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interfacial相关的网络例句

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与 interfacial 相关的网络例句 [注:此内容来源于网络,仅供参考]

The microcapsules with polyurea shell for functionally thermal fluid application were synthesized by interfacial polymerization with isophorone diisocyanate and tetraethylenepentamine as wall material precursor in an emulsion system.

1前言功能热流体是在单相流体中混入其它材料形成的一种集储热与强化传热功能于一身的新型储传热介质[1]。

Electrochemical behaviors on the surface of jamesonite in an acidic solution of pH4.0 buffer solution containing diethyl dithiocarbamate were investigated by the methods of cyclic voltammetry and AC impedance.The changes of the reactions,electrochemical adsorption,passivation action,electrochemical impedance and interfacial capacitance on jamesonite were discussed under the different conditions of electrode potentials.

用循环伏安和交流阻抗法,研究了脆硫锑铅矿在含乙硫氮的pH 4.0缓冲溶液中的表面电化学行为,讨论了在不同电位下脆硫锑铅矿表面的反应、电化学吸附、钝化作用、电化学阻抗、微分电容的变化。

As a part of this key program from China Natural Science Foundation, this research focuses on the electrochemical reactions and oxidization products on the surfaces of jamesonite and marmatite, and on the change of their interfacial structures and their electrochemical mechanisms by various methods of thermodynamic, electrochemistry (such as Tafel, constant potential step, cycle voltammetry, AC impedance) and IR, UV spectra when the collectors, adjusting reagents act with the sulfide minerals in the flotation system so that the electrochemical conditions to float selectively the minerals can be decided.

本研究作为该国家自然科学重点基金项目的一部分,采用热力学、电化学(Tafel、循环伏安、恒电位阶跃和交流阻抗法)以及光谱等多种研究手段,集中研究了浮选体系中脆硫锑铅矿、铁闪锌矿表面的电化学反应及氧化产物,研究这两种矿物与捕收剂、调整剂相互作用时的界面结构变化及电化学机理,阐明了使药剂选择性捕收或选择性抑制这些硫化矿物的电化学条件。

The interfacial energy as a resistance of martensitic transformation is less than 10% of the critical driving force.

体系的共格界面能作为马氏体相变临界驱动力△Gγ→εMs中的阻力项所占的比例小于10%。

Reverse osmosis composite membrane was prepared by interfacial polymerization of metaphenylene diamine with trimesoyl chloride on the surface of polysulfone support.

以聚砜超滤膜为支撑膜,间苯二胺为水相功能单体,均苯三甲酰氯为油相功能单体,通过界面聚合法制备了反渗透复合膜。

Through designing of composition and structure of the bioactive graded coating,innerstress and its distribution in the coating were analyzed and calculated, the resultsshowed that when composition distribution coefficient n was 1.5, a reasonable stressdistribution could be got, that was at the beginning of deposition the suspension containingrichly BG granules was used so that a rich BG granules layer, a good transitional layerbetween BG layer at the bottom and the coating could be obtained at the titanium alloy side,the bottom of the coating; the stress value near the interface and surface and its character,pressure stress or tensile stress, were decided by the character of its composition itself.Changing composition distribution coefficient n could only change the variation tendency ofstress in the coating, but did not change the stress distribution rule in the coating. Thethinner the coating is, the sharper stress variation in the coating is, which does not mean thatthicker coating is better because the thicker the coating is, the little the permitteddeformation of coating is, so the coating thickness should be thinner, for example, about50μm for bending applications, but for applications only bearing pure shear stress, such asroot of tooth implant, the coating can be thicker little, for instance, about 80~100μm. The study on electrification characteristic and electrophoresis deposition of HAand BG granules in aqueous and non-aqueous solution system found that EPD almost didn'toccur in aqueous solution system. However, because HA granules take position charges inabsolute alcohol, a homogeneous EPD be carried out on the cathode titanium alloy slice, but taking negative charge in absolute alcohol the BG granules not be deposited on the cathode. A guided HA crystallizing, 100~300nm, on surface of the BG granules be realized by metathetical reaction, which cover BG granules with HA microcrystals and make the covered BG granules taking position charges in absolute alcohol, sequentially realize the EPCD of the BG and HA granules on the cathode, so it is feasible to make a titanium alloy/BG/HA bioactive graded coating by making use of EPCD technology. The corrosion experiment of rich boron bioglass coating and plasma spray coating showed that split phase, rich boron and rich silicon phase, occurred during its preparation. In basic medium the corrosion behavior of 〓 BG coating showed uniformity corrosion, the corrosion mostly occurred at rich boron phase area, therefore batch formula design of BGshould avoid the occurring of split phase. The corrosion appearance of plasma spray coatingappeared a non-uniform corrosion, mostly occurred at the edge of the laminated HA moltendrops, and emerged an accelerated corrosion tendency, which will easyly lead to corrosioncrackles extending to the interface and the happening of osmotic interfacial corrosion, thatmay be one of the major reasons leading to the coating cracking-off in the later period. Thetesting results of thermal expansion coefficient of 〓 and 〓BG showed the thermalexpansion coefficient of 〓 BG matched with that of titanium alloy better, and 〓 BG couldsinter with titanium alloy into densification enamel layer at low temperature (720℃).

将Ti6Al4V合金在1000℃下进行真空热处理会降低其力学性能,且合金内的V元素会向表面富集,因此,钛合金真空热处理和表面涂层的烧结温度不能过高,即应低于其相转变点;通过对生物活性梯度涂层的组成和结构的设计,分析和计算了梯度涂层内的应力大小和分布,结果表明:对于本研究,当成分分布系数n=1.5时,可以获得较合理的涂层力学性能,即在沉积开始时,采用富含BG颗粒的悬浮液,以便在钛合金侧获得同底层BG有良好过渡的富BG涂层;梯度涂层界面和表面的应力大小、性质由材料组成本身的性质决定,改变成分分布系数,只能改变涂层内应力变化的趋势;涂层的厚薄不影响涂层内的应力分布规律,但涂层越薄,涂层内的应力变化越快,但这并不意味着涂层越厚越好,因为涂层越厚,涂层允许的变形越小,对于应用于弯曲受力部位的涂层而言,涂层应薄一点为好(50μm);而对于仅纯受剪切应力的部位,如牙根种植体,涂层可适当加厚(80~100μm);通过对HA和BG颗粒在水溶液体系和非水溶液体系中的带电特性和电泳沉积的研究发现,它们在水溶液体系中很难发生电沉积;在无水乙醇溶液中,HA颗粒带正电,可在阴极钛合金片上发生均匀的电泳沉积,而BG颗粒则带负电荷;利用复分解反应法,可以制得100~300nm的HA,通过诱导HA在BG颗粒表面结晶,可对BG颗粒进行表面包覆,获得了被HA包覆的BG颗粒,改变了BG颗粒表面的带电特性,使BG和HA颗粒在无水乙醇中均带上正电荷,从而实现了HA和BG颗粒在阴极上的共沉积。

Then obtain heavy magnesium water solution, add interfacial active agent and ammonia to solution, via hydrothermal treatment and filtration washing, dry to gain nemaline magnesium hydroxide.

得到重镁水溶液,向溶液中加入表面活性剂和氨水,经过水热处理,过滤洗涤后、干燥得到纤维状氢氧化镁。

The stability of GA-PBCA-NP was also studied.ResultsDue to the agglomerationg of nanoparticles with no stabilizer,it was difficult to preparate.GA-PBCA-NP produced by the two methods both had spheric and smooth outer appearance,uniform distribution,nonadherence and stability.The diameter,ebeding ratio and drug loading in GA-PBCA-NP produced by emulsification polymerization and interfacial polymerization methods were 90~600 nm and 200 nm,60.49% and 73.87%,18.15% and 22.23%,respectively.

结果未添加稳定剂的纳米球表面粘连团聚现象严重,难以成球;乳化聚合法制备的GA-PBCA-NP在透射电镜下观察表面圆整光滑,粒子之间不团聚,不黏连,粒径范围在90~600 nm,包封率为60.49%,载药量为18.15%;界面缩聚法制得的纳米粒表面圆整光滑,粒子之间不团聚,不黏连,粒径大小均匀,都在200 nm左右,包封率为73.87%,载药量为22.23%,两种方法制备的稳定性都较好。

GA-PBCA-NP produced by the two methods both had spheric and smooth outer appearance,uniform distribution,nonadherence and stability.The diameter,ebeding ratio and drug loading in GA-PBCA-NP produced by emulsification polymerization and interfacial polymerization methods were 90~600 nm and 200 nm,60.49% and 73.87%,18.15% and 22.23%,respectively.ConclusionIt is important to add dextran 70 in preparation.

结果未添加稳定剂的纳米球表面粘连团聚现象严重,难以成球;乳化聚合法制备的GA-PBCA-NP在透射电镜下观察表面圆整光滑,粒子之间不团聚,不黏连,粒径范围在90~600 nm,包封率为60.49%,载药量为18.15%;界面缩聚法制得的纳米粒表面圆整光滑,粒子之间不团聚,不黏连,粒径大小均匀,都在200 nm左右,包封率为73.87%,载药量为22.23%,两种方法制备的稳定性都较好。

Using a model of concrete in which the aggregates are spherical and nonconductive particles, the ratio of the interfacial transition zone electrical conductivity and the matrix electrical conductivity σ_/σ_ were calculated.

利用一个将骨料看成非电导球形颗粒的混凝土模型,计算了界面过渡区的电导率与水泥浆基体电导率的比值。

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推荐网络例句

The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了,排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意,我建议我们在价格上大家各让一半。

After an hour and no pup, look for continued contractions and arching of the back with no pup as a sign of trouble.

一个小时后,并没有任何的PUP ,寻找继续收缩和拱的背面没有任何的PUP作为一个注册的麻烦。