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1.
In this research, a float-sink test was applied to a Late Permian high-sulfur coal collected from Pu’an coalfield, Southwest in Guizhou, China. To investigate the occurrence modes and the mobility of various trace elements, as well as the cleaning potential of some harmful elements in density separation, coal quality parameters and concentrations of 46 elements of 7 density fractionated samples were determined and statistically analyzed. Results show that larger size and higher density fractions have higher total sulfur content and ash yield than the smaller and lower ones. In fact, most (74.39 %) of the total sulfur occurs in the inorganic matter. Affinity and correlation analysis show that Mo and Ni have apparently strong organic affinity, whereas Rh, Cs, Sr, Co, Nb, Zr, V, Ga, Sc, Be, Ge, Hf, Th, U, Ag, As, In, Cu, Cd, Ta, Li, TI, and Ba are mostly in the heavy fractions. Rare earth element (REE) patterns for the seven density fractions present good uniformity and show that they are of right-inclined pattern type characterized by Light REE (LREE, La ~ Eu) enrichment relative to Heavy REE (HREE, Gd ~ Lu) and pronounced negative δ Eu anomalies. This suggests that REE was mainly derived from basalt-weathered materials. LRREE/HREE ratio variations reveal that LREE has stronger affinity with the organic matter relative to the HREE, while high LRREE/HREE in heavy fractions may be related to pyrite. Supposing the maximum sulfur content of the cleaned coal is 1.00 %, the theoretical removal ratios of Co, TI, and Ba are as high as 90.94, 93.73, and 92.29 %, respectively, while those of As, Ni and Mo are only 56.33, 48.85, and 45.05 %, respectively. As these figures change with different maximum sulfur contents required for the cleaned coal, not only the decrease of sulfur and ash in coal washing, but also the mobility of some harmful trace elements should be taken into consideration.  相似文献   

2.
A study of near surface sediments from the Dan River (southeastern USA) was conducted to assess the use of magnetic properties as proxies of coal ash after a recent spill. The watershed geology is diverse and potentially contributes magnetic minerals to riverbed sediment from diabase dikes in the Dan River Triassic Basin and from granitic gneiss outside the basin. Coal ash is heterogeneous, including aluminosilicate spheres, amorphous particles and carbonaceous rods and lacy particles. The magnetic fraction of ash from the failed storage pond is up to 17 wt% and is mostly composed of black spheres with maghemite and magnetite. Ash was detected in riverbed sediment from quiet water settings such as inside of meander bends, the confluence of tributary streams and near islands between the spill site and 20 miles downstream in the Schoolfield Reservoir, Danville, VA. The strong magnetic signal is detected above background in riverbed samples and is strongly positively correlated with total ash; elevated low field magnetic susceptibility (χ LF) is evident in samples with ≥ 12% ash content. Anhysteretic remanent magnetization and hysteresis parameters delineate native sediment, ash-bearing sediment, and diabase dikes. Between 20 and 70 miles downstream of the spill site, ash concentrations were either buried or too low due to dilution with native sediment to be detected with χ LF in riverbed samples.  相似文献   

3.
The high cost of traditional stabilizing agents such as lime and cement has led to the research on industrial and agricultural wastes as suitable alternatives. Rice growing areas of Kenya accumulate large quantities of rice husk which pose serious disposal problems. When burnt as a means of disposal, the rice husk ash formed is difficult to coagulate and thus contribute to air and water pollution, require a large space for disposal, and cause respiratory health problems when inhaled. Red coffee soil poses serious engineering problems such as swelling due to wetting, shrinkage due to drying, low bearing capacity, and differential settlement leading to cracks and needs improvement for strength and stability in service. Red coffee soil and rice husks samples were obtained from Gatundu and Mwea, respectively. The rice husk was burnt at temperatures between 500 and 700 °C to ensure maximal formation of siliceous component. Chemical analysis on the rice husk ash gave the sum of SiO2, Fe2O3, and Al2O3 as 85.5 % indicating that it has pozzolanic activity. Rice husk ash was applied at 4, 6, 8, and 10 % by weight of dry soil. Plasticity index, liquid limit, and linear shrinkage decreased from 26.1, 67.1, and 13.0 % for lean sample to 18.5, 63.6, and 9.2 %, for 10 % rice husk ash stabilized samples, whereas plastic limit increased from 41.0 to 45.15 %. The soaked California bearing ratio value for rice husk ash stabilized samples increased from 5 to 22 % corresponding to soil subgrade class S4. However, lime-stabilized samples gave higher values.  相似文献   

4.
Coal, a fossil fuel, is the largest source of energy for the generation of electricity in India. In order to study the potential environmental hazards by coal based power plants, particulate matters were collected using Stack Monitoring Kit and gaseous pollutants by Automatic Flue Gas Analyzer. The morphological and chemical properties, mineralogical composition and particle size distributions have been determined by SEM–EDX, XRD and CILAS. The data revealed the presence of particulate matters, SO2, NOx in the range of 236–315, 162–238, 173–222 mg/Nm3 respectively. The emission of CO2 was in the range of 43,004–60,115 Nm3/h with an average of 52,830 Nm3/h. Among the elements, Fe > Mn > Al > Zn > B > Ni > Cr > Cu were present in substantially higher proportion than Pb > Mo > Cd > Se > As > Hg. It was found that most of the elements were concentrated on fly ash surface rather than coal, bottom ash and pond ash. This variation may be attributed to the fineness of fly ash particles with large surface ratio to mass. Mineralogical studies of coal and fly ash by X-ray diffraction revealed the presence of mullite, quartz, cristobalite and maghemite. Presence of mullite and quartz found in fly ash indicate the conversion of complex minerals to mullite and quartz at high temperature. Transfer Coefficient was calculated to determine the ratio of the enrichment of trace elements in fly or bottom ash with respect to coal and pond ash.  相似文献   

5.
运用电感耦合等离子体质谱和煤质分析等技术方法,对内蒙古胜利煤田0-1号钻孔揭露的早白垩世1、2和4号煤层(共20个煤分层,1个夹矸)进行了研究。结果显示,1、2号煤层的挥发分产率大于44%,透光率小于50%,煤类为褐煤;4号煤层挥发分产率42%,透光率53%,煤类为次烟煤(长焰煤);1、2号煤层灰分和硫含量较高,4号煤层灰分和硫含量较低。与世界煤微量元素含量平均值相比,1、2和4号煤层中Sb富集,V、Zr、Nb、Hf、W等元素轻微富集,其它微量元素的含量接近或低于世界煤含量的平均值。1、2和4号煤层中稀土元素和钇(REY)含量较低,根据上地壳标准值(La/Lu)N比值,所有煤分层均显示重稀土富集类型特征,而煤中泥岩夹矸则显示轻稀土富集类型特征。  相似文献   

6.
Sixty-five natural gas samples were collected from 19 oil-gasfields in the Qaidam basin, China. The chemical composition and carbon isotope values of the samples were measured, and the geochemical characteristics and origin of the natural gases were studied. The gases can be divided into biogenic gases, sapropelic oil-type gases, mixed type oil-type gases, coal-type gases and mixed gas. The δ13Ci values of the biogenic gases are very small and the C2+ contents of them are very low, ranging from -68.2‰ to -61.8‰ and 0.06% to 0.20% respectively. They have heavy δD and δ13Cco2> showing a CC>2 reduction pathway. They are distributed in the East depression region and derived from the Quaternary source rocks. The sapropelic oil-type gases have small δ13C2 values and high C2+ ranging from -36.6‰ to -28.6‰ and from 33.01% to 47.15% respectively. The mixed type oil-type gases have <5I3C2 values and C2+ contents varying from -28.6‰ to -24.8‰ and from 4.81% to 26.06% respectively. Both sapropelic oil-typ  相似文献   

7.
The first combined mineralogical and geochemical investigation of coal ashes from the Northwest Thrace Coal Basin, Turkey, was performed as a case study. The coal ash samples were obtained at 525 °C (group I), 750 °C (group II), and 1000 °C (group III) ashing temperatures from coal samples from the basin and were studied in terms of their mineralogical and geochemical composition using XRD and ICP-MS methods. The determination of the mineralogical composition was done for all of the groups; the geochemical analysis was carried out only for group II. In accordance with the high SiO2, Fe2O3, CaO, and SO3 content of the ash, quartz (SiO2), hematite (Fe2O3), and anhydrite (CaSO4) are the major crystalline phases for all of the ash groups. The other minerals are muscovite, thenardite, tridymite, calcite, wollastonite, anorthite, cristobalite, gibbsite, ternesite, mullite, nahcolite, and nacrite. High-temperature phases such as mullite, wollastonite, and anorthite were observed at 750 and 1000 °C. According to the (Fe2O3 + CaO + MgO+ K2O+ Na2O)/(SiO2 + Al2O3+ TiO2) ratios varying from 0.19 to 5.65, the ashes are highly prone to slagging. Compared to average values of low-rank coal ashes, the contents of V, Cr, Co, Ni, Zn, As, Rb, Sr, Mo, Cs, W, and U of the ash are higher, whereas the total content of rare earth elements (REEs) (Σ 163.7 ppm) are lower. Based on upper continental crust normalization, As, Se, Th, and U are enriched in all of the samples. The higher trace element contents in the ashes might be considered as a possible health hazard. The correlation analyses indicated that Ca is associated with anhydrite and As with hematite. The correlation analyses also showed that newly formed Al and Ca silicates may contain the elements such as Ti, K, Na, Cr, Sn, and Pb.  相似文献   

8.
The objective of the study is to investigate spatio-temporal variations of PM10, PM2.5, and PM1 concentrations at seven residential sites, located in the vicinity of opencast coal projects, Basundhara Garjanbahal Area (BGA), India. Meteorological parameters such as wind speed, wind direction, relative humidity, and temperature were collected simultaneously with PM concentrations. Mean concentrations of PM10 in the range 215 ± 169–526 ± 412 μg m?3, PM2.5 in the range of 91 ± 79–297 ± 107 μg m?3, PM1 in the range of 68 ± 60–247 ± 84 μg m?3 were obtained. Coarse fractions (PM2.5–10) varied from 27 to 58% whereas fine fractions (PM1–2.5 and PM1) varied in the range of 51–73%. PM2.5 concentration was 41–74% of PM10 concentration, PM1 concentration was 31–62% of PM10 concentration, and PM1 concentration was 73–83% of PM2.5 concentration. Role of meteorology on PM concentrations was assessed using correlation analysis. Linear relationships were established among PM concentrations using least square regression analysis. With the aid of principal component analysis, two components were drawn out of eight variables, which represent more than 75% of variance. The results indicated that major sources of air pollutants (PM10, PM2.5, PM1, CO, CO2) at the residential sites are road dust raised by vehicular movement, spillage of coal generated during transportation, spontaneous combustion of coal, and biomass burning in village area.  相似文献   

9.
The review presented covers: (a) historical introduction; (b) some analytical comments; (c) some peculiarities of the As geochemistry in environment; (d) an estimation of coal Clarke value of As; (e) some coals enriched in As; (f) mode of As occurrence in coal; (g) factors influencing the As distribution in coal matter and coal bed; (h) genetic topics; (i) some topics related to environmental impact of As by the coal combustion.The World average As content in coals (coal Clarke of As) for the bituminous coals and lignites are, respectively, 9.0±0.8 and 7.4±1.4 ppm. On an ash basis, these contents are higher: 50±5 and 49±8 ppm, respectively. Therefore, As is a very coalphile element: it has strong affinity to coal matter — organic and (or) inorganic but obligatory authigenic. The coalphile affinity of As is like that for Ge or S.There is strong regional variability of As distribution due to geologic variability of the individual coal basins. For example, bituminous coals in Eastern Germany, Czech Republic and SE China are enriched in As, whereas the coals in South Africa or Australia are very depleted compared to coal Clarke of As. In general, some relationship exists between As content and its mode of occurrence in coals. Typically, at high As content, sulphide sites dominate (pyrite and other more rare sulphides), whereas at low As content, Asorg dominates, both being authigenic. A contribution of the terrigenic As (in silicates) is usually minor and of the biogenic Asbio (derived from coal-forming plants) is poorly known.Both organic and inorganic As can exist not only as chemically bound form but also in the sorbed (acid leacheable) arsenate form. With increasing coal rank, sorbed exchangeable arsenate content decreases, with a minimum in the coking coals (German data: the Ruhr coals).Relations of As content in coal to ash yield (or its partitioning in sink–float fractions) and to coal petrographic composition are usually complicated. In most cases, these relations are controlled by main site (form) of As — Aspyr or Asorg. If Aspyr dominates, an As accumulation in heavy fractions (or in high-ash coals) is observed, and if Asorg dominates, it is enriched in medium-density fractions (or low- and medium-ash coals). Arsenic is in part accumulated in the inertinite vs. vitrinite (Asorg ?).There are four genetic types of As accumulation on coal: two epigenetic and two syngenetic: (1) Chinese type—hydrothermal As enrichment, sometimes similar to known Carlin type of As-bearing telethermal gold deposits; (2) Dakota type—hypergene enrichment from ground waters draining As-bearing tufa host rocks; (3) Bulgarian type—As enrichment resulting from As-bearing waters entered coal-forming peat bogs from sulphide deposit aureoles; (4) Turkish type—volcanic input of As in coal-forming peat bog as exhalations, brines and volcanic ash.During coal combustion at power plants, most of the initial As in coal volatilizes into the gaseous phase. At the widely used combustion of pulverized coal, most of Asorg, Aspyr and “shielded” As-bearing micromineral phases escape into gaseous and particulate phase and only minor part of Asclay remains in bottom ash. The dominant fraction of escaping As is in fly ash. Because 97–99% of the fly ash is collected by electrostatic precipitators, the atmospheric emission of As (solid phase and gaseous) is usually assumed as rather minor (10–30% from initial As in coal). However, fly ash disposal creates some difficult environmental problems because it is potentially toxic in natural waters and soils. The As leaching rate from ash disposal is greatly controlled by the ash chemistry. In natural environment, As can be readily leached from acid (SiO2-rich) bituminous coal ashes but can be very difficult from alkali (CaO-rich) lignite ashes.If the Aspyr form dominates, conventional coal cleaning may be an efficient tool for the removing As from coal. However, organic-bound or micromineral arsenic (“shielded” grains of As-bearing sulphides) are not removed by this procedure.Some considerations show that “toxicity threshold” of As content in coal (permissible concentration for industrial utility) may be in the range 100–300 ppm As. However, for different coals (with different proportions of As-forms), and for different combustion procedures, this “threshold” varies.  相似文献   

10.
Eighteen basalts and some volcanic gases from the submarine and subaerial parts of Kilauea volcano were analyzed for the concentration and isotope ratios of sulfur. By means of a newly developed technique, sulfide and sulfate sulfur in the basalts were separately but simultaneously determined. The submarine basalt has 700 ± 100 ppm total sulfur with δ34SΣs of 0.7 ± 0.1 ‰. The sulfate/sulfide molar ratio ranges from 0.15 to 0.56 and the fractionation factor between sulfate and sulfide is +7.5 ± 1.5‰. On the other hand, the concentration and δ34SΣs values of the total sulfur in the subaerial basalt are reduced to 150 ± 50 ppm and ?0.8 ± 0.2‰, respectively. The sulfate to sulfide ratio and the fractionation factor between them are also smaller, 0.01 to 0.25 and +3.0‰, respectively. Chemical and isotopic evidence strongly suggests that sulfate and sulfide in the submarine basalt are in chemical and isotopic equilibria with each other at magmatic conditions. Their relative abundance and the isotope fractionation factors may be used to estimate the ?o2 and temperature of these basalts at the time of their extrusion onto the sea floor. The observed change in sulfur chemistry and isotopic ratios from the submarine to subaerial basalts can be interpreted as degassing of the SO2 from basalt thereby depleting sulfate and 34S in basalt.The volcanic sulfur gases, predominantly SO2, from the 1971 and 1974 fissures in Kilauea Crater have δ34S values of 0.8 to 0.9%., slightly heavier than the total sulfur in the submarine basalts and definitely heavier than the subaerial basalts, in accord with the above model. However, the δ34S value of sulfur gases (largely SO2) from Sulfur Bank is 8.0%., implying a secondary origin of the sulfur. The δ34S values of native sulfur deposits at various sites of Kilauea and Mauna Loa volcanos, sulfate ions of four deep wells and hydrogen sulfide from a geothermal well along the east rift zone are also reported. The high δ34S values (+5 to +6%.o) found for the hydrogen sulfide might be an indication of hot basaltseawater reaction beneath the east rift zone.  相似文献   

11.
Major ions showed high concentrations, ionic strength and chemical activity in the surface waters of Govind Ballabh Pant Sagar reservoir. Various geochemical ratios showed the dominance of silicate over carbonate weathering and major ions such as Na+ + K+ account for about 52 % of the cation budget. The high Na+ and K+ showed sedimentation of rock/coal particles consisting of highly weathered silicate minerals contributed by the discharge of mine water, fly ash mixing during transportation, etc. Further, Ca2+ + Mg2+/Na+ + K+ ratio was <1 (0.92) indicating the occurrence of silicate weathering in the reservoir catchment. The comparative assessment showed that the proportion of Ca2+ + Mg2+/Na+ + K+ tends to be lower along the coal mining belts compared to non-coal mining regions in the world. The Ca2+/SO4 2? ratio <1 revealed not only H2CO3 but H2SO4 also acting as a source of protons for rock weathering. The cause underlying these differences can be related directly to geological substrate and anthropogenic activities.  相似文献   

12.
Fresh submarine basalt glasses from Galapagos Ridge, FAMOUS area, Cayman Trough and Kilauea east rift contain 22 to 160 ppm carbon and 0.3 to 2.8 ppm nitrogen, respectively, as the sums of dissolved species and vesicle-filling gases (CO2 and N2). The large range of variation in carbon content is due to combined effect of depth-dependency of the solubility of carbon in basalt melt and varying extents of vapour loss during magma emplacement as well as in sample crushing. The isotopic ratios of indigenous carbon and nitrogen are in very narrow ranges,?6.2 ± 0.2% relative to PDB and +0.2 ± 0.6 %. relative to atmospheric nitrogen, respectively. In basalt samples from Juan de Fuca Ridge, however, isotopically light carbon (δ13C = around ?24%.) predominates over the indigenous carbon; no indigenous heavy carbon was found. Except for Galapagos Ridge samples, these ocean-floor basalts contain 670 to 1100 ppm sulfur, averaging 810 ppm, in the form of both sulfide and sulfate, whereas basalts from Galapagos Ridge are higher in both sulfur (1490 and 1570 ppm) and iron (11.08% total iron as FeO). The δ34S values average +0.3 ± 0.5%. with average fractionation factor between sulfate and sulfide of +7.4 ± 1.6%.. The sulfate/sulfide ratios tend to increase with increasing water content of basalt, probably because the oxygen fugacity increases with increasing water content in basalt melt.  相似文献   

13.
This study investigated the removal efficiency of pharmaceuticals from aqueous solutions supported on chemically treated fly ash. The coal fly ash was supplied by the electric power station in Krakow, Poland. There are plenty of studies showing the utilization of fly ash as a low-cost adsorbent for wastewater containing heavy metals or dyes. Adsorption and immobilization of pharmaceuticals and personal care products on fly ash is a relatively new method but it is a very promising one. In this study, the adsorptive removal of diclofenac, ketoprofen, carbamazepine, bezafibrate, bisphenol A, 17α-ethinyl estradiol and estriol by HCl- and NaOH-treated fly ash was assessed. Chemical treatment of fly ash changed structures of particles and enhanced specific surface areas. HCl-treated fly ash was characterized by the highest BET specific surface area 47.9 m2 g?1 and unburned carbon content 8.1%. Isotherms for all compounds except for 17α-ethinyl estradiol (EE2) and estriol (E3) were linear. Higher linear regression coefficients (R 2) obtained for isotherms of EE2 and E3 show that the Freundlich model better describes their sorption. Adsorption coefficients K d varied between 109.5 (L kg?1) for bisphenol A and 471.5 (L kg?1) for bezafibrate. Freundlich constants (K F) for EE2 and E3 were 62.3 and 119.9 (µg1?1/n L1/n kg?1), respectively. Acid treatment of fly ash increased adsorption of diclofenac, ketoprofen, carbamazepine, bezafibrate and bisphenol A. Comparison of the octanol–water partitioning coefficients (log K OW) with the partitioning coefficients normalized on unburned carbon content (log K UC) revealed similarities but no strong correlation. The increasing of unburned carbon increased sorption of compounds to fly ash.  相似文献   

14.
The history of life on Earth is critically dependent on the carbon, sulfur and oxygen cycles of the lithosphere – hydrosphere – atmosphere – biosphere system. An Archean oxygen-poor greenhouse atmosphere developed through: (i) accumulation of CO2 and CH4 from episodic injections of CO2 from volcanic activity, volatilised crust impacted by asteroids and comets, metamorphic devolatilisation processes and release of methane from sediments; and (ii) little CO2 weathering-capture due to both high temperatures of the hydrosphere (low CO2 solubility) and a low ratio of exposed continents to oceans. In the wake of the Sturtian glaciation, enrichment in oxygen and appearance of multicellular eukaryotes heralded the onset of the Phanerozoic where greenhouse conditions were interrupted by periods of strong CO2-sequestration through intensified capture of CO2 by marine plants, onset of land plants and burial of carbonaceous shale and coal (Late Ordovician; Carboniferous – Permian; Late Jurassic; Late Tertiary – Quaternary). The progression from Late Mesozoic and Early Tertiary greenhouse conditions to Late Tertiary – Quaternary ice ages was related to the sequestration of CO2 by rapid weathering of the emerging Alpine and Himalayan mountain chains. A number of peak warming and sea-level-rise events include the Late Oligocene, mid-Miocene, mid-Pliocene and Pleistocene glacial terminations. The Late Tertiary – Quaternary ice ages were dominated by cyclic orbital-forcing-triggered terminations which involved CO2-feedback effects from warming seas and the biosphere and albedo flips due to ice-sheet melting. Since ca AD 1750 human emissions were ～305 Gt of carbon, as compared with ～750 Gt C in the atmosphere. The emissions constitute ～12% of the terrestrial biosphere and ～10% of the known global fossil fuel reserve of ～4000 Gt C, whose combustion would compare to the ～ 4600 Gt C released to the atmosphere during the K – T impact event 65 million years ago, with associated ～65% mass extinction of species. The current growth rate of atmospheric greenhouse gases and global mean temperatures exceed those of Pleistocene glacial terminations by one to two orders of magnitude. The relationship between temperatures and sea-levels for the last few million years project future sea-level rises toward time-averaged values of at least 5 m per 1°C. The instability of ice sheets suggested by the Dansgaard – Oeschinger glacial cycles during 50 – 20 ka, observed ice melt lag effects of glacial terminations, spring ice collapse dynamics and the doubling per-decade of Greenland and west Antarctic ice melt suggest that the Intergovernmental Panel on Climate Change's projected sea-level rises (<59 cm) for the 21st century may be exceeded. The biological and philosophical rationale underlying climate change and mass extinction perpetrated by an intelligent carbon-emitting mammal species may never be known.  相似文献   

15.
The isotopic compositions of S (δ34S) and C (δ13C) were determined for the coal utilized by a power plant and for the fly ash produced as a by-product of the coal combustion in a 220-MW utility boiler. The coal samples analyzed represent different lithologies within a single mine, the coal supplied to the power plant, the pulverized feed coal, and the coal rejected by the pulverizer. The ash was collected at various stages of the ash-collection system in the plant. There is a notable enrichment in 34S from the base to the top of the coal seam in the mine, with much of the variation due to an upwards enrichment in the δ34S values of the pyrite. Variations in δ34S and in the amount of pyritic S in the coal delivered to the plant show that there was a change of source of coal supplied to the plant, between week one and week two of monitoring, supporting a previous study based on metal and sulfide geochemistry for the same plant. The fly ash has a more enriched δ34S than the pulverized coal and, in general, the δ34S is more enriched in fly ashes collected at cooler points in the ash-collection system. This pattern of δ34S suggests an increased isotopic fractionation due to temperature, with the fly ash becoming progressively depleted in 34S and the flue gas S-containing components becoming progressively enriched in 34S with increasing temperatures. Substantially less variation is seen in the C isotopes compared to S isotopes. There is little vertical variation in δ13C in the coal bed, with δ13C becoming slightly heavier towards the top of the coal seam. An 83–93% loss of solid phase C occurs during coal combustion in the transition from coal to ash owing to loss of CO2. Despite the significant difference in total C content only a small enrichment of 0.44–0.67‰ in 13C in the ash relative to the coal is observed, demonstrating that redistribution of C isotopes in the boiler and convective passes prior to the arrival of the fly ash in the ash-collections system is minor.  相似文献   

16.
To evaluate the impact of invading seagrass on biogeochemical processes associated with sulfur cycles, we investigated the geochemical properties and sulfate reduction rates (SRRs) in sediments inhabited by invasive warm affinity Halophila nipponica and indigenous cold affinity Zostera marina. A more positive relationship between SRR and below-ground biomass (BGB) was observed at the H. nipponica bed (SRR = 0.6809 × BGB ? 4.3162, r 2 = 0.9878, p = 0.0006) than at the Z. marina bed (SRR = 0.3470 × BGB ? 4.0341, r 2 = 0.7082, p = 0.0357). These results suggested that SR was more stimulated by the dissolved organic carbon (DOC) exuded from the roots of H. nipponica than by the DOC released from the roots of Z. marina. Despite the enhanced SR in spring-summer, the relatively lower proportion (average, 20%) of acid-volatile sulfur (AVS) in total reduced sulfur and the strong correlation between total oxalate-extractable Fe (Fe(oxal)) and chromium-reducible sulfur (CRS = 0.2321 × total Fe(oxal) + 1.8180, r 2 = 0.3344, p = 0.0076) in the sediments suggested the rapid re-oxidation of sulfide and precipitation of sulfide with Fe. The turnover rate of the AVS at the H. nipponica bed (0.13 day?1) was 2.5 times lower than that at the Z. marina bed (0.33 day?1). Together with lower AVS turnover, the stronger correlation of SRR to BGB in the H. nipponica bed suggests that the extension of H. nipponica resulting from the warming of seawater might provoke more sulfide accumulation in coastal sediments.  相似文献   

17.
While the Intergovernmental Panel on Climate Change classifies coal as anthracite, bituminous coal, and sub-bituminous coal, Korea only distinguishes coal as anthracite and bituminous coal while sub-bituminous coal is considered bituminous coal. As a result, Korea conducted research in the CO2 emission factors of anthracite and bituminous coal, but largely ignored sub-bituminous coal. Therefore, the purpose of this research is to develop the CO2 emission factor of sub-bituminous coal by classifying sub-bituminous coal from resources of bituminous coal activities collected in Korea between 2007 and 2011. The 2007–2011 average carbon content of sub-bituminous coal was analyzed to be 69.63 ± 3.11 %, the average hydrogen content 4.97 ± 0.37 %, the inherent moisture 12.60 ± 4.33 %, the total moisture 21.91 ± 5.45 %, and the dry-based gross calorific value was analyzed to be 5,914 ± 391 kcal/kg; using these analyzed values, the as-received net calorific value was found to be 20.75 ± 7.59 TJ/Gg and the CO2 emission factor was found to be 96,241 ± 4,064 kg/TJ. In addition, the 62.7 million ton amount for the 2009 greenhouse gas emission from sub-bituminous coal as estimated with the analyzed value of this study is an amount that is equivalent to 11.1 % of the 2009 total greenhouse gas emission amount of 564.7 million tons, and this amount is larger than the 9.3 % for the industrial processes sector, 3.3 % for the agricultural sector and 2.5 % for the waste sector. Therefore, it is important to reflect the realities of Korea when estimating the greenhouse gas emission from such sub-bituminous coals.  相似文献   

18.
Fly ash is a product arising from coal combustion in thermal power plants. It represents a major source of environmental pollution. It is well known by its chemical composition rich of SiO2 and Al2O3. With the aim of preserving the environment against this contamination, fly ash was used along with the starting materials for producing glass cordierite (2MgO, 2Al2O3, 5SiO2). Four formulations were developed by mixing the silica gel, magnesium chloride (MgCl2.6H2O) and fly ash in the percentages enclosing the stoichiometry of cordierite (2MgO, 2Al2O3, 5SiO2). Different experimental techniques (DTA/TGA, X-ray diffraction, FTIR and SEM) were used to characterise the prepared formulations. The results shown that for all formulations, a cordierite phase was obtained at 1200 °C along with several secondary phases such as mullite, cristobalite, silicon oxide, enstatite and spinel. At 1300 °C, pure indialite (α-cordierite) was obtained along with a small amount of spinel. The four formulations sintered at 1200 °C exhibit a homogenous morphology and high porosity. The acicular-shaped indialite grains were observed in both formulations with excess of alumina and excess of magnesia.  相似文献   

19.
Lake Erie is biologically the most active lake among the Great Lakes of North America, experiencing seasonal harmful algal blooms (HABs). The early detection of HABs in the Western Basin of Lake Erie (WBLE) requires a more efficient and accurate monitoring tool. Remote sensing is an efficient tool with high spatial and temporal coverage that can allow accurate and timely detection of the HABs. The WBLE is heavily influenced by the surrounding terrestrial ecosystem via rivers such as the Sandusky River and the Maumee River. As a result, the optical properties of the WBLE are influenced by multiple color producing agents (CPAs) such as phytoplankton, colored dissolved organic matter (CDOM), organic detritus, and terrigenous inorganic particles. The diversity of the CPAs and their non-linear interactions makes these waters optically complex, and the task of optical remote sensing for retrieving estimates of CPAs more challenging. Chlorophyll a, which is the primary light harvesting pigment in all phytoplankton, is used as a proxy for algal biomass. In this study, several published remote sensing algorithms and band ratio models were applied to the reflectance data from the full resolution MERIS sensor to remotely estimate chlorophyll a concentrations in the WBLE. Efficiency of the sensor and the algorithms performance were tested through a least squares regression and residual analysis. The results indicate that, among the suite of existing bio-optical models, the Simis semi-analytical algorithm provided the best model results for measures of algal biomass in the optically complex WBLE with R 2 of 0.65, RMSE 0.85 μg/l, (n = 71, P < 0.05). The superior results of this model in detecting chlorophyll a are attributed to several factors including optimizing spectral regions that are less sensitive to CDOM and the incorporation of correction factors such as absorption effects due to pure water (a w), backscatter (b b) from suspended matter and interference due to phycocyanin (δ), a major accessory pigment in the WBLE.  相似文献   

20.
The formation environment of the main coal seam in Shengli coal mine is analyzed, and the effect of coal ash parameters on the coal-forming environment is mainly discussed according to gray component parameters combined with other coal quality test analysis data. Results show that the hydrodynamic conditions of the main coal during coal accumulation have a general pattern of strong northeast and weak southwest, and lakeside swamp is generally in the retrograde process from south to north. The No.5 coal seam is a water entry cycle, and the No.5lower coal is a water withdrawal cycle. The No.6 thick coal seam is formed in the peat swamp environment where the water is shallow and the groundwater activity is weak. The input of terrestrial debris material was most abundant in the formation period of No.5lower coal, followed by No.5 coal, and that in No.6 coal is the least. Vertically, the peat swamp environment changed from weak reduction to weak oxidation to strong reducing environment. The ash yield was low to high to low from bottom to top. The organic sulfur is the main type of sulfur in the main coal seam. The weaker the hydrodynamic condition, the higher the organic sulfur content in the reduction environment, while lower organic sulfur content in the oxidation environment. The peat swamp water of No.5lower coal is medium alkaline, and the peat swamp water of No.5 and No. 6 coals is weakly alkaline or acidic.  相似文献   

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