Four types of nanoparticles,amorphous carbon,ironⅢoxide,SiO2,and amino-coated SiO2,were tested to determine changes in tetrahydrofuran-water(THF-water)clathrate hydrate nucleation and agglomeration.Rates were experim...Four types of nanoparticles,amorphous carbon,ironⅢoxide,SiO2,and amino-coated SiO2,were tested to determine changes in tetrahydrofuran-water(THF-water)clathrate hydrate nucleation and agglomeration.Rates were experimentally found to determine their viability for preventing natural gas hydrates from developing during offshore drilling operations.THF-water clathrates were chosen as a model to represent gas hydrate growth at atmospheric pressure.Concentrations of each nanoparticle between 0.15%and 1.0%by weight were tested as a kinetic inhibitor to hydrate formation.Tests were repeated at various temperatures below the formation temperature of 4.4℃for THF-water clathrate hydrates.Measurements were made to identify how the concentration of THF affects the clathrate hydrates forming under static conditions between20%and 30%by mole of THF.The primary tests in this study were performed using a 20:80 THF/water ratio.Temperature increases during hydrate nucleation for THF-water were measured between-5 and 3℃.The range of ideal nanoparticle concentrations was found to be between 0.15%and 0.45%by weight for optimal static,kinetic inhibition of hydrate nucleation.At approximately 0.3%by weight,the most significant inhibition was observed under static conditions for all four types of nanoparticles tested.We found that functionalized amino-coated SiO2 nanoparticles,across all tests,significantly increased the time required for the formation of THF-water clathrate hydrates compared to the other three non-functionalized nanoparticles.The amorphous carbon and ironⅢoxide nanoparticles performed similarly across each test and were both the least effective in their inhibition of the clathrate hydrates of the four nanoparticles studied compared to a control.展开更多
Single-crystalline samples of Eu/Ba-filled Sn-based type-Ⅷ clathrate are prepared by the Ga flux method with different stoichiometric ratios. The electrical transport properties of the samples are optimized by Eu dop...Single-crystalline samples of Eu/Ba-filled Sn-based type-Ⅷ clathrate are prepared by the Ga flux method with different stoichiometric ratios. The electrical transport properties of the samples are optimized by Eu doping. Results indicate that Eu atoms tend to replace Ba atoms. With the increase of the Eu initial content, the carrier density increases and the carrier mobility decreases, which leads to an increase of the Seebeck coefficient. By contrast, the electrical conductivity decreases. Finally, the sample with Eu initial content of x = 0.75 behaves with excellent electrical properties, which shows a maximal power factor of 1.51 mW·m^-1K^-2 at 480K, and the highest ZT achieved is 0.87 near the temperature of 483K.展开更多
N-type Si-based type-Ⅰ clathrates with different Ga content were synthesized by combining the solid-state reaction method,melting method and spark plasma sintering (SPS) method.The effects of Ga composition on high...N-type Si-based type-Ⅰ clathrates with different Ga content were synthesized by combining the solid-state reaction method,melting method and spark plasma sintering (SPS) method.The effects of Ga composition on high temperature thermoelectric transport properties were investigated.The results show that at room temperature,the carrier concentration decreases, while the carrier mobility increases slightly with increasing Ga content.The Seebeck coefficient increases with increasing Ga content. Among all the samples,Ba7.93Ga17.13Si28.72exhibits higher Seebeck coefficient than the others and reaches -135μV·K^-1 at 1000 K.The sample prepared by this method exhibits very high electrical conductivity,and reaches 1.95x 10^5 S·m^-1 for Ba8.01Ga16.61Si28.93 at room temperature.The thermal conductivity of all samples is almost temperature independent in the temperature range of 300-1000 K,indicating the behaviour of a typical metal.The maximum ZT value of 0.75 is obtained at 1000 K for the compound Ba7.93Ga17.13Si28.72.展开更多
Single-crystal samples of type-VIII BasGa16-xCuxSn30 (x = 0, 0.03, 0.06, 0.15) clathrates were prepared using the Sn-flux method. At room temperature the carrier density, n, is 3.5-5 × 10^19 cm^-3 for all the s...Single-crystal samples of type-VIII BasGa16-xCuxSn30 (x = 0, 0.03, 0.06, 0.15) clathrates were prepared using the Sn-flux method. At room temperature the carrier density, n, is 3.5-5 × 10^19 cm^-3 for all the samples, the carrier mobility, μH, increases to more than twice that of BasGa16Sn30 for all the Cu doping samples, and consequently the electrical conductivity is enhanced distinctly from 1.90×10^4 S/m to 4.40 ×10^4 S/m, with the Cu composition increasing from x = 0 to x = 0.15. The Seebeck coefficient,α, decreases slightly with the increases in Cu composition. The values are about 0.72 W/mK at 300 K and are almost invariant with temperature up to 500 K for the samples with x = 0 and x = 0.03. The lattice thermal conductivity, μL, decreases from 0.59 W/InK for x = 0 to 0.50 W/mK for x = 0.03 at 300 K. The figure of merit for x = 0.03 reaches 1.35 at 540 K.展开更多
The site occupancies and thermoelectric properties of tin-based clathrates Cs8M4Sn44□2 (M = Zn, Cd, Hg) and CssSn44□2 were studied by the first principle calculations. We had provided an efficient way to probe the...The site occupancies and thermoelectric properties of tin-based clathrates Cs8M4Sn44□2 (M = Zn, Cd, Hg) and CssSn44□2 were studied by the first principle calculations. We had provided an efficient way to probe the relationship between the crystalline structure and power factor. Detailed analyses indicated the p states of Sn at 16i and 24k sites together with the p states of M substitute contributed significantly to the maximum power factor, yet Cs atoms nearly did not. The dangling bonds of vacancies in Cs8Snn44□2 are also discussed. The power factors of p- and n-type CssMaSn42 and Cs8Sn44□2 at optimal temperature and carder concentration are predicted. Our results suggest that Cs8ZnaSn44□2 is a promising candidate at the 5.25 ×10^19 cm-3 hole carrier concentration as a high temperature thermoelectric material that is competitive to the state-of-art Ge-based clathrate thermoelectric materials.展开更多
Bulk materials Ba_(8)Ga_(16)In_(x)Ge_(30-x)(x=0.5,1.0,1.5)were prepared by High-Pressure and High-Temperature(HPHT)method and the crystal structure has been confirmed by X-ray diffraction and cell refinement.The actua...Bulk materials Ba_(8)Ga_(16)In_(x)Ge_(30-x)(x=0.5,1.0,1.5)were prepared by High-Pressure and High-Temperature(HPHT)method and the crystal structure has been confirmed by X-ray diffraction and cell refinement.The actual In composition was much lower than the starting composition,and lattice constants increased with the increase of substitution.As the temperature increased,the Seebeck coefficient and electrical resistivity increased first and then decreased,while the thermal conductivity was the opposite,which leads to significant enhancement on thermoelectric properties of the clathrates.The substitution of indium elements decreased the seebeck coefficient and electrical resistivity,and also changed the microstructure of the compounds.A minimum thermal conductivity of 0.84Wm^(-1)1K^(-1)was obtained,and a good ZT value of 0.52 was achieved.The grain boundaries and lattice defects generated by high pressure can effectively scatter phonons of different frequencies,which reduce the lattice thermal conductivity.展开更多
In this paper, biochar (BC) was used as raw material, activated by deionizing aqueous solution, NaCl solution, CA solution and HCl solution respectively. Epichlorohydrin (EPI) was used as crosslinking agent, and β-cy...In this paper, biochar (BC) was used as raw material, activated by deionizing aqueous solution, NaCl solution, CA solution and HCl solution respectively. Epichlorohydrin (EPI) was used as crosslinking agent, and β-cyclodextrin (β-CD) was used to modify biochar (BC). The prepared modified biochar materials were labeled with β-CDBC, β-CDBC-Na, β-CDBC-CA and β-CDBC-H, respectively. The infrared spectrum, X-ray diffractometer, scanning electron microscope and specific surface area of the four modified materials were tested. The results showed that the C-O stretching vibration peak at 1020 cm<sup>−</sup><sup>1</sup> of the modified materials was slightly offset compared with that of biochar. The characteristic absorption peaks of XRD pattern decrease obviously at 2θ = 26.7˚ and 29.5˚. It can be obviously observed on the electron microscope image that the surface is loaded or formed clathrates, and BET data and graphs also show that the specific surface area of the modified biochar is larger. Therefore, β-cyclodextrin successfully modified biochar and formed clathrates on the surface of biochar or was loaded in the pore structure of biochar, especially β-CDBC-CA achieved better modification effect. Because biochar and β-cyclodextrin raw materials are cheap, easy to prepare and green, and less prone to secondary pollution, it has a good advantage in environmental governance.展开更多
Intermetallic clathrates are materials characterized by a large cage structure where guest atoms can move anharmonically,providing these materials exotic thermoelectric properties.Unfortunately,the dynamical and atomi...Intermetallic clathrates are materials characterized by a large cage structure where guest atoms can move anharmonically,providing these materials exotic thermoelectric properties.Unfortunately,the dynamical and atomic nature of the rattling phonons,and their interactions with the electronic structure,are not fully understood.Here,we report that a germanium isotope effect can trigger an inherent guest rattling and cage distortion in clathrate Ba8Ga16Ge30(BGG).Raman-scattering spectroscopy and advanced electron microscopy demonstrate that the atomic germanium isotope effect induces an offcentre rattling at the 6d sites as well as a tetrakaidecahedron deformation which is anisotropic for ntype BGG but isotropic for p-type BGG.The present findings indicate that the large n-type germanium isotope effect arises from the strong electron-phonon coupling,which opens up a novel avenue for manipulating dynamical motions of phonons via atomic isotope engineering.展开更多
It has been recognized that a small amount of propane mixed with methane can change greatly in not only the thermodynamics but also the structural properties of gas hydrate.However,its mechanism is still not well unde...It has been recognized that a small amount of propane mixed with methane can change greatly in not only the thermodynamics but also the structural properties of gas hydrate.However,its mechanism is still not well understood yet.In this research,structure-Ⅱ(sⅡ)hydrate is synthesized using a methanepropane gas mixture with an initial mole ratio of 99:1,and it is found that large(5~(12)6~4)cages are cooccupied by multiple gases based on the rigid structure analysis of neutron diffraction data.The first principles calculation and molecular dynamics simulation are conducted to uncover the molecular mechanism for sⅡmethane-propane hydrate formation,revealing that the presence of propane inhibits the formation of structure-Ⅰ(sⅠ)hydrate but promotes sⅡhydrate formation.The results help to understand the accumulation mechanism of natural gas hydrate and benefit to optimize the condition for gas storage and transportation in hydrate form.展开更多
Green alga Enteromorpha clathrata(E.clathrata)contains a variety of bioactive compounds,including polysaccharides,polyphenols and fat-soluble pigments etc.,among which polyphenols exhibit a wide range of medicinal pro...Green alga Enteromorpha clathrata(E.clathrata)contains a variety of bioactive compounds,including polysaccharides,polyphenols and fat-soluble pigments etc.,among which polyphenols exhibit a wide range of medicinal properties.E.clathrata polyphenols(ECPs)have shown various biological activities such as antioxidant,anti-inflammatory and antidiabetic effects;however,the potential of ECPs as an anti-cancer reagent remains unclear.The aim of this study was to investigate the anti-tumor activity and underlying mechanisms of ECPs on hepatocellular carcinoma.The cytotoxicity of Hepa1-6 cells was determined by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT)and lactate dehydrogenase(LDH)assay.Flow cytometry and fluorescence microscope analysis of cell apoptosis after annexin V-fluorescein isothiocyanate(FITC)/propidium iodide(PI)staining.2',7'-dichlorodihydrofluorescein diacetate(DCFH-DA)assay was used for intracellular reactive oxygen species(ROS)detection.caspase-9 activity was determined using cspase-9 colorimetric assay.Mitochondrial transmembrane potential(Δψm)was measured using JC-1.Western blot and quantitative real-time PCR(qPCR)were used to assess the expressions of the apoptosis regulators Bax,Bcl-2,cytochrome c and caspase-3.It was found that ECPs showed a dose-dependent cytotoxicity against Hepa1-6 cells by inducing apoptosis.The apoptosis in ECPs-treated Hepa1-6 cells was accompanied by the loss of mitochondrial membrane potential,elevated ROS generation,increased release of mitochondrial cytochrome c,and up-regulation of caspase-9 and caspase-3.The expressions of Bax(pro-apoptotic molecule)and Bcl-2(apoptosis suppressor)were up-regulated and down-regulated,respectively,at both mRNA and protein levels.These molecular alterations revealed that ECPs caused apoptosis of cells through the mitochondrial pathway,suggesting that ECPs are potential candidates to be developed for liver cancer treatment.展开更多
Recently,a new phase C'_(1) H_(2) hydrate was experimentally identified.In this work,the diffusive behaviors of H_(2) in C'_(1)phase clathrate hydrate are explored using classic molecular dynamics(MD)simulatio...Recently,a new phase C'_(1) H_(2) hydrate was experimentally identified.In this work,the diffusive behaviors of H_(2) in C'_(1)phase clathrate hydrate are explored using classic molecular dynamics(MD)simulations.It reveals that the cage occupancy by H_(2) molecule negligibly influences the C'_(1) phase clathrate structure but greatly dictates the diffusion coefficient of H_(2)molecule.Due to the small cage size and small windows connecting the neighboring cages in C'_(1) phase clathrate,nonoccupancy of the neighboring cages is demanded to enable the diffusion of H_(2) molecule that is primarily dominated by hopping mechanism.Moreover,the analysis of diffusive free energy landscape reveals lower energy barrier of H_(2) molecule in C'_(1) phase clathrate hydrate than that of other gases in conventional clathrate hydrates,and that H_(2) molecule travels through the windows between neighboring cages with preferential molecular orientation.This study provides critical physical insights into the diffusion behaviors of H_(2) in the C'_(1) phase clathrate hydrate,and implies that the C'_(1) clathrate hydrate is a promising solid structure for the next-generation H_(2) storage.展开更多
CO2 capture by hydrate formation is a novel gas separation technology, by which CO2 is selectively engaged in the cages of hydrate and is separated with other gases, based on the differences of phase equilibrium for C...CO2 capture by hydrate formation is a novel gas separation technology, by which CO2 is selectively engaged in the cages of hydrate and is separated with other gases, based on the differences of phase equilibrium for CO2 and other gases. However. rigorous temperature and pressure, high energy cost and industrialized hydration separator dragged the development of the hydrate based CO2 capture. In this paper, the key problems in CO2 capture from the different sources such as shifted synthesis gas, flue gas and sour natural gas or biogas were analyzed. For shifted synthesis gas and flue gas, its high energy consumption is the barrier, and for the sour natural gas or biogas (CO2/CH4 system), the bottleneck is how to enhance the selectivity of CO2 hydration. For these gases, scale-up is the main difficulty. Also, this paper explored the possibility of separating different gases by selective hydrate formation and reviewed the progress of CO2 separation from shifted synthesis gas, flue gas and sour natural gas or biogas.展开更多
The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon ...The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon nanotubes,on the kinetics of methane hydrate formation was investigated in this work.The experiments were carried out at a pressure of 4.5 MPa and a temperature of 0 ℃ in a batch reactor.By adding nanostructures,the induction time decreases,and the shortest induction time appeares at certain concentrations of reduced graphene oxide with SDS and graphene oxide,that is,at a concentration of 360 ppm for reduced graphene oxide with SDS and 180 ppm for graphene oxide,with a 98% decrease in induction time compared to that in pure water.Moreover,utilization of carbon nanostructures increases the amount and the rate of methane consumed during the hydrate formation process.Utilization of multi-walled carbon nanotubes with a concentration of 90 ppm showes the highest amount of methane consumption.The amount of methane consumption increases by 173% in comparison with that in pure water.The addition of carbon nanostructures does not change the storage capacity of methane hydrate in the hydrate formation process,while the percentage of water conversion to hydrate in the presence of carbon nanotubes increases considerably,the greatest value of which occurres at a 90 ppm concentration of carbon nanotubes,that is,a 253% increase in the presence of carbon nanotubes compared to that of pure water.展开更多
Gas hydrate is a new technology for energy gas(methane/hydrogen)storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methan...Gas hydrate is a new technology for energy gas(methane/hydrogen)storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methane,the main problems are low formation rateand storage capacity,which can be solved by strengthening mass andheat transfer,such as adding additives,stirring,bubbling,etc.Onekind of additives can change the equilibrium curve to reduce the formation pressure of methane hydrate,and the other kind of additivesis surfactant,which can form micelle with water and increase the interface of water-gas.Dry water has the similar effects on the methanehydrate as surfactant.Additionally,stirring,bubbling,and sprayingcan increase formation rate and storage capacity due to mass transferstrengthened.Inserting internal or external heat exchange also canimprove formation rate because of good heat transfer.For hydrogen,the main difficulties are very high pressure for hydrate formed.Tetrahydrofuran(THF),tetrabutylammonium bromide(TBAB) andtetrabutylammonium fluoride(TBAF) have been proved to be able todecrease the hydrogen hydrate formation pressure significantly.展开更多
Study on the microscopic structure of clathrate hydrate has made significant progress in the past decades.This review aims to summarize the state of the art of the experimental characterization of guest molecular occu...Study on the microscopic structure of clathrate hydrate has made significant progress in the past decades.This review aims to summarize the state of the art of the experimental characterization of guest molecular occupancy in clathrate hydrate cages,which is an important area of the microscopic structures.The characterizing method and features of different guest molecular,such as hydrocarbon,carbon dioxide,hydrogen and inhibitor/promoter,in different hydrate cages have been extensively reviewed.A comprehensive use of advanced technologies such as X-ray diffraction,Raman spectroscopy and nuclear magnetic resonance may provide better understanding on the compositions and microscopic mechanisms of clathrate hydrate.展开更多
Using transient plane source technique, we measured THF hydrate thermal conductivity from 243 K to 263 K. The sample THF solution is over saturated in order to avoid the effect of ice. And also to avoid the effect of ...Using transient plane source technique, we measured THF hydrate thermal conductivity from 243 K to 263 K. The sample THF solution is over saturated in order to avoid the effect of ice. And also to avoid the effect of crystal anisotropy, the THF hydrate was crushed to measure. In the test temperature value increases with the temperature increasing.展开更多
In this paper, the effect of adding different concentrations of kinetic inhibitors on the induction time of hydrogen sulfide hydrate formation in a reactor equipped with automatic adjustable temperature controller is ...In this paper, the effect of adding different concentrations of kinetic inhibitors on the induction time of hydrogen sulfide hydrate formation in a reactor equipped with automatic adjustable temperature controller is studied. A novel method namely "sudden cooling" is used for performing the relevant measurements, in which the induction time of H2S hydrate in the presence/absence of PVP and L-tyrosine with different concentrations (100, 500, and 1000 ppm) is determined. As a result, PVP with the concentration of 1000 ppm in aqueous solution is detected as a more suitable material for increasing the induction time of H2S hydrate formation among the investigated kinetic hydrate inhibitors.展开更多
文摘Four types of nanoparticles,amorphous carbon,ironⅢoxide,SiO2,and amino-coated SiO2,were tested to determine changes in tetrahydrofuran-water(THF-water)clathrate hydrate nucleation and agglomeration.Rates were experimentally found to determine their viability for preventing natural gas hydrates from developing during offshore drilling operations.THF-water clathrates were chosen as a model to represent gas hydrate growth at atmospheric pressure.Concentrations of each nanoparticle between 0.15%and 1.0%by weight were tested as a kinetic inhibitor to hydrate formation.Tests were repeated at various temperatures below the formation temperature of 4.4℃for THF-water clathrate hydrates.Measurements were made to identify how the concentration of THF affects the clathrate hydrates forming under static conditions between20%and 30%by mole of THF.The primary tests in this study were performed using a 20:80 THF/water ratio.Temperature increases during hydrate nucleation for THF-water were measured between-5 and 3℃.The range of ideal nanoparticle concentrations was found to be between 0.15%and 0.45%by weight for optimal static,kinetic inhibition of hydrate nucleation.At approximately 0.3%by weight,the most significant inhibition was observed under static conditions for all four types of nanoparticles tested.We found that functionalized amino-coated SiO2 nanoparticles,across all tests,significantly increased the time required for the formation of THF-water clathrate hydrates compared to the other three non-functionalized nanoparticles.The amorphous carbon and ironⅢoxide nanoparticles performed similarly across each test and were both the least effective in their inhibition of the clathrate hydrates of the four nanoparticles studied compared to a control.
基金Supported by the National Natural Science Foundation of China under Grant No 51262032
文摘Single-crystalline samples of Eu/Ba-filled Sn-based type-Ⅷ clathrate are prepared by the Ga flux method with different stoichiometric ratios. The electrical transport properties of the samples are optimized by Eu doping. Results indicate that Eu atoms tend to replace Ba atoms. With the increase of the Eu initial content, the carrier density increases and the carrier mobility decreases, which leads to an increase of the Seebeck coefficient. By contrast, the electrical conductivity decreases. Finally, the sample with Eu initial content of x = 0.75 behaves with excellent electrical properties, which shows a maximal power factor of 1.51 mW·m^-1K^-2 at 480K, and the highest ZT achieved is 0.87 near the temperature of 483K.
基金Project supported by the National Basic Research Program of China (Grant Nos 2007CB607501 and 2007CB607503)Yunnan Natural Science Fund (Grant No 2008CD114)
文摘N-type Si-based type-Ⅰ clathrates with different Ga content were synthesized by combining the solid-state reaction method,melting method and spark plasma sintering (SPS) method.The effects of Ga composition on high temperature thermoelectric transport properties were investigated.The results show that at room temperature,the carrier concentration decreases, while the carrier mobility increases slightly with increasing Ga content.The Seebeck coefficient increases with increasing Ga content. Among all the samples,Ba7.93Ga17.13Si28.72exhibits higher Seebeck coefficient than the others and reaches -135μV·K^-1 at 1000 K.The sample prepared by this method exhibits very high electrical conductivity,and reaches 1.95x 10^5 S·m^-1 for Ba8.01Ga16.61Si28.93 at room temperature.The thermal conductivity of all samples is almost temperature independent in the temperature range of 300-1000 K,indicating the behaviour of a typical metal.The maximum ZT value of 0.75 is obtained at 1000 K for the compound Ba7.93Ga17.13Si28.72.
基金Project supported by the National Natural Science Foundation of China(Grant No.50902119)
文摘Single-crystal samples of type-VIII BasGa16-xCuxSn30 (x = 0, 0.03, 0.06, 0.15) clathrates were prepared using the Sn-flux method. At room temperature the carrier density, n, is 3.5-5 × 10^19 cm^-3 for all the samples, the carrier mobility, μH, increases to more than twice that of BasGa16Sn30 for all the Cu doping samples, and consequently the electrical conductivity is enhanced distinctly from 1.90×10^4 S/m to 4.40 ×10^4 S/m, with the Cu composition increasing from x = 0 to x = 0.15. The Seebeck coefficient,α, decreases slightly with the increases in Cu composition. The values are about 0.72 W/mK at 300 K and are almost invariant with temperature up to 500 K for the samples with x = 0 and x = 0.03. The lattice thermal conductivity, μL, decreases from 0.59 W/InK for x = 0 to 0.50 W/mK for x = 0.03 at 300 K. The figure of merit for x = 0.03 reaches 1.35 at 540 K.
基金Supported by the 973 program(No.2010CB933501)NNSFC(Nos.20973175,21233009,and 21103190)
文摘The site occupancies and thermoelectric properties of tin-based clathrates Cs8M4Sn44□2 (M = Zn, Cd, Hg) and CssSn44□2 were studied by the first principle calculations. We had provided an efficient way to probe the relationship between the crystalline structure and power factor. Detailed analyses indicated the p states of Sn at 16i and 24k sites together with the p states of M substitute contributed significantly to the maximum power factor, yet Cs atoms nearly did not. The dangling bonds of vacancies in Cs8Snn44□2 are also discussed. The power factors of p- and n-type CssMaSn42 and Cs8Sn44□2 at optimal temperature and carder concentration are predicted. Our results suggest that Cs8ZnaSn44□2 is a promising candidate at the 5.25 ×10^19 cm-3 hole carrier concentration as a high temperature thermoelectric material that is competitive to the state-of-art Ge-based clathrate thermoelectric materials.
基金This workwas financially supported by National Natural Science Foundation of China(51171070)the Project of Jilin Science and Technology Development Plan(20170101045JC).
文摘Bulk materials Ba_(8)Ga_(16)In_(x)Ge_(30-x)(x=0.5,1.0,1.5)were prepared by High-Pressure and High-Temperature(HPHT)method and the crystal structure has been confirmed by X-ray diffraction and cell refinement.The actual In composition was much lower than the starting composition,and lattice constants increased with the increase of substitution.As the temperature increased,the Seebeck coefficient and electrical resistivity increased first and then decreased,while the thermal conductivity was the opposite,which leads to significant enhancement on thermoelectric properties of the clathrates.The substitution of indium elements decreased the seebeck coefficient and electrical resistivity,and also changed the microstructure of the compounds.A minimum thermal conductivity of 0.84Wm^(-1)1K^(-1)was obtained,and a good ZT value of 0.52 was achieved.The grain boundaries and lattice defects generated by high pressure can effectively scatter phonons of different frequencies,which reduce the lattice thermal conductivity.
文摘In this paper, biochar (BC) was used as raw material, activated by deionizing aqueous solution, NaCl solution, CA solution and HCl solution respectively. Epichlorohydrin (EPI) was used as crosslinking agent, and β-cyclodextrin (β-CD) was used to modify biochar (BC). The prepared modified biochar materials were labeled with β-CDBC, β-CDBC-Na, β-CDBC-CA and β-CDBC-H, respectively. The infrared spectrum, X-ray diffractometer, scanning electron microscope and specific surface area of the four modified materials were tested. The results showed that the C-O stretching vibration peak at 1020 cm<sup>−</sup><sup>1</sup> of the modified materials was slightly offset compared with that of biochar. The characteristic absorption peaks of XRD pattern decrease obviously at 2θ = 26.7˚ and 29.5˚. It can be obviously observed on the electron microscope image that the surface is loaded or formed clathrates, and BET data and graphs also show that the specific surface area of the modified biochar is larger. Therefore, β-cyclodextrin successfully modified biochar and formed clathrates on the surface of biochar or was loaded in the pore structure of biochar, especially β-CDBC-CA achieved better modification effect. Because biochar and β-cyclodextrin raw materials are cheap, easy to prepare and green, and less prone to secondary pollution, it has a good advantage in environmental governance.
基金National Natural Science Foundation of China(NSFC)(grant no.11274234)R.A.thanks the financial supports from NSFC(grant no.51771126)+4 种基金Youth Foundation of Science&Technology Department of Sichuan Province(grant no.2016JQ0051)Sichuan University Talent Introduction Research Funding(grant no.YJ201537)Sichuan University Outstanding Young Scholars Research Funding(grant no.2015SCU04A20)P.R.and S.-F.W.acknowledge support from NSFC(grant nos.11274362 and 11674371)the Ministry of Science and Technology of China(grant nos.2015CB921000,2016YFA0401000 and 2016YFA0300300).J.T.thank Xiangjun Wei and Xiaolong Li for their useful discussion on PXRD data.
文摘Intermetallic clathrates are materials characterized by a large cage structure where guest atoms can move anharmonically,providing these materials exotic thermoelectric properties.Unfortunately,the dynamical and atomic nature of the rattling phonons,and their interactions with the electronic structure,are not fully understood.Here,we report that a germanium isotope effect can trigger an inherent guest rattling and cage distortion in clathrate Ba8Ga16Ge30(BGG).Raman-scattering spectroscopy and advanced electron microscopy demonstrate that the atomic germanium isotope effect induces an offcentre rattling at the 6d sites as well as a tetrakaidecahedron deformation which is anisotropic for ntype BGG but isotropic for p-type BGG.The present findings indicate that the large n-type germanium isotope effect arises from the strong electron-phonon coupling,which opens up a novel avenue for manipulating dynamical motions of phonons via atomic isotope engineering.
基金supported by the National Key Research and Development Program of China(2016YFA0401503 and 2018YFA0305700)the National Natural Science Foundation of China(11575288,91934303,21935001 and 11775011)+4 种基金the Strategic Priority Research ProgramKey Research Program of Frontier Sciences of the Chinese Academy of Sciences(XDB33000000,XDB25000000 and QYZDBSSW-SLH013)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(Y202003)the China Geological Survey(DD20190234)the Scientific Instrument Developing Project(ZDKYYQ20170001)of the Chinese Academy of Sciences。
文摘It has been recognized that a small amount of propane mixed with methane can change greatly in not only the thermodynamics but also the structural properties of gas hydrate.However,its mechanism is still not well understood yet.In this research,structure-Ⅱ(sⅡ)hydrate is synthesized using a methanepropane gas mixture with an initial mole ratio of 99:1,and it is found that large(5~(12)6~4)cages are cooccupied by multiple gases based on the rigid structure analysis of neutron diffraction data.The first principles calculation and molecular dynamics simulation are conducted to uncover the molecular mechanism for sⅡmethane-propane hydrate formation,revealing that the presence of propane inhibits the formation of structure-Ⅰ(sⅠ)hydrate but promotes sⅡhydrate formation.The results help to understand the accumulation mechanism of natural gas hydrate and benefit to optimize the condition for gas storage and transportation in hydrate form.
基金the National Key R&D Program of China(No.2018YFD0901105)the Ningbo Natural Science Foundation(No.202003N4128)the Scientific Research Foundation of Graduate School of Ningbo University(No.IF2021085)。
文摘Green alga Enteromorpha clathrata(E.clathrata)contains a variety of bioactive compounds,including polysaccharides,polyphenols and fat-soluble pigments etc.,among which polyphenols exhibit a wide range of medicinal properties.E.clathrata polyphenols(ECPs)have shown various biological activities such as antioxidant,anti-inflammatory and antidiabetic effects;however,the potential of ECPs as an anti-cancer reagent remains unclear.The aim of this study was to investigate the anti-tumor activity and underlying mechanisms of ECPs on hepatocellular carcinoma.The cytotoxicity of Hepa1-6 cells was determined by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT)and lactate dehydrogenase(LDH)assay.Flow cytometry and fluorescence microscope analysis of cell apoptosis after annexin V-fluorescein isothiocyanate(FITC)/propidium iodide(PI)staining.2',7'-dichlorodihydrofluorescein diacetate(DCFH-DA)assay was used for intracellular reactive oxygen species(ROS)detection.caspase-9 activity was determined using cspase-9 colorimetric assay.Mitochondrial transmembrane potential(Δψm)was measured using JC-1.Western blot and quantitative real-time PCR(qPCR)were used to assess the expressions of the apoptosis regulators Bax,Bcl-2,cytochrome c and caspase-3.It was found that ECPs showed a dose-dependent cytotoxicity against Hepa1-6 cells by inducing apoptosis.The apoptosis in ECPs-treated Hepa1-6 cells was accompanied by the loss of mitochondrial membrane potential,elevated ROS generation,increased release of mitochondrial cytochrome c,and up-regulation of caspase-9 and caspase-3.The expressions of Bax(pro-apoptotic molecule)and Bcl-2(apoptosis suppressor)were up-regulated and down-regulated,respectively,at both mRNA and protein levels.These molecular alterations revealed that ECPs caused apoptosis of cells through the mitochondrial pathway,suggesting that ECPs are potential candidates to be developed for liver cancer treatment.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.12172314,11772278,and 11904300)the Jiangxi Provincial Outstanding Young Talents Program(Grant No.20192BCBL23029)+2 种基金the Fundamental Research Funds for the Central Universities(Xiamen University:Grant Nos.20720210025 and 20720220023)the Research Council of Norway(Grant No.262644)the 111 project(Grant No.B16029)。
文摘Recently,a new phase C'_(1) H_(2) hydrate was experimentally identified.In this work,the diffusive behaviors of H_(2) in C'_(1)phase clathrate hydrate are explored using classic molecular dynamics(MD)simulations.It reveals that the cage occupancy by H_(2) molecule negligibly influences the C'_(1) phase clathrate structure but greatly dictates the diffusion coefficient of H_(2)molecule.Due to the small cage size and small windows connecting the neighboring cages in C'_(1) phase clathrate,nonoccupancy of the neighboring cages is demanded to enable the diffusion of H_(2) molecule that is primarily dominated by hopping mechanism.Moreover,the analysis of diffusive free energy landscape reveals lower energy barrier of H_(2) molecule in C'_(1) phase clathrate hydrate than that of other gases in conventional clathrate hydrates,and that H_(2) molecule travels through the windows between neighboring cages with preferential molecular orientation.This study provides critical physical insights into the diffusion behaviors of H_(2) in the C'_(1) phase clathrate hydrate,and implies that the C'_(1) clathrate hydrate is a promising solid structure for the next-generation H_(2) storage.
基金the National Natural Science Foundation of China(Grant No.51176051 and 51106054)the National Basic Research Program of China(973 Program,No.2009CB219504-03)
文摘CO2 capture by hydrate formation is a novel gas separation technology, by which CO2 is selectively engaged in the cages of hydrate and is separated with other gases, based on the differences of phase equilibrium for CO2 and other gases. However. rigorous temperature and pressure, high energy cost and industrialized hydration separator dragged the development of the hydrate based CO2 capture. In this paper, the key problems in CO2 capture from the different sources such as shifted synthesis gas, flue gas and sour natural gas or biogas were analyzed. For shifted synthesis gas and flue gas, its high energy consumption is the barrier, and for the sour natural gas or biogas (CO2/CH4 system), the bottleneck is how to enhance the selectivity of CO2 hydration. For these gases, scale-up is the main difficulty. Also, this paper explored the possibility of separating different gases by selective hydrate formation and reviewed the progress of CO2 separation from shifted synthesis gas, flue gas and sour natural gas or biogas.
文摘The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon nanotubes,on the kinetics of methane hydrate formation was investigated in this work.The experiments were carried out at a pressure of 4.5 MPa and a temperature of 0 ℃ in a batch reactor.By adding nanostructures,the induction time decreases,and the shortest induction time appeares at certain concentrations of reduced graphene oxide with SDS and graphene oxide,that is,at a concentration of 360 ppm for reduced graphene oxide with SDS and 180 ppm for graphene oxide,with a 98% decrease in induction time compared to that in pure water.Moreover,utilization of carbon nanostructures increases the amount and the rate of methane consumed during the hydrate formation process.Utilization of multi-walled carbon nanotubes with a concentration of 90 ppm showes the highest amount of methane consumption.The amount of methane consumption increases by 173% in comparison with that in pure water.The addition of carbon nanostructures does not change the storage capacity of methane hydrate in the hydrate formation process,while the percentage of water conversion to hydrate in the presence of carbon nanotubes increases considerably,the greatest value of which occurres at a 90 ppm concentration of carbon nanotubes,that is,a 253% increase in the presence of carbon nanotubes compared to that of pure water.
基金supported by the National 863 Program (2007AA03Z229)the Fundamental Research Funds for the Central Universities (2009ZM0185)
文摘Gas hydrate is a new technology for energy gas(methane/hydrogen)storage due to its large capacity of gas storage and safe.But industrial application of hydrate storage process was hindered by someproblems.For methane,the main problems are low formation rateand storage capacity,which can be solved by strengthening mass andheat transfer,such as adding additives,stirring,bubbling,etc.Onekind of additives can change the equilibrium curve to reduce the formation pressure of methane hydrate,and the other kind of additivesis surfactant,which can form micelle with water and increase the interface of water-gas.Dry water has the similar effects on the methanehydrate as surfactant.Additionally,stirring,bubbling,and sprayingcan increase formation rate and storage capacity due to mass transferstrengthened.Inserting internal or external heat exchange also canimprove formation rate because of good heat transfer.For hydrogen,the main difficulties are very high pressure for hydrate formed.Tetrahydrofuran(THF),tetrabutylammonium bromide(TBAB) andtetrabutylammonium fluoride(TBAF) have been proved to be able todecrease the hydrogen hydrate formation pressure significantly.
基金Supported by the National Natural Science Foundation of China(51706248,51876222)National Key R&D Program of China(2017YFC0307304)
文摘Study on the microscopic structure of clathrate hydrate has made significant progress in the past decades.This review aims to summarize the state of the art of the experimental characterization of guest molecular occupancy in clathrate hydrate cages,which is an important area of the microscopic structures.The characterizing method and features of different guest molecular,such as hydrocarbon,carbon dioxide,hydrogen and inhibitor/promoter,in different hydrate cages have been extensively reviewed.A comprehensive use of advanced technologies such as X-ray diffraction,Raman spectroscopy and nuclear magnetic resonance may provide better understanding on the compositions and microscopic mechanisms of clathrate hydrate.
文摘Using transient plane source technique, we measured THF hydrate thermal conductivity from 243 K to 263 K. The sample THF solution is over saturated in order to avoid the effect of ice. And also to avoid the effect of crystal anisotropy, the THF hydrate was crushed to measure. In the test temperature value increases with the temperature increasing.
文摘In this paper, the effect of adding different concentrations of kinetic inhibitors on the induction time of hydrogen sulfide hydrate formation in a reactor equipped with automatic adjustable temperature controller is studied. A novel method namely "sudden cooling" is used for performing the relevant measurements, in which the induction time of H2S hydrate in the presence/absence of PVP and L-tyrosine with different concentrations (100, 500, and 1000 ppm) is determined. As a result, PVP with the concentration of 1000 ppm in aqueous solution is detected as a more suitable material for increasing the induction time of H2S hydrate formation among the investigated kinetic hydrate inhibitors.