scholarly journals Geochemical Study of Weathered Coal, a Co-Substrate for Bioremediation of South African Coal Discard Dumps

Minerals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 772 ◽  
Author(s):  
Yvonne van Breugel ◽  
Ashton Keith Cowan ◽  
Harilaos Tsikos

Coal mining creates large volumes of waste in the form of discard coal that is stockpiled. In South Africa, rehabilitation of coal discard dumps remains a challenge due to reliance on topsoil for establishment of vegetation. Exploitation of fungal bio liquefaction/degradation of coal resulted in the emergence of Fungcoal as a bioprocess for the rehabilitation of coal discard dumps and opencast spoils. In this process, a suite of fungi is used to bio liquefy/degrade recalcitrant waste coal to form a soil-like material which promotes reinvigoration of the microbial component, grass growth, and re-vegetation. Here, the role of outcrop weathered coal as a mineral/carbon source to ensure biologically induced humic acid-like substance enrichment of discard and spoil to increase efficacy of fungi-plant mutualism and stimulate revegetation without the need for topsoil was investigated. Mineralogical, elemental, and pyrolysis gas chromatography-mass spectroscopic analyses show that outcrop weathered coal has decreased volatile material and increased humics, ash, and mineral bound water in comparison to bituminous coal. These changes occur coincidently with decreased C, N, and H contents, and a substantial increase in O concentration. No apparent stoichiometric relationship between sulphur and iron oxide content of weathered coal could be discerned suggesting little residual pyrite in this material and a dominance of oxy-hydroxides of Fe. Organic analysis showed weathered coal to be enriched in C-16 and C-18 fatty acids and the presence of the indicator, 17α(H),21β(H)-homohopane but not the β,β-stereoisomer, was interpreted to indicate that bacteria may only have been active prior to transformation of hard coal into weathered coal.

2020 ◽  
Vol 7 (2) ◽  
pp. 405-416
Author(s):  
Jacob Taiwo Olawale ◽  
Oghenekume Gerald Edeki ◽  
Ashton Keith Cowan

Author(s):  
Christian Storm ◽  
Helmut Rüdiger ◽  
Hartmut Spliethoff ◽  
Klaus R. G. Hein

Biomass and sewage sludge are attracting increasing interest in power plant technology as a source of carbon dioxide-neutral fuels. A new way to reduce the consumption of fossil fuels could be the co-combustion or co-gasification of coal and biomass or coal and sewage sludge. In both cases, pyrolysis is the first step in the technical process. In order to obtain detailed information about the pyrolysis of coal/biomass and coal/sewage sludge mixtures as well as unblended fuels, the ‘Institut für Verfahrenstechnik und Dampfkesselwesen (IVD)’ at the University of Stuttgart has carried out investigations using an electrically heated entrained flow reactor. One application of substitution of fossil fuels could be the utilization of pyrolysis gas or gas generated in a gasification process as a reburn fuel in conventional boilers fired with fossil fuels. Investigation showed that generated gas from coal, biomass and sewage sludge pyrolysis and gasification have high NOx reduction efficiencies compared to methane or low calorific gases using it as a reburn fuel in coal fired boilers. In order to take advantage of this pretreatment process the release of organic as well as of mineral compounds during the pyrolysis or gasification has to be investigated. For coal pyrolysis and gasification the reactions are known since there was a lot of research all over the world. Biomass or sewage sludge have other structures compared to fossil fuels and contain alkali, chlorine and other problematic compounds, like heavy metals. The release of those elements and of the organic matter has to be investigated to characterize the gas and the residual char. The optimum process parameters regarding the composition of the generated gas and the residual char have to be found out. The IVD has studied the co-pyrolysis of biomass and sewage sludge together with a high volatile hard coal. The main parameters to be investigated were the temperature of the pyrolysis reactor (400°C–1200°C) and the coal/biomass and coal/sewage sludge blends. Besides co-pyrolysis experiments test runs with unmixed main fuels were carried out with the hard coal, straw as biomass, and a sewage sludge. It was expected that the high reactivity of biomass and sewage sludge would have an effect on the product composition during co-pyrolysis. The test runs provided information about fuel conversion efficiency, pyrolysis gas and tar yield, and composition of pyrolysis gas and tar. Besides gas and tar analysis investigations regarding the path of trace elements, like heavy metals, alkali, chlorine and nitrogen components, during the pyrolysis process varying different parameters have been carried out. The fuel nitrogen distribution between pyrolysis gas, tar and char has been analyzed as well as the ash composition and thus the release of mineral components during pyrolysis. Increasing reaction temperatures result in a higher devolatilization for all fuels. Biomass shows a devolatilization of up to 80% at high temperatures. Hard coal shows a weight toss of approx. 50% at same temperatures. Sewage sludge devolatilizes also up to 50%, which is nearly a total release of organic matter, because of the high ash content of about 50% in sewage sludge. Gaseous hydrocarbons have a production maximum at about 800°C reaction temperature for all feedstocks. Carbon monoxide and hydrogen are increasingly formed at high pyrolysis temperatures due to gasification reactions. Mineral elements are released during straw pyrolysis, but within the hot gas filtration unit further recombination reactions and condensation of elements on panicles take place. There is no release of mineral elements during sewage sludge pyrolysis and only a slight release of heavy metals at high pyrolysis temperatures. The effect of co-pyrolysis depends on the feedstocks used in association with the panicle size. The co-pyrolysis test runs showed that a synergetic effect exists when using sewage sludge and hard coal. There is a higher char production related to the unmixed fuels; gas and tar formation are lowered. Co-pyrolysis test runs with biomass and coal did not show this effect on the pyrolysis products. Reasons for this behaviour could be a difference in particle size and material structure which influences the devolatilization velocity of the fuels used or the relatively short residence time in the entrained flow reactor. It seems possible that coal pyrolysis is influenced by the reaction atmosphere, generated in co-pyrolysis. In the co-pyrolysis of coal and sewage sludge, the sludge degases much faster than coal because of the structure of sewage sludge and its small panicle. The coal pyrolysis taking place afterwards in the reaction tube occurs in a different atmosphere, compared to the mono-pyrolysis experiments. The devolatilization of coal in the co-pyrolysis experiments together with straw was not disturbed by the gaseous products of straw pyrolysis, because the large straw particles showed a delayed degasing compared to the coal particles.


Author(s):  
Nyamsuren B ◽  
Barsbold Kh ◽  
Buyan-Ulzii B ◽  
Baasanjargal T ◽  
Enkhsaruul B

Bench-scale methanation experiments were performed using the mixture gases evolved in pyrolysis of Tavantolgoi weathered coal and of Baganuur thermal coal. The methanation reactor was composed of the parts of feed gas desulfurization, fixed bed main reactor, condenser and dryer of product gases. The preliminary desulfurized feed gas passed through the fixed bed methanation reactor with the three layers of Ni/Al2O3 catalyst mixed with different amounts of quartz in order to avoid from overheating in upper level of the catalyst. Methanation experiments of pyrolysis gases were performed at temperatures of 250°С and 350˚°С, in a pressure of 3 bar with a GHSV of 9000 h-1. In methanation of pyrolysis gas from the Tavantolgoi weathered coal, CH4 content was increased 10 times from 3.20% to 34.4% at 250°С, however CH4 content was increased 3 times from 9.60% to 29.4% during the methanation of Baganuur coal pyrolysis gas at 350°С. Тавантолгойн болон Багануурын нүүрсний пиролизын хийн метанжуулалтын томруулсан туршилт Хураангуй: Энэхүү судалгааны ажлаар Тавантолгойн ордын исэлдсэн давхаргын нүүрс болон Багануурын ордын үндсэн давхаргын нүүрсний пиролизоос үүссэн хийг метанжуулах томруулсан (бэнч) хэмжээний туршилтыг хийж гүйцэтгэв. Метанжуулалтын томруулсан төхөөрөмж нь хүхэргүйжүүлэгч, конденсатор, чийг шингээгч болон хөдөлгөөнгүй үет реактор бүхий урвалын систем байхаар зохион бүтээсэн. Нүүрсний пиролизын хийг кварцтай хольж Ni/Al2O3 катализаторын гурван үеэр нэвтрүүлж, дулаан дамжуулалтын усгүй шийдлийг хэрэглэсэн. Метанжуулалтын томруулсан туршилтыг 250°С болон 350˚°С температуруудад, 3 бар даралтанд, 9000 h-1 түүхий эдийн урсгал хурдтай нөхцөлд хийж гүйцэтгэв. Тавантолгойн ордын исэлдсэн давхаргын нүүрсний пиролизын хийг метанжуулахад бүтээгдэхүүн хий дэх метаны агуулга 3.20%-иас 34.4% хүрч 10 дахин ихсэж, харин Багануурын нүүрсний хийнээс үүссэн метаны агуулга 9.60%-иас 29.4% болж 3 дахин ихэслээ. Хэдийгээр метанжуулах процессын температур харьцангуй нам байсан боловч Тавантолгойн ордын исэлдсэн давхаргын нүүрсний пиролизын хийн метанжуулалтын дүнд үүссэн метан хийн агуулга нь Багануурын ордын үндсэн давхаргын нүүрсний пиролизын хийтэй харьцуулахад 5.01%-иар их байлаа.


2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Yoshimi Kamiya ◽  
Takayuki Honda ◽  
Atsushi Ohbuchi ◽  
Tetsuo Miyakoshi

Organic analysis and inorganic analysis are generally based on different physical principles, and for this reason it is difficult to analyze resins and pigments simultaneously. For these reasons, we have performed Py-GC/MS measurements of red-, yellow-, and green-colored lacquer films applied to lacquerware items to assess the feasibility of simultaneously detecting resin ingredients together with certain pigments. We have also compared our findings to the results of SEM-EDS, X-ray fluorescence spectrometry (XRF), and X-ray diffractometry (XRD) measurements. XRD analysis yielded molecular-level information (information on binding states) regarding mercury (Hg) and iron (Fe); however, the information obtained for arsenic (As) and sulfur (S) was insufficient. In contrast, Py-GC/MS analyses simultaneously yielded molecular-level information on arsenic (As) and sulfur (S) together with detection of the primary ingredients of the lacquer. For this reason, it shows that several pieces of information is provided easily and quickly when the colored lacquer cultural heritage is measured using the Py-GC/MS method.


2019 ◽  
Vol 5 (12) ◽  
pp. 37-46
Author(s):  
K. Chalov ◽  
Yu. Lugovoy ◽  
Yu. Kosivtsov ◽  
E. Sulman

This paper presents a study of the process of thermal degradation of crosslinked polyethylene. The kinetics of polymer decomposition was studied by thermogravimetry. Crosslinked polyethylene showed high heat resistance to temperatures of 400 °C. The temperature range of 430–500 °C was determined for the loss of the bulk of the sample. According to thermogravimetric data, the decomposition process proceeds in a single stage and includes a large number of fracture, cyclization, dehydrogenation, and other reactions. The process of pyrolysis of a crosslinked polymer in a stationary-bed metal reactor was investigated. The influence of the process temperature on the yield of solid, liquid, and gaseous pyrolysis products was investigated. The optimum process temperature was 500 °C. At this temperature, the yield of liquid and gaseous products was 85.0 and 12.5% (mass.), Respectively. Samples of crosslinked polyester decomposed almost completely. The amount of carbon–containing residue was 3.5% by weight of the feedstock. With increasing temperature, the yield of liquid products decreased slightly and the yield of gaseous products increased, but their total yield did not increase. For gaseous products, a qualitative and quantitative composition was determined. The main components of the pyrolysis gas were hydrocarbons C1–C4. The calorific value of pyrolysis gas obtained at a temperature of 500 °C was 17 MJ/m3. Thus, the pyrolysis process can be used to process crosslinked polyethylene wastes to produce liquid hydrocarbons and combustible gases.


2001 ◽  
Vol 6 (1) ◽  
pp. 9-19 ◽  
Author(s):  
A. Buikis ◽  
J. Cepitis ◽  
H. Kalis ◽  
A. Reinfelds ◽  
A. Ancitis ◽  
...  

The mathematical model of wood drying based on detailed transport phenomena considering both heat and moisture transfer have been offered in article. The adjustment of this model to the drying process of papermaking is carried out for the range of moisture content corresponding to the period of drying in which vapour movement and bound water diffusion in the web are possible. By averaging as the desired models are obtained sequence of the initial value problems for systems of two nonlinear first order ordinary differential equations. 


2013 ◽  
Vol 58 (2) ◽  
pp. 449-463 ◽  
Author(s):  
Mieczysław Żyła ◽  
Agnieszka Dudzińska ◽  
Janusz Cygankiewicz

Ethane constitutes an explosive gas. It most often accompanies methane realizing during exploitation and mining works. In this paper the results of ethane sorption have been discussed on three grain classes of six selected hard coal samples collected from active Polish coalmines. On the basis of obtained results, it has been stated that the tested hard coals prove differentiated sorption power with reference to ethane. Te extreme amount of ethane is sorbed by low carbonized hard coal from “Jaworzno” coalmine. This sort of coal shows great porosity, and great content of oxygen and moisture. The least amount of ethane is sorbed by hard coal from “Sośnica” coalmine. This sort of coal possesses relatively a great deal of ash contents. Together with the process of coal disintegration, the amount of sorbed ethane increases for all tested coal samples. Between tested coals there are three medium carbonized samples collected from “Pniówek”, “Chwałowice” “Zofiówka” coalmines which are characterized by small surface values counted according to model BET from nitrogen sorption isotherms determined at the temperature of 77.5 K. The samples of these three coals prove the highest, from between tested coals, increase of ethane sorption occurring together with their disintegration. These samples disintegrated to 0,063-0,075 mm grain class sorb ethane in the amount corresponding with the sorption quantity of low carbonized coal from “Jaworzno” coalmine in 0.5-0.7 mm grain class. It should be marked that the low carbonized samples collected from “Jaworzno” and Wesoła” coalmines possess large specific surface and great porosity and belong to coal group of “loose” spatial structure. Regarding profusion of sorbed ethane on disintegrated medium carbonized samples from “Pniówek”, “Zofiówka”, “Chwałowice” coalmines it can be supposed that in the process of coal disintegration, breaking their “compact’ structure occurs. Loosened structure of medium carbonized coals results in increasing accessibility of ethane particles to sorption centres both electron donors and electron acceptors which are present on hard coal surface. The surface sorption centre increase may result in formation a compact layer of ethane particles on coal surface. In the formed layer, not only the strengths of vertical binding of ethane particles with the coal surface appear but also the impact of horizontal strengths appears which forms a compact layer of sorbed ethane particles. The surface layer of ethane particles may lead to explosion.


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