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Monday, July 27, 2020 | History

2 edition of Autoxidation of hydrocarbons and polyolefins found in the catalog.

Autoxidation of hydrocarbons and polyolefins

Leo Reich

Autoxidation of hydrocarbons and polyolefins

kinetics and mechanisms

by Leo Reich

  • 51 Want to read
  • 35 Currently reading

Published by M. Dekker in New York .
Written in English

    Subjects:
  • Oxidation.,
  • Hydrocarbons.,
  • Polyolefins.,
  • Chemical kinetics.

  • Edition Notes

    Includes bibliographies.

    Statement[by] Leo Reich [and] Salvatore S. Stivala.
    ContributionsStivala, Salvatore S., 1923- joint author.
    Classifications
    LC ClassificationsQD281.O9 R44
    The Physical Object
    Paginationxi, 527 p.
    Number of Pages527
    ID Numbers
    Open LibraryOL5609846M
    LC Control Number68017424

    Effect of formic acid and formates on the oxidation of hydrocarbons and hydrocarbon polymers In order to ascertain the nature of the inhibiting action of the products of hydrocarbon oxidation, a kinetic study was made of the oxidation of cetane, a hydrocarbon serving as a model of the polyethylene chain, at –°C. AUTOXIDATION. A second method is to use molecular oxygen as oxidant and to initiate an autoxidation reaction by using a metal ion which will readily undergo a one electron oxidation. Among the former reagents, two commonly used compounds are the potassium salts of the dichromate and permanganate : D. M. Roundhill.

    Hydrocarbons, the essential component of petroleum-based fuels, are likely during storage to react with atmospheric oxygen and with one another. Products which originate from oxygenation will undergo further changes, resulting in change of coloration, the presence of non-volatile, macromolecular substances (gum), Cited by: 2. Polyolefin, any of a class of synthetic resins prepared by the polymerization of olefins. Olefins are hydrocarbons (compounds containing hydrogen [H] and carbon [C]) whose molecules contain a pair of carbon atoms linked together by a double bond. They are most often derived from natural gas or from.

    Cobalt acetate bromide in acetic acid solution is an extraordinarily active catalyst for the autoxidation of hydrocarbons. Carboxylic acids and ketones are readily prepared in high yields at moderate temperatures and at atmospheric pressure. In addition, benzylic and allylic groups can be converted Cited by: PDF ( K) PDF-Plus ( K) Citing articles; Absolute rate constants for hydrocarbon autoxidation. XIII. Aldehydes: photo-oxidation, co-oxidation, and inhibitionCited by:


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Autoxidation of hydrocarbons and polyolefins by Leo Reich Download PDF EPUB FB2

Autoxidation of Hydrocarbons and Polyolefins [Leo and Stivala, Salvatore S. Reich] on *FREE* shipping on qualifying : Reich, Leo and Stivala, Salvatore S. Autoxidation of Hydrocarbons and Polyolefins: Kinetics and Mechanisms by Leo Reich; Salvatore S.

Stivala and a great selection of related books, art and collectibles available now at Open Library is an open, editable library catalog, building towards a web page for every book ever published.

Autoxidation of hydrocarbons and polyolefins by Leo Reich; 1 edition; First published in ; Subjects: Hydrocarbons, Oxidation, Chemical kinetics, Polyolefins. Stanford Libraries' official online search tool for books, media, journals, databases, government documents and more.

Autoxidation of hydrocarbons and polyolefins; kinetics and mechanisms in SearchWorks catalog. Additional Physical Format: Online version: Reich, Leo. Autoxidation of hydrocarbons and polyolefins. New York, M. Dekker, (OCoLC) Material Type.

Autoxidation of hydrocarbons and polyolefins: Kinetics and mechanisms. By Leo Reich and Salvatore S. Stivala, Marcel Dekker, Inc., 95 Madison Ave., New York, NYxi + pp.

× cm. Price $ Autoxidation of hydrocarbons and polyolefins: Kinetics and mechanisms. By Leo Reich and Salvatore. This contribution summarizes our recent efforts to unravel the radical chemistry of autoxidations. Abstraction of the weakly bonded αH-atom of the primary Autoxidation of hydrocarbons and polyolefins book product by chain carrying peroxyl radicals is identified as the source of major end products such as alcohol and ketone/aldehyde.

In the case of cyclohexane autoxidation, this reaction is even responsible for the Cited by: The kinetics and mechanism of metal-catalyzed autoxidation. Journal of the American Oil Chemists’ Society48 (9), DOI: /BF Gerald Lundeen, Robert Livingston.

CHEMILUMINESCENCE OF HYDROCARBON OXIDATION. Photochemistry and Photobiology4 (6), DOI: / by: Potassium superoxide was found to initiale autoxidations of fluorene, diphenylmethane, and distyrylmethane.

In each case the oxidation results in the formation of ketones as primary products. Kinetics of the fluorene and diphenylmethane oxidations showed typical sigmoidal autoxidation Cited by: 5. Autoxidation (auto-oxidation) is a complex oxidation mechanism that proceeds through a free radical chain process.

It is a common degradation mechanism for unsaturated fats, but a number of drugs containing carbon–carbon double bonds also undergo autoxidation. On the autoaccelerated character of the branched oxidation of polyolefins. Macromolecular Symposia(1), DOI: /masy John Scheirs, Stephen W.

Bigger, Norman C. Billingham. A review of oxygen uptake techniques for measuring polyolefin by:   This book is comprised of 35 chapters and begins with an analysis of the chain processes taking place during the oxidation of hydrocarbons and how to stimulate slow chain branching reactions.

The role of peroxides in the kinetics of liquid-phase oxidation processes is then considered, along with several elementary stages of the liquid-phase Book Edition: 1. Autoxidation, the free radical chain reaction that nominally inserts O 2 into hydrocarbons to give peroxides, is primarily responsible for the degradation of all organic materials.

Peroxyl radicals propagate autoxidation mainly by abstraction of labile H-atoms from the hydrocarbons, whereas radical-trapping antioxidants (RTAs) Cited by: 6.

Autoxidation. Autoxidation is a chain reaction, starting with the formation of a free radical (initiation), continuing with the propagation of the reaction with the formation of more and more free radicals and unstable molecules and ending with reactions between the free radicals to form stable molecules (termination).

Abstract. The oxidation and autoxidation of adamantane, norbornane and cyclohexane can be photochemically promoted by ceric ammonium nitrate in acetonitrile at room temperature, both processes being extremely efficient and selective with adamantane.

The oxidation and autoxidation of some cycloalkanes in MeCn, at room temperature, Cited by: Photocatalytic oxidation of hydrocarbons proceeds according to mechanisms usually involved in photodegradation of organic pollutants.

Under some specific conditions it can, however, be used as a synthetic method. Oxidation of cyclohexane at TiO 2, studied by Almquist and Biswas, 25 is a good example of such a process.

On the origin of the byproducts in the autoxidation of cyclohexane to cyclohexanol and cyclohexanone. Recueil des Travaux Chimiques des Pays-Bas89 (7), DOI: /recl O.

Cicchetti. Mechanisms of oxidative photodegradation and of UV stabilization of polyolefins., DOI: /BFbCited by: A) Technologically significant reactions (oleochemistry) 1. esterification enzymatic (lipases) (book 1, tab) H 2 H 2 R C H 2 C H 2 C H 2 C H C H R 1 2 olejová general mechanism of hydrocarbon chain autoxidation (radical reaction) 1.

induction stage. Autoxidation, or air oxidation, is one of the simplest functionalization reactions of alkanes. In general, hydroperoxides are the first-formed products, but these can decompose under the conditions of the reaction to give the ketone and alcohol. 78 The reagents used to initiate the reaction are usually O -centered radicals or even O 2 itself.

Heterogeneous features of autooxidation of hydrocarbon polymers. Polymer Degradation and Stability72 (1), DOI: /S(00) Yurii A Mikheev, Gennadii E Zaikov.

Heterophase mechanisms of thermal oxidation of polymers. New by:. The nature and mechanism of formation of the thiobarbituric acid (TBA)-reactive material produced in the autoxidation of polyunsaturated fatty acids (PUFA) or their esters has been studied.

On the basis of chemical studies andCited by:   IN view of current interest in the autoxidation of hydrocarbons, it seems desirable to record briefly some observations made in these laboratories concerning the autoxidation of by: 7.Propagation and termination rate constants have been measured for autoxidation of benzyl phenyl ether, benzyl-t-butyl ether, isopropyl ether, and benzyl the case of isopropyl ether and benzyl ether, estimates have been made of inter- and intramolecular propagation rate by: