Zobrazeno 1 - 10
of 11
pro vyhledávání: '"John L. Cawse"'
Publikováno v:
Die Makromolekulare Chemie. 185:709-723
Novel furan-based diisocyanates (2a – c) were reacted with 1-butanol and basic kinetic studies were made. The results were compared with those obtained from 4,4′-methylenediphenylene diisocyanate (1) under similar conditions. The kinetics of thes
Publikováno v:
Journal of Applied Polymer Science. 31:1549-1565
Publikováno v:
British Polymer Journal. 17:233-238
The synthesis and development of novel, furan-based diisocyanates (FDI) and myrcene-based polyols (PM) with potential for polyurethane production are presented. Pure FDI compounds, similar in structure to 4,4'-methylenediphenylene diisocyanate (MDI)
Publikováno v:
Polymer. 28:368-374
A reactive liquid rubber based on hydroxy-functionalized polymyrcene was used to modify a highly-crosslinked, glassy polyurethane network. During the polymerization, the products formed from the reacting liquid rubber and the polyurethane matrix comp
Publikováno v:
Journal of Applied Polymer Science. 33:2231-2248
Two hydroxy-functionalized liquid rubbers, one a commercially available polybutadiene (PB) and the other a specially synthesized polymyrcene (PM), have been converted into homopolyurethane elastomers by reaction with 4,&4prime;-diphenylmethane diisoc
Publikováno v:
Die Makromolekulare Chemie. 185:697-707
Furan-based diisocyanates and diamines were prepared unambiguously as potential monomers for polyurethane and polyamide production, starting from methyl furoate and furfurylamine, respectively. The syntheses were optimized and the product identity wa
Publikováno v:
ACS Symposium Series ISBN: 9780841215627
Adhesives from Renewable Resources
Adhesives from Renewable Resources
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e93a5da2df4608e4f9ef3131d09a997
https://doi.org/10.1021/bk-1989-0385.ch030
https://doi.org/10.1021/bk-1989-0385.ch030
Publikováno v:
Journal of Applied Polymer Science. 33:1445-1446
A range of hydroxy-terminated polymyrcenes has been prepared using hydrogen peroxide initiated polymerization of pyrolysate grade, β-myrcene in n-butanol solution at 100°C. An oligomeric fraction, containing a large proportion of dimeric material f
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