Silica aerogels were prepared at ambient drying by using ethanol/trimethylchlorosilane （TMCS）/heptane solution as pore water exchange and surface modification of the wet gel before drying. The obtained silica aeroge...Silica aerogels were prepared at ambient drying by using ethanol/trimethylchlorosilane （TMCS）/heptane solution as pore water exchange and surface modification of the wet gel before drying. The obtained silica aerogels exhibit a sponge-like structure with uniform pore size distribution. The effects of heat-treatment on the hydrophobicity, specific surface area and other properties were investigated. The results indicated that the hydrophobicity of silica aerogels could be maintained up to 350℃. With increasing heating temperature, hydrophobicity decreased, and became completely hydrophilic after heat-treatment at 500℃. Brunaueremmitt-teller （BET） surface area results indicated that the specific surface area of silica aerogels increased with increasing heating temperature in the range of 150-500℃. The effects of heat-treatment on the morphology and chemical bonding state of silica aerogels were investigated by scanning electron microscopy （SEM）, differential temperature analysis （DTA） and Fourier-transform infrared spectroscopy （FT-IR）.展开更多
A simple,fast and cost-effective method for monolithic carbon aerogels(CAs) preparation was proposed through sol-gel polycondensation of resorcinol with fo rmaldehyde in a basic aqueous solution followed by ambient pr...A simple,fast and cost-effective method for monolithic carbon aerogels(CAs) preparation was proposed through sol-gel polycondensation of resorcinol with fo rmaldehyde in a basic aqueous solution followed by ambient pressure drying without solvent exchange,and carbonization.The microstructure and network strength of CAs were tailored by adju sting the catalyst concentration([resorcinol]/[sodium carbonate] in the range of 300-2000),water content([deionized water]/[resorcinol] equals to 17 and 24,respectively),and gelation temperature(Tgel in the range of 30-90℃).Resultantly,the CAs with a wide range of density(0.30-1.13 g/cm3),high specific surface area(465-616 m2/g),high compressive strength(6.5-147.4 MPa)and low thermal conductivity(0.065-0.120 W·m-1 K-1) were obtained in this work.Moreover,the largesized CAs(100×100×20 mm3) can also be prepared by this method since the formed robust skeleton network can resist shrinkage/collapse of pore structure and prevent cracking during drying.The improved mechanical strength and monolithic forming abilities could be mainly attributed to the uniform arrangement of carbon particles and pores,fine particle size,abundant network structure and enhanced particle neck.展开更多
Three-dimensional graphene-based aerogels have promising applications in oil adsorption and environmental restoration.However,current research of graphene-based aerogels is often hindered by high preparation cost,poor...Three-dimensional graphene-based aerogels have promising applications in oil adsorption and environmental restoration.However,current research of graphene-based aerogels is often hindered by high preparation cost,poor mechanical properties and low recycling efficiency.Here,superelastic graphene aerogel(SGA)was prepared through one-step freezing and twice hydrothermal reduction followed by drying under ambient pressure.The simple atmospheric drying provides a possibility for large-scale preparation of high performance graphene-based aerogels.The prepared SGA not only has the ability of highly repeatable compression rebound,but also exhibits excellent oil adsorption performance.And the overall performance of SGA is better than most of graphenebased aerogels prepared by freeze drying.After the SGA was cyclically compressed with 70%strain for 300 times,it can return to the original shape and height substantially.SGA retained about 90%of the initial adsorption capacity after 50 cycles of adsorption and compression regeneration for cyclohexane.展开更多
Carbon aerogels were synthesized via ambient pressure drying process using resorcinolformaldehyde as precursor and P123 to strengthen their skeletons. CO2 activation technology was implemented to improve surface areas...Carbon aerogels were synthesized via ambient pressure drying process using resorcinolformaldehyde as precursor and P123 to strengthen their skeletons. CO2 activation technology was implemented to improve surface areas and adjust pore size distribution. The synthesis process was optimized, and the morphology, structure, adsorption properties and electrochemical behavior of different samples were characterized. The CO2-activated samples achieved a high specific capacitance of 129.2 F/g in 6 M KOH electrolytes at the current density of 1 m A/cm^2 within the voltage range of 0-0.8 V. The optimized activation temperature and duration were determined to be 950 ℃ and 4 h, respectively.展开更多
An ambient pressure synthesis of SiO2/TiO2 binary aerogel was prepared through the low-cost precursors of titanium tetrachloride（TiCl4） and sodium silicate（Na2O·nSiO2）.After gelation,solvent exchange and surf...An ambient pressure synthesis of SiO2/TiO2 binary aerogel was prepared through the low-cost precursors of titanium tetrachloride（TiCl4） and sodium silicate（Na2O·nSiO2）.After gelation,solvent exchange and surface modification were performed simultaneously and the modified gel was finally dried under ambient pressure.Microstructural analyses by transmission electron microscope（TEM） indicate that fabricated SiO2/TiO2 aerogel composite shows similar sponge-like nanostructure as silica aerogel,and the Brunauer-EmmettTeller（BET） analysis shows that the specific surface area of the composite reaches 605 m^2/g,and the average pore size is 9.7 nm.Such binary aerogel exhibits significant photocatalytic performance in this paper for treating model pollutant of methyl orange（MO）,and the decolorizing efficiency of MO is detected as 84.9%after 210 mins exposure to UV light irradiation.Degraded gel suspends in the water so as to separate from solution for reuse,and after 4 times recycling,70%degradation efficiency can be easily reached when composite catalyzed system is exposed for 210 mins under UV irradiation.展开更多
Silica aerogels were prepared by sol-gel technique from industrial silicon derivatives （polyethoxydisiloxanes, E40）, followed by silylation and drying under ambient pressure. The specific surface area, pore size dis...Silica aerogels were prepared by sol-gel technique from industrial silicon derivatives （polyethoxydisiloxanes, E40）, followed by silylation and drying under ambient pressure. The specific surface area, pore size distribution and thermal conductivity of the silica aerogels were investigated and the results showed that the diameter of the silica particles is about 6 nm and the average pore size of the silica aerogels is 14.7 nm. The specific surface area of which is about 1000 m^2.g^-1 and the thermal conductivity is about 0.014 wm^-l.K^-1 at room temperature and pressure of 1.01×10^5 Pa. The Si-CH3 groups were also detected on the internal surface of the silica aerogels, which show hydrophobic. Silica aerogels derived by this technique is low cost and have wide applications.展开更多
The synthesis procedures and physical properties of the ambient dried hydrophobic silica aerogels by using different contents of ethanol （EtOH）/trimethylchlorosilane （TMCS）/n-Hexane as surface modification agent w...The synthesis procedures and physical properties of the ambient dried hydrophobic silica aerogels by using different contents of ethanol （EtOH）/trimethylchlorosilane （TMCS）/n-Hexane as surface modification agent were investigated. One-step solvent exchange and surface modification were simultaneously progressed by immersing silica hydrogels in EtOH/TMCS/n-Hexane solution. It is found that microstructures as well as properties of silica aerogels like porosity, specific density and specific surface area are affected by the contents of surface modification agent in the sol from the results of SEM, TEM morphology, FT-IR chemical structure, BET surface area and BJH pore size analyses. The volume of TMCS is of 10% and 20% of hydrogels, and the final product is hydrophilic xerogels. When TMCS＇s percent （v/v） is elevated to 75 %-100%, hydrophobic silica aerogels with good performance are synthesized, the porosities of aerogels are in the range of 93.5%-95.8% and the average pore size diameter is less than 20 nm.展开更多
In this work, Chinese fir samples with a size of 400 mm (L) by 50 mm (W) 30 mm (H) weretaken as specimens, and drying rate and energy consumption were compared under the conditions, inwhich the absolute pressure was 0...In this work, Chinese fir samples with a size of 400 mm (L) by 50 mm (W) 30 mm (H) weretaken as specimens, and drying rate and energy consumption were compared under the conditions, inwhich the absolute pressure was 0.02 , 0.04 , 0.06 and 0.10 MPa, respectively, and the temperature was80 oC. The results showed that, when the moisture content (MC) of the samples was above fibersaturation point (FSP), the vacuum drying rate was 0.96-1.24 times as high as the ambient pressuredrying rate. However, when it was below FSP, the vacuum drying rate was 1.26-1.32 times as high as theambient pressure drying rate. At the same time, when the MC was above FSP, the energy consumptionof vacuum drying was 81.1%-95.9% of that of ambient pressure drying; when the MC was below FSP,the energy consumption of vacuum drying was 62.40%-69.40% of that of ambient pressure drying.Therefore, the vacuum drying was superior to the ambient pressure drying in terms of drying rate andenergy consumption.展开更多
Diatomite was used as raw material to prepare sodium silicate with a modulus of 3.1 by alkali dissolution method and the resulted sodium silicate solution was employed as a precursor. Methyl methaerylate monomers were...Diatomite was used as raw material to prepare sodium silicate with a modulus of 3.1 by alkali dissolution method and the resulted sodium silicate solution was employed as a precursor. Methyl methaerylate monomers were introduced in wet gels through solution-immersion, and upon heating at 70 ℃, the mesoporous surfaces throughout the skeletal framework were coated with the polymer layer. PMMA modified silica aerogels were successfully synthesized via ambient pressure drying. The properties were investigated by FT- IR, NMR, TGA, nitrogen adsorption-desorption, FESEM and nano-indentation, etc. Results indicate that with the increasing of PMMA incorporated into silica aerogels, the bulk density and the BET surface area increase, the porosity decreases. Through the observation of FESEM, it is found that the interconnecting pores and the big pores add, the pore size distribution expands from 5-17 to 28-150 urn. By comparison, the PMMA modified silica aerogels achieve a 52-fold increase in hardness and a 10-fold increase in modulus.展开更多
Multi-walled carbon nanotube doped silica aerogels（MWCNT-SAs） were synthesized from a wet gel of well-dispersed MWCNT by one-step solvent exchange/surface modification and ambient pressure drying（APD）. Waterglass ...Multi-walled carbon nanotube doped silica aerogels（MWCNT-SAs） were synthesized from a wet gel of well-dispersed MWCNT by one-step solvent exchange/surface modification and ambient pressure drying（APD）. Waterglass was employed as a precursor to prepare wet gel. The content of MWCNT varied from 0 to 15% volume by wet gel. The surface group, thermal stability and microstructure of pure silica aerogel and MWCNT-SAs were investigated by FTIR, DTA, and TEM. Experimental results show that MWCNT-SAs are hydrophobic when the temperature is below 400 ℃, MWCNT-SAs exhibit a mesoporous network structure, and they achieve the largest scale with least shrinkage and lowest density when doped with 5 vol% MWCNT.展开更多
Here we present an economical ambient pressure drying method of preparing monolithic silica aerogels from methyltrimethoxysilane precursor while using sodium bicarbonate solution as the exchanging solvent.We prepared ...Here we present an economical ambient pressure drying method of preparing monolithic silica aerogels from methyltrimethoxysilane precursor while using sodium bicarbonate solution as the exchanging solvent.We prepared silica aerogels with a density and a specific surface area of 0.053 g·cm^(-3) and 423 m^(2)·g^(-1) respectively.The average pore diameter of silica aerogels is 23 nm as the pore specific volume is 1.11 cm^(3)·g^(-1),Further,the contact angle between water droplet and the surface of silica aerogels in specific condition can be as high as 166°,which indicates a super-hydrophobic surface of aerogels.展开更多
Titanium oxides have been considered promising anode materials for lithium-ion batteries(LIBs).However,the poor conductivity and low specific capacity of bulk titanium oxides limit their application.In this study,a ca...Titanium oxides have been considered promising anode materials for lithium-ion batteries(LIBs).However,the poor conductivity and low specific capacity of bulk titanium oxides limit their application.In this study,a carbon dot-modified TiO_(2)@SiO_(2)aerogel was successfully fabricated through a facile ambient pressure drying strategy and used as an anode material of LIBs.Benefiting from the crosslinking of carbon dots and the surface modification of SiO_(2),the as-prepared hierarchical aerogel exhibited a high initial discharge capacity of 974 mAh g^(−1)and maintained a capacity of 299 mAh g^(−1)after 100 cycles at 0.1 A g^(−1).It also retained a discharge capacity of 111 mAh g^(−1)with a CE of 99.9%at 3 A g^(−1).The carbon dot-modified cross-linking skeleton contributes to the structural integrity of the TiO_(2)@SiO_(2)aerogel during repeated insertion/extraction of lithium ions,guaranteeing outstanding cycling and high-rate performance.This ambient pressure drying strategy provides a facile and feasible way to produce high-performance aerogel anode materials for lithium-ion storage.展开更多
文摘Silica aerogels were prepared at ambient drying by using ethanol/trimethylchlorosilane （TMCS）/heptane solution as pore water exchange and surface modification of the wet gel before drying. The obtained silica aerogels exhibit a sponge-like structure with uniform pore size distribution. The effects of heat-treatment on the hydrophobicity, specific surface area and other properties were investigated. The results indicated that the hydrophobicity of silica aerogels could be maintained up to 350℃. With increasing heating temperature, hydrophobicity decreased, and became completely hydrophilic after heat-treatment at 500℃. Brunaueremmitt-teller （BET） surface area results indicated that the specific surface area of silica aerogels increased with increasing heating temperature in the range of 150-500℃. The effects of heat-treatment on the morphology and chemical bonding state of silica aerogels were investigated by scanning electron microscopy （SEM）, differential temperature analysis （DTA） and Fourier-transform infrared spectroscopy （FT-IR）.
基金supported by the Major Program of Aerospace Advanced Manufacturing Technology Research Foundation of NSFC and CASC, China Grant No. U1537204National Natural Science Foundation of China Grant No. 51802313 and 51902315+2 种基金National Science and Technology Major Project (2017-VI-0020-0093)Research Fund of Youth Innovation Promotion Association of CAS, China Grant No. 2014171National Key R&D Program of China Grant No. 2018YFF01013600。
文摘A simple,fast and cost-effective method for monolithic carbon aerogels(CAs) preparation was proposed through sol-gel polycondensation of resorcinol with fo rmaldehyde in a basic aqueous solution followed by ambient pressure drying without solvent exchange,and carbonization.The microstructure and network strength of CAs were tailored by adju sting the catalyst concentration([resorcinol]/[sodium carbonate] in the range of 300-2000),water content([deionized water]/[resorcinol] equals to 17 and 24,respectively),and gelation temperature(Tgel in the range of 30-90℃).Resultantly,the CAs with a wide range of density(0.30-1.13 g/cm3),high specific surface area(465-616 m2/g),high compressive strength(6.5-147.4 MPa)and low thermal conductivity(0.065-0.120 W·m-1 K-1) were obtained in this work.Moreover,the largesized CAs(100×100×20 mm3) can also be prepared by this method since the formed robust skeleton network can resist shrinkage/collapse of pore structure and prevent cracking during drying.The improved mechanical strength and monolithic forming abilities could be mainly attributed to the uniform arrangement of carbon particles and pores,fine particle size,abundant network structure and enhanced particle neck.
基金the financial support of National Natural Science Foundation of China (22078366)
文摘Three-dimensional graphene-based aerogels have promising applications in oil adsorption and environmental restoration.However,current research of graphene-based aerogels is often hindered by high preparation cost,poor mechanical properties and low recycling efficiency.Here,superelastic graphene aerogel(SGA)was prepared through one-step freezing and twice hydrothermal reduction followed by drying under ambient pressure.The simple atmospheric drying provides a possibility for large-scale preparation of high performance graphene-based aerogels.The prepared SGA not only has the ability of highly repeatable compression rebound,but also exhibits excellent oil adsorption performance.And the overall performance of SGA is better than most of graphenebased aerogels prepared by freeze drying.After the SGA was cyclically compressed with 70%strain for 300 times,it can return to the original shape and height substantially.SGA retained about 90%of the initial adsorption capacity after 50 cycles of adsorption and compression regeneration for cyclohexane.
基金Funded by the National High Technology Research and Development Program(863 Program)(No.2013AA050905),China Academy of Engineering Physics,Mianyang,China
文摘Carbon aerogels were synthesized via ambient pressure drying process using resorcinolformaldehyde as precursor and P123 to strengthen their skeletons. CO2 activation technology was implemented to improve surface areas and adjust pore size distribution. The synthesis process was optimized, and the morphology, structure, adsorption properties and electrochemical behavior of different samples were characterized. The CO2-activated samples achieved a high specific capacitance of 129.2 F/g in 6 M KOH electrolytes at the current density of 1 m A/cm^2 within the voltage range of 0-0.8 V. The optimized activation temperature and duration were determined to be 950 ℃ and 4 h, respectively.
基金Funded by the National Natural Science Foundation of China(NSFC)(Nos.51278073,51308079 and 51408073)
文摘An ambient pressure synthesis of SiO2/TiO2 binary aerogel was prepared through the low-cost precursors of titanium tetrachloride（TiCl4） and sodium silicate（Na2O·nSiO2）.After gelation,solvent exchange and surface modification were performed simultaneously and the modified gel was finally dried under ambient pressure.Microstructural analyses by transmission electron microscope（TEM） indicate that fabricated SiO2/TiO2 aerogel composite shows similar sponge-like nanostructure as silica aerogel,and the Brunauer-EmmettTeller（BET） analysis shows that the specific surface area of the composite reaches 605 m^2/g,and the average pore size is 9.7 nm.Such binary aerogel exhibits significant photocatalytic performance in this paper for treating model pollutant of methyl orange（MO）,and the decolorizing efficiency of MO is detected as 84.9%after 210 mins exposure to UV light irradiation.Degraded gel suspends in the water so as to separate from solution for reuse,and after 4 times recycling,70%degradation efficiency can be easily reached when composite catalyzed system is exposed for 210 mins under UV irradiation.
基金This work was supported by tile National Natural Science Foundation of China(Grant No.20133040,59802007,69978017)Chinese National Foundation of High Technology(2002AA842052)+2 种基金Shanghai Committee of Science and Technology(055211010,0352nm022,0352nm056)Shanghai Key Subject Programme,Shanghai Phospher Program(05QMH1413)Trans-Century Training Programme Foundation for the Talents by the State Education Commission.
文摘Silica aerogels were prepared by sol-gel technique from industrial silicon derivatives （polyethoxydisiloxanes, E40）, followed by silylation and drying under ambient pressure. The specific surface area, pore size distribution and thermal conductivity of the silica aerogels were investigated and the results showed that the diameter of the silica particles is about 6 nm and the average pore size of the silica aerogels is 14.7 nm. The specific surface area of which is about 1000 m^2.g^-1 and the thermal conductivity is about 0.014 wm^-l.K^-1 at room temperature and pressure of 1.01×10^5 Pa. The Si-CH3 groups were also detected on the internal surface of the silica aerogels, which show hydrophobic. Silica aerogels derived by this technique is low cost and have wide applications.
基金Funded by the National Mega-Project of Scientific & Technical Sup-porting Programs, Ministry of Science & Technology of China(No.2006BAJ04A 04)the Science Foundation of Liaoning Province,China (No.20062147)
文摘The synthesis procedures and physical properties of the ambient dried hydrophobic silica aerogels by using different contents of ethanol （EtOH）/trimethylchlorosilane （TMCS）/n-Hexane as surface modification agent were investigated. One-step solvent exchange and surface modification were simultaneously progressed by immersing silica hydrogels in EtOH/TMCS/n-Hexane solution. It is found that microstructures as well as properties of silica aerogels like porosity, specific density and specific surface area are affected by the contents of surface modification agent in the sol from the results of SEM, TEM morphology, FT-IR chemical structure, BET surface area and BJH pore size analyses. The volume of TMCS is of 10% and 20% of hydrogels, and the final product is hydrophilic xerogels. When TMCS＇s percent （v/v） is elevated to 75 %-100%, hydrophobic silica aerogels with good performance are synthesized, the porosities of aerogels are in the range of 93.5%-95.8% and the average pore size diameter is less than 20 nm.
基金supported by National Natural Science Foundation of China - The Key Theory Study on Vacuum-superheated Vapor Wood Drying (30871978)
文摘In this work, Chinese fir samples with a size of 400 mm (L) by 50 mm (W) 30 mm (H) weretaken as specimens, and drying rate and energy consumption were compared under the conditions, inwhich the absolute pressure was 0.02 , 0.04 , 0.06 and 0.10 MPa, respectively, and the temperature was80 oC. The results showed that, when the moisture content (MC) of the samples was above fibersaturation point (FSP), the vacuum drying rate was 0.96-1.24 times as high as the ambient pressuredrying rate. However, when it was below FSP, the vacuum drying rate was 1.26-1.32 times as high as theambient pressure drying rate. At the same time, when the MC was above FSP, the energy consumptionof vacuum drying was 81.1%-95.9% of that of ambient pressure drying; when the MC was below FSP,the energy consumption of vacuum drying was 62.40%-69.40% of that of ambient pressure drying.Therefore, the vacuum drying was superior to the ambient pressure drying in terms of drying rate andenergy consumption.
基金Supported by the the National Natural Science Foundation of China(No.51278086)Petro China Innovation Fundation(No.2013D-5006-0606)+3 种基金the Program for New Century Excellent Talents in University by Ministry of Education of the People’s Republic of China(No.NCET-12-0084)Liaoning BaiQianWan Talents of Science and Technology Program(No.2012921073)Henan Open and Cooperation Project of Scienceand Technology(No.142106000023)Dalian Plan Projects of Science and Technology(No.2013A16GX113)
文摘Diatomite was used as raw material to prepare sodium silicate with a modulus of 3.1 by alkali dissolution method and the resulted sodium silicate solution was employed as a precursor. Methyl methaerylate monomers were introduced in wet gels through solution-immersion, and upon heating at 70 ℃, the mesoporous surfaces throughout the skeletal framework were coated with the polymer layer. PMMA modified silica aerogels were successfully synthesized via ambient pressure drying. The properties were investigated by FT- IR, NMR, TGA, nitrogen adsorption-desorption, FESEM and nano-indentation, etc. Results indicate that with the increasing of PMMA incorporated into silica aerogels, the bulk density and the BET surface area increase, the porosity decreases. Through the observation of FESEM, it is found that the interconnecting pores and the big pores add, the pore size distribution expands from 5-17 to 28-150 urn. By comparison, the PMMA modified silica aerogels achieve a 52-fold increase in hardness and a 10-fold increase in modulus.
基金Funded by the Fundamental Research Funds for the Central Universities (No.DUT11NY11)the State Key Laboratory of Coastal and Offshore Engineering (No.LP1109)
文摘Multi-walled carbon nanotube doped silica aerogels（MWCNT-SAs） were synthesized from a wet gel of well-dispersed MWCNT by one-step solvent exchange/surface modification and ambient pressure drying（APD）. Waterglass was employed as a precursor to prepare wet gel. The content of MWCNT varied from 0 to 15% volume by wet gel. The surface group, thermal stability and microstructure of pure silica aerogel and MWCNT-SAs were investigated by FTIR, DTA, and TEM. Experimental results show that MWCNT-SAs are hydrophobic when the temperature is below 400 ℃, MWCNT-SAs exhibit a mesoporous network structure, and they achieve the largest scale with least shrinkage and lowest density when doped with 5 vol% MWCNT.
文摘Here we present an economical ambient pressure drying method of preparing monolithic silica aerogels from methyltrimethoxysilane precursor while using sodium bicarbonate solution as the exchanging solvent.We prepared silica aerogels with a density and a specific surface area of 0.053 g·cm^(-3) and 423 m^(2)·g^(-1) respectively.The average pore diameter of silica aerogels is 23 nm as the pore specific volume is 1.11 cm^(3)·g^(-1),Further,the contact angle between water droplet and the surface of silica aerogels in specific condition can be as high as 166°,which indicates a super-hydrophobic surface of aerogels.
基金supported by the National Key Research and Development Project(2019YFC1907801)the Innovation-Driven Project of Central South University(No.2020CX007).
文摘Titanium oxides have been considered promising anode materials for lithium-ion batteries(LIBs).However,the poor conductivity and low specific capacity of bulk titanium oxides limit their application.In this study,a carbon dot-modified TiO_(2)@SiO_(2)aerogel was successfully fabricated through a facile ambient pressure drying strategy and used as an anode material of LIBs.Benefiting from the crosslinking of carbon dots and the surface modification of SiO_(2),the as-prepared hierarchical aerogel exhibited a high initial discharge capacity of 974 mAh g^(−1)and maintained a capacity of 299 mAh g^(−1)after 100 cycles at 0.1 A g^(−1).It also retained a discharge capacity of 111 mAh g^(−1)with a CE of 99.9%at 3 A g^(−1).The carbon dot-modified cross-linking skeleton contributes to the structural integrity of the TiO_(2)@SiO_(2)aerogel during repeated insertion/extraction of lithium ions,guaranteeing outstanding cycling and high-rate performance.This ambient pressure drying strategy provides a facile and feasible way to produce high-performance aerogel anode materials for lithium-ion storage.
