CS210654B2 - Viscous solution - Google Patents

Viscous solution Download PDF

Info

Publication number: CS210654B2
Authority: CS; Czechoslovakia
Prior art keywords: carbon atoms; compound; diol; viscose; viscose solution
Prior art date: 1974-09-23

Application number

CS756359A

Other languages

Czech (cs)

English (en)

Inventor

Svante L Wahlen

Original Assignee

Berol Kemi Ab

Priority date (The priority date 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 date listed.)

1974-09-23

Filing date

1975-09-19

Publication date

1982-01-29

1975-09-19 Application filed by Berol Kemi Ab filed Critical Berol Kemi Ab

1982-01-29 Publication of CS210654B2 publication Critical patent/CS210654B2/cs

Links

229920000297 Rayon Polymers 0.000 claims abstract description 28
150000001875 compounds Chemical class 0.000 claims abstract description 26
239000004094 surface-active agent Substances 0.000 claims abstract description 18
229920002678 cellulose Polymers 0.000 claims abstract description 13
239000001913 cellulose Substances 0.000 claims abstract description 13
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 6
125000006353 oxyethylene group Chemical group 0.000 claims abstract description 3
239000011347 resin Substances 0.000 claims description 12
229920005989 resin Polymers 0.000 claims description 12
239000002736 nonionic surfactant Substances 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 4
239000007795 chemical reaction product Substances 0.000 claims description 4
239000000835 fiber Substances 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
-1 neionogsnní Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
238000000926 separation method Methods 0.000 claims description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
150000008040 ionic compounds Chemical class 0.000 claims 1
229910052757 nitrogen Inorganic materials 0.000 claims 1
DWANEFRJKWXRSG-UHFFFAOYSA-N 1,2-tetradecanediol Chemical compound CCCCCCCCCCCCC(O)CO DWANEFRJKWXRSG-UHFFFAOYSA-N 0.000 abstract description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract description 5
BTOOAFQCTJZDRC-UHFFFAOYSA-N 1,2-hexadecanediol Chemical compound CCCCCCCCCCCCCCC(O)CO BTOOAFQCTJZDRC-UHFFFAOYSA-N 0.000 abstract description 4
ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 abstract description 4
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 description 2
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 description 2
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 description 2
125000001165 hydrophobic group Chemical group 0.000 abstract 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-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
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 8
230000000694 effects Effects 0.000 description 8
125000002947 alkylene group Chemical group 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
238000000034 method Methods 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000003513 alkali Substances 0.000 description 3
XWAMHGPDZOVVND-UHFFFAOYSA-N 1,2-octadecanediol Chemical compound CCCCCCCCCCCCCCCCC(O)CO XWAMHGPDZOVVND-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
229940074993 carbon disulfide Drugs 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
239000004627 regenerated cellulose Substances 0.000 description 2
238000002834 transmittance Methods 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 class OC(C(C)O)SC(C(C)O)O IQJUADKJXUPKJE-UHFFFAOYSA-N 0.000 description 1
DSCJWPCDWPRRIR-UHFFFAOYSA-N 1-(2,3-dihydroxynonadecylsulfanyl)nonadecane-2,3-diol Chemical compound CCCCCCCCCCCCCCCCC(O)C(O)CSCC(O)C(O)CCCCCCCCCCCCCCCC DSCJWPCDWPRRIR-UHFFFAOYSA-N 0.000 description 1
229940126062 Compound A Drugs 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
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
238000005282 brightening Methods 0.000 description 1
QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 1
150000001767 cationic compounds Chemical class 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000010411 cooking Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000005517 mercerization Methods 0.000 description 1
PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
238000012163 sequencing technique Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
229940035024 thioglycerol Drugs 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000004711 α-olefin 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)

CS756359A 1974-09-23 1975-09-19 Viscous solution CS210654B2 (en)

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
CS210654B2 true CS210654B2 (en)	1982-01-29

Family

ID=20322199

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS756359A CS210654B2 (en)	1974-09-23	1975-09-19	Viscous solution

Country Status (13)

Country	Link
US (1)	US4025353A (fr)
JP (1)	JPS5157758A (fr)
AU (1)	AU475845B2 (fr)
BE (1)	BE833603A (fr)
CA (1)	CA1032304A (fr)
CS (1)	CS210654B2 (fr)
DE (1)	DE2541961C3 (fr)
ES (1)	ES441331A1 (fr)
FR (1)	FR2285425A1 (fr)
GB (1)	GB1525627A (fr)
NL (1)	NL162408C (fr)
SE (1)	SE421530B (fr)
SU (1)	SU730313A3 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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 DE DE2541961A patent/DE2541961C3/de not_active Expired
- 1975-09-19 JP JP50114220A patent/JPS5157758A/ja active Granted
- 1975-09-19 SU SU752177198A patent/SU730313A3/ru active
- 1975-09-19 AU AU85034/75A patent/AU475845B2/en not_active Expired
- 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 FR FR7528790A patent/FR2285425A1/fr active Granted
- 1975-09-19 BE BE160188A patent/BE833603A/fr not_active IP Right Cessation
- 1975-09-19 CS CS756359A patent/CS210654B2/cs unknown
- 1975-09-22 CA CA235,997A patent/CA1032304A/fr 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
GB1525627A (en)	1978-09-20
BE833603A (fr)	1976-01-16
AU475845B2 (en)	1976-09-02
SU730313A3 (ru)	1980-04-25
US4025353A (en)	1977-05-24
ES441331A1 (es)	1977-08-01
CA1032304A (fr)	1978-06-06
DE2541961C3 (de)	1980-02-14
NL7511215A (nl)	1976-03-25
SE421530B (sv)	1982-01-04
FR2285425B1 (fr)	1978-12-08
JPS535060B2 (fr)	1978-02-23
DE2541961B2 (de)	1979-06-21
DE2541961A1 (de)	1976-04-01
AU8503475A (en)	1976-09-02
NL162408C (nl)	1980-05-16
FR2285425A1 (fr)	1976-04-16
SE7411920L (sv)	1976-03-24
JPS5157758A (en)	1976-05-20

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US20220119554A1 (en)	2022-04-21	Method for producing a viscose solution and a viscose solution produced thereby and a method for producing viscose fiber
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