Epoxy resins, analysis

Shear-stress-shear-strain curves typical of fiber-reinforced epoxy resins are quite nonlinear, but all other stress-strain curves are essentially linear. Hahn and Tsai [6-48] analyzed lamina behavior with this nonlinear deformation behavior. Hahn [6-49] extended the analysis to laminate behavior. Inelastic effects in micromechanics analyses were examined by Adams [6-50]. Jones and Morgan [6-51] developed an approach to treat nonlinearities in all stress-strain curves for a lamina of a metal-matrix or carbon-carbon composite material. Morgan and Jones extended the lamina analysis to laminate deformation analysis [6-52] and then to buckling of laminated plates [6-53]. 

Viscoelastic characteristics of composite materials usually result from a viscoelastic-matrix material such as epoxy resin. General stress analysis of viscoelastic composites was discussed by Schapery [6-54]. An important application to laminated plates was made by Sims [6-55]. 

FIGURE 5.2 Analysis of epoxy resin, three columns AMGEL 10 A, AMGEL Iff A, AMGEL SOOA 300 X 7.8 mm, eluant THF, flow rate I ml/min, temperature 30°C, detector (DRI). 

FIGURE I 1.7 Chromatogram of an amine-based epoxy resin. The analysis of an amine-based epoxy resin was obtained on a column bank of 7.8 x 300 mm Styragel HR O.S, HR I, HR 2, and HR 3 columns. (Courtesy of Waters Corp.)... 

FIGURE 13.28 Different epoxy resins run in chloroform, analysis times of 160 min, and column temperature maintained at 50°C. 

Network properties and microscopic structures of various epoxy resins cross-linked by phenolic novolacs were investigated by Suzuki et al.97 Positron annihilation spectroscopy (PAS) was utilized to characterize intermolecular spacing of networks and the results were compared to bulk polymer properties. The lifetimes (t3) and intensities (/3) of the active species (positronium ions) correspond to volume and number of holes which constitute the free volume in the network. Networks cured with flexible epoxies had more holes throughout the temperature range, and the space increased with temperature increases. Glass transition temperatures and thermal expansion coefficients (a) were calculated from plots of t3 versus temperature. The Tgs and thermal expansion coefficients obtained from PAS were lower titan those obtained from thermomechanical analysis. These differences were attributed to micro-Brownian motions determined by PAS versus macroscopic polymer properties determined by thermomechanical analysis. 

Lauchli, A., Spurr, A.R. Wittkop, R.W. (1970). Electron probe analysis of freeze substituted, epoxy resin embedded tissue for ion transport studies in plants. Planta, 95, 341-50. 

In a study of dental silicate cements, Kent, Fletcher Wilson (1970) used electron probe analysis to study the fully set material. Their method of sample preparation varied slightly from the general one described above, in that they embedded their set cement in epoxy resin, polished the surface to flatness, and then coated it with a 2-nm carbon layer to provide electrical conductivity. They analysed the various areas of the cement for calcium, silicon, aluminium and phosphorus, and found that the cement comprised a matrix containing phosphorus, aluminium and calcium, but not silicon. The aluminosilicate glass was assumed to develop into a gel which was relatively depleted in calcium. 

Aromatic amines formed from the reduction of azo colorants in toy products were analysed by means of HPLC-PDA [703], Drews et al. [704] have applied HPLC/ELSD and UV/VIS detection for quantifying SFE and ASE extracts of butyl stearate finish on various commercial yarns. From the calibrated ELSD response the total extract (finish and polyester trimer) is obtained and from the UV/VIS response the trimer only. Representative SFE-ELSD/UV finish analysis data compare satisfactorily to their corresponding SFE gravimetric weight recovery results. GC, HPLC and SEC are also used for characterisation of low-MW compounds (e.g. curing agents, plasticisers, by-products of curing reactions) in epoxy resin adhesives. 

High Resolution Transmission Electron Microscopy (HRTEM, Philips CM20, 200 kV) was applied to get structural and nanotextural information on the fibers, by imaging the profile of the aromatic carbon layers in the 002-lattice fringe mode. A carbon fiber coated with pyrolytic carbon was incorporated in epoxy resin and a transverse section obtained by ultramicrotomy was deposited on a holey carbon film. An in-house made image analysis procedure was used to get quantitative data on the composite. 

Three industries were suspected to cause the BDE-209 contamination along the Vero River the first one, a textile industry which produced polyester fibers treated with flame retardants, the second one produced epoxy resins, and the third one is focused on the polyamide polymerization. Moreover, the effluent of the industrial park at the discharge site to the Vero River was also analyzed. Analysis of industrial effluents of each industry revealed that industry focused on the polyamide polymerization is the main responsible of the BDE-209 contamination, with concentration levels around 2,600 ng/L (Table 5). Nevertheless, the two other industries also contribute in some way to the total contamination. 

Bromide analysis, of water, 26 41 Bromide ions, in development solution, 79 205-206 Bromides, 4 319-330 thorium, 24 763 titanium, 25 54 tungsten, 25 379 uranium, 25 439 Bromimide, 4 299, 319 Brominated additive flame retardants, 77 461-468, 471-473t Brominated Anthanthrone Orange, pigment for plastics, 7 367t Brominated aromatic compounds, 7 7 459 Brominated bisphenol A-based epoxy resins, 70 366... 

See also Epoxy coatings Epoxy chalcone, 10 450 12,13-Epoxy-cis-9-octadecenoic (vernolic) acid, physical properties, 5 35t Epoxy coatings, 10 436 450 17 845. See also Epoxy can coatings for corrosion protection, 7 199 markets for, 10 442-449 performance of, 10 423 waterborne, 10 439 Epoxy composites, 10 450, 451 Epoxy compounds, photoinitiated polymerization of, 23 716 Epoxy content analysis, 10 385 Epoxy cresol novolac (ECN) resins, 10 367, 369... 

The first moment of the distribution is Pt0T the total, cumulative molar concentration of polymeric material. As the molecular weight of polymeric species increases, branching and crosslinking reactions yield a thermoset resin. Chromatography analysis of epoxy resin extracts confirms the expected population density distribution described by Equation 4, as is shown in Figure 2. Formulations and cure cycles appear in Table II. 

For quality cured thermoset resins, approximately one percent of the mass is soluble when subjected to long-term leaching with tetrahydrofuran. Equilibrium is approached in two weeks resin swell is not visually noticeable. The monomeric, chemical structures are such that the hydrocarbon resins exhibit more pronounced viscoelastic properties whereas, the epoxy resins are similar to elastic bodies when subjected to tensile testing at room temperature. Therein, LRF 216 is less sensitive to flaws and is more nonlinear in tensile or compressive stress-strain analysis. 

Size Exclusion Chromatography Analysis of Epoxy Resin Cure Kinetics... 

Patrikis. A.K., Andrews, M.C. and Young, R.J. (1994). Analysis of the single fiber pull-out test by the use of Raman spectroscopy part I Pull-out of aramid fibers from an epoxy resin. Composites Sci. Technol. 52, 387 396. 

The epoxy resin formed by tetraglycidyl 4,4 -diamino diphenyl methane and 4,4 -diamino diphenyl sulfone was characterized by dynamic mechanical analysis. Epoxy specimens were exposed to varying dose levels of ionizing radiation (0.5 MeV electrons) up to 10,000 Hrads to assess their endurance in long-term space applications. Ionizing radiation has a limited effect on the mechanical properties of the epoxy. The most notable difference was a decrease of approximately 40°C in Tg after an absorbed dose of 10,000 Mrads. Sorption/desorption studies revealed that plasticization by degradation products was responsible for a portion of the decrease in Tg. 

Glass transition temperatures (Tg s) were detemined using a Dupont DSC 910 attached to a 9900 data analysis system. For off-stoichiometric studies, epoxy resin and diamine were cured in situ within a hermetically sealed DSC pan (sample tak from 25 C - 300 C at lO C/min), then cooled rapidly back to 25 C, and finally scanned from 40 C - 220 c to record the Tg. All samples were scanned under nitrogen atmosphere at a rate of 10 C/min. 

Cure Kinetics. The cure kinetics of the mixed system to the B-stage were determined by the method outlined by Senich, MacKnight and Schneider (7) for two epoxy resins cured with dicyandianide by dynamic spring analysis (DSA). Senich et al. (7) used the elapsed time to the loss peak maximum of tan delta as a measure of the rate of the reaction at each temperature and for each frequency. The slope of an Arrhenius plot of In (tmax) vs. 1/T was then used to determine the activation energy. 

Figure 8. GPC analysis of low molecular weight epoxy resin.

Solvent absorption measurement has been shown to be a sensitive and useful test method in the manufacture of epoxy powder coatings. A test method was defined and the effects of time and temperature of immersion described. It was shown that solvent absorption is a measure of raw material properties (EEW of the epoxy resin, and CTBN elastomer type and concentration), the homogeneity of the extrudate, as well as the state of cure. The information obtained from solvent absorption measurements has proven to be extremely important not only in quality control analysis but also in providing an insight into the structure function relationships in epoxy resin chemistry. 

The relevant properties of these materials for the torsional-mechanical analysis are listed in Table 8.11. On the basis of specific elastic modulus and specific shear modulus, the best materials are the graphite-fiber-reinforced epoxy resin, followed by either of the alloys, then the Kevlar fiber-reinforced epoxy. The chopped glass sheet molding compound is obviously not a good choice. 

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