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81.
对中国石油吉林石化公司300 kt/a乙烯装置汽油加氢二段反应器接管与筒体焊接接头的缺陷进行详细分析。阐明了缺陷的产生是由于在焊接过程中焊缝熔合区内形成马氏体、增碳层并伴有δ-铁素体的分解而使熔合区内及焊缝处的材质脆化。由于选用焊接材料的错误,产生较高的焊接残余应力致使焊缝开裂。分析了焊缝马氏体、增碳层及δ-铁素体分解的原因。  相似文献   
82.
纳米SiOx改性不饱和聚酯树脂   总被引:3,自引:0,他引:3  
用纳米SiOx粒子对298#不饱和聚脂(UPR)进行增强、增韧改性,发现随粒子用量增加,树脂凝胶时间、粘度增大;粒子用量为0.5%时树脂有脆韧转变现象;用量为3%时,拉伸强度和断裂延伸率分别提高约33%和60%。用KH-570偶联剂进行表面处理有助于提高纳米SiOx粒子在UPR中的均匀分散。  相似文献   
83.
The effects of homopolymer and copolymer compositions and structures in styrene/n-butyl acrylate (Sty/BA) latices on sodium dioctyl sulfosuccinate (SDOSS) surfactant mobility and its preferential concentration at the film–air (F–A) and film–substrate (F–S) interfaces were examined using attenuated total reflectance Fourier transform infrared (ATR FTIR) spectroscopy. It appears that the SDOSS concentration at the F–S interface is highest when the Sty/BA feed ratio is 50/50, and the excess of Sty results in migration of SDOSS surfactant to the F–A interface. This behavior is attributed to the increased glass transition temperature and diminished compatibility between surfactant molecules and copolymer latex. This study also shows that the primary factors that influence exudation to either F–A or F–S interfaces are surface tension of the substrate, glass transition temperature, water flux during coalescence, and compatibility between latex components. © 1995 John Wiley & Sons, Inc.  相似文献   
84.
We have found that not only block copolymers but also ionomers can self-assemble in a selective solvent to form surfactant-free nanoparticles. The self-assembly can be induced by chemical reaction, polymer-polymer complexation, and microphase inversion in addition to the temperature. A recently developed microwave method for the preparation of uniform surfactant-free polymeric nanoparticles is also reviewed. Our results have revealed that for a given dispersion, the particle surface area occupied per stabilizer (surfactant, polymer chains, and ionic groups) is close to a constant.  相似文献   
85.
Blends of statistical copolymers containing ethylene/hexene (PEH) and ethylene/butene (PEB) exhibited the behavior of upper critical solution temperature (UCST). The interplay between the early and intermediate stage liquid-liquid phase separation (LLPS) and crystallization of the PEH/PEB 50/50 blend was studied by time-resolved simultaneous small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD) techniques. Samples were treated by two different quench procedures: in single quench, the sample was directly quenched from 160 °C to isothermal crystallization temperature of 114 °C; while in double quench, the sample was firstly quenched to 130 °C for 20 min annealing, where LLPS occurred, and then to 114 °C. It was found that in the early stage of crystallization, the integrated values of Iq2 and crystallinity, Xc, in the double quench procedure were consistently higher than those in the single quench procedure, which could be attributed to accelerated nucleation induced by enhanced concentration fluctuations and interfacial tension. In the late stage of crystallization, some morphological parameters were found to crossover and then reverse, which could be explained by retardation of lamellar growth due to phase separation formed during the double quench procedure. This phenomenon was also confirmed by DSC measurements in blends of different compositions at varying isothermal crystallization temperatures. The crystal lamellar thickness determined by SAXS showed a good agreement with TEM observation. Results indicated that the early stage LLPS in the PEH/PEB blend prior to crystallization indeed dictated the resulting lamellar structures, including the average size of lamellar stack and the stack distribution. There seemed to be little variation of lamellar thickness and long period between the two quenching procedures (i.e., single quench versus double quench).  相似文献   
86.
A series of new polyamides 3a–d containing aryl-azo, ether and sulfone groups in the main chain were synthesized from bis[4-(4-aminophenoxy)phenyl sulfone] 1 and several azo aromatic diacyl chlorides 2a–d by the low temperature solution polycondensation technique. FTIR spectroscopy, nuclear magnetic resonance (NMR) and elemental analyses confirmed the structure of these polymers. Owing to the aryl and amide groups in the main chain, these polymers exhibit photochromic properties as well as excellent thermal stabilities. The transition temperatures (T g) are between 242 and 265 °C, and the char yields at 800 °C in nitrogen atmosphere were above 39%. Based on incorporation of flexible ether linkages and polar sulfone groups, the polyamides show desirable solubility in organic solvents such as DMAc, N,N-dimethylformamide (DMF), N-methyl-2-pyrroidinone (NMP) and dimethylsulfoxide (DMSO). And it is exemplified that polyamide containing 2 and 2′ substitutes performed better solubility. Funded by the National Natural Science Foundation of China (No. 50572081)  相似文献   
87.
88.
摘 要 研究目的:从西方经济学的原理出发,通过对我国土地资源配置中市场失灵和政府失灵问题的分 析,寻求在市场和政府的双重作用机制下土地资源高效配置的实现途径。研究方法:文献资料分析法、比 较分析法。研究结果:在市场经济条件下,单纯地依靠市场或政府,不可能实现我国土地资源的优化配置, 必须将二者结合起来,以规划的宏观调控来弥补和矫正市场失灵的缺陷,但是当前的土地利用规划存在失 效的负面影响。研究结论:应该从加强土地利用规划的政府宏观调控与完善土地市场机制两个途径入手, 实现土地资源的高效配置。  相似文献   
89.
The exponential p-moment stability of stochastic impulsive differential equations is addressed. A new theorem to ensure the p-moment stability is established for the trivial solution of the stochastic impulsive differential system. As an application of the theorem proposed, the problem of controlling chaos of Lorenz system which is excited by parameter white-noise excitation is considered using impulsive control method. Finally, numerical simulation results are given to verify the feasibility of our approach. Supported by the National Natural Science Foundation of China (Grant No. 10772046)  相似文献   
90.
针对传统开关电源存在的控制芯片供电方式耗能较大、反馈电路光耦有效输入电流范围窄两个问题,对传统电源电路进行了改进,设计并实现了一款性能优良的48V转+5V、±15V,输出功率25W的三路输出反激式开关电源。样机输出电压精度为0.2%(+5V)、0.53%(+15V)、0.6%(-15V),输出电压纹波为20mV(+5V)、50mV(+15V)、60mV(-15V),电压精度和纹波率均满足小于1%的要求;测试表明:该电源性能优良,具有效率高,稳压精度高,负载调整率高等优点,有很高的生产应用价值。  相似文献   
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