ES218247A1 - Improvements in or relating to linear polyamides - Google Patents

Improvements in or relating to linear polyamides

Info

Publication number
ES218247A1
ES218247A1 ES0218247A ES218247A ES218247A1 ES 218247 A1 ES218247 A1 ES 218247A1 ES 0218247 A ES0218247 A ES 0218247A ES 218247 A ES218247 A ES 218247A ES 218247 A1 ES218247 A1 ES 218247A1
Authority
ES
Spain
Prior art keywords
polyamide
group
diamines
dibasic acids
linear polyamides
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
ES0218247A
Other languages
Spanish (es)
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of ES218247A1 publication Critical patent/ES218247A1/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
    • C08G69/265Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids from at least two different diamines or at least two different dicarboxylic acids
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04BTRANSMISSION
    • H04B7/00Radio transmission systems, i.e. using radiation field
    • H04B7/02Diversity systems; Multi-antenna system, i.e. transmission or reception using multiple antennas
    • H04B7/04Diversity systems; Multi-antenna system, i.e. transmission or reception using multiple antennas using two or more spaced independent antennas
    • H04B7/08Diversity systems; Multi-antenna system, i.e. transmission or reception using multiple antennas using two or more spaced independent antennas at the receiving station
    • H04B7/0802Diversity systems; Multi-antenna system, i.e. transmission or reception using multiple antennas using two or more spaced independent antennas at the receiving station using antenna selection
    • H04B7/0831Compensation of the diversity switching process for non-uniform properties or faulty operations of the switches used in the diversity switching process

Landscapes

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

Abstract

Linear polyamides are prepared from (a) a solid mixture of the stereo-isomers of bis-(aminocyclohexyl) methane and (b) a mixture of 100 mol. of sebacic acid with 12.5-77.5 mols. of adipic acid. Up to 15 per cent of the polyamide-forming ingredients may be the conventional diamines, dibasic acids or a monoamino-monocarboxylic acid or caprolactam. Some or all of the polyamide-forming ingredients may be present as derivatives or the diamines and dibasic acids may be used as preformed salts. A monofunctional amide-forming reactant may be present, as described in Specification 495,790, [Group IV]. The products are particularly suitable for transparent films or wire-coating enamels. The usual reaction procedures are employed. A number of specific examples are given. Specifications 619,706, [Group IV (b)] and 619,707 also are referred to.
ES0218247A 1953-11-16 1954-11-05 Improvements in or relating to linear polyamides Expired ES218247A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3167753A GB760025A (en) 1953-11-16 1953-11-16 Improvements in or relating to linear polyamides

Publications (1)

Publication Number Publication Date
ES218247A1 true ES218247A1 (en) 1955-06-01

Family

ID=38524561

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0218247A Expired ES218247A1 (en) 1953-11-16 1954-11-05 Improvements in or relating to linear polyamides

Country Status (5)

Country Link
BE (1) BE533330A (en)
ES (1) ES218247A1 (en)
FR (1) FR1118435A (en)
GB (1) GB760025A (en)
NL (1) NL83393C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2732928A1 (en) * 1977-07-21 1979-02-01 Bayer Ag TRANSPARENT POLYAMIDE
DE2737257A1 (en) * 1977-08-18 1979-03-01 Bayer Ag TRANSPARENT POLYAMIDE
DE2855928A1 (en) * 1978-12-23 1980-07-10 Bayer Ag NEW COPOLYAMID

Also Published As

Publication number Publication date
NL83393C (en) 1956-11-15
BE533330A (en) 1958-04-11
GB760025A (en) 1956-10-31
FR1118435A (en) 1956-06-05

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