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Exposure thermal

Vessel heads can be made from explosion-bonded clads, either by conventional cold- or by hot-forming techniques. The latter involves thermal exposure and is equivalent in effect to a heat treatment. The backing metal properties, bond continuity, and bond strength are guaranteed to the same specifications as the composite from which the head is formed. AppHcations such as chemical-process vessels and transition joints represent approximately 90% of the industrial use of explosion cladding. [Pg.150]

The effect of temperature on PSF tensile stress—strain behavior is depicted in Figure 4. The resin continues to exhibit useful mechanical properties at temperatures up to 160°C under prolonged or repeated thermal exposure. PES and PPSF extend this temperature limit to about 180°C. The dependence of flexural moduli on temperature for polysulfones is shown in Figure 5 with comparison to other engineering thermoplastics. [Pg.466]

Some of the chemicals mentioned above and others, such as chlorinated mbber or paraffin, antimony trioxide, calcium carbonate, calcium borate, pentaerythrithol, alumina trihydrate, titanium dioxide, and urea—melamine—formaldehyde resin, may be used to formulate fire retardant coatings. Many of these coatings are formulated in such a way that the films intumesce (expand) when exposed to fire, thus insulating the wood surface from further thermal exposure. Fire retardant coatings are mostly used for existing constmction. [Pg.329]

Crosslinking has been claimed to improve thermal resistance of the cyanoacrylate adhesive [18]. However, in other reports [6], little or no improvement in thermal resistance of the adhesive was demonstrated by the addition of a difunctional monomer. As seen in Fig. 2, the addition of varying amounts of crosslinker 7 provided no improvement in the tensile adhesive strength of ethyl cyanoacrylate on steel lapshears after thermal exposure at 121 °C for up to 48 h. [Pg.852]

Fig. 2. Adhesion tests after thermal exposure with ECA crosslinked with the dicyanoacrylate ester of butanediol, 7. Fig. 2. Adhesion tests after thermal exposure with ECA crosslinked with the dicyanoacrylate ester of butanediol, 7.
Fig. 5. Lapshear strengths for ECA and DEMM monomer mixtures after thermal exposure. Fig. 5. Lapshear strengths for ECA and DEMM monomer mixtures after thermal exposure.
An example of this improvement in toughness can be demonstrated by the addition of Vamac B-124, an ethylene/methyl acrylate copolymer from DuPont, to ethyl cyanoacrylate [24-26]. Three model instant adhesive formulations, a control without any polymeric additive (A), a formulation with poly(methyl methacrylate) (PMMA) (B), and a formulation with Vamac B-124 (C), are shown in Table 4. The formulation with PMMA, a thermoplastic which is added to modify viscosity, was included to determine if the addition of any polymer, not only rubbers, could improve the toughness properties of an alkyl cyanoacrylate instant adhesive. To demonstrate an improvement in toughness, the three formulations were tested for impact strength, 180° peel strength, and lapshear adhesive strength on steel specimens, before and after thermal exposure at 121°C. [Pg.857]

The impact strength data for ambient temperature and 121°C cure are shown in Fig. 6. While the addition of the rubber does not initially improve impact strength, it does increase over time at ambient temperature, and after thermal exposure, this improvement is even greater. [Pg.857]

The addition of Vamac B-124 to ethyl cyanoacrylate has a more pronounced effect on peel strength, both at ambient temperature and after thermal exposure. After 24 h at ambient temperature, the peel strength of the rubber-toughened formulation is almost 40% greater than the control formulation A without rubber. After heating the test specimens for 2 h at 121°C, the peel strength of formulation A, is almost non-existent, while that of C has increased significantly, as seen in Fig. 7. [Pg.857]

Fig. 6. Impact strengths for ECA, ECA/PMMA, and ECA/Vamac B-124, in the text respectively indicated by A, B and C, with and without thermal exposure at 121°C. Fig. 6. Impact strengths for ECA, ECA/PMMA, and ECA/Vamac B-124, in the text respectively indicated by A, B and C, with and without thermal exposure at 121°C.
ISO DIS 12894 Selection of an appropriate system of medical supervision for different types of thermal exposure EIrgonomics of the thermal environment Medical supervision of individuals exposed to hot or cold environment ... [Pg.375]

Incorporated in methacrylate and unsaturated polyester cast resins, P.R.88 not only withstands several hours of thermal exposure during processing but is also resistant to the peroxides which are used as catalysts. Some types accelerate the polymerization process, i.e., the hardening of the plastic. [Pg.500]

Eye bums are a process that develops during a chemical or thermal exposure that is of exceeding mass, contact time, chemical reactivity, and temperature until the exhaustion of the protective mechanisms of the eye. The most plastic description of this process can be given in images that are obtained by optical coherence tomography [5]. [Pg.65]

No further cross-linking of the 3-APTHS is observed as a function of thermal exposure to temperatures up to 120°C. [Pg.320]

One of the main reasons for the recent interest in organic sulfur in sedimentary organic matter is the growing evidence that it plays a role in the petroleum generation process. Organically-bound sulfur has been implicated in the formation of low API gravity, asphaltene-rich petroleums at a low level of thermal exposure (1). Recent studies indicate that... [Pg.532]

Thermal Exposures. The thermal aging tests on coated and uncoated samples were conducted in Precision forced convection ovens. Temperature uniformity was 1 C, which was determined with a thermocouple array that was mounted in the oven containing a set of dummy samples. No change in temperature uniformity was observed as a result of removing samples periodically for analysis. Test temperatures were 150°C, 110 C, 90°C, 80°C and 70°C for... [Pg.111]

Thermal Exposures. The thermally Induced changes in tensile properties of coated and uncoated silk fabric, expressed as percent retained breaking-load, strain-to-break and energy-to-break in Figures 2,3, and 4, respectively, are shown with the lines representing the calculated exponential decline. [Pg.115]

Bench-scale reaction-to-fire tests are used to characterize the behavior of materials under more severe thermal exposure conditions that are representative of the growing pre-flashover stage of a compartment fire. These tests essentially determine how a material responds to the temperatures and heat fluxes in a growing fire. In these tests, the fire conditions are simulated with a radiant panel or by inserting the specimen into a small furnace. A pilot may be used to ignite the flammable gases and vapors that are generated as a result of thermal decomposition of the... [Pg.354]

Finally, a small furnace is sometimes used to create the desired thermal exposure conditions. A furnace arrangement is ideal when the objective is to create a constant or specified time-varying temperature environment. [Pg.359]


See other pages where Exposure thermal is mentioned: [Pg.70]    [Pg.855]    [Pg.859]    [Pg.90]    [Pg.106]    [Pg.149]    [Pg.211]    [Pg.617]    [Pg.240]    [Pg.617]    [Pg.11]    [Pg.11]    [Pg.134]    [Pg.305]    [Pg.316]    [Pg.121]    [Pg.20]    [Pg.295]    [Pg.63]    [Pg.91]    [Pg.99]    [Pg.108]    [Pg.203]    [Pg.99]    [Pg.274]    [Pg.352]    [Pg.355]    [Pg.358]   
See also in sourсe #XX -- [ Pg.115 , Pg.116 , Pg.117 , Pg.118 , Pg.119 , Pg.120 , Pg.121 , Pg.122 , Pg.123 ]

See also in sourсe #XX -- [ Pg.47 , Pg.48 ]




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Microwave exposure thermal

Thermal exposure magnitude

Thermal exposure procedure

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