Properties of aliphatic hyperbranched polyesters in dilute solutions
Author(s) -
Jasna Vuković,
M. D. Lechner,
Slobodan Jovanović
Publication year - 2007
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc0712493v
Subject(s) - dispersity , branching (polymer chemistry) , dimethylacetamide , chemistry , polyester , molar mass , hydroxymethyl , solvent , intrinsic viscosity , trimethylolpropane , polymer chemistry , tmpta , organic chemistry , monomer , polymer , polyurethane , acrylate
The results of an investigation of the influence of the synthesis procedure, number of pseudo generations and degree of branching of hydroxy-functional ali- phatic hyperbranched polyesters (AHBP) on the values of limiting viscosity num- ber, (η), hydrodynamic radius, Rη, molar mass and polydispersity index, Q, are pre- sented in this paper. Two series of AHBP, synthesized from 2,2-bis(hydroxyme- thyl)propionic acid and di-trimethylolpropane using a pseudo-one-step and a one-step procedure were investigated. The obtained results show that the values of (η) and Rη for all examined samples are the highest in a 0.7 mass % solution of LiCl in N,N-di- methylacetamide (LiCl/DMAc), which indicates that this solvent is the best from the investigated ones. The values of (η) in N-methyl-2-pyrrolidinone (NMP) increa- sed up to the sixth pseudo generation, after which a slight decrease occurred as the consequence of the presence of side-reaction products, formed during the synthesis. The appearance of these side-reaction products was also confirmed from the charac- teristic GPC chromatograms. For the samples of AHBP synthesized using the pseu- do-one-step procedure, a good linear dependence between log (η) and log Mw was obtained up to the fifth pseudo generation, when LiCl/DMAc, NMP and DMAc were used as solvents. The values of the "shrinking" factor, g', were calculated for all investigated AHBPs.
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