Method for activating catalyst for chlorine production
a catalyst and chlorine technology, applied in the field of activating catalysts for chlorine production, can solve the problems that the activity of catalysts with decreased activity cannot be recovered sufficiently, and achieve the effect of cost-effective production
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reference example 1
(a) Preparation of Fresh Catalyst
[0028]50 Parts by weight of titanium oxide [STR-60R manufactured by Sakai Chemical Industry Co., Ltd., 100% rutile type], 100 parts by weight of α-alumina [AES-12 manufactured by Sumitomo Chemical Co., Ltd.], 13.2 parts by weight of a titania sole [CSB manufactured by Sakai Chemical Industry Co., Ltd., titania content: 38% by weight] and 2 parts by weight of methyl cellulose [Metolose 65SH-4000 manufactured by Shin-Etsu Chemical Co., Ltd.] were mixed and pure water was added, followed by kneading. The resultant mixture was extruded into a cylindrical body having a diameter of 3.0 mmφ, dried and then ground into pieces each having a length of 4 to 6 mm. The resultant shaped body was calcined in air at 800° C. for 3 hours to obtain a carrier including a mixture of titanium oxide and α-alumina. The carrier was impregnated with an aqueous solution of ruthenium chloride, dried and then calcined in air at 250° C. for 2 hours to obtain a bluish gray support...
example 1
(a) Activation Treatment of Deteriorated Catalyst
[0030](Contact Treatment with Reducing Gas)
[0031]A nickel reaction tube having an inner diameter of 13 mm was filled with 1 g of the deteriorated catalyst of Reference Example 1(b) and then filled with 12 g of α-alumina spheres [SSA995 manufactured by NIKKATO CORPORATION] as a preheating layer at the gas inlet side of a catalyst layer. While feeding nitrogen gas at a rate of 80 ml / min, the reaction tube was immersed in a salt bath using a molten salt [potassium nitrate / sodium nitrite=1 / 1 (weight ratio)] as a heat medium, thereby adjusting the temperature of the catalyst layer to 350° C. Next, feed of the nitrogen gas was stopped, and carbon monoxide gas was fed at a rate of 3.2 ml / min (0.009 mol / h) and nitrogen gas was fed at a rate of 28.8 ml / min (0.08 mol / h) for 2 hours.
(b) Evaluation of Activated Catalyst
[0032]After the activation treatment (a), feed of the carbon monoxide gas was stopped and nitrogen gas was fed at a rate of 80 ml...
example 2
(a) Activation Treatment of Deteriorated Catalyst
[0033](Contact Treatment with Reducing Gas)
[0034]A nickel reaction tube having an inner diameter of 13 mm was filled with 1 g of the deteriorated catalyst of Reference Example 1(b) and then filled with 12 g of α-alumina spheres [SSA995 manufactured by NIKKATO CORPORATION] as a preheating layer at the gas inlet side of a catalyst layer. While feeding nitrogen gas at a rate of 80 ml / min, the reaction tube was immersed in a salt bath using a molten salt [potassium nitrate / sodium nitrite=1 / 1 (weight ratio)] as a heat medium, thereby adjusting the temperature of the catalyst layer to 350° C. Next, feed of the nitrogen gas was stopped, and carbon monoxide gas was fed at a rate of 3.2 ml / min (0.009 mol / h) and nitrogen gas was fed at a rate of 28.8 ml / min (0.08 mol / h) for 2 hours.
(Contact Treatment with Oxidizing Gas)
[0035]After the contact treatment with the reducing gas, feed of the carbon monoxide gas was stopped, and oxygen was fed at a r...
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