Bio-SR工艺去除硫化氢气体的研究

采用Bio-SR工艺,利用铁盐吸收与氧化亚铁硫杆菌的联合作用对H2S进行脱除实验。通过改进微生物的培养条件,减少了83.9%的沉淀量,一定程度上解决了挂膜后生物填料塔易堵塞的问题,保证了填料塔的连续运行。在实验选取工况下,硫化氢脱除率可达到98.4%以上,当吸收液中Fe3+浓度为5.5～6 g/L、H2S进气浓度为1 g/m3、通气量为0.08～0.12 m3/h时效果最佳,反应器可持续高效地运行。此外,对进气浓度、通气量与硫化氢去除率之间的相关性进行了进一步研究,其结果有利于反应器及运行参数的优化设计。     

Nitrogen mass flow in China's animal production system and environmental implications

China's economic boom in recent decades has stimulated consumer demand for animal products and consequently, a vast expansion in animal production. From 1978 to 2006, the number of animals increased by 322% for pigs, 209% for poultry, and 2770% for dairy cattle. The objective of the present study was to quantify nitrogen mass flow in China's animal production system at the national scale and to elucidate potential environmental implications. A comprehensive analysis was performed combining statistical records with data from the scientific literature and supplemental survey information. Results indicate that approximately 18 Mt of N flowed through the Chinese animal production system in 2006. Nitrogen input to the system was from various feed materials, including 6.8 Mt (38% of total) from roughage, 4.4 Mt (24%) from byproducts, 2.3 Mt (13%) from cereal grains, and 1.6 Mt (9%) each from crop residues and oilseed cakes, with the remaining N (16%) obtained from other feedstuffs. Nitrogen outputs from the system included edible animal products (2.4 t, 13% of total), nonedible animal parts (e.g., bones, skins) (3.8 Mt, 21%), and excreta (12 Mt, 66%). At the national level, the excreta would average 28 Mg (as excreted) and 90 kg N ha(-1) of cropland. However, at the provincial level, it varied from 1 Mg ha(-1) (5 kg N ha(-1)) in Qinghai to 97 Mg ha(-1) (243 kg N ha(-1)) in Sichuan. In regions with excreta in the intermediate rate (e.g., Hebei Province, 115 kg N ha(-1)) or high rare (e.g., Sichuan Province, 243 kg N ha(-1)), animal manure contributes significantly to nutrients polluting groundwater and/or surface waters. It is crucial for China to develop and implement proper management practices to maximum the beneficial use of the 12 Mt excreta N while minimizing its environmental footprint.     

微波功率、辐射时间及污泥量对污泥微波干燥效能的综合影响研究

通过正交实验探讨了微波功率、辐射时间及污泥量对污泥微波干燥效能的综合影响研究,实验结果表明:在微波功率为140～580 W,辐射时间为5～20 min,污泥量为200～350 g的实验条件下,微波功率、辐射时间及两者之间的交互作用对污泥微波干燥效能影响高度显著,污泥量影响不显著;并得出微波功率、辐射时间对污泥含水率综合影响的定量正交回归方程。     

Fluoride removal performance of a novel Fe-Al-Ce trimetal oxide adsorbent

A trimetal oxide was developed as a fluoride adsorbent by coprecipitation of Fe(II), Al(III) and Ce(IV) salt solutions with a molar ratio of 1:4:1 under alkaline condition. The material retained amorphous structure and maintained relatively stable fluoride adsorption performance at calcination temperatures lower than 600 degrees C. The optimum pH range for fluoride adsorption was 6.0-6.5 and the adsorbent also showed high defluoridation ability around pH 5.5-7.0, which is preferable for actual application. A high fluoride adsorption capacity of 178 mg g(-1) was acquired under an equilibrium fluoride concentration of 84.5 mg l(-1), adsorbent dose of 150 mg l(-1) and pH 7.0. The adsorption isotherm could be better described by the two-site Langmuir model than the one-site model, suggesting the existence of two types of active sites on the adsorbent surface. Coexistence of high concentrations of phosphate or arsenate only led to partial inhibition of fluoride adsorption, which further suggests the existence of heterogeneous adsorption sites. Sulfate and chloride did not affect fluoride adsorption, and nitrate influenced it only when the concentration of NO(3)(-)-N exceeded 50 mg l(-1). A high desorption efficiency of 97% was achieved by treating fluoride loaded Fe-Al-Ce oxide with NaOH solution at pH 12.2. A column experiment using the adsorbent fabricated into 1mm pellets was performed at an initial fluoride concentration of 5.5 mg l(-1), space velocity of 5h(-1) and pH of 5.8, and 2240 bed volumes were treated with the effluent fluoride under 1.0 mg l(-1).     

Determination of benzene, toluene, ethylbenzene, xylenes in water at sub-ng l-1 levels by solid-phase microextraction coupled to cryo-trap gas chromatography-mass spectrometry

A trace analytical method of benzene, toluene, ethylbenzene and xylenes (BTEX) in water has been developed by using headspace solid-phase microextraction (HS-SPME) coupled to cryo-trap gas chromatography-mass spectrometry (GC-MS). The chromatographic peak shape for BTEX was improved by using cryo-trap equipment. The HS-SPME experimental procedures to extract BTEX from water were optimized with a 75 microm carboxen/polydimethylsiloxane (CAR/PDMS)-coated fiber at a sodium chloride concentration of 267 g l(-1), extraction for 15 min at 25 degrees C and desorption at 290 degrees C for 2 min. Good linearity was verified in a range of 0.0001-50 microg l(-1) for each analyte (r(2)=0.996-0.999). The limits of detection (LODs) of BTEX in water reached at sub-ng l(-1) levels. LODs of benzene, toluene, ethylbenzene, m/p-xylene and o-xylene were 0.04, 0.02, 0.05, 0.01 and 0.02 ng l(-1), respectively. The proposed analytical method was successfully used for the quantification of trace BTEX in ground water. The results indicate that HS-SPME coupled to cryo-trap GC-MS is an effective tool for analysis of BTEX in water samples at the sub-ng l(-1) level.     

Influence of changes in hydrodynamic conditions on cadmium transport in tidal river network of the Pearl River Delta, China

With rapid economic development, the Pearl River Delta (PRD) of China has experienced a series of serious heavy metal pollution events. Considering complex hydrodynamic and pollutants transport process, one-dimensional hydrodynamic model and heavy metal transport model were developed for tidal river network of the PRD. Then, several pollution emergency scenarios were designed by combining with the upper inflow, water quality and the lower tide level boundary conditions. Using this set of models, the temporal and spatial change process of cadmium (Cd) concentration was simulated. The influence of change in hydrodynamic conditions on Cd transport in tidal river network was assessed, and its transport laws were summarized. The result showed the following: Flow changes in the tidal river network were influenced remarkably by tidal backwater action, which further influenced the transport process of heavy metals; Cd concentrations in most sections while encountering high tide were far greater than those while encountering middle or low tides; and increased inflows from upper reaches could intensify water pollution in the West River (while encountering high tide) or the North River (while encountering middle or low tides).     

北京地区采暖期SO2熏烟型污染及评估

随着北京城市建设的发展，为了保护环境，北京市的新建生活区均采用集中供热系统。燃烧后的有害气体通过烟排向大气，经过高空稀释后的烟气可以降低污染负荷，但是在某此气象条件下仍然造成了地面局部污染，本文在北京市丰台区一个生活小区的供热系统污染源环境影响评价的基础上，讨论了熏烟污染的发生及危害。     

垃圾卫生填埋场卫生防护距离标准研究

根据我国大气环境质量标准，参照美国，日本等国对居住区的污染物容许浓度，提出了佛山市南海狮中垃圾卫生填埋卫生防护距离标准的建议值。     

Kinetic analysis of anaerobic phosphorus release during biological phosphorus removal process

Enhanced biological phosphorus removal (EBPR) is a commonly used and sustainable method for phosphorus removal from wastewater. Poly-β-hydroxybutyrate (PHB), polyphosphate, and glycogen are three kinds of intracellular storage polymers in phosphorus accumulation organisms. The variation of these polymers under different conditions has an apparent influence on anaerobic phosphorus release, which is very important for controlling the performance of EBPR. To obtain the mechanism and kinetic character of anaerobic phosphorus release, a series of batch experiments were performed using the excessively aerated sludge from the aerobic unit of the biological phosphorus removal system in this study. The results showed that the volatile suspended solid (VSS) had an increasing trend, while the mixed liquid suspended sludge (MLSS) and ashes were reduced during the anaerobic phosphorus release process. The interruption of anaerobic HAc-uptake and phosphorus-release occurs when the glycogen in the phosphorus-accumulating-organisms is exhausted. Under the condition of lower initial HAc-COD, HAc became the limiting factor after some time for anaerobic HAc uptake. Under the condition of higher initial HAc-COD, HAc uptake was stopped because of the depletion of glycogen in the microorganisms. The mean ratio of Δρ _P/Δρ _PHB, Δρ _GLY/Δρ _PHB, Δρ _P/ΔCOD, was 0.48, 0.50, 0.44, and 0.92, respectively, which was nearly the same as the theoretical value. The calibrated kinetic parameters of the HAc-uptake and phosphorus-release model were evaluated as follows: Q _HAc,max was 164 mg/(g · h), Q _P,max was 69.9 mg/(g · h), K _gly was 0.005, and KCOD was 3 mg/L. An apparently linear correlation was observed between the ratio of Δρ _P/ΔCOD and pH of the solution, and the equation between them was obtained in this study. Translated from Acta Scientiae Circumstantiae, 2005, 25(9), 1164–1169 [译自: 环境科学学报]     

环境水样中的痕量NO-2的化学发光分析法

本文将亚硝酸根在酸性介质中氧化亚铁氰化钾为铁氰化钾和鲁米诺-铁氰化钾-尿酸化学发光反应偶合一起,建立了一种间接测定亚硝酸根的新方法.讨论了酸度、反应物浓度、干扰离子等因素的影响.方法的检出限为5.0×l0-9g/mL,对环境水样样品进行了平行测定(n＝11),其相对标准偏差为1.9～3.3%,线性范围为l.0×l0-7～1.0×l0-5g/mL,回收率为94.45～105.5%.方法简便,易于操作,并具有较高的灵敏度和选择性,结果令人满意.