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ChemicalBook CAS DataBase List 1,8-DIMETHYLNAPHTHALENE

1,8-DIMETHYLNAPHTHALENE synthesis

8synthesis methods
-

Yield:91-20-3 3.11 %Chromat. ,91-57-6 15.68 %Chromat. ,90-12-0 3.71 %Chromat. ,939-27-5 0.57 %Chromat. ,1127-76-0 0.26 %Chromat. ,581-42-0 4.86 %Chromat. ,582-16-1 4.58 %Chromat. ,575-43-9 2.92 %Chromat. ,571-61-9 0.39 %Chromat. ,569-41-5 0.12 %Chromat.

Reaction Conditions:

with hydrogen;chromium corundum at 20 - 475; under 44929.5 Torr;Conversion of starting material;

Steps:

4 Example 4 (Hydrodealkylation)
Example 4 (Hydrodealkylation) A part of Fraction-17 and Residue shown in Table 3 are mixed to prepare the feedstock(Blend-A) for hydrodealkylation. A 50 g amount of Cr2O3/Al2O3 type catalyst produced by Sud-Chemie AG is charged into a tubular reactor. The reactor is heated gradually from ambient temperature to 662F (350 °C) to dry the catalyst while supplying hydrogen gas. Thereupon Blend-A is fed to the reactor at the rate of 50 g/hr and 1.0 hr-1 in WHSV, while supplying hydrogen gas at 1.25 cf/hr (0.034 m3/hr). Hydrodealkylation is carried out at 887F (475 °C) and 854 psig (5.99 MPa). The product is analyzed by GC and the results of hydrodealkylation are summarized in Table 4 below. As shown in Table 4, Cr2O3/Al2O3 type catalyst is effective to enrich 2,6-DMN from 2,6-DMN lean feed.

References:

KABUSHIKI KAISHA KOBE SEIKO SHO;EXXONMOBIL OIL CORPORATION EP1165473, 2004, B1 Location in patent:Page 9-10

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