C08F222/1067

Acrylic emulsions modified with functional (meth)acrylates to enable crosslinking

The present invention provides a method for crosslinking an acrylic emulsion with a (meth)acrylate monomer or a (meth)acrylate oligomer including adding a base acrylic emulsion to a vessel, adding at least one (meth)acrylate crosslinker to the vessel, incorporating the at least one (meth)acrylate crosslinker into the base acrylic emulsion to create a two-phase system including water and a phase including crosslinkers of the at least one (meth)acrylate crosslinker inside acrylic emulsion particles of the base acrylic emulsion, applying the two-phase system to a surface, and curing the two-phase system to create a final system including a continuous film and crosslinked crosslinkers.

Low diameter optical fiber

Small-radius coated optical fibers having large mode field diameter and low bending losses. The coated fiber may have an outer radius of 110 μm or less, while providing a mode field diameter of 9.0 μm or greater and a bending loss when wrapped about a 15 mm mandrel of 0.5 dB/km or less at wavelength of 1550 nm. The coated fiber may have a mode field diameter of 9.2 μm or greater and may have a bending loss at 1550 nm of 0.25 dB/km or less when wrapped about a 20 mm mandrel or a bending loss at 1550 nm of 0.02 dB/km or less when wrapped about a 30 mm mandrel.

COMPOSITE MATERIALS INCLUDING CERAMIC FIBERS AND NANOCLUSTERS, DENTAL PRODUCTS, KITS, AND METHODS OF MAKING AND USING SAME

The present disclosure provides a composite material. The composite material includes 20 to 40 weight percent (wt. %) of a polymerizable component; 6 to 40 wt. % of ceramic fibers; and 30 to 70 wt. % of nanoclusters. Each of the ceramic fibers has a diameter and a length, the ceramic fibers having an arithmetic mean diameter of 0.3 micrometers to 5 micrometers, and the length of fifty percent of the ceramic fibers (based on a total number of the ceramic fibers) is at least 10 micrometers and the length of ninety percent of the ceramic fibers is no greater than 500 micrometers. The present disclosure also provides a method of making the composite material. The method includes obtaining components and admixing the components to form a composite material. Further, the present disclosure provides a method of using a composite material including placing a composite material near or on a tooth surface, changing the shape of the composite material near or on a tooth surface, and hardening the composite material. In addition, the present disclosure provides dental products and kits. Hardened composite materials can exhibit high strength.

Fast Curing Epoxy Acrylic Liquid Shim

The present disclosure provides two part, room-temperature curable hybrid epoxy/(meth)acrylate compositions, comprising: (a) a first component, comprising (meth)acrylate monomers, crosslinkers, epoxy curatives, and optional free radical accelerator, tougheners, fillers and additives, and inhibitors; and (b) a second component, comprising epoxy resins, methacrylate free radical initiators, and optional tougheners, fillers and additives. The compositions provide among other advantageous properties fast cure rate, extremely high compression properties, and good thermal cycling performance.

Fast Curing Epoxy Acrylic Liquid Shim

The present disclosure provides two part, room-temperature curable hybrid epoxy/(meth)acrylate compositions, comprising: (a) a first component, comprising (meth)acrylate monomers, crosslinkers, epoxy curatives, and optional free radical accelerator, tougheners, fillers and additives, and inhibitors; and (b) a second component, comprising epoxy resins, methacrylate free radical initiators, and optional tougheners, fillers and additives. The compositions provide among other advantageous properties fast cure rate, extremely high compression properties, and good thermal cycling performance.

DENTAL MATERIALS USING THERMOSET POLYMERS

Provided herein are crosslinked polymers useful in orthodontic appliances and light polymerizable liquid compositions and formulations useful for making crosslinked polymers. Also provided are methods of making an orthodontic appliance comprising a cross-linked polymer formed by a direct fabrication technique.

HIGH TEMPERATURE RESISTANT PHOTOCURABLE MATERIAL FOR 3D INKJET PRINTING AND PREPARATION METHOD THEREOF, 3D PRINTING PRODUCT AND 3D PRINTER
20210253764 · 2021-08-19 ·

The present application provides a high temperature resistant photocurable material for 3D inkjet printing, a preparation method thereof, a 3D printing product and a 3D printer, which relates to 3D printing technology. The high temperature resistant photocurable material for 3D inkjet printing includes the following components: 60-99 parts by weight of first vinyl compounds, 0-39 parts by weight of second vinyl compounds, and 0.5-4 parts by weight of free radical photoinitiators, where: the first vinyl compounds have a non-reactive cyclic structure, and the non-reactive cyclic structure does not have photopolymerization properties under initiations of the free radical photoinitiators; the second vinyl compounds do not have the non-reactive cyclic structure, and the number of methylene on a main chain are not less than 3.

HIGH TEMPERATURE RESISTANT PHOTOCURABLE MATERIAL FOR 3D INKJET PRINTING AND PREPARATION METHOD THEREOF, 3D PRINTING PRODUCT AND 3D PRINTER
20210253764 · 2021-08-19 ·

The present application provides a high temperature resistant photocurable material for 3D inkjet printing, a preparation method thereof, a 3D printing product and a 3D printer, which relates to 3D printing technology. The high temperature resistant photocurable material for 3D inkjet printing includes the following components: 60-99 parts by weight of first vinyl compounds, 0-39 parts by weight of second vinyl compounds, and 0.5-4 parts by weight of free radical photoinitiators, where: the first vinyl compounds have a non-reactive cyclic structure, and the non-reactive cyclic structure does not have photopolymerization properties under initiations of the free radical photoinitiators; the second vinyl compounds do not have the non-reactive cyclic structure, and the number of methylene on a main chain are not less than 3.

TWO-PART, CYANOACRYLATE/FREE RADICALLY CURABLE ADHESIVE SYSTEMS

Two-part cyanoacrylate/free radically curable adhesive systems demonstrating improved toughness are provided.

TWO-PART, CYANOACRYLATE/FREE RADICALLY CURABLE ADHESIVE SYSTEMS

Two-part cyanoacrylate/free radically curable adhesive systems demonstrating improved toughness are provided.