Abstract: Organic polymers which are "hydroxyphenyl-substituted" and "ether-substituted" polypyrroles ("PP") linked through N-adjacent C atoms, are disclosed which are compactable, extrudable and are also electrical conductors. When such PPs are prepared by electrochemical deposition with an appropriate electrolyte, they are also soluble in commonly available solvents, provided at least one of the 3- or 4- positions of the pyrrole nucleus is substituted with a substituent having either a hydroxyphenyl, or an ether structure. By choice of the hydroxyphenyl and/or ether substituent on one of the substitutable positions (3- or 4-) of the pyrrole nucleus, or both, the PP may be tailored for use either as a semiconductor having a conductivity in the range from about 10.sup.-5 to about 10.sup.-2 S/cm, or a relatively good conductor having a conductivity in the range from about 10.sup.-2 to about 10.sup.2 S/cm.

Abstract: Under particular conditions, a cationic ring-opening polymerization of an oxirane monomer selected from the group consisting of an acyclic glycidyl ether, a cyclic glycidyl ether, and a haloalkyl epoxide, in the presence of a hydroxyl-containing backbone of a polymer ("HCB") and a particular catalyst, produces a polymerization having `living polymerization` characteristics, provided the OH groups are aliphatic OH groups and not aromatic OH groups. The result is a graft copolymer the molecular weight (mol wt) of which is directly proportional to the conversion of the monomer. The HCB, which may have from 1 to about 400 pendant OH groups, and more preferably at least 7 pendant OH groups, provides grafting sites for the grafting segments. Where a grafted segment contains halogen, the segment may be aminated. If the HCB is hydrophobic, the aminated block copolymer is amphiphilic.

Abstract: A universal cement composition is disclosed suitable for both natural and synthetic rubber based tire compounds which solves the tack and cured adhesion problems heretofore encountered at the tread splice region of radial and bias/belted tires. The composition disclosed contains 75 to 90 parts by weight ("wt") of a cis-polybutadiene elastomer, 10 to 25 parts by wt of natural rubber, 5 to 30 parts by wt of a phenolic tackifying resin, and 40 to 80 parts by wt of a fine reinforcing carbon black and has an AMEDA carbon black dispersion rating of from 96 to 99 percent.

Abstract: Vinyl chloride (VC) resins, particularly poly(vinyl chloride) (PVC) and chlorinated poly(vinyl chloride) (CPVC) are reinforced with glass fibers which have been sized with a particular aminosilane coupling agent and an alkylene oxide-containing film former. This combination of sizing components, among all others, generates allylic Cl atoms in the VC chain of the polymer. Though the VC resin contains an adequate amount of stabilizer to counter the formation of such allylic Cl atoms in the mass of the resin, enough are generated near the surface of the glass to cause a reaction with the aminosilane so as to bond the glass fibers to the VC resin so strongly that a composite only fails in coherent failure. The sizing consists essentially of (i) an aminosilane coupling agent having a reactive amine moiety which upon reaction with the VC resin results in a compound having a peak in a proton magnetic resonance spectra at 5.

Abstract: Elastomer compositions are provided which contain high molecular weight water-insoluble humic acid humates. The compositions show improved bloom resistance in both the uncured and the vulcanized or otherwise cured state. Methods to make sponge rubber are also disclosed in which the humic acid humate is the gas producing agent. A predominantly humic acid humate containing composition maintains a clean mold, and curing an uncured article coated with the humate at elevated temperature will clean metal molds which have dirty surfaces, particularly when green coated articles are vulcanized in contact with the mold's surfaces.

Abstract: A pneumatic radial tire is provided with a tread having from 1 part by weight of hydrated amorphous fine-particle silica per 3 parts of carbon black tread reinforcing filler, to about 3 parts by weight of the silica to 1 part of the carbon black. The amount of silica present is preferably in the range from about 18 parts to about 50 parts by weight per 100 parts of natural or synthetic rubber. When such a tread is compounded with a mercaptosilane in which the mercapto group is reversibly blocked, the tread provides reduced rolling resistance without loss of traction. Such reduction in rolling resistance without loss of traction is not observed when the silica is not coupled with the mercaptosilane coupling agent.

Abstract: A random copolymer which consists essentially of a copolymer of (i) acrylic acid or methacrylic acid (together "(meth)acrylic"), (ii) acrylamide or methacrylamide (together "(meth)acrylamide"), and (iii) and alkoxyalkyl (meth)acrylate ester ("AAE") present in specified relative proportions, is soluble in water, and is surprisingly effective in the treatment of industrial process water used in recirculating water systems, particularly with respect to inhibiting the deposition of calcium phosphate on surfaces of equipment used in such systems.

Abstract: A wire rack is mounted on the inner surface of a door of a cabinet at a suitable height, and a plastic bag with integral handle-loops is suspended from the rack without supporting the body of the bag. The wire rack comprises a main wire member and a wire bail which interconnects ends of the main wire member. The bail is used to store individual bags to be used, or a package of unused bags. The main member has tab-shaped protrusions formed by the sides of the main member, and the handle-loops are slipped around the tab-shaped protrusions so as to hold the bag in an open-mouthed material-receiving attitude.

Abstract: An infant's swing is disclosed which has a simple construction including a stationary main frame and a reciprocable infant-swinging structure. The swing may be operated with a commercially available rechargeable or alkaline battery or transformer supplying current at no more than about 24 volts. The low voltage current is used to actuate a solenoid fixedly mounted on the main frame in a unique manner so as to use a compensating extensible spring. This spring drivingly engages an infant's seat while simultaneously compensating for the difference between the linear velocity of the solenoid's plunger and the angular velocity of hangers supporting the reciprocable seat. Current is supplied to the solenoid in pulses having a duration of less than about 0.5 second so as to conserve the battery. The swing may also be operated with a D-C transformer providing current at about 2 amperes and preferably 3 or 4 volts.

Abstract: A simple economical multistage vulcanization process is disclosed for producing premium anomaly-free tires wherein the inner liner or curing bladder is supplied with dead end water and steam sequentially in several stages at high pressures which assure thorough diffusion of entrapped air. The internal steam pressure is 250 to 300 psig in stage I to effect rapid heat transfer, the internal water pressure in stage II is from 300 to 450 psig, and the internal steam pressure is 250 psig or higher in the first part of stage III. The overall cycle time for curing radial passenger car tires in "Bag-O-Matic" presses is reduced one minute or more by using internal steam pressures from 250 to 300 psig in stage I and III and reducing the steam pressure near the end of stage III to boil off the residual water.

Abstract: Cycloalk-2-enes and cycloalk-2-ene-dienes are found to be Michael acceptors which react with tosylmethylisocyanide to form bicyclo fused-ring compounds. A wide variety of substituents may be introduced on the alkylene ring with the aid of the carbonyl group(s) on the fused-ring compound.These carbonyl-containing bicyclo fused-ring compounds may be reduced to provide monomers which may be electrodeposited as substituted polypyrroles ("PP") which are electrically conductive, compactable and extrudable organic polymers. By choice of substituents on the alkylene ring which bridges the 3- and 4- carbon atoms of the pyrrole ring, the PP may be tailored for use either as a semiconductor having a conductivity in the range from about 10.sup.-5 to about 10.sup.-2 S/cm, or a relatively good conductor having a conductivity in the range from about 10.sup.-2 to about 10.sup.2 S/cm.

Abstract: Under particular conditions, a cationic ring-opening polymerization of a first oxirane monomer selected from the group consisting of an acyclic glycidyl ether, a cyclic glycidyl ether, and a haloalkyl epoxide, in the presence of a hydroxyl-containing organic material ("HCM"), for example a polymer (referred to herein as a `hydroxyl-prepolymer`), and a particular catalyst, produces a polymerization having `living polymerization` characteristics. The result is that molecular weight (mol wt) of the resulting polymer is directly proportional to the conversion of the monomer to said resulting polymer. This HCM serves as a chain propagator which initially furnishes OH groups as propagation sites. Subsequently, a second oxirane monomer, different from said first, is sequentially polymerized to yield a block copolymer. Branched block copolymers, or linear block copolymers of a HCM and (a) one or more glycidyl ethers, or (b) a haloalkyl epoxide and at least one glycidyl ether, may be prepared.

Abstract: Oxidation of chlorinated hydrocarbons ("CHC") is effected in a fluidized bed of alumina catalyst-support on which is deposited a "soft" metal as the active catalytic ingredient, and the bed is fluidized with a nitrogen-free oxygen-containing stream of HCl gas, in conjunction with steam. The steam, in a particular range of proportions relative to the HCl, stifles the production of free Cl without blinding the active catalyst sites so that conversion of the CHCs is always at least 95%. The process comprises contacting the CHCs in the vapor phase with a fluidized bed of a catalyst-support on which is deposited an effective amount of iron, or copper, or both, in an active form, sufficient to convert in excess of 95% of the CHC on a molar basis, and the bed is fluidized with HCl, superheated steam and oxygen substantially free of nitrogen.In a particular embodiment using a single ("catoxid") reactor, the effluent is purged of water, unconverted CHCs, CO.sub.

Abstract: An inclined hearth incinerator for the incineration of municipal, and industrial/commercial solid waste optionally in conjunction with sludge, with a controlled amount of combustion air allows the even distribution of underfire air to an upper hearth of plural stepped hearths in the floor of the incinerator. A clean-out assembly includes a piston which automatically cleans out feed-tubes for combustion air. The feed-tubes are protected by being embedded in the hearth, or being disposed beneath the hearth. The piston and a ram on the hearth may be interconnected for reciprocation by an actuating means so as to provide synchronous to-and-fro movement of the piston and ram.

Abstract: Reinforcing fabrics or cords, particularly those made from adhesive activated (AA) polyester yarn, or non-adhesive activated (non-AA) polyester yarn, or aramid yarn, maybe coated in a first of two dips in a two-step (double-dip) process, or more preferably in a single-step (single-dip) process, with an adhesive dispersion comprising a solid finely divided reversibly blocked polyisocyanate (RBP), having a majority of its primary particles smaller than 1 micron in average diameter, when the RBP is held in suspension as a substantially homogeneous dispersion with the aid of a hydrocarbyl disperser. The RBP is so held with less agitation than is required to produce a vortex in the dispersion. There is no "flaking" on the fabric after it is dried at a temperature higher than 250.degree. F. for less than about 3 minutes, and heat-set at a temperature above that at which the RBP is unblocked.

Abstract: Non-adhesive activated ("non-AA") polyester cord, or aramid cord, and fabrics made therefrom, may be coated in a two-step process, the first step of which is conventional. In the novel second step, after the cord is conventionally pre-coated in the first step, it is dipped in a R/F-free latex of a diene polymer in which an acrylic resin having a mol wt. in the range from about 100,000 to about 1,000,000 is dispersed. The acrylic resin resin is a copolymer selected from the group consisting of two or more monomers, one of which is (meth)acrylic acid and another is a lower alkyl(meth)acrylic acid ester, the monomers having the configuration ##STR1## wherein, R represents H, methyl, ethyl, Cl or CN, and, X represents hydroxyl (OH), hydroxymethylamino (NHCH.sub.2 OH), or alkoxy (O-alkyl) having from 1 to 4 carbon atoms; and, optionally, in addition the copolymer may include a vinyl aromatic monomer having from 8 to about 18 carbon atoms.

Abstract: Novel polysubstituted 2-keto-1,4-diazacycloalkanes are powerful stabilizers for materials subject to ultraviolet (UV) light degradation, particularly for polyolefins. The cyclic 2-keto compounds of this invention have (a) a fixed two-carbon bridge between the N.sup.1 and N.sup.4 atoms of the diaza ring, the remaining portion of the ring having a variable length bridge of two or more carbon atoms, (b) and N-adjacent carbonyl in the fixed two-carbon bridge, and (c) at least one N.sup.4 -adjacent carbon atom of the diaza ring is polysubstituted, that is, has two substituents which may be cyclizable.Compositions containing (a) the polysubstituted 2-keto-1,4-diazacycloalkanes of this invention, and (b) prior art polysubstituted 2-keto-1,4-diazacycloalkanes, exhibit excellent stability to UV light.

Abstract: A known base-induced catalytic ketoform synthesis can now be carried out without sacrificing the directivity of the prior art process, but non-catalytically, that is, in the absence of the phase transfer catalyst heretofore required, provided the ketone/araldehyde is present in large excess from about 2 to about 25 times the calculated molar amount necessary to yield the reaction product. This synthesis obviates the problems of separating and recovering a phase transfer catalyst used in the prior art process.

Abstract: A process is taught in which a flexible, reinforcing travelling web may be uniformly, thinly transfer-coated, on both sides of the web simultaneously, with a low-viscosity liquid or mixture of monomers which may or may not wet the web, but does not wet the surface of a substrate on which the web and mixture are deposited. The liquid or mixture is first curtain-coated on an applicator curtain against which the web moves in controlled contact. An apparatus is provided for transfer-coating a travelling web with a low-viscosity liquid which is first curtain-coated on an applicator curtain.