A directional passive air sampler for monitoring polycyclic aromatic hydrocarbons (PAHs) in air mass

A passive air sampler was developed for collecting polycyclic aromatic hydrocarbons (PAHs) in air mass from various directions. The airflow velocity within the sampler was assessed for its responses to ambient wind speed and direction. The sampler was examined for trapped particles, evaluated quantitatively for influence of airflow velocity and temperature on PAH uptake, examined for PAH uptake kinetics, calibrated against active sampling, and finally tested in the field. The airflow volume passing the sampler was linearly proportional to ambient wind speed and sensitive to wind direction. The uptake rate for an individual PAH was a function of airflow velocity, temperature and the octanol-air partitioning coefficient of the PAH. For all PAHs with more than two rings, the passive sampler operated in a linear uptake phase for three weeks. Different PAH concentrations were obtained in air masses from different directions in the field test.     

Modified Fenton reaction for trichlorophenol dechlorination by enzymatically generated H2O2 and gluconic acid chelate

Glucose oxidase is a well-known enzyme that catalyzes the oxidation of β-d-glucose to produce gluconic acid and hydrogen peroxide. Fenton reaction is a powerful oxidation technology used for the oxidation of groundwater pollutants. For the application of Fenton reaction in groundwater remediation, successful operation of Fenton reaction near neutral pH, and on-site generation of both H₂O₂ and chelate will be beneficial. The focus of this experimental study was to couple the glucose oxidation reaction with chelate-based Fenton reaction. The idea was to use the hydrogen peroxide and chelate gluconic acid generated during glucose oxidation for the dechlorination of 2,4,6-trichlorophenol (TCP) by Fenton reaction. The oxidation of glucose was achieved using the enzyme in free and immobilized forms. The rate of production of hydrogen peroxide was determined for each system, and was used to estimate the time required for complete consumption of glucose during the process, thus avoiding any traces of glucose in the Fenton reaction. In the case of free enzyme reaction, separation of the enzyme was achieved using an ultrafiltration membrane before initiating the Fenton reaction. The oxidation of TCP by Fenton reaction was performed at varying ratios of gluconic acid/Fe, and its effect on the decomposition of TCP and H₂O₂ was studied. TCP degradation was studied both in terms of parent compound degradation and free chloride generation.     

Occurrence and fate of pesticides in four contrasting agricultural settings in the United States

Occurrence and fate of 45 pesticides and 40 pesticide degradates were investigated in four contrasting agricultural settings--in Maryland, Nebraska, California, and Washington. Primary crops included corn at all sites, soybeans in Maryland, orchards in California and Washington, and vineyards in Washington. Pesticides and pesticide degradates detected in water samples from all four areas were predominantly from two classes of herbicides--triazines and chloroacetanilides; insecticides and fungicides were not present in the shallow ground water. In most samples, pesticide degradates greatly exceeded the concentrations of parent pesticide. In samples from Nebraska, the parent pesticide atrazine [6-chloro-N-ethyl-N'-(1-methylethyl)-1,3,5-triazine-2,4-diamine] was about the same concentration as the degradate, but in samples from Maryland and California atrazine concentrations were substantially smaller than its degradate. Simazine [6-chloro-N,N'-diethyl-1,3,5-triazine-2,4-diamine], the second most detected triazine, was detected in ground water from Maryland, California, and Washington. Metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide] rarely was detected without its degradates, and when they were detected in the same sample metolachlor always had smaller concentrations. The Root-Zone Water-Quality Model was used to examine the occurrence and fate of metolachlor at the Maryland site. Simulations accurately predicted which metolachlor degradate would be predominant in the unsaturated zone. In analyses of relations among redox indicators and pesticide variance, apparent age, concentrations of dissolved oxygen, and excess nitrogen gas (from denitrification) were important indicators of the presence and concentration of pesticides in these ground water systems.     

Municipal waste compost as an alternative to cattle manure for supplying potassium to lowland rice

The importance of the use of potassium in agriculture is increasing in South Asia for making most productive use of the nutrient in terms of economic returns. Nutrient supply traditionally by cattle manure is constrained by its insufficient availability. Municipal waste compost may be an alternative source of nutrient supplements. Field experiments were conducted at the Experimental Farm of Calcutta University, West Bengal, India during the wet seasons of 1997, 1998 and 1999 on flooded lowland rice. Potassium fractions in municipal waste compost and cattle manure were determined by sequential extraction and also the potassium uptake by rice to compare the effectiveness of municipal waste compost with traditional manure. Potassium was significantly bound to the organic matter in municipal waste compost. Potassium uptake by rice grain and straw increased significantly with the combined application of organics and fertilizers and it was higher in grain than in straw. Water-soluble and non-exchangeable potassium contents of municipal waste compost and cattle manure were highly correlated with the uptake of potassium by straw and grain. Exchangeable and residual potassium were also significantly correlated with the uptake of potassium by straw and grain of rice. Much higher uptake of K in rice straw and rain resulted from applying the manures in conjunction with fertilizers than when applied singly.     

Analysis of pollution status of River Illo,Ota, Nigeria

An assessment of the pollution status of River Illo, located within River Owo catchments area in Ota, Ogun State, Nigeria, was carried out. The River’s response to deoxygenation due to BOD loading from an abattoir and its dissolved oxygen (DO) level was predicted using the modified Streeter-Phelps model. The average concentrations of measured parameters at the sampling stations include: 2.24 mg/l of DO, 312.85 mg/l of BOD, 782.86 mg/l of chemical oxygen demand, and 620.76 g/l of total solids. The DO model for River Illo showed a positive correlation between measured and calculated DO, while the dissolved oxygen curve gave a double spoon shape of two major segments with distinct zones of degradation, decomposition, and recovery. The self-purification factor (f) for both segments ranged between 0.8 and 1.1 depicting River Illo as a slow moving or sluggish river. The above results revealed slow reaeration of the water body while full recovery from pollution was difficult. The treatment of River Illo before usage is very essential to ensure public health safety of users from waterborne diseases.     

Modification of ferrite–manganese oxide sorbent by doping with cerium oxide

Fe–Mn oxide and Ce-doped Fe–Mn oxide sorbents were studied on the structural and desulfurization behavior in COS removal from syngas. The effects of cerium oxide on the Fe–Mn oxides have been investigated by XRD, BET, TPR, XPS and TEM methods. Analysis data show that the Ce-doped sorbent has larger specific surface area and better particles’ dispersion compared with non-modified Fe–Mn sorbent. The addition of Ce improves the reduction performance of Fe–Mn species. The desulfurization experiments show that the desulfurization activity of sorbent can be increased because of the promotion of the structural and redox properties by ceria doped. The Ce-doped sorbent can reduce COS from 15,000 ppmv to less than 0.1 ppmv at 325 °C and a space velocity of 1000 h⁻¹.     

Lysimeter Experiments to Investigate the Fate of Chemicals in Soils – Comparison of Five Different Lysimeter Systems

Several lysimeter scenarios and approaches exist to study the fate of agro-chemicals or contaminants from deposition in soil columns. In many systems just transport and leaching of the parent compound is followed, in some systems the leaching and transport of the metabolites is investigated as well. In more sophisticated lysimeter systems the volatilization and also the mineralization of the applied chemicals can be additionally monitored. Depending on the lysimeter system used and on the fact whether the applied chemicals are ¹⁴C-labeled or not, different results and various interpretations of the results might be achieved. Different lysimeter systems are described in this paper and a real dataset of a specific lysimeter experiment was transferred and evaluated in a virtual approach in the different lysimeter systems in order to show the advantages and disadvantages of the various systems.     

Magnetic mapping of fly-ash pollution and heavy metals from soil samples around a point source in a dry tropical environment

The Singrauli region in the southeastern part of Uttar Pradesh, India is one of the most polluted industrial sites of Asia. It encompasses 11 open cast coalmines and six thermal power stations that generate about 7,500 MW (about 10% of India’s installed generation capacity) electricity. Thermal power plants represent the main source of pollution in this region, emitting six million tonnes of fly-ash per annum. Fly-ash is deposited on soils over a large area surrounding thermal power plants. Fly-ashes have high surface concentrations of several toxic elements (heavy metals) and high atmospheric mobility. Fly ash is produced through high-temperature combustion of fossil fuel rich in ferromagnetic minerals. These contaminants can be identified using rock-magnetic methods. Magnetic susceptibility is directly linked to the concentration of ferromagnetic minerals, primarily high values of magnetite. In this study, magnetic susceptibility of top soil samples collected from surrounding areas of a bituminous-coal-fired power plant were measured to identify areas of high emission levels and to chart the spatial distribution of airborne solid particles. Sites close to the power plant have shown higher values of susceptibility that decreases with increasing distance from the source. A significant correlation between magnetic susceptibility and heavy metal content in soils is found. A comparison of the spatial distribution of magnetic susceptibility with heavy-metal concentrations in soil samples suggests that magnetic measurements can be used as a rapid and inexpensive method for proxy mapping of air borne pollution due to industrial activity.     

自催化法合成聚天冬氨酸

以马来酸酐和乙酸铵为原料，在微波条件下用自催化法合成了聚天冬氨酸（PASP）。通过正交实验确定了最佳合成条件：n（乙酸铵）：n（马来酸酐）=1．2，微波功率为1200W，反应时间为10min。在最佳合成条件下，PASP的收率为91．6％，PASP的黏均相对分子质量约为1．5×10^4。经红外光谱表征和核磁共振氢谱测试结果表明，PASP的各种主要官能团表现明显。当Ca^2＋质量浓度为250mg／L、PASP加入量为3mg／L时，PASP的阻垢率达到95％，表明PASP具有较好的阻垢性能。     

氯苯嘧啶醇在水体中的光解机制研究

以太阳光为实验光源研究了氯苯嘧啶醇在水溶液中的光解,考察了pH、水体类型、溶解氧及卤素离子等对其光解的影响.结果表明,氯苯嘧啶醇在水溶液中的光解符合一级动力学方程,在不同水体中氯苯嘧啶醇光解的速率大小顺序为:重蒸水>水库水>湖水>池塘水;氯苯嘧啶醇光解的半衰期随着溶液pH的增大而延长,当pH为5、7、9、11时光解半衰期分别为5.00、6.86、7.45、7.53 h;3种卤素离子对氯苯嘧啶醇光解有很大的影响,均表现出强的猝灭作用,3种离子的猝灭能力的大小顺序为Ⅰ->Br->Cl-;溶解氧和三重态光猝灭剂山梨酸均对氯苯嘧啶醇在水中的光解没有影响,而三重态光敏剂丙酮则对其光解有较强的猝灭作用,表明氯苯嘧啶醇在水中的光解主要以直接光解为主,光解过程不经历三重态.