Indirect mineral carbonation of blast furnace slag with(NH4)2SO4 as a recyclable extractant

Large quantities of COand blast furnace slag are discharged in the iron and steel industry. Mineral carbonation of blast furnace slag can offer substantial COemission reduction and comprehensive utilisation of the solid waste. In this study, a recyclable extractant,（NH）SO, was used to extract calcium and magnesium from blast furnace slag（main phases of gehlenite and akermanite） by using low-temperature roasting to fix COthrough aqueous carbonation. The process parameters and efficiency of the roasting extraction, mineralisation, and Al recovery were investigated in detail. The results showed that the extractions of Ca, Mg, and Al can reach almost 100% at an（NH4）SO-to-slag mass ratio of 3:1 and at 370°C in 1 h. Adjusting the p H value of the leaching solution of the roasted slag to 5.5 with the NHreleased during the roasting resulted in 99% Al precipitation, while co-precipitation of Mg was lower than 2%. The Mg-rich leachate after the depletion of Al and the leaching residue（main phases of CaSOand SiO） were carbonated using（NH）COand NHHCOsolutions, respectively, under mild conditions. Approximately 99% of Ca and 89% of Mg in the blast furnace slag were converted into CaCOand（NH）Mg（CO）·4 HO,respectively. The latter can be selectively decomposed to magnesium carbonate at 100-200 °C to recover the NHfor reuse. In the present route, the total COsequestration capacity per tonne of blast furnace slag reached up to 316 kg, and 313 kg of Al-rich precipitate, 1000 kg of carbonated product containing CaCOand SiO, and 304 kg of carbonated product containing calcium carbonate and magnesium carbonate were recovered simultaneously. These products can be used, respectively, as raw materials for the production of electrolytic aluminium, cement, and light magnesium carbonate to replace natural resources.

Indirect mineral carbonation of titanium-bearing blast furnace slag coupled with recovery of TiO_2 and Al_2O_3

Large quantities of CO2 and blast furnace slag are discharged in the iron and steel industry. Mineral carbonation of blast furnace slag can offer substantial CO2 emission reduction and comprehensive utilization of the solid waste. This paper describes a novel route for indirect mineral carbonation of titanium-bearing blast furnace （TBBF） slag, in which the TBBF slag is roasted with recyclable （NH4）2SO4 （AS） at low temperatures and converted into the sulphates of various valuable metals, including calcium, magnesium, aluminium and titanium. High value added Ti-and Al-rich products can be obtained through stepwise precipitation of the leaching solution from the roasted slag. The NH3 produced during the roasting is used to capture CO2 from flue gases. The NH4HCO3 and （NH4）2CO3 thus obtained are used to carbonate the CaSO4-containing leaching residue and MgSO4-rich leaching solution, respectively. In this study, the process parameters and efficiency for the roasting, carbonation and Ti and Al recovery were investigated in detail. The results showed that the sulfation ratios of calcium, magnesium, titanium and aluminium reached 92.6%, 87% and 84.4%, respectively, after roasting at an AS-to-TBBF slag mass ratio of 2：1 and 350℃ for 2 h. The leaching solution was subjected to hydrolysis at 102℃ for 4 h with a Ti hydrolysis ratio of 95.7%and the purity of TiO2 in the calcined hydrolysate reached 98 wt%. 99.7% of aluminium in the Ti-depleted leaching solution was precipitated by using NH3. The carbonation products of Ca and Mg were CaCO3 and （NH4）2Mg（CO3）2·4H2O, respectively. The latter can be decomposed into MgCO3 at 100-200℃ with simultaneous recovery of the NH3 for reuse. In this process, approximately 82.1% of Ca and 84.2% of Mg in the TBBF slag were transformed into stable carbonates and the total CO2 sequestration capacity per ton of TBBF slag reached up to 239.7 kg. The TiO2 obtained can be used directly as an end product, while the Al-rich precipitate and the two carbonation products can act, respectively, as raw materials for electrolytic aluminium, cement and light magnesium carbonate production for the replacement of natural resources.

Ultra-fine grinding and mechanical activation of mine waste rock using a high-speed stirred mill for mineral carbonation

CO2sequestration by mineral carbonation can permanently store CO2and mitigate climate change. However, the cost and reaction rate of mineral carbonation must be balanced to be viable for industrial applications. In this study, it was attempted to reduce the carbonation costs by using mine waste rock as a feed stock and to enhance the reaction rate using wet mechanical activation as a pre-treatment method. Slurry rheological properties, particle size distribution, specific surface area, crystallinity, and CO2 sequestration reaction efficiency of the initial and mechanically activated mine waste rock and olivine were characterized. The results show that serpentine acts as a catalyst, increasing the slurry yield stress, assisting new surface formation, and hindering the size reduction and structure amorphization. Mechanically activated mine waste rock exhibits a higher carbonation conversion than olivine with equal specific milling energy input. The use of a high-speed stirred mill may render the mineral carbonation suitable for mining industrial practice.

CO_(2) mineralization by typical industrial solid wastes for preparing ultrafine CaCO_(3): A review

Mineral carbonation is a promising CO_(2) sequestration strategy that can utilize industrial wastes to convert CO_(2) into high-value CaCO_(3).This review summarizes the advancements in CO_(2) mineralization using typical industrial wastes to prepare ultrafine CaCO_(3).This work surveys the mechanisms of CO_(2) mineralization using these wastes and its capacities to synthesize CaCO_(3),evaluates the effects of carbonation pathways and operating parameters on the preparation of CaCO_(3),analyzes the current industrial application status and economics of this technology.Due to the large amount of impurities in solid wastes,the purity of CaCO_(3) prepared by indirect methods is greater than that prepared by direct methods.Crystalline CaCO_(3) includes three polymorphs.The polymorph of CaCO_(3) synthesized by carbonation process is determined the combined effects of various factors.These parameters essentially impact the nucleation and growth of CaCO_(3) by altering the CO_(2) supersaturation in the reaction system and the surface energy of CaCO_(3) grains.Increasing the initial pH of the solution and the CO_(2)flow rate favors the formation of vaterite,but calcite is formed under excessively high pH.Vaterite formation is favored at lower temperatures and residence time.With increased temperature and prolonged residence time,it passes through aragonite metastable phase and eventually transforms into calcite.Moreover,polymorph modifiers can decrease the surface energy of CaCO_(3) grains,facilitating the synthesis of vaterite.However,the large-scale application of this technology still faces many problems,including high costs,high energy consumption,low calcium leaching rate,low carbonation efficiency,and low product yield.Therefore,it is necessary to investigate ways to accelerate carbonation,optimize operating parameters,develop cost-effective agents,and understand the kinetics of CaCO_(3) nucleation and crystallization to obtain products with specific crystal forms.Furthermore,more studies on life cycle assessment(LCA)should be conducted to fully confirm the feasibility of the developed technologies.

Basalt Petrology, Water Chemistry, and Their Impact on the CO_(2) Mineralization Simulation at Leizhou Peninsula Sites, Southern China

Mineral carbonation, which precipitates dissolved carbon dioxide(CO_(2)) as carbonate minerals in basaltic groundwater environments, is a potential technique for negative emissions. The Leizhou Peninsula in southwest Guangdong province has extensive basalt, indicating a promising potential for CO_(2) storage through rapid mineralization. However, understanding of the basic geological setting, potential, and mechanisms of CO_(2) mineralization in the basalts of the Leizhou Peninsula is still limited. The mineralization processes associated with CO_(2)storage at two candidate sites in the area are investigated in this paper: Yongshi Farm and Tianyang Basin(of the dried maar lake). Petrography,rock geochemistry, basalt petrophysical properties, and groundwater hydrochemistry analyses are included in the study. Numerical simulation is used to examine the reaction process and its effects. The results show that basalts in the study areas mainly comprise plagioclase, pyroxene, and Fe–Ti oxides, revealing a total volume fraction exceeding 85%. Additionally, small amounts of quartz and fayalite are available, with volume fractions of 5.1% and 1.0%, respectively. The basalts are rich in divalent metal cations, which can form carbonate minerals, with an average of approximately 6.2 moles of metal cations per 1 kg of rock. The groundwater samples have a pH of 7.5–8.2 and are dominated by the Mg–Ca–HCO3 type. The basalts demonstrate a porosity range of 10.9% to 28.8%, with over 70% of interconnected pores. A 20-year geochemical simulation revealed that CO_(2) injection dissolves primary minerals, including anorthite, albite, and diopside, while CO_(2)mineralization dissolves precipitation secondary minerals, such as calcite, siderite, and dolomite. Furthermore, a substantial rise in pH from 7.6to 10.6 is observed in the vicinity of the injected well, accompanied by a slight reduction in porosity from 20% to 19.8%. Additionally, 36.8% of the injected CO_(2) underwent complete mineralization within five years, revealing an increasing percentage of 66.1% if the experimental period is extended to 20 years. The presence of abundant divalent metal cations in basalts and water-bearing permeable rocks in the Leizhou Peninsula supports the potential for mineral carbonation in basalts, as indicated by the geochemical simulation results. Additional research is necessary to identify the factors that influence the CO_(2) mineralization, storage, and sensitivity analysis of basalt in the Leizhou Peninsula.

A review of in situ carbon mineralization in basalt

Global warming has greatly threatened the human living environment and carbon capture and storage(CCS)technology is recognized as a promising way to reduce carbon emissions.Mineral storage is considered a reliable option for long-term carbon storage.Basalt rich in alkaline earth elements facilitates rapid and permanent CO_(2) fixation as carbonates.However,the complex CO_(2)-fluid-basalt interaction poses challenges for assessing carbon storage potential.Under different reaction conditions,the carbonation products and carbonation rates vary.Carbon mineralization reactions also induce petrophysical and mechanical responses,which have potential risks for the long-term injectivity and the carbon storage safety in basalt reservoirs.In this paper,recent advances in carbon mineralization storage in basalt based on laboratory research are comprehensively reviewed.The assessment methods for carbon storage potential are introduced and the carbon trapping mechanisms are investigated with the identification of the controlling factors.Changes in pore structure,permeability and mechanical properties in both static reactions and reactive percolation experiments are also discussed.This study could provide insight into challenges as well as perspectives for future research.

Research progress of CO_(2) capture and mineralization based on natural minerals

Natural minerals,such as kaolinite,halloysite,montmorillonite,attapulgite,bentonite,sepiolite,forsterite,and wollastonite,have considerable potential for use in CO_(2) capture and mineralization due to their abundant reserves,low cost,excellent mechanical prop-erties,and chemical stability.Over the past decades,various methods,such as those involving heat,acid,alkali,organic amine,amino sil-ane,and ionic liquid,have been employed to enhance the CO_(2) capture performance of natural minerals to attain high specific surface area,a large number of pore structures,and rich active sites.Future research on CO_(2) capture by natural minerals will focus on the full utiliza-tion of the properties of natural minerals,adoption of suitable modification methods,and preparation of composite materials with high specific surface area and rich active sites.In addition,we provide a summary of the principle and technical route of direct and indirect mineralization of CO_(2) by natural minerals.This process uses minerals with high calcium and magnesium contents,such as forsterite(Mg_(2)SiO_(4)),serpentine[Mg_(3)Si_(2)O(OH)_(4)],and wollastonite(CaSiO_(3)).The research status of indirect mineralization of CO_(2) using hydro-chloric acid,acetic acid,molten salt,and ammonium salt as media is also introduced in detail.The recovery of additives and high-value-added products during the mineralization process to increase economic benefits is another focus of future research on CO_(2) mineralization by natural minerals.

CO_2 Sequestration from flue gas by direct aqueous mineral carbonation of wollastonite

Emission of carbon dioxide is considered to be the main cause of the greenhouse effect. Mineral carbonation, an important part of the CCS technology, is an attractive option for long-term CO2 sequestration. In this study, wollastonite was chosen as the feedstock and the feasibility of direct aqueous mineral carbonation in the simulated flue gas was investigated via a series of experimental studies carried in a stirred reactor. X-ray diffraction （XRD）, X-ray fluorescence spectroscopy （XRF）, ion chro- matography （IC） and thermal decomposition were used to determine the carbonation conversion. The influences of various factors, including reaction temperature, reaction pressure, solution composition, heat-treatment and particle size, were dis- cussed. Concurrently, the effects of SO2 and NO presented in simulated flue gas were also investigated and a possible mecha- nism was used to explain the results. Experimental results show that reaction temperature, reaction pressure and particle size can effectively improve the carbonation reaction. Addition of 0.6 M NaHCO3 was also proved to be beneficial to the reaction and heat-treatment is not needed for wollastonite to get a higher carbonation conversion. Compared with carbonation in puri- fied CO2 gas, CO2 sequestration directly from simulated flue gas by mineral carbonation is suggested to have a certain degree of economic feasibility in the conditions of medium and low-pressure. A highest carbonation conversion of 35.9% is gained on the condition of T=150℃, P=40 bar and PS 〈30 μ in distilled water for 1 h.

Two-step accelerated mineral carbonation and decomposition analysis for the reduction of CO_2 emission in the eco-industrial parks

Carbon dioxide（CO2） emissions are a leading contributor to the negative effects of global warming. Globally, research has focused on effective means of reducing and mitigating CO2 emissions. In this study, we examined the efficacy of eco-industrial parks（EIPs） and accelerated mineral carbonation techniques in reducing CO2 emissions in South Korea.First, we used Logarithmic Mean Divisia Index（LMDI） analysis to determine the trends in carbon production and mitigation at the existing EIPs. We found that, although CO2 was generated as byproducts and wastes of production at these EIPs, improved energy intensity effects occurred at all EIPs, and we strongly believe that EIPs are a strong alternative to traditional industrial complexes for reducing net carbon emissions. We also examined the optimal conditions for using accelerated mineral carbonation to dispose of hazardous fly ash produced through the incineration of municipal solid wastes at these EIPs. We determined that this technique most efficiently sequestered CO2 when micro-bubbling, low flow rate inlet gas, and ammonia additives were employed.

CO_(2) sequestration through direct aqueous mineral carbonation of red gypsum

In this study,the physical and chemical characteristics and direct aqueous mineral carbonation of red gypsum have been investigated.The characterization studies showed that red gypsum is a very potential feedstock for mineral carbonation.It is mainly consisted of CaO,Fe2O3 and SO3 along with some impurities.On the other hand,the carbonation results showed that direct aqueous carbonation of red gypsum resulted in CaCO3 and FeCO3 production,however,the carbonates purity and carbonation efficiency are still very low.

A combination process of mineral carbonation with S02 disposal for simulated flue gas by magnesia-added seawater

The desulfurization by seawater and mineral carbonation have been paid more and more attention.In this study,the feasibility of magnesia and seawater for the integrated disposal of S02 and C02 in the simulated flue gas was investigated.The process was conducted by adding MgO in seawater to reinforce the absorption of S02 and facilitate the mineralization of C02 by calcium ions.The influences of various factors,including digestion time of magnesia,reaction temperature,and salinity were also investigated.The results show that the reaction temperature can effectively improve the carbonation reaction.After combing S02 removal process with mineral carbonation,Ca^2+removal rate has a certain degree of decrease.The best carbonation condition is to use 1.5 times artificial seawater(the concentrations of reagents are 1.5 times of seawater)at 80℃and without digestion of magnesia.The desulfurization rate is close to 100%under any condition investigated,indicating that the seawater has a sufficient desulfurization capacity with adding magnesia.This work has demonstrated that a combination of the absorption of S02 with the absorption and mineralization of C02 is feasible.

Origin of carbonate minerals and impacts on reservoir quality of the Wufeng and Longmaxi Shale, Sichuan Basin

The Ordovician-Silurian Wufeng and Longmaxi Shale in the Sichuan Basin were studied to understand the genesis and diagenetic evolution of carbonate minerals and their effects on reservoir quality. The results of geochemical and petrological analyses show that calcite grains have a negative Ce anomaly indicating they formed in the oxidizing environment of seawater. The high carbonate mineral contents in the margin of basin indicate that calcite grains and cores of dolomite grains appear largely to be of detrital origin. The rhombic rims of dolomite grains and dolomite concretions with the δ^(13)C of –15.46‰ and the enrichment of middle rare earth elements were formed during the sulfate-driven anaerobic oxidation of methane. The calcite in radiolarian were related to the microbial sulfate reduction for the abundant anhedral pyrites and δ^(13)C value of –11.34‰. Calcite veins precipitated in the deep burial stage with homogenization temperature of the inclusions ranging from 146.70 ℃ to 182.90 ℃. The pores in shale are mainly organic matter pores with pore size mainly in the range of 1–20 nm in diameter. Carbonate minerals influence the development of pores through offering storage space for organic matter. When calcite contents ranging from 10% to 20%, calcite grains and cement as rigid framework can preserve primary pores. Subsequently, the thermal cracking of liquid petroleum in primary pores will form organic matter pores. The radiolarian were mostly partially filled with calcite, which combining with microcrystalline quartz preserved a high storage capacity.

Effects of Nitrogen Treatments on Organic Carbon Mineralization of Citrus Orchard Soil

[Objective] This study aimed to investigate the effect of soil organic carbon mineralization at different temperature on the amount of nitrogen application, in order to provide references for the establishment of carbon circulation model for orchard eco-system. [Method] The effects of nitrogen treatments on soil organic carbon mineralization of citrus orchard soil were investigated under 10, 20, 30 ℃ by laboratory simulated experiment. [Result] The mineralization rate decreased quickly at the be- ginning of the experiment but remained stable at the late period under three temper- ature treatments. The amounts of CO2 ranged from 1 328.25-2 219.42 mg/kg under three temperature condition, and the amount of soil organic carbon mineralization of 100 mg/kg （N4） treatment was the greatest, while that of CK was the lowest. High level nitrogen treatment （N4 and N3） were significant higher than the lower level nitro- gen treatment （N2 and N1）. The soil organic carbon mineralization rate increased with the temperature from 10 to 30℃. The dependence of soil carbon mineralization to temperature （Q10） was different under different nitrogen treatments that the Qlo value of N2 treatment was the lowest while that of the N4 treatment was the greatest. The soil organic carbon mineralization in Citrus orange orchard soil was affected significantly by high level nitrogen treatment, but with no significance under lower nitrogen treatment. [Conclusion] The dependence of soil carbon mineralization to temperature （Q10） increased with the increasing nitrogen input. The combination of nitrogen with temperature may increase the CO2 emission from Citrus orchard soil.

Benefaction from Carbonation of Flue Gas CO_(2) as Coal Mining Filling

CO2 capturing, transport and sequestration by pressurized water dissolution and reacting by natural alkali lime and magnesia in coal fly ash or other sources become an industrial advantageous sequestration option resulting in green waste solutions or solid fines. Mg and Ca containing minerals are reacting with CO2 to form carbonates. Various types of fly ash materials may react with CO2 to form carbonate regarding ash composition and reaction parameters. Mineral sequestration of CO2 will also allow using the products in cement industry or as cement material in constructions with low cost. This paper discussed progress on coal mining filling by carbonation method using coal fly ash of Soma, Yatagan, Afsin Elbistan Power Stations. Other filler materials containing coal mine waste shale, fly ashes and foam concrete, and additives were searched for pretreatment methods to enhance cement reactivity;and in analyzing the structural changes to identify reaction paths and potential barriers.

Effects of Temperature,Soil Moisture,Soil Type and Their Interactions on Soil Carbon Mineralization in Zoigê Alpine Wetland,Qinghai-Tibet Plateau

Wetland stores substantial amount of carbon and may contribute greatly to global climate change debate. However, few researches have focused on the effects of global climate change on carbon mineralization in Zoige alpine wetland, Qinghai-Tibet Plateau, which is one of the most important peatlands in China. Through incubation experiment, this paper studied the effects of temperature, soil moisture, soil type （marsh soil and peat soil） and their interactions on CO2 and CH4 emission rates in Zoige alpine wetland. Results show that when the temperature rises from 5℃ to 35℃, CO2 emission rates increase by 3.3-3.7 times and 2.4-2.6 times under non-inundation treatment, and by 2.2-2.3 times and 4.1-4.3 times under inundation treatment in marsh soil and peat soil, respectively. Compared with non-inundation treatment, CO2 emission rates decrease by 6%-44%, 20%-60% in marsh soil and peat soil, respectively, under inundation treatment. CO2 emission rate is significantly affected by the combined effects of the temperature and soil type （p 〈 0.001）, and soil moisture and soil type （p 〈 0.001）, and CH4 emission rate was significantly affected by the interaction of the temperature and soil moisture （p 〈 0.001）. Q10 values for CO2 emission rate are higher at the range of 5 ℃-25℃ than 25 ℃-35℃, indicating that carbon mineralization is more sensitive at low temperature in Zoige alpine wetland.

Artificial root exudates and soil organic carbon mineralization in a degraded sandy grassland in northern China

Plant root exudates contain various organic and inorganic components that include glucose, citric and oxalic acid. These components affect rhizosphere microbial and microfaunal activities, but the mechanisms are not fully known. Studies concerned from degraded grassland ecosystems with low soil carbon（C） contents are rare, in spite of the global distribution of grasslands in need of restoration. All these have a high potential for carbon sequestration, with a reduced carbon content due to overutilization. An exudate component that rapidly decomposes will increase soil respiration and CO2 emission, while a component that reduces decomposition of native soil carbon can reduce CO2 emission and actually help sequestering carbon in soil. Therefore, to investigate root exudate effects on rhizosphere activity, citric acid, glucose and oxalic acid（0.6 g C/kg dry soil） were added to soils from three biotopes（grassland, fixed dune and mobile dune） located in Naiman, Horqin Sandy Land, Inner Mongolia, China） and subjected to a 24-day incubation experiment together with a control. The soils were also analyzed for general soil properties. The results show that total respiration without exudate addition was highest in grassland soil, intermediate in fixed dune and lowest in mobile dune soil. However, the proportion of native soil carbon mineralized was highest in mobile dune soil, reflecting the low C/N ratio found there. The exudate effects on CO2-C emissions and other variables differed somewhat between biotopes, but total respiration（including that from the added substrates） was significantly increased in all combinations compared with the control, except for oxalic acid addition to mobile dune soil, which reduced CO2-C emissions from native soil carbon. A small but statistically significant increase in pH by the exudate additions in grassland and fixed dune soil was observed, but there was a major decrease from acid additions to mobile dune soil. In contrast, electrical conductivity decreased in grassland and fixed dune soil and increased in mobile dune. Thus, discrete components of root exudates affected soil environmental conditions differently, and responses to root exudates in soils with low carbon contents can differ from those in normal soils. The results indicate a potential for, e.g., acid root exudates to decrease decomposition rate of soil organic matter in low carbon soils, which is of interest for both soil restoration and carbon sequestration.

Predicting dynamics of soil organic carbon mineralization with a double exponential model in different forest belts of China

The dynamics of soil organic carbon （SOC） was analyzed by using laboratory incubation and double exponential model that mineralizable SOC was separated into active carbon pools and slow carbon pools in forest soils derived from Changbai and Qilian Mountain areas. By analyzing and fitting the CO2 evolved rates with SOC mineralization, the results showed that active carbon pools accounted tor 1.0% to 8.5% of SOC with an average of mean resistant times （MRTs） for 24 days, and slow carbon pools accounted for 91% to 99% of SOC with an average of MRTs for 179 years. The sizes and MRTs of slow carbon pools showed that SOC in Qilian Mountain sites was more difficult to decompose than that in Changbai Mountain sites. By analyzing the effects of temperature, soil clay content and elevation on SOC mineralization, results indicated that mineralization of SOC was directly related to temperature and that content of accumulated SOC and size of slow carbon pools from Changbai Mountain and Qilian Mountain sites increased linearly with increasing clay content, respectively, which showed temperature and clay content could make greater effect on mineralization of SOC.

A kinetic approach to evaluate salinity effects on carbon mineralization in a plant residue-amended soil

The interaction of salinity stress and plant residue quality on C mineralization kinetics in soil is not well understood. A laboratory experiment was conducted to study the effects of salinity stress on C mineralization kinetics in a soil amended with alfalfa, wheat and corn residues. A factorial combination of two salinity levels （0.97 and 18.2 dS/m） and four levels of plant residues （control, alfalfa, wheat and corn） with three replications was performed. A first order kinetic model was used to describe the C mineralization and to calculate the potentially mineralizable C. The CO2-C evolved under non-saline condition, ranged from 814.6 to 4842.4 mg CO2-C/kg in control and alfalfa residue-amended soils, respectively. Salinization reduced the rates of CO2 evolution by 18.7%, 6.2% and 5.2% in alfalfa, wheat and corn residue-amended soils, respectively. Potentially mineralizable C （Co） was reduced significantly in salinized alfalfa residue-treated soils whereas, no significant difference was observed for control treatments as well as wheat and corn residue-treated soils. We concluded that the response pattern of C mineralization to salinity stress depended on the plant residue quality and duration of incubation.

The dating and temperature measurement technologies for carbonate minerals and their application in hydrocarbon accumulation research in the paleouplift in central Sichuan Basin, SW China

A new method for reconstructing the geological history of hydrocarbon accumulation is developed, which are constrained by U-Pb isotope age and clumped isotope((35)47) temperature of host minerals of hydrocarbon-bearing inclusions. For constraining the time and depth of hydrocarbon accumulation by the laser in-situ U-Pb isotope age and clumped isotope temperature, there are two key steps:(1) Investigating feature, abundance and distribution patterns of liquid and gaseous hydrocarbon inclusions with optical microscopes.(2) Dating laser in-situ U-Pb isotope age and measuring clumped isotope temperature of the host minerals of hydrocarbon inclusions. These technologies have been applied for studying the stages of hydrocarbon accumulation in the Sinian Dengying gas reservoir in the paleo-uplift of the central Sichuan Basin. By dating the U-Pb isotope age and measuring the temperature of clumped isotope((35)47) of the host minerals of hydrocarbon inclusions in dolomite, three stages of hydrocarbon accumulation were identified:(1) Late Silurian: the first stage of oil accumulation at(416±23) Ma.(2) Late Permian to Early Triassic: the second stage of oil accumulation between(248±27) Ma and(246.3±1.5) Ma.(3) Yanshan to Himalayan period: gas accumulation between(115±69) Ma and(41±10) Ma. The reconstructed hydrocarbon accumulation history of the Dengying gas reservoir in the paleo-uplift of the central Sichuan Basin is highly consistent with the tectonic-burial history, basin thermal history and hydrocarbon generation history, indicating that the new method is a reliable way for reconstructing the hydrocarbon accumulation history.

Composition and mineralization of soil organic carbon pools in four single-tree species forest soils

Forest soil carbon （C） is an important compo- nent of the global C cycle. However, the mechanism by which tree species influence soil organic C （SOC） pool composition and mineralization is poorly understood. To understand the effect of tree species on soil C cycling, we assessed total, labile, and recalcitrant SOC pools, SOC chemical composition by 13C nuclear magnetic resonance spectroscopy, and SOC mineralization in four monoculture plantations. Labile and recalcitrant SOC pools in surface （0-10 cm） and deep （40-60 cm） soils in the four forests contained similar content. In contrast, these SOC pools exhibited differences in the subsurface soil （from 10 to 20 cm and from 20 to 40 cm）. The alkyl C and O-alkyl C intensities of SOC were higher in Schima superba and Michelia macclurei forests than in Cunninghamia lanceolata and Pinus massoniana forests. In surface soil, S. superba and M. macclurei forests exhibited higher SOC mineralization rates than did P. massoniana and C.lanceolata forests. The slope of the straight line between C60 and labile SOC was steeper than that between C60 and total SOC. Our results suggest that roots affected the composition of SOC pools. Labile SOC pools also affected SOC mineralization to a greater extent than total SOC pools.