Preparation of Ag3PO4/CoWO4 S-scheme heterojunction and study on sonocatalytic degradation of tetracycline

In this study, 0.6Ag₃PO₄/CoWO₄ composites were synthesized by hydrothermal method. The prepared materials were systematically characterized by techniques of scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), N₂ adsorption/desorption, and UV–vis diffuse reflectance spectrum (DRS). Furthermore, the sonocatalytic degradation performance of 0.6Ag₃PO₄/CoWO₄ composites towards tetracycline (TC) was investigated under ultrasonic radiation. The results showed that, combined with potassium persulfate (K₂S₂O₈), the 0.6Ag₃PO₄/CoWO₄ composites achieved a high sonocatalytic degradation efficiency of 97.89 % within 10 min, which was much better than bare Ag₃PO₄ or CoWO₄. By measuring the electrochemical properties, it was proposed that the degradation mechanism of 0.6Ag₃PO₄/CoWO₄ is the formation of S-scheme heterojunction, which increases the separation efficiency of electron-hole pairs (e^--h⁺) and generates more electrons and holes, thereby enhancing the degradation activity. The scavenger experiments confirmed that hole (h⁺) was the primary active substance in degrading TC, and free radicals (OH) and superoxide anion radical (O₂^–) were auxiliary active substances. The results indicated that 0.6Ag₃PO₄/CoWO₄ nanocomposites could be used as an efficient and reliable sonocatalyst for wastewater treatment.     

核壳Fenton催化剂CuFe_2O_4@PDA-Cu的制备、表征及其活化H_2O_2降解染料的性能

为得到新型高效多相催化剂,有效去除废水中的染料,以Cu(Ac)_2与CuFe_2O_4@PDA为原料制备了催化剂CuFe_2O_4@PDA-Cu.通过IR、XRD、XPS、UV-Vis、DRS技术对催化剂的性能进行了表征,考察了温度、H_2O_2用量、催化剂用量、pH值、盐等对催化活性的影响.利用HPLC测定降解产物,采用自由基捕获和抑制实验进行机理验证,发现催化剂是核壳结构.温度升高、pH值升高、H_2O_2和催化剂用量的增加均有利于提高催化活性;氯化物、硫酸盐、硝酸盐和磷酸盐不影响催化效果,溴化物和亚硝酸盐降低了催化效果.得到的最优降解条件为:T=30℃,催化剂用量10mg·L~(-1),pH=9,过氧化氢用量10mmol·L~(-1),染料浓度30mg·L~(-1).最优条件下催化剂可循环使用4次以上;甲基橙、茜素红和罗丹明B的去除率为100%;染料R0213、O0118和B0115的去除率大于60%.降解产物有草酸、马来酸和CO_2.甲基橙、茜素红和罗丹明B降解后COD_(Mn)=2~4mg·L~(-1).水杨酸捕获·OH生成2.5-二羟基苯甲酸,叔丁醇抑制染料降解.结果表明,催化剂可活化H_2O_2产生·OH,·OH攻击染料分子开环降解直至矿化.该研究为开发高效多相催化剂,有效去除废水中的染料提供了科学依据.     

Hybrid Isothermal Model for the Ferrohydrodynamic Chemically Reactive Species

A hybrid isothermal model for the homogeneous-heterogeneous reactions in ferrohydrodynamic boundary layer flow is established. The characteristics of Newtonian heating and magnetic dipole in a ferrofluid due to a stretchable surface is analyzed for three chemical species. It is presumed that the isothermal cubic autocatalator kinetic gives the homogeneous reaction and the first order kinetics gives the heterogeneous (surface) reaction. The analysis is carried out for equal diffusion coefficients of all autocatalyst and reactions. Heat flux is examined by incorporating Fourier's law of heat conduction. Characteristics of materialized parameters on the magneto-thermomechanical coupling in the flow of a chemically reactive species are investigated. Further, the heat transfer rate and friction drag are depicted for the ferrohydrodynamic chemically reactive species. It is evident that the Schmidt number has increasing behavior on the rate of heat transfer in the boundary layer. Comparison with available results for specific cases is found an excellent agreement.     

HL-2M偏滤器CFC/CuCrZr靶板的非晶钎焊工艺研究

在采用商用的STEMET-1101非晶钎料、温度为710~750°C的真空钎焊下，对CFC/OFC(氯氟烃/无氧铜)复合块与CuCrZr(铬锆铜)的钎焊进行了研究。首先，通过X-射线衍射(XRD)和差式扫描量热分析对钎料的结构和熔化行为进行了表征；然后，通过光学显微镜、电子探针微分析和拉伸试验等方法对焊缝的组织形貌、元素成分分布、相结构和力学性能进行了分析；最后，通过高热负荷装置对CFC/OFC/CuCrZr钎焊模块的热疲劳性能进行测试。结果表明，在710~750°C钎焊温度内焊缝由Cu固溶体、(Cu, Ni)3P和Ni(Cu ,Cr)2P金属间化合物组成，焊缝平整无裂纹；特别是在750°C/15min情况下，抑制了焊缝金属间化合物的连续分布，OFC/CuCrZr的焊接强度大于OFC的抗拉强度，CuCrZr/CuCrZr的结合强度为210MPa，并呈现部分韧性断裂。在750°C/15min情况下制备的CFC/Cu/CuCrZr模块可以承受1000次7MW·m^-2的循环热负荷。     

Condensed Mode Cooling of Ethylene Polymerization in Fluidized Bed Reactors

This review gives an overview of the evolution of the technology of condensed mode cooling, primarily for the case of ethylene polymerization on supported catalysts in fluidized bed reactors. It is well known that this mode of heat removal is quite effective in allowing polyolefin manufacturers to increase significantly production rates. What is perhaps less well understood are all of the issues that, in addition to the effect of the latent heat of vaporization of injected liquid components, also have an impact on the rate of production and behavior of the reactor. However, the liquid components injected into the reactor can vaporize rapidly under full‐scale conditions, leaving behind several heavy components (with respect to ethylene) that have numerous effects on how the particles behave, on the reaction rate, and on fluidization, fouling, and other parameters related to reactor and process performance.     

Mechanical Properties Comparison of Various Ratios of L-Lactide Grafted Sisal Fibers and Untreated Sisal Fibers Reinforced Poly (lactic acid) Composites

Composites composed of the mixed fibers of L-lactide (LA) grafted sisal fiber (SF-g-LA) and untreated sisal fiber (USF) in a poly (lactic acid) (PLA) matrix were prepared with SF-g-LA/USF fibers ratios of 0, 1:9, 3:7, 5:5, 7:3, 9:1, and 1. The mechanical properties and the interfacial performance of the mixed SF reinforced PLA composites were investigated. The results of the study showed that the introduction of SF-g-LA improved the tensile strength, tensile modulus, flexural strength and flexural modulus of the mixed SF reinforced PLA composites compared with pure PLA or PLA composites with only USF, resulting from the improved interfacial adhesion between SF-g-LA and the PLA matrix. In addition, the introduction of some amount of USF enhanced the reinforcing efficiency of the mixed SF in the composites compared to the PLA composites with only SF-g-LA, owing to the good mechanical properties of USF itself. Furthermore, as for the tensile strength and tensile modulus of the mixed SF reinforced PLA composites, the optimal ratio of SF-g-LA and USF was 7:3, whereas for the flexural modulus of the mixed SF reinforced PLA composites, the optimal mixed ratio of SF-g-LA and USF was 3:7.     

石墨烯基吸附剂的设计及其对水中抗生素的去除

抗生素的大量使用,所带来的环境污染问题受到广泛关注。吸附法因去除效率高、普遍适用性强,呈现出广阔的应用前景,开发新型吸附剂是高效能吸附处理的关键。近年来石墨烯优良的物理和化学性质以及吸附性能,使其成为重要的抗生素吸附剂。由于石墨烯自身的局限性以及对石墨烯吸附剂处理效能和稳定性的要求,基于石墨烯设计开发了多种石墨烯基吸附材料。而目前基于水体中抗生素的石墨烯基复合材料的设计、合成及其吸附作用机制缺乏相关的系统性综述。本文综述了目前水体中抗生素的危害,针对石墨烯基复合吸附材料中,广泛关注的磁性石墨烯吸附剂、聚合物/石墨烯吸附剂、三维石墨烯凝胶和石墨烯/生物炭吸附剂的设计和制备方法进行了总结和概述,并阐述了石墨烯基吸附材料对水体中抗生素的主要吸附作用机制。最后,本文对石墨烯基吸附材料去除水体中抗生素未来的发展方向进行了展望。