Patent classifications
C08C19/38
RECYCLABLE CROSS-LINKED DIENE ELASTOMERS COMPRISING FURANYL GROUPS AND PRECURSORS THEREOF
Disclosed are new precursors of recyclable cross-linked diene elastomers including chain-end units with furanyl groups, their use in the preparation of the recyclable elastomers and their process of preparation. Also disclosed are new recyclable cross-linked diene elastomers, their preparation process and their uses.
Cross-linking agents containing isocyanate groups for nitrile rubbers
By the use of special cross-linkers that contain at least two isocyanate groups, hydroxyl group-containing optionally hydrogenated nitrile rubber polymers can be successfully cross-linked. Preferred cross-linkers contain allophanate, biuret, uretdione, uretonimine, bridged carbamate, carbodiimide, isocyanurate, iminooxadiazinedione or oxadiazinetrione structural elements.
Cross-linking agents containing isocyanate groups for nitrile rubbers
By the use of special cross-linkers that contain at least two isocyanate groups, hydroxyl group-containing optionally hydrogenated nitrile rubber polymers can be successfully cross-linked. Preferred cross-linkers contain allophanate, biuret, uretdione, uretonimine, bridged carbamate, carbodiimide, isocyanurate, iminooxadiazinedione or oxadiazinetrione structural elements.
PROCESS FOR SURFACE TREATMENT OF SILICONE RUBBER ARTICLE
A process for surface treatment of a silicone rubber article includes the steps of: (a) surface-treating the silicone rubber article with ultraviolet radiation to permit hydrogen groups on a surface of the silicone rubber article to be converted to hydroxyl groups; and (b) subjecting the surface-treated silicone rubber article to another surface treatment with a poly(fluoroalkylene oxide) ether trialkoxy silane-based composition to permit a chemical reaction therebetween.
PROCESS FOR SURFACE TREATMENT OF SILICONE RUBBER ARTICLE
A process for surface treatment of a silicone rubber article includes the steps of: (a) surface-treating the silicone rubber article with ultraviolet radiation to permit hydrogen groups on a surface of the silicone rubber article to be converted to hydroxyl groups; and (b) subjecting the surface-treated silicone rubber article to another surface treatment with a poly(fluoroalkylene oxide) ether trialkoxy silane-based composition to permit a chemical reaction therebetween.
Farnesene-based macromonomers and methods of making and using the same
A macromonomer precursor is provided that includes a polymeric chain derived from farnesene and a single functional terminal end. The functional terminal end may include a hydroxyl group, an amino group, an epoxy group, an isocyanato group, or a carboxylic acid group. The terminal end of the macromonomer precursor may then be reacted with a (meth)acrylate to form a macromonomer having a (meth)acrylate functionalized terminal end that may be (co)polymerized with radically polymerizable monomers, such as alkyl(meth)acrylate monomers. Alternatively, a copolymer may be obtained by first deriving a poly(meth)acrylate from (meth)acrylate monomers having reactive groups that would allow the macromonomer precursors to be grafted onto the poly(meth)acrylate in a second step. The resulting copolymer may be incorporated as an additive in various formulations, such as a lubricant, a hydraulic fluid, a cosmetic composition, and an adhesive composition.
Farnesene-based polymers and liquid optically clear adhesive compositions incorporating the same
A low viscosity polymer having a linear or branched backbone derived from farnesene monomers and at least one terminal-end functionalized with a hydroxyl group. This polymer may be further hydrogenated to reduce unsaturation and acrylated, such that it may be incorporated into a LOCA composition. The LOCA composition may be used in a laminated screen assembly, such as a touch screen, for electronic devices by adhering the LOCA composition between an optically transparent layer, such as a cover glass, and a display. The cured LOCA composition has a refractive index similar to the optically transparent layer. A method of making the low viscosity polymer for the LOCA composition includes anionically polymerizing farnesene monomers, quenching a living end of the polymer to provide the hydroxyl-terminated polymer; hydrogenating the hydroxyl-terminated polymer; and reacting the at least partially saturated hydroxyl-terminated polymer with at least one reagent to provide an acrylate terminated hydrogenated polymer.
Farnesene-based polymers and liquid optically clear adhesive compositions incorporating the same
A low viscosity polymer having a linear or branched backbone derived from farnesene monomers and at least one terminal-end functionalized with a hydroxyl group. This polymer may be further hydrogenated to reduce unsaturation and acrylated, such that it may be incorporated into a LOCA composition. The LOCA composition may be used in a laminated screen assembly, such as a touch screen, for electronic devices by adhering the LOCA composition between an optically transparent layer, such as a cover glass, and a display. The cured LOCA composition has a refractive index similar to the optically transparent layer. A method of making the low viscosity polymer for the LOCA composition includes anionically polymerizing farnesene monomers, quenching a living end of the polymer to provide the hydroxyl-terminated polymer; hydrogenating the hydroxyl-terminated polymer; and reacting the at least partially saturated hydroxyl-terminated polymer with at least one reagent to provide an acrylate terminated hydrogenated polymer.
Organosilicon compound and production process therefor
An organosilicon compound represented by formula (1), which has, per alkoxysilyl group, a plurality of epoxy groups each capable of reacting with an organic resin moiety to form a bond and which hence is useful as a primer, a resin modifier, etc. ##STR00001##
(In the formula, the R.sup.1 moieties each independently represent an (un)substituted C.sub.1-10 alkyl group, etc.; the R.sup.2 moieties each independently represent an (un)substituted C.sub.1-10 alkyl group, etc.; the R.sup.3 moieties each independently represent a hydrogen atom or a methyl group; A.sup.1 represents a single bond, O, S, NH, or a divalent linking group containing a heteroatom; A.sup.2 represents a single bond or an (un)substituted C.sub.1-20 divalent hydrocarbon group optionally containing a heteroatom; a and c are each independently a number greater than 0; b, d, e, and f are each independently a number of 0 or greater; and m is an integer of 1 to 3. The repeating units may have been linked in any order.)
Adhesive Composition For Optical Use And Adhesive Film For Optical Use Comprising Adhesive Layer Comprising Photocured Product Thereof
The present specification provides an adhesive composition for optical use, including a polybutadiene rubber having a reactive group including one or more selected from the group consisting of a hydroxy group and a (meth)acrylate group, the reactive group bonded to a main chain thereof, and an adhesive film for optical film, including an adhesive layer including a photocured product of the adhesive composition for optical use.