C08G18/7621

ALDIMINES AND USES THEREOF
20230038642 · 2023-02-09 ·

The present invention relates to compounds having one of the following formulae (I) and (II):

##STR(I)##

##STR(II)##

and also to the uses thereof.

Silicate modified polymer foam material for filling and sealing

A silicate modified polymer foam material for filling and sealing contains prepolymerized isocyanate and a silicate modified aqueous solution with a mass ratio in a range of 1:(1.2-1.4). In the prepolymerized isocyanate, a mass percentage of P is 4.4%, a mass percentage of N is 7.9%, and a mass percentage of —NCO is 11.9%. The silicate modified aqueous solution includes liquid sodium silicate, small molecule alcohol, water and a catalyst, wherein the liquid sodium silicate, the small molecule alcohol, the water and the catalyst account for 63-66%, 17-20%, 14-17% and 1.5-2.5% of the weight of the silicate modified aqueous solution respectively. A method of preparing the silicate modified polymer foam material for filling and sealing includes mixing the prepolymerized isocyanate with the silicate modified aqueous solution.

Structural flame retardant high strength low exothermic polymer grouting material for consolidating

A structural flame retardant high strength low exothermic polymer grouting material for consolidating, belonging to a technical field of polyurethane material, is produced by combined the polyether polyol and the modified isocyanate in a weight ratio of 100:(100-160), leading to internal reaction temperature ≤100° C., strength ≥60 mPa, bonding ≥3 mPa, oxygen index ≥28% while no halogen and no effect on water quality, odor level (80° C.) ≤3.5, and fog test ≤5 mg (which means no physical additive flame retardant is diffused into the environment). In particular, with no halogen, which is known as environmental hormones, in the plasticizers, there will be less combustion smoke, wherein the present invention will not release corrosive or irritating hydrogen halide gas, nor produce toxic carcinogens polybrominated benzoxins and polybrominated dibenzofurans, thereby avoiding the long-term impact of the material on the environment.

Silicate-modified high-toughness and low-heat polymer grouting material for reinforcement

The present invention relates to a silicate-modified high-toughness and low-heat polymer grouting material for reinforcement, which belongs to the technical field of materials. About 60% by weight of the raw materials of the silicate modified grouting material of the present invention is the silicate modified aqueous solution, and about 40% is the structural flame retardant isocyanate, and main components of the polymer grouting material are classified into inorganic components according to the main total proportion. The silicate-modified high-toughness and low-heat polymer grouting material for reinforcement of the present invention has excellent flame retardancy and compressive performance, wherein a compressive strength is ≥60 MPa, an oxygen index is ≥30%, and a maximum reaction temperature is ≤100° C., an odor grade (80° C.) is ≤3.5, a fog test is ≤5 mg (no physical additive flame retardant diffuses to the environment), bonding is ≥3 MPa, a shear strength is ≥20 MPa, and a tensile strength is ≥20 MPa.

NOVEL POLYETHER POLYOL BLENDS, A PROCESS FOR THEIR PREPARATION, FOAMS PREPARED FROM THESE POLYETHER POLYOL BLENDS AND A PROCESS FOR THEIR PREPARATION

This invention relates to a novel polyether polyol blend having an overall hydroxyl number of 56 mg KOH/g to 140 mg KOH/g, an overall functionality of greater than 2, and an overall content of copolymerized oxyethylene of 20% to 40% by weight. These novel polyether polyol blends may also be in-situ formed novel polyether polyol blends. A process for preparing these novel polyether polyol blends is also disclosed. These novel polyether polyol blends are suitable for preparing viscoelastic flexible polyurethane foams, and in a process for preparing viscoelastic foams.

Prepolymer of elastomer material for screw drilling tool and preparation method thereof

A prepolymer of elastomer material for screw drilling tools and a preparation method thereof are provided. The prepolymer includes component A and component B, wherein the component A includes hydroxyl-terminated liquid rubber, polytetrahydrofuran diol, and polyether polyol; the component B includes at least one of an isocyanate, a cyanate, and a cyano compound; the mass ratio of the hydroxyl-terminated liquid rubber, polytetrahydrofuran diol, and polyether polyol is (0.2-1.0): (0.2-1.0): (0.2-1.0). Different molecular segments of different proportions are introduced through structural design, such that the molecular structure of the prepolymer has both rigid and flexible segments, thus to achieve an adjustable and controllable structure of the prepolymer; and the introduction of active groups makes the prepolymer to show good reactivity and processability. Therefore, a reactive elastomer material having excellent properties such as hardness, tear strength, and tensile strength can be obtained used as an elastomer material for screw drilling tools.

INHIBITION OF CRYSTALLIZATION IN POLYURETHANE RESINS
20230007999 · 2023-01-12 ·

A resin composition useful for additive manufacturing is provided, which resin composition may exhibit improved shelf life through inhibition of crystallization. Such resin composition may include a crystallization inhibitor as taught herein, and/or a prepolymer produced by reaction of an isocyanate with multiple isomers and comprising a lower percentage of the structurally symmetric isomer. Methods of forming a three-dimensional object using such resin composition are also provided.

Compressible non-reticulated polyurea polishing pad

The invention provides a polishing pad suitable for polishing at least one of semiconductor, optical, magnetic or electromechanical substrates. It includes a polyurea polishing layer and a polyurea matrix. The polyurea has a soft segment being a copolymer of aliphatic fluorine-free polymer groups and a fluorocarbon having a length of a least six carbons. The polyurea matrix being cured with a curative agent and including gas or liquid-filled polymeric microelements. The polyurea matrix has a bulk region and a transition region adjacent the bulk region that extends to the polishing layer. The polymeric microelements in the transition region decrease in thickness as they approach the polishing layer with thickness of the compressed microelements adjacent the polishing layer being less than fifty percent of a diameter of the polymeric microelements in the bulk region. The polishing layer remains hydrophilic during polishing in shear conditions.

Polycarbodiimide compound, production method therefor, and resin composition

There are provided a carbodiimide compound excellent in storage stability, and performance as a crosslinking agent, and a method for producing the same, and a resin composition excellent in the film forming properties and solvent resistance of a coating made at low temperature. A polycarbodiimide compound derived from an aliphatic diisocyanate compound having at least one primary isocyanate group, the polycarbodiimide compound having a structure in which all ends are capped with an organic compound having a functional group that reacts with an isocyanate group, carbodiimide group concentration A (%) and weight average molecular weight Mw satisfying the following formula (1), and a resin composition comprising the carbodiimide compound and an aqueous resin having a predetermined acid value at a predetermined ratio.
(A/Mw)×1000≥0.55  (1).

Partially coated films and packages formed from same

The present invention provides coated films and packages formed from such films. In one aspect, a partially coated film comprises (a) a film having two outer surfaces, wherein a first outer surface is provided by a film layer that comprises from 70 to 100 percent by weight of a polyolefin having a density of 0.860 to 0.965 g/cm.sup.3; and (b) a coating on the first outer surface of the film comprising polyurethane, wherein the coating covers less than 25% of the surface area of the first outer surface of the film and wherein the coated portion of the film exhibits an Elmendorf tear in at least one of the machine direction or cross direction that is at least 20% less than the Elmendorf tear of the uncoated portion in the same direction, with the Elmendorf tear being measured in accordance with ASTM D1922.