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Poly , methyl-capped

In the JKR experiments, a macroscopic spherical cap of a soft, elastic material is in contact with a planar surface. In these experiments, the contact radius is measured as a function of the applied load (a versus P) using an optical microscope, and the interfacial adhesion (W) is determined using Eqs. 11 and 16. In their original work, Johnson et al. [6] measured a versus P between a rubber-rubber interface, and the interface between crosslinked silicone rubber sphere and poly(methyl methacrylate) flat. The apparatus used for these measurements was fairly simple. The contact radius was measured using a simple optical microscope. This type of measurement is particularly suitable for soft elastic materials. [Pg.94]

Figure 1. 60 MHz NMR Spectra of Hydroxy Terminated-(2), Trimethyl-siloxyl End-Capped-(3) and Trimethylsiloxyl End-Capped/N-oxidized-(4) Poly(methyl 3-pyridinylsiloxane). Figure 1. 60 MHz NMR Spectra of Hydroxy Terminated-(2), Trimethyl-siloxyl End-Capped-(3) and Trimethylsiloxyl End-Capped/N-oxidized-(4) Poly(methyl 3-pyridinylsiloxane).
A very versatile and important methodology for controlling the properties of polysiloxanes involves hydrosilylation [eqn (10.33)]. Reaction of poly(methyl-hydrosiloxane) or poly(methylhydrosiloxane)-poly(dimethylsiloxane) copolymers with vinyl-capped species allows the introduction of side groups which give rise to a variety of interesting properties. [Pg.195]

Poly(methyl methacrylate) films Pyridine-soluble, phenyl-capped Cd incorporated in polymers... [Pg.135]

In another recent example, dtrate-capped Au NPs are modified with 1-dodeca-nethiol in a first step. These premade nanoparticles were encapsulated with block copolymers such as poly(styrene-block-acrylic acid) (PS-b-PAA) and poly(methyl-methacrylate-block-acrylic acid) (PMMA-b-PAA) leading to core-shell hybrid materials. The Au NP diameters are 12 and 31 nm with average shell thickness of about 15 nm [121] (Scheme 3.18). [Pg.157]

Fig. 7a and b. Separation of poly(methyl methacrylate) oligomers, (a) Gradient elution of methyl-capped oligomers on a silica column (250 x 3.2 mm do = 6 nm dP = 5 pm). Gradient butyl chloride/ acetonitrile (1-20% in 20 min) UV detection at 254 nm. (b) Gradient elution of hydrogen-capped oligomers under the same conditions as in Fig. 7 a. (From Ref.28) with permission)... [Pg.173]

Scheme 13.S End-capping of poly-methyl methacrylate (poly-MMA) formed by ATRP by silyl enol ethers. Scheme 13.S End-capping of poly-methyl methacrylate (poly-MMA) formed by ATRP by silyl enol ethers.
Dithienothiophenes give cation polymeric radicals capable of further copolymer addition" while polystryene with a narrow polydispersity has been prepared through the use of an end-capped photoactive anthryl group. ° Large differences in radical termination rates have been found to be responsible for the marked variations in molecular weights of polymer from the UV flash polymerisation of 1,3-butadiene. tra 5-l,2-bis(5-Phenyl-2-oxazolyl)ethene has been found to exhibit low laser conversion efficiency due to preferential dimerisation while thermally activated patterns can be formed on the surface of poly(methyl methacrylate) by coating with photodimerisable 9-anthraldehyde. " ... [Pg.355]

Fig. 15.2.35. Solid state C CP/MAS spectra of three samples of poly(methyl methacrylate) crosslinked with 5 (lower), 20 (mid) and 50 (top) % of f-butyl acrylate end-capped oligomer containing ca. 2-3 HDDA repeat units. Fig. 15.2.35. Solid state C CP/MAS spectra of three samples of poly(methyl methacrylate) crosslinked with 5 (lower), 20 (mid) and 50 (top) % of f-butyl acrylate end-capped oligomer containing ca. 2-3 HDDA repeat units.
Synthesis of poly(methyl methacrylate)"b-polyisobutylene-b-poly(methyl methacrylate) (PMMA-b-PIB-b-PMMA) triblock copolymers was also performed (see Table I). First, a series of DPE-capped telechelic PIBs were prepared by using a difiinctional initiator (tBuDiCumCl) for LCCP of IB. [Pg.129]

Genomic RNA. The viral genome is a positive-stranded RNA of approximately 11,700 nucleotides and has the structural features of messenger RNA (ie, mRNA, a 5 methylated cap [m7GpppA] and a poly-A tract at the 3 end).77 As a complete and functional mRNA, genomic RNA purified from virions is fully infectious when artificially introduced (ie, transfected) into susceptible cells. Similarly, RNA transcribed from a full-length complementary DNA (cDNA) clone of an alphavirus is also infectious,... [Pg.569]

Cain et al. (1978) have extended this method to allow the homostabilization between identical surfaces to be studied. The apparatus developed by them is shown schematically in Fig. 13.15. The central elements of the apparatus were two hemispherically capped silicone rubber cylinders which had been silvered and coated with a thin layer (ca 5 of poly(methyl methacrylate) (see insert... [Pg.308]

Living polymerization of azo monomers is one of the most effective ways to prepare well-defined azo BCs. Generally, a monodispersed macroinitiator should be prepared first. It is then used as an initiator for the subsequent polymerization of azo monomers. Finkelmann and Bohnert (1994) first reported the synthesis of LC-side chain AB azo BCs by direct anionic polymerization of an azo monomer. As shown in Scheme 12.1, the polymerization of polystyrene (PS)-based diblock copolymers was carried out from a PS-lithium capped with 1,1-diphenylethylene (DPE), whereas the poly(methyl methacrylate) (PMMA)-based diblock copolymers were prepared by addition of methyl methacrylate (MMA) monomers to the living azo polyanion, obtained by reaction of l,l-diphenyl-3-methylpentylithium (DPPL) with the azo monomer in tetrahydrofuran (THF) at lower temperature. By this method, a series of well-defined azo BCs were obtained with controlled molecular weights and narrow polydispersities (Lehmann et al., 2000). [Pg.413]

The metallocene-ATRP route has been expanded by Matsugi etal. [164], to produce polyethylene-b-poly(methyl methacrylate). In the first step, hydroxyl-functionalized polyethylene was successfully prepared through the copolymerization of ethylene with aluminum-capped allyl alcohol, using a specific zirconium metaUocene/methylaluminoxane catalyst system. In the next step, the terminal alcohol was converted to hahde by 2-bromoisobutyryl bromide to obtain bromide-functionalized polyethylene, which could initiate the ATRP of MMA (Scheme 11.40). The block copolymers obtained exhibited unique morphological features that depended on the content of PMMA segment. Moreover, the block copolymers effectively compatibiUzed the corresponding homopolymer blend at the nanometer level. [Pg.337]

For example, methyl methacrylate block copolymers are much less studied than those of styrene. Anion chain transfer occurs at the pendent ester group, drastically reducing the yield of block copolymers. Poly(methyl methacrylate-b-isoprene) has been prepared, however, by using an ingenious chain cap of l,l -diphenylethyl-ene(27,28). i l diphenylethylene will not anionically homopolymerize, therefore it adds only one mer to the macroanion. This anion is more stable in the presence of methyl methacrylate, but will initiate further polymerization. Other workers have reported the preparation of isoprene-methyl methacrylate block copolymers by sequential addition to "living" polyisoprene anions(29,30),... [Pg.91]

Hergenrother and Ambrose have prepared butadiene-imide and butadiene-caprolactam(73,74)block copolymers using polybutadiene capped on each terminus by isocyanate groups. Poly(ethylene-propylene adipate-b-methyl methacrylate) was prepared by heating hydroxy terminated poly(methyl methacrylate) with the isocyanate terminated reaction products of hydroxy terminated poly(ethylene-propylene... [Pg.94]

PVC blends with CPE were patented and commercialized in 1956 as HostaliF. Blends with CSR soon followed. By the mid-1970s, the emphasis shilted toward blends with acrylic elastomers. Ternary alloys were developed, viz., of PVC with CPE and poly(methyl methacrylate-co-butyl acrylate) (MMBA) (Maruyama et al. 1977) or PVC, CPVC, and either MABS or a mixture of PMMA with imidized-PMMA or imidized-SMA (Soby et al. 1994). These blends have been used for outdoor applications, flame-retardant wall coverings, and automobile interiors. Injection molded components include gullies in sewage systems, caps for road reflector posts and bench slats, etc. Evolution of these blends is traced in Table 1.29. [Pg.59]

Lee L-H, Chen W-C (2001) High-refiactive-index thin films prepared liom trialkoxysilane-capped poly(methyl methacrylate) — titania materials. Chem Mater 13(3) 1137-1142... [Pg.174]

Tunable Near-IR Optical Properties from Trialkoxysilane-Capped Poly(methyl methacrylate)-Silica Waveguide Materials... [Pg.307]

Figure /. Scheme for preparing optical planar waveguides from trialkoxysilane-capped poly (methyl methacrylate )-silica materials. [Pg.309]


See other pages where Poly , methyl-capped is mentioned: [Pg.3]    [Pg.709]    [Pg.80]    [Pg.78]    [Pg.637]    [Pg.771]    [Pg.338]    [Pg.249]    [Pg.95]    [Pg.96]    [Pg.106]    [Pg.360]    [Pg.569]    [Pg.68]    [Pg.308]    [Pg.318]   
See also in sourсe #XX -- [ Pg.78 ]




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Trialkoxysilane-capped poly(methyl material

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