Abstract: A modified bitumen consisting of a polyurethane wherein the polyisocyanate or polyisocyanate-dominated polyurethane prepolymer (or prepolymers) is first reacted with the bitumen to take advantage of the bitumen's hydroxyl and amine functionality and form an isocyanate-bitumen adduct to form a weatherproofing product.

Abstract: Modified lignin products, processes for making them, and their use to produce rigid polyurethane or polyisocyanurate foams are disclosed. The processes comprise heating a lignin source with a nitrogen source and a starved concentration of a C1-C5 aldehyde to give a reaction mixture comprising a Mannich condensation product, neutralizing the reaction mixture, and isolating the modified lignin product. The process is performed at a mass ratio of lignin source to nitrogen source within the range of 1:1 to 1:5 and at a molar ratio of nitrogen source to C1-C5 aldehyde within the range of 3.5:1 to 1:1. Polyol blends and performance additives that contain the modified lignin products are described. Rigid foams that process well and incorporate up to 60 wt. %, based on the amount of polyol component, of the modified lignin contribute to excellent flame retardancy and low-temperature R-value performance.

Abstract: Provided are a resin composition including a compound represented by Formula (1) and a resin, a film and a filter including the resin composition, a liquid crystal display device and a solid-state imaging element including the filter, and a compound suitable as a light absorbing component of the resin composition and the filter. In Formula (1), Dye represents a colorant structural part obtained by removing n1 hydrogen atoms from a squarylium compound having a specific structure. Q1 is a structural part in which energy levels of a highest occupied molecular orbital and a lowest unoccupied molecular orbital satisfy a specific condition. L1 represents a divalent linking group and n1 represents an integer of 1 to 4.

Abstract: A quinacridone solid solution pigment that allows a colored product to have high chroma and a properly yellowish hue and has a controlled particle diameter, and a method for producing the quinacridone solid solution pigment. In the method, a water-containing crude quinacridone solid solution is produced by a co-cyclization reaction of a diarylaminoterepththalic acid and a dialkylarylaminoterephthalic acid in polyphosphoric acid, then the resulting water-containing crude quinacridone solid solution having a mass ratio of unsubstituted quinacridone to a 2,9-dialkylquinacridone of 85:15 to 60:40 is dried, thereby obtaining a powdery, crude quinacridone solid solution having a water content of less than 1%. Then, the resulting powdery, crude quinacridone solid solution is heated in a liquid medium that does not dissolve the crude quinacridone solid solution. Also, a pigment dispersion liquid and an inkjet ink each containing the obtained quinacridone solid solution pigment are provided.

Abstract: A method for preparing carbon black from pyrolysis char of waste tires by a molten salt thermal treatment and a product thereof are provided. The method includes heating one or two groups of a metal chloride salt group and a metal sulfate group to obtain a molten salt; adding pyrolysis char of waste tires into the molten salt and subjecting same to a molten salt thermal treatment under a preset reaction atmosphere; after the reaction is complete, separating the reaction product to obtain a secondary molten salt and treated pyrolysis char, washing the treated pyrolysis char with hot water and then drying same so as to obtain carbon black, and at the same time, recycling the secondary molten salt.

Abstract: Systems and methods of making carbon particles with thermal transfer gas. A method of making carbon particles may comprise heating a thermal transfer gas by Joule heating and contacting the thermal transfer gas with a reactive hydrocarbon feedstock gas to generate the carbon particles and hydrogen gas. A method of making carbon particles may comprise heating a thermal transfer gas with the aid of Joule heating and mixing the thermal transfer gas with a hydrocarbon feedstock gas to generate the carbon particles.

Abstract: An object is to provide a printing ink that has high environmental friendliness and is excellent in quick dry-curability of a coating when a plasma is used as a curing system. A solution is to provide an ink composition for plasma curing including a photocatalyst compound and/or a composite of a metal component and a photocatalyst compound and to provide an additive for an ink composition for plasma curing, the additive including a photocatalyst compound and/or a composite of a metal component and a photocatalyst compound.

Abstract: The present invention provides a water-based black ink, utilizing biochar as the black pigment. The black inks of the invention contain high bio-renewable carbon content (BRC), preferably 100% BRC. The inks exhibit the physical properties required to perform according to the requirements of rotogravure and flexographic printing.

Abstract: Provided are an active energy ray-curable ink including a photopolymerization initiator including a compound represented by Formula (1) and at least one of a monomer A composed of a photopolymerizable monomer having a molecular weight of 400 or more or a monomer B composed of a photopolymerizable monomer having a molecular weight of 130 or more and less than 400, and an image recording method. L1 represents an organic group having 20 or less carbon atoms and a valence of n, and n represents an integer of 3 to 8. AO represents an alkyleneoxy group having 2 or 3 carbon atoms, and m represents an integer of 0 to 15. L2 represents a single bond, an oxygen atom, a sulfur atom, or —NR11—. R11 represents a substituent. X represents an oxygen atom or a sulfur atom, and n R1's and n R2's each independently represent a substituent.

Abstract: Disclosed is an ink comprising a transparent matrix being UV curable and heat scalable, and at least one pigment component. The ink in its UV-cured state has a peel strength in the range of about 6 to 8 N/cm, wherein this adhesiveness is achievable by means of a further lamination step under the influence of pressure and heat so that the ink acts as a hot glue. Further disclosed is a safety structure comprising a semitransparent layer being formed at least partially by the UV-cured ink, and a secure article comprising the safety structure. Further disclosed is a use of the ink for silkscreen printing.

Abstract: Thermoset compositions and methods for forming three-dimensional articles via an additive fabrication process, and articles made therefrom are disclosed herein. In an embodiment, a composition comprises a first network-forming component comprising a first oligomer comprising a backbone and having at least 2 polymerizable groups, one or more first network monomers, and a first network initiator. The backbone of the first oligomer comprises a polyepoxide based on Bisphenol A, F, or S, a polyepoxide based on hydrogenated Bisphenol A, F, or S, a polycarbonate, or a polyimide. The composition may further comprise a second network-forming component.

Abstract: Provided is an aqueous ink composition for writing instruments which is excellent in an antibacterial property and an antifungal property without damaging storage stability and writing performances. The aqueous ink composition for writing instruments according to the present invention is characterized in that at least particles comprising principally a polymer represented by the following Formula (I) are contained as an active ingredient and that a content thereof is 0.1 to 30 mass %: wherein R is an alkyl group having 2 to 8 carbon atoms.

Abstract: There is provided an ink composition that can form a color filter pixel unit with high external quantum efficiency. An ink composition containing light-emitting nanocrystal particles, light-diffusing particles, and at least two monomers with an ethylenically unsaturated group, wherein the at least two monomers include two monomers with Hansen solubility parameters ?d, ?p, and ?h that satisfy the following conditions: 16.0 MPa0.5??d<18.0 MPa0.5; 2.5 MPa0.5??p<5.5 MPa0.5; 2.5 MPa0.5??h<8.0 MPa0.5.

Abstract: An inkjet textile printing ink includes coloring particles and an aqueous medium. The coloring particles each include a core and a shell layer covering the core. The core contains a polyester resin and a dye. The shell layer contains a specific resin with a non-ring-opened oxazoline group and an amide ester group. The polyester resin preferably includes a non-crystalline polyester resin.

Abstract: The ink composition comprises pigment particles and a stimulus responsive dispersing agent for dispersing said pigment particles in a protic polar solvent, for instance for inkjet printing, which stimulus responsive dispersing agent comprises an anchoring part for anchoring to said pigment particles, a stimulus responsive part as shown in formula (XXa) or (XXb) and a hydrophilic part for solvent stabilization of the pigment, wherein the stimulus responsive part upon exposure to a stimulus initiates decomposition of the stimulus responsive dispersing agent. The paper with the printed ink can be deinked in an industrial deinking process.

Abstract: A fluororesin material including a melt-fabricable fluororesin, the fluororesin material having a dielectric constant of 2.1 or less and a dielectric loss tangent of 0.00030 or less at 12 GHz. Also disclosed is a fluororesin material for high-frequency transmission including the fluororesin material and a coated electric wire for high-frequency transmission including a solid insulating coating layer made of the fluororesin material.

Abstract: Provided is a coating film having excellent durability and wear resistance, and utility as mold surface release coating. The coating film has excellent releasability (non-adhesiveness) over a long period of time. Further provided is a coating composition capable of forming such a coating film, the coating composition containing a fluoropolymer and an oil that is a liquid at 25° C., wherein the decomposition temperature of the oil is higher than the melting point of the fluoropolymer.

Abstract: Coated substrates comprising a topcoat are disclosed. The coated substrate may be substantially free of PVC while having performance comparable to a coated substrate comprising PVC. The topcoat may comprise a base polymer comprising a polyvinylpyrrolidone copolymer, such as polyvinylpyrrolidone/vinyl acetate. The base polymer may also comprise a cationic acrylic resin. The topcoat may also comprise a pigment system and optionally, a crosslinking system.

Abstract: To provide a fluorinated ether compound, a fluorinated ether composition and a coating liquid excellent in chemical resistance, an article having a surface layer excellent in chemical resistance and a method for producing it, and a method for producing a fluorinated ether compound excellent in chemical resistance. A fluorinated ether compound which has a first partial structure represented by the following formula (1) and a second partial structure represented by the following formula (2), and which has at least five first partial structures, or has at least two second partial structures: —ORf12—??(1) —ORf13—??(2) wherein Rf12 is a C1-6 fluoroalkylene group, and Rf13 is a group having a fluorinated cyclic structure which may have a hetero atom.

Abstract: A quick-drying solvent-free sag-resistant polyurethane waterproof coating and preparation method therefor, raw materials therefor comprising a polyurethane prepolymer, a plasticizer, a dispersant, a filler, a dehydrant, a catalyst, a defoamant, and an oxazolidine reactive diluent. The catalyst is composed of pentamethyl dipropylene triamine, tetramethylethylenediamine, and 1,8-diazabicyclo[5.4.0]undecene. Raw materials of the polyurethane prepolymer comprise a polyether diol, a polyether triol, an isocyanate, and a chain extender. The prepolymer is prepared by means of the following method: 1) measuring out the raw materials for the polyurethane prepolymer, and reacting the polyether diol with the isocyanate until reaction is complete; 2) then adding the polyether triol for reaction until reaction is complete; 3) then adding the chain extender for reaction, completing preparation.

Abstract: Coated substrates include a metal substrate and a polytriazole polymer applied to a surface of the metal substrate. The polytriazole polymer may include substituted phenyls, substituted benzyls, or both substituted phenyls and substituted benzyls. The substituted phenyls and the substituted benzyls may be independently substituted with hydrogen, bromo, fluoro, chloro, iodo, hydroxy, methyl, trifluoromethyl, dimethylamino, tert-butyl, carboxyl, triphenylmethyl, tris(4-fluorophenyl)methyl, tris(4-methylphenyl)methyl, (4-hydroxyphenyl)diphenylmethyl, and difluoromethoxy groups. The polytriazole polymer may have a degree of polymerization from 50 to 400.

Abstract: A window includes a base layer and a first coating layer. The first coating layer is disposed on a first surface of the base layer. The first coating layer is a single layer. The first coating layer includes a siloxane-based compound. The siloxane-based compound includes fluorine and silica.

Abstract: Compositions comprising asphalt and corn oil are provided, as are the shingles made using the compositions, methods for making the compositions, and methods for making the shingles. The compositions comprise mixtures of asphalt and corn oil, and the mixtures are oxidized to attain desirable properties.

Abstract: Provided are an organic solvent composition having excellent solvency for and compatibility with a resin, and a paint composition including the same. Specifically, the paint composition including the same is prepared, due to the difference in evaporation rate of the organic solvent composition, the compatibility with the resin may be further improved.

Abstract: The present disclosure provides a high-temperature nano-composite coating and a preparation method thereof, and a small bag flexible packaging coating. The high-temperature nano-composite coating provided by the present disclosure controls the fiber length. Moreover, high-temperature reinforcing filler and high-temperature expansion filler are introduced, to make the coating have ultra-high strength at high temperature without cracks caused by shrinkage at high-temperature. In addition, nanopowder, high-temperature skeleton filler and other additives are introduced to make the coating be uniform and stable and reach a slurry state similar to toothpaste. There is no precipitation and stratification during the placement process. Small packaging can be realized to facilitate construction and operation. Besides, the coating has a good bonding to furnace lining, and will not fall off from the furnace lining, thereby prolonging the service life of the furnace lining.

Abstract: Provided is hollow resin particles having higher compressive strength and more excellent heat insulating properties and heat resistance than before. The hollow resin particles each having one or two or more hollow portions, wherein a number average particle diameter is from 0.1 ?m to 9.0 ?m, a void ratio is from 70% to 99%, and an amount of the volatile organic compound contained is 5% by mass or less.

Abstract: A polishing liquid containing: abrasive grains; a first nitrogen-containing compound; a second nitrogen-containing compound; and water, in which the first nitrogen-containing compound contains at least one selected from the group consisting of (I) a compound having an aromatic ring containing one nitrogen atom in the ring and a hydroxyl group, (II) a compound having an aromatic ring containing one nitrogen atom in the ring and a functional group containing a nitrogen atom, (III) a compound having a 6-membered ring containing two nitrogen atoms in the ring, (IV) a compound having a benzene ring and a ring containing a nitrogen atom in the ring, and (V) a compound having a benzene ring to which two or more functional groups containing a nitrogen atom are bonded, and an HLB value of the second nitrogen-containing compound is 7 or more.

Abstract: An adhesive composition for use in debonding with light irradiation, which composition can achieve debonding through irradiation with light, characterized in that the adhesive composition contains an adhesive component (S) and a light-absorbing organic compound (X); and the light-absorbing organic compound (X) contains, in the molecule thereof, one or more aromatic rings, one or more rings each containing a heteroatom forming the ring, and one or more groups selected from among a carbonyl group and a thiocarbonyl group.

Abstract: A bio-electrode composition contains (A) a silicone bonded to an ionic polymer and having a structure containing a T unit shown by the following general formula (T1): (R0SiO3/2) (T1), the structure excluding a cage-like structure. In the formula, R0 represents a linking group to the ionic polymer. The ionic polymer is a polymer containing a repeating unit having a structure selected from the group consisting of salts of ammonium, lithium, sodium, potassium, and silver formed with any of fluorosulfonic acid, fluorosulfonimide, and N-carbonyl-fluorosulfonamide. Thus, the present invention provides a bio-electrode composition capable of forming a living body contact layer for a bio-electrode which is excellent in electric conductivity, biocompatibility, stretchability, and adhesion, soft, light-weight, and manufacturable at low cost, and which prevents significant reduction in the electric conductivity even when wetted with water or dried.

Abstract: An adhesive composition contains an acid anhydride group-containing oil or fat (A) and a curing agent (B) having a reactive group reactive with an acid anhydride group. A laminate is obtained by placing an adhesive layer between a first substrate and a second substrate, and the adhesive layer includes the aforementioned adhesive composition. A package is obtained by forming a bag from a laminate obtained by placing an adhesive layer between a first substrate and a second substrate, and the adhesive layer includes the aforementioned adhesive composition.

Abstract: A method of activating a surface of a plastics substrate formed from: (a) polyaryletherketone such as polyether ether ketone (PEEK) polyether ketone ketone (PEKK), polyether ketone (PEK); polyether ether ketone ketone (PEEKK); or polyether ketone ether ketone ketone (PEKEKK); (b) a polymer containing a phenyl group directly attached to a carbonyl group, for example polybutadiene terephthalate (PBT) optionally wherein the carbonyl group is part of an amide group, such as polyarylamide (PARA); (c) polyphenylene sulfide (PPS); or (d) polyetherimide (PEI); for subsequent bonding, the method comprising the step of exposing the surface to actinic radiation wherein the actinic radiation: includes radiation with wavelength in the range from about 10 nm to about 1000 nm; the energy of the actinic radiation to which the surface is exposed is in the range from about 0.5 J/cm2 to about 300 J/cm2.

Abstract: A reactive PSA film that includes: (a) a polymeric film former matrix; (b) one or more reactive components; and (c) a reagent selected from an initiator, a curing agent and an activator. The component (b) is present at a mass fraction of ?30%, as based on the sum of (a), (b) and (c). Further, ?50 wt % of the film former matrix is a crystallizable polymer which: (i) exhibits a crystallization enthalpy of <1 J/g in a DSC measurement on cooling at 10K/min from at least 30K above a peak temperature of the melting peak of the polymer or ?100° C., whichever is greater; and (ii) exhibits a crystallite fusion enthalpy of ?15 mJ/mg in its pure state in a first heating curve of a DSC measurement at 10K/min and after storage for ?one month from 15 to 25° C. and relative humidity from 30 to 70%.

Abstract: Disclosed is a composition comprising at least one interpolymer dispersed within an aqueous medium, the interpolymer comprising at least one unsaturated monomer and at least one selected from the group consisting of at least one conjugated acid, at least one mono-ester of a conjugated acid, and mixtures thereof, and, optionally, at least one surfactant configured to stabilize the interpolymer within the aqueous medium. The conjugated acid may be derived from a naturally-occurring oil, such as tung oil. There is also provided a method for preparing a composition, comprising forming an interpolymer comprising the at least one unsaturated monomer and the at least one selected from the group consisting of at least one conjugated acid, at least one mono-ester of a conjugated acid, and mixtures thereof. There is still further provided a pressure sensitive adhesive comprising the composition prepared according to the disclosed method.

Abstract: A double-sided pressure-sensitive adhesive tape having excellent impact resistance, excellent reworkability, and excellent alcohol resistance. The double-sided pressure-sensitive adhesive tape includes: a base material layer; and pressure-sensitive adhesive layers arranged on both surface sides of the base material layer, wherein the pressure-sensitive adhesive layers are each formed from a pressure-sensitive adhesive composition, wherein the pressure-sensitive adhesive composition contains at least one kind selected from the group consisting of a monomer component (m) and a polymer component (P) obtained by polymerizing the monomer component (m), wherein the monomer component (m) contains 50 wt % or more of butyl (meth)acrylate, wherein a ratio of a thickness of the base material layer to a total thickness of the double-sided pressure-sensitive adhesive tape is less than 35%, and wherein the double-sided pressure-sensitive adhesive tape has a force, which is generated at 100% strain at 23° C.

Abstract: The invention relates to a high-performance sky blue thermally activated delayed fluorescent material, manufacturing method thereof, and application thereof, which solves the problems of the prior art. Through clever molecular design, a series of sky-blue thermally activated delayed fluorescent materials with less singlet-triplet energy level difference, high luminous efficiency, and fast-rate reverse intersystem crossing constant were synthesized, while fine-tuning of the structure and spectrum thereof were realized.

Abstract: Provided herein are organic-inorganic hybrid-perovskites, including metal halide perovskites having a 1D crystal structure. The metal halide perovskites may be luminescent. The metal halide perovskites may include a dopant, including an emitter dopant. Methods of forming metal halide perovskites, and devices including the metal halide perovskites also are provided.

Abstract: A hydrogen-bonded organic framework nanosheet, a preparation method and application thereof are provided. The preparation method includes in a small heat-resistant glass container, mixing 1,2,4,5-tetrakis (4-carboxyphenyl) benzene (H4TCPB) with N,N-dimethylformamide (DMF), heating until the solid is dissolved, placing the uncapped small glass container in a large heat-resistant glass container filled with some water, sealing the large glass container, standing and heating the large glass container in a constant-temperature oven to obtain colorless crystals, suction filtering to obtain a solid material, drying, grinding, and then dispersing the solid material in a solvent, performing ultrasonication in an ice-water bath, centrifuging to discard supernatant, and drying to obtain the hydrogen-bonded organic framework nanosheets.

Abstract: This specification discloses methods of enhancing the stability and performance of Eu2+ doped narrow band red emitting phosphors. In one embodiment the resulting phosphor compositions are characterized by crystallizing in ordered structure variants of the UCr4C4 crystal structure type and having a composition of AE1?xLi3?2yAl1+y?zSizO4?4y?zN4y+z:Eux (AE=Ca, Sr, Ba, or a combination thereof, 0<x<0.04, 0?y<1, 0<z<0.05, y+z?1). It is believed that the formal substitution (Al,O)+ by (Si,N)+ reduces the concentration of unwanted Eu3+ and thus enhances properties of the phosphor such as stability and conversion efficiency.

Abstract: Disclosed are films comprising Ag, In, Ga, and S (AIGS) nanostructures and at least one ligand bound to the nanostructures. In some embodiment, the AIGS nanostructures have a photon conversion efficiency of greater than 32% and a peak wavelength emission of 480-545 nm. In some embodiments, the nanostructures have an emission spectrum with a FWHM of 24-38 nm.

Abstract: A scintillation compound can include a rare earth element that is in a divalent (RE2+) or a tetravalent state (RE4+). The scintillation compound can include another element to allow for better change balance. The other element may be a principal constituent of the scintillation compound or may be a dopant or a co-dopant. In an embodiment, a metal element in a trivalent state (M3+) may be replaced by RE4+ and a metal element in a divalent state (M2+). In another embodiment, M3+ may be replaced by RE2+ and M4+. In a further embodiment, M2+ may be replaced by a RE3+ and a metal element in a monovalent state (M1+). The metal element used for electronic charge balance may have a single valance state, rather than a plurality of valence states, to help reduce the likelihood that the valance state would change during formation of the scintillation compound.

Abstract: A method for producing a cholesteric liquid crystal based shell is provided. The method comprises producing a cholesteric liquid crystal shell, solidifying the cholesteric liquid crystal shell so as to obtain a solid shell and perforating the solid shell. Also provided is a cholesteric liquid crystal based solid shell comprising a perforation. A coating composition comprising a plurality of cholesteric liquid crystal based solid shells, an item comprising a tag that comprises the cholesteric liquid crystal based solid shells and a method for authenticating the item are also provided.

Abstract: A liquid crystal polyester comprising a repeating unit (A1) represented by the formula (A1) and a repeating unit (A2) represented by the formula (A2). A molar ratio (phenolic hydroxyl groups derived from the repeating unit (A2)/phenolic hydroxyl groups derived from the repeating unit (A1)) is 1 or lower, as calculated by 1H-NMR. A ratio [repeating unit (A2)/repeating unit (A1)] is 1.2 or larger. The number of the repeating unit (A1) is 20% or more and the number of the repeating unit (A2) is 58% or more based on 100% of a total number of all repeating units of the liquid crystal polyester. A flow starting temperature of the liquid crystal polyester is 250° C. or more. —O—Ar11—CO—??(A1) —O—Ar12—CO—??(A2) Ar11 represents a phenylene group and Ar12 represents a naphthylene group. A hydrogen atom is optionally substituted.

Abstract: An abrasive particle including a shaped abrasive particle including a body having a plurality of abrasive particles bonded to at least one surface of the body of the shaped abrasive particle.

Abstract: A method of forming a shaped abrasive particle including extruding a mixture into a form, applying a dopant material to an exterior surface of the form, and forming a precursor shaped abrasive particle from the form.

Abstract: A magnetizable abrasive particle is presented. The magnetizable abrasive particle has a ceramic particle having an outer surface. The magnetizable abrasive particle also has a magnetic coating layer applied to the outer surface of the ceramic particle prior to sintering. The sintered magnetizable particle is responsive to a magnetic field.

Abstract: A method of electrochemical redox refrigeration includes inducing a flow of an electrochemical refrigerant that is in contact with a first electrode to a second electrode; applying an electrical potential difference between the first electrode and the second electrode, wherein the electrochemical refrigerant is oxidized at one of the first electrode and second electrode and reduced at another of the first electrode and second electrode; wherein the first electrode is at least partially thermally isolated from Joule heating in the electrochemical refrigerant and from activation losses in the second electrode by an action of the flow of the electrochemical refrigerant.

Abstract: A drilling fluid comprises an aqueous solution; a clay-based component comprising layered silicate; and a viscosifier additive comprising poly(acrylamide-co-diallyldimethylammonium chloride) (poly(AAm-co-DMAC)) polymer. The polymer comprises a number average molecular weight of from 10,000 g/mol to 2,000,000 g/mol. The layered silicate and poly(AAm-co-DMAC) reacts to form a silicate-poly(AAm-co-DMAC) complex within the aqueous solution. A mass ratio of the poly(AAm-co-DMAC) to the layered silicate is 1 to 8.

Abstract: A method is disclosed that includes adding a recirculation chemical composition to a hydrocarbon containing stream, wherein the recirculation chemical composition may be an emulsion breaker. The method may also include separating the hydrocarbon containing stream into a stream containing water and a stream containing oil; contacting the stream containing oil in a water wash unit; and removing residual emulsion breaker from the stream containing oil.

Abstract: The invention describes the use of both low-density oxidized polyethylene wax (LDoxPE) and high-density oxidized polyethylene wax (HDoxPE) as rheological additives in oil-based drilling fluids (OBF). This includes both 100% oil and invert emulsion drilling fluids in which the continuous phase is diesel oil, mineral oil, synthetic esters, synthetic olefins, or other organic fluid.

Abstract: A well cementing method is described for improving cementing quality by controlling the hydration heat of cement slurry. By controlling the degree and/or rate of hydration heat release from cement slurry, the method improves the hydration heat release during formation of cement with curing of cement slurry, improves the binding quality between the cement and the interfaces, and in turn improves the cementing quality at the open hole section and/or the overlap section. The cementing method improves cementing quality of oil and gas wells and reduces the risk of annular pressure.