| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 522068000 | Specified rate-affecting material contains oxygen | 9 |
| 20090062418 | NOVEL PHOTOINITIATORS - A photoinitiator compound is functionalized with alkoxy groups so as to be soluble in alkoxy-containing monomers. The photoinitiator has a formula of R | 03-05-2009 |
| 20090281207 | DE-POLLUTING AND SELF-CLEANING EPOXY SILOXANE COATING - De-polluting, self-cleaning coating compositions are disclosed which comprise photocatalytic titanium dioxide and a binder comprising an epoxy siloxane polymer. The compositions produce durable, self-cleaning coatings with photocatalytic activity against pollutants in the air, such as NO | 11-12-2009 |
| 20110082229 | CARBOXYL RESIN, HARDENING COMPOSITION CONTAINING CARBOXYL RESIN, AND HARDENED MATERIAL THEREOF - A carboxyl resin according to the present invention is obtained by a process including following steps: epoxy groups on a resin (a) having two or more epoxy groups in one molecule is made to react with 0.3-0.85 mol of a monocarboxylic acid (b) per one epoxy-group equivalent weight to obtain a reaction product (c); the epoxy group or groups on the reaction product (c) are made to react with 0.15-0.95 mol of a polybasic acid (d) per one epoxy-group equivalent weight to obtain a reaction product (e); and the epoxy group or groups on the reaction product (e) are further made to react with 1.0-5.0 mol of a monocarboxylic acid (f) per one epoxy-group equivalent weight. The carboxyl resin thus obtained has an acid value within a range from 20 to 200 mgKOH/g and is soluble in an organic solvent. | 04-07-2011 |
| 20110092609 | PHOTOSENSITIVE POLYMERIC NETWORKS - The present invention related to amorphous photosensitive networks. The networks are characterized by good shape memory properties. | 04-21-2011 |
| 20160030298 | COMPOSITE MATERIAL HAVING REDUCED DEGRADATION OF PASTY PROPERTY - A composite material including silanated filler and mixed polymerizable monomer, having a stable pasty property which keeps well and has a consistent usability. A composite material containing a silanated filler, a polymerizable monomer, and a polymerization initiator, and may be produced by a process which includes in order of a mixed polymerizable monomer preparing step, a mixed polymerizable monomer preserving step, a composite material preparing step, a composite material preserving step, a composite material filling step, and a small quantity preserving container preserving step. | 02-04-2016 |
| 20160083589 | COMPOSITIONS FOR THREE-DIMENSIONAL (3D) PRINTING - A composition for three-dimensional printing includes a precursor to a soft polymer block having a glass transition temperature (T | 03-24-2016 |
| 20160120764 | BISGMA-FREE ORTHODONTIC ADHESIVES - Three adhesives formulated with Trimethylolpropane Trimethacrylate (TMPTMA) that do not contain BisGMA were developed, whereby the mutagenic and teratogenic risk by the release of bisphenol A is eliminated, and presented a better performance compared to the three commercial adhesives prepared with BisGMA (Adhesive A, Adhesive C and Adhesive B). The invention provides an adhesive used in one-step and provides a system which is formed by a primer and a slurry. The adhesives of the invention were compared with two commercial controls. They were physically characterized by assessing: hardening time, adhesion stress, elastic modulus, sorption and solubility at different pHs (6.8 and 7.7); by the obtained values premature detachments, white lesions below the appliance and microfiltration are avoided; its fluidity, film thickness were evaluated and were compared with those obtained from the three commercial adhesives. Storage stability and thermogravimetric analysis were assessed. The prepared adhesives with TMPTMA are photopolymerizables, thereby providing enough time to the operator to place the appliance in proper position, it is easy to handle, capable of supporting orthodontic biomechanics, has low elastic modulus, enables transitions of heavy arches reducing the risk of involuntary detachment of the appliances, have low viscosity, penetrates on both the brace retentions as those made with acid etching on enamel surface. Presenting adhesion to both the base of the attachments as well as to the enamel, its film thickness is minimal and does not alter the prescription system. When the appliance is removed at the end of the treatment, it does not cause structural damage to the enamel because the adhesive remains on the enamel and can be removed easily with a rotary instrument. | 05-05-2016 |
| 522069000 | Phenolic, e.g., hydroquinone, etc. | 2 |
| 20080214691 | Low-viscosity allophanates containing actinically curable groups - A process for preparing binders containing allophanate groups which contain, at the oxygen atom of the allophanate group that is bonded via two single bonds, organic radicals with activated groups capable of participating in a polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation; the process includes reacting A) one or more compounds containing uretdione groups with B) one or more OH-functional compounds which contain groups capable of participating in a polymerization reaction with ethylenically unsaturated compounds on exposure to actinic radiation, and C) optionally further NCO-reactive compounds, and D) in the presence of one or more compounds containing phenoxide groups, as catalysts. The binders can be used in preparing coatings, coating materials, coating compositions, adhesives, printing inks, casting resins, dental compounds, sizes, photoresists, stereolithography systems, resins for composite materials and sealants. | 09-04-2008 |
| 20140187663 | TELECHELIC MACROMER, METHOD FOR PRODUCING TELECHELIC MACROMER AND COMPOSITION CONTAINING TELECHELIC MACROMER - A telechelic macromer is disclosed having (meth)acrylic end-groups and a core. The macromer defined by Formula 1 comprises a core Y (Formulas 2 to 9) that is linked to (meth)acrylic groups by urethane, ester or anhydride bonds and has iodine value ranging from 5 to 75. The method involves a chemical reaction carried out in solvent, ranging 6-24 hours, wherein the precursor of a core (Formulas 2 and 3) reacts in two stages with compounds forming urethane bonds, or wherein the precursor of a core (Formulas 4 to 8) reacts in one stage with compounds forming ester bonds, or wherein the precursor of a core defined by Formula 9 reacts in one stage with compounds forming anhydride bonds. The urethane, ester and anhydride moieties comprise groups capable of free radical polymerization isolating the final product by evaporation. The composition disclosed provides the macromer, a photoinitiator and possibly a reactive diluent. | 07-03-2014 |
