The hierarchically structured ZSM-5 monolith was prepared through transforming the skeletons of the macroporous silica gel into ZSM-5 by the steam-assisted conversion method. The morphology and monolithic shapes of ma...The hierarchically structured ZSM-5 monolith was prepared through transforming the skeletons of the macroporous silica gel into ZSM-5 by the steam-assisted conversion method. The morphology and monolithic shapes of macroporous silica gel were well preserved. The hierarchically structured ZSM-5 monolith exhibited the hierarchical porosity, with mesopores and macropores existing inside the macroporous silica gel, and micropores formed by the ZSM-5. The products have been characterized properly by using the XRD, SEM and N2 adsorption–desorption methods.展开更多
The effect of drying techniques on the microstructure,morphology and pore structure of porous silica gels was studied in the paper.The gels were prepared by using sol-gel process and different drying routes:freeze-dry...The effect of drying techniques on the microstructure,morphology and pore structure of porous silica gels was studied in the paper.The gels were prepared by using sol-gel process and different drying routes:freeze-drying (FD),low pressure drying (LPD),high temperature drying (HTD) and chemical modification & ambient drying (CMD) techniques.Observation under pore distribution and structural properties showed that CMD technique leads to homogenous mesoporous silica material with specific surface area of 745 m2/g,and the average pore size around 20 nm,while LPD and HTD result in loosely packed particles with non-isotropic aggregation pattern.The specific surface areas of LPD and HTD samples are 419 and 513 m2/g respectively,and the pore size distribution of the samples are observed distributing widely in range of 10-100 nm.Freeze drying method is a new but prospective way to prepare mesoporous silica.The specific area of FD sample is around 500 m2/g.By the comparison for the properties of the gels,this paper wants to induce a further interest in finding a proper method to synthesize the porous silica gels for low price use.展开更多
Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based compos...Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based composites were compared with adding different silica gel particle size and proportion.The morphological characteristics,the isothermal equilibrium moisture content curve,moisture absorption and desorption rate,moisture absorption and desorption stability,and humidity-conditioning performance were tested and analyzed.The experimental results show that,compared with pure-gypsum,the surface structure of the gypsum-based composites is relatively loose,the quantity,density and aperture of the pores in the structure increase.The absorption and desorption capacity increase along with the increase of silica gel particle size and silica gel proportion.When 3 mm silica gel particle size is added with a mass ratio of 40%,the maximum equilibrium moisture content of humidity-controlling composites is 0.161 g/g at 98% relative humidity(RH),3.22 times that of pure-gypsum.The moisture absorption and desorption rates are increased,the equilibrium moisture absorption and desorption rates are 2.68 times and 1.61 times that of pure-gypsum at 58.5% RH,respectively.The gypsum-based composites have a good stability,which has better timely response to dynamic humidity changes and can effectively regulate indoor humidity under natural conditions.展开更多
In this paper,a novel mesoporous silica gel evenly doped by Prussian blue nanoparticles(PBMSG) was successfully synthesized by using N,N-dimethylamide as template with a large Barrett-Emmett-Teller(BET) surface area o...In this paper,a novel mesoporous silica gel evenly doped by Prussian blue nanoparticles(PBMSG) was successfully synthesized by using N,N-dimethylamide as template with a large Barrett-Emmett-Teller(BET) surface area of 505 m^(2)/g and an average pore size of 2.9 nm.The static adsorption experiments showed that the equilibration time of PBMSG for Cs^(+) was about 30 min.The adsorption isotherm of PBMSG for Cs^(+) accorded with Langmuir model and the theoretical maximum adsorption capacity was80.0± 2.9 mg/g.When the initial concentration of Cs^(+) was 1.00 mg/L,the adsorption partition coefficient Kd could reach 3.5 × 10^4 mL/g After adsorption,Cs+ could be eluted by dilute hydrochloric acid(pH2) with an efficiency of 89.8%,while no K^(+),Fe^(3+),Fe^(2+) was eluted.PBMSG exhibited good selectivity toward Cs^(+) and Rb^(+).In the presence of high concentration of K^(+),the selective adsorption of PBMSG could change the mass ratio of K^(+),Rb^(+) and Cs^(+) from 96.63:0.83:1.00-1.12:0.73:1.00.The separation of Cs^(+) and Rb^(+) from K^(+) with similar concentration(100 mg/g) was realized by column experiment.This indicated that PBMSG was suitable for rapid recovery of low concentration of rubidium and cesium from complex matrixes,such as wastewater and salt lake brine,etc.展开更多
Chlorophyll a(naturally occurring Mg porphyrene)has been entrapped in nano/porous silica gel using sol-gel method at room temperature,producing a stable composite.HR TEM observationreveals regular nanoscale[around 15-...Chlorophyll a(naturally occurring Mg porphyrene)has been entrapped in nano/porous silica gel using sol-gel method at room temperature,producing a stable composite.HR TEM observationreveals regular nanoscale[around 15-20 nm diameter]distribution of aggregated polycrystalinechlorophylla within porous silica matrix.UV-vis study also corroborates the presence of variousaggregated chlorophyll a species within the system.Low field measurement shows almost 400times enhancement of dielectric constant(1700)with incorporation of only 0.125 mg/ml of chlorophyll and the loss is 0.5 at room temperature at 100 Hz.The dielectric constant of the composite reaches 2500 as chlorophyll concentration becomes 1 mg/ml.Observed strong space charge response to the external field and strong frequency dispersion of the dielectric properties ofthe composite can be attributed to the long-range electron delocalization[nomadic polarization]in chlorophyl a aggregates.The electric modulus(M*)formalism used in this study enabled us todistinguish and separate various relaxation processes.It is found that with increasing chlorophyll concentration D.C.relaxation time decreases exponentially at room temperature.It is shown that observed relaxations do not perfectly follow the Debye response in high frequency region due toheterogeneous distribution of chlorophyll aggregates.The low values of room temperature acti-vation energy calculated from Arrhenius plot reveal that polaronic hopping phenomena is absent at grain-interfacial region due to low thermal energy.展开更多
The adsorption of Pb(II)on silica gel synthesized from chemical glass bottle waste has been studied.The effect of independent variables(adsorbent dose,initial concentration of Pb(II),contact time,and pH)on the Pb(II)r...The adsorption of Pb(II)on silica gel synthesized from chemical glass bottle waste has been studied.The effect of independent variables(adsorbent dose,initial concentration of Pb(II),contact time,and pH)on the Pb(II)removal from water was evaluated and optimized using the Response Surface Methodology(RSM).Under optimized conditions(adsorbent dose:20 mg;contact time:30 min;initial Pb(II)concentration:120 mg.L^(−1);and pH:8),the removal of Pb(II)was 99.77%.The adsorption equilibrium data obtained from the batch experiment were investigated using different isotherm models.The Langmuir isotherm model fits the experimental data.This shows that the surface of the silica gel synthesized from chemical bottles waste was covered by a Pb(II)monolayer.XRF analysis showed that the synthesized silica gel had a SiO_(2) content of 75.63%.Amorphous silica was observed from XRD analysis.SEM-EDX characterization showed that Pb was adsorbed on the silica gel surface.SEM analysis showed that silica gel has irregular particles with a surface area of 297.08 m2.g^(−1) with a pore radius of 15.74 nm calculated from BET analysis.展开更多
This research focuses on the effective removal of methylene blue dye using silica gel synthesized from chemical glass bottle waste as an environmentally friendly and cost-effective adsorbent.The adsorption process was...This research focuses on the effective removal of methylene blue dye using silica gel synthesized from chemical glass bottle waste as an environmentally friendly and cost-effective adsorbent.The adsorption process was optimized using Box-Behnken Design(BBD)and Response Surface Methodology(RSM)to investigate the influence of pH(6;8 and 10),contact time(15;30 and 45 min),adsorbent mass(30;50 and 70 mg),and initial concentration(20;50 and 80 mg/L)of the adsorbate on the adsorption efficiency.The BBD was conducted using Google Colaboratory software,which encompassed 27 experiments with randomly assigned combinations.The silica gel synthesized from chemical glass bottle was characterized by XRD,FTIR,SEM-EDX and TEM.The adsorption result was measured by spectrophotometer UV-Vis.The optimized conditions resulted in a remarkable methylene blue removal efficiency of 99.41%.Characterization of the silica gel demonstrated amorphous morphology and prominent absorption bands characteristic of silica.The Langmuir isotherm model best described the adsorption behavior,revealing chemisorption with a monolayer coverage of methylene blue on the adsorbent surface,and a maximum adsorption capacity of 82.02 mg/g.Additionally,the pseudo-second-order kinetics model indicated a chemisorption mechanism during the adsorption process.The findings highlight the potential of silica gel from chemical glass bottle waste as a promising adsorbent for wastewater treatment,offering economic and environmental benefits.Further investigations can explore its scalability,regenerability,and reusability for industrial-scale applications.展开更多
Mesoporous poly (styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis wasachieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydrid...Mesoporous poly (styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis wasachieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymerin the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template orpore-forming agent, followed by ethanol extraction. Characterization results from nitrogen sorption isotherms and powder X-ray diffraction indicate that polymer-modified mesoporous materials with large specific surface areas (e.g. 900 m^2/g) andpore volumes (e.g. 0.6 cm^3/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, porevolumes and pore diameters of the hybrid materials increase.展开更多
Porous silica was synthesized via the sol-gel process using clay obtained locally from Ijero-Ekiti in Ekiti State, Nigeria and compared with silica synthesized under similar conditions from sodium metasilicate (Na2SiO...Porous silica was synthesized via the sol-gel process using clay obtained locally from Ijero-Ekiti in Ekiti State, Nigeria and compared with silica synthesized under similar conditions from sodium metasilicate (Na2SiO3) obtained comer- cially. The clay was initially refluxed with sodium hydroxide (NaOH) for 2 hours to extract SiO2 to form Na2SiO3, which was subsequently hydrolyzed to form a gel. The gel obtained was washed with deionized water to get rid of im-purities, dried and calcined at 800°C for 3 hours. The obtained silica powders were characterized using atomic absorp-tion spectrophotometer, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results showed that the vibrational modes and diffraction patterns of the silica derived from com-mercial Na2SiO3 and that prepared from clay were similar containing pure amorphous SiO2. The morphology of the commercially obtained silica showed better arrangement of particles and exhibited slightly lesser porosity (62.4%) compared to that derived from clay which had a porosity of 65.5%. The result indicates that clay has a potential for use as an environmentally safe and economic starting material for preparing porous silica instead of high quality precursors.展开更多
The phase separation and gel formation behavior in an alkoxy-derived silica sol-gel system containing C16EO15 has been investigated. Various gel morphologies similar to other sol-gel systems containing organic additiv...The phase separation and gel formation behavior in an alkoxy-derived silica sol-gel system containing C16EO15 has been investigated. Various gel morphologies similar to other sol-gel systems containing organic additives were obtained by changing the preparation conditions. Micrometer-range interconnected porous gels were obtained by freezing transitional structures of phase sepa- ration in the sol-gel process. The dependence of the resulting gel morphology on several important reaction parameters such as the starting composition, reaction temperature and acid catalyst concentration was studied in detail. The experimental results indicate that the gel morphology is mainly determined by the time relation between the onset of phase separation and gel formation.展开更多
Structural strengthening of the nano porous silica films has been reported. The films were prepared with a base/acid two-step catalyzed TEOS-based sol-gel processing and dip-coating, and then baked in the mixed gas of...Structural strengthening of the nano porous silica films has been reported. The films were prepared with a base/acid two-step catalyzed TEOS-based sol-gel processing and dip-coating, and then baked in the mixed gas of ammonia and water vapor. The silica films were characterized with TEM, AFM, FTIR, spectrophotometer, ellipsometer, and abrasion test, respectively. The experimental results have shown that the films have a nanostructure with a low refractive index and can form an excellent scratch-resistant broadband anti-reflectance. The two-step catalysis noticeably strengthens the films, and the mixed gas treatment further improves mechanical strength of the silica network. Finally the strengthening mechanism has been discussed.展开更多
Biogas can be used as an alternative energy source for producing heat and electricity;however, volatile methylsiloxanes(VOSiC) present in biogas can severely damage heat exchangers, turbines and gas engines. Consequen...Biogas can be used as an alternative energy source for producing heat and electricity;however, volatile methylsiloxanes(VOSiC) present in biogas can severely damage heat exchangers, turbines and gas engines. Consequently, e cient removal of VOSiC from biogas that is used as a biofuel is required. In this work, acetylated silica gel(Ac@SG) was synthesized,via treatment of microporous silica gel(SG) with acetic anhydride as an adsorbent, for removal of VOSiC from biogas,and characterized with XRD, SEM–EDS, N2-BET and FT-IR. This Ac@SG adsorbent exhibited a meso-/microporous structure and hydrophobic surface, indicating it was a more e cient adsorbent for removing hexamethyldisiloxane(L2) and octamethylcyclotetrasiloxane(D4) from biogas samples than conventional SG. It was found that the adsorption capacities of Ac@SG reached 304 mg L2/g for hexamethyldisiloxane and 916 mg D4/g for octamethylcyclotetrasiloxane at lower temperatures in the experimental range, and water had no significant e ect on its absorption e ciency. The used Ac@SG could be easily regenerated by heating it at 110 °C, and the adsorption capacity of recycled Ac@SG for hexamethyldisiloxane and octamethylcyclotetrasiloxane was kept constant in four recycle adsorption experiments.展开更多
In this paper, nitrogen-doped hierarchical porous carbon(N-HPC) was prepared from polyaniline(PANI)/silica self-aggregates. H-bonding between N\\H groups in aniline/PANI and \\OH groups in nano silica template led to ...In this paper, nitrogen-doped hierarchical porous carbon(N-HPC) was prepared from polyaniline(PANI)/silica self-aggregates. H-bonding between N\\H groups in aniline/PANI and \\OH groups in nano silica template led to a self-assembly type, which enabled the formation of uniform N-HPC nanoparticles. Silica self-aggregates provided macroporous channels resulted in a decreased diffusion distance. After removing the hard template,the N-HPC had a high surface area(899 m^2·g^(-1)). Owing to two co-existed synergetic energy-storage mechanisms and the hierarchical porous structure, the obtained N-HPC exhibited a high specific capacitance of 218.75 F·g^(-1) at 0.5 A·g^(-1), compared with the nonporous nitrogen-doped carbon(N-C) derived from pure PANI. Moreover, the N-HPC electrode demonstrated excellent cycle life, retaining 99% of its initial specific capacitance after 1000 cycles.展开更多
Hybrid drug delivery systems(DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybr...Hybrid drug delivery systems(DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybrid thermoresponsive DDS were fully characterized and loaded with a model drug. The in vitro drug release tests are carried out at below and above the lower critical solution temperature(LCST) of the copolymer. The results have revealed that due to the presence of small diameter(~1.3 nm) micropores at the periphery of the particles, the collapsed globules of the thermoresponsive copolymer above its LCST hinders the complete release of the drug which resulted in a reverse thermoresponsive drug release profile by the hybrid DDS.展开更多
A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid(2,4-D) was prepared by a surface imprinting technique in combination with a sol-gel process.The 2,4-D-imprin...A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid(2,4-D) was prepared by a surface imprinting technique in combination with a sol-gel process.The 2,4-D-imprinted amino-functionalized silica sorbent was characterized by FT-IR,nitrogen adsorption and static adsorption experiments.The selectivity of the sorbent was investigated by a batch competitive binding experiment using an aqueous 2,4-D and 2,4-dichlorophenol(2,4-DCP) mixture or using an aqueous 2,4-D and 2,4dichlorophenylacetic acid(DPAC) mixture.The largest selectivity coefficient for 2,4-D in the presence of 2,4-DCP was found to be over 18,the largest relative selectivity coefficient between 2,4-D and 2,4-DCP over 9.The static uptake capacity and selectivity coefficient of the 2,4-D-imprinted functionalized sorbent are higher than those of the non-imprinted sorbent.The imprinted functionalized silica gel sorbent offered a fast kinetics for the extraction/stripping of 2,4-D,73% of binding capacity(200 mg/L 2,4-D onto 20 mg of imprinted sorbent) was obtained within 5 min and the adsorbed 2,4-D can be easily stripped by the mixture solution of ethanol and 6 mol/L HCl(V:V =1:1).In a test of five extraction/stripping cycles,the adsorption capacity of the sorbent was all above 93% of that of the fresh sorbent.Experimental result showed the potential of molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-D.展开更多
Deoxynivalenol(DON) is a type B trichothecenes mycotoxin produced by several Fusarium species, often found in foodstuffs for humans and animals. DON is in great demand for the toxicological researches both in vivo and...Deoxynivalenol(DON) is a type B trichothecenes mycotoxin produced by several Fusarium species, often found in foodstuffs for humans and animals. DON is in great demand for the toxicological researches both in vivo and in vitro. In this work, wheat culture was inoculated with a Fusarium graminearum PH-1 strain for DON production. The solvent system for crude extraction was acetonitrile-water(84:16, v/v). A simple two-step silica gel column chromatography was employed to separate the DON mycotoxin from wheat culture, combined with preparative high performance liquid chromatography(preparative HPLC) to purify the compound. The solvent system for the second silica gel column chromatography was methylene chloride-methanol(17:1, v/v), which provided a good elution effect selected on thin layer chromatography(TLC). The target compound was identified by HPLC, and the chemical structure was confirmed by mass spectrometry(MS) and ~1H and ^(13)C nuclear magnetic resonance(NMR) spectroscopy. A total of 433 mg of purified DON was obtained from 1 kg of wheat culture, with a purity of 99.01%. The study had provided an easy-operating and cost-effective method to isolate an expensive compound in a simple way.展开更多
A novel adsorbent (AMPS-silica) was synthesized by bounding AMPS (2-acrylamido-2-methylpropanesulfonic acid) onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent was ...A novel adsorbent (AMPS-silica) was synthesized by bounding AMPS (2-acrylamido-2-methylpropanesulfonic acid) onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent was characterized by nitrogen adsorption/desorption measurement, thermogravimetric analysis (TGA) and potentiometric titration analysis. The TGA result indicated that the surface modification reactions introduced some organic functional groups onto the surface of silica. The surface area of AMPSsilica was 389.7 m2/g. The adsorbent was examined for copper ion removal in series of batch adsorption experiments. Results showed that the adsorption of Cu2+ onto AMPS-silica was pH dependent, and the adsorption capacity increased with increasing pH from 2 to 6. The adsorption kinetics showed that Cu2+ adsorption was fast and the data fitted well with a pseudo secondorder kinetic model. The adsorption of Cu2+ onto AMPS-silica obeyed both Freundlich and Langmuir isotherms, with r2 = 0.993 and r2 = 0.984, respectively. The maximum Cu2+ adsorption capacity was 19.9 mg/g. The involved mechanism might be the adsorption through metal binding with organic functional groups such as carboxyl, amino and sulfonic groups. Cu2+ loaded on AMPS-silica could be desorbed in HNO3 solution, and the adsorption properties remain stable after three adsorption-desorption cycles.展开更多
In this work,a series of polyethyleneimine(PEI) functionalized commercial silica gel were prepared by wet impregnation method and used as CO 2 sorbent.The as-prepared sorbents were characterized by N 2 adsorption,FT-I...In this work,a series of polyethyleneimine(PEI) functionalized commercial silica gel were prepared by wet impregnation method and used as CO 2 sorbent.The as-prepared sorbents were characterized by N 2 adsorption,FT-IR and SEM techniques.CO 2 capture was tested in a fixed bed reactor using a simulated flue gas containing 15.1% CO 2 in a temperature range of 25-100 C.The effects of sorption temperature and amine content on CO 2 uptake of the adsorbents were investigated.The silica gel with a 30 wt% PEI loading manifested the largest CO 2 uptake of 93.4 mg CO 2 /g adsorbent(equal to 311.3 mg CO 2 /g PEI) among the tested sorbents under the conditions of 15.1%(v/v) CO 2 in N 2 at 75 C and atmospheric pressure.Moreover,it was rather low-cost.In addition,the PEI-impregnated silica gel exhibited stable adsorption-desorption behavior during 5 consecutive test cycles.These results suggest that the PEI-impregnated silica gel is a promising and cost-effective sorbent for CO 2 capture from flue gas and other stationary sources with low CO 2 concentration.展开更多
文摘The hierarchically structured ZSM-5 monolith was prepared through transforming the skeletons of the macroporous silica gel into ZSM-5 by the steam-assisted conversion method. The morphology and monolithic shapes of macroporous silica gel were well preserved. The hierarchically structured ZSM-5 monolith exhibited the hierarchical porosity, with mesopores and macropores existing inside the macroporous silica gel, and micropores formed by the ZSM-5. The products have been characterized properly by using the XRD, SEM and N2 adsorption–desorption methods.
基金Sponsored by the National Mega-Project of Scientific & Technical Supporting Programs,Ministry of Science &Technology of China (Grant No.2006BAJ04A04)the Science Foundation of Liaoning Province,China (Grant No. 2008S190)
文摘The effect of drying techniques on the microstructure,morphology and pore structure of porous silica gels was studied in the paper.The gels were prepared by using sol-gel process and different drying routes:freeze-drying (FD),low pressure drying (LPD),high temperature drying (HTD) and chemical modification & ambient drying (CMD) techniques.Observation under pore distribution and structural properties showed that CMD technique leads to homogenous mesoporous silica material with specific surface area of 745 m2/g,and the average pore size around 20 nm,while LPD and HTD result in loosely packed particles with non-isotropic aggregation pattern.The specific surface areas of LPD and HTD samples are 419 and 513 m2/g respectively,and the pore size distribution of the samples are observed distributing widely in range of 10-100 nm.Freeze drying method is a new but prospective way to prepare mesoporous silica.The specific area of FD sample is around 500 m2/g.By the comparison for the properties of the gels,this paper wants to induce a further interest in finding a proper method to synthesize the porous silica gels for low price use.
基金Funded by the National Natural Science Foundation of China(No.51678254)。
文摘Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based composites were compared with adding different silica gel particle size and proportion.The morphological characteristics,the isothermal equilibrium moisture content curve,moisture absorption and desorption rate,moisture absorption and desorption stability,and humidity-conditioning performance were tested and analyzed.The experimental results show that,compared with pure-gypsum,the surface structure of the gypsum-based composites is relatively loose,the quantity,density and aperture of the pores in the structure increase.The absorption and desorption capacity increase along with the increase of silica gel particle size and silica gel proportion.When 3 mm silica gel particle size is added with a mass ratio of 40%,the maximum equilibrium moisture content of humidity-controlling composites is 0.161 g/g at 98% relative humidity(RH),3.22 times that of pure-gypsum.The moisture absorption and desorption rates are increased,the equilibrium moisture absorption and desorption rates are 2.68 times and 1.61 times that of pure-gypsum at 58.5% RH,respectively.The gypsum-based composites have a good stability,which has better timely response to dynamic humidity changes and can effectively regulate indoor humidity under natural conditions.
基金National NaturalScience Foundation of China (No.U1507203)Science Challenge Project (No.TZ2016004)。
文摘In this paper,a novel mesoporous silica gel evenly doped by Prussian blue nanoparticles(PBMSG) was successfully synthesized by using N,N-dimethylamide as template with a large Barrett-Emmett-Teller(BET) surface area of 505 m^(2)/g and an average pore size of 2.9 nm.The static adsorption experiments showed that the equilibration time of PBMSG for Cs^(+) was about 30 min.The adsorption isotherm of PBMSG for Cs^(+) accorded with Langmuir model and the theoretical maximum adsorption capacity was80.0± 2.9 mg/g.When the initial concentration of Cs^(+) was 1.00 mg/L,the adsorption partition coefficient Kd could reach 3.5 × 10^4 mL/g After adsorption,Cs+ could be eluted by dilute hydrochloric acid(pH2) with an efficiency of 89.8%,while no K^(+),Fe^(3+),Fe^(2+) was eluted.PBMSG exhibited good selectivity toward Cs^(+) and Rb^(+).In the presence of high concentration of K^(+),the selective adsorption of PBMSG could change the mass ratio of K^(+),Rb^(+) and Cs^(+) from 96.63:0.83:1.00-1.12:0.73:1.00.The separation of Cs^(+) and Rb^(+) from K^(+) with similar concentration(100 mg/g) was realized by column experiment.This indicated that PBMSG was suitable for rapid recovery of low concentration of rubidium and cesium from complex matrixes,such as wastewater and salt lake brine,etc.
文摘Chlorophyll a(naturally occurring Mg porphyrene)has been entrapped in nano/porous silica gel using sol-gel method at room temperature,producing a stable composite.HR TEM observationreveals regular nanoscale[around 15-20 nm diameter]distribution of aggregated polycrystalinechlorophylla within porous silica matrix.UV-vis study also corroborates the presence of variousaggregated chlorophyll a species within the system.Low field measurement shows almost 400times enhancement of dielectric constant(1700)with incorporation of only 0.125 mg/ml of chlorophyll and the loss is 0.5 at room temperature at 100 Hz.The dielectric constant of the composite reaches 2500 as chlorophyll concentration becomes 1 mg/ml.Observed strong space charge response to the external field and strong frequency dispersion of the dielectric properties ofthe composite can be attributed to the long-range electron delocalization[nomadic polarization]in chlorophyl a aggregates.The electric modulus(M*)formalism used in this study enabled us todistinguish and separate various relaxation processes.It is found that with increasing chlorophyll concentration D.C.relaxation time decreases exponentially at room temperature.It is shown that observed relaxations do not perfectly follow the Debye response in high frequency region due toheterogeneous distribution of chlorophyll aggregates.The low values of room temperature acti-vation energy calculated from Arrhenius plot reveal that polaronic hopping phenomena is absent at grain-interfacial region due to low thermal energy.
文摘The adsorption of Pb(II)on silica gel synthesized from chemical glass bottle waste has been studied.The effect of independent variables(adsorbent dose,initial concentration of Pb(II),contact time,and pH)on the Pb(II)removal from water was evaluated and optimized using the Response Surface Methodology(RSM).Under optimized conditions(adsorbent dose:20 mg;contact time:30 min;initial Pb(II)concentration:120 mg.L^(−1);and pH:8),the removal of Pb(II)was 99.77%.The adsorption equilibrium data obtained from the batch experiment were investigated using different isotherm models.The Langmuir isotherm model fits the experimental data.This shows that the surface of the silica gel synthesized from chemical bottles waste was covered by a Pb(II)monolayer.XRF analysis showed that the synthesized silica gel had a SiO_(2) content of 75.63%.Amorphous silica was observed from XRD analysis.SEM-EDX characterization showed that Pb was adsorbed on the silica gel surface.SEM analysis showed that silica gel has irregular particles with a surface area of 297.08 m2.g^(−1) with a pore radius of 15.74 nm calculated from BET analysis.
基金funded by Directorate of Research and Community Service(DRPM,Direktorat Riset dan Pengabdian Kepada Masyarakat)ITS through the ITS Research Local Grant(No.1727/PKS/ITS/2023).
文摘This research focuses on the effective removal of methylene blue dye using silica gel synthesized from chemical glass bottle waste as an environmentally friendly and cost-effective adsorbent.The adsorption process was optimized using Box-Behnken Design(BBD)and Response Surface Methodology(RSM)to investigate the influence of pH(6;8 and 10),contact time(15;30 and 45 min),adsorbent mass(30;50 and 70 mg),and initial concentration(20;50 and 80 mg/L)of the adsorbate on the adsorption efficiency.The BBD was conducted using Google Colaboratory software,which encompassed 27 experiments with randomly assigned combinations.The silica gel synthesized from chemical glass bottle was characterized by XRD,FTIR,SEM-EDX and TEM.The adsorption result was measured by spectrophotometer UV-Vis.The optimized conditions resulted in a remarkable methylene blue removal efficiency of 99.41%.Characterization of the silica gel demonstrated amorphous morphology and prominent absorption bands characteristic of silica.The Langmuir isotherm model best described the adsorption behavior,revealing chemisorption with a monolayer coverage of methylene blue on the adsorbent surface,and a maximum adsorption capacity of 82.02 mg/g.Additionally,the pseudo-second-order kinetics model indicated a chemisorption mechanism during the adsorption process.The findings highlight the potential of silica gel from chemical glass bottle waste as a promising adsorbent for wastewater treatment,offering economic and environmental benefits.Further investigations can explore its scalability,regenerability,and reusability for industrial-scale applications.
基金the National Natural Science Foundation of China(Grant No.20133040)the Chinese National Foundation of High Technology(2002AA842052)+1 种基金the Shanghai Nanotechnology Promotion Center(0352nm022,0352nm056)the Shanghai International Cooperation Program and Trans-Century Training Programme Foundation for the Talents by the State Education Commission.
基金Project supported by the National Natural Science Foundation of China (No. 29874002) and the Outstanding Young Scientist Award from National Natural Science Foundation of China (No. 29825504)
文摘Mesoporous poly (styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis wasachieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymerin the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template orpore-forming agent, followed by ethanol extraction. Characterization results from nitrogen sorption isotherms and powder X-ray diffraction indicate that polymer-modified mesoporous materials with large specific surface areas (e.g. 900 m^2/g) andpore volumes (e.g. 0.6 cm^3/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, porevolumes and pore diameters of the hybrid materials increase.
文摘Porous silica was synthesized via the sol-gel process using clay obtained locally from Ijero-Ekiti in Ekiti State, Nigeria and compared with silica synthesized under similar conditions from sodium metasilicate (Na2SiO3) obtained comer- cially. The clay was initially refluxed with sodium hydroxide (NaOH) for 2 hours to extract SiO2 to form Na2SiO3, which was subsequently hydrolyzed to form a gel. The gel obtained was washed with deionized water to get rid of im-purities, dried and calcined at 800°C for 3 hours. The obtained silica powders were characterized using atomic absorp-tion spectrophotometer, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results showed that the vibrational modes and diffraction patterns of the silica derived from com-mercial Na2SiO3 and that prepared from clay were similar containing pure amorphous SiO2. The morphology of the commercially obtained silica showed better arrangement of particles and exhibited slightly lesser porosity (62.4%) compared to that derived from clay which had a porosity of 65.5%. The result indicates that clay has a potential for use as an environmentally safe and economic starting material for preparing porous silica instead of high quality precursors.
文摘The phase separation and gel formation behavior in an alkoxy-derived silica sol-gel system containing C16EO15 has been investigated. Various gel morphologies similar to other sol-gel systems containing organic additives were obtained by changing the preparation conditions. Micrometer-range interconnected porous gels were obtained by freezing transitional structures of phase sepa- ration in the sol-gel process. The dependence of the resulting gel morphology on several important reaction parameters such as the starting composition, reaction temperature and acid catalyst concentration was studied in detail. The experimental results indicate that the gel morphology is mainly determined by the time relation between the onset of phase separation and gel formation.
基金the National Natural Science Foundation of China(No:69978017,20133040)Shanghai Key Subject Programme,Chinese Foundation of High Technology(2002AA842052)Shanghai Natural Science Foundation(02ZE14101)as well as Shanghai Nanotechnology Promotion Center(0159um039).
文摘Structural strengthening of the nano porous silica films has been reported. The films were prepared with a base/acid two-step catalyzed TEOS-based sol-gel processing and dip-coating, and then baked in the mixed gas of ammonia and water vapor. The silica films were characterized with TEM, AFM, FTIR, spectrophotometer, ellipsometer, and abrasion test, respectively. The experimental results have shown that the films have a nanostructure with a low refractive index and can form an excellent scratch-resistant broadband anti-reflectance. The two-step catalysis noticeably strengthens the films, and the mixed gas treatment further improves mechanical strength of the silica network. Finally the strengthening mechanism has been discussed.
基金financial support from the National Natural Science Foundation of China (21677046)the Natural Science Foundation of Hebei Province (B2017205146)
文摘Biogas can be used as an alternative energy source for producing heat and electricity;however, volatile methylsiloxanes(VOSiC) present in biogas can severely damage heat exchangers, turbines and gas engines. Consequently, e cient removal of VOSiC from biogas that is used as a biofuel is required. In this work, acetylated silica gel(Ac@SG) was synthesized,via treatment of microporous silica gel(SG) with acetic anhydride as an adsorbent, for removal of VOSiC from biogas,and characterized with XRD, SEM–EDS, N2-BET and FT-IR. This Ac@SG adsorbent exhibited a meso-/microporous structure and hydrophobic surface, indicating it was a more e cient adsorbent for removing hexamethyldisiloxane(L2) and octamethylcyclotetrasiloxane(D4) from biogas samples than conventional SG. It was found that the adsorption capacities of Ac@SG reached 304 mg L2/g for hexamethyldisiloxane and 916 mg D4/g for octamethylcyclotetrasiloxane at lower temperatures in the experimental range, and water had no significant e ect on its absorption e ciency. The used Ac@SG could be easily regenerated by heating it at 110 °C, and the adsorption capacity of recycled Ac@SG for hexamethyldisiloxane and octamethylcyclotetrasiloxane was kept constant in four recycle adsorption experiments.
基金Supported by the National Natural Science Foundation of China(21401079,21501069)Fundamental Research Funds for Central Universities(JUSRP51626B)+2 种基金the Natural Science Foundation of Jiangsu Province of China(BK20140158,BK20161128,BK20161166)Natural Science Fund for Colleges and Universities in Jiangsu Province(18KJD430008,17KJD430005,17KJB430032)the Top-notch Academic Programs Project of Jiangsu Higher Education Institutions(PPZY2015B181)
文摘In this paper, nitrogen-doped hierarchical porous carbon(N-HPC) was prepared from polyaniline(PANI)/silica self-aggregates. H-bonding between N\\H groups in aniline/PANI and \\OH groups in nano silica template led to a self-assembly type, which enabled the formation of uniform N-HPC nanoparticles. Silica self-aggregates provided macroporous channels resulted in a decreased diffusion distance. After removing the hard template,the N-HPC had a high surface area(899 m^2·g^(-1)). Owing to two co-existed synergetic energy-storage mechanisms and the hierarchical porous structure, the obtained N-HPC exhibited a high specific capacitance of 218.75 F·g^(-1) at 0.5 A·g^(-1), compared with the nonporous nitrogen-doped carbon(N-C) derived from pure PANI. Moreover, the N-HPC electrode demonstrated excellent cycle life, retaining 99% of its initial specific capacitance after 1000 cycles.
文摘Hybrid drug delivery systems(DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybrid thermoresponsive DDS were fully characterized and loaded with a model drug. The in vitro drug release tests are carried out at below and above the lower critical solution temperature(LCST) of the copolymer. The results have revealed that due to the presence of small diameter(~1.3 nm) micropores at the periphery of the particles, the collapsed globules of the thermoresponsive copolymer above its LCST hinders the complete release of the drug which resulted in a reverse thermoresponsive drug release profile by the hybrid DDS.
基金supported by the Natural Science Foundation of Zhejiang Province (No.Y505073)the Scientific Project of Zhejiang Province (No.2008C22012)
文摘A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid(2,4-D) was prepared by a surface imprinting technique in combination with a sol-gel process.The 2,4-D-imprinted amino-functionalized silica sorbent was characterized by FT-IR,nitrogen adsorption and static adsorption experiments.The selectivity of the sorbent was investigated by a batch competitive binding experiment using an aqueous 2,4-D and 2,4-dichlorophenol(2,4-DCP) mixture or using an aqueous 2,4-D and 2,4dichlorophenylacetic acid(DPAC) mixture.The largest selectivity coefficient for 2,4-D in the presence of 2,4-DCP was found to be over 18,the largest relative selectivity coefficient between 2,4-D and 2,4-DCP over 9.The static uptake capacity and selectivity coefficient of the 2,4-D-imprinted functionalized sorbent are higher than those of the non-imprinted sorbent.The imprinted functionalized silica gel sorbent offered a fast kinetics for the extraction/stripping of 2,4-D,73% of binding capacity(200 mg/L 2,4-D onto 20 mg of imprinted sorbent) was obtained within 5 min and the adsorbed 2,4-D can be easily stripped by the mixture solution of ethanol and 6 mol/L HCl(V:V =1:1).In a test of five extraction/stripping cycles,the adsorption capacity of the sorbent was all above 93% of that of the fresh sorbent.Experimental result showed the potential of molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-D.
基金supported by the National Natural Science Foundation of China (31402268)the Natural Science Foundation of Jiangsu Province of China (BK20140691)+1 种基金Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), ChinaThe Introduction of International Advanced Agricultural Science and Technology Project from the Ministry of Agriculture of China (2012-Z22)
文摘Deoxynivalenol(DON) is a type B trichothecenes mycotoxin produced by several Fusarium species, often found in foodstuffs for humans and animals. DON is in great demand for the toxicological researches both in vivo and in vitro. In this work, wheat culture was inoculated with a Fusarium graminearum PH-1 strain for DON production. The solvent system for crude extraction was acetonitrile-water(84:16, v/v). A simple two-step silica gel column chromatography was employed to separate the DON mycotoxin from wheat culture, combined with preparative high performance liquid chromatography(preparative HPLC) to purify the compound. The solvent system for the second silica gel column chromatography was methylene chloride-methanol(17:1, v/v), which provided a good elution effect selected on thin layer chromatography(TLC). The target compound was identified by HPLC, and the chemical structure was confirmed by mass spectrometry(MS) and ~1H and ^(13)C nuclear magnetic resonance(NMR) spectroscopy. A total of 433 mg of purified DON was obtained from 1 kg of wheat culture, with a purity of 99.01%. The study had provided an easy-operating and cost-effective method to isolate an expensive compound in a simple way.
基金supported by the Fundation for Creative Research Groups of China (No. 50621804)
文摘A novel adsorbent (AMPS-silica) was synthesized by bounding AMPS (2-acrylamido-2-methylpropanesulfonic acid) onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent was characterized by nitrogen adsorption/desorption measurement, thermogravimetric analysis (TGA) and potentiometric titration analysis. The TGA result indicated that the surface modification reactions introduced some organic functional groups onto the surface of silica. The surface area of AMPSsilica was 389.7 m2/g. The adsorbent was examined for copper ion removal in series of batch adsorption experiments. Results showed that the adsorption of Cu2+ onto AMPS-silica was pH dependent, and the adsorption capacity increased with increasing pH from 2 to 6. The adsorption kinetics showed that Cu2+ adsorption was fast and the data fitted well with a pseudo secondorder kinetic model. The adsorption of Cu2+ onto AMPS-silica obeyed both Freundlich and Langmuir isotherms, with r2 = 0.993 and r2 = 0.984, respectively. The maximum Cu2+ adsorption capacity was 19.9 mg/g. The involved mechanism might be the adsorption through metal binding with organic functional groups such as carboxyl, amino and sulfonic groups. Cu2+ loaded on AMPS-silica could be desorbed in HNO3 solution, and the adsorption properties remain stable after three adsorption-desorption cycles.
文摘In this work,a series of polyethyleneimine(PEI) functionalized commercial silica gel were prepared by wet impregnation method and used as CO 2 sorbent.The as-prepared sorbents were characterized by N 2 adsorption,FT-IR and SEM techniques.CO 2 capture was tested in a fixed bed reactor using a simulated flue gas containing 15.1% CO 2 in a temperature range of 25-100 C.The effects of sorption temperature and amine content on CO 2 uptake of the adsorbents were investigated.The silica gel with a 30 wt% PEI loading manifested the largest CO 2 uptake of 93.4 mg CO 2 /g adsorbent(equal to 311.3 mg CO 2 /g PEI) among the tested sorbents under the conditions of 15.1%(v/v) CO 2 in N 2 at 75 C and atmospheric pressure.Moreover,it was rather low-cost.In addition,the PEI-impregnated silica gel exhibited stable adsorption-desorption behavior during 5 consecutive test cycles.These results suggest that the PEI-impregnated silica gel is a promising and cost-effective sorbent for CO 2 capture from flue gas and other stationary sources with low CO 2 concentration.
