SU730313A3 - Вискоза - Google Patents
Вискоза Download PDFInfo
- Publication number
- SU730313A3 SU730313A3 SU752177198A SU2177198A SU730313A3 SU 730313 A3 SU730313 A3 SU 730313A3 SU 752177198 A SU752177198 A SU 752177198A SU 2177198 A SU2177198 A SU 2177198A SU 730313 A3 SU730313 A3 SU 730313A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- carbon atoms
- viscose
- diol
- compound
- adduct
- Prior art date
Links
- 229920000297 Rayon Polymers 0.000 title claims abstract description 30
- 239000004094 surface-active agent Substances 0.000 claims abstract description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 229920002678 cellulose Polymers 0.000 claims abstract description 11
- 239000001913 cellulose Substances 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- 125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 7
- 125000006353 oxyethylene group Chemical group 0.000 claims abstract description 5
- 239000011347 resin Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 230000008021 deposition Effects 0.000 claims description 4
- 239000013543 active substance Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract description 4
- DWANEFRJKWXRSG-UHFFFAOYSA-N 1,2-tetradecanediol Chemical compound CCCCCCCCCCCCC(O)CO DWANEFRJKWXRSG-UHFFFAOYSA-N 0.000 abstract 2
- 125000001165 hydrophobic group Chemical group 0.000 abstract 2
- BTOOAFQCTJZDRC-UHFFFAOYSA-N 1,2-hexadecanediol Chemical compound CCCCCCCCCCCCCCC(O)CO BTOOAFQCTJZDRC-UHFFFAOYSA-N 0.000 abstract 1
- IBYGKBNZASXIED-UHFFFAOYSA-N 1-(2,3-dihydroxynonadecylsulfonyl)nonadecane-2,3-diol Chemical compound CCCCCCCCCCCCCCCCC(O)C(O)CS(=O)(=O)CC(O)C(O)CCCCCCCCCCCCCCCC IBYGKBNZASXIED-UHFFFAOYSA-N 0.000 abstract 1
- SAVLJVRYWVRUGO-UHFFFAOYSA-N 1-(2,3-dihydroxypentadecoxy)pentadecane-2,3-diol Chemical compound CCCCCCCCCCCCC(O)C(O)COCC(O)C(O)CCCCCCCCCCCC SAVLJVRYWVRUGO-UHFFFAOYSA-N 0.000 abstract 1
- FVTTWONDGJFJST-UHFFFAOYSA-N 1-(2-hydroxy-3-sulfanylpentadecoxy)-3-sulfanylpentadecan-2-ol Chemical compound CCCCCCCCCCCCC(S)C(O)COCC(O)C(S)CCCCCCCCCCCC FVTTWONDGJFJST-UHFFFAOYSA-N 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 abstract 1
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 abstract 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ZMRUPTIKESYGQW-UHFFFAOYSA-N propranolol hydrochloride Chemical compound [H+].[Cl-].C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 ZMRUPTIKESYGQW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000047 product Substances 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 4
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000001935 peptisation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- HBGYGPVHYBGCKG-UHFFFAOYSA-N 1-(1,2-dihydroxypropoxy)propane-1,2-diol Chemical class CC(O)C(O)OC(O)C(C)O HBGYGPVHYBGCKG-UHFFFAOYSA-N 0.000 description 1
- IQJUADKJXUPKJE-UHFFFAOYSA-N 1-(1,2-dihydroxypropylsulfanyl)propane-1,2-diol Chemical compound OC(C(C)O)SC(C(C)O)O IQJUADKJXUPKJE-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000009278 visceral effect Effects 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/22—Cellulose xanthate
- C08L1/24—Viscose
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7411920A SE421530B (sv) | 1974-09-23 | 1974-09-23 | Viskoslosning samt sett for framstellning av en viskoslosning |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU730313A3 true SU730313A3 (ru) | 1980-04-25 |
Family
ID=20322199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752177198A SU730313A3 (ru) | 1974-09-23 | 1975-09-19 | Вискоза |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4025353A (https=) |
| JP (1) | JPS5157758A (https=) |
| AU (1) | AU475845B2 (https=) |
| BE (1) | BE833603A (https=) |
| CA (1) | CA1032304A (https=) |
| CS (1) | CS210654B2 (https=) |
| DE (1) | DE2541961C3 (https=) |
| ES (1) | ES441331A1 (https=) |
| FR (1) | FR2285425A1 (https=) |
| GB (1) | GB1525627A (https=) |
| NL (1) | NL162408C (https=) |
| SE (1) | SE421530B (https=) |
| SU (1) | SU730313A3 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE455505B (sv) * | 1983-05-05 | 1988-07-18 | Berol Kemi Ab | Sett att forbettra en viskoslosnings filtrerbarhet |
| SE511842C2 (sv) * | 1997-04-18 | 1999-12-06 | Akzo Nobel Surface Chem | Sätt att framställa en viskoslösning |
| SE511094C2 (sv) * | 1997-12-05 | 1999-08-02 | Akzo Nobel Nv | Användning av en alkoxilerad polyamintensid som spinnbadsadditiv i viskosprocessen |
| JP6417502B2 (ja) * | 2015-04-23 | 2018-11-07 | サンノプコ株式会社 | マーセル化促進剤及びビスコースレーヨン製造方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2519227A (en) * | 1941-04-19 | 1950-08-15 | American Viscose Corp | Manufacture of yarns and the like |
| US3423499A (en) * | 1965-02-18 | 1969-01-21 | Fmc Corp | Process for spinning modified xanthated polymers |
| US3708364A (en) * | 1970-07-06 | 1973-01-02 | Oreal | Non-ionic surface-active agents derived from fatty chain diols and method of preparing same |
-
1974
- 1974-09-23 SE SE7411920A patent/SE421530B/xx unknown
-
1975
- 1975-09-19 FR FR7528790A patent/FR2285425A1/fr active Granted
- 1975-09-19 JP JP50114220A patent/JPS5157758A/ja active Granted
- 1975-09-19 BE BE160188A patent/BE833603A/xx not_active IP Right Cessation
- 1975-09-19 GB GB38608/75A patent/GB1525627A/en not_active Expired
- 1975-09-19 ES ES441331A patent/ES441331A1/es not_active Expired
- 1975-09-19 SU SU752177198A patent/SU730313A3/ru active
- 1975-09-19 CS CS756359A patent/CS210654B2/cs unknown
- 1975-09-19 AU AU85034/75A patent/AU475845B2/en not_active Expired
- 1975-09-19 DE DE2541961A patent/DE2541961C3/de not_active Expired
- 1975-09-22 CA CA235,997A patent/CA1032304A/en not_active Expired
- 1975-09-22 US US05/615,648 patent/US4025353A/en not_active Expired - Lifetime
- 1975-09-23 NL NL7511215.A patent/NL162408C/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA1032304A (en) | 1978-06-06 |
| DE2541961A1 (de) | 1976-04-01 |
| JPS535060B2 (https=) | 1978-02-23 |
| AU8503475A (en) | 1976-09-02 |
| JPS5157758A (en) | 1976-05-20 |
| CS210654B2 (en) | 1982-01-29 |
| US4025353A (en) | 1977-05-24 |
| SE7411920L (sv) | 1976-03-24 |
| ES441331A1 (es) | 1977-08-01 |
| NL162408C (nl) | 1980-05-16 |
| FR2285425B1 (https=) | 1978-12-08 |
| AU475845B2 (en) | 1976-09-02 |
| GB1525627A (en) | 1978-09-20 |
| BE833603A (fr) | 1976-01-16 |
| NL7511215A (nl) | 1976-03-25 |
| SE421530B (sv) | 1982-01-04 |
| FR2285425A1 (fr) | 1976-04-16 |
| DE2541961B2 (de) | 1979-06-21 |
| DE2541961C3 (de) | 1980-02-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5567496B2 (ja) | 界面活性剤として有用なアルキレンオキシドでキャップされた第２級アルコールアルコキシレート | |
| US4476037A (en) | Free flow, readily dilutable aqueous concentrates of a tenside of the sulfate and sulfonate type | |
| CA2282365C (en) | Polyoxyalkylene monoethers with reduced water affinity | |
| EP3020749B1 (de) | Verfahren zur herstellung von platin enthaltenden zusammensetzungen | |
| EP2588437B1 (en) | Branched secondary alcohol alkoxylate surfactants and process to make them | |
| SU730313A3 (ru) | Вискоза | |
| DE69837482T2 (de) | Entschäumende zusammensetzungen | |
| DE69609405T2 (de) | Verfahren zur alkoxylierung von fluorierten alkoholen | |
| GB2129004A (en) | Poloxyalkylene ethers of glycerol or 1,2-propane diol which are esterified with a fatty acid and/or isostearic acid their preparation and their use as thickeners or solubilisers | |
| TW200922968A (en) | An alkoxylate composition and a process for preparing the same | |
| SU1097201A3 (ru) | Способ разделени водосодержащих нефт ных эмульсий | |
| DE1745514A1 (de) | Sulfatoorganooxyalkylsiloxanverbindungen | |
| EP0346736A2 (de) | Polyether | |
| EP2571923B1 (de) | Derivate von tris(2-hydroxyphenyl)methan, deren herstellung und verwendung | |
| US2692877A (en) | Acetylation of wood pulp | |
| CN107108964A (zh) | 溶解纸浆组合物及粘胶丝制造方法 | |
| DE68918379T2 (de) | Eindickende Mittel für wässerige Systeme. | |
| DE1467552A1 (de) | Schaumarme Spuel- und Reinigungsmittel | |
| US5124074A (en) | Anti-foaming agent | |
| DE2246598B2 (de) | Schmieröl | |
| CN108654512A (zh) | 一种低泡非离子表面活性剂及其制备方法与应用 | |
| JP2999789B2 (ja) | ポリエーテル類の製造方法 | |
| WO1982000039A1 (en) | Methods of foam inhibition or depression | |
| DE19728900A1 (de) | Hydrophile Glykoside | |
| CN116099238A (zh) | 一种有机硅消泡剂的制备方法及其产物和应用 |