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Additional, in industrial respect, ion exchange fiber can become activator carrier as activator, use at catalysis certain and organic reaction; Can use as dehydrating agent and grease depart material; Use as water sorbent, take off with what divide at the water in storehouse except; Use as material of sex hygiene suction blood, can make radioactivity is absorbed and defend material; Use ion exchange fiber the adsorption to the bacterium and antiseptic ability, make underwear of deodorant insole, health care wait.

另外,在工业方面,离子交换纤维可作为催化剂成催化剂载体,用于催化某些有机反应;可用作脱水剂和油水分离材料;用作水吸附(物质表面吸住周围介质中的分子或离子现象)剂,用于仓库中水分的脱除;用作吸血性卫生材料,可制成放射性吸收和防护材料;利用离子交换纤维对细菌的吸附(物质表面吸住周围介质中的分子或离子现象)和杀菌能力,制成防臭鞋垫、保健内衣等。

From the analysis of theory and technique character of ion-implantation and the energies, the implant range and straggle of nitrogen ions in 4H-SiC calculated by TRIM, the method to calculate the channel depth of 4H-SiC MESFET is present based on the energy diagram's analysis of implanted layer.

通过研究离子注入的理论和工艺特性,以及蒙特卡洛分析软件TRIM对氮离子注入4H-SiC的能量、深度和偏差等参数的分析,在注入层的能带理论分析的基础上,提出了计算离子注入4H-SiC MESFET器件的沟道深度的方法,以及离子注入工艺参数,包括能量、剂量的确定方法。

The study of the effect of Glycerol on survival of the E.coli shew Glycerol could protect E.coli and improve dry, vacuum and implantational survival rate during ion beam implanting the E.coli. The whole survival rate of protected the E.coli implanted by 30keV N+ was 530-10000 times higher than unprotect ones. Glycerol changed bacteria outer color and survival rate curve. At the same doses, the color of the E.coli protected by five and one percent Glycerol was white or yellow, lighter than unprotected. In addition, the survival rate curve of the E.coli with Glycerol located above one without Glycerol, and the peak of which was higher and delayed at dose.

在研究甘油对低能离子注入E.coli存活的影响时,发现甘油保护可以提高E.coli的干燥存活率,真空存活率以及注入存活率,使得整个30keY氮离子注入后E.coli的最终存活率提高530-10000倍;甘油保护引起离子注入后的菌体颜色发生变化,在相同的剂量下,未用甘油保护的菌体颜色最深,1%甘油保护菌体颜色次之,5%甘油保护菌体颜色最浅;另外,甘油可以引起离子注入E.coli的"马鞍型"存活率曲线发生变化,甘油保护的E.coli存活曲线大致位于未用甘油保护的存活曲线的上面。

The research progresses in degradation technologies of benzene or some of its derivatives in water are reviewed.The macroscopical reaction mechanism of HNO2(NO2-)and C6H5Br in aqueous solution has been studied.Different influence factors have been discussed,including different pH condition,initial concentration,irradiation time,different anions and the optimization of experimental conditions.By using liquid chromatography,the degradation rate of bromobenzene has been qualitatively analyzed.The concentration variations of Br~and NO2- have been analyzed by using ion chromatography.

本文介绍了苯及其衍生物对水环境所造成的污染和危害,研究了365nm光照下HNO2(NO2-)与C6H5Br混合溶液的宏观反应过程,初步考察了混合体系中溴苯的降解及衰减行为,较为系统地探讨了影响溴苯降解过程的各种影响因素,包括溶液的pH值、初始浓度、光照时间、不同离子的影响以及实验条件的优化,并利用液相色谱法进行定量研究溴苯的降解率,利用离子色谱法分析检测实验过程中溴离子和亚硝酸根离子的变化。

The organoboron compounds in this paper are based on triarylboranes, boronic acids and boronic esters. The structure-property relationship and sensing mechanism are elucidated. Organoboron compounds as Lewis acid can be used as fluoride probe with high sensitivity and selectivity because they have a unique LUMO in which the π-conjugation is divergently extended through the vacant p-orbital of the boron atom. The complexation of the boron π-electron systems with fluoride ion would interrupt the π-conjugation extended through the boron atom, causing the change of photophysical properties.

介绍了基于三芳基硼化合物、硼酸和硼酸酯的有机硼化合物在氟离子检测中的应用,评述了这些化合物的结构和检测性能之间的关系,讨论了检测机理,即有机硼化合物中硼原子空的p轨道使其作为路易斯酸能够选择性地结合氟离子,硼原子与氟离子的结合破坏了硼中心与芳香取代基的p-π共轭,引起有机硼化合物光物理性质的变化,从而实现对氟离子的高选择性检测。

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。

The new opinion and mechanism that the simultaneously adsorption of complex pollution of both organic and heavy metals will be achieved on soil modified with amphoteric surface modifying agent, which have both charged group and organophilic group on one ASMA molecule, were proposed at first time, and its rationality was testified at the same time; The 50% was the critical CTMAB modifying ratio of soil CEC at which the organophilic bond modifying mechanism was emerged; The thermodynamic characteristics of adsorption of OPT and HMP on OMS were discovered ; The study revealed the surface peculiarity of OMS that the modifying agent were distributed at uneven scatter mode and multi-characters surface were coexisted on surface of OMS, revealed the adsorption peculiarity of OMS that multi-mechanisms were coexisted, confirmed the unequal charge amount modifying mode of OMS in which dual-modifying mechanism of both ion exchange and OPB were processed at the same time, and confirmed that the adsorption hobby to CTMAB was higher than that to Ca2+ on Lou soil.

首次提出了用两性表面修饰剂对土壤进行修饰改性,利用两性表面修饰剂所具有的荷电基团和疏水基团达到对土壤中有机、重金属污染物同时吸附的思路和机理,并通过实验证实了所提设想的合理性;发现了土壤CEC值的50%修饰比例是CTMAB开始显现以疏水键机制对土土样表面进行修饰的临界点;揭示了有机修饰改性土对有机物、重金属吸附过程的热力学特征,填补了该项研究工作的空白;阐明了修饰剂在改性土表面呈分散态的非均匀分布,改性土表面具有不同性质表面共存的表面特征和对污染物多机制共存的吸附特征,确定了阳离子表面修饰剂在土表面的修饰是一种离子交换和疏水键结合两种机制相伴并行且为非等电荷量交换的修饰反应模式,以及土具有对CTMAB的吸附偏好性远大于对钙离子吸附偏好性的特征。

The results showed that the interactions between Al(superscript 3+), Fe(superscript 3+), polysilicic acid, the polynuclear hydroxy complexes of Al(superscript 3+), Fe(superscript 3+) and SO(superscript 2- subscript 4) had a compositive effect of electric neutralization, adsorption and bridge on the coagulating properties.

结果表明,含硅多核无机高分子絮凝剂的混凝作用是铁离子、铝离子、聚硅酸、铝铁离子的水解聚合物以及它们和硫酸根离子相互作用的产物对废水中胶体悬浮物颗粒的电中和、吸附架桥及粘附卷扫等综合作用的结果。

Three kinds of ionic liquid were used to support the acetylacetone at the C3 position directly according to the method indicated above. These synthesized ionic liquid supported acetylacetone catalysts include imidazolium salts ionic liquid supported acetylacetone catalysts, pyridinium salts ionic liquid supported acetylacetone catalysts and ammonium salts ionic liquid supported acetylacetone catalysts. All these catalysts were characterized by ~1H-NMR,~(13)C-NMR, IR and elementary analysis.

采用设计过程中预期能够提高乙酰丙酮金属催化剂催化氧化活性的修饰方式,合成了三类离子液体支载的乙酰丙酮金属催化剂:咪唑型离子液体支载乙酰丙酮金属催化剂、吡啶型离子液体支载乙酰丙酮金属催化剂、胺型离子液体支载乙酰丙酮金属催化剂,并采用核磁共振氢谱、碳谱,红外光谱及元素分析来对这些新型的催化剂进行了表征。

Results of meausred radioluminescence spectra show that energy transfer mechanisms occurring from Gd3+ cations towards Tb3+ emssion centers as well as the cross relaxation among Tb3+ cations within the certain concentration range exert tremendous effects on the emission intensity of glasses.

Tb3+离子的掺杂浓度范围为1-5 mol %。玻璃样品的X射线激发发射光谱结果显示,发生在玻璃基质中由Gd3+离子向发光中心Tb3+离子的能量转移机制以及在一定浓度范围内Tb3+离子之间的交叉驰豫过程对玻璃的发光性能有重要影响。

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