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Benzyl Methacrylate (benzyl + methacrylate)

Distribution by Scientific Domains

Polymers and Materials Science	80%

Selected Abstracts

Synthesis and properties of mesogen-jacketed liquid crystalline polymers containing bistolane mesogen

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 21 2010
Zhen Lin Zhang
Abstract On the basis of the concept of mesogen-jacketed liquid crystalline polymers, a series of new methacrylate monomers, (2,5- bis[2-(4,-alkoxyphenyl) ethynyl] benzyl methacrylate (MACn, n = 4, 6, 8, 10, and 12) and 2,5- bis[2-(6,-decanoxynaphthyl) ethynyl] benzyl methacrylate (MANC10), and their polymers, PMACn (n = 4, 6, 8, 10, and 12) and PMANC10 were synthesized. The bistolane mesogen with large ,-electron conjugation were side-attached to the polymer backbone via short linkages. Various characterization techniques such as differential scanning calorimetry, wide-angle X-ray diffraction, and polarized light microscopy were used to study their mesomorphic phase behavior. The polymer PMACn with shorter flexible substituents (n = 4) forms the columnar nematic (,N) phase, but other polymers with longer flexible tails (n = 6, 8, 10, and 12) can develop into a smetic A (SA) phase instead of a ,N phase. The PMANC10 containing naphthyl can also form a well-defined SA phase. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 [source]

Dynamic mechanical properties and morphology of poly(benzyl methacrylate)/epoxy thermoset blends

POLYMER ENGINEERING & SCIENCE, Issue 9 2010
Margarita G. Prolongo
Poly(benzyl methacrylate) (PBzMA)/epoxy thermoset blends of composition 5 to 25 wt% of PBzMA were prepared curing with 4,4,diaminodiphenylmethane (DDM), to study the influence of composition on the morphology and dynamic-mechanical properties of the blends. The cured blends are phase separated in PBzMA-rich phase and epoxy rich-phase. As the PBzMA content increases, the morphology evolves from nodular, to combined and to totally inverted. The analysis of the ,-mechanical relaxations indicates that the glass transition temperatures (Tg) of PBzMA and of epoxy in the blends are different from the neat polymers, this is related to a noncomplete phase separation on curing. The profiles of the loss modulus-temperature curves are correlated with the change in morphology that appears increasing the PBzMA content. The storage modulus-temperature curves are highly dependent on the morphology of the samples. The storage modulus-composition dependence is predicted using several models for two phase composites. POLYM. ENG. SCI., 50:1820,1830, 2010. © 2010 Society of Plastics Engineers [source]

Ternary miscibility in blends of three polymers with balanced binary interactions

POLYMER ENGINEERING & SCIENCE, Issue 3 2003
E. M. Woo
This study demonstrates and discusses ternary miscibility in a three-polymer blend system based on balanced binary interactions. A truly miscible ternary blend comprising poly(,-caprolactone) (PCL), poly(benzyl methacrylate) (PBzMA), and poly(vinyl methyl ether) (PVME), was discovered and reported. Miscibility with phase homogeneity (excluding the PCL crystalline domain) in a wide composition range has been demonstrated using criteria of thermal transition behavior, cloud point, and microscopy characterization. At ambient temperature, the three-polymer ternary system is completely miscible within the entire composition range (i.e., no immiscibility loop). However, at slightly elevated temperatures above the ambient. phase separation readily occurred in this originally miscible ternary blend. A quite low "lower critical solution temperature" (LCST) near 75°C was found for the ternary blend, which is much lower than any of those for the binary pairs. Balanced interactions with no offsetting ,, among the three binary pairs were a key factor leading to a ternary miscible system. [source]

Porous polymer monolith for surface-enhanced laser desorption/ionization time-of-flight mass spectrometry of small molecules

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 13 2004
Dominic S. Peterson
Porous poly(butyl methacrylate- co -ethylene dimethacrylate), poly(benzyl methacrylate- co -ethylene dimethacrylate), and poly(styrene- co -divinylbenzene) monoliths have been prepared on the top of standard sample plates used for matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry and the modified plates were used for laser desorption/ionization mass spectrometry (LDI-MS). The hydrophobic porous surface of these monoliths enables the transfer of sufficient energy to the analyte to induce desorption and ionization prior to TOFMS analysis. Both UV and thermally initiated polymerization using a mask or circular openings in a thin gasket have been used to define spot locations matching those of the MALDI plates. The desorption/ionization ability of the monolithic materials depends on the applied laser power, the solvent used for sample preparation, and the pore size of the monoliths. The monolithic matrices are very stable and can be used even after long storage times in a typical laboratory environment without observing any deterioration of their properties. The performance of the monolithic material is demonstrated with the mass analysis of several small molecules including drugs, explosives, and acid labile compounds. The macroporous spots also enable the archiving of samples. Copyright © 2004 John Wiley & Sons, Ltd. [source]