主要产物

The reaction of benzoic acid and ethylenediamine was studied under different conditions.

在不同条件下考察了苯甲酸与乙二胺的反应，对反应产物、主要副产物及反应中间体进行了分离和鉴定，通过熔点测定、元素分析和红外光谱分析，确定了产物为2-苯基咪唑啉，主要副产物为二苯甲酰乙二胺，中间体之一为乙二胺与苯甲酸形成的双盐。

The Dabie Mountains are unique among ultrahigh pressure metamorphic terranes in having the most profound post collisional plutonism The Mesozoic shoshonitic and calc alkaline intrusive rocks can be divided into three groups with different isotopic ages, rock assemblages and chemical features Group I consists of late Triassic (~ 210 Ma) mafic monzodiorites It could have been generated by partial melting of enriched subcontinental lithosphere mantle due to slab breakoff Group II consists ma...

第 I组，主要由晚三叠世（约210 Ma）二长闪长岩辉长岩体组成，它可能是在板片断离过程中富集的大陆岩石圈地幔部分熔融的产物；第I I组，由中侏罗世－早白垩世（160～120 Ma）的角闪石英二长岩、黑云母二长花岗岩和正长花岗岩组成，主要是由幔源岩浆的分离结晶与地壳混染共同作用的产物；第II I组，以白垩纪（125～95 Ma）的花岗岩和花岗斑岩为代表，是在热穹窿作用过程中大别杂岩深熔作用和高度演化的产物。

The contents are mainly divided into three parts: The first part describes mechanism and metabolism rule of natural products and its classification ; The second part is about the growth and development of plants and their mutual relationship, natural biological active substances which are produced in the course of defending plant diseases and insect damages. The third part is not only the function and principle of medicine, anticancer and antioxygen activity of different kinds of natural products such as resin ,essential oil, high molecule, grease and so on but also their application. The fourth is security problem of Plant Natural Products. Through the lessons, we can correctly understand and use the relationship between plants and environment.

其课程分为13章，内容主要分为4大部分，一是阐述植物天然产物的发生机理和代谢规律，介绍相关主要植物种类，并对天然产物进行化学分类；二是讲述植物天然产物和自身生长发育之间的关系、天然产物如何影响植物之间的相互关系、以及植物如何利用天然生物活性物质抵御病虫害的威胁；三是详细描述了各种天然产物，如植物自身生长发育过程中所产生的活性物质、植物与其它生物之间的相互关系中所产生的生物活性物质、植物毒性物质、植物药理活性物质、植物抗生物质、植物树脂、植物精油、植物高分子、植物油脂、植物抗氧化活性成分等，并阐述它们的药理活性、抗癌性、抗氧化性等对人类健康起作用的的功能和原理；四是提出了植物天然产物的安全性问题，并介绍相关案例和介绍相关法规；在此基础上还专门讲述了树脂、精油、高分子、以及油脂类等天然产物的应用。

Or FR4 PCB, bromide exsited mainly in pyrolysis gas and gas products mainly consisted of CO, CO2, propylene, 2-methacrylate, bromomethane, and a small amount of acetone, C1-C3 halogenation alkyls. The pyrolysis gas could be reclaimed as fules after debromide treatment. Pyrolysis liquid products consisted of 8.333% water and 91.667% oil component.

R4板中溴元素主要存在于气体产物中，气体产物主要为CO、CO2、丙烯、2-甲基丙烯、溴甲烷以及其他小分子烯烷烃产物，气体产物可通过除溴无害化处理作可燃气回收；液体产物中含有8.333%的水和油质成分。

To the product yield is mainly studied in the brominating process, and the best synthesizing process conditions is obtained; the effect of the selection, quantity of the solvent, the reaction temperature, reaction time, and the catalyzer to the product yield is researched in the process of ketalization and the relative preferable process conditions has been got.

在脱溴反应中，主要研究了溶剂的用量、溶剂配比、物料配比、反应时间和反应温度等对目标产物得率的影响；在选择性溴化反应中，主要研究了溶剂和溴化剂的选择、物料配比、溶剂的用量等参数对产物质量和得率的影响，最终得到了合成的最佳工艺条件；在缩酮化反应中，主要研究了溶剂的选择、溶剂的用量、反应温度、反应时间和催化剂的选择等参数对产物得率的影响，并得到合成的较佳工艺条件。

The hydrolysates from oat xylan using Xyn Ⅰ Xyn Ⅱ and their mixture for hydrolysis were analysed by HPLC. It was showed that Xyn Ⅰ hydrolyzed mainly the unsubstituted regions of oat xylan, and hydrolytes were high xylooligosaccharides; whereas Xyn Ⅱ exhibited greater catalytic versatility than Xyn Ⅰ and were able to attack substituted regions of the polysaccharide and showed greater activity to low xylooligosaccharides than Xyn Ⅰ to give xylobiose as the main hydrolysate. The purified xylanases were acidic enzymes.

以纯化酶组分及其混合物水解燕麦木聚糖，采用高效液相色谱分析相应的水解产物，结果表明，Xyn Ⅰ降解燕麦木聚糖时，主要降解作用发生在底物中没有取代基的区域，水解产物的聚合度较高；Xyn Ⅱ对底物具有更强的适应性，能降解底物中有取代基的区域，相对Xyn Ⅰ酶组分，Xyn Ⅱ酶组分对低聚合度的木聚糖的活性更高，木二糖为主要降解产物。

Research on thermodynamics and kinetics of pyrolysis reaction mechanism Kinetic and thermodynaimic research of the pyrolysis reaction mechanism of toluene was conducted at different temperature range 298-1223K. The result shows that the pyrolysis reaction firstly occurs at the methyl on the benzene ring, and produces benzyl.

裂解机理的热力学与动力学研究在298K-1223K的温度范围内对甲苯热解机理的热力学和动力学研究结果表明，热解首先发生在苯环甲基C-H键上并生成卞基自由基，主要产物为联二甲苯，反应的活化能ΔE〓=402.27kJ/mol。

In this work, nanostructure samples of La1-xCaxMnO3（x=0.2、0.3、0.4、0.5）were prepared by hydrothermal-precipitation method . The structural characterization of the powder samples were done by X-ray diffraction. XRD patterns showed that all the samples ate single perovskite-type phase withoutother impurity or secondary phase. The shape and size of samples were performed on Scanning Electron Microscopy. SEM photographs investigated that temperature of hydrothermal effects the phase of samples and alkalinity of the reaction mixture by ΔTad-T curve measurement device at low magnetic fielded

本论文采用水热共沉淀退火法制备了La1-xCaxMnO3（x=0.2、0.3、0.4、0.5）系纳米结构，用X射线衍射仪确定产物为单相钙钛矿结构，无任何杂峰及第二相；用扫描电子显微镜与透射电子显微镜分析了产物的大小和形貌，发现水热温度对产物的形成起决定作用，随着温度的升高，产物由薄膜状向丝状转变，而溶液的碱度可控制产物的形貌和大小，当碱度为6.35mol/L，水热温度为240 C时，La0.6Ca0.4MnO3的主要形貌为纳米丝并有少量纳米颗粒，纳米丝平均直径为40nm；最后测量了粉末样品在低磁场（1.4T）下的磁热效应，发现水热共沉淀退火法制备样品的最大绝热温度明显高于球磨法制备样品的最大绝热温变。

Therefore, pDCs accumulated in spleens from HIV patients with high proviral loads, but they did not seem to be the main IFN- producers.

因此，浆细胞样树突状细胞在高前病毒载量的HIV阳性患者的脾脏内聚集，但并没有IFN等主要产物。

XRD and EDS analysis indicate that at static condition, the composition of the scale is CO3, while the scale changes to CO3 at dynamic conditions. The increment in flow rate increased the thickness of the scale remarkably, but had little influence on the hardness and Young's modulus of the scale. The fracture toughness of the scale exhibited the lowest value at the flow rate of 0.5 m/s whereas the adhesion strength increased with increasing the flow rate.

结果表明，静态条件下形成的腐蚀产物膜的主要成分为CO3，动态条件下的主要成分为CO3；介质的流动能够促进腐蚀产物膜的形成，但对膜的硬度以及杨氏模量影响不大；腐蚀产物膜的断裂韧性随着流速的增大先下降后上升，流动状态下内层腐蚀产物膜的致密性较好，膜与基体的结合强度较高。

If you are unfortunate enough to the lovelorn, please tell me, I will help you out, really, please contact me!

如果你不幸失恋了，请告诉我，我会帮助你摆脱困境，真的，请联系我啦！

China's plan to cut energy intensity by 20 percent and pollutant discharges by 10 percent between 2006 and 2010 is a case in point.

中国计划在2006年到2010间降低20%的能源强度和减少10%的主要污染物排放，就是一个这样的例子。