The rising prevalence of drug-resistant Gram-positive pathogens,particularly methicillin-resistant Staphy-lococcus aureus(MRSA)and vancomycin-resistant Enterococci(VRE),poses a substantial clinical challenge.Biofilm-a...The rising prevalence of drug-resistant Gram-positive pathogens,particularly methicillin-resistant Staphy-lococcus aureus(MRSA)and vancomycin-resistant Enterococci(VRE),poses a substantial clinical challenge.Biofilm-associated infections exacerbate this problem due to their inherent antibiotic resistance and complex structure.Current antibiotic treatments struggle to penetrate biofilms and eradicate persister cells,leading to prolonged antibiotic use and increased resistance.Host defense peptides(HDPs)have shown promise,but their clinical application is limited by factors such as enzymatic degradation and difficulty in largescale preparation.Synthetic HDP mimics,such as poly(2-oxazoline),have emerged as effective alter-natives.Herein,we found that the poly(2-oxazoline),Gly-POX_(20),demonstrated rapid and potent activity against clinically isolated multidrug-resistant Gram-positive strains.Gly-POX_(20) showed greater stability under physiological conditions compared to natural peptides,including resistance to protease degradation.Importantly,Gly-POX_(20) inhibited biofilm formation and eradicated mature biofilm and demonstrated superior in vivo therapeutic efficacy to vancomycin in a MRSA biofilm-associated mouse keratitis model,suggesting its potential as a novel antimicrobial agent against drug-resistant Gram-positive bacteria,especially biofilm-associated infections.展开更多
Consisting of natural histidine residues,polyhistidine(PHis)simulates functional proteins.Traditional approaches towards PHis require the protection of imidazole groups before monomer synthesis and polymerization to p...Consisting of natural histidine residues,polyhistidine(PHis)simulates functional proteins.Traditional approaches towards PHis require the protection of imidazole groups before monomer synthesis and polymerization to prevent degradation and side reactions.In the contribution,histidine N-thiocarboxyanhydride(His-NTA)is directly synthesized in aqueous solution without protection.With the self-catalysis of the imidazole side group,the ring-closing reaction to form His-NTA does not require any activating reagent(e.g.,phosphorus tribromide),which is elucidated by density functional theory(DFT)calculations.His-NTA directly polymerizes into PHis bearing unprotected imidazole groups with designable molecular weights(4.2-7.7 kg/mol)and low dispersities(1.10-1.19).Kinetic experiments and Monte Carlo simulations reveal the elementary reactions and the relationship between the conversion of His-NTA and time during polymerization.Block copolymerization of His-NTA with sarcosine N-thiocarboxyanhydride(Sar-NTA)demonstrate versatile construction of functional polypept(o)ides.The triblock copoly(amino acid)PHis-b-PSar-b-PHis is capable to reversibly coordinate with transition metal ions(Fe^(2+),Co^(2+),Ni^(2+),Cu^(2+)and Zn^(2+))to form pH-sensitive hydrogels.展开更多
The increasing deployment of electronics in everyday life has generated great concerns regarding the effective disposal of waste from these components.Here,we focused on a facile sustainable and economical strategy to...The increasing deployment of electronics in everyday life has generated great concerns regarding the effective disposal of waste from these components.Here,we focused on a facile sustainable and economical strategy to provide ideas for this issue.This strategy relied on using appropriate mechanical treatment and sodium lignosulfonate coating to improve the dispersion and interfacial compatibility of bamboo fibers in poly(lactic acid).By optimising the particle size and concentration of sodium lignosulphonate,high value-added and green composites were prepared using sectional pressurization with a venting procedure.The treated composite displayed an ultra-smooth surface(roughness of 0.592 nm),impressive transient properties(disintegration and degradation behaviour after 30 d),and outstanding ultraviolet(UV)shielding properties(100%).These properties hold the promise of being an excellent substrate for electronic devices,especially for high-precision processing,transient electronics,and UV damage prevention.The satisfactory interfacial compatibility of the composites was confirmed by detailed characterisation regarding the related physicochemical properties.This investigation offers a sustainable approach for producing high value-added green composites from biomass and biomass-derived materials.展开更多
Polyfluoroarenes represent an essential group of compounds in the fields of medical and material chemistry.It is still a challenge to synthesize alkylated polyfluoroarenes.Herein,a Ni-catalyzed reductive alkylation of...Polyfluoroarenes represent an essential group of compounds in the fields of medical and material chemistry.It is still a challenge to synthesize alkylated polyfluoroarenes.Herein,a Ni-catalyzed reductive alkylation of polyfluoroarenes with alkyl halides under mild conditions is reported.Polyfluoroarenes(3~6 F)can reacted smoothly with a diverse range of alkyl halides,such as primary,secondary,and tertiary alkyl iodides.The efficient formation of C(sp2)—C(sp3)can be achieved through the combination of Ni catalysis and(Bpin)2/K2CO3 as terminal reductant.展开更多
Although the efficiency of poly(ethylene terephthalate)(PET)degradation has been successfully improved by depolymerase engineering,mostly by using Goodfellow-PET(gf-PET)as a substrate,efforts to degrade unpretreated P...Although the efficiency of poly(ethylene terephthalate)(PET)degradation has been successfully improved by depolymerase engineering,mostly by using Goodfellow-PET(gf-PET)as a substrate,efforts to degrade unpretreated PET materials with high crystallinity remain insufficient.Here,we endeavored to improve the degradation capability of a WCCG mutant of leaf-branch compost cutinase(LCC)on a unpretreated PET substrate(crystallinity>40%)by employing iterative saturation mutagenesis.Using this method,we developed a high-throughput screening strategy appropriate for unpretreated substrates.Through extensive screening of residues around the substrate-binding groove,two variants,WCCG-sup1 and WCCG-sup2,showed good depolymerization capabilities with both high-(42%)and low-crystallinity(9%)substrates.The WCCG-sup1 variant completely depolymerized a commercial unpretreated PET product in 36 h at 72℃.In addition to enzyme thermostability and catalytic efficiency,the adsorption of enzymes onto substrates plays an important role in PET degradation.This study provides valuable insights into the structure-function relationship of LCC.展开更多
Poly(butylene succinate-co-furandicarboxylate)(PBSF)and poly(butylene adipateco-furandicarboxylate)(PBAF)are novel furandicarboxylic acid-based biodegradable copolyesters with great potential to replace fossil-derived...Poly(butylene succinate-co-furandicarboxylate)(PBSF)and poly(butylene adipateco-furandicarboxylate)(PBAF)are novel furandicarboxylic acid-based biodegradable copolyesters with great potential to replace fossil-derived terephthalic acid-based copolyesters such as poly(butylene succinate-co-terephthalate)(PBST)and poly(butylene adipate-co-terephthalate)(PBAT).In this study,quantum chemistry techniques after molecular dynamics simulations are employed to investigate the degradationmechanism of PBSF and PBAF catalyzed by Candida antarctica lipase B(CALB).Computational analysis indicates that the catalytic reaction follows a four-step mechanism resembling the ping-pong bibi mechanism,with the initial two steps being acylation reactions and the subsequent two being hydrolysis reactions.Notably,the first step of the hydrolysis is identified as the rate-determining step.Moreover,by introducing single-point mutations to expand the substrate entrance tunnel,the catalytic distance of the first acylation step decreases.Additionally,energy barrier of the rate-determining step is decreased in the PBSF system by site-directed mutations on key residues increasing hydrophobicity of the enzyme’s active site.This study unprecedently show the substrate binding pocket and hydrophobicity of the enzyme’s active site have the potential to be engineered to enhance the degradation of copolyesters catalyzed by CALB.展开更多
Poly(ethylene 2,5-furandicarboxylate)(PEF),a bioplastic synthesized via the polymerization of 2,5-furandicarboxylic acid(FDCA)with ethylene glycol,can be served as a substitute to petroleum-based polyethylene terephth...Poly(ethylene 2,5-furandicarboxylate)(PEF),a bioplastic synthesized via the polymerization of 2,5-furandicarboxylic acid(FDCA)with ethylene glycol,can be served as a substitute to petroleum-based polyethylene terephthalate(PET)due to its enhanced material properties.However,the fabrication of PEF with stable and desirable properties is still a challenge,largely due to the impurities in FDCA.In this study,a highly efficient purification strategy for FDCA was proposed,utilizing a dioxane/H_(2)O binary solvent system for effective crystallization.Furthermore,PEFs were synthesized from FDCA with varying impurity and the effects of these impurities were systematically characterized.The results revealed that impurities in FDCA could result in PEFs with relatively poor thermal properties.This study provides crucial insights for the impact of impurities on PEF properties and FDCA purification.展开更多
Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interfac...Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.展开更多
Poly(octamethylene citrate)(POC)is a promising bioelastomer material in the biomedical field.However,its thermosetting nature poses a significant challenge to processing and molding,especially manufacturing the POC-ba...Poly(octamethylene citrate)(POC)is a promising bioelastomer material in the biomedical field.However,its thermosetting nature poses a significant challenge to processing and molding,especially manufacturing the POC-based elastomer particles as potential,degradable and toughened fillers.Firstly,a Pickering emulsion with a pre-polymer(pre-POC)solution in dimethyl carbonate as a dispersed oil phase,a Pullulan(PUL)aqueous solution as a continuous water phase,and chitin nanocrystal(ChiNC)as a particle-type emulsifier was constructed.Secondly,the POC-based core/shell structured microspheres were prepared by spray-drying of the emulsions,and characterized by a scanning electron microscope and a transmission electron microscope.Finally,the POC-based core/shell structured microspheres were used as elastomer fillers to strengthen and toughen a chitosan film,resulting in 26%increase in the tensile strength and 45%increase in the strain at break;the POC-based core/shell structured microsphere as a double-layer drug release system was built in which the hydrophilic drug of tetracycline hydrochloride(TCH)was released from the outer layer and the hydrophobic drug of curcumin was released from the inner layer,roughly following the Ritger-Peppas model.展开更多
Poly(vinyl alcohol)(PVA)is a biodegradable and environmentally friendly material known for its gas barrier characteristics and solvent resistance.However,its flammability and water sensitivity limit its application in...Poly(vinyl alcohol)(PVA)is a biodegradable and environmentally friendly material known for its gas barrier characteristics and solvent resistance.However,its flammability and water sensitivity limit its application in specialized fields.In this study,phytic acid(PA)was introduced as a halogen-free flame retardant and biochar(BC)was introduced as a reinforcement to achieve both flame resistance and mechanical robustness.We thoroughly investigated the effects of BC particle sizes(100-3000 mesh)and addition amounts(0 wt%-10 wt%),as well as PA addition amounts(0 wt%-15 wt%),on the properties of PVA composite films.Notably,the PA10/1000BC5 composite containing 10 wt%PA and 5 wt%1000 mesh BC exhibited optimal properties.The limiting oxygen index increased to 39.2%,and the UL-94 test achieved a V-0 rating.Additionally,the PA10/1000BC5 composite film demonstrated significantly enhanced water resistance,with a swelling ratio reaching 800%without dissolving,unlike that of the control PVA.The water contact angle was 70°,indicating that hydrophilic properties remained essentially unaffected.Most importantly,the tensile modulus and elongation at break were 213 MPa and 281.7%,respectively,nearly double those of the PVA/PA composite film.This study presents an efficient and straightforward method for preparing PVA composite films that are flame-retardant,tough,and waterresistant,expanding their potential applications in various fields.展开更多
Semicrystalline polymers usually undergo multilevel microstructural evolutions with annealing and stretching processes,which is es-sential to tailor the physical properties of the polymer.Here,poly(butylene carbonate)...Semicrystalline polymers usually undergo multilevel microstructural evolutions with annealing and stretching processes,which is es-sential to tailor the physical properties of the polymer.Here,poly(butylene carbonate)(PBC)sheets were prepared via isothermal annealing and unidirectional pre-stretching processes,then the changes of PBC in crystallinity,mechanical properties,thermal properties and microscopic changes before and after annealing and stretching were measured,as well as the relationship between microstructure and macroscopic proper-ties before and after stretching.The strengthening mechanism of PBC was also described.It was demonstrated that shish-kabab structure emerged under the pre-stretching process.With the increase of the tensile ratio,the crystallinity,structure and mechanical properties are in-creased differently.Among them,the crystallinity and tensile strength after annealing-stretching treatment increased to 24.45%and 104.5 MPa,respectively,which were about 1.55 times and 3.4 times of those-without any treatment.展开更多
The sulfonated poly(α-methyl styrene-b-isobutylene-b-α-methyl styrene)copolymers(S-ASIBS)with the average molar percentage of sulfonic acid(-SO_(3)H)groups(SP)ranging from 3.6 mol%to 14.3 mol%could be synthesized by...The sulfonated poly(α-methyl styrene-b-isobutylene-b-α-methyl styrene)copolymers(S-ASIBS)with the average molar percentage of sulfonic acid(-SO_(3)H)groups(SP)ranging from 3.6 mol%to 14.3 mol%could be synthesized by sulfonation of ASIBS with acetyl sulfate.The hydrophilic ionic channels were generated for proton exchange membranes(PEMs)by ion aggregation of-SO_(3)H groups and microphase separation between hydrophobic polyisobutylene and hydrophilic sulfonated poly(α-methyl styrene)segments in S-ASIBS.The proton transport ability was improved while oxidative stability was decreased by increasing SP in S-ASIBS.The appropriate SP of about 12.7 mol%in S-ASIBS provides the available PEMs with high proton transport ability,low methanol permeability and good oxidative stability.The absence of active tertiary hydrogen atoms along S-ASIBS copolymer chains avoids their attack by peroxy radicals.The residual rates of weight(RW)and proton conductivity(Rσ)of S-ASIBS-12.7 membrane after oxidation treatment for 916 h were 84.3%and 88.1%respectively,near to those of commercial Nafion 117(RW=87.9%,Rσ=90.3%).The membrane electrode assembly(MEA)could be prepared by using various S-ASIBS as PEMs for direct methanol fuel cell.The single cell with S-ASIBS-12.7 MEA behaves high performance of open circuit voltage(OCV)of 548 mV and peak power density(Pmax)of 36.1 mW·cm^(-2),which is similar to those of Nafion 117(OCV=506 mV,P_(max)=35.6 mW·cm^(-2)).To the best of our knowledge,this is the first example of advanced S-ASIBS membrane with high proton conductivity,excellent fuel barrier property and remarkable oxidative stability for promising PEMs.展开更多
Poly(L-lactic acid)(PLLA)has been widely concerned because of its excellent biodegradability and biocompatibility.However,the poor crystallization ability of PLLA during the molding process not only leads to weak mech...Poly(L-lactic acid)(PLLA)has been widely concerned because of its excellent biodegradability and biocompatibility.However,the poor crystallization ability of PLLA during the molding process not only leads to weak mechanical properties but also reduces the processing efficiency,which limits the application of PLLA greatly.Enhancing crystallization ability of PLLA via introducing inorganic nanoparticles usually sacrifices biodegradability or transparency.Here,the microfine fibers with stereocomplex(SC)crystallites were incorporated into PLLA film to tailor the crystallization ability of PLLA as well as the mechanical properties.The results confirmed that the crystallization ability of PLLA matrix under different circumstances could be greatly enhanced by a few amounts of SC crystalline fibers,and synchronously enhanced tensile strength and ductility were also achieved,especially at relatively high temperature.Due to the relatively homogeneous dispersion of SC crystalline fibers and the similar refractive index between components,the PLLA-based film also exhibited high transparency,up to 85%-90%depending on the content of SC crystalline fibers.This work provides guidance for manufacturing transparent PLLA-based packaging materials with good crystallization capability and mechanical properties.展开更多
This article provided a preparation protocol for poly(lactic acid)(PLA)/modified epoxidized soybean oil(ECP)/nano-magnesium oxide(n-MgO)ternary composites and studied their mechanical and antibacterial properties.By m...This article provided a preparation protocol for poly(lactic acid)(PLA)/modified epoxidized soybean oil(ECP)/nano-magnesium oxide(n-MgO)ternary composites and studied their mechanical and antibacterial properties.By means of an organic synthesis technique,epoxidized soybean oil(ESO)is chemically grafted to PLA to synthesize ESO chemically plastically modified PLA,abbreviated ECP.To fabricate PLA/ECP/n-MgO composite materials,ECP acts as a plasticizer and a compatibilizer simultaneously,and n-MgO acts as an enhancer.Then scanning electron microscopy,X-ray diffraction,differential scanning calorimetry,universal tester,and antibacterial research were exploited to characterize the morphology,thermal resistance,mechanical properties,and antibacterial performance of PLA/ECP/n-MgO composites.The experimental results show that ECP acts as a plasticizer by causing heterogeneous nucleation,which increases PLA's crystallinity.Evenly distributed n-MgO can greatly improve PLA's antibacterial qualities.Furthermore,ECP and n-MgO work together to improve the positive aspects of PLA/ECP/n-MgO composites,with PLA/ECP/n-MgO 100/1/0.5 composites having the best overall properties.While improving the mechanical performance and toughness of PLA,this work offers a prospective approach and foundational database for the creation of multifunctional biodegradable composites.展开更多
Oxidative stress,characterized by the excessive accumulation of reactive oxygen species(ROS),is linked to various pathological conditions,including myocardial infarction,cancer,and neurodegenerative diseases.Addressin...Oxidative stress,characterized by the excessive accumulation of reactive oxygen species(ROS),is linked to various pathological conditions,including myocardial infarction,cancer,and neurodegenerative diseases.Addressing ROS-induced cell damage has become a critical focus of biomedical research.In this study,a thermo-sensitive poly(amino acid)hydrogel,composed of poly(ethylene glycol)-block-poly(l-methionine),was prepared for cytoprotection through ROS scavenging.The sol-to-gel transition mechanism of the hydrogel was elucidated,and its potent antioxidant properties and cell protective effects were validated using hydrogen peroxide(H_(2)O_(2))-induced oxidative stress and oxygen-glucose deprivation(OGD)models.The hydrogel significantly mitigated H_(2)O_(2)-induced damage in L929 cells,doubling their survival rate.Additionally,it scavenged approximately 35.8%of the ROS during OGD,reducing mitochondrial oxidative damage and resulting in a 29.4%decrease in apoptotic cell number.These findings underscore the potential biomedical applications of thermo-sensitive poly(amino acid)hydrogels,particularly in treating oxidative stress-related cell damage.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
Considering large volume variation and dissolution issues of some promising electrode materials for chloride ion batteries(CIB),the construction of solid polymer electrolytes(SPE)for efficient chloride ion transport i...Considering large volume variation and dissolution issues of some promising electrode materials for chloride ion batteries(CIB),the construction of solid polymer electrolytes(SPE)for efficient chloride ion transport is intriguing.However,this is hindered by low ionic conductivity of chloride SPEs and poor cycling performance of CIBs.Herein,an in-situ polymerized and cross-linked poly(ethylene gly-col)diacrylate-based chloride SPE with a low plasticizer content of succinonitrile is designed,yielding a room-temperature ionic conductivity of 7.6×10^(−5) S cm^(−1),which is higher than that of previously re-ported SPEs for CIBs.Moreover,the use of the asprepared SPE achieves an integrated organic cathode with significantly enhanced rate performance and capacity retention of 96.1%after 100 cycles at room temperature,which is much higher than 49.9%(80 cycles)of the cathode in the CIB with a sandwiched structure.These improved properties are also superior to that of other reported cathodes coupled with different chloride SPEs.The chloride ion transfer mechanism of the cathode is revealed by X-ray photo-electron spectroscopy and energy dispersive spectroscopy.展开更多
Low ionic conductivity is a major obstacle for polymer solid-state electrolytes.In response to this issue,a design concept of enhanced regional electric potential difference(EREPD)is proposed to modulate the interacti...Low ionic conductivity is a major obstacle for polymer solid-state electrolytes.In response to this issue,a design concept of enhanced regional electric potential difference(EREPD)is proposed to modulate the interaction of nanofillers with other components in the composite polymer solid-state electrolytes(CPSEs).While ensuring the periodic structure of the graphdiyne(GDY)backbone,methoxysubstituted GDY(OGDY)is prepared by an asymmetric substitution strategy,which increases the electric potential differences within each repeating unit of GDY.The staggered distributed electron-rich regions and electron-deficient regions on the two-dimensional plane of OGDY increase the free Li^(+)concentration through Lewis acid-base pair interaction.The adjacent ERRs and EDRs form uniformly distributed EREPDs,creating a continuous potential gradient that synergistically facilitates the efficient migration of Li^(+).Impressively,the OGDY/poly(ethylene oxide)(PEO)exhibits a high ionic conductivity(1.1×10^(-3)S cm^(−1))and ion mobility number(0.71).In addition,the accelerated Li^(+)migration promotes the formation of uniform and dense SEI layers and inhibits the growth of lithium dendrites.As a proof of concept,Li||Li symmetric cell and Li||LiFePO_(4)full cell and pouch cell assembled with OGDY/PEO exhibit good performance,highlighting the effectiveness of our EREPD design strategy for improving CPSEs performance.展开更多
Most commercial plastics cannot easily degrade,which raises a number of sustainability issues.To address the current problem of plastic pollution,the research and development of easily degradable and recyclable polyme...Most commercial plastics cannot easily degrade,which raises a number of sustainability issues.To address the current problem of plastic pollution,the research and development of easily degradable and recyclable polymers has become an attractive subject.Herein,a new monomer of thiosalicylic methyl glycolide(TSMG)was synthesized using one-pot method and high molecular weight poly(thiosalicylic methyl glycolide)(PTSMG,M_(n) up to 300 kDa)can be obtained via the ring-opening polymerization(ROP)of TSMG.PTSMG exhibits good closed-loop recyclability and hydrolytic degradability,where PTSMG can generate pristine monomers through sublimation thermal depolymerization conditions due to the presence of thiophenol ester bond in the polymer chains,and can be degraded rapidly in aqueous solution,which provides a potential solution to the current plastic pollution problem.展开更多
基金financially supported by the National Key Research and Development Program of China(no.2022YFC2303100)National Natural Science Foundation of China(nos.T2325010,22305082,52203162,and 22075078)+1 种基金Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism(Shanghai Municipal Education Commission),the Fundamental Research Funds for the Central Universities(nos.JKVD1241029 and JKD01241701)Open Research Fund of State Key Laboratory of Polymer Physics and Chemistry(Changchun Institute of Applied Chemistry,Chinese Academy of Sciences),the Open Project of Engineering Research Center of Dairy Quality and Safety Control Technology(Ministry of Education,no.R202201).
文摘The rising prevalence of drug-resistant Gram-positive pathogens,particularly methicillin-resistant Staphy-lococcus aureus(MRSA)and vancomycin-resistant Enterococci(VRE),poses a substantial clinical challenge.Biofilm-associated infections exacerbate this problem due to their inherent antibiotic resistance and complex structure.Current antibiotic treatments struggle to penetrate biofilms and eradicate persister cells,leading to prolonged antibiotic use and increased resistance.Host defense peptides(HDPs)have shown promise,but their clinical application is limited by factors such as enzymatic degradation and difficulty in largescale preparation.Synthetic HDP mimics,such as poly(2-oxazoline),have emerged as effective alter-natives.Herein,we found that the poly(2-oxazoline),Gly-POX_(20),demonstrated rapid and potent activity against clinically isolated multidrug-resistant Gram-positive strains.Gly-POX_(20) showed greater stability under physiological conditions compared to natural peptides,including resistance to protease degradation.Importantly,Gly-POX_(20) inhibited biofilm formation and eradicated mature biofilm and demonstrated superior in vivo therapeutic efficacy to vancomycin in a MRSA biofilm-associated mouse keratitis model,suggesting its potential as a novel antimicrobial agent against drug-resistant Gram-positive bacteria,especially biofilm-associated infections.
基金financially supported by the National Natural Science Foundation of China(Nos.22271252 and 22201105)。
文摘Consisting of natural histidine residues,polyhistidine(PHis)simulates functional proteins.Traditional approaches towards PHis require the protection of imidazole groups before monomer synthesis and polymerization to prevent degradation and side reactions.In the contribution,histidine N-thiocarboxyanhydride(His-NTA)is directly synthesized in aqueous solution without protection.With the self-catalysis of the imidazole side group,the ring-closing reaction to form His-NTA does not require any activating reagent(e.g.,phosphorus tribromide),which is elucidated by density functional theory(DFT)calculations.His-NTA directly polymerizes into PHis bearing unprotected imidazole groups with designable molecular weights(4.2-7.7 kg/mol)and low dispersities(1.10-1.19).Kinetic experiments and Monte Carlo simulations reveal the elementary reactions and the relationship between the conversion of His-NTA and time during polymerization.Block copolymerization of His-NTA with sarcosine N-thiocarboxyanhydride(Sar-NTA)demonstrate versatile construction of functional polypept(o)ides.The triblock copoly(amino acid)PHis-b-PSar-b-PHis is capable to reversibly coordinate with transition metal ions(Fe^(2+),Co^(2+),Ni^(2+),Cu^(2+)and Zn^(2+))to form pH-sensitive hydrogels.
基金supported by the National Natural Science Foundation of China(Nos.31971741 and 31760195)the Yunnan Fundamental Research Projects(Nos.2018FB066 and 202001AT070141)the Yunnan Agricultural Basic Research Special Projects(No.202101BD070001-086).
文摘The increasing deployment of electronics in everyday life has generated great concerns regarding the effective disposal of waste from these components.Here,we focused on a facile sustainable and economical strategy to provide ideas for this issue.This strategy relied on using appropriate mechanical treatment and sodium lignosulfonate coating to improve the dispersion and interfacial compatibility of bamboo fibers in poly(lactic acid).By optimising the particle size and concentration of sodium lignosulphonate,high value-added and green composites were prepared using sectional pressurization with a venting procedure.The treated composite displayed an ultra-smooth surface(roughness of 0.592 nm),impressive transient properties(disintegration and degradation behaviour after 30 d),and outstanding ultraviolet(UV)shielding properties(100%).These properties hold the promise of being an excellent substrate for electronic devices,especially for high-precision processing,transient electronics,and UV damage prevention.The satisfactory interfacial compatibility of the composites was confirmed by detailed characterisation regarding the related physicochemical properties.This investigation offers a sustainable approach for producing high value-added green composites from biomass and biomass-derived materials.
文摘Polyfluoroarenes represent an essential group of compounds in the fields of medical and material chemistry.It is still a challenge to synthesize alkylated polyfluoroarenes.Herein,a Ni-catalyzed reductive alkylation of polyfluoroarenes with alkyl halides under mild conditions is reported.Polyfluoroarenes(3~6 F)can reacted smoothly with a diverse range of alkyl halides,such as primary,secondary,and tertiary alkyl iodides.The efficient formation of C(sp2)—C(sp3)can be achieved through the combination of Ni catalysis and(Bpin)2/K2CO3 as terminal reductant.
文摘Although the efficiency of poly(ethylene terephthalate)(PET)degradation has been successfully improved by depolymerase engineering,mostly by using Goodfellow-PET(gf-PET)as a substrate,efforts to degrade unpretreated PET materials with high crystallinity remain insufficient.Here,we endeavored to improve the degradation capability of a WCCG mutant of leaf-branch compost cutinase(LCC)on a unpretreated PET substrate(crystallinity>40%)by employing iterative saturation mutagenesis.Using this method,we developed a high-throughput screening strategy appropriate for unpretreated substrates.Through extensive screening of residues around the substrate-binding groove,two variants,WCCG-sup1 and WCCG-sup2,showed good depolymerization capabilities with both high-(42%)and low-crystallinity(9%)substrates.The WCCG-sup1 variant completely depolymerized a commercial unpretreated PET product in 36 h at 72℃.In addition to enzyme thermostability and catalytic efficiency,the adsorption of enzymes onto substrates plays an important role in PET degradation.This study provides valuable insights into the structure-function relationship of LCC.
基金supported by the Joint Funds of the National Natural Science Foundation of China(No.U21A20320)the National Natural Science Foundation of China(No.22106102)was also sponsored by the special fund of State Environmental Protection Key Laboratory of Environmental Health Impact Assessment of Emerging Contaminants(No.SEPKLEHIAEC-202203).
文摘Poly(butylene succinate-co-furandicarboxylate)(PBSF)and poly(butylene adipateco-furandicarboxylate)(PBAF)are novel furandicarboxylic acid-based biodegradable copolyesters with great potential to replace fossil-derived terephthalic acid-based copolyesters such as poly(butylene succinate-co-terephthalate)(PBST)and poly(butylene adipate-co-terephthalate)(PBAT).In this study,quantum chemistry techniques after molecular dynamics simulations are employed to investigate the degradationmechanism of PBSF and PBAF catalyzed by Candida antarctica lipase B(CALB).Computational analysis indicates that the catalytic reaction follows a four-step mechanism resembling the ping-pong bibi mechanism,with the initial two steps being acylation reactions and the subsequent two being hydrolysis reactions.Notably,the first step of the hydrolysis is identified as the rate-determining step.Moreover,by introducing single-point mutations to expand the substrate entrance tunnel,the catalytic distance of the first acylation step decreases.Additionally,energy barrier of the rate-determining step is decreased in the PBSF system by site-directed mutations on key residues increasing hydrophobicity of the enzyme’s active site.This study unprecedently show the substrate binding pocket and hydrophobicity of the enzyme’s active site have the potential to be engineered to enhance the degradation of copolyesters catalyzed by CALB.
基金supported by the National Natural Science Foundation of China(22378338,U22A20421)the Project for Science and Technology Plan of Fujian Province of China(2024H4007)。
文摘Poly(ethylene 2,5-furandicarboxylate)(PEF),a bioplastic synthesized via the polymerization of 2,5-furandicarboxylic acid(FDCA)with ethylene glycol,can be served as a substitute to petroleum-based polyethylene terephthalate(PET)due to its enhanced material properties.However,the fabrication of PEF with stable and desirable properties is still a challenge,largely due to the impurities in FDCA.In this study,a highly efficient purification strategy for FDCA was proposed,utilizing a dioxane/H_(2)O binary solvent system for effective crystallization.Furthermore,PEFs were synthesized from FDCA with varying impurity and the effects of these impurities were systematically characterized.The results revealed that impurities in FDCA could result in PEFs with relatively poor thermal properties.This study provides crucial insights for the impact of impurities on PEF properties and FDCA purification.
基金financially supported by the National Natural Science Foundation of China(Nos.22172028,21903015,and 22403017)Natural Science Foundation of Fujian Province of China(No.2022J05041)。
文摘Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.
文摘Poly(octamethylene citrate)(POC)is a promising bioelastomer material in the biomedical field.However,its thermosetting nature poses a significant challenge to processing and molding,especially manufacturing the POC-based elastomer particles as potential,degradable and toughened fillers.Firstly,a Pickering emulsion with a pre-polymer(pre-POC)solution in dimethyl carbonate as a dispersed oil phase,a Pullulan(PUL)aqueous solution as a continuous water phase,and chitin nanocrystal(ChiNC)as a particle-type emulsifier was constructed.Secondly,the POC-based core/shell structured microspheres were prepared by spray-drying of the emulsions,and characterized by a scanning electron microscope and a transmission electron microscope.Finally,the POC-based core/shell structured microspheres were used as elastomer fillers to strengthen and toughen a chitosan film,resulting in 26%increase in the tensile strength and 45%increase in the strain at break;the POC-based core/shell structured microsphere as a double-layer drug release system was built in which the hydrophilic drug of tetracycline hydrochloride(TCH)was released from the outer layer and the hydrophobic drug of curcumin was released from the inner layer,roughly following the Ritger-Peppas model.
基金supported by the Zhejiang Provincial"Vanguard"and"Leading Goose"R&D Program(No.2025C02203)the Zhejiang Provincial Natural Science Foundation of China(No.LTGS24C130001)the Fund for Key Scientific Research in the Public Interest of Ningbo(No.2024S009)。
文摘Poly(vinyl alcohol)(PVA)is a biodegradable and environmentally friendly material known for its gas barrier characteristics and solvent resistance.However,its flammability and water sensitivity limit its application in specialized fields.In this study,phytic acid(PA)was introduced as a halogen-free flame retardant and biochar(BC)was introduced as a reinforcement to achieve both flame resistance and mechanical robustness.We thoroughly investigated the effects of BC particle sizes(100-3000 mesh)and addition amounts(0 wt%-10 wt%),as well as PA addition amounts(0 wt%-15 wt%),on the properties of PVA composite films.Notably,the PA10/1000BC5 composite containing 10 wt%PA and 5 wt%1000 mesh BC exhibited optimal properties.The limiting oxygen index increased to 39.2%,and the UL-94 test achieved a V-0 rating.Additionally,the PA10/1000BC5 composite film demonstrated significantly enhanced water resistance,with a swelling ratio reaching 800%without dissolving,unlike that of the control PVA.The water contact angle was 70°,indicating that hydrophilic properties remained essentially unaffected.Most importantly,the tensile modulus and elongation at break were 213 MPa and 281.7%,respectively,nearly double those of the PVA/PA composite film.This study presents an efficient and straightforward method for preparing PVA composite films that are flame-retardant,tough,and waterresistant,expanding their potential applications in various fields.
基金supported by the Sichuan Provincial Regional Innovation Cooperation Project(No.2024YFHZ0159).
文摘Semicrystalline polymers usually undergo multilevel microstructural evolutions with annealing and stretching processes,which is es-sential to tailor the physical properties of the polymer.Here,poly(butylene carbonate)(PBC)sheets were prepared via isothermal annealing and unidirectional pre-stretching processes,then the changes of PBC in crystallinity,mechanical properties,thermal properties and microscopic changes before and after annealing and stretching were measured,as well as the relationship between microstructure and macroscopic proper-ties before and after stretching.The strengthening mechanism of PBC was also described.It was demonstrated that shish-kabab structure emerged under the pre-stretching process.With the increase of the tensile ratio,the crystallinity,structure and mechanical properties are in-creased differently.Among them,the crystallinity and tensile strength after annealing-stretching treatment increased to 24.45%and 104.5 MPa,respectively,which were about 1.55 times and 3.4 times of those-without any treatment.
基金financially supported by the National Natural Science Foundation of China (No. 21774006)
文摘The sulfonated poly(α-methyl styrene-b-isobutylene-b-α-methyl styrene)copolymers(S-ASIBS)with the average molar percentage of sulfonic acid(-SO_(3)H)groups(SP)ranging from 3.6 mol%to 14.3 mol%could be synthesized by sulfonation of ASIBS with acetyl sulfate.The hydrophilic ionic channels were generated for proton exchange membranes(PEMs)by ion aggregation of-SO_(3)H groups and microphase separation between hydrophobic polyisobutylene and hydrophilic sulfonated poly(α-methyl styrene)segments in S-ASIBS.The proton transport ability was improved while oxidative stability was decreased by increasing SP in S-ASIBS.The appropriate SP of about 12.7 mol%in S-ASIBS provides the available PEMs with high proton transport ability,low methanol permeability and good oxidative stability.The absence of active tertiary hydrogen atoms along S-ASIBS copolymer chains avoids their attack by peroxy radicals.The residual rates of weight(RW)and proton conductivity(Rσ)of S-ASIBS-12.7 membrane after oxidation treatment for 916 h were 84.3%and 88.1%respectively,near to those of commercial Nafion 117(RW=87.9%,Rσ=90.3%).The membrane electrode assembly(MEA)could be prepared by using various S-ASIBS as PEMs for direct methanol fuel cell.The single cell with S-ASIBS-12.7 MEA behaves high performance of open circuit voltage(OCV)of 548 mV and peak power density(Pmax)of 36.1 mW·cm^(-2),which is similar to those of Nafion 117(OCV=506 mV,P_(max)=35.6 mW·cm^(-2)).To the best of our knowledge,this is the first example of advanced S-ASIBS membrane with high proton conductivity,excellent fuel barrier property and remarkable oxidative stability for promising PEMs.
基金supported by the Sichuan Science and Technology Program(No.2023ZHCG0050)the China Postdoctoral Science Foundation(No.2023M742883)+2 种基金the Science and Technology Innovation Fund for Basic Scientific Research Operating Expenses of Central Universities(No.2682023CX002)the New Interdisciplinary Cultivation Fund of SWJTU(No.2682022KJ040)SEM characterizations were supported by the Analytical and Testing Center of Southwest Jiaotong University。
文摘Poly(L-lactic acid)(PLLA)has been widely concerned because of its excellent biodegradability and biocompatibility.However,the poor crystallization ability of PLLA during the molding process not only leads to weak mechanical properties but also reduces the processing efficiency,which limits the application of PLLA greatly.Enhancing crystallization ability of PLLA via introducing inorganic nanoparticles usually sacrifices biodegradability or transparency.Here,the microfine fibers with stereocomplex(SC)crystallites were incorporated into PLLA film to tailor the crystallization ability of PLLA as well as the mechanical properties.The results confirmed that the crystallization ability of PLLA matrix under different circumstances could be greatly enhanced by a few amounts of SC crystalline fibers,and synchronously enhanced tensile strength and ductility were also achieved,especially at relatively high temperature.Due to the relatively homogeneous dispersion of SC crystalline fibers and the similar refractive index between components,the PLLA-based film also exhibited high transparency,up to 85%-90%depending on the content of SC crystalline fibers.This work provides guidance for manufacturing transparent PLLA-based packaging materials with good crystallization capability and mechanical properties.
基金Funded by the National Natural Science Foundation of China(No.21104031)the Education Department of Hunan province in 2020(No.20C1589)。
文摘This article provided a preparation protocol for poly(lactic acid)(PLA)/modified epoxidized soybean oil(ECP)/nano-magnesium oxide(n-MgO)ternary composites and studied their mechanical and antibacterial properties.By means of an organic synthesis technique,epoxidized soybean oil(ESO)is chemically grafted to PLA to synthesize ESO chemically plastically modified PLA,abbreviated ECP.To fabricate PLA/ECP/n-MgO composite materials,ECP acts as a plasticizer and a compatibilizer simultaneously,and n-MgO acts as an enhancer.Then scanning electron microscopy,X-ray diffraction,differential scanning calorimetry,universal tester,and antibacterial research were exploited to characterize the morphology,thermal resistance,mechanical properties,and antibacterial performance of PLA/ECP/n-MgO composites.The experimental results show that ECP acts as a plasticizer by causing heterogeneous nucleation,which increases PLA's crystallinity.Evenly distributed n-MgO can greatly improve PLA's antibacterial qualities.Furthermore,ECP and n-MgO work together to improve the positive aspects of PLA/ECP/n-MgO composites,with PLA/ECP/n-MgO 100/1/0.5 composites having the best overall properties.While improving the mechanical performance and toughness of PLA,this work offers a prospective approach and foundational database for the creation of multifunctional biodegradable composites.
基金financially supported by the National Key R&D Program of China(No.2022YFB3808000)the National Natural Science Foundation of China(No.U21A2099)+2 种基金the Science and Technology Development Program of Jilin Province(No.20240101002JJ)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(No.Y2023066)the Plan for Enhancing Health Science and Technology Capacity in Jilin Province(No.2020J041).
文摘Oxidative stress,characterized by the excessive accumulation of reactive oxygen species(ROS),is linked to various pathological conditions,including myocardial infarction,cancer,and neurodegenerative diseases.Addressing ROS-induced cell damage has become a critical focus of biomedical research.In this study,a thermo-sensitive poly(amino acid)hydrogel,composed of poly(ethylene glycol)-block-poly(l-methionine),was prepared for cytoprotection through ROS scavenging.The sol-to-gel transition mechanism of the hydrogel was elucidated,and its potent antioxidant properties and cell protective effects were validated using hydrogen peroxide(H_(2)O_(2))-induced oxidative stress and oxygen-glucose deprivation(OGD)models.The hydrogel significantly mitigated H_(2)O_(2)-induced damage in L929 cells,doubling their survival rate.Additionally,it scavenged approximately 35.8%of the ROS during OGD,reducing mitochondrial oxidative damage and resulting in a 29.4%decrease in apoptotic cell number.These findings underscore the potential biomedical applications of thermo-sensitive poly(amino acid)hydrogels,particularly in treating oxidative stress-related cell damage.
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supported by the National Natural Science Foundation of China(No.52222211)“333”Project of Jiangsu Province,and the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD).
文摘Considering large volume variation and dissolution issues of some promising electrode materials for chloride ion batteries(CIB),the construction of solid polymer electrolytes(SPE)for efficient chloride ion transport is intriguing.However,this is hindered by low ionic conductivity of chloride SPEs and poor cycling performance of CIBs.Herein,an in-situ polymerized and cross-linked poly(ethylene gly-col)diacrylate-based chloride SPE with a low plasticizer content of succinonitrile is designed,yielding a room-temperature ionic conductivity of 7.6×10^(−5) S cm^(−1),which is higher than that of previously re-ported SPEs for CIBs.Moreover,the use of the asprepared SPE achieves an integrated organic cathode with significantly enhanced rate performance and capacity retention of 96.1%after 100 cycles at room temperature,which is much higher than 49.9%(80 cycles)of the cathode in the CIB with a sandwiched structure.These improved properties are also superior to that of other reported cathodes coupled with different chloride SPEs.The chloride ion transfer mechanism of the cathode is revealed by X-ray photo-electron spectroscopy and energy dispersive spectroscopy.
基金supported by the National Key Research and Development Project of China(2022YFA1204500,2022YFA1204503,2018YFA0703501)the National Natural Science Foundation of China(22275115,21875274,11704024)+4 种基金the Natural Science Foundation of Shandong Province(ZR2024ZD02)Natural Science Foundation of Hebei Province(B2020201006)Hebei Province Innovation Capability Enhancement Plan Project(22567620H)Young Scholarship Funding of Shandong University.Post-graduate Innovation Fund Project of Open Laboratory Project Fund of Hebei University(HBU2025SS010)Basic Research Project of Shandong University-Xin’an Group Silicon-Based High-End New Materials Institute.
文摘Low ionic conductivity is a major obstacle for polymer solid-state electrolytes.In response to this issue,a design concept of enhanced regional electric potential difference(EREPD)is proposed to modulate the interaction of nanofillers with other components in the composite polymer solid-state electrolytes(CPSEs).While ensuring the periodic structure of the graphdiyne(GDY)backbone,methoxysubstituted GDY(OGDY)is prepared by an asymmetric substitution strategy,which increases the electric potential differences within each repeating unit of GDY.The staggered distributed electron-rich regions and electron-deficient regions on the two-dimensional plane of OGDY increase the free Li^(+)concentration through Lewis acid-base pair interaction.The adjacent ERRs and EDRs form uniformly distributed EREPDs,creating a continuous potential gradient that synergistically facilitates the efficient migration of Li^(+).Impressively,the OGDY/poly(ethylene oxide)(PEO)exhibits a high ionic conductivity(1.1×10^(-3)S cm^(−1))and ion mobility number(0.71).In addition,the accelerated Li^(+)migration promotes the formation of uniform and dense SEI layers and inhibits the growth of lithium dendrites.As a proof of concept,Li||Li symmetric cell and Li||LiFePO_(4)full cell and pouch cell assembled with OGDY/PEO exhibit good performance,highlighting the effectiveness of our EREPD design strategy for improving CPSEs performance.
基金supported by the National Key R&D Program of China(No.2023YFA1506804)the National Natural Science Foundation of China(Nos.22471110,22171111,22131007 and 22071093)+1 种基金the Science Foundation of Gansu Province of China(No.22JR5RA406)the Fundamental Research Funds for the Central Universities(No.lzujbky-2023-15)。
文摘Most commercial plastics cannot easily degrade,which raises a number of sustainability issues.To address the current problem of plastic pollution,the research and development of easily degradable and recyclable polymers has become an attractive subject.Herein,a new monomer of thiosalicylic methyl glycolide(TSMG)was synthesized using one-pot method and high molecular weight poly(thiosalicylic methyl glycolide)(PTSMG,M_(n) up to 300 kDa)can be obtained via the ring-opening polymerization(ROP)of TSMG.PTSMG exhibits good closed-loop recyclability and hydrolytic degradability,where PTSMG can generate pristine monomers through sublimation thermal depolymerization conditions due to the presence of thiophenol ester bond in the polymer chains,and can be degraded rapidly in aqueous solution,which provides a potential solution to the current plastic pollution problem.
