查询词典 interfacial

The demulsification mechanism of PAMAM belongs to displacing mechanism. Acylamino groups of PAMAM of integral having strong polarity can take place chemical adsorption with the materials of strong polarity in the exterior of oil drop and be participated in into the membrane, which will result in adsorbed crude surfactant and other active materials to be partially displaced and reduce the intensity of interfacial film between oil and water.

其机理是由于整代的PAMAM具有强极性的酰胺基团，能与油滴表面的强极性的物质发生化学吸咐作用，参与成膜，能把原来吸咐的天然活性剂分子和其它活性物质部分顶替，削弱油水界面膜强度。

HREM studies show that TiB〓/Al interface is atomically flat, smooth and free from any interfacial phases.

HREM观察发现，TiB〓和α-Al之间不存在固定的晶体学取向关系。

The research results indicated that the viscosity of the autogenetic foam system has good thermal stability, the system has favorable ability to reduce the viscosity and interfacial tension of the heavy oil, the displacement of the system for the heavy oil is good and it has good mobility control ability for the mobility in layers and interlayers,.

研究结果表明，自生泡沫体系粘度具有较好的热稳定性，并具有良好的稠油降粘和降界面张力能力，驱替稠油能力强，具有很强的层内层间流度控制能力。

The properties of the oil displacement using the autogenetic foam combination system have been researched through the viscosity reduction, interfacial tension, thermal stability and rheological experiments.

通过降粘实验、界面张力实验、热稳定性实验以及流变实验研究了自生泡沫复合体系的驱油性质。

The structural and photocatalytic properties of TiO〓 as well as surface acidity were greatly improved by sulfation. SO〓〓/TiO〓 solid superacid with Hammett constant Ho less than -12.14 was prepared by treating the TiO〓 with 1.0mol. L〓 sulfuric acid solution and then calcining at 450℃ for 3h. When compared to unmodified TiO〓, the SO〓〓/TiO〓 superacid catalyst exhibited higher anatase content, smaller crystal size, higher specific surface area, centralized pore size distribution, and the blue-shifted band edge of uv-vis adsorption spectra. Furthermore, the SO〓〓/TiO〓 superacid also showed excellent reaction activity and stability for CH〓Br photocatalytic decomposition even under the moist reaction conditions. The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

All the results indicate that interfacial polymerization between isocyanate and amine to form polyurea wall material is a quick, effective way for capsulation of wax.

实验结果表明由异氰酸酯与胺反应形成聚脲囊壁材料是一种快速、有效的包裹石蜡的方法。

The chemical structure of the product was characterized by means of the melting point and IR. The results show that tetraethylammonium bromide which was used as a phase transfer catalyst in this reaction had optimization effect on the interfacial diffusive reaction of BTC and PNP. Higher concentration of sodium hydroxide, lower temperature and a higher dosage of BTC produced a small amount of 4-nitrophenyl chloroformate, while lower concentration of sodium hydroxide and a lower dosage of BTC made reaction incomplete, which affected the yield.

结果表明，在碳酸二（4-硝基苯基）酯合成中使用的相转移催化剂四乙基溴化铵对受界面扩散控制的BTC气与对硝基酚钠反应有良好的相转移催化效果；氢氧化钠质量分数较低时，酚钠盐向溶有BTC的油相扩散速度较小，较高时会产生氯甲酸对硝基苯酯；温度较低、BTC量较高时，会产生少量氯甲酸对硝基苯酯，BTC用量较低会使反应不完全，这些都影响着收率。

The demonstrate in can asking to develop a process of course (safeguard a map by development staff for example, a of the ID interfacial element and tiring-room or correspondence of a group of operations rises), what I need to solve now is how to let the system discovers automatically and maintain these relationships Read above oneself problem, discovery had a direct result to be told to the system,"Authority " the ID that is an interface element and the URL that a group of tiring-room serve (take no account of data to visit attributive temporarily), attributive ={id, comId, urls, desc} such, how can problem translate into realize the definition of attributive, let him user input ComId, Urls?

当然可以要求开发过程中指明（例如由开发人员维护一个映射，把界面元素的ID和后台的一个或者一组操作对应起来），我现在需要解决的是如何让系统自动发现和维护这些关系读了上面自己的问题，发现有了个直观的答案对于系统来讲，&权&就是一个界面元素的ID和一组后台服务的URL（暂时不考虑数据访问权限），权限={id，comId，urls，desc}这样，问题转化为如何能够实现权限的定义，让用户自己输入comId、urls吗？

The interfacial conglutinative behavior between glass fiber and Polyvinyl chloride was analyzed by molecular dynamic simulation.

通常对聚合物基复合材料的研究多着重于宏观力学性能[1]，而较少涉及复合材料多相性所导致的微观行为。

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。