低SO_2氧化率脱硝催化剂的开发

介绍了SCR脱硝催化剂中V2O5对SO2的氧化及SO2氧化对脱硝催化剂及其下游设备的危害,分析了脱硝催化剂中V2O5对SO2氧化的原理和影响因素,探讨了低SO2氧化率脱硝催化剂开发方面的研究成果。     

铁屑还原－鼓风氧化－石灰凝沉法脱除硫酸生产废水中的砷

比较了硫酸生产废水的几种除砷方法，认为铁屑还原－鼓风氧化－石灰凝沉工艺是可行的，此法具有处理量大、处理效果好、运行费用低等优点。     

矿化垃圾生物覆盖层减少垃圾填埋场CH4、N2O和CO2释放的效应研究

对利用矿化垃圾构建生物覆盖层以削减填埋场温室气体的释放问题进行了深入研究,分析了环境因素对CH4释放的作用,考察了作为生物覆盖层材料的矿化垃圾的厚度变化对CH4氧化的影响.结果表明,温度为5～45℃时,矿化垃圾对CH4的氧化速率平均值分别约为黏性土和砂性土的2.35和4.71倍,CH4氧化速率随温度的升高而增加,并在35℃时达到最大值.当含水率w为16％ ～ 24％时,纯矿化垃圾覆盖层、半矿化垃圾覆盖层和砂性土覆盖层CH4氧化能力均达到最大.砂性土覆盖层和半矿化垃圾覆盖层CH4释放通量平均值分别为纯矿化垃圾覆盖层的329.8倍（P＜0.05）和91.7倍（P＜0.05）,添加矿化垃圾填料会增加覆盖层N2O释放通量,纯矿化垃圾覆盖层N2O（以N计）释放通量平均值分别为半矿化垃圾覆盖层和砂性土覆盖层的2.1倍（P＜0.05）和3.5倍（P＜0.05）.     

不同加热方式下催化氧化甲苯的性能研究

研究考察了微波单模腔、多模腔与传统电炉三种不同加热方式下甲苯的催化氧化性能,分析不同加热方式下进出口气体温度和固定床反应温度的变化,并对实验前后的Cu-Mn-Ce/TiO2-分子筛催化剂进行了扫描电镜、X射线衍射和比表面积等表征测试.研究表明,相同工艺条件下电炉加热、微波多模腔与单模腔加热对甲苯的去除效率分别为77%、83%和94%,对应的床层反应温度为265℃、215℃和145℃,微波加热的选择性、"热点效应"和偶极极化作用提高了甲苯的降解效率并降低其氧化温度和工艺处理能耗,微波单模腔内高的能量密度显著提高了甲苯的氧化效率并降低反应温度.催化剂表征发现,微波加热对催化剂结构与活性组分的分布几乎没有影响,而电炉加热则导致催化剂表面烧结与活性组分团聚,微波加热下催化剂更大的比表面积有利于甲苯的吸附与氧化降解.     

Quantity and activity of ammonia-oxidizing archaea and bacteria and their contribution to ammonia oxidation in farmland soil of Qinghai-Tibet Plateau北大核心CSCD

Ammonia oxidation, the first and rate-limiting step of nitrification, is mainly performed by ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB). However, the activities of AOA and AOB in soil and their relative contribution to ammonia oxidation are unclear, and whether there is a significant correlation between the quantity of AOA and AOB and the ammonia oxidation rate is also controversial. In this study, quantitative PCR combined with acetylene (C2H2) and 1-octyne inhibition methods were used to determine the quantity and activity of AOA and AOB in wheat, highland barley, and oilseed rape soils in Nyingchi, Lhatse, Sangzhuzi, and Sangri counties on the Qinghai-Tibet Plateau. The results showed that the quantity of AOB ((2.34 ± 0.84) ×105 - (2.65 ± 1.07) ×106 copies g-1 dry soil) was significantly higher than that of AOA ((0.20 ± 0.10) ×104 - (4.02 ± 0.39) ×104 copies g-1 dry soil) in all the soil samples. Soil pH was the key factor affecting the quantity of AOB, and the total phosphorus and ammonium nitrogen in soil were the key factors affecting the quantity of AOA. The rates of ammonia oxidation in the farmland soils of Lhatse (2.42 ± 0.73 mg kg-1 d-1) and Sangzhuzi (3.24 ± 1.15 mg kg-1 d-1) were significantly higher than those in the soils of Nyingchi (1.17 ± 0.43 mg kg-1 d-1) and Sangri counties (0.88 ± 0.57 mg kg-1 d-1). The rates of ammonia oxidation in the farmland soils of Lhatse and Sangzhuzi were dominated by AOB, while those in the farmland soils of Nyingchi and Sangri counties were dominated by AOA. For crops, the ammonia oxidation rates of wheat and oilseed rape soils in all four regions were significantly higher than those of highland barley soil, whereas the activity of AOA and AOB was not influenced by crops. The ratio of nitrogen to phosphorus was the key factor influencing AOA activity, whereas soil pH and total carbon were the main factors influencing AOB activity. Additionally, the quantities of AOA and AOB were not significantly correlated with the total ammonia oxidation rates and AOA and AOB activity. Overall, our study suggests that both AOA and AOB play important roles in ammonia oxidation in farmland soils of the Qinghai-Tibet Plateau. Moreover, it is unreliable to predict the activity of AOA and AOB and their relative contribution to ammonia oxidation directly based on their number of amoA genes, and the activity of AOA and AOB should be directly and accurately measured. These results are important for understanding ammonia nitrogen removal processes, slowing nitrate loss, and reducing the emission of the greenhouse gas nitrous oxide in the farmland ecosystem of the Qinghai-Tibet Plateau. © 2022 Science Press. All rights reserved.     

Semi-closed synthesis of nitrogen and oxygen Co-doped mesoporous carbon for selective aqueous oxidation

Heteroatom-doped meso/micro-porous carbon materials are conventionally produced by harsh carbonization under an inert atmosphere involving specific precursors, hard/soft templates, and heteroatom-containing agents. Herein, we report a facile synthesis of N and O co-doped meso/micro-porous carbon (NOMC) by template-free carbonization of a small-molecule precursor in a semi-closed system. The semi-closed carbonizaiton process yields hydrophilic NOMCs with large surface area in a high yield. The porous structure as well as the elemental composition of NOMCs can be modulated by changing the holding time at a particular temperature. NOMCs as metal-free heterogeneous catalysts can selectively oxidize benzyl alcohol and its derivatives into aldehydes/ketones with>85％conversion in aqueous solution, which is much higher than that of the control sample obtained in tube furnace (21％conversion), mainly due to their high N content, high percentage of pyridinic N, and large surface area. The presence of O-containing moieties also helps to improve the hydrophilicity and dispersion ability of catalysts and thus facilitates the mass transfer process during aqueous oxidation. The NOMC catalysts also dispayed excellent activity for a wide range of substrates with a selectivity of>99％.     

The role of primary and secondary air pollutants in atmospheric pollution: Athens urban area as a case study

The question to what extent primary and secondary air pollutants are relevant to atmospheric pollution and their effects on human health and the quality of the environment can be answered in a straight-forward manner: atmospheric processes, including oxidation procedures, particle formation and equilibria, determine the fate of primary emissions and, in most cases, the secondary products of these processes are the more important ones concerning their effects on human health and the quality of the environment. The formation of secondary products represents the critical property determining the establishment of certain air standards, rather than the actually emitted substance, although there are notable exceptions. In this paper, a review concerning transformation of primary pollutants as studied in the atmosphere of Athens is used to enlighten matters that may need further attention by the responsible authorities and stakeholders for the control and reduction of atmospheric pollution.     

纳米光催化氧化测定不同水体化学需氧量的研究

采用简便的沉淀法制备的纳米氧化锌为光催化荆,重铬酸钾为光生电子接受体,研究了纳米氧化锌-重铬酸钾体系测定COD的方法.COD值在1～100mg/L之间有良好的线性关系,线性方程为y=0.0007χ 0.0069,相关系数为r=0.9992,检测限为0.66mg,L.采用本方法和CODM.国标法对不同水体样品进行比较测定发现,对低COD值样品本方法加标回收率在96.3%～100.6%之间,变异系数Cv%=1.1～3.4,准确度和精密度均优于CODMn国标法,弥补了低COD值样品国标法(CODmn)测定不准确的不足,且单个样品测定时间短,具有推广应用价值.     

Distribution of Iron, Manganese, Zinc and Atrazine in Groundwater in Parts of Palar and Cheyyar River Basins, South India

A study was carried out in a part of Palar and Cheyyar river basin to evaluate the current status of iron, manganese, zinc and atrazine concentrations, their origin and distribution in groundwater. Groundwater samples were collected during post-monsoon (March 1998 and February 1999) and pre-monsoon (June 1999) periods from 41 sampling wells distributed throughout the study area. The groundwater samples were analyzed for trace metals using AAS and atrazine using HPLC. The concentration of the trace elements in groundwater is predominant during pre-monsoon period. Distribution pattern indicates that the concentration of these elements increases from west to northeast and towards Palar river. Lower concentrations in the central part may be due to recharge of fresh water from the lakes located here. During most of the months, as there is no flow in Palar river, the concentrations of trace elements in groundwater are high. Drinking water standards indicate that Mn and Zn cross the permissible limit recommended by EPA during the pre-monsoon period. A comparison of groundwater data with trace element chemistry of rock samples shows the abundance of trace elements both in the rock and water in the order of Fe > Mn > Zn and Fe > Zn > Mn. This indicates that iron in groundwater is derived from lithogenic origin. Further, Fe, Mn and Zn have good correlation in rock samples, while it is reverse in the case of water samples, indicating the non-lithogenic origin of Mn and Zn. Atrazine (a herbicide) was not detected in any of the groundwater samples in the study area, perhaps due to low-application rate and adsorption in the soil materials.     

龙口褐煤对Ni^2＋,Mn^2＋,Hg^2＋等重金属离子的吸附特性

本文以龙口褐煤作吸附剂,对重金属离子Ｎｉ＾２,Ｍｎ＾２＋,Ｈｇ＾２＋的单组分水溶液进行吸附研究,探讨了吸附剂的吸附性能,影响吸附的因素和吸附机理。结果表明：褐煤对Ｎｉ＾２＋,Ｍｎ＾２＋,Ｈｇ＾２＋的吸附均表现出Ｌａｎｇｍｕｉｒ特征,ＰＨ值是影响吸附的一个重要因素。