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991.
大丝束聚丙烯腈基预氧丝炭化研究   总被引:1,自引:0,他引:1  
采用正交实验法研究了炭化温度、炭化时间、升温速率等因素对两种聚丙烯腈基预氧丝炭化产物结构和性能的影响.结果表明,进口东邦48 K大丝束聚丙烯腈基预氧丝环化程度优于国产吉林6 K小丝束聚丙烯腈基预氧丝,在炭化温度950℃,升温速率4℃/min,保温时间10 min条件下,炭化可取得最佳性能,炭化产物纤维拉伸强度达2.96 GPa,而国产吉林6 K小丝束在炭化温度1 100℃,升温速率4℃/min,保温时间5 min条件下炭化产物性能最佳,产物炭纤维拉伸强度近3.80 GPa.伴随两种预氧丝炭化过程,纤维颜色加深,表面缺陷减少,拉伸断裂模式均由假塑性向脆性过渡,为复合材料低成本开发中预氧丝坯体制备与炭化工艺提供了参考依据.  相似文献   
992.
用DSC研究了高T_e超导体B_(2-r)Pb_rSr_2Ca_2Cu_sO_v(x=0,0.2,0.4,0.6)从室温至600℃范围内的相变。在320℃和440℃附近有二个吸热蜂,每一个峰对应一个相变过程。440℃附近的相变是不可递的,其原子激活能为1.37eV,是由高T_e相向低T_e相的转变。而320℃附近的相变则与超结构的形成有关。  相似文献   
993.
介绍 4 0 0 kt/ a硫酸系统电除雾器总体结构及工艺设计参数 ,投入运行后 ,除雾效率低 ,介绍对存在问题的分析及解决过程 ,并介绍 2点成功经验  相似文献   
994.
A series of noncyclic acetal-linked cleavable surfactants were simply prepared by condensation of aldehydes with poly(ethylene glycol) monomethyl ethers. All of the products were characterized by1H nuclear magnetic resonance. Their hydrophile-lipophile balance, surface tension, cloud point, critical micelle concentration, and foam height were determined. Hydrolysis kinetic studies, followed by gas chromatography, showed that they had higher hydrolytic reactivity in acidic solution than cyclic acetal-linked cleavable surfactants.  相似文献   
995.
Isothermal storage of NO2 and subsequent reduction with different reducing agents (H2, CO or H2 + CO) in a lean NO x trap catalyst was tested by Temperature Programmed Desorption (TPD) and Temperature Programmed Reduction (TPR) experiments at temperatures representative of automotive “cold-start” conditions (<200 °C) using a commercial NO x trap catalyst. Results from the TPR experiments revealed that no reduction of stored NO2 to N2 was observed at 100–180 °C, and at 200 °C 10% reduction only of NO2 to N2 was measured. A special affinity of H2 to form NH3 was observed during the reduction of stored NO2. The formation of NH3 increases with increasing amount of stored NO2 and decreases with increasing storage temperature. Direct relation exists between the amount of adsorbed and/or stored NO2 and the formation of H2O and NH3.  相似文献   
996.
Rubber‐toughened polypropylene (PP)/org‐Montmorillonite (org‐MMT) nanocomposite with polyethylene octene (POE) copolymer were compounded in a twin‐screw extruder at 230°C and injection‐molded. The POE used had 25 wt % 1‐octene content and the weight fraction of POE in the blend was varied in the range of 0–20 wt %. X‐ray diffraction analysis (XRD) revealed that an intercalation org‐MMT silicate layer structure was formed in rubber‐toughened polypropylene nanocomposites (RTPPNC). Izod impact measurements indicated that the addition of POE led to a significant improvement in the impact strength of the RTPPNC, from 6.2 kJ/m2 in untoughened PP nanocomposites to 17.8 kJ/m2 in RTPPNC containing 20 wt % POE. This shows that the POE elastomer was very effective in converting brittle PP nanocomposites into tough nanocomposites. However, the Young's modulus, tensile strength, flexural modulus, and flexural strength of the blends decreased with respect to the PP nanocomposites, as the weight fraction of POE was increased to 20 wt %. Scanning electron microscopy (SEM) was used for the investigation of the phase morphology and rubber particles size. SEM study revealed a two‐phase morphology where POE, as droplets was dispersed finely and uniformly in the PP matrix. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3441–3450, 2006  相似文献   
997.
对目前甲醇吹除气中氢回收的两种方法进行了比较、分析。  相似文献   
998.
用5-硝基糠叉二醋酸酯与环己酮在60%H3PO4溶液中缩合制得标题物。反应混合物在100℃下搅拌反应5h得61%的2,6-双(5-硝基-2-糠叉)环己酮。分别经IR、1HNMR、MS、UV、TLC和元素分析进行了表征和鉴定。  相似文献   
999.
The high melting point of poly(1,4‐cyclohexanedicarboxylic anhydride) [poly(CHDA)] is a disadvantage, in that it is intractable in the melting process of a drug delivery system. This report relates to diols introduced into the polyanhydride main chain to decrease its melting point. Various poly(ester anhydride)s containing ethylene glycol, 1,3‐propanediol, 1,4‐butanediol, or 1,6‐hexandiol [poly(CHDA–XDO)] were synthesized by the esterification reaction and melt polycondensation. FTIR, DSC, WAXD, and intrinsic viscosity of polymers were recorded and hydrolytic degradation, as well as in vitro drug delivery, was conducted. The results show that the samples are stable in an anhydrous environment at room temperature and degrade in water following a surface erosion mechanism. The degradation period of poly(CHDA–XDO) ranged from 130 to 320 h as a result of the different diols and amounts of XDO introduced. The in vitro drug delivery gave 130–350 h of stable delivery along with the typical surface erosion mechanism. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2509–2514, 2002  相似文献   
1000.
Adults of a generalist herbivore, the lubber grasshopper,Romalea guttata, can be converted to functional specialists by feeding them exclusively on catnip,Nepeta cataria. No obvious adverse effects on adult development resulted from this enforced monophagy. Notwithstanding the fact thatR. guttata has had no coevolutionary relationship with this Eurasian mint, it readily sequesters compounds that are identical to or derived from the terpenoid lactones that are characteristic ofN. cataria. R. guttata appears to both biomagnify minor allelochemicals and to sequester metabolites of theNepeta terpenes in its paired defensive glands. The levels of autogenously produced phenolics are not affected by feeding onN. cataria and the defensive secretions of catnip-fed grasshoppers are more repellent to ants than those of wild-fed acridids. Metabolites of theN. cataria monoterpenes are sequestered in the defensive glands when catnip is added to the natural diet ofR. guttata. The ability of a generalist,R. guttata, to facilely bioaccumulate a potpourri of foreign allelochemicals when feeding in a specialist mode is analyzed in terms of its biochemical, physiological, and functional significance. Sequestration is examined as a response to the enteric effronteries represented by the phytochemicals that can be characteristic of the overload in a monophagous diet.  相似文献   
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