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calomel相关的网络例句

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与 calomel 相关的网络例句 [注:此内容来源于网络,仅供参考]

Under the optimum conditions, the analytes could be separated within 17 min in a 75 cm length capillary at a separation voltage of 18 kV in a 10 mmol/L borate buffer (pH 8.2). A 300 μm diameter carbon disk electrode generated a good response at+ 0.95 V vs. saturated calomel electrode (SCE for all analytes. The relationship between peak currents and analyte concentrations was linear over about three orders of magnitude with detection limits (S/N=3) ranging from 78 μg/L to 110 μg/L for all analytes.

在优化的实验条件下,以直径300μm的碳圆盘电极为工作电极,检测电位为+0.95V,在10mmol/L硼酸盐(pH8.2)的运行缓冲溶液中,上述6种活性成分能在17min内实现很好的基线分离,被测物浓度与峰电流在3个数量级范围呈良好的线性关系,检出限(S/N=3)范围为78~110μg/L。

To pretreatment human hair samples by burning oxygen bottles, with a total strength as absorbent, and then use of fluoride ion electrode as directed electrode, and saturated calomel electrode as the reference electrode. To determine with improved Gran's Drawing with a satisfactory result.

用氧瓶燃烧法预处理人发样品,以总离子强度剂兼作吸收剂,然后直接用氟离子选择电极作指示电极,饱和甘汞电极作参比电极,用改进Gran's作图法进行测定,结果满意。

Films with large and homogenous grain size and ratio of Cu/In approaching 1 were obtained at deposition potentials of -0.7 and -0.75 V vs the saturated calomel electrode and Na-citrate concentration of 500 mmol/L.

当沉积电位为-0.7和-0.75V vs.SCE、柠檬酸钠浓度为500mM时,能制得颗粒尺寸大且均一、Cu/In接近1的预制层。

Aturated calomel electrode, the calibration curves for all polycarboxylic acids studied were linear with 2~3-orders of magnitude and all the detection limits (s/n=3) were below 15 fmol except malonic acid.

CE获得了选择性的、灵敏的检测,检测限在15fmol(丙二酸97.5fmol)以下,线性范围达2~3数量级。

A three-electrode system composed of TiO2/Ni as the working electrode, porous nickel as the counter electrode and saturated calomel electrode as the reference electrode was used for the photoelectrocatalytic degradation of sulfosalicylic acid under anodic bias potential.

建立了以刮浆工艺制得的TiO2/Ni为工作电极、泡沫镍为对电极、饱和甘汞电极为参比电极的光电催化反应体系,研究了在磺基水杨酸的光电催化降解过程中,外加电压和溶液PH值对降解速率的影响。

CV data showed that Sbad on Au electrode yielded oxidation and reduction features at about 0.15 V vs saturated calomel electrode, SCE.

用电化学循环伏安法和电化学石英晶体微天平技术研究了Sb在Au电极上不可逆吸附的电化学过程。

The determination of.K_2O in raw materials for ceramic industry has been made by direct measurement with volinomycin potassium electrode as indicator electrode and calomel electrode as reference electrode.

以缬氨霉钾电极作指示电极,甘汞电极作参比电极,用直读法测定了陶瓷原材中的K_2O。

CV data showed that Sb on Au electrode yielded oxidation and reduction features at about 0.15 V (vs saturated calomel electrode, SCE).

研究结果表明,在-0.25V到0.18V范围内,Sb可在Au电极上稳定吸附,并且在0.15V附近出现特征氧化还原峰。

A 125W UV lamp (365nm) was used as light source. The photoelectrochemical system consisted of three electrodes. As follows, Ti/TiO2 thin film was used as the working electrode, graphite electrode as the counter electrode and saturated calomel electrode as the reference electrode. Methyl orange was used as the objective substance. The photoelectrocatalytic degradation of Methyl orange on the Ti/TiO2 thin film was studied .The effects of some factors such as external bias potential, ventilation were also observed.

并以125W紫外线高压汞灯为光源,Ti/TiO2薄膜为工作电极,石墨电极为辅助电极,饱和甘汞电极为参比电极,建立了三电极的光电催化体系,甲基橙溶液为降解对象,并对其在Ti/TiO2薄膜电极上的光电催化降解进行了研究,观察外加电压、通空气等外加因素对甲基橙降解速率的影响。

In this thesis, multi-wall carbon nanotubeswas worked as a modified agent. The working electrode was a glassy carbon electrode or graphite electrode. A saturated calomel electrode and a platinum electrode were used as the reference and the auxiliary electrode respectively. Some pharmaceutics'electro-chemical behavior has been studied with great details. The main researches were summarized as follows: The acid-treated CNT was successfully dispersed into the DMF by using ultrasound technology.

本论文以多壁碳纳米管为修饰剂,以玻碳电极和石墨电极为工作电极,铂丝电极为对电极,饱和甘汞电极为参比电极,研究了几种药物的电化学行为及其检测方法,取得了以下研究结果:以N,N-二甲基甲酰胺为分散介质,将酸化后的MWNT超声分散于DMF中,获得分散液。

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