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Magnesium hydroxides polymerization

F. Molesky in Recent Advances in Flame Retardamy of Polymeric Materials, Stamford, Coim., 1990 F. Molesky, "The Use of Magnesium Hydroxide for Flame Retarded Low Smoke Polypropylene," Polyolefins IHInternational Conference, Feb. 24,1991, Houston, Tex. [Pg.463]

Melamine resins are used from this group of thermosets for the manufacture of food contact materials. The melamine can be used in mixtures with urea and in some applications with phenol (< 1 %). The polymerization process is catalyzed in the presence of organic acids (e.g. acetic acid, lactic acid, tartaric acid, citric acid), hydrochloric acid, sulfuric acid, phosphoric acid, sodium and potassium hydroxide, ammonia, calcium or magnesium hydroxide as well as salts of these substances (total < 1 %) which cause the elimination of water and lead to a cured resin system. Stearic acid can be used as a lubricant as can zinc, calcium and magnesium salts, esters of montanic acid with ethandiol and 1,3-butandiol, as well as silicone oil (total < 1 %). [Pg.36]

From Formaldehyde.—Historically and physiologically, the most important synthesis of hexose mono-saccharoses is from formaldehyde. In 1861 Butlerow found that dioxymethylene (tri-oxymethylene), produced by polymerizing formaldehyde, yielded with hot lime water a sweet substance to which he gave the name of methylenitan. The substance reduced Fehling s solution, but was optically inactive and non-fermentable with yeast zymase. Later, Loew obtained a sweet, non-fermentable syrup by the direct action of lime-water on formaldehyde. This substance he called formose. He afterward obtained what he considered another sugar by the action of magnesium hydroxide upon formaldehyde. This substance was fermentable by yeast and to it he gave the name of methose. In 1887, Fischer and Tafel... [Pg.340]

All of these catalysts were active for ethylene polymerization. The average activity values are shown in Table 44. The activity was mostly unaffected by the presence of alkaline earth metal hydroxide, with the exception of barium hydroxide, which lowered the polymer yield by about 50%. Magnesium hydroxide caused a major change in the physical structure of the catalyst, which is an indication that a new material, perhaps magnesium silicate, was formed, with smaller primary particles. It is not clear whether the Cr(VI) becomes attached to the new material or whether it remains with the silica phase, perhaps now etched or otherwise changed. [Pg.393]

The reaction is carried out with the dihalide suspended in an aqueous magnesium hydroxide phase. The value of x is slightly above 2. A typical polymerization system also includes up to 2% 1,2,3-trichloro-propane. The polymerization occurs readily yielding a polymer with a very high molecular weight. [Pg.512]

The flammability and smoke generation of the floor coverings including the polymeric sheets can be improved using aluminum trihydrate and magnesium hydroxide. These compoimds release water at elevated temperatures. Also phosphorous compoimds, borates, and zinc oxide are improving the fire characteristics of PLA-based systems. [Pg.277]

The polymerization process generally is carried out in an aqueous solution containing sodium sulfide and small amounts of magnesium hydroxide catalyst [S]. The dihalide is mixed gradually with the aqueous solution while heating the reaction mixture at about 70-80°C. [Pg.741]

Subsequently, Patrick, solved the production problem by using a novel suspension polymerization technique. The Thiokol suspension based on a magnesium hydroxide slurry was readily purified and coagulated by acidification in the same manner as the coagulation of natural rubber latex. Since the Prohibition Act had not been repealed, it was easy to obtain glass lined tanks from an abandoned Kansas City brewery and to start the large scale production of Thiokol in 1929. [Pg.114]

The polysulfide polymers are prepared as a suspension by condensation of the dihalide monomer with polysulfide in aqueous solution [18]. Bis-2-dichloro-ethyl formal is the monomer usually used, and 0.1-0.4% 1,2,3-trichloropropane is added as a crosslinking monomer [19]. In conducting polymerization, the standard practice is to feed the dihalide monomer into the aqueous polysulfide solution containing specific suspending and nucleating agents. A combination of an alkyl naphthalene sulfonate with magnesium hydroxide sol prepared in situ is commonly used. [Pg.459]

Addition to PE-HD/MDH composites (samples numbers 10-18) polymeric coupling agent PE-g-MA resulted in a significant improvement in the mechanical properties of the magnesium hydroxide modified by fatty acids. [Pg.98]

The decohesion fracture observed in PE-HD/MH1 50 composite prepared without PE-g-MA, was changed to cohesion failure of PE-HD/MDHl 50/PE-g-MA 2 composite with the addition of polymeric coupling agent. This improvement in adhesion was particularly reflected in the mechanical properties, and improvement in both strength and modulus of high-density polyethylene composites containing surface modified by fatty acids magnesium hydroxide and PE-g-MA. [Pg.99]

Flame retardance of ethylene-vinyl acetate copolymer can be achieved using magnesium hydroxide incorporated in the polymeric matrix. The adduct of a small amount of zinc borate as synergistic agent in the formulation increases the fire-proofing properties. Multinuclei solid-state NMR appears as a means to characterise materials before and after combustion. It was shown that endothermic dehydration, water vapour evolved and formation of a glassy coating provided the flame retardancy of interest to the polymer matrix. 12 refs. EUROPEAN COMMUNITY EUROPEAN UNION FRANCE WESTERN EUROPE... [Pg.123]

Polymer-Magnesium Hydroxide Nanocomposites by Emulsion Polymerization... [Pg.180]


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See also in sourсe #XX -- [ Pg.189 ]




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Emulsion polymerization magnesium hydroxides

Magnesium hydroxide

Polymer-Magnesium Hydroxide Nanocomposites by Emulsion Polymerization

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