Abstract: There is disclosed a process for the preparation of sulfenimides comprising: mixing, in a hydrocarbon solvent, a sulfenamide of the formula with an aldehyde of the formula R4CHO where X is a sulfur atom, a —C═N— group, or a —C═C— group, R1 and R2 are independently selected from the group consisting of hydrogen, alkyl, and aryl or may be joined to form a saturated or unsaturated ring or aromatic ring, R3 is alkyl or cycloalkyl, and R4 is a hydrocarbon radical wherein the carbon bearing the aldehyde function is bonded only to other carbon atoms, a substituted or unsubstituted aryl ring, or a heteroaromatic ring; and heating the mixture at a temperature and for a period of time sufficient to convert the sulfenamide to the sulfenimide.

Abstract: An axially elongated extruder screw includes a screw body having an axially extending extruding portion defined by a feed section at an inlet end of the screw, a metering section at an outlet end of the screw and a barrier section between the feed and metering sections. At least one helical primary flight extends about and is coaxial with the screw body. The primary flight and the screw body cooperate to form a channel in the feed section for conveying resinous material to the barrier section. The barrier section includes at least one helical secondary flight extending from the primary flight about the screw body which in turn defines a first surface of revolution between the primary and secondary flights. At least one helical tertiary flight is positioned between the primary and secondary flights and also extends about the screw body which defines a second helical surface of revolution between the secondary and tertiary flights.

Abstract: A polyurethane elastomer is disclosed that comprises the reaction product of: A) a prepolymer of at least one diisocyanate and at least one polyether polyol selected from the group consisting of a homopolymer of ethylene oxide, a homopolymer of propylene oxide, and a copolymer of ethylene oxide and propylene oxide, wherein free diisocyanate has been reduced to a level of less than 1% of the prepolymer; B) at least one alkylated8 aromatic diamine in a quantity sufficient to react with about 50% to about 105% of the available isocyanate content in the prepolymer; and C) at least one catalyst in a quantity sufficient to reduce the pot life to no more than two minutes; whereby said elastomer possesses high resilience and clarity and can be processed safely and at low cost.

Abstract: Dissolved silanes, silicones and silicates from solvents used in the slurry phase Direct Synthesis of alkoxysilanes are removed by adding a compatabilizing agent and water to generate filterable precipitates and reusable solvent. The solvents are thereby remediated and made suitable for reuse in Direct Synthesis processes. Foaming is reduced with the remediated solvent and silicon conversion rates are higher. The precipitates are easily filtered and retain negligible quantities of solvent.

Abstract: Disclosed herein is a method for making compounds having the structural formulae (I) or (II): ##STR1## wherein: X is a) phenyl; lower phenylalkoxy; phenoxy; or benzyl; or b) one substituent from group a) and one or more substituents selected from C.sub.1 -C.sub.4 alkoxy; hydroxyl; halogen; lower alkyl; and lower alkylthio; or c) along with the phenyl to which it is attached, forms a multiple fused ring heterocycle such as dibenzofuranyl; Y is H, C.sub.1 -C.sub.4 alkanoyl, C.sub.1 -C.sub.4 haloalkanoyl dialkoxyphosphoryl, alkylaminocarbonyl, haloalkylsulfonyl, or C.sub.1 -C.sub.4 alkoxy carbonyl; and R is H, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, C.sub.3 -C.sub.6 cycloalkoxy, haloalkyl, alkoxyalkyl, arylalkoxy, alkenyl, alkylthio, alkoxycarbonyl, alkylamino, heteroaryl, arylalkyl, haloalkoxy, aryloxy, or C.sub.3 -C.sub.

Abstract: A metallocene catalyst is provided which comprises the product obtained by combining (a) a metallocene procatalyst, preferably one containing a bridging group possessing at least two bulky groups, and (b) a cation-generating cocatalyst. A process for activating a metallocene procatalyst is also provided which comprises combining the metallocene procatalyst with the components of a cation-generating cocatalyst.

Abstract: A process for the preparation of derivatives of halo-but-2-enoic acids and esters high in 2-ene content, several of which are novel. The esters and their derivatives are useful as promoters for the polymerization of ethylene or the copolymerization of ethylene with .alpha.-olefins and, optionally, nonconjugated polyenes. The promoters can also be combined with transition metal compounds, e.g., vanadium, to form combination promoter-catalyst compounds.

Abstract: A cation-generating cocatalyst is provided for activating a metallocene procatalyst. The cocatalyst comprises (1) a metal- and/or metalloid-containing first component, e.g., an aluminum compound, (2) a neutral metal- and/or metalloid-containing second component, e.g., a borane compound, and (3) an anionic metal- and/or metalloid-containing third component, e.g., a metal containing borate.

Abstract: A method for evaluating the polymer growth inhibition ability of a compound or compounds is disclosed wherein the method comprises:A) weighing a dry seed of insoluble polymer capable of growing via a living polymerization mechanism;B) subjecting the seed of insoluble polymer to conditions capable of causing a living polymer to grow via a living polymerization mechanism;C) drying the seed; andD) weighing the seed a second time to determine any increase in weight;wherein the polymer growth inhibition ability of the compound or compounds is inversely proportional to any increase found in weight of the seed.

Abstract: The present invention is directed to novel alkyl glyceryl ether disulfonate compositions (ADEDS), alkylphenol polyethoxy sulfate-sulfonates, and ethoxylated alkylphenol sulfonates, and novel methods of preparation and uses thereof.

Abstract: This invention describes the use of novel blocked mercaptosilanes, wherein the hydrogen atom of the mercaptan functionality has been substituted, in filled polymers. The blocked mercaptosilanes described are unique in that they allow the mixing of fillers with organic polymers to proceed while remaining inert toward coupling to the polymer. The coupling reactions of these blocked mercaptosilicon compounds are triggered by addition of an appropriate deblocking agent, which preferably is tetramethylthiuram monosulfide.

Abstract: A motor mounting apparatus supports a motor relative to a base for relative rotation about a pivot axis to control tension in an endless loop driving element. A driving element emcompasses a drive member driven by the motor about a drive member axis and a driven member coupled to a load and driven by the driving member about a driven member axis to transmit power from the motor to the load. The apparatus includes a threaded shaft rotatable by a user about a shaft axis. The shaft axis is fixed relative to a first of the base and motor. A rider is carried by the threaded shaft so that rotation of the threaded shaft about the shaft axis produces longitundinal translation of the rider along the shaft axis relative to such first one of the base and motor. A rigid link has a first end pivotally coupled to the rider and a second end pivotally coupled to a second one of the base and motor.

Abstract: A process is disclosed for the direct preparation of alkanediol-diaminobenzoates comprising transesterifying an alkyl-p-aminobenzoate with a diol in the presence of a transesterification catalyst.

Abstract: A film extruder employing an internal deckle system including a pair of rectangular metal bars disposed in the pre-land area of the die one above the other with the opposing edges of each bar having a tapered surface. The tapered surfaces cause the bars to increase or decrease the total with of the flag when one of the bars is moved and to provide sufficient sealing pressure to effectively seal off the pre-land area. Preferable, the tapered wedge flags are disposed below the usual plug at each end of the extruder and apply sealing pressure against a deckle rod adjustably placed below the tapered wedge bars.

Abstract: A lubricating oil additive is disclosed that comprises the reaction product of:(a) an unsaturated or saturated ester or acid,(b) a diamine of the formula: ##STR1## (c) carbon disulfide, and (d) a molybdenum compound,wherein R.sub.8 is an alkyl group of 1 to 40 carbon atoms, R.sub.9 and R.sub.10 are independently selected aliphatic or aromatic moieties, W is oxygen, sulfur, or --CH.sub.2 --. The additive imparts friction modification and beneficial antiwear, extreme pressure, and oxidation stability properties to the lubricating oil.

Abstract: Phenolic amides, useful as stabilizers for organic materials such as polyols and polyurethanes, possess the general formula ##STR1## wherein n is 0 to 3, R.sub.1 is alkyl of from 1 to about 6 carbon atoms, R.sub.2 is hydrogen or alkyl of from 1 to about 6 carbon atoms, R.sub.3 is hydrogen or hydrocarbyl of up to about 20 carbon atoms, optionally containing one or more heterocyclic groups, R.sub.4 is hydrocarbyl of up to about 20 carbon atoms, optionally containing one or more heterocyclic groups, or R.sub.3 and R.sub.4 together with the nitrogen atom to which they are bonded are joined together to form a heterocyclic group, optionally containing one or more additional heterocyclic atoms.

Abstract: A method of (co)polymerizing vinyl and/or diene monomers comprising contacting the monomers with a (co)polymeriztion composition under conditions effective to (co)polymerize the monomers, wherein the (co)polymerization composition comprises: (a) an organic peroxide component, and (b) a heteropoly acid, in an amount effective to lower the onset temperature of decomposition of the organic peroxide component with the proviso that if the heteropoly acid is phosphomolybdic acid the organic peroxide is not a peroxydicarbonate.

Abstract: The present invention is directed to an improvement in a wire or cable system comprising a wire or cable portion, an insulation composition surrounding the wire or cable portion, a filler material surrounding the insulation composition and a jacket composition surrounding the filler material wherein either the insulation composition, the jacket composition, or both comprise at least one antioxidant, wherein the improvement comprises the inclusion in the filler material of a stabilizing mixture comprising at least two antioxidants, selected from at least two members of the group consisting of:(a) metal dithiocarbamate salts,(b) amine antioxidants, and(c) sterically hindered phenolic antioxidants,wherein the stabilizing mixture is present in the filler material in an amount that is effective for the reduction of the oxidation of the cable filling material, thereby reducing deterioration of the jacket and/or insulation.

Abstract: The present invention provides amine/amide catalysts for use in catalyzing the formation of polyurethane. The amine/amide catalysts, which have low fugitivity due to their reactivity with isocyanates, and good catalytic activity, have the structure ##STR1## wherein Q is C.sub.z H.sub.2z+1, or (CH.sub.2).sub.n N(R.sup.3).sub.k T, T is a monovalent C.sub.1 -C.sub.4 alkyl, amino-C.sub.1 -C.sub.4 -alkyl, mono-C.sub.1 -C.sub.4 -alkylamino-C.sub.1 -C.sub.4 -alkyl, or di-C.sub.1 -C.sub.4 -alkylamino-C.sub.1 -C.sub.4 -alkyl group, or T is a divalent alkyl, amine substituted alkyl, alkylaminoalkyl, or alkoxyalkyl group which forms with the nitrogen atom shown in structure (I) to which T is attached a cyclic structure which incorporates up to 6 carbon atoms in the ring as well as the nitrogen atom shown in structure (I), which cyclic structure may be substituted with C.sub.1 to C.sub.4 alkyl;k=0 or 1, being 1 if T is a monovalent group and 0 if T is a divalent group; R.sup.2 .dbd.H or C.sub.z H.sub.2z+1 ; R.sup.3 .dbd.

Abstract: An impact modifier for thermoplastic polyamides comprises:(A) an elastomeric olefin copolymer; and(B) a resinous olefin homopolymer or copolymerwherein at least one of (A) and (B) is maleated; andwherein the melt flow index of the resulting composition measured at 230.degree. C. and 2.16 kg weight is at least 3 g per 10 minutes.