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hydrophobic相关的网络例句

查询词典 hydrophobic

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

The polymethyl methacrylate material with super-hydrophobic surface of the invention is prepared in the following steps: 1 the polymethyl methacrylate material is first put into diamine solution, so that the ester group on the surface of the material has ammonolysis reaction with diamine molecules; 2 and then, the product of the step 1 is put into long chain fatty acid solution to be treated and the solvent is volatilized, so as to obtain the polymethyl methacrylate material with super-hydrophobic surface.

本发明具有超疏水表面的聚甲基丙烯酸甲酯材料,是按照如下步骤进行制备的:1将聚丙烯酸甲酯材料先置于二胺溶液中使聚丙烯酸甲酯材料表面的酯基与二胺分子发生氨解反应;2然后,将其置于长链脂肪酸溶液中进行处理,挥发掉溶剂,得到具有超疏水表面的聚甲基丙烯酸甲酯材料。

In this paper,all work are developed based on HP model(3-dimensional hydrophobic -hydrophilic model).

本文的工作是在三维HP模型(3-dimensional hydrophobic-hydrophilic model)的基础上开展的。

The experimental results show that hydrophobic association increases obviously with increasing polymer concentration, hydrophobe content, hydrophobic side chain length and temperature. The Critical aggregate concentration of P(AM/NaAA/C_8AM) with different hydrophobic content is 1.5-3g/L. Strong ass...

结果表明,随聚合物浓度、疏水单体摩尔分数、疏水侧链长和温度的增加,疏水缔合作用增强;不同疏水单体含量的P(AM/NaAA/C8AM)的临界缔合浓度为1.5~3.0 g/L;表面活性剂十二烷基硫酸钠与P(AM/NaAA/C8AM)发生了强烈的疏水相互作用,形成混合胶束,得到SDS的临界胶束浓度为8×10-3 mol/L;由于聚合物链上羧基的存在,使其具有良好的 pH敏感性,随 pH值的增大,P(AM/NaAA/C8AM)的疏水缔合作用呈现先减弱后恒定再增强的变化。

The experimental results show that hydrophobic association increases obviously with increasing polymer concentration, hydrophobe content, hydrophobic side chain length and temperature. The Critical aggregate concentration of P (AM/NaAA/C8AM) with different hydrophobic content is 1.5~3g/L. Strong association between surfactant sodium dodecyl sulfate and P (AM/NaAA/C8AM) occurs through the formation of mixed micelles. The CMC of SDS is 8×10^(-3)mol/L. Moreover, because of the presence of-COOH group, the terpolymers have pH-responsive characterization. The hydrophobical association changes greatly with increasing pH.

结果表明,随聚合物浓度、疏水单体摩尔分数、疏水侧链长和温度的增加,疏水缔合作用增强;不同疏水单体含量的P(AM/NaAA/C8AM)的临界缔合浓度为1.5~3.0g/L;表面活性剂十二烷基硫酸钠与P(AM/NaAA/C8AM)发生了强烈的疏水相互作用,形成混合胶束,得到SDS的临界胶束浓度为8×l0^(-3)mol/L;由于聚合物链上羟基的存在,使其具有良好的pH敏感性,随pH值的增大,P(AM/NaAA/C8AM)的疏水缔合作用呈现先减弱后恒定再增强的变化。

From the calculations, it can be found that the van der Waals interactions, the hydrophobic interactions, as well as the H-bonding interactions are crucial for the ligand binding. The 4-phenylamino group can produce strong van der Waals adn hydrophobic interactions with the nonpolar side chains of the residues deep in the binding cleft. The R^1 and R^2 substituents on the bicyclic chromophore can also produce strong van der Waals and hydrophobic interactions with the residues located at the exterior part of the binding pocket. Moreover, the two N atoms of the quinazoline can form H-bonds with EGFR, which will produce significant contribution to biological activities. The calculated nonbonded interactions between anilinoquinazolines and EGFR, as well as the information obtained from the predicted complexes, can interpret the structure-activities of the inhibitors well, which can afford us important information for structure-based drug design.

从模拟结果得到的抑制剂和靶酶之间的相互作用模式表明范德华相互作用、疏水相互作用以及氢键相互作用对抑制剂的活性都有重要的影响,抑制剂的苯胺部分位于活性口袋的底部,能够与受体残基的非极性侧链产生很强的范德华和疏水相互作用,抑制剂双环上的取代基团也能和活性口袋外部的部分残基形成一定的范德华和疏水性相互作用,而抑制剂喹唑啉环上的氮原子能和周围的残基形成较强的氢键相互作用,对抑制剂的活性有较大的影响,计算得到抑制剂和靶酶之间的非键相互作用能以及抑制剂和靶酶之间的相互作用信息能够很好地解释抑制剂活性和结构的关系,为全新抑制剂的设计提供了重要的结构信息。

Cation group has the capability of charge neutrality and this would make oily wastewater demulsify and remove oil easily. Hydrophobic group would improve hydrophobic-oleophilic nature of the oil granule. Simultaneously, wetting reversed agent would change wetting performance of oil granule, enhance conglutination capability between air bubble and oil granule. And Frother would form bigger foam layer on the water, so it could prevnt granule with air bubble from rolling downward.Using the hydrophobic polymeric flocculant as one of ingredients for flotation agent formula, the flotation agent has good treatment effect.

浮选剂配方中的疏水性高分子絮凝剂分子链上带有的阳离子基团起到电中和作用,使含油污水易于破乳除油,而疏水基团能增强颗粒的疏水性能;润湿反转剂能改变颗粒的润湿性,增强气泡与颗粒的粘附能力;起泡剂在水面能形成强度较大的泡沫层,起阻止带气絮粒向下翻动的作用。

Hydrophobic-hydrophilic macroporous polydivinylbenzene/polyacrylethylenediamine interpenetrating polymer networks (PDVB/PAEM IPN) were prepared by the sequential suspension polymerization method. These were composed of two networks, of which one was hydrophobic and the other was hydrophilic. The objective of this work was to study the adsorption thermodynamics and adsorption kinetics of this hydrophobic- hydrophilic IPN. The focus was on adsorption isotherms of vanillin at different temperatures, and these fit well into the Freundlich adsorption isotherm. The isosteric adsorption enthalpy, adsorption Gibbs free energies and the adsorption entropy could be calculated according to thermodynamic functions.

采用分步悬浮聚合法制备了具有疏水性能的聚二乙烯基苯(polydivinylbenzene, PDVB)为第一网,具有亲水性能的聚丙烯酰乙二胺(polyacrylethylenediamine, PAEM)为第二网的疏水/亲水大孔聚二乙烯基苯/聚丙烯酰乙二胺互穿聚合物网络(interpenetrating polymer networks, IPN),研究这类疏水/亲水IPN组成的树脂对吸附质的吸附热力学和吸附动力学;测定了该树脂对香兰素在不同温度下的吸附等温线,吸附等温线符合Freundlich等温吸附方程,利用热力学函数关系计算出了吸附焓、自由能和熵变。

The hydrophobic and hydrophilic organic fractions each accounted for about 50% of DOC of the secondary effluent samples. Hydrophobic acids were the largest group accounting for 42%, followed by hydrophilic acids and non-acid hydrophilic matters at 26% and 24%, respectively; nonacid hydrophobic matters at 8% were the smallest group.

实验结果表明:当生化出水中有机物浓度以DOC表征时,水中硫水性物质与亲水性物质各占50%,其中疏水酸浓度最高,约为42%,其次为亲水酸和非酸亲水物质,分别占25%和24%,非酸疏水物质仅为8%。

SPMDs filled with triolein, and goldfish were simultaneously exposed to nine moderately hydrophobic hydrophobic chlorophenols and nine weakly hydrophobic nitroaromatics respectively, from water in laboratory continuous-flow experiments.

针对氯酚和硝基芳烃两类、各九种有毒有机污染物,在实验室内分别进行了流动体系下SPMD模拟采样动力学研究,并和鱼体富集进行平行比较,探讨了半渗透膜采样技术对中、低等疏水性污染物进行监测的可行性和机理。

The results of its fluorescence probe showed that when the guanidine hydrochloride concentration in denaturation solution was about 1.0 mol/L,there existed some stable hydrophobic regions,which could interact with a hydrophobic reagent 8-anilino-1-naphthalene sulfonic acid,in the partially folded intermediate of Bacillus amyloliquefaciensα-amylase;with the denaturation concentration increasing,the stable hydrophobic regions disappered.the results of fluorescence quenching using acrylamide and potassium iodide as quenchers showed that using acrylamide as quenchers,with the protein denaturation extent increasing,the number of Trp that can be quenched increased untill all the Trp residues were quenched;Using potassium iodide as quenchers,with the maximum number(8) of tryptophan residues in a partially folded intermediate Bacillus amyloliquefaciensα-amylase molecule could be quenched by potassium iodide;with the denaturation concentration increasing,the number of Trp that can be quenched decreased to 5.the results of their protein electrophoreses and SEC showed that no aggregate or aggregate precipitation of Bacillus amyloliquefaciensα-amylase formed during the whole unfolding/refolding procedure of Bacillus amyloliquefaciensα-amylase induced by guanidine hydrochloride or urea.

ANS外源荧光探针结果表明:盐酸胍诱导的芽孢杆菌α-淀粉酶分子去折叠过程中存在着能够与探针分子1-苯胺基-8-萘磺酸结合的稳定的疏水区域;而随着芽孢杆菌α-淀粉酶分子在盐酸胍溶液中变性程度的加深,这一疏水区域逐步被瓦解。丙烯酰胺和碘化钾猝灭结果表明:在盐酸胍溶液中,随着芽孢杆菌α-淀粉酶分子变性程度的进一步加深,其分子内能够被丙烯酰胺接近的色氨酸残基逐渐增多,直至全部被猝灭。但位于芽孢杆菌α-淀粉酶分子表面的能够被碘化钾猝灭的色氨酸残基,在中间态芽孢杆菌α-淀粉酶分子中数目达到最大的8个,而随着其分子变性程度的进一步加深,反而减少至5个。

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