CH636635A5 - Antistatikum und verfahren zu dessen herstellung. - Google Patents

Antistatikum und verfahren zu dessen herstellung. Download PDF

Info

Publication number: CH636635A5
Authority: CH; Switzerland
Prior art keywords: antistatic; compounds; ether; water; bischlorohydrin
Prior art date: 1977-09-30

Application number

CH1008978A

Other languages

German (de)

English (en)

Inventor

Guenter Pusch

Original Assignee

Pfersee Chem Fab

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.)

1977-09-30

Filing date

1978-09-27

Publication date

1983-06-15

1978-09-27 Application filed by Pfersee Chem Fab filed Critical Pfersee Chem Fab

1983-06-15 Publication of CH636635A5 publication Critical patent/CH636635A5/de

Links

238000000034 method Methods 0.000 title claims description 6
238000004519 manufacturing process Methods 0.000 title description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 38
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 23
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 18
150000001875 compounds Chemical class 0.000 claims description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 7
239000002216 antistatic agent Substances 0.000 claims description 6
239000000975 dye Substances 0.000 claims description 6
230000000694 effects Effects 0.000 claims description 6
229920002994 synthetic fiber Polymers 0.000 claims description 6
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 5
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
239000000463 material Substances 0.000 claims description 5
239000012209 synthetic fiber Substances 0.000 claims description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
150000008044 alkali metal hydroxides Chemical class 0.000 claims description 4
239000007859 condensation product Substances 0.000 claims description 4
239000000047 product Substances 0.000 claims description 4
238000010992 reflux Methods 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
150000002170 ethers Chemical class 0.000 claims description 3
239000002657 fibrous material Substances 0.000 claims description 3
239000000049 pigment Substances 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
239000003513 alkali Substances 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
239000011734 sodium Substances 0.000 claims description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
239000004593 Epoxy Substances 0.000 claims 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
239000002253 acid Substances 0.000 claims 2
150000001412 amines Chemical class 0.000 claims 2
238000009833 condensation Methods 0.000 claims 2
230000005494 condensation Effects 0.000 claims 2
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims 2
239000000243 solution Substances 0.000 claims 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
150000007513 acids Chemical class 0.000 claims 1
229910001854 alkali hydroxide Inorganic materials 0.000 claims 1
150000001339 alkali metal compounds Chemical class 0.000 claims 1
125000003277 amino group Chemical group 0.000 claims 1
239000007864 aqueous solution Substances 0.000 claims 1
239000003054 catalyst Substances 0.000 claims 1
XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical group CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 claims 1
-1 chlorohydrin ethers Chemical class 0.000 claims 1
230000008021 deposition Effects 0.000 claims 1
230000006866 deterioration Effects 0.000 claims 1
238000007046 ethoxylation reaction Methods 0.000 claims 1
230000004720 fertilization Effects 0.000 claims 1
150000003944 halohydrins Chemical group 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
229920000233 poly(alkylene oxides) Chemical group 0.000 claims 1
229920000768 polyamine Polymers 0.000 claims 1
229910052700 potassium Inorganic materials 0.000 claims 1
239000011591 potassium Substances 0.000 claims 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
239000000203 mixture Substances 0.000 description 6
239000004744 fabric Substances 0.000 description 5
230000003068 static effect Effects 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 3
239000000835 fiber Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000004753 textile Substances 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
XJMWHXZUIGHOBA-UHFFFAOYSA-N azane;propanoic acid Chemical compound N.CCC(O)=O XJMWHXZUIGHOBA-UHFFFAOYSA-N 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
229940043276 diisopropanolamine Drugs 0.000 description 1
KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical compound [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
MSJMDZAOKORVFC-UAIGNFCESA-L disodium maleate Chemical compound [Na+].[Na+].[O-]C(=O)\C=C/C([O-])=O MSJMDZAOKORVFC-UAIGNFCESA-L 0.000 description 1
235000019524 disodium tartrate Nutrition 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000001053 orange pigment Substances 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
238000007747 plating Methods 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
FIJPWGLOBMXXSF-UHFFFAOYSA-M potassium;2-hydroxyacetate Chemical compound [K+].OCC([O-])=O FIJPWGLOBMXXSF-UHFFFAOYSA-M 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
238000002791 soaking Methods 0.000 description 1
HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
KYKFCSHPTAVNJD-UHFFFAOYSA-L sodium adipate Chemical compound [Na+].[Na+].[O-]C(=O)CCCCC([O-])=O KYKFCSHPTAVNJD-UHFFFAOYSA-L 0.000 description 1
235000011049 sodium adipate Nutrition 0.000 description 1
UDWXLZLRRVQONG-UHFFFAOYSA-M sodium hexanoate Chemical compound [Na+].CCCCCC([O-])=O UDWXLZLRRVQONG-UHFFFAOYSA-M 0.000 description 1
239000001433 sodium tartrate Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/55—Epoxy resins
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2618—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen
- C08G65/2621—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups
- C08G65/2624—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups containing aliphatic amine groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
- C08G65/33306—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group acyclic

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Coloring (AREA)

CH1008978A 1977-09-30 1978-09-27 Antistatikum und verfahren zu dessen herstellung. CH636635A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2744021A DE2744021C3 (de)	1977-09-30	1977-09-30	Konzentriertes wäßriges Mittel zum Antistatischmachen von synthetischen Fasermaterialien und dessen Verwendung

Publications (1)

Publication Number	Publication Date
CH636635A5 true CH636635A5 (de)	1983-06-15

Family

ID=6020307

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1008978A CH636635A5 (de)	1977-09-30	1978-09-27	Antistatikum und verfahren zu dessen herstellung.

Country Status (8)

Country	Link
BE (1)	BE870828A (fr)
CH (1)	CH636635A5 (fr)
DE (1)	DE2744021C3 (fr)
ES (1)	ES473782A1 (fr)
FR (1)	FR2404662A1 (fr)
GB (1)	GB2004890B (fr)
IT (1)	IT1107458B (fr)
SE (1)	SE7810186L (fr)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2042453A1 (en) *	1970-08-27	1972-03-02	Rotta Chem Fab Theodor	Condensates of reaction products of alkylene polyamines - with epichlorohydrine, and chlorohydrin ethers of polyalkylene glycol
CH548481A (fr) *	1971-12-03	1974-04-30
CH568435B5 (fr) *	1973-09-06	1975-10-31	Sandoz Ag
DE2432296B2 (de) *	1974-07-05	1978-04-20	Bayer Ag, 5090 Leverkusen	Flüssige, wässrige Zubereitungen von Fettsäure-Alkanolamin-Kondensaten und deren Verwendung

1977
- 1977-09-30 DE DE2744021A patent/DE2744021C3/de not_active Expired
1978
- 1978-09-27 CH CH1008978A patent/CH636635A5/de not_active IP Right Cessation
- 1978-09-27 IT IT51274/78A patent/IT1107458B/it active
- 1978-09-27 GB GB7838409A patent/GB2004890B/en not_active Expired
- 1978-09-28 SE SE7810186A patent/SE7810186L/xx unknown
- 1978-09-28 BE BE190760A patent/BE870828A/fr not_active IP Right Cessation
- 1978-09-29 ES ES473782A patent/ES473782A1/es not_active Expired
- 1978-09-29 FR FR7828039A patent/FR2404662A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
DE2744021A1 (de)	1979-04-05
IT1107458B (it)	1985-11-25
GB2004890A (en)	1979-04-11
GB2004890B (en)	1982-03-17
SE7810186L (sv)	1979-03-31
FR2404662A1 (fr)	1979-04-27
DE2744021B2 (de)	1980-08-14
ES473782A1 (es)	1979-04-16
IT7851274A0 (it)	1978-09-27
DE2744021C3 (de)	1981-06-11
BE870828A (fr)	1979-01-15

Legal Events

Date	Code	Title	Description
1985-05-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

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DE1147910B (de)	1963-05-02	Verfahren zur Verringerung der Ansammlung elektrostatischer Ladungen auf hydrophoben Stoffen
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DE1419042A1 (de)	1969-03-27	Verfahren zur Ausruestung von geformten Gebilden
DE1940178A1 (de)	1971-03-04	AEthansulfonsaeurederivate
DE2256234A1 (de)	1973-05-24	Kationische oberflaechenaktive verbindungen, verfahren zu ihrer herstellung und ihre verwendung fuer die behandlung von textilmaterialien
DE2206983B2 (de)	1975-11-20	Mittel und Verfahren zum gleichzeitigen antistatischen und schmutzabweisenden Ausrüsten von Fasermateralien
DE1060595B (de)	1959-07-02	Verfahren zur Herstellung von Egalisiermitteln fuer das Faerben von Textilien
DE1619542B1 (de)	1971-02-04	Verfahren zum Färben von stickstoffhaltigen Fasermaterialien
EP0221855B1 (fr)	1990-07-11	Sels d'ammonium diquaternaire, leur préparation et leur utilisation comme agent de finition pour textiles
EP0057398B1 (fr)	1984-06-13	Procédé pour le post-traitement de teintures de matière fibreuse rendue résistant au feutrage par un apprêt
CH313159A (de)	1956-03-31	Verfahren zur Herstellung beständiger Färbe- und Abziehbäder
DE2949212C2 (fr)	1989-02-16
DE1469344C3 (de)	1973-10-31	Verfahren zur antistatischen Aus rustung von faserigen Materialien
CH636635A5 (de)	1983-06-15	Antistatikum und verfahren zu dessen herstellung.
EP0093361B1 (fr)	1987-03-18	Composés alcoxyalcoylés d'ammonium quaternaire, procédé de préparation et utilisation
DE1619082A1 (de)	1970-02-12	Verfahren zur permanenten antistatischen Ausruestung von Textilmaterial
DE1619182B2 (de)	1977-07-14	Verfahren zum weichmachen von textilien
EP0824156B1 (fr)	2003-08-27	Polymères dérivés de l'urée, solubles dans l'eau, ayant des groupements ammonium quaternaire, et leur utilisation
DE894099C (de)	1953-10-22	Verfahren zum Verbessern der Nassechtheiten von Faerbungen und Drucken
DE2335674C3 (de)	1978-09-21	Verfahren und Mittel zum Präparieren von Fasern
DE1930768A1 (de)	1971-01-07	Verfahren zur Permanentausruestung von Cellulosefasern enthaltenden Textilmaterialien
DE2442250A1 (de)	1975-03-13	Verfahren zur ausruestung von natuerlichen und synthetischen fasermaterialien
DE1619082C (de)	1972-06-15	Verwendung von wasserlöslichen oder in Wasser dispergierbaren hartbaren Konden sationsprodukten zur permanenten antista tischen Ausrüstung von Textilmaterial
DE1469280C (de)	1973-06-20	Verwendung wasseriger Zubereitungen von Salzen von N,N disubstituierten Saure amiden von Di oder Tricarbonsäuren zum Weichmachen von Textilien
DE1419042C (de)	1972-08-03	Verfahren zur permanenten antistatischen Ausrüstung von geformten Gebilden