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北京石油化工学院2026年研究生招生接收调剂公告
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[求助] 求助炭黑方面的几句文献翻译(中译英)

炭黑的增强作用机理
目前,关于炭黑的增强作用机理主要有分子
链滑动理论、结合胶理论、填料网络理论以及范
得华网络理论等。

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zb6824785: 金币+5, 翻译EPI+1, ★★★★★最佳答案 2013-12-15 12:12:48
The mechanism of carbon black enhancement
The mechanism of carbon black enhancement are presently  Perturbed hard-chain theory , crystal colloid theory,  filler  network theory and Van Der Waals network theory.
1??·??????????í??van der Waals theory
Abstract
Generalized van der Waals theory is used to establish a partition function that considers the effect of density on rotational and vibrational motions in addition to translational degrees of freedom. A three-parameter equation of state is derived from this partition function. The equation of state is applicable to small, spherical (argon-like) molecules and also to large, structurally complex molecules, including polymers. Parameters are presented for three polymers and twenty-two common fluids including light hydrocarbons, heavy hydrocarbons, nitrogen, carbon dioxide, hydrogen, carbon monoxide, hydrogen sulfide, sulfur dioxide, and water. The equation of state gives good liquid densities, and vapor pressures, and fair second virial coefficients.
2??Perturbed hard-chain theory ·?×????????í??
Perturbed hard-chain theory: An equation of state for fluids containing small or large molecules
Samil Beret†, J. M. PrausnitzArticle first published online: 17 JUN 2004

DOI: 10.1002/aic.690210612

Copyright © 1975 American Institute of Chemical Engineers
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3??Molecular Network Theories ?????????í?? ?òLodge's molecular network theories
Rheological Equations from Molecular Network Theories Rent: Rent this article for
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Buy: USD28.00  10.1122/1.549276By Pierre J. Carreau1
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Affiliations: 1 Chemical Engineering Department, The University of Wisconsin, Madison, Wisconsin View the Scitation page for University of Wisconsin.
Trans. Soc. Rheol. 16, 99 (1972); https://dx.doi.org/10.1122/1.549276  Previous ArticleTable of ContentsNext Article   

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Lodge's molecular network theories are quite successful in describing the linear viscoelastic behavior of polymer solutions and melts, but cannot account for the rate?\of?\strain dependence of various material functions. By allowing the junction?\creation rate and the probability of loss of junctions to depend on the second invariant of the rate?\of?\strain tensor, more realistic constitutive equations were obtained. Two rheological models are proposed by assuming two different mechanisms for the effect of the rate of strain on the kinetics of the network. The experimental data on three fluids (representative of eight viscoelastic fluids) are used to test the models in various flow situations. For steady simple shearing and small?\amplitude, sinusoidal simple shearing, both model A and model B are capable of fitting the four functions ??,−(?? 11 −?? 22 ),  ????, andG'  rather well over many decades of shear rate or frequency. For suddenly changing flow experiments model A is inadequate. Model B however appears to be the only rheological equation which can fit simultaneously the steady shear, complex viscosity, stress growth, and stress relaxation functions. For stress growth, the agreement with the experimental data is remarkable, especially after the other models were shown to fail drastically. Finally, an interpretation of the stress growth and relaxation phenomena is given in the light of the modified theory.
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