GB1180238A - Synthetic Resins and Substrates Treated Therewith - Google Patents
Synthetic Resins and Substrates Treated TherewithInfo
- Publication number
- GB1180238A GB1180238A GB2761766A GB2761766A GB1180238A GB 1180238 A GB1180238 A GB 1180238A GB 2761766 A GB2761766 A GB 2761766A GB 2761766 A GB2761766 A GB 2761766A GB 1180238 A GB1180238 A GB 1180238A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- groups
- acid
- secondary amine
- anhydride
- 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
-
- 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
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
1,180,238. Water soluble resins. HERCULES Inc. 7 Sept., 1967 [21 June, 1966], No. 27617/66. Heading C3R. [Also in Division D1] An amphionic/cationic condensation product is prepared by reacting: (I) a linear saturated organic polymer containing a plurality of secondary amine groups separated by hydrocarbon chains which are interrupted by carbonamide groups, successively with: (II) a compound selected from halogenoalkanoic acids, halogenoalkanesulphonic acids, #-sulphatoethanesulphonic acid, vinylsulphonic acid, #- sulphopropionic acid anhydride, ortho-sulphobenzoic acid anhydride, maleic anhydride, succinic anhydride or phthalic anhydride, with the said secondary amino groups to convert them to groups of the structure: N-X-R-Y in which X is a carbonyl, sulphonyl or alkylene residue; R is a hydrocarbon residue, preferably an alkylene residue and Y represents -SO 3 H or -COOH (or salts thereof) thereby to form a branched chain polymer, and (III) an epihalohydrin. Reaction may be effected in any order with II and III but the first of them must be reacted in conditions such that a substantial proportion (e.g. 50-95%) of the secondary amine groups are available to take part in the second reaction. The polymer may also be reacted with (IV) a reactive derivative of a compound: in which B is selected from -CHROH, -CHR<SP>1</SP>OH and -COOH; A is selected from - CHROH, -CHR<SP>1</SP>OH, -COOH and -OQ in which Q is phenyl, naphthyl or alkyl; R and R<SP>1</SP> are hydrogen or saturated hydrocarbon groups; n is an integer of at least 3. Reaction with (IV) may take place with up to 30% of the available secondary amine groups. (I) may be a water soluble polymer derived from reaction of 1 mole of a polyalkylene polyamine containing at least one secondary amine group with 0À8 to 1À2 moles of an alkane dicarboxylic acid, e.g. adipic acid and diethylenetriamine. (IV) may be derived from the reaction of polyethylene glycol (M.W. 1500) and epichlorohydrin. The products are used to impregnate natural or synthetic fibrous materials, e.g. wool or flannel cloth to impart shrink resistant and antistatic properties.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2761766A GB1180238A (en) | 1966-06-21 | 1966-06-21 | Synthetic Resins and Substrates Treated Therewith |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2761766A GB1180238A (en) | 1966-06-21 | 1966-06-21 | Synthetic Resins and Substrates Treated Therewith |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1180238A true GB1180238A (en) | 1970-02-04 |
Family
ID=10262512
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2761766A Expired GB1180238A (en) | 1966-06-21 | 1966-06-21 | Synthetic Resins and Substrates Treated Therewith |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1180238A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2159484A1 (en) * | 1971-11-12 | 1973-06-22 | Bayer Ag |
-
1966
- 1966-06-21 GB GB2761766A patent/GB1180238A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2159484A1 (en) * | 1971-11-12 | 1973-06-22 | Bayer Ag | |
US3932363A (en) * | 1971-11-12 | 1976-01-13 | Bayer Aktiengesellschaft | Polyamines containing acid groups |
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