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Edité par J Applied Physics, 1967
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Ajouter au panierPamphlet. Etat : Very Good. Vol 38, No 2, pp. 475-482, Illus, 4to, Extracted from orig Vol, thus begins with title page, trimmed & stapled pamphlet, else VG.
Edité par Plenum Press, 1971
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Ajouter au panierHardcover. Etat : Very Good. Etat de la jaquette : Good. hardback in very good condition in good dust jacket.

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Etat : New. pp. 508.

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Paperback. Etat : Brand New. 507 pages. 9.25x6.10x1.02 inches. In Stock.

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Etat : Gut. Zustand: Gut | Seiten: 508 | Sprache: Englisch | Produktart: Bücher | For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than the glassy state. It is generally assumed that networks possess an av erage composition to which average properties may be assigned; from such a continuum view, a powerful analysis of such properties as modulus, swelling, birefringence and thermoelasticity has emerged. In the years following the rise of polymer characterization (the late 40's and early 50's), many scientists began to study ap parent relations between the properties of linear polymer molecules and the networks obtainable therefrom. This search was also stimu lated by the wide range of applications of polymer networks in com mercial elastomers, thermosets and coatings. Frequently, these data were confidently matched with curves obtained from statisti cally describable models of networks of ghost chains, uniformly distributed in space. More recently, it has become apparent that polymer chains in networks are not as ideal as assumed in the formulation of statis tical models, and there has been a shift in emphasis towards the less than ideal, perturbed and possibly inhomogeneous networks which are more frequently encountered in practice. The continuum approach, however, had to be developed before inhomogeneous systems could be described; the present volume, therefore, contains both views.…

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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than the glassy state. It is generally assumed that networks possess an av erage composition to which average properties may be assigned; from such a continuum view, a powerful analysis of such properties as modulus, swelling, birefringence and thermoelasticity has emerged. In the years following the rise of polymer characterization (the late 40's and early 50's), many scientists began to study ap parent relations between the properties of linear polymer molecules and the networks obtainable therefrom. This search was also stimu lated by the wide range of applications of polymer networks in com mercial elastomers, thermosets and coatings. Frequently, these data were confidently matched with curves obtained from statisti cally describable models of networks of ghost chains, uniformly distributed in space. More recently, it has become apparent that polymer chains in networks are not as ideal as assumed in the formulation of statis tical models, and there has been a shift in emphasis towards the less than ideal, perturbed and possibly inhomogeneous networks which are more frequently encountered in practice. The continuum approach, however, had to be developed before inhomogeneous systems could be described; the present volume, therefore, contains both views. 508 pp. Englisch.…

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Etat : New. Print on Demand pp. 508 49:B&W 6.14 x 9.21 in or 234 x 156 mm (Royal 8vo) Perfect Bound on White w/Gloss Lam.

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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than t.…

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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than the glassy state. It is generally assumed that networks possess an av erage composition to which average properties may be assigned; from such a continuum view, a powerful analysis of such properties as modulus, swelling, birefringence and thermoelasticity has emerged. In the years following the rise of polymer characterization (the late 40's and early 50's), many scientists began to study ap parent relations between the properties of linear polymer molecules and the networks obtainable therefrom. This search was also stimu lated by the wide range of applications of polymer networks in com mercial elastomers, thermosets and coatings. Frequently, these data were confidently matched with curves obtained from statisti cally describable models of networks of ghost chains, uniformly distributed in space. More recently, it has become apparent that polymer chains in networks are not as ideal as assumed in the formulation of statis tical models, and there has been a shift in emphasis towards the less than ideal, perturbed and possibly inhomogeneous networks which are more frequently encountered in practice. The continuum approach, however, had to be developed before inhomogeneous systems could be described; the present volume, therefore, contains both views.…

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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than the glassy state. It is generally assumed that networks possess an av erage composition to which average properties may be assigned; from such a continuum view, a powerful analysis of such properties as modulus, swelling, birefringence and thermoelasticity has emerged. In the years following the rise of polymer characterization (the late 40's and early 50's), many scientists began to study ap parent relations between the properties of linear polymer molecules and the networks obtainable therefrom. This search was also stimu lated by the wide range of applications of polymer networks in com mercial elastomers, thermosets and coatings. Frequently, these data were confidently matched with curves obtained from statisti cally describable models of networks of ghost chains, uniformly distributed in space. More recently, it has become apparent that polymer chains in networks are not as ideal as assumed in the formulation of statis tical models, and there has been a shift in emphasis towards the less than ideal, perturbed and possibly inhomogeneous networks which are more frequently encountered in practice. The continuum approach, however, had to be developed before inhomogeneous systems could be described; the present volume, therefore, contains both views.Libri GmbH, Europaallee 1, 36244 Bad Hersfeld 508 pp. Englisch.…