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Resin matrices

Piezocomposite transducers are an advancement of piezoelectric ceramics. Instead of the classic piezoceramic material, a compound of polymer and piezoceramic is used for the composite element to improve specific properties. The 1-3 structure, which is nowadays mostly used as transducer material, refers to parallel ceramic rods incorporated in an epoxy-resin matrix (see Fig. 1). [Pg.707]

Fig. 5. Chemistry of cyclized mbbei—bis-a2ide negative acting resist, (a) Preparation of cyclized mbber resin from polyisoprene (b) photochemistry of aromatic bis-a2ide sensiti2ers. The primary photoproduct is a highly reactive nitrene which may combine with molecular oxygen to form oxygenated products, or may react with the resin matrix by addition or insertion to form polymer—polymer linkages. Fig. 5. Chemistry of cyclized mbbei—bis-a2ide negative acting resist, (a) Preparation of cyclized mbber resin from polyisoprene (b) photochemistry of aromatic bis-a2ide sensiti2ers. The primary photoproduct is a highly reactive nitrene which may combine with molecular oxygen to form oxygenated products, or may react with the resin matrix by addition or insertion to form polymer—polymer linkages.
Composites. Various composite materials have evolved over the years as a significant class of high performance textile products. The prototype composite is carbon fiber with an epoxy resin matrix for stmctural akcraft components and other aerospace and military appHcations. Carbon fiber composites ate also used in various leisure and spotting items such as golf clubs, tennis rackets, and lightweight bicycle frames. However, other types of appHcations and composites ate also entering the marketplace. For example, short ceUulose fiber/mbbet composites ate used for hoses, belting, and pneumatic tire components. [Pg.71]

Gopolymerization. The chemistry of the resin matrix, the type and degree of porosity, the particle size, and the particle size distribution are estabhshed in the copolymerization step. Formulations and operating procedures must be strictiy foHowed. Reaction vessels must be weH designed. Mistakes made during copolymerization are rarely corrected during functionalization. [Pg.372]

A polyester-type fluorescent resin matrix (22) is made by heating trimellitic anhydride, propylene glycol, and phthaUc anhydride with catalytic amounts of sulfuric acid. Addition of Rhodamine BDC gives a bright bluish red fluorescent pigment soluble in DME and methanol. It has a softening point of 118°C. Exceptional heat resistance and color brilliance are claimed for products of this type, which are useful for coloring plastics. [Pg.301]

The thermoplastic or thermoset nature of the resin in the colorant—resin matrix is also important. For thermoplastics, the polymerisation reaction is completed, the materials are processed at or close to their melting points, and scrap may be reground and remolded, eg, polyethylene, propjiene, poly(vinyl chloride), acetal resins (qv), acryhcs, ABS, nylons, ceUulosics, and polystyrene (see Olefin polymers Vinyl polymers Acrylic ester polymers Polyamides Cellulose ESTERS Styrene polymers). In the case of thermoset resins, the chemical reaction is only partially complete when the colorants are added and is concluded when the resin is molded. The result is a nonmeltable cross-linked resin that caimot be reworked, eg, epoxy resins (qv), urea—formaldehyde, melamine—formaldehyde, phenoHcs, and thermoset polyesters (qv) (see Amino resins and plastics Phenolic resins). [Pg.456]

The addition—reaction product of bisphenol A [80-05-07] and glycidyl methacrylate [106-91-2] is a compromise between epoxy and methacrylate resins (245). This BSI—GMA resin polymerizes through a free-radical induced covalent bonding of methacrylate rather than the epoxide reaction of epoxy resins (246). Mineral fillers coated with a silane coupling agent, which bond the powdered inorganic fillers chemically to the resin matrix, are incorporated into BSI—GMA monomer diluted with other methacrylate monomers to make it less viscous (245). A second monomer commonly used to make composites is urethane dimethacrylate [69766-88-7]. [Pg.493]

Composite Resins. Many composite restorative resins have incorporated fluoride into the filler particles. One commonly used material, yttrium trifluoride [13709-49-4] is incorporated as a radiopaque filler to aid in radiographic diagnosis, and is also responsible for slow release of fluoride from the composites (280). This same effect is achieved with a barium—alumina—fluoro-siUcate glass filler in composite filling and lining materials. Sodium fluoride [7681-49-4] has also been used in composites by incorporating it into the resin matrix material where it provides long-term low level release (281-283). [Pg.494]

The individual laminae used by Tsai [4-6] consist of unidirectional glass fibers in a resin matrix (U.S. Polymeric Co. E-787-NUF) with moduli given in Table 2-3. A series of special cross-ply laminates was constructed with M = 1,2,3,10 for two-layered laminates and M = 1,2,5,10 for three-layered laminates. The laminates were subjected to axial loads and bending moments whereupon surface strains were measured. Accordingly, the stiffness relations as strains and curvatures in terms of forces and moments, that is. [Pg.230]

Multi-walled CNTs (MWCNTs) are produced by arc discharge between graphite electrodes but other carbonaceous materials are always formed simultaneously. The main by-product, nanoparticles, can be removed utilizing the difference in oxidation reaction rates between CNTs and nanoparticles [9]. Then, it was reported that CNTs can be aligned by dispersion in a polymer resin matrix [10]. However, the parameters of CNTs are uncontrollable, such as the diameter, length, chirality and so on, at present. Furthermore, although the CNTs are observed like cylinders by transmission electron microscopy (TEM), some reports have pointed out the possibility of non-cylindrical structures and the existence of defects [11-14]. [Pg.76]

B. Strength, Modulus, and Chemical Stability of Fiber and Resin Matrix... [Pg.819]

In one series of laboratory tests carried out to find the optimum wear resistance of heavy-duty epoxy resin flooring compositions, a number of different abrasion resistant materials were evaluated using BS 416, employing three different epoxy resin binders which themselves had significantly differing chemical compositions and mechanical properties. The results of this work, which was carried out under dry conditions, are given in Table 9.1. As can be seen from the table, the selection of the abrasion-resistant material and the resin matrix both influence the abrasion resistance of the system, although the abrasive material incorporated appears to play a more cmcial role. [Pg.105]

Specific strength Epoxy-novolac Resin matrix for filament wound motor case... [Pg.119]

Thermal decomposition of the matrix material offers a simple way of recovering the relatively expensive reinforcing fibres from a fibre-reinforced laminate. The epoxy resin matrix was made to decompose by thermal treatment in air or nitrogen, this treatment allowing the carbon fibres to be recovered without damage. [Pg.47]

Liquid rubbers In order to improve the flexibihty of short glass fiber-reinforced epoxy composites, Kaynak et al. [53] modified the epoxy resin matrix with hydroxyl-terminated polybutadiene (HTPB) liquid mbber. A silane coupling agent was also used to improve the interfacial adhesion between glass fibers and epoxy matrix. However, Humpidge et al. [54] reported some unique processing problems for the resulting pasty mixmres when short textile fibers were incorporated in a hquid mbber medium. [Pg.354]

ASTM D 3171-90 describes a standard test method for fibre content determination of resin-matrix composites by matrix digestion in a hot medium, such as HNO3 or H2SO4/H2O2 [53],... [Pg.600]

ASTM D 3171-90, Standard Test Method for Fiber Content of Resin-Matrix Composites by Matrix Digestio, Annual Book of ASTM Standards, ASTM, West Conshohocken, PA (1998), Vol. 15.03. [Pg.680]

Several cases of interaction between anion exchange resins and nitric acid causing rapid release of energy or explosion have occurred [1]. The cause has been attributed to oxidative degradation of the organic resin matrix and/or nitration of... [Pg.1588]


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See also in sourсe #XX -- [ Pg.532 ]

See also in sourсe #XX -- [ Pg.414 ]




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Chemistry and properties of vinylester resins as matrix materials

Composite matrix resins

Composite matrix resins, adhesives

Composite resins matrix phase

Composites Thermosetting resin matrix

Compositions, polymer composites matrix resin

Compression resin transfer moulding (CRTM) in polymer matrix composites

Cross-linked epoxy resin matrix

Cyclized rubber matrix resins

Damage, interfacial matrix resin

Epoxide adhesives matrix resins

Hydrophilic resin matrix

Matrix epoxy resins

Matrix resin PEEKS

Matrix resin capability

Matrix resin continuous phase

Matrix resin damage

Matrix resin novolac

Matrix resin novolac copolymer

Matrix resin outstanding processing

Matrix resin poly

Matrix resin polyamide

Matrix resin polyethylene

Matrix resin polypropylene

Matrix resin properties

Matrix resin requirements

Matrix resin thermoplastic resins

Matrix resin thermosetting resins

Moisture sensitivity of matrix resins

No-matrix resins

Polyester resins as a matrix material

Polyimide matrix resins, synthesis

Polymer (Resin) Matrices

Polymer matrix resin, undesirable

Polyurethane Resin matrix

Processing with Thermosetting Resin Matrices

Requirements, matrix resins capability

Requirements, matrix resins properties

Resin matrices alkali

Resin matrices mechanical properties

Resin matrices rating values

Resin matrices reinforced resins

Resin matrices tensile strength

Resin matrices, thermoplastic

Resins matrix materials

Resins polymeric matrix

Types resin-matrix

Vinyl ester resin matrix

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