反应

Effects on the reaction of factors such as reactant ratio, reaction time, and reaction temperature were investigated, and optimum reaction conditions were determined as follows: mole ratio of cyanuric chloride to ethylamine to sodium hydroxide to sodium methyl mercaptide was 1:2.1:2.0:1.7, and the temperature and time of the first, second, and third substitution reactions were -2, 0, and 82℃ and 30, 60, and 180 min, respectively.

讨论了原料配比、反应时间和反应温度等因素对反应的影响，获得了较佳的反应条件。较佳反应条件为三聚氯氰：乙胺：氢氧化钠：甲硫醇钠＝l：2.1：2.0：1.7，第一、第二、第三取代反应的反应温度和反应时间分别为-2℃、0℃、82℃和30、60、180min。

Results show that 4-oxo-β-ionone is the major product with yield of 53.5% under the conditions as follows: reaction temperature 45℃, reaction time 24 h, the molar ratio of n: n(NaClO3): n 20: 100: 3, and pH value of solution in 1-3; on the other hand, 5,6-epoxy-β-ionone is major product with yield of 25.4% when reaction temperature is 40℃, reaction time is 24 h, the molar ratio of n: n(NaClO3): n is 20: 120: 5, and pH values of solution is 3. The excessive β-ionone can be recovered by vacuum distillation for reusing again. 4-oxo-β-ionone and 5,6-epoxy-3-ionone were purified by recrystallization and silica gel column chromatograph respectively with the purity over 98%.

研究结果表明：氯酸钠氧化β-紫罗兰酮的反应主要生成4-氧代－β-紫罗兰酮和5，6-环氧－β-紫罗兰酮，经重结晶和硅胶柱层析分离，纯度高于98%；4-氧代－β-紫罗兰酮的有利合成条件是反应温度为45℃，反应时间为24h，溶液的pH值为1~3，反应物配比n：n(NaClO3)：n为20：100：3，最佳收率为53.5%；5，6-环氧－β-紫罗兰酮有利的合成条件是反应温度为40℃，反应时间为24h，溶液的pH值为3，反应物配比n：n(NaClO3)：n为20：120：5，其收率为25.4%；未反应的β-紫罗兰酮经减压蒸馏回收后可重复使用。

A new general kinetic equation was derived in which the effect of the removal of condensation water was taken into account completely, and was applied to the polyesterification kinetic study of AA/HPHP and AA/NPG. It was found that the reaction order of self-catalyzed polyesterification was not constant. For these polyesterifications, the reaction order was 2.5 at a low temperature, while 3.0 at a high temperature.

考虑缩合水的排除对反应体系的影响，用体积浓度单位推导出一个新的聚酯反应总包动力学方程，并应用到AA/HPHP和AA/NPG两个聚酯化反应的动力学研究中，研究发现，自催化聚酯反应的反应级数并不是固定值，对于AA/HPHP和AA/NPG两个聚酯化反应而言，低温时反应级数为2.5，高温时反应级数为3.0。

We projected the possible reaction pathways of the isomeric reaction system for n-pentane, n-hexane and n-heptane according to the products which had been explored in the experiment and the Hydrogen Overfall Hypothesis put forward by ZhongCun YuShi and Teng YunanXun for the isomerization of n-paraffins.

根据实验检测到的产物以及由中村育世、藤元薰等人所提出的正构烷烃异构化的氢溢流机理，首先设计了正戊烷、正己烷、正庚烷异构反应体系可能反应通道。(1)正戊烷异构反应体系可能反应通道(2)正己烷异构反应体系可能反应通道(3)正庚烷异构反应体系可能反应通道

Master the Keto-Enol tautomerism; reactions of enols:α-H substitution reactions;α-halogenation of aldehydes and ketones;α-bromination of carboxylic acids; acidity ofα-H atoms: enolate ion formation; reactivity of enolate ions; alkylation of enolate ions; mechanism of carbonyl condensation reactions;condensations of aldehydes and ketones: the Aldol reaction; dehydration of Aldol products; the Claisen condensation reaction; the Michael addition.

熟练掌握酮式－烯醇式互变异构；烯醇的反应：α-H的活性；醛酮的α卤代反应；羧酸的α-溴代反应；α-H的酸性：烯醇负离子的形成；烯醇负离子的反应；烯醇负离子的烃基化；羰基化合物的缩合反应机理；醛酮的缩合反应－Aldol缩合；Aldol缩合产物的脱水反应； Cleisen 酯缩合反应；麦克尔加成反应。

Therefore esterification crosslinked reactionbetween polyearboxylic acid and wood can be quantitatively determined.According toexperiment results of stereoscopic configuration choices by crosslinking agents,crosslinkingreaction between model of reaction intermediate and wood,and the intermediate characteristic incrosslinking reaction,crosslinking reaction intermediate was proofed.We can infercrosslinking reactions between polycarboxylicacid and wood want through a mechanism of twosteps reaction process,the first cyclic anhydrides were formed as intermediates by dehydratingbetween hydroxyls in polycarboxylic acids,second esters were occurred by substitution reactionbetween wood hydroxyls and cyclic anhydrides.

从而可全面定量表征木材与多元羧酸类化合物的酯化交联反应；依据交联剂立体构型选择性、反应中间体模型物与木材的交联反应和交联反应中间体的波谱特征实验结果，证实了交联反应中间体，因此可以推测：多元羧酸类化合物与木材化学组分的交联反应是经历两步反应的机理，首先多元羧酸中相邻羧基的羟基之间脱水形成五元环酸酐中间体，然后木材的羟基与酸酐发生亲核取代反应形成酯。

The reaction kinetics of poly urethane formation and that of trimerization of isocyanate in a system of modified by urethane were studied by FTIR.

采用傅里叶快速红外光谱技术研究了氨酯改性聚异氰脲酸酯反应体系中氨酯、聚异氰脲酸酯生成的反应动力学，结果表明，在该反应体系中，氨酯反应和异氰酸酯的三聚反应是同步发生并同步进行的，其中三聚反应是一级反应；氨酯对异氰酸酯是一级反应，对聚醚二元醇为0级反应。

The reaction kinetics of polyurethane formation and that of trimerization of isocyanate in a system of polyisocyanurate modified by urethane were studied by FTIR. The results show that the two competing reactions occurred and progressed simultaneously, and the trimerization was found to be first order, and the polyurethane formation was first order with respect to the isocyanate concentration and zero order with respect to the polyol concentration.

采用傅里叶快速红外光谱技术研究了氨酯改性聚异氰脲酸酯反应体系中氨酯、聚异氰脲酸酯生成的反应动力学，结果表明，在该反应体系中，氨酯反应和异氰酸酯的三聚反应是同步发生并同步进行的，其中三聚反应是一级反应；氨酯对异氰酸酯是一级反应，对聚醚二元醇为0级反应。

And therefore it has the potential applications in green chemistry and chemical process,organic reactions areas.The literature review section of the thesis gave a brief introduction of the important applications in the green chemical process as well as the status of organic reactions research in NCW,and also summarized the applications in different kind of reactions such as hydrolysis,dehydration/hydration,alkylation,acylation, Diels-Alder reactions,rearrangements,condensations,hydrogen isotope exchange reaction,oxidation-reduction reaction,organometallic reactions.

论文的综述部分简要介绍了近临界水在绿色化工过程中的重要应用价值和国内外在近临界水中进行有机化学反应的研究现状，以及以近临界水作为反应溶剂或催化剂在水解反应、脱水/水合反应、烷基化、酰基化、Diels-Alder反应、重排反应、缩合、氢同位素交换反应、氧化还原反应、有机金属反应等反应类型中的应用。

By esterification, saponification, doubledecomposition and formulation, liquid rare earth of monoisooctyl phthalate complex heat stabilizer was prepared with phthalic anhydride, isooctyl alcohol, sodium hydrate, rare earth chloride, mixed solvent and other reagents. The optimum conditions are: the temperature of esterfication is 130～140℃,and the reaction time is 1h. The temperature and time of saponification is 60℃ and 10min respectively. The temperature of double decomposition is 60～70℃,and the reaction ti...

摘 要：以邻苯二甲酸酐、异辛醇、氢氧化钠、氯化稀土、混合溶剂、助剂为原料，通过酯化反应、皂化反应、复分解反应以及复配制备了以邻苯二甲酸单异辛酯稀土为主要成分的液态稀土复合热稳定剂，其工艺条件为：酯化反应的温度控制在 130～ 14 0℃，反应时间为 1h ；皂化反应的温度为 6 0℃，反应时间为 5min ；复分解反应的温度在 6 0～ 70℃，反应时间为 1h ；水洗温度控制在 6 0～ 6 5℃；混合溶剂的用量为 5 0 %，稀土含量为 6 0 3%；在复配过程中，采用亚磷酸酯作为辅助热稳定剂，其用量为 5 %～ 7%，PVC中加入 2 %的这种稀土复合热稳定剂，在185℃下，其热稳定时间为 4 5min。

Objective To investigate the effects of interleukin-1 β converting enzyme gene on the biologic characteristics of ovarian cancer cells.

目的 探讨白细胞介素-1 β转换酶的表达，对卵巢癌细胞生物学特性的影响。

Campylobacter: This illness is the most commonly identified cause of diarrheal illness in the world.

弯曲：这种病是最常见的原因查明腹泻病，在世界上。