Embodiments of organic peroxide formulations provide significant improvements in surface tackiness (often including tack-free surfaces) when curing elastomers in the presence of oxygen. The peroxide formulations may include, for example, one or more compounds selected from sulfur-containing compounds, organophosphite compounds, HALS (Hindered Amine Light Stabilizer) compounds, aliphatic allyl urethane compounds, and blends comprising nitroxides (e.g., 4-hydroxy-TEMPO) and quinones (e.g., mono-tert-butylhydroquinone).

Embodiments of organic peroxide formulations provide significant improvements in surface tackiness (often including tack-free surfaces) when curing elastomers in the presence of oxygen. The peroxide formulations may include, for example, one or more compounds selected from sulfur-containing compounds, organophosphite compounds, HALS (Hindered Amine Light Stabilizer) compounds, aliphatic allyl urethane compounds, and blends comprising nitroxides (e.g., 4-hydroxy-TEMPO) and quinones (e.g., mono-tert-butylhydroquinone).

The electrophotographic electroconductive member includes a support having an electroconductive outer surface, and an electroconductive layer on the surface of the support. The electroconductive layer has a matrix containing a crosslinked product of a first rubber, and domains dispersed in the matrix, and the domains each contain a crosslinked product of a second rubber and electroconductive particles. The matrix has a volume resistivity R1 of more than 1.0×10.sup.12 Ω.Math.cm, and the domains each have a volume resistivity R2 lower than the volume resistivity R1 of the matrix. The electroconductive layer further has a pore, and an inner wall of the pore is constituted by a part of the matrix and a part of the domains. The domains constituting the inner wall protrude into the pore at sites on the inner wall.

The electrophotographic electroconductive member includes a support having an electroconductive outer surface, and an electroconductive layer on the surface of the support. The electroconductive layer has a matrix containing a crosslinked product of a first rubber, and domains dispersed in the matrix, and the domains each contain a crosslinked product of a second rubber and electroconductive particles. The matrix has a volume resistivity R1 of more than 1.0×10.sup.12 Ω.Math.cm, and the domains each have a volume resistivity R2 lower than the volume resistivity R1 of the matrix. The electroconductive layer further has a pore, and an inner wall of the pore is constituted by a part of the matrix and a part of the domains. The domains constituting the inner wall protrude into the pore at sites on the inner wall.

Thermally vulcanisable, meltable adhesives and processes have a meltable polybutadiene-polyurethane, ground sulphur and optionally at least one vulcanisation accelerator, at least one filling material, at least one epoxide resin, at least one tackifier resin, bitumen, at least one softener and further auxiliary and additive materials, wherein said adhesives and processes can be thermally vulcanised within a temperature range of 130° C. to 230° C., such that same, as well as an adhesive strip produced from same, can be used for adhesion and/or sealing in the automotive industry, as well as in structural work on oiled sheet metal, and in the painting line on e-coated or otherwise painted sheet metal, for example, for crimp fold adhesion, for crimp fold sealing, for seam sealing, for lining adhesion, for hole closure and much more.

Thermally vulcanisable, meltable adhesives and processes have a meltable polybutadiene-polyurethane, ground sulphur and optionally at least one vulcanisation accelerator, at least one filling material, at least one epoxide resin, at least one tackifier resin, bitumen, at least one softener and further auxiliary and additive materials, wherein said adhesives and processes can be thermally vulcanised within a temperature range of 130° C. to 230° C., such that same, as well as an adhesive strip produced from same, can be used for adhesion and/or sealing in the automotive industry, as well as in structural work on oiled sheet metal, and in the painting line on e-coated or otherwise painted sheet metal, for example, for crimp fold adhesion, for crimp fold sealing, for seam sealing, for lining adhesion, for hole closure and much more.

The present disclosure discloses a high-performance rubber damping material and a method for preparing the same, relating to the technical field of damping materials. The method for preparing the high-performance rubber damping material includes: grafting hydroxyethyl methacrylate and lignin to a rubber molecular chain of natural rubber latex through graft copolymerization reaction, so as to obtain a high-performance rubber damping material. This method adopts natural rubber latex as a base material, the hydroxyethyl methacrylate and lignin are grafted to the rubber molecular chain of natural rubber latex through graft copolymerization reaction, to form a semi-interpenetrating network structure.

The present disclosure discloses a high-performance rubber damping material and a method for preparing the same, relating to the technical field of damping materials. The method for preparing the high-performance rubber damping material includes: grafting hydroxyethyl methacrylate and lignin to a rubber molecular chain of natural rubber latex through graft copolymerization reaction, so as to obtain a high-performance rubber damping material. This method adopts natural rubber latex as a base material, the hydroxyethyl methacrylate and lignin are grafted to the rubber molecular chain of natural rubber latex through graft copolymerization reaction, to form a semi-interpenetrating network structure.

The present invention provides a tire having a good balance of fuel efficiency, chipping resistance, and steering stability.

The present invention provides a tire having a good balance of fuel efficiency, chipping resistance, and steering stability.