Polypeptide Multilayer Films: Role of Molecular Structure and Charge

Langmuir ◽  
2004 ◽  
Vol 20 (11) ◽  
pp. 4540-4547 ◽  
Author(s):  
Donald T. Haynie ◽  
Shantanu Balkundi ◽  
Naveen Palath ◽  
Kiran Chakravarthula ◽  
Komal Dave
Keyword(s):  
Molecular Structure ◽  
Multilayer Films

Crystal and molecular structure of d,l-dethiobiotin. Role of sulfur in biotin stereochemistry

1976 ◽  
Vol 98 (16) ◽  
pp. 4983-4990 ◽  
Author(s):  
Cheng-San Chen ◽  
R. Parthasarathy ◽  
George T. DeTitta
Keyword(s):  
Molecular Structure ◽  
Crystal And Molecular Structure

Subsequent and Subsidiary? Rethinking the Role of Applications in Establishing Quantum Mechanics

2015 ◽  
Vol 45 (5) ◽  
pp. 641-702 ◽  
Author(s):  
Jeremiah James ◽  
Christian Joas
Keyword(s):  
Molecular Structure ◽  
Quantum Mechanics ◽  
Quantum Theory ◽  
Classical Mechanics ◽  
Theory Construction ◽  
Science Pedagogy ◽  
Old Quantum Theory ◽  
The Common ◽  
Complete Quantum

As part of an attempt to establish a new understanding of the earliest applications of quantum mechanics and their importance to the overall development of quantum theory, this paper reexamines the role of research on molecular structure in the transition from the so-called old quantum theory to quantum mechanics and in the two years immediately following this shift (1926–1928). We argue on two bases against the common tendency to marginalize the contribution of these researches. First, because these applications addressed issues of longstanding interest to physicists, which they hoped, if not expected, a complete quantum theory to address, and for which they had already developed methods under the old quantum theory that would remain valid under the new mechanics. Second, because generating these applications was one of, if not the, principal means by which physicists clarified the unity, generality, and physical meaning of quantum mechanics, thereby reworking the theory into its now commonly recognized form, as well as developing an understanding of the kinds of predictions it generated and the ways in which these differed from those of the earlier classical mechanics. More broadly, we hope with this article to provide a new viewpoint on the importance of problem solving to scientific research and theory construction, one that might complement recent work on its role in science pedagogy.

The role of strain-induced structural changes on the mechanical behavior of PA6/PE multilayer films under uniaxial drawing

Polymer ◽  
2012 ◽  
Vol 53 (23) ◽  
pp. 5336-5346 ◽  
Author(s):  
N. Sallem-Idrissi ◽  
V. Miri ◽  
A. Marin ◽  
R. Seguela ◽  
J.-M. Lefebvre ◽  
...  
Keyword(s):  
Mechanical Behavior ◽  
Structural Changes ◽  
Multilayer Films

scholarly journals Role of package headspace on multilayer films subjected to high hydrostatic pressure

2019 ◽  
Vol 32 (5) ◽  
pp. 247-257 ◽  
Author(s):  
Saleh Al‐Ghamdi ◽  
Barbara Rasco ◽  
Juming Tang ◽  
Gustavo V. Barbosa‐Cánovas ◽  
Shyam S. Sablani
Keyword(s):  
Hydrostatic Pressure ◽  
High Hydrostatic Pressure ◽  
Multilayer Films

The Role of Molecular Structure of Phenylalanine Peptides on the Formation of Vertically Aligned Ordered Bionanostructures: Implications for Sensing Application

2020 ◽  
Vol 3 (5) ◽  
pp. 4305-4313
Author(s):  
Vefa Sahibbeyli ◽  
Dilara B. Yildiz ◽  
Gözde Papir ◽  
Yavuz Dede ◽  
Gokhan Demirel
Keyword(s):  
Molecular Structure ◽  
Vertically Aligned ◽  
Sensing Application

The Role of Intermolecular Forces in the Mechanism of High-Elastic Deformation. I. The Molecular Mechanism and an Equation for the Kinetics of High Elastic Deformation

1951 ◽  
Vol 24 (2) ◽  
pp. 336-343
Author(s):  
B. A. Dogadkin ◽  
G. M. Bartenev ◽  
M. M. Reznikovskii˘
Keyword(s):  
Molecular Structure ◽  
Molecular Mechanism ◽  
Elastic Deformation ◽  
Approximate Equation ◽  
Intermolecular Forces ◽  
Joint Application ◽  
Balanced Configurations ◽  
Kinetics Of ◽  
Constant Deformation

Abstract 1. The molecular mechanism of the relaxation of deformation of high-elastic polymers has been studied. 2. It is shown that the slow relaxation, which is typical of high-elastic polymers, may be best explained as a restoration process, which either partial or complete (depending on the degree of development of side chains in the molecular structure formed by the main valence chains) of the balanced configurations of the molecular chains. 3. It is shown that the rate of the relaxation process in this case is determined by the molecular activity of the particular polymer. 4. An approximate equation for the kinetics of high-elastic deformation which expresses qualitatively the mechanical properties of high-elastic polymers is proposed. 5. Hypotheses concerning the relation between the time of relaxation and the unbalanced stress are advanced. Equation (2) is derived as characteristic of this relation. 6. It is shown that the joint application of Equations (1) and (2) makes it possible to describe qualitatively the relaxation of stress at constant deformation.

Sign in / Sign up

Export Citation Format

Share Document