Abstract: Disclosed is a method of selective preparation of ditertiary butyl peroxide from tertiary butyl hydroperoxide and t-butanol which comprises reacting said tertiary butyl hydroperoxide and t-butanol over a Beta-zeolite catalyst under hydroperoxide conversion conditions.

Abstract: A process for separating phthalimido-peroxycaproic acid (PAP) from solutions in organic solvents, wherein the organic solvents have a solubility in water equal to or lower to 10% by weight, is provided. The process employs the following steps:(a) dispersing the solution in an aqueous medium to form a suspension;(b) bubbling an inert gas into the resulting suspension; and(c) recovering PAP from the suspension.

Abstract: A process for the separation of ditertiary butyl peroxide form tertiary butanol is provided which includes the step of dehydrating the tertiary butanol to isobutylene and water.

Abstract: The present invention provides a process for the production of dialkyl peroxides by reaction of an alcohol and/or an olefin with an organic hydroperoxide, using a solid acidic zeolite catalyst.

Abstract: The present invention provides a process the production of dialkyl peroxides by reaction of an alcohol and/or an olefin with an organic hydroperoxide, using an acidic resin catalyst, especially a highly cross-linked hydrophobic acidic resin catalyst.

Abstract: A method for conjointly preparing tertiary butyl alcohol and ditertiary butyl peroxide wherein a solution of a tertiary butyl hydroperoxide feedstock in tertiary butyl alcohol is charged to a hydroperoxide decomposition reaction zone containing a catalytically effective amount of a hydroperoxide decomposition catalyst consisting essentially of palladium supported on pelleted carbon, and is brought into contact with the catalyst in liquid phase under hydroperoxide decomposition reaction conditions to convert the tertiary butyl hydroperoxide to decomposition products, principally tertiary butyl alcohol and ditertiary butyl peroxide.

Abstract: The invention relates to a compound having the Formula (I) ##STR1## in which n=1, 2, 3 or 4 and m=1, 2, 3, 4, 5, 6, 7 or 8. The invention also relates to a method for the preparation of the above-described compound by bringing a cycloalkyl hydroperoxide having 5 to 12 carbon atoms into contact with a cycloalkene having 5-8 carbon atoms, under the influence of a metal compound as catalyst, the metal being chosen from groups VIB, VIIB and VIII of the periodic system. The reaction takes place at a temperature of 0.degree.-80.degree. C.

Abstract: An integrate process is provided for the production of ditertiary butyl peroxide wherein isobutane oxidate containing tertiary butyl alcohol and tertiary butyl hydroperoxide is reacted in the presence of an aqueous acidic catalyst, the reaction mixture is phase separated, the aqueous catalyst is recovered and recycled, and the product peroxide is recovered from the organic phase by water extraction.

Abstract: The present invention relates to surface-active peroxides which can be employed as emulsifying initiators for the preparation of low-electrolyte polymer dispersions having a low tendency to foam.

Abstract: The present invention provides a process for the production of dialkyl peroxides by reaction of an alcohol and/or an olefin with an organic hydroperoxide, using an inorganic heteropoly and/or isopoly acid catalyst.

Abstract: A substantially water-free, non-dusting and flowable composition comprising an organic peroxide, a hydrocarbyl phthalate, and at least one phlegmatization agent is provided wherein the phlegmatization agent is selected from the group consisting of a polyester and a glycol-based aliphatic carboxylic acid ester, and mixtures thereof. The composition is prepared by: (1) substantially dissolving the hydrocarbyl phthalate and phlegmatization agent in a solvent to form a plasticizer mixture; (2) substantially dissolving the organic peroxide in the plasticizer mixture to form an organic peroxide-plasticizer mixture; (3) cooling the organic peroxide-plasticizer mixture whereby a crystallized composition is formed; and (4) recovering the crystallized composition.

Abstract: A process for the preparation of an aqueous suspension of a solid free-radical forming initiator, a plant for the preparation, an initiator suspension and use of the suspension in polymerization of ethylenically unsaturated monomers. The process for the preparation of the suspension comprises the steps of:(a) heating the initiator to its melting point;(b) finely dividing the initiator in water while it is in a molten state;(c) rapid cooling so that the initiator is in a molten state for a period of time which is less than about 5 minutes.The initiator suspension has very small particles and a narrow particle size distribution whereby at least 50% by weight of the particles are smaller than 5 .mu.m and at least 90% by weight of the particles are smaller than 10 .mu.m.

Abstract: The mixture consists of at least one organic peroxide, at least one hydroquinone derivative of the general formulae I and/or II and/or III ##STR1## wherein R and R.sup.1, which may be identical or different, stand for H or t-alkyl, and X stands, for example, for C.sub.1-18 -alkylene, and a crosslinkage promoter, and permits the crosslinkage of polymers and at the same time extends the scorch time, which must be understood as the processing time.

Abstract: The peroxides which include the O.sup.17 isotope, especially the hydrogen peroxides and peroxides and hydroperoxides prepared therefrom, are well adapted as nonradioactive labeled compounds for use in the medicinal and biological arts.

Abstract: This invention relates to an improved process for preparing dihydroperoxyalkanes and, particularly, dimethyldihydroperoxyhexane. The improvement resides in utilizing a tetrahydrofuran derivative which is a liquid as a feedstock. This feedstock then is reacted with hydrogen peroxide in the presence of sulfuric acid to form the dihydroperoxide.

Abstract: Described herein is an isocyanate-reactive compound containing at least one linkage of the formula:--X--X--wherein X is independently in each occurrence --NR--, --S--, or --O--; R is independently in each occurrence hydrogen, C.sub.1-10 alkyl, aryl, or arylene; and at least one N, S, or O atom of the above formula is bonded to an aryl or arylene group. Also disclosed are isocyanate-reactive compositions containing the above compound and flexible polyurethane foams prepared therefrom.

Abstract: Multifunctional cyclobutarene peroxide polymerization initiators comprising at least one cyclobutarene moiety linked through the aromatic ring to at least one peroxide containing group which catalyze free radical polymerizations, as well as participate in cyclobutarene initiated ring opening polymerizations. The cyclobutarene peroxides of this invention are useful for the production of cross-linked, branched and graft polymeric compositions.

Abstract: Imidopercarboxylic acids or salts thereof of the formula ##STR1## in which A denotes a group of the formula ##STR2## n denotes the number 0, 1 or 2, R.sup.1 denotes hydrogen, chlorine, bromine, C.sub.1 -C.sub.20 -alkyl, C.sub.2 -C.sub.20 -alkenyl, aryl, or alkylaryl,R.sup.2 denotes hydrogen, chlorine, bromine or a group of the formula --SO.sub.3 M, --CO.sub.2 M, CO.sub.3 M or OSO.sub.3 M.M denotes hydrogen, an alkali metal or ammonium ion or the equivalent of an alkaline earth metal ion andX denotes C.sub.3 -C.sub.19 -alkylene or arylene, preferably phenylene.These compounds are suitable as stable peroxide compounds in bleaching, oxidizing and cleaning agents.

Abstract: The present invention relates to a novel antioxidant-peroxide compound of Structure A,(Y--[R--OO--X).sub.x --An].sub.y Ain which the definitions of X, Y, R, An, x, and y are given in the Summary of the Invention section, for example, t-butyl peroxy-3-(3,5-di-t-butyl-4-hydroxypheneyl) propionate, processes for producing polymeric composition of enhanced oxidative stability via initiation of polymerization of ethylenically unsaturated monomers, curing of elastomers and unsaturated polyester resins, modification of polypropylene and other polymers and copolymers, and crosslinking of olefin polymers and copolymers, and the resulting polymers having enhanced oxidative stability.

Abstract: 2-Hydrazono-4,6-dinitrobenzthiazolones of the formula ##STR1## in which X.sub.1 represents hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -hydroxyalkyl, C.sub.1 -C.sub.4 -sulphoalkyl or C.sub.1 -C.sub.4 -sulphatoalkyl, andX.sub.2 represents hydrogen or --SO.sub.2 X.sub.3, whereX.sub.3 may represent hydrogen, C.sub.1 -C.sub.8 -alkyl or optionally substituted aryl andX.sub.1 also represents a double bond between the cyclic nitrogen atom and the carbon atom 2 according to the formula II below: ##STR2## where X.sub.2 has the meaning specified under the above formula. These hydrazones may be employed in the preparation of azo dyestuffs and as color formers for detecting of biological substances, and in the determination of H.sub.2 O.sub.2.

Abstract: Terpene peroxides of formula: ##STR1## in which R denotes a tertiary alkyl radical substituted, if desired, by one or more phenyl radicals, a cycloalkyl radical or a trialkylsilyl radical, R.sub.1, R.sub.2 and R.sub.3, which are identical or different, each denote hydrogen or an aliphatic radical optionally containing one or more double or triple bonds and optionally substituted, and R.sub.4 denotes an aliphatic radical optionally containing one or more double or triple bonds and optionally substituted or R.sub.3 denotes hydrogen and R.sub.2 and R.sub.4 together form an alkylene radical which may be substituted by one or more methyl radicals, are obtained by reaction of a hydroperoxide of formula R--OOH with a compound of formula: ##STR2## the operation being carried out in a basic aprotic solvent.

Abstract: Disclosed is a process for the preparation of tert. alkyl-tert. aralkyl peroxides with the general formula ##STR1## where R represents an alkyl radical with 1 to 4 C-atoms, R', R" and R'" represent the same or different alkyl radicals with 1 to 5 C-atoms and n is a number from 1 to 3, by reacting an olefin with the general formula ##STR2## with a tert. alkyl hydroperoxide with the general formula ##STR3## where R, R' and R" and R'" and n having the meaning indicated above the presence of aqueous hydrochloric acid.

Abstract: In general, inorganic or organic peroxyacids are unstable in the presence of a nonionic surfactant, so that it was not feasible to contemplate storing liquid compositions containing both components. It has now been discovered that storable compositions containing both components can be obtained by the use of particulate potassium-4-sulphoperoxybenzoic acid dispersed in the liquid nonionic surfactant containing phase. Additionally, the compositions can also include a dispersed particulate water-insoluble builder such as zeolite or water-soluble builder such as STPP. It is preferable to include a small amount of a chelating peroxidic stabilizer such as dipicolinic acid or 1,1,1-hydroxyethylidene diphosphonic acid.

Abstract: An aqueous suspension of a solid organic peroxide is produced by mixing a solid organic peroxide having a difference of at least 5.degree. C. between the melting point and the thermal decomposition temperature thereof with a protective colloid, a surface active agent, and water thereby forming an aqueous emulsion and subsequently cooling this aqueous emulsion.

Abstract: Increased energy costs have stimulated a demand for peroxygen compounds that are effective at ambient to hand-hot temperatures, but peroxyacids and acyl peroxides tend to suffer from one or more of poor thermal stability, or sensitivity to impact, thereby rendering their manufacture or storage hazardous, or from poor solubility. The instant invention provides a salt of the formula (in anhydrous form): ##STR1## The salt can be incorporated in low temperature bleaching compositions, in washing compositions, in sanitizing compositions or in disinfection/sterilization compositions.

Abstract: Disclosed are novel blends of peroxides that have melting points of about 5.degree. C. and lower. The blends consist essentially of (1) t-butyl cumyl peroxide, (2) bis(.alpha.-t-butylperoxyisopropyl)benzene, and (3) dicumyl peroxide.

Abstract: This invention relates to production of singlet oxygen and includes means and methods for storage and retrieval thereof as well as continuous production from ground state oxygen. With respect to storage and retrieval of singlet oxygen, certain aromatic acceptor compounds are oxidized to yield solid endoperoxides which, in turn, are decomposed to yield singlet oxygen and regenerate the acceptor. Continuous production of singlet oxygen occurs through irradiation of dye sensitizers with electromagnetic radiation causing activation thereof and excitation of flowing ground state oxygen.

Abstract: The present invention relates to the provision in solid form of the magnesium salt of certain aromatic, cycloaliphatic or conjugated aliphatic compounds containing a peroxycarboxylic acid group and a carboxylate group, and optionally also an alkyl, carboxylate, sulphonate, nitro, chloro or bromo group, which can be employed as bleaching agents. One especially referred example is magnesium monoperoxyphthalate having the formula: ##STR1## The invention also provides processes for the preparation of the salts, by reaction between a magnesium compound and the organic peroxyacid/carboxylate compound in a solvent from which the salt precipitates, the latter preferably being obtained by reaction between hydrogen peroxide and the corresponding anhydride under controlled reaction conditions of temperature and reagent ratios.

Abstract: A method for the preparation of benzoyl peroxide in crystalline form, which crystals may range in size below 10 microns, comprises forming a first solution of the benzoyl peroxide in a precipitate promoting material, adding the first solution to a second solution comprising an aqueous solution of a dispersant, to precipitate the benzoyl peroxide in the desired crystalline form, and finally recovering the crystalline benzoyl peroxide from the first and second solutions. The precipitate promoting material may be selected from sulfur-containing aliphatic ethers, long-chain aliphatic and araliphatic ethers, ethylene oxide derivatives, and mixtures thereof. The dispersant may be selected from cellulosic derivatives, anionic surfactants, nonionic surfactants, colloidal inorganic materials, and mixtures thereof. The present method may be performed at room temperature and is therefore safe and energy conservative.

Abstract: The present invention relates to the provision in solid form of the magnesium salt of certain aromatic, cycloaliphatic or conjugated aliphatic compounds containing a peroxycarboxylic acid group and a carboxylate group, and optionally also an alkyl, carboxylate, sulphonate, nitro, chloro or bromo group, which can be employed as bleaching agents. One especially referred example is magnesium monoperoxyphthalate having the formula: ##STR1## The invention also provides processes for the preparation of the salts, by reaction between a magnesium compound and the organic peroxyacid/carboxylate compound in a solvent from which the salt precipitates, the latter preferably being obtained by reaction between hydrogen peroxide and the corresponding anhydride under controlled reaction conditions of temperature and reagent ratios.

Abstract: A process for the preparation of dicumyl peroxide by reaction of dimethylbenzyl hydroperoxide (cumene hydroperoxide) with dimethyl phenyl carbinol in the presence of a catalytic quantity of a phosphorous halide or oxyhalide is described. This catalyst gives good yields of the useful reaction product and a high selectivity.

Abstract: A process for the preparation of dicumyl peroxide by reaction of dimethylbenzyl hydroperoxide (cumene hydroperoxide) with methyl cumyl ether is described. The reaction is carried out in the presence of a catalytic quantity of Lewis or Bronsted acids, the methanol which forms as a by-product being removed as the reaction proceeds. Furthermore, the reaction is carried out in a reaction medium consisting of the methyl cumyl ether itself, which is employed in quantities greater than the stoichiometric quantity required for the reaction with the cumene hydroperoxide.

Abstract: A process for preparing peroxidic mixtures, more particularly mixtures of ketone peroxides useful as polymerization initiators for unsaturated polyester resins, is disclosed. The process comprises in situ peroxidation of one or more ketone compounds with hydrogen peroxide, in a solvent which is a ketone peroxide formulation.

Abstract: Compounds of the formula IA.multidot.m B (I)whereinA is a compound of the formula II or III ##STR1## m is a rational number between 0.1 and 4.0, and B is H.sub.2 O.sub.2, N.sub.2 H.sub.4 or NH.sub.2 OH, andR.sub.1 is an unsubstituted or substituted aliphatic or aromatic hydrocarbon radical which has 3-30 C atoms and which can be interrupted by oxygen or sulfur atoms,R.sub.2 is hydrogen or C.sub.1 -C.sub.30 alkyl,X is --O-- or --SO.sub.2 -- and, in the case where B is N.sub.2 H.sub.4 or NH.sub.2 OH, also --S-- or --SO--,Y is the direct bond, ##STR2## Q is --CH.sub.2, --CH(OH)--CH.sub.2 -- or --CH(CH.sub.2 --OH)--, and n is 1, 2, 3, 4, 5, 6, 7 or 8.

Abstract: An aliphatic or cycloaliphatic hydroperoxide, an olefin such as a 1-aromatic-1-substituted ethylene and a halide corresponding to the ethylene are reacted under essentially anhydrous conditions, in the absence of a free acid, at a temperature below the decomposition temperature of the halide to obtain a peroxide corresponding to the hydroperoxide and the ethylene.Preferably the product peroxide is recovered by treating the reaction product mixture with aqueous alkali metal hydroxide to destroy the halide and hydroperoxide therein; then distilling the treated mixture in the presence of a substantial amount of liquid water at sub-atmospheric pressure to remove overhead impurities.Example: Dicumyl peroxide is prepared by reacting at about 30.degree. C for about 5 hours cumene hydroperoxide, .alpha.-methylstyrene and cumyl chloride, which compounds has been charged to the reaction zone in a mole ratio of 1.25: 0.86: 0.

Abstract: A novel class of compounds having the formula ##STR1## where Z is a substituted carbonate or carbamate, D is an alkynyl or an alkyl, and the R's may be alkyl.