环境因素对长寿湖底泥释磷影响的模拟实验研究

肥水养殖显著增加了长寿湖底泥中的磷含量。为了解肥水养殖积累在湖泊底泥中磷的释放情况,以长寿湖大坝口枯水期底泥为实验材料,模拟研究了不同环境条件(上覆水pH、温度、DO含量和扰动)下湖泊底泥的释磷特征。结果表明,在弱碱性条件下,底泥释磷量随上覆水pH的升高而升高;温度升高有利于底泥磷的释放,温度每升高5℃,第21天时底泥释磷量增大0.0045～0.0074 mg/L;DO含量降低有利于底泥中铁/铝结合态磷的释放;扰动对底泥磷的释放没有明显影响。研究表明,网箱养殖增加了底泥中的有机磷含量,促进有机磷向无机磷转化,增大了底泥中磷的释放风险。     

改造现有工艺回收地面计量天然气

为解决牙哈作业区A区块3口井在见水后含水上升较快、单井产液量增加、现有装置处理能力不足,导致A区块所有生产井不能全部进站的问题,同时为提高最终采收率,需要延长见水时间,见水后控制含水的上升趋势。这就要求掌握含水井的生产动态,而现有装置无法对单井的含水进行计量,塔里木油田公司牙哈作业区A区块建造集中试采装置,文章介绍了改造前后的工艺流程及改造效果。     

石化废水深度处理用臭氧催化氧化体系的研究＊

文章就臭氧催化氧化体系在石化废水处理中的作用进行了深入研究,对催化剂载体、催化剂配伍体系以及臭氧的投加方式进行了优化筛选。根据实验,多元催化掺杂体系较一元催化体系氧化效果好,CODCr的去除率可由一元催化时的20%提高到多元催化时的33%;在臭氧的投加方式上,分段投加要优于单级投加,臭氧投加分配比例为6∶3∶1时,CODCr的去除率可由单一投加时的9%提高到分级投加时的19%。     

Restoration of hyper-eutrophic water with a modularized and air adjustable constructed submerged plant bed

A modularized and air adjustable constructed submerged plant bed (CSPB) which can be used to restore the eutrophic water is introduced in this paper. This plant bed helps hydrophyte grow under poor conditions such as frequently changed water depth, impaired water transparency, algae bloom and substantial duckweed in summer, which are not naturally suitable for growing hydrophyte. This pilot study in Waihuan River of Tianjin, China, revealed that reduction of Chemical Oxygen Demand (COD), Total Nitrogen (TN) and Total Phosphorus (TP) by the use of CSPB could be reached 30%–35%, 35%–40%, 30%–40% respectively in the growing season (from March to October) and 5%–10%, 5%–15%, 7%–20% respectively in the winter (from November to February) when the detention time was 6 d. The relationships between the concentration of COD, TN, TP and the detention time fit the first-order kinetic equation well and the coefficients of determination (R²) were all above 0.9. The attenuation coefficients k of the kinetic equation were a function of the water temperature. When the water temperature was quite low or quite high, k was not significantly changed with increasing or decreasing water temperature. While when the temperature was in a moderate range, an increase or decrease of water temperature would lead to a rapid increase or decrease in k.     

The concentrations, distribution and sources of PAHs in agricultural soils and vegetables from Shunde, Guangdong, China

The concentrations, distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in 30 agricultural soil and 16 vegetable samples collected from subtropical Shunde area, an important manufacturing center in China. The total PAHs ranged from 33.7 to 350 μg/kg in soils, and 82 to 1,258 μg/kg in vegetables. The most abundant individual PAHs are phenanthrene, fluoranthene, chrysene, pyrene and benzo(b)fluoranthene for soil samples, and anthracene, naphthalene, phenanthrene, pyrene and chrysene for vegetable samples. Average vegetable–soil ratios of total PAHs were 2.20 for leafy vegetables and 1.27 for fruity vegetables. Total PAHs in vegetable samples are not significantly correlated to those in corresponding soil samples. Principal component analyses were conducted to distinguish samples on basis of their distribution in each town, soil type and vegetable specie. Relatively abundant soil PAHs were found in town Jun’an, Beijiao, Chencun, Lecong and Ronggui, while abundant vegetable PAHs were observed in town Jun’an, Lecong, Xingtan, Daliang and Chenchun. The highest level of total PAHs were found in vegetable soil, followed by pond sediment and “stacked soil” on pond banks. The PAHs contents in leafy vegetables are higher than those in fruity vegetables. Some PAH compound ratios suggest the PAHs derived from incomplete combustion of petroleum, coal and refuse from power generation and ceramic manufacturing, and paint spraying on furniture, as well as sewage irrigation from textile industries. Soil PAHs contents have significant logarithmic correlation with total organic carbon, which demonstrates the importance of soil organic matter as sorbent to prevent losses of PAHs.     

Characterization and diurnal variation of size-resolved inorganic water-soluble ions at a rural background site

Water-soluble inorganic ions in aerosol samples have been studied. The sample collection took place during summer in 2003 at a European background site which is operating within the framework of the European Monitoring and Evaluation Program. Gent type PM10 stacked filter unit (SFU) samplers were operated in parallel on a day and night basis to collect particles in separate coarse (2.0-10 microm) and fine (<2.0 microm) size fractions. Particulate masses were measured gravimetrically; the filters from one of the SFU samplers were analyzed by particle-induced X-ray emission spectrometry (PIXE) and instrumental neutron activation analysis (INAA). Filters from the other SFU sampler were analyzed by ion chromatography (IC) for major inorganic anions (MSA-, NO2(-), NO3(-), Cl-, Br-, SO4(2-), oxalate) and cations (Na+, K+, NH4(+), Mg2+, Ca2+). The water-soluble inorganic ions measured were responsible for 44% and 16% of the total fine and coarse particulate mass, respectively. In the fine size fraction, the main ionic components were SO4(2-) and NH4(+) accounting for about 90% of fine ionic mass. In the coarse fraction the main ionic components were Ca2+ and NO3(-), followed by SO4(2-). Significant day and night difference in the mass concentrations was observed only for fine NO3(-). The molar ratios of fine NH4(+) to SO4(2-) indicated their complete neutralization to (NH4)2SO4. According to the cation-to-anion ratios the coarse particles were alkaline, while the fine particles were slightly acidic or neutral. By comparing the corresponding concentrations obtained from PIXE/INAA and IC, we determined the water-extractable part of the individual species. We also investigated the effect of long-range transported air masses on the local air concentrations, and we found that the air quality of this background monitoring station was affected by regional pollution sources.     

Kinetics of peanut shell pyrolysis and hydrolysis in subcritical water

Biomass is recognized as an important solution to energy and the environmental problems related to fossil fuel usage. The rational utilization of biomass waste is important not only for the prevention of environmental issues, but also for the effective utilization of natural resources. Pyrolysis and hyrolysis in subcritical water are promising processes for biomass waste conversion. This paper deals with hydrolysis and pyrolysis of peanut shells. Hydrolysis and pyrolysis kinetics of peanut shell wastes were investigated for the in-depth exploration of process mechanisms and for the control of the reactions. Hydrolysis kinetics was conducted in a temperature range of 180–240 °C. A simplified kinetic model to describe the hydrolysis of peanut shells was proposed. Hydrolysis activation energy as well as the pre-exponential factor was determined according to the model. The target products of peanut shell hydrolysis, reducing sugars, can reach up to 40.5 % (maximum yield) at 220 °C and 180 s. Pyrolysis characteristics were investigated. The results showed that three stages appeared in this thermal degradation process. Kinetic parameters in terms of apparent pyrolysis activation energy and pre-exponential factor were obtained by the Coats–Redfern method.     

不同类型电镀液中阴离子的离子色谱法检测

采用抑制型电导离子色谱法检测电镀液中的常见阴离子.色谱条件是: IonPac AS11-HC阴离子交换色谱柱,淋洗液自动发生装置在线产生KOH梯度淋洗,抑制型电导检测.检测限(S/N=3)在0.29-15.3 μg·l-1,阴离子F-,Cl-,MSA-,NO-3,SO2-4,PO3-4和CrO2-4的线性范围均在两个数量级以上,RSD在5%以下,回收率为92%-110%,具有灵敏度高,选择性好,重现性佳等特点,用于实际样品的检测,结果令人满意.     

玉米芯为碳源实现酸性矿山废水生物处理

引入了一种新的碳源——玉米芯，对SRB法处理酸性矿山废水进行了更加深入的探索，分析了各种参数条件对s暖一还原效果的影响，确定了常温下这种碳源所需要的最适宜工况条件，探讨了硫酸盐矿山废水的水质资源化问题，并对山西矿山废水的生物治理进行了可行性实验验证。实验证明，玉米芯为碳源时，矿山废水中SO^2-4的出水值可达221．1mg／L，金属离子的浓度也都达到了生活饮用水的质量标准，所以玉米芯可作为酸性矿山废水资源化生物处理的合适有效碳源。     

风险评价标准值初探

提出了风险指标和ALARP原则的含义,从风险评价的ALARP原则出发,得出个人风险评价标准值和社会风险评价标准值的制定方法。