GB1085666A - Modified polycarbonamides - Google Patents

Modified polycarbonamides

Info

Publication number
GB1085666A
GB1085666A GB1964965A GB1964965A GB1085666A GB 1085666 A GB1085666 A GB 1085666A GB 1964965 A GB1964965 A GB 1964965A GB 1964965 A GB1964965 A GB 1964965A GB 1085666 A GB1085666 A GB 1085666A
Authority
GB
United Kingdom
Prior art keywords
acid
naphthalene
potassium
carboxylic acid
sulphonate
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
Application number
GB1964965A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Co
Original Assignee
Monsanto Co
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.)
Filing date
Publication date
Application filed by Monsanto Co filed Critical Monsanto Co
Publication of GB1085666A publication Critical patent/GB1085666A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/42Polyamides containing atoms other than carbon, hydrogen, oxygen, and nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyamides (AREA)
  • Artificial Filaments (AREA)

Abstract

Fibre-forming linear polycarbonamides are characterized by recurring carbonamide linkages as an integral part of the polymer chain and containing as a component part of the polymer chain between 0.1 and 2.0 mole percentage based on the weight of the polycarbonamide of chain terminal units of the structure: <FORM:1085666/C3/1> wherein n is 0 or an integer from 1 to 6, Z is <FORM:1085666/C3/2> , X is hydrogen or alkyl of 1 to 6 carbon atoms and M is hydrogen, the ammonium radical or an alkali metal. They may be prepared by polymerizing a polycarbonamideforming composition selected from (A) substantially equimolecular proportions of a dibasic acid of the formula HOOC-R-COOH and a diamine of the formula <FORM:1085666/C3/3> and (B) a monoaminomonocarboxylic acid having the formula <FORM:1085666/C3/4> and (C) polycarbonamide forming derivatives of (A) and (B) wherein R is a divalent hydrocarbon radical and X is hydrogen or alkyl of 1 to 6 carbon atoms, in the presence of between 0.1 and 2.0 mole per cent based on the weight of the polycarbonamide of a monofunctional disulphonated compound of the formula <FORM:1085666/C3/5> where n and M are as above and Y is -OH, -Cl or OR1, R1 being a monovalent hydrocarbon radical such that R1-OH is volatile below the decomposition temperature of the polycarbonamide formed. Many examples of the dibasic acids, diamines, monoaminomonocarboxylic acids and monofunctional disulphonated compounds are listed but the examples describe the preparation of polycarbonamides from (a) di(potassium sulphonate)-naphthalene-2-carboxylic acid and hexamethylene diammonium adipate, (b) di(potassium sulphonate)-naphthalene-2-carboxylic acid and epsiloncaprolactam, (c) di(potassium sulphonate)-naphthalene-2-carboxylic acid and hexamethylene diammonium sebacate, (d) di(sulphonic acid) naphthalene-2-carboxylic acid and hexamethylene diammonium adipate and (e) di-(ammonium sulphonate) - naphthalene - 2- carboxylic acid and hexamethylene diammonium adipate.ALSO:Di(potassium sulphonate) - naphthalene - 2 - carboxylic acid may be prepared by reacting 2-naphthoic acid with fuming sulphuric acid followed by slow addition of potassium bicarbonate. The precipitated product so formed may be redissolved in water, treated with activated charcoal and precipitated by the addition of potassium chloride. The corresponding disulphonic acid may be prepared from the potassium salt by passing the salt through a cation-exchange resin. On treating the disulphonic acid with ammonia in aqueous solution, the corresponding ammonium salt is formed.
GB1964965A 1964-05-08 1965-05-10 Modified polycarbonamides Expired GB1085666A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US36668864A 1964-05-08 1964-05-08

Publications (1)

Publication Number Publication Date
GB1085666A true GB1085666A (en) 1967-10-04

Family

ID=23444071

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1964965A Expired GB1085666A (en) 1964-05-08 1965-05-10 Modified polycarbonamides

Country Status (7)

Country Link
BE (1) BE663649A (en)
DE (1) DE1570968A1 (en)
GB (1) GB1085666A (en)
IL (1) IL23495A (en)
LU (1) LU48553A1 (en)
NL (2) NL6505840A (en)
SE (1) SE321578B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999019382A1 (en) * 1997-10-14 1999-04-22 E.I. Du Pont De Nemours And Company Substituted polyamides and process for preparing the same
US6274697B1 (en) 1998-10-02 2001-08-14 E. I. Du Pont De Nemours And Company Process and product for making polyamides
US6277948B1 (en) 1998-10-02 2001-08-21 E. I. Du Pont De Nemours And Company Process and product for making polyamides
CN116355209A (en) * 2023-05-31 2023-06-30 泰和新材集团股份有限公司 Preparation method and application of high-whiteness meta-aramid polymer

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999019382A1 (en) * 1997-10-14 1999-04-22 E.I. Du Pont De Nemours And Company Substituted polyamides and process for preparing the same
US6274697B1 (en) 1998-10-02 2001-08-14 E. I. Du Pont De Nemours And Company Process and product for making polyamides
US6277948B1 (en) 1998-10-02 2001-08-21 E. I. Du Pont De Nemours And Company Process and product for making polyamides
CN116355209A (en) * 2023-05-31 2023-06-30 泰和新材集团股份有限公司 Preparation method and application of high-whiteness meta-aramid polymer
CN116355209B (en) * 2023-05-31 2023-08-15 泰和新材集团股份有限公司 Preparation method and application of high-whiteness meta-aramid polymer

Also Published As

Publication number Publication date
SE321578B (en) 1970-03-09
NL128829C (en)
BE663649A (en) 1965-11-08
DE1570968A1 (en) 1970-01-29
LU48553A1 (en) 1965-11-10
IL23495A (en) 1968-09-26
NL6505840A (en) 1965-11-09

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