吸附

This result laid a foundation of theory and experiment for the development of mordenite sorbent to separate ethene.NaY was firstly modified using two ion-exchange and two calcinations method which was heated by microwave.

首次采用微波加热二次离子交换二次焙烧的方法改性NaY分子筛，制得CeY、CeY、CuY、AgY、KY、MgY和SrY，并用于吸附噻吩和苯，其中CeY分子筛对噻吩具有最好的吸附容量和选择性。

But it is not correct that the adsorbed phase is considered as saturated liquid for multicomponent supercritical adsorption equilibrium.

但是，现有模型的共同缺点是把吸附相看作为饱和液体，这种处理方法对超临界多组分吸附平衡是不合理的。

The nickelous chloride both may use in to galvanize, and is prepares the galvanization chemical thionamic acid nickel the important raw material, lead is affects the electronickelling quality a important attribute, in the present industry 331 ion exchange resin deleading effect still could not arrive in the electronickelling the lead content standard, used pocket weak basicity resin XSC312 after the screening experiment determination to take from the nickelous chloride solution intermediate ion exchange except the micro lead resin, inspected the material fluid pH value, the contact duration in the ionic exchange column to the ionic exchange adsorption lead influence, has determined the resin adsorption capacity and inspected the resin analysis performance.

氯化镍既可用于电镀，又是制备电镀化学品氨基磺酸镍的重要原料，其中的铅是影响电镀镍质量的一个重要因素，现行工业中的331离子交换树脂除铅效果尚不能到电镀镍中铅含量标准，经过筛选试验确定采用大孔弱碱性树脂XSC312作为从氯化镍溶液中离子交换除微量铅树脂，在离子交换柱中考察了料液pH值、接触时间对离子交换吸附铅的影响，测出了树脂的吸附容量并考察了树脂的解析性能。

Results showed that single ozone oxidation can only remove about 50% nitrobenzol, single active carbon absorption can reduce nitrobenzol to a standard index mark when empty-bed station time exceeded 15 minutes, but ozone oxidation-active carbon absorption technology can remove nitrobenzol completely when the time exceeded 10 minutes.

研究发现：单独采用0 氧化能去除约50％的硝基苯；单独采用活性炭吸附，在空床停留时间大于15 min时可使出水指标达到标准要求；而对于O 氧化一活性炭吸附工艺，当停留时间在10 min 以上时，可完全去除水中的硝基苯。

In our work, Activated Carbon and Bentonite are selected as adsorbents in this process to degrade nitrophenol wastewater and slightly-polluted potable water. This paper investigates operation parameters; reaction mechanism; carbon modification and reaction kinetic model.

本文分别采用活性炭和膨润土作为吸附剂，以硝基酚污染物和低浓度微污染源水为处理对象，对该体系的工艺参数、反应机理、吸附剂改性、有机污染物降解途径以及反应动力学模型等方面进行了系统的研究。

The paper is concerned with its experimental study on the mechanism and effect of Nocardia amarae used as adsorbent for removing Pb2+ from the waste water by way of biosorption-flotation.

以苦味诺卡氏菌作为Pb2+吸附剂，研究了采用生物吸附-浮选法去除废水中Pb2+的效果及其作用机理。

Nonfouling mechanism of polymer materials and recent research progress of protein-resistant polymer preparation and surface modification are reviewed.

本文对聚合物材料表面阻抗蛋白质吸附的机理进行了归纳，介绍了阻抗蛋白质吸附的材料制备及表面修饰的相关研究进展。

For the tetracene overlayer near to a monolayer, formation of a parquet-like pattern was observed.

当分子长轴取向垂直于[1-210]方向并且其质心位于密排原子列上两个Ru原子的短桥位时，该位置是它的次佳吸附位，在该位置的吸附能为4.19 eV。

When the coverage is increased,the aspartic acid molecules can finally form an overlayer with uniform contrast but could never form any ordered structures.

随着覆盖度的提高，天冬氨酸分子最终在Cu(0 0 1)表面形成一均匀衬度的吸附层，但并不形成有序吸附结构，也不能使台阶发生小面化。

In the initial stage of the bioleaching, when the bacteria are not active, the chemical oxidation of ferric irons to the solid sulfide minerals is primary; While in the whole course of the bioleaching, it is very limited; ferric irons inhibit the bacterial activity, lower the oxidational ability of the bacteria to ferrous irons in the liquid phase; ferric irons and their precipitations reduce the quantities of the attached bacteria and their activity, and have bad influence on the direct bioleaching action.

结果表明，在浸出的初始阶段，Fe3+的化学氧化作用是主要的；但在整个金属浸出过程中，Fe3+的化学氧化作用是很有限的；Fe3+对T.f菌有一定的抑制作用，降低了它们对液相中Fe2+的氧化能力；Fe3+及其沉淀使细菌在固体矿物颗粒表面的吸附量减少，降低了吸附细菌的活性，从而影响了细菌的直接氧化浸出作用。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新