Search results for "Polymer fractionation"

Fractionation of unsubstituted cellulose from solutions in either Ni-tren or (N,N-dimethylacetamide + LiCl)

2000

Starting from solutions of unsubstituted cellulose (Avicel PH101, M w = 30.1 kg/mol and M w /M n = 3 or Solucell 500, M w = 230 kg/mol, M w /M n = 2.8) in either Nitren (0.8 M aqueous solution of the dihydroxotris(2-aminoethly)amine nickel(II) complex) or in a mixed solvent DMAc+LiCl (consisting of N,N-dimethylacetamide plus lithium chloride) it was investigated whether the segregation of a second phase caused by the addition of suitable precipitants leads to polymer fractionation. With Ni-tren the long chains accumulate in the precipitate formed upon the addition of sulfuric acid; as the pH falls below 9, the solution is free of cellulose. Nevertheless this route option for fractionation m…

Characterization of melt-polymerized polycarbonate: preparative fractionation, branching distribution and simulation

2001

Melt-polymerized bisphenol-A polycarbonate materials characterized by a low degree of branching were fractionated according to molecular weight by the continuous polymer fractionation (CPF) method. The distribution of two types of end-groups and in-chain salicylate moieties arising from thermal rearrangement reactions were assessed across the molecular weight distribution by analysis of the fractions. Experimentally determined branching densities of the fractions agreed well with a molecular simulation based on a random sampling polycondensation model. Both simulation and experiments showed that the branching density increases with molecular weight in the experimentally accessible range. (C…

Molar Mass Distribution and Size of Hydroxyethyl Starch Fractions Obtained by Continuous Polymer Fractionation

2002

By the use of continuous polymer fractionation (CPF) the initial polymer can be separated into fractions of different molar masses, which makes it possible to obtain hydroxyethyl starch (HES) fractions tailor-made for specific application. Two samples of HES (HES A and HES B) were fractionated by means of CPF. By size-exclusion chromatography-multi-angle laser light-scattering-differential refractive index (SEC/ MALLS/DRI) measurements it was shown that CPF is able to remove the low-molar-mass components and to adjust the samples to various desired molar masses with lower polydispersities than the original samples. In terms of the weight-average mean molar mass M w , the sol fractions have …

Continuous polymer fractionation

1994

Continuous polymer fractionation of poly(methyl vinyl ether) and a new Kuhn-Mark-Houwink relation

1995

Continuous polymer fractionation (CPF) — a new large-scale method — was applied to the technical poly(methyl vinyl ether) (PVME) using toluence as solvent and petroleum ether as non-solvent. Two different devices served as fractionation apparatus, namely a column packed with glass beads and a set of mixer-settler extractors. Advantages and draw-backs of these devices are discussed. The experiments yielded numerous PVME fractions, varying in molar mass from 22 to 87 kg/mol and in molecular non-uniformity U = (M¯w/Mn) – 1 from 0,25 to 0,41 according to gel-permeation chromatography as compared with ca. U = 1,30 for the starting material. The following Kuhn-Mark-Houwink relation was establishe…

Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Preparative fractionation and characterization of polycarbonate/eugenol-siloxane copolymers

2002

Bisphenol-A polycarbonate/eugenol-siloxane copolymers were fractionated at the preparative scale by the continuous polymer fractionation (CPF) technique. It is the first example of copolymer fractionation by CPF. The distribution of siloxane species across the fractions was assessed for copolymers differing in initial siloxane concentration and block length. On- and off-line combinations of size exclusion chromatography and infrared spectroscopy were used to analyze chemical composition (CC) of the unfractionated samples across the molecular weight distribution enabling comparison with the fractions. A polycarbonate-siloxane copolymer containing 10 wt% of very short siloxane blocks (dp = 2)…

CPF: A New Method for Large Scale Fractionation

1986

The paper demonstrates how the Continous Polymer Fractionation (CPF) functions and how it has been applied to polyvinylchlorid.

1985

A new Continuous Polymer Fractionation method, called CPF, is described. The polymer to be fractionated is dissolved in a solvent/non-solvent mixture, and this solution (feed) is extracted continuously by a second liquid (extracting agent), which contains the same solvent components as the feed. In the case of PVC, the fractionation was carried out with a pulsed counter current extraction apparatus and THF/water was used as solvent/non-solvent mixture. Fractionation is achieved by the fact that the molecules are distributed over the counter current phases according to their chain length; the feed leaves the column as gel and the extracting agent as sol. First some explorative experiments we…

1990

The countercurrent extraction method recently developed for the continuous polymer fractionation (CPF) was applied to linear polyethylene (Mw = 55 kg/mol; Mn = 16,7 kg/mol). At temperatures higher than 130°C, moderately concentrated solution of polyethylene were extracted to remove the low-molecular-weight components. Discontinuous fractionation experiments served to detect the best suited solvents. Diphenyl ether was chosen to demonstrate that the present extraction can be performed even with the same single solvent used to prepare the feed. For very high-molecular-weight polymers, mixed solvents are, however, normally better than single ones, since they allow an easier tailoring of thermo…