含钒废渣生产五氧化二钒的沉钒废水的处理研究

简要介绍了含钒废渣生产五氧化二钒的工艺,阐述了沉钒废水对人体和环境的危害,陈述了两种工艺沉钒废水的主要成分及浓度,分析了共性和特性。并针对不同的生产方法及沉钒废水的性质,分别选择制定合理的废水处理方案,为环境影响评价工作提供一定的科学依据。     

浙江油田管5井区块注水处理研究

浙江油田管5井区块属于低渗透区块,油田开发过程中产出水悬浮物(SS)、硫酸盐还原菌(SRB)、腐生菌(TGB)等指标严重超标。未经处理的油田污水如果直接注入到地层中,注入水中的悬浮颗粒会伤害油层的渗透率,导致注水井的吸水能力降低和油井产能下降,从而影响开发效果。因而,对其油田产出水采用内压式中空纤维超滤工艺处理。文章介绍了注水处理工艺及流程,结果表明:超滤工艺出水水质:SS为0.25mg/L,SRB菌数为0,铁细菌数为17个/mL,腐生菌数0,相关水质指标符合《碎屑岩油藏注水水质推荐指标及分析方法》(SY/T5329-94)的要求。     

1,2,4,5-四氯苯 C 18 Empore TM 膜/水分配系数的研究

研究了1,2,4,5-四氯苯在C18膜／水相之间的分配规律。1,2,4,5-四氯苯在：25℃,80r／min条件下恒温震荡96h可达分配平衡,温度和盐度对1,2,4,5-四氯苯C18膜／水的分配过程影响很小,1,2,4,5-四氯苯C18膜／水分配平衡时间受溶液体积和容器容积的影响,但不受溶液中C18膜膜量的影响,推测脂溶性小于或接近1,2,4,5-四氯苯的有机污染物在恒温震荡条件下C18膜与水之间的分配96h可达到平衡。     

Characterization and assessment of “Kullar Domestic Wastewater Treatment Plant” wastewaters

We investigated conventional characterization of wastewaters of the "Kullar Domestic Wastewater Treatment Plant." In the study of conventional characterization; 23 composite samples, which were taken during 10 months, were used and analysed as COD, BOD5, TKN, NH3-N, SS, VSS, TP, RP, TS, Alkalinity, oil and grease, detergent, chloride parameters. For determine of the plant efficiency, 8 output grab samples were taken. The COD and BOD5 values of influent, respectively, ranging from 37 to 1,056 mg/L and 8 to 140 mg/L in total wastewater. The meanly BOD5/COD ratio was calculated as 0.34 in total wastewaters.     

Dissipation,half-lives,and mass spectrometric identification of chlorpyrifos and its two metabolites on field-grown collard and kale

The persistence and fate of chlorpyrifos and its two metabolites, chlorpyrifos-oxon and the 3, 5, 6-trichloro-2-pyridinol (TCP) break-down product were investigated on kale and collard leaves under field conditions. A simultaneous extraction and quantification procedure was developed for chrorpyrifos and its two main metabolites. Residues of chlorpyrifos, chlorpyrifos oxon, and TCP were determined using a gas chromatograph (GC) equipped with an electron capture detector (GC/ECD). Chlorpyrifos metabolites were detectable up to 23 days following application. Residues were confirmed using a GC equipped with a mass selective detector (GC/MSD) in total ion mode. Initial residues of chlorpyrifos were greater on collard (14.5 µg g^?1) than kale (8.2 µg g^?1) corresponding to half-lives (T_1/2) values of 7.4 and 2.2 days, respectively. TCP, the hydrolysis product, was more persistent on collards with an estimated T_1/2 of 6.5 days compared to kale (T_1/2 of 1.9 days).     

Development on whose terms?: CSR discourse and social realities in Papua New Guinea's extractive industries sector

The emergence of Corporate Social Responsibility (CSR) in the extractive industries represents a bid to legitimize the sector after decades of environmental disasters and the trampling of indigenous rights. But whilst the rise in CSR has meant safer technologies and better stakeholder engagement, there is little evidence of any real socio-economic development at the grassroots. This paper examines the uneasy relationship existing between the strategic ‘business model’ of CSR and the brand of development it delivers. Using evidence from two multinational extractive industries in Papua New Guinea, we show how weaknesses in CSR practice come from greater emphasis on meeting global ‘performance standards’ than on the specificities of the social contexts in which strategies are implemented. These weaknesses, we argue, lead to ill-conceived and inappropriate development programmes that generate inequality, fragmentation, and social and economic insecurity. We conclude that greater engagement with affected communities will facilitate the development of more mutually beneficial and appropriate CSR strategies.     

焦化废水BOD5接种质量控制

接种是BOD5质量控制关键。为了提高生物毒性较大的焦化废水BOD5测定结果的精密度和准确度,本文采用焦化废水活性污泥制备接种液,考察了接种底质和接种量对测定结果的影响。接种量为3～5mL/L时,BOD5值达到了GB 7488-1987质控要求。2个月的稳定性考察实验以及对随机水样的测定结果表明,该方法制备的接种液活性高、稳定性好,对改进焦化废水BOD5的监测有一定的现实指导意义。     

5:3 Polyfluorinated acid aerobic biotransformation in activated sludge via novel "one-carbon removal pathways"

The polyfluorinated carboxylic acids 5:3 acid (C₅F₁₁CH₂CH₂CO₂H) and 7:3 acid (C₇F₁₅CH₂CH₂CO₂H) are major products from 6:2 FTOH (C₆F₁₃CH₂CH₂OH) and 8:2 FTOH (C₈F₁₇CH₂CH₂OH) aerobic biotransformation, respectively. The 5:3 and 7:3 acids were dosed into domestic WWTP activated sludge for 90 d to determine their biodegradability. The 7:3 acid aerobic biodegradability was low, only 1.7 mol% conversion to perfluoroheptanoic acid (PFHpA), whereas no transformation was observed previously in soil. In stark contrast, 5:3 acid aerobic biodegradability was enhanced 10 times in activated sludge compared to soil. The 5:3 acid was not activated by acyl CoEnzyme A (CoA) synthetase, a key step required for further α- or ß-oxidation. Instead, 5:3 acid was directly converted to 4:3 acid (C₄F₉CH₂CH₂CO₂H, 14.2 mol%) and 3:3 acid (C₃F₇CH₂CH₂CO₂H, 0.9 mol%) via “one-carbon removal pathways”. The 5:3 acid biotransformation also yielded perfluoropentanoic acid (PFPeA, 5.9 mol%) and perfluorobutanoic acid (PFBA, 0.8 mol%). This is the first report to identify key biotransformation intermediates which demonstrate novel one-carbon removal pathways with sequential removal of CF₂ groups. Identified biotransformation intermediates (10.2 mol% in sum) were 5:3 Uacid, α-OH 5:3 acid, 5:2 acid, and 5:2 Uacid. The 5:2 Uacid and 5:2 acid are novel intermediates identified for the first time which confirm the proposed pathways. In the biodegradation pathways, the genesis of the one carbon removal is CO₂ elimination from α-OH 5:3 acid. These results suggest that there are enzymatic mechanisms available in the environment that can lead to 6:2 FTOH and 5:3 acid mineralization. The dehydrogenation from 5:3 acid to 5:3 Uacid was the rate-limiting enzymatic step for 5:3 acid conversion to 4:3 acid.     

Volatile organic compounds at swine facilities: A critical review

Volatile organic compounds (VOCs) are regulated aerial pollutants that have environmental and health concerns. Swine operations produce and emit a complex mixture of VOCs with a wide range of molecular weights and a variety of physicochemical properties. Significant progress has been made in this area since the first experiment on VOCs at a swine facility in the early 1960s. A total of 47 research institutions in 15 North American, European, and Asian countries contributed to an increasing number of scientific publications. Nearly half of the research papers were published by U.S. institutions.Investigated major VOC sources included air inside swine barns, in headspaces of manure storages and composts, in open atmosphere above swine wastewater, and surrounding swine farms. They also included liquid swine manure and wastewater, and dusts inside and outside swine barns. Most of the sample analyses have been focusing on identification of VOC compounds and their relationship with odors. More than 500 VOCs have been identified. About 60% and 10% of the studies contributed to the quantification of VOC concentrations and emissions, respectively. The largest numbers of VOC compounds with reported concentrations in a single experimental study were 82 in air, 36 in manure, and 34 in dust samples.The relatively abundant VOC compounds that were quantified in at least two independent studies included acetic acid, butanoic acid (butyric acid), dimethyl disulfide, dimethyl sulfide, iso-valeric, p-cresol, propionic acid, skatole, trimethyl amine, and valeric acid in air. They included acetic acid, p-cresol, iso-butyric acid, butyric acid, indole, phenol, propionic acid, iso-valeric acid, and skatole in manure. In dust samples, they were acetic acid, propionic acid, butyric acid, valeric acid, p-cresol, hexanal, and decanal. Swine facility VOCs were preferentially bound to smaller-size dusts.Identification and quantification of VOCs were restricted by using instruments based on gas Chromatography (GC) and liquid chromatography (LC) with different detectors most of which require time-consuming procedures to obtain results. Various methodologies and technologies in sampling, sample preparation, and sample analysis have been used. Only four publications reported using GC based analyzers and PTR-MS (proton-transfer-reaction mass spectrometry) that allowed continuous VOC measurement. Because of this, the majority of experimental studies were only performed on limited numbers of air, manure, or dust samples. Many aerial VOCs had concentrations that were too low to be identified by the GC peaks.Although VOCs emitted from swine facilities have environmental concerns, only a few studies investigated VOC emission rates, which ranged from 3.0 to 176.5 mg d⁻¹ kg⁻¹ pig at swine finishing barns and from 2.3 to 45.2 g d⁻¹ m⁻² at manure storages. Similar to the other pollutants, spatial and temporal variations of aerial VOC concentrations and emissions existed and were significantly affected by manure management systems, barn structural designs, and ventilation rates.Scientific research in this area has been mainly driven by odor nuisance, instead of environment or health concerns. Compared with other aerial pollutants in animal agriculture, the current scientific knowledge about VOCs at swine facilities is still very limited and far from sufficient to develop reliable emission factors.     

Cyclic volatile methylsiloxanes in fish from the Baltic Sea

Laboratory studies suggest that the cyclic volatile methylsiloxanes (cVMS) octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6) will persist in the aquatic environment and bioaccumulate in fish. Here these cVMS were measured in herring collected in the Swedish waters of the Baltic Sea and the North Sea and in grey seals from the Baltic Proper. D4, D5, and D6 were present in herring muscle at concentrations around 10, 200, and 40 ng g⁻¹ lipid weight, respectively. The ratio of these concentrations was similar to the relative magnitude of estimated emissions to water, suggesting that the efficiency of overall transfer through the environment and food web was similar (within a factor 2–3) for the three chemicals. The concentrations of D5 and D6 were similar in herring caught in the highly populated Baltic Proper and in the less populated Bothnian Sea and Bothnian Bay. The D4 concentrations were lower at the most remote northern station, suggesting that D4 is less persistent than D5 and D6. Herring from the North Sea had lower levels of all three chemicals. The concentrations of D4, D5 and D6 in grey seal blubber were lower than the lipid normalized concentrations in herring, indicating that they do not biomagnify in grey seals.