Primary composite structure

Military aircraft have made much more use of primary composite structures than on commercial transport aircraft, but most new general aviation aircraft since the resurgence of this industry a decade ago have made even more extensive use of composites, co-cured and bonded, in their primary structures. Their smaller size favors this method of manufacture. 

Considerations of the primary chemical structure (e.g., molecular composition, backbone microstructure, chain length, crosslinking) of urethane polymers are... 

StructurPly I and II by Multi-Axial are thermoplastic matrix resin prepregs used in the construction of primary-load-carrying composite structures. Unlike the few hours typically required by the thermoset resin materials to cure, StructurPly needs a few minutes at 196°C. 

Physical models of fuel cell operation contribute to the development of diagnoshc methods, the rational design of advanced materials, and the systematic ophmization of performance. The grand challenge is to understand relations of primary chemical structure of materials, composition of heterogeneous media, effective material properties, and performance. For polymer electrolyte membranes, the primary chemical structure refers to ionomer molecules, and the composition-dependent phenomena are mainly determined by the uptake and distribuhon of water. 

Fig. 17. Composite structural motions of subunits can be described with translation, libration, and screw-axis (TLS) analysis of the NCP. Analysis of the histone subunits are shown here, (a) Composite motion of histones H2A (blue) and H2B (blue) considered as individual elements and combined as H2A H2B dimer (red). Note for the individual histones that the axis of motion is parallel with the medial a-helix of the histone. The origin of the TLS axes are within the structural positions of the histone. The composite motion for the H2A H2B dimer is dominated by the motion of H2A, as is seen in the similarity of orientation and position of the two axes, (b) The orientation and motion of the two H2A H2B dimers appear symmetric across the dyad axis of the NCP. (c) H3 H4 composite motions when considered as dimers (blue) and as the tetramer (red). Interpretation is more complex because of the asymmetric magnitude of motion for the two dimers, and the different position in the axis of primary motion for the tetramer. These motions are most likely the consequence of packing interactions, described in greater detail in the text.

The effect of k on d is most clearly demonstrated in the experiment by Fukada and Date (1970) on the polyester resin film, filled with powdered barium titanate and polarized under a d.c. field. The strong piezoelectricity, as shown in Fig. 29, is ascribed to the polarization charge of the ceramic filler and heterogeneous strain due to the composite structure. The real part d exhibits a maximum at 90° C and d" has a peak and a succeeding dip at this temperature where the primary relaxation of polyester resin occurs. The behavior of d and d" is quite similar to that of k and k" in Fig. 16, respectively, in which decreasing X = an corresponds to increasing temperature. 

It can be readily appreciated that there will be an element of overlap between the broad categories above and in particular with evolving complex hybrid systems. The classification is intended as a point of reference and for ease of understanding the vast possibilities that exist with nanosystems without the need for constant reclassification as far as possible. These structures may be further differentiated according to their primary composition ... 

These results provide insight into the potential biogeochemical and trophic impacts of shifting compositions and quantities of new N compounds impHcated in marine eutrophication. Both the amount and makeup of new N play critical roles in determining the magnitude and composition of primary producers. Structural and functional modifications of the primary producer community strongly influence... 

Description. Proteins are polyelectrolytes, but they occur in such a bewildering variety of composition, structure, and properties that physicochemical polymer theory is of limited use for understanding them. The properties ultimately depend on the primary structure of a protein, i.e., what amino acid residues occur and in what sequence. The 20 amino acid building blocks differ in several respects. The most important general properties may be their charge, which determines the charge of the protein as a function of pH and the hydrophobicity, which is of prime importance for conformation and solubility. 

A polysaccharide can be added as a component in a protein system to produce a protein-polysaccharide composite structure. Tolstoguzov (2003) reviewed the main function of protein and polysaccharide in protein-polysaccharide food formulation. Generally, polysaccharides have less surface activity in comparison to proteins. This inferiority is related to their low flexibility and monotonic repetition of the monomer units in the backbone. The low surface activity of polysaccharides results in their inability to form a primary adsorbed layer in the system. The nature of interactions between polysaccharides and adsorbed proteins, as well as their influence on colloid stability, can either stabilize or destabilize the emulsions. Attractive protein-polysaccharide interactions can enhance the emulsion stability by forming a thicker and stronger steric-stabilizing layer. In contrast, the attractive interactions... 

In other words, the sum of functional properties depends on the physicochemical characteristics of the whole system containing the working protein. The determinant properties of the protein itself are the amino acid composition, structure (primary, secondary, tertiary, quaternary), and conformational stability the charge of the molecule and its dimensions, shape, and topography the extent of polarity and hydrophobicity, and the nature of protein-protein interactions. 

---