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991.
Nitin Y VaidyaChang Dae Han 《Polymer》2002,43(10):3047-3059
The temperature-composition phase diagrams for six pairs of diblock copolymer and homopolymer are presented, putting emphasis on the effects of block copolymer composition and the molecular weight of added homopolymers. For the study, two polystyrene-block-polyisoprene (SI diblock) copolymers having lamellar or spherical microdomains, a polystyrene-block-polybutadiene (SB diblock) copolymer having lamellar microdomains, and a series of polystyrene (PS), polyisoprene (PI), and polybutadiene (PB) were used to prepare SI/PS, SI/PI, SB/PS, and SB/PB binary blends, via solvent casting, over a wide range of compositions. The shape of temperature-composition phase diagram of block copolymer/homopolymer blend is greatly affected by a small change in the ratio of the molecular weight of added homopolymer to the molecular weight of corresponding block (MH,A/MC,A or MH,B/MC,B) when the block copolymer is highly asymmetric in composition but only moderately even for a large change in MH,A/MC,A ratio when the block copolymer is symmetric or nearly symmetric in composition. The boundary between the mesophase (M1) of block copolymer and the homogeneous phase (H) of block copolymer/homopolymer blend was determined using oscillatory shear rheometry, and the boundary between the homogeneous phase (H) and two-phase liquid mixture (L1+L2) with L1 being disordered block copolymer and L2 being macrophase-separated homopolymer was determined using cloud point measurement. It is found that the addition of PI to a lamella-forming SI diblock copolymer or the addition of PB to a lamella-forming SB diblock copolymer gives rise to disordered micelles (DM) having no long-range order, while the addition of PS to a lamella-forming SB diblock copolymer retains lamellar microdomain structure until microdomains disappear completely. Thus, the phase diagram of SI/PI or SB/PB blends looks more complicated than that of SI/PS or SB/PS blends. 相似文献
992.
In Kim 《乙烯基与添加剂工艺杂志》2007,13(2):71-75
Electrically conductive acrylonitrile‐butadiene rubbers (NBRs) containing carbon black (CB) as conductive filler were prepared in order to investigate their electrical and mechanical properties. The effects of conductive CB loading, temperature, acrylonitrile content, crosslinking density of vulcanizates, and plasticizer on conductivity were studied. The change in electrical conductivity of NBRs with different amounts of CB showed that there is a certain critical point (percolation threshold) where a significant decrease in electrical resistivity (increase in conductivity) is observed. Mechanical properties such as tensile strength, elongation to break, and surface hardness of vulcanized NBRs were measured. It was found that the percolation threshold was 5 phr of CB for the NBR/CB composites. J. VINYL ADDIT. TECHNOL., 13:71–75, 2007. © 2007 Society of Plastics Engineers. 相似文献
993.
994.
在自由基聚合中,生成间规立构的趋势稍优先于等规立构。通常认为,碳碳双键上取代基的体积效应和极性效应,是加成反应的立体定向力;而作者则认为,极性呈静电排斥效应是决定间规立构含量较优的主要因素。取代基的体积效应具有两个因素同时决定着立体异构的形成,其一是热力学因素,即体积的排斥效应使间规立构含量增加;另一是动力学因素,即在加成反应瞬间影响链末端碳碳单键内旋转的自由度。因此,取代基的存在不仅使得间规立构占主导,而且取代基体积越小,则自由基的碳碳单键内旋转越容易,形成间规立构的比例亦越高;反之则内旋转不自由,形成随机取向(即无规立构)的比例增加。 相似文献
995.
Copoly(ehtylene terephthalate/imide)s (PETI) were prepared by melt polycodensation of bis(2-hydroxyethyl)terephthalate (BHET) and imide containing comonomer, 4,4′-bis[(4-carbo-2-hydroxyethoxy)phthalimido]diphenylmethane (BHEI) with Sb2O3 as catalyst at 280°C under vacuum (~ 1 mm Hg). The change of Tm with an increase of the BHEI repeat unit in the PETI copolymer was analyzed by the Flory equation. On isothermal crystallization, a longer induction time and a lower activation energy than for the PET homopolymer were observed with an increasing amount of BHEI repeat unit. The Avrami exponent, n, increased from 1.5 to 2.3 as the content of BHEI or crystallization temperature was increased. The Avrami rate constant K decreased with the increase of the BHEL unit. On nonisothermal crystallization, the Ozawa equation and Lawton plot were used to investigate the effect of BHEI units on the crystallization kinetics of PETI copolymers. From the change of the cooling crystallization function and the result of the Lawton plot, it was found that the BHEI unit effectively decreases the rate of crystallization. 相似文献
996.
Miscibility and crystallization of poly-p-phenylene terephthalamide (PPTA)/nylon 6 and nylon 66 composites prepared by coagulation of isotropic ternary sulfuric acid solutions were studied. The apparent crystallinity of nylon 6 and nylon 66 in molecular composites was investigated by differential scanning calorimetry and Fourier transform infrared spectroscopy. The solvation of nylon 6 crystals in PPTA matrix was observed when the PPTA content exceeds 70 wt%. Cross-hydrogen bonding seems to be responsible for the virtual disappearance of nylon 6 crystals. Specific interaction between PPTA and nylon 6 macromolecules and phase separation during thermal treatment has been discussed. 相似文献
997.
矩阵是一种重要的数学方法,在数学领域有其独特的作用。根据正定实对称矩阵的一个重要不等式及均值不等式在矩阵方面的一个重要性质,对国际数学竞赛和不同书刊中有关不等式进行探讨。通过对比,体现了在解某类不等式问题时运用矩阵解题的优势。 相似文献
998.
掺钡白钨矿型CaWO4:Ba2+荧光材料的制备与表征 总被引:1,自引:0,他引:1
以氯化钙、氯化钡和硝酸钠为原料,采用沉淀法制备出纯CaWO4、BaWO4粉体,采用固相反应法制备出CaWO4:Ba2+(CaxBa1-xWO4)粉体,研究了钡离子的掺杂量对CaWO4:Ba2+荧光材料的发光性能的影响.通过XRD、FT-IR对样品的晶体尺寸进行表征,以及PL分析了样品的发光特性.研究结果表明:掺杂后钨酸盐中的晶胞参数随Ba2+的掺杂量增加而增大,且晶体结构中WO2-4四面体构型发生畸变;钨酸钙的在370 cm-1、430 cm-1附近有明显发光,当钡离子掺入量较低时,CaWO4:Ba2+的发光强度增加,但当钡离子掺入量增加时,发光强度却下降. 相似文献
999.
为研究尾矿库漫顶溃决动态演化过程与溃口发展机理及规律,通过3组相似模型试验,对溃口展宽过程和演变机理进行了系统分析,提出了尾矿坝漫顶模式下溃口展宽速率的幂函数公式,并讨论了库水位上升阶段浸润线的变化过程及溃决阶段不同浸润线埋深条件下流速、流量、溃口宽度的变化过程。研究结果表明:尾矿坝的溃决过程可分为坝面漫流与冲沟形成、坝体崩塌与溃口快速扩张及稳定泄流3个阶段;浸润线埋深对流量、流速及溃口最终宽度有较大影响,排渗失效时峰值流量及溃口最终宽度接近正常排渗时的1.5倍,峰值流速可达1.2~1.3倍;降低浸润线高度可以延缓溃决泥石流到达下游的时间,紧急撤离时间也可延长3 min左右;提出的幂函数公式计算值与实测值吻合较好。 相似文献
1000.
Single-crystal silicon wafers ((1 1 1) and (1 0 0)p-type) were abraded at room temperature 300 °C, and 600 °C by a polycrystalline partially stabilized zirconia ball in a ball-on reciprocating flat geometry. The sliding direction was 1 1 0. The friction coefficient was recorded as a function of reciprocating strokes and the deformation mode of the silicon. The friction coefficient at room temperature decreased with the number of strokes, and this variation was less affected by the number of strokes at the higher temperatures. The wear track width and depth were measured at the three temperatures. Wear increases as the temperature is raised to 300 and 600 °C. Optical and scanning electron microscopy of the subsurface damage reveals that cracks are generated at RT and 300 °C and dislocations are produced at 600 °C. The change in deformation mode with temperature from brittle fracture to plastic deformation accounts for the differences in wear. 相似文献