Contribution of covalent bond force to pressure in polymer melts

1989 ◽  
Vol 91 (5) ◽  
pp. 3168-3173 ◽  
Author(s):  
J. Gao ◽  
J. H. Weiner
Author(s):  
C. Julian Chen

This chapter discusses the physics and properties of four types of atomic forces occurring in STM and AFM: the van der Waals force, the hard core repulsion, the ionic bond, and the covalent bond. The general mathematical form of the van der Waals force between a tip and a flat sample is derived. The focus of this chapter is the covalent-bond force, which is a key in the understanding of STM and AFM. The concept of covalent bond is illustrated by the hydrogen molecular ion, the prototypical molecule used by Pauling to illustrate Heisenberg’s concept of resonance. The Herring-Landau perturbation theory of the covalent bond, an analytical incarnation of the concept of resonance, is presented in great detail. It is then applied to molecules built from many-electron atoms, to show that the perturbation theory can be applied to practical systems to produce simple analytic results for measurable physical quantities with decent accuracy.


Author(s):  
C. Julian Chen

This chapter presents a unified theory of tunneling phenomenon and covalent bond force, as a result of the similarity between the Bardeen theory of tunneling and the Herring-Landau theory of the covalent bond. Three general theoretical treatments are presented, which show that tunneling conductance is proportional to the square of the covalent bond interaction energy, or equivalently, the square of covalent bond force. The constant of proportionality is related to the electronic properties of the materials. For the case of a metal tip and a metal sample, an explicit equation contains only measurable physical quantities is derived. Several experimental verifications are presented. The equivalence of covalent bond energy and tunneling conductance provides a theoretical explanation of the threshold resistance observed in atom-manipulation experiments, and points to a method of predicting the threshold resistance for atom manipulation. Theory of imaging wavefunctions with AFM is discussed.


2000 ◽  
Vol 113 (6) ◽  
pp. 2497-2503 ◽  
Author(s):  
Lionel Garnier ◽  
Bernard Gauthier-Manuel ◽  
Eric W. van der Vegte ◽  
Jaap Snijders ◽  
Georges Hadziioannou

Author(s):  
James F. Hainfeld ◽  
Frederic R. Furuya

Glutaraldehyde is a useful tissue and molecular fixing reagents. The aldehyde moiety reacts mainly with primary amino groups to form a Schiff's base, which is reversible but reasonably stable at pH 7; a stable covalent bond may be formed by reduction with, e.g., sodium cyanoborohydride (Fig. 1). The bifunctional glutaraldehyde, (CHO-(CH2)3-CHO), successfully stabilizes protein molecules due to generally plentiful amines on their surface; bovine serum albumin has 60; 59 lysines + 1 α-amino. With some enzymes, catalytic activity after fixing is preserved; with respect to antigens, glutaraldehyde treatment can compromise their recognition by antibodies in some cases. Complicating the chemistry somewhat are the reported side reactions, where glutaraldehyde reacts with other amino acid side chains, cysteine, histidine, and tyrosine. It has also been reported that glutaraldehyde can polymerize in aqueous solution. Newer crosslinkers have been found that are more specific for the amino group, such as the N-hydroxysuccinimide esters, and are commonly preferred for forming conjugates. However, most of these linkers hydrolyze in solution, so that the activity is lost over several hours, whereas the aldehyde group is stable in solution, and may have an advantage of overall efficiency.


Author(s):  
Raja Subramanian ◽  
Kenneth S. Vecchio

The structure of stacking faults and partial dislocations in iron pyrite (FeS2) have been studied using transmission electron microscopy. Pyrite has the NaCl structure in which the sodium ions are replaced by iron and chlorine ions by covalently-bonded pairs of sulfur ions. These sulfur pairs are oriented along the <111> direction. This covalent bond between sulfur atoms is the strongest bond in pyrite with Pa3 space group symmetry. These sulfur pairs are believed to move as a whole during dislocation glide. The lattice structure across these stacking faults is of interest as the presence of these stacking faults has been preliminarily linked to a higher sulfur reactivity in pyrite. Conventional TEM contrast analysis and high resolution lattice imaging of the faulted area in the TEM specimen has been carried out.


Author(s):  
S. Kirchanski ◽  
D. Branton

We have investigated the effect of integral membrane proteins upon the fracturing of frozen lipid bilayers. This investigation has been part of an effort to develop freeze fracture labeling techniques and to assess the possible breakage of covalent protein bonds during the freeze fracture process. We have developed an experimental protocol utilizing lectin affinity columns which should detect small amounts of covalent bond breakage during the fracture of liposomes containing purified (1) glycophorin (a transmembrane glycoprotein of human erythrocyte membranes). To fracture liposomes in bulk, frozen liposomes are ground repeatedly under liquid nitrogen. Failure to detect any significant covalent bond breakage (contrary to (2)) led us to question the effectiveness of our grinding procedure in fracturing and splitting lipid bilayers.


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