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The results showed that the half of decay time of methyl parathion in Chinese cabbage was 2.91 days.

喷药后,在第零天、第一天、第二天、第三天、第五天、第七天分别取样,用气相色谱法分析测定甲基对硫磷在小白菜上的残留量,得出甲基对硫磷残留量与时间的关系。

The optimum pH value for enzymatic hydrolysis of methyl parathion was 8. 6~8. 8, the optimum temperature was 15℃.

甲基对硫磷水解酶水解甲基对硫磷的最适pH均为8.6~8.8,最佳反应温度为15℃。

Methyle β cyclodextrin was simply synthesized, and the impacts on the solubilization of methyl parathion and carbofuran were investigated.

摘 要:研究了甲基化β环糊精的一种简单制备方法及其对甲基对硫磷和呋喃丹的增溶作用。

Na〓 inhibited enzyme activity strongly. The kinetic parameters of Km and kcat against methyl parathion at 25℃ was 68. 6±5. 1μmol/L and 45 ±6 S〓 respectively.

Na〓对甲基对硫磷水解酶有较强的抑制作用。25℃时该酶对甲基对硫磷的米氏常数Km为68.6±5.1μmol/L,kcat为45±6 S〓。

With trimethyl,4-dodecylbenezyl ammonium chloride and 18-crown-6 as pase-transfer catalysts, the azidation of polyepichlorohydrin in poly and H2O were studied. The reaction discipline and mechanism were discussed. The results show that the system with trimethyl, 4-dodecylbenezyl ammonium chloride as phase transfer catalyst and PEG as medium is a safe and effective approach to glycidyl azide polymer preparation, and azidational ratio of PECH can reach 97% above within 15 h.

研究了氯化十二烷基苄基三甲基铵和18-冠-6为相转移催化剂时端羟基聚环氧氯丙烷在聚环氧乙烷和水为介质中的叠氮化反应,探讨了反应规律和反应机理,结果表明:以PECH为介质,十二烷基苄基三甲基氯化铵(TMDA-1)为相转移催化剂的反应体系,可在15h内使PECH叠氮化转化率达到97%以上,无主链断裂等副反应,是一条较为安全快速的制备叠氮粘合剂的方法。

Auto-immune type: also known as methyl-dopa-type, hemolytic disease can be medication from 3 months to 4 years later, on behalf of drug: a - methyl-dopa, levodopa, phenytoin, phenacetin, chlorpromazine, indomethacin, etc.

自身免疫型:又称甲基多巴型,溶血发病可在服药3个月至4年后,代表药物有:a--甲基多巴、左旋多巴、苯妥英钠、非那西丁、氯丙嗪、吲哚美辛等

Saturated Ag/AgCl. Furthermore, in situ UV-Vis spectra showed that the electrocopolymerization between m-toluidine and p-phenylenediamine was performed. The p-phenylenediamine might react with m-toluidine to yield more active intermediates, which not only promote polymerization but also accelerate polymerization. In addition, through that p-phenylenediamine could be incorporated into copolymer to make the copolymer have a phenazine or phenazine like cyclic structure, which was proved by the FTIR of polymers.

在恒电位电解的条件下,相应的原位紫外-可见光谱和聚合物的傅立叶变换红外光谱表明间甲基苯胺和对苯二胺能发生电化学共聚反应,由于对苯二胺可能与间甲基苯胺形成了具有较强反应活性的中间体,使得对苯二胺的加入不但促进和加速了聚合反应,而且还结合进聚合物中形成了phenazine或类似于phenazine的环结构。

Two kinds of dsDNA intercalating fluorescent dyes, [Ru2]2+(phen = 1,10-phenanlinthroline; dppz = dipyrido [3,2-a:2',3'-c] phenazine) and BOBO-3 2,2\'-1,3-propanediylbis[(dimethyliminio-3,1-propanediyl -1(4H)-pyridinyl-4-ylidenemethy-lidynebis[3-methyl]-benzothiazoe were employed in this chapter, and two non-covalent labeled fluorescence sensing systems for thrombin determination were successfully developed and compared based on its 29-mer aptamer.

本章利用dsDNA嵌入式荧光染料[Ru2]2+(phen = 1,10-二氮菲; dppz =吡啶[3,2-a:2',3'-c]吩嗪)及BOBO-32,2\'-1,3-丙二基二[(二甲基亚氨基-3,1-丙二基-1(4H)-吡啶基-4-(丙-1,3-二烯基二[3-甲基]-苯并噻唑),基于适配体29-mer,分别建立了两种凝血酶检测体系[Ru(phen2]2+及BOBO-3检测体系。

Solvent dosage is 10mL/ gram epichlorohydrin. The yield of 5-chloromethyl-2-oxazolidinone was more than 65.2%. 5-Chloromethyl-2-oxazolidinone and sodium phenolate were condensated to give 5-phenoxymethyl-2-oxazolidinone after taking off the sodium chloride in yield of 63.0%~78.0%. Dimethylsulfoxide was used as the solvent, and orthogonal experiment to the reaction condition had been carried out.

用5-氯甲基-2-噁唑烷酮和酚钠缩合,脱去氯化钠后生成5-芳氧甲基-2-噁唑烷酮类化合物,选用二甲亚砜为溶剂,对反应条件进行了正交实验,最佳条件为:反应温度120℃、反应时间20h、物料配比1:1,产率为63.0%~78.0%。

Spinodals of polystyrene/poly/poly(2,6 dimethyl 1,4 phenylene oxide) were simulated over a wide temperature range and the calculated resul...

将上述方法用于已知状态方程参数的三元均聚物共混物聚苯乙烯/聚甲基乙烯基醚/聚2,6-二甲基1,4-苯撑氧中,得到一系列不同温度下的spinodal相图,预测结果与文献报导吻合。在此基础上进一步研究了聚合物的分子量对体系相行为的影响。

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