钨钴硬质合金电化学蚀刻加工研究

对YG6硬质合金电化学蚀刻工艺进行了研究,提出了采用光致抗蚀剂作保护膜,在生成一定钝化膜的情况下进行电化学蚀刻的方法.在一定的蚀刻深度范围内,该工艺的可控性好、腐蚀区表面质量较好.     

Electrochemical release testing of a stainless steel in a glucose solution using thin layer activation

The contamination of consumer products, e.g. food, during production, storage and/or transport, due to release of chemicals caused by contact with technical components is of some concern. Various methods can be used to study the release of these chemicals. These include those using radiotracers, such as thin layer activation (TLA). A dedicated facility combining TLA with electrochemical tests is presented. Its use is illustrated with Ni and Cr release during electrochemical testing of 316L stainless steel in a glucose solution. TLA offers various advantages, which include area selectivity, high sensitivity, and the possibility for in situ and on-line monitoring of elements. Due to the complementarity of TLA with the conventional electrochemical methods it contributes to a better understanding of the underlying release processes. Additionally, the usefulness of TLA to develop more reliable test methodology is indicated.     

A组分变化对AB2型储氢合金组织结构及电化学性能的影响

设计了两种成分AB2型合金,（Zr1-XTiX）（NiVMnCo）2＋α,采用XRD、SEM、TEM以及电化学性能测试方法分别对它们的铸态、快淬态及快淬态经过773 K、973 K和1 173 K退火处理的合金进行研究,结果表明,在AB2型储氢合金中加入少量Ti,可以增加电极的放电容量,提高循环寿命。熔体旋转快淬制备的非晶态合金电极的电化学性能差。快淬样品经过退火后,可获得纳米晶结构,能够大幅度提高电极材料的放电容量（370 mAh/g）和循环寿命（300次循环后容量衰减3%）。     

Electrochemical oxidation analysis for dressing bronze-bonded diamond grinding wheels

Electrochemical dressing of fine-grained metal-bonded diamond grinding wheels enables to grind hard and brittle materials in the ductile mode. Optical surfaces can be manufactured by grinding, which reduces the need for subsequent, time-consuming polishing work. When using metal-bonded grinding wheels, the emerging oxides regulate the electrochemical dissolution. Bronze-bonded grinding wheels are more suitable for grinding cemented carbides and ceramics than iron-bonded grinding wheels, as it is easier to modify their chemical composition to suit a specific grinding task. They can also be sintered at lower temperatures, which reduces the risk of thermal damage to the diamond. In this paper, the dissolution and the oxidation of different bronze alloys are characterized for the electrochemical dressing process. The relevant evaluation criteria are the oxide layer thickness, the electrical behavior and the different emerging bronze alloy oxides. This work is funded by the German Research Association DFG within the Transregional Collaborative Research Center SFB/TR4 “Process Chains for the Replication of Complex Optical Elements”.     

Comparative study of bis-piperidiniummethyl-urea and mono-piperidiniummethyl-urea as volatile corrosion inhibitors for mild steel

Bis-piperidiniummethyl-urea (BPMU) and mono-piperidiniummethyl-urea (MPMU) were developed as novel volatile corrosion inhibitors (VCIs). Their vapor corrosion inhibition property was evaluated by volatile inhibiting sieve test (VIS) and vapor inhibiting ability test (VIA). Volatile weight-loss test in a closed space was used to compare their volatility. Electrochemical impedance spectroscopy of a volatile corrosion inhibitor monitor (VCIM) was applied to study the effect of BPMU and MPMU on the corrosion inhibition of mild steel in thin electrolyte layer. The results show that BPMU has the better protection effect compared with MPMU. Adsorption of BPMU and MPMU on steel surface was investigated by X-ray photoelectron spectroscopy (XPS). It was shown that one BPMU molecule has two N atoms to coordinate with one Fe atom, and that one MPMU molecule has one N atom to coordinate with one Fe atom. The quantum chemical parameters were obtained by PM3 semi-empirical method. BPMU has the smaller HOMO-LUMO energy gap and the smaller net positive charge intensities of 4N and 8N atoms in its molecule.     

用丝束电极研究SO_4~(2-)对纯铝缝隙腐蚀的影响

采用动电位极化和丝束电极技术测量了纯铝在2mol/L NaCl和2mol/L NaCl 0.8mol/L Na2SO4溶液中的极化曲线、缝隙内外的自腐蚀电位和电化学阻抗分布,研究了SO42-对铝缝隙腐蚀的影响。结果表明,在NaCl溶液中,缝隙内的铝为阳极、缝隙外为阴极;随浸泡时间增加,腐蚀不均匀性增加。加入Na2SO4后,减小了缝隙内外腐蚀电位差,显著降低了铝的腐蚀速度。Na2SO4是中性溶液中铝的吸附型缓蚀剂,延缓了缝隙腐蚀的发生。     

A novel electrochemical testing method and its use in the investigation of the self-repairing ability of temporarily protective oil coating

A novel electrochemical method using a wire beam electrode was developed to investigate self-repairing ability of temporarily protective oil coating. Results showed that inhibited oil coatings had the ability of self-repairing, and oil-soluble inhibitors had direct effect on the self-repairing ability of oil coating. The degradation processes that were related to the underfilm corrosion of oil coating could also be realized by investigating the self-repairing ability of oil coating.     

Electrochemical DNA biosensor for the detection of interaction between di[azino-di(5,6-azafluorene)-κ-NN′]dichlormanganous and DNA

A new Mn(II) complex of MnL₂Cl₂ (L = azino-di(5,6-azafluorene)-κ²-NN′) was synthesized and utilized as an electrochemical indicator for the determination of hepatitis B virus (HBV) based on its interaction with MnL₂Cl₂. The electrochemical behavior of interaction of MnL₂Cl₂ with salmon sperm DNA was investigated on glassy carbon electrode (GCE). In the presence of salmon sperm DNA, the peak current of [MnL₂]²⁺ was decreased and the peak potential was shifted positively without appearance of new peaks. The binding ratio between [MnL₂]²⁺ and salmon sperm DNA was calculated to be 2:1 and the binding constant was 3.72 × 10⁸ mol² L⁻². The extent of hybridization was evaluated on the basis of the difference between signals of [MnL₂]²⁺ with probe DNA before and after hybridization with complementary sequence. Control experiments performed with non-complementary and mismatch sequence demonstrated the good selectivity of the biosensor. With this approach, a sequence of the HBV could be quantified over the range from 1.76 × 10⁻⁸ to 1.07 × 10⁻⁶ mol L⁻¹, with a linear correlation of r = 0.9904 and a detection limit of 6.80 × 10⁻⁹ mol L⁻¹. Additionally, the binding mechanism was preliminarily discussed. The mode of interaction between MnL₂Cl₂ and DNA was found to be primary intercalation binding.     

Electrochemical deposition of polypyrrole/graphene oxide composite on microelectrodes towards tuning the electrochemical properties of neural probes

By exploiting the electrostatic interaction between positively charged pyrrole cation radicals and negatively charged graphene oxide (GO) sheets, we prepared polypyrrole/graphene oxide (PPy/GO) composite films by a one-step electrochemical process. We studied the effects of the polymerization current density and the GO content in electrolyte on the formation of PPy/GO coatings onto platinum neural microelectrode sites. As compared with pure PPy film, PPy/GO coatings show a rougher surface feature with micrometer-scale bulges. The impedance of the PPy/GO coated Pt electrode is only about 10% of the bare Pt electrode at the biological relevant 1 kHz, while the charge capacity density is more than two orders of the magnitude of the bare Pt electrode. Moreover, the PPy/GO coated Pt electrodes show higher performance than the PPy coated electrodes for the application of neural probe.     

Aptamer biosensor for label-free impedance spectroscopy detection of thrombin based on gold nanoparticles

This paper presents a simple electrochemical impedance spectroscopy (EIS) aptasensor based on an anti-thrombin-aptamer as a molecular recognition element. Improvement in sensitivity was achieved by utilizing gold nanoparticles (AuNPs), which were self-assembled on the surface of a bare electrode by using 1,6-Hexanedithiol as a medium. To quantify the amount of thrombin, changes in the interfacial electron transfer resistance (R_et) of the aptasensor were monitored using the redox couple of an [Fe(CN)₆]^3−/4− probe. The plot of (Reti−Ret₀)/Ret₀ against the logarithm of thrombin concentration is linear with over the range from 0.1 nM to 30 nM with a detection limit of 0.013 nM. Meanwhile, the packing density of aptamers was determined by cyclic voltammetric (CV) studies of redox cations (e.g., [Ru(NH₃)₆]³⁺) which were electrostatically bound to the DNA phosphate backbones. The results indicate that the total amount of aptamer probes immobilized on the gold nanoparticle surface is sixfold higher than that on the bare electrode. The aptasensor also showed good selectivity for thrombin without being affected by the presence of other proteins.