Aqueous zinc ion batteries are regarded as one of the most promising candidates for large-scale energy stor-age due to their high safety,cost-effectiveness,and environ-mental friendliness.However,uncontrolled zinc den...Aqueous zinc ion batteries are regarded as one of the most promising candidates for large-scale energy stor-age due to their high safety,cost-effectiveness,and environ-mental friendliness.However,uncontrolled zinc dendrite growth and side reactions of the zinc anode decrease the sta-bility of Zn batteries.We report the synthesis of an air-oxid-ized carbon nanotube(O-CNT)film by chemical vapor de-position followed by heat treatment in air which is used as a protective layer on the Zn foil to suppress zinc dendrite growth.The increase in the hydrophilicity of the O-CNT film caused by air oxidation facilitates zinc deposition between the film and the anode instead of deposition on the film surface.The porous structure of the O-CNT film homogenizes the Zn^(2+)ion flux and the electric field on the surface of the Zn foil,leading to the uniform deposition of Zn.As a result,a O-CNT@Zn symmetric cell has a much better cycling stability with a life of more than 3000 h at 1 mA cm^(−2) with a capacity of 1 mAh cm^(−2),and values of more than 2000 h and 1 mAh cm^(−2) at 5 mA cm^(−2).In addition,a O-CNT@Zn||Mn^(2+)inserted hydrated vanadium pentoxide(MnVOH)full cell has a better rate per-formance than a Zn||MnVOH cell,achieving a high discharge capacity of 194 mAh g^(−1) at a high current density of 8 A g^(−1).In a long-term cycling test,the O-CNT@Zn||MnVOH full cell has a capacity retention of 58.8%after 2000 cycles at a current density of 5 A·g^(−1).展开更多
To enhance the hydrophilicity and antistatic properties of the polyethylene terephthalate(PET)fabric,the lawsone dye was employed in dyeing the PET fabric.It was dissolved in ethanol/deionized water mixture and deioni...To enhance the hydrophilicity and antistatic properties of the polyethylene terephthalate(PET)fabric,the lawsone dye was employed in dyeing the PET fabric.It was dissolved in ethanol/deionized water mixture and deionized water separately,forming different lawsone dye solutions(LDSs).The study investigated how the compounds in the LDS improve the surface properties and color durability of the PET fabric,resulting in increased dye uptake.An infrared dyeing machine was utilized to expedite the reactions between the lawsone dye and the PET fabric.Additionally,the chemical composition of the dyed PET fabric was verified using techniques such as Fourier transform infrared(FTIR)spectroscopy,X-ray photoelectron spectroscopy(XPS),X-ray diffraction(XRD)and ultraviolet-visible(UV-Vis)spectrophotometry.The K/S value was measured to assess color durability.After dyeing,the PET fabric exhibited high hydrophilicity which improved the hygroscopicity of the PET fabric and thus the conductivity of the PET fabric surface increased,thereby providing an antistatic effect.展开更多
The use of biomass feedstocks for the manufacture of high-performance polymers can help expand their range of applications and reduce their dependence on finite fossil resources.However,improving the heat resistance a...The use of biomass feedstocks for the manufacture of high-performance polymers can help expand their range of applications and reduce their dependence on finite fossil resources.However,improving the heat resistance and hydrophilicity of bio-based polyesters remains a significant challenge.Herein,we introduce N,N'-trans-1,4-cyclohexane-bis(pyrrolidone-4-methylcarboxylate)(CBPC),a novel bio-based tricyclic dibasic ester synthesized from renewable dimethyl itaconic acid and trans-1,4-cyclohexane diamine via an aza-Michael addition reaction.As a unique comonomer,CBPC features a rigid tricyclic backbone that significantly enhances chain packing and thermal stability,whereas its pyrrolidone side groups impart tunable polarity and improved hydrophilicity.Using CBPC,diphenyl carbonate,and 1,4-butylene glycol,a series of PBCC copolymers with 10 mol%-30 mol%CBPC was synthesized via ester-exchange and melt polycondensation methods.Incorporation of CBPC raised the melting temperature(Tm)from 56.8℃to 225.8℃and the initial decomposition temperature(Td5%)from 258.0℃to 306.7℃,positioning PBCC among the most heat-resistant bio-based polyesters reported.Additionally,the pyrrolidone units enabled transformation from hydrophobic to hydrophilic.This study demonstrates that CBPC is an effective and innovative building block for the design of bio-based polymers with enhanced thermal and surface properties,offering a promising strategy for the development of high-performance sustainable materials.展开更多
The synthesis of functionalized rubber copolymers is a topic of great research interest.In this study,we present a novel approach for the direct construction ofα-functionalized 3,4-polyisoprene through polymerization...The synthesis of functionalized rubber copolymers is a topic of great research interest.In this study,we present a novel approach for the direct construction ofα-functionalized 3,4-polyisoprene through polymerization of polar monomers and isoprene monomer.Theα-functionalized 3,4-polyisoprene was successfully synthesized via in situ sequential polymerization using the iron-based catalytic system(Fe(acac)_(3)/IITP/AliBu_(3)),exhibiting high activity and resistance to polar monomers without requiring protection of polar groups.The structure ofα-functionalized 3,4-polyisoprene was confirmed by proton nuclear magnetic resonance spectroscopy(^(1)H-NMR)and two-dimensional diffusion-ordered spectroscopy(2D DOSY)spectra analysis.The introduction of polar groups,particularly hydroxyl groups,enhanced the hydrophilicity of the copolymer.This was evidenced by a decrease in the water contact angle from 106.9°to 96.4°with increasing hydroxyl content in the copolymer.展开更多
Hydrophilicity is critical in Nafion membranes during fuel cell operation as insufficient membrane hydration leads to brittle behavior and a drop in proton conductivity.The incorporation of APTS(3-(aminopro pyl)trieth...Hydrophilicity is critical in Nafion membranes during fuel cell operation as insufficient membrane hydration leads to brittle behavior and a drop in proton conductivity.The incorporation of APTS(3-(aminopro pyl)triethoxysilane)into exfoliated graphene oxide(EGO)by covalent functionalization to be used as filler into Nafion membranes allows higher hydrophilicity for these membranes.This is associated with promoting hydroxyl,carbonyl,siloxane,silane,and amine groups within the EGO-APTS matrix.The incorporation of these materials as Fuel Cell MEAs leads to a significant reduction of the ohmic resistance measured at high frequency resistance(HFR)in electrochemical impedance spectroscopy(EIS)experiments and achieves maximum power densities of 1.33 W cm^(-2)at 60℃ at 100%RH(APTS-EGO,0.2 wt%)and1.33 W cm^(-2)at 60℃ at 70%RH(APTS-EGO,0.3 wt%),which represents an improvement of 190%compared to the commercial Nafion 212 when utilizing low humidification conditions(70%).Moreover,the as-synthesized membrane utilizes lower Nafion ionomer mass,which,in conjunction with the excellent cell performance,has the potential to decrease the cost of the membrane from 87 to 80￡/W as well as a reduction of fluorinated compounds within the membrane.展开更多
Constructing multi-dimensional hydrogen bond(H-bond)regulated single-molecule systems with multiemission remains a challenge.Herein,we report the design of a new excited-state intramolecular proton transfer(ESIPT)feat...Constructing multi-dimensional hydrogen bond(H-bond)regulated single-molecule systems with multiemission remains a challenge.Herein,we report the design of a new excited-state intramolecular proton transfer(ESIPT)featured chromophore(HBT-DPI)that shows flexible emission tunability via the multidimensional regulation of intra-and intermolecular H-bonds.The feature of switchable intramolecular Hbonds is induced via incorporating several hydrogen bond acceptors and donors into one single HBT-DPI molecule,allowing the“turn on/off”of ESIPT process by forming isomers with distinct intramolecular Hbonds configurations.In response to different external H-bonding environments,the obtained four types of crystal/cocrystals vary in the contents of isomers and the molecular packing modes,which are mainly guided by the intermolecular H-bonds,exhibiting non-emissive features or emissions ranging from green to orange.Utilizing the feature of intermolecular H-bond guided molecular packing,we demonstrate the utility of this fluorescent material for visualizing hydrophobic/hydrophilic areas on large-scale heterogeneous surfaces of modified poly(1,1-difluoroethylene)(PVDF)membranes and quantitatively estimating the surface hydrophobicity,providing a new approach for hydrophobicity/hydrophilicity monitoring and measurement.Overall,this study represents a new design strategy for constructing multi-dimensional hydrogen bond regulated ESIPT-based fluorescent materials that enable multiple emissions and unique applications.展开更多
The stability of oil-dominated emulsions,including oil-based drilling fluids and crude oils,is crucial for mitigating gas hydrate risks in the petroleum and natural gas industries.Nanoparticles can stabilize oilwater ...The stability of oil-dominated emulsions,including oil-based drilling fluids and crude oils,is crucial for mitigating gas hydrate risks in the petroleum and natural gas industries.Nanoparticles can stabilize oilwater systems(Pickering emulsions)by residing at the oil-water interface.However,their effects on the kinetics of hydrate formation in these systems remain unclear.To address this,we experimentally investigated how hydrophilic and hydrophobic nano-CaCO_(3) influence CH4 hydrate formation within dynamic oil-water systems.A series of hydrate formation experiments were conducted with varying water cuts and different concentrations of nano-CaCO_(3) at a particle size of 20 nm,under 3℃ and 6 MPa.The induction time,hydrate formation volume,and hydrate growth rate were measured and calculated.The results indicate that hydrophilic nano-CaCO_(3) generally inhibits hydrate formation,particularly at high water cuts,while hydrophobic nano-CaCO_(3) can significantly inhibit or even prevent hydrate formation at low water cuts.Water cut strongly influences the kinetics of hydrate formation,and nanoparticle concentration also impacts the results,likely due to changes in oil-water interface stability caused by nanoparticle distribution.This study will offer valuable insights for designing deepwater oilbased drilling fluids using nanoparticles and ensuring safe multiphase flow in deepwater oil and gas operations.展开更多
The Nd-doped TiO2 thin films with higher hydrophilic and photocatalytic activities were prepared on glass slides by an acid-catalyzed sol？gel method. The effects of Nd doping on crystalline phase, surface composition...The Nd-doped TiO2 thin films with higher hydrophilic and photocatalytic activities were prepared on glass slides by an acid-catalyzed sol？gel method. The effects of Nd doping on crystalline phase, surface composition and optical property were investigated by means of techniques such as X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Fourier transform infrared spectroscopy （FT-IR）, optical contact angle tester and UV-Vis spectroscopy. The results show that Nd doping obviously influences the hydrophilic and photocatalytic activities of TiO2thin films. Nd doping could cause the TiO2 lattice distortion, inhibit phase transition from anatase to rutile, cause red shift of the absorption spectrum edge, produce hydroxyl radicals （·OH）, and accelerate surface hydroxylation, which result in a significant improvement in the hydrophilicity and photoreactivity of Nd-doped TiO2 thin films. When the content of Nd is 0.1% （mass fraction）, TiO2 thin films achieve the smallest grain size （about 15 nm）, and the hydrophilic and photocatalytic activities of TiO2 thin film reach the maximum, the contact angle is only 8.1°, and 92% of methylene blue is finally degraded. Moreover, the modification mechanism of Nd doping was also discussed.展开更多
Titania films with nano-sized pores were prepared on the NaOH？HCl pretreated NiTi alloy substrate by sol？gel method.A crack-free film is obtained for the sample with a dense inner layer and a porous outside layer（s...Titania films with nano-sized pores were prepared on the NaOH？HCl pretreated NiTi alloy substrate by sol？gel method.A crack-free film is obtained for the sample with a dense inner layer and a porous outside layer（sample TC1＋1）.The X-ray diffraction shows that the titania films are composed of anatase,and a little Ni4Ti3 phase in the heat treated substrate is also detected.The X-ray photoelectron spectroscopy results indicate that the titania film completely covered the NiTi substrate for sample TC1＋1.The sample TC1＋1 is hydrophilic with a contact angle about 20°,and UV illumination treatment for 15 min further decreases the contact angle to（9.2±3.2）°.The potentiodynamic polarization test in 0.9% NaCl solution reveals a better corrosion resistance of sample TC1＋1 than the polished NiTi sample.展开更多
Ta-containing TiO2 films with Ta contents of 5%, 20%, 33% （mole fraction） were sol-gel coated on the surface roughened Ti6AI4V alloy by dip coating method for biomedical applications. The Ta-TiO2 films on 1.5 mol/L ...Ta-containing TiO2 films with Ta contents of 5%, 20%, 33% （mole fraction） were sol-gel coated on the surface roughened Ti6AI4V alloy by dip coating method for biomedical applications. The Ta-TiO2 films on 1.5 mol/L NaOH-HCI pretreated substrate are adherent, but there are cracks for the sample with 33% Ta. X-ray photoelectron spectroscopy results show that Ti and Ta exist as TiP2 and Ta205 in the film, and A1 element is not detectable. X-ray diffraction and Raman scattering analyses reveal that the addition of Ta decreases crystallization of the films. Potentiodynamic polarization test in a Ca-free Hank＇s balanced solution demonstrates that the coating samples markedly improve the corrosion resistance compared with the polished sample. The addition of Ta impedes UV light-induced hydrophilic conversion of the coating samples. The sample with 20% Ta has enough film integrity and hydrophilic conversion rate, and is expected to possess good biological properties.展开更多
The electrochemical deposition technique was applied to achieve porous silicon （PS） surface passivated with Ag deposition for improving the properties of PS photoluminescence. The relation of Ag depositing forms to ...The electrochemical deposition technique was applied to achieve porous silicon （PS） surface passivated with Ag deposition for improving the properties of PS photoluminescence. The relation of Ag depositing forms to current density and the effect of PS hydrophilic surface on deposition uniformity were investigated. The experimental results indicated that there were two critical current densities （maximum and minimum） in which Ag was absent and electroplated on PS surface correspondingly, and the range of current density for deposition of Ag on porous silicon was from 50 μA/cm^2 to 400 μA/cm^2. The process of changing PS surface from hydrophobic into hydrophilic had positive effect on Ag deposition uniformity. Under the same experimental conditions, PS hydrophobic surface presented uneven Ag deposition.However, hydrophilic surface treated with SC-1 solution was even. Finally, the effect of PS surface passivation with Ag even deposition on photoluminescence intensity and stabilization of PS was studied. It was discovered that Ag passivation inhibited the degradation of PL intensity effectively. In addition, excessive Ag deposition had a quenching effect on room-temperature visible photoluminescence of PS.展开更多
A range of poly（ε-caprolactone）/poly（N-vinyl-2-pyrrolidone） amphiphilic block copolymers with well-defined hydrophilic chain length were synthesized by the living/controlled reversible addition fragmentation chai...A range of poly（ε-caprolactone）/poly（N-vinyl-2-pyrrolidone） amphiphilic block copolymers with well-defined hydrophilic chain length were synthesized by the living/controlled reversible addition fragmentation chain transfer polymerization method. The composition and struc- ture of the targeted resultants were characterized with 1H NMR, 13C NMR, FT-IR spec- troscopy and gel permeation chromatography. The various block copolymers were success- fully employed to fabricate the spherical micelle with core-shell morphological structure. The poly（N-vinyl-2-pyrrolidone） block-dependent characteristics of the copolymeric micelles were investigated by fluorescence spectroscopy, dynamic light scattering, and transmission electron microscopy. The solubilization of the hydrophobic ibuprofen as a model drug in the micelle solution was also explored. It was found that the drug loading contents are related to the micellar morphology structure determined by hydrophilic chain length in the copolymer.展开更多
Porous polyvinylidene fluoride（PVDF）membranes blended with LiCl are prepared through the phase inversion method to obtain a good support layer for air dehumidification.The hydrophilicity of the resulting membrane is...Porous polyvinylidene fluoride（PVDF）membranes blended with LiCl are prepared through the phase inversion method to obtain a good support layer for air dehumidification.The hydrophilicity of the resulting membrane is evaluated by water contact angle measurements and vapor adsorption tests.The moisture permeation performance of the membrane is measured by permeation tests in terms of total mass transfer coefficients and moisture permeability rates.It is found that water contact angles and water vapor adsorption capacities increase with the increasing LiCl content in the casting solution.As the LiCl content increases,the total mass transfer coefficient increases slightly at a low LiCl content（below 2.5%）and then improves greatly at a high LiCl content（above 2.5%）,whereas the moisture permeation rate increases.The results demonstrate that LiCl can remarkably improve the hydrophilicity of PVDF membranes,and then greatly enhance moisture permeation performance.展开更多
Polyetheretherketone (PEEK) is known as one of the “super-engineering plastics” and is used as an intervertebral disk spacer in the body. PEEK has a hydrophobic surface (water contact angle (WCA) > 80°) and ...Polyetheretherketone (PEEK) is known as one of the “super-engineering plastics” and is used as an intervertebral disk spacer in the body. PEEK has a hydrophobic surface (water contact angle (WCA) > 80°) and high chemical resistance, and it is thus difficult to perform any surface treatment, such as hydrophilization. In this study, we aimed to form a hydrophilic surface on PEEK without coating layers by using hydroprocessing (aqueous solution processing), and we examined the osteoconductivity and anti-inflammatory properties of surface-treated PEEK in vivo compared with Ti implants. The WCA value of PEEK reached ~20° using a combination of immersion in a solution of >16.2 M H2SO4 and ultraviolet irradiation (172 nm). In in vivo testing, the hydrophilization of PEEK by surface modification without a coating layer improved the osteoconductivity and anti-inflammatory properties. The relationship between the bone-implant contact ratio and the WCA values of the surface-modified PEEK agreed well with that of the surface-treated Ti.展开更多
Liposomes were prepared by adding hydrophilic agents PEG PE, rigidity agent SM in the bilayer membrane for mimetic red cell membrane. In PBS or serum, release of calcein content from liposomes dramatically decreased,...Liposomes were prepared by adding hydrophilic agents PEG PE, rigidity agent SM in the bilayer membrane for mimetic red cell membrane. In PBS or serum, release of calcein content from liposomes dramatically decreased, which demonstrated increasing membrane stability by adding PEG PE or SM. The ratio b/R of the remains of liposomes in blood to that in RES was used as a parameter of biodistribution in vivo. At 2 h after iv injection, b/R of modified liposomes was enhanced 6.5～13.1 fold. Their clearance half life from blood circulation was delayed 1.6～5.8 fold. The modification of liposome membrane by PEG PE or SM is the favorable condition for drug liposomes to target the non RES.展开更多
Invasion of drilling fluid into natural gas hydrate deposits during drilling might damage the reservoir,induce hydrate dissociation and then cause wellbore instability and distortion of the data from well logging. Add...Invasion of drilling fluid into natural gas hydrate deposits during drilling might damage the reservoir,induce hydrate dissociation and then cause wellbore instability and distortion of the data from well logging. Adding nanoparticles into drilling fluid is an effective method in reducing the invasion of drilling fluid and enhancing borehole stability. However, the addition of nanoparticles might also introduce hydrate formation risk in borehole because they can act as the "seeds" for hydrate nucleation. This paper presents an experimental study of the effect of hydrophilic silica nanoparticle on gas hydrate formation in a dynamic methane/liquid-water system. In the experiment, the ultrapure water with and without1.0 wt%–6.0 wt% concentrations of silica nanoparticles, grain sizes of 20 and 50 nm, were pressurized by methane gas under varied conditions of temperature and pressure. The induction time, the gas consumption, and the average rate of gas consumption in the system were measured and compared to those in ultrapure water. The results show that a concentration of 4.0 wt% hydrophilic SiO_2 particles with a grain size of 50 nm has a relatively strong inhibition effect on hydrate formation when the initial experimental condition is 5.0 °C and 5.0 MPa. Compared to ultrapure water, the hydrophilic nano-SiO_2 fluid increases the induction time for hydrate formation by 194% and decreases the amount and average rate of hydrate formation by 10% and 17%, respectively. This inhibition effect may be attributed to the hydrophilicity,amount and aggregation of silica nanoparticle according to the results of water activity and zeta potential measurements. Our work also elucidates hydrophilic, instead of hydrophobic, nanoparticles can be added to the drilling fluid to maintain wellbore stability and to protect the hydrate reservoir from drilling mud damage, because they exhibit certain degree of hydrate inhibition which can reduce the risk of hydrate reformation and aggregation during gas hydrate or deep water drilling if their concentration can be controlled properly.展开更多
Polyethersulfone(PES) is widely used as biomaterials due to its thermal stability,mechanical strength,and chemical inertness.Nevertheless,their blood compatibility is still not adequate for hemodialysis and blood puri...Polyethersulfone(PES) is widely used as biomaterials due to its thermal stability,mechanical strength,and chemical inertness.Nevertheless,their blood compatibility is still not adequate for hemodialysis and blood purification.In this study,the sulfonated polyethersulfone(SPES) was synthesized through an electrophilic substitution reaction,and PES/SPES blending membranes were prepared.The characterization of the SPES was studied by FTIR.The water adsorption and water contact angle experiments show that the hydrophilicity of PES/SPES blend membrane was improved as for the sulfonate group existing in the SPES.Moreover,PES/SPES blend membrane could effectively reduce bovine serum albumin adsorption and prolong the blood coagulation time compared with the PES membrane,thereby improving blood compatibility.展开更多
基金supported by the National Natural Science Foundation of China(22179093 and21905202)。
文摘Aqueous zinc ion batteries are regarded as one of the most promising candidates for large-scale energy stor-age due to their high safety,cost-effectiveness,and environ-mental friendliness.However,uncontrolled zinc dendrite growth and side reactions of the zinc anode decrease the sta-bility of Zn batteries.We report the synthesis of an air-oxid-ized carbon nanotube(O-CNT)film by chemical vapor de-position followed by heat treatment in air which is used as a protective layer on the Zn foil to suppress zinc dendrite growth.The increase in the hydrophilicity of the O-CNT film caused by air oxidation facilitates zinc deposition between the film and the anode instead of deposition on the film surface.The porous structure of the O-CNT film homogenizes the Zn^(2+)ion flux and the electric field on the surface of the Zn foil,leading to the uniform deposition of Zn.As a result,a O-CNT@Zn symmetric cell has a much better cycling stability with a life of more than 3000 h at 1 mA cm^(−2) with a capacity of 1 mAh cm^(−2),and values of more than 2000 h and 1 mAh cm^(−2) at 5 mA cm^(−2).In addition,a O-CNT@Zn||Mn^(2+)inserted hydrated vanadium pentoxide(MnVOH)full cell has a better rate per-formance than a Zn||MnVOH cell,achieving a high discharge capacity of 194 mAh g^(−1) at a high current density of 8 A g^(−1).In a long-term cycling test,the O-CNT@Zn||MnVOH full cell has a capacity retention of 58.8%after 2000 cycles at a current density of 5 A·g^(−1).
文摘To enhance the hydrophilicity and antistatic properties of the polyethylene terephthalate(PET)fabric,the lawsone dye was employed in dyeing the PET fabric.It was dissolved in ethanol/deionized water mixture and deionized water separately,forming different lawsone dye solutions(LDSs).The study investigated how the compounds in the LDS improve the surface properties and color durability of the PET fabric,resulting in increased dye uptake.An infrared dyeing machine was utilized to expedite the reactions between the lawsone dye and the PET fabric.Additionally,the chemical composition of the dyed PET fabric was verified using techniques such as Fourier transform infrared(FTIR)spectroscopy,X-ray photoelectron spectroscopy(XPS),X-ray diffraction(XRD)and ultraviolet-visible(UV-Vis)spectrophotometry.The K/S value was measured to assess color durability.After dyeing,the PET fabric exhibited high hydrophilicity which improved the hygroscopicity of the PET fabric and thus the conductivity of the PET fabric surface increased,thereby providing an antistatic effect.
基金financially supported by the Provincial Project of Science and Technology(No.2023112258)Tianshan Talent Training Program(No.2024TSYCCX0112)+1 种基金Talent Introduction and Start Foundation for Young Scientists of Shihezi University(No.2022ZK004)Program for Young Innovative Talents of Shihezi University(No.CXFZ202302)。
文摘The use of biomass feedstocks for the manufacture of high-performance polymers can help expand their range of applications and reduce their dependence on finite fossil resources.However,improving the heat resistance and hydrophilicity of bio-based polyesters remains a significant challenge.Herein,we introduce N,N'-trans-1,4-cyclohexane-bis(pyrrolidone-4-methylcarboxylate)(CBPC),a novel bio-based tricyclic dibasic ester synthesized from renewable dimethyl itaconic acid and trans-1,4-cyclohexane diamine via an aza-Michael addition reaction.As a unique comonomer,CBPC features a rigid tricyclic backbone that significantly enhances chain packing and thermal stability,whereas its pyrrolidone side groups impart tunable polarity and improved hydrophilicity.Using CBPC,diphenyl carbonate,and 1,4-butylene glycol,a series of PBCC copolymers with 10 mol%-30 mol%CBPC was synthesized via ester-exchange and melt polycondensation methods.Incorporation of CBPC raised the melting temperature(Tm)from 56.8℃to 225.8℃and the initial decomposition temperature(Td5%)from 258.0℃to 306.7℃,positioning PBCC among the most heat-resistant bio-based polyesters reported.Additionally,the pyrrolidone units enabled transformation from hydrophobic to hydrophilic.This study demonstrates that CBPC is an effective and innovative building block for the design of bio-based polymers with enhanced thermal and surface properties,offering a promising strategy for the development of high-performance sustainable materials.
基金financially supported by the National Key R&D Program of China(No.2022YFB3704701)the National Key R&D Program of China(No.2022YFC2603502)+1 种基金Natural Science Foundation of Shandong Province(No.ZR2022QE271)the financial support from the Taishan Scholars Program(No.tsqn202211165)。
文摘The synthesis of functionalized rubber copolymers is a topic of great research interest.In this study,we present a novel approach for the direct construction ofα-functionalized 3,4-polyisoprene through polymerization of polar monomers and isoprene monomer.Theα-functionalized 3,4-polyisoprene was successfully synthesized via in situ sequential polymerization using the iron-based catalytic system(Fe(acac)_(3)/IITP/AliBu_(3)),exhibiting high activity and resistance to polar monomers without requiring protection of polar groups.The structure ofα-functionalized 3,4-polyisoprene was confirmed by proton nuclear magnetic resonance spectroscopy(^(1)H-NMR)and two-dimensional diffusion-ordered spectroscopy(2D DOSY)spectra analysis.The introduction of polar groups,particularly hydroxyl groups,enhanced the hydrophilicity of the copolymer.This was evidenced by a decrease in the water contact angle from 106.9°to 96.4°with increasing hydroxyl content in the copolymer.
基金financially supported by the UK Research Council EPRSC EP/W03395X/1the Program grant SynHiSel EP/V047078/1the Hydrogen and Fuel Cells Hub(H_(2)FC SUPERGEN)EP/P024807/1。
文摘Hydrophilicity is critical in Nafion membranes during fuel cell operation as insufficient membrane hydration leads to brittle behavior and a drop in proton conductivity.The incorporation of APTS(3-(aminopro pyl)triethoxysilane)into exfoliated graphene oxide(EGO)by covalent functionalization to be used as filler into Nafion membranes allows higher hydrophilicity for these membranes.This is associated with promoting hydroxyl,carbonyl,siloxane,silane,and amine groups within the EGO-APTS matrix.The incorporation of these materials as Fuel Cell MEAs leads to a significant reduction of the ohmic resistance measured at high frequency resistance(HFR)in electrochemical impedance spectroscopy(EIS)experiments and achieves maximum power densities of 1.33 W cm^(-2)at 60℃ at 100%RH(APTS-EGO,0.2 wt%)and1.33 W cm^(-2)at 60℃ at 70%RH(APTS-EGO,0.3 wt%),which represents an improvement of 190%compared to the commercial Nafion 212 when utilizing low humidification conditions(70%).Moreover,the as-synthesized membrane utilizes lower Nafion ionomer mass,which,in conjunction with the excellent cell performance,has the potential to decrease the cost of the membrane from 87 to 80￡/W as well as a reduction of fluorinated compounds within the membrane.
基金supported by the National Key R&D Program of China(No.2021YFC2103600)the National Natural Science Foundation of China(Nos.21878156,21978131,22275085,and 22278224)+2 种基金the Natural Science Foundation of Jiangsu Province(Nos.BK20200089 and BK20200691)the Project of Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)the State Key Laboratory of Materials-Oriented Chemical Engineering(No.KL21-08).
文摘Constructing multi-dimensional hydrogen bond(H-bond)regulated single-molecule systems with multiemission remains a challenge.Herein,we report the design of a new excited-state intramolecular proton transfer(ESIPT)featured chromophore(HBT-DPI)that shows flexible emission tunability via the multidimensional regulation of intra-and intermolecular H-bonds.The feature of switchable intramolecular Hbonds is induced via incorporating several hydrogen bond acceptors and donors into one single HBT-DPI molecule,allowing the“turn on/off”of ESIPT process by forming isomers with distinct intramolecular Hbonds configurations.In response to different external H-bonding environments,the obtained four types of crystal/cocrystals vary in the contents of isomers and the molecular packing modes,which are mainly guided by the intermolecular H-bonds,exhibiting non-emissive features or emissions ranging from green to orange.Utilizing the feature of intermolecular H-bond guided molecular packing,we demonstrate the utility of this fluorescent material for visualizing hydrophobic/hydrophilic areas on large-scale heterogeneous surfaces of modified poly(1,1-difluoroethylene)(PVDF)membranes and quantitatively estimating the surface hydrophobicity,providing a new approach for hydrophobicity/hydrophilicity monitoring and measurement.Overall,this study represents a new design strategy for constructing multi-dimensional hydrogen bond regulated ESIPT-based fluorescent materials that enable multiple emissions and unique applications.
基金supported by the National Natural Science Foundation of China(No.42402319,51704266)the Anhui Provincial Natural Science Foundation(No.2308085QE151)+3 种基金the Natural Science Research Project of Anhui Educational Committee(No.2023AH051222)Young Talent Nurturing Program of Anhui Association For Science and Technology(No.RCTJ202403)the Open Foundation of the Innovation Base of Fine Mine Prospecting and Intelligent Monitoring Technology(No.2023-MPIM-01)partly supported by the Open Fund of Engineering Research Center of Rock-Soil Drilling&Excavation and Protection(No.202407).
文摘The stability of oil-dominated emulsions,including oil-based drilling fluids and crude oils,is crucial for mitigating gas hydrate risks in the petroleum and natural gas industries.Nanoparticles can stabilize oilwater systems(Pickering emulsions)by residing at the oil-water interface.However,their effects on the kinetics of hydrate formation in these systems remain unclear.To address this,we experimentally investigated how hydrophilic and hydrophobic nano-CaCO_(3) influence CH4 hydrate formation within dynamic oil-water systems.A series of hydrate formation experiments were conducted with varying water cuts and different concentrations of nano-CaCO_(3) at a particle size of 20 nm,under 3℃ and 6 MPa.The induction time,hydrate formation volume,and hydrate growth rate were measured and calculated.The results indicate that hydrophilic nano-CaCO_(3) generally inhibits hydrate formation,particularly at high water cuts,while hydrophobic nano-CaCO_(3) can significantly inhibit or even prevent hydrate formation at low water cuts.Water cut strongly influences the kinetics of hydrate formation,and nanoparticle concentration also impacts the results,likely due to changes in oil-water interface stability caused by nanoparticle distribution.This study will offer valuable insights for designing deepwater oilbased drilling fluids using nanoparticles and ensuring safe multiphase flow in deepwater oil and gas operations.
基金Projects(51162022,21201098)supported by the National Natural Science Foundation of ChinaProject(GJJ14126)supported by Jiangxi Provincial Education Department,ChinaProject(2012019)supported by the Test Foundation of Nanchang University,China
文摘The Nd-doped TiO2 thin films with higher hydrophilic and photocatalytic activities were prepared on glass slides by an acid-catalyzed sol？gel method. The effects of Nd doping on crystalline phase, surface composition and optical property were investigated by means of techniques such as X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Fourier transform infrared spectroscopy （FT-IR）, optical contact angle tester and UV-Vis spectroscopy. The results show that Nd doping obviously influences the hydrophilic and photocatalytic activities of TiO2thin films. Nd doping could cause the TiO2 lattice distortion, inhibit phase transition from anatase to rutile, cause red shift of the absorption spectrum edge, produce hydroxyl radicals （·OH）, and accelerate surface hydroxylation, which result in a significant improvement in the hydrophilicity and photoreactivity of Nd-doped TiO2 thin films. When the content of Nd is 0.1% （mass fraction）, TiO2 thin films achieve the smallest grain size （about 15 nm）, and the hydrophilic and photocatalytic activities of TiO2 thin film reach the maximum, the contact angle is only 8.1°, and 92% of methylene blue is finally degraded. Moreover, the modification mechanism of Nd doping was also discussed.
基金Project(xjj2011096)supported by the Fundamental Research Fund for the Central Universities,ChinaProject(201107)supported by the Open Project Program of State Key Laboratory of Metastable Materials Science and Technology,ChinaProject(50901058)supported by the National Natural Science Foundation of China
文摘Titania films with nano-sized pores were prepared on the NaOH？HCl pretreated NiTi alloy substrate by sol？gel method.A crack-free film is obtained for the sample with a dense inner layer and a porous outside layer（sample TC1＋1）.The X-ray diffraction shows that the titania films are composed of anatase,and a little Ni4Ti3 phase in the heat treated substrate is also detected.The X-ray photoelectron spectroscopy results indicate that the titania film completely covered the NiTi substrate for sample TC1＋1.The sample TC1＋1 is hydrophilic with a contact angle about 20°,and UV illumination treatment for 15 min further decreases the contact angle to（9.2±3.2）°.The potentiodynamic polarization test in 0.9% NaCl solution reveals a better corrosion resistance of sample TC1＋1 than the polished NiTi sample.
基金Project(xjj2011096)supported by the Fundamental Research Fund for the Central Universities,ChinaProjects(50901058,51374174)supported by the National Natural Science Foundation of China
文摘Ta-containing TiO2 films with Ta contents of 5%, 20%, 33% （mole fraction） were sol-gel coated on the surface roughened Ti6AI4V alloy by dip coating method for biomedical applications. The Ta-TiO2 films on 1.5 mol/L NaOH-HCI pretreated substrate are adherent, but there are cracks for the sample with 33% Ta. X-ray photoelectron spectroscopy results show that Ti and Ta exist as TiP2 and Ta205 in the film, and A1 element is not detectable. X-ray diffraction and Raman scattering analyses reveal that the addition of Ta decreases crystallization of the films. Potentiodynamic polarization test in a Ca-free Hank＇s balanced solution demonstrates that the coating samples markedly improve the corrosion resistance compared with the polished sample. The addition of Ta impedes UV light-induced hydrophilic conversion of the coating samples. The sample with 20% Ta has enough film integrity and hydrophilic conversion rate, and is expected to possess good biological properties.
文摘The electrochemical deposition technique was applied to achieve porous silicon （PS） surface passivated with Ag deposition for improving the properties of PS photoluminescence. The relation of Ag depositing forms to current density and the effect of PS hydrophilic surface on deposition uniformity were investigated. The experimental results indicated that there were two critical current densities （maximum and minimum） in which Ag was absent and electroplated on PS surface correspondingly, and the range of current density for deposition of Ag on porous silicon was from 50 μA/cm^2 to 400 μA/cm^2. The process of changing PS surface from hydrophobic into hydrophilic had positive effect on Ag deposition uniformity. Under the same experimental conditions, PS hydrophobic surface presented uneven Ag deposition.However, hydrophilic surface treated with SC-1 solution was even. Finally, the effect of PS surface passivation with Ag even deposition on photoluminescence intensity and stabilization of PS was studied. It was discovered that Ag passivation inhibited the degradation of PL intensity effectively. In addition, excessive Ag deposition had a quenching effect on room-temperature visible photoluminescence of PS.
文摘A range of poly（ε-caprolactone）/poly（N-vinyl-2-pyrrolidone） amphiphilic block copolymers with well-defined hydrophilic chain length were synthesized by the living/controlled reversible addition fragmentation chain transfer polymerization method. The composition and struc- ture of the targeted resultants were characterized with 1H NMR, 13C NMR, FT-IR spec- troscopy and gel permeation chromatography. The various block copolymers were success- fully employed to fabricate the spherical micelle with core-shell morphological structure. The poly（N-vinyl-2-pyrrolidone） block-dependent characteristics of the copolymeric micelles were investigated by fluorescence spectroscopy, dynamic light scattering, and transmission electron microscopy. The solubilization of the hydrophobic ibuprofen as a model drug in the micelle solution was also explored. It was found that the drug loading contents are related to the micellar morphology structure determined by hydrophilic chain length in the copolymer.
基金The National Natural Science Foundation of China(No.50676034)the National High Technology Research and Development Program of China(863 Program)(No.2008AA05Z206)
文摘Porous polyvinylidene fluoride（PVDF）membranes blended with LiCl are prepared through the phase inversion method to obtain a good support layer for air dehumidification.The hydrophilicity of the resulting membrane is evaluated by water contact angle measurements and vapor adsorption tests.The moisture permeation performance of the membrane is measured by permeation tests in terms of total mass transfer coefficients and moisture permeability rates.It is found that water contact angles and water vapor adsorption capacities increase with the increasing LiCl content in the casting solution.As the LiCl content increases,the total mass transfer coefficient increases slightly at a low LiCl content（below 2.5%）and then improves greatly at a high LiCl content（above 2.5%）,whereas the moisture permeation rate increases.The results demonstrate that LiCl can remarkably improve the hydrophilicity of PVDF membranes,and then greatly enhance moisture permeation performance.
文摘Polyetheretherketone (PEEK) is known as one of the “super-engineering plastics” and is used as an intervertebral disk spacer in the body. PEEK has a hydrophobic surface (water contact angle (WCA) > 80°) and high chemical resistance, and it is thus difficult to perform any surface treatment, such as hydrophilization. In this study, we aimed to form a hydrophilic surface on PEEK without coating layers by using hydroprocessing (aqueous solution processing), and we examined the osteoconductivity and anti-inflammatory properties of surface-treated PEEK in vivo compared with Ti implants. The WCA value of PEEK reached ~20° using a combination of immersion in a solution of >16.2 M H2SO4 and ultraviolet irradiation (172 nm). In in vivo testing, the hydrophilization of PEEK by surface modification without a coating layer improved the osteoconductivity and anti-inflammatory properties. The relationship between the bone-implant contact ratio and the WCA values of the surface-modified PEEK agreed well with that of the surface-treated Ti.
文摘Liposomes were prepared by adding hydrophilic agents PEG PE, rigidity agent SM in the bilayer membrane for mimetic red cell membrane. In PBS or serum, release of calcein content from liposomes dramatically decreased, which demonstrated increasing membrane stability by adding PEG PE or SM. The ratio b/R of the remains of liposomes in blood to that in RES was used as a parameter of biodistribution in vivo. At 2 h after iv injection, b/R of modified liposomes was enhanced 6.5～13.1 fold. Their clearance half life from blood circulation was delayed 1.6～5.8 fold. The modification of liposome membrane by PEG PE or SM is the favorable condition for drug liposomes to target the non RES.
基金supported by National Youth Top-notch Talent Support Programthe National Natural Science Foundationof China(41672367,51704266)+2 种基金China Geological Survey Project(DD20160216)Qingdao National Laboratory for Marine Science and Technology Open Fund(QNLM2016ORP0203)Experimental Apparatus Improvement Program of CUG(SJ-201613)
文摘Invasion of drilling fluid into natural gas hydrate deposits during drilling might damage the reservoir,induce hydrate dissociation and then cause wellbore instability and distortion of the data from well logging. Adding nanoparticles into drilling fluid is an effective method in reducing the invasion of drilling fluid and enhancing borehole stability. However, the addition of nanoparticles might also introduce hydrate formation risk in borehole because they can act as the "seeds" for hydrate nucleation. This paper presents an experimental study of the effect of hydrophilic silica nanoparticle on gas hydrate formation in a dynamic methane/liquid-water system. In the experiment, the ultrapure water with and without1.0 wt%–6.0 wt% concentrations of silica nanoparticles, grain sizes of 20 and 50 nm, were pressurized by methane gas under varied conditions of temperature and pressure. The induction time, the gas consumption, and the average rate of gas consumption in the system were measured and compared to those in ultrapure water. The results show that a concentration of 4.0 wt% hydrophilic SiO_2 particles with a grain size of 50 nm has a relatively strong inhibition effect on hydrate formation when the initial experimental condition is 5.0 °C and 5.0 MPa. Compared to ultrapure water, the hydrophilic nano-SiO_2 fluid increases the induction time for hydrate formation by 194% and decreases the amount and average rate of hydrate formation by 10% and 17%, respectively. This inhibition effect may be attributed to the hydrophilicity,amount and aggregation of silica nanoparticle according to the results of water activity and zeta potential measurements. Our work also elucidates hydrophilic, instead of hydrophobic, nanoparticles can be added to the drilling fluid to maintain wellbore stability and to protect the hydrate reservoir from drilling mud damage, because they exhibit certain degree of hydrate inhibition which can reduce the risk of hydrate reformation and aggregation during gas hydrate or deep water drilling if their concentration can be controlled properly.
基金Supported by the Special Fund for International Cooperation Projects of China (2005DFA50160)
文摘Polyethersulfone(PES) is widely used as biomaterials due to its thermal stability,mechanical strength,and chemical inertness.Nevertheless,their blood compatibility is still not adequate for hemodialysis and blood purification.In this study,the sulfonated polyethersulfone(SPES) was synthesized through an electrophilic substitution reaction,and PES/SPES blending membranes were prepared.The characterization of the SPES was studied by FTIR.The water adsorption and water contact angle experiments show that the hydrophilicity of PES/SPES blend membrane was improved as for the sulfonate group existing in the SPES.Moreover,PES/SPES blend membrane could effectively reduce bovine serum albumin adsorption and prolong the blood coagulation time compared with the PES membrane,thereby improving blood compatibility.
