A new type of rubidium ion-imprinted polymer has been synthesized by the surface-imprinting technique using methacrylic acid as the functional monomer,the rubidium ion as the template,methanol as the solvent,and silic...A new type of rubidium ion-imprinted polymer has been synthesized by the surface-imprinting technique using methacrylic acid as the functional monomer,the rubidium ion as the template,methanol as the solvent,and silica as a carrier.Ethylene glycol dimethacrylate and 2,2-azobisisobutyronitrile were used as acrosslinker and an initiator,respectively.In addition,based on the macrocyclic effect of crown ethers,the 18-crown-6 ligand was introduced as a ligand to fix the template ions better.Scanning electron microscopy,zeta-potential analysis,Fourier transform infrared spectroscopy,thermogravimetric analysis,and X-ray photoelectron spectroscopy were performed to characterize the ion-imprinted polymer.The effects of the preparation and adsorption conditions on the adsorption performance of the rubidium ion-imprinted polymer were investigated.The results indicated that the rubidium ion-imprinted polymer has high selectivity and faster kinetics than other adsorbents,with an equilibrium adsorption capacity of 200.19 mg·g^(-1)at 298 K within 25 min.The sorption isotherm was well described by the Freundlich isotherm model,while the adsorption kinetics fitted the pseudo-second-order kinetic model.Consecutive adsorption-desorption experiments showed that the ion-imprinted polymer had good chemical stability and reusability.展开更多
Since the application in fuel cell,the electrochemical adsorption of hydroxyl has received considerable attention in recent years.While most research mainly focus on the room temperature,in this paper,the electrochemi...Since the application in fuel cell,the electrochemical adsorption of hydroxyl has received considerable attention in recent years.While most research mainly focus on the room temperature,in this paper,the electrochemical adsorption of hydroxyl in alkaline solution at high temperature was investigated.An unusual oxidation peak was observed at-0.27 V,suggesting new behavior of hydroxyl adsorption occurred.As is known two kinds of cation hydrated clusters exist in alkaline solution,(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H and(H_(2)O)_xM^(+)-O_(ad)H.For K^(+)and Cs^(+),the cluster shows unstable structure due to the weak interaction between hydrated cation and OH^(-)especially at high temperature.However,For Li^(+),Na^(+)the cluster structure would be stable,as the interaction force between the hydrated cation and OH^(-)is so strong.It was revealed that the unusual oxidation peak has some relationship with the(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H cluster(K^(+)and Cs^(+))absorbed at Pt electrode surface.When the temperature was raised,(H_(2)O)_(x-1)M^(+)-H_(2)O-and-O_(ad)H was disconnected,then the O_(ad)H absorbed at Pt surface got oxidated.Based on the SEM observation,it was showed the unusual electrochemical oxidation reaction would generate platinum oxides,blocking the reactive sites at Pt electrode surface,thus reducing the electrochemical reactivity of Pt electrode.Accordingly,parameters of alkaline concentration and temperature were systematically studied,it was found that increase temperature or alkaline concentration was in favor of the unusual oxidation reaction.This study provides more understanding of hydroxyl adsorption behavior at Pt electrode surface for the high temperature water solution environment.展开更多
In this study,the benign target double terpyridine parts based amphiphilic ionic molecules(AIMs 1,2)and the reference single terpyridine segment included AIMs(AIMs 3,4)were synthesized through a multi-step method,and ...In this study,the benign target double terpyridine parts based amphiphilic ionic molecules(AIMs 1,2)and the reference single terpyridine segment included AIMs(AIMs 3,4)were synthesized through a multi-step method,and the molecular structures were fully characterized.The excellent anticorrosion of the target AIMs for copper surface in H_(2)SO_(4) solution was demonstrated by the electrochemistry analysis,which was more superior over those of the reference AIMs.The standard adsorption free energy changes of the target AIMs calculated by the adsorption isotherms were lower than -40 kJ·mol^(-1),suggesting an intensified chemical adsorption on metal surface.The molecular modeling and molecular dynamic computation of the studied AIMs were performed,demonstrating that the target AIMs exhibited lower highest occupied molecular orbital-lowest unoccupied molecular orbital energy gaps and greater adsorption energies than the reference ones.The chemical adsorption of the AIMs on metal surface was revealed by various spectroscopic methods including scanning electron microscopy,atomic force microscopy,Fourier transform infrared spectroscopy,attenuated total reflection infrared spectroscopy,Raman and X-ray diffraction.展开更多
The characteristics of Pb^2+ adsorption on the surface of birnessites with different average oxidation states (AOS) of Mn, synthesized under acidic and alkali conditions, were investigated. The results indicated th...The characteristics of Pb^2+ adsorption on the surface of birnessites with different average oxidation states (AOS) of Mn, synthesized under acidic and alkali conditions, were investigated. The results indicated that the amount of adsorbed Pb^2+ increased with the increase of Mn AOS in birnessites. The amount of Pb〉 adsorbed positively correlated with the amount of released Mn^2+, H^+, and K^+ (r = 0.9962 〉 0.6614, n = 14, ct = 0.01). The released Mn^2+, H^+, and K^+ were derived mostly from the corresponding cations adsorbed on the vacant sites. The maximum amount of adsorbed Pb^2+ increased with the increasing vacant cation sites, leading to an increase of the total amount of released Mn^2+, H^+, and K^+, and the increased likelihood for two Pb^2+ adsorbed in the region of one side of a vacant site.展开更多
The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the i...The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the increase in the NaClO4 concentration at first and eventually was little affected by the latter. The adsorption of Cl- was almost linearly related with the quantity of NaCl added to the system, while the OHrelease-NaCl curve varied with the soil type and the concentration of NaClO4. The logarithm of the quantity of released OH- was linearly related with the pH. The ratio of released OH- to adsorbed Cl- was larger in dilute NaClO4 solutions than in concentrated solutions and decreased with increasing NaCl.展开更多
Mesoporous silica cocoon materials(MSNCs) and MgO doped mesoporous silica cocoons(MgO-MSNCs) with the cocoon-like hierarchical morphology and different alkalinities were synthesized as carriers for acidic drugs. Indom...Mesoporous silica cocoon materials(MSNCs) and MgO doped mesoporous silica cocoons(MgO-MSNCs) with the cocoon-like hierarchical morphology and different alkalinities were synthesized as carriers for acidic drugs. Indomethacin(IMC) was selected as a model drug and loaded into carriers. All materials and the drug-loaded samples were characterized by nitrogen adsorption, FTIR spectroscopy, transmission electron microscopy(TEM), powder X-Ray diffraction(XRD) and differential scanning calorimetry(DSC). The effect of the Mg/Si molar ratio on the kinetics and equilibrium of IMC adsorption on MgO-MSNCs was thoroughly examined, and it was found that the increase in the Mg/Si molar ratio resulted in an increasing IMC adsorption rate due to the increased affinity between alkaline MgO-MSNCs and weak acid IMC. The adsorption kinetics fitted a pseudo second-order model well. The Freundlich isotherm showed a better fit, indicating that the coverage of IMC on the surface of MgO-MSNCs was heterogeneous. The maximum adsorption capacity of adsorbent was calculated by the Langmuir isotherm equation. The Temkin equation provided further support that the IMC adsorption on MgO-MSNCs was dominated by a chemisorption process. MgO-MSNCs also have the advantage of allowing an adjustment of the drug release rate of weak acid drug. The cytotoxicity assay indicated good biocompatibility of MgO-MSNCs. Our research on MgO-MSNCs carriers demonstrated their potential therapeutic benefit for safe and effective management of IMC adsorption and in vitro release.展开更多
An exact solution has been obtained for the release kinetics of a solute from a cylindrical non-erodible polymeric matrix into a finite external volume when the initial solute loading is greater than the solubility li...An exact solution has been obtained for the release kinetics of a solute from a cylindrical non-erodible polymeric matrix into a finite external volume when the initial solute loading is greater than the solubility limit in the matrix. The moving boundary solution is derived based on the combination of variable method. The formulas of the moving boundary and the fractional solute release are given. The moving boundary and the fractional solute release profiles have been calculated at various solute loading levels and different external volumes. The obtained results show that as the external fluid volume increases, the fractional release at any time and the maximum fractional release increase. In addition, for a given external volume, as initial drug loading increases, the fractional release at any time decreases.展开更多
Careful measurements of the dilute solution viscosities of polyethylene glycol and polyvinyl alcohol in water were carried out. The reduced viscosities of both polymer solutions plot upward curves at extremely dilute ...Careful measurements of the dilute solution viscosities of polyethylene glycol and polyvinyl alcohol in water were carried out. The reduced viscosities of both polymer solutions plot upward curves at extremely dilute concentration levels similar to the phenomena observed for many polymer solutions in the early 1950's. Upon observation of the changes of the flow times of pure water in and the wall surface wettability of the viscometer after measuring solution viscosity, a view was formed that the observed viscosity abnormality at extremely dilute concentration regions is solely due to the effect of adsorption of polymer chains onto the wall surface of viscometer. A theory of adsorption effect based on the Langmuir isotherms was proposed and a mathematical; analysis for data treatment was performed. The theory could adequately describe the existing viscosity data. It seems necessary to correct the viscosity result of dilute polymer solutions measured by glass capillary viscometer by taking into account the effect of adsorption in all cases.展开更多
In this study,seven coal-based activated carbons(ACs)were adopted to remove trimethylamine(TMA)in an aqueous solution as environmentally friendly and harmless adsorbents.The results showed that columnar AC(CAC)had a c...In this study,seven coal-based activated carbons(ACs)were adopted to remove trimethylamine(TMA)in an aqueous solution as environmentally friendly and harmless adsorbents.The results showed that columnar AC(CAC)had a clear scale and honeycomb structures with few fragments and micropores,contributing to superior TMA removal capacity compared to granular AC(GAC)(71.67%for 6.0 mm CAC and 69.92%for 40–60 mesh GAC).In addition,the process of adsorption was accompanied by desorption,and the recommended absorbed time was 120–180 min.The short time to achieve equilibrium indicated that adsorption was kinetically controlled,and pseudo-second-order kinetics was more appropriate than pseudo-first-order kinetics in explaining the adsorption mechanism in both water and oyster enzymatic hydrolysate.The intraparticle diffusion model presented that the adsorption processes could be divided into three steps for GAC and two steps for CAC.The adsorption processes were consistent with the Freundlich model,indicating the existence of physisorption and chemisorption as multilayer adsorption.The results indicated that AC,especially CAC,has great potential for TMA elimination in aquatic product processing.展开更多
Effects of NH+ concentration, solution/soil ratio and temperature on NH+ adsorption were studied in a Eum-OrthicAnthrosol. The slopes of the soil NH+ adsorption isotherms and the fitted n, the coefficient for the adso...Effects of NH+ concentration, solution/soil ratio and temperature on NH+ adsorption were studied in a Eum-OrthicAnthrosol. The slopes of the soil NH+ adsorption isotherms and the fitted n, the coefficient for the adsorption intensity,and k, the coefficient related to adsorption capacity, of the Freundlich equation increased with increasing solution/soilratio (SSR) and with decreasing temperature (T). For the range of experimental conditions, the value of δq/δc, the rateof change of the amount of NH+ adsorbed in the soil solid phase (q) with respect to the equilibrium concentration of NH+in soil solution (c), was 0.840, indicating that q increased with increasing c. From 2 to 45℃, δq/δSSR, the rate of changeof q with respect to SSR, decreased from 2.598 to 1.996, showing that q increased with increasing SSR, while its increasingrate decreased with temperature. From SSR 1:1 to 20:1, δq/δT, the rate of change of q with respect to T, decreasedfrom -0.095 to -0.361, indicating that q decreased with increasing temperature, and at the same time the negative effectof temperature became larger as SSR increased. Thus under the experimental conditions the order of importance indetermining the amount of NH+ adsorbed in the soil solid phase was δq/δSSR > δq/δc > |δq/δT|, indicating that thegreatest effect on the amount of NH^4+ adsorbed was with the solution/soil ratio; the equilibrium concentration of NH+had a lesser effect; and temperature had the least effect.展开更多
For the diffusion-controlled adsorption,the expression of dynamic surface adsorption(t)was obtained by solving the diffusion equation.Two cases,i.e.the short and long time limits,were mainly discussed in this paper.Fr...For the diffusion-controlled adsorption,the expression of dynamic surface adsorption(t)was obtained by solving the diffusion equation.Two cases,i.e.the short and long time limits,were mainly discussed in this paper.From the measured dynamic surface tension of aqueous surfactant sodium dodecyl sulfate(SDS) solutions at25 °C,the adsorption kinetics of SDS at air/solution interface was studied.It was proved that for both of the short and long time limits,the adsorption process of SDS was controlled by diffusion.展开更多
A fast and selective adsorbent for Hg(II) from aqueous solutions using thiourea(TU) functionalized polypropylene fiber grafted acrylic acid(PP-g-AA),PP-g-AA-TU fibers,was characterized by Fourier transform infrared sp...A fast and selective adsorbent for Hg(II) from aqueous solutions using thiourea(TU) functionalized polypropylene fiber grafted acrylic acid(PP-g-AA),PP-g-AA-TU fibers,was characterized by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy.The adsorption behavior of the functionalized chelating fibers for Hg(II) was investigated by static adsorption experiments,and the effects of some essential factors on adsorption of Hg(II) were examined,such as pH,initial concentration,adsorption time,coexisting cations,and temperature.The results showed that the adsorptive equilibrium could be achieved in 10 min,and the equilibrium adsorption quantity of PP-g-AA-TU fibers was 20 times that of PP-g-AA fibers.The PP-g-AA-TU fibers showed a very high adsorption rate and a good selectivity for Hg(II) over a wide range of p H.The adsorption isotherm can be well described with Langmuir model,with the maximum adsorption capacity for Hg(II) up to52.04 mg·g^(-1)and the removal of Hg(II) more than 97%.The kinetic data indicate that the adsorption process is best-fitted into the pseudo-second-order model.展开更多
A novel nanocomposite bioadsorbent rectorite/chitosan was prepared by controlling different mass ratios of chitosan to rectorite using the water phase intercalation technique. The structure of the bioadsorbent was cha...A novel nanocomposite bioadsorbent rectorite/chitosan was prepared by controlling different mass ratios of chitosan to rectorite using the water phase intercalation technique. The structure of the bioadsorbent was characterized by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM), Transmission electron microscopy (TEM), respectively. The results showed that the chitosan had been inserted into the rectorite layer successfully. The adsorption properties of the nanocomposite adsorbent toward CHCl3 from aqueous solution were investigated. Adsorption results showed that both nanocomposite adsorbents with weight ratio of rectorite to chitosan of 3:1 and 5:1 exhibited higher adsorption capacities.展开更多
The adsorption of decylmethylsulfoxide(DEMS)onto carbon black and the effects of temperature,salt(NaCl)and acid (HCl)have been measured.Typical two plateaux type adsorption isotherms were obtained.Applying the two ste...The adsorption of decylmethylsulfoxide(DEMS)onto carbon black and the effects of temperature,salt(NaCl)and acid (HCl)have been measured.Typical two plateaux type adsorption isotherms were obtained.Applying the two step model of surfactant adsorption on solid/liquld interface and the general adsorption isotherm equation[9]the experimental results were interpreted qualitatively and quantitatively.展开更多
Palygorskite(PG)adsorbent with superior adsorption property and ion-exchange ability is highly desired in the field of dye removal.However,it generates high amounts of precipitation due to the granular form,resulting ...Palygorskite(PG)adsorbent with superior adsorption property and ion-exchange ability is highly desired in the field of dye removal.However,it generates high amounts of precipitation due to the granular form,resulting in secondary pollution after adsorption.Herein,the novel high porosity PG-based nanofibers that are easy for operating and retrieving have been fabricated using effective solution blowing and subsequent calcination.The obtained highly efficient adsorption nanofibers exhibit large specific surface area about 170.50 m^(2)/g with average diameter from 243 nm to 365 nm.Based on the abovementioned nanofibrous structure and negatively charged PG,the solution blowing of PG-based nanofibers(SBPNs)showed high adsorption capacity for methylene blue(MB)(112.36 mg/g).In addition,the adsorption of SBPNs is well described by the Langmuir isotherm model.This work provides new SBPNs forming process for the fields of dye removal,which may achieve the production of PG adsorbents at the industrial level.展开更多
This study aimed to develop controlled release formulation of Thiabendazole for reduced contaminations to soil water and agricultural produces. The idea behind this work was based on changing the ionization status of ...This study aimed to develop controlled release formulation of Thiabendazole for reduced contaminations to soil water and agricultural produces. The idea behind this work was based on changing the ionization status of Thiabendazole molecule throughout pH changes to become a cation then adsorbing it to bentonite clay surfaces. Equilibrium concentrations of Thiabendazole in the adsorption solutions were determined by HPLC. Results showed that Thiabendazole was better adsorbed in clay at the lowest pH value (pH 3). Furthermore, raising the temperature of the adsorption reaction increased the adsorbed amount of Thiabendazole. Release experiments showed that Thiabendazole is extremely slower at pH 3 than at pH 5.5 or pH 9. These promising results suggest that application of Thiabendazole clay based formulation may reduce the applied rate and that the released fraction consequently may reduce the environmental contamination. It is also advantageous to use these formulations in the acidic soil for plant disease control.展开更多
基金supported by the National Natural Science Foundation of China(22125802 and 22078010)Beijing Natural Science Foundation(2222017)Big Science Project from BUCT(XK180301)。
文摘A new type of rubidium ion-imprinted polymer has been synthesized by the surface-imprinting technique using methacrylic acid as the functional monomer,the rubidium ion as the template,methanol as the solvent,and silica as a carrier.Ethylene glycol dimethacrylate and 2,2-azobisisobutyronitrile were used as acrosslinker and an initiator,respectively.In addition,based on the macrocyclic effect of crown ethers,the 18-crown-6 ligand was introduced as a ligand to fix the template ions better.Scanning electron microscopy,zeta-potential analysis,Fourier transform infrared spectroscopy,thermogravimetric analysis,and X-ray photoelectron spectroscopy were performed to characterize the ion-imprinted polymer.The effects of the preparation and adsorption conditions on the adsorption performance of the rubidium ion-imprinted polymer were investigated.The results indicated that the rubidium ion-imprinted polymer has high selectivity and faster kinetics than other adsorbents,with an equilibrium adsorption capacity of 200.19 mg·g^(-1)at 298 K within 25 min.The sorption isotherm was well described by the Freundlich isotherm model,while the adsorption kinetics fitted the pseudo-second-order kinetic model.Consecutive adsorption-desorption experiments showed that the ion-imprinted polymer had good chemical stability and reusability.
基金the National Key Research and Development Program of China(2020YFC1909703)S&T Program of Hebei Province(21284402Z)+1 种基金Fangchenggang Key Research and Development(AB20014008)Lvliang Key Research and Development Program(2020GXZDYF7)。
文摘Since the application in fuel cell,the electrochemical adsorption of hydroxyl has received considerable attention in recent years.While most research mainly focus on the room temperature,in this paper,the electrochemical adsorption of hydroxyl in alkaline solution at high temperature was investigated.An unusual oxidation peak was observed at-0.27 V,suggesting new behavior of hydroxyl adsorption occurred.As is known two kinds of cation hydrated clusters exist in alkaline solution,(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H and(H_(2)O)_xM^(+)-O_(ad)H.For K^(+)and Cs^(+),the cluster shows unstable structure due to the weak interaction between hydrated cation and OH^(-)especially at high temperature.However,For Li^(+),Na^(+)the cluster structure would be stable,as the interaction force between the hydrated cation and OH^(-)is so strong.It was revealed that the unusual oxidation peak has some relationship with the(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H cluster(K^(+)and Cs^(+))absorbed at Pt electrode surface.When the temperature was raised,(H_(2)O)_(x-1)M^(+)-H_(2)O-and-O_(ad)H was disconnected,then the O_(ad)H absorbed at Pt surface got oxidated.Based on the SEM observation,it was showed the unusual electrochemical oxidation reaction would generate platinum oxides,blocking the reactive sites at Pt electrode surface,thus reducing the electrochemical reactivity of Pt electrode.Accordingly,parameters of alkaline concentration and temperature were systematically studied,it was found that increase temperature or alkaline concentration was in favor of the unusual oxidation reaction.This study provides more understanding of hydroxyl adsorption behavior at Pt electrode surface for the high temperature water solution environment.
基金the National Natural Science Foundation of China (21376282,21676035,21878029)Chongqing Science and Technology Commission (cstc2018jcyjAX0668)+2 种基金Shandong Province Natural Science Foundation (ZR2020QB18)China Postdoctoral Science Foundation (22012 T50762&2011 M501388)Graduate Student Research Innovation Project,Chongqing University (CYB18046)。
文摘In this study,the benign target double terpyridine parts based amphiphilic ionic molecules(AIMs 1,2)and the reference single terpyridine segment included AIMs(AIMs 3,4)were synthesized through a multi-step method,and the molecular structures were fully characterized.The excellent anticorrosion of the target AIMs for copper surface in H_(2)SO_(4) solution was demonstrated by the electrochemistry analysis,which was more superior over those of the reference AIMs.The standard adsorption free energy changes of the target AIMs calculated by the adsorption isotherms were lower than -40 kJ·mol^(-1),suggesting an intensified chemical adsorption on metal surface.The molecular modeling and molecular dynamic computation of the studied AIMs were performed,demonstrating that the target AIMs exhibited lower highest occupied molecular orbital-lowest unoccupied molecular orbital energy gaps and greater adsorption energies than the reference ones.The chemical adsorption of the AIMs on metal surface was revealed by various spectroscopic methods including scanning electron microscopy,atomic force microscopy,Fourier transform infrared spectroscopy,attenuated total reflection infrared spectroscopy,Raman and X-ray diffraction.
基金supported by the National Natural Science Foundation of China (No. 40471070)the National Excellent Doctoral Dissertation of China(No. 200767)
文摘The characteristics of Pb^2+ adsorption on the surface of birnessites with different average oxidation states (AOS) of Mn, synthesized under acidic and alkali conditions, were investigated. The results indicated that the amount of adsorbed Pb^2+ increased with the increase of Mn AOS in birnessites. The amount of Pb〉 adsorbed positively correlated with the amount of released Mn^2+, H^+, and K^+ (r = 0.9962 〉 0.6614, n = 14, ct = 0.01). The released Mn^2+, H^+, and K^+ were derived mostly from the corresponding cations adsorbed on the vacant sites. The maximum amount of adsorbed Pb^2+ increased with the increasing vacant cation sites, leading to an increase of the total amount of released Mn^2+, H^+, and K^+, and the increased likelihood for two Pb^2+ adsorbed in the region of one side of a vacant site.
文摘The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the increase in the NaClO4 concentration at first and eventually was little affected by the latter. The adsorption of Cl- was almost linearly related with the quantity of NaCl added to the system, while the OHrelease-NaCl curve varied with the soil type and the concentration of NaClO4. The logarithm of the quantity of released OH- was linearly related with the pH. The ratio of released OH- to adsorbed Cl- was larger in dilute NaClO4 solutions than in concentrated solutions and decreased with increasing NaCl.
基金supported by the National Basic Research Pro-gram of China(973 Program)(No.2015CB932100)National Natural Science Foundation of China(No.81473165)Liaoning Provincial Key Laboratory of Drug Preparation De-sign&Evaluation of Liaoning Provincial Education Depart-ment(No.LZ2015068)
文摘Mesoporous silica cocoon materials(MSNCs) and MgO doped mesoporous silica cocoons(MgO-MSNCs) with the cocoon-like hierarchical morphology and different alkalinities were synthesized as carriers for acidic drugs. Indomethacin(IMC) was selected as a model drug and loaded into carriers. All materials and the drug-loaded samples were characterized by nitrogen adsorption, FTIR spectroscopy, transmission electron microscopy(TEM), powder X-Ray diffraction(XRD) and differential scanning calorimetry(DSC). The effect of the Mg/Si molar ratio on the kinetics and equilibrium of IMC adsorption on MgO-MSNCs was thoroughly examined, and it was found that the increase in the Mg/Si molar ratio resulted in an increasing IMC adsorption rate due to the increased affinity between alkaline MgO-MSNCs and weak acid IMC. The adsorption kinetics fitted a pseudo second-order model well. The Freundlich isotherm showed a better fit, indicating that the coverage of IMC on the surface of MgO-MSNCs was heterogeneous. The maximum adsorption capacity of adsorbent was calculated by the Langmuir isotherm equation. The Temkin equation provided further support that the IMC adsorption on MgO-MSNCs was dominated by a chemisorption process. MgO-MSNCs also have the advantage of allowing an adjustment of the drug release rate of weak acid drug. The cytotoxicity assay indicated good biocompatibility of MgO-MSNCs. Our research on MgO-MSNCs carriers demonstrated their potential therapeutic benefit for safe and effective management of IMC adsorption and in vitro release.
文摘An exact solution has been obtained for the release kinetics of a solute from a cylindrical non-erodible polymeric matrix into a finite external volume when the initial solute loading is greater than the solubility limit in the matrix. The moving boundary solution is derived based on the combination of variable method. The formulas of the moving boundary and the fractional solute release are given. The moving boundary and the fractional solute release profiles have been calculated at various solute loading levels and different external volumes. The obtained results show that as the external fluid volume increases, the fractional release at any time and the maximum fractional release increase. In addition, for a given external volume, as initial drug loading increases, the fractional release at any time decreases.
基金This work was supported by the National Basic Research Project-Macromolecular Condensed State,and the National Natural Science Foundationof China
文摘Careful measurements of the dilute solution viscosities of polyethylene glycol and polyvinyl alcohol in water were carried out. The reduced viscosities of both polymer solutions plot upward curves at extremely dilute concentration levels similar to the phenomena observed for many polymer solutions in the early 1950's. Upon observation of the changes of the flow times of pure water in and the wall surface wettability of the viscometer after measuring solution viscosity, a view was formed that the observed viscosity abnormality at extremely dilute concentration regions is solely due to the effect of adsorption of polymer chains onto the wall surface of viscometer. A theory of adsorption effect based on the Langmuir isotherms was proposed and a mathematical; analysis for data treatment was performed. The theory could adequately describe the existing viscosity data. It seems necessary to correct the viscosity result of dilute polymer solutions measured by glass capillary viscometer by taking into account the effect of adsorption in all cases.
基金the National Key R&D Program of China(No.2018YFC0311202)the Key-Area Research and Development Program of Guang-dong Province(No.2020B1111030004)+4 种基金the Science and Technology Program of Guangzhou,China(Nos.201804010364 and 201804010321)the Key Special Project for Introduced Talents Team of Southern Marine Science and Engineering Guangdong Laboratory(Guangzhou)(No.GML2019ZD0406)the National Key R&D Program of China(No.2018YFC0311202)the Natural Science Foun-dation of Guangdong Province,China(Nos.2018A030313088,2018A030313626)the Academician Work-station Foundation for Young Scientists of Chinese Aca-demy of Sciences Guangzhou Branch(No.20180313).
文摘In this study,seven coal-based activated carbons(ACs)were adopted to remove trimethylamine(TMA)in an aqueous solution as environmentally friendly and harmless adsorbents.The results showed that columnar AC(CAC)had a clear scale and honeycomb structures with few fragments and micropores,contributing to superior TMA removal capacity compared to granular AC(GAC)(71.67%for 6.0 mm CAC and 69.92%for 40–60 mesh GAC).In addition,the process of adsorption was accompanied by desorption,and the recommended absorbed time was 120–180 min.The short time to achieve equilibrium indicated that adsorption was kinetically controlled,and pseudo-second-order kinetics was more appropriate than pseudo-first-order kinetics in explaining the adsorption mechanism in both water and oyster enzymatic hydrolysate.The intraparticle diffusion model presented that the adsorption processes could be divided into three steps for GAC and two steps for CAC.The adsorption processes were consistent with the Freundlich model,indicating the existence of physisorption and chemisorption as multilayer adsorption.The results indicated that AC,especially CAC,has great potential for TMA elimination in aquatic product processing.
基金Project supported by the National Natural Science Foundation of China (No. 49901009).
文摘Effects of NH+ concentration, solution/soil ratio and temperature on NH+ adsorption were studied in a Eum-OrthicAnthrosol. The slopes of the soil NH+ adsorption isotherms and the fitted n, the coefficient for the adsorption intensity,and k, the coefficient related to adsorption capacity, of the Freundlich equation increased with increasing solution/soilratio (SSR) and with decreasing temperature (T). For the range of experimental conditions, the value of δq/δc, the rateof change of the amount of NH+ adsorbed in the soil solid phase (q) with respect to the equilibrium concentration of NH+in soil solution (c), was 0.840, indicating that q increased with increasing c. From 2 to 45℃, δq/δSSR, the rate of changeof q with respect to SSR, decreased from 2.598 to 1.996, showing that q increased with increasing SSR, while its increasingrate decreased with temperature. From SSR 1:1 to 20:1, δq/δT, the rate of change of q with respect to T, decreasedfrom -0.095 to -0.361, indicating that q decreased with increasing temperature, and at the same time the negative effectof temperature became larger as SSR increased. Thus under the experimental conditions the order of importance indetermining the amount of NH+ adsorbed in the soil solid phase was δq/δSSR > δq/δc > |δq/δT|, indicating that thegreatest effect on the amount of NH^4+ adsorbed was with the solution/soil ratio; the equilibrium concentration of NH+had a lesser effect; and temperature had the least effect.
文摘For the diffusion-controlled adsorption,the expression of dynamic surface adsorption(t)was obtained by solving the diffusion equation.Two cases,i.e.the short and long time limits,were mainly discussed in this paper.From the measured dynamic surface tension of aqueous surfactant sodium dodecyl sulfate(SDS) solutions at25 °C,the adsorption kinetics of SDS at air/solution interface was studied.It was proved that for both of the short and long time limits,the adsorption process of SDS was controlled by diffusion.
基金Supported by the Tianjin and MOST Innovation Fund for Small Technology-based Firms(14ZXCXGX00724,13C26211200305)Science and Technology Support Program(13ZCZDSF00100)
文摘A fast and selective adsorbent for Hg(II) from aqueous solutions using thiourea(TU) functionalized polypropylene fiber grafted acrylic acid(PP-g-AA),PP-g-AA-TU fibers,was characterized by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy.The adsorption behavior of the functionalized chelating fibers for Hg(II) was investigated by static adsorption experiments,and the effects of some essential factors on adsorption of Hg(II) were examined,such as pH,initial concentration,adsorption time,coexisting cations,and temperature.The results showed that the adsorptive equilibrium could be achieved in 10 min,and the equilibrium adsorption quantity of PP-g-AA-TU fibers was 20 times that of PP-g-AA fibers.The PP-g-AA-TU fibers showed a very high adsorption rate and a good selectivity for Hg(II) over a wide range of p H.The adsorption isotherm can be well described with Langmuir model,with the maximum adsorption capacity for Hg(II) up to52.04 mg·g^(-1)and the removal of Hg(II) more than 97%.The kinetic data indicate that the adsorption process is best-fitted into the pseudo-second-order model.
文摘A novel nanocomposite bioadsorbent rectorite/chitosan was prepared by controlling different mass ratios of chitosan to rectorite using the water phase intercalation technique. The structure of the bioadsorbent was characterized by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM), Transmission electron microscopy (TEM), respectively. The results showed that the chitosan had been inserted into the rectorite layer successfully. The adsorption properties of the nanocomposite adsorbent toward CHCl3 from aqueous solution were investigated. Adsorption results showed that both nanocomposite adsorbents with weight ratio of rectorite to chitosan of 3:1 and 5:1 exhibited higher adsorption capacities.
文摘The adsorption of decylmethylsulfoxide(DEMS)onto carbon black and the effects of temperature,salt(NaCl)and acid (HCl)have been measured.Typical two plateaux type adsorption isotherms were obtained.Applying the two step model of surfactant adsorption on solid/liquld interface and the general adsorption isotherm equation[9]the experimental results were interpreted qualitatively and quantitatively.
基金National Natural Science Foundation of China(No.51473121)Science and Technology Plans of Tianjin,China(No.20YDTPJC03180)National Undergraduate Training Programs for Innovation and Entrepreneurship,China(No.202010058069)。
文摘Palygorskite(PG)adsorbent with superior adsorption property and ion-exchange ability is highly desired in the field of dye removal.However,it generates high amounts of precipitation due to the granular form,resulting in secondary pollution after adsorption.Herein,the novel high porosity PG-based nanofibers that are easy for operating and retrieving have been fabricated using effective solution blowing and subsequent calcination.The obtained highly efficient adsorption nanofibers exhibit large specific surface area about 170.50 m^(2)/g with average diameter from 243 nm to 365 nm.Based on the abovementioned nanofibrous structure and negatively charged PG,the solution blowing of PG-based nanofibers(SBPNs)showed high adsorption capacity for methylene blue(MB)(112.36 mg/g).In addition,the adsorption of SBPNs is well described by the Langmuir isotherm model.This work provides new SBPNs forming process for the fields of dye removal,which may achieve the production of PG adsorbents at the industrial level.
基金Supported by the National Natural Science Foundation of China (No.20466002), the Program of Ministry of Education for New Century Excellent Talents (NCET-04-0989), the Doctor Funds of Xinjiang Bingtuan (04BSZJ04) and the Shihezi University's. Key Scientific and Technological Project (ZDGG2004-01).
文摘This study aimed to develop controlled release formulation of Thiabendazole for reduced contaminations to soil water and agricultural produces. The idea behind this work was based on changing the ionization status of Thiabendazole molecule throughout pH changes to become a cation then adsorbing it to bentonite clay surfaces. Equilibrium concentrations of Thiabendazole in the adsorption solutions were determined by HPLC. Results showed that Thiabendazole was better adsorbed in clay at the lowest pH value (pH 3). Furthermore, raising the temperature of the adsorption reaction increased the adsorbed amount of Thiabendazole. Release experiments showed that Thiabendazole is extremely slower at pH 3 than at pH 5.5 or pH 9. These promising results suggest that application of Thiabendazole clay based formulation may reduce the applied rate and that the released fraction consequently may reduce the environmental contamination. It is also advantageous to use these formulations in the acidic soil for plant disease control.