Experimental study on the control of black smoke pollution from the ceramic kilns based on the mechanism of the surfactant and coagulant

Aiming at the characteristics of carbon black, a new method of controlling the black smoke from the industrial coal-burning ceramic kilns by wetting was brought forward. The carbon black in the flue of coal-burning ceramic kiln was collected for the experiments, and its physical and chemical properties were studied in detail. In order to change the sedimentation and wettability state of the carbon black, the complex solution of the coagulant and surfactant was applied. After a series of orthogonal experiments, the complex solutions with better effects were chosen. Then, the sedimentation percentage of carbon black treated by the selected complex solutions was measured. The optimized complex solutions included Na₂SO₄ (100 mmol/L), sodium dodecyl benzenesulfonate (SDBS) (1.2 mmol/L) and polyacrylamide (PAM) (40 mg/L). After carbon black was absorbed, the complex solutions were clear and colorless. The complex solutions can be recycled, and the sedimentation percentage of carbon black is 94%.     

多轴差分吸收光谱仪对大气污染物SO2、NO2、O3的立体监测

多轴差分吸收光谱仪（MAX—DOAS）是用来监测大气中痕量气体成分的专用仪器,它能同时自动监测SO2、NO2和03三种污染气体,得到的垂直柱浓度对研究污染物的时空分布特点具有重要意义。分析了2011年5月下旬至2012年4月中旬期间MAX—DOAS在重庆市的测量数据,结果表明：夏季SO2的柱浓度高于其它季节,并在每个季节都出现了峰值：SO2与NO2之间浓度变化趋势相同,且最大小时浓度值都集中在上午;O3垂直柱浓度受气象条件和臭氧前体物的影响呈夏季高、秋冬低的季节性变化;通过多元回归建立了O3柱浓度与气象因素、前体物的关系式。     

活性污泥工艺的多目标优化分析

研究了多目标优化方法在活性污泥工艺优化中应用的可行性,以国际水协(IWA)发布的基准仿真模型BSM1的工艺流程为对象,以出水水质、过程能耗和反应池体积的指标为优化目标,以反应池池容(5个)、混合液回流量、污泥回流量、污泥排放量、反应池氧气传质系数(3个)等11个变量为决策变量,构建了基于BSM1的多目标优化模型,并利用MatLab非支配排序遗传算法NSGA-II进行求解,获得了BSM1多目标优化模型的Pareto解.研究结果表明,在Dry进水条件下,通过将体积指标增大4.1%,可以明显改善出水水质指标(降低81.5%),能耗指标也能得到一定改善(降低13.3%);在3种进水条件(Dry,Rain,Storm)下,相对于BSM1工艺参数的缺省值,利用本研究的优化解作为工艺参数,均能不同程度改善出水水质、降低能耗.研究结果显示,在活性污泥过程不同目标之间进行权衡可以通过多目标优化方法来实现.     

Ten-year emission characteristics of atmospheric pollutants from incineration of sacrificial offerings in China

The incineration of sacrificial offerings is a significant widely practiced custom that is also a kind of neglected air pollution source in China. Our results showed that the emission factors of particulate matter, SO₂, CO, NO_x, and VOCs emitted from the incineration of sacrificial offerings with purification systems were reduced by 95%, 19%, 9%, 82%, and 42%, respectively, compared with those without a purification system, revealing a significant effect of the flue gas purification system on reducing particulate matter and gaseous pollutants. The emission level of air pollutants from the incineration of sacrificial offerings remained stable before 2013 and then showed a remarkable decrease after the implementation of China´s Air Pollution Prevention Action Plan in 2013. The emissions of TSP (total suspended particulate), PM₁₀, PM_2.5, and NO_x in 2009 were 8222, 6106, 5656 and 15,878 ton, respectively, obviously higher than 3434, 2551, 2305 and 8579 ton in 2019. Such trend was affected by both the quantity of incineration and the installation rate of purification systems after the Emission Standard of Air Pollutants for Crematory (GB 13801-2015) issued in China. Distinct spatial distribution of atmospheric pollutants from incineration of sacrificial offerings was found with higher in the east and south of China than the west and north of China, which is proportional to the regional economy and population. The maximum ground-level concentration typically occurred at 0.12-0.2 km from the pollution source, posing potential health risks to people entering and exiting funeral and burial sites and nearby residents.     

Association of emergency room visits for respiratory diseases with sources of ambient PM2.5

Previous studies have reported associations of short-term exposure to different sources of ambient fine particulate matter(PM_(2.5)) and increased mortality or hospitalizations for respiratory diseases. Few studies, however, have focused on the short-term effects of source-specific PM_(2.5) on emergency room visits(ERVs) of respiratory diseases. Source apportionment for PM_(2.5) was performed with Positive Matrix Factorization(PMF) and generalized additive model was applied to estimate associations between source-specific PM_(2.5) and respiratory disease ERVs. The association of PM_(2.5) and total respiratory ERVs was found on lag4(RR = 1.011, 95%CI: 1.002, 1.020) per interquartile range(76 μg/m~3) increase.We found PM_(2.5) to be significantly associated with asthma, bronchitis and chronic obstructive pulmonary disease(COPD) ERVs, with the strongest effects on lag5(RR = 1.072,95%CI: 1.024, 1.119), lag4(RR = 1.104, 95%CI: 1.032, 1.176) and lag3(RR = 1.091, 95%CI: 1.047,1.135), respectively. The estimated effects of PM_(2.5) changed little after adjusting for different air pollutants. Six primary PM_(2.5) sources were identified using PMF analysis, including dust/soil(6.7%), industry emission(4.5%), secondary aerosols(30.3%), metal processing(3.2%),coal combustion(37.5%) and traffic-related source(17.8%). Some of the sources were identified to have effects on ERVs of total respiratory diseases(dust/soil, secondary aerosols, metal processing, coal combustion and traffic-related source), bronchitis ERVs(dust/soil) and COPD ERVs(traffic-related source, industry emission and secondary aerosols). Different sources of PM_(2.5) contribute to increased risk of respiratory ERVs to different extents, which may provide potential implications for the decision making of air quality related policies, rational emission control and public health welfare.     

陈化处理对棉花秸秆生物炭理化性质的影响

为探讨陈化处理对秸秆生物炭理化性质的影响,采用冻融和干湿方法分别对不同热解温度(350、500和650℃)下制备的棉花秸秆生物炭进行陈化处理,对比分析新鲜和陈化生物炭的理化性质.结果表明,热解温度、环境温度、湿度和陈化时间是影响生物炭理化性质的主要因素.陈化处理可以加速生物炭表面发生氧化反应,增加生物炭表面的酸性官能团,进而降低生物炭的pH值.生物炭经过陈化处理后,其C含量减少,O含量增加,这也归因于生物炭的氧化反应.陈化处理可以增加生物炭的比表面积和微孔体积,且新鲜和陈化生物炭的孔隙结构主要以介孔为主.陈化处理还可以破坏生物炭表面较完整的形状,降低生物炭的稳定性.     

Quantitative assessment of polycyclic aromatic hydrocarbons in sewage sludge from wastewater treatment plants in Qingdao, China

In this study, 16 polycyclic aromatic hydrocarbons (PAHs) were detected in sewage sludge samples from four wastewater treatment plants (WWTPs) in Qingdao, China. These WWTPs differ in the type of treatment used and in the origin of the wastewater. The total amounts of PAHs in digested sludges ranged from 1.9645 to 6.5752 mg/kg, which did not exceed the projected European Union cut-off limits (6 mg/kg) for sludge found in farmland, except for the Haibohe WWTP. Significant differences were observed in overall PAH values between WWTPs receiving domestic effluents and those receiving industrial effluents. The total amounts of PAHs in digested sludge from the Licunhe and Haibohe WWTPs, which mainly received industrial effluents, were markedly higher than those of the Tuandao and Huangdao WWTPs, which received only domestic effluents. The distribution of PAH compounds in digested sludges were analysed. At the Tuandao, Huangdao and Licunhe WWTPs, 2-, 3-, 4-benzene rings were predominant, accounting for 100%, 99.8% and 99.0% of the sum concentration of 16 PAHs (∑PAHs), respectively. At the Haibohe WWTP, a large number of high molecular weight PAHs (5-, 6-benzene rings) were observed, accounting for 30% of the ∑PAHs. The sum of seven carcinogenic PAHs (∑PAHs-c) ranged from 0.8694 to 3.0389 mg/kg in four WWTPs. The highest value was found in the Haibohe WWTP. Moreover, the PAH concentrations in sludges from the different treatment processes in the Licunhe and Tuandao WWTPs are discussed.     

三峡库区荔枝,龙眼的适宜性评价与开发利用

荔枝、龙眼等南亚热带水果是三峡库区的特色水果，不论从栽培历史和当地的气候条件看都适宜在库区的川江河谷地段种植；恢复和发展荔枝、龙眼生产的主要技术措施有：加速品种更新改造、搞好种植区划和发展规划以及合理增加投入和加强储藏保鲜技术研究与应用等。     

Diurnal variations of polycyclic aromatic hydrocarbons associated with PM2:5 in Shanghai, China

Forty-eight daily time interval PM2:5 samples were collected from December 2006 to January 2008 in an urban site in Shanghai, China. Concentrations and compositions of polycyclic aromatic hydrocarbons (PAHs) were analyzed with GC-MS to study the diurnal and seasonal variations and to identify the main emitting sources. The diurnal variation of the PAHs concentrations was greater in the late autumn and winter sampling days, and was greatly influenced by meteorological conditions such as wind speed and ambient temperature. The concentration of PAHs in the mornings (6:30–10:00) increased distinctly, and was high in the late autumn and winter sampling days, indicating the contribution from vehicle emissions during rush hours. The diurnal variation of the high molecular weight PAHs did not seem to be controlled by the shift of gas-particle partitioning due to temperature variation, instead, it could be indicative of the variation in the source. Statistical analyses showed that the concentrations of PAHs were negatively correlated with temperature and wind speed, and positively correlated with relative humidity. Diagnostic ratios of PAHs suggested mixed emission sources of petroleum and coal/biomass combustion for PAHs in the PM2:5 in Shanghai.     

Enhanced ozonation of dichloroacetic acid in aqueous solution using nanometer ZnO powders

Nanometer zinc oxide (ZnO) powders were used as a catalyst to enhance the ozonation for the degradation of dichloroacetic acid (DCAA) in aqueous solution. The batch experiments were carried out to investigate the e ects of key factors such as catalyst dosage, ozone dosage, solution pH and tert-butyl alcohol (t-BuOH) on the degradation e ciency of DCAA. Density functional theory (DFT) was adopted to explore the mechanism of generating hydroxyl radical (.OH) on the ZnO surface. The results showed that adsorption and ozonation processes were not e ective for DCAA removal, and the addition of ZnO catalyst improved the degradation e ciency of DCAA during ozonation, which caused an increase of 22.8% for DCAA decomposition compared to the case of ozonation alone after 25 min. Under the same experimental conditions, the DCAA decomposition was enhanced by increasing catalyst dosage from 100 to 500 mg/L and ozone dosage from 0.83 to 3.2 mg/L. The catalytic ozonation process is more pronounced than the ozonation process alone at pH 3.93, 6.88, and 10. With increasing the concentration of t-BuOH from 10 to 200 mg/L, the degradation of DCAA was significantly inhibited in the process of catalytic ozonation, indicating that ZnO catalytic ozonation followed .OH reaction mechanism. Based on the experimental results and DFT analysis, it is deduced that the generation of .OH on the ZnO surface is ascribed to the adsorption of molecule ozone followed by the interaction of adsorbed ozone with active sites of the catalyst surface. It is also concluded that ZnO may be an e ective catalyst for DCAA removal, which could promote the formation of .OH derived from the catalytic decomposition of ozone.