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4The obtained solid alkali catalyst was applied to biodiesel preparation with colza oil and used oil as materials respectively and the technics was optimized by sigle-factor and orthogoral experiments with esterification rate as the index. The optimal technique conditions using colza oil were: the amount of solid catalyst 12%, the mol ratio of methanol to oil 9:1, reaction temperature 65℃, reaction time 3h, under which the esterification rate reached to 94.48%.

4以菜籽油和煎炸废油为原料,利用固体碱催化剂催化制备生物柴油,以转化率为考察指标,采用单因素和正交试验对工艺进行优化,得到以菜籽油为原料时制备的最佳工艺参数为固体催化剂投入量2.5%,醇油摩尔比9∶1,反应温度65℃,反应时间3h,转化率达到93.9%;以煎炸废油为原料时最佳工艺参数为反应温度65℃,反应时间3h,固体催化剂投入量4%,醇油摩尔比6∶1,转化率达到91.2%。

The effects of different factors on the laser-induced graft polymerization on the PET surface were analyzed, and the mechanisms were discussed. The factors were: 1 Monomers with smaller molecules resulted in better modification than polymeric monomers. Acrylamide monomer was chosen as hydrophilic modifier finally; 2 Higher concentration of the monomer solution favored the graft reaction; 3 With the increasing laser fluence, the surface hydrophilicity of PET films increased at first, then decreased. More laser pulses led to a more hydrophilic surface; 4 Benzophenone as a photosensitizer hindered the graft polymerization; 5 The homopolymer retardant of ammonium iron sulfate hexahydrate in a proper concentration retarded the formation of homopolymers and promotes the graft copolymerization; 6 The solvent of monomer solution also affected the graft reaction. Different solvents functioned in different ways. Ethanol can promote the graft reaction because of the activity of hydrogen in its structure; 7 pH value of the monomer solution affects the polymerization rate, and a lower pH value was favorable to the graft reaction.

这些影响因素的作用分别为:1小分子单体的表面改性效果好,确定以丙烯酰胺为亲水性改性单体;2较高的单体溶液浓度有利于接枝反应;3激光能量密度增大,薄膜表面亲水性先显著增强,后又减弱;激光脉冲次数越多,改性后表面亲水性越强;4光敏剂BP对PET表面接枝聚合反应有阻碍作用;5适当浓度的均聚物抑制剂六水合硫酸铁铵能减少单体均聚物的生成,促进接枝聚合;6单体溶液的溶剂也影响接枝聚合的反应进程,不同溶剂的影响作用原理不同,含较活泼氢的乙醇能促进接枝反应;7溶液pH值影响单体聚合速率,pH值较低有利于接枝反应。

At present,the rate laws and reaction mechanisms of pyrite oxidation,pyrite and chalcopyrite formation,uraninite and magnetite dissolution in aqueous solutions are mainly studied,and it is discovered that (1)oxidation rate of pyrite controlled by surface reaction assume fractional dependence on Fe3+ and O2 molalities in acid solutions;(2)Pyrite cannot nucleate directly from solutions below 300 ℃,it can only form initially through sulfidation of a FeS precursor. The rate equation of reaction between FeS and H2S to form pyrite is of the second order;(3)Chalcopyrite is formed by reactions of pyrrhotite or pyrite with Cu2+,the former proceeds via a series of mediate metastable phases of Cu-Fe sulfide,whereas the rate equation of the latter is apparently of the first order which is controlled by surface reaction;(4)The nonlinear behavior of magnetite dissolution at acid pH can be represented by a shrinking core model coupling with surface reaction and diffusion transport.

目前主要研究了水溶液中黄铁矿氧化、黄铁矿和黄铜矿形成、晶质铀矿和磁铁矿溶解的速率定律和反应机理,发现:(1)酸性溶液中黄铁矿的氧化速率对Fe3+和O2浓度呈分数依赖并受表面反应的控制;(2)低于300 ℃时黄铁矿不能从溶液中直接成核,而需初始地通过FeS先驱物的硫化生成,FeS与H2S反应形成黄铁矿的速率方程为二级;(3)磁黄铁矿或黄铁矿与Cu2+反应均可形成黄铜矿,前者经历了一系列准稳的Cu-Fe硫化物的中间物,后者的速率方程为表观一级并受表面反应的控制;(4)酸性pH时磁铁矿的非线性溶解行为可采用表面反应扩散输运耦合的收缩核模型来描述。

After analyzing the reaction mechanism through literature, we think the reaction from diethanolamine to iminodiatic salt is composed of two steps—reaction from alcohol to aldehyde and the disproportionation reaction of the aldehyde. The selectivity, conversion, rate of this reaction are mainly attributed to the capability of this catalyst.

通过查阅文献资料,分析了反应机理,认为二乙醇胺脱氢生成酸是由两步反应组成─醇脱氢生成醛与醛的歧化,催化剂的性能是影响反应转化率、选择性及反应速度的主要因素,确定了采用沉淀法制备Cu/ZrO2做催化剂。

The results showed that the degrdation rate of fluorobenzene by TiO2/SnO2 coating rosed from 71.9% to 90.1% compared with pure TiO2 coating. The apparent rate constant k of the photocatalytic degradation is related to the initial concentration of fluorobenzene and the reaction order is zero. The corresponding degradation rate of aldehyde with the concentration of 100ppm rosed from 69.2% to 91.4% and the reaction order is one.

结果表明:与未改性涂料相比,SnO2改性涂料的活性对氟苯的降解率由71.9%提高到90.1%,反应表观速率常数与降解液初始浓度有关,光催化降解氟苯属于零级反应;对100ppm乙醛的降解率由69.2%提高到91.4%,光催化降解乙醛属于一级反应。

Study result suggest: The change of stock in RFCCU directly affect gasoline content. Gasoline content can be reduced through increasing the equilibrium activity of catalyst, controlling reaction level, increasing recirculating rate of gasoline and stability of gasoline level. Conclusions drawn from experiment is that optimization of operating condition has great effect on lowering olefine content of gasoline which can be reduced from 60% to 50%.Reducing reaction temperature is useful for lowering olefine content of gasoline, when the reaction temperature is raised, thermal cracking rate is higher than catalytic cracking rate, so that olefine content is increased. Raising catalyst-to-oil ratio is good for lowering olefine content. With conversion rate increased, the yield of LPG and coke is raised, the yield of gasoline is increased firstly and then decreased slightly, hydrogen transfer index is increased, so the olefine content is decreased.

研究结果表明:催化裂化装置的原料的变化直接影响到催化汽油的烯烃含量;可以通过优化催化装置的操作条件来降低催化汽油中的烯烃含量,其中通过提高催化剂平衡活性、控制反应深度、增加汽油回炼量、汽油深度稳定可以降低催化汽油烯烃含量,优化工艺条件对降低催化汽油烯烃含量有较大作用,汽油烯烃含量由60%降至50%左右;降低反应温度有利于降低催化汽油的烯烃含量,当反应温度的提高,热裂化反应速度提高的幅度大于催化裂化反应速度提高的幅度,汽油烯烃含量增加;剂油比的提高有利于降低催化汽油的烯烃含量,转化率提高,液化气产率提高,汽油收率先增加后略有下降,焦炭产率增加,氢转移反应指数提高,汽油烯烃含量下降;反应时间对产品分布及汽油烯烃含量有影响,增加提升管反应时间,液化汽、汽油产率提高,干气和焦炭产率增加。

As the concentration of FeO increasing, the rate of decarburizing and reaction-dissolving of refractory rises sharply. Meanwhile gas production rate of reduction reaction is increased and motion and foaming of molten slag are also speeded up. The corrosion feature of refractory containing graphite carbon is that the most severity area is slag level (interface of slag-gas phas -refractory) and slag-metal interface comes second, and the lowest corrosion rate is the area of iron-bath.

熔体的组成、温度及熔体与耐火材料间的相对运动对耐火材料的侵蚀产生着很大影响,而熔渣中FeO浓度是最主要的因素,FeO浓度提高,使耐火材料脱碳和反应熔蚀速度呈直线上升,熔体中还原产生气体量增加,熔体涨泡及运动速度提高,这些作用都加快了熔体对耐火材料的侵蚀。

In this paper, the roles of variable γ and R in Arrhenius law applications are reconsidered, and their effects on the chemical reaction rate are demonstrated by simulating one-dimensional C-J and two-dimensional cellular detonations.

本文研究了变化的比热比和气体常数对Arrhenius 定律应用的影响,并通过对一维C-J爆轰波的热力学特性和二维非定常爆轰波的胞格的数值研究证实了该影响的存在性和重要性。

Based on both western scholars' study such as Taylor on a monetary policy reaction function and Chinese condition, this article makes a new forwardlooking monetary policy reaction function, in terms of market interest rate, regulated interest rate and interest rate spread.

本文在泰勒等西方学者对货币政策反应函数研究的基础上,构造一个适合我国国情的前瞻性货币政策反应函数,从市场利率、管制利率以及两者利差三个层次,通过该反应函数对我国货币政策的实证检验结果发现,一方面,该反应函数能够很好地描述同业拆借利率、存贷款利率和两者利差的具体走势,能够为我国货币政策的制定提供一个参考尺度,以衡量货币政策的松紧。

At equilibrium,the rate of the metal dissolution is equal to the rate of the cathodic reaction,and the rate of the reaction is directly proportional to the current density by Faradar's law ;therefore:(6)and the Nernst equation can be rewritten(7)where B is a constant and i0 is the exchange current density,which is defined as the anodiccurrent density at the standard electrode potential.

在平衡,金属溶解的率与负极反应的率是相等的,并且反应的率与电流密度直接地是比例由Faradar的法律;因此:(6)和能斯脱等式可以被重写(7) B是常数的地方,并且i0是交换电流密度,被定义作为正极电流密度在标准电极电位。

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Breath, muscle contraction of the buttocks; arch body, as far as possible to hold his head, right leg straight towards the ceiling (peg-leg knee in order to avoid muscle tension).

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