Acrylic glass

The interaction of solutes (especially adsorption) with the filter material and the retained particles. The problem is especially serious with trace elements (heavy metals) that adsorb especially at pH values of 7 and above on filter walls and on the filter materials (glass, acrylic copolymers, cellulose esters, polycarbonates etc.). One also needs to consider that... 

Filters can be grouped on the basis of different characteristics. For example, they can be grouped on the basis of the design capacity of the filters according to the particle concentration or loading [Svarovsky, 1981] or they can be grouped on the basis of the materials of the filters, e.g., fabric or nonfabric [Cooper and Freeman, 1982], Most filters in use are bag filters, which are fabric. The common fabric materials include cotton, polyester, wool, asbestos, glass, acrylic, polytetrafluoroethylene (Teflon), poly (m-phenylene isophthalate) (Nomex), polycaprolactam (Nylon), and polypropylene. 

CHi=CMeCOOH. Colourless prisms m.p. 15-16 C, b.p. 160-5 C. Manufactured by treating propanone cyanohydrin with dilute sulphuric acid. Polymerizes when distilled or when heated with hydrochloric acid under pressure, see acrylic acid polymers. Used in the preparation of synthetic acrylate resins the methyl and ethyl esters form important glass-like polymers. 

CH =C(CH3)C02Me. Colourless liquid b.p. lOO C. Manufactured by healing acetone cyanohydrin with methanol and sulphuric acid. It is usually supplied containing dissolved polymerization inhibitor, on removal of which it is readily polymerized to a glass-like polymer. See acrylate resins. 

CHjlCH COOH. Colourless liquid having an odour resembling that of ethanoic acid m.p. 13 C, b.p. I4I°C. Prepared by oxidizing propenal with moist AgO or treating -hy-droxypropionitrile with sulphuric acid. Slowly converted to a resin at ordinary temperatures. Important glass-like resins are now manufactured from methyl acrylate, see acrylic resins. Propenoic acid itself can also be polymerized to important polymers - see acrylic acid polymers. 

Acrylic acid derivatives. Acrylic esters polymerise readily under the influence of oxygen, peroxides, light or heat to give colourless, glass-Uke plastics. 

This process yields satisfactory monomer, either as crystals or in solution, but it also produces unwanted sulfates and waste streams. The reaction was usually mn in glass-lined equipment at 90—100°C with a residence time of 1 h. Long residence time and high reaction temperatures increase the selectivity to impurities, especially polymers and acrylic acid, which controls the properties of subsequent polymer products. 

Acryflc acid, alcohol, and the catalyst, eg, sulfuric acid, together with the recycle streams are fed to the glass-lined ester reactor fitted with an external reboiler and a distillation column. Acrylate ester, excess alcohol, and water of esterification are taken overhead from the distillation column. The process is operated to give only traces of acryflc acid in the distillate. The bulk of the organic distillate is sent to the wash column for removal of alcohol and acryflc acid a portion is returned to the top of the distillation column. If required, some base may be added during the washing operation to remove traces of acryflc acid. 

Below T polymers are stiff, hard, britde, and glass-like above if the molecular weight is high enough, they are relatively soft, limp, stretchable, and can be somewhat elastic. At even higher temperatures they flow and are tacky. Methods used to determine glass-transition temperatures and the reported values for a large number of polymers may be found in References 7—9. Values for the T of common acrylate homopolymers are found in Table 1. 

This type of adhesive is generally useful in the temperature range where the material is either leathery or mbbery, ie, between the glass-transition temperature and the melt temperature. Hot-melt adhesives are based on thermoplastic polymers that may be compounded or uncompounded ethylene—vinyl acetate copolymers, paraffin waxes, polypropylene, phenoxy resins, styrene—butadiene copolymers, ethylene—ethyl acrylate copolymers, and low, and low density polypropylene are used in the compounded state polyesters, polyamides, and polyurethanes are used in the mosdy uncompounded state. 

T is the glass-transition temperature at infinite molecular weight and is the number average molecular weight. The value of k for poly(methyl methacrylate) is about 2 x 10 the value for acrylate polymers is approximately the same (9). A detailed discussion on the effect of molecular weight on the properties of a polymer may be found in Reference 17. 

Other examples of DAP copolymerizations of industrial interest include copolymerization with MMA in emulsion (50) and for light focusing rods (51) with vinyl naphthalene for lenses (52) with epoxy acrylates and glass fibers (53) epoxy acrylates and coatings (54) with diacetone acrylamide (55) with ahphatic diepoxide compounds (56) triaHyl cyanurate in lacquers for printed circuits (57) and DAIP with MMA (58). 

Fig. 3. Effect of comonomer stmcture on the glass-transition temperature of VDC copolymers (72), where A represents acrylonitrile B, methyl acrylate ...

In cases where the copolymers have substantially lower glass-transition temperatures, the modulus decreases with increasing comonomer content. This results from a drop in crystallinity and in glass-transition temperature. The loss in modulus in these systems is therefore accompanied by an improvement in low temperature performance. However, at low acrylate levels (< 10 wt %), T increases with comonomer content. The brittle points in this range may therefore be higher than that of PVDC. 

Fig. 3. Elastomer properties as a function of monomer composition, butyl acrylate (BA), ethyl acrylate (FA), and methoxyethyl acrylate (MEA). (a), (—) glass-transition temperature (------------) swelling in ASTM No. 3 oil (b) (-) residual elongation at break, %, after heat aging.

Medium 20,000-50,000 4 Acrylic resins, plastics, PVC, ammonium chloride, DMT, copper compounds, lead Ferroalloys, fluorspar, nickel Iron, potash, glass-making mixtures... 

Butyl acrylate [I4I-32-2J M 128.2, b 59 /25mm, d 0.894, n 1.4254. Washed repeatedly with aqueous NaOH to remove inhibitors such as hydroquinone, then with distilled water. Dried with CaCl2. Fractionally distd under reduced pressure in an all-glass apparatus. The middle fraction was sealed under nitrogen and stored at 0° in the dark until used [Mallik and Das J Am Chem Soc 82 4269 I960]. 

Deformation of low molecular weight polymer or polymer precursor such as in the casting of acrylic sheet and preparation of glass-reinforced laminates. 

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