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961.
This study aims at quantifying the nano-size effect in terms of elastic and thermal properties in nano-reinforced polymers. Nano-reinforced PMMA with 4% volume fraction of silica nanoparticles was prepared using particle diameters of 15 nm, 25 nm, 60 nm, 150 nm and 500 nm. Uniaxial tensile tests showed an increase in Young's modulus with decreasing particle diameter when the volume fraction was kept constant. This increase is the signature of the nano-size effect on the macroscopic mechanical properties. Conversely to mechanical properties, the presence of particles in the matrix induced a decrease in glass transition, possibly due to weak interactions between the matrix and silica nanoparticles. 相似文献
962.
Synthesis of poly(isopropenylphenoxy propylene carbonate) and its facile side‐chain functionalization into hydroxy‐polyurethanes
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Chun Chieh Huang Ching Hsuan Lin Shenghong A. Dai 《Journal of polymer science. Part A, Polymer chemistry》2016,54(6):802-808
4‐Isopropenyl phenol ( 4‐IPP ) is a versatile dual functional intermediate that can be prepared readily from bisphenol‐A ( BPA ). Through etherification with epichlorohydrin to the phenolic group of 4‐IPP , it can be converted into 4‐isopropenyl phenyl glycidyl ether ( IPGE ). On further reaction with carbon dioxide in the presence of tetra‐n‐butyl ammonium bromide ( TBAB ) as the catalyst, IPGE was transformed into 4‐isopropenylphenoxy propylene carbonate ( IPPC ) in 90% yield. Cationic polymerization of IPPC with strong acid such as trifluoromethanesulfonic acid or boron trifluoride diethyl etherate as the catalyst at ?40 °C gave a linear poly(isopropenylphenoxy propylene carbonate), poly( IPPC ), with multicyclic carbonate groups substituted uniformly at the side‐chains of the polymer. The cyclic carbonate groups of poly( IPPC ) were further reacted with different aliphatic amines and diamines resulting in formation of polymers with hydroxy‐polyurethane on side‐chains. Syntheses, characterizations of poly( IPPC ) and its conversion into hydroxy‐polyurethane crosslinked polymers were presented. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 802–808 相似文献
963.
From superhydrophobic‐ to superhydrophilic‐patterned poly(vinylidene fluoride‐co‐chlorotrifluoroethylene) architectures as a novel platform for biotechnological applications
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Vanessa F. Cardoso Ana R. Machado Vânia C. Pinto Paulo J. Sousa Gabriela Botelho Graça Minas Senentxu Lanceros‐Méndez 《Journal of Polymer Science.Polymer Physics》2016,54(18):1802-1810
The manufacture of three‐dimensional patterned electroactive poly(vinylidene fluoride‐co‐chlorotrifluoroethylene) microstructures with tailored architecture, morphology, and wettability is presented. The patterned microstructures are fabricated using a simple, effective, low cost, and reproducible technique based on microfluidic technology. These novel structures can represent innovative platforms for advanced strategies in a wide range of biotechnological applications, including tissue engineering, drug delivery, microfluidic, and sensors and actuators devices. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 1802–1810 相似文献
964.
David R. Harding Holly Goodrich Aaron Caveglia Mitchell Anthamatten 《Journal of Polymer Science.Polymer Physics》2014,52(14):936-945
Knowing the mechanical properties of UV‐curable resins at cryogenic conditions is important to ongoing fusion‐energy research and to emerging aerospace applications. The tensile and interfacial shear strengths of two commercially available UV‐curable resins were measured at room‐temperature and cryogenic conditions for both bulk and reduced (subnanoliter) specimen volumes. The tensile properties of cured specimens are remarkably sensitive to both testing temperature and specimen size. For one type of resin, the cold (?150 °C) tensile strength of subnanoliter specimens is ~9× larger (179 ± 19 MPa) than bulk values at room temperature. The interfacial shear strength between SiC fibers and small volumes of resin volumes is comparable to the bulk, room‐temperature tensile strength, but it varies over a wide range at ?150 °C (15–53 MPa). All resins were fully cured, and an analysis of fractured surfaces revealed microstructural features. The enhanced strength in microscopic specimens may be related to inhomogeneous stress fields that develop during cure. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52, 936–945 相似文献
965.
《Journal of separation science》2017,40(2):506-513
A simple one‐pot approach based on molecularly imprinted polymer shells dispersed on the surface of silica for simultaneous determination of rhodamine B and dibenzyl phthalate (DBzP) has been developed. Highly dense molecularly imprinted polymer shells were formed in the mixture of acetonitrile and toluene by the copolymerization of methacrylic acid and ethylene glycol dimethacrylate, as well as two templates, rhodamine B and dibenzyl phthalate, directed by the vinyl end groups functional monolayer at surface silica microspheres after 3‐methacryloxypropyl trimethoxysilane modification. The obtained imprinted polymer shells showed large average pore diameter (102.5 nm) and about 100 nm shell thickness. The imprinted particles also showed high imprinting factor (αRhB = 3.52 and αDBzP = 3.94), rapid binding kinetics, and excellent selective affinity capacity for rhodamine B and dibenzyl phthalate containing another three competitors in mixed solution. Moreover, the imprinted particles coupled with ultra high performance liquid chromatography was successfully applied to simultaneous analysis of rhodamine B and dibenzyl phthalate in two spiked beverage samples with average recoveries in the range of 88.0−93.0% for rhodamine B and 84.0–92.0% for dibenzyl phthalate with the relative standard deviation lower than 5.1%. 相似文献
966.
Encapsulation of materials in particles dispersed in water has many applications in nutritional foods, imaging, energy production and therapeutic/diagnostic medicine. Ultrasonic technology has been proven effective at creating encapsulating particles and droplets with specific physical and functional properties. Examples include highly stable emulsions, functional polymeric particles with environmental sensitivity, and microspheres for encapsulating drugs for targeted delivery. This article provides an overview of the primary mechanisms arising from ultrasonics responsible for the formation of these materials, highlighting examples that show promise particularly in the development of foods and bioproducts. 相似文献
967.
Suchismita Guha Matti Knaapila Dhanashree Moghe Zuzana Konôpková Mika Torkkeli Martin Fritsch Ullrich Scherf 《Journal of Polymer Science.Polymer Physics》2014,52(15):1014-1023
The role of high pressure on a low molecular weight nematic liquid crystalline organic semiconductor, ethyl‐hexyl substituted polyfluorene (PF2/6) is investigated using photoluminescence (PL), Raman scattering, and X‐ray scattering studies at pressures from 1 to 8 GPa. The PL and the Raman data under pressure are consistent with each other with no abrupt changes in the pressure coefficients of PL or Raman peaks. The PL energies redshift and broaden, consistent with both enhanced intra‐ and interchain interactions. The Raman peak positions yield pressure coefficients similar to other phenyl based π‐conjugated polymers. The broadening of a doublet peak in the 1135 cm?1 region indicates a more planar backbone conformation with increasing pressure. X‐ray scattering indicates that the torsion angle between adjacent repeats reduces with increasing pressure and reverts back with decompression. The intermolecular structure is weakly ordered (frozen nematic) and essentially maintained with increasing pressure, in contrast to a high molecular weight PF2/6. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52, 1014–1023 相似文献
968.
Structure and Photoelectric Characteristics of Functional Polymers and of Compositions Based on Them 总被引:1,自引:0,他引:1
The electronic processes in disordered organic solids were analyzed, classified, and summarized. They include the photogeneration of charge pairs, electron transport, geminal and bimolecular recombination, and the capture of charge carriers in local electronic states. General criteria were formulated for the targeted search for and the creation of new prospective polymers and their compositions with organic pigments and related compounds having specific photoelectric characteristics for electrographic and holographic media, photoelectric converters, and electroluminescent and photorefractive devices. 相似文献
969.
The process of growth of an individual cavity in a viscoelastic adhesive layer has been investigated experimentally. The formation
of cavities was caused by the application of a negative pressure on a very confined layer with a flat-ended probe. The cavities
appeared in the bulk of the adhesive layer and were observed for a range of values of applied stress approximately ten times
higher than the shear modulus of the adhesive layer. Depending on the loading rate, the shape of the growing cavity changed
from a flat disc to a more spherical shape. Furthermore, the growth rate of the cavity radius was consistent with a constant
strain rate at the edge of the cavity, which suggests a constant level of stress at the edge of the cavity.
Received 5 June 2002
RID="a"
ID="a"Current address: Ethicon, Johnson & Johnson, Route 22 West, P.O. Box 151, Somerville, NJ 08876-0151, USA.
RID="b"
ID="b"e-mail: costantino.creton@espci.fr 相似文献
970.
Sun Xiaoying Yang Xiaohui Liu Yunhang Wang Xinling 《Journal of polymer science. Part A, Polymer chemistry》2004,42(10):2356-2364
A multiarm star polymer was synthesized through the grafting of oligo polyglycol with urethane chain end units onto the core of hyperbranched polyglycerol (HPG), which was obtained through the cationic ring‐opening polymerization of glycidol. Samples were characterized with 13C NMR, liquid chromatography/mass spectrometry, vapor pressure osmometry, and Raman spectroscopy. The degree of branching of HPG was 0.54, and the number of arms grafting onto HPG was 4. The urethane of the arms mainly reacted with the terminal hydroxy groups of HPG. The differences between the spin–spin relaxation times indicated that the terminal segments of the star were more flexible than those of the core. Grafting polyglycol polyurethane (soft segments of polyurethane is polyglycol) onto HPG improved its dimensional stability. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2356–2364, 2004 相似文献