Enhancing catalytic activity of multi-enzyme in vitro through substrate channeling effect is promis-ing yet challenging.Herein,conjugated microporous polymers(CMPs)-scaffolded integrated en-zyme cascade systems(I-ECSs...Enhancing catalytic activity of multi-enzyme in vitro through substrate channeling effect is promis-ing yet challenging.Herein,conjugated microporous polymers(CMPs)-scaffolded integrated en-zyme cascade systems(I-ECSs)are constructed through co-entrapping glucose oxidase(GOx)and horseradish peroxidase(HRP),in which hydrogen peroxide(H_(2)O_(2)) is the intermediate product.The interplay of low-resistance mass transfer pathway and appropriate pore wall-H_(2)O_(2) interactions facilitates the directed transfer of H_(2)O_(2),resulting in 2.4-fold and 5.0-fold elevation in catalytic activ-ity compared to free ECSs and separated ECSs,respectively.The substrate channeling effect could be regulated by altering the mass ratio of GOx to HRP.Besides,I-ECSs demonstrate excellent stabili-ties in harsh environments and multiple recycling.展开更多
A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by...A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by Klebsiella aerogenes were found to be 0.25 mol/L calcium acetate,4%inoculum level,and pH 7.Following that,the monosaccharides and proteins contained in the extracellular polymeric substances(EPS)of Klebsiella aerogenes were identified.The effects of additional identified monosaccharide and proteins on the crystalline form conversion of CaCO_(3) crystals were investigated,and the additional monosaccharides were found to promote the crystalline form conversion of CaCO_(3) crystals from vaterite to calcite.Specifically,adding 1.00 g/L glucuronic acid was observed to enhance the conversion of crystalline phases of CaCO_(3) crystals to calcite completely after 5 d.Meanwhile,additional catalase was observed to contribute to the regular morphology of CaCO_(3) crystals without affecting their crystalline phases.The results indicate that the additional glucuronic acid influences the crystalline forms of CaCO_(3) crystals significantly.展开更多
The variation of microbial community structure was investigated for the tank bioleaching process of Pb-Zn-Sn chalcopyrite concentrate in the presence of mixed moderately thermophilic bacteria. The parameters, such as ...The variation of microbial community structure was investigated for the tank bioleaching process of Pb-Zn-Sn chalcopyrite concentrate in the presence of mixed moderately thermophilic bacteria. The parameters, such as pH value, solution potential and concentrations of metal ions, were determined by the method of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to analyze the succession of microbial community. The results showed that a final copper extraction rate of 85.6% could be obtained after tank bioleaching for 30 d. The Acidithiobacillus caldus was the dominant population with abundance of about 73.80%in the initial stage, then Sulfobacillus thermosulfidooxidans dominated from the 18th day to the end of bioleaching, while the abundance of Leptospirillum ferriphilum changed slightly. A higher solution potential within a certain range and appropriate concentration of ferric ions were essential for this tank bioleaching of chalcopyrite.展开更多
A novel porous coordination polymer,iron naphthalenedicarboxylate Fe(OH)(1,4-NDC)·2H2O is hydrothermally synthesized by the reaction of FeSO4·7H2O and 1,4-naphthalenedicarboxylic acid(1,4-H2NDC) at 150...A novel porous coordination polymer,iron naphthalenedicarboxylate Fe(OH)(1,4-NDC)·2H2O is hydrothermally synthesized by the reaction of FeSO4·7H2O and 1,4-naphthalenedicarboxylic acid(1,4-H2NDC) at 150℃.The compound crystallizes in a tetragonal space group P42/nmc:a=2.1447(4) nm,c=0.68849(14) nm,V=3.1669(11) nm3,Z=8,R=0.0845,wR=0.1829.The crystal structure exhibits a three-dimensional framework which is composed of infinite chains of corner-sharing octahedral Fe(OH)2O4 with 1,4-NDC ligands forming two types of channels with square-shaped cross-sections.The large channels present a cross-section of 0.76 nm×0.76 nm,while the small channels are about 0.30 nm×0.30 nm.No structural transformation occurs after removing the guest water molecules,while a robust structure generates with permanent porosity.The adsorption measurements show that the anhydrous sample of the compound can adsorb CO2 into its pores.The adsorption isotherms for methanol,acetone,tetrahydrofuran and benzene are also measured.展开更多
To design an accelerated method to evaluate thymopentin release from PLGA microspheres in vitro. Microspheres were prepared by double emulsion technique, using poly(lactide-co-glycolide) (PLGA) as carrier. At high...To design an accelerated method to evaluate thymopentin release from PLGA microspheres in vitro. Microspheres were prepared by double emulsion technique, using poly(lactide-co-glycolide) (PLGA) as carrier. At higher medium temperature (45℃, 50℃ and 55℃), an accelerated release testing in short time was studied and correlated with the conventional release (37℃) in vitro. The release in vitro of thymopentin from PLGA microspheres at 45 ℃, 50℃ and 55℃ was significantly accelerated (P 〈 0.05). In particular, at 50℃, an accelerated release (30 h) of the hydrophilic peptide from the PLGA matrix was achieved and correlated well with the conventional release (30 d). An accelerated release testing in vitro at higher temperature could be used to monitor thymopentin release from PLGA microspheres.展开更多
Aim Ciprofloxacin polylactic acid microspheres (CFX-PLA-MS) were preparedusing solvent evaporation method from a solid-in-oil-in-water emulsion system. Methods Orthogonalexperiment was used to optimize the method of C...Aim Ciprofloxacin polylactic acid microspheres (CFX-PLA-MS) were preparedusing solvent evaporation method from a solid-in-oil-in-water emulsion system. Methods Orthogonalexperiment was used to optimize the method of CFX-PLA-MS preparation. Microspheres werecharacterized in terms of morphology, size, encapsulation efficiency, drug loading and in vitro drugrelease. Results The physical state of CFX-PLA-MS was determined by scanning electron microscopy(SEM) and differential scanning calorimetry (DSC) . Microspheres formed were spherical with smoothsurfaces. Drug was enveloped in microspheres without mixing physically with PLA. The averageparticle size was 280.80 ± 0.15 μm, with over 90% of microspheres falling in the range of 250 -390 μm. The encapsulation efficiency was 65.8% ± 0.58% and the drug loading was 34.1% ± 0.51% .In vitro release study revealed a profile of sustained release of Ciprofloxacin from CFX-PLA-MS. Theaccumulated release percentage and half-life (T_(1/2) of Ciprofloxacin microspheres were 84.0% in53.2 h, and 31.9 h, respectively. Higuchi equation was Q= -0.0043 + 0.003 9 t^(1/2), r = 0.9941.Conclusion Ciprofloxacin microspheres have been successfully prepared and sustained release of CFXfrom microspheres is achieved.展开更多
The polymerization of styrene is monitored by pyrene excimer formation. The ratio of monomer to excimer intensities ( I m/ I e) of pyrene increases as polymerization proceeds. The increase of I m/ I e...The polymerization of styrene is monitored by pyrene excimer formation. The ratio of monomer to excimer intensities ( I m/ I e) of pyrene increases as polymerization proceeds. The increase of I m/ I e is ascribed to the increase of microviscosity surrounding the probes forming excimer during polymerization. The linear relationship between the changing rate of I m/ I e and the polymerization rate of styrene is obtained. Therefore, I m/ I e may be used to monitor the progress of the polymerization of styrene.展开更多
Cetyl-chitosan, prepared by reacting chitosan with chlorocetane under alkaline condition, is soluble and spontaneously forms nanoparticles about 100 nm in diameter. Infrared spectra (IR) revealed that there was a subs...Cetyl-chitosan, prepared by reacting chitosan with chlorocetane under alkaline condition, is soluble and spontaneously forms nanoparticles about 100 nm in diameter. Infrared spectra (IR) revealed that there was a substitution reaction mainly on the amine groups of chitosan (CS). By using paracetamol (PCTM) as a model drug, the balanced release concentration of PCTM in phosphate buffer solution (pH=7.4) can be decreased with the increase of degree of substitution alkyl and can be reduced effectively even under a lower PCTM loading.展开更多
Aim PLA/PLGA was used as biodegradable and biocompatible carriers to achieve sustained release of estradiol (E 2). Methods Microcapsules (MC) were prepared by an emulsification solvent extraction method, and then ...Aim PLA/PLGA was used as biodegradable and biocompatible carriers to achieve sustained release of estradiol (E 2). Methods Microcapsules (MC) were prepared by an emulsification solvent extraction method, and then the properties and in vitro drug release behavior of MC were examined. An analysis of variance (ANOVA) was used to test the statistical significance. Then, multiple comparisons were made with a T method between levels to examine the significance of difference further. For all the results a P value 】0 05 was considered statistically insignificant . Results Under the same conditions, the water adding speed and the particle size had significant effects ( P 【0 01) on the entrapment efficiency of MC; the water adding speed and the concentration of PLA in the oil phase had significant effects ( P 【0 01) on the diameter MC in medium. Release of E 2 from MC was influenced significantly ( P 【0 01) by the water adding speed and the type and molecule weight of the polymers. But the differences between levels of the variates were not all significant. Conclusion E 2 PLA/PLGA MC with various properties can be formed when the formulation and the technology were changed accordingly.展开更多
The composition and sequence distribution of monomeric units in polyester polyether multiblock copolymer were studied by pyrolysis? gas chromatography (PGC) and pyrolysis gas chromatography/mass spectrometry (PGC/M...The composition and sequence distribution of monomeric units in polyester polyether multiblock copolymer were studied by pyrolysis? gas chromatography (PGC) and pyrolysis gas chromatography/mass spectrometry (PGC/MS). PGC was applied to study the F t curve of the multiblock copolymer and PGC/MS was used to separate and identify the pyrolyzates. DTA experiment was used to study the decomposition temperature. The results show that the beginning point of elastomer’s decomposition was about 300?℃ and the decomposition temperature of most of the sample was 550?℃. Many pyrolyzates were produced because of the breaking of weak bonds in the sample. The possible microstructure was verified and the pyrolysis pathway of the copolymer was investigated.展开更多
The main objective of this paper focuses on the changes that occur in the strength and microstructural properties of sodium silicate activated fly ash based geopolymer due to varying the sulfate salt and water content...The main objective of this paper focuses on the changes that occur in the strength and microstructural properties of sodium silicate activated fly ash based geopolymer due to varying the sulfate salt and water content.A series of tests including X-ray diffraction,Fourier transform infrared spectroscopy,scanning electron microscopy,physical adsorption and unconfined compressive strength were used to investigate this effect.The results indicate that the higher water content has an adverse effect on the alkali activation and microstructural properties of geopolymer,so the optimum mass ratio of sodium sulfate in alkali-activated geopolymer under different water-to-binder ratios shows a“peak shifting”phenomenon,i.e.,the higher the water-to-binder ratio,the higher the optimum mass ratio.Lower presence of sodium sulfate has no significant effect on the alkali-activated geopolymer systems;higher addition of sodium sulfate,however,could cause the symmetrical stretching vibration of Si—O and the symmetrical stretching vibration of Si—O—Si and Al—O—Si,and promote the formation of N-A-S-H gels.Furthermore,the cement effect of the gel and sodium sulfate aggregate could improve the integrity of pore structure obviously.The maximum strength of geopolymer curing at ambient temperature was 52 MPa.This study obtains the rule that the strength properties of alkali-activated geopolymers vary with the water-to-binder ratio and sodium sulfate content.The feasibility of geopolymer co-activated by sodium sulfate and sodium silicate was investigated,and reference for engineering application of alkali-activated geopolymer in salt-bearing areas was provided.展开更多
Acryionitrilv-methyi mcthacrylate copolymer was synthesized in aqueous solution by Redox. The copolymer was mixed with 10 - 40 wt% of microencapsulated n-octadecane (MieroPCMs) in water. Copolymer films containing M...Acryionitrilv-methyi mcthacrylate copolymer was synthesized in aqueous solution by Redox. The copolymer was mixed with 10 - 40 wt% of microencapsulated n-octadecane (MieroPCMs) in water. Copolymer films containing Mi- eroPCMs were cast at room temperature in N, N- imethyiformamide solution. The copolymer of acrylonitrile-methyl methacrylate and the copolymer films containing MicroPC- Ms were characterized by using Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Thermosravimetrlc Analyzer (TG), X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM), etc. The mierocapsules in the films are evenly distributed in the copolymer matrix. The heat-absorbing temperatures and heat-evolving temperatures of the films are almost the same as that of the MieroPCMs, respectively, and fluctuate in a slight range. In addition, the enthalpy efficiency of MieroPCMs rises with the contents of MicroPCMs increasing. The crystallirdty of the film increases with the contents of MicroPOMs increasing.展开更多
Paramagnetic polymer microspheres were synthesized by the inverse suspension polymerizationmethod through polymerization of glycidyl methacrylate,ally glycidyl ether and methacrylamide onthe surface of silica‐coated ...Paramagnetic polymer microspheres were synthesized by the inverse suspension polymerizationmethod through polymerization of glycidyl methacrylate,ally glycidyl ether and methacrylamide onthe surface of silica‐coated Fe3O4nanoparticles using N,N’‐methylene‐bis(acrylamide)as across‐linking agent.Penicillin G acylase(PGA)was covalently immobilized on the surface of theparamagnetic microspheres by reacting the amino groups of the PGA molecules with the epoxygroups of the paramagnetic polymer microspheres.The effect of the SiO2coating and the amount ofparamagnetic Fe3O4nanoparticles on the initial activity and the operational stability of the immobilizedPGA was investigated.The results indicated that SiO2played an important role in the polymerization process and paramagnetic polymer microspheres with a SiO2‐coated Fe3O4nanoparticles mass content of7.5%are an optimal support material for PGA immobilization.Immobilized PGA on the paramagnetic polymer microspheres shows a high initial activity of430U/g(wet)and retains99%of its initial activity after recycling10times.Furthermore,immobilized PGA exhibits high thermal stability,pH stability and excellent reusability,which can be rapidly recycled by the aid of magnet.?2018,Dalian Institute of Chemical Physics,Chinese Academy of Sciences.Published by Elsevier B.V.All rights reserved.展开更多
文摘Enhancing catalytic activity of multi-enzyme in vitro through substrate channeling effect is promis-ing yet challenging.Herein,conjugated microporous polymers(CMPs)-scaffolded integrated en-zyme cascade systems(I-ECSs)are constructed through co-entrapping glucose oxidase(GOx)and horseradish peroxidase(HRP),in which hydrogen peroxide(H_(2)O_(2)) is the intermediate product.The interplay of low-resistance mass transfer pathway and appropriate pore wall-H_(2)O_(2) interactions facilitates the directed transfer of H_(2)O_(2),resulting in 2.4-fold and 5.0-fold elevation in catalytic activ-ity compared to free ECSs and separated ECSs,respectively.The substrate channeling effect could be regulated by altering the mass ratio of GOx to HRP.Besides,I-ECSs demonstrate excellent stabili-ties in harsh environments and multiple recycling.
基金supported by the National Natural Science Foundation of China(Nos.U20A20267,U1967210,12275123)Hunan Provincial Science Fund for Distinguished Young Scholars,China(No.2022JJ10041)the Program of Science and Technology Department of Hunan Province,China(Nos.2020 TJ-Q03,2022SK2077).
文摘A strain of Klebsiella aerogenes(K.aerogenes)capable of decomposing calcium acetate for CaCO_(3) biomineralization was screened,and the optimum conditions for producing the maximum mass of CaCO_(3) crystals induced by Klebsiella aerogenes were found to be 0.25 mol/L calcium acetate,4%inoculum level,and pH 7.Following that,the monosaccharides and proteins contained in the extracellular polymeric substances(EPS)of Klebsiella aerogenes were identified.The effects of additional identified monosaccharide and proteins on the crystalline form conversion of CaCO_(3) crystals were investigated,and the additional monosaccharides were found to promote the crystalline form conversion of CaCO_(3) crystals from vaterite to calcite.Specifically,adding 1.00 g/L glucuronic acid was observed to enhance the conversion of crystalline phases of CaCO_(3) crystals to calcite completely after 5 d.Meanwhile,additional catalase was observed to contribute to the regular morphology of CaCO_(3) crystals without affecting their crystalline phases.The results indicate that the additional glucuronic acid influences the crystalline forms of CaCO_(3) crystals significantly.
基金Project (51374248) supported by the National Natural Science Foundation of ChinaProject (NCET-13-0595) supported by the Program for New Century Excellent Talents in University,China+3 种基金Project (2012AA061501) supported by the High-tech Research and Development Program of ChinaProject (2010CB630905) supported by the National Basic Research Program of ChinaProject (20120162120010) supported by the Research Fund for the Doctoral Program of Higher Education of ChinaProject (CSUZC2012020) supported by the Open-End Fund for the Valuable in Central South University,China
文摘The variation of microbial community structure was investigated for the tank bioleaching process of Pb-Zn-Sn chalcopyrite concentrate in the presence of mixed moderately thermophilic bacteria. The parameters, such as pH value, solution potential and concentrations of metal ions, were determined by the method of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to analyze the succession of microbial community. The results showed that a final copper extraction rate of 85.6% could be obtained after tank bioleaching for 30 d. The Acidithiobacillus caldus was the dominant population with abundance of about 73.80%in the initial stage, then Sulfobacillus thermosulfidooxidans dominated from the 18th day to the end of bioleaching, while the abundance of Leptospirillum ferriphilum changed slightly. A higher solution potential within a certain range and appropriate concentration of ferric ions were essential for this tank bioleaching of chalcopyrite.
基金The Natural Science Foundation of Jiangsu Province(No.BK2009262)the Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry
文摘A novel porous coordination polymer,iron naphthalenedicarboxylate Fe(OH)(1,4-NDC)·2H2O is hydrothermally synthesized by the reaction of FeSO4·7H2O and 1,4-naphthalenedicarboxylic acid(1,4-H2NDC) at 150℃.The compound crystallizes in a tetragonal space group P42/nmc:a=2.1447(4) nm,c=0.68849(14) nm,V=3.1669(11) nm3,Z=8,R=0.0845,wR=0.1829.The crystal structure exhibits a three-dimensional framework which is composed of infinite chains of corner-sharing octahedral Fe(OH)2O4 with 1,4-NDC ligands forming two types of channels with square-shaped cross-sections.The large channels present a cross-section of 0.76 nm×0.76 nm,while the small channels are about 0.30 nm×0.30 nm.No structural transformation occurs after removing the guest water molecules,while a robust structure generates with permanent porosity.The adsorption measurements show that the anhydrous sample of the compound can adsorb CO2 into its pores.The adsorption isotherms for methanol,acetone,tetrahydrofuran and benzene are also measured.
文摘To design an accelerated method to evaluate thymopentin release from PLGA microspheres in vitro. Microspheres were prepared by double emulsion technique, using poly(lactide-co-glycolide) (PLGA) as carrier. At higher medium temperature (45℃, 50℃ and 55℃), an accelerated release testing in short time was studied and correlated with the conventional release (37℃) in vitro. The release in vitro of thymopentin from PLGA microspheres at 45 ℃, 50℃ and 55℃ was significantly accelerated (P 〈 0.05). In particular, at 50℃, an accelerated release (30 h) of the hydrophilic peptide from the PLGA matrix was achieved and correlated well with the conventional release (30 d). An accelerated release testing in vitro at higher temperature could be used to monitor thymopentin release from PLGA microspheres.
基金National Natural Science Foundation of Guangdong Province (020885,980504).
文摘Aim Ciprofloxacin polylactic acid microspheres (CFX-PLA-MS) were preparedusing solvent evaporation method from a solid-in-oil-in-water emulsion system. Methods Orthogonalexperiment was used to optimize the method of CFX-PLA-MS preparation. Microspheres werecharacterized in terms of morphology, size, encapsulation efficiency, drug loading and in vitro drugrelease. Results The physical state of CFX-PLA-MS was determined by scanning electron microscopy(SEM) and differential scanning calorimetry (DSC) . Microspheres formed were spherical with smoothsurfaces. Drug was enveloped in microspheres without mixing physically with PLA. The averageparticle size was 280.80 ± 0.15 μm, with over 90% of microspheres falling in the range of 250 -390 μm. The encapsulation efficiency was 65.8% ± 0.58% and the drug loading was 34.1% ± 0.51% .In vitro release study revealed a profile of sustained release of Ciprofloxacin from CFX-PLA-MS. Theaccumulated release percentage and half-life (T_(1/2) of Ciprofloxacin microspheres were 84.0% in53.2 h, and 31.9 h, respectively. Higuchi equation was Q= -0.0043 + 0.003 9 t^(1/2), r = 0.9941.Conclusion Ciprofloxacin microspheres have been successfully prepared and sustained release of CFXfrom microspheres is achieved.
文摘The polymerization of styrene is monitored by pyrene excimer formation. The ratio of monomer to excimer intensities ( I m/ I e) of pyrene increases as polymerization proceeds. The increase of I m/ I e is ascribed to the increase of microviscosity surrounding the probes forming excimer during polymerization. The linear relationship between the changing rate of I m/ I e and the polymerization rate of styrene is obtained. Therefore, I m/ I e may be used to monitor the progress of the polymerization of styrene.
文摘Cetyl-chitosan, prepared by reacting chitosan with chlorocetane under alkaline condition, is soluble and spontaneously forms nanoparticles about 100 nm in diameter. Infrared spectra (IR) revealed that there was a substitution reaction mainly on the amine groups of chitosan (CS). By using paracetamol (PCTM) as a model drug, the balanced release concentration of PCTM in phosphate buffer solution (pH=7.4) can be decreased with the increase of degree of substitution alkyl and can be reduced effectively even under a lower PCTM loading.
文摘Aim PLA/PLGA was used as biodegradable and biocompatible carriers to achieve sustained release of estradiol (E 2). Methods Microcapsules (MC) were prepared by an emulsification solvent extraction method, and then the properties and in vitro drug release behavior of MC were examined. An analysis of variance (ANOVA) was used to test the statistical significance. Then, multiple comparisons were made with a T method between levels to examine the significance of difference further. For all the results a P value 】0 05 was considered statistically insignificant . Results Under the same conditions, the water adding speed and the particle size had significant effects ( P 【0 01) on the entrapment efficiency of MC; the water adding speed and the concentration of PLA in the oil phase had significant effects ( P 【0 01) on the diameter MC in medium. Release of E 2 from MC was influenced significantly ( P 【0 01) by the water adding speed and the type and molecule weight of the polymers. But the differences between levels of the variates were not all significant. Conclusion E 2 PLA/PLGA MC with various properties can be formed when the formulation and the technology were changed accordingly.
文摘The composition and sequence distribution of monomeric units in polyester polyether multiblock copolymer were studied by pyrolysis? gas chromatography (PGC) and pyrolysis gas chromatography/mass spectrometry (PGC/MS). PGC was applied to study the F t curve of the multiblock copolymer and PGC/MS was used to separate and identify the pyrolyzates. DTA experiment was used to study the decomposition temperature. The results show that the beginning point of elastomer’s decomposition was about 300?℃ and the decomposition temperature of most of the sample was 550?℃. Many pyrolyzates were produced because of the breaking of weak bonds in the sample. The possible microstructure was verified and the pyrolysis pathway of the copolymer was investigated.
基金Project(51878322)supported by the National Natural Science Foundation of ChinaProject(18YF1FA112)supported by Key Research and Development Program of Gansu Province,China。
文摘The main objective of this paper focuses on the changes that occur in the strength and microstructural properties of sodium silicate activated fly ash based geopolymer due to varying the sulfate salt and water content.A series of tests including X-ray diffraction,Fourier transform infrared spectroscopy,scanning electron microscopy,physical adsorption and unconfined compressive strength were used to investigate this effect.The results indicate that the higher water content has an adverse effect on the alkali activation and microstructural properties of geopolymer,so the optimum mass ratio of sodium sulfate in alkali-activated geopolymer under different water-to-binder ratios shows a“peak shifting”phenomenon,i.e.,the higher the water-to-binder ratio,the higher the optimum mass ratio.Lower presence of sodium sulfate has no significant effect on the alkali-activated geopolymer systems;higher addition of sodium sulfate,however,could cause the symmetrical stretching vibration of Si—O and the symmetrical stretching vibration of Si—O—Si and Al—O—Si,and promote the formation of N-A-S-H gels.Furthermore,the cement effect of the gel and sodium sulfate aggregate could improve the integrity of pore structure obviously.The maximum strength of geopolymer curing at ambient temperature was 52 MPa.This study obtains the rule that the strength properties of alkali-activated geopolymers vary with the water-to-binder ratio and sodium sulfate content.The feasibility of geopolymer co-activated by sodium sulfate and sodium silicate was investigated,and reference for engineering application of alkali-activated geopolymer in salt-bearing areas was provided.
基金Supported by National Natural Science Foundation of China (No.50573058) and Specialized Research Found for the Doctoral Programof Higher Education (No.20050058004)
文摘Acryionitrilv-methyi mcthacrylate copolymer was synthesized in aqueous solution by Redox. The copolymer was mixed with 10 - 40 wt% of microencapsulated n-octadecane (MieroPCMs) in water. Copolymer films containing Mi- eroPCMs were cast at room temperature in N, N- imethyiformamide solution. The copolymer of acrylonitrile-methyl methacrylate and the copolymer films containing MicroPC- Ms were characterized by using Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Thermosravimetrlc Analyzer (TG), X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM), etc. The mierocapsules in the films are evenly distributed in the copolymer matrix. The heat-absorbing temperatures and heat-evolving temperatures of the films are almost the same as that of the MieroPCMs, respectively, and fluctuate in a slight range. In addition, the enthalpy efficiency of MieroPCMs rises with the contents of MicroPCMs increasing. The crystallirdty of the film increases with the contents of MicroPOMs increasing.
基金This work was supported by the National Natural Science Foundation of China(91545103)Shu Guang Project of Shanghai Municipal Education Commission and Shanghai Education Development Foundation(10SG30)the Fundamental Research Funds for the Central Universities(222201717003)~~
文摘Paramagnetic polymer microspheres were synthesized by the inverse suspension polymerizationmethod through polymerization of glycidyl methacrylate,ally glycidyl ether and methacrylamide onthe surface of silica‐coated Fe3O4nanoparticles using N,N’‐methylene‐bis(acrylamide)as across‐linking agent.Penicillin G acylase(PGA)was covalently immobilized on the surface of theparamagnetic microspheres by reacting the amino groups of the PGA molecules with the epoxygroups of the paramagnetic polymer microspheres.The effect of the SiO2coating and the amount ofparamagnetic Fe3O4nanoparticles on the initial activity and the operational stability of the immobilizedPGA was investigated.The results indicated that SiO2played an important role in the polymerization process and paramagnetic polymer microspheres with a SiO2‐coated Fe3O4nanoparticles mass content of7.5%are an optimal support material for PGA immobilization.Immobilized PGA on the paramagnetic polymer microspheres shows a high initial activity of430U/g(wet)and retains99%of its initial activity after recycling10times.Furthermore,immobilized PGA exhibits high thermal stability,pH stability and excellent reusability,which can be rapidly recycled by the aid of magnet.?2018,Dalian Institute of Chemical Physics,Chinese Academy of Sciences.Published by Elsevier B.V.All rights reserved.