Changes in physical and chemical properties of three soil types in India as a result of amendment with fly ash and sewage sludge

The use of coal fly ash and domestic sewage sludge in agriculture is being considered as one of the methods for recycling of these wastes in an environmental beneficial manner. Mixtures with soil were prepared at different proportions of fly ash and sludge, either alone or in combination at a maximum application rate of 52 t ha^-1. The changes in the selected properties and heavy metal contents of three soil types in India were studied after incubating the respective mixtures for 90 days at near field capacity moisture level. Sewage sludge, due to its acidic and saline nature, high organic matter and heavy metals content, had more impact on soil properties than the fly ash. Sludge application produced several changes including an increase in available nitrogen, organic carbon, salinity and water-holding capacity of the soils. The concentrations of major cations and heavy metals also increased because of the sludge application and the pH was decreased. However, the levels of individual metal concentrations in all the mixture types were below the allowable limits prescribed by several environmental agencies. Using fly ash either alone or in equal quantity with sewage sludge had little influence on soil properties and heavy metal content. The relative availability (RA) of heavy metals in three soils amended with 52 t ha^-1 of sewage sludge was observed to be highest in oxisol, followed by alfisol and vertisol.     

粉煤灰和二灰对桂林红黏土力学性质的影响

为了研究粉煤灰和二灰掺量及养护时间对桂林红黏土的改良效果,进行了直剪试验、固结试验以及电镜扫描试验。试验结果表明,粉煤灰的掺入提高了红黏土的抗剪强度,但超过一定量（18%粉煤灰掺量）反而会降低红黏土黏聚力,各掺量粉煤灰红黏土随养护龄期的延长,抗剪强度呈先增后缓趋势。二灰改良红黏土,在早期强度剧增,且强度随养护时间增长而大幅增加,一定龄期内,二灰红黏土黏聚力随二灰掺量呈先增后减趋势。粉煤灰和二灰的掺入均增大了红黏土的压缩模量,且随养护时间的延长而逐渐增大。红黏土中随粉煤灰、石灰的加入,发生一系列物理化学反应,从微观结构分析得知土中孔隙减少,结构性较素红黏土好。     

Impact of biochar,bentonite, and compost on physical and chemical characteristics of a sandy soil

In this study, bentonite (Ben), compost (Com), and biochar (Bio) were used as soil amendments to enhance sandy soil physical properties. A soil column experiment was conducted in a laboratory. Application rates were 3% (weight/weight) of Bio (T₁), Ben (T₂), and Com (T₃). Furthermore, mixtures 1.5% and 1.5% of Bio and Ben (T₄), Ben and Com (T₅), and Bio and Com (T₆), and a mixture 1%, 1%, and 1% of Bio, Ben, and Com (T₇) in addition to control treatment were adopted. The mixtures of amendments and sandy soil were concentrated at the top 10 cm of columns. Results revealed that the cumulative evaporation was reduced by 2.3% and 5.7% as a result of using T₃ and T₅, respectively. However, the remaining treatments enhanced the cumulative evaporation. The application of amendments increased the capacity of the soil to maintain water by 35.4%, 24.4%, 13.3%, and 10.2%, for soils treated with T₅, T₃, T₇, and T₄, respectively. The water content at field capacity had the highest increase in the top 10 cm when treatment T₃ was used. Although T₃ (compost) was the most efficient for enhancing soil physical properties, this study recommends T₅ and T₇ to improve hydraulic properties of sandy soils. This is due to the fact that biochar and bentonite remain in the soil for a longer period and resist biodegradation while compost overcomes the negative impact of soil chemical properties as a result of biochar and bentonite additions.     

Effects of coal storage in air on physical and chemical properties of coal and on gas adsorption

This paper investigates changes in the high-volatile bituminous Lower Block Coal Member from Indiana owing to moisture availability and oxidation in air at ambient pressure and temperature over storage time. Specifically, it investigates changes in chemistry, in surface area, and pore structure, as well as changes in methane and carbon dioxide adsorption capacities. Our results document that the methane adsorption capacity increased by 40%, whereas CO₂ adsorption capacity increased by 18% during a 13-month time period. These changes in adsorption are accompanied by changes in chemistry and surface area of the coal.The observed changes in adsorption capacity indicate that special care must be taken when collecting samples and preserving coals until adsorption characteristics are measured in the laboratory. High-pressure isotherms from partially dried coal samples would likely cause overestimation of gas adsorption capacities, lead to a miscalculation of coal-bed methane prospects, and provide deceptively optimistic prognoses for recovery of coal-bed methane or capture of anthropogenic CO₂.     

Impact of co-combustion of petroleum coke and coal on fly ash quality: Case study of a Western Kentucky power plant

Petroleum coke has been used as a supplement or replacement for coal in pulverized-fuel combustion. At a 444-MW western Kentucky power station, the combustion of nearly 60% petroleum coke with moderate- to high-sulfur Illinois Basin coal produces fly ash with nearly 50% uncombusted petroleum coke and large amounts of V and Ni when compared to fly ash from strictly pulverized coal burns. Partitioning of the V and Ni, known from other studies to be concentrated in petroleum coke, was noted. However, the distribution of V and Ni does not directly correspond to the amount of uncombusted petroleum coke in the fly ash. Vanadium and Ni are preferentially associated with the finer, higher surface area fly ash fractions captured at lower flue gas temperatures. The presence of uncombusted petroleum coke in the fly ash doubles the amount of ash to be disposed, makes the fly ash unmarketable because of the high C content, and would lead to higher than typical (compared to other fly ashes in the region) concentrations of V and Ni in the fly ash even if the petroleum coke C could be beneficiated from the fly ash. Further studies of co-combustion ashes are necessary in order to understand their behavior in disposal.     

Evaluation of the use of modified coal ash as a potential sorbent for organic waste streams

Fly ash was modified by hydrothermal treatment with 7 M NaOH. The resultant product displayed an 8-fold increase in surface area. The primary crystalline component of the modified fly ash was identified by X-ray diffraction to be hydroxysodalite (Na₆Al₆Si₆O₂₄8H₂O). The cation exchange capacity of the modified ash was significantly increased over that of the raw fly ash (188 vs 2 meq g⁻¹). Adsorption experiments showed that the modified fly ash adsorbed a cationic dye (methylene blue) to a much greater extent than an anionic dye (alizarin sulfonate). Saturation adsorption revealed that the capacity of the ash for methylene blue had increased 10-fold during modification when compared to the raw ash. Adsorption is thus ascribed to be a surface effect rather than involving incorporation into the channels of the hydroxysodalite structure.     

From in-situ coal to fly ash: a study of coal mines and power plants from Indiana

This paper presents data on the properties of coal and fly ash from two coal mines and two power plants that burn single-source coal from two mines in Indiana. One mine is in the low-sulfur (<1%) Danville Coal Member of the Dugger Formation (Pennsylvanian) and the other mines the high-sulfur (>5%) Springfield Coal Member of the Petersburg Formation (Pennsylvanian). Both seams have comparable ash contents (11%). Coals sampled at the mines (both raw and washed fractions) were analyzed for proximate/ultimate/sulfur forms/heating value, major oxides, trace elements and petrographic composition. The properties of fly ash from these coals reflect the properties of the feed coal, as well as local combustion and post-combustion conditions. Sulfur and spinel content, and As, Pb and Zn concentrations of the fly ash are the parameters that most closely reflect the properties of the source coal.     

Characterization of fly ash from a power plant and surroundings by micro-Raman spectroscopy

Fly ash samples were collected from a Portuguese power plant that burns low-sulphur coals from South Africa, U.S.A., Colombia, and Australia. The fly ashes were collected from the hoppers of the economizers, air heaters, electrostatic precipitators, and from the stack. The power plant air monitoring system was also sampled. The fly ash characterization was conducted by micro-Raman spectroscopy (MRS). The micro-Raman spectroscopic analysis permitted an efficient identification and characterization of different inorganic and organic materials present in fly ash: quartz, hematite, magnetite, calcite, glass, aluminium and calcium oxides, and different types of organic constituents.The study of the structural evolution of the unburned carbon/char material during their path through the power plant, though the use of Raman spectra and Raman parameters reveal that despite the high temperatures they reached, these materials are still structurally disordered. However, a structural evolution occurs in the char from the economizer up to the electrostatic precipitators where the char is structurally more disordered.The different features of the Raman spectra observed for carbon particles collected from the stack, together with the high range of variation of the Raman parameters, confirm the existence of different carbon particles in the stack, i.e., char and others (probably soot).The filters from the surroundings contain a variety of carbon particles with Raman parameters different from the ones obtained in the fly ash hoppers and stack. These are diesel particles as indicated by the values of W_D1, FWHM_D1, FWHM_G, W_G and ID1/IG obtained.     

Chemical and petrographical characterization of feed coal, fly ash and bottom ash from the Figueira Power Plant, Paraná, Brazil

The aim of the present study is the petrographic and chemical characterization of the coal at the Figueira Power Plant, Paraná, Brazil, prior and after the beneficiation process and the chemical characterization of fly and bottom ashes generated in the combustion process.Petrographic characterization was carried out through maceral analysis and vitrinite reflectance measurements. Chemical characterization included proximate analysis, determination of calorific value and sulphur content, ultimate analysis, X-ray diffraction, X-ray fluorescence, Inductively Coupled Plasma — Mass Spectrometry (ICP-MS) and Inductively Coupled Plasma — Atomic Emission Spectrometry (ICP-AES) analysis, and determination of Total Organic Carbon (TOC) content.Vitrinite reflectance analyses indicate a high volatile B/C bituminous coal (0.61 to 0.73% Rrandom). Maceral analyses show predominance of the vitrinite maceral group (51.6 to 70.9 vol.%, m.m.f). Except of the Run of mine (ROM) coal sample, the average calorific value of the coals is 5205 kcal/kg and ash yields range from 21.4 to 38.1 wt.%. The mineralogical composition (X-ray diffraction) of coals includes kaolinite, quartz, plagioclase and pyrite, whereas fly and bottom ashes are composed by mullite, ettringite, quartz, magnetite, and hematite. Analyses of major elements from coal, fly and bottom ashes indicate a high SiO₂, Al₂O₃, and Fe₂O₃ content. Trace elements analysis of in-situ and ROM coals by ICP-MS and ICP-AES show highest concentration in Zn and As. Most of the toxic elements such as As, Cd, Cr, Mo, Ni, Pb, and Zn are significantly reduced by coal beneficiation. Considering the spatial distribution of trace elements in the beneficiated coal samples, which were collected over a period of three months, there appears to be little variation in Cd and Zn concentrations, whereas trace elements such as As, Mo, and Pb show a larger variation.In the fly and bottom ashes, the highest concentrations of trace elements were determined for Zn and As. When compared with trace element concentrations in the feed coal, fly ashes show a significant enrichment in most trace elements (As, B, Be, Cd, Co, Cr, Cu, Li, Mn, Mo, Ni, Pb, Sb, Tl, and Zn), suggesting a predominantly volatile nature for these elements. In contrast, Sn is distributed evenly within the different ash types, whereas U shows depleted concentration in both bottom and fly ash samples.According to the International Classification of in-seam coals the Cambuí coals are of para/ortho bituminous rank of low grade (except for the ROM sample), and are characterized by the predominance of vitrinite macerals.     

Petrology of subbituminous feed coal as a guide to the capture of mercury by fly ash—influence of depositional environment

The mercury and maceral content of subbituminous feed coals burned at six Canadian power plants was measured and compared to the mercury and carbon content of corresponding fly ashes. The fly ashes were collected from electrostatic precipitator (ESP) pollution controls used at the power plants. Four feed coals from the Upper Cretaceous to Tertiary age Scollard Formation were deposited in freshwater depositional environment and contain 35–44% inertinite. Two feed coals from the Upper Cretaceous age Horseshoe Canyon Formation were deposited in a brackish water environment and contain 14% inertinite.The data show that abundant inertinite equates to more unburned carbon in ESP fly ash, and to enhanced capture of mercury in cold-side ESP fly ash. This indicates that the inertinite content of a coal seam may be indicative of the percentage of unburned carbon and the percentage of mercury captured by a cold-side ESP.     

Study on the distribution of PAHs in fly ash from coal and residual char combustion in a pressurized fluidized bed

Direct coal combustion not only has a low utilizing efficiency, but also produces a large amount of pollutants such as particulate, CO2, SO2, NOx, polycyclic aromatic hydrocarbons （PAHs）, PCDD/PCDFs, and so on. Coal gasification is a clean coal technology that presents good prospects for coal use, mainly for producing electricity with a high coal conversion efficiency and low environmental impact. However, there is a problem about the minimization of PAHs in coal gasification or direct coal combustion. PAHs are harmful to the environment and human health due to their high degree of mutagenicity and carcinogenicity when they enter human bodies through breathing, eating, and drinking. It is said that about 75%-90% cancers of human beings are mainly caused by PAHs. So the US EPA has prioritized 16 PAH compounds as hazardous air pollutants; these compounds are naphthalene （NAP）, acenaphthylene （AcPy）, acenaphthene （AcP）, fluorene （Flu）, phenanthrene （PhA）, anthracene （ANT）, fluoranthene （FluA）, pyrene （Pyr）, benzo （a） anthracene （BaA）, chrysene （Chr）, benzo （b） fluoranthene （BbF）, benzo （k） fluoranthene （BkF）, benzo （a） pyrene （BaP）, indeno（1,2,3,-cd） pyrene [In（1,2,3-cd） P], dibenzo （a,h） anthracene （DbA）, and benzo （ghi） perylene （BghiP）. The residual char is one of the main products during coal gasification, and then it is brought into the combustion chamber to combust. To investigate the distribution of PAHs in fly ash, the combustion of coal and residual char was tested in a pressurized spouted fluidized bed. After Soxhlet extraction and K-D concentration, the contents of 16 PAHs recommended by US EPA in coal, residual char, and fly ash, were analyzed by a HPLC coupled with fluorescence and diode-array detection.     

Mercury capture by selected Bulgarian fly ashes: Influence of coal rank and fly ash carbon pore structure on capture efficiency

Mercury capture by fly ash C was investigated at five lignite- and subbituminous-coal-burning Bulgarian power plants (Republika, Bobov Dol, Maritza East 2, Maritza East 3, and Sliven). Although the C content of the ashes is low, never exceeding 1.6%, the Hg capture on a unit C basis demonstrates that the low-rank-coal-derived fly ash carbons are more efficient in capturing Hg than fly ash carbons from bituminous-fired power plants. While some low-C and low-Hg fly ashes do not reveal any trends of Hg versus C, the 2nd and, in particular, the 3rd electrostatic precipitator (ESP) rows at the Republika power plant do have sufficient fly ash C range and experience flue gas sufficiently cool to capture measurable amounts of Hg. The Republika 3rd ESP row exhibits an increase in Hg with increasing C, as observed in other power plants, for example, in Kentucky power plants burning Appalachian-sourced bituminous coals. Mercury/C decreases with an increase in fly ash C, suggesting that some of the C is isolated from the flue gas stream and does not contribute to Hg capture. Mercury capture increases with an increase in Brunauer-Emmett-Teller (BET) surface area and micropore surface area. The differences in Hg capture between the Bulgarian plants burning low-rank coal and high volatile bituminous-fed Kentucky power plants suggests that the variations in C forms resulting from the combustion of the different ranks also influence the efficiency of Hg capture.     

Investigation of the changes in magnetic and chemical properties of soil during plant growth in a controlled environment

Changes in magnetic and chemical properties of soil during the growth of tomato plants (Lycopersicon esculentum) are examined in this study. The synthetic soils, prepared from sand, topsoil and organic material, were treated with magnetite powder (<5 μm) in order to simulate metal contamination. Six soil treatments were prepared from two soil types: controls, low-contamination and high-contamination treatments (0.01 and 0.05 g of magnetite powder/kg soil, respectively). Overall, the contaminated soils had a greater decrease in magnetic susceptibility (MS) than the controls, and the difference in MS decrease between the treatments was found to be statistically significant for both soil types. Potential reasons for the overall MS decrease were explored, and among them, trace element uptake by plants probably had a minor contribution as the concentration differences of Fe and other trace elements (Ni, Mn) between treatments were not statistically significant. In soils, oxidized and weakly magnetic minerals (maghemite, goethite and hematite) were common after plant growth, when compared with the untreated (background) soil. Such mineral transformations could have contributed to the overall MS decrease. The results show that exposure to Fe contaminants can affect plant growth and suggest that plant growth can measurably change the magnetic properties of their growth media. While the potential variables affecting plant growth were controlled as much as possible, there still remains the potential that biotic and abiotic chemical reactions could have affected the results. Thus, continuous monitoring of the changes in soil magnetic and chemical properties in more complex soil–plant systems is needed.     

碱渣与粉煤灰拌合物的岩土工程及环境特性研究

碱渣是氨碱法生产纯碱时产生的工业废料,仅天津碱厂历年堆积的碱渣占地已达数平方公里。碱渣与其它材料（如粉煤灰等）拌和可制成工程土,代替一般工程土作为道路基础或大面积填垫材料的途经。对碱渣制工程土的化学成分,岩土工程性质和对环境的影响进行了研究,对碱渣土回填场地的地基承载能力和长期稳定性进行了测试。研究成果可以使这种工程土得到合理利用,从而减轻工业废料-碱渣的堆积和污染问题     

Comparison of physical and chemical properties of maceral groups separated by density dradient centrifugation

Eight coals have been selected for study of the physical and chemical properties of the maceral group . The density-gradient centrifugation technique was employed to affect maceral group separation. The maximum reflectance method of Ting and Lo was used for estimating the reflectance of very small coal particles. The reflectograms were used to characterize the separated maceral fractions. The density, elemental composition, reflectance, NMR parameters of aromaticity, protonated aromatic carbon content and ƒ_stuggereda^stuggeredH of the maceral groups were compared. Variations in the aromatic structure of the maceral groups are discussed as well as the observation that ƒ_stuggereda and ƒ_stuggereda^stuggeredH change with particle density.     

Measuring reactive pools of Cd,Pb and Zn in coal fly ash from the UK using isotopic dilution assays

Large volumes of coal fly ash are continually being produced and stockpiled around the world and can be a source of environmentally sensitive trace elements. Whilst leaching tests are used for regulatory purposes, these provide little information about the true geochemical behaviour and ‘reactivity’ of trace elements in coal ash because they are poorly selective. Isotope dilution (ID) assays are frequently used in soil geochemistry as a means of measuring the reactive pools of trace metals that are in equilibrium with soil pore waters. This paper examines the applicability of multi-element ID assays in measuring the labile or reactive pool of Cd, Pb and Zn in a range of fresh and weathered fly ash, where pH is generally much more alkaline than in soils. The method generally worked well using 0.0005 M EDTA as a background electrolyte as it provided robust analytical ICP-MS measurements as well as fulfilling the important principle of ID that non-labile metal should not be solubilised. Reactive pools were equivalent to 0.5–3% of the total Pb pool and 4–13% of the total Cd pool. For Zn, where samples had pH < 11.5, the reactive Zn pool varied between 0.3% and 2%; when fresh ash samples with pH > 11.5 were tested, the method failed as the spiked isotope appeared to be sorbed or precipitated. Ash weathering was found to exert little impact on the lability of Cd, Pb and Zn. Isotope dilution results were compared with 0.43 M HNO₃ and 0.05 M EDTA extractions, these commonly being used as analogues of the ID assay, and concluded that these can be used as fast, cost-effective and simple proxies for the ID assays. Results suggest that ID methods can be used to enhance knowledge of trace element behaviour in fresh and weathered fly ash.     

粉煤灰增强回填碱渣工程特性的试验研究

碱渣与饱和卤水混合制成浆体回填到盐矿废弃盐腔可同时解决碱渣处理问题和地下废弃盐腔存在的地质隐患。回填碱渣强度是影响充填效果的重要因素。因此,为了提高回填碱渣强度,采用掺入粉煤灰制成复合碱渣对其强度特性进行改良。针对不同粉煤灰掺合比的碱渣开展了组成、力学和细观试验。研究结果表明：（1）掺入粉煤灰能明显改善碱渣的强度,使其黏聚力、内摩擦角都大幅提高,抗剪强度大幅增加;（2）粉煤灰掺合比越大,增强效果越明显,但强度并非随掺合比呈线性变化,对黏聚力而言,在0～20%内的掺合比下增加速度最快,而对内摩擦角则在20%～30%的掺合比区间增加最快,对抗剪强度而言,0～20%的掺合比内增加最明显;（3）粉煤灰掺入还可显著改善碱渣的压缩固结特性,使其固结系数大幅提高,从而提高碱渣固结速度,缩短充填工期,其中在0～10%的掺合比内对压缩固结特性改善最显著;（4）矿物组成分析表明,粉煤灰掺入改变了矿物组成,使得亲水性矿物含量急剧锐减,进而改变了其沉积特性。而细观分析则表明,粉煤灰掺入使碱渣从絮凝团细观结构变成了粉煤灰充当骨架的充填结构,且粒间支撑和拉联效应明显。从增强效果提高、压缩固结特性增强、控制成本和工期综合分析表明,最优掺合比为20%左右,建议工程中以不高于20%的掺合比作为实用掺合比即可取得较为理想的充填增强效果。该研究为揭示碱渣增强机制及废弃盐腔碱渣充填工艺优化提供了有益参考。     

Effects of biochar and bio-fertilizer on yield and qualitative properties of soybean and some chemical properties of soil

This study attempted to examine the effects of biochar amendment together with bio-fertilizer on soybean yield and its qualitative properties, as well as a few chemical properties of soil through a factorial randomized complete block design at three replications in east of Golestan Province (Iran) during 2014. The two factors under study included the following: (1) biochar amendment (in four levels of 0, 2.5, 8, and 16 tons per hectare), (2) bio-fertilizer containing phosphorus and sulfur growth-promoting rhizobacteria (in two levels of inoculation and non-inoculation) applied through foliar feeding. The results of analysis of variance indicated that interactions of biochar amendment and bio-fertilizer on harvest index and grain yield were significant (p ≤?0.01). According to the results of this study, the highest harvest index and oil content were 56.9, and 17.7%, respectively, in the treatment of 8 tons per hectare biochar and inoculation with bio-fertilizer. The lowest harvest index and the lowest oil content were in the control treatment. The interaction of biochar and bio-fertilizer on bulk density and cation exchange capacity was significant (p ≤?0.01). The results of this study demonstrated that biochar affected the amount of residual nitrogen in the soil after harvest, cation exchange capacity (CEC), acidity (pH), and electrical conductivity (EC). The highest grain yield (3440 kg/ha) was in the 8-ton biochar treatment with inoculated bio-fertilizer. Our study concludes that the biochar and bio-fertilizers can improve grain yield of soybean till 51% relative to the control.