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Magnesium methyl carbonate, methoxy

Figure 24 Comparison of isothermal chemiluminescence intensity for pullulan (1) and pullulan impregnated by methoxy magnesium methyl carbonate (2) from a 5% solution in methanol initial molar mass of pullulan 404 kg/mol, oxygen atmosphere, temperature 190°C. Figure 24 Comparison of isothermal chemiluminescence intensity for pullulan (1) and pullulan impregnated by methoxy magnesium methyl carbonate (2) from a 5% solution in methanol initial molar mass of pullulan 404 kg/mol, oxygen atmosphere, temperature 190°C.
The most successful nonaqueous deacidification treatment is the Wei T o process which uses solutions of methoxy magnesium methyl carbonate in alcohol and Freon as the starting materials (33). The spray deacidification of the solution on books is now in use at the... [Pg.19]

The methoxy magnesium methyl carbonate (H COMgOCOOCH,) after being deposited in the fibers by the solvents, reacts witn water from the air to form a mixture of magnesium carbonate (MgCO ), magnesium hydroxide [Mg(OH )], and magnesium oxide (MgO) ... [Pg.22]

Wei T o Process. Wei T o process is the only mass deacidification process currently available commercially. The "liquid gas" deacidification solution of this process consists of methoxy magnesium methyl carbonate dissolved in a mixture of Freon and methyl alcohol. The process has been proven by six years of production operation at the National Library and Public Archives of Canada. It utilizes a less complex system than the DEZ process to achieve deacidification. National Library and Public Archives of Canada are satisfied with the deacidification results. [Pg.27]

Wei To 2 (deacidifier) Wei To Corp. Methoxy magnesium methyl carbonate... [Pg.96]

Carboxylation of activated CH groups with MMMC (methoxy magnesium methyl carbonate) 1 (Szarvasy) and addition of the resulting activated groups to C=N bonds (Schopf) (see 1st edition). [Pg.356]

In the presence of methoxy magnesium methyl carbonate, the chemiluminescence emission in pullulan and cellulose increased significantly. It may be attributed to the decomposition of dioxetanes, with higher quantum yield of emission, which were formed from peroxidation of terminal semiacetal groups in the presence of MgO. [Pg.114]

Fithium tetrahydroaluminate, Fluoroamides, 0075 Lithium tetrahydroaluminate, Water, 0075 Lithium, 1,2-Diaminoethane, Tetralin, 4675 Magnesium, Barium carbonate, Water, 4685 Maleic anhydride, Bases, or Cations, 1400 Mercaptoacetonitrile, 0763 t Methanol, Hydrogen, Raney nickel catalyst, 0482 4-Methoxy-3-nitrobenzoyl chloride, 2911 Methoxyacetyl chloride, 1161 t Methyl formate, Methanol, Sodium methoxide, 0830 3-Methyl-2-penten-4-yn-l-ol, 2378 Nitric acid, 4430... [Pg.2357]


See other pages where Magnesium methyl carbonate, methoxy is mentioned: [Pg.121]    [Pg.22]    [Pg.95]    [Pg.143]    [Pg.145]    [Pg.141]    [Pg.377]    [Pg.377]    [Pg.377]    [Pg.428]    [Pg.490]    [Pg.144]    [Pg.1122]    [Pg.36]    [Pg.237]    [Pg.238]    [Pg.423]    [Pg.15]    [Pg.69]    [Pg.253]    [Pg.666]    [Pg.6]    [Pg.271]   
See also in sourсe #XX -- [ Pg.31 , Pg.31 , Pg.91 ]




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5-Methoxy-4-methyl

Carbon methylation

Magnesium carbonate

Magnesium methyl carbonate

Magnesium methylate

Methyl carbonates

Methyl carbons

Methyl magnesium

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