Hermans’ theory

Herman Pines and Luke A. Schaap The Use of X-Ray K-Absorption Edges in the Study of Catalytically Active Solids Robert A. Van Nordstrand The Electron Theory of Catalysis on Semiconductors Th. Wolkenstein... 

Herman, Z.S. Recent Advances in Simple Valence-Bond Theory and the Theory of Hybrid Bond Orbitals Int. J. Quantum Chem. 1983, 23, 921-943. 

Boerhaave, Herman. A new method of chemistry including the history, theory and practice of the art translated from the original Latin of Dr. Boerhaave s Elementa Chemise, as published by himself. To which are added, notes and an appendix, shewing the necessity and utility of enlarging the bounds of chemistry. .. By Peter Shaw. .. 2nd ed ed. Edited by Peter Shaw. London T. T. Longman, 1741. 2 vols... 

Boerhaave, Herman. A new method of chemistry including the theory and practice of that art laid down on mechanical priciples, and accommodated to the uses of life. The whole making a clear and rational system of chemical philosophy. To which is prefix d a critical history of chemistry and chemists, from the origin of the art to the present time. Written by the very learned H. Boerhaave. .. translated from the printed ed., collated with the best manuscript copies. By P. Shaw, M.D. and E. Chambers. .. with additional notes and sculptures. 3rd ed ed. Translated by Peter Shaw and Ephraim Chambers. London J. Osborn T. Longman, 1727. 2 vols (xvi, 383, 335, [43] p.)... 

Boerhaave, Herman. Dr. Boerhaave s Academical lectures on the theory of physic. Being a genuine translation of his institutes and explanatory comment, collated and adjusted to each other, as they were dictated to his students at the University of Leyden. .. London , 1742-1746. 6 vols... 

Martin, M., Herman, D.P., Guiochon, G. (1986). Probability theory for number of mixture components resolved by n independent columns. Anal. Chem. 58, 2200-2207. 

This observation is expected from theory, as the observed thickness distributions are exactly the functions by which one-dimensional short-range order is theoretically described in early literature models (Zernike and Prins [116] J. J. Hermans [128]). From the transformed experimental data we can determine, whether the principal thickness distributions are symmetrical or asymmetrical, whether they should be modeled by Gaussians, gamma distributions, truncated exponentials, or other analytical functions. Finally only a model that describes the arrangement of domains is missing - i.e., how the higher thickness distributions are computed from two principal thickness distributions (cf. Sect. 8.7). Experimental data are fitted by means of such models. Unsuitable models are sorted out by insufficient quality of the fit. Fit quality is assessed by means of the tools of nonlinear regression (Chap. 11). 

The Hot Big Bang theory of the Universe was pioneered by George Gamow, R. A. Alpher and R. C. Herman in the late 1940s and early 50s. They supposed that during the first few minutes of the (then radiation-dominated) Universe, matter was originally present in the form of neutrons and that, after some free decay, protons captured neutrons and successive captures, followed by /3-decays, built up all the elements (Alpher Herman 1950). 

G. Gamow, R. Alpher and R. Herman develop Hot Big Bang theory and suggest all elements created by neutron captures in early Universe. W. Baade distinguishes two stellar populations. 

The early focus of polymer related education was then also largely empirical. The first formal course in polymer chemistry which balanced theory with practice was probably one associated with Herman Mark given at the Polytechnic shortly after his arrival. Ray Seymour offered such a course at the University of Chattanooga in 1945. 

LS-11. I. Prigogine and R. Herman, Kinetic Theory of Vehicular Traffic, Elsevier, New York. 

TFL.5. R. L. Anderson, R. Herman, and 1. Prigogine, On the statistical distribution function theory... 

TFL.6.1. Prigogine, R. Herman, and T. Lam, Kinetic theory of vehicular traffic. Comparison with Data, Transportation Sci. 6(4) (1972). 

C. Buess-Herman, S. Bare, M. Poelman, Ordered organic adlayers at electrode surfaces in Interfacial Electrochemistry. Theory, Experiment and Applications (Ed. A. Wi ckowski), Marcel Dekker, New York-Basel, 1999, p. 427. 

At all levels of theory, the N-acetyl group of N-acetyl-N-arylnitrenium ions is rotated out of the plane of the aromatic ring, although to different extents." The N-acetyl group destabilizes the ion by ca. 20 kcal/mol relative to an N-methyl substituent in comparison with the neutral amide and amine precursors. This destabilization was attributed by Ford and Herman to loss of resonance in the amide precursor on going to the nitrenium ion, not to inductive destabilization of the ion by the acyl group. 

Figure 7.4 The crosses are computed from Mie theory. Scalar diffraction theory and geometrical optics predict the limiting value 1.067. From Bohren and Herman, 1979.

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