Hg removal from flue gas over different zeolites modified by FeCl3

The elemental mercury removal abilities of three different zeolites (NaA, NaX, HZSM-5) impregnated with iron(III) chloride were studied on a lab-scale fixed-bed reactor. X-ray diffraction, nitrogen adsorption porosimetry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and temperature programmed desorption (TPD) analyses were used to investigate the physicochemical properties. Results indicated that the pore structure and active chloride species on the surface of the samples are the key factors for physisorption and oxidation of Hg⁰, respectively. Relatively high surface area and micropore volume are beneficial to efficient mercury adsorption. The active Cl species generated on the surface of the samples were effective oxidants able to convert elemental mercury (Hg⁰) into oxidized mercury (Hg^2 +). The crystallization of NaCl due to the ion exchange effect during the impregnation of NaA and NaX reduced the number of active Cl species on the surface, and restricted the physisorption of Hg⁰. Therefore, the Hg⁰ removal efficiencies of the samples were inhibited. The TPD analysis revealed that the species of mercury on the surface of FeCl₃–HZSM-5 was mainly in the form of mercuric chloride (HgCl₂), while on FeCl₃–NaX and FeCl₃–NaA it was mainly mercuric oxide (HgO).     

空气资源评估方法及其在城市环境总体规划中的应用

从空气污染气候学的角度,提出了空气资源禀赋的概念、评估方法、等级划分及分区管控的理念.同时,以宜昌城市环境总体规划为例,利用MM5耦合CALMET模式对大气环境系统进行解析,计算了宜昌市域范围高时空分辨率(1 km×1 km)通风系数A值分布,并作为空气资源禀赋等级分区的依据.在此基础上,将空气资源分区的结果与地理信息系统相结合,给出其空间分布,强化了分区管控政策的空间落地.评估结果表明,宜昌地区空气资源禀赋等级共分为4级,A值在8以上的空气资源禀赋充裕的地区,约占市域面积的30.3%;较好和一般的地区,A值分别在5~8和3~5之间,约占34.1%和34.8%;A值在1~3之间空气资源禀赋稀少的地区,仅占0.8%.本研究提出的空气资源禀赋分区方法具有较强的合理性,预期在城市中长期发展过程中的产业布局与分级调控中具有较好的应用前景.     

Ti/SnO2-Sb2O5/PbO2电极的制备及降解不同污染物性能研究

采用溶胶凝胶法和电沉积法分别制备了Ti/SnO2-Sb2O5/PbO2电极的中间层和表面活性层,并通过XRD和SEM对电极的中间层和表面活性层进行了相关表征.结果表明,制得的电极表面为β型PbO2,表面形貌均匀致密.同时,采用线性伏安扫描和交流阻抗测试对电极的电化学性能进行了测试.结果表明,电解液中污染物的存在可提高电极的析氧电位,中间层的制备可以有效提高电极的催化性能.另外,通过测定电极对苯酚、靛蓝胭脂红、甲基橙3种不同类型污染物的去除率、COD去除率,研究了该电极对不同类型有机物的降解规律.结果表明,在相同条件下该电极对靛蓝胭脂红的去除速率较高且所需电压最低,降解1 h时靛蓝胭脂红去除率即达100%,甲基橙降解3 h时其COD去除率高达55%.     

黄曲霉A5p1脱色类黑精及其机理初探:葡萄糖氧化酶的作用

类黑精是一种高分子难降解色素污染物质,在糖蜜酒精废水中大量存在.选取在前期研究中对糖蜜酒精废水具有较好脱色作用的黄曲霉(Aspergillus flavus)A5p1(保藏号CGMCC.4292),以合成的类黑精为对象研究脱色机理,试图为实际废水的生物脱色提供理论基础.结果显示,此菌株对合成类黑精具有生物吸附和生物降解的双重作用,以后者为主,最高脱色率可达65%.相较于漆酶、依赖/不依赖于锰的过氧化物酶等常规氧化脱色酶,此菌株中的产过氧化氢酶对脱色起主要作用,而且脱色过程中作为产过氧化氢酶之一的葡萄糖氧化酶与类黑精脱色率之间存在着一定的正相关性.添加葡萄糖氧化酶激活剂和抑制剂进行验证,发现葡萄糖氧化酶酶活力、过氧化氢产量和脱色率三者之间呈相关性变化.初步推测,葡萄糖氧化酶是黄曲霉A5p1生物降解脱色类黑精的关键酶之一.     

羟基氧化铁催化臭氧氧化对滤后水卤乙酸生成势的影响

考察了滤后水经过单独臭氧氧化和羟基氧化铁(FeOOH)催化臭氧氧化后5种卤乙酸生成势(HAA5FP)的生成情况.研究了氧化时间、溴离子浓度、滤后水pH值、碱度和O3投量对2种氧化方式下HAA5FP的影响规律.发现该滤后水氯化后的HAA种类为二氯乙酸(DCAA)、三氯乙酸(TCAA)及溴离子存在时有二溴乙酸(DBAA).无溴离子存在时,催化臭氧氧化在5～20min内使得HAA5FP比臭氧氧化后的降低9.5%～18.3%.溴离子浓度增加使HAA5FP减少,催化臭氧氧化后HAA5FP也比臭氧氧化后低更多.中性pH时,催化臭氧氧化比臭氧氧化有更明显的控制HAA5FP的优势.重碳酸盐碱度升高使HAA5FP降低,且2种氧化后HAA5FP的差别减小.O₃/TOC比值为0.45～1.43的臭氧投量范围内,催化臭氧氧化后HAA5FP比臭氧氧化后减少11.2%～28.0%.催化臭氧氧化对滤后水HAA5FP的影响与FeOOH催化臭氧生成羟基自由基的特点密切相关.     

Preparation and characterization of Fe2O3-CeO2-TiO2/γ-Al2O3 catalyst for degradation dye wastewater

In order to develop a catalyst with high activity for catalytic wet oxidation （CWO） process at room temperature and atmospheric pressure, Fe2O3-CeO2-TiO2/γ-Al2O3 catalyst was prepared by consecutive impregnation method and the prepared parameters were optimized. The structure of the catalyst was characterized by BET, XRF, SEM and XPS technologies, and the actual wastewater was used to investigate the catalytic activity of Fe2O3-CeO2-TiO2/γ-Al2O3 in CWO process. The experimental results showed that the prepared catalyst exhibited good catalytic activity when the doping amount of Ti was 1.0 wt% （the weight ratio of Ti to carriers）, and the middle product, Fe2O3-CeO2-TiO2/γ-Al2O3, was calcined in 450℃ for 2 h. The CWO experiment for treating actual dye wastewater indicated that the COD, color and TOC of actual wastewater were decreased by 62.23%, 50.12% and 41.26% in 3 h, respectively, and the ratio of BOD5/COD was increased from 0.19 to 0.30.     

β-Cyclodextrin and its derivatives-enhanced solubility and biodegradation of 2-nitrobiphenyl

This paper investigated the effects of β-cyclodextrins （I3-CD） and its two derivatives, hydroxypropyl-β-cyclodextrin （HPCD） and carboxymethyl-β-cyclodextrin （CMCD）, on the solubility and biodegradation of 2-nitrophenyl by an A cinetbacter sp. Results showed that β-CD, HPCD and CMCD could not be utilized by A cinetbacter sp. as sole carbon source and none of the CDs had toxic effects on the growth of the bacteria in the experiments; all the CDs could enhance the apparent solubility and accelerate the biodegradation of 2-nitrobipheny. It showed that biodegradation-accelerating effects of CDs on 2-nitrobiphenyl were correlated with their solubility-enhancing effects. Among three CDs investigated, CMCD had the most obvious effects both on the apparent solubility and the biodegradation, followed by β-CD and HPCD.