6种挥发性有机物在甲苯驯化微生物中的好氧生物降解性能

利用振荡摇瓶法测定了6种典型挥发性有机物,甲苯、邻二甲苯、间二甲苯、对二甲苯、苯和氯苯在甲苯驯化微生物中的好氧生物降解性能.结果表明,在本研究的液相浓度范围内(甲苯＜174mg/L,邻二甲苯＜149mg/L,间二甲苯＜129mg/L,对二甲苯＜133mg/L,苯＜234mg/L,氯苯＜146mg/L),3种二甲苯、苯和氯苯的降解速率随其初始浓度的增大而增加,符合一级反应,这5种VOCs未对微生物产生明显的抑制或毒害作用;甲苯的液相浓度大于85mg/L时,其降解速率不随初始浓度的增大而改变,其降解规律符合Monod方程.     

Employment of passive sampling in monitoring indoor air quality in selected residences in a Tri-city area in Poland

Time-weighted average concentrations of selected volatile compounds were measured in chosen residences in a Tri-City area of Poland by means of passive sampling. The results were compared to those obtained by dynamic technique – sorption tubes filled with Tenax TA sorbent. Results obtained by employing the two techniques were similar. Total volatile organic compound (TVOC) parameters were also determined. An attempt was also made to evaluate the influence of outdoor air pollutants on indoor air quality.     

Study of sorptive properties of trap systems for selective enrichment of volatile organic compounds from tobacco smoke samples

There is a dearth of data on the consumer product concentrations of iron, lead, and nickel for accurate comparison to be made. The levels of these elements were determined in 85 samples of six different classes of personal care products commonly used in Nigeria using atomic absorption spectrophotometry. The results of the analysis showed that the range of the mean concentrations of Fe was 0.485–1.108 ppm, Pb ND–0.163 ppm, and Ni ND-0.160 ppm. The analytical data have demonstrated that the selected consumer products are possible sources of iron, lead, and nickel exposure. Users can be exposed to these metals directly through dermal contact or inhalation. The regulations relating to cosmetic products give no limit values for heavy metals in cosmetic products, hence, it was difficult to establish if the values obtained in this study are safe or not. Prolonged use of soaps, creams, and detergent containing these elements may pose threat to human health and the environment. This could be responsible for various skin diseases such as allergic skin, follicular and pigmentary disorders, which are common among the users (exposed groups) of these products in Nigeria. A body of evidence has presented a rare example of systemic allergic dermatitis caused by topical application of a mercury-containing cosmetic to the upper lip of a 32-year-old Turkish patient.     

Male reproductive toxicity of organophosphorous compounds: a review

Fertility is declining in many countries and there has been substantial interest in the potential adverse effects of exposure to environmental hazardous chemicals, including pesticides on male reproduction. Organophosphorous compounds (organophosphates, OP) constitute a heterogeneous category of chemicals specifically designed for the control of pests or plant diseases. OP are known to produce reproductive toxicity, resulting in a decrease in the fertility levels of humans and animals. This review article mainly focused on toxicity of some OP such as acephate, chlorpyrifos, diazinon, dimethoate, fenitrothion, malathion, and monocrotophos especially dealing with reproductive toxicity in males. Furthermore, this review deals with mode of action and clinical syndromes of OP. Considerable lab studies on animals concluded that OP produce adverse effects on male reproductive system.     

Detection and quantitation of trace levels of low molecular weight halocarbons (LMHs) associated with commercial sodium humate

Examination of vapor above commercial sodium humate and above 10wt% aqueous humate solution by gas chromatography (GC) revealed the presence of chloroform and trichloroethylene. Further examination of the aqueous humate by the purge and trap procedure confirmed the association of chloroform and trichloroethylene with the humate. GC/mass spectrometry analyses of methylene chloride extract of the humate established the association of LMHs with the humate. Improved headspace capillary GC technique showed that the humate contained not only chloroform, trichloroethylene but several other LMHs in the range 190 to 4000ng·kg^‐1.     

Aqueous high‐temperature chemistry of arsenic‐containing compounds in water at 300°C

Arsenic compounds, and especially organo‐arsenic derivatives, are highly toxic and many have been manufactured as chemical warfare agents. This study was designed to provide background information relevant to the potential application of aquathermolysis techniques for the detoxification of such potent military warfare agents. Six arsenic‐containing compounds with structural features which mimic known agents were studied in neutral superheated water: 4‐aminophenylarsine oxide, 4‐arsanilic acid, 4‐nitrophenylarsonic acid, 5, 10‐dihydro‐10‐ethylphenarsazine, tetraphenylarsonium chloride hydrate, and (3‐cyanopropyl)dimethyl(2‐phenethyl)arsonium bromide. Most of these compounds were moderately susceptible to hydrolysis for 1h at 300°C. o‐ and p‐Aminosubsituted arsenic compounds were more reactive than compounds with an electron‐withdrawing group substituent. Aromatic C—As bonds were more resistant to cleavage than aliphatic C—As bonds.     

Source and material balance of total organic halogen pollution in the Ayase River system,Japan

The total organic halogen (TOX) pollution in the highly polluted Ayase River system was investigated. Using the concentration of coexisting linear undecylbenzenesulfonate and the difference in the flowing water volume between summer and winter, the fractions of domestic and agricultural wastewaters in the whole water column were calculated and the variety of the TOX sources in the river was estimated. The river carried about 100 kgCl of TOX materials in one day; about 50 kgCl of the materials was from residential area in the basin. The contribution of agricultural drainage from paddy field was not negligible in summer. Highly contribution of industrial wastewater was observed in a tributary Furuayase River basin while the amount of TOX loaded in the area was widely varied; 0–105 kgCl of the materials was discharged as industrial wastewater.     

珠江三角洲印刷行业VOCs组分排放清单及关键活性组分

根据珠江三角洲地区印刷行业活动数据和不锈钢罐采样-气质联用技术,获取了印刷工艺VOCs成分谱,建立了该地区2010年印刷行业VOCs组分排放清单,研究了不同工艺排放的臭氧生成潜势. 结果表明:该地区2010年印刷行业VOCs排放总量达8591.26t,深圳、东莞、佛山排放量较大.凹印是印刷行业主要VOCs排放工艺,排放量达5762.01t;平印和凸印次之,分别为1954.01和37.82t.不同工艺排放的VOCs组分差异较大,平印工艺排放的VOCs成分中异丙醇含量最多(306.58t),其次为正庚烷(115.87t);苯和甲苯是凸印工艺排放的VOCs成分中含量最大的2种化合物,分别达5.58和4.83t;乙酸乙酯是凹印工艺排放的VOCs成分中的首要化合物,达2482.85t.凸印工艺排放的VOCs单位浓度臭氧潜势最大,达1.30μg/m3,平印和凹印较小,分别为0.89和0.72μg/m3,各工艺排放的含氧有机物对臭氧生成潜势的贡献均为最大.      

Microbial Potential for the Anaerobic Transformation of Simple Homocyclic and Heterocyclic Compounds in Sediments of the Tsengwen River

The ability of microbial populations to mediate the anaerobic transformation of four aromatic compounds (aniline, benzoic acid, pyridine, and quinoline) in sediments of the Tsengwen River was examined. Along the river, from a freshwater (0.0° salinity) to an oceanic (37.0° salinity) environment, five sampling stations were chosen to collect the sediment. Sediment slurries were incubated in an anaerobic mineral salts medium that was amended with multiple electron acceptors, including manganese (IV) and ferric (III) oxides, and the concentrations of the aromatic substrates were followed over a 3- to 4-month period. Most sediment samples showed a complete loss of benzoic acid and quinoline (0.12–0.21 mM) within approximately three months. Pyridine was transformed after a lag period of 53 days in the sediment slurries from the freshwater environment which had been amended with both metal oxide (either Fe (OH)₃ or MnO₂) and inhibitor (either BESA or molybdate). Pyridine was not transformed in other sediment slurries. No significant metabolism of aniline was apparent in any of the sediments.