Experimental investigation on high temperature wettability and structural behaviour of SAW fluxes using MgO–TiO2–SiO2 and Al2O3–MgO–SiO2 flux system

To establish the relationship between wettability and structure with the change in SAW flux composition, the contact angle measurement study was performed at 1700 K. For MgO–TiO₂–SiO₂ and Al₂O₃–MgO–SiO₂ flux system the wetting behaviour was studied by evaluating the contact angle as well as surface tension properties. Sessile drop method was used to determine the wetting properties of SAW fluxes. Twenty-one SAW fluxes were designed & developed by applying mixture design approach of design of experiments. Chemical, phase and structural properties of SAW fluxes were measured using modern techniques such as X-ray fluorescence (XRF), X-ray diffraction (XRD) & Fourier Transform Infra-red spectroscopy (FTIR). As per the calculated contact angle value, different surface tension values for MgO–TiO₂–SiO₂ and Al₂O₃–MgO–SiO₂ flux system was calculated using Young's & Boni's equations. Using Dupre's equation the adhesion energy for twenty-one basic fluxes was also calculated. Measured contact angle value increased with increase in the TiO₂/MgO & TiO₂/Al₂O₃ flux ratio. Lower contact angle gives higher wettability between the flux and the heating substrate. With increase of TiO₂/SiO₂ ratio up to 1.5 to 2.0 the calculated surface tension value is decreasing while after that it is increased with increase in TiO₂/SiO₂ ratio.     

Reactive wetting behavior and mechanism of AlN ceramic by CuNi-Xwt%Ti active filler metal

In order to propel the application of the developed CuNi-Xwt%Ti active filler metal in AlN brazing and get the universal reactive wetting mechanism between liquid metal and solid ceramic, the reactive wetting behavior and mechanism of AlN ceramic by CuNi-Xwt%Ti active filler metal were investigated. The results indicate that, with the increasing Ti content, surface tension for liquid CuNi-Xwt%Ti filler metal increases at low-temperature interval, but very similar at high-temperature interval, which influence the wetting behavior on AlN ceramic obviously. CuNi/AlN is the typical non-reactive wetting system, the wetting process including rapid wetting stage and stable stage. The wettability is depended on surface tension of the liquid CuNi filler metal completely. However, the wetting process of CuNi-8wt.%Ti/AlN and CuNi-16 wt%Ti/AlN reactive wetting system is composed by three stages, which are rapid wetting stage decided by surface tension, slow wetting stage caused by interfacial reaction and stable stage. For CuNi-8wt.%Ti/AlN and CuNi-16 wt%Ti/AlN reactive wetting system, although the surface tension of liquid filler metal is the only factor to influence the instant wetting angle θ₀ at rapid wetting stage, the reduced free energy caused by interfacial reaction at slow wetting stage plays the decisive role in influencing the final wettability.     

湿法磷酸净化脱砷的研究现状

随着食品、医药及电子行业的不断发展，磷酸及磷酸盐的市场需求量不断增大，并且对磷酸的品质要求也越来越高，尤其是对湿法磷酸中砷杂质的要求，湿法磷酸中砷的含量将直接影响其在磷精细化工领域的应用，因此湿法磷酸中砷的高效、安全去除是亟待解决的一大难题。本文主要对湿法净化磷酸脱砷技术的研究情况进行综述，比较了几种湿法净化磷酸脱砷工艺的优缺点，介绍了较常见的化学沉淀法、结晶法，以及新兴的电沉积法、垂直区域熔融法和微反应器脱砷工艺的应用前景，并指出这些新兴的脱砷工艺将成为今后湿法磷酸的净化脱砷的发展方向，如能解决将这些脱砷工艺在实际中的问题，将会对磷酸工业的发展提供一个更有力的支持。     

煤化工烟道气毒性成分对Chlorella pyrenoidosa生长和细胞成分的影响

探究煤化工烟道气中毒性成分对微藻的影响是利用微藻固定煤化工烟道气CO₂实现减排的关键。本文利用不同浓度的NaHS、Na₂SO₃和NH₃·H₂O培养Chlorella pyrenoidosa（C. pyrenoidosa），以探究煤化工烟道气主要毒性成分H₂S、SO₂和NH₃气体水溶物的毒性。实验结果表明：NaHS、Na₂SO₃和NH₃·H₂O浓度分别低于1mmol/(L·d)、40mmol/(L·d)和7mmol/(L·d)时对C. pyrenoidosa生长无抑制作用，而且Na₂SO₃[＜40mmol/(L·d)]会显著促进 C. pyrenoidosa的生长；NaHS 添加4mmol/(L·d)时会在生长初期抑制C. pyrenoidosa的生长，NH₃·H₂O添加35mmol/(L·d)则会直接造成藻细胞的破碎死亡。与对照组相比，NaHS和Na₂SO₃浓度分别低于1mmol/(L·d)、10mmol/(L·d)时对C. pyrenoidosa的细胞成分无影响；NaHS添加4mmol/(L·d)使藻蛋白含量提高7.13%；Na₂SO₃添加40mmol/(L·d)使藻蛋白降低13.45%，总糖含量提高42.90%；NH₃·H₂O的添加会使藻蛋白含量降低，总糖含量提高。微藻生物质整体蛋白质含量较高，可作为蛋白饲料来源。研究结果表明，C. pyrenoidosa对煤化工烟道气中的主要毒性气体有较好的耐受性，利用煤化工烟道气培养微藻具有可行性。     

小型特种精细化工过程自动化和信息化研究发展趋势探讨

针对采取小批量间歇性批次生产方式、工艺介质腐蚀性强、危险性大的小型特种精细化工生产工艺研究试验过程自动化、信息化程度不高，导致工艺研究试验中获取数据较少、过程机理研究不够透彻、人工操作多、安全风险高、研究试验消耗大及效率不高等问题，综述了期待通过智能控制、在线分析、模拟仿真和虚拟制造、工况监测及预测性维护以及信息管理和生产调度等关键技术的研究和应用，提高小型特种精细化工生产工艺过程的自动化和信息化程度，实现小型特种精细化工生产工艺过程的数字化、虚拟化和智能化，降低生产安全风险和试验消耗，提高小型特种精细化工生产工艺研究试验的成功率和效率，达到小型特种精细化工生产工艺过程的数字化设计和精准生产的目标。     

改良剂对重金属污染根际土壤理化性质影响的研究进展

针对现阶段土壤中重金属污染较为严重的问题及各类修复方法各有利弊的现状,分析了近年来相关学者对于改良剂对重金属污染根际土壤理化性质影响的研究进展,研究了常见有机和无机改良剂对重金属胁迫下根际土壤pH值、氧化还原电位(Eh)、酶活性、化学性质、微生物菌落种群等理化性质的影响以及对重金属的化学沉淀和溶解平衡的影响。后期应加强超富集植物与一般植物根际、非根际理化性质的差异研究;土壤中重金属种类及污染程度与根际土壤理化性质的关系研究;土壤中其他环境因子的影响以及根际土壤中重金属的作用机理方面的研究。     

用于水质净化的氧化石墨烯膜研究进展

氧化石墨烯膜具有超高的水通量、可控的层间距以及卓越的分离性能，这些优异的特性使氧化石墨烯膜有望成为新一代膜材料并用于水环境中物质的精确分离。对氧化石墨烯膜的研究已经取得了许多重要的成果，本文系统地阐述了用于水质净化的氧化石墨烯膜的结构特性和构效关系，总结了氧化石墨烯膜典型的制备方法，重点介绍了氧化石墨烯膜的改性方式，概述了氧化石墨烯膜在多种水环境中的应用，总结并展望了氧化石墨烯膜的发展方向，为设计和合成高性能氧化石墨烯膜用于水质净化提供新的思路。     

Reproducible,biocompatible medical materials from biologically derived polysaccharides: Processing and Characterization

Natural polysaccharides like chitosan and dextran have garnered considerable interest in biomedical applications due to their biocompatibility, biodegradability, and nontoxicity. Nonetheless, the development of a reproducible class of medical devices from these materials is challenging and has had limited success. Chitosan and dextran are inherently variable and synthesis using these materials is prone to inconsistencies. In this study, we put forward a robust product development regimen that allows these natural materials to be developed into a reproducible class of biomaterials. First, an array of validated characterization methods (Proton Nuclear Magnetic Resonance, titrations, Ultraviolet spectroscopy, Size Exclusion Chromatography—Multi-Angle Light Scattering, Size Exclusion Chromatography—Refractive Index, and proprietary methods) were developed that allowed rigorous specifications to be set for unprocessed chitosan and dextran, chitosan and dextran intermediates, and chemically modified materials—acrylated chitosan (aCHN) and oxidized dextran (oDEX). Second, a robust and reproducible synthesis scheme involving various in-process controls was developed to chemically modify the unprocessed polysaccharides. Third, purification methods to remove byproducts and low-molecular-weight impurities for both aCHN and oDEX were developed. The study presents a viable strategy for converting variable, natural materials into a reproducible class of biomaterials that can be applied in various biomedical applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48454.     

Synthesis method of novel Gd2O3@Fe3O4 nanocomposite modified by dextrose capping agent

In current study, gadolinium oxide was heterogeneously formed on the surface of iron oxide nanoparticles and further modified with dextrose capping agent to be used in biomedical applications, especially for contrast enhancement in MR images. First, two types of iron oxide nanoparticles were prepared at 25 and 80 ^°C via simple coprecipitaion method. Then, gadolinium oxide nanoparticles were synthesized through a consecutive precipitation process on previously formed iron oxide seeds in an aqueous media and subsequent annealing at 300 ^°C. Finally, dextrose was used as capping agent to stabilize nanocomposites in a colloidal suspension. X-ray diffraction (XRD), Scanning and Transmission electron microscopy, Dynamic Laser Scattering (DLS), Fourier-Transform Infrared Spectroscopy (FTIR), and Magnetometery (VSM) techniques were employed for nanocomposites investigation and MTT-assay method used for viability assessment of colloidal samples. Measurements based on Scherrer equation from XRD patterns showed that increasing coprecipitation temperature resulted bigger iron oxide crystallites. The iron oxide crystallite size was increased from 15.1 to 28.1 nm. Precipitation process led to gadolinium oxide formation with 30.7 and 38.8 nm crystallite sizes, respectively. TEM images revealed that iron oxide agglomerates were encapsulated in gadolinium oxide surroundings. Hydrodynamic size of the coated nanoparticles with dextrose was 208 and 247 nm. In VSM examinations, nanocomposites did not display coercive field and the saturation magnetization was 1.93 emu/g. MTT-assay results showed 80% viability in 285 μg nanocomposites containing 96.9 μg [Fe] and 11.4 μg [Gd].     

Surface engineering of CeO2–TiO2 composite electrode for enhanced electron transport characteristics and alkaline hydrogen evolution reaction

Herein, we report the fine tuning of electrocatalytic characteristics of CeO₂–TiO₂ composite by surface engineering to reduce overpotential and to improve exchange current density for enhanced alkaline hydrogen evolution reaction (HER). The enhanced electrocatalytic activity of the surface engineered CeO₂–TiO₂ composite through Ni and P decoration is attributed to the improved electron transport ability. The surface roughness characteristics and surface composition of electroactive species are tuned to generate high electronic conductivity on the surface engineered composite electrode surface. The developed hard electrode with leptokurtic surface (S_ku > 3) exhibited a high average roughness value (Sa) of 3 μm due to incorporation of the mesoporous catalyst material into it. Tuning of a compact and continuous electrode surface with critical composition of elements Ni (52 at.%), P (20 at.%), Ce (9 at.%) and Ti (8 at.%) furnishes the high conductivity (contact potential difference = 0.83 V) to the electrode. The developed electrode with surface engineered CeO₂–TiO₂ catalyst exhibited a low overpotential of −111 mV (at a high current density of 250 mA cm⁻²) and high exchange current density (1.6 × 10⁻¹ mA cm⁻²) with low charge transfer resistance (615 Ω cm²). High electrocatalytic activity and stability of the surface engineered CeO₂–TiO₂ catalyst electrode during alkaline (32 w/v.% NaOH) HER ensure its promising performance and applicability for long term HER.