ZrCo alloy holds great promise for hydrogen isotope storage,yet its susceptibility to poisoning by impurity gases,especially CO,poses a challenge.This susceptibility arises due to the electron acceptor nature of the s...ZrCo alloy holds great promise for hydrogen isotope storage,yet its susceptibility to poisoning by impurity gases,especially CO,poses a challenge.This susceptibility arises due to the electron acceptor nature of the surface Co element and the formation of the d-πfeedback bond,thereby impeding the surface hydrogen dissociation.Accordingly,we propose a novel local activity modulation strategy,where substituent elements are sacrificed to protect the active Co sites for hydrogen dissociation.Considering CO absorption capacity,solid solubility,and hydrogen affinity,we selected V,Cr,and Mn as microalloying elements and successfully prepared the single-phase ZrCo_(0.97)(VCrMn)_(0.03)alloy.Compared to pristine ZrCo,ZrCo_(0.97)(VCrMn)_(0.03)demonstrates significantly enhanced poisoning resistance.Notably,the hydrogenation kinetics of ZrCo_(0.97)(VCrMn)_(0.03)is 2.4 times higher than that of ZrCo in 4 bar H_(2)+5000 ppm CO.Interestingly,the controllable in situ formation of the Co_(2)C phase shell structure during cycling further safeguards the surface reactivity of ZrCo_(0.97)(VCrMn)_(0.03).Consequently,its capacity retention ratio after 25 cycles has been improved to 74.5%from 55.3%of the ZrCo alloy.These findings suggest that micro-alloying engineering could be a promising strategy for surface activity modulation to enhance the anti-poisoning properties of hydrogen storage materials.展开更多
Fluorosurfactants are the key ingredients in the formulations of aqueous film-forming foams(AFFFs)for extinguishing flammable liquids,thus developing high-efficient and low-toxic fluorosurfactants is desirable in AFFF...Fluorosurfactants are the key ingredients in the formulations of aqueous film-forming foams(AFFFs)for extinguishing flammable liquids,thus developing high-efficient and low-toxic fluorosurfactants is desirable in AFFFs application.Herein,a series of hyperbranched polymeric fluorosu rfactants(HPFs)were successfully synthesized through sequentially modifying hyperbranched polyethylenimine(PEI)with the hydrophilic poly(ethylene glycol)(PEG)chains and the hydrophobic C6/C4-based perfluoroalkyl chains,which were verified by FTIR,^(1)H-and^(19)F-NMR.The surface tensions of all the HPFs in water were measured,and the corresponding physicochemical parameters were interpreted.It was found that the surface activities of HPFs could be tuned through adjusting the ratio of PEG to perfluoroalkyl chains,the length of perfluoroalkyl chains,the molecular weight of PEI core,but not the PEG chain length.In the binary mixture of HPFs with the commercial small molecule fluorosurfactant Capstone^(TM)1157(C1157),a strong synergism led to the elevation of surface activity,which was attributed to the efficient encapsulation of C1157 vips by the compact hyperbranched HPFs as the hosts.The utilization of HPF/C1157 as fluorosurfactant ingredients in AFFF formulations could realize much higher fire-extinguishing efficiency towards flammable oils than the control AFFFs prepa red from the polymeric Capstone^(TM)1460 or the neat C1157.展开更多
The magnetism and surface behaviour of Pt-Dy/γ-Al_2O_3 catalysts were studied respectively by means of a Faraday magnetic balance and the method of carbon disulfide.The ferromagnetic impurity in the support,γ-Al_2O_...The magnetism and surface behaviour of Pt-Dy/γ-Al_2O_3 catalysts were studied respectively by means of a Faraday magnetic balance and the method of carbon disulfide.The ferromagnetic impurity in the support,γ-Al_2O_3,at low temperature was corrected for the first time.The magnetic susceptibilities of the cat- alysts follow the sequence in different stage of preparation:χ_(uncalcined)<χ_(calcined)<χ_(reduced). The magnetic susceptibilities of the catalysts decrease as they adsorb hydrogen,cyclohexane or benzene. There is a correlation between the aromatization yield of cyclohexane or heptane on these catalysts and the magnetic susceptibility of the catalysts.Since addition of Dy increases the number of adsorption sites and the relevant proportions of weak adsorption sites,the abilities of sulfur-resistance and cyclohexane dehydrogenation are improved.In Pt-Dy/γ-A:_2O_3 catalysts,Dy improves the aromatization activity and stability of the catalyst and plays the role of the electron promoter.展开更多
A key feature that distinguishes cancer cells from all other cells is their capability to spread throughout the body.Although how cancer cells collectively migrate by following molecular rules which influence the stat...A key feature that distinguishes cancer cells from all other cells is their capability to spread throughout the body.Although how cancer cells collectively migrate by following molecular rules which influence the state of cell-cell adhesion contacts has been comprehensively formulated,the impact of physical interactions on cell spreading remains less understood.Cumulative effects of physical interactions exist as the interplay between various physical parameters such as(1)tissue surface tension,(2)viscoelasticity caused by collective cell migration,and(3)solid stress accumulated in the cell aggregate core region.This review aims to point out the role of these physical parameters in cancer cell spreading by considering and comparing the rearrangement of various mono-cultured cancer and epithelial model systems such as the fusion of two cell aggregates.While epithelial cells undergo volumetric cell rearrangement driven by the tissue surface tension,which directs cell movement from the surface to the core region of two-aggregate systems,cancer cells rather perform surface cell rearrangement.Cancer cells migrate toward the surface of the two-aggregate system driven by the solid stress while the surface tension is significantly reduced.The solid stress,accumulated in the core region of the two-aggregate system,is capable of suppressing the movement of epithelial cells that can undergo the jamming state transition;however,this stress enhances the movement of cancer cells.We have focused here on the multi-scale rheological modeling approaches that aimed at reproducing and understanding these biological systems.展开更多
The chemical structure of newly synthesized cationic surfactants based on Schiff base was confirmed using Fourier transform infrared spectroscopy,proton nuclear magnetic resonance spectroscopy,and mass spectroscopy.Th...The chemical structure of newly synthesized cationic surfactants based on Schiff base was confirmed using Fourier transform infrared spectroscopy,proton nuclear magnetic resonance spectroscopy,and mass spectroscopy.The synthesized surfactants were used in the synthesis of silver nanoparticles by a simple one-step method.The silver nanoparticle（AgNPs） formation was confirmed using transmission electron microscopy（TEM）,electron diffraction（SAED）,dynamic light scattering（DLS）,and energy dispersive X-ray spectroscopy（EDX）.The structure of the surfactant played an important role in the synthesis process.Increasing the hydrophobic chain length,the stability,and the amount of surfactant increased the quantity of AgNPs formed.The surface activity of the synthesized cationic surfactants was determined using surface tension measurements at three different temperatures.The synthesized surfactants showed a high tendency toward adsorption and micellization.Increasing the hydrophobic chain length of the synthesized surfactant increased its adsorption.Screening the synthesized cationic surfactants and their nano-form against bacteria and fungi showed that they are highly effective.The silver nanoparticles enhanced the biological activity of the synthesized cationic surfactants.展开更多
In this paper,we examine an illegal wireless communication network consisting of an illegal user receiving illegal signals from an illegal station and propose an active reconfigurable intelligent surface(ARIS)-assiste...In this paper,we examine an illegal wireless communication network consisting of an illegal user receiving illegal signals from an illegal station and propose an active reconfigurable intelligent surface(ARIS)-assisted multi-antenna jamming(MAJ)scheme denoted by ARIS-MAJ to interfere with the illegal signal transmission.In order to strike a balance between the jamming performance and the energy consumption,we consider a so-called jamming energy efficiency(JEE)which is defined as the ratio of achievable rate reduced by the jamming system to the corresponding power consumption.We formulate an optimization problem to maximize the JEE for the proposed ARIS-MAJ scheme by jointly optimizing the jammer’s beamforming vector and ARIS’s reflecting coefficients under the constraint that the jamming power received at the illegal user is lower than the illegal user’s detection threshold.To address the non-convex optimization problem,we propose the Dinkelbach-based alternating optimization(AO)algorithm by applying the semidefinite relaxation(SDR)algorithm with Gaussian randomization method.Numerical results validate that the proposed ARIS-MAJ scheme outperforms the passive reconfigurable intelligent surface(PRIS)-assisted multi-antenna jamming(PRIS-MAJ)scheme and the conventional multiantenna jamming scheme without RIS(NRIS-MAJ)in terms of the JEE.展开更多
The soot surface growth plays significant role on the soot mass accumulation,which starts with H(hydrogen)atom abstraction forming activated soot surface sites,and is followed by the acetylene addition process.In this...The soot surface growth plays significant role on the soot mass accumulation,which starts with H(hydrogen)atom abstraction forming activated soot surface sites,and is followed by the acetylene addition process.In this study,the effect of the mixture inhomogeneity and combustion temperature on the soot surface activity and soot formation was investigated by developing a new multi-step phenomenological(MSP)soot model of diesel engines.A new detailed soot surface growth mechanism was proposed by correlation analysis of combustion parameters with soot formation.The inhomogeneity coefficient of soot surface activityαCH and the specific rate of soot surface growth R CH were derived to highlight the effect of inhomogeneity of mixture and combustion temperature on soot formation.The predicted diesel engine-out soot agreed well with experimental findings in wide ranges of combustion conditions.In the case of lower engine load with single fuel injection and higher EGR(exhaust gas recirculation)rate,it had quiet homogeneous mixtures before ignition when the combustion temperature dominated the soot surface activity.At medium engine load with multi-pulse fuel injections,it got mixture slightly stratified before ignition and revealed that the mixture inhomogeneity became more dominated on soot surface activity than the combustion temperature.An increased soot surface activity led to increased soot emission.Under the full engine loads with single fuel injection but quite high boost pressure over 0.4 MPa,it led to the combustion conditions of higher mixture density and higher mixture heat capacity,which benefits the mixture homogeneity.The decay rate of soot surface activity became lower due to the decreased combustion temperature and the soot surface activity decreased due to improved mixture homogeneity.In addition,the lowered intake oxygen concentration due to usage of EGR played a role to lower the specific rate of soot surface growth R CH,but to increase the soot surface activityαCH.展开更多
Mixing hydrocarbon surfactants with fluorocarbon surfactants is still an important strategy to improve the economic benefits and performances of fluorocarbon surfactants and expand their range of application.Herein,we...Mixing hydrocarbon surfactants with fluorocarbon surfactants is still an important strategy to improve the economic benefits and performances of fluorocarbon surfactants and expand their range of application.Herein,we prepared a novel kind of hydrocarbon-fluorocarbon surfactant mixtures via mixing a cationic surfactant,cetyltrimethylammonium bromide(CTAB),with a tri-block nonionic short-chain fluorocarbon surfactant(F_(9)EG_(13)F_(9))in aqueous solution.The results showed that adding a small CTAB amount to F_(9)EG_(13)F_(9)(the molar fraction of CTAB in the mixture(x_(1))was 0.2)could greatly reduce its critical micelle concentrations(cmc)from 0.408mmol/L to 0.191 mmol/L.At this x_(1),the contact angle of the mixture was the minimum(57.7°)at 100 s on polytetrafluoroethylene film,which was even lower than that of F_(9)EG_(13)F_(9).Besides,CTAB/F_(9)EG_(13)F_(9) mixtures possessed better colloidal stability and solubilization ability toward hydrophobic dye(SudanІ)than F_(9)EG_(13)F_(9).The outstanding performances of binary surfactant mixtures benefited from the non-ideal mixing and strong synergistic effect evidence that CTAB/F_(9)EG_(13)F_(9) surfactant mixtures could be used in practical applications instead of individual F_(9)EG_(13)F_(9),thereby reducing the used cost of F_(9)EG_(13)F_(9).展开更多
α‐,β‐,δ‐,andγ‐MnO2nanocrystals are successfully prepared.We then evaluated the NH3selective catalytic reduction(SCR)performance of the MnO2catalysts with different phases.The NOx conversion efficiency decrease...α‐,β‐,δ‐,andγ‐MnO2nanocrystals are successfully prepared.We then evaluated the NH3selective catalytic reduction(SCR)performance of the MnO2catalysts with different phases.The NOx conversion efficiency decreased in the order:γ‐MnO2>α‐MnO2>δ‐MnO2>β‐MnO2.The NOx conversion with the use ofγ‐MnO2andα‐MnO2catalysts reached90%in the temperature range of140–200°C,while that based onβ‐MnO2reached only40%at200°C.Theγ‐MnO2andα‐MnO2nanowire crystal morphologies enabled good dispersion of the catalysts and resulted in a relatively high specific surface area.We found thatγ‐MnO2andα‐MnO2possessed stronger reducing abilities and more and stronger acidic sites than the other catalysts.In addition,more chemisorbed oxygen existed on the surface of theγ‐MnO2andα‐MnO2catalysts.Theγ‐MnO2andα‐MnO2catalysts showed excellent performance in the low‐temperature SCR of NO to N2with NH3.展开更多
In this paper,the effect of sodium laurate(SL)on the properties of sodium lauroyl glutamate(SLG),such as surface activity,foam,wetting,emulsification,and resistance to hard water,has been systematically investigated.T...In this paper,the effect of sodium laurate(SL)on the properties of sodium lauroyl glutamate(SLG),such as surface activity,foam,wetting,emulsification,and resistance to hard water,has been systematically investigated.The results showed that the critical micelle concentration(cmc)of SLG was 0.30 mmol/L,and the surface tension at the cmc(γcmc)was 34.95 mN/m.With the increase of SL content,the efficiency of SLG solution in reducing the surface tension was decreased.When the SL content was increased,there was no significant change in the foaming ability and foam stability of SLG solutions.The increase of SL content improved both the emulsification and wettability of SLG,but reduced its water resistance.展开更多
Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morpho...Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morphology simulation with an enhanced agglomerate model to establish a mathematical framework elucidating pore evolution,Pt utilization,and oxygen transport in catalyst layers.Results demonstrate dominant local mass transport resistance governed by three factors:(1)active site density dictating oxygen flux;(2)ionomer film thickness defining shortest transport path;(3)ionomer-to-Pt surface area ratio modulating practical pathway length.At low ionomer-to-carbon(I/C)ratios,limited active sites elevate resistance(Factor 1 dominant).Higher I/C ratios improve the ionomer coverage but eventually thicken ionomer films,degrading transport(Factors 2–3 dominant).The results indicate that larger carbon particles result in a net increase in local transport resistance by reducing external surface area and increasing ionomer thickness.As the proportion of Pt situated in nanopores or the Pt mass fraction increases,elevated Pt density inside the nanopores exacerbates pore blockage.This leads to the increased transport resistance by reducing active sites,and increasing ionomer thickness and surface area.Lower Pt loading linearly intensifies oxygen flux resistance.The model underscores the necessity to optimize support morphology,Pt distribution,and ionomer content to prevent pore blockage while balancing catalytic activity and transport efficiency.These insights provide a systematic approach for designing high-performance mesoporous carbon catalysts.展开更多
The lack of the early phase gelation property has limited the application of anhydrite as building material products. The use of additives, however, activates the anhydrite surfaces and results in the occurrence of ea...The lack of the early phase gelation property has limited the application of anhydrite as building material products. The use of additives, however, activates the anhydrite surfaces and results in the occurrence of early phase gelation. Under different surface modification conditions,the solubility of anhydrite in water has been measured and it has indicated a correlation between the anhydrite surface activity and its solubility in water. This relationship can be utilized to further study the anhydrite surface activation.展开更多
From April 21st to 23rd,the 2025 China Surfactant Industry Conference was successfully held in Hangzhou.The conference was hosted by China Research Institute of Daily Chemical,and the National Engineering Research Cen...From April 21st to 23rd,the 2025 China Surfactant Industry Conference was successfully held in Hangzhou.The conference was hosted by China Research Institute of Daily Chemical,and the National Engineering Research Center for Surfactant,undertaken by the National Productivity Promotion Center for Surfactant and Detergent Industry and the China Daily Chemical Industry Information Center,specially co-organized by Zanyu Technology Group Co.,Ltd,and jointly co-organized by the China Surface Active Agent Industry Alliance (SAA),the Malaysian Palm Oil Board (MPOB),the Roundtable on Sustainable Palm Oil (RSPO),and the American Oil Chemists’ Society (AOCS).展开更多
Isomorphic substitution of ferric ion(Fe~(3+))by aluminum ion(Al~(3+))in iron(hydro)oxides is ubiquitous in natural environments.Aluminum substitution inevitably leads to changes in the microstructures,physicochemical...Isomorphic substitution of ferric ion(Fe~(3+))by aluminum ion(Al~(3+))in iron(hydro)oxides is ubiquitous in natural environments.Aluminum substitution inevitably leads to changes in the microstructures,physicochemical properties,and surface reactions of iron(hydro)oxides,which may have great impacts on the sequestration of nutrients and contaminants in soils and aquatic environments.Over the past decades,the structural properties and surface reactivity of Al-substituted iron(hydro)oxides have been intensively studied.Iron(hydro)oxides in various structural forms and with different Al substitution amounts present high application potentials in addressing environmental issues.A timely summary of the structural properties and interfacial reactions of the most common and representative Al-substituted iron(hydro)oxides is of significance.Herein,the effects of Al substitution on the structural properties and surface activities of iron(hydro)oxides were clarified according to the microstructure,crystal facets,surface site type and density,interfacial reaction mechanisms,and modeling parameters of iron(hydro)oxides.This review systematically elucidates how Al substitution affects the structural properties and surface reactions of iron(hydro)oxides,including the well crystallized goethite and hematite and the poorly crystallized ferrihydrite,providing theoretical guidance for further exploration of the mineralogical characteristics and environmental geochemical behaviors of iron(hydro)oxides.展开更多
The Pt decorated Ni/C nanocatalysts were prepared for hydrogen oxidation reaction（HOR） in fuel cell.By regulating the contents of Pt and Ni in the catalyst,both the composition and the structure affected the electro...The Pt decorated Ni/C nanocatalysts were prepared for hydrogen oxidation reaction（HOR） in fuel cell.By regulating the contents of Pt and Ni in the catalyst,both the composition and the structure affected the electrochemical catalytic characteristics of the Pt-Ni/C catalysts.When the Pt mass content was 3.1% percent and that of Ni was 13.9% percent,the Pt-Ni/C-3 catalyst exhibited a larger electrochemically active surface area and a higher exchange current density toward HOR than those of pure supported platinum sample.Our study demonstrates a feasible approach for designing the more efficient catalysts with lower content of noble metal for HOR in fuel cell.展开更多
This paper considers a multi-antenna ac-cess point(AP)transmitting secrecy message to a single-antenna user in the presence of a single-antenna illegal eavesdropper(Eve)and proposes a double ac-tive reconfigurable int...This paper considers a multi-antenna ac-cess point(AP)transmitting secrecy message to a single-antenna user in the presence of a single-antenna illegal eavesdropper(Eve)and proposes a double ac-tive reconfigurable intelligent surfaces(DARISs)as-sisted physical layer security(PLS)scheme denoted by DARISs-PLS to protect the secrecy message trans-mission.We formulate a secrecy rate maximization problem for the proposed DARISs-PLS scheme by considering a power budget constraint for the two ac-tive reconfigurable intelligent surfaces(ARISs)and AP.To address the formulated optimization problem,we jointly optimize the reflecting coefficients for the two ARISs and the beamforming at the AP in an it-erative manner by applying Dinkelbach based alter-nating optimization(AO)algorithm and a customized iterative algorithm together with the semidefinite re-laxation(SDR).Numerical results reveal that the pro-posed DARISs-PLS scheme outperforms the dou-ble passive reconfigurable intelligent surfaces-assisted PLS method(DPRISs-PLS)and single ARIS-assisted PLS method(SARIS-PLS)in terms of the secrecy rate.展开更多
Gelatinase A (MMP-2) is considered to play a critical role in cell migration and invasion. The proteinase is secreted from the cell as an inactive zymogen. In vivo it is postulated that activation of progelationase A ...Gelatinase A (MMP-2) is considered to play a critical role in cell migration and invasion. The proteinase is secreted from the cell as an inactive zymogen. In vivo it is postulated that activation of progelationase A (proMMP-2) takes place on the cell surface mediated by membrane-type matrix metalloproteinases (MT-MMPs). Recent studies have demonstrated that proMMP-2 is recruited to the cell surface by interacting with tissue inhibitor of metalloproteinases-2 (TIMP-2) bound to MT1MMP by forming a ternary complex. bee MT1-MMP closely located to the ternary complex then activates proMMP-2 on the cell surface. MT1-MMP is found in cultured invasive cancer cells at the invadopodia. The MTMMP/TIMP-2/ MMP- 2 system t bus provides localized expression of proteolysis of the extracellular matrix required for cell migration.展开更多
YAG laser welding with surface activating flux has been investigated, and the influencing factors and mechanism are discussed. The results show that both surface activating flux and surface active element S have fanta...YAG laser welding with surface activating flux has been investigated, and the influencing factors and mechanism are discussed. The results show that both surface activating flux and surface active element S have fantastic effects on the YAG laser weld shape, that is to obviously increase the weld penetration and D/W ratio in various welding conditions. The mechanism is thought to be the change of weld pool surface tension temperature coefficient, thus, the change of fluid flow pattern in weld pool due to the flux.展开更多
Boron is a very promising and highly attractive fuel because of high calorific value. However, the practical applications in explosives and propellants of boron have been limited by long ignition delay time and low co...Boron is a very promising and highly attractive fuel because of high calorific value. However, the practical applications in explosives and propellants of boron have been limited by long ignition delay time and low combustion efficiency. Herein, nano-Al and graphene fluoride(GF) as surface activated materials are employed to coat boron(B) particles to improve ignition and combustion performance. The reaction heat of nano-Al coated B/KNO_(3)and GF coated B/KNO_(3)are 1116.83 J/g and 862.69 J/g, respectively, which are higher than that of pure B/KNO_(3)(823.39 J/g). The ignition delay time of B/KNO_(3)could be reduced through nano-Al coating. The shortest ignition delay time is only 75 ms for B coated with nano-Al of 8 wt%, which is much shorter than that of pure B/KNO_(3)(109 ms). However, the ignition delay time of B/KNOcoated with GF has been increased from 109 to 187 ms. B coated with GF and nano-Al shown significantly influence on the pressure output and flame structure of B/KNO_(3). Furthermore, the effects of B/O ratios on the pressure output and ignition delay time have been further fully studied. For B/KNO_(3)coated with nano-Al and GF, the highest pressures are 88 KPa and 59 KPa for B/O ratio of 4:6, and the minimum ignition delay time are 94 ms and 148 ms for B/O ratio of 7:3. Based on the above results, the reaction process of boron coated with GF and nano-Al has been proposed to understand combustion mechanism.展开更多
A novel C/Pb composite has been successfully prepared by electmless plating to reduce the hydrogenevolution and achieve the high reversibility of the anode of lead-carbon battery （LCB）. The depositedlead on the surf...A novel C/Pb composite has been successfully prepared by electmless plating to reduce the hydrogenevolution and achieve the high reversibility of the anode of lead-carbon battery （LCB）. The depositedlead on the surface of C/Pb composite was found to be uniform and adherent to carbon surface. Becauselead has been stuck on the surface of C/Pb composite, the embedded structure suppresses the hydrogenevolution of lead-carbon anode and strengthens the connection between carbon additive and sponge lead.Compared with the blank anode, the lead-carbon anode with C/Pb composite displays excellent charge-discharge reversibility, which is attributed to the good connection between carbon additives and leadthat has been stuck on the surface of C/Pb composite during the preparation process. The addition of CIPb composite maintains a solid anode structure with high specific surface area and power volume, andthereby, it plays a significant role in the highly reversible lead-carbon anode.展开更多
基金financially supported by the National Key Research and Development Program of China(2022YFE03170002)the National Natural Science Foundation of China(52071286,U203020852171223)。
文摘ZrCo alloy holds great promise for hydrogen isotope storage,yet its susceptibility to poisoning by impurity gases,especially CO,poses a challenge.This susceptibility arises due to the electron acceptor nature of the surface Co element and the formation of the d-πfeedback bond,thereby impeding the surface hydrogen dissociation.Accordingly,we propose a novel local activity modulation strategy,where substituent elements are sacrificed to protect the active Co sites for hydrogen dissociation.Considering CO absorption capacity,solid solubility,and hydrogen affinity,we selected V,Cr,and Mn as microalloying elements and successfully prepared the single-phase ZrCo_(0.97)(VCrMn)_(0.03)alloy.Compared to pristine ZrCo,ZrCo_(0.97)(VCrMn)_(0.03)demonstrates significantly enhanced poisoning resistance.Notably,the hydrogenation kinetics of ZrCo_(0.97)(VCrMn)_(0.03)is 2.4 times higher than that of ZrCo in 4 bar H_(2)+5000 ppm CO.Interestingly,the controllable in situ formation of the Co_(2)C phase shell structure during cycling further safeguards the surface reactivity of ZrCo_(0.97)(VCrMn)_(0.03).Consequently,its capacity retention ratio after 25 cycles has been improved to 74.5%from 55.3%of the ZrCo alloy.These findings suggest that micro-alloying engineering could be a promising strategy for surface activity modulation to enhance the anti-poisoning properties of hydrogen storage materials.
基金the Key Research and Development Project of the Ministry of Science and Technology of China(No.2022YFC3004900)。
文摘Fluorosurfactants are the key ingredients in the formulations of aqueous film-forming foams(AFFFs)for extinguishing flammable liquids,thus developing high-efficient and low-toxic fluorosurfactants is desirable in AFFFs application.Herein,a series of hyperbranched polymeric fluorosu rfactants(HPFs)were successfully synthesized through sequentially modifying hyperbranched polyethylenimine(PEI)with the hydrophilic poly(ethylene glycol)(PEG)chains and the hydrophobic C6/C4-based perfluoroalkyl chains,which were verified by FTIR,^(1)H-and^(19)F-NMR.The surface tensions of all the HPFs in water were measured,and the corresponding physicochemical parameters were interpreted.It was found that the surface activities of HPFs could be tuned through adjusting the ratio of PEG to perfluoroalkyl chains,the length of perfluoroalkyl chains,the molecular weight of PEI core,but not the PEG chain length.In the binary mixture of HPFs with the commercial small molecule fluorosurfactant Capstone^(TM)1157(C1157),a strong synergism led to the elevation of surface activity,which was attributed to the efficient encapsulation of C1157 vips by the compact hyperbranched HPFs as the hosts.The utilization of HPF/C1157 as fluorosurfactant ingredients in AFFF formulations could realize much higher fire-extinguishing efficiency towards flammable oils than the control AFFFs prepa red from the polymeric Capstone^(TM)1460 or the neat C1157.
文摘The magnetism and surface behaviour of Pt-Dy/γ-Al_2O_3 catalysts were studied respectively by means of a Faraday magnetic balance and the method of carbon disulfide.The ferromagnetic impurity in the support,γ-Al_2O_3,at low temperature was corrected for the first time.The magnetic susceptibilities of the cat- alysts follow the sequence in different stage of preparation:χ_(uncalcined)<χ_(calcined)<χ_(reduced). The magnetic susceptibilities of the catalysts decrease as they adsorb hydrogen,cyclohexane or benzene. There is a correlation between the aromatization yield of cyclohexane or heptane on these catalysts and the magnetic susceptibility of the catalysts.Since addition of Dy increases the number of adsorption sites and the relevant proportions of weak adsorption sites,the abilities of sulfur-resistance and cyclohexane dehydrogenation are improved.In Pt-Dy/γ-A:_2O_3 catalysts,Dy improves the aromatization activity and stability of the catalyst and plays the role of the electron promoter.
基金This work was supported by the Ministry of Education,Science and Technological Development of The Republic of Serbia(Contract No.451-03-68/2022-14/200135).
文摘A key feature that distinguishes cancer cells from all other cells is their capability to spread throughout the body.Although how cancer cells collectively migrate by following molecular rules which influence the state of cell-cell adhesion contacts has been comprehensively formulated,the impact of physical interactions on cell spreading remains less understood.Cumulative effects of physical interactions exist as the interplay between various physical parameters such as(1)tissue surface tension,(2)viscoelasticity caused by collective cell migration,and(3)solid stress accumulated in the cell aggregate core region.This review aims to point out the role of these physical parameters in cancer cell spreading by considering and comparing the rearrangement of various mono-cultured cancer and epithelial model systems such as the fusion of two cell aggregates.While epithelial cells undergo volumetric cell rearrangement driven by the tissue surface tension,which directs cell movement from the surface to the core region of two-aggregate systems,cancer cells rather perform surface cell rearrangement.Cancer cells migrate toward the surface of the two-aggregate system driven by the solid stress while the surface tension is significantly reduced.The solid stress,accumulated in the core region of the two-aggregate system,is capable of suppressing the movement of epithelial cells that can undergo the jamming state transition;however,this stress enhances the movement of cancer cells.We have focused here on the multi-scale rheological modeling approaches that aimed at reproducing and understanding these biological systems.
文摘The chemical structure of newly synthesized cationic surfactants based on Schiff base was confirmed using Fourier transform infrared spectroscopy,proton nuclear magnetic resonance spectroscopy,and mass spectroscopy.The synthesized surfactants were used in the synthesis of silver nanoparticles by a simple one-step method.The silver nanoparticle（AgNPs） formation was confirmed using transmission electron microscopy（TEM）,electron diffraction（SAED）,dynamic light scattering（DLS）,and energy dispersive X-ray spectroscopy（EDX）.The structure of the surfactant played an important role in the synthesis process.Increasing the hydrophobic chain length,the stability,and the amount of surfactant increased the quantity of AgNPs formed.The surface activity of the synthesized cationic surfactants was determined using surface tension measurements at three different temperatures.The synthesized surfactants showed a high tendency toward adsorption and micellization.Increasing the hydrophobic chain length of the synthesized surfactant increased its adsorption.Screening the synthesized cationic surfactants and their nano-form against bacteria and fungi showed that they are highly effective.The silver nanoparticles enhanced the biological activity of the synthesized cationic surfactants.
基金supported in part by the National Natural Science Foundation of China under Grant 62071253,Grant 62371252 and Grant 62271268in part by the Jiangsu Provincial Key Research and Development Program under Grant BE2022800in part by the Jiangsu Provincial 333 Talent Project.
文摘In this paper,we examine an illegal wireless communication network consisting of an illegal user receiving illegal signals from an illegal station and propose an active reconfigurable intelligent surface(ARIS)-assisted multi-antenna jamming(MAJ)scheme denoted by ARIS-MAJ to interfere with the illegal signal transmission.In order to strike a balance between the jamming performance and the energy consumption,we consider a so-called jamming energy efficiency(JEE)which is defined as the ratio of achievable rate reduced by the jamming system to the corresponding power consumption.We formulate an optimization problem to maximize the JEE for the proposed ARIS-MAJ scheme by jointly optimizing the jammer’s beamforming vector and ARIS’s reflecting coefficients under the constraint that the jamming power received at the illegal user is lower than the illegal user’s detection threshold.To address the non-convex optimization problem,we propose the Dinkelbach-based alternating optimization(AO)algorithm by applying the semidefinite relaxation(SDR)algorithm with Gaussian randomization method.Numerical results validate that the proposed ARIS-MAJ scheme outperforms the passive reconfigurable intelligent surface(PRIS)-assisted multi-antenna jamming(PRIS-MAJ)scheme and the conventional multiantenna jamming scheme without RIS(NRIS-MAJ)in terms of the JEE.
基金supported by the National Natural Science Foundation of China through its key project funding CNFS(Grant No.51236005)the Ministry of Science and Technology through its 973 National Key Project(Grant No.2013CB228401)
文摘The soot surface growth plays significant role on the soot mass accumulation,which starts with H(hydrogen)atom abstraction forming activated soot surface sites,and is followed by the acetylene addition process.In this study,the effect of the mixture inhomogeneity and combustion temperature on the soot surface activity and soot formation was investigated by developing a new multi-step phenomenological(MSP)soot model of diesel engines.A new detailed soot surface growth mechanism was proposed by correlation analysis of combustion parameters with soot formation.The inhomogeneity coefficient of soot surface activityαCH and the specific rate of soot surface growth R CH were derived to highlight the effect of inhomogeneity of mixture and combustion temperature on soot formation.The predicted diesel engine-out soot agreed well with experimental findings in wide ranges of combustion conditions.In the case of lower engine load with single fuel injection and higher EGR(exhaust gas recirculation)rate,it had quiet homogeneous mixtures before ignition when the combustion temperature dominated the soot surface activity.At medium engine load with multi-pulse fuel injections,it got mixture slightly stratified before ignition and revealed that the mixture inhomogeneity became more dominated on soot surface activity than the combustion temperature.An increased soot surface activity led to increased soot emission.Under the full engine loads with single fuel injection but quite high boost pressure over 0.4 MPa,it led to the combustion conditions of higher mixture density and higher mixture heat capacity,which benefits the mixture homogeneity.The decay rate of soot surface activity became lower due to the decreased combustion temperature and the soot surface activity decreased due to improved mixture homogeneity.In addition,the lowered intake oxygen concentration due to usage of EGR played a role to lower the specific rate of soot surface growth R CH,but to increase the soot surface activityαCH.
基金National Natural Science Foundation of China(No.22078207)Sichuan Science and Technology Program(2021ZHCG0042)Fundamental Research Funds for the Central Universities(China).
文摘Mixing hydrocarbon surfactants with fluorocarbon surfactants is still an important strategy to improve the economic benefits and performances of fluorocarbon surfactants and expand their range of application.Herein,we prepared a novel kind of hydrocarbon-fluorocarbon surfactant mixtures via mixing a cationic surfactant,cetyltrimethylammonium bromide(CTAB),with a tri-block nonionic short-chain fluorocarbon surfactant(F_(9)EG_(13)F_(9))in aqueous solution.The results showed that adding a small CTAB amount to F_(9)EG_(13)F_(9)(the molar fraction of CTAB in the mixture(x_(1))was 0.2)could greatly reduce its critical micelle concentrations(cmc)from 0.408mmol/L to 0.191 mmol/L.At this x_(1),the contact angle of the mixture was the minimum(57.7°)at 100 s on polytetrafluoroethylene film,which was even lower than that of F_(9)EG_(13)F_(9).Besides,CTAB/F_(9)EG_(13)F_(9) mixtures possessed better colloidal stability and solubilization ability toward hydrophobic dye(SudanІ)than F_(9)EG_(13)F_(9).The outstanding performances of binary surfactant mixtures benefited from the non-ideal mixing and strong synergistic effect evidence that CTAB/F_(9)EG_(13)F_(9) surfactant mixtures could be used in practical applications instead of individual F_(9)EG_(13)F_(9),thereby reducing the used cost of F_(9)EG_(13)F_(9).
基金supported by the National Natural Science Foundation of China(51502221)~~
文摘α‐,β‐,δ‐,andγ‐MnO2nanocrystals are successfully prepared.We then evaluated the NH3selective catalytic reduction(SCR)performance of the MnO2catalysts with different phases.The NOx conversion efficiency decreased in the order:γ‐MnO2>α‐MnO2>δ‐MnO2>β‐MnO2.The NOx conversion with the use ofγ‐MnO2andα‐MnO2catalysts reached90%in the temperature range of140–200°C,while that based onβ‐MnO2reached only40%at200°C.Theγ‐MnO2andα‐MnO2nanowire crystal morphologies enabled good dispersion of the catalysts and resulted in a relatively high specific surface area.We found thatγ‐MnO2andα‐MnO2possessed stronger reducing abilities and more and stronger acidic sites than the other catalysts.In addition,more chemisorbed oxygen existed on the surface of theγ‐MnO2andα‐MnO2catalysts.Theγ‐MnO2andα‐MnO2catalysts showed excellent performance in the low‐temperature SCR of NO to N2with NH3.
文摘In this paper,the effect of sodium laurate(SL)on the properties of sodium lauroyl glutamate(SLG),such as surface activity,foam,wetting,emulsification,and resistance to hard water,has been systematically investigated.The results showed that the critical micelle concentration(cmc)of SLG was 0.30 mmol/L,and the surface tension at the cmc(γcmc)was 34.95 mN/m.With the increase of SL content,the efficiency of SLG solution in reducing the surface tension was decreased.When the SL content was increased,there was no significant change in the foaming ability and foam stability of SLG solutions.The increase of SL content improved both the emulsification and wettability of SLG,but reduced its water resistance.
基金supported by the Program of Ministry of Science and Technology of China(No.2023YFB2504200)support of Shanghai Rising-Star Program(Grant No.24QB2703200)the Major Science and Technology Projects of Yunnan Province(No.202302AH360001).
文摘Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morphology simulation with an enhanced agglomerate model to establish a mathematical framework elucidating pore evolution,Pt utilization,and oxygen transport in catalyst layers.Results demonstrate dominant local mass transport resistance governed by three factors:(1)active site density dictating oxygen flux;(2)ionomer film thickness defining shortest transport path;(3)ionomer-to-Pt surface area ratio modulating practical pathway length.At low ionomer-to-carbon(I/C)ratios,limited active sites elevate resistance(Factor 1 dominant).Higher I/C ratios improve the ionomer coverage but eventually thicken ionomer films,degrading transport(Factors 2–3 dominant).The results indicate that larger carbon particles result in a net increase in local transport resistance by reducing external surface area and increasing ionomer thickness.As the proportion of Pt situated in nanopores or the Pt mass fraction increases,elevated Pt density inside the nanopores exacerbates pore blockage.This leads to the increased transport resistance by reducing active sites,and increasing ionomer thickness and surface area.Lower Pt loading linearly intensifies oxygen flux resistance.The model underscores the necessity to optimize support morphology,Pt distribution,and ionomer content to prevent pore blockage while balancing catalytic activity and transport efficiency.These insights provide a systematic approach for designing high-performance mesoporous carbon catalysts.
文摘The lack of the early phase gelation property has limited the application of anhydrite as building material products. The use of additives, however, activates the anhydrite surfaces and results in the occurrence of early phase gelation. Under different surface modification conditions,the solubility of anhydrite in water has been measured and it has indicated a correlation between the anhydrite surface activity and its solubility in water. This relationship can be utilized to further study the anhydrite surface activation.
文摘From April 21st to 23rd,the 2025 China Surfactant Industry Conference was successfully held in Hangzhou.The conference was hosted by China Research Institute of Daily Chemical,and the National Engineering Research Center for Surfactant,undertaken by the National Productivity Promotion Center for Surfactant and Detergent Industry and the China Daily Chemical Industry Information Center,specially co-organized by Zanyu Technology Group Co.,Ltd,and jointly co-organized by the China Surface Active Agent Industry Alliance (SAA),the Malaysian Palm Oil Board (MPOB),the Roundtable on Sustainable Palm Oil (RSPO),and the American Oil Chemists’ Society (AOCS).
基金financially supported by the National Natural Science Foundation of China(Nos.42207352,42007020,and 42007015)the Natural Science Fund for Excellent Young Scholars of Hainan Province,China(No.324YXQN421)。
文摘Isomorphic substitution of ferric ion(Fe~(3+))by aluminum ion(Al~(3+))in iron(hydro)oxides is ubiquitous in natural environments.Aluminum substitution inevitably leads to changes in the microstructures,physicochemical properties,and surface reactions of iron(hydro)oxides,which may have great impacts on the sequestration of nutrients and contaminants in soils and aquatic environments.Over the past decades,the structural properties and surface reactivity of Al-substituted iron(hydro)oxides have been intensively studied.Iron(hydro)oxides in various structural forms and with different Al substitution amounts present high application potentials in addressing environmental issues.A timely summary of the structural properties and interfacial reactions of the most common and representative Al-substituted iron(hydro)oxides is of significance.Herein,the effects of Al substitution on the structural properties and surface activities of iron(hydro)oxides were clarified according to the microstructure,crystal facets,surface site type and density,interfacial reaction mechanisms,and modeling parameters of iron(hydro)oxides.This review systematically elucidates how Al substitution affects the structural properties and surface reactions of iron(hydro)oxides,including the well crystallized goethite and hematite and the poorly crystallized ferrihydrite,providing theoretical guidance for further exploration of the mineralogical characteristics and environmental geochemical behaviors of iron(hydro)oxides.
基金supported by the National Natural Science Foundation of China (21476145)~~
文摘The Pt decorated Ni/C nanocatalysts were prepared for hydrogen oxidation reaction（HOR） in fuel cell.By regulating the contents of Pt and Ni in the catalyst,both the composition and the structure affected the electrochemical catalytic characteristics of the Pt-Ni/C catalysts.When the Pt mass content was 3.1% percent and that of Ni was 13.9% percent,the Pt-Ni/C-3 catalyst exhibited a larger electrochemically active surface area and a higher exchange current density toward HOR than those of pure supported platinum sample.Our study demonstrates a feasible approach for designing the more efficient catalysts with lower content of noble metal for HOR in fuel cell.
基金supported in part by the National Natural Science Foundation of China under Grant 62071253,Grant 62371252 and Grant 62271268in part by the Jiangsu Provincial Key Research and Development Program under Grant BE2022800in part by the Jiangsu Provincial 333 Talent Project.
文摘This paper considers a multi-antenna ac-cess point(AP)transmitting secrecy message to a single-antenna user in the presence of a single-antenna illegal eavesdropper(Eve)and proposes a double ac-tive reconfigurable intelligent surfaces(DARISs)as-sisted physical layer security(PLS)scheme denoted by DARISs-PLS to protect the secrecy message trans-mission.We formulate a secrecy rate maximization problem for the proposed DARISs-PLS scheme by considering a power budget constraint for the two ac-tive reconfigurable intelligent surfaces(ARISs)and AP.To address the formulated optimization problem,we jointly optimize the reflecting coefficients for the two ARISs and the beamforming at the AP in an it-erative manner by applying Dinkelbach based alter-nating optimization(AO)algorithm and a customized iterative algorithm together with the semidefinite re-laxation(SDR).Numerical results reveal that the pro-posed DARISs-PLS scheme outperforms the dou-ble passive reconfigurable intelligent surfaces-assisted PLS method(DPRISs-PLS)and single ARIS-assisted PLS method(SARIS-PLS)in terms of the secrecy rate.
文摘Gelatinase A (MMP-2) is considered to play a critical role in cell migration and invasion. The proteinase is secreted from the cell as an inactive zymogen. In vivo it is postulated that activation of progelationase A (proMMP-2) takes place on the cell surface mediated by membrane-type matrix metalloproteinases (MT-MMPs). Recent studies have demonstrated that proMMP-2 is recruited to the cell surface by interacting with tissue inhibitor of metalloproteinases-2 (TIMP-2) bound to MT1MMP by forming a ternary complex. bee MT1-MMP closely located to the ternary complex then activates proMMP-2 on the cell surface. MT1-MMP is found in cultured invasive cancer cells at the invadopodia. The MTMMP/TIMP-2/ MMP- 2 system t bus provides localized expression of proteolysis of the extracellular matrix required for cell migration.
文摘YAG laser welding with surface activating flux has been investigated, and the influencing factors and mechanism are discussed. The results show that both surface activating flux and surface active element S have fantastic effects on the YAG laser weld shape, that is to obviously increase the weld penetration and D/W ratio in various welding conditions. The mechanism is thought to be the change of weld pool surface tension temperature coefficient, thus, the change of fluid flow pattern in weld pool due to the flux.
基金supported by the National Natural Science Foundation of China (11872341 and 22075261)。
文摘Boron is a very promising and highly attractive fuel because of high calorific value. However, the practical applications in explosives and propellants of boron have been limited by long ignition delay time and low combustion efficiency. Herein, nano-Al and graphene fluoride(GF) as surface activated materials are employed to coat boron(B) particles to improve ignition and combustion performance. The reaction heat of nano-Al coated B/KNO_(3)and GF coated B/KNO_(3)are 1116.83 J/g and 862.69 J/g, respectively, which are higher than that of pure B/KNO_(3)(823.39 J/g). The ignition delay time of B/KNO_(3)could be reduced through nano-Al coating. The shortest ignition delay time is only 75 ms for B coated with nano-Al of 8 wt%, which is much shorter than that of pure B/KNO_(3)(109 ms). However, the ignition delay time of B/KNOcoated with GF has been increased from 109 to 187 ms. B coated with GF and nano-Al shown significantly influence on the pressure output and flame structure of B/KNO_(3). Furthermore, the effects of B/O ratios on the pressure output and ignition delay time have been further fully studied. For B/KNO_(3)coated with nano-Al and GF, the highest pressures are 88 KPa and 59 KPa for B/O ratio of 4:6, and the minimum ignition delay time are 94 ms and 148 ms for B/O ratio of 7:3. Based on the above results, the reaction process of boron coated with GF and nano-Al has been proposed to understand combustion mechanism.
基金the financial support provided by the National Natural Science Foundation of China (No.21573093)the National Key Research and Development Program (No.2017YFB0307501)Guangdong Innovative and Entrepreneurial Research Team Program (No.2013C092)
文摘A novel C/Pb composite has been successfully prepared by electmless plating to reduce the hydrogenevolution and achieve the high reversibility of the anode of lead-carbon battery （LCB）. The depositedlead on the surface of C/Pb composite was found to be uniform and adherent to carbon surface. Becauselead has been stuck on the surface of C/Pb composite, the embedded structure suppresses the hydrogenevolution of lead-carbon anode and strengthens the connection between carbon additive and sponge lead.Compared with the blank anode, the lead-carbon anode with C/Pb composite displays excellent charge-discharge reversibility, which is attributed to the good connection between carbon additives and leadthat has been stuck on the surface of C/Pb composite during the preparation process. The addition of CIPb composite maintains a solid anode structure with high specific surface area and power volume, andthereby, it plays a significant role in the highly reversible lead-carbon anode.
