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Reaction adhesives

In the crosslinked state, epoxy resins are highly resistant to chemicals, temperature, and solvents and are also endowed with good electrical properties. They are therefore employed, for example, as casting resins in electro- and electronic industry as well as resistant lacquers and coatings. Moreover, they possess excellent adhesive power for many plastics, wood, and metals ( reaction adhesives two-component adhesives ). [Pg.326]

Use Ester exchange reactions adhesion of paints, rubber, and plastics to metals condensation catalyst. [Pg.1224]

PUR adhesives have shown the most annual growth of all adhesive types at 3.5%. The absolute volume/year for these products exceeds that of aU other reaction adhesives. As is the case in all PUR chemical applications, the PUR adhesives show a variety not found with other reaction adhesives. [Pg.231]

Corhesive is a solvent-free, two-component reaction adhesive system for use with polyurethanes, plasma treated silicones and certain metals (Tables 4.4, 4,12, 4.13, and 4.14). [Pg.316]

Davidson, A., Alderson, S. (2009). An introduction to solution and reaction adhesives for fossil preparation. In M. A. Brown, J. F. Kane, W. G. Parker (Eds.), Methods in Fossil Preparation, First Annual Fossil Preparation and Collections symposium. Petrified Forest Proceedings (pp. 53-62). [Pg.136]

FIGURE 8.3 Examples of monomers used in acrylic reaction adhesives, e.g. anaerobic and ultraviolet curing types. [Pg.173]

Assembly adhesives are either available as dispersions or as one-component reaction adhesives in cartridges or tubes. [Pg.93]

Via cations UV epoxides cure rapidly via a cationic reaction (ca. 30-90 s). Oxygen does not inhibit the reaction. Adhesive which emanates from the joint forms a dry surface. The UV absorption is usually in the wavelength region between 320 and 450 nm. [Pg.993]

Resins formed from the reaction of poly(vinyl alcohol) with aldehydes. The formal derivative (from methanal) is used in wire coatings and adhesives and the bulyral (from butanal) is used in metal paints, wood-sealers, adhesives and in safety glass interlayers. [Pg.323]

Aluminum complex greases, obtained by the reaction of aluminum isopropylate with a mixture of benzoic acid and fatty acids. These greases have a remarkable resistance to water, very good adhesion to metallic surfaces, good mechanical stability properties and resistance to temperature. They are less common than the first two types. [Pg.281]

Epoxy Resins. The chemistry of epoxy resin adhesives is quite varied. However, the most widely used is that formed from the reaction of 4,4 -isopropyhdene diphenol (bisphenol A) [80-05-7] and epichlorohydrin [106-89-8] C H CIO. This epoxy resin is more commonly known as... [Pg.232]

The two-part epoxy adhesive, readily available in hardware stores or other consumer outlets, comes in two tubes. One tube contains the epoxy resin, the other contains an amine hardener. Common diamine room temperature epoxy curing agents are materials such as the polyamides, available under the trade name Versamid. These polyamides are the reaction products of dimer acids and aUphatic diamines such as diethylenetriamine [111-40-0] ... [Pg.232]

Phenolic Resins. Phenohc resins (qv) are formed by the reaction of phenol [108-95-2] C H O, and formaldehyde [50-00-0] CH2O. If basic conditions and an excess of formaldehyde are used, the result is a resole phenohc resin, which will cure by itself Hberating water. If an acid catalyst and an excess of phenol are used, the result is a novolac phenohc resin, which is not self-curing. Novolac phenohc resins are typically formulated to contain a curing agent which is most often a material known as hexamethylenetetraamine [100-97-0] C H22N4. Phenohc resin adhesives are found in film or solution... [Pg.233]

Acryhc stmctural adhesives have been modified by elastomers in order to obtain a phase-separated, toughened system. A significant contribution in this technology has been made in which acryhc adhesives were modified by the addition of chlorosulfonated polyethylene to obtain a phase-separated stmctural adhesive (11). Such adhesives also contain methyl methacrylate, glacial methacrylic acid, and cross-linkers such as ethylene glycol dimethacrylate [97-90-5]. The polymerization initiation system, which includes cumene hydroperoxide, N,1S7-dimethyl- -toluidine, and saccharin, can be apphed to the adherend surface as a primer, or it can be formulated as the second part of a two-part adhesive. Modification of cyanoacrylates using elastomers has also been attempted copolymers of acrylonitrile, butadiene, and styrene ethylene copolymers with methylacrylate or copolymers of methacrylates with butadiene and styrene have been used. However, because of the extreme reactivity of the monomer, modification of cyanoacrylate adhesives is very difficult and material purity is essential in order to be able to modify the cyanoacrylate without causing premature reaction. [Pg.233]

In the area of moleculady designed hot-melt adhesives, the most widely used resins are the polyamides (qv), formed upon reaction of a diamine and a dimer acid. Dimer acids (qv) are obtained from the Diels-Alder reaction of unsaturated fatty acids. Linoleic acid is an example. Judicious selection of diamine and diacid leads to a wide range of adhesive properties. Typical shear characteristics are in the range of thousands of kilopascals and are dependent upon temperature. Although hot-melt adhesives normally become quite brittle below the glass-transition temperature, these materials can often attain physical properties that approach those of a stmctural adhesive. These properties severely degrade as the material becomes Hquid above the melt temperature. [Pg.235]

Health and safety information is available from the manufacturer of every adhesive sold in the United States. The toxicology of a particular adhesive is dependent upon its components, which mn the gamut of polymeric materials from natural products which often exhibit low toxicity to isocyanates which can cause severe allergic reactions. Toxicological information may be found in articles discussing the manufacture of the specific chemical compounds that comprise the adhesives. [Pg.236]


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See also in sourсe #XX -- [ Pg.155 ]




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