Behavior and analysis of Cesium adsorption on montmorillonite mineral

The adsorption of Cs by montmorillonite and the effects of experimental conditions on adsorption were investigated by using ¹³⁴Cs as a radioactive tracer. Additionally, the Cs-adsorbed and the modified montmorillonite were analyzed by X-ray Diffractometer System (XRD) and Scanning Electron Microscopy (SEM). The results showed that the adsorption of Cs by montmorillonite was efficient in the initial concentration (C₀) of 30 μg/L Cs nitrate solution with 20 g/L montmorillonite at room temperature. In this condition, more than 98% Cs⁺ ions could be adsorbed at pH 8. The adsorption equilibrium was achieved within 5 min and the relationship between the concentration of Cs⁺ in aqueous solutions and adsorption capacities of Cs⁺ can be described by the Langmuir adsorption isotherm. The adsorption rate would decrease when temperature increase from 0 °C to 50 °C or in presence of coexistent K⁺, Na⁺ and Ca²⁺, while modification by (NH₄)₂SO₄, [Ag(NH₃)₂]⁺, [Cu(NH₃)₄]²⁺ or 450 °C could improve the adsorption abilities of montmorillonite for Cs⁺. However, more than 89% of adsorbed Cs⁺ on montmorillonite could be desorbed by 2 mol/L HNO₃ solutions. The XRD and SEM analysis further showed that the structure of the Cs-adsorbed or modified montmorillonite were different from that of the original one.     

Development and analysis of high-performance green concrete in the urban infrastructure

Cement production accounts for approximately 5% of total global CO₂ emissions from all human activities. In addition, the consumption of virgin aggregates for concrete infrastructure has created virgin material scarcity issues in many areas of the USA. High-performance green concrete (HPGC) with fly ash and recycled aggregates can help reduce the demand for material inputs and reduce pollution outputs associated with bulk material flow of urban concrete. Structural and durability tests showed that HPGC containing fly ash and 50% recycled aggregate (100% of the coarse aggregate fraction) performed equally or better than 100% ordinary Portland cement concrete with the same cementitious content. Durability improvements were more significant with Class F than Class C fly ash. For both Class F and Class C fly ash, greater per cent replacement of Portland cement with fly ash led to slower and lower strength gain, but still within acceptable strength criteria for Colorado Department of Transportation Class B concrete. This paper quantifies the sustainability of HPGC in urban infrastructure by addressing structural performance, environmental, economic and resource depletion impacts.     

Phosphorus removal by fly ash

The aim of this work was to investigate the possible use of fly ash generated from thermic power stations in the removal of phosphorus contained in aqueous solutions. A series of batch tests were conducted and the influence of temperature, phosphate concentration, and fly ash dosage on phosphate removal were investigated. The effect of adsorption dosage was not significant at any temperature applied. Phosphate removal in excess of 99% was obtained in these studies. Maximum removals were achieved at 40°C. The tests were also carried out on a continuous basis in an adsorption column. It was found that fly ash is an efficient adsorbent for phosphate removal. This was expected due to the high concentration of calcite present in the fly ash (338 g/kg). The phosphate removal decreased to 80.4% at the end of 72 h.     

Assessment of surface area normalisation for interpreting distribution coefficients (Kd) for uranium sorption

Adsorption of radionuclides on soils and sediments is commonly quantified by distribution coefficients (K_d values). This paper examines the relationship between K_d values for uranium(VI) adsorption and the specific surface area (SSA) of geologic materials. We then investigate the potential applicability of normalising uranium (U) K_d measurements using the SSA, to produce ‘K_a values’ as a generic expression of the affinity of U for the surface. The data for U provide a reasonably coherent set of K_a values on various solid phases, both with and without ligands. The K_a representation provides a way of harmonising datasets obtained for materials having different specific surface areas, and accounting for the effects of ligands in different systems. In addition, this representation may assist in developing U sorption models for complex materials. However, a significant limitation of the K_a concept is that sorption of radionuclides at trace levels can be dominated by interactions with specific surface sites, whose abundances are not reflected by the SSA. Therefore, calculated K_a values should be interpreted cautiously.     

The chemistry of smog formation: A review of current knowledge

This paper describes smog chemistry and the methods used to develop our knowledge of its complex chemistry. These methods employ computer modeling, fundamental chemistry, smog chamber experiments, sophisticated analytical instrumentation, and process analysis techniques. The photochemistry leading to smog formation involves a kinetically controlled and coupled competitive process. The essential pathway for formation of nitrogen oxides starts with emissions composed primarily of NO, which are converted to NO₂, mostly via reactions with peroxy radicals; NO₂ is converted to photochemically inert nitric acid primarily by reaction with OH. Organics in smog chemistry are eventually oxidized to CO₂ and water; before this, they typically react with OH to form peroxy radicals. The peroxy (RO₂·) radicals couple the organic and nitrogen chemistry by converting NO to NO₂; the RO₂· radicals are converted to RO radicals, which typically lead to oxygenated intermediate organics that continue through OH·---RO₂·---RO· cycles. These OH·---RO₂·---RO· cycles produce CO, CO₂, and radical products. The radical products, which usually derive from photolysis of oxygenated intermediate organic products, are central to the overall process of smog formation. This is because the balance of these radicals affects the rapidity and severity of smog development. The radical balance is, in turn, controlled by the sources and sinks that depend on the HC/NO_x ratio, the types of organics, and the light flux. With only a rudimentary understanding of smog chemistry as a process, many of the effects observed from precursor controls can be explained and the basic shape of Empirical Kinetics Modeling Approach (EKMA) isopleth curves can be accounted for. The next step beyond this basic level of understanding involves a host of subprocesses composed of a complex series of chemical reactions. Current research in smog chemistry centers on the assessment and elucidation of these complex subprocesses. Atmospheric models currently in use rely on condensed chemical mechanisms. All such modern mechanisms treat the same basic processes, but differ both in their method of condensation and in their manner of addressing the complex subprocesses of smog chemistry.     

Detection and average content levels of carcinogenic and mutagenic compounds from the particulates on diesel and gasoline engine mufflers

Carcinogenic and mutagenic compounds, which were extracted from the particulates that adhered to inner surfaces of diesel and gasoline engine mufflers, were quantified by the series method of Soxhlet extraction, liquid-liquid partition, thin-layer chromatography, and spectrofluorometry. Mutagenic activity of their neutral and acidic fractions was tested in the improved Ames assay by the preincubation method with Salmonella typhimurium TA98 in the presence and absence of metabolic activation system (S-9 mix). The average content levels (μg/g tar) of polycyclic aromatic hydrocarbons from gasoline engine cars were greater than those from diesel engine vehicles. However, the levels of nitro derivatives of PAHs and polycyclic quinones from the diesel engines were greater than from the gasoline engines. Mutagenic activity of the diesel acidic fraction was the highest among the diesel and gasoline fractions, and was significantly higher in the absence of the S-9 mix. Furthermore, the relative value (R_{c = 0}) of infrared absorption of carbonyl stretching vibration to that of methylene asymmetric stretching vibration of the diesel acidic fraction was the highest among the diesel and gasoline fractions. These results strongly suggest that highly direct-acting mutagens in the acidic fraction are at higher levels in diesel emission particulates than those from gasoline, and that these mutagens are carboxylic acid, aldehyde, and alcohol derivatives of PAHs and NPAHs.     

Properties of alkali-activated fly ash: high performance to lightweight

Alkali ash material (AAM) concrete is a unique material that is sustainable and cost-effective because it utilises waste fly ash, and has properties superior to other concrete products. The AAM concrete described here is produced from the addition of inexpensive chemicals to fly ash. AAM can be used to create a wide range of materials including high performance concrete (HPC-AAM) and lightweight (LW-AAM). The high performance AAM provides rapid strength gain along with high ultimate strengths of more than 110 MPa (16000 psi). LW-AAM can produce materials with densities ranging from 1200 to 2200 kg/m³ and compressive strengths from 2 (290 psi) to 65 MPa (9500 psi). Both HPC-AAM and LW-AAM have far better environmental resistance than Portland cement concrete, resisting attack from sulphuric acid (H₂SO₄), hydrochloric acid (HCl) and organic acids. AAMs resists freeze–thaw attack and high abrasion, possesses low chloride permeability and does not exhibit alkali silica reactivity.     

Leachability of elements from sub-bituminous coal fly ash from India

Environmental concerns regarding the potential contamination of soil, surface and ground water due to the presence of soluble metal species in the ash pond leachate is of great importance. Serial batch leaching was carried out simulating the rainwater condition of the study area to understand the behaviour of elements during leaching. The leachates were analysed for the elements Al, Ca, K, Mg, Na, P, S, Si, As, Ba, Fe, Mn, Mo, Ti, V, Pb, Zn, Co, Cr, Cu, Ni and Cd by inductively coupled plasma optical emission spectrometer (ICP-OES). It was found that Cd, Co, Cr and Ni did not leach from the ash while Cu and Pb concentrations were insignificant in the leachate regardless of liquid to solid (L/S) ratio. Most of the elements showed maximum concentrations at lower L/S ratio and then decreased with increasing L/S. The total cumulative concentrations of As, Mn and Mo were found to be higher than the World Health Organization (WHO) recommended values for drinking water while the concentrations of Fe, Mn and As exceeded the maximum allowable concentrations prescribed by the United States Environmental Protection Agency (USEPA). The pre and the post leached ash samples were analysed for morphology, specific surface area and mineralogical changes. Analysis of post-leached fly ash indicated changes in the specific surface area and morphology but no change in mineralogy.     

Introduction to and experimental conditions during the first year of the GMR chronic inhalation studies of diesel exhaust

A chronic exposure study was initiated to determine the effects of diesel exhaust on the health of experimental animals. For this purpose, test atmospheres of clean air (control) or freshly diluted diesel exhaust at concentrations of 250, 750, and 1500 μg/m³ were supplied to four 12.6 m³ inhalation chambers which housed rats and guinea pigs. Diesel aerosol size and concentration, as well as chamber temperature and relative humidity, were continually monitored and controlled to maintain the exposure dose levels and an environment of 22±2°C and 50%±20% relative humidity. The concentrations of CO and NO_x were found to be 5.8±1.0 mg/m³ and 7.9±1.0 mg/m³ above ambient in the chamber containing 1500 μg/m³ of particulate. Animals were supplied from the chambers, on a random basis, for both intramural and extramural studies throughout the exposure period. The experiment ran uninterrupted for over twelve months with mean diesel particle mass concentrations within 2% of the target values.     

江苏天目湖表层沉积物中多环芳烃污染特征与来源

区别于长江三角洲地区众多的大型天然浅水湖泊，江苏天目湖是一个较深的水库型湖泊，也是重要的城乡生活及工农业水源地之一。为了解天目湖表层沉积物中多环芳烃（PAHs）污染状况， 2006年在天目湖全湖采集7个点位的表层沉积物样品，利用GC/MS分析了16种优控PAHs。结果表明：天目湖表层沉积物中16种优控PAHs总量介于28750~71393 ng/g（干重），平均值为45852 ng/g；在空间分布上，北部受污染程度高于南部，主要是北部旅游业快速发展导致污染物排放的影响；沉积物中总有机碳含量与PAHs总量呈显著相关；利用特征化合物指数对PAHs的来源进行判别，指示天目湖表层沉积物中PAHs的主要来源是木材、煤的不完全燃烧。与不同地区水体沉积物PAHs含量对比表明，天目湖PAHs污染处于一个低至中等程度。基于沉积物中多环芳烃的环境质量标准，仅有1个样点芴浓度超过风险效应低值，但远小于毒性风险效应中值，因此沉积物中多环芳烃的生态风险较小。然而天目湖表层沉积物中的PAHs的污染程度已超过南水北调东线所经过的南四湖，而且天目湖湖水较深，湖水交换周期比较长，其PAHs污染应引起重视，需制定切实措施保护江苏“最后一泓净水”。     

Trace element and radionuclide mass balances at a coal-fired electric generating station

Coal, bottom ash, and fly ash from Milliken Station, a coal-fired 270 MW power plant, were analyzed for 20 elements (Ag, Al, As, Be, Cd, Co, Cr, Cu, Ga, Hg, Mn, Ni, Pb, Sb, Se, Sn, Te, Tl, V, and Zn) and the major natural radionuclides (²³⁸U series, ²³²Th series, and ⁴⁰K). Mass balance calculations showed that most of the Hg, and some of the Sb and Se, were unaccounted for by ash collection, suggesting their possible discharge into the atmosphere. Silver, As, Hg, Pb, Cd, and Zn were more concentrated in the fly ash than in the bottom ash while all of the other elements were equally distributed, by concentration, between the ash fractions. The radionuclides showed a 46% higher concentration in fly ash than in bottom ash, and ²¹⁰Pb was enriched in the fly ash relative to the other radionuclides by a factor of 2.4. Mass balance calculations indicated a balance within statistical error for the radionuclides, except for ²¹⁰Pb.     

红枫湖地表水中多环芳烃的分布及来源

将固相微萃取与气相色谱联用，对贵阳红枫湖水样中16种美国环境保护署优控的多环芳烃进行分析。结果表明：红枫湖水中16种多环芳烃总量为0167 1~0336 4 μg/L，与国内其它水系相比，湖中存在多环芳烃轻度污染。7种（萘、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘和苯并(ghi)苝）多环芳烃的总量未超出中国城市供水行业对多环芳烃规定的限值，但作为饮用水源，红枫湖水中的苯并(a)芘含量已超出我国标准GB3838-2002中生活饮用水地表水源地的苯并(a)芘限值，并且苯并(a)蒽、〖JX-*9〗〖SX（B-25x〗〖HT7，5”〗艹〖〗〖HT6”，5”〗屈〖HT5”〗〖SX）〗〖JX*9〗、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘的含量也超过了美国环境保护署地表水水质标准限值。通过多环芳烃特征参数的比值，分析了红枫湖水中多环芳烃的污染来源。污染源分析表明，湖中多环芳烃的主要来源为燃烧源，包括木材、煤以及化石燃料的燃烧，同时也有一部分多环芳烃是来源石油类物质的输入.     

红枫湖地表水中多环芳烃的分布及来源

将固相微萃取与气相色谱联用,对贵阳红枫湖水样中16种美国环境保护署优控的多环芳烃进行分析。结果表明：红枫湖水中16种多环芳烃总量为0167 1~0336 4 μg/L,与国内其它水系相比,湖中存在多环芳烃轻度污染。7种（萘、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘和苯并(ghi)苝）多环芳烃的总量未超出中国城市供水行业对多环芳烃规定的限值,但作为饮用水源,红枫湖水中的苯并(a)芘含量已超出我国标准GB3838-2002中生活饮用水地表水源地的苯并(a)芘限值,并且苯并(a)蒽、〖JX-*9〗〖SX（B-25x〗〖HT7,5”〗艹〖〗〖HT6”,5”〗屈〖HT5”〗〖SX）〗〖JX*9〗、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘的含量也超过了美国环境保护署地表水水质标准限值。通过多环芳烃特征参数的比值,分析了红枫湖水中多环芳烃的污染来源。污染源分析表明,湖中多环芳烃的主要来源为燃烧源,包括木材、煤以及化石燃料的燃烧,同时也有一部分多环芳烃是来源石油类物质的输入.     

Size dependent cytotoxicity of fly ash particles

Fly ash samples were collected from the electrostatic precipitator of a coal-fired power plant in Hong Kong. The particles of the respirable range (smaller than 10 μm) were divided into 4 groups according to their particle size (mass median aerodynamic diameters). The surface morphology and the metal contents (Fe, Mn, Al and Zn) of fly ash particles were examined by a scanning electron microscope and an inductively coupled plasma spectrophotometer, respectively. The particles were very heterogenous in size and shape as well as the concentration of metals. The cytotoxicity of these four groups of fly ash particles was evaluated using an in vitro rat alveolar macrophages culture assay. The viability of alveolar macrophages was lower when incubated with smaller size particles. This relationship was also reflected by the damage of the surface morphology of the cells and the release of cytoplasmic (lactate dehydrogenase) and lysosomal (acid phosphatase and β-glucuronidase) marker enzymes into the culture media.     

Assessment of hydrothermally modified fly ash for the treatment of methylene blue dye in the textile industry wastewater

Dyes and pigments are one of the major water pollutants and if not discharged properly cause ecological disturbance. Considering this, the current study investigates the application of thermal power plant by-product, i.e., fly ash for the elimination of a hazardous methylene blue dye from its synthetic aqueous solution. Experiments were conducted in batch mode to study the effect of pH, temperature, adsorbent dose and contact time. Highest dye removal (94.3%) was achieved at pH 10 using adsorbent dose of 10 g/L in 90 min of contact time at 40 °C. However, for cost-effective operation at neutral pH and room temperature (30 °C), it yields 89.3% dye removal having similar dose and contact time. Equilibrium isotherms for adsorption were analyzed by Langmuir and Freundlich, Temkin and Dubinin–Radushkevich isotherm equations. The results revealed that the best fit model of adsorption closely followed Langmuir adsorption. Based on adsorption isotherm models, thermodynamics parameters ΔG, ΔH and ΔS were calculated. The negative value of ΔG and ΔH revealed that adsorption process was exothermic, spontaneous and physical. The present work suggests that through simple process hydrothermally modified fly ash has the potential to be used as cost-effective and efficient adsorbent for the treatment of wastewater from textile industries.     

Escaping radioactivity from coal-fired power plants (CPPs) due to coal burning and the associated hazards: a review

Coal, like most materials found in nature, contains trace quantities of the naturally occurring primordial radionuclides, i.e. of ⁴⁰K and of ²³⁸U, ²³²Th and their decay products. Therefore, the combustion of coal results in the released into the environment of some natural radioactivity (1.48 TBq y⁻¹), the major part of which (99 %) escapes as very fine particles, while the rest in fly ash. The activity concentrations of natural radionuclides measured in coals originated from coal mines in Greece varied from 117 to 435 Bq kg⁻¹ for ²³⁸U, from 44 to 255 Bq kg⁻¹ for ²²⁶Ra, from 59 to 205 Bq kg⁻¹ for ²¹⁰Pb, from 9 to 41 Bq kg⁻¹ for ²²⁸Ra (²³²Th) and from 59 to 227 Bq kg⁻¹ for ⁴⁰K. Fly ash escapes from the stacks of coal-fired power plants in a percentage of 3-1% of the total fly ash, in the better case. The natural radionuclide concentrations measured in fly ash produced and retained or escaped from coal-fired power plants in Greece varied from 263 to 950 Bq kg⁻¹ for ²³⁸U, from 142 to 605 Bq kg⁻¹ for ²²⁶Ra, from 133 to 428 Bq kg⁻¹ for ²¹⁰Pb, from 27 to 68 Bq kg⁻¹ for ²²⁸Ra (²³²Th) and from 204 to 382 Bq kg⁻¹ for ⁴⁰K. About 5% of the total ash produced in the coal-fired power plants is used as substitute of cement in concrete for the construction of dwellings, and may affect indoor radiation doses from external irradiation and the inhalation of radon decay products (internal irradiation) is the most significant. The resulting normalized collective effective doses were 6 and 0.5 man-Sv (GW a)⁻¹ for typical old and modern coal-fired power plants, respectively.     

Radiological impact of coal-fired power generation

A radiological impact assessment was carried out at the 4000 MW Nanticoke Thermal Generating Station on the north shore of Lake Erie and at an ash disposal site in Metropolitan Toronto, both operated by Ontario Hydro. Analyses were performed on feed coal, fly ash and bottom ash and on samples of air filters, precipitation, water, soil and vegetation in the vicinity of the generating station. The measured radionuclide levels in the vicinity of the generating station showed no evidence of enhancement from station emissions. There were no indications that leaching of radionuclides or emanation of radon gas from ash disposal sites would be a problem. There was evidence, however, of higher radionuclide concentrations on the finer ash particles. Furthermore, the use of fly ash in building materials could lead to enhanced radiation levels. Atmospheric dispersion and radiation dose calculations were also carried out. Predicted concentrations in air were all less than 1% of background values. The committed dose equivalent from one year of operation was estimated to be 0·27 μSv at the site boundary and 0·11 μSv at 10 km east of the site.     

Population exposure to airborne thorium at the high natural radiation areas in India

High natural radiation areas in the coastal and peninsular India were studied for airborne thorium and resultant population exposure due to inhalation. Four locations covering three states viz., Ayiramthengu and Neendakara in Kerala, Kudiraimozhi in Tamil Nadu and Bhimilipatnam in Andhra Pradesh were investigated. External gamma radiation fields 1 m above the monazite ore bodies ranged from 200 to 3000 nGy h^-1. Soil samples showed ²³²Th specific activity varying from 0·1 to 1·5 Bq g^-1 with surface alpha activity in the range of 1·0–12·5 Bq cm^-2. Suspended particulates in the samples ranged from 60–140 μg m^-3 with ²³²Th showing a wider variation of <0·03–0·3 mBq m^-3. There was poor correlation between suspended particulates and long-lived alpha airborne activity . The resuspension factors for ²³²Th were in the range of 1·5×10^-8–7·9×10^-7 cm^-1. Higher resuspension was correlated with dry sand dunes. The upper limits for Committed Effective Dose (CED) due to inhalation of airborne ²³²Th at the respective high natural radiation areas were estimated to range from 50±30 to 300±130 μSv (5–30 mrem) per year per adult member of public assuming an activity median aerodynamic diameter of 1 μm for the airborne particulates.     

PAH emission from the incineration of three plastic wastes

A batch-type, controlled-air incinerator was used for the treatment of polyvinyl chloride (PVC), high-density polyethylene (HDPE), and polypropylene (PP) plastic wastes. The concentration and composition of 21 individual polycyclic aromatic hydrocarbons (PAHs) in the raw wastes, flue gas (gas and particle phases), and ash were determined. Stack flue-gas samples were collected by a PAH stack-sampling system. Twenty-one individual PAHs were analyzed primarily by a gas chromatograph/mass spectrometer (GC/MS). The CO concentration correlated well with the total PAH (R2 > .89), and thus can be used as a surrogate indicator for PAH emission. Excess amounts of air supply in the incineration of plastic wastes could decrease not only the concentration of the PAHs in the bottom ash but also the emission factor (EF) of the total PAH in the stack flue gas. Of the three plastic wastes, HDPE was found to have the highest mean EF of the total PAHs (462.3 mg/kg waste) from the stack flue gas. Incinerating PVC would result in a higher EF of PAHs (195.4 mg/kg waste) in the bottom ash. When PVC plastic wastes were incinerated, higher-ringed PAHs constituted a larger percentage in the bottom ash as compared to those from PP and HDPE plastics. By judging the output and input (O/I) ratio of the PAHs from the incineration trials of plastic wastes, the PAHs involved in incineration of three plastic wastes were almost entirely destroyed; and a low residual amount between 0.00018 and 0.00032 remained in the emission.     

Predicting fly ash resistivity—an evaluation

Recently a technique for predicting fly ash resistivity from an as-received, ultimate coal analysis and the chemical composition of the coal ash produced by simple laboratory ignition was published. This paper evaluates this technique by comparing predicted resistivity data with laboratory measured values, in situ resistivity data, and precipitator performance information acquired from 12 field test programs. Considering the precision of measurement generally encountered in precipitator technology and the limited amount of certain laboratory data available, the results are encouraging and the evaluation is favorable.