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Wacker-Chemie liquid phase

Figure 2. Mechanism for Wacker-Chemie Liquid Phase Acetaldehyde and Vinyl... Figure 2. Mechanism for Wacker-Chemie Liquid Phase Acetaldehyde and Vinyl...
The direct liquid phase oxidation of ethylene was developed in 1957—1959 by Wacker-Chemie and Farbwerke Hoechst in which the catalyst is an aqueous solution of PdQ2 and CuCl2 (86). [Pg.51]

The liquid-phase oxidation of ethylene to acetaldehyde was pioneered by the Consortium fiir Elektrochemische Industrie G.m.b.H. Industrially, the single-stage process was developed mainly by Farbwerke Hoechst A. G. and the two-stage process by Wacker Chemie G.m.b.H. itself. Both processes are licensed by Aldehyd G.m.b.H., jointly owned by Wacker Chemie G.m.b.H. and Farbwerke Hoechst G.m.b.H. The basic patents of these two companies on the Wacker process are listed in Table IV. In addition to these patents, which have given Wacker Chemie G.m.b.H. and Farbwerke Hoechst a dominant role in this field, other companies hold some patents in this area (Table X). How many of the patents listed in Tables IX and X are commercially important cannot be judged, based on the open literature alone. [Pg.69]

In 1960, quickly after the introduction of the Celanese process, Wacker-Chemie commercialized a liquid phase vinyl acetate process which represented and extension of its earlier acetaldehyde process wherein acetic acid was simply substituted for water. (See equation [19]. This chemical transformation is also referred to as oxidative acetoxylation.) As shown in Figure 2, wherein R=Ac, the liquid phase oxidative acetoxylation of ethylene utilized the same catalytic cycle as the Wacker-Chemie acetaldehyde process. [Pg.376]

Because the solubility coefficients of carbon in the solid and the liquid phase are almost the same, zone melting, which is used to prepare high-purity crystals of many other elements, is not suitable in the case of boron. Technical boron, which is often taken as the ingredient for the preparation of boron compounds, contains up to about 0.5% carbon. However, in several preparative methods for boron compounds the carbon content may be reduced by secondary chemical or physical reactions. The purest P-rhombohedral boron crystals that have become available up to now were produced by Wacker-Chemie, Munich, FRG. Despite the claimed purity of 99.9999% with respect to other elements, even this high-purity boron contains carbon in concentrations of typically 30 to 80 ppm. Therefore, apart from boron carbide containing carbon as a determining bonding partner, in the assessment of the properties of boron and boron compounds attention must be paid to the fact that a certain, usually unknown carbon content could have influenced the properties determined. [Pg.599]


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