Search results for "Plastics"
showing 10 items of 2724 documents
Synthesis of well-defined polymeric activated esters
2008
Monomers bearing an activated ester group can be polymerized under various controlled polymerization techniques, such as ATRP, NMP, RAFT polymerization, or ROMP. Combining the functionalization of polymers via polymeric activated esters with these controlled polymerization techniques generate possibilities to realize highly functionalized polymer architectures. Within this highlight two different research areas of activated esters in polymer science will be discussed: (i) the preparation of defined reactive polymer architectures by controlled polymerization techniques and (ii) the preparation of defined reactive thin films. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6…
Synthesis of Functional Inorganic−Organic Hybrid Polymers Based on Poly(silsesquioxanes) and Their Thin Film Properties
2008
New stable and adherent coating materials have been synthesized on the basis of inorganic/organic hybrid polymers. As the inorganic part, different poly(silsesquioxanes) (PSSQ) have been functionalized to act as polymeric chain transfer agents (CTAs) for a reversible addition fragmentation chain transfer polymerization, thereby determining the starting point of a controlled radical polymerization of vinyl-type monomers. Using two different CTAs acrylates, we have successfully polymerized methacrylates and styrene under RAFT polymerization conditions. Different monomers were copolymerized in such an organic block to incorporate multiple functionalities. The variation of the block ratios and …
Mechanical relaxation in miscible polymer systems: the glass transition regime in poly(vinylmethylether) (PVME)-cross-polystyrene (PS) semi-interpene…
1990
Abstract Miscible semi-interpenetrating polymer networks (semi-IPN) of varying composition are prepared by crosslinking polystyrene containing few maleic anhydride groups with a diamine in the presence of linear poly(vinylmethylether) (PVME). The resulting PVME-c-P(ScoMA) semi-IPNs are characterized by their thermal and thermomechanical behaviour. Comparison with the corresponding uncrosslinked material proves that weak crosslinking has a negligible effect on the location of the glass transition as measured by d.s.c. Both the Tg data and the temperatures of the loss modulus maximum E″ (at 1 rad/s) show the same non-linear curved composition dependence. Contrary to this the tan δ maximum var…
Amphiphilic poly(ether urethanes) carrying associative terpyridine side groups with controlled spacing
2021
The rational design of transiently crosslinked polymer gels requires a profound understanding of how molecular and topological factors determine the mechanical and dynamic material properties. To refine so-far established structure–property relations, complementary and versatile model sytems are still a crucial prerequisiste. In this study, the synthesis of a metallo-supramolecular associating terpyridine-diol (referred to as sticker) and its incorporation into poly(ethylene glycol) (pEG) based polyurethanes (PU) with strictly alternating vs. random sequences and variable sticker spacings is described. Synergetic effects resulting from the proximity of multiple neighboring urethane and stic…
Controlling supramolecular polymerization through multicomponent self-assembly
2016
The self-assembly into supramolecular polymers is a process driven by reversible non-covalent interactions between monomers, and gives access to materials applications incorporating mechanical, biological, optical or electronic functionalities. Compared to the achievements in precision polymer synthesis via living and controlled covalent polymerization processes, supramolecular chemists have only just learned how to developed strategies that allow similar control over polymer length, (co)monomer sequence and morphology (random, alternating or blocked ordering). This highlight article discusses the unique opportunities that arise when coassembling multicomponent supramolecular polymers, and …
An Improved Rapid Synthesis of Oligo(p -benzamide) Block Copolymers
2008
We describe a new synthesis that allows the preparation of oligo(p-benzamide)s up to the heptamer on solid support without the need of semi-temporary amide N-protective groups. With increase in length, the solubility of oligo(p-benzamide)s reduces dramatically. Even the tetra(p-benzamide) is not soluble in common organic solvents. Therefore, solution syntheses of oligomers beyond the tetramer are not feasible. As will be shown in this paper, solid supported synthesis allows the preparation of even longer oligomers (up to the heptamer) in good yields. The high dilution on the solid support is most likely responsible for their pseudo-solution-like reactivity and the prevention of aggregation.…
Excess viscosity and glass transition
2001
Abstract Literature data on the viscosity of solutions of poly(butyl methacrylate) (PBMA) and poly(methyl methacrylate) (PMMA) in diethyl phthalate (DEP) for different temperatures, including the range around and below T g , the glass transition temperatures of the pure polymers, were evaluated by means of an approach that uses surface fractions as composition variables. The discussion of these results together with information on solutions of the isomeric polymers, poly(vinyl acetate) (PVAc) and poly(methyl acrylate) (PM(A)), in the same solvent testifies that the previously published relations remain valid for T T g . They enable the determination of viscosities of the pure polymers below…
Crystallization kinetics in relation to polymer processing
1993
Phase distribution of quenched samples has been determined by a deconvolution procedure of WAXS spectra in a wide range of cooling rates. The informations collected together with isothermal and DSC results provide a very wide set of data on the crystallization kinetics of polymers relevant which covers conditions encountered in most polymer processing operations. They have been compared with predictions of a non-isothermal crystallization model assuming two independent and parallel crystallization processes competing during solidification.
Effect of bulkiness and lewis acidity of aluminium compounds on the anionic polymerization of methyl methacrylate in toluene
1996
The bulkiness and the Lewis acidity of added aluminium compounds strongly affect the polymerization of methyl methacrylate in toluene at −78°C. The polymerization strongly deviates from ‘ideal’ first-order kinetics, i.e. the first-order time-conversion plots are kinked at low monomer conversions. Additionally, for the more bulky and more Lewis-acid aluminium alkyls, the time-conversion plots show a further downward curvature. This curvature is not the result of a termination reaction because the polymers are free of side products like β-ketoesters or vinyl ketone units. The molecular weight distributions and tacticities of the resulting polymers are also affected. Dependent on the aluminium…
Antibacterial chitosan-based blends with ethylene–vinyl alcohol copolymer
2010
Abstract This study reports for the first time about the formulation, morphology, water barrier and the antimicrobial activity of high and low molecular weight chitosonium-acetate based solvent-cast blends with ethylene–vinyl alcohol (EVOH) copolymers. The blends based on the low molecular weight chitosan grade showed enhanced phase morphology, transparency, enhanced water barrier properties, up to 86% water permeability reduction compared to pure chitosonium-acetate films, as well as excellent antimicrobial activity. When the fraction of low molecular weight chitosan exceeded the phase inversion in the blend, phase segregation became noticeable but good interfacial adhesion was still obser…