Moist-electric generation,a green and environmentally friendly energy harvesting technology,is undoubt-edly one of the effective methods to alleviate energy shortages and environmental damage.However,the lack of fiber...Moist-electric generation,a green and environmentally friendly energy harvesting technology,is undoubt-edly one of the effective methods to alleviate energy shortages and environmental damage.However,the lack of fiber-like moist-electric generators(MEGs)that combine continuous power generation and high electrical output performance has constrained the development of moist-electric in the fields of flexi-ble wearable and self-power supplies.In this work,sodium alginate(SA)/multi-walled carbon nanotubes(MWCNT)fibers with axial heterogeneous(axi-he)of oxygen-containing functional groups(Ocfgs)are prepared through a mold forming method in assistance with the coagulation process.The interaction be-tween axi-he MEG and moisture is investigated by analyzing the electrical signal changes of dried MEG under moisture stimulation.The maximum output voltage and current of axi-he MEG can reach 0.35 V and 1.92μA under the stimulation of moisture.Based on the regulation of Ocfgs,axi-he MEG has a con-tinuous high moist-electric performance and environmental adaptability.The maximum output power density(Pmo)of axi-he MEG with a length of only 2 cm can reach 27.37μW cm-2 at RH=90%,which exceeds most of the MEGs reported in literature.Meanwhile,a continuous output voltage of 0.33-0.37 V for more than 15 h can be obtained from this axi-he MEG.Thus,the axi-he MEG from Ocfg distribution design and mold forming method provides a new way of clean energy generation using moisture from the ambient environment,exhibiting enormous potential in energy supply for Internet of Things(IoT)devices.展开更多
A facile method for the preparation of sodium alginate（SA）/carboxyl-functionalized graphene（G-COOH）composite hydrogel was developed. Based on the coordination ability of lanthanide ions to the carboxyl groups, a s...A facile method for the preparation of sodium alginate（SA）/carboxyl-functionalized graphene（G-COOH）composite hydrogel was developed. Based on the coordination ability of lanthanide ions to the carboxyl groups, a series of hydrogel derived from different ratios of SA and G-COOH was fabricated by neodymium（Nd3＋） ions coordination. A relatively uniform layered structure was recorded by SEM at the interior of SA/G-COOH hydrogel. Several parameters such as water content, swelling ratio（SR）, tensile test and solvent resistance were also investigated. The SA/G-COOH composite hydrogel showed excellent mechanical strength, and the tensile strength of SA/G-COOH composite hydrogel reaches 53.72 MPa at high water content. Due to the coordination ability of Nd3＋ ions, the hydrogel also exhibited an excellent solvent resistance and stability.展开更多
The presence of toxic dyes in the aqueous medium has threatened environmental safety,and thereby re-moving them from wastewater in an efficient way is highly desired.Herein,the efficient biosorbents were successfully ...The presence of toxic dyes in the aqueous medium has threatened environmental safety,and thereby re-moving them from wastewater in an efficient way is highly desired.Herein,the efficient biosorbents were successfully fabricated via a facile physical gelation process of sodium alginate(SA)and carboxymethyl chitosan(CMCTS)in an acidic aqueous solution.The as-prepared hydrogel beads not only displayed water superabsorbent properties and pH-responsive swelling characters but also exhibited excellent methylene blue(MB)adsorption capacity removal efficiency with experimental maximum MB adsorption capacity of 2518 and 1005 mg g-1,which are comparable with most reported lignocellulosic and alginate-based hydrogels.The MB adsorption process fitted well in different kinetic and isotherm models and became more heterogeneous in concentrated MB solutions as verified by principal component analysis results.The adsorption mechanism was proposed,and the high dye absorbency was attributed to the strong electro-static forces between adsorbents and adsorbates.Our current study provides a promising and sustainable composite hydrogels platform targeted to dye decontamination.展开更多
Krill oil is effective in reducing blood lipid levels,particularly in individuals with severe hyperlipidemia.However,poor water insolubility and stability limited its usage.This study investigated a method for encapsu...Krill oil is effective in reducing blood lipid levels,particularly in individuals with severe hyperlipidemia.However,poor water insolubility and stability limited its usage.This study investigated a method for encapsulating Antarctic krill oil using alginate(ALG)and gelatin(GLN)to enhance its stability and bioactivity.The encapsulation efficiency,functional group integrity,swelling rate,and lipid-lowering activity were assessed.Results indicated that the optimal encapsulation conditions were identified with an ALG:GLN ratio of 2:1(m/m),coagulation bath of 9%CaCl_(2),and a nozzle size of 750μm,resulting in 69.34%encapsulation efficiency.Fourier-transform infrared spectroscopy confirmed successful encapsulation.The ALG-GLN shell materials enriched astaxanthin in krill oil and protected it from harsh gastric conditions,enabling targeted intestinal release.In a high-fat diet-induced rat model,krill oil microcapsules significantly reduced triglycerides(TG),total cholesterol(TC),and low-density lipoprotein-cholesterol(LDL-C)levels while increasing high-density lipoprotein-cholesterol(HDL-C)levels compared to unencapsulated krill oil.Additionally,the microcapsules elevated nitric oxide(NO)levels,enhanced superoxide dismutase(SOD)activity,and reduced malondialdehyde(MDA)levels,liver and perirenal fat weight.Therefore,encapsulating Antarctic krill oil in alginate-gelatin hydrogel offers a promising strategy for managing hyperlipidemia and associated metabolic disorders.展开更多
A novel macroparticle magnesium-modified biochar/yttrium alginate(Mg-BC/SA-Y)hybrid biogel composite was successfully developed through a facile solution reaction of magnesium-modified BC and yttrium alginate polymer,...A novel macroparticle magnesium-modified biochar/yttrium alginate(Mg-BC/SA-Y)hybrid biogel composite was successfully developed through a facile solution reaction of magnesium-modified BC and yttrium alginate polymer,and its properties were characterized.The obtained Mg-BC/SA-Y biogel beads have a particle size of approximately 1.5 mm,featuring abundant network pores and an uneven,distinctive surface.The performance and mechanisms of Mg-BC/SA-Y for phosphate adsorption were thoroughly investigated.The findings indicate that Mg-BC/SA-Y removes up to 95.7%of phosphate at pH4.0 and 298 K,and also achieves a phosphate removal efficiency of over 80%within a pH range of3.0-11.0.The adsorption capacity of Mg-BC/SA-Y for phosphate is nearly four times that of BC.The spontaneous adsorption processes and endothermic adsorption behavior can be elucidated by the pseudo-second-order rate and Langmuir equations,respectively.Phosphate adsorption is almost unaffected by water ionic strength and common coexisting ions,except for the influence of highconcentration F-ions.The recyclable biogel beads can be reused after adsorbing phosphate,and represent excellent stability and practicability in real water.The mechanisms of ligand exchange,innersphere complexation and electrostatic attraction are involved in phosphate removal.Mg-BC/SA-Y biogel polymer is a desirable and sustainable biosorbent for treating water with excessive phosphate levels and reducing pollution and carbon emissions.展开更多
Based on the characteristics of laser-induced surface ignition,energetic photosensitive films show promising potential to meet the ignition requirements of various energetic materials(EMs).In this study,DATNBI/ferric ...Based on the characteristics of laser-induced surface ignition,energetic photosensitive films show promising potential to meet the ignition requirements of various energetic materials(EMs).In this study,DATNBI/ferric alginate(DI/FeA),DI/cobalt alginate(DI/CoA),and DI/nickel alginate(DI/Ni A)films are fabricated by employing sodium alginate(SA)with a three-dimensional network structure as the film matrix,via ionic cross-linking of SA with Fe^(3+),Co^(2+),and Ni^(2+)ions.The study demonstrates that the ionic cross-linking enhances the hydrophobic performance of the films,with the water contact angle increasing from 82.1° to 123.5°.Concurrently,the films'near-infrared(NIR)light absorption improved.Furthermore,transition metal ions facilitate accelerated electron transfer,thereby catalyzing the thermal decomposition of DATNBI.Under 1064 nm laser irradiation,the DI/Fe A film exhibits exceptional combustion performance,with an ignition delay time as low as 76 ms.It successfully acts as an NIR laser ignition medium to initiate the self-sustained combustion of CL-20.This study demonstrates the synergistic realization of enhanced hydrophobicity,improved photosensitivity,and promoted catalytic decomposition through microstructural design of the material,providing new insights for the design of additive-free EMs in laser ignition applications.展开更多
Porous carbons hold broad application prospects in the domains of electrochemical energy storage devices and sensors.In this study,porous carbon derived from sodium alginate-encapsulated ZIF-8(SA/ZIF-8-C)was suc-cessf...Porous carbons hold broad application prospects in the domains of electrochemical energy storage devices and sensors.In this study,porous carbon derived from sodium alginate-encapsulated ZIF-8(SA/ZIF-8-C)was suc-cessfully prepared by blending ZIF-8 particles with sodium alginate,forming hydrogel beads in the presence of divalent metal ions,and subsequently subjecting them to high-temperature pyrolysis.Various characterization techniques were employed to evaluate the properties of the prepared materials.The introduction of a carbon framework on ZIF-8-derived particles effectively enhanced the conductivity of the prepared materials.The SA/ZIF-8(1.0)-C sample heated at 800℃exhibited a specific capacitance of up to 208 F g^(-1)at a current density of 0.5 A g^(-1)and outstanding cyclic stability.Even after 10,000 charge and discharge cycles,its capacitance retention rate remained as high as 87.14%.The symmetric supercapacitor constructed with the composite demonstrated an excellent energy density of 14.58 Wh kg^(-1)at a power capacity of 403.85 W kg^(-1).The implementation of this study provides new ideas and inspiration for the development of high-performance supercapacitors.展开更多
Alginate-based magnetic micro/millirobots have demonstrated significant potential for biomedical applications due to their flexible structures and capacity to carry various types of cargo,such as cells,enabling target...Alginate-based magnetic micro/millirobots have demonstrated significant potential for biomedical applications due to their flexible structures and capacity to carry various types of cargo,such as cells,enabling targeted therapy to specific diseased regions within the body.Their active therapy is typically achieved through magnetic actuation and magnetic heating,while monitored by medical imaging methods like CT which pose additional risks due to radiation exposure.In the last decades,a novel imaging method for superparamagnetic materials,known as magnetic particle imaging(MPI),has been under active development,offering not only positional tracking but also the ability to measure concentration and temperature.Here,we report the world's first MPI-traceable magnetic hydrogel robots,which employ a combination of iron oxide nanoflowers,NdFeB powder,and calcium alginate.Unlike previous magnetic alginate robots composed of a single magnetic material,the synergistic combination of NdFeB and nanoflowers enables these robots to exhibit triple magnetic functionalities:magnetic heating,locomotion at low magnetic fields,and tracking,all of which can be controlled using a single all-in-one electromagnetic coil system.The effects of various magnetization fields,as well as different concentrations of NdFeB and nanoflowers on the robots'magnetic properties were analyzed.This led to the development of three types of triple-function robots(spiral,droplet,and hybrid),with experimental results demonstrating biocompatibility,a magnetic heating temperature increase of over 10℃in plasma fluid under a magnetic field of 13 kA·m^(-1)at 200 kHz,locomotion speeds of up to 25 mm·s^(-1)in fields below 2 mT,and an MPI tracking error of 2.8 mm with a selection field of 0.4 mT·mm^(-1).Additionally,the robots'capacity for localized thermal therapy and selectively targeted cell delivery,as well as their locomotion within a medical phantom against a maximum flow of 50 mm·s^(-1)were demonstrated.展开更多
Self-healing(SH)polymer composites are a transformative achievement in polymer material technology that offers significant potential to extend the lifespan and reliability of materials.This work presents a novel appro...Self-healing(SH)polymer composites are a transformative achievement in polymer material technology that offers significant potential to extend the lifespan and reliability of materials.This work presents a novel approach to developing a hybrid natural-synthetic reinforced polymer composite with SH behavior using urea-free,non-toxic,environment-friendly material encapsulating resin,and hardener within a multicavity microcapsule(MC).This MC offers multiple healing because of its multicavity structure.These Xerogel MCs are integrated into hybrid bamboo/recycled glass fiber reinforced epoxy composite(25 wt% and 40 wt%)and were evaluated for their flexural strength,healing efficiency,moisture absorption,and thermal behavior.The results demonstrated that the composite containing 40 wt% exhibited the highest initial flexural strength and modulus retention after multiple healing cycles,approaching 80.67% and 61.34% respectively at 1st and 2nd cycles of healing efficiency.The behavior of self-healing hybrid composites(SHHC)in different environmental conditions was also investigated.Thermal Analysis TGA and DTA done on hybrid and other SH composites.Scanning electron microscopy shows the surface morphology of Xerogel MCs before and after damage,composite fractured surface,and how Healing Agent(HA)gets released and acquires surface after fracture.To ensure functional groups and chemical reactions between each component of the composite,FTIR analysis confirmed the successful encapsulation of HA inside MC.展开更多
In order to improve the substrate diffusion properties and stability of an immobilized enzyme alginate microgels modified with TiO2 nanoparticles were employed as the enzyme immobilizing support.Ionotropic gelation wa...In order to improve the substrate diffusion properties and stability of an immobilized enzyme alginate microgels modified with TiO2 nanoparticles were employed as the enzyme immobilizing support.Ionotropic gelation was applied for the preparation of hybrid gels while Ca2＋ Ce3＋ Ni2＋Cu2＋and Fe3＋were employed as the crosslinkers.Papain was selected as the model enzyme. UV-Vis spectroscopy was employed to investigate the activity of papain to evaluate kinetics and stability.Analysis results show that the highest affinity the lowest Michaelis-Menten constant Km =11.0 mg/mL and the highest stability are obtained when using Cu2＋as the crosslinker.The effect of the mass ratio of TiO2 to papain on the stability and leakage of papain is also investigated and the results show that 10∶1 TiO2∶papain is optimal because the proper use of TiO2 can reduce enzyme leakage and ensure enzyme stability.Preparing Cu/alginate/TiO2 hybrid gels via ionotropic gelation can provide a satisfactory diffusion capability and enzyme stability.展开更多
Polymer binder plays a pivotal role in electrochemical performance of high-capacity silicon(Si)anode that usually suffers from severe capacity fading due to enormous substantial volume change of Si during cycling.In a...Polymer binder plays a pivotal role in electrochemical performance of high-capacity silicon(Si)anode that usually suffers from severe capacity fading due to enormous substantial volume change of Si during cycling.In an effort to find efficient polymer binder that could mitigate such capacity fading,alginate-carboxymethyl chitosan(Alg-C-chitosan)composite polymer was investigated as a low-cost watersoluble binder for silicon anodes in lithium-ion batteries.The electrostatic interaction between carboxylate(-COO-)of Alg and protonated amines(-NH3+)of C-chitosan forms a selfhealing porous scaffold structure.Synergistic effect on the enhanced porous scaffold structure and self-healing electrostatic interaction of Alg-C-chitosan binder effectively can tolerate the tremendous volume change of Si and maintain an integrated electrode structure during cycling process.The Si nanopowder electrodes with Alg-C-chitosan composite binder exhibit an excellent cycling stability,with a capacity of750 mAh·g-1 remaining after 100 th cycling.In addition,an extraordinary areal capacity of 3.76 mAh·cm-2 is achieved for Si-based anodes with Alg-C-chitosan binder.展开更多
To achieve effective decolorization of reactive dyes,laccase immobilization was investigated.Laccase 0.2%(m/V)(Denilite IIS) was trapped in beads of alginate/gelatin blent with polyethylene glycol(PEG),and then the su...To achieve effective decolorization of reactive dyes,laccase immobilization was investigated.Laccase 0.2%(m/V)(Denilite IIS) was trapped in beads of alginate/gelatin blent with polyethylene glycol(PEG),and then the supporters were activated by cross-linking with glutaraldehyde.The results of repeated batch decolorization showed that gelatin and appropriate concentration of glutaraldehyde accelerated the decolorization of Reactive Red B-3BF(RRB);PEG had a positive effect on enzyme stability and led to an inc...展开更多
Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental frien...Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin （kaolin/CA）, was prepared using a sol-gel method. The effects of contact time, pH, adsorbent dose, and temperature on Cu2＋ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2＋ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.展开更多
基金supported by the National Natural Science Foundation of China(No.22073015)the National Key R&D Program of China(No.2022YFB3704600).
文摘Moist-electric generation,a green and environmentally friendly energy harvesting technology,is undoubt-edly one of the effective methods to alleviate energy shortages and environmental damage.However,the lack of fiber-like moist-electric generators(MEGs)that combine continuous power generation and high electrical output performance has constrained the development of moist-electric in the fields of flexi-ble wearable and self-power supplies.In this work,sodium alginate(SA)/multi-walled carbon nanotubes(MWCNT)fibers with axial heterogeneous(axi-he)of oxygen-containing functional groups(Ocfgs)are prepared through a mold forming method in assistance with the coagulation process.The interaction be-tween axi-he MEG and moisture is investigated by analyzing the electrical signal changes of dried MEG under moisture stimulation.The maximum output voltage and current of axi-he MEG can reach 0.35 V and 1.92μA under the stimulation of moisture.Based on the regulation of Ocfgs,axi-he MEG has a con-tinuous high moist-electric performance and environmental adaptability.The maximum output power density(Pmo)of axi-he MEG with a length of only 2 cm can reach 27.37μW cm-2 at RH=90%,which exceeds most of the MEGs reported in literature.Meanwhile,a continuous output voltage of 0.33-0.37 V for more than 15 h can be obtained from this axi-he MEG.Thus,the axi-he MEG from Ocfg distribution design and mold forming method provides a new way of clean energy generation using moisture from the ambient environment,exhibiting enormous potential in energy supply for Internet of Things(IoT)devices.
基金supported by the National Natural Science Foundation of China under Grant Nos.21274020 and 21304019
文摘A facile method for the preparation of sodium alginate（SA）/carboxyl-functionalized graphene（G-COOH）composite hydrogel was developed. Based on the coordination ability of lanthanide ions to the carboxyl groups, a series of hydrogel derived from different ratios of SA and G-COOH was fabricated by neodymium（Nd3＋） ions coordination. A relatively uniform layered structure was recorded by SEM at the interior of SA/G-COOH hydrogel. Several parameters such as water content, swelling ratio（SR）, tensile test and solvent resistance were also investigated. The SA/G-COOH composite hydrogel showed excellent mechanical strength, and the tensile strength of SA/G-COOH composite hydrogel reaches 53.72 MPa at high water content. Due to the coordination ability of Nd3＋ ions, the hydrogel also exhibited an excellent solvent resistance and stability.
文摘The presence of toxic dyes in the aqueous medium has threatened environmental safety,and thereby re-moving them from wastewater in an efficient way is highly desired.Herein,the efficient biosorbents were successfully fabricated via a facile physical gelation process of sodium alginate(SA)and carboxymethyl chitosan(CMCTS)in an acidic aqueous solution.The as-prepared hydrogel beads not only displayed water superabsorbent properties and pH-responsive swelling characters but also exhibited excellent methylene blue(MB)adsorption capacity removal efficiency with experimental maximum MB adsorption capacity of 2518 and 1005 mg g-1,which are comparable with most reported lignocellulosic and alginate-based hydrogels.The MB adsorption process fitted well in different kinetic and isotherm models and became more heterogeneous in concentrated MB solutions as verified by principal component analysis results.The adsorption mechanism was proposed,and the high dye absorbency was attributed to the strong electro-static forces between adsorbents and adsorbates.Our current study provides a promising and sustainable composite hydrogels platform targeted to dye decontamination.
基金funded by the National Key Research and Development Program of China(2023YFF1103804)the Academic Research Projects of Beijing Union University(ZK20202516).
文摘Krill oil is effective in reducing blood lipid levels,particularly in individuals with severe hyperlipidemia.However,poor water insolubility and stability limited its usage.This study investigated a method for encapsulating Antarctic krill oil using alginate(ALG)and gelatin(GLN)to enhance its stability and bioactivity.The encapsulation efficiency,functional group integrity,swelling rate,and lipid-lowering activity were assessed.Results indicated that the optimal encapsulation conditions were identified with an ALG:GLN ratio of 2:1(m/m),coagulation bath of 9%CaCl_(2),and a nozzle size of 750μm,resulting in 69.34%encapsulation efficiency.Fourier-transform infrared spectroscopy confirmed successful encapsulation.The ALG-GLN shell materials enriched astaxanthin in krill oil and protected it from harsh gastric conditions,enabling targeted intestinal release.In a high-fat diet-induced rat model,krill oil microcapsules significantly reduced triglycerides(TG),total cholesterol(TC),and low-density lipoprotein-cholesterol(LDL-C)levels while increasing high-density lipoprotein-cholesterol(HDL-C)levels compared to unencapsulated krill oil.Additionally,the microcapsules elevated nitric oxide(NO)levels,enhanced superoxide dismutase(SOD)activity,and reduced malondialdehyde(MDA)levels,liver and perirenal fat weight.Therefore,encapsulating Antarctic krill oil in alginate-gelatin hydrogel offers a promising strategy for managing hyperlipidemia and associated metabolic disorders.
基金Project supported by the National Natural Science Foundation of China(21167011)the Natural Science Foundation of Inner Mongolia Autonomous Region,China(2020LH02009)the Collaborative Innovation Center for Water Environment Security of Inner Mongolia Autonomous Region,China(XTCX003)。
文摘A novel macroparticle magnesium-modified biochar/yttrium alginate(Mg-BC/SA-Y)hybrid biogel composite was successfully developed through a facile solution reaction of magnesium-modified BC and yttrium alginate polymer,and its properties were characterized.The obtained Mg-BC/SA-Y biogel beads have a particle size of approximately 1.5 mm,featuring abundant network pores and an uneven,distinctive surface.The performance and mechanisms of Mg-BC/SA-Y for phosphate adsorption were thoroughly investigated.The findings indicate that Mg-BC/SA-Y removes up to 95.7%of phosphate at pH4.0 and 298 K,and also achieves a phosphate removal efficiency of over 80%within a pH range of3.0-11.0.The adsorption capacity of Mg-BC/SA-Y for phosphate is nearly four times that of BC.The spontaneous adsorption processes and endothermic adsorption behavior can be elucidated by the pseudo-second-order rate and Langmuir equations,respectively.Phosphate adsorption is almost unaffected by water ionic strength and common coexisting ions,except for the influence of highconcentration F-ions.The recyclable biogel beads can be reused after adsorbing phosphate,and represent excellent stability and practicability in real water.The mechanisms of ligand exchange,innersphere complexation and electrostatic attraction are involved in phosphate removal.Mg-BC/SA-Y biogel polymer is a desirable and sustainable biosorbent for treating water with excessive phosphate levels and reducing pollution and carbon emissions.
基金supported by Research Fund of SWUST for PhD(Grant No.22zx7175)Sichuan Science and Technology Program(Grant No.2024NSFSC1097)。
文摘Based on the characteristics of laser-induced surface ignition,energetic photosensitive films show promising potential to meet the ignition requirements of various energetic materials(EMs).In this study,DATNBI/ferric alginate(DI/FeA),DI/cobalt alginate(DI/CoA),and DI/nickel alginate(DI/Ni A)films are fabricated by employing sodium alginate(SA)with a three-dimensional network structure as the film matrix,via ionic cross-linking of SA with Fe^(3+),Co^(2+),and Ni^(2+)ions.The study demonstrates that the ionic cross-linking enhances the hydrophobic performance of the films,with the water contact angle increasing from 82.1° to 123.5°.Concurrently,the films'near-infrared(NIR)light absorption improved.Furthermore,transition metal ions facilitate accelerated electron transfer,thereby catalyzing the thermal decomposition of DATNBI.Under 1064 nm laser irradiation,the DI/Fe A film exhibits exceptional combustion performance,with an ignition delay time as low as 76 ms.It successfully acts as an NIR laser ignition medium to initiate the self-sustained combustion of CL-20.This study demonstrates the synergistic realization of enhanced hydrophobicity,improved photosensitivity,and promoted catalytic decomposition through microstructural design of the material,providing new insights for the design of additive-free EMs in laser ignition applications.
基金supports from the National Natural Science Foundation of China(22075034,22178037,and 22478047)Natural Science Foundation of Liaoning Province of China(2021-MS-303)the China Scholarship Council(CSC No 202008210171).
文摘Porous carbons hold broad application prospects in the domains of electrochemical energy storage devices and sensors.In this study,porous carbon derived from sodium alginate-encapsulated ZIF-8(SA/ZIF-8-C)was suc-cessfully prepared by blending ZIF-8 particles with sodium alginate,forming hydrogel beads in the presence of divalent metal ions,and subsequently subjecting them to high-temperature pyrolysis.Various characterization techniques were employed to evaluate the properties of the prepared materials.The introduction of a carbon framework on ZIF-8-derived particles effectively enhanced the conductivity of the prepared materials.The SA/ZIF-8(1.0)-C sample heated at 800℃exhibited a specific capacitance of up to 208 F g^(-1)at a current density of 0.5 A g^(-1)and outstanding cyclic stability.Even after 10,000 charge and discharge cycles,its capacitance retention rate remained as high as 87.14%.The symmetric supercapacitor constructed with the composite demonstrated an excellent energy density of 14.58 Wh kg^(-1)at a power capacity of 403.85 W kg^(-1).The implementation of this study provides new ideas and inspiration for the development of high-performance supercapacitors.
基金supported by a Korea University Grantby the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)with Grant Number 2022R1A2C1003381。
文摘Alginate-based magnetic micro/millirobots have demonstrated significant potential for biomedical applications due to their flexible structures and capacity to carry various types of cargo,such as cells,enabling targeted therapy to specific diseased regions within the body.Their active therapy is typically achieved through magnetic actuation and magnetic heating,while monitored by medical imaging methods like CT which pose additional risks due to radiation exposure.In the last decades,a novel imaging method for superparamagnetic materials,known as magnetic particle imaging(MPI),has been under active development,offering not only positional tracking but also the ability to measure concentration and temperature.Here,we report the world's first MPI-traceable magnetic hydrogel robots,which employ a combination of iron oxide nanoflowers,NdFeB powder,and calcium alginate.Unlike previous magnetic alginate robots composed of a single magnetic material,the synergistic combination of NdFeB and nanoflowers enables these robots to exhibit triple magnetic functionalities:magnetic heating,locomotion at low magnetic fields,and tracking,all of which can be controlled using a single all-in-one electromagnetic coil system.The effects of various magnetization fields,as well as different concentrations of NdFeB and nanoflowers on the robots'magnetic properties were analyzed.This led to the development of three types of triple-function robots(spiral,droplet,and hybrid),with experimental results demonstrating biocompatibility,a magnetic heating temperature increase of over 10℃in plasma fluid under a magnetic field of 13 kA·m^(-1)at 200 kHz,locomotion speeds of up to 25 mm·s^(-1)in fields below 2 mT,and an MPI tracking error of 2.8 mm with a selection field of 0.4 mT·mm^(-1).Additionally,the robots'capacity for localized thermal therapy and selectively targeted cell delivery,as well as their locomotion within a medical phantom against a maximum flow of 50 mm·s^(-1)were demonstrated.
文摘Self-healing(SH)polymer composites are a transformative achievement in polymer material technology that offers significant potential to extend the lifespan and reliability of materials.This work presents a novel approach to developing a hybrid natural-synthetic reinforced polymer composite with SH behavior using urea-free,non-toxic,environment-friendly material encapsulating resin,and hardener within a multicavity microcapsule(MC).This MC offers multiple healing because of its multicavity structure.These Xerogel MCs are integrated into hybrid bamboo/recycled glass fiber reinforced epoxy composite(25 wt% and 40 wt%)and were evaluated for their flexural strength,healing efficiency,moisture absorption,and thermal behavior.The results demonstrated that the composite containing 40 wt% exhibited the highest initial flexural strength and modulus retention after multiple healing cycles,approaching 80.67% and 61.34% respectively at 1st and 2nd cycles of healing efficiency.The behavior of self-healing hybrid composites(SHHC)in different environmental conditions was also investigated.Thermal Analysis TGA and DTA done on hybrid and other SH composites.Scanning electron microscopy shows the surface morphology of Xerogel MCs before and after damage,composite fractured surface,and how Healing Agent(HA)gets released and acquires surface after fracture.To ensure functional groups and chemical reactions between each component of the composite,FTIR analysis confirmed the successful encapsulation of HA inside MC.
基金The National Natural Science Foundation of China(No.21005016)the Foundation of Educational Commission of Jiangsu Province(No.JHB2011-2)
文摘In order to improve the substrate diffusion properties and stability of an immobilized enzyme alginate microgels modified with TiO2 nanoparticles were employed as the enzyme immobilizing support.Ionotropic gelation was applied for the preparation of hybrid gels while Ca2＋ Ce3＋ Ni2＋Cu2＋and Fe3＋were employed as the crosslinkers.Papain was selected as the model enzyme. UV-Vis spectroscopy was employed to investigate the activity of papain to evaluate kinetics and stability.Analysis results show that the highest affinity the lowest Michaelis-Menten constant Km =11.0 mg/mL and the highest stability are obtained when using Cu2＋as the crosslinker.The effect of the mass ratio of TiO2 to papain on the stability and leakage of papain is also investigated and the results show that 10∶1 TiO2∶papain is optimal because the proper use of TiO2 can reduce enzyme leakage and ensure enzyme stability.Preparing Cu/alginate/TiO2 hybrid gels via ionotropic gelation can provide a satisfactory diffusion capability and enzyme stability.
基金financially supported by the National Natural Science Foundation of China (No. 51404032)the National High Technology Research and Development Program of China(No. 2013AA050904)
文摘Polymer binder plays a pivotal role in electrochemical performance of high-capacity silicon(Si)anode that usually suffers from severe capacity fading due to enormous substantial volume change of Si during cycling.In an effort to find efficient polymer binder that could mitigate such capacity fading,alginate-carboxymethyl chitosan(Alg-C-chitosan)composite polymer was investigated as a low-cost watersoluble binder for silicon anodes in lithium-ion batteries.The electrostatic interaction between carboxylate(-COO-)of Alg and protonated amines(-NH3+)of C-chitosan forms a selfhealing porous scaffold structure.Synergistic effect on the enhanced porous scaffold structure and self-healing electrostatic interaction of Alg-C-chitosan binder effectively can tolerate the tremendous volume change of Si and maintain an integrated electrode structure during cycling process.The Si nanopowder electrodes with Alg-C-chitosan composite binder exhibit an excellent cycling stability,with a capacity of750 mAh·g-1 remaining after 100 th cycling.In addition,an extraordinary areal capacity of 3.76 mAh·cm-2 is achieved for Si-based anodes with Alg-C-chitosan binder.
基金supported by the National Hi-Tech Research and Development Program(863)of China(No.2007AA02Z218)the Open Project Program of Key Lab-oratory of Eco-Textiles,Jiangnan University,Ministry of Education,China(No.KLET0625) the Youth Fundof Jiangnan University(No.2006LQN002).
文摘To achieve effective decolorization of reactive dyes,laccase immobilization was investigated.Laccase 0.2%(m/V)(Denilite IIS) was trapped in beads of alginate/gelatin blent with polyethylene glycol(PEG),and then the supporters were activated by cross-linking with glutaraldehyde.The results of repeated batch decolorization showed that gelatin and appropriate concentration of glutaraldehyde accelerated the decolorization of Reactive Red B-3BF(RRB);PEG had a positive effect on enzyme stability and led to an inc...
基金supported by the National Natural Science Foundation of China (No. 50802045,20975056/B050902)the Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry,and the Middleaged and Youth Scientist Incentive Foundation of Shandong Province (No.BS09018)
文摘Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin （kaolin/CA）, was prepared using a sol-gel method. The effects of contact time, pH, adsorbent dose, and temperature on Cu2＋ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2＋ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.
