三聚硫氰酸单钠盐的制备及应用研究进展

三聚硫氰酸单钠盐是一种新型的多官能团化精细化学品。介绍了三聚硫氰酸单钠盐的制备方法,以及其在橡胶硫化、橡胶与金属的硫化粘合等领域的应用研究进展。     

Fabrication of bacterial cellulose with high efficient loading of Ag and TiO2 nanoparticles for removing organic dyes

As a new advanced oxidation technology, photocatalytic technology has broad application prospects in the field of wastewater treatment. However, in the actual use process, there will be difficulties in catalyst recovery and reuse. This article successfully prepared bacterial cellulose (BC) loaded silver and titanium dioxide nanoparticles (Ag-plated TiO₂/BC composite pellicle) by in situ embedding method. BC not only works as the carrier to load TiO₂ and Ag NPs but also adsorbs dyes to promote the reaction. As a reusable photocatalytic film, it is convenient to use and recycle in terms of testing and characterization compared with powders. The results show that Ag and TiO₂ nanoparticles were closely embedded in BC. We evaluated the photocatalytic degradation performance of the catalyst on methylene blue (MB), active red X-3B, and Rhodamine B. When the reaction time was 2 h, the dye removal rates were 71%, 68%, and 82.6%. At the same time, through the inhibition zone experiment, it was found that the material has a certain inhibitory effect on both Escherichia coli and Staphylococcus aureus. Therefore, the supported catalyst prepared by this method has the advantages of high catalytic activity, relatively stable property, easy recovery, and tailorability, making it potentially applicable in sewage post-treatment links.     

镀液温度实时控制系统的设计与实现

针对镀液温度变化的非线性和滞后性,设计了采用专家规则的镀液温度实时控制系统。该系统在实时监测的基础上,构建了综合评判镀液温度偏差和镀液温度偏差变化率的专家规则,实现了镀液温度的自适应快速调节。仿真分析结果表明,该系统克服了非线性和滞后性的不良影响,能够实现镀液温度的实时控制。     

SiC nanoparticles incorporation in electroless NiP-Graphene oxide nanocomposite coatings

The presence of SiC nanoparticles within the Graphene oxide (GO) incorporated electroless deposited NiP layers (NiP-GO) on carbon steel substrate was studied in this work. The effect of co-deposition of GO nanoplatelets and/or SiC nanoparticles on the morphology and structure of the heat-treated NiP coatings were investigated by scanning electron microscope and X-ray diffraction, respectively. The results revealed that the heat-treated NiP and NiP–SiC coatings consisted of Ni and Ni₃P phases, whereas the NiP-GO also contains the intermediated Ni₂P and Ni₁₂P₅ metastable phases due to the incomplete precipitation of Ni₃P. Such metastable phases are significantly decreased by the incorporation of SiC nanoparticles in NiP-GO coatings. The mechanical properties of the coatings were characterized by microhardness measurement and “pin on disk” wear test. The corrosion tests were conducted in aqueous 3.5 %wt NaCl using electrochemical measurement for Ni–P, NiP-GO, NiP–SiC, and NiP-GO-xSiC coatings. By co-deposition of SiC nanoparticles, the hardness of NiP-GO is significantly increased and the wear loss is reduced, especially at a high sliding distance during the wear test. The corrosion behavior of the NiP-GO coatings containing different amounts of SiC nanoparticles has been investigated.     

A highly active composite electrocatalyst Ni–Fe–P–Nb2O5/NF for overall water splitting

This work demonstrates a facile Nb₂O₅-decorated electrocatalyst to prepare cost-effective Ni–Fe–P–Nb₂O₅/NF and compared HER & OER performance in alkaline media. The prepared electrocatalyst presented an outstanding electrocatalytic performance towards hydrogen evolution reaction, which required a quite low overpotential of 39.05 mV at the current density of ?10 mA cm^?2 in 1 M KOH electrolyte. Moreover, the Ni–Fe–P–Nb₂O₅/NF catalyst also has excellent oxygen evolution efficiency, which needs only 322 mV to reach the current density of 50 mA cm^?2. Furthermore, its electrocatalytic performance towards overall water splitting worked as both cathode and anode achieved a quite low potential of 1.56 V (10 mA cm^?2).     

Pre-activation of SBA-15 intermediate barriers with Pd nuclei to increase thermal and mechanical resistances of pore-plated Pd-membranes

Thermal and mechanical resistances of palladium composite membranes prepared by Electroless Pore-Plating (ELP-PP) and containing SBA-15 as intermediate layer were improved by doping the silica material with Pd nuclei before its incorporation on the composite membrane. Textural properties of synthesized SBA-15 materials (both raw and doped ones) were analyzed by XRD, N₂ adsorption-desorption at 77 K and TEM, while the main properties of the composite membrane were determined by SEM and gravimetric analyses. Moreover, membrane permeation tests were also carried out with pure gases, hydrogen and nitrogen, and binary mixtures of them at temperature of 400 °C and pressure driving forces in the range of 0.5–2.5 bar. The use of bare SBA-15 intermediate layer leads to the appearance of cracks on the Pd layer during permeation experiments at high temperature. In contrast, the use of Pd-doped SBA-15 particles avoids this problem, thus improving both thermal and mechanical resistances of the composite ELP-PP Pd-membrane. Following this preparation method, an estimated Pd thickness of 7.1 μm was obtained, reaching a hydrogen permeance of 3.81·10^?4 mol s^?1 m^?2 Pa^?0.5 and ensuring an ideal H₂/N₂ separation factor higher than 2550 at 400 °C.     

Ni-Zn-P镀层在黏液形成菌中的结垢和腐蚀特性

利用化学镀层对换热面常用的碳钢材料进行表面改性,得到晶胞细致的Ni-Zn-P镀层。将得到的Ni-Zn-P试样与碳钢试样、Ni-P试样进行比较。在黏液形成菌菌悬液中进行微生物污垢和腐蚀实验,进而分析3种试样的抗微生物污垢特性和腐蚀特性。利用称重法记录3种试样的污垢沉积变化情况和光电比浊法记录黏液形成菌的生长情况。利用扫描电镜观察试样在污垢静置实验后的表面形貌,分析比较实验前后表面形貌的变化。利用电化学方法研究试样在黏液形成菌菌悬液中的腐蚀情况。实验结果表明,Ni-Zn-P镀层抗微生物污垢特性和耐腐蚀性稍好于Ni-P镀层,Ni-Zn-P镀层表面微生物污垢附着量相较于Ni-P镀层和碳钢分别减小24.1%和67.7%,Ni-Zn-P镀层表面腐蚀失重量相较于Ni-P镀层和碳钢分别减小5%和84.6%。由于Ni-Zn-P镀层的保护,碳钢表面抗微生物污垢特性和耐腐蚀性得到明显提高。     

Coating the porous Al2O3 substrate with a natural mineral of Nontronite-15A for fabrication of hydrogen-permeable palladium membranes

Substrate surface modification is a key pretreatment during fabrication of composite palladium membranes for hydrogen purification in hydrogen energy applications. The suspension of a natural porous material, Nontronite-15A mineral, without any organic additives was employed in dip-coating of the porous Al₂O₃ substrate. The Nontronite-15A mineral was characterized by SEM, XRD, TG−DSC and granulometry analysis. The surface and cross-section of the coated porous Al₂O₃ tubes were observed by SEM, and their pore size distribution and nitrogen flux were also measured. Palladium membranes were fabricated over the coated Al₂O₃ tubes by a suction-assisted electroless plating. The optimal loading amount of the Nontronite-15A mineral is just to fill in and level up the surface cavities of the Al₂O₃ substrate rather than to form an extra continuous layer. A thin and selective palladium membrane was successfully obtained, and its permeation performances were tested. The kinetic analyses on the hydrogen flux indicate that the hydrogen permeation behavior exhibits typical characteristics for most of the palladium membranes. During the stability test at 450 °C for 192 h, no membrane damage was detected, and the hydrogen flux increased slightly.     

Enhancement of oxidation and wear resistance of Fe-based amorphous coatings by surface modification of feedstock powders

Surface oxidation of the in-flight powders during the preparation of amorphous coatings in high velocity oxygen fuel process causes the formation of oxygen-rich intersplat regions. These regions are brittle in nature and can dramatically deteriorate the mechanical performance of the coatings. To solve this problem, the starting FeCrMoCBY amorphous feedstock powders were modified by electroless plating a thin layer of Ni–W–P amorphous phase. It was found that the covering of the Ni–W–P layer can significantly reduce the oxygen content in the resultant Fe-based amorphous coatings. The wear resistance of the coatings with and without the modification of Ni–W–P thin layer was comparatively studied by ball-on-disk wear tests against Si₃N₄ counterpart in air. It revealed that the wear of two types of coatings follows the same oxidation wear mechanism but the modified coating exhibits much better wear resistance due to the improved oxidation resistance.     

Microstructure and properties of open-cell Ni–Sn–P alloy foams prepared by electroless plating

In this study, open-cell Ni–Sn–P alloy foams were prepared by electroless plating. The influence of tin content on the surface morphology and properties of Ni–Sn–P alloy foams were investigated. The surface structure of Ni–Sn–P alloy foams became more uniform and compact with the increase of Sn content. The X-ray diffraction result showed that Ni–Sn–P alloy foams gradually transformed from an amorphous structure into crystallization with the increase of heat-treatment temperature. The introduction of Sn significantly enhanced the corrosion resistance of Ni–P coatings in 3.5 wt% NaCl solution, the corrosion current density decreased from 5.022 to 0.805 μA/cm² and the corrosion potential shifted positively from −0.423 to −0.294 V after adding 5.96 wt% Sn to Ni–P coatings. However, the corrosion resistance of Ni–Sn–P foams was deteriorated after heat treatment. Adding Sn to the Ni–P system slightly weakened the compressive strength of Ni–P binary foams. Nevertheless, significant improvement in the antioxidant performance of Ni–Sn–P alloy foams was indicated by the reduction of the mass change rate in that the mass change rate of Ni–P foams obviously reduced from 5.15% to 0.25% after adding 5.96 wt% Sn.