Download Physico-Chemical Constants of Binary Systems in Concentrated by Jean Timmermans PDF

By Jean Timmermans

A compilation of numerical information released in regards to the focused binary suggestions of natural compounds, with a minimum of one being a hydroxyl spinoff, this e-book serves as a reference advisor for scientists and chemical engineers. writer authorised every kind of drugs, parts or compounds, aside from steel alloys and selected arbitrarily platforms among 10 and ninety percentage by means of weight. In each one part, the binary combinations are introduced jointly in nice divisions, in line with the measure of physico-chemical similitude in their elements. In each one of those divisions, the binary combos are indexed based on the order of the 1st part, and for every of them, in response to the order of the second one part. the information has been reproduced below the identify of the writer, with the yr of ebook.

The platforms were prepared in 4 different types, one for every quantity:

  • Both elements are natural compounds, excepting hydroxyl derivatives.
  • Both elements are natural compounds, one a minimum of being a hydroxyl by-product.
  • At least one of many elements is a metal compound.
  • All different structures.
  • Content:
    • entrance subject
    observe for clients
    • Preface to quantity 2
    • desk of Contents
    •Section H. Hydrocarbons + Hydroxyl Derivatives
    21. Hydrocarbons + Alcohols
    22. fragrant Hydrocarbons + Oximes and Alcohols
    23. Hydrocarbons + Phenols
    24. Hydrocarbons + Acids
    •Section I. Halogen Derivatives CO, CO2, CS2, and so on. + Hydroxyl Derivatives
    25. Halogen Derivatives + Alcohols
    26. Halogen Derivatives + Phenols and Acids
    27. CO2, CS2, and so forth. + Hydroxyl Derivatives
    •Section J. Oxygen Derivatives + Hydroxyl Derivatives
    28. Ether Oxides + Hydroxyl Derivatives
    29. Ketones + Hydroxyl Derivatives
    30. Anhydrides and Esters + Hydroxyl Derivatives
    •Section okay. Nitrogen Derivatives + Hydroxyl Derivatives
    31. Nitrogen Derivatives + Alcohols
    32. Nitrogen Derivatives + Phenols
    33. Nitrogen Derivatives + Acids
    •Section L. combined Oxygen-Nitrogen Derivatives + Hydroxyl Derivatives
    34. Oxygen-Nitrogen Derivatives + Alcohols
    35. Oxygen-Nitrogen Derivatives + Phenols
    36. Oxygen-Nitrogen Derivatives + Acids
    •Section M. Hydroxyl Derivatives
    37. Hydroxyl Derivatives of other Species
    38. Alcohols and Phenols
    39. Acids
    • Symbols and Abbreviations

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    Additional info for Physico-Chemical Constants of Binary Systems in Concentrated Solutions, Volume 2 - Two Organic Compounds

    Example text

    Polymorphic forms. Rastogi and Varma, 1956. mold 0 10 20 30 40 50 Dv. ( c d m o l e ) mold Dv. t. t. t. T. 8 b. t. t. t. 4263 k b. t . 3 METHYLCYCLOHEXAN E t 2-METHYL-1-P ROPANETHIOL 42 nethylcyclohexane ( C 7 H l 4 ) ( b . t . 10 (cc/g) Le c a t, 1949 2nd Cornp. t. t. % b. t. 4 47. 8 ( C4HlOS ) c,H,, Oethylcyclohexane ( Denyer, F i d l e r and Lowry, 1949 Alcohols. t . 8083 20 2nd comp. 7 + Alcohols ) Lecat , 1949 2nd Comp. t . t. 2 _ _ _ I - Bu ty l a 1coho 1 Isobutyl alcohol tert. 45 2nd Comp.

    T. t. t. t. 3 0 Tichacek, Kmak and Drickamer, 1956 d t D therm. 40° 20 50 80 Jahn, 1891. +I. 80 +O. 8696 ------------ _ l p l _ I - Properties of phases . -- --_ Density . 8724 s'. 86 100 T c i t e l b a m , Gortalova and Ganclina, 1950 no1 . 317 359 362 362 360 361 359 359 354 347 326 . n- -. L. S. 7872 Shakhparonov and Shlenkina, 1954. mols'. 18 1. 8 t c n y e r r t u r e c o e f f i c i e n t of t h e d i l a t a t i o n (volucie). conipressibility c o e f f i c i e n t . 3 575. 514 28. 4476 1 .

    T. 5 769 763 421 423 241 243 T y r e r , 1912 ss L L. t . 5 b . t .

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