The thioacetamide derivative(TD)-composite preservation system(TDCPS)exhibits superior preservation effects on natural rubber latex(NRL)and significantly enhances its vulcanization efficiency and mechanical properties...The thioacetamide derivative(TD)-composite preservation system(TDCPS)exhibits superior preservation effects on natural rubber latex(NRL)and significantly enhances its vulcanization efficiency and mechanical properties.This study primarily investigated the principal chemical groups and mechanism of action of TDCPS in promoting NRL vulcanization through a comparative analysis.The results indicated that the key functional groups(thioamide and pyridine)in TDCPS synergistically accelerated crosslinking,reducing the vulcanization time by 41.18%compared to the high-ammonia(HA)preservation system.At an optimal TDCPS dosage of 5 mmol·L^(−1),vulcanized films achieved a tensile strength of 34.18 MPa,with a sulfur content of 1.5 phr further improving the strength by 42.26%.TD outperformed the conventional accelerators 2-imidazolidinethione(ETU)and 3-hydroxypyridine(3-Hp)in promoting the crosslinking density and mechanical performance while eliminating ammonia-related environmental risks.This eco-friendly system demonstrates the industrial potential for sustainable rubber production.展开更多
This study delves into the pivotal role of sulfur vulcanization in defining the mechanical characteristics of natural rubber(NR)latex-dipped products.Utilizing sulfur vulcanization,known for its operational simplicity...This study delves into the pivotal role of sulfur vulcanization in defining the mechanical characteristics of natural rubber(NR)latex-dipped products.Utilizing sulfur vulcanization,known for its operational simplicity and cost-effectiveness,we examine its ability to enhance product elasticity and mechanical strength through various sulfidic bond formations such as mono-,di-,and polysulfidic bonds.Different vulcanization systems and sulfur contents were evaluated for their influence on the mechanical attributes of latex films,employing three types of NR latex,namely concentrated NR(CNR),deproteinized NR(DPNR),and small rubber particle NR(SRP),each representing distinct non-rubber components(NRCs).The study utilized advanced atomic force microscopy(AFM)equipped with PeakForce Quantitative Nanomechanical Mapping(QNM)to visualize and measure Young’s modulus distribution across the film of pre-vulcanized latex.Our findings reveal that films by CNR processed using the conventional vulcanization(CV)system exhibited enhanced tensile strength and elongation at break.It even showed a lower crosslink density than those processed using the efficient vulcanization(EV)system.Interestingly,DPNR films showed a more uniform distribution of Young’s modulus,correlating well with their superior mechanical strength.In contrast,SRP films showed excessive network structure formation in the particles due to accelerated vulcanization rates,hampering subsequent post-vulcanization interparticle crosslinking in film formation and remaining more rigid.The overall results Illustrate clearly that the ultimate mechanical properties of the latex films are strongly dependent on the type of sulfidic bonds formed.This research reveals further the very intricate relationship between the vulcanization methods,sulfur content,and latex type in optimizing the mechanical performance of NR latex products.It provides valuable insights for industry practices aimed at improving the quality and performance of latex-dipped goods.展开更多
A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and...A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and Mo2S3 nanoparticles were integrated at the edges of Co3O4 nanosheets,creating a rich,heterogeneous interface that enhances the synergistic effects of each component.In an alkaline electrolyte,the synthesized CoMoNiO-S/NF-110 exhibited superior electrocatalytic performance for oxygen evolution reaction(OER),achieving current densities of 100 and 200 mA·cm^(-2) with low overpotentials of 199.4 and 224.4 mV,respectively,outperforming RuO2 and several high-performance Mo and Ni-based catalysts.This excellent performance is attributed to the rich interface formed between the components and active sites exposed by the defect structure.展开更多
Recycling of waste rubber(WR)is crucial for the sustainable development of the rubber industry.The enhancement of interfacial interactions is the main strategy for waste polymer recycling.However,there is a lack of me...Recycling of waste rubber(WR)is crucial for the sustainable development of the rubber industry.The enhancement of interfacial interactions is the main strategy for waste polymer recycling.However,there is a lack of methods for enhancing the interfacial interactions for WR recycling because WR contains abundant inert C―H bonds.Herein,we designed thioctic acid inverse vulcanization copolymers to endow recycled WR with dynamic disulfide interfacial interactions,significantly improving the mechanical properties of recycled WR.These disulfide interfacial interactions among the recycled WR tend to exchange,which dramatically increases the fractocohesive length and prevents stress concentration near the crack tips.When recycled WR is subjected to external stress,the loads are redistributed across a broad region of adjacent regions instead of being concentrated on a limited length scale,which resists crack propagation.This work effectively recycled WR,providing a strategy for solvent-free reaction-derived inverse vulcanization copolymers to improve the toughness of WR recycling.展开更多
基金the Ministry of Agriculture and Rural Affairs of Chinathe Department of Science and Technology of the Hainan Province for their support+2 种基金financially supported by the National Key R&D Program of China(No. 2022YFD2301201)Hainan Province Science and Technology Special Fund (No. ZDYF2024XDNY284)Earmarked Fund for China Agriculture Research System (No.CARS-33-JG1)
文摘The thioacetamide derivative(TD)-composite preservation system(TDCPS)exhibits superior preservation effects on natural rubber latex(NRL)and significantly enhances its vulcanization efficiency and mechanical properties.This study primarily investigated the principal chemical groups and mechanism of action of TDCPS in promoting NRL vulcanization through a comparative analysis.The results indicated that the key functional groups(thioamide and pyridine)in TDCPS synergistically accelerated crosslinking,reducing the vulcanization time by 41.18%compared to the high-ammonia(HA)preservation system.At an optimal TDCPS dosage of 5 mmol·L^(−1),vulcanized films achieved a tensile strength of 34.18 MPa,with a sulfur content of 1.5 phr further improving the strength by 42.26%.TD outperformed the conventional accelerators 2-imidazolidinethione(ETU)and 3-hydroxypyridine(3-Hp)in promoting the crosslinking density and mechanical performance while eliminating ammonia-related environmental risks.This eco-friendly system demonstrates the industrial potential for sustainable rubber production.
基金supported by Mahidol University(Fundamental Fund:fiscal year 2024 by the National Science Research and Innovation Fund(NSRF),FF-078/2567)Academy of Tropical Agricultural Sciences for Science and Technology Innovation Team of National Tropical Agricultural Science Center(No.CATASCXTD202401)the National Research Council of Thailand(NRCT)via the Royal Golden Jubilee Ph.D.Program(No.PHD/0150/2560)。
文摘This study delves into the pivotal role of sulfur vulcanization in defining the mechanical characteristics of natural rubber(NR)latex-dipped products.Utilizing sulfur vulcanization,known for its operational simplicity and cost-effectiveness,we examine its ability to enhance product elasticity and mechanical strength through various sulfidic bond formations such as mono-,di-,and polysulfidic bonds.Different vulcanization systems and sulfur contents were evaluated for their influence on the mechanical attributes of latex films,employing three types of NR latex,namely concentrated NR(CNR),deproteinized NR(DPNR),and small rubber particle NR(SRP),each representing distinct non-rubber components(NRCs).The study utilized advanced atomic force microscopy(AFM)equipped with PeakForce Quantitative Nanomechanical Mapping(QNM)to visualize and measure Young’s modulus distribution across the film of pre-vulcanized latex.Our findings reveal that films by CNR processed using the conventional vulcanization(CV)system exhibited enhanced tensile strength and elongation at break.It even showed a lower crosslink density than those processed using the efficient vulcanization(EV)system.Interestingly,DPNR films showed a more uniform distribution of Young’s modulus,correlating well with their superior mechanical strength.In contrast,SRP films showed excessive network structure formation in the particles due to accelerated vulcanization rates,hampering subsequent post-vulcanization interparticle crosslinking in film formation and remaining more rigid.The overall results Illustrate clearly that the ultimate mechanical properties of the latex films are strongly dependent on the type of sulfidic bonds formed.This research reveals further the very intricate relationship between the vulcanization methods,sulfur content,and latex type in optimizing the mechanical performance of NR latex products.It provides valuable insights for industry practices aimed at improving the quality and performance of latex-dipped goods.
文摘A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and Mo2S3 nanoparticles were integrated at the edges of Co3O4 nanosheets,creating a rich,heterogeneous interface that enhances the synergistic effects of each component.In an alkaline electrolyte,the synthesized CoMoNiO-S/NF-110 exhibited superior electrocatalytic performance for oxygen evolution reaction(OER),achieving current densities of 100 and 200 mA·cm^(-2) with low overpotentials of 199.4 and 224.4 mV,respectively,outperforming RuO2 and several high-performance Mo and Ni-based catalysts.This excellent performance is attributed to the rich interface formed between the components and active sites exposed by the defect structure.
基金financially supported by the National Natural Science Foundation of China(No.52363007)。
文摘Recycling of waste rubber(WR)is crucial for the sustainable development of the rubber industry.The enhancement of interfacial interactions is the main strategy for waste polymer recycling.However,there is a lack of methods for enhancing the interfacial interactions for WR recycling because WR contains abundant inert C―H bonds.Herein,we designed thioctic acid inverse vulcanization copolymers to endow recycled WR with dynamic disulfide interfacial interactions,significantly improving the mechanical properties of recycled WR.These disulfide interfacial interactions among the recycled WR tend to exchange,which dramatically increases the fractocohesive length and prevents stress concentration near the crack tips.When recycled WR is subjected to external stress,the loads are redistributed across a broad region of adjacent regions instead of being concentrated on a limited length scale,which resists crack propagation.This work effectively recycled WR,providing a strategy for solvent-free reaction-derived inverse vulcanization copolymers to improve the toughness of WR recycling.
