176 resultados para 1,15-C30 Diol
Resumo:
本工作用DSC方法对三种不同支化度的茂金属短链支化聚乙烯的等温、非等温结晶行为进行了研究 .样品为乙烯和己烯 1的共聚物 ,短支链主要为正丁基 ,分子量Mw =2 0 ,0 0 0 ,Mw/Mn<1 15 ,支化度 (每10 0 0C中CH3 数目 )分别为 1 6、10 4、40 .实验结果表明 ,茂金属短链支化聚乙烯结晶方式Ⅰ Ⅱ转变温度随支化度增加而降低 ,分别为 119 8℃、115 9℃、113 3℃ ;同时支链的存在降低了二次成核速率 ,增大了方式Ⅰ的结晶范围 ,总的结晶速度随支化度增大而减小
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对苯酚类化合物结构与活性ID50进行了三维构效关系研究 ,取得了满意的结果。其中ID50为引起半数梨形化合物四膜虫生长受到抑制所需的苯酚类化合物的浓度。
Resumo:
Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to examine the morphology of blends of PA1010 and polypropylene (PP) compatibilized with polypropylene grafted with glycidyl methacrylate (PP-g-GMA). It is found that the morphologies are dependent on the content of glycidyl methacrylate in PP-g-GMA and the mixing time. The size of the dispersed PP particles decreases as the content of GMA in the PP-g-GMA increases for binary blends of PA1010 and PP-g-GMA. Similar results are obtained for changing the mixing time. Ternary blends of PA1010, PP, and PP-g-GMA indicate that morphologies depend on the content of glycidyl metyacrylate in the PP-g-GMA and the miscibility of PP and PP-g-GMA. By changing the content of GMA in PP-g-GMA, it was possible to introduce significant changes of morphology. A matrix removal TEM method is used to investigate the interfacial structure of PA1010/PP blends containing PP-g-GMA as a compatibilizer. This technique shows the reaction product between PA1010 and PP-g-GMA to be located at interface as a surrounding layer around domain particles. SEM observation on the interface shows that the adhesion between PA1010 and pure PP is very weak and their interface boundary is sharp. For the samples of PA1010 and PP-g-GMA, it was found that the interface was not so obvious, and the reaction between PA1010 and PP-g-GMA strengthens the interface significantly. (C) 1997 Elsevier Science Ltd.
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Phenol hydroxylation catalyzed by iron(II)-1,10-phenanthroline is investigated through kinetics, ESR, W-Vis as well as cyclic voltammogram studies. The optimum reaction conditions are obtained for diphenols production. Radical substitution mechanism is first proposed to explain the effects of pH, reaction medium and other factors on the phenol hydroxylation with H2O2 as oxidant, and found that the coexisting of iron(II)-1,10-phenanthroline and iron(III)-1,10-phenanthroline is the key for phenol hydroxylation to occur with H2O2 as oxygen donor.
Resumo:
利用CO2-TPD方法考察了Ti-La-Li系多元氧化物催化剂的表面碱性,实验发现:C2 选择性与表面碱强度呈顺变关系,而CH4 转化率与CO2 的脱附峰面积呈顺变关系.同时,利用XPS,O2-TPD等方法对该体系催化剂的表面活性氧种进行了表征与研究,结果表明:催化剂的表面晶格氧与C2 选择性有关,表面吸附氧与甲烷转化(包括偶联和深度氧化)有关.O2 -TPD实验发现催化剂的表面存在三种氧:α( 100℃≤t≤450℃),β(450℃
Resumo:
In the structure of 4,10,16,22-tetraamino-6,12,18,24-tetramethyl-5,11,1 7,23-tetraaza-1,7,13,19-tetraazoniapentacyclo[19.3.1. 1(3,7).1(9,13).1(15,19)]octacosa-1(25),3,5,- 7(26),9,11,13(27),15,17,19(28),21,23-dodecaene dichloride dihydroxide octahydrate, C
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The crystal structures and Mossbauer spectra of various mixed oxides LaFe1-xMnxO3 and LaFe1-xCoxO3 (x = 0 to 0.9) are determined and measured at room temperature. The results indicate that the crystal structure of both the La-Fe-Mn-O and the La-Fe-Co-O sy
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本文用R_2O_3(R=Y,Gd,La),V_2O_6,Nb_2O_5和高温固相反应法合成了复合钒铌酸盐RVMb_2O_3,并以此为基质研究了Eu~(3+)和Dy~(3+)在其中的光谱性质.实验表明,Eu~(3+)在这三个化合物中均处于偏离反演对称中心的格位上,Eu~(3+)的荧光强度的红/横比(R/O)和Dy~(3+)的黄/蓝比(Y/B)均随R~(3+)的电荷半径比的减小而下降.同时还研究了Bi~(3+)和温度对Dy~(3+)的发射强度的影响.
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本文研究了神经递质多巴胺(DA)在AQ聚合物薄膜修饰组合微盘电极上的电化学行为。结果表明,在pH7.0的磷酸缓冲溶液中,修饰组合微盘电极经电化学处理后,DA的氧化还原峰电位差较小(约为80mV),氧化峰、还原峰的峰形比较对称。在选定条件下,DA的伏安溶出峰电流与浓度在1.0×10~(-6)~8.0×10~(-6)mol/L范围内呈线性关系。厚的AQ膜修饰组合微电极可基本上消除抗坏血酸的干扰。利用AQ膜修饰的微盘电极测定DA和肾上腺素(E)在膜中的扩散系数,分别为4.1X10~(-8)cm~2/s和2.4×10~(-8)cm~2/s。
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应用GC-MS、PGC-MS、ESR和IR等分析方法测定了α-蒎烯等离子体聚合过程中气相产物的组成及其聚合物结构。根据分析结果,提出a-蒎烯等离子体聚合机理是自由基聚合反应机理。
Resumo:
The structure of quenched isotactic polypropylene (iPP) films, including samples etched with fuming nitric acid (FNA), has been studied by infrared (IR) spectra, wide-angle x-ray diffraction (WAXD), small-angle x-ray scattering (SAXS), and differential scanning calorimetry (DSC) measurements. The changes of IR, SAXS, DSC, and WAXD results induced by annealing for etched samples have been compared with those for unetched ones. The IR absorbance spectrum of the quenched iPP etched by FNA did not change. In addition, the SAXS intensity did not increase when these samples were annealed, indicating that the total (IR) crystallinity (i.e., the content of chain segments in the helical conformations) of the etched samples does not increase. However, WAXD patterns of the samples changed in a manner similar to those of the unetched one, from the original two blurred diffraction peaks to the sharp crystal patterns of alpha-form iPP, suggesting that the mesomorphic (or liquid crystal-like) phase has reorganized to alpha-form crystals. It is concluded that the change of WAXD of quenched iPP films during annealing results mainly from transformation of order in the mesomorphic phase, rather than only from an increase of crystal size. In other words, mesomorphic-form iPP is not constituted by any known crystals (such as alpha or beta crystals) in small sizes; its WAXD pattern reflects truly the degree of order in the mesomorphic phase.
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Dysprosium and ytterbium monophosphides have been prepared by the solid state reaction. The optical and electrical properties have been studied. Evidence that DyP and YbP are semiconductors has been obtained from the study of the absorption spectrum, the negative temperature coefficient of resistance and the rectifying effect. Their energy gaps are determined as 1.15 eV for DyP and 1.30 eV for YbP, electric conduction type is n-type, resistivities are about 10(-2) ohm cm and Hall mobility is 8.5-80 cm2/Vs. The p-n junction is formed on the LnP/Si.
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本文利用FTIR、固体高分辨~(13)C-NMR、共振拉曼光谱及紫外-可见光谱等手段,研究了聚苯胺掺杂前后的结构变化,指出质子酸的掺杂使聚苯胺中的醌亚胺单元和苯二胺单元发生部分的氧化还原反应,生成了具有一定电荷分布的共轭体系。
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Three members of the tetraspanin/TM4SF superfamily were cloned from Chinese shrimp, Fenneropenaeus chinensis. The deduced amino acid sequences of the three proteins have typical motifs of the tetraspanin/TM4SF superfamily. Phylogenetic analysis of the proteins, together with the known tetraspanins of invertebrates and vertebrates, revealed that they belong to different tetraspanin subfamilies: CD9, CD63 and tetraspanin-3. The three cloned genes of CD9, CD63 and tetraspanin-3 showed apparently different tissue distributions. The CD9 gene (FcCD9) was specifically expressed in the hepatopancreas. While for the CD63 gene (FcCD63), the highest expression was detected in nerves, epidermis and heart, with low expression in haemocytes, ovary, gill, hepatopancreas and stomach and no expression in intestine, muscle and lymphoid organ. Compared with FcCD9 and FcCD63, the tetraspanin-3 gene (FcTetraspanin-3) was more broadly expressed and its highest expression was detected in the intestine. Its expression in nerves was lower than in the intestine, but was higher than in other tissues. Expression in haemocytes, ovary and muscle was much lower than in other tissues. The expression profiles of FcCD9, FcCD63 and FcTetraspanin-3 in different tissues, including haemocytes, lymphoid organ and hepatopancreas, were compared by real-time PCR when shrimp were challenged by live white spot syndrome virus (WSSV) and heat-inactivated WSSV. All three tetraspanins were markedly up-regulated in the live WSSV-challenged shrimp tissues. The data suggested that the three cloned members of TM4SF superfamily in Chinese shrimp may play a key role in the route of WSSV infection.
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Superoxide dismutase (SOD; EC 1.15.1.1) is an enzyme that protects against oxidative stress from superoxide radicals in living cells. This enzyme had been isolated, purified and partially characterized from muscle tissue of the shrimp Macrobrachium nipponense. The purification was achieved by heat treatment, ammonium sulfate fractionated precipitation and column chromatograph on DEAE-cellulose 32. Some physiological and biochemical characterization of it was tested. The molecular weight of it was about 21.7 kDa, as judged by SDS-polyacrylamide gel electrophoresis. The purified enzyme had an absorption peak of 278 nm in ultraviolet region, and the enzyme remained stable at 25-45 degreesC within 90 min. However, it was rapidly inactivated at higher temperature. Treatment of the enzyme with 1 mM ZnCl2, SDS and 1 mM or 10 mM mercaptoethanol showed some increasing activity. However, the enzyme activity was obviously inhibited by 10 mM CaCl2, CuSO4, ZnCl2 and 1 mM CaCl2 and 10 mM K2Cr2O7. SOD activity did not show significantly variation after incubated with 1 mM CaCl2, EDTA and 10 MM SDS. The enzyme was insensitive to cyanide and contained 1.03 +/- 0.14 atoms of manganese per subunit shown in atomic absorption spectroscopy, which revealed that purified SOD was Mn superoxide dismutase. (C) 2004 Elsevier B.V. All rights reserved.