Effect of pickling process on removal of oxide layer on the surface of ferritic stainless steel

Oxide layer formed on stainless steel surface can result in a decrease in surface quality. Thus, it must be removed. In this paper, we investigated the effect of different pickling processes on removal of the oxide layer. Ferritic stainless steel was used as raw material. After it received annealing treatment, the components and structure of the oxide layer formed on its surface were studied. Then, the annealed stainless steel was pickled in hydrochloric acid solution system and mixed acid solution system, respectively. Results are as follows. The oxide layer on stainless steel surface has a thickness of 15–35?μm. With increase in hydrochloric acid concentration in hydrochloric acid pickling solution, the weight loss rate of stainless steel increases and is always greater than that in mixed acid pickling system. In addition, the surface of the stainless steel pickled in hydrochloric acid is smoother than that pickled in mixed acid. Furthermore, compared with channels in the oxide layer created during mixed acid pickling, those created during hydrochloric acid pickling are more, leading to shorter removal time. These results are important for increasing the pickling efficiency and improving the surface quality of stainless steel.     

Characterization of La0.995Ca0.005NbO4/Ni anode functional layer by electrophoretic deposition in a La0.995Ca0.005NbO4 electrolyte based PCFC

The Electrophoretic Deposition (EPD) technique has been applied to the preparation of a porous La_0.995Ca_0.005NbO₄/Ni composite anode layer, deposited on a porous pre-sintered La_0.995Ca_0.005NbO₄/Ni support. Powders of La_0.995Ca_0.005NbO₄ and NiO were suspended in a solution of acetylacetone, iodine and water. Selectivity in the composition of the deposited layer was analyzed as a function of the suspension compositions and deposition conditions. A quasi-symmetrical cell was produced by depositing La_0.995Ca_0.005NbO₄ electrolyte layer on the anode layer by EPD, and by applying a porous La_0.995Ca_0.005NbO₄/Ni counter electrode on the dense electrolyte layer by brushing. The performance of the electrodes was evaluated by electrochemical impedance spectroscopy in 3% wet H_2.     

Investigations of electrochemical double layer capacitor (EDLC) materials – a comparison of test methods

A comparison between various methods for determining the capacitance and resistance of electrochemical double layer capacitors (EDLC) with cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), galvanostatic charge‐discharge methods and cell voltage jump experiments are presented. Therefore, a commercially available electrochemical double layer capacitor was used. For the validation of the screw cell measurements the electrode foils were isolated and extracted from the commercial capacitor. The results support the adequacy of the screw cell tests for electrode materials on a laboratory scale. The comparison of methods shows in part strong differences. The reasons will therefore be discussed. Consequently, the determination of specific values requires methods which respect the influence of the actual tests or measurement frequency and exhibit the importance of an internationally accepted specification for electrochemical double layer capacitors material investigation.     

Multi-scale characteristics of magnesium potassium phosphate cement modified by metakaolin

Workability and early-ages mechanical properties are important indicators of magnesium potassium phosphate cement (MKPC) as a repair material. The effect of metakaolin (MK) on the setting time, fluidity and early-ages strength of MKPC paste was studied, and its influence mechanism was analyzed through pore structure, microstructure and nanomechanical properties. The results show that 10% and 20% of MK prolong the setting time of MKPC paste, but excessive MK shortens the setting time of MKPC paste. Meanwhile, incorporating MK reduces the fluidity of MKPC paste, and the early-ages strength of MKPC specimens increases when the substitution ratio of MK is 10%. When 10% of MK is incorporated to the MKPC paste, the 30-d shrinkage of the sample is only 69% of the control group. Meanwhile, a proper amount of MK can improve the pore structure of the MKPC specimen and make its microstructure denser by generating amorphous aluminosilicate phosphate gel. It is observed from the nano-scale characteristics that incorporating 10% MK can reduce the content of pore phase and unreacted MgO phase, and increase the volume fraction of hydration products.     

关于建筑工程转换层的施工技术探究

建筑物的不同结构形式相互连接的关键点是结构转换层。转换层不仅是结构下部分的封顶，还是结构上部分的基础部分，在建筑物体系中起着非常重要的连接作用，拥有直接的受力和传力，且造价较低，在建筑工程中应用广泛。结合实际工程案例，对建筑工程转换层的施工技术进行探讨和分析。     

A surface modification layer capable of tolerating substrate contamination on transparent electrodes of organic electronic devices

An organic molecule, hexaazatriphenylene hexacarbonitrile (HAT-CN), is found that it can be used not only as a hole-injecting material but also a surface modification material to clean contaminated substrate electrodes for the fabrication of organic electronic devices. As an example, HAT-CN can modify or “clean” indium-tin-oxide (ITO) anode surface in organic light-emitting diodes (OLEDs). Negative effect from ITO surface contamination on the electroluminescence performance of OLEDs can be dramatically reduced with this modification layer. As a result, the OLEDs with the same device architecture but with different ITO surface conditions, even with intentional contamination, can all exhibit substantially identical and superior electroluminescence performance. The surface modification function of this material is feasibly useful for the real fabrications of OLEDs as well as for advanced research on other organic electronic devices.     

EPR and Raman study of silicon layers obtained by gas detonation spraying

We demonstrate availability of gas detonation deposition spraying (GDS) to obtain silicon layers that can be used for production of solar cells. Silicon powder remaining as secondary raw material of silicon and/or silicon production is used during GDS. To study defects and structural perfection of initial powders and obtained layers, electron paramagnetic resonance (EPR) and Raman spectroscopy are used. It is shown that one part of EPR spectra displays resonances originating from different nearest-neighbor configurations of silicon dangling bonds, whereas an increase of the total number of paramagnetic defects in GDS silicon layer is related to the rise of conduction electrons or electrons filled band tail states. Thermal annealing of layers in hydrogen ambience further reduces the number of silicon dangling bonds owing to their passivation. Based on the results of X-ray diffraction, EPR and Raman spectroscopy it is assumed that the GDS Si layers are composed of randomly oriented and partially oxidized monocrystalline silicon grains. It is found that optical and photoelectric properties of the layers obtained indicate a possibility to apply them for solar cells production.     

Stability Indicating HPTLC Determination of Linezolid as Bulk Drug and in Pharmaceutical Dosage Form

Abstract

A simple, selective, precise, and stability-indicating high-performance thin layer chromatographic method of analysis of Linezolid both as a bulk drug and in formulations was developed and validated in pharmaceutical dosage form. The method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of toluene–acetone (5:5, v/v). This system was found to give compact spots for Linezolid (R_f value of 0.29 ± 0.01). Linezolid was subjected to acidic, alkali hydrolysis, oxidation, and photodegradation. The degraded products also were well separated from the pure drug. Densitometric analysis of Linezolid was conducted in the absorbance mode at 254 nm. The linear regression data for the calibration plots showed good linear relationship with r² = 0.997 ± 0.001 in the concentration range of 300–800 ng/spot. The mean value of correlation coefficient, slope, and intercept were 0.998 ± 0.003, 0.15 ± 0.009, and 19.52 ± 1.66 respectively. The method was validated for precision, accuracy, ruggedness, and recovery. The limits of detection and quantification were 20 ng/spot and 50 ng/spot, respectively. The drug undergoes degradation under acidic and basic conditions, oxidation and photo degradation. All the peaks of degraded product were resolved from the standard drug with significantly different R_f values. This indicates that the drug is susceptible to acid–base hydrolysis, oxidation, and photo degradation. Statistical analysis proves that the method is reproducible and selective for the estimation of the said drug. Because the method could effectively separate the drug from its degradation products, it can be used as a stability indicating one.     

Decalcification of activated paper sludge – Fly ash-Portland cement blended pastes in pure water

Decalcification in pure water of ternary Portland cement (TPC) pastes, containing thermally activated paper sludge and fly ash, has been evaluated from the leaching of Ca²⁺ in pure water at the temperature of 20 °C during 90 days. Monitoring of calcium loss showed that the leaching kinetics are controlled by diffusion. The degradation of the material over time is estimated from the calcium effective diffusivity. A similar study of plain ordinary Portland cement (OPC) pastes was carried out for comparison. The results showed lower effective diffusion coefficients of calcium in the case of the TPC pastes. This behaviour is related to its microstructure, which is denser than that of OPC as a result of the pozzolanic activity of both additions.