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Methylene Spacers (methylene + spacer)
Selected AbstractsFormation and Properties of Responsive Siloxane-Based Polymeric Surfaces with Tunable Surface Reconstruction KineticsADVANCED FUNCTIONAL MATERIALS, Issue 3 2009Julie Ann Crowe-Willoughby Abstract Here, the formation of responsive polymeric materials with tunable response time is reported. These structures are fabricated by chemically modifying poly(vinylmethyl siloxane) (PVMS) networks with alkanethiols bearing a hydrophilic end-group (COOH or OH). The response time is facilitated by the liquid nature of the PVMS backbone and increases with increase in length of the methylene spacer (CH2)n in the alkanethiol pendent group. While for n,=,2 and 6, the surface reconstructs almost instantaneously, specimens with n,=,11 resist reconstruction because of strong van der Waals forces, leading to the formation of semi-crystalline regions. It is demonstrated that the responsive nature of PVMSS(CH2)11OH can be fine-tuned by varying the temperature; it possesses a faster response at temperatures above the melting point of the S(CH2)11OH moiety. [source] Synthesis and characterization of dicyanate monomers containing methylene spacersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008G. Anuradha Abstract The bisphenols containing methylene spacer were prepared by treating eugenol/2-allyl phenol with 2,6-dimethyl phenol/guiacol/o -cresol in the presence of AlCl3. All the bisphenols were converted to their respective cyanate esters by treating with CNBr. The structural confirmation was done by FTIR, 1H NMR, 13C NMR spectral methods, and elemental analysis. Thermal characterization was done by DSC and TGA. DSC transition shows that the Tg is in the range of 208,239°C. The Tg is highest for the cyanate ester Cy(b) with symmetric structure. The Tg of the cured network depends on the length and symmetry of the monomer, Tg being higher for shorter and the para-substituted monomers. The T10 values are in the range of 364,381°C. The char yield is in the range of 47,53%. From the char yield, the limiting oxygen index (LOI) value was determined, which is used to confirm the flame retardancy of the cyanate ester resins. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Synthesis, characterization, and in vitro degradation of liquid-crystalline terpolyesters of 4-hydroxyphenylacetic acid/3-(4-hydroxyphenyl)propionic acid with terephthalic acid and 2,6-naphthalene diolJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 11 2002V. S. Prasad Abstract Melt-processable liquid-crystalline terpolyesters of 4-hydroxyphenylacetic acid (HPAA) and 3-(4-hydroxyphenyl)propionic acid (HPPA) with terephthalic acid and 2,6-naphthalene diol were synthesized by one-step acidolysis melt polycondensation followed by postpolymerization and were characterized with viscosity studies, Fourier transform infrared (FTIR) and NMR spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), polarized light microscopy, and wide-angle X-ray diffraction. The melting behaviors and liquid-crystalline transition temperatures of the terpolyesters were dependent on the composition of the HPAA/HPPA content. The transition temperatures of the polyesters could be effectively reduced by the introduction of an even number of built-in short methylene spacers in combination with the 2,6-naphthalene offset structure. A terpolyester with an HPPA content of 33% (NTP33) showed optimum properties for the glass-transition temperature, around 71 °C, and the melting temperature, near 240 °C, with a Schlieren nematic texture. The polymer showed excellent flow behavior in a Brabender plasticorder. It was also thermally stable up to 400 °C. NTP33 showed 2.5% in vitro hydrolytic degradation in buffer solutions of pH 10 at 60 °C after 540 h. Considerable enzymatic degradation was also observed with porcine pancreas lipase/buffer solutions in comparison with Candida rugosa lipase after 60 days. The degradation was also followed with FTIR, DSC, and TGA. Apart from the temperature and pH of the buffer solution, several structural parameters, such as the aromatic content, crystallinity percentage, and composition of the polymer, affected the degradation behavior. FTIR studies indicated the involvement of chain scission during degradation. Scanning electron microscopy studies further showed that surface erosion also played a major role in the degradation. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1845,1857, 2002 [source] Copolymerization of ethylene with aromatic vinyl monomers using metallocenesPOLYMER INTERNATIONAL, Issue 4 2001K Rajesh Kumar Abstract Copolymerization of ethylene with styrene, allyl benzene and 4-phenyl-1-butene was examined using different metallocene catalysts. We separated the bulky phenyl group of styrene from its double bond using methylene spacers and studied the effect on its copolymerization behaviour with ethylene. The extent of incorporation of the comonomer is in the order 4-phenyl-1-butene,>,allyl benzene,>,styrene for all catalysts. The comonomer incorporation was found to be less than 10,mol% under the experimental conditions employed in the present study. © 2001 Society of Chemical Industry [source] | ||||||||||