高压静电分选Ag与PET的实验研究

为了提高高压静电分选Ag与聚对苯二甲酸乙二醇酯(polyethylene terephthalate,简称PET)的效率,寻求可产生较佳分选效率的电压、转速、极间距和电晕线角度。采用自制的线辊式静电分选机,通过单因素实验和部分因子实验,研究了不同条件下Ag与PET的分选效率。结果表明:将Ag与PET从二者混合物中有效分选出来的电压为25~30k V、转速为60~75 r/min、极间距为60~70 mm、电晕极角度为50~60°;当电压为30 k V、转速为75 r/min、电晕极距离为70 mm和电晕极角度为60°时,Ag的分选效率达到了最大值为99.60%,PET的分选效率也达到了最大值为99.98%,为线辊式静电分选机结构设计与参数优化提供了参考。     

吸油烟机油烟捕集和空气性能的模拟与试验研究

应用计算流体动力学(CFD)模拟吸油烟机油烟捕集和空气性能,捕集结果和测量基本吻合。改滤网为分离器,使烟机油脂分离度和分离器占烟机分离度提高2.3%和15.8%,减少叶轮和蜗壳的清洗。计算的风量和功率与实验结果的误差分别为18.9%和8.4%。提出改进机箱空间,并采用空心叶轮和蜗壳后盖板挖槽方案。     

电子废弃物中贵重金属的回收技术研究

目前电子废弃物数量巨大,对生态环境产生了严重的危害,并且其中的贵重金属成分的潜在价值很高,所以,对电子废弃物中的贵重金属的回收迫在眉睫。总结了电子废弃物处理的传统技术,包括机械处理、火法和湿法冶金技术等。针对以上方法的特点及流程,从技术上和经济上分析其存在的问题,以及对环境造成的影响。另外,详细介绍了生物技术和超临界流体萃取技术在回收贵重金属方面的研究和发展趋势。最后,简要评述了国内电子废弃物处理所面临的问题,并提出了可能的解决方案。     

Improved method for analyzing the degradation of estrogens in water by solid-phase extraction coupled with ultra performance liquid chromatography-ultraviolet detection

We established an improved method for the determination of four estrogens including estriol (E3), 17 -estradiol (E2), 17 -ethynylestrodiol (EE2) and estrone (E1) in water. The method consisted of solid-phase extraction (0.5 L water) and subsequent analysis of analytes by ultra-performance liquid chromatography (UPLC) with an ultraviolet detector (UVD). Base-line separation was achieved for all studied estrogens using a column (50 mm 2.1 mm) packed with 1.7 m particle size stationary phase. Recovery was higher than 88% and detection limits ranged between 12.5–23.7 ng/L for the four estrogens, with the RSD ranging from 7% to 11%. The method was successfully applied to determine E2 and EE2 in simulated natural water, which found that about 70% of E2 was degraded (with a half-life of about 30 hr) within 48 hr and about 55% of EE2 was degraded (with a half-life of about 36 hr). Low levels of E1 were found, however E3 was undetectable during the process.     

Synthesis and adsorption performance of lead ion-imprinted micro-beads with combination of two functional monomers

Synthesis and high adsorption and selectivity performance of lead ion-imprinted micro-beads with combination of two functional monomers.     

分离高浓度污泥产酸发酵液的自生动态膜形成机制

采用自生生物动态膜分离高浓度污泥发酵液,研究了动态膜的形成过程及其对污泥发酵液的分离效果.结果表明,自生动态膜的形成过程受污泥浓度的影响较小,污泥浓度仅影响初始膜通量,不影响稳定时的膜通量.膜通量随着滤布孔径和搅拌速度的增大而增大.动态膜的形成过程符合死端过滤模型,分别由以下4个过程构成:先通过与膜基材孔径相似的污泥颗粒堵塞膜基材孔,其后在膜基材上形成单层污泥,进而在膜基材上形成多层污泥,最后,大颗粒污泥继续沉积到污泥层上.动态膜形成后,对污泥颗粒和溶解性COD(SCOD)的截留率分别为98%和28%,对挥发性脂肪酸(volatile fatty acids,VFAs)的渗透率在82%以上,胞外聚合物(extracellular polymeric substances,EPS)中的蛋白质是动态膜的主要成分.     

BiOCl-(NH4)3PW12O40复合光催化剂制备及其光催化降解污染物机制

光生电子和空穴的分离效率是影响光催化性能的重要因素.氯氧铋是典型的层状纳米光催化剂,却因光生电子和空穴的快速复合所表现出的低量子效率而受到使用限制.本文通过两步的水热法合成了BiOCl-(NH_4)_3PW_(12)O_(40)复合光催化剂.以甲基橙(MO)为模拟污染物进行光催化活性测试.结果表明,在氙灯模拟的太阳光照射下,Bi与W的原子比为1∶1时,其催化效果最佳.通过自由基猝灭实验对催化剂光降解MO的催化机制进行了研究,发现BiOCl是由空穴,羟基自由基和超氧自由基共同作用来对MO进行降解;而复合催化剂则主要以羟基自由基和超氧自由基为活性物种来降解MO.通过对反应前后的催化剂进行XPS分析,证明了磷钨酸铵可以接收BiOCl产生的光生电子.通过光电流测试,表明复合光催化剂的光生电子的转移和分离效率有了较大的提高,从而提高了光催化活性.     

新OG系统旋流脱水器气液分离特性数值研究

根据旋流脱水器的内部流动特性,基于欧拉-拉格朗日方法,对旋流脱水器内部气液两相流动进行了数值计算和分析,研究了液滴直径、进口质量含气率和湍流扩散效应对流场分布、脱水效率、出口质量含气率和出口液滴粒度分布的影响.结果表明：当质量流量一定时,旋流脱水器进出口压降随着进口质量含气率的增加而显著提高.对于单一直径的液滴,在不考虑湍流扩散效应的情况下,脱水效率随进口质量含气率的增加而增加.当考虑湍流扩散效应时,对于直径较小的液滴（0.1~1μm）,这种规律刚好是相反的,连续相速度的增加提升了湍流扩散速度,使湍流运动更加紊乱,但脱水效率高于不考虑湍流扩散效应时的计算结果.在混合粒径条件下,随着进口质量含气率的增加,脱水效率和出口质量含气率增加,计算表明湍流扩散效应有利于混合直径液滴的分离.随着进口质量含气率的增加,液滴质量分数的峰值逐渐向小粒径方向移动,粒径分布范围逐渐减小.     

Role of NO in Hg oxidation over a commercial selective catalytic reduction catalyst V2O5–WO3/TiO2

Experiments were conducted in a fixed-bed reactor that contained a commercial catalyst, V₂O₅–WO₃/TiO₂, to investigate mercury oxidation in the presence of NO and O₂. Mercury oxidation was improved by NO, and the efficiency was increased by simultaneously adding NO and O₂. With NO and O₂ pretreatment at 350°C, the catalyst exhibited higher catalytic activity for Hg⁰ oxidation, whereas NO pretreatment did not exert a noticeable effect. Decreasing the reaction temperature boosted the performance of the catalyst treated with NO and O₂. Although NO promoted Hg⁰ oxidation at the very beginning, excessive NO counteracted this effect. The results show that NO plays different roles in Hg⁰ oxidation; NO in the gaseous phase may directly react with the adsorbed Hg⁰, but excessive NO hinders Hg⁰ adsorption. The adsorbed NO was converted into active nitrogen species (e.g., NO₂) with oxygen, which facilitated the adsorption and oxidation of Hg⁰. Hg⁰ was oxidized by NO mainly by the Eley–Rideal mechanism. The Hg⁰ temperature-programmed desorption experiment showed that weakly adsorbed mercury species were converted to strongly bound ones in the presence of NO and O₂.     

Bioinspired and biomimetic membranes for water purification and chemical separation: A review

•The history of biological and artificial water channels is reviewed. •A comprehensive channel characterization platform is introduced. •Rationale designs and fabrications of biomimetic membranes are summarized. •The advantages, limitations, and challenges of biomimetic membranes are discussed. •The prospect and scalable solutions of biomimetic membranes are discussed. Bioinspired and biomimetic membranes that contain biological transport channels or attain their structural designs from biological systems have been through a remarkable development over the last two decades. They take advantage of the exceptional transport properties of those channels, thus possess both high permeability and selectivity, and have emerged as a promising solution to existing membranes. Since the discovery of biological water channel proteins aquaporins (AQPs), extensive efforts have been made to utilize them to make separation membranes–AQP-based membranes, which have been commercialized. The exploration of AQPs’ unique structures and transport properties has resulted in the evolution of biomimetic separation materials from protein-based to artificial channel-based membranes. However, large-scale, defect-free biomimetic membranes are not available yet. This paper reviews the state-of-the-art biomimetic membranes and summarizes the latest research progress, platform, and methodology. Then it critically discusses the potential routes of this emerging area toward scalable applications. We conclude that an appropriate combination of bioinspired concepts and molecular engineering with mature polymer industry may lead to scalable polymeric membranes with intrinsic selective channels, which will gain the merit of both desired selectivity and scalability.