查询词典 reaction

The intervention of chemotherapy could worsen the quality of life during the treatment of neo-adjuvant chemotherapy combined with surgery which may be attributed to the side reaction, but such adverse reaction may not affect actually the postoperative subjective feeling; On the other hand, the colorectal surgery may not decrease the quality of life although which could lead more early postoperative uncomforting.

MDT诊治模式下新辅助化疗联合手术综合治疗过程中，化疗干预手段会使生存质量降低，这可能与其副反应相关，但其不良反应可能并不会实际影响到术后患者的部分主观感受；而结直肠癌外科手术干预可能是造成患者术后近期内更多的不适感的主要原因，但并不会额外增加综合治疗后患者的生存质量负担。

On elementary theory of non-thermal plasma, the mechanism of VOCs destruction was decided: under the action of activated particles (such as high-energy electrons, ozone, radicals, etc) produced by discharge reaction, a series of physical and chemical reaction will take place, the result is that harmful VOCs is decomposed into unharmful substance.

根据电晕放电等离子体的基本理论，得出了等离子体处理VOCs的机制：在放电产生的活性粒子(如高能电子、臭氧、自由基等)的作用下，发生一系列的物理化学反应，使有害的VOCs转化成无害的物质。

The unimolecular decomposition and dehydrogenation of ethanol initiate the branched chain reaction, and the 3 isomers of radical C2H5O determine the direction of the reaction chain branching.

乙醇氧化经裂解反应、脱氢反应最终形成支链反应，乙氧基C2H5O的三种同分异构体在链分支中决定了链分支的进行方向。

Monomolecular reaction; unimolecular reaction

Re： qq280027真正求教关于单词的问题：单分子反应

Examining the reaction mechanism of Co Mo/TiO 2 catalyst and various factors effecting the said reaction,this paper showed that the new type catalyst is noted for its non presulfurizing process and excellent initial activity,unpossessed by traditional Co Mo/Al 2O 3 hydro conversion catalyst in the process of hydrodesulfurization.

讨论了新型Co┐Mo／TiO2加氢转化催化剂的反应机理和影响反应的诸因素，结果表明，新型催化剂与传统Co┐Mo／Al2O3加氢转化催化剂相比具有不预硫化和高初活性的特

Rational reaction condition is that ratio of the Cu(superscript 2+) schiff base complex of disproportionated rosin amine is 3%, urushiol concentration is 68.8 g/L, the system of reaction reacts 36 h at 30℃ in alcohol dissolvent.

结果表明，氧化聚合反应的理想条件是以乙醇为溶剂，加入3%歧化松香胺席夫碱－铜配合物催化剂，漆酚浓度为0.0688g/ml，在30℃下反应36h后，漆酚聚合物的沉淀得率为51.3%。

The effects of reaction temperature, space velocity, molar ratio of water to methanol, and reaction time on the performance of the micro reactor were investigated.

试验研究分析了反应温度、进料速度、水醇比（水和甲醇的物质的量的比）、反应时间对甲醇水蒸气重整制氢微型反应器性能的影响。

The results show that a little amount of heteropolymolybdovanadophosphate can remarkably speed the degradation, the best conditions of the oxidative degradation of chitosan with hydrogen peroxide catalized by heteropolymolybdovanadophosphate in homogeneous condition are as follows: the ratio of catalyst and chitosan is 1 to 10, concentration of hydrogen peroxide is 0.15%, the temperature is 80℃, reaction time is 2h. 0.2g chitosan was degraded under the best condition and the molecular weight by viscometry was degraded from 1460000 to 7812. then water-soluble chitosan was obtained by this method; The heterogeneous method is a high efficient way, the best condition of this method are as follows: the ratio of catalyst and chitosan is 2 to 100, the volume of 30% hydrogen peroxide is about 3mL, the temperature is 90℃, reaction time is 5min～30min.

研究结果表明，适量磷钼钒的存在可显著加速壳聚糖的降解，磷钼钒催化过氧化氢均相氧化降解壳聚糖的适宜反应条件是：催化剂与壳聚糖的质量比为1∶10、过氧化氢百分浓度为0.15％、反应温度为80℃、反应时间为2h，在此条件下对0.2g溶解在100 mL 0.5％稀醋酸中的壳聚糖进行降解，可使壳聚糖的粘均分子量由原来的146万下降到七千多(7812)，成为水溶性低分子量壳聚糖，从而达到应用的要求；在异相条件下以磷钼钒为催化剂催化过氧化氢氧化降解壳聚糖是一种高效快速的方法，此法降解壳聚糖的最佳反应条件是：催化剂与壳聚糖的质量比为2∶100；30％过氧化氢的用量为3mL左右；反应温度为90℃、反应时间为5min～30min。

Methoxystilbene and 2-methoxy-4'-nitrostilbene were synthesized from benzyl chloride and nitrobenzyl chloride by the Wittig reaction, and used as intermediates for the synthesis of the final product fluorescent whitener FP4,4'-bis(2-methoxystyrylbiphenyl via reduction and diazotisation of the latter followed by reaction with the former in the presence of NaOH.

以氯化苄和对硝基氯苄为原料，经Wittig反应合成中间体：2-甲氧基-二苯乙烯和2-甲氧基-4'-硝基-二苯乙烯。后者经还原反应、重氮化反应后，在氢氧化钠存在下与前者反应生成最终产品荧光增白剂FP4，4'-双-2-(甲氧基苯乙烯基联苯。为该类荧光增白剂的合成开辟了一条新路线

Started from D-tyrosine, we obtained the tetramic acid 96 using Jouin reaction. The assembly of the second fragment 109 was stared from 1,4-butandiol,using asymmetric alkylation reaction developed by Oppolzer as a key step. Coupling of the tetramic acid 96 with 109 provided the key intermediate 110 according to Yoshii\'s procedure. After remove protective group and Sharpless epoxidation, we obtained the key intermediate 113. Its macrocyclization to form the final product is in progress.

本论文的第二章主要对Macrocidin A开展了合成工作，我们从D构型的酪氨酸出发，经过官能团转换；利用Jouin反应生成Tetramic acid 96，另外一个片断从1，4-丁二醇开始经过多步反应生成碘化物104，利用Oppolzer发展的手性樟脑磺酰胺为辅基参与的不对称烷基化反应，引入手性甲基，生成关键中间体109，接着通过Yoshii发展的方法连接96和109生成110，经过Sharpless不对称环氧化反应建立环氧化合物，然后脱去保护基得到关环前体113，分子内的Mitsunobu反应进行关大环反应正在进行之中。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。