Abstract: A resorcinolic novolac resin composition comprising the reaction product of (i) an aldehyde or ketone, and (ii) aralkyl-substituted resorcinol and resorcinol, where the moles of the aralkyl-substituted resorcinol to the total moles of the resorcinol and aralkyl-substituted resorcinol is 0.01:1 to 0.4:1.

Abstract: A rubber composition comprises at least one phenol/aldehyde resin based on at least one aromatic polyphenol comprising at least one aromatic ring bearing at least two hydroxyl functions in the meta position relative to one another, the two positions ortho to at least one of the hydroxyl functions being unsubstituted, and at least one aromatic polyaldehyde selected from 1,3-benzenedicarboxaldehyde, 1,4-benzenedicarboxaldehyde and mixtures of these compounds, the rubber composition having a nominal secant modulus at 10% elongation, measured according to standard ASTM D 412, 1998, of greater than or equal to 25 MPa.

Abstract: A positive-type photosensitive resin composition includes (A) a phenol resin modified by a compound having an unsaturated hydrocarbon group having 4 to 100 carbon atoms; (B) a compound that produces an acid by light; (C) a thermal crosslinking agent; and (D) a solvent. The positive-type photosensitive resin composition according to the present invention can be developed by an alkaline aqueous solution, and an effect thereof is that a resist pattern having sufficiently high sensitivity and resolution, excellent adhesion, and good thermal shock resistance can be formed.

Abstract: A polyolefin-polybutadiene block-copolymer and a tire tread composition comprising the polyolefin-polybutadiene block-copolymer, the composition comprising, by weight of the composition, within the range from 15 to 60 wt % of a styrenic copolymer, processing oil, filler, a curative agent, and from 4 to 20 wt % of a polyolefin-polybutadiene block-copolymer, wherein the polyolefin-polybutadiene block-copolymer is a block copolymer having the general formula PO-XL-fPB; where “PO” is a polyolefin block having a weight average molecular weight within the range from 1000 to 150,000 g/mole, the “fPB” is a functionalized polar polybutadiene block having a weight average molecular weight within the range from 500 to 30,000 g/mole, and “XL” is a cross-linking moiety that covalently links the PO and fPB blocks; and wherein the maximum Energy Loss (Tangent Delta) of the immiscible polyolefin domain is a temperature within the range from ?30° C. to 10° C.

Abstract: The invention relates to a rubber composition comprising a rubber and a processing additive wherein the processing additive is a functional reactive diluent having at least one functional group in the molecule which is not an olefinic unsaturation, to a process of compounding such rubber compositions, and to the use thereof.

Abstract: Organic gels of resorcinol-formaldehyde type, carbon-based materials of adjusted porosity derived therefrom by pyrolysis. Such materials may be used, in particular, for the production of electrodes.

Abstract: The present invention is a method for manufacturing a rubber composition containing a rubber component, a resin, a reinforcing filler and a crosslinking agent, and the method contains: a first step of adding the resin to the rubber component to produce a master batch; a second step of kneading the master batch with the reinforcing filler to produce a filled master batch; and a third step of kneading the filled master batch with the crosslinking agent, thereby providing a rubber composition having higher elasticity and large breaking elongation.

Abstract: A resol-type para-octylphenol-formaldehyde co-condensation resin and a method for producing the same are provided, the resol-type para-octylphenol-formaldehyde co-condensation resin having a content of a para-octylphenol monomer of 1 wt. % or less, having a total content of an aliphatic hydrocarbon, a halogenated aliphatic hydrocarbon, an aromatic hydrocarbon, a halogenated aromatic hydrocarbon, and an alcohol having 1 to 8 carbon atoms of 1 wt. % or less, the aliphatic hydrocarbon, the halogenated aliphatic hydrocarbon, the aromatic hydrocarbon, the halogenated aromatic hydrocarbon, and the alcohol having a boiling point of 60° C. or more, having a softening point of 70 to 105° C., and having an acid value of 20 to 28 KOHmg/g. The resol-type para-octylphenol-formaldehyde co-condensation resin can be used as a resin cross-linking agent for a rubber.

Abstract: Provided are a rubber composition for a tire cord topping, a breaker edge strip, a breaker cushion, or a strip adjacent to cords, which achieves a balanced improvement in handling stability, fuel economy, durability, ride quality, and adhesion; and pneumatic tires including the same. The rubber composition includes: an isoprene-based rubber; a phenol resin and/or an alkylphenol resin; and a partial condensate of HMMM and/or a partial condensate of HMMPME, wherein an amount of the isoprene-based rubber is 60% by mass or higher per 100% by mass of the rubber component; and a combined amount of the phenol resin and the alkylphenol resin is 2-3.9 parts by mass, a combined amount of the partial condensate of HMMM and the partial condensate of HMMPME is 0.5-5 parts by mass, and an amount of silica is at most 15 parts by mass, each per 100 parts by mass of the rubber component.

Abstract: A resin composition which has low stress, and good adhesive property in high temperature and high moisture environments and which is useful in adhesive applications in low stress, high moisture sensitivity level electronic packages. Preferably, a flexible epoxy anhydride adduct modified solid bismaleimide and solid benzoxazine resin composition that can survive high temperature and high moisture conditions and maintain good adhesion strength and minimize the stress resulting from a coefficient of thermal expansion mismatch between a silicon die and a substrate which is Ball Grid Array solder mask or a smart card polyethylene terephthalate or silver or copper metal lead frame.

Abstract: Toughened thermosetting resins comprising thermosetting resins and rubber particles having an average particle size in the range of 20 to 500nm. The toughened resins are obtained by mixing a fully vulcanized powdery rubber having an average particle size in the range of 20 to 500nm with thermosetting resin prepolymers and then curing them. The toughened thermosetting resins comprise rubber phases having a small, uniform and stable particle size, which results in a very significant toughening effect, especially when crazes rapidly grow (as in a standard Izod impact test). The toughened thermosetting resins are excellent in impact resistance, strength, modulus and heat resistance, and when appropriately toughened, the thermosetting resins can be enhanced in terms of impact strength, glass transition temperature and heat distortion temperature.

Abstract: The present invention is directed to pneumatic tire comprising at least one component, the at least one component comprising a rubber composition comprising: at least one diene-based rubber; and from 1 to 50 phr of a particulate polyamide having a particle size of from 0.1 to 1 micron, wherein the particulate polyamide is substantially spherical and wherein the particulate polyamide has a melting temperature greater than 210° C. as measured by ISO 11357.

Abstract: Provided is a rubber composition that comprises a rubber component of at least one of natural rubber and synthetic rubber and a resin composition containing a novolak-type resorcin resin and a resol-type phenolic resin in which the content of the dimethylene ether group is within a specific range. Not using hexamethylenetetramine or hexamethoxymethylmelamine as a curing agent, the curability and the thermal stability of the resin composition have been enhanced; and the rubber composition has characteristics of high elasticity, large elongation at breakage and low heat generation. Also provided is a tire which comprises the rubber composition in the tire bead part thereof and, therefore, has improved durability in use thereof while concerning for the environmental safety.

Abstract: A method of using at least one polymerisable resin R1 is disclosed. According to some aspects, the resin R1 is selected from the group consisting of epoxidised polybutadiene resins, epoxidised polyisoprene resins, epoxidised polysiloxane resins, epoxidised triglyceride resins and epoxidised polyether resins. The resin R1 having at the non-polymerised state a total mass loss (TML) value lower than about 10%, a recovered mass loss (RML) value lower than about 10%, and a collected volatile condensable material (CVCM) value lower than about 1%, as determined in accordance with standard ECSS-Q-70-02A of the European Space Agency. The resin R1 also characterized by an epoxide equivalent weight of about 100 to 600 g/mole. The resin is configured for the manufacture of a composite material for use in space, and more specifically, a composite material of a Gossamer structure. Polymerisable resin compositions are also disclosed which are useful in the manufacture of composite materials for use in space.

Abstract: Ink receiving particles is provided. The ink receiving particles includes polymer particles, the polymer particles including a resin including an acidic group and a polyoxyethylene chain, the acidic group at least partially having a salt structure.

Abstract: Organic gels of resorcinol-formaldehyde type, carbon-based materials of adjusted porosity derived therefrom by pyrolysis. Such materials may be used, in particular, for the production of electrodes.

Abstract: A composite prepared using a thermosettable epoxy resin composition having, as components: (1) an epoxy resin; (2) an epoxidized cycloaliphatic dicyclopentadiene phenolic resin; (3) an optional epoxidized bisphenol-A novolac resin; (4) an optional oligomeric butadiene; (5) an optional organic solvent; and (6) an alkylphenol novolac resin, the alkylphenol novolac resin serving as a curing agent. The composite so prepared may have good physical properties and superior a electrical properties as compared to conventional composites, such as laminates. The prepregs used to make the laminates may have a better surface appearance as well.

Abstract: Aspects of the invention include a method of curing a rubber composition comprising providing a rubber; intimately contacting a curative agent with the rubber; wherein the curative agent consists essentially of a phenol formaldehyde resin, a metal oxide and a carboxylic acid metal salt. Another aspect of the present invention is to a method of curing a rubber composition comprising providing a rubber; intimately contacting a curative agent with the rubber; wherein the curative agent comprises a phenol formaldehyde resin and carboxylic acid metal salt; and wherein halogen-donating species are absent from the rubber and curative agent.

Abstract: Described herein is a composition preparation process of forming an unkneaded mixture of (a) 100 parts by weight of an ethylene-?-olefin-unconjugated polyene copolymer rubber synthesized with a metallocene catalyst, (b) 20 to 350 parts by weight of a crystalline olefin resin, (c) 2 to 25 parts by weight of an alkylphenol-formaldehyde resin, and (d) 5 to 120 parts by weight of at least one polymer selected from the group consisting of a copolymer of a vinyl aromatic compound with a conjugated diene compound, a hydrogenated copolymer obtained by hydrogenating a copolymer of a vinyl aromatic compound with a conjugated diene compound, and a hydrogenated polymer obtained by hydrogenating a polymer of a conjugated diene compound, and kneading the formed unkneaded mixture to form a thermoplastic elastomer composition. This process produces a composition that is excellent in compression set and oil resistance at high temperatures and in flexibility and moldability.

Abstract: There is disclosed a glass-fiber coating liquid for forming a coating layer on a glass fiber cord, prepared in the form of an emulsion by dispersing a phenol resin, a vinylpyridine-stylene-butadiene copolymer (B) and a chlorosulfonated polyethylene (C) into water to form a coating layer on a glass fiber cord, wherein the phenol resin is a monohydroxybenzene-formaldehyde resin (A) obtained by reaction of monohydroxybenzene (D) and formaldehyde (E).

Abstract: A composition comprising (i) a dynamically-cured rubber, (ii) from about 20 to about 300 parts by weight of a thermoplastic resin per 100 parts by weight rubber, (iii) from 0.2 to 0.9 parts by weight stannous chloride per 100 parts by weight rubber, and (iv) from 0.25 to 4.0 parts by weight metal oxide per 100 parts by weight rubber.

Abstract: As a rubber composition having an elasticity further increased as compared with the conventional rubber composition while preventing the lowering of the fracture resistance, there is provided a rubber composition comprising a rubber component of at least one of natural rubber and synthetic diene rubbers and a phenolic resin compounded therein and represented by the following formula (I): (wherein R0 is a hydrogen atom, an alkyl group, a phenyl group or a methylol group, and each of R1 and R2 is an arylene group, an alkylene group having a carbon number of 2-10, an aralkylene group, a cycloalkenylene group or a cycloalkadienylene group, and n is 0-10).

Abstract: A modified alkylresorcinol resin is prepared by reacting one or more alkylresorcinols with one or more aldehydes and optionally an olefinically unsaturated compound. The reaction may be carried out in the presence of a catalyst. The resulted modified alkylresorcinol resin can be used as a methylene acceptor that reacts with methylene donors in vulcanizable rubber compositions.

Abstract: A vulcanizable adhesive composition, which comprises 100 parts by weight of phenolxylylene resin or phenolbiphenyl resin, 10 to 1,000 parts by weight of resol-type phenol resin, 0 to 1,000 parts by weight of novolak-type phenol resin, 10 to 1,000 parts by weight of unvulcanized nitrile rubber and 10 to 500 parts by weight of chlorinated polyethylene, is effectively applied to (hydrogenated) nitrile rubber with a nitrile content of 18 to 48%, and has a suppression effect on a decrease in the adhesiveness even if exposed to dip in various cryogenic liquids such as flon gas, polyalkylene glycol, water, etc. for a long time.

Abstract: A thermoplastic composition includes a functionalized poly(arylene ether) and a copolymer of (a) ethylene or an ?-olefin, and (b) an alkyl(meth)acrylate. Optional components in the composition include an impact modifier and a flame retardant. The composition is useful for fabricating wire and cable insulation.

Abstract: A modified resorcinol resin is prepared by reacting a phenolic compound (e.g., resorcinol) with an olefinically unsaturated compound (e.g., styrene) and two types of aldehyde: a formaldehyde and an alkyl aldehyde (e.g., butyraldehyde). The reaction is typically carried out in the presence of an acid catalyst. The resulting resin has a lower softening point and can be used as a methylene acceptor compound in a vulcanizable rubber composition.

Abstract: A curable composition includes a functionalized poly(arylene ether); an alkenyl aromatic monomer; an acryloyl monomer; and a polymeric additive having a glass transition temperature less than or equal to 100° C. and a Young's modulus less than or equal to 1000 megapascals at 25° C. The polymeric additive is soluble in the combined functionalized poly(arylene ether), alkenyl aromatic monomer, and acryloyl monomer at a temperature less than or equal to 50° C. The composition exhibits low shrinkage on curing and improved surface smoothness. It is useful, for example, in the manufacture of automotive body panels.

Abstract: A silane-modified phenolic resin is prepared by reacting a phenolic compound (e.g., resorcinol) with an aldehyde to produce a phenolic novolak resin. The phenolic novolak resin is further reacted with at least one silane compound to produce the silane-modified phenolic resin. The reaction is typically carried out in the presence of an acid or base catalyst. The resulting resin has a lower softening point and can be used as a methylene acceptor compound in a vulcanizable rubber composition.

Abstract: 0.3-5.0 parts by weight of phenol resin, sulfur, and vulcanizing accelerator are added to 100 parts by weight of EPDM rubber. They are kneaded, and the EPDM rubber is vulcanized and molded. Generation of blooming can be suppressed without inhibiting the vulcanizing speed and the vulcanizing start timing.

Abstract: 0.3-5.0 parts by weight of phenol resin, sulfur, and vulcanizing accelerator are added to 100 parts by weight of EPDM rubber. They are kneaded, and the EPDM rubber is vulcanized and molded. Generation of blooming can be suppressed without inhibiting the vulcanizing speed and the vulcanizing start timing.

Abstract: A procedure for removing a water-insoluble finish from aramide fibers, wherein the aramide fibers are present as short-cut, random fibers or flat textile materials and are treated with an agent that contains at least one hydrophilic fluid.

Abstract: A modified resorcinol resin is prepared by reacting a phenolic compound (e.g., resorcinol) with an olefinically unsaturated compound (e.g., styrene) and two types of aldehyde: a formaldehyde and an alkyl aldehyde (e.g., butyraldehyde). The reaction is typically carried out in the presence of an acid catalyst. The resulting resin has a lower softening point and can be used as a methylene acceptor compound in a vulcanizable rubber composition.

Abstract: The invention relates to rubber compounds comprising at least one double bond-containing rubber, additions of rubber gels, phenolic resin adducts or phenol/formaldehyde condensation products, such as resols or novolaks, and optionally, further fillers and rubber auxiliary substances, and the vulcanizates and molded rubber articles produced from them. The rubber compounds according to the present invention are characterized in the uncrosslinked state by good processability (compound viscosity ML 1+4/100° C.<60 ME) and in the vulcanized state by Shore-A hardness values/23° C.>60, high impact resilience values E/23° C.>60% and a low specific density. The vulcanizates are suitable for the production of industrial rubber articles and for various tire components, such as roll coverings, conveyor belt coverings, belts, spinning cops, seals, golf ball cores, shoe soles and bead compounds, tire carcasses, subtread compounds and tire sidewalls.

Abstract: A process for reducing the heat evolution on dynamic stressing of vulcanised rubber products, using for this purpose, in vulcanizable rubber mixtures, mixtures made from non-selfcuring novolaks A and from unetherified or partially etherified triazine resins B, as a combination of reinforcing resin and curing agent.

Abstract: The present invention relates to a rubber stock for bead wire compounds comprising (A) based on 100 parts by weight of rubber (1) from about 5 to about 40 weight percent of a carboxylated acrylonitrile-diene rubber having an acrylonitrile content ranging from about 15 to 45 percent by weight; and (2) from about 60 to about 95 weight percent of a non-carboxylated rubber selected from the group consisting of natural rubber, polyisoprene, polybutadiene, styrene-butadiene rubber, styrene-isoprene-butadiene rubber, styrene-isoprene rubber, isoprene-butadiene rubber and mixtures thereof; (B) from about 0.1 to about 10 phr of a methylene acceptor; and (C) from about 0.1 to about 10 phr of a methylene donor.

Abstract: 0.3-5.0 parts by weight of phenol resin, sulfur, and vulcanizing accelerator are added to 100 parts by weight of EPDM rubber. They are kneaded, and the EPDM rubber is vulcanized and molded. Generation of blooming can be suppressed without inhibiting the vulcanizing speed and the vulcanizing start timing.

Abstract: Methods for preparing formaldehyde-free resorcinol resins are disclosed. The methods generally comprise reacting resorcinol first with dicyclopentadiene and then reacting that mixture with an olefinic compound. The resins produced by this method are also disclosed, as are rubber compositions utilizing the present resins. The resins are characterized as having a free resorcinol content of about 1 wt. % or less, and yielding a suitable softening point when used in rubber applications.

Abstract: A process for forming a thermoplastic vulcanizate compromising the steps of dynamically vulcanizing a rubber within a blend that comprises the rubber and a thermoplastic polymer, where said step of vulcanizing is carried out by using a phenolic resin in the presence of a catalyst system formed by combining a metal halide and a metal carboxylate. Also, a thermoplastic vulcanizate having low moisture pick-up with a technologically useful cure.

Abstract: A method for increasing the damping properties of tire rubber comprising the steps of adding an unsaturated damping additive to a vulcanizable composition of matter, and processing the vulcanizable composition of matter containing the damping additive into tire rubber.

Abstract: A vulcanizate that has improved damping properties where the vulcanizate is prepared by the steps comprising blending an unsaturated damping additive within a vulcanizable composition of matter, wherein the vulcanizable composition of matter includes a vulcanizable elastomer, and effecting vulcanization of the elastomer.

Abstract: A vulcanized rubber composition which comprises the vulcanization reaction product of 100 parts by weight of at least one natural or synthetic rubber; 0.1 to 25 parts by weight of sulfur and/or a sufficient amount of a sulfur donor to provide the equivalent of 0.1 to 25 parts by weight of sulfur; 10-100 parts by weight of at least one silica filler; 0.1 to 5 parts by weight of at least one anti-reversion coagent comprising at least two groups selected from citraconimide and/or itaconimide groups; and a sufficient amount of a least one cure-improving resin to significantly increase the delta torque of the rubber composition during the vulcanization process as compared to the delta torque of a similar rubber composition in the absence of the cure-improving resin, is disclosed. Also disclosed is a process for the vulcanization of this rubber composition, and articles of manufacture comprising the vulcanized rubber composition.

Abstract: A high modulus composition based on a mixture of a hydrogenated acrylonitrile butadiene rubber which has been modified with either zinc methacrylate or a combination of zinc oxide and methacrylic acid and an unmodified hydrogenated acrylonitrile butadiene rubber for use in high load-bearing synchronous drive belts and belts made therewith.

Abstract: A vehicle for lithographic printing ink is prepared by using an improved binder resin of petroleum resin-modified phenol resin, in which the melt viscosity of the binder resin is maintained below a certain level to improve the workability in polymerization process and the misting in printing press is reduced by using the improved binder resin. In the preparation of the binder resin, acid modified hydrocarbon resin (A) is prepared by reacting components (a) mainly comprising five-membered cyclic compounds or their Diels-Alder reaction products with the components (b) comprising unsaturated carboxylic acids or their anhydrides, and said acid modified hydrocarbon resin (A) is then reacted with phenol resin (B) in which portions of the phenol resin are fed one after another, thereby producing said binder resin having the properties of: high weight average molecular weight, low melt viscosity and low ratio of melt viscosity to solution viscosity.

Abstract: Phenolic resin curatives having a majority of dibenzyl ether linkages were unexpectedly found to be very effective in curing unsaturated rubbers in a blend of a crystalline polyolefin and said rubber. Their effectiveness exceeds that of conventional phenolic resins for many thermoplastic vulcanizate compositions allowing for the reformulation of the recipes with lower amounts of curatives and equivalent or superior physical properties in the resulting thermoplastic vulcanizate.

Abstract: A vulcanizable elastomer having at least one pendant reactive amino group. The elastomer is vulcanized by using a phenolic-resin curative essentially in the absence of an activation catalyst, to form a vulcanizate. Also provided is a thermoplastic elastomeric vulcanizable composition of matter, employing the elastomer having the pendent reactive amino group, which may be dynamically vulcanized without the use of an activation catalyst. Further provided is a method for vulcanizing an elastomer having at least one pendent reactive amino group by utilizing a phenolic vulcanizing agent without the use of a catalyst.

Abstract: An improved oxazolidine-based hardener to be used with a resorcinol resin or a tannin resin as the adhesive for the bonding of wood articles. Preferably, an oxazolidine is combined with particulate silica, and the resin is combined with a base such as NaOH. The adhesive based on the improved hardener can be used to glue wood particles to pass wet strength requirements after the glue is cured at room temperature for under 24 hours. The improved hardener composition is storage stable; it can be prepared anytime before its use and, thus, eliminate the need to prepare a hardener immediately prior to the glue use. Since it is formaldehyde-free; it eliminates the safety issues associated with handling formaldehyde or paraformaldehyde. Also, the hardener provides flexible gel time or working time. Since the resins can be cured at room temperature, heating in an oven is not needed but could be used to reduce curing time. If radio frequencies are used to cure the resins, the exposure time can be reduced.

Abstract: An adhesive tape for electronic parts, comprising(a) a heat resistant base film, and(b) an adhesive layer laminated on at least one surface of said base film, said adhesive layer comprising(i) a resol type phenol resin, and(ii) an acrylonitrile/butadiene copolymer,in a proportion of from 100 to 500 parts by weight of said resol type phenol resin per 100 parts by weight of said acrylonitrile/butadiene copolymer,said resol type phenol resin being selected from the group consisting of bisphenol A type resins, alkylphenol type resins, phenol type resins and their co-condensed type phenol resins which contain as the phenol component at least one member selected from the group consisting of bisphenol A, alkylphenols and phenol.

Abstract: There is provided a co-condensation product obtainable by subjecting a p-alkylphenol to reaction with formaldehyde in the presence of an alkali catalyst to prepare a resol type condensate, and subjecting the resulting resol type condensate to reaction with a m-substituted phenol such as resorcin in the presence of an acid catalyst, wherein the content of the m-substituted phenol is not higher than 4% by weight, and the content of a component having a molecular weight not higher than 1,000 excluding both the p-alkylphenol and the m-substituted phenolis at least 25% by weight based on the total weight of the co-condensation product. This co-condensation product is low in fuming and in hygroscopic properties, exhibits excellent adhesiveness in vulcanizing adhesion between rubber and a reinforcing material, and further provides a vulcanized rubber article of high hardness.

Abstract: An adhesive tape for electronic parts, comprising (a) a heat resistant base film, and (b) an adhesive layer laminated on at least one surface of said base film, said adhesive layer comprising(i) a resol type phenol resin, and(ii) an acrylonitrile/butadiene copolymer,in a proportion of from 100 to 500 parts by weight of said resol phenol resin per 100 parts by weight of said acrylonitrile/butadiene copolymer, said resol type phenol resin being selected from the group consisting of bisphenol A type resins, alkylphenol type resins, phenol type resins and their co-condensed type phenol resins which contain as the phenol component at least one member selected from the group consisting of bisphenol A, alkylphenols and phenol.

Abstract: Hydrogenated butadiene polymers having terminal functional groups have minimum viscosity at any molecular weight when the 1,2-addition is between 30% and 70% Hydrogenated butadiene polymers having about two terminal hydroxyl groups per molecule have surprisingly lower viscosities at 30% to 70% 1,2-addition than similar polymers having either higher or lower amounts of 1,2-addition. The polymers are useful in making coatings, sealants, binders, and block copolymers with polyesters, polyamides, and polycarbonates.