Improving the interfacial interaction between rubber and silica nanoparticles, and simultaneously reducing free sulfur and preventing migration and volatilization of a rubber vulcanizing agent, commercial sulfur compound aliphatic ether polysulfide (VA-7) was chemically attached to the silica surface to obtain a functionalized nanoparticle (silica-s-VA7). Functional nanoparticles can not only effectively crosslink rubber without sulfur as a novel vulcanizator, but are also evenly dispersed in the rubber matrix and improve the dispersion of the remaining pristine silica as an interfacial compatibilizer. In addition, the thicker immobilized polymer layer and prominent crosslinking density of SBR nanocomposites simultaneously demonstrate that the novel vulcanizing agent silica-s-VA7 gives rise to significant improvement on the rubber⁻filler interfacial adhesion on account of the covalent linkages of organic and inorganic interfaces between elastomer and nanofillers. We envisage that this strategy may provide a new avenue to implement high-efficiency design for a multifunctional rubber-vulcanizing agent through an organic and inorganic hybridization mechanism.
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http://dx.doi.org/10.3390/polym10101138 | DOI Listing |
Polymers (Basel)
January 2025
College of Mechanical and Electrical Engineering, Qingdao University, Qingdao 266071, China.
Currently, in the domestic practice of retreading tires using vulcanization tanks, some tanks exhibit uneven temperature distributions leading to low retreading success rates. To address that, this paper simulated the temperature and velocity fields during the heating process of vulcanization tanks for waste tire retreading. The results indicated that a higher heating power reduces the time required for the vulcanizing agent to reach the vulcanization condition, but it also increases the difference in tire temperature in the tank, with a severely uneven distribution of the temperature field.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Nordbayerisches NMR-Zentrum, Universität Bayreuth, 95447 Bayreuth, Germany.
Rubbers prepared from technical poly(butadiene) and natural poly(isoprene) are studied by field-cycling (FC) H NMR relaxometry to elucidate the changes of the relaxation spectrum. Starting with the non-cross-linked polymer successively cross-links are introduced via sulfur or peroxide vulcanization. Applying an advanced home-built relaxometer allows one to probe entanglement dynamics in addition to Rouse dynamics.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
School of Physics and Electronic Sciences, Hunan Provincial Key Laboratory of Flexible Electronic Materials Genome Engineering, Changsha University of Science and Technology, Changsha 410114, PR China. Electronic address:
Developing a catalytic nanoenzyme activated by the tumor microenvironment (TME) shows excellent potential for in situ cancer treatment. However, the rational design of a cascade procedure to achieve high therapeutic efficiency remains challenging. In this study, the colorectal TME-responsive multifunctional cascade nanoenzyme CuO@MnO@glucose oxidase (GOx)@hyaluronic acid (HA) was developed to target in situ cancer starvation/chemodynamic therapy (CDT)/photothermal therapy (PTT).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Polymer Chemistry Research group, Centre of Macromolecular Chemistry (CMaC) and Laboratory of Organic Synthesis, Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University, Krijgslaan, 281-S4, Ghent, 9000, Belgium.
Recycling thermosetting materials presents itself as a major challenge in achieving sustainable material use. Dynamic covalent cross-linking of polymers has emerged as a viable solution that can combine the structural integrity of thermosetting materials with the (re-)processability of thermoplastics. Thioether linkages between polymer chains are quite common, and their use dates back to the vulcanization of rubbers.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, Tennessee 37996, United States.
The achievement of sufficient dispersion of vulcanization accelerators is critical to tailoring superior cross-linked elastomers. Modern recipes rely on multicomponent formulations with silica particles covered by coupling agents. We study the molecular properties of select accelerators in polyisoprene melts and their affinity for functionalized surfaces via extensive all-atom molecular dynamics simulations.
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