Mercury oxidation and adsorption characteristics of potassium permanganate modified lignite semi-coke

The adsorption characteristics of virgin and potassium permanganate modified lignite semi-coke （SC） for gaseous Hg were investigated in an attempt to produce more effective and lower price adsorbents for the control of elemental mercury emission. Brunauer-Emmett- Teller （BET） measurements, X-ray powder diffraction （XRD） and X-ray photoelectron spectroscopy （XPS） were used to analyze the surface physical and chemical properties of SC, Mn-SC and Mn-H-SC before and after mercury adsorption. The results indicated that potassium permanganate modification had significant influence on the properties of semi-coke, such as the specific surface area, pore structure and surface chemical functional groups. The mercury adsorption efficiency of modified semi-coke was lower than that of SC at low temperature, but much higher at high temperature. Amorphous Mn7＋, Mn6＋ and Mn4＋ on the surface of Mn-SC and Mn-H-SC were the active sites for oxidation and adsorption of gaseous Hg~, which oxidized the elemental mercury into Hg2＋ and captured it. Thermal treatment reduced the average oxidation degree of Mn2＋ on the surface of Mn-SC from 3.80 to 3.46. However, due to the formation of amorphous MnOx, the surface oxidation active sites for gaseous Hg0 increased, which gave Mn-H-SC higher mercury adsorption efficiency than that of Mn-SC at high temperature.

The Advantages of Methane Production by Combined Fermentation of Lignite and Wheat Straw

Biogasification of coal is important for clean utilization of coal. Experiments on the fermentation of single lignite, single straw and their mixture were performed to explore the variation characteristics of gas production potential, microbial community and methanogenic metabolic pathways of mixture. Research has shown that mixed fermentation of lignite and straw significantly promoted biomethane production. The abundance of hydrolytic acidifying functional bacteria genera (Sphaerochaeta, Lentimicrobium) in mixed fermentation was higher than that in the fermentation of single lignite and single straw. The abundance of some key CAZy metabolic enzyme gene sequences in mixed fermentation group was increased, which was favorable to improve methane production. Aceticlastic methanogenesis was the most critical methanogenic pathway and acetic acid pathway was more competitive in methanogenic mode during peak fermentation. Macrogenomics provided theoretical support for the claim that mixed fermentation of coal and straw promoted biomethane metabolism, which was potentially valuable in expanding methanogenesis from mixed fermentation of lignite with different biomasses.

Change in Grain-Size Composition of Lignite under Cyclic Freezing-Thawing and Wetting-Drying

The paper presents the change in grain-size composition of lignite under cyclic freezing-thawing (FTC) and wetting-drying (WDC). The article shows that in the spring and autumn periods the lignites can be subjected to repeated freezing-thawing and wetting-drying, which determines the possibility of changing their grain-size composition and structure. Experimental studies in laboratory conditions on the influence of cyclic freezing-thawing (FTC) and wetting-drying (WDC) on the quality indicators of lignites have been carried out, their granulometric (fractional) composition has been studied. Freezing-thawing cycle conditions are as follows (FTC): minimum exposure temperature: -20°C;maximum: +5°C;relative humidity: 30%;number of processing cycles: 3. Wetting-drying cycles are as follows (WDC): drying temperatures are +20, +40, +60, +80°C, drying time 90 minutes, the coals are further subjected to rain (soaking) for a period of water saturation to humidity of 30% - 40% and dry again. The number of wetting-drying cycles is 3 times. The tests have revealed the destructive effects of FTC and WDC on the samples of lower metamorphic grade coal, and the cycles of wet-dry lead to the much higher yield of fine sizes (-6+0;-13+0 mm) than the cycles of freeze-thaw. Furthermore, it is found that the increase in the yield of fines depends on the heating temperature: coal disintegration proceeds more intensively at a higher temperature of drying.

Effectiveness of Combined Biochar and Lignite with Poultry Litter on Soil Carbon Sequestration and Soil Health

Healthy soils are important to ensure satisfactory crop growth and yield. Poultry litter (PL), as an organic fertilizer, has proven to supply the soil with essential macro and micronutrients, enhance soil fertility, and improve crop productivity. Integrating this treatment has the potential to improve soil physical and biological properties by increasing soil carbon, C. However, rapid decomposition and mineralization of PL, particularly in the hot and humid southeastern U.S., resulted in losing C and reduced its effect on soil health. Biochar and lignite have been proposed to stabilize and mitigate C loss through application of fresh manure. However, their combined effects with PL on C sequestration and soil health components are limited. A field experiment was conducted on Leeper silty clay loam soil from 2017 to 2020 to evaluate the combined effect on soil properties when applying biochar and lignite with PL to cotton (Gossypium hirsutum L.). The experimental design was a randomized complete block involving nine treatments replicated three times. Treatments included PL and inorganic nitrogen, N, fertilizer with or without biochar and lignite, and an unfertilized control. Application rates were 6.7 Mgkg⋅ha−1 for PL, 6.7 Mgkg⋅ha−1 for biochar and lignite and 134 kg⋅ha−1 for inorganic N fertilizer. Integration of PL and inorganic fertilizer with biochar and lignite, resulted in greater soil infiltration, aggregate stability, plant available water, reduced bulk density and penetration resistance as compared to the sole applications of PL and inorganic fertilizer.

Kinetics of recovering germanium from lignite ash with chlorinating roasting methods

A process of recovering Ge by chlorinating masting was put forward. GeCl4 was separated and recovered from lignite ash because of its low boiling point. Kinetic analysis indicates that the chlorinating roasting process fits with the unreacted-core shrinking model and the reaction rate equation corresponds to 1 - 2a/3 - （1 - a）2/3 = kt. The apparent activation energy Ea is calculated to be 22.36 kJ·mol^-1. The diffusion of product layer serves as the rate-controlling step in this process. When the roasting temperature is 250℃, the roasting time is 60 min, the con- centration of hydrochloric acid is 10 mol/L, and the ratio of liquid to solid is 10 （mHCl/ash = 10）, and 90% Ge in lignite ash can be recovered.

Effect of impregnation methods on sorbents made from lignite for desulfurization at middle temperature

With lignite after vacuum drying as the raw material,a series of Zn-based sorbents were prepared by static impregnation,ultrasonic-assisted impregnation,bubbling-assisted impregnation and high-pressure impregnation.The physical properties and the desulfurization performances of Zn-based sorbents were studied systematically by XRD,BET,AAS characterization techniques and the fixed-bed desulfurization evaluation apparatus.The sorbents obtained by high-pressure impregnation method have a larger specific surface area,pore volume and pore diameter comparing with other methods,which is conducive to the sulfidation reaction of hydrogen sulfide gas in the sorbent.The effects of pressure during the high-pressure impregnation and concentration of Zn(NO3)2 precursor solution on the sorbents properties and desulfurization behavior were investigated.The higher the impregnation pressure and the concentration of impregnation solution are,the greater the amount of the active components are uploaded.However,overhigh impregnation pressure can cause collapse and blocking of the carrier pore.The optimal operating condition of high-pressure impregnation method for preparing the sorbents was the impregnation pressure of 20 atm and the solution concentration of 41%.Under that condition,the sorbent had the best desulfurization ability with a sulfur capacity of 13.94 gS/100 gsorbent and a breakthrough time of 54 h.Its desulfurization precision and efficiency of removing H2S before sorbent breakthrough from the middle temperature gases of 400℃ can reach【5 ppm and】99%,respectively.Sorbents could be regenerated under the condition of 1 vol%O2,20 vol% H2O,0.5 vol% NH3,and N2balance gas.The regenerated sorbent could be used for repeated absorption of H2S with a slight decrease in desulfurization effect.

Bio-solubilization of Chinese lignite II:protein adsorption onto the lignite surface

Lignite bio-solubilization is a promising technology for converting solid lignite into oil.This study concerns the adsorption of lignite-solubilizing enzymes onto the lignite surface.Adsorption capacity, infrared spectral analysis and driving forces analysis are studied as a way to help understand the bio-solubilization mechanism.The results show that the amount of lignite bio-solubilization is proportional to the amount of adsorbed lignite-solubilizing enzymes.An increase in lignite-solubilizing enzyme adsorption of 10% leads to a 7% increase in lignite bio-solubilization.However, limited amounts of enzymes can be adsorbed by the lignite, thus resulting in low percentages of bio-solubilization.Infrared spectral analysis shows that side chains, such as hy-droxyl and carbonyl, of the lignite structure are the main, and necessary, structures where lignite-solubilizing enzymes attachto the lignite.Furthermore, driving force analysis indicates that the electrostatic force between lignite and enzymes is the main adsorption mechanism.The forces are influenced by solution pH levels, the zeta potential of the lignite and the isoelectric points of the en-zymes.

Improving slurryability, rheology,and stability of slurry fuel from blending petroleum coke with lignite

Petroleum coke and lignite are two important fossil fuels that have not been widely used in China. Petroleum coke-lignite slurry （PCLS）, a mixture of petro- leum coke, lignite, water, and additives, efficiently utilizes the two materials. In this study, we investigate the effects of the proportion （7） of petroleum coke on slurryability, rheo- logical behavior, stability, and increasing temperature characteristics of PCLSs. The results show that the fixed- viscosity solid concentration （COo） increases with increasing 7. The ~Oo of lignite-water slurry （LWS, ~ = 0） is 46.7 %, compared to 71.3 % for the petroleum coke-water slurry （PCWS, c~ --- i00 %）, while that of PCLS is in between the two values. The rheological behavior of PCLS perfectly fits the power-law model. The PCWS acts as a dilatant fluid. As decreases, the slurry behaves first as an approximate Newtonian fluid, and then turns into a pseudo-plastic fluid that exhibits shear-thinning behavior. With increasing ct, the rigid sedimentation and water separation ratio （WSR） increase, indicating a decrease in the stability of PCLS. When α is 60-70 %, the result is a high-quality slurry fuel for industrial applications, which has high slurryability （ω0 = 57-60 %）, good stability （WSR 〈 2 %）, and superior pseudo-plastic behavior （n = 0.9）.

Characterization of nitrogen-containing aromatics in Baiyinhua lignite and its soluble portions from thermal dissolution

Soluble portions(SPs) 1-4(SP1-SP4) were afforded from sequentially dissolution and alkanolyses of Baiyinhua lignite(BL) in cyclohexane,CH3OH,CH3CH2OH,and(CH3)2CHOH at 300℃.They were analyzed with a gas chromatograph/mass spectrometer and quadrupole exactive orbitrap mass spectrometer(QEOTMS) with an atmosphere pressure chemical ionization source in positive-ion mode,while BL was characterized with an X-ray photoelectron spectrometer(XRPES).The results show that the yields of SP2 and SP3 are much higher than those of SP1 and SP4,and the total SP yield is ca.39.0%.According to the analysis with XRPES,pyrrolic nitrogen atoms are the most abundant nitrogen existing forms in BL.Thousands of nitrogen-containing aromatics(NCAs) were resolved with QEOTMS and their molecular masses are mainly in the range of 200-450 u.The main NCAs are N1O1 and N1O2 class species with double bond equivalent values of 4-18 and carbon numbers of 7-30.The nitrogen atoms appear in pyridine s,quinolines,benzoquinolines or acridine,and dibenzoquinolines or naphthoquinolines,while the oxygen atoms exist in methoxy and furan rings.

Eocene lignites from Cambay basin, Western India： An excellent source of hydrocarbon

In the present paper lignites from the Cambay basin have been studied for their hydrocarbon potential.The samples were collected from three lignite fieldse Vastan, Rajpardi and Tadkeshwar, and were investigated by petrography, chemical analyses and Rock-Eval pyrolysis. The results are well comparable with the empirically derived values. The study reveals that these ‘low rank C＇ lignites are exceedingly rich in reactive macerals（huminite t liptinite） while inertinite occurs in low concentration. These high volatile lignites generally have low ash yield except in few sections. The Rock-Eval data indicates the dominance of kerogen type-III with a little bit of type-II. The study reveals that the lignites of Vastan（lower and upper seams） and Tadkeshwar upper seam are more gas-prone while Rajpardi and Tadkeshwar lower seams are oil-prone. Further, the fixed hydrocarbons are several times higher than the free hydrocarbons. The relation between TOC and fixed hydrocarbon indicates that these lignites are excellent source rock for hydrocarbon which could be obtained mainly through thermal cracking. The empirically derived values reveal a high conversion（94e96%） and high oil yield（64e66%） for these lignites.

Lignite oxidative desulphurization Notice 1.Process condition selection

The process of lignite desulphurization via its treatment by an oxidant(air or air–steam mixture)has been studied.The research objective was useful determination of steam application in oxidative lignite desulphurization.It has been proved that the water steam should be included in the oxidant composition to increase the hydrogen sulphide and combustible constituent content in the gases obtained during the processes under research.The impact of factors which affect the reactions between solid(in our case–lignite)and gaseous reagent(oxidant,i.e.air and or air–steam mixture)upon the research process has been investigated,if these reactions occur in the kinetic area.Such factors are linear rate of oxidant movement and coal grain size.The values of oxidant movement linear rate and coal grain size,which the reaction transfer from pyrite sulphur and organic content of lignite from diffusion into kinetic area occurs by,have been determined.Under these‘‘transfer’’conditions,the values of coefficients of oxidant mass transfer(β,m/s)as well as Sherwood criteria and boiling layer differences have been calculated.

Impact of impregnation pressure on desulfurization performance of Zn-based sorbents supported on semi-coke

High-pressure impregnation, a new preparation method for sorbents to remove H2S from hot coal gas, is introduced in this paper. Semi-coke （SC） and ZnO is selected as the support and active component of sorbent, respectively. The sorbent preparation process includes high-pressure impregnation, filtration, ovendry and calcination. The aim of this research is to primarily study the effects of the impregnation pressure on physical properties and desulfurization ability of the sorbent. The desulfurization experiment was carried out in a fixed-bed reactor at 500 ~C and a simulated coal gas used in this work was composed of CO （33 vol%）, H2 （39 vol%）, H2S （300 ppm in volume）, and N2 （balance）. Experimental results show that the pore structure of the SC support can be improved effectively and ZnO active component can be uniformly dispersed on the support, with the small particle size of 10-500 nm. Sorbents prepared using high-pressure impregnation have better desulfurization capacity and their active components have higher utilization rate. P20-ZnSC sorbent, obtained by high-pressure impregnation at 20 atm, has the best desulfurization ability with a sulfur capacity of 7.54 g S/100g sorbent and a breakthrough time of 44 h. Its desulfurization precision and efficiency of removing H2S from the middle temperature gases can reach 〈 1 ppm and 〉99.7%, respectively, before sorbent breakthrough.

Investigation on activated semi-coke desulfurization

An activated semi coke with industrial scale size was prepared by high pressure hydrothermal chemistry activation, HNO 3 oxidation and calcination activation in proper order from Inner Mongolia Zhalainuoer semi coke, which is rich in resource and cheap in sale. SO 2 adsorption capacity on this activated semi coke was assessed in the fixed bed in the temperature range of 60—170℃, space velocity range of 500—1300 h -1 , SO 2 concentration of 1000—3000 ppmv, and N 2 as balance. The surface area, elemental and proximate analysis for both raw semi coke and activated semi cokes were measured. The experimental results showed that the activated semi coke has a high adsorption capacity for sulfur dioxide than the untreated semi coke. This may be the result of increase of surface area on activated semi coke and surface oxygen functional groups with basicity characteristics. Comparison to result of FTIR, it is known that group of —C—O—C? ?may be active center of SO 2 catalytic adsorption on activated semi coke.

The Adsorption of Phenol by Lignite Activated Carbon

The feasibility and adsorption effect of lignite activated carbon for phenol removal from aqueous solutions were evaluated and investigated. A series of tests were performed to look into the influence of various experimental parameters such as contact time, initial phenol concentration, temperature, and pH value on the adsorption of phenol by lignite activated carbon. The experimental data were fitted well with the pseudo-second-order kinetic model. The adsorption is an endothermic process and conforms to Freundlich thermodynamic model. The results indicate that the lignite activated carbon is suitable to be used as an adsorbent material for adsorption of phenol from aqueous solutions.

Combustion characteristics of Daqing oil shale and oil shale semi-cokes

Thermo-gravimetric-analysis(TGA) was used to analyze the combustion characteristics of an oil shale and semi-cokes prepared from it.The effect of prior pyrolysis and TGA heating rate on the combustion process was studied.Prior pyrolysis affects the initial temperature of mass loss and the ignition temperature.The ignition temperature increases as the volatile content of the sample decreases.TG/DTG curves obtained at different heating rates show that heating rate has little effect on ignition temperature.But the peak of combustion shifts to higher temperatures as the heating rate is increased.The Coats-Redfern integration method was employed to find the combustion-reaction kinetic parameters for the burning of oil shale and oil shale semi-coke.

Evaluating performance of lignite pillars with 2D approximation techniques and 3D numerical analyses

This paper attempts to investigate the use of approximate 2D numerical simulation techniques for the evaluation of lignite pillar geomechanical response, formed via the room and pillar mining method.Performance and applicability of the developing methodology are assessed through benchmarking with a more direct and accurate 3D numerical model. This analysis utilizes an underground lignite mine which is being developed in soft rock environment. Through the decisions made for the optimum room and pillar layout, the design process highlights the strong points and the weaknesses of 2D finite element analysis, and provides useful recommendations for future reference. The interpretations of results demonstrate that 2D approximation techniques come near quite well to the actual 3D problem.However, external load approximation technique seems to fit even better with the respective outcomes from the 3D analyses.

Geochemistry of Kasnau-Matasukh lignites, Nagaur Basin, Rajasthan （India）

The distribution and verticals variation of geochemical components in the Kasnau-Matasukh lignites of Nagaur Basin, Rajasthan, were investigated using microscopy, proximate and ultimate analyses, Rock-Eval Pyrolysis, X-ray diffraction and Fourier Transform Infrared analyses, and major/minor/trace element determination. The relationship of elements with ash content and with macerals have also been discussed. These lignites are stratified, black, dominantly composed of huminite group macerals with subordinated amounts of liptinite and inertinite groups. They are classified as type-III kerogen and are mainly gas prone in nature. The concentration （in vol%） of mineral matter is seen to increase towards upper part of seam and so is the concentration （in wt%） of the volatile matter, elemental carbon and sulphur. The common minerals present in these lignitesare mixed clay layer, chlorite, and quartz as identified by X-ray diffraction study. Compared with world average in brown coal, the bulk concentration of Cu is anomalously high in most of the samples while Cd is 2-3 times high and Zn is high in one band. Based on interrelationship, different pyrite forms are noticed to have different preferential enrichment of various elements. The concentration of disseminated pyrite is more than the other pyrite forms and is followed by discrete pyrite grains and massive pyrite.

Enhanced-hydrogen gas production through underground gasification of lignite

Underground coal gasification is one of the clean technologies of in-situ coal utilization.Hydrogen production from underground gasification of lignite was investigated in this study based on simulation experiments.Pyrolysis of lignite, gasification activity, oxygen-steam gasification and the effect of groundwater influx were studied.As well, the advantages of lignite for stable underground gasification were analyzed.The results indicate that lignite has a high activity for gasification.Coal pyrolysis is an important source of hydrogen emission.Under special heating conditions, hydrogen is released from coal seams at temperatures above 350 °C and reaches its maximum value between 725 and 825 °C.Gas with a hydrogen concentration of 40% to 50% can be continuously obtained by oxygen-steam injection at an optimum ratio of steam to oxygen, while lignite properties will ensure stable gasification.Groundwater influx can be utilized for hydrogen preparation under certain geological conditions through pressure control.Therefore, enhanced-hydrogen gas production through underground gasification of lignite has experimentally been proved.

Bio-solubilization of Chinese lignite I:extra-cellular protein analysis

A white rot fungus strain, Trichoderma sp.AH, was isolated from rotten wood in Fushun and used to study the mechanism of lignite bio-solubilization.The results showed that nitric acid pretreated Fushun lignite was solubilized by T.sp.AH and that extracellular proteins from T.sp.AH were correlated with the lignite bio-solubilization results.In the presence of Fushun lignite the extracellular protein concentration from T.sp.AH was 4.5 g/L while the concentration was 3 g/L in the absence of Fushun lignite.Sodium dodecyl sulfate polyacrylamide gel electrophoresis(SDS-PAGE) of the extracellular proteins detected at least four new protein bands after the T.sp.AH had solubilized the lignite.Enzyme color reactions showed that extracellular proteins from T.sp.AH mainly consisted of phenol-oxidases, but that lignin decomposition enzymes such as laccase, peroxidase and manganese peroxidases were not present.

Effects of ultrasound on the desulfurization performance of hot coal gas over Zn-Mn-Cu supported on semi-coke sorbent prepared by high-pressure impregnation method

Zn-Mn-Cu/SC（U） sorbent was hydrothermally synthesized by ultrasound-assisted high-pressure impregnation method with semi-coke（SC）as support and the mixed solution of zinc nitrate,manganese nitrate and copper nitrate as active component precursors.The desulfurization performances of hot coal gas on the prepared sorbent at a mid-temperature of 500°C were tested in fixed-bed reactor.Morphology and pore structure of the prepared sorbent were also characterized by TEM,N2adsorption/desorption isotherms and XRD.For comparison,the sorbent of Zn-Mn-Cu/SC prepared by conventional high-pressure impregnation was also evaluated and characterized in order to study the effects of ultrasound treatment.Zn-Mn-Cu/SC（U） sorbent prepared by high-pressure impregnation under ultrasound-assisted condition showed a better desulfurization performance than Zn-Mn-Cu/SC.It could remove H2 S from 1000×10-6m3/m3 to 0.1×10-6m3/m3 at 500°C and maintained for 12.5 h with the sulfur capacity of 7.74%,in which both the breakthrough time and sulfur capacity were about 32% and 51% higher than those of Zn-Mn-Cu/SC sorbent.The introduction of ultrasound during high-pressure impregnation process greatly improved the morphology and pore structure of the sorbent.The ultrasonic treatment made particle size of active components smaller and made them more evenly disperse on semi-coke support,which provided more opportunities to contact with H2S in coal-based gases.However,there were no any difference in compositions and existing forms of active components on the Zn-Mn-Cu/SC and Zn-Mn-Cu/SC（U） sorbents.