An inherent problem with natural gas production or transmission is the formation of gas hydrates, which can lead to safety hazards for production/transportation systems, and substantial economic risks. Hydrate inhibit...An inherent problem with natural gas production or transmission is the formation of gas hydrates, which can lead to safety hazards for production/transportation systems, and substantial economic risks. Hydrate inhibition with different inhibitors such as, methanol, ethylene glycol （EG）, triethylene glycol （TEG）, and sodium chloride solution continues to play a critical role in many operations. An understanding of when the hydrates form in the presence of these hydrate inhibitors, is therefore necessary to overcome hydrate problems. Several thermodynamic models have been proposed for predicting the hydrate formation conditions in aqueous solutions containing methanol/glycols and electrolytes. However, available models have limitations that include the types of liquid, compositions of fluids, and inhibitors used. The aim of this study is to develop a simple-to-use correlation for accurate prediction of hydrate-forming pressures of pure alkanes in the presence of different hydrate inhibitors, where the obtained results illustrate good agreement with the reported experimental data.展开更多
Recent experimental results and kinetic modeling of fast flow gas-phase oxidation of methane and other lower alkanes to methanol and other oxygenates are discussed, alongside with prospects and possible areas for appl...Recent experimental results and kinetic modeling of fast flow gas-phase oxidation of methane and other lower alkanes to methanol and other oxygenates are discussed, alongside with prospects and possible areas for applications of the processes.展开更多
Mitigation of the deleterious environmental impacts associated with CO_(2) emissions requires the development of more sustainable processes for synthesizing fuels and chemicals.Selective conversion of abundant yet dif...Mitigation of the deleterious environmental impacts associated with CO_(2) emissions requires the development of more sustainable processes for synthesizing fuels and chemicals.Selective conversion of abundant yet difficult to activate molecules such as CO_(2) and surplus light alkanes from shale gas to desirable products can potentially reduce reliance upon conventional fossil-based feedstocks.Therefore,co-conversion of CO_(2) with abundant light alkanes such as methane and ethane using atmospheric-pressure.展开更多
China University of Petroleum(East China)has developed an inexpensive and environmentally friendly TiO2 catalyst for dehydrogenation of low-carbon alkanes,which is an excellent substitute for the Pt series catalysts(w...China University of Petroleum(East China)has developed an inexpensive and environmentally friendly TiO2 catalyst for dehydrogenation of low-carbon alkanes,which is an excellent substitute for the Pt series catalysts(with high production cost)and Cr series catalysts(with toxicity)coupled with apparent technical and economic benefits and high applicability.展开更多
Spray auto-ignition experiments were carried out in a constant volume combustion chamber for some pure alkanes(n-paraffins with different chain length, cyclohexane, n-butyl cyclohexane, and isooctane) and blends of n-...Spray auto-ignition experiments were carried out in a constant volume combustion chamber for some pure alkanes(n-paraffins with different chain length, cyclohexane, n-butyl cyclohexane, and isooctane) and blends of n-decane with Standard Blended Fuel(isooctane/n-heptane) and product gasoline. Test results showed that the reaction activity of n-paraffins was relatively high. Meanwhile, the auto-ignition characteristics differed significantly with the molecular structures of alkanes. Adding different volume fractions of n-decane to Standard Blended Fuel and product gasoline could improve the fuel reaction activity at varying degree. Finally, functional groups effects were used to simulate the relationship between the molecular topology and the auto-ignition quality.展开更多
This review paper aims at analysing the state of the art for partial oxidation and oxidative dehydrogenation（ODH） reactions of lower alkanes C–Cinto olefins and oxygenated products（aldehydes, anhydrides,carboxylic...This review paper aims at analysing the state of the art for partial oxidation and oxidative dehydrogenation（ODH） reactions of lower alkanes C–Cinto olefins and oxygenated products（aldehydes, anhydrides,carboxylic acids） on metal oxide catalysts with cations of variable oxidation state, such as Mo and V in particular. Key parameters to be met by the catalysts, such as their redox properties, their structural aspects, active sites composed of ensembles of atoms isolated one from the others, mechanisms of reactions, are discussed. Main features of the different reactions of C–Calkanes and catalysts are analysed and their generalisation for determining more active and more selective catalysts is attempted. Prospective views for the future of the domain are proposed.展开更多
The combination of a low cost source of Biofine＇s levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable co...The combination of a low cost source of Biofine＇s levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable compounds for transportation sector. The present review illustrates the development of different approaches to one–pot synthesis of fuel-like alkanes from lignocellulose derived carboxylic acids where particular focus is given to valeric acid consecutive decarboxylative coupling（ketonization） and ketone hydrodeoxygenation in a single reactor over one catalyst bed. The key factors that influence the catalytic performance on both ketonization and hydrodeoxygenation steps as well as their cross-influence will be clarified to provide insights for the design of more efficient catalysts for the one-pot transformation. Valeric acid is considered as a potential acid source from viewpoint of cost effectiveness and feasibility of such transformation with reasonable alkane yield. The both reaction mechanisms and kinetics will also be discussed to understand deeply how the selective C–C coupling and following C=O hydrogenation can be achieved.展开更多
Ultra-long n-alkanes are highly valuable in both scientific research and as major constituents of specialty high-melting-point waxes.Unlike conventional methods(e.g.,Fischer–Tropsch(FT),ethylene oligomerization,and p...Ultra-long n-alkanes are highly valuable in both scientific research and as major constituents of specialty high-melting-point waxes.Unlike conventional methods(e.g.,Fischer–Tropsch(FT),ethylene oligomerization,and polyethylene cracking)typically resulting in wide n-alkane distributions,the elaborate design strategy presented herein allows the direct synthesis of pure,long n-alkanes using a modular splicing method with acetone,furfural,and fatty acid anhydrides or acyl chlorides as bio-blocks.The herein approach is based on a simple four-step catalytic reaction scheme involving C–C chain elongation and C–O bond activation.The synthesized pure n-alkanes had a carbon chain length as high as C_(49)(total yield of 49%).The synthesis approach also allows to selectively prepare n-alkanes with even and odd carbon numbers ranging from C15 to C_(49).This process represents a great breakthrough in the synthesis of long-chain pure n-alkanes,surpassing the carbon number limitations reported in previous methodologies.展开更多
Exploration and development of large gas fields is an important way for a country to rapidly develop its natural gas industry.From 1991 to 2020,China discovered 68 new large gas fields,boosting its annual gas output t...Exploration and development of large gas fields is an important way for a country to rapidly develop its natural gas industry.From 1991 to 2020,China discovered 68 new large gas fields,boosting its annual gas output to 1925×108m3in 2020,making it the fourth largest gas-producing country in the world.Based on 1696 molecular components and carbon isotopic composition data of alkane gas in 70 large gas fields in China,the characteristics of carbon isotopic composition of alkane gas in large gas fields in China were obtained.The lightest and average values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become heavier with increasing carbon number,while the heaviest values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become lighter with increasing carbon number.Theδ^(13)C_(1)values of large gas fields in China range from-71.2‰to-11.4‰(specifically,from-71.2‰to-56.4‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-18.9‰for coal-derived gas,and from-35.6‰to-11.4‰for abiogenic gas).Based on these data,theδ^(13)C_(1)chart of large gas fields in China was plotted.Moreover,theδ^(13)C_(1)values of natural gas in China range from-107.1‰to-8.9‰,specifically,from-1071%o to-55.1‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-13.3‰for coal-derived gas,and from-36.2‰to-8.9‰for abiogenic gas.Based on these data,theδ^(13)C_(1)chart of natural gas in China was plotted.展开更多
A computer-aided ionic liquid design(CAILD) study is presented for the frequently encountered alkane/cycloalkane separations in petrochemical industry. Exhaustive experimental data are first collected to extend the UN...A computer-aided ionic liquid design(CAILD) study is presented for the frequently encountered alkane/cycloalkane separations in petrochemical industry. Exhaustive experimental data are first collected to extend the UNIFAC-IL model for this system, where the proximity effect in alkanes and cycloalkanes is considered specifically by defining distinct groups. The thermodynamic performances of a large number of ILs for 4 different alkane/cycloalkane systems are then compared to select a representative example of such separations. By applying n-heptane/methylcyclohexane extractive distillation as a case study, the CAILD task is cast as a mixed-integer nonlinear programming(MINLP) problem based on the obtained task-specific UNIFAC-IL model and two semi-empirical models for IL physical properties. The top 5 IL candidates determined by solving the MINLP problem are subsequently introduced into Aspen Plus for process simulation and economic analysis, which finally identify 1-hexadecyl-methylpiperidinium tricyanomethane([C_(16)MPip][C(CN)_3]) as the best entrainer for this separation.展开更多
Recently abiogenic alkanes have been found in various locations in the world and other celestial bodies. The chemical composition of abiogenic alkane gases varies widely. The content of methane is low and nearly no C2...Recently abiogenic alkanes have been found in various locations in the world and other celestial bodies. The chemical composition of abiogenic alkane gases varies widely. The content of methane is low and nearly no C2+ is found in the abiogenic alkane gases from fluid inclusions in volcanic rocks or hot springs in China. In the unsedimented submarine hydrothermal vent system C1/C2+ ratios are much greater than those for the thermogenic gases, mostly >800 and in some cases up to 8,000. In the Songliao Basin, China, C1/C2+ of some abiogenic gases are often less than 150. Abiogenic alkane gases which have been found in nature often have carbon isotopic reversal among C1–C4 alkanes (δ13C1>δ13C2>δ13C3>δ13C4), whereas both regular and reversed hydrogen isotope distribution pattern among C1–C4 alkanes have been reported. The δ13C of abiogenic methane is mainly greater than ?30‰ though laboratory synthesized methane can have δ13C as low as ?57‰, and its δD1 values vary widely and overlap with biogenic gases. High 3He/4He ratios often indicate the addition of mantle-derived helium and are related to abiogenic gases. However, some biogenic gases can also have high 3He/4He ratios up to 8. The CH4/3He end-member is often lower than 106 for abiogenic alkane gases while greater than 1013 for biogenic gases, and the values between these two end-members often reflect the mixing of biogenic and abiogenic gases.展开更多
To study the composition, affecting factors of the stable hydrogen isotopes of alkane gases and their application to identification of the natural gas origin and maturities, the chemical and isotopic compositions of 1...To study the composition, affecting factors of the stable hydrogen isotopes of alkane gases and their application to identification of the natural gas origin and maturities, the chemical and isotopic compositions of 118 gas samples of Carboniferous- Permian in the Ordos Basin, and of Triassic in the Sichuan Basin, combined with 68 gas samples from the Sinian and Cambrian reservoirs in the Sichuan Basin, and Ordovician and Siliurian reservoirs of Tarim Basin, are analyzed comprehensively. The following conclusions are obtained:(1) Natural gases in the study area and strata of the Ordos and Sichuan basins are dominated by alkane gases, and the dryness coefficients and maturities of the Carboniferous-Permian gases in the Ordos Basin are higher than the gases in the Triassic Xujiahe Formation of the Sichuan Basin, while the hydrogen isotopes of the latter ones are much enriched in 2H than the former.(2) The δ2HCH4-C1/C2+3 genetic identification diagram of natural gas was drawn, and the diagrams of hydrogen isotopic differences between the heavy alkane gases and methane vs. hydrogen isotopes of alkane gases can also be used in natural gas genetic identification.(3) The δ2HCH4-Ro formulas of coal-formed gas in different areas of the two basins are given, and the δ2HC2H6-δ2HCH4 is a new index for maturity, and the (δ2HC2H6-δ2HCH4)-Ro formula of the coal-formed gas can be used to calculate the maturity of the natural gas.(4) The stable hydrogen isotopes of alkane gases are affected by parent materials in source rocks, maturity, mixing and the aqueous medium conditions, among which the aqueous paleo-salinity is the key factor. To sum up, the hydrogen isotopes of alkane gases are affected by multiple factors, and they are significant to the identification of the origin, and maturity of natural gas, and the water environment during the deposition of source rocks.展开更多
This paper presents a review of low molecular weight alkane-fed solid oxide fuel cells(SOFCs),which,unlikely the conventional use of SOFCs for only power production,are utilized to cogenerate produce useful chemicals ...This paper presents a review of low molecular weight alkane-fed solid oxide fuel cells(SOFCs),which,unlikely the conventional use of SOFCs for only power production,are utilized to cogenerate produce useful chemicals at the same time.The cogeneration processes in SOFC have been classified according to the different types of fuel.C_(2)and C_(3)alkenes and synthesis gas are the main cogenerated chemicals together with electricity.The chemicals and energy cogeneration in a fuel cell reactor seems to be an effective alternative to conventional reactors for only chemicals production and conventional fuel cells for only power production.Although,the use of SOFCs for chemicals and energy cogeneration has proved successful in the industrial setting,the development of new catalysts aimed at obtaining the desired chemicals together with the production of a high amount of energy,and optimizing SOFC operation conditions is still a challenge to enhance system performance and make commercial applications workable.展开更多
By using a simplified Coulomb explosion model, the laser-driven Coulomb explosion processes of three deuterated alkane clusters, i.e., deuterated methane（CD4）N, ethane（C2D6）N and propane（C3D8）N clusters are simu...By using a simplified Coulomb explosion model, the laser-driven Coulomb explosion processes of three deuterated alkane clusters, i.e., deuterated methane（CD4）N, ethane（C2D6）N and propane（C3D8）N clusters are simulated numerically.The overrun phenomenon that the deuterons overtake the carbon ions inside the expanding clusters, as well as the dependence of the energetic deuterons and fusion neutron yield on cluster size, is discussed in detail. Researches show that the average kinetic energy of deuterons and neutron yield generated in the Coulomb explosion of（C2D6）N cluster are higher than those of（CD4）N cluster with the same size, in qualitative agreement with the reported conclusions from the experiments of（C2 H6）N and（CH4）N clusters. It is indicated that（C2D6）N clusters are superior to（CD4）N clusters as a target for the laser-induced nuclear fusion reaction to achieve a higher neutron yield. In addition, by comparing the relevant data of（C3D8）N cluster with those of（C2D6）N cluster with the same size, it is theoretically concluded that（C3D8）N clusters with a larger competitive parameter might be a potential candidate for improving neutron generation. This will provide a theoretical basis for target selection in developing experimental schemes on laser-driven nuclear fusion in the future.展开更多
Although naphthenes have long been identified as important feedstock components for the production of light olefins and aromatics in fluid catalytic cracking units,their cacking mechanism and microscopic reaction netw...Although naphthenes have long been identified as important feedstock components for the production of light olefins and aromatics in fluid catalytic cracking units,their cacking mechanism and microscopic reaction networks,such as activation modes,ring-opening paths,and the production of aromatics,remain debated.In this context,we reported experimental and computational work aimed at elucidating the reaction network of naphthenes in fluid catalytic cracking using cyclohexane as the model naphthene.First,the main reactions for the formation of highly selective and value-added products such as light olefins and aromatics were discussed.Then,the proportions of cyclohexane activation via(i)the non-classical carbonium mechanism and(ii)the classical carbenium mechanism were analyzed by data fitting methods,which revealed that around 32.6%of cyclohexane was initiated by path(i),and the remaining naphthene was activated by path(ii).Moreover,our DFT results showed that the ring opening of cyclohexane through pathway(i)was more difficult than that through path(ii),and ring opening followed by the ring contraction of cyclohexane carbenium ions was the most energetically favorable route among the different ring-opening ways.展开更多
文摘An inherent problem with natural gas production or transmission is the formation of gas hydrates, which can lead to safety hazards for production/transportation systems, and substantial economic risks. Hydrate inhibition with different inhibitors such as, methanol, ethylene glycol （EG）, triethylene glycol （TEG）, and sodium chloride solution continues to play a critical role in many operations. An understanding of when the hydrates form in the presence of these hydrate inhibitors, is therefore necessary to overcome hydrate problems. Several thermodynamic models have been proposed for predicting the hydrate formation conditions in aqueous solutions containing methanol/glycols and electrolytes. However, available models have limitations that include the types of liquid, compositions of fluids, and inhibitors used. The aim of this study is to develop a simple-to-use correlation for accurate prediction of hydrate-forming pressures of pure alkanes in the presence of different hydrate inhibitors, where the obtained results illustrate good agreement with the reported experimental data.
基金support from Russian Foundation for Basic Research(Grant No 03-03-32105)is gratefully acknowledged.
文摘Recent experimental results and kinetic modeling of fast flow gas-phase oxidation of methane and other lower alkanes to methanol and other oxygenates are discussed, alongside with prospects and possible areas for applications of the processes.
基金financially supported by the Yale Center for Natural Carbon Capturesupport from the U.S. Department of Energy, Office of Basic Energy Sciences, under Contract No. DE-SC0012704。
文摘Mitigation of the deleterious environmental impacts associated with CO_(2) emissions requires the development of more sustainable processes for synthesizing fuels and chemicals.Selective conversion of abundant yet difficult to activate molecules such as CO_(2) and surplus light alkanes from shale gas to desirable products can potentially reduce reliance upon conventional fossil-based feedstocks.Therefore,co-conversion of CO_(2) with abundant light alkanes such as methane and ethane using atmospheric-pressure.
文摘China University of Petroleum(East China)has developed an inexpensive and environmentally friendly TiO2 catalyst for dehydrogenation of low-carbon alkanes,which is an excellent substitute for the Pt series catalysts(with high production cost)and Cr series catalysts(with toxicity)coupled with apparent technical and economic benefits and high applicability.
基金funded by the National Key Research and Development Program (2017YFB0306505)
文摘Spray auto-ignition experiments were carried out in a constant volume combustion chamber for some pure alkanes(n-paraffins with different chain length, cyclohexane, n-butyl cyclohexane, and isooctane) and blends of n-decane with Standard Blended Fuel(isooctane/n-heptane) and product gasoline. Test results showed that the reaction activity of n-paraffins was relatively high. Meanwhile, the auto-ignition characteristics differed significantly with the molecular structures of alkanes. Adding different volume fractions of n-decane to Standard Blended Fuel and product gasoline could improve the fuel reaction activity at varying degree. Finally, functional groups effects were used to simulate the relationship between the molecular topology and the auto-ignition quality.
文摘This review paper aims at analysing the state of the art for partial oxidation and oxidative dehydrogenation（ODH） reactions of lower alkanes C–Cinto olefins and oxygenated products（aldehydes, anhydrides,carboxylic acids） on metal oxide catalysts with cations of variable oxidation state, such as Mo and V in particular. Key parameters to be met by the catalysts, such as their redox properties, their structural aspects, active sites composed of ensembles of atoms isolated one from the others, mechanisms of reactions, are discussed. Main features of the different reactions of C–Calkanes and catalysts are analysed and their generalisation for determining more active and more selective catalysts is attempted. Prospective views for the future of the domain are proposed.
基金partly supported by Russian Academy of Science Project No. V.46.4.4Part of work related to metal oxides was supported by RFBR grant 15-03-09329
文摘The combination of a low cost source of Biofine＇s levulinic acid with available way of valeric acid synthesis opens up new opportunities for valeric acid as a promising bio-derived source for synthesis of valuable compounds for transportation sector. The present review illustrates the development of different approaches to one–pot synthesis of fuel-like alkanes from lignocellulose derived carboxylic acids where particular focus is given to valeric acid consecutive decarboxylative coupling（ketonization） and ketone hydrodeoxygenation in a single reactor over one catalyst bed. The key factors that influence the catalytic performance on both ketonization and hydrodeoxygenation steps as well as their cross-influence will be clarified to provide insights for the design of more efficient catalysts for the one-pot transformation. Valeric acid is considered as a potential acid source from viewpoint of cost effectiveness and feasibility of such transformation with reasonable alkane yield. The both reaction mechanisms and kinetics will also be discussed to understand deeply how the selective C–C coupling and following C=O hydrogenation can be achieved.
基金supported by National Natural Science Foundation of China(General Program,No.22372060)Shanghai Municipal Science and Technology Commission Project(No.22dz1209300)National Natural Science Youth Fund(No.22205065)。
文摘Ultra-long n-alkanes are highly valuable in both scientific research and as major constituents of specialty high-melting-point waxes.Unlike conventional methods(e.g.,Fischer–Tropsch(FT),ethylene oligomerization,and polyethylene cracking)typically resulting in wide n-alkane distributions,the elaborate design strategy presented herein allows the direct synthesis of pure,long n-alkanes using a modular splicing method with acetone,furfural,and fatty acid anhydrides or acyl chlorides as bio-blocks.The herein approach is based on a simple four-step catalytic reaction scheme involving C–C chain elongation and C–O bond activation.The synthesized pure n-alkanes had a carbon chain length as high as C_(49)(total yield of 49%).The synthesis approach also allows to selectively prepare n-alkanes with even and odd carbon numbers ranging from C15 to C_(49).This process represents a great breakthrough in the synthesis of long-chain pure n-alkanes,surpassing the carbon number limitations reported in previous methodologies.
基金Supported by the National Natural Science Foundation of China(41472120)General Project of National Natural Science Foundation of China(42272188)+1 种基金Special Fund of PetroChina and New Energy Branch(2023YQX10101)Petrochemical Joint Fund of Fund Committee(U20B6001)。
文摘Exploration and development of large gas fields is an important way for a country to rapidly develop its natural gas industry.From 1991 to 2020,China discovered 68 new large gas fields,boosting its annual gas output to 1925×108m3in 2020,making it the fourth largest gas-producing country in the world.Based on 1696 molecular components and carbon isotopic composition data of alkane gas in 70 large gas fields in China,the characteristics of carbon isotopic composition of alkane gas in large gas fields in China were obtained.The lightest and average values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become heavier with increasing carbon number,while the heaviest values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become lighter with increasing carbon number.Theδ^(13)C_(1)values of large gas fields in China range from-71.2‰to-11.4‰(specifically,from-71.2‰to-56.4‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-18.9‰for coal-derived gas,and from-35.6‰to-11.4‰for abiogenic gas).Based on these data,theδ^(13)C_(1)chart of large gas fields in China was plotted.Moreover,theδ^(13)C_(1)values of natural gas in China range from-107.1‰to-8.9‰,specifically,from-1071%o to-55.1‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-13.3‰for coal-derived gas,and from-36.2‰to-8.9‰for abiogenic gas.Based on these data,theδ^(13)C_(1)chart of natural gas in China was plotted.
基金financial support from National Natural Science Foundation of China(21776074,21576081,and21861132019)
文摘A computer-aided ionic liquid design(CAILD) study is presented for the frequently encountered alkane/cycloalkane separations in petrochemical industry. Exhaustive experimental data are first collected to extend the UNIFAC-IL model for this system, where the proximity effect in alkanes and cycloalkanes is considered specifically by defining distinct groups. The thermodynamic performances of a large number of ILs for 4 different alkane/cycloalkane systems are then compared to select a representative example of such separations. By applying n-heptane/methylcyclohexane extractive distillation as a case study, the CAILD task is cast as a mixed-integer nonlinear programming(MINLP) problem based on the obtained task-specific UNIFAC-IL model and two semi-empirical models for IL physical properties. The top 5 IL candidates determined by solving the MINLP problem are subsequently introduced into Aspen Plus for process simulation and economic analysis, which finally identify 1-hexadecyl-methylpiperidinium tricyanomethane([C_(16)MPip][C(CN)_3]) as the best entrainer for this separation.
基金supported by the China Postdoctoral Science Foundation (20070420393)China Postdoctoral Special Science Foundation (20081095)PetroChina Science and Technology Project (07-01C-01-07)
文摘Recently abiogenic alkanes have been found in various locations in the world and other celestial bodies. The chemical composition of abiogenic alkane gases varies widely. The content of methane is low and nearly no C2+ is found in the abiogenic alkane gases from fluid inclusions in volcanic rocks or hot springs in China. In the unsedimented submarine hydrothermal vent system C1/C2+ ratios are much greater than those for the thermogenic gases, mostly >800 and in some cases up to 8,000. In the Songliao Basin, China, C1/C2+ of some abiogenic gases are often less than 150. Abiogenic alkane gases which have been found in nature often have carbon isotopic reversal among C1–C4 alkanes (δ13C1>δ13C2>δ13C3>δ13C4), whereas both regular and reversed hydrogen isotope distribution pattern among C1–C4 alkanes have been reported. The δ13C of abiogenic methane is mainly greater than ?30‰ though laboratory synthesized methane can have δ13C as low as ?57‰, and its δD1 values vary widely and overlap with biogenic gases. High 3He/4He ratios often indicate the addition of mantle-derived helium and are related to abiogenic gases. However, some biogenic gases can also have high 3He/4He ratios up to 8. The CH4/3He end-member is often lower than 106 for abiogenic alkane gases while greater than 1013 for biogenic gases, and the values between these two end-members often reflect the mixing of biogenic and abiogenic gases.
基金Supported by the China National Science and Technology Major Project(2016ZX05004-001)
文摘To study the composition, affecting factors of the stable hydrogen isotopes of alkane gases and their application to identification of the natural gas origin and maturities, the chemical and isotopic compositions of 118 gas samples of Carboniferous- Permian in the Ordos Basin, and of Triassic in the Sichuan Basin, combined with 68 gas samples from the Sinian and Cambrian reservoirs in the Sichuan Basin, and Ordovician and Siliurian reservoirs of Tarim Basin, are analyzed comprehensively. The following conclusions are obtained:(1) Natural gases in the study area and strata of the Ordos and Sichuan basins are dominated by alkane gases, and the dryness coefficients and maturities of the Carboniferous-Permian gases in the Ordos Basin are higher than the gases in the Triassic Xujiahe Formation of the Sichuan Basin, while the hydrogen isotopes of the latter ones are much enriched in 2H than the former.(2) The δ2HCH4-C1/C2+3 genetic identification diagram of natural gas was drawn, and the diagrams of hydrogen isotopic differences between the heavy alkane gases and methane vs. hydrogen isotopes of alkane gases can also be used in natural gas genetic identification.(3) The δ2HCH4-Ro formulas of coal-formed gas in different areas of the two basins are given, and the δ2HC2H6-δ2HCH4 is a new index for maturity, and the (δ2HC2H6-δ2HCH4)-Ro formula of the coal-formed gas can be used to calculate the maturity of the natural gas.(4) The stable hydrogen isotopes of alkane gases are affected by parent materials in source rocks, maturity, mixing and the aqueous medium conditions, among which the aqueous paleo-salinity is the key factor. To sum up, the hydrogen isotopes of alkane gases are affected by multiple factors, and they are significant to the identification of the origin, and maturity of natural gas, and the water environment during the deposition of source rocks.
文摘This paper presents a review of low molecular weight alkane-fed solid oxide fuel cells(SOFCs),which,unlikely the conventional use of SOFCs for only power production,are utilized to cogenerate produce useful chemicals at the same time.The cogeneration processes in SOFC have been classified according to the different types of fuel.C_(2)and C_(3)alkenes and synthesis gas are the main cogenerated chemicals together with electricity.The chemicals and energy cogeneration in a fuel cell reactor seems to be an effective alternative to conventional reactors for only chemicals production and conventional fuel cells for only power production.Although,the use of SOFCs for chemicals and energy cogeneration has proved successful in the industrial setting,the development of new catalysts aimed at obtaining the desired chemicals together with the production of a high amount of energy,and optimizing SOFC operation conditions is still a challenge to enhance system performance and make commercial applications workable.
基金supported by the National Natural Science Foundation of China(Grant No.11005080)
文摘By using a simplified Coulomb explosion model, the laser-driven Coulomb explosion processes of three deuterated alkane clusters, i.e., deuterated methane（CD4）N, ethane（C2D6）N and propane（C3D8）N clusters are simulated numerically.The overrun phenomenon that the deuterons overtake the carbon ions inside the expanding clusters, as well as the dependence of the energetic deuterons and fusion neutron yield on cluster size, is discussed in detail. Researches show that the average kinetic energy of deuterons and neutron yield generated in the Coulomb explosion of（C2D6）N cluster are higher than those of（CD4）N cluster with the same size, in qualitative agreement with the reported conclusions from the experiments of（C2 H6）N and（CH4）N clusters. It is indicated that（C2D6）N clusters are superior to（CD4）N clusters as a target for the laser-induced nuclear fusion reaction to achieve a higher neutron yield. In addition, by comparing the relevant data of（C3D8）N cluster with those of（C2D6）N cluster with the same size, it is theoretically concluded that（C3D8）N clusters with a larger competitive parameter might be a potential candidate for improving neutron generation. This will provide a theoretical basis for target selection in developing experimental schemes on laser-driven nuclear fusion in the future.
基金This work was performed with the financial support of Sinopec Research Institute of Petroleum Processing(RIPP,Proj.R17022).
文摘Although naphthenes have long been identified as important feedstock components for the production of light olefins and aromatics in fluid catalytic cracking units,their cacking mechanism and microscopic reaction networks,such as activation modes,ring-opening paths,and the production of aromatics,remain debated.In this context,we reported experimental and computational work aimed at elucidating the reaction network of naphthenes in fluid catalytic cracking using cyclohexane as the model naphthene.First,the main reactions for the formation of highly selective and value-added products such as light olefins and aromatics were discussed.Then,the proportions of cyclohexane activation via(i)the non-classical carbonium mechanism and(ii)the classical carbenium mechanism were analyzed by data fitting methods,which revealed that around 32.6%of cyclohexane was initiated by path(i),and the remaining naphthene was activated by path(ii).Moreover,our DFT results showed that the ring opening of cyclohexane through pathway(i)was more difficult than that through path(ii),and ring opening followed by the ring contraction of cyclohexane carbenium ions was the most energetically favorable route among the different ring-opening ways.
