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Types resin-matrix

Duolite A-7 2.2 1.12 Phenolic type resin. High porosity and hydrophilic matrix. pH range is 0 to 6. [Pg.1113]

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]

Polymer-based, synthetic ion-exchangers known as resins are available commercially in gel type or truly porous forms. Gel-type resins are not porous in the usual sense of the word, since their structure depends upon swelhng in the solvent in which they are immersed. Removal of the solvent usually results in a collapse of the three-dimensional structure, and no significant surface area or pore diameter can be defined by the ordinaiy techniques available for truly porous materials. In their swollen state, gel-type resins approximate a true molecular-scale solution. Thus, we can identify an internal porosity p only in terms of the equilibrium uptake of water or other liquid. When crosslinked polymers are used as the support matrix, the internal porosity so defined varies in inverse proportion to the degree of crosslinkiug, with swelhng and therefore porosity typically being more... [Pg.1500]

The resins can be divided into two groups having major structural differences gel and macroreticular . In the case of gel type resins if the beads are totally dry, then the polymeric matrix collapses and the polystyrene chains will be as close as atomic forces allow. Therefore, swelling ability of the reactants is a prerequisite for catalysis by gel resins. Gel resins are characterized by a divinyl benzene content that is generally below 12%. [Pg.127]

From this result on MRS, we expected that a combination of phenolic-resin-based resist and aqueous alkaline developer would lead to etching-type dissolution and non-swelling resist patterns. In this paper, we report on a new non-swelling negative electron beam resist consisting of an epoxy novolac, azide compound and phenolic resin matrix (EAP) and discuss the radiation chemistry of this resist. [Pg.424]

Following this initial period of polyimide development, interest reached a steady-state and remained there until the late 1970s. During this time a major impetus to the polyimide area was provided by the aerospace industry. The need for composite matrix resins as well as structural adhesives with excellent oxidative and thermal stability appeared to be at least partially met by polyimide type resins. Ultimately, requirements of high flow and low void content in relatively thick parts directed these efforts into different directions. Another upswing occurred in the early 1980s with the potential application of... [Pg.114]

Pretreatment for fillers. When used as a surface treatment for fillers or reinforcing materials, in which the silane is applied to the filler or fibre before incorporation into a resin matrix, the same factors as for pretreatment primers apply. In addition, the particle size and the absence/presence of water are important, and in a sense this application is only a variation on the former. It should be noted that silane treated fillers may have, or impart, different rheological properties to non-treated fillers, particularly particulates. A major disadvantage of this approach is that a general purpose silane may have to be used by a manufacturer rather than one specifically tailored to the use of a particular resin type and less than optimum properties are likely to be achieved in some cases. [Pg.25]

Resin Matrix Type Physical structure Capacity (meq/mL) Dry wt (%) ... [Pg.528]

Fillers may be added to low-viscosity resins by conventional sigma-blade mixer or the same type of equipment used for mixing paint systems. Three roll mills are generally employed for more viscous systems to obtain thorough wetting of the filler by the resin matrix. [Pg.393]

In the CTBN-epoxy resin system without bisphenol A we believe product (IV) type may be dissolved and distributed throughout the matrix. Because the solubility parameter difference between product (IV) and the epoxy resin matrix is less than with the bisphenol A modified epoxy resin matrix, we do not observe the second small particle size in this system. [Pg.340]

Type Chemically bonded functional group Resin/matrix Trade name... [Pg.150]

Many monomers can be grafted by redox polymerization to the magnetic core [magnetic material embedded in poly(vinyl alcohol) matrix nominally 100% cross-linked with glutaraldehyde] to get whisker-type resins " . Acrylic acid and acryl-... [Pg.95]


See other pages where Types resin-matrix is mentioned: [Pg.301]    [Pg.301]    [Pg.373]    [Pg.379]    [Pg.301]    [Pg.527]    [Pg.74]    [Pg.783]    [Pg.215]    [Pg.218]    [Pg.227]    [Pg.447]    [Pg.9]    [Pg.552]    [Pg.9]    [Pg.29]    [Pg.320]    [Pg.214]    [Pg.527]    [Pg.45]    [Pg.373]    [Pg.374]    [Pg.375]    [Pg.379]    [Pg.100]    [Pg.275]    [Pg.69]    [Pg.389]    [Pg.229]    [Pg.1322]    [Pg.142]    [Pg.117]    [Pg.59]    [Pg.679]   
See also in sourсe #XX -- [ Pg.103 ]




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