有反应

We define the ADR and the ADRcompensation in the theory research. The paper goes into detail about the ADR theory basis andthe responsibility constitution of other countries and provides the theory basis in order to make itclear why the victims should get the compensation and who should undertake the responsibility.(3)According to the analysis of the data statistical and the investigation, most reports come from themedical institutions while the reports from the production and operation enterprises are extremelyfew, only making up 1%. The speakers are mostly doctors. The serious ADR is about 2% andoccur at different ages. 50 -year-old middle-aged persons and old persons suffer from the ADReasily. In those reports, the ADR caused by using the one drug is about 90%; the ADR caused bythe anti-infection medicine ranks first due to using it wide in clinical medicine and applyingunreasonably. The intravenous injection easily causes the ADR.

对各国药品不良反应损害补偿的理论基础和责任构成进行阐述，为解决为什么要对药品不良反应受害者进行补偿、由谁承担责任提供了理论依据。3、我国药品不良反应现状研究方面，药品不良反应数据统计分析调查，发现报告主要来源于医疗机构，生产和经营企业报告数量极少，企业的报告数只占总数的1％，报告人都是以医生为主，严重不良反应发生的比例占药品不良反应报告总数的2％左右，不同年龄段都有药品不良反应发生，其中年龄大于50岁的中老年人发生的几率最大，在药品不良反应报告总数中，主要是使用一种药品的情形，占90％左右，抗感染药物占各类药物的首位，这与抗感染药物在临床广泛及不合理应用有关，静脉给药一直高居引起药品不良反应给药途径之首。

Reducing afterblowing and using the carburant with low nitrogen content are important measure. The kinetics of nitrogen removal from liquid steel under vacuum with reaction between carbon and oxygen was studied on the multi-function induction furnace. The following conclusions were obtained by experiments: The nitrogen removal was obtained by the nitrogen transfer through the liquid steel diffusion layer at 67Pa and 110Pa pressure, and by the gas-liquid surface chemical reaction at 2000P.

结果表明：真空度对脱氮机理有影响，67Pa～110Pa时脱氮为一级反应，2000Pa时脱氮为二级反应，1340Pa时为混合控制；即使在。1％的条件下，碳氧反应亦可显著提高脱氮速度常数促进深脱氮，在RH内通过加强碳氧反应来提高脱氮率理论上是可行的；当钢液内存在内生或外来固态粒子时，有利于钢液中CO及N〓气泡的形成及排除，这时气泡内p〓≈0，有可能使钢液中氮含量低干与系统真空度平衡的氮含量。

The region between the circular brown band generated by cell lipid exosmosis and the band of the wound in the non-transgenic cotton Z35's leaves, is wider than that of the transgenic cotton T-34's leaves, and no micro-HR was found in Z35, the intensity of leaves wilting is much serious, by contrast, micro BR was found around the wound region within the transgenic cotton leaves inoculated with the pathogen, but the micro-HR was not found in the transgenic cotton treated with water and around wound region of non-transgenic cotton Z35 leaves which showed that there was micro-HR defence in transgenic hpa1xoo cotton.

棉花黄萎病菌侵染叶片后，非转基因棉花叶部伤口周围细胞无微过敏性反应，受病原菌侵染的叶片萎蔫程度较重；转hpa1xoo基因棉花叶部伤口周围细胞有微过敏反应，叶部刺伤处仅有较小的坏死斑，且不相连，发病较轻，而清水处理的转基因棉花与非转基因棉花叶片中伤口周围均无微过敏反应，说明病原菌侵染诱导转hpa1xoo基因棉花产生微过敏防御反应，转hpa1xoo基因棉花较非转基因棉花有较强的抗病性。

The whole sintering process of SHS converter fettling materials can be divided into three steps. The first step is the decomposition reaction of carbonates and sodium nitrate, which is an endothermic reaction. The second step is the SHS reaction, i. e. thermite reaction, the metal of Al reacts with CO〓, O〓, NO〓, Fe〓O〓 to form Al〓O〓. The speed of thermite reaction is very quick, and accompanied with large amount of heat emission and temperature rise. The third step is the reaction of spinels formation. The Al〓O〓 produced by SHS reacts with MgO to form spinels.

整个SHS补炉料的烧结过程分三步进行：第一步为碳酸盐、硝酸钠的分解反应，属于吸热反应；第二步为SHS反应即铝热反应，金属铝粉与CO〓、O〓、NO〓、Fe〓O〓等反应生成Al〓O〓，反应速度很快，并伴随有巨大的放热和温度升高；第三步为合成尖晶石的反应，SHS反应产物Al〓O〓与MgO反应生成尖晶石。

In this study, the UV-spectra of AITC and its thioureas , and kinetic properties of piperidine, morpholine and diethyl amine reacted with AITC were investigated.

AITC与胺反应转化为硫脲后，最大吸收峰强度有了极大的提高，摩尔吸光系数增加了十余倍；利用我们的发现，我们以光度法研究了该反应的动力学，证明该反应为二级反应，并求得了反应速率常数和反应活化能等参数；同时，讨论了反应机理。

The results show that:First, concentration of hydrogen peroxide have the most obvious influence to oil yield and carbon black yield,with the increase of concentration of hydrogen peroxide the oil yield first increase then decrease,when concentration of hydrogen peroxide is 8.19% or so,the oil yield reach to the biggest value, and with the increase of concentration of hydrogen peroxide carbon black yield decrese;Then,reaction time have more obvious influence to oil yield and carbon black yield,oil yield increase but carbon black yield decrease with the increase of reaction time;Thirdly,reaction tempreture have some influence to oil yield and carbon black yield,samely,oil yield increase but carbon black yield decrease with the increase of reaction tempreture;Finally,reaction pressure does almost no influence on oil yield and carbon black yield.

研究结果表明：过氧化氢质量浓度对产油率和炭黑产率的影响最为显著，产油率随过氧化氢质量浓度的提高先提高后降低，在过氧化氢质量浓度为8.19%左右时达到最大值，炭黑产率随过氧化氢质量浓度的提高而降低；反应时间对产油率和炭黑产率的影响也比较显著，产油率随反应时间的增加而提高，炭黑产率随反应时间的增加而降低；反应温度对产油率和炭黑产率也有一定的影响，产油率随反应温度的提高而相应地提高，炭黑产率随反应温度的提高而降低；在本文实验范围内，反应压力对产油率和炭黑产率基本上没有影响。

A one-step method for the synthesis of aromatic indolizine derivatives byintramolecular 1,5-dipolar cyclization reaction of 2-(2-arylethenyl)pyridinium N-ylidesin the presence of an oxidant has been studied for the first time. In the presence ofelectron-deficient olefins, however, 2-(2-phenylethenyl)pyridinium N-ylides underwent1,3-dipolar cycloadditions and then aromatized in situ by TPCD to produce indolizinederivatives, indicating 1,3-dipolar cycloaddition proceed more readily than 1 ,5-dipolarcyclization in these conditions. Pyridinium disubstituted N-ylides, readily obtainedfrom corresponding pridinium and β-chlorovinyl ketone, underwent thermalintramolecular 1,5-dipolar cyclization to give indolizine derivatives easily.Indolizinecarbaldehyde derivatives were synthesized starting from 2-pyridinecarbaldehyde in four-steps involving 1,3-dipolar cycloaddition reaction.

本文首次研究了2-(2-芳基乙烯基)吡啶N-叶立德在氧化剂存在下的分子内1，5-偶极环化反应，采用一锅法合成了中氮茚衍生物；研究了这些N-叶立德的1，5-偶极环化和1，3-偶极环加成反应的选择性，发现当有缺电子烯烃存在时，优先进行1，3-偶极环加成反应，而不再发生分子内1，5-偶极环化反应；由β-氯乙烯酮方便地得到了烯丙基N-叶立德，他们在加热时进行分子内1，5-偶极环化反应而得到中氮茚衍生物；由2-吡啶甲醛为起始原料，通过1，3-偶极环加成反应等四步反应，得到了重要的中氮茚甲醛衍生物，这些反应都具有条件温和和操作简便的特点，是合成中氮茚衍生物的新方法。

From the potential energy profile, it can be predicted that, the dominant channel of this reaction consists of three steps: the two reactants first form a three-membered ring intermediate (INT1) through a barrier-free exothermic reaction of 19.2 kJ/mol; three-membered ring intermediate (INT1) isomerizes to a four-membered ring silylene(P2) via the transition state (TS2) with an energy barrier of 22.8 kJ/mol; four-membered ring silylene(P2) further reacts with ethene(R2) to form a silicic bis-heterocyclic compound (P3), which is also a barrier-free exothermic reaction of 132.2 kJ/mol.

用CCSD//MP2/6-31G*方法研究了单重态二甲基亚烷基硅烯与乙烯生成硅杂双环化合物环加成反应的机理，根据该反应的势能面可以预言，该反应的主反应通道有三步组成：第一步是两反应物（R1， R2）首先生成了一三元环中间体（INT1），它是一无势垒的放热反应，放出的能量为19.2 kJ/mol；第二步是三元环中间体(INT1)经过渡态TS2异构化为了四元环硅烯（P2），其势垒为22.8 kJ/mol；第三步是四元环硅烯（P2）进一步与乙烯(R2)反应生成了硅杂双环化合物（P3），该反应也是一无势垒的放热反应，放出的能量为132.2 kJ/mol。

The aniline HDN was strongly stressed by the presence of quinoline and DHQ and the HDN of quinoline proceeds exclusively via a pathway which involves fully saturated intermediates on the MCM-41-supported nickel phosphides. The HDN activity of nickel phosphide catalyst was dramatically reduced by the presence of H2S and DBT, probably due to the strong adsorption of H_2S and DBT on active sites which inhibited the adsorption of quinoline.

喹啉和DHQ对苯胺的HDN反应有强烈的抑制作用，喹啉在磷化镍催化剂上几乎全部通过完全加氢饱和路径进行反应。H_2S和二苯并噻吩强烈地吸附在磷化镍催化剂活性中心上，阻碍了反应物分子的吸附，从而对喹啉的HDN反应有强烈的抑制作用。

Two kinds of catalytic oxidations for naphthalene with Fenton reagent and POD catalyst were studied, and the results showed that there were some common points: Fe ion and OH radical all participated in two kinds of catalytic oxidations and α-naphthol was found.

通过Fenton试剂及POD催化H〓O〓与萘的反应过程分析，可以确定两种反应之间有一些相同点，它们是两种反应过程中均有Fe离子及·OH自由基参与，且反应过程中均有α萘酚生成。

With Death guitarist Schuldiner adopting vocal duties, the band made a major impact on the scene.

随着死亡的吉他手Schuldiner接受主唱的职务，乐队在现实中树立了重要的影响。

But he could still end up breakfasting on Swiss-government issue muesli because all six are accused of nicking around 45 million pounds they should have paid to FIFA.

不过他最后仍有可能沦为瑞士政府&议事餐桌&上的一道早餐，因为这所有六个人都被指控把本应支付给国际足联的大约4500万英镑骗了个精光。