Polymethylmethacrylate copolymers

Poly styrene-block -polybutadiene-feZoc/ -polymethylmethacrylate copolymers, 7 645... 

The ruthenium catalyst RuCl2(= CHPh)(PCy3)2 is able to promote both alkene metathesis polymerization (ROMP) and atom transfer polymerization (ATRP) [80,81]. The bifunctional catalyst A was designed to promote both ROMP of cyclooctadiene (COD) and ATRP of methyl methacrylate (MMA). Thus, catalyst A was employed to perform both polymerizations in one pot leading to diblock polybutadiene/polymethylmethacrylate copolymer (58-82% yield, PDI = 1.5). After polymerization the reaction vessel was exposed to hydrogen (150 psi, 65 °C, 8h), under conditions for Ru(H2)(H)Cl(PCy3)2 to be produced, and the hydrogenation of diblock copolymer could attain 95% [82] (Scheme 36). 

Lin CX, Zhan HY, Liu MH, Habibi Y, Fu SY, Lucia LA (2013) RAFT synthesis of cellulose-g-polymethylmethacrylate copolymer in an ionic liquid. J Appl Polym Sci 127 4840-4849... 

Where transparency is required, a range of polymers is available. Polystyrene is the least expensive but polymethylmethacrylate has an outstanding high light transmission combined with excellent weathering properties. Also to be considered are the polycarbonates, glass-clear polyamides, SAN, butadiene-styrene block copolymers, MBS polymers, plasticised PVC, ionomers and cellulose esters such as cellulose acetate. 

ACPA azobis(4-cyanopentanoic acid) AIBN azobis isobutyronitrile) BPO benzoyl peroxide DVB divinyl benzene, EGA 2-ethylcyano-acrylate HPC hydroxypropyl cellulose MMA methyl methacrylate PAAc polyacrylic acid PEI polyethyleneimine, PEO/PPO polyethylene oxide/polypyropylene oxide copolymer PVME polyvinylmethylether PVP polyvinylpyrrolidone K-30 DMSO dimethylsulfoxide PGA polyglutaraldehyde CMS chloromethylstyrene PMMA-g-OSA polymethylmethacrylate grafted oligostearic acid. 

The soapless seeded emulsion copolymerization method was used for producing uniform microspheres prepared by the copolymerization of styrene with polar, functional monomers [115-117]. In this series, polysty-rene-polymethacrylic acid (PS/PMAAc), poly sty rene-polymethylmethacrylate-polymethacrylic acid (PS/ PMMA/PMAAc), polystyrene-polyhydroxyethylmeth-acrylate (PS/PHEMA), and polystyrene-polyacrylic acid (PS/PAAc) uniform copolymer microspheres were synthesized by applying a multistage soapless emulsion polymerization process. The composition and the average size of the uniform copolymer latices prepared by multistage soapless emulsion copolymerization are given in Table 11. 

Polymeric particles can be constructed from a number of different monomers or copolymer combinations. Some of the more common ones include polystyrene (traditional latex particles), poly(styrene/divinylbenzene) copolymers, poly(styrene/acrylate) copolymers, polymethylmethacrylate (PMMA), poly(hydroxyethyl methacrylate) (pHEMA), poly(vinyltoluene), poly(styrene/butadiene) copolymers, and poly(styrene/vinyltoluene) copolymers. In addition, by mixing into the polymerization reaction combinations of functional monomers, one can create reactive or functional groups on the particle surface for subsequent coupling to affinity ligands. One example of this is a poly(styrene/acrylate) copolymer particle, which creates carboxylate groups within the polymer structure, the number of which is dependent on the ratio of monomers used in the polymerization process. 

Two chemically modified types of NR (graft copolymers of NR and polymethylmethacrylate, and epoxidised NR) exhibit useful properties. The former are used in adhesive systems, and for the production of hard compounds, whilst the latter has probably still to find its market niche. 

Chemical modification of polymers (J.) still remains a field of continuously increasing importance in macromolecular chemistry. In spite of its high diversification, it may be divided into 2 distinct but complementary main research lines a) the fundamental study of the chemical reactivity of macromolecular chains b) the synthesis of new homopolymers and copolymers, and the functionalization of linear or crosslinked polymers. Some of these facets have been reviewed in the last years (2-6), and the purpose of this presentation is to illustrate a number of characteristic topics both from fundamental and applied points of view, through some literature data and through our own studies on nucleophilic substitution of polymethylmethacrylate (PMMA). 

A radical anion is formed at the cathode and the radical and anion portions polymerize independently, producing polymethylmethacrylate block on the anion and a copolymer on the free-radical portion. 

The following plain example might demonstrate the usefulness of the e° data. In benzene (e° = 0.32) polystyrene samples are eluted from a silica column, whereas polymethylmethacrylates and its copolymers are not. In THF (0.57) even PMMA homopolymers leave the column. Hence, THF is strong enough to prevent PMMA from adsorption. In chloroform (0.40) random copolymers with no more than 50%... 

The concept of using block copolymers for preparation of nanoscopically structured material and surfaces was advanced further by introducing a third block in the chain structure [29]. One of the consequences of the multiphilicity and versatility of the ABC triblock copolymers is their tremendous richness and diversity in morphology. One of the most peculiar structures is shown in Fig. 28 where the helices of a polybutadiene microphase are wound around columns of polystyrene which are embedded in a matrix of polymethylmethacrylate. Complementary to the TEM studies of the bulk morphology (Fig. 28a,b), SFM has been used to image the surface structure of the triblock copolymer films. Figure 28c shows the wrapped PS cylinders oriented parallel to the surface, where one... 

Hahm J et al (1998) Defect evolution in ultrathin films of polystyrene-block-polymethylmethacrylate diblock copolymers observed by atomic force microscopy. J Chem Phys 109(23) 10111-10114... 

The fire-retardant mechanisms identified for the various phosphorus moieties in these polymethylmethacrylate (PMMA) and PS copolymers investigated can be summarized as follows ... 

For high viscous systems the indication of a phase transition is remarkable more difficult as for the low viscous system (3). Fig. 6 shows a typical example of the system 8.5 % PMMA/91.5 % SAN (Polymethylmethacrylate/Styrene acrylonitrile copolymer). 

Besides the use of micromolecular multiinitiators, block copolymers can be obtained from macromolecular initiators. In a first step, a polymeric initiator is generally synthesized by reacting a mono- or difunctional polymer with a functional initiator. Various macromolecular initiators were prepared in this way including quite different sequences polystyrene [13, 18, 19, 25, 26], poly(dimethylsiloxane) [27], polymethylmethacrylate) [13,15,28], polyvinylacetate [28], polyvinylchloride [29, 30], polyesters [30], polycarbonate [31,32], polybutadiene [13, 25, 33], polyamide [34], polyethylene glycol) [35] or polyaromatic [36], An excellent review of the synthesis and uses of such macroinitiators was written by Nuyken and Voit [37]. Thus, only few typical examples are going to be mentioned below. 

The "comb" dispersing agent was a graft copolymer of polymethylmethacrylate-methacrylic acid (methoxypolyethylene oxide methacrylate) supplied by ICI Paints Division (Slough) and used as received. The exact molecular weight of the polymer is not known, but it is ejqpected to be in the region of 20-30,000 (as indicated by ICI Paints Division). The of the polyethylene chains was 750. 

Acrylate resists such as polymethylmethacrylate (PMMA) have been used extensively in electron beam lithography because of their excellent resolution and contrast, despite their limited dry etch resistance and low sensitivity (1). Copolymers of PMMA, containing chemical groups more sensitive to radiation induced degradation, have also been studied and have shown up to a four-fold improvement in sensitivity (2). One approach has been to form a crosslinked gel, in-situ on the wafer, which contains radiation sensitive crosslinks and leads to improved sensitivity and improved contrast during development (3-7). 

In addition to these irregularities, Winey et al. (1996) have found that in random and alternating copolymers of styrene and methyl methacrylate, the sequence distribution of monomers along the backbone of the polymer strongly affects its miscibility with polystyrene and polymethylmethacrylate homopolymers, even when the overall ratio of styrene/methyl methacrylate in the copolymer chain is held constant. A strictly alternating sequence of monomers in the copolymer was found to be more miscible with the ho-miopolymers than is a copolymer with a random sequence distribution. These results... 

Second generation. Systems with reduced or no molding shrinkage developed for automotive and other commercial applications Polyvinyl acetates Polymethylmethacrylate and copolymers Polyvinyl chloride-vinyl acetate copolymers Styrene-butadine copol5uners Cellulose acetate but5rate Modified polyvinyl acetates... 

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