Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Eugene E. Schrier"'
Publikováno v:
The Journal of Physical Chemistry. 84:350-354
Publikováno v:
The Journal of Physical Chemistry. 81:674-679
Autor:
Evelyn R. Stimson, Eugene E. Schrier
Publikováno v:
Journal of Chemical & Engineering Data. 19:354-358
(1) Cheung, H.. Zander, E. H. , Chem. Eng. Progr.. Symp. Ser.. 64 ( 8 8 ) , 34 (1968). Francis, A. W., J. Arner. Chem. SOC., 58, 1099 (1954). Gupta, V. S., PhD thesis, The Pennsylvania State University, University Park, Pa., 1969. Huie, N. C.. PhD th
Publikováno v:
The Journal of Physical Chemistry. 82:1703-1707
Autor:
R.A. Robinson, Eugene E. Schrier
Publikováno v:
Journal of Solution Chemistry. 3:493-501
Three systems of the type amino acid or peptide-sodium chloride-water have been investigated over wide solute molality ranges using the isopiestic vapor pressure method. The amino acid employed was L-α-alanine, while the peptides were diglycine and
Autor:
Martha Y. Schrier, Eugene E. Schrier
Publikováno v:
Biochemistry. 15:2607-2612
Isopiestic vapor pressure measurements have been used to obtain free energies of transfer of ribonuclease A from dilute buffer to solutions of either urea or guanidine hydrochloride (GdnHCl) over a wide cosolute concentration range. The free energies
Autor:
Evelyn R. Stimson, Eugene E. Schrier
Publikováno v:
Biopolymers. 14:509-520
The enthalpies of transfer, ΔHtr, of a series of amides from water to aqueous solutions of either guanidinium hydrochloride (GuHCl) or potassium iodide were obtained from calorimetric measurements at 25°C. The amides were studied at molalities arou
Publikováno v:
Journal of the American Chemical Society. 86:3444-3449
Autor:
Eugene E. Schrier, Lois D. Mackey
Publikováno v:
The Journal of Physical Chemistry. 72:733-736
Autor:
Eugene E. Schrier, Martha Y. Spink
Publikováno v:
The Journal of Chemical Thermodynamics. 2:821-832
The dependence of solute activity coefficients on composition in systems, MCl(component 1) + acetone(component 2) + water, has been investigated over a wider range of solute molalities than any salt + non-electrolyte system previously studied. The sa