Water-soluble matter in PM2.5 in a coastal city over China: Chemical components, optical properties, and source analysis

Although marine and terrestrial emissions simultaneously affect the formation of atmospheric fine particles in coastal areas, knowledge on the optical properties and sources of water-soluble matter in these areas is still scarce. In this work, taking Qingdao, China as a typical coastal location, the chemical composition of PM_2.5 during winter 2019 was analyzed. Excitation-emission matrix fluorescence spectroscopy was combined with parallel factor analysis model to explain the components of water-soluble atmospheric chromophores of PM_2.5. Our analysis indicated that NO₃⁻, NH₄⁺ and SO₄²⁻ ions accounted for 86.80% of the total ion mass, dominated by NO₃⁻. The ratio of [NO₃⁻]/[SO₄²⁻] was up to 2.42 ± 0.84, suggesting that mobile sources play an important role in local pollutants emission. The result of positive correlation between Abs₃₆₅ with K⁺ suggests that biomass burning is an important source of water-soluble organic compounds (WSOC). Six types of fluorophores (C1-C6), all humic-like substances, were identified in WSOC. Humification index, biological index and fluorescence index in winter were 1.66 ± 0.34, 0.51 ± 0.44 and 1.09 ± 0.78, respectively, indicating that WSOC in Qingdao were mainly terrestrial organic matters. Overall, although the study area is close to the ocean, the contribution of terrestrial sources to PM_2.5, especially vehicle exhaust and coal combustion, is still much higher than that of marine sources. Our study provides a more comprehensive understanding of chemical and optical properties of WSOC based on PM_2.5 in coastal areas, and may provide ground for improving local air quality.     

Identification and characterization of Fe3O4/peroxodisulfate advanced oxidation products from sulfameter

Sulfonamides (SAs) are one of the most widely used antibiotics and their residuals in the environment could cause some negative environmental issues. Advanced oxidation such as Fenton-like reaction has been widely applied in the treatment of SAs polluted water. Degradation rates of 95%-99.7% were achieved in this work for the tested 8 SAs, including sulfisomidine, sulfameter (SME), phthalylsulfathiazole, sulfamethoxypyridazine, sulfamonomethoxine, sulfisoxazole, sulfachloropyridazine, and sulfadimethoxine, in the Fe₃O₄/peroxodisulfate (PDS) oxidation system after the optimization of PDS concentration and pH. Meanwhile, it was found that a lot of unknown oxidation products were formed, which brought up the uncertainty of health risks to the environment, and the identification of these unknown products was critical. Therefore, SME was selected as the model compound, from which the oxidation products were never elucidated, to identify these intermediates/products. With liquid chromatography-high resolution tandem mass spectrometry (LC-HRMS/MS), 10 new products were identified, in which 2-amino-5-methoxypyrimidine (AMP) was confirmed by its standard. The investigation of the oxidation process of SME indicated that most of the products were not stable and the degradation pathways were very complicated as multiple reactions, such as oxidation of the amino group, SO₂ extrusion, and potential cross-reaction occurred simultaneously. Though most of the products were not verified due to the lack of standards, our results could be helpful in the evaluation of the treatment performance of SAs containing wastewater.     

Oxidative stress and genotoxicity of 1-methyl-3-octylimidazolium chloride on loach (Misgurnus anguillicaudatus)

This study was a preliminary step to evaluate the acute toxicity of 1-methyl-3-octylimidazolium chloride ([C₈mim]Cl) on loach (Misgurnus anguillicaudatus) by determining the effects on hepatic antioxidant enzyme activities and by the comet assay. The results showed that [C₈mim]Cl had acute toxicity at concentrations above 20 mg L^?1, inducing oxidative stress and genotoxicity on fish liver cells. In respect to enzyme activities, [C₈mim]Cl induced changes in the activities of superoxide dismutase, catalase, and glutathione content the livers of fish exposed at 20–80 mg L^?1. [C₈mim]Cl at the same exposure level caused a remarkable increase in malondialdehyde level. The comet assay indicated that [C₈mim]Cl at 20–80 mg L^?1 induced genotoxicity in liver cells. With increased exposure concentration and time, the two comet parameters trailing rate and tail moment were significantly increased, with significant differences (P < 0.05) observed between control group and each treatment group. The present study shows that ionic liquids can be a threat to the health of aquatic organism when accidentally released to aquatic ecosystems.     

钼冶炼工艺的循环经济探讨

钼是重要的稀有金属之一,主要通过氧化分解辉钼矿来提取。我国普遍使用反射炉、回转窑等焙烧设备生产氧化钼,造成了严重的SO2污染和资源浪费问题。为改变辉钼矿焙烧分解工艺的污染状况,硝酸高压分解、碱性高压氧分解、次氯酸钠分解和电氧化分解等辉钼矿湿法工艺相继被开发出来。但是这工艺往往只关注在如何获取金属钼等资源,而忽视了辉钼矿中占40%的硫资源。从循环经济角度分析了不同辉钼矿分解工艺的物质流向,探讨符合清洁生产和循环经济精神的工艺革新方向,提出了纯氧氧化焙烧和浓硫酸氧化两种新工艺。     

Chemical dynamics of the Sava riverine system

Presented here is a study of the geochemical dynamics of the entire River Sava watershed, a major tributary of the River Danube which has not previously been investigated. The sampling was performed at 33 selected locations along the main channel of the stream and at its largest tributaries during three sampling seasons (fall 2005, spring 2006 and fall 2006), going from headwater locations to the mouth near the confluence with the Danube. Almost 80% of the solutes are derived from carbonate mineral weathering and represent over 50% of specific HCO(3)(-) flux normalized to unit basin area at the mouth of the Danube. Statistical analysis indicates that agricultural and industrial sources contribute significantly to increased Na(+), K(+), Cl(-), SO(4)(2-) and NO(3)(-) concentrations in tributary waters. Different processes control the water chemistry along the course of the Sava's drainage-the upper reaches are largely regulated by contributions from carbonate mineral weathering, the middle reaches are influenced by agricultural activity and biological processes related to eutrophication, while the lower reaches tend to have more pronounced parameters related to the industrial processing along with leakages from municipal sanitary systems of these higher population density areas.     

臭氧-BAF组合工艺对石化行业废水深度处理的中试研究

采用臭氧-曝气生物滤池（BAF）组合工艺对中石化九江分公司二级生化出水进行深度处理中试实验。探讨了臭氧投加量、进水水质冲击负荷等因素对该组合工艺出水COD、NH₄⁺-N的影响。中试结果表明，在该水质条件下，臭氧最佳投加量为20~25 mg/L；组合工艺处理后出水COD低于40 mg/L，NH₄⁺-N低于5 mg/L，达到中水回用设计标准；该组合工艺能够经受一定冲击负荷。     

漆酶对活性黑KN-B和直接大红染料的脱色性能

利用白腐真菌漆酶对活性黑KN-B和直接大红2种偶氮染料进行脱色实验。考察反应时间、加酶量、pH值、染料浓度、温度对脱色率的影响，研究了ABTS介体以及金属离子存在下的脱色效果，并分析了漆酶脱色的动力学性能以及其对偶氮染料的降解规律。结果表明，活性黑KN-B和直接大红脱色适宜条件为：反应时间为30 min，加酶量8 U/mL，pH=7，染料浓度分别为50 mg/L和80 mg/L，温度40~45℃。ABTS介体对酶促偶氮染料脱色没有明显促进作用。Fe²⁺对漆酶脱色有较强的抑制作用；Cu²⁺对漆酶催化活性黑KN-B促进作用较大，对直接大红影响较小。漆酶对2种染料的脱色反应符合米氏方程，其催化活性黑KN-B和直接大红染料的K_m值分别为114.81 mg/L，317.5 mg/L，v_max值分别为6.57 mg/（L·min）和26.0 mg/（L·min）。     

碱预处理污泥产酸效果及其生物群落研究

为了提高污泥水解酸化过程中的挥发酸产量,获取污水脱氮除磷所需的内碳源,以深圳市罗芳污水厂的二沉池污泥为研究对象,采用不同的碱量对其进行预处理。通过测定碱预处理污泥水解酸化过程中的挥发酸浓度,并采用聚合酶链式反应-变性梯度凝胶电泳(polymerase chain reaction denature gradient gel electrophoresis,PCR-DGGE)技术对参与碱预处理污泥水解酸化产酸过程的主要微生物种群进行分析,结果表明,当碱投加量为0.20 g NaOH/g VSS时,初始溶出的蛋白浓度为1 780 mg/L;水解酸化15 d时,挥发酸总量达到3 473 mg/L;参与产酸的主要细菌属于Firmicutes、Proteobacteria、Bacteroidetes三个门类。     

稠油污水回用锅炉处理工艺的应用

新疆油田公司稠油污水处理普遍采用成熟的离子调整旋流反应水处理技术,污水处理后达到回用锅炉水质标准SY/T 0097-2000《稠油油田采出水用于蒸汽发生器给水处理设计规范》,供给油田专用高压注汽锅炉用水。采用相同技术建成的采油一厂稠油处理站污水回用锅炉处理工艺投用后,处理后污水回用锅炉,减少了含油污水的外排,充分利用了稠油污水的热能,取得了良好的经济和社会效益。