RU2114940C1 - Усовершенствованный способ приготовления нитей из поли-(м-фениленизофталамида) - Google Patents
Усовершенствованный способ приготовления нитей из поли-(м-фениленизофталамида) Download PDFInfo
- Publication number
- RU2114940C1 RU2114940C1 RU95118153A RU95118153A RU2114940C1 RU 2114940 C1 RU2114940 C1 RU 2114940C1 RU 95118153 A RU95118153 A RU 95118153A RU 95118153 A RU95118153 A RU 95118153A RU 2114940 C1 RU2114940 C1 RU 2114940C1
- Authority
- RU
- Russia
- Prior art keywords
- hcl
- solution
- polymer
- phenyleneisophthalamide
- amide
- Prior art date
Links
- YCGKJPVUGMBDDS-UHFFFAOYSA-N 3-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2C=3C=C2C=CC=3)=C1 YCGKJPVUGMBDDS-UHFFFAOYSA-N 0.000 title abstract description 3
- 238000004519 manufacturing process Methods 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims abstract description 42
- 239000002904 solvent Substances 0.000 claims abstract description 31
- 150000001408 amides Chemical class 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 20
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003456 ion exchange resin Substances 0.000 claims abstract description 12
- 229920003303 ion-exchange polymer Polymers 0.000 claims abstract description 12
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract description 11
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229940018564 m-phenylenediamine Drugs 0.000 claims abstract description 11
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 9
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 9
- 239000004571 lime Substances 0.000 claims abstract description 9
- 238000006386 neutralization reaction Methods 0.000 claims abstract description 6
- 150000001412 amines Chemical class 0.000 claims abstract description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical group CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 20
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 229920000889 poly(m-phenylene isophthalamide) Polymers 0.000 claims description 13
- 239000006227 byproduct Substances 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 238000005342 ion exchange Methods 0.000 claims description 3
- 229920006158 high molecular weight polymer Polymers 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 39
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 14
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000007787 solid Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000015271 coagulation Effects 0.000 description 5
- 238000005345 coagulation Methods 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical class C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 238000004804 winding Methods 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
- D01F6/605—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
- B01J41/04—Processes using organic exchangers
- B01J41/07—Processes using organic exchangers in the weakly basic form
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Polyamides (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/039.564 | 1993-03-29 | ||
| US08/039,564 US5340519A (en) | 1993-03-29 | 1993-03-29 | Preparation of poly(m-phenylene isophthalamide) filaments |
| US08/039,564 | 1993-03-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU95118153A RU95118153A (ru) | 1997-09-20 |
| RU2114940C1 true RU2114940C1 (ru) | 1998-07-10 |
Family
ID=21906141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU95118153A RU2114940C1 (ru) | 1993-03-29 | 1994-03-28 | Усовершенствованный способ приготовления нитей из поли-(м-фениленизофталамида) |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5340519A (enExample) |
| EP (1) | EP0692038B1 (enExample) |
| JP (1) | JP3299757B2 (enExample) |
| AU (1) | AU677053B2 (enExample) |
| BR (1) | BR9406502A (enExample) |
| CA (1) | CA2159181C (enExample) |
| DE (1) | DE69428591T2 (enExample) |
| ES (1) | ES2164101T3 (enExample) |
| RU (1) | RU2114940C1 (enExample) |
| SG (1) | SG43318A1 (enExample) |
| TW (1) | TW272998B (enExample) |
| UA (1) | UA35613C2 (enExample) |
| WO (1) | WO1994023099A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2302605A1 (en) | 1997-09-09 | 1999-03-18 | E.I. Du Pont De Nemours And Company | Wholly aromatic synthetic fibers spun from a liquid-crystalline polymer solution, a process for preparing the same fibers and use of the same fibers |
| WO2001029296A1 (fr) * | 1999-10-21 | 2001-04-26 | Teijin Limited | Procédé de production de fibres polyamides méta-aromatiques |
| DE10331772A1 (de) * | 2003-07-11 | 2005-02-03 | Basf Ag | Verfahren zur Herstellung von Diaminodiarylmethanen |
| CN101275308B (zh) * | 2007-03-26 | 2010-06-02 | 上海特安纶纤维有限公司 | 全间位芳香族聚砜酰胺纤维的制造方法 |
| US7771638B2 (en) * | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | Rapid plasticization of quenched yarns |
| US7771637B2 (en) * | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | High-speed meta-aramid fiber production |
| US7771636B2 (en) * | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | Single stage drawing for MPD-I yarn |
| US7780889B2 (en) * | 2007-12-19 | 2010-08-24 | E.I. Du Pont De Nemours And Company | Multistage draw with relaxation step |
| CN101285214B (zh) * | 2008-03-18 | 2011-11-09 | 东华大学 | 一种低含盐的芳纶1313湿法纺制纤维法 |
| CN102534840B (zh) * | 2010-12-29 | 2014-11-12 | 圣欧芳纶（江苏）股份有限公司 | 制备间位芳纶纤维的方法 |
| CN103668533B (zh) * | 2013-11-28 | 2016-06-22 | 圣欧芳纶（江苏）股份有限公司 | 一种聚间苯二甲酰间苯二胺纤维及其制备方法 |
| CN110218309B (zh) * | 2019-06-05 | 2022-04-26 | 赣州龙邦材料科技有限公司 | 一种胶体状芳纶聚合物及其制备方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3498955A (en) * | 1967-07-06 | 1970-03-03 | Monsanto Co | Neutralization of polymerization solutions of aromatic polyamides |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3063966A (en) * | 1958-02-05 | 1962-11-13 | Du Pont | Process of making wholly aromatic polyamides |
| DE2313308A1 (de) * | 1973-03-17 | 1974-09-19 | Hoechst Ag | Verfahren zur herstellung von faeden, fasern und folien aus aromatischen polyamiden |
| SU494036A1 (ru) * | 1974-05-30 | 1978-11-15 | Предприятие П/Я Г-4059 | Способ получени ароматических полиамидов |
| US4342715A (en) * | 1980-10-29 | 1982-08-03 | Teijin Limited | Process for preparing wholly aromatic polyamide shaped articles |
| US4758649A (en) * | 1986-05-21 | 1988-07-19 | Kuraray Co., Ltd. | Heat resistant organic synthetic fibers and process for producing the same |
| JPH03296530A (ja) * | 1990-04-16 | 1991-12-27 | Toray Ind Inc | 芳香族ポリアミド溶液の製造法 |
-
1993
- 1993-03-29 US US08/039,564 patent/US5340519A/en not_active Expired - Lifetime
-
1994
- 1994-03-28 RU RU95118153A patent/RU2114940C1/ru active
- 1994-03-28 ES ES94912845T patent/ES2164101T3/es not_active Expired - Lifetime
- 1994-03-28 EP EP94912845A patent/EP0692038B1/en not_active Expired - Lifetime
- 1994-03-28 JP JP52216894A patent/JP3299757B2/ja not_active Expired - Fee Related
- 1994-03-28 AU AU65233/94A patent/AU677053B2/en not_active Ceased
- 1994-03-28 CA CA002159181A patent/CA2159181C/en not_active Expired - Fee Related
- 1994-03-28 UA UA95094342A patent/UA35613C2/uk unknown
- 1994-03-28 WO PCT/US1994/003145 patent/WO1994023099A1/en not_active Ceased
- 1994-03-28 DE DE69428591T patent/DE69428591T2/de not_active Expired - Fee Related
- 1994-03-28 BR BR9406502A patent/BR9406502A/pt not_active IP Right Cessation
- 1994-03-28 SG SG1996008242A patent/SG43318A1/en unknown
- 1994-04-06 TW TW083102981A patent/TW272998B/zh active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3498955A (en) * | 1967-07-06 | 1970-03-03 | Monsanto Co | Neutralization of polymerization solutions of aromatic polyamides |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3299757B2 (ja) | 2002-07-08 |
| US5340519A (en) | 1994-08-23 |
| TW272998B (enExample) | 1996-03-21 |
| CA2159181C (en) | 2003-05-13 |
| EP0692038A1 (en) | 1996-01-17 |
| CA2159181A1 (en) | 1994-10-13 |
| WO1994023099A1 (en) | 1994-10-13 |
| EP0692038B1 (en) | 2001-10-10 |
| ES2164101T3 (es) | 2002-02-16 |
| UA35613C2 (uk) | 2001-04-16 |
| AU6523394A (en) | 1994-10-24 |
| JPH08508548A (ja) | 1996-09-10 |
| DE69428591D1 (de) | 2001-11-15 |
| BR9406502A (pt) | 1996-01-02 |
| DE69428591T2 (de) | 2002-07-18 |
| AU677053B2 (en) | 1997-04-10 |
| SG43318A1 (en) | 1997-10-17 |
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