秦皇岛市重点工业企业VOCs排放及分布特征

工业企业挥发性有机物(VOCs)污染排放对大气环境影响日益突出,工业源VOCs污染防治成为环境保护的重点工作。为进一步提高秦皇岛市工业源挥发性有机物(VOCs)治理的科学性、针对性和有效性,对2019年秦皇岛市重点排污企业VOCs的排污量、区域分布、排放行业等进行了详细调查分析:秦皇岛市重点工业源VOCs排放总量为6875.83t,排放量最大的区域是秦皇岛经济技术开发区,占比51.1%;排放量最大的行业是交通运输设备制造业,占总排放量的33.5%;溶剂使用源的排放量最大,占比52.3%。     

Organochlorine and heavy metals in newborns: Results from the Flemish Environment and Health Survey (FLEHS 2002–2006)

To collect regional information on internal levels of pollutants in humans in Flanders, 1196 mother–child pairs were systematically recruited in 2002–2003 via 25 maternities across Flanders. Cd, Pb, PCB congeners 118, 170, 138, 153 and 180, p,p′-DDE — a key metabolite of DDT- and hexachlorobenzene (HCB) were measured in cord blood or plasma. Cd was detected in 64% of the samples (geometric mean 0.21 µg/L cord blood). p,p′-DDE (110 ng/g plasma lipids) and Pb (14.7 µg/L blood), were measurable in nearly all samples. The individual PCB congeners could be detected in 40 to 81% of the newborns (138 + 153 + 180 = 64.4 ng/g plasma lipids). HCB (18.9 ng/g plasma lipids) and dioxin-like compounds measured by DR-CALUX® (23 pg CALUX-TEQ/g lipids) were above detection limit in more than 75% of the samples. Age and smoking habits of the mothers, did not influence the cord blood Pb and Cd levels. The organochlorines increased 4 to 9% per year of the mother's age (partial R² = 0.05 to 0.22). Mothers had 2.6% less PCBs in cord blood (partial R² = 0.02) for each unit increase in pre-pregnancy BMI. Season of delivery, breastfeeding previous children or consumption of local dairy products, were minor determinants. Up to 20% of the variability in organochlorine concentrations was explained by residence area. It was concluded that the place of birth in Flanders is an important determinant of the load of pollutants measured at the start of life. This underlines the validity of human biomonitoring on (relatively) small geographical scale.     

Biomagnification of anthropogenic and naturally-produced organobrominated compounds in a marine food web from Sydney Harbour, Australia

Polybrominated diphenyl ethers (PBDEs) and naturally-produced organobrominated compounds, such as methoxylated PBDEs (MeO-PBDEs), have been scarcely studied in the Southern Hemisphere. Yet, sources of the latter group of compounds were found in Southern regions, specifically in Australia. The environmental distribution and biomagnification potential of organobrominated compounds were therefore investigated in a representative aquatic food chain (invertebrates and fish) from the Sydney Harbour, Australia. Mean PBDE concentrations ranged from 6.4 ng/g lipid weight (lw) in squid to 115 ng/g lw in flounder. BDE 47 was the dominant congener, followed by BDE 100. Mean levels of MeO-PBDEs (sum of congeners 2’-MeO-BDE 68 and 6-MeO-BDE 47) were as high as 110 ng/g lw in tailor, with a slight dominance of 2’-MeO-BDE 68. Polybrominated hexahydroxanthene derivates (PBHDs), another class of naturally-produced compounds, were found at variable concentrations and ranged from 4.7 ng/g lw in fanbelly and 146 ng/g lw in tailor. The tribrominated PBHD isomer dominated in the samples, except for luderick and squid. The lower levels of PBDEs found in luderick from the harbour compared to those obtained from the upper Parramatta River indicated a terrestrial (anthropogenic) origin of PBDEs, while the higher levels of MeO-PBDEs and PBHDs in the samples from the harbour confirmed the marine (natural) origin of these compounds. The highest trophic magnification factor (TMF) was found for sum PBDEs (3.9), while TMFs for sum MeO-PBDEs and sum PBHDs were 2.9 and 3.4, respectively. This suggests that biomagnification occurs in the studied aquatic food chain for anthropogenic brominated compounds, but also for the naturally-produced organobromines.     

典型涂料制造企业VOCs排放量核算与排放特征分析

采集了上海地区8家不同类型的涂料制造企业中不同生产环节有组织排放的废气样本,分析其VOCs组分特征和活性VOCs物种,并应用3种实际排放量核算方法计算企业的VOCs年排放量,分析了其与排污许可排放量的关系。结果表明：1)涂料制造行业排放废气的特征组分为芳香烃、OVOCs、卤代烃,占全部VOCs质量浓度的56.2%~99.1%,乙酸乙酯、乙酸丁酯、4-乙基甲苯、间/对二甲苯、甲苯、甲乙酮是涂料制造行业VOCs排放的典型物种;2)基于MIR值法的计算结果,芳香烃和OVOCs是涂料制造行业排放VOCs的主要活性组分,累计OFP贡献率达36.0%~99.8%,其中,4-乙基甲苯(52.1%)、氯乙烯(48.1%)、乙酸丁酯(47.9%)、乙酸乙酯(42.6%)、间/对二甲苯(41.3%)是各类涂料工艺废气中OFP贡献率最高的物质,除苯系物、乙酸酯类化合物外,氯乙烯、甲乙酮、四氢呋喃也是涂料制造过程中值得关注的活性物质;3)涂料制造企业车间的有组织废气VOCs排放量占全厂VOCs排放量的75.0%以上,其次是实验室废气,VOCs排放量为3.5%~16.8%。在VOCs实际排放量核算中,使用实测法的核算结果与物料衡算法接近,且计算简便,在正常运行时均低于许可排放限值;而产污系数法所核算数值较许可排放限值更高,在现阶段可作为一项惩罚性计算方法。     

吸附法净化工业VOCs的研究进展

挥发性有机化合物(VOCs)是大气中PM2.5及O3的关键前体物,大多易燃易爆,部分属有毒有害物质,会造成大气环境污染,有损人群健康.吸附法因简单高效及低成本等优点被广泛应用于VOCs的净化.综述了工业VOCs的类型及特点,分析了影响VOCs吸附净化效果的主要因素,如吸附材料、吸附剂物化参数(比表面积、孔结构、表面官能...     

Determination of Q1, an unknown organochlorine contaminant, in human milk, Antarctic air, and further environmental samples

Q1, an organochlorine component with the molecular formula C(9)H(3)Cl(7)N(2) and of unknown origin was recently identified in seal blubber samples from the Namibian coast (southwest of Africa) and the Antarctic. In these samples, Q1 was more abundant than PCBs and on the level of DDT residues. Furthermore, Q1 was more abundant in seals from the Antarctic than the Arctic. To prove this assumption, gas chromatography-electron-capture negative ion mass spectrometry (GC/ECNI-MS), which is sensitive and selective for Q1, allowed for screening of traces of Q1 even in samples with particularly high levels of other organochlorine contaminants. Q1 was isolated by high-performance liquid chromatography (HPLC) from a skua liver sample. A 1:1 mixture with trans-nonachlor in electron-capture detectors (ECDs) was used to determine the relative response factor with ECNI-MS. The ECNI-MS response of Q1 turned out to be 4.5 times higher than that of trans-nonachlor in an ECD. With GC/ECNI-MS in the selected ion-monitoring mode, four Antarctic and four Arctic air samples were investigated for the presence of Q1. In the Antarctic air samples, Q1 levels ranged from 0.7 to 0.9 fg/m(3). In Arctic air samples, however, Q1 was below the detection limit (<0.06 fg/m(3) or 60 ag/m(3)). We also report on high Q1 levels in selected human milk samples (12-230 microg/kg lipid) and, therefore, suggested that the unknown Q1 is an environmental compound whose origin and distribution should be investigated in detail. Our data confirm that Q1 is a bioaccumulative natural organochlorine product. Detection of a highly chlorinated natural organochlorine compound in air and human milk is novel.     

含氮芳香化合物的厌氧生物降解研究回顾

回顾了硝基芳香化合物和偶氮化合物在厌氧条件下的生物脱毒、转化和矿化作用的研究成果。这些研究表明 ,由于硝基和偶氮基具有强烈的吸电子性 ,好氧条件下很难降解。但是 ,硝基和偶氮基芳香化合物在产甲烷菌群作用下较易还原脱毒 ,转化为相应的芳香胺类 ,其毒性要小几个数量级 ,因而有些毒性很高的芳香化合物废水可利用厌氧反应器处理 ,而且反应过程中发现一些芳香胺类化合物可被完全矿化 ,表明一些含氮芳香化合物可作为厌氧菌的碳源和能源 ,在厌氧条件下被完全生物降解。     

单环硝基芳香化合物好氧生物降解及其遗传学研究进展

硝基芳香化合物是环境中难降解的有机污染物之一 ,对环境的污染日益严重 ,利用生物技术对这类有机物进行降解是行之有效的新途径。针对几种单环硝基芳香化合物好氧降解的微生物、降解途径以及降解过程中的主要酶、降解性质粒、基因定位等分子遗传学的研究进展进行了综述     

Antifungal and anti-aflatoxigenic activity of Heliopsis longipes roots and affinin/spilanthol against Aspergillus parasiticus by downregulating the expression of alfD and aflR genes of the aflatoxins biosynthetic pathway

Abstract

In the present study, ethanolic extract from Heliopsis longipes roots and affinin/spilanthol against Aspergillus parasiticus growth and aflatoxins production were studied in relation to the expression of aflD and aflR, two key genes of aflatoxins biosynthetic pathway. Phytochemical analysis of the ethanolic extract by GC-EIMS identified affinin/spilanthol (7.84?±?0.27?mg g^?1) as the most abundant compounds in H. longipes roots. The antifungal and anti-aflatoxigenic assays showed that affinin/spilanthol at 300?µg mL^?1 produced the higher inhibition of radial growth (95%), as well as, the higher aflatoxins production inhibition (61%) in comparison to H. longipes roots (87% and 48%, respectively). qRT-PCR revealed that the expression of aflD and aflR genes showed a higher downregulation in affinin/spilanthol at 300?µg mL^?1. The expression ratio of alfD was suppressed by affinin/spilanthol in 79% and aflR in 84%, while, a lower expression ratio suppressed by H. longipes was obtained, alfD (55%) and aflR (59%). Affinin/spilanthol possesses higher antifungal and anti-aflatoxigenic activity against A. parasiticus rather than H. longipes roots, and this anti-aflaxotigenic activity occurring via downregulation of the aflD and aflR genes. Thus, H. longipes roots and affinin/spilanthol can be considered potent antifungal agents against aflatoxigenic fungus, especially, affinin/spilanthol.     

ENHANCEMENTS OF NONPOINT SOURCE MONITORING OF VOLATILE ORGANIC COMPOUNDS IN GROUND WATER1

ABSTRACT: The U.S. Geological Survey (USGS) has compiled a national retrospective data set of analyses of volatile organic compounds (VOCs) in ground water of the United States. The data are from Federal, State, and local nonpoint‐source monitoring programs, collected between 1985–95. This data set is being used to augment data collected by the USGS National Water‐Quality Assessment (NAWQA) Program to ascertain the occurrence of VOCs in ground water nationwide. Eleven attributes of the retrospective data set were evaluated to determine the suitability of the data to augment NAWQA data in answering occurrence questions of varying complexity. These 11 attributes are the VOC analyte list and the associated reporting levels for each VOC, well type, well‐casing material, type of openings in the interval (screened interval or open hole), well depth, depth to the top and bottom of the open interval(s), depth to water level in the well, aquifer type (confined or unconfined), and aquifer lithology. VOCs frequently analyzed included solvents, industrial reagents, and refrigerants, but other VOCs of current interest were not frequently analyzed. About 70 percent of the sampled wells have the type of well documented in the data set, and about 74 percent have well depth documented. However, the data set generally lacks documentation of other characteristics, such as well‐casing material, information about the screened or open interval(s), depth to water level in the well, and aquifer type and lithology. For example, only about 20 percent of the wells include information on depth to water level in the well and only about 14 percent of the wells include information about aquifer type. The three most important enhancements to VOC data collected in nonpoint‐source monitoring programs for use in a national assessment of VOC occurrence in ground water would be an expanded VOC analyte list, recording the reporting level for each analyte for every analysis, and recording key ancillary information about each well. These enhancements would greatly increase the usefulness of VOC data in addressing complex occurrence questions, such as those that seek to explain the reasons for VOC occurrence and nonoccurrence in ground water of the United States.