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cyclic voltammetry
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  循环伏安法
     The linear range is 5.0×10~(-6)~3. 0×10~(-3)mol/L (R=0.999) with the detection limit of 2.0×10~(-6) mol/L for cyclic voltammetry.
     用循环伏安法测定H_2O_2,线性范围为5.0×10~(-6)~3.0×10~(-3)mol/L(R=0.999),检出限为2.0×10~(-6)mol/L。
短句来源
     Methods The Electrochemical Properties of Alkylcobaloxime Complexes RCo (DMG)2·L, were R=n-C 3H 7、i-C 4H 9、n-C 4H 9、n-C 5H 11 、c-C 6H 11 、Ph CH 2 and L=H 2O containing the equatorical ligand dimethylglyoxime were studied by cyclic voltammetry.
     方法 用循环伏安法研究了钴肟类模型化合物RCo(DMG) 2 ·L(R =n -C3 H7、i-C4 H9、n -C4 H9、n -C5H11、c -C6H11、PhCH2 、Cl,DMG =丁二酮肟 ,L =H2 O)的电化学性质。
短句来源
     The electrochemical behavior of 0. 01 mol·dm-3 Pr(CH3SO3)3-0.01 mol·dm-3 NiCl2-0.01 mol·dm-3 FeCl2-3.0 mol·dm-3 urea-DMSO was investigated by cyclic voltammetry.
     利用循环伏安法研究了0.01 mol·dm-3Pr(CH3SO3)3-0.01mol·dm-3NiCl2-0.01 mol·dm-3FeCl2-3.0 mol·dm-3尿素-DMSO体系的电化学行为。
     The mode of Eu(bpy) 3+ 3 interacted with DNA in solution is studied by cyclic voltammetry and differential pulse voltammetry.
     用循环伏安法和差示脉冲伏安法研究了金属配合物Eu(bpy) 3+3 与DNA的作用模式 ,表明Eu(bpy) 3+3 以静电模式与DNA作用 .
短句来源
     The influence of the axial organic base on the electrochemical oxidation and reduction of the coenzyme B1 2 model compounds [R Co(salen) L ],where R=n- C3 H7,i- C4H9; L =H2 O, py,γ- pic was studied by means of cyclic voltammetry.
     用循环伏安法研究了辅酶 B1 2 模型化合物 RCo(salen) L (R=n- C3 H7,i- C4H9;L=H2 O,py,γ-pic)的电化学行为 ,讨论了轴向碱基 L对氧化还原电位的影响。
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  循环伏安
     Study on the Cyclic Voltammetry of LiCo_(1-X)M_XO_2
     LiCo_(1-X)M_XO_2的循环伏安性能研究
短句来源
     Study on the Aqueous System I~--I_2 -X~- (X=F, C1,Br) by Cyclic Voltammetry
     水溶液中I~-I_2-X~-(X=F、Cl、Br)体系的循环伏安研究
短句来源
     Cyclic voltammetry study on spinel LiMn_2O_4
     尖晶石型LiMn_2O_4电极循环伏安研究
短句来源
     From the voltage profile and cyclic voltammetry, the redox processes occurring at ~3.7 and ~4.4 V were assigned to the Ni2+/4+ and Co3+/4+ couples, respectively.
     循环伏安曲线上3.7V和4.4V的氧化还原过程对应于Ni2+/4+和Co3+/4+氧化还原电对的反应.
短句来源
     Effect of pH on Cyclic Voltammetry of Self-assembled Monolayers of Cysteamine in Fe(CN)_6~(3-/4-) Solution
     pH对半胱胺自组装膜在Fe(CN)_6~(3-/4-)溶液中的循环伏安的影响
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  “cyclic voltammetry”译为未确定词的双语例句
     CYCLIC VOLTAMMETRY STUDY ON ANTIMALARIAL MECHANISM OF ARTEMISININ(QINGHAOSU)DERIVATIVES
     CYCLIC VOLTAMMETRY STUDY ON ANTIMALARIAL MECHANISM OF ARTEMISININ(QINGHAOSU)DERIVATIVES
短句来源
     Methods The cyclic voltammetry(CV) of p-hydroquinone and conjoint p-hydroquinone with serum protein at L-cysteine bodified golden electrode in 0.05 mol/L Na2HPO4-0.05 mol/L NaH2PO4-0.10 mol/L NaCl buffer solution(pH=7.30) was studied in this paper.
     方法在0.05 mol/L Na2HPO4-0.05 mol/L NaH2PO4-0.10 mol/L NaCl缓冲溶液中(pH=7.30),观察对苯二酚及牛血清白蛋白与对苯二酚结合后在L-半胱氨酸修饰金电极上的电化学行为。
短句来源
     The peak current is proportional to the concentration of L-Cys in the range of 2.0×10~(-6)~3.0×10~(-4) mol/L with a detection limit of 5.5×10~(-7) mol/L by means of cyclic voltammetry at the SWNT modified electrode.
     峰电流与L-半胱氨酸的浓度在2.0×10-6~3.0×10-4mol/L范围内有良好的线性关系,检出下限为5.5×10-7mol/L。
短句来源
     Adsorption and Oxidation of 1, 2-Propanediol at Pt/S_(ad) Electrode Using Cyclic Voltammetry and EQCM
     Pt/S_(ad)电极上1,2-丙二醇吸附和氧化的CV和EQCM研究
短句来源
     The linear range is from 5.0×10~(-9) to 5.0×10~(-7) mol/L with the detection limit of 1.0×10~(-9) mol/L. The sensitization of the surfactant was studied with cyclic voltammetry and normal pulse polarography.
     利用此波可测定痕量安非他酮,线性范围为5.0×10-9~5.0×10-7mol/L,检测下限达1.0×10-9mol/L.
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  cyclic voltammetry
The electrochemical behavior of the system was also studied by cyclic voltammetry, and the experiment results showed that the electrode process was an irreversible absorptive with two electrons participating.
      
Ionic liquid like 1-butyl-3-methyl-imidazolium tetrafluorobrate ([BMIM]BF4) has been used as solvent and electrolyte for the electropolymerization of aniline at glassy carbon electrode by cyclic voltammetry.
      
The electrochemical behavior of compounds in nonaqueous solution DMF was carried out by means of cyclic voltammetry.
      
The NB-CNT/ glasssy carbon (GC) electrode was fabricated by modifying NB-CNT nanocomposite on the GC electrode surface and its electrochemical properties were investigated by cyclic voltammetry.
      
absorption peak from the electronic spectra is red shifted and the intensity is weakened and that the values of peak current from cyclic voltammetry are decreased significantly in the presence of DNA compared with that in the absence of DNA.
      
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This paper reports the anodic stripping voltammetry of trace amount of arsenic on the gold film which is deposited on a glassy graphite electrode. In 1 M sulfuric acid medium, it shows a peak of stripping current of arsenic at +0.15 V~+0.25 V (vs. 1N. Ag-AgCl). A linear relation between the peak height and the concentration of arsenic in the range of 1.0~10~(-9)M to 6.0×10~(-6)M was observed, the sensitivity of this method is about 200 times higher than that of the colorimetry of arsenic with silver diethyldithio-carbamate....

This paper reports the anodic stripping voltammetry of trace amount of arsenic on the gold film which is deposited on a glassy graphite electrode. In 1 M sulfuric acid medium, it shows a peak of stripping current of arsenic at +0.15 V~+0.25 V (vs. 1N. Ag-AgCl). A linear relation between the peak height and the concentration of arsenic in the range of 1.0~10~(-9)M to 6.0×10~(-6)M was observed, the sensitivity of this method is about 200 times higher than that of the colorimetry of arsenic with silver diethyldithio-carbamate. On the other hand, we have studied the electrode process with the triangle cyclic voltammetry. It shows that the electrode reaction is irreversible and the deposition of arsenic on the gold film electrode is probably due to the formation of intermetallic compound of arsenic with gold.

本文报道了痕量砷在玻璃态石墨电极为基体的金膜电极上的阳极溶出伏安法,在1M硫酸介质中,于+0.20V左右得到一个砷的溶出峰,峰高与砷的浓度在1.0×10~(-9)M~6.0×10~(-6)M范围内有良好的线性关系。定量下限达1.0×10~(-9)M,相当于0.075ppb,比DDC银法灵敏度高出200多倍。本文并用三角波周期伏安法观察了电极反应过程,证明电极反应属不可逆反应。此外认为砷在电极上的浓集是由于形成了砷-金的金属间化合物。

Zinc plating bath containing Water Glass-DPE (III) is a new technique used in zinc plating. This bath possesses stability and may produce bright deposit. It compares favourably with cyanide zinc plating. The fundamental principles are studied qualitatively and semi-quantitatively employing techniques of single linear sweep, cyclic voltammetry and polarography. The results indicate that electrode reaction is controlled both by the rates of electron transfer and the preceding chemical reaction. The electroactive...

Zinc plating bath containing Water Glass-DPE (III) is a new technique used in zinc plating. This bath possesses stability and may produce bright deposit. It compares favourably with cyanide zinc plating. The fundamental principles are studied qualitatively and semi-quantitatively employing techniques of single linear sweep, cyclic voltammetry and polarography. The results indicate that electrode reaction is controlled both by the rates of electron transfer and the preceding chemical reaction. The electroactive species, as in the case of alkaline zincate plating, is Zn(OH)_2 Or Zn(OH)_3~-. The reason why water glass can enhance the cathodic polarization is due to the formation of mixed ligand complexes.

水玻璃锌酸盐镀锌是一种镀锌新工艺。该镀液性能稳定,镀层质量优良,可与氰化物镀液媲美。本文用动电位极化曲线法,循环伏安法以及极谱等方法对水玻璃碱性镀锌原理进行了定性和半定量的研究。实验结果表明:锌在水玻璃碱性液中电沉积的电活性粒子仍然是Zn(oH)_2、Zn(oH)_3~-,而且电沉积反应受电化学步骤和前置转化步骤共同控制。水玻璃增大镀液的阴极极化作用是由于锌能与硅结合成混合配体络合物的缘故。

The anodic stripping voltammetry of trace amounts of germanium on the gold film deposited on a glassy graphite electrode was reported. In boric acid buffer solution, at pH 10, two peaks of stripping current of germanium appear at -0.90 V and-0.17V (vs. 1N Ag-AgCl)respectively, the first peak is used for quantitative analysis. A linear relationship exists between the peak height and the concentration of germanium in the range of 1.0×10~(-8)~1.0×10~(-6)M. The detection limit is about 5.0×10~(-9)M(or 0.36 ppb)....

The anodic stripping voltammetry of trace amounts of germanium on the gold film deposited on a glassy graphite electrode was reported. In boric acid buffer solution, at pH 10, two peaks of stripping current of germanium appear at -0.90 V and-0.17V (vs. 1N Ag-AgCl)respectively, the first peak is used for quantitative analysis. A linear relationship exists between the peak height and the concentration of germanium in the range of 1.0×10~(-8)~1.0×10~(-6)M. The detection limit is about 5.0×10~(-9)M(or 0.36 ppb). We have further studied the electrode process by means of triangle cyclic voltammetry and proved that the electrode reaction is irreversible and show that the first peak is due to the oxidation of metallic germanium to divalent germanium ion and the second peak due to the oxidation of divalent ions to tetravalent ions. The deposition of germanium on the gold film electrode is possibly due to the formation of an alloy of germanium and gold.

本文报道了痕量锗在玻璃石墨电极为基体的金膜电极上的阳极溶出伏安法.找出在pH10的硼砂缓冲溶液中于-1.90V和-1.17V(对1NAg-AgCl)左右出现两个溶出峰.取第一峰高为定量分析的基础.锗的浓度在1.0×10~(-8)~1.0×10~(-6)M范围内有良好的线性关系.检出下限为5.0×10~(-9)M,相当于0.36ppb.本文用三角波周期伏安法观察了电极反应过程,证明电极反应为不可逆反应,并确定第一峰为金属锗氧化为二价锗,第二峰为二价锗氧化为四价锗.此外认为锗在电极上的富集是由于形成了金锗合金.

 
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