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

By Jean Timmermans

A compilation of numerical information released in regards to the centred 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 accredited all types of drugs, components or compounds, except for metal alloys and selected arbitrarily structures among 10 and ninety percentage through weight. In each one part, the binary combinations are introduced jointly in nice divisions, in keeping with the measure of physico-chemical similitude in their elements. In each one of those divisions, the binary combos are indexed in accordance with the order of the 1st part, and for every of them, in accordance with the order of the second one part. the knowledge has been reproduced less than the identify of the writer, with the yr of ebook.

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

  • Both parts 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 steel 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 on. + Hydroxyl Derivatives
    •Section J. Oxygen Derivatives + Hydroxyl Derivatives
    28. Ether Oxides + Hydroxyl Derivatives
    29. Ketones + Hydroxyl Derivatives
    30. Anhydrides and Esters + Hydroxyl Derivatives
    •Section ok. 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

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    T. t.. t. m. t . t. t. 65 L e c a t , 1933. t. t. t. 8 1 + Alcohols m r t , 1949 2-Pinene ( CloH,6) ( b . t . 8 ) + Alcohols 2nd Conp. lai,,e A2 ~ ~ , . lt ~ . t. D t Kix L e c a t , 1949 2nd Coixp. t. t. 5 (10%) (35%) (50%) TURPENTINE d t ETHYL ALCOHOL 50 Turpentine d ( CloH,6) + Ethyl alcohol ( C,HgO ) -- . XXII. 40° Oximes : s e e page 46 . t. 94 -------- ----p ) ---- I - 50 volb ) ----------. t. 365 -- - TURPENTINE d t ETHYL ALCOHOL 50 Turpentine d ( CloH,6) + Ethyl alcohol ( C,HgO ) -- . XXII.

    T. t. t. t. 5 Giecalone, 1942 Pickeiing. t. 610 I . 9 0 - 4.. 9. 82 dew. t. 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).

    T. 76708 98. 8009L? 117, 2. 0 37 CYCLOHEXANE t PROPYL ALCOHOL _ _ _ _ _ ~ Cyclohcxane ( C 6 H 1 2 1 + Propyl a l c o h o l ( C,H80 1 ~______ "D no156 D t mix b. t. 000 f + Duty1 a l c o h o l ( CUH1,0 ) L e c a t , 1949 - % b. t . 75 7 9 . 8 0 4 100 Cyclohexane ( C 6 I l I 2 1 + Isopropyl a l c o h o l ( C,Il,O ; L c c a t , 1949 Sniyth and S t o o p s , 1929 % b. t. t. 0 31 . 3, . 236 2. 028 farnis, 1943 mol% d 220 0 Cyclohexane ( C 6 H I 2 ) ( b . t . 000 + Alcohols Lecat, 1949 II 2nd Comp. t.

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