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Thickness methacrylate

The principal structural features are as follows ceiling and walls are 1/4" thick methacrylate plastic floor and structural elements were aluminum. Approximate dimensions are 1 x 2 x 3 M. A heat exchanger supplied by external chilled water provided temperature and humidity control. Sensors buried in the vermiciiite or sand support medium allowed monitoring of soil moisture content. Carbon dioxide was provided from external cylinders, and nutrient was supplied to each plant through a sealed bulkhead. Alternatively, solid inorganic nutrient was provided from a pellet buried in the sand/vermiculite soil medium, and the condensed water of transpiration recycled and distributed to each plant by means of an automatic dispenser controlled by a preset timer. This system was probably most satisfactory from the viewpoint of eliminating periodic additions of external liquid nutrient and subsequent withdrawal of the condensed water of transpiration. [Pg.194]

Pentaerythritol is used in self-extinguishing, non dripping, flame-retardant compositions with a variety of polymers, including olefins, vinyl acetate and alcohols, methyl methacrylate, and urethanes. Phosphoms compounds are added to the formulation of these materials. When exposed to fire, a thick foam is produced, forming a fire-resistant barrier (see Elame retardants) (84—86). [Pg.466]

Table 4. Electrical Properties of 6.35-mm Thick Poly(methyl methacrylate) Sheet ... Table 4. Electrical Properties of 6.35-mm Thick Poly(methyl methacrylate) Sheet ...
Fig. 4.55. Experimental and calculated (dashed line) RAIR-spectra for poly(methyl methacrylate) films 3270 + 100 nm, 362 30 nm, and 78 + 15 nm thick (a) p-polarized light incident at 60° (b) s-polarized light incident at 60°, after [4.266]. Fig. 4.55. Experimental and calculated (dashed line) RAIR-spectra for poly(methyl methacrylate) films 3270 + 100 nm, 362 30 nm, and 78 + 15 nm thick (a) p-polarized light incident at 60° (b) s-polarized light incident at 60°, after [4.266].
The chlorinated surface of glass then acted as a coinitiator, and when photochemically treated with metal carbonyl in the presence of MMA monomer, a thin layer of 0.4 /Am thickness of poly(methyl methacrylate) was obtained. [Pg.255]

Sanding is carried out at this stage and, after clean-up, the final colour or top-coat is applied. There is some variation in the resin chemistry used. Alkyds crosslinked with melamine-formaldehyde are widely used for non-metallic pigmentation. Metallics are usually based on acrylics for better durability. The acrylic may be thermoset with melamine-formaldehyde or a thermoplastic lacquer (plasticised copolymer of methyl methacrylate). A thickness of about 50ftm is applied and stoved for 20 min at 130°C (lacquers receive a bake-sand-bake process for a smoother appearance). [Pg.627]

Tri-n-butyltin methacrylate (TBTM) was synthesized by chemists at the David Taylor Naval Ship Research and Development Center (DTNSRDC), Annapolis, Maryland. The methods of Dyckman et al. (1 ) and Montermoso et al. (2 ) were used, in which 30 g methacrylic acid was slowly added to 103.8 g bis(tri-n-butyltin) oxide in 300 mL benzene in a flask equipped with a stirrer and reflux condenser. Cooling kept the temperature below 25°C. After all acid had been added, the solution was heated gradually and maintained at 30°C while the water of reaction was removed in vacuo and benzene was added to replace the benzene lost during this period. When the solution became clear, the benzene was removed and the resulting pale yellow viscous liquid was diluted with 100 mL ether and cooled to -20°C. The product separated as long, thick, transparent needles. The yield was close to theoretical and the ra.p. was 18°C. [Pg.485]

Table IV compares the X-ray exposure characteristics (at 8.3 X, Al Kai,2 emission line) of the halogenated resists and of PMMA Elvacite 20U1. It can be seen that poly(2-ehloroethyl methacrylates) and poly(2-bromoethyl methacrylates) exhibit a low sensitivity unlike poly(2-fluoroethyl methacrylates) and poly(2-, 2-,2-trifluoroethyl methacrylates) which are more sensitive than PMMA as shown in Figures 2a, 2b, 2c, 2d where the dose-thickness curves of these resists are plotted. The low sensitivity of the PC1EMA and PBrEMA samples may be explained by some competing crosslinking reactions which could occur during exposure as a result of C-Cl and C-Br homolytic bond scissions as noted by Tada... Table IV compares the X-ray exposure characteristics (at 8.3 X, Al Kai,2 emission line) of the halogenated resists and of PMMA Elvacite 20U1. It can be seen that poly(2-ehloroethyl methacrylates) and poly(2-bromoethyl methacrylates) exhibit a low sensitivity unlike poly(2-fluoroethyl methacrylates) and poly(2-, 2-,2-trifluoroethyl methacrylates) which are more sensitive than PMMA as shown in Figures 2a, 2b, 2c, 2d where the dose-thickness curves of these resists are plotted. The low sensitivity of the PC1EMA and PBrEMA samples may be explained by some competing crosslinking reactions which could occur during exposure as a result of C-Cl and C-Br homolytic bond scissions as noted by Tada...
Figure 2.54 The geometry of one of the substrates employed by Murray and Allara in their spacer experiments. PMMA = polymelhyl methacrylate spacer of thickness J, PNBA = monolayer of p-nitrobcnzoic acid. The mass thicknesses of the other layers are CaF, = 800 A. Al = 2500 A. Al = oxide c. 30 A, Ag = 200 A. From Murray and Allara (1982). Figure 2.54 The geometry of one of the substrates employed by Murray and Allara in their spacer experiments. PMMA = polymelhyl methacrylate spacer of thickness J, PNBA = monolayer of p-nitrobcnzoic acid. The mass thicknesses of the other layers are CaF, = 800 A. Al = 2500 A. Al = oxide c. 30 A, Ag = 200 A. From Murray and Allara (1982).
Czymmek KJ, Bourett TM, Howard RJ. Immunolocalisation of tubulin and actin in thick-sectioned fungal hyphae after freeze-substitution fixation and methacrylate de-embedment. JMicrosc 1996 181 153-161. [Pg.89]

TiCU readily functionalizes hydrophilic polymers such as poly(vinyl alcohol), m-ciesol novolac and methacrylic acid copolymers as well as moderately hydrophobic polymers such as poly(methyl methacrylate), poly(vinyl acetate), poly(benzyl methacrylate) and fully acetylated m-cresol novolac. HCI4 did not react with poly(styrene) to form etch resistant films indicating that very hydrophobic films follow a different reaction pathway. RBS analysis revealed that Ti is present only on the surface of hydrophilic and moderately hydrophobic polymer films, whereas it was found diffused through the entire thickness of the poly(styrene) films. The reaction pathways of hydrophilic and hydrophobic polymers with HCI4 are different because TiCl is hydrolysed by the surface water at the hydrophilic polymer surfaces to form an etch resistant T1O2 layer. Lack of such surface water in hydrophobic polymers explains the absence of a surface TiC>2 layer and the poor etching selectivities. [Pg.208]

Unsaturated polyester and methacrylate casting resins are normally cured with organic peroxides. The polyester casting resins are dissolved in monostyrene, and temperatures up to 200°C are reached in their polymerization. Thick-walled articles in particular are often exposed to heat for a long period of time. The required heat resistance of the organic pigments used is governed by this. [Pg.176]


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See also in sourсe #XX -- [ Pg.209 ]




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