMRZ-UHFFFAOYSA-N 0.000 description 1
- MMAXOAIHEPNELR-UHFFFAOYSA-N n,n-dimethylcyclohexanamine oxide Chemical compound C[N+](C)([O-])C1CCCCC1 MMAXOAIHEPNELR-UHFFFAOYSA-N 0.000 description 1
- OZYPPHLDZUUCCI-UHFFFAOYSA-N n-(6-bromopyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=CC(Br)=N1 OZYPPHLDZUUCCI-UHFFFAOYSA-N 0.000 description 1
- TTYJLIYVYBNXAP-UHFFFAOYSA-N n-cyclohexyl-n-methylcyclohexanamine oxide Chemical compound C1CCCCC1[N+]([O-])(C)C1CCCCC1 TTYJLIYVYBNXAP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
- D01F2/08—Composition of the spinning solution or the bath
- D01F2/10—Addition to the spinning solution or spinning bath of substances which exert their effect equally well in either
Definitions
- One modification which is frequently employed consists in using substances which facilitate the production of the viscose, for example, at the time of xanthation, by shortening the time required for xanthate formation by emulsifying the carbon disulphide and/ or dispersing impurities in extremely fine form in the viscose, so that, for example, satisfactory filtration is guaranteed.
- An improvement in the filament-drawing capacity is apparent with these additives.
- the disadvantageous deposition of impurities from the viscose and/or from the spinning bath at the spinnerets is avoided. On account of the products added to the spinning baths or products reaching the baths from the viscose, the said baths remain free from clouding substances which otherwise usually sediment.
- amine oxides of the general formula cording to the invention are, for example dimethyl lauryl, diethyloctyl, tributyl, dimethyl butyl, triisopropyl, triiso- 3,114,592 Patented Dec. 17, 1963 octyl, methoxyethylmethyl lauryl, dimethyl stearyl, diethyl oleyl, dimethyl cyclohexyl, dicyclohexyl methyl and dimethyl phenyl amine oxides.
- Example 0.2 g. of dimethyl laurylamine oxide are added per litre to a viscose normally used for the production of textile filaments.
- the eflfect of the additive is that the viscose becomes completely transparent, can easily be filtered and shows excellent filament-drawing capacity. Its surface tension is also reduced by at least 50% and, on spinning into a conventional Miiller bath, it does not cause any incrustation of the spinnerets. Impurities in the precipitation bath are also avoided.
- Example 2 If an unripe viscose is processed, as in Example 1, using 0.8 g./l. of diethyloctylamine oxide, the effects mentioned in Example 1 are also produced. In addition, the milkiness which always occurs when processing unripe viscose is avoided.
- Example 3 0.5 g./l. of dimethyl laurylamine oxide are added to a normal viscose to which a matting agent or a spinning dye-stuff has been added.
- the amine oxide can also be added by first of all being mixed with the pigment, the mixture then being incorporated in the viscose. If this viscose is spun in the usual manner, more intensive matting or dyeing effects are produced than those obtained when amine oxide is not used. It is obvious that the amine oxide produces an improved dispersion of the pigment in the viscose, whereby a better utilisation of the pigment is obtained.
- Example 4 If 2 g./l. of tributylamine oxide are added to a viscose normally used for the production of cord filaments, the stretchability is improved to a surprising degree and thereby a cord rayon with a high strength value is produced.
- amine oxide selected from the group consisting of Dimethyl laurylamine oxide
- Dimethyl cyclohexylamine oxide Dicyclohexyl methylamine oxide, and Dimethyl phenylamine oxide.
- a process for the production of spun hydrated cellulose which comprises the steps of adding to viscose 0.2 g./l. referred to the viscose of an amine oxide of the formula Ra wherein R R R are selected from the group consisting of alkyl, cycloalkyl, alkoxyalkyl, and phenyl, the sum of the C atoms of the R substituents being from 6 to 24, introducing the viscose through spinnerets into a spinning bath and recovering the spun hydrated cellulose therefrom.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC21918A DE1217544B (de) | 1960-07-15 | 1960-07-15 | Verfahren zur Herstellung von Fasern aus Hydratcellulose |
DEC0027744 | 1962-08-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3114592A true US3114592A (en) | 1963-12-17 |
Family
ID=25969320
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US123116A Expired - Lifetime US3114592A (en) | 1960-07-15 | 1961-07-11 | Process for the production of elements made of hydrated cellulose |
Country Status (5)
Country | Link |
---|---|
US (1) | US3114592A (en, 2012) |
BE (2) | BE635885A (en, 2012) |
DE (1) | DE1217544B (en, 2012) |
GB (2) | GB947115A (en, 2012) |
NL (2) | NL296702A (en, 2012) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2179195A (en) * | 1935-02-16 | 1939-11-07 | American Enka Corp | Manufacture of artificial silk |
US2422021A (en) * | 1940-07-29 | 1947-06-10 | Ind Rayon Corp | Manufacture of thread or the like |
US2519227A (en) * | 1941-04-19 | 1950-08-15 | American Viscose Corp | Manufacture of yarns and the like |
-
0
- BE BE605928D patent/BE605928A/xx unknown
- BE BE635885D patent/BE635885A/xx unknown
- NL NL266943D patent/NL266943A/xx unknown
- NL NL296702D patent/NL296702A/xx unknown
-
1960
- 1960-07-15 DE DEC21918A patent/DE1217544B/de active Pending
-
1961
- 1961-07-11 US US123116A patent/US3114592A/en not_active Expired - Lifetime
- 1961-07-12 GB GB25290/61A patent/GB947115A/en not_active Expired
-
1963
- 1963-08-19 GB GB32700/63A patent/GB998293A/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2179195A (en) * | 1935-02-16 | 1939-11-07 | American Enka Corp | Manufacture of artificial silk |
US2422021A (en) * | 1940-07-29 | 1947-06-10 | Ind Rayon Corp | Manufacture of thread or the like |
US2519227A (en) * | 1941-04-19 | 1950-08-15 | American Viscose Corp | Manufacture of yarns and the like |
Also Published As
Publication number | Publication date |
---|---|
BE635885A (en, 2012) | |
NL266943A (en, 2012) | |
NL296702A (en, 2012) | |
DE1217544B (de) | 1966-05-26 |
GB998293A (en) | 1965-07-14 |
GB947115A (en) | 1964-01-22 |
BE605928A (en, 2012) |
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