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181.
A series of fracture mechanics tests of a set of random and impact copolymers of polypropylene, in which the ethylene content was varied, is described. The plane strain toughness is found to change from the homopolymer value, but thereafter to be independent of ethylene content. The yield stress of the impact copolymers decreases markedly with ethylene content, while that for random copolymers increases only slightly. This is reflected in toughness values in tension. A comparison with the behavior of other rubber-modified materials is made and it is concluded that crazing is an important mechanism in polypropylene and is perhaps more rate and temperature sensitive than in acrylonitrile-butadiene-styrene (ABS). 相似文献
182.
Fernando A. Oliveira Neri Alves José A. Giacometti Carlos J. L. Constantino Luiz H. C. Mattoso Ana M. O. A. Balan Aldo E. Job 《应用聚合物科学杂志》2007,106(2):1001-1006
This work describes the preparation and characterization of composite materials obtained by the combination of natural rubber (NR) and carbon black (CB) in different percentages, aiming to improve their mechanical properties, processability, and electrical conductivity, aiming future applications as transducer in pressure sensors. The composites NR/CB were characterized through optical microscopy (OM), DC conductivity, thermal analysis using differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMA), thermogravimetry (TGA), and stress–strain test. The electrical conductivity varied between 10?9 and 10 S m?1, depending on the percentage of CB in the composite. Furthermore, a linear (and reversible) dependence of the conductivity on the applied pressure between 0 and 1.6 MPa was observed for the sample with containing 80 wt % of NR and 20% of CB. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
183.
The polymerization of α-methylstyrene (αMeSty) initiated by HI/I2 or HI in the presence of liquid sulfur dioxide has been investigated. The number-average molecular weight increased with
the monomer concentration for reactions initiated by the HI/I2 system. I2 also participates in the initiation process, increasing the number-average polymer chain at higher monomer concentration.
HI alone is also able to initiate the polymerization of αMeSty in the presence of SO2. With this initiator, transfer reaction can be minimized in systems containing low amount of SO2.
Received: 19 December 1996/Revised: 27 January 1997/Accepted 29 January 1997 相似文献
184.
This article reports the design and deployment of two optical‐fiber temperature sensors based on the fiber Fabry–Perot etalon. The first involved the use of an extrinsic fiber Fabry–Perot sensor, but in this instance, the coefficient of thermal expansion of the reflector and/or capillary was chosen to offer a mismatch. Hence, the cavity length could increase or decrease according to the coefficient of thermal expansion of the fiber and/or capillary. For comparison, single‐mode and multimode optical‐fiber Bragg gratings were also used as temperature sensors. The Fabry–Perot sensors operated from ?50 to 410°C. The accuracy of the measurements was up to ±0.5°C with a low‐cost charged‐coupling‐device spectrometer. The sensors also worked effectively in a microwave oven and in a composite panel in an autoclave. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 83–95, 2004 相似文献
185.
The lower halides of zinc, namely, ZnCl2 , ZnBr2 , and ZnI2 , may act as network formers in glasses that also contain modifying alkali halides such as KCI, KBr, KI, NaI, or CsI. Compositions which contain only Br− or I− anions are of particular interest because of their extended infrared transmission, which includes the ∼10-μm region, in addition to full visible transparency. A series of modified zinc halide glasses were prepared and characterized by differential scanning calorimetry, middle and far Fourier transform infrared spectroscopy, and polarized Raman spectroscopy. T g values were characteristically low, around 40°C. Bulk glass infrared transmission up to 15 to 20 μm was recorded. The most probable glass structures are discussed and compared to oxide glass models. An attenuation of 0.001 dB/km has been projected as a possible intrinsic minimum for optical fibers operating near ∼6 μm. 相似文献
186.
G. L. Chen C. Guyon Z. X. Zhang B. Da Silva P. Da Costa S. Ognier D. Bonn M. Tatoulian 《Microfluidics and nanofluidics》2014,16(1-2):141-148
In this paper, tricobalt tetraoxide (Co3O4) catalyst was coated on the polydimethylsiloxane microchannel by the plasma-enhanced metal-organic chemical vapor deposition technology. The obtained Co3O4 film was characterized by SEM, XRD, XPS, and TEM, and the results show that the as-deposited Co3O4 film was initially composed of many cauliflowers-shaped microclusters. Also, the microcauliflower was transformed from an amorphous phase to a crystal phase when the Co3O4 film was treated by Ar and O2 plasma for more than 20 min, and the crystal lattice line occurred on the surface of nano-sized-Co3O4 particles. Meanwhile, the interface of Co3O4 particles with diameter between 3 and 12 nm became obvious and some nano-catkin structures were also formed on the Co3O4 film. The ratio of Co3+/Co2+ in the spinel-type Co3O4 was nearly 2, and the nano-particles predominantly expose their {311}, {111}, and {220} planes. These morphologies and structure characteristics were found to be ideal for increasing the catalytic activity efficiency of Co3O4 for CO oxidation, and the catalytic stability of Co3O4 coated on the organic microreactor lasted nearly 85 h for trace CO oxidation at room temperature. 相似文献
187.
Luiz C.A Oliveira 《Carbon》2004,42(11):2279-2284
In this work, hydrogen peroxide reactions, i.e. H2O2 decomposition and oxidation of organics in aqueous medium, were studied in the presence of activated carbon. It was observed that the carbon pre-treatment with H2 at 300, 500, 700 and 800 °C resulted in an increase in activity for both reactions. The carbons were characterized by BET nitrogen adsorption, thermogravimetric analyses (TG), temperature programmed reduction (TPR), electron paramagnetic resonance (EPR), iodometric titration and determination of the acid/basic sites. TPR experiments showed that activated carbon reacts with H2 at temperatures higher than 400 °C. The treatment produces a slight increase in the surface area. EPR analyses indicate the absence of unpaired electrons in the carbon. Iodometric titrations and TG analyses suggested that the treatment with H2 generates reduction sites in the carbon structure, with concentration of approximately 0.33, 0.53, 0.59, 0.65 and 0.60 mmol/g for carbons treated at 25, 300, 500, 700 and 800 °C, respectively. It was also observed the appearance of basic sites which might be related to the reduction sites. It is proposed that these reducing sites in the carbon can activate H2O2 to generate HO* radicals which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. 相似文献
188.
新品种的间苯二酚-甲醛树脂中的游离间苯二酚含量极低,且不再具有吸湿性。考察了间苯二酚-甲醛树脂(Penacolite B-20-S)、硼酰化钴和不溶性硫黄的用量对钢丝粘合胶与镀铜钢丝粘合性能的影响。结果表明,树脂/钴盐粘合体系比单纯的钴盐粘合体系的粘合性能好得多。仅考虑粘合性能时,粘合体系最佳配方为:Penacolite B-20-S树脂4,硼酰化钴(活性钴)0.1,不溶性硫黄(活性)7.1,HMMM(活性)2.66。 相似文献
189.
Luis Carlos Ferreira Jr.Marcos A.S. Costa Pedro Ivo C. GuimarãesLuiz Claudio de Santa Maria 《Polymer》2002,43(14):3857-3862
Styrene polymerization was carried out with Ni(acac)2/MAO and Ni(acac)2/SiO2/MAO. The influence of reaction parameters (Al/Ni mole ratio, catalyst concentration, temperature and time polymerization) on styrene polymerization was evaluated. It was observed that both catalytic systems were affected by reaction parameters and that the heterogeneous catalyst presented higher activity than the homogeneous one. Polystyrenes with different molecular weight, stereoregularity and polydispersity were obtained. These results suggest that different active catalyst species could have been present. In addition, two types of methylaluminoxane (MAO) with different molecular weights were also evaluated as cocatalyst. As a result, the catalyst activity and stereospecificity were strongly affected by the MAO type. 相似文献
190.
A laboratory‐sized two‐roll mill was used to incorporate rice husk ash into natural rubber (NR). A conventional vulcanization system was used for curing and cure studies were carried out on a Monsanto rheometer. Physical testing of the NR vulcanizates involved determining tensile and tear resistances and hardness. Swelling behavior of NR compounds and scanning electron microscopy were used to investigate the interaction between rice husk ash and natural rubber. Also, dynamical mechanical thermal analysis was used to assess filler–rubber interactions in terms of storage modulus (E′) and loss tangent (tan δ). For comparison purposes, two commercial fillers, precipitated silica (Zeosil‐175) and carbon black (N774), were also used. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2331–2346, 2002 相似文献