Characterization of High Performance Composite Matrices

Author(s):  
Roger J. Morgan
Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 2983
Author(s):  
He Xiang ◽  
Yaming Jiang ◽  
Yexiong Qi ◽  
Jialu Li

In order to characterize the process-induced distortions of 3D thin shell composites with complex shape, the multilayered biaxial weft knitted (MBWK) fabric reinforced high-performance composite helmet was selected as the research object, and the 3D laser scanning machine was used to scan the helmet surface, then the 3D scanning data was compared with the CAD model to evaluate the deformation. The results and discussion indicated that the conventional method was workable, but the speed of convergence was slow and the calculation results were easy to drop into local optimization. According to detailed analysis, a measurement method focusing on the principle of “Feature Distance” was developed. The measurement results shown that this method can not only give accurate results, but also reduce working procedure and greatly save the computing resources, which is proved to be a feasible approach for the deformation measurement foundation of 3D thin shell textile composites.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Dan Rosu ◽  
Constantin N. Cascaval ◽  
Liliana Rosu

AbstractVinyl ester resins are unsaturated polyesters, widely used as matrix for high performance composite materials. The paper presents the synthesis and characterization of some vinyl ester resin/hydroxyapatite bioactive compositions using an unsaturated copolyester based on turpentine oil as reactive diluent. The vinyl ester oligomer /unsaturated copolyester/hydroxyapatite structural complex was characterized from the morphological point of view, water absorbtion, density measurements and volume contraction. The water uptake is dependent on the concentration in vinyl ester resin. The increase of the vinyl ester resin content in the bioactive composite leads to the increase of the density, respectively to a significant decrease of the volume contraction


2014 ◽  
Vol 529 ◽  
pp. 117-121 ◽  
Author(s):  
An Qing Fu ◽  
Yang Zhou ◽  
Ming Jie Zhu ◽  
Yao Rong Feng ◽  
Xun Ji Li ◽  
...  

In this work, the permeability of high performance composite coating (HPCC) and its containing layers fusion bonded epoxy (FBE) and middle density polyethylene (MDPE) to dissolved CO2 was investigated. The obtained results showed that the permeability to dissolved CO2 of HPCC, FBE, and MDPE are in order of HPCC<FBE<MDPE, the corresponding values of three coatings are 1.27 × 10-11 mol/atm⋅m⋅s, 1.54 × 10-11, and 3.51×10-10 mol/atm⋅m⋅s, respectively. The measurement methodology of dissolved CO2 permeability on organic coatings is feasible based on the present work.


1984 ◽  
Vol 51 (01) ◽  
pp. 016-021 ◽  
Author(s):  
S Birken ◽  
G Agosto ◽  
B Lahiri ◽  
R Canfield

SummaryIn order to investigate the early release of NH2-terminal plasmic fragments from the Bβ chain of fibrinogen, substantial quantities of Bβ 1-42 and Bβ 1-21 are required as immunogens, as radioimmunoassay standards and for infusion into human volunteers to determine the half-lives of these peptides. Towards this end methods that employ selective proteolytic cleavage of these fragments from fibrinogen have been developed. Both the N-DSK fragment, produced by CNBr cleavage of fibrinogen, and Bβ 1-118 were employed as substrates for plasmin with the finding of higher yields from N-DSK. Bβ 1-42 and Bβ 1-21 were purified by gel filtration and ion-exchange chromatography on SP-Sephadex using volatile buffers. When the purified preparation of Bβ 1-42 was chromatographed on reverse-phase high performance liquid chromatography, two peaks of identical amino acid composition were separated, presumably due either to pyroglutamate or to amide differences.


1998 ◽  
Author(s):  
A. Crasto ◽  
D. Anderson ◽  
R. Esterline ◽  
K. Han ◽  
C. Hill

1992 ◽  
Vol 57 (10) ◽  
pp. 2151-2156 ◽  
Author(s):  
Peter Chabreček ◽  
Ladislav Šoltés ◽  
Hynek Hradec ◽  
Jiří Filip ◽  
Eduard Orviský

Two methods for the preparation of high molecular weight [3H]hyaluronic acid were investigated. In the first one, hydrogen atoms in the molecule were replaced by tritium. This isotopic substitution was performed in aqueous solution using Pd/CaCO3 as the catalyst. In the second method, the high molecular weight hyaluronic acid was alkylated with [3H]methyl bromide in liquid ammonia at a temperature of -33.5 °C. High-performance gel permeation chromatographic separation method was used for the isolation and characterization of the high molecular weight [3H]hyaluronic acid. Molecular weight parameters for the labelled biopolymers were Mw = 128 kDa, Mw/Mn = 1.88 (first method) and Mw = 268 kDa, Mw/Mn = 1.55 (second method). The high molecular weight [3H]hyaluronic acid having Mw = 268 kDa was degraded further by specific hyaluronidase. Products of the enzymatic depolymerization were observed to be identical for both, labelled and cold biopolymer. This finding indicates that the described labelling procedure using [3H]methyl bromide does not induce any major structural rearrangements in the molecule.


Sign in / Sign up

Export Citation Format

Share Document