GB917232A - Poly-n-acrylylpiperidine filaments - Google Patents
Poly-n-acrylylpiperidine filamentsInfo
- Publication number
- GB917232A GB917232A GB41926/60A GB4192660A GB917232A GB 917232 A GB917232 A GB 917232A GB 41926/60 A GB41926/60 A GB 41926/60A GB 4192660 A GB4192660 A GB 4192660A GB 917232 A GB917232 A GB 917232A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acrylylpiperidine
- poly
- spun
- filaments
- methylene chloride
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- 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
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
-
- 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
- D01F6/74—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polycondensates of cyclic compounds, e.g. polyimides, polybenzimidazoles
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
Abstract
Filaments are made by the solution-spinning of poly-N-acrylylpiperidine. Solutions of crystalline poly-N-acrylylpiperidine in chlorinated hydrocarbon solvents or mixtures thereof, e.g. methylene chloride, chloroform, tetrachlorethane, chlorobenzene, and mixtures of methylene chloride with either chloroform or chlorobenzene, may be wet-spun into any of the following coagulants:- acetone, aqueous acetone, tetrahydrofuran, methyl ethyl ketone, N:N-dimethylformamide, N:N-dimethylacetamide, cyclohexane and isopropyl alcohol. Chlorinated hydrocarbon solvents boiling below 70 DEG C. are preferred. Alternatively, solutions of crystalline poly-N-acrylylpiperidine in lower fatty acids, e.g. formic or acetic acid, may be wet-spun into water or aqueous alkali. Coagulated wetspun filaments may be stretched in a hot glycerol bath at, e.g. over 60 DEG C., dried, wound-up, and then further stretched, e.g. over a hot plate at temperatures above 130 DEG C. In an example, a 20% w./v. solution of poly-N-acrylylpiperidine in methylene chloride is spun into a coagulating bath of N:N-dimethylformamide at 20 DEG C., and the coagulated filaments are drawn 100% in a glycerol bath at 120 DEG C. After drying, the filaments are further drawn at a draw ratio of 2:1 over a hot plate at 180 DEG C. Crystalline poly-N-acrylylpiperidine may also be dissolved in chloroform or methylene chloride and dry-spun into hot air at a temperature above 40 DEG C. In an example, a 40% w./v. solution of poly-N-acrylylpiperidine in methylene chloride at 38 DEG C. is dry-spun into air at 44 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB41926/60A GB917232A (en) | 1960-12-06 | 1960-12-06 | Poly-n-acrylylpiperidine filaments |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB41926/60A GB917232A (en) | 1960-12-06 | 1960-12-06 | Poly-n-acrylylpiperidine filaments |
Publications (1)
Publication Number | Publication Date |
---|---|
GB917232A true GB917232A (en) | 1963-01-30 |
Family
ID=10422008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB41926/60A Expired GB917232A (en) | 1960-12-06 | 1960-12-06 | Poly-n-acrylylpiperidine filaments |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB917232A (en) |
-
1960
- 1960-12-06 GB GB41926/60A patent/GB917232A/en not_active Expired
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