共查询到20条相似文献，搜索用时 31 毫秒
1.
V. A. Avramenko S. Yu. Bratskaya A. S. Yakushevich A. V. Voit V. V. Ivanov S. I. Ivannikov 《Geochemistry International》2012,50(5):437-446
Brown coals with high Au and PGE concentrations from six deposits in the southern Russian Far East were analyzed for elemental
composition, acid-base properties, and the molecular-size distribution of humic acids (HA). The ash contents of the coals
were determined to be negatively correlated with their Au concentrations, and the content of “organic Au” (which is chemically
bound to humic substances, HS) reaches 95%. The most probable mode of Au occurrence in the brown coals is submicrometer-sized
particles of elemental gold stabilized by HA. Quantum-mechanical calculations of interactions between Au(0) clusters with
model HS fragments confirm that HS could be originally strongly chemically adsorbed on the surface of elemental gold particles.
Different stability of colloids during centrifuging of alkali extracts of the gold-bearing brown coals was proved to be likely
responsible for the selective separation of free HA and those bound with gold particles, and this can be used to develop a
technology for gold recovery from coals without decomposing their organic matrix. 相似文献
2.
S.I. Arbuzov L.P. Rikhvanov S.G. Maslov V.S. Arhipov A.M. Belyaeva 《International Journal of Coal Geology》2006,68(3-4):127-134
One hundred twenty-two samples of Jurassic and Paleogene brown coals and 1254 peat samples from the south-eastern region of the Western-Siberian platform were analyzed for gold by the neutron-activation method. Mean content of Au in Jurassic coals is 30 ± 8 ppb, in Paleogene coals is 10.6 ± 4.8 ppb, and in peat is 6 ± 1.4 ppb. Concentrations of gold as high as 4.4 ppm were found in coal ash and 0.48 ppm in the peat ash. Coal beds with anomalous gold contents were found at Western-Siberian platform for the first time.Negative correlation between gold and ash yield in coals and peat and highest gold concentrations were found in low-ash and ultra-low-ash coals and peat. Primarily this is due to gold's association with organic matter.For the investigation of mode of occurrence of Au in peat the bitumen, water-soluble and high-hydrolyzed substances, humic acids, cellulose and lignin were extracted from it. It was determined that in peat about 95% of gold is combined with organic matter. Forty to sixty percent of Au is contained in humic acids and the same content is in lignin. Bitumens, water-soluble and high-hydrolyzed substances contain no more than 1% of general gold quantity in peat.The conditions of accumulation of high gold concentrations were considered. The authors suggest that Au accumulation in peat and brown coals and the connection between anomalous gold concentrations and organic matter in low-ash coals and peat can explain a biogenic–sorption mechanism of Au accumulation. The sources of formation of Au high concentration were various Au–Sb, Au–Ag Au–As–Sb deposits that are abundant in the Southern and South-Eastern peripheries of the coal basin. 相似文献
3.
The relationship between noble metal mineralization and carbonaceous rocks (black shales and brown coals) is considered. We have confirmed the previous conclusions of multistage syn- and epimetamorphic formation of gold-bearing deposits in black shales and syn- and epigenetic accumulation of noble metals in brown coals. The gold and PGE in the brown coals of the Verkhnii Amur region and Primorye were presumably derived by disintegration of adjacent ore sources in the Cenozoic. Addition studies and sampling are required at the coal and graphite objects of the Russian Far East to solve this problem. 相似文献
4.
This paper presents a review of the genetic types and geochemical processes that have formed ‘metalliferous’ coals around the world. Primary attention is given to elements in coal that are currently being extracted from coal as raw material (Ge and U) or have, in our opinion, the best chance for such use (REE, Ag, Au, and PGE). Coals with anomalously high concentrations of other metals having potential for economic by-product recovery (Be, Sc, V, Ga, Sb, Cs, Mo, W, and Re) are briefly considered. Original data and a survey of the literature indicate that metalliferous coals are in many coal basins. Ore formation in coal-bearing structures may occur during peat accumulation, during diagenesis of the organic matter, or by epigenesis. Various metals are supplied to sedimentary basins as minerals that are transported by water and wind or as ionic species in surface water and descending and ascending underground water and may be incorporated into peat or coals. The modes of occurrence of metals in the enriched coals are diverse. The data presented in this review indicates that metalliferous coals should be regarded as promising for economic recovery for by-products in the course of coal mining and combustion. 相似文献
5.
淤泥富含大量有机质,受微生物作用,有机质会逐步分解出腐殖酸;同时,腐殖酸又会影响有机质降解,进而影响淤泥固化效果。为此,通过维持恒定的碱性缓冲溶液环境（pH=9.0）,将淤泥浸泡其中,观测其有机质含量的变化过程。结果表明,碱性缓冲溶液既能加快有机质分解,也能消耗腐殖酸,使溶液保持为碱性状态;当有机质分解完成,腐殖酸也释放结束,降解过程大约持续28 d。通过掺入水泥和石灰固化淤泥,发现含有机质的固化淤泥,其强度随养护时间会先增长后衰减,但预降解有机质的固化淤泥强度不会衰减。由此说明,通过碱性缓冲溶液预降解淤泥有机质,可以提升固化土耐久性。 相似文献
6.
A. A. Cherepanov 《Russian Journal of Pacific Geology》2008,2(2):110-121
The distribution and speciation of gold and platinum in ash-cinder wastes of the thermal power plants of Khabarovsk krai and Primorye are considered in terms of the research methods and the results obtained. The Au and PGE contents attain 2 g/t and higher, being 0.8–1.5 g/t on average. The ash of brown coal from the Pavlovka, Khurmuli, and some other fields is characterized by elevated PGE contents. The causes of discrepancies in the analytical determination of noble metals in coaly and carbonaceous rocks are considered. Accumulation of noble metals in coal is caused largely by their sorption on carbonaceous matter. The content of noble metals in ash-cinder wastes depends on their grade in the burnt coal. The latter, in turn, depends on the metallogenic characteristics of the coalfield. Gold and platinum are of economic importance, and a special technology for their recovery should to be worked out. 相似文献
7.
A. S. Yakushevich S. Yu. Bratskaya V. V. Ivanov N. V. Polyakova V. A. Avramenko 《Geochemistry International》2013,51(5):405-412
We studied a number of chemical characteristics in the coals of the Spetsugli germanium-bearing area of the Pavlovskoe coalfield in southern Primorye. It was found that the coals show variable contents of ash, extractable organic matter (OM), and germanium. No less than 60% germanium in the coals are bound to mobile OM, including 25–60% in complex compounds of humic acids and 8–39% in the low-molecular-weight fraction of OM not precipitated by acids. It was shown that germanium can be partly accumulated in coals as organic compounds owing to the dissolution of the mineral forms of germanium by humic acids. 相似文献
8.
W. R. Jackson G. D. Bongers P. J. Redlich G. Favas Y. Fei A. F. Patti R. B. Johns 《International Journal of Coal Geology》1996,32(1-4)
It has been proposed that Victorian brown coal can be considered as a two-component structure — a lignocellulosic “host”, containing various amounts of weakly bound or entrapped “guest” material together with very small amounts of inorganic and/or mineral matter. The latter predominantly consists of wax esters and/or terpenoid material. In this paper we describe attempts to gain structural information regarding the more complex, “host” component of the coal. Our initial model compound has been humic acid that can be readily obtained from the coal by alkaline extraction. It has been found that “pure” humic acid, free from material associated with the “guest” components of the coal, can be obtained by a highly selective, low-yielding alkaline extraction. This humic acid has been studied by nmr spectroscopy and pyrolysis gas chromatography-mass spectroscopy (py-gc/ms). The products arising from py-gc/ms have been compared with those obtained from similar pyrolysis of whole coals. Alkylation of humic acids using alkyl halides in the presence of base has been successfully carried out and reactivity of the resulting materials compared with those of the parent coal and humic acid. 相似文献
9.
M.A. Rashid 《Chemical Geology》1974,13(2):115-123
Humic acids isolated from marine sediments were found to be effective in absorption of various metal ions through chelation, cation exchange and surface adsorption. The quantities of metal ions complexed varied from 40 to 205 mg/g of organic matter. In the presence of equal concentrations of Co, Cu, Mn, Ni and Zn in the reaction media, humic acid and peatmoss, a rich source of humic compounds, showed preferential absorption for Cu. Copper constituted more than 50% of the metal ions complexed by organic matter. As compared with the other metal ions, its bonding strength was very firm because it could not be displaced by ferric ion or cation exchange reagents.Peatmoss, a rich source of humic acid, was found to absorb significant quantities of various metal ions. Under laboratory conditions each kg of peat absorbed about 1500 mg of various metal ions from solutions containing equal concentrations of Co, Cu, Mn, Ni and Zn. However, in the field trials with sea water, absorption of metals was limited to Zn (28.7 mg/kg), Cu (3.66 mg/kg) and Fe (2.0 mg/kg). Under-saturation of sea water for transition metals and super-saturation for alkali and alkaline earth metals appears to be a bottleneck in the effective utilization of peat as a means of recovery of metals from sea water. 相似文献
10.
The role of organic ligands in metal complexing in natural waters has received little attention because of uncertainties regarding both the abundance and nature of dissolved organic carbon compounds. Recent data show that the bulk of dissolved organic matter in natural waters consists of highly oxidized and chemically and biologically stable polymeric compounds closely resembling soil humic substances. Average molar concentrations of these aquatic humics in major U.S. rivers range from 5 × 10?6to 3 × 10?5 moles 1?1. Fractional elution of soil organic matter by meteoric waters may be considered to be the main process contributing to the presence of humic matter in rivers. The aquatic humic polymers participate in complex formation through ionizable functional groups with a range of differential acidities. The stabilities of metal-humic complexes in natural waters are higher than those of the corresponding inorganic metal complexes. Quantitative evaluation of the metal-organic interactions can be approached by applying variable equilibrium functions which take into account the differential physico-chemical characteristics of the active complexing sites on the polymer molecule. Assuming an average humic concentration of 10 mg 1?1, complexation of trace metals can be significant even in the presence of excess concentrations of major cations. 相似文献
11.
陆架边缘海是“河口—陆架”体系重要的碳汇,黏土矿物作为主要载体将有机质与金属元素吸附于表面或层间,通常表现为粒度、有机质和金属元素含量之间高度正相关。本文通过分析南黄海中部沉积物粒度、总有机碳、主微量元素,探讨三者之间分布特征和相互关系,进一步开展金属元素、有机质与黏土矿物吸附模拟实验,结果表明,酸性条件（pH=4）下适量的金属离子（Zn2+、Ni2+、Pb2+）明显促进伊利石对腐殖酸（有机质主要组成部分）吸附,腐殖酸吸附量达到20.06 mg/g,其中金属离子加入使腐殖酸吸附量提高6.25%;同时碱性条件（pH=8）下金属离子也能够促进伊利石对腐殖酸吸附,腐殖酸吸附量达到15.7 mg/g,金属离子加入使腐殖酸吸附量提高38.9%。金属离子的阳离子键桥作用促进伊利石吸附腐殖酸,且酸性环境下腐殖酸的吸附量高于碱性环境。证实了陆架边缘海背下金属元素的参与对黏土矿物吸附腐殖酸具有明显促进作用,有利于在全球碳循环过程形成边缘海“碳库”,同时海洋酸化可能造成海洋溶解有机质降低和重金属离子浓度升高,对陆架边缘海海洋生态系统平衡构成威胁。 相似文献
12.
A review with 227 references of the title subject is presented. It is divided into two main sections, viz., nature and properties of humic matter, and water—metal—sediment interactions.The first section deals with the essential properties of organic matter which occurs naturally in drainage sediments and waters. Discussion of the basic molecular structure of humic and fulvic acids is followed by some details of the chemical nature of functional groups within these structures which are important in metal-ion adsorption and complexing reactions which these materials can undergo. Information is also presented for colloidal and polyelectrolyte properties, complexation properties, and finally a summary discussion of metal-ion—humic-acid, metal-ion—fulvic-acid stability constants for both single ligand and mixed ligand systems completes the section.The second section comprises discussions of some specific aspects of interactions between metals, sediments and waters, including metal and organic speciation studies; sorption interactions between organic matter, clays and humic acids; chemical reaction between humic acids, heavy-metal minerals, clays and other silicate minerals; metal-ion adsorption—desorption studies, oxidation—reduction reactions between metal ions and humic acids; effects of sulphide ion on some of the above interactions and finally a summary of some relevant field geochemical dispersion studies.This second section describes both laboratory and field studies for each aspect. 相似文献
13.
A dialysis procedure was used to assess the distribution coefficients of ∼50 major and trace elements (TEs) between colloidal (1 kDa–0.22 μm) and truly dissolved (<1 kDa) phases in Fe- and organic-rich boreal surface waters. These measurements allowed quantification of both TE partitioning coefficients and the proportion of colloidal forms as a function of solution pH (from 3 to 8). Two groups of elements can be distinguished according to their behaviour during dialysis: (i) elements which are strongly associated with colloids and exhibit significant increases of relative proportion of colloidal forms with pH increase (Al, Ba, Cd, Co, Cr, Cu, Fe, Ga, Hf, Mn, Ni, Pb, rare earth elements (REEs), Sr, Th, U, Y, Zn, Zr and dissolved organic C) and (ii) elements that are weakly associated with colloids and whose distribution coefficients between colloidal and truly dissolved phases are not significantly affected by solution pH (As, B, Ca, Cs, Ge, K, Li, Mg, Mo, Na, Nb, Rb, Sb, Si, Sn, Ti, V). Element speciation was assessed using the Visual MINTEQ computer code with an implemented NICA-Donnan humic ion binding model and database. The model reproduces quantitatively the pH-dependence of colloidal form proportion for alkaline-earth (Ba, Ca, Mg, Sr) and most divalent metals (Co, Cd, Mn, Ni, Pb, Zn) implying that the complexation of these metals with low molecular weight organic matter (<1 kDa fraction) is negligible. In contrast, model prediction of colloidal proportion (fraction of 1 kDa–0.22 μm) of Cu2+ and all trivalent and tetravalent metals is much higher than that measured in the experiment. This difference may be explained by (i) the presence of strong metal-binding organic ligands in the <1 kDa fraction whose stability constants are several orders of magnitude higher than those of colloidal humic and fulvic acids and/or (ii) coprecipitation of TE with Fe(Al) oxy(hydr)oxides in the colloidal fraction, whose dissolution and aggregation controls the pH-dependent pattern of TE partitioning. Quantitative modeling of metal – organic ligand complexation and empirical distribution coefficients corroborate the existence of two colloidal pools, formerly reported in boreal surface waters: “classic” fulvic or humic acids binding divalent transition metals and alkaline-earth elements and large-size organo-ferric colloids transporting insoluble trivalent and tetravalent elements. 相似文献
14.
BAO Zhiwei Jayanta GUHA 《《地质学报》英文版》2007,81(1):121-134
The Lannigou deposit is a large-sized sedimentary rock-hosted disseminated gold （SRHDG） deposit located in the Youjiang Basin. It is hosted by the Middle Triassic turbidite. Wall rock alterations, including silicification, pyritization, arsenopyritization, carbonatization and argillization, commonly occur along fractures. PGE study demonstrates that either Permian basalts or Triassic ultrabasic intrnsives are unlikely to be the main source of gold mineralization. Coupled with the lack of other nmgmatic activity in the vicinity of the mining area, an amagmatic origin is proposed. Organic matter compositions and GC-MS analysis of the ores and host rocks show that the organics in the ores and the host rocks have a common source; the organic matter in the ores was mainly indigenous. The positive correlation between S2 and Au contents, along with the common occurrence of organic inclusions, suggest involvement of organic matter in the ore-forming process in terms of promoting Au leaching from the source rocks, making colloidal Au migration possible, as well as hydrocarbon reduction of sulphate. Geological and geochemical characteristics of the Lannigou deposit suggest that it was formed through circulation of meteoric water and probably less importantly organic bearing formation water driven by high geothermal gradient caused by late Yanshanian extension, which leached Au from the source bed, and then migrated as Au-bisnlfides and colloidal Au, culminating in deposition by reduction-adsorption and surface complexation of gold onto the growth surface of arsenlan pyrite. 相似文献
15.
The sedimentary humic acid or its acid-hydrolysate, consisting of various amino acids, was found effective in dissolving unusually large quantities of metals (up to 682 mg/g of organic matter) from their insoluble salts. The presence of humic acid in the reaction media which had favorable conditions for the precipitation of metals as carbonates, hydroxides or sulfides, prevented the formation of insoluble metal salts. Infrared analysis suggests that the metals added to various anionic systems and humic acid do not react with the anion. The most likely mechanism of reaction appears to be a complex formation between metals and organic matter which keeps the metal in solution.The enhanced solubility and consequent decrease in precipitation of metals under the influence of humic compounds, as evidenced in these studies should play a leading role in the accumulation of metals in sedimentary deposits. 相似文献
16.
Characteristics and distributions of humic acid (HA) and soil organic matter (SOM) in a yellow soil profile and a limestone soil profile of the southwest China Karst area were systematically investigated to reveal their evolutions in different soils of the study area. The results showed that characteristics and distribution of SOM along the two soil profiles were notably different. Total organic carbon (TOC) contents of soil samples decreased just slightly along the limestone soil profile but sharply along the yellow soil profile. TOCs of the limestone soils were significantly higher than those of the corresponding yellow soils, and C/N ratios of SOMs showed a similar variation trend to that of TOCs, indicating that SOM can be better conserved in the limestone soil than in the yellow soil. The soil humic acids were exhaustively extracted and further fractionated according to their apparent molecular weights using ultrafiltration techniques to explore underlying conservation mechanisms. The result showed that C/N ratios of HAs from different limestone soil layers were relatively stable and that large molecular HA fractions predominated the bulk HA of the top soil, indicating that HA in the limestone profile was protected while bio and chemical degradations were retarded. Combined with organic elements contents and mineral contents of two soils, we concluded that high calcium contents in limestone soils may play a key role in SOM conservation by forming complexation compounds with HAs or/and enclosing SOMs with hypergene CaCO3 precipitation. 相似文献
17.
M. Narayanasamy D. Dhanasekaran G. Vinothini N. Thajuddin 《International Journal of Environmental Science and Technology》2018,15(1):119-132
Printed circuit boards contain precious metals. They are produced in large volumes, rendering them an important component of the electronic waste. In view of the heterogeneity of the metals present, reprocessing of electronic waste is a heinous task. The present study focused on leaching of valuable metals from electronic waste printed circuit boards using Aspergillus niger DDNS1. The adaptation phases began at 0.1, 0.5 and 1.0% of fine powder of printed circuit boards with 10% inoculum and were optimized with three effective factors, viz. initial pH, particle size and pulp density, to achieve the maximum simultaneous recovery of the valuable metals. The interactions of these metals were also deciphered using scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, Fourier transform infrared spectrum and atomic absorption spectroscopy. The results indicated that extraction of the precious metals was accomplished mainly through the unique organic acids originating from A. niger DDNS1. The initial pH played an important role in the extraction of the precious metals and the metals precipitate formation. The leaching rate of the metals was generally higher at low powder dosage of printed circuit boards. The toxicity of the printed circuit boards had little effect on two-step bioleaching at the pulp density of 0.1% compared to one-step bioleaching. The two-step bioleaching process was followed under organic acid-forming conditions for the maximum mobilization of metals. Thus, the precious metals from printed circuit boards could be mobilized through fungal bioleaching which promises an important industrial application in recycling of electronic wastes. 相似文献
18.
Manzur Ahmed Herbert Volk Simon C. George Mohinudeen Faiz Linda Stalker 《Organic Geochemistry》2009,40(7):810-831
Organic geochemical and petrological assessment of coals/coaly shales and fine grained sediments, coupled with organic geochemical analyses of oil samples, all from Permo–Triassic sections of the Southern Sydney Basin (Australia), have enabled identification of the source for the widely distributed oil shows and oil seeps in this region. The Permian coals have higher hydrogen indices, higher liptinite contents, and much higher total organic matter extract yields than the fine grained sediments. A variety of source specific parameters obtained from n-alkanes, regular isoprenoids, terpanes, steranes and diasteranes indicate that the oil shows and seeps were generated and expelled predominantly from higher plant derived organic matter deposited in oxic environments. The source and maturity related biomarkers and aromatic hydrocarbon distributions of the oils are similar to those of the coals. The oil-coal relationship also is demonstrated by similarities in the carbon isotopic composition of the total oils, coal extracts, and their individual n-alkanes. Extracts from the Permo–Triassic fine grained sediments, on the other hand, have organic geochemical signatures indicative of mixed terrestrial and prokaryotic organic matter deposited in suboxic environments, which are significantly different from both the oils and coal extracts. The molecular signatures indicating the presence of prokaryotic organic matter in some of the coal extracts and oils may be due to thin sections of possibly calcareous lithologies interbedded within the coal measures. The genetic relationship between the oils and coals provides new evidence for the generation and expulsion of oils from the Permian coals and raises the possibility for commercial oil accumulations in the Permian and Early Triassic sandstones, potentially in the deeper offshore part of the Sydney Basin. 相似文献
19.
A new method is proposed to characterize the complexation properties of colloids and metal–colloid interactions in natural waters. Based on the association of ultrafiltration with isotopic tracing, this method could quantify the pool of elements in an exchangeable position and also address the kinetic aspects of these exchanges. Basically, it consists of the comparison of isotopic compositions between the bulk sample and a succession of filtrates through time. Exchanges between colloidal humic acids (HA) and metals were first characterized, before applying such manipulations on natural waters. A few elements, representative of a wide range of complexation properties, were chosen: Cu, Zn, Cd, Pb, Sr, Nd, Ni, Th and U. In the case of humic acids, very small (less than 10% of isotopes), but significant isotopic shifts were observed compared to the isotopic equilibrium. It means that more than 90% of the isotopes were exchanged just after addition of isotopic tracers. Experiments on natural organic-rich waters (Mengong and Nyong streams) indicate isotopic composition variations close to those of humic acids. On the contrary, ultrafiltration performed on the total Sanaga River water (including suspended matter “SM”) shows an important isotopic shift between the filtered and unfiltered solutions. It means that in the case of the Sanaga River, a significant part of the chemical elements did not exchange. 相似文献
20.
Three Australian brown coals have been separated into humin and humic acid fractions and studied by high resolution solid state 13C NMR spectroscopy and Fourier transform IR spectroscopy. The aromatic rings of the humic acids are highly substituted showing that extensive cross linking must have occurred during formation from wood lignin and tannin. However, the humins contain more aliphatic carbon and hydrogen than the corresponding humic acids. This shows that little cross linking has occurred with other components of the brown coal such as resins, waxes cutin and algal detritus, and cross linking has not rendered the aromatics alkali insoluble. The kinetics of extraction are complex and not simple first order. This is reflected in the chemical composition of the humic acid which is extraction temperature dependent. We also observed that there is a conversion of aromatic carbon to aliphatic carbon and gas during extraction, probably by alkaline oxidation, resulting in ring opening. A range of suitable model compounds have been studied to confirm this finding. Such a mechanism may account for the modification of lignin in oxidising environments such as those occurring in the initial stages of coalification (lignite or brown coal formation) and in soils. 相似文献