PL104341B1 - Sposob wytwarzania kopolieteroestroamidu odpowiedniego na przedze i wlokna antystatyczne - Google Patents
Sposob wytwarzania kopolieteroestroamidu odpowiedniego na przedze i wlokna antystatyczne Download PDFInfo
- Publication number
- PL104341B1 PL104341B1 PL19301876A PL19301876A PL104341B1 PL 104341 B1 PL104341 B1 PL 104341B1 PL 19301876 A PL19301876 A PL 19301876A PL 19301876 A PL19301876 A PL 19301876A PL 104341 B1 PL104341 B1 PL 104341B1
- Authority
- PL
- Poland
- Prior art keywords
- glycol
- polyamide
- antistatic
- weight
- fibers
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title claims description 30
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 56
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 19
- 239000004952 Polyamide Substances 0.000 claims description 18
- 229920002647 polyamide Polymers 0.000 claims description 18
- -1 aliphatic diols Chemical class 0.000 claims description 8
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- 229920000571 Nylon 11 Polymers 0.000 claims description 5
- 229920002292 Nylon 6 Polymers 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- DOVJROOSBVOVCS-UHFFFAOYSA-N ethane-1,1,1,2,2-pentol Chemical compound OC(O)C(O)(O)O DOVJROOSBVOVCS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004953 Aliphatic polyamide Substances 0.000 claims 1
- 229920003231 aliphatic polyamide Polymers 0.000 claims 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 21
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 10
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 7
- 229910052753 mercury Inorganic materials 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 239000001361 adipic acid Substances 0.000 description 5
- 239000012298 atmosphere Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 241000208202 Linaceae Species 0.000 description 3
- 235000004431 Linum usitatissimum Nutrition 0.000 description 3
- MLTWWHUPECYSBZ-UHFFFAOYSA-N ethene-1,1,2-triol Chemical group OC=C(O)O MLTWWHUPECYSBZ-UHFFFAOYSA-N 0.000 description 3
- 125000001033 ether group Chemical group 0.000 description 3
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 3
- 150000003951 lactams Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 125000003827 glycol group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 238000006384 oligomerization reaction Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005829 trimerization reaction Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- MEPBGQNZBKRPSN-UHFFFAOYSA-N 2-iminodecanoic acid Chemical compound N=C(C(=O)O)CCCCCCCC MEPBGQNZBKRPSN-UHFFFAOYSA-N 0.000 description 1
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
- 241001214176 Capros Species 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 206010033307 Overweight Diseases 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004959 Rilsan Substances 0.000 description 1
- 241000546339 Trioxys Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- UPNPFJPZTJQZJM-UHFFFAOYSA-N icosane-1,2-diamine Chemical compound CCCCCCCCCCCCCCCCCCC(N)CN UPNPFJPZTJQZJM-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
Classifications
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
-
- 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
- D01F6/82—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from polyester amides or polyether amides
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)
- Polyamides (AREA)
- Artificial Filaments (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7531828A FR2328060A1 (fr) | 1975-10-17 | 1975-10-17 | Copolyetheresteramides comme fibres et filaments antistatiques |
| FR7628248A FR2364982A2 (fr) | 1976-09-21 | 1976-09-21 | Copolyetheresteramides comme fibres et filaments antistatiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL104341B1 true PL104341B1 (pl) | 1979-08-31 |
Family
ID=26219104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL19301876A PL104341B1 (pl) | 1975-10-17 | 1976-10-14 | Sposob wytwarzania kopolieteroestroamidu odpowiedniego na przedze i wlokna antystatyczne |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS5288624A (enrdf_load_stackoverflow) |
| BR (1) | BR7606915A (enrdf_load_stackoverflow) |
| CA (1) | CA1091387A (enrdf_load_stackoverflow) |
| DD (1) | DD126932A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2646752C3 (enrdf_load_stackoverflow) |
| GB (1) | GB1518060A (enrdf_load_stackoverflow) |
| IT (1) | IT1083965B (enrdf_load_stackoverflow) |
| NL (1) | NL7611468A (enrdf_load_stackoverflow) |
| PL (1) | PL104341B1 (enrdf_load_stackoverflow) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2716004C3 (de) * | 1977-04-09 | 1987-01-22 | Hüls AG, 4370 Marl | Thermoplastische Formmassen auf der Basis von Polylaurinlactam und deren Verwendung zur Herstellung von Rohren |
| FR2401947A1 (fr) * | 1977-09-02 | 1979-03-30 | Ato Chimie | Procede de preparation de polyether-ester-amides sequences utilisables, entre autres, comme produits a mouler, a extruder ou a filer |
| FR2497518A1 (fr) * | 1981-01-05 | 1982-07-09 | Ato Chimie | Compositions adhesives thermofusibles a base de copolyetheramides sequences |
| JPS58206628A (ja) * | 1982-05-27 | 1983-12-01 | Toray Ind Inc | ポリエ−テルエステルアミドの製造方法 |
| JPS58210925A (ja) * | 1982-06-02 | 1983-12-08 | Toray Ind Inc | ポリエ−テルエステルアミドの製造方法 |
| JPS59213724A (ja) * | 1983-05-18 | 1984-12-03 | Toray Ind Inc | 脂肪族ポリアミドエラストマ |
| JPS60110724A (ja) * | 1983-11-18 | 1985-06-17 | Daicel Chem Ind Ltd | ポリエ−テルエステルアミドの製造方法 |
| JPS61155426A (ja) * | 1984-12-28 | 1986-07-15 | Res Dev Corp Of Japan | 抗血栓性を有する医療用材 |
| JP4054151B2 (ja) | 1999-01-18 | 2008-02-27 | 日本ポリペンコ株式会社 | 帯電防止性ポリエステルアミド樹脂成形体 |
| EP1351867A1 (en) | 2001-01-15 | 2003-10-15 | Ciba SC Holding AG | Antistatic flexible intermediate bulk container |
| WO2004065471A2 (en) | 2003-01-24 | 2004-08-05 | Ciba Specialty Chemicals Holding Inc. | Antistatic composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1495800A1 (de) * | 1964-05-13 | 1969-05-29 | Bayer Ag | Verfahren zur Herstellung von Polyaetheresteramiden |
| BE755378A (fr) * | 1969-08-27 | 1971-02-01 | Bayer Ag | Polyesteramides, leur procede de preparation et leurs applications a laformation de fibres, fils, feuilles et analogues |
-
1976
- 1976-10-13 GB GB4255076A patent/GB1518060A/en not_active Expired
- 1976-10-14 PL PL19301876A patent/PL104341B1/pl unknown
- 1976-10-15 NL NL7611468A patent/NL7611468A/xx not_active Application Discontinuation
- 1976-10-15 JP JP12301776A patent/JPS5288624A/ja active Granted
- 1976-10-15 IT IT2834676A patent/IT1083965B/it active
- 1976-10-15 DD DD19529376A patent/DD126932A5/xx unknown
- 1976-10-15 BR BR7606915A patent/BR7606915A/pt unknown
- 1976-10-15 CA CA263,477A patent/CA1091387A/fr not_active Expired
- 1976-10-15 DE DE19762646752 patent/DE2646752C3/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5288624A (en) | 1977-07-25 |
| DE2646752C3 (de) | 1982-04-08 |
| BR7606915A (pt) | 1977-08-30 |
| DE2646752B2 (de) | 1981-05-21 |
| CA1091387A (fr) | 1980-12-09 |
| DE2646752A1 (de) | 1977-04-28 |
| IT1083965B (it) | 1985-05-25 |
| JPS5522567B2 (enrdf_load_stackoverflow) | 1980-06-18 |
| DD126932A5 (enrdf_load_stackoverflow) | 1977-08-24 |
| GB1518060A (en) | 1978-07-19 |
| NL7611468A (nl) | 1977-04-19 |
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