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The plastic deformation mechanism operating in polymer glasses is analyzed. The whole process consists of two main stages: nucleation of special shear defects, called PSTs (plastic shear transformations), and their disappearance. The important feature of plastic deformation of glasses is the storage of a large amount of internal energy ΔUdef upon straining. Such energy storage is the critical issue for mechanical performance of polymeric material: if the amount of stored energy is high, the appearance of macroscopic failure is very probable while glassy materials collecting a small amount of stored deformation energy are quite ductile. It is proposed that the rate of disappearance of PSTs is a key factor in dissipation of stored deformation energy. A parameter describing the dissipation ability of material upon deformation is introduced. 相似文献
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T. Nakajima-KambeN.G. Edwinoliver H. MaedaK. Thirunavukarasu M.K. GowthamanK. Masaki S. MahalingamN.R. Kamini 《Polymer Degradation and Stability》2012,97(2):139-144
A lipase from Aspergillus niger MTCC 2594 was purified 53.8-fold to homogeneity by hydrophobic interaction chromatography using octyl sepharose and the enzyme showed two protein bands with apparent molecular mass of 35 and 37 kDa respectively. The lipase exhibited maximum activity at pH 7.0 and 37 °C and was stable between pH 4.0 and 10.0 and temperatures up to 50 °C. The values of Km and Vmax were 3.83 mM and 32.21 μmol/min/mg respectively, using olive oil as substrate. Lipase encoding gene, lipA, coded for 297 amino acid residues with conserved pentapeptide sequence, G-H-S-L-G, was cloned and expressed in Pichia pastoris. Although lipA showed high homology with the known Aspergillus lipases, it exhibited differences in putative lid domain. Both native and recombinant lipases have potential for degradation of poly(lactic acid) and poly(ε-caprolactone), and the present study will serve as a baseline of initial studies for its exploitation in polymer degradation. 相似文献
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Direct loading of polymer matrices in plastic microchips for rapid DNA analysis: A comparative study
C Hurth J Gu M Aboud MD Estes AR Nordquist B McCord F Zenhausern 《Electrophoresis》2012,33(16):2604-2611
We report the design and performance validation of microfluidic separation technologies for human identification using a disposable plastic device suitable for integration into an automated rapid DNA analysis system. A fabrication process for a 15-cm long hot-embossed plastic microfluidic devices with a smooth semielliptical cross section out of cyclic olefin copolymer is presented. We propose a mixed polymer solution of 95% w/v hydroxyethylcellulose and 5% w/v polyvinylpyrrolidone for a final polymer concentration of 2.5 or 3.0% to be used as coating and sieving matrix for DNA separation. This formulation allows preparing the microchip without pretreatment in a single-loading step and provides high-resolution separation (≈1.2 bp for fragments <200 bp), which is superior to existing commercial matrices under the same conditions. The hot-embossed device performance is characterized and compared to injection-molded devices made out of cyclic olefin copolymer based on their respective injector geometry, channel shape, and surface charges. Each device design is assessed by fluorescence videomicroscopy to evaluate the formation of injection plugs, then by comparing electropherograms for the separation of a DNA size standard relevant to human identification. 相似文献
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Simultaneous screening and determination eight phthalates in plastic products for food use by sonication-assisted extraction/GC-MS methods 总被引:7,自引:0,他引:7
Studies on determination of eight kinds of phthalates, e.g. di-ethyl phthalate (DEP), di-propyl phthalate (DPP), di-isobutyl phthalate (DIBP), di-butyl phthalate (DBP), benzyl butyl phthalate (BBP), di-cyclohexyl phthalate (DCHP), di-(2-ethylhexyl) phthalate (DEHP), di-octyl phthalate (DOP), in 25 kinds of plastic products for food use, including packaging bags, packaging film, containers, boxes for microwave oven use, sucking tubes, spoons, cups, plates, etc. by gas chromatography in combination with mass spectrometry detector (GC-MS) in electronic ionisation mode (EI) with selected-ion monitoring (SIM) acquisition method (GC-MS (EI-SIM)) have been carried out. Methods have been developed for both qualitative and quantitative analysis of phthalates. Extraction, clean-up and analysis procedure have been optimized. Determination of samples were performed after frozen in liquid nitrogen and sonication-assisted extraction with hexane, clean-up with LC-C18 SPE and analyzed by GC-MS methods. The base peak (m/z = 149) of all the phthalates was selected for the screening studies. The characteristic ions, 121, 177, 222 for DEP; 191, 209 for DPP; 57, 223 for DIBP; 104 for DBP; 91, 132, 206 for BBP; 55, 167 for DCHP; 113, 167, 279 for DEHP; 279 for DOP were chosen for quantitative studies. These techniques are possible to detect phthalates at the level of 10.0 μg/kg. Overall recoveries were 82-106% with R.S.D. values at 3.8-10.2%. Only one of the 25 examined samples was free from phthalates. The rest 24 samples were found to contain at least three or more of these phthalates. The predominant phthalate detected in the studied samples was DEHP. 相似文献
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Summary The behaviour of codeine reineckate and codeine tetraphenylborate membrane electrodes has been observed with a respectiveNernstian response of 58 and 56 mV/decade for 9.3×10–5–1.3×10–3
M codeine sulfate solutions. The workingpH ranges were 5–8 and 4–8, respectively. The selectivity towards sugars, amines, amino acids, cations, and some pharmaceutical compounds was found to be satisfactory. The isothermal temperature coefficient was 0.0014 V/°C. The electrodes were applied successfully for the determination of codeine in some pharmaceutical dosage forms with a relative standard deviation range of 0.16–0.30% and an average recovery of 98.6±0.6%.
Herstellung und Charakterisierung einer codeinselektiven Elektrode
Zusammenfassung Das Verhalten von Codeinreineckat- und Codeintetraphenylboratmembranelektroden in 9.3×10–5–1.3×10–3 M Codeinsulfatlösungen wurde untersucht (Nernstscher Response: 58 bzw. 56 mV/Dekade). Der verwendetepH-Bereich für die beiden Elektroden war 5–8 bzw. 4–8. Ihre Selektivität gegenüber Zuckern, Aminen, Aminosäuren, Kationen und einigen pharmazeutisch aktiven Verbindungen ist zufriedenstellend. Der isotherme Temperaturkoeffizient beträgt 0.0014V/°C. Die Elektroden wurden erfolgreich zur Bestimmung von Codein in einigen pharmazeutischen Präparaten eingesetzt (relative Standardabweichung: 0.16–0.30%).相似文献