Transfeer of organic pollutants during sewage-seawater mixing

The transfer processes of organic pollutants during sewage-seawater mixing were simulated in three different mixing systems. The release rate of organic matter from sewage particles to seawater was found to be about 0.02–0.04 d⁻¹. The release processes can be simulated by an exchange-equilibrium kinetic model. Degradation of COD was observed in all three mixing systems and can be described by a first order kinetic equation. The degradation rate constantk ranged between 0.04 and 0.07 d⁻¹. These results have provided important parameters for estimation of environmental capacity.     

A review of pollutants in the sea-surface microlayer (SML): a unique habitat for marine organisms

Boundary layers between different environmental compartments represent critical interfaces for biological, chemical and physical processes. The sea-surface microlayer (uppermost 1-1000 microm layer) forms the boundary layer interface between the atmosphere and ocean. Environmental processes are controlled by the SML, and it is known to play a key role in the global distribution of anthropogenic pollutants. Due to its unique chemical composition, the upper organic film of the SML represents both a sink and a source for a range of pollutants including chlorinated hydrocarbons, organotin compounds, petroleum hydrocarbons, polycyclic aromatic hydrocarbons (PAH) and heavy metals. These pollutants can be enriched in the SML by up to 500 times relative to concentrations occurring in the underlying bulk water column. The SML is also a unique ecosystem, serving as an important habitat for fish eggs and larvae. Concentration ranges and enrichment factors of pollutants in the SML in different areas of the world's oceans have been critically reviewed, together with available toxicity data for marine biota found within the SML. Overall, the SML is highly contaminated in many urban and industrialized areas of the world, resulting in severe ecotoxicological impacts. Such impacts may lead to drastic effects on the marine food web and to fishery recruitment in coastal waters. Studies of the toxicity of fish eggs and larvae exposed to the SML contaminants have shown that the SML in polluted areas leads to significantly higher rates of mortality and abnormality of fish embryos and larvae.     

内蒙古自治区主要城市空气质量状况分析

文章利用呼和浩特市、包头市、乌海市、赤峰市、东胜区2007年1月1日到2011年12月31日5a空气主要污染物SO2、NO2、PM10浓度资料,统计分析了各城区主要污染物的分布特征,得到:⑴总体来看,乌海市空气质量较差,其次是包头市,东胜区最好;⑵PM10浓度值变化幅度最大,日最大值均出现在3—5月的沙尘日中,SO2最大值都出现在冬季采暖期;⑶各地均是12月出现污染日数最多,其次是1月;⑷从2007年开始,空气质量状况逐年好转。     

区段控制浓度的一种定量化模型研究

该文就总量控制工作进行理论探讨,提出控制平均浓度的排污等效模型,同时对计算区段控制浓度的确定进行定量化模型研究。该模型简便、易操作、实用性强,具有一定的理论意义和实用价值。     

Analyses of the Compositional Characteristics and Sources of the Organochlorine Pesticides in the Surface Sediments of Guanghai Bay,Taishan City,Guangdong Province

Organochlorine pesticides (OCPs) are a class of toxic and harmful persistent organic pollutants widely found in environment. Hexachlorocyclohexane (HCHs) and DDTs are two of the most widely used OCPs (Qiu et al., 2004), so it is important to find out their compositional characteristics and sources in surface sediments. Guanghai Bay is located in the south of Guanghai Bay Industrial Park in Taishan City, Guangdong Province. It borders Huangmaohai to the east and Zhenhai Bay to the west, covering an area of about 236 square kilometers. In this study, surface sediments were collected at 16 sites in Guanghai Bay (Fig. 1). After the surface sediments were pretreated, GC‐MS was used to analyze OCPs. A total of 14 OCPs were detected and their content was shown in Table 1. The concentration of ΣOCPs ranged between 0.507～0.860ng·g‐1, with an average of 0.680 ng?g‐1. In general, the content of ΣOCPs was the highest at No. A12 site. The concentrations of these 14 detected OCPs ordered as dieldrin > epoxy heptachlor > P, P'‐DDD > γ‐HCH >endrin >aldrin > P, P'‐DDE >mirex >hexachlorobenzene >P, P'‐DDT > α‐HCH > δ‐HCH >β‐HCH > heptachlor.     

某废弃煤矿有机污染场地地下水修复治理中试研究

某废弃煤矿竖井经倾倒有机废液,导致环境污染事件,造成巷道及采空区内地下水污染。本文结合场地实际情况,选取倾倒竖井(事故井)及周边区域为中试区域,采用“抽出处理+原位氧化循环”两阶段联合修复技术对污染场地开展中试研究。本文介绍了场地污染概况、地下水修复中试方案设计和实施,以及对修复效果进行评价。结果表明,中试处理后地下水中COD和二氯甲烷最高去除率分别为97.88%和99.74%。中试试验表明, “抽出处理+原位氧化循环”两阶段修复技术,对处理矿区内巷道及采空区等复杂地层结构下深层地下水中有机污染物具有较好的去除效果,可以结合现场实际情形对整个污染场区进行规模应用。     

Investigating the Changes in Air Pollutant Emissions over the Beijing-Tianjin-Hebei Region in February from 2014 to 2019 through an Inverse Emission Method

In recent years, China has implemented several measures to improve air quality. The Beijing-Tianjin-Hebei(BTH)region is one area that has suffered from the most serious air pollution in China and has undergone huge changes in air quality in the past few years. How to scientifically assess these change processes remain the key issue in further improving the air quality over this region in the future. To evaluate the changes in major air pollutant emissions over this region, this paper employs ens...     

不同人为源排放清单对大气污染物浓度数值模拟的影响:以浙江省为例

应用大气化学模式WRF-Chem(Weather Research and Forecast-Chemistry),分别选用亚洲排放源清单INTEX-B(Intercontinental Chemical Transport Experiment-Phase B)、REASv2.1(Regional Emission inventory in Asia version 2.1)以及全球排放源清单HTAP_v2(Hemispheric Transport of Air Pollution version 2),对浙江省2013年12月进行模拟,分别记为IN、RE和HT试验,研究人为源排放清单对大气污染物浓度数值模拟的影响。结果表明,3组试验合理的反映出PM2.5(空气动力学当量直径小于等于2.5μm的颗粒物,即细颗粒物)、PM10(空气动力学当量直径小于等于10μm的颗粒物,即可吸入颗粒物)和NO_2近地面浓度的时空分布特征,相关系数为0.5~0.8,85%以上的模拟值落在观测值的0.5~2倍范围内,但对SO_2近地面浓度模拟较差。IN、RE、HT试验对PM2.5和PM10的模拟偏差均成递减趋势,约为30%、16%和6%,HT试验的模拟值更加接近观测。INTEX-B清单中PM2.5的一次排放与二次气溶胶前提物SO_2均高于REAS与HTAP清单,因此会导致更多的硫酸盐生成,从而进一步增加PM2.5浓度。HTAP_v2清单中较低的NH3排放会抑制硝酸盐的生成,从而有助于降低PM2.5浓度。3个清单的基准年与模拟年的差异对SO_2浓度模拟的准确性影响更大,INTEX-B清单中SO_2排放量明显高于REASv2.1与HTAP_v2清单,尤其在浙北和沿海工业发达地区,导致IN试验模拟的SO_2在这些地区存在明显高估。3组试验模拟的NO_2浓度偏差最小且更为接近(-8%~4%),主要原因是3个清单在浙江省的NOx排放十分一致。从3组试验结果之间的差异程度来看,浙江省范围内PM2.5、PM10、SO_2和NO_2逐日浓度模拟值之间的平均差异程度分别约为14%、15%、51%和16%,最大差异程度分别为69%、78%、137%和132%。月均浓度与逐日浓度的平均差异程度基本一致,但最大差异程度明显更低。总体来看3组试验模拟的PM2.5、PM10与NO_2的差异程度明显低于SO_2。     

粉煤灰中污染离子淋释试验及其运移模型

通过对不同介质条件下粉煤灰中污染离子的淋释实验,得出一些离子淋释规律,在此基础上,对粉煤灰中淋释污染离子在地下水中的浓度变化从理论上给出两种数学模型      

Direct Conversion of Food Waste into 3D Porous Carbon Traps for Selective Adsorption of Cationic Dyes

Conversion of waste biomass into valuable functional materials accomplishes the concept of circular economy in the development of sustainable waste management, and also recovery of such resources possibly reduces the requirement of feedstocks. In this scenario, the development of methodologies toward the direct conversion of the raw biomass into solid adsorbent materials without the use of any templates is highly desirable, but exceptionally challenging due to the complexity of the process. Here the direct synthesis of 3D porous carbon traps by a simple, cost-effective, and template-free process starting from a kitchen-based recipe and fermented food waste is described. Precisely, a robust carbon trap is formed with a spongy structure and highly interconnected hierarchical pores after the pyrolysis of a rice-based foam in the air. The developed materials float on water and interact efficiently with cationic dyes at static conditions. Importantly, such performance of the 3D carbon traps is not affected in the presence of anionic dyes, indicating the excellent selectivity towards the adsorption of cationic dyes. The adsorbent can be easily recovered and reused for up to 3 cycles without releasing any byproducts, thus, without causing hazardous risk of any secondary pollution to the environment.