本文讨论了卤间化合物的形成规律及其反应活性。
This paper discussed the forming rules and their reaction activities of interhalogen compounds.
烯烃的双键：重点是反应活性。
这些原子有较高的反应活性。
酸催化比碱催化具有更高的反应活性。
Activity of acid catalyst was higher than that of base catalyst.
同时提供了提高磷矿反应活性的一些措施。
And some measures to improve reaction activity of phosphate rock is offered.
结果表明，改性体系的固化反应活性略有降低；
The results showed that the curing activity was slowly depressed.
而且和苯环衍生的硫恶唑啉相比反应活性相对较高。
In addition, these ligands showed higher activity than thioether deveritives of phenyl oxazolines.
实验研究了石油焦气化反应活性和孔比表面积的关系。
The relationship of gasification reactivity and pore specific surface area of petroleum coke is studied.
考察了碱金属碳酸盐类助剂和溶剂对反应活性的影响。
Moreover, the effects of alkali metal carbonate promoters and the solvents were investigated at the same time.
麦草碱木素在碱催化下经脱甲基改性可提高其反应活性。
The reactivity of wheat straw soda lignin(WSSL) can be improved by demethylation modification.
结果表明，随着非质子溶剂极性的增大，反应活性增加。
The results show that the activity increases with the rise of polarity of nonprotic solvent.
芳环的存在可以增加与其相连的仲碳和叔碳的反应活性。
The reactivity of tertiary and secondary C connected to the arene ring was increased obviously.
结论液化后芦竹组分与苯酚发生化学反应，反应活性增强。
Conclusion After liquefaction the giant reed composition happened chemical reaction with phenol and the reaction activity was enhanced.
根据晶种理论和水化物脱水相的反应活性分析了熟料烧成机理。
The clinker burning mechanism according to the crystal seeds theory and the activity of the dehydrated phase are analysed.
结果表明，FS存在结构羟基，其中一些羟基具有化学反应活性。
The results showed that structural hydroxyls existed on FS and some of those were active.
在溶胀煤的液化反应中，极性溶胀溶剂明显提高了煤的反应活性。
In the liquefying reaction of swollen coal, polar solvent enhanced the reaction activity.
研究了DCPD酚环氧树脂与酸酐及胺类固化剂的固化反应活性。
It was studied on the curing activity of DCPD phenol epoxy resin with anhydrides and amines.
用溶胶-凝胶法制备的纳米氧化镍具有较好的乙烷氧化脱氢低温反应活性。
Nano size nickel oxide prepared by sol-gel method has better ethane oxidative dehydrogenation activity at lower temperature than by other methods.
在同样的反应条件下，高碳数烯烃的反应活性要高于低碳数烯烃的反应活性。
It was also found that the big molecule olefins were more reactive than the low carbon olefins under same operating conditions.
结果表明，纯化产物的纯度可达95 %以上，并具有良好的免疫学反应活性。
The result showed that purification rate of the purified product was higher than 95%, and it had immunological reactive activity.
H2O2也是具有高度反应活性的羟基游离基的前体，并参与降解过程。收藏。
The H2O2 also is a precursor of the highly reactive hydroxyl radical, which participates in wood degradation.
发现不同的底物结构上的差异可能造成选择性脱除乙酰基保护反应活性的差异。
Furthermore, the reaction condition of the selective removal of acetyl group in the presence of caffeoyl group was optimized.
同时还考查了催化剂组成、激光功率及熔炼时间与丙烯歧化反应活性之间的关系。
Then it discusses the relations of catalytic activity with composition of the catalyst, laser power and melting time.
气化化学反应活性较强的煤，气化反应温度相对较低，其正常炉出煤气温度也相应较低。
If the chemical reactivity of coal is strong, the gasification reaction temperature will be relatively low and the gas outlet temperatures will also be lower.
磷矿中碳酸盐的含量及在磷矿晶体中的存在状况对磷矿的酸解反应活性有着较大的影响。
The content of carbonate and its presence status in phosphate ore have large effect on acid decomposition activity of phosphate ore.
发生炉正常炉出煤气温度与气化用煤的化学反应活性和气化用煤的挥发分及水分含量相关。
The normal gas outlet temperature of coal gasifier is related to chemical reactivity, volatile matter and moisture content of gasification coal.
采用共沉淀法在多种条件下分别制备氧化铁及其负载金催化剂，测定其水煤气变换反应活性。
Both iron oxide and its supported gold catalyst for water-gas shift reaction were prepared under various conditions through co-precipitation method.
反应活性与室温下的氧相似。在常温常压下NF 3是相对不活泼的，显示出很低的反应活性。
Reactivity is similar to that of oxygen at room temperature. NF3 is relatively inert at ambient temperature and pressure conditions and exhibits little, if any, reactivity.
在人工双层膜囊泡表面，构建了一个通过人工受体的分子识别行为控制酶反应活性的超分子体系。
Functionalized lipid bilayer vesicles on which molecular recognition by an artificial receptor synchronized with catalytic reaction by an enzyme were prepared in aqueous media.
在人工双层膜囊泡表面，构建了一个通过人工受体的分子识别行为控制酶反应活性的超分子体系。
Functionalized lipid bilayer vesicles on which molecular recognition by an artificial receptor synchronized with catalytic reaction by an enzyme were prepared in aqueous media.
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