Search results for "MOLA"
showing 10 items of 1216 documents
Molecular dynamics of discotic charge-transfer complexes, dielectric spectroscopy and2H NMR studie
1994
Abstract Using a combination of solid state 2H NMR spectroscopy on selectively deuteriated samples and dielectric spectroscopy, the molecular dynamics of discotic charge-transfer (CT) complexes were investigated. These complexes show particular thermodynamic and flow properties. Considered were mixtures of low molar mass donors and acceptors, low molar mass donors with main chain acceptor polymers and covalently linked donor-acceptor twins with different lengths of the spacer. A main result is that correlated rotational motions of discotic molecules or groups about the columnar axis are observed in all systems except for the twin with the short spacer. This type of motion seems to be a gene…
Synthesis, characterization and properties of functional star and dendritic block copolymers of ethylene oxide and glycidol with oligoglycidol branch…
2009
Abstract Well-defined, four-arm star block copolymers of ethylene oxide and glycidol were prepared via controlled anionic polymerization using protected glycidol. The length of the poly(ethylene oxide) block was varied from DP = 10 to 50, while the length of the short polyglycidol block remained nearly constant, at DP = 4–6. Star block copolymers with hydroxyl groups at the ends of the arms after conversion to the corresponding alkoxides were used as multifunctional macroinitiators for the sequential polymerization of ethylene oxide and protected glycidol. After deprotection, the branched block copolymers of ethylene oxide and glycidol had narrow molar mass distributions and multiple hydrox…
Injection moldability and properties of compatibilized PA6/LDPE blends
2004
An ethylene-acrylic acid copolymer (EAA), either alone or combined with a low molar mass bis-oxazoline compound (PBO), has been used as a compatibilization promoter for blends of polyamide-6 (PA6) with low-density polyethylene (LDPE). The effect of compatibilization on blend processability in injection molding operations and on the properties of the molded specimens has been studied. In the absence of compatibilization, the injection molded articles were shown to have low-quality surface appearance and poor mechanical properties. Both these characteristics were appreciably improved as a result of reactive compatibilization of the blends with EAA and, even more, with the EAA-PBO couple. In f…
Blends of PDMS and random copolymers of dimethylsiloxane and methylphenylsiloxane: Phase separation in the quiescent state and under shear
1999
The miscibility of random copolymers (COP), consisting of dimethylsiloxane and methylphenylsiloxane units, with poly(dimethylsiloxane)s (PDMS) was studied in the absence and in the presence of shear experimentally as well as theoretically. Blends of COP 0.86 28 with PDMS 33 (subscripts: volume fraction of DMS in the copolymer, numbers after the abbreviations: weight average molar masses in kg/mol) were investigated far from critical conditions on the PDMS side of the phase diagram. According to these experiments the two phase regime increases by shear without exception and the maximum effects grow from 3 to 12 K as the PDMS concentration increases. Theoretical calculations were performed un…
Untersuchungen zur Reaktionsfähigkeit statistisch verteilter Estergruppierungen in Copolymeren aus Styrol und Acrylsäureestern
1974
Die Aminolyse der ortho- und para-Nitrophenylester von Propionsaure, Isobuttersaure, 4-Phenylbuttersaure und 4-Phenylvaleriansaure sowie von Copolymeren aus Styrol und geringen Mengen Acrylsaure wurde mit Butylamin in Dioxan untersucht. Bei grosem Aminuberschus reagieren die niedermolekularen Ester streng nach erster Ordnung, wobei die Reaktionsgeschwindigkeit durch Zugabe von Polystyrol nicht beeinflust wird. Fur Copolymere, deren Reaktionsgeschwindigkeit deutlich geringer ist, erhalt man dagegen keine Beziehung erster Ordnung, obwohl die Anfangsgeschwindigkeit der Gesamtkonzentration der Estergruppen direkt proportional ist. Bei den Copolymeren erhalt man annahernd die gleichen Aktivierun…
Reactive blending of a functionalized polyethylene with a semiflexible liquid crystalline copolyester
1996
Reactive blends (50/50 w/w) of a low molar mass polyethylene containing free carboxylic groups (PEox) and a semiflexible liquid crystalline polyester (SBH 1 : 1 : 2, by Eniricerche) have been prepared at 240 degrees C in a Brabender mixer, in the presence of Ti(OBu)(4) catalyst, for different mixing times (15, 60, and 120 min). In order to prove the formation of a PE-g-SBH copolymer, the blends have been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been analyzed by Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG and DTG), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM)…
ALTMET Polymerization of Amino Acid-Based Monomers Targeting Controlled Drug Release
2016
Giving the imminent necessity of a new generation of biodegradable and biocompatible polymers prepared from feedstock, the synthesis of a potentially biodegradable amino acid-based copolymer by the alternating diene metathesis (ALTMET) strategy is herein presented. The reaction was tailored to minimize isomerization and deactivation of ruthenium catalysts by intramolecular coordination with the amide carbonyl group of the amino-acid-based monomer. Alternated l-lysine–phosphoester copolymers with molar masses higher than 18 000 g/mol were obtained using Hoveyda–Grubbs second-generation and Umicore M2 catalysts. The copolymer was further used to prepare nanoparticles loaded with rifampicin (u…
Hyperbranched Poly(ethylene glycol) Copolymers: Absolute Values of the Molar Mass, Properties in Dilute Solution, and Hydrodynamic Homology
2015
Hyperbranched poly(ethylene glycol) copolymers were synthesized by random anionic ring-opening multibranching copolymerization of ethylene oxide with glycidol as a branching agent, leading to poly(ethylene glycol) structure with glycerol branching points. Extending the available range of molar masses by novel synthesis strategies, a limited extent of control over the degree of polymerization was achieved by variation of the solvent in this copolymerization. Generally, absolute molar mass characterization of hyperbranched polymers still represents an unresolved challenge. A series of the hyperbranched poly(ethylene glycol)-co-(glycerol) copolymers (hbPEGs) of a wide range of molar masses (14…
Reactive compatibilization of PA6/LDPE blends with an ethylene–acrylic acid copolymer and a low molar mass bis-oxazoline
2003
Abstract A sample of polyamide-6 (PA) was blended with low density polyethylene (LDPE) in the 80/20 wt/wt ratio, either without and with 2 phr of an ethylene–acrylic acid copolymer (EAA), Which was known to behave as a compatibilizer precursor, and the effect of the addition of small amounts (0.2 or 0.35 phr) of a fourth component, 2,2′-(1,3-phenylene)-bis(2-oxazoline) (PBO), was investigated. The reactions of PBO with EAA, PA and their blends were studied by recording as a function of time the torque applied to the blending apparatuses and by studying the solubility behavior of the products in formic acid. The PALDPE blends were prepared in a co-rotating twin screw extruder and were charac…
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…