解磷微生物对煤系废弃物粉煤灰的改良效应

燃煤产生大量的粉煤灰虽会严重污染环境,但却含有植物生长必需的营养元素,将其资源化生物利用是一条很好的途径.从粉煤灰和农田土壤中分离筛选出 2 株解磷细菌 CA 和 SL,以紫花苜蓿为供试植物,通过盆栽试验研究接种解磷细菌对粉煤灰基质的改良作用.研究表明,加入解磷细菌后,对粉煤灰基质有一定的改良作用,促进了植物生长,增加了对粉煤灰中难溶性磷的吸收利用,降低了粉煤灰 pH,增加了根际细菌和真菌的数量.从粉煤灰中筛选分离出的菌株 CA的改良作用更显著,苜蓿的地上干重比对照提高了45.1%.解磷微生物的应用对于实现废弃物粉煤灰场的生态恢复提供了新的技术与潜力.     

不同基质人工湿地去除重金属Cd的研究

以粉煤灰(F)、河砂(S)、河砂+粉煤灰(S+F)为基质,搭配水芹(Oenanthe javanica)、灯芯草(Juncus effusus)和水葫芦(Eichhornia crassipes),研究人工湿地对废水中Cd的净化效果。结果表明,3种基质对Cd均有明显的去除效果。其中,F基质去除效果最好,但出水pH和电导率较高,且水芹和水葫芦相对电导率(REC)和丙二醛(MDA)较高,表明植物生长受到影响。S基质对Cd去除率最低,但植物生长状态良好。S+F基质发生协同作用,有利于植物生长,去除Cd效果也较好,评估为最佳人工湿地基质。人工湿地中不同基质各层全量Cd、有效态Cd分布情况均为上层中层下层。     

植物-微生物联合修复石油污染土壤的实验研究

筛选高效石油降解菌并考察菌株的石油降解能力,通过植物-微生物联合修复石油污染土壤室内实验,在修复过程中测定了土壤中细菌和固氮菌,碱解氮、速效磷和速效钾的含量变化,同时采用傅立叶变换离子回旋共振质谱(ESI FT-ICR MS)考察了植物-微生物联合修复效果。结果表明,菌株3#、4#的生长适应性较强,其混合菌的降解效果最好,将其混合菌液与植物进行植物-微生物联合修复不同浓度的石油污染土壤,经过150 d的温室降解,最高降解率达到73.47%。ESI FT-ICR MS分析结果表明,与空白组相比,植物组的O1、O2和N1类等化合物相对丰度都发生了显著变化,石油污染物得到一定程度的生物降解。     

染料降解菌的脱色特性、降解酶系及基因定位研究进展

本文分析了当前染料废水微生物降解优势菌的降解效果及降解机制等，介绍了三种染料降解酶的催化机理和影响因素，阐明了某些降解菌中的质粒可以控制不同结构染料的脱色。最终指出了提高菌株应用价值的两种途径：一是筛选或构建出具有多功能性的超级菌；二是在不改变染料性质的前提下，向其分子结构中引入特定取代基团，以提高其生物降解性。     

樟脑废水高效优势降解菌的选育及降解效果

针对樟脑废水，从活性污泥中筛选出降解樟脑废水的高效优势菌，通过分离纯化，优选出三株适应能力强、生长旺盛的菌株，分别为ZH-1，ZH-2、TZH-2。经初步鉴定分别为动胶菌属、假单胞菌属、短杆菌属。试验测定了单株菌和混合菌对樟脑废水的降解效果，结果表明，混合菌的降解效果最为明显，降解率为75．23％。     

利用Rank氧电极筛选焦化废水功能菌的探索

介绍了一种利用Rank氧电极筛选焦化废水功能菌的方法。实验所用焦化废水中含有结构不明的成色有机物，从驯化后的活性污泥中分离到一组对该物质有效的菌株，利用Rank氧电极测定其对该物质的活性大小，筛选出活性较好的菌种用于废水生化处理的进一步研究。对于结构不明的物质降解，这种方法具有快速、简捷、灵敏度高等优点。可广泛应用于功能菌的筛选等方面。     

镉污染土壤的植物修复研究进展

镉会影响植物正常生长,经食物链富集,则会对动物和人体造成危害。植物修复是一种生态友好的修复手段,能有效修复镉污染土壤。因此,开展镉污染土壤植物修复的系统研究非常必要。通过研究发现,目前针对镉污染土壤的植物修复的研究主要集中于两方面:一方面是镉超积累植物和镉富集性植物的筛选,另一方面是植物-微生物联合修复技术的强化。目前已筛选出镉超积累植物11种,镉富集性植物31种,已研究出针对镉污染土壤的植物-微生物匹配组合11个,镉耐性菌16种。     

城市污水中高效COD去除菌对微藻生长的促进作用研究

利用城市污水培养微藻生产柴油既有助于去除污染物,又可回收能源,是解决环境污染与能源危机的研究热点之一。从城市污水处理系统中筛选有利于微藻生长的高效COD去除菌,并考察其对微藻生长的促进作用。研究结果表明:在筛选的38株菌中有5株为高效COD去除菌,分别命名为L2、L8、L11、W2、W5,5个菌株对COD的去除率均达到80%左右。在原污水培养条件下,菌株L11对微藻的生长具有显著的促进作用,与空白组相比,稳定期微藻产量提高了97.7%,微藻平均生长速率提高了12.7%,油脂产量提高了75.8%。菌株L11与微藻共培养不仅可以提高微藻产量,同时有利于使污水中的COD维持在较低水平。     

牛粪堆肥升温菌剂的筛选及其作用机制

以糖、淀粉、蛋白质、纤维素培养基及菌株增殖倍数、菌株性能等为筛选方法,从牛粪低温堆肥中筛选不同原料重要功能菌并组成功能菌剂;以不同类别原料菌及单菌株发酵实验对升温机制进行研究。结果表明,芽孢杆菌、假单胞菌、纤维单胞菌及小孢霉菌等为重要功能菌;菌剂起温快,升温效果好,48 h堆体即由低温进入中温,5 d达到高温,腐熟时间可缩短至约17~18 d;糖功能菌升温效果最为显著,淀粉及蛋白质功能菌次之,纤维素功能菌升温能力较弱;菌株利用各种原料能力越强,增殖速度越快,对升温作用越大。各菌株充分利用基质各成分,紧密协同和促进,是低温堆体发酵升温的主要作用机制。     

畜禽养殖污水中高效氨氮降解菌的筛选、鉴定及生长条件研究

从养殖污水中分离纯化得到1株高效氨氮降解菌,对其进行形态特征、生理生化、16S rDNA序列分析以及最佳生长条件研究,并将菌株投入养殖污水降解污水中的氨氮。结果表明：AN4菌株在NH4＋-N初始质量浓度为50 mg/L的条件下,24 h内的氨氮降解率为92.5%;初步鉴定该菌株为苍白杆菌属（Ochrobactrum sp.）,菌株的16S rDNA序列在Gen-Bank的登录号为GU345782;AN4菌株在装液量为60.64 mL,pH为7.06,葡萄糖为6.0 g/L的条件下培养,菌株的降解率可以达到94.28%;菌株对养殖污水中氨氮的降解率为12.3%。苍白杆菌菌属能够降畜禽养殖污水中的氨氮还未见报道,AN4菌株的筛选获得为生物降解养殖污水中的氨氮又提供了一种新型菌株。     

Influence of plant growth promoting bacteria and its mutant on heavy metal toxicity in Brassica juncea grown in fly ash amended soil

In this study a metal tolerant plant growth promoting bacteria, NBRI K28 Enterobacter sp. was isolated from fly ash (FA) contaminated soils. The strain NBRI K28 and its siderophore overproducing mutant NBRI K28 SD1 were found capable of stimulating plant biomass and enhance phytoextraction of metals (Ni, Zn and Cr) from FA by metal accumulating plant i.e. Brassica juncea (Indian mustard). Concurrent production of siderophores, Indole acetic acid (IAA) and phosphate solubilization revealed its plant growth promotion potential. The strain also exhibited 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase activity. In most of the cases mutant of NBRI K28, exerted more pronounced effect on metal accumulation and growth performance of B. juncea plants than wild type.     

Release of mercury vapor from coal combustion ash

The long-term stability of Hg in coal combustion by-products (CCBs) was evaluated at ambient and near-ambient temperatures. Six CCB samples with atypically high levels of total Hg were selected for study assuming a greater potential for release of measurable amounts of Hg vapor. The samples selected included two fly ash samples from U.S. eastern bituminous coal, two fly ash samples from South African low-rank coal, one fly ash from Powder River Basin (PRB) subbituminous coal blended with petroleum coke, and one PRB subbituminous coal fly ash incorporated with flue gas desulfurization material. Air scrubbed of Hg was passed through compacted 100-g aliquots of each sample at 1 mL/min and vented to a gold-coated quartz trap to collect released Hg vapor. The samples were maintained at ambient and near-ambient (37 degrees C) temperatures. All samples released low-picogram levels of Hg after 90 days. No pattern was evident to link the total Hg content to the rate of release of Hg vapor. An average of 0.030 pg Hg/g CCB/day was released from the samples, which equates to 2.2 x 10(-8) lb Hg/ton CCB/year. If this were applied to a coal-fired power plant production of 200,000 tons of fly ash per year, there would be a maximum potential release of 0.0044 lb, or 2.00 g, of Hg per year. Experiments are continuing to determine long-term vapor release of Hg from CCBs. All samples have been set up in duplicate at ambient temperature with an improved apparatus to reevaluate results reported in this article.     

Release of Mercury Vapor from Coal Combustion Ash

Abstract

The long-term stability of Hg in coal combustion byproducts (CCBs) was evaluated at ambient and near-ambient temperatures. Six CCB samples with atypically high levels of total Hg were selected for study assuming a greater potential for release of measurable amounts of Hg vapor. The samples selected included two fly ash samples from U.S. eastern bituminous coal, two fly ash samples from South African low-rank coal, one fly ash from Powder River Basin (PRB) subbituminous coal blended with petroleum coke, and one PRB subbituminous coal fly ash incorporated with flue gas desulfurization material.

Air scrubbed of Hg was passed through compacted 100-g aliquots of each sample at 1 mL/min and vented to a gold-coated quartz trap to collect released Hg vapor. The samples were maintained at ambient and near-ambient (37 °C) temperatures. All samples released low-picogram levels of Hg after 90 days. No pattern was evident to link the total Hg content to the rate of release of Hg vapor. An average of 0.030 pg Hg/g CCB/day was released from the samples, which equates to 2.2 x 10^-8 lb Hg/ton CCB/year. If this were applied to a coal-fired power plant production of 200,000 tons of fly ash per year, there would be a maximum potential release of 0.0044 lb, or 2.00 g, of Hg per year. Experiments are continuing to determine long-term vapor release of Hg from CCBs. All samples have been set up in duplicate at ambient temperature with an improved apparatus to reevalu-ate results reported in this article.     

Utilization of coal fly ash as a slow-release granular medium for soil improvement

This work proposes a new potential application of waste coal fly ash as a K fertilizer support. Fly ash was reacted with KOH to facilitate the impregnation of K as well as to enhance the bonding force. In particular, the applied process resulted in a significant slow-releasing characteristic of fertilizer elements. To examine the effect of K impregnation, a few detailed leaching tests were carried out in terms of process variables such as reaction time and temperature, sintering time and temperature, and KOH concentration. The current experiment presented an optimum preparation condition that is competitive with conventional commercial fertilizers. The manufactured ash fertilizers inhibited release of the K elements. It was also found through the continuous leaching test with pure water that the ash fertilizer had excellent moisture absorbability. However, the effects of some trace elements in fly ash on soil health and crop productivity as well as environmental considerations need to be established with long-term studies.     

An assessment of the significance of mercury release from coal fly ash

Some mercury (Hg) naturally present in coal is retained in the fly ash remaining after combustion. Concern has been raised regarding the potential for release of this Hg to the environment. The exchange of Hg between fly ash and the atmosphere was measured in the laboratory and in situ at a fly ash landfill. All samples of fly ash used in the laboratory study, with the exception of that derived from lignite-type coal, acted as a sink for atmospheric Hg. Deposition rates were found to increase as air Hg concentrations increased and to decrease with incident light and increased temperature. Addition of water to fly ash samples resulted in re-emission of deposited atmospheric Hg. Deposition was the dominant flux measured in situ at a fly ash landfill. Atmospheric Hg was deposited to all samples collected as part of two demonstration projects using carbon injection for enhanced Hg capture. Hg concentrations of extracts derived using U.S. Environmental Protection Agency Method 1312 (Synthetic Precipitation Leaching Procedure) were < or = 14.4 ng/L. Data developed demonstrate that fly ash, including that collected from Hg removal projects, will release little Hg to the air or water, and under certain conditions, absorbs Hg from the air.     

Heavy metal leaching from coal fly ash amended container substrates during Syngonium production

Coal fly ash has been proposed to be an alternative to lime amendment and a nutrient source of container substrates for ornamental plant production. A great concern over this proposed beneficial use, however, is the potential contamination of surface and ground water by heavy metals. In this study, three fly ashes collected from Florida, Michigan, and North Carolina and a commercial dolomite were amended in a basal substrate. The formulated substrates were used to produce Syngonium podophyllum Schott 'Berry Allusion' in 15-cm diameter containers in a shaded greenhouse. Leachates from the containers were collected during the entire six months of plant production and analyzed for heavy metal concentrations. There were no detectable As, Cr, Hg, Pb, and Se in the leachates; Cd and Mo were only detected in few leachate samples. The metals constantly detected were Cu, Mn, Ni, and Zn. The total amounts of Cu, Mn, Ni, and Zn leached during the six-month production period were 95, 210, 44, and 337 microg per container, indicating that such amounts in leachates may contribute little to contamination of surface and ground water. In addition, plant growth indices and fresh and dry weights of S. podophyllum 'Berry Allusion' produced from fly ash and dolomite-amended substrates were comparable except for the plants produced from the substrate amended with fly ash collected from Michigan which had reduced growth indices and fresh and dry weights. Thus, selected fly ashes can be alternatives to commercial dolomites as amendments to container substrates for ornamental plant production. The use of fly ashes as container substrate amendments should represent a new market for the beneficial use of this coal combustion byproduct.     

An Assessment of the Significance of Mercury Release from Coal Fly Ash

Abstract

Some mercury (Hg) naturally present in coal is retained in the fly ash remaining after combustion. Concern has been raised regarding the potential for release of this Hg to the environment. The exchange of Hg between fly ash and the atmosphere was measured in the laboratory and in situ at a fly ash landfill. All samples of fly ash used in the laboratory study, with the exception of that derived from lignite-type coal, acted as a sink for atmospheric Hg. Deposition rates were found to increase as air Hg concentrations increased and to decrease with incident light and increased temperature. Addition of water to fly ash samples resulted in re-emission of deposited atmospheric Hg. Deposition was the dominant flux measured in situ at a fly ash landfill. Atmospheric Hg was deposited to all samples collected as part of two demonstration projects using carbon injection for enhanced Hg capture. Hg concentrations of extracts derived using U.S. Environmental Protection Agency Method 1312 (Synthetic Precipitation Leaching Procedure) were ≤14.4 ng/L. Data developed demonstrate that fly ash, including that collected from Hg removal projects, will release little Hg to the air or water, and under certain conditions, absorbs Hg from the air.     

A new method to assess mercury emissions: a study of three coal-fired electric-generating power station configurations

U.S. Environmental Protection Agency (EPA) Method 7473 for the analysis of mercury (Hg) by thermal decomposition, amalgamation, and atomic absorption spectroscopy has proved successful for use in Hg assessment at coal-fired power stations. In an analysis time of approximately 5 min per sample, this instrumental methodology can directly analyze total Hg--with no discrete sample preparation--in the solid matrices associated with a coal-fired power plant, including coal, fly ash, bottom ash, and flue gas desulfurization (FGD) material. This analysis technique was used to investigate Hg capture by coal combustion byproducts (CCBs) in three different coal-fired power plant configurations. Hg capture and associated emissions were estimated by partial mass balance. The station equipped with an FGD system demonstrated 68% capture on FGD material and an emissions estimate of 18% (11 kg/yr) of total Hg input. The power plant equipped with low oxides of nitrogen burners and an electrostatic precipitator (ESP) retained 43% on the fly ash and emitted 57% (51 kg/yr). The station equipped with conventional burners and an ESP retained less than 1% on the fly ash, emitting an estimated 99% (88 kg/yr) of Hg. Estimated Hg emissions demonstrate good agreement with EPA data for the power stations investigated.     

A New Method to Assess Mercury Emissions: A Study of Three Coal-Fired Electric-Generating Power Station Configurations

Abstract

U.S. Environmental Protection Agency (EPA) Method 7473 for the analysis of mercury (Hg) by thermal decomposition, amalgamation, and atomic absorption spectroscopy has proved successful for use in Hg assessment at coal-fired power stations. In an analysis time of ～5 min per sample, this instrumental methodology can directly analyze total Hg—with no discrete sample preparation—in the solid matrices associated with a coal-fired power plant, including coal, fly ash, bottom ash, and flue gas desulfurization (FGD) material. This analysis technique was used to investigate Hg capture by coal combustion byproducts (CCBs) in three different coal-fired power plant configurations. Hg capture and associated emissions were estimated by partial mass balance. The station equipped with an FGD system demonstrated 68% capture on FGD material and an emissions estimate of 18% (11 kg/yr) of total Hg input. The power plant equipped with low oxides of nitrogen burners and an electrostatic precipitator (ESP) retained 43% on the fly ash and emitted 57% (51 kg/yr). The station equipped with conventional burners and an ESP retained less than 1% on the fly ash, emitting an estimated 99% (88 kg/yr) of Hg. Estimated Hg emissions demonstrate good agreement with EPA data for the power stations investigated.     

Trace Element Inputs from a Coal Burning Power Plant to Adjacent Terrestrial and Aquatic Environments

Inputs of trace elements derived from coal ash to terrestrial and aquatic environments were investigated near an 83 MW coal-burning power plant. Comparisons were made between terrestrial inputs of trace elements through aerial deposition during 23 years before installation of electrostatic precipitators and aquatic inputs from ash disposal basins after installation. A gaussian plume model was used to predict deposition patterns of 29 trace elements in coal ash about the power plant. Detectable increases of only Sr, As, Sb, and Be in surface soils within 3 km of the power plant were predicted. Concentrations measured in surface soils were largely consistent with these predictions. Measurements of aerial deposition of Cd, Pb, Cu, and Mn at a site 5.5 km distant were similar to those in other rural areas and indicated that little of the measured Cd, Cu, Mn, or Pb was derived from fly ash. Concentrations of 12 heavy metals in effluents from the basin receiving ash were comparable to those predicted in rainfall deposited nearest the plant. It is concluded that at other coal combustion facilities, basin disposal could be a more serious contamination threat to aquatic environments than aerial dispersal of ash.