2012
DOI: 10.1080/10601325.2012.687968
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Synthesis of Novel Polyether Polyol by Using Double Metal Cyanide

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Cited by 10 publications
(6 citation statements)
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“…At higher EO fractions (>78%), turbid solutions were observed, caused by the crystallization of long PEO homopolymer fractions. In 2012, Sun et al reported the homopolymerization of epichlorohydrin (ECH) with tri-(2-hydroxyethyl) isocyanurate as an initiator, followed by the use of PECH as chain extender for PU elastomers . Recently, the homopolymerization of racemic ECH, S -ECH, and R -ECH was reinvestigated by Zhang et al Regioregular PECH was obtained with a head-to-tail content exceeding 99%, molecular weights ranging from 900 to 2700 g/mol and PDIs of 1.42 to 1.72.…”
Section: Polymerization Of Alkylene Oxides: Methodsmentioning
confidence: 99%
“…At higher EO fractions (>78%), turbid solutions were observed, caused by the crystallization of long PEO homopolymer fractions. In 2012, Sun et al reported the homopolymerization of epichlorohydrin (ECH) with tri-(2-hydroxyethyl) isocyanurate as an initiator, followed by the use of PECH as chain extender for PU elastomers . Recently, the homopolymerization of racemic ECH, S -ECH, and R -ECH was reinvestigated by Zhang et al Regioregular PECH was obtained with a head-to-tail content exceeding 99%, molecular weights ranging from 900 to 2700 g/mol and PDIs of 1.42 to 1.72.…”
Section: Polymerization Of Alkylene Oxides: Methodsmentioning
confidence: 99%
“…In 2012, Gu et al polymerized ECH with DMC catalysts using an isocyanate as an initiator to make a polyurethane elastomer. 53 In 2014, Wei et al prepared regioregular PECH with controlled molecular weights up to 4.2 kg/mol with Đ > 1.4 using DMC catalysts. 36 By using racemic mixtures or enantiopure ECH, the authors were able to make thermoplastic or semi-crystalline PECH, respectively.…”
Section: Double Metal Cyanide Catalystsmentioning
confidence: 99%
“…Elemental analyses were performed by using an ICP-AES instrument (Leeman Labs) and a Vario MACRO instrument (Elementar). 1 H NMR and 13 C NMR spectra of the products were obtained on a Bruker Advance DMX 400 MHz and 125 MHz spectrometer with TMS as internal reference respectively. Average-number molecular weight (M n ) and molecular weight distribution (M w /M n ) were determined by using a PL-GPC 220 chromatograph (Polymer Laboratories Ltd.) equipped with an HP 1100 pump from Agilent Technologies.…”
Section: Characterizationmentioning
confidence: 99%
“…Due to the chloromethyl and two terminated hydroxyl groups, polyepichlorohydrin [poly(ECH)] diol is widely used as a precursor for making functionalized polymers. The terminated hydroxyls could react with di-or tri-isocyanates to give linear or cross-linked polyurethane materials, 1 while the nucleophilic substitution of -Cl by azide (-N 3 ) would result in the formation of glycidylazide polymer, which could be used as an energetic binder. 2 For most of the disclosed catalysts, like Lewis acids of BF 3 etherate, 3 SnCl 4 , 4 or SbCl 5 , 5 inorganic acid of sulfuric acid, 6 trialkyl oxonium salt of triethyloxonium tetrauoroborate, 7 and super acid esters of CF 3 SO 3 R or FSO 3 R, 8 generally, a protic compound co-initiator is essentially required.…”
Section: Introductionmentioning
confidence: 99%