Search results for "Mono"
showing 10 items of 6843 documents
Radiation grafting functionalization of poly (vinylidene fluoride) to compatibilize its blends with polyolefin ionomers
1998
Blends of a crystalline vinylidene fluoride copolymer (PVDF) and a polyolefin ionomer were produced by melt mixing and characterized by a variety of techniques to examine the effect of increasing the level of salt formation on morphology. The PVDF component was also grafted with methacrylic acid by irradiating the polymer powder and subsequently treating it with an aqueous monomer solution. The effect of neutralizing the acid in both polymer components to produce the corresponding zinc salt was also investigated. Compatibilization was accomplished by the addition of zinc acetyl acetonate (ZnAcAc) to the mixture. This increased the viscosity of the polyolefin ionomer phase, comparable to tha…
Characterization of monopolymer blend of virgin and recycled polyamide 6
2002
It is a common industrial practice to blend virgin polymer with the same recycled polymer coming from plastic scraps that, in general, has not undergone relevant degradation. In this work, the characteristics of blends of virgin and recycled polyamide have been considered by changing the amount of recycled polymer and the presence of humidity and a stabilizer. Neither dry nor wet stabilized recycled polyamide samples show significant variations of the molecular weight, but the melt Newtonian viscosity of the blends are slightly different from that predicted by an additive rule, despite the same chemical nature of the two components. This holds true even more for the humid unstabilized sampl…
Phase identification of triphenylene-based discotic monomer and its main chain polymers
1998
Abstract A monomer, 2,3,6,7,10,11-hexakispentyloxy triphenylene (HPT) possesses a triphenylene core as a discotic mesogen. Polymers containing this discotic mesogen have been studied using wide-angle X-ray and electron diffraction. HPT is known to show a discotic liquid crystal phase, noted as Dho (h for hexagonal bidimensional lattice, o for ordered molecular spacing in each column). In this paper, however, HPT liquid crystalline phases, heated up from the crystalline state and cooled down from the isotropic state, were characterized in the diameter dimensions. In addition. the diameters of the columns are close to a parameter of two separate crystals. A core orientation was, therefore, pr…
Polysiloxane-backbone block copolymers in a one-pot synthesis: a silicone platform for facile functionalization.
2012
Block copolymers consisting exclusively of a silicon-oxygen backbone are synthesized by sequential anionic ring-opening polymerization of different cyclic siloxane monomers. After formation of a poly(dimethylsiloxane) (PDMS) block by butyllithium-initiated polymerization of D3, a functional second block is generated by subsequent addition of tetramethyl tetravinyl cyclotetrasiloxane (D4(V) ), resulting in diblock copolymers comprised a simple PDMS block and a functional poly(methylvinylsiloxane) (PMVS) block. Polymers of varying block length ratios were obtained and characterized. The vinyl groups of the second block can be easily modified with a variety of side chains using hydrosilylation…
Some linear and branched macromolecules by ring-opening polymerization
1993
In the first part the ring-opening polymerization of some macrocyclic ether-acetals is briefly described. Of special interest are acetal polymers with functional groups, for instance C=C-double bonds. Appropriate unsaturated monomers and their polymerizability are discussed. The second part deals with the polymerization of oxazolines, substituted in 2- and/or 4-position. Branched polymers are obtained by copolymerization of 2-ethyl-2-oxazoline with 2-hexyl-2-oxazoline or 2-undecyl-2-oxazoline. The properties of the random copolymers and corresponding block copolymers are compared. By a “mixed mechanism technique” a block copolymer composed of a poly(tert -butyl methacrylate) block and a pol…
Living Polymer Chains with Predictable Molecular Weight and Dispersity via Carbanionic Polymerization in Continuous Flow: Mixing Rate as a Key Parame…
2016
Aiming at systematic variation of the parameter dispersity, Đ (or “polydispersity”), living polymers with predictable dispersity (Đ = 1.15–2.20) and controlled molecular weights (Mn = 3200–18 500 g mol–1) were prepared via carbanionic polymerization. The approach relies on a continuous flow reactor equipped with a tangential four-way jet micromixing device. By varying the total flow rate, the mixing efficiency of the initiator (sec-BuLi) and the corresponding vinyl monomers is controlled, resulting in polymers with predefined dispersity, while the number-average molecular weight, Mn, is kept constant. In this manner living polystyrene (PS), poly(p-methylstyrene) (PpMeS), and poly(2-vinylpyr…
Polydispersity and Molecular Weight Distribution of Hyperbranched Graft Copolymers via “Hypergrafting” of ABm Monomers from Polydisperse Macroinitiat…
2013
The hypergrafting strategy designates the synthesis of hyperbranched graft copolymers (HGCs) in a grafting-from approach, using ABm monomers, from multifunctional, polydisperse macroinitiator cores by slow monomer addition. Hypergrafting leads to complex polymer topologies with defined molecular weight, degree of branching (DB), and polydispersity (PD). By a generating function formalism, a generally applicable equation for the PD of HGCs (PD = PDf + (m – 1)/f) is derived, where PDf is the polydispersity of the core and f its average functionality. In addition, the complete molecular weight distribution function has been calculated for varied m and f as well as for a given distribution of i…
Block Copolymers Build-up of Electron and Hole Transport Materials
2004
In this article we describe the synthesis of various monomers modified with triphenyl-1,3,5-triazine side groups as electron transport moieties. By nitroxide-mediated polymerization with a TEMPO unimer it was possible to obtain polymers with a narrow polydispersity. Furthermore, by living radical polymerization block copolymers were obtained from these monomers. Therefore, microphase separated structures are accessible which possess hole conducting moieties in one phase and electron conducting moieties in the other phase.
Functional Diblock Copolymers for the Integration of Triboluminescent Materials into Polymer Matrices
2008
This work describes the synthesis and use of new diblock copolymers to integrate functional inorganic particles into a polymer matrix. These diblock copolymers were synthesized by nitroxide-mediated polymerization (NMP) from styrene and two styrene-like monomers with protected functional groups for the later connection to the functional inorganic material. It was possible to keep the polydispersity of the block copolymers around or below 1.2 and to preset the length of the functional block to about 20 monomers or 10 mol-% of monomers. The groups for the surface functionalization (amino groups or chelating ligands) were obtained in their free form by polymer analogous reactions. As an exampl…
Mechanistic study on the metallocene-based tandem catalytic coordinative chain transfer polymerization for the synthesis of highly branched polyolefi…
2021
Abstract Creation and control of long-chain branches (LCBs) in coordination polymerization of olefins is an enduring focus of research in both academia and industry. We have recently introduced a tandem catalytic coordinative chain transfer polymerization reaction where upon the concerted function of the polymerization catalyst, the chain transfer agent (CTA), and the displacement catalyst, a highly branched microstructure can be formed. Here we introduce a new tandem catalytic system using Et(Ind)2ZrCl2 as the polymerization catalyst. Despite the optimal reaction temperature for the cooperative function of catalyst components is lower than the ideal temperature for the productivity of the …