Loaded quaternary ammonium salt and metal chloride catalyst and preparation method thereof
A quaternary ammonium salt and catalyst technology, which is applied in the field of supported quaternary ammonium salt and metal chloride catalysts and their preparation, can solve the problems of low activity of non-precious metal catalysts, high cost of gold and precious metal catalysts, easy deactivation and loss of mercury catalysts, etc. Achieve the effect of reducing carbon deposition and coking, low cost and less by-products
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[0029] Example 1: Weigh 1.05g of copper chloride and 2g of tetrabutylammonium chloride, dissolve them in 10mL of water, stand for 2h at 90°C, and then filter and separate to obtain the complex; using an equal volume impregnation method, the above obtained complex The substance is dissolved in 10 mL of water to completely dissolve to obtain a catalyst impregnation solution. Add 5 g of porous coal-based activated carbon support to the catalyst impregnation solution under stirring, and immerse in an oven at 60°C for 10 hours. Finally, the sample is dried in an oven at 120°C for 12 hours. The active carbon supported quaternary ammonium salt and metal chloride catalyst is prepared.
[0030] The catalyst prepared above was placed in a fixed bed reactor for activity, selectivity and stability evaluation. The reaction conditions were 140°C, molar ratio of hydrogen chloride and acetylene of 1.5:1, and acetylene space velocity of 180h -1 The acetylene conversion rate of the catalyst is 60.8...
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[0031] Example 2: Weigh 0.61g of bismuth chloride and 0.05g of 2-hydroxyethyltrimethylammonium chloride, dissolve them in 10mL of ethanol, stand for 10 hours at 60°C, and then filter and separate to obtain the complex; adopt equal volume impregnation method , Dissolve the obtained complex in 10 mL of water to completely dissolve the catalyst impregnation solution, add 5 g of porous wood activated carbon support to the catalyst impregnation solution under stirring, and soak in a 60 ℃ oven for 24 hours. Finally, the sample is at 60 ℃ After drying in an oven for 12 hours, the activated carbon supported quaternary ammonium salt and metal chloride catalyst was prepared.
[0032] The catalyst prepared above was used for infrared characterization, and the infrared spectrum is attached figure 1 Shown at 1050cm -1 There is a characteristic peak of C-N stretching vibration; at 1460cm -1 And 1380cm -1 There is a characteristic peak of C-C stretching vibration of alkyl chain; at 1500cm -1 The...
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[0034] Example 3: Weigh 0.88g of cobalt chloride and 1g of trimethylammonium hydantoin hydrochloride, dissolve in 10mL of acetonitrile, stand for 12h at 30°C, and then filter and separate to obtain the complex; The obtained complex was dissolved in 10 mL of water to completely dissolve to obtain a catalyst impregnation solution; 5g of porous coconut shell activated carbon carrier was added to the above catalyst impregnation solution under stirring, and immersed in an oven at 40°C for 12 hours. Finally, the sample was dried in an oven at 100°C 12h, the activated carbon supported quaternary ammonium salt and metal chloride catalyst was prepared.
[0035] The catalyst prepared above was used for infrared characterization, and the infrared spectrum is attached figure 2 Shown at 1050cm -1 There is a characteristic peak of C-N stretching vibration; at 1460cm -1 And 1380cm -1 There is a characteristic peak of C-C stretching vibration of alkyl chain nearby; at 1700cm -1 And 3400cm -1 The...
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