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Recent research findings show that under the circumstance of traumatic hemorrhagenic shock, in such viscera as liver, lung and small intestine, large numbers of polymorphonuclear neutrophil will congregate, sequestrate and even infiltrate, which result in tissue edema and inflammation. At the same time, due to the fact that PMN delays its apoptosis and can not be removed in time, secondary necrosis will occur and release great amount of toxic substances, such as absorbent oxygen and free radicals, which will amplify inflammation. All the above constitute the major cause of SIRS, MODS and MOF.

近来研究发现在创伤失血性休克的情况下,机体内各脏器普遍可观察到大量中性粒细胞的聚集、扣押甚至浸润,造成组织水肿,出现炎症反应,同时由于PMN凋亡延迟,不能及时被清除而发生继发性坏死,释放大量的活性氧、自由基等毒性产物使炎症反应进一步扩大,是创伤引发全身炎症反应综合征、多脏器功能不全甚至衰竭的主要途径。

However, when reaction time is fixed, this system can follow Lambert-Beer Law within visible spectrum. Furthermore, it can not be affected by temperature. Based on these findings, CTAB Turbidness Method, a quick method to determine hyaluronic acid contents in fermentation broth is established.

研究表明,随着反应时间延长,反应体系的吸光度逐渐升高,但当反应时间固定后,在可见光区反应体系能较好的遵循朗伯-彼尔定律,并且不受温度的影响。

The experimental results from cyclic voltammetry and constant-potential electrolysis show that the mechanism of the reaction was two molecules and three steps electrochemical process with eight-electrons transferred: anion radical arose in the first step; two-electrons were transferred in the second step and accompanied with coupling reaction of radicals and protonation and dehydrate, the main product was azoxybenzene; two-electrons were transferred in the third step, and azobenzene was achieved.

研究结果表明,硝基苯在铂电极上的电还原反应为双分子八电子三步骤电化学过程:第一步反应为准可逆单电子转移步骤,产生阴离子自由基;第二步为二电子转移步骤,并伴有随后的双分子不可逆自由基偶合反应和快速质子化及脱水反应,主要产物为氧化偶氮苯;第三步是二电子转移产生偶氮苯的过程。

RESULTS:In the Chenxiang Lubailu table,the identification of bismuthic salt positive result with dilute nitric acid instead of hydrochloric acid and the white precepitation formed in identification of magnesian was bismuth hydroxide sediments,it was easy and accurate to identify bismuthic salt by adding ascorbic acid.

结果:该片中的铋盐碘化钾鉴别反应,用稀硝酸代替盐酸做溶剂,呈正反应;镁盐氯化铵-磷酸氢二钠鉴别反应,加氨试液后,析出的白色沉淀不是Mg2,而是Bi3,该沉淀在氯化铵试液中不溶,干扰镁盐鉴别;铋盐含量测定项,用加抗坏血酸掩蔽剂的方法,排除Fe3+的干扰,使终点颜色稳定,易于准确判断。

The results of the experiment show that the main non-enzymatic browning reactions are Maillard and caramelization reaction, and VC or polyphenol does not play an important role in the color formation.

结果显示:美拉德反应和焦糖化是主要的非酶褐变反应,VC、多酚类物质对颜色形成不起主要的贡献作用;果糖和蔗糖在非酶褐变反应中起重要的作用,葡萄糖的作用几乎可忽略不计。

In this article, high DS and low viscosity carboxymethyl starch was prepared in aqueous media through the reaction between corn starch with acid treatment and etherifying agent, the effect of acid treatment time, liquor/material ratio, the amount of sodium hydroxide, the amount of monochloroacetic acid, etherification time, and reaction tempera.

以玉米淀粉为原料,采用酸化-醚化复合变性的方法在水相中制备高取代度低黏度羧甲基淀粉,探讨了酸化时间、液固比、NaOH用量、ClCH2COOH用量、醚化反应时间、反应温度对羧甲基化过程的影响,研究发现,对原淀粉进行酸化,可以在不增加其它反应试剂用量的基础上提高产物的取代度,但是酸化时间不应过长。

The compoud 1 can be converted to intramolecular coupled cyclic olefine (2) as a main product in the presence of iron catalyst.

控制反应条件,在铁催化下可以生成偶联烯烃化的环烯产物(2 )为主要产物;不加催化剂,加热回流反应得到分子内亲核取代反应产物环丙烷化合物 3

These results show that the ring expansion of cyclopropylsilylene C3H5SiH to silacyclobutene is easy to occur with a barrier of 113.4kJ/mol, while the 1,2-H shift is not competitive to the ring expansion for its much higher barrier.

结果表明,环丙基硅烯经过113.4kJ/mol的势垒扩环重排为硅杂环丁烯为自发反应;而其1,2-氢迁移重排反应热垒为190.0kJ/mol,是非自发反应,难于进行,不能与扩环重排相竞争。

In addition, some transformation reactions of imines were also examined.

而且在水相中,反应速率有较大程度提高,反应条件更加温和,一些在有机相中不能发生的反应在水相中也能顺利进行。

On the other hand, steam can be used to restrain the side reaction such as hydrogen transfer reaction so as to increase the yield of light olefins by diluting the concentration of the reactant. In addition, minor steam can react with the feed hydrocarbon resulting in the decrease of coke and the formation of active hydrogen without the increase of hydrogen gas and light saturates that is not desirable.

另一方面,水蒸气不仅仅具有降低烃分压的作用,抑制了氢转移反应等副反应,对于低碳烯烃的产率有好的影响,而且在反应过程中,少量参与了反应,与烃类发生了水煤气反应,生成了活泼氢,不仅降低了焦碳的产率,并且没有提高氢气、低碳烷烃等不希望得到的产物。

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