US20100183499A1 - Method for activating catalyst for chlorine production - Google Patents

Method for activating catalyst for chlorine production Download PDF

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US20100183499A1
US20100183499A1 US12/669,757 US66975708A US2010183499A1 US 20100183499 A1 US20100183499 A1 US 20100183499A1 US 66975708 A US66975708 A US 66975708A US 2010183499 A1 US2010183499 A1 US 2010183499A1
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catalyst
gas
rate
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Youhei Uchida
Kohei Seki
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Sumitomo Chemical Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/90Regeneration or reactivation
    • B01J23/96Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the noble metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/04Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/04Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/10Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst using elemental hydrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/04Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/12Treating with free oxygen-containing gas
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B7/00Halogens; Halogen acids
    • C01B7/01Chlorine; Hydrogen chloride
    • C01B7/03Preparation from chlorides
    • C01B7/04Preparation of chlorine from hydrogen chloride
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04Alumina
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/063Titanium; Oxides or hydroxides thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46Ruthenium, rhodium, osmium or iridium
    • B01J23/462Ruthenium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/0201Impregnation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Definitions

  • the present invention relates to a method for activating a catalyst for use in the production process of chlorine, which production process comprises oxidizing hydrogen chloride with oxygen.
  • the present invention also relates to a method for producing chlorine by oxidizing hydrogen chloride with oxygen using the catalyst activated by the method.
  • Japanese Unexamined Patent Publication No. 2007-7521 discloses a method for activating a catalyst having decreased activity by bringing the catalyst into contact with a gas substantially composed only of oxygen and/or an inert gas.
  • An object of the present invention is to provide a method which can effectively recover the activity of a catalyst having decreased activity.
  • the present invention provides a method for activating a catalyst for use in the production process of chlorine, which process comprises oxidizing hydrogen chloride with oxygen, characterized in that a catalyst having decreased activity is treated by contacting with a reducing gas containing carbon monoxide and/or hydrogen.
  • the present invention also provides a method for producing chlorine by oxidizing hydrogen chloride with oxygen in the presence of the catalyst activated by the above method.
  • the activity of a catalyst having decreased activity can be recovered, and chlorine can be produced cost-effectively by reusing the catalyst activated by the present method.
  • the catalyst to be subjected to the activation treatment in the present invention is a catalyst for use in the production of chlorine, which process comprises oxidizing hydrogen chloride with oxygen (hereinafter said catalyst merely referred to as catalyst).
  • the catalyst includes, for example, a copper catalyst, a chromium catalyst and a ruthenium catalyst.
  • Suitable examples of the copper catalyst include a catalyst generally referred to as Dracon catalysts, comprising various compound(s), as a third component, in addition to copper chloride and potassium chloride.
  • Suitable examples of the chromium catalyst include catalysts containing chromium oxide disclosed in Japanese Unexamined Patent Publication No. 61-136902, Japanese Unexamined Patent Publication No. 61-275104, Japanese Unexamined Patent Publication No. 62-113701 and Japanese Unexamined Patent Publication No. 62-270405.
  • Suitable examples of the ruthenium catalyst include catalysts containing ruthenium oxide disclosed in Japanese Unexamined Patent Publication No. 9-67103, Japanese Unexamined Patent Publication No. 10-338502, Japanese Unexamined Patent Publication No. 2000-281314, Japanese Unexamined Patent Publication No. 2002-79093 and Japanese Unexamined Patent Publication No. 2002-292279.
  • the method of the present invention is suitably used for the ruthenium catalyst, particularly the catalyst containing ruthenium oxide.
  • the catalyst containing ruthenium oxide may be, for example, a catalyst composed substantially only of ruthenium oxide, or a supported ruthenium oxide in which ruthenium oxide is supported on a carrier such as alumina, titania, silica, zirconia, niobium oxide or activated carbon, or a complex oxide composed of ruthenium oxide and other oxides, such as alumina, titania, silica, zirconia and niobium oxide.
  • the production of chlorine using the catalyst described above is usually performed by a continuous method under vapor phase conditions while feeding hydrogen chloride and oxygen in a fixed bed reactor filled with a catalyst or a fluidized bed reactor in which the catalyst is fluidized.
  • the reaction temperature is usually from 100 to 500° C., and preferably from 200 to 400° C., while the reaction pressure is usually from about 0.1 to 5 MPa.
  • an oxygen source air may be used, or pure oxygen may be used.
  • oxygen is theoretically required in an amount of 1 ⁇ 4 mol per mol of hydrogen chloride.
  • oxygen is used in an amount of 0.1 to 10 times larger than that of the theoretical amount.
  • the feed rate of hydrogen chloride is usually from about 10 to about 20,000 h ⁇ 1 in terms of a volume feed rate (as converted at 0° C. and 1 atm) of the gas per volume of catalyst layer, namely, GHSV.
  • Examples of the hydrogen chloride-containing gas which can be used as a hydrogen chloride source include a gas produced by the reaction of hydrogen and chlorine, a gas generated by heating hydrochloric acid, various by-product gasses generated by a thermal decomposition reaction or combustion reaction of a chlorine compound, a carbonylation reaction of an organic compound using phosgene, a chlorination reaction of an organic compound using chlorine and production of chlorofluoroalkane, and flue gases generated from an incinerator.
  • the thermal decomposition reaction of a chlorine compound includes, for example, a reaction in which vinyl chloride is produced from 1,2-dichloroethane and a reaction in which tetrafluoroethylene is produced from chlorodifluoromethane;
  • the carbonylation reaction of an organic compound using phosgene includes, for example, a reaction in which isocyanate is produced from amine, and a reaction in which a carbonate ester is produced from a hydroxy compound;
  • the chlorination reaction of an organic compound using chlorine includes, for example, a reaction in which allyl chloride is produced from propylene, a reaction in which ethyl chloride is produced from ethane and a reaction in which chlorobenzene is produced from benzene.
  • the production of chlorofluoroalkane includes, for example, production of dichlorodifluoromethane and trichloromonofluoromethane by the reaction of carbon tetrachloride and hydrogen fluoride, and production of dichlorodifluoromethane and trichloromonofluoromethane by the reaction of methane, chlorine and hydrogen fluoride.
  • the activity of the catalyst gradually decreases.
  • An unexpected decrease in catalytic activity can be caused by operating error during operation and trouble of equipment. For example, when it becomes difficult to control the reaction temperature and thus the catalyst is exposed to high temperature for a long time, or feed of oxygen is stopped and thus the catalyst is contacted with hydrogen chloride for a long time in the absence of oxygen, the activity of the catalyst may decease. Furthermore, also when initiation of feed of oxygen is delayed upon starting up or stop of feed of hydrogen chloride is delayed upon temporary stop of the reaction and thus the catalyst is contacted with hydrogen chloride for a long time in the absence of oxygen, the activity of the catalyst may decrease.
  • hydrogen chloride generated as a by-product when amine is reacted with phosgene to produce isocyanate may contain impurities such as carbonyl sulfide derived from phosgene, hydrogen sulfide, carbon disulfide and sulfur oxide. When such hydrogen chloride is used as a raw material for the oxidation reaction, the catalytic activity may decrease.
  • a contact treatment with a reducing gas containing carbon monoxide and/or hydrogen is performed so as to recover the activity of a catalyst having decreased activity.
  • the present invention is suitably employed for a catalyst whose activity is decreased as a result of using hydrogen chloride containing a sulfur component as a raw material for the oxidation reaction, among catalysts having decreased activity.
  • the reducing gas containing carbon monoxide and/or hydrogen may be a gas composed only of carbon monoxide, a gas composed only of hydrogen, or a mixture of gases of carbon monoxide and hydrogen.
  • the reducing gas may contain an inert gas in addition to these gases.
  • the inert gas as used herein is a neutral component which substantially does not exhibit neither oxidizability nor reducibility to catalyst, and does not also substantially exhibits neither acidity nor basicity, and examples thereof include steam, nitrogen, argon, helium and carbon dioxide. If necessary, a mixture of two or more kinds of them can also be used.
  • nitrogen is preferably used as the inert gas.
  • the concentration of carbon monoxide and/or hydrogen in the reducing gas is usually from 0.1 to 100% by volume, and preferably from 1 to 20% by volume. When the concentration is low, it takes a long time for activation of catalyst.
  • the temperature at which a catalyst having decreased activity is treated by contacting with the reducing gas namely, the temperature of the contact treatment with the reducing gas is usually from 100 to 500° C., and preferably from 150 to 450° C. When the temperature is too low, it takes a long time for activation of catalyst. In contrast, when the temperature is too high, a catalyst component is likely to be vaporized.
  • the pressure at which the Contact treatment with the reducing gas is performed is usually from 0.01 to 3 MPa, and preferably from 0.1 to 1 MPa.
  • the contact treatment with the reducing gas may be performed by a fixed bed method or a fluidized bed method.
  • the feed rate of the reducing gas is usually from about 1 to about 100,000 h ⁇ 1 in terms of a volume feed rate (as converted at 0° C. and 1 atm) of the gas per volume of a catalyst layer, namely, GHSV.
  • the time of the contact treatment with the reducing gas is usually from about 0.5 to about 100 hours.
  • Said oxidizing gas is a gas containing an oxidizing substance and typically includes an oxygen-containing gas.
  • an oxygen source air and pure oxygen are usually used and can be diluted with the inert gas described above, if necessary.
  • nitrogen is preferably used.
  • the oxygen concentration in the gas is usually from 0.1 to 100% by volume, and preferably from 10 to 100% by volume.
  • the temperature of the contact treatment with the oxidizing gas is usually from 200 to 500° C., and preferably from 250 to 450° C. when the temperature is too low, it takes a long time for activation of catalyst. When the temperature is too high, a catalyst component is readily vaporized.
  • the pressure at which the contact treatment with the oxidizing is performed is usually from 0.1 to 3 MPa, and preferably from 0.1 to 1 MPa.
  • the contact treatment with the oxidizing gas may be performed by a fixed bed method or a fluidized bed method.
  • the feed rate of the oxidizing gas is usually from about 1 to 100,000 h ⁇ 1 in terms of a volume feed rate (calculated at 0° C. under 1 atmospheric pressure) of a gas per volume of a catalyst layer, namely, GHSV.
  • the time of the contact treatment with the oxidizing gas is usually from about 0.5 to about 100 hours.
  • catalyst activation can be more effectively accomplished by (1) treating a catalyst having decreased activity by contacting with water, thereafter with the reducing gas, and then with the oxidizing gas; (2) treating a catalyst having decreased activity by contacting with the reducing gas, thereafter contacted with water, and then contacted with the oxidizing gas; or (3) treating a catalyst having decreased activity by contacting with the reducing gas, thereafter contacting with the oxidizing gas, and then contacted with water.
  • the method of (1) is more preferred.
  • the water to be used in the contact treatment with water is preferably high-purity water, such as distilled water, ion-exchange water or ultrapure water.
  • high-purity water such as distilled water, ion-exchange water or ultrapure water.
  • the temperature of the contact treatment with water is usually from 0 to 100° C., and preferably from 10 to 90° C. When the temperature is too low, the catalyst sometimes cannot be sufficiently activated.
  • the pressure at which the contact treatment with water is performed is usually from 0.1 to 1 MPa, and preferably atmospheric pressure.
  • the contact treatment with water may be performed by a fixed bed method or a batch-wise method. When the contact treatment is performed by a fixed bed method, the feed rate of water is usually from about 0.01 to 100 h ⁇ 1 in terms of a volume feed rate (as converted at 0° C. and 1 atm) of a liquid per volume of catalyst, namely, LHSV.
  • the time of the contact treatment is usually from about 0.5 to 100 hours. In the fixed bed method, water may be circulated.
  • the amount of water used when the contact treatment is performed by a batch-wise method is usually from about 1 to 100 parts by weight based on 1 part by weight of the catalyst, and the time of the contact treatment is usually from about 0.5 to 120 hours.
  • the number of the contact treatment is usually from about 1 to 10 times.
  • the catalyst thus activated can be reused for the reaction of oxidizing hydrogen chloride with oxygen.
  • a cost of the catalyst can be reduced and chlorine can be produced cost-effectively by activating and reusing the catalyst in such a manner.
  • an advantageously employed process comprises performing an oxidation reaction while feeding material gas including hydrogen chloride and oxygen in a reactor filled with a catalyst, stopping feed of the material gas when the activity of the catalyst is decreased to such extent that it becomes difficult to continue the operation, performing the activation treatment of the present invention while the reactor is filled with the catalyst, restarting feed of the material gases, performing the oxidation reaction, and optionally repeating these activation treatments and oxidation reactions.
  • an advantageously employed process comprises continuously or intermittently extracting portion of a catalyst from a reactor while performing the oxidation reaction, activating the catalyst in a separate vessel, and returning the activated catalyst to the reactor, namely, process of circulating the catalyst between a reactor and a vessel for an activation treatment.
  • a feed rate (ml/min) of a gas is expressed by a value as converted at 0° C. and 1 atm unless otherwise specified.
  • titanium oxide [STR-60R manufactured by Sakai Chemical Industry Co., Ltd., 100% rutile type]
  • ⁇ -alumina AES-12 manufactured by Sumitomo Chemical Co., Ltd.
  • CSB a titania sole
  • methyl cellulose Metalolose 65SH-4000 manufactured by Shin-Etsu Chemical Co., Ltd.
  • the resultant mixture was extruded into a cylindrical body having a diameter of 3.0 mm ⁇ , 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 ⁇ -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 supported ruthenium oxide in which ruthenium oxide is supported on the carrier at a supporting ratio of about 2% by weight.
  • the resultant supported ruthenium oxide fresh catalyst was analyzed by ICP spectrometry. As a result, the sulfur content was 0.02% by weight.
  • a reactor was filled with the fresh catalyst obtained in Reference Example 1(a).
  • a deteriorated catalyst was prepared by performing an oxidation reaction while feeding a material gas including hydrogen chloride (containing 130 ppb by volume of a sulfur component) and oxygen in the reactor.
  • the deteriorated catalyst was extracted and analyzed by ICP spectrometry. As a result, the sulfur content was 0.14% by weight.
  • feed of the carbon monoxide gas was stopped and nitrogen gas was fed at a rate of 80 ml/min (0.21 mol/h), and then the temperature of the catalyst layer was adjusted within a range from 281 to 282° C.
  • feed of the nitrogen gas was stopped and an oxidation reaction was performed at a catalyst layer temperature of 281 to 282° C. by feeding hydrogen chloride gas (containing 19 ppb by volume of a sulfur component) at a rate of 80 ml/min (0.21 mol/h) and oxygen gas at a rate of 40 ml/min (0.11 mol/h).
  • conversion ratio (%) of hydrogen chloride ⁇ production rate (mol/l) of chlorine ⁇ 2/(feed rate (mol/h) of hydrogen chloride) ⁇ 100
  • feed of the oxygen was stopped and nitrogen gas was fed at a rate of 80 ml/min (0.21 mol/h), and then the temperature of the catalyst layer was adjusted within a range from 281 to 282° C.
  • feed of the nitrogen gas was stopped and an oxidation reaction was performed at a catalyst layer temperature of 281 to 282° C. by feeding hydrogen chloride gas (containing 19 ppb by volume of a sulfur component) at a rate of 80 ml/min (0.21 mol/h) and oxygen gas at a rate of 40 ml/min (0.11 mol/h).
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 300° C. in the contact treatment with the reducing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the reducing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • the activated catalyst was evaluated in the same manner as in Example 2(b). The results are shown in Table 1. After the evaluation, the catalyst was analyzed by ICP spectrometry. As a result, the sulfur content was 0.08% by weight.
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 280° C. in the contact treatment with the oxidizing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • the activated catalyst was evaluated in the same manner as in Example 2(b). The results are shown in Table 1. After the evaluation, the catalyst was analyzed by ICP spectrometry. As a result, the sulfur content was 0.12% by weight.
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 300° C. in the contact treatment with the reducing gas of Example 2(a) and the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the oxidizing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the oxidizing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • Example 2(a) Under the same conditions as in Example 2(a), except that the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the reducing gas of Example 2(a) and the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the oxidizing gas of Example 2(a), an activation treatment of a catalyst was performed.
  • a quartz reaction tube having an inner diameter of 14 mm was filled with 2.4 g of the deteriorated catalyst of Reference Example 1(b). While feeding nitrogen gas at a rate of 90 ml/min in the reaction tube, the temperature of a catalyst layer was adjusted to 350° C. in an electric furnace. Subsequently, while feeding the nitrogen gas at the same rate, hydrogen gas was fed at a rate of 10 ml/min (0.027 mol/h), followed by maintaining for 1.5 hours. After stopping feed of the hydrogen gas, the temperature was adjusted to 100° C. or lower while feeding the nitrogen gas, and the catalyst was withdrawn.
  • a nickel reaction tube having an inner diameter of 13 mm was filled with 1 g of the catalyst obtained by the above contact treatment with the reducing gas and then filled with 12 g of ⁇ -alumina spheres [SSA995 manufactured by NIKKATO CORPORATION] as a preheating layer at the gas inlet side of a catalyst layer.
  • oxygen was fed at a rate of 40 ml/min (0.009 mol/h) and nitrogen gas was fed at a rate of 160 ml/min (0.43 mol/h) for 2 hours.
  • Example 9(a) Under the same conditions as in Example 9(a), except that the temperature of a catalyst layer was adjusted to 200° C. and the maintaining time was adjusted to 2 hours in the contact treatment with the reducing gas of Example 9(a), an activation treatment of a catalyst was performed.
  • Example 9(a) Under the same conditions as in Example 9(a), except that the temperature of a catalyst layer was adjusted to 250° C. in the contact treatment with the reducing gas of Example 9(a), an activation treatment of a catalyst was performed.
  • the activated catalyst was evaluated in the same manner as in Example 2(b). The results are shown in Table 1. After the evaluation, the catalyst was analyzed by ICP spectrometry. As a result, the sulfur content was 0.09% by weight.
  • Example 9(a) Under the same conditions as in Example 9(a), except that the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the reducing gas of Example 9(a), an activation treatment of a catalyst was performed.
  • Example 9(a) Under the same conditions as in Example 9(a), except that the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the reducing gas of Example 9(a) and the temperature of a catalyst layer was adjusted to 400° C. in the contact treatment with the oxidizing gas of Example 9(a), an activation treatment of a catalyst was performed.
  • 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 ⁇ -alumina spheres [SSA995 manufactured by NIKKATO CORPORATION] as a preheating layer at the gas inlet side of a catalyst layer.
  • 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 ⁇ -alumina spheres [SSA995 manufactured by NIKKATO CORPORATION] as a preheating layer at the gas inlet side of a catalyst layer.
  • oxygen was fed at a rate of 40 ml/min (0.009 mol/h) and nitrogen gas was fed at a rate of 160 ml/min (0.43 mol/h) for 2 hours.
  • a nickel reaction tube having an inner diameter of 13 mm was filled with 1 g of the water-treated catalyst obtained above and then filled with 12 g of ⁇ -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 in the reaction tube, 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.

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120087855A1 (en) * 2009-06-10 2012-04-12 Basf Se Process for the oxidation of hydrogen chloride over a catalyst having a low surface roughness
US20130207055A1 (en) * 2010-09-10 2013-08-15 Toagosei Co., Ltd. Additive for molding of ceramic material

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5189954B2 (ja) * 2008-10-30 2013-04-24 住友化学株式会社 塩素の製造方法
US9610567B2 (en) * 2008-12-30 2017-04-04 Basf Se Process for regenerating a catalyst comprising ruthenium oxide for the oxidation of hydrogen chloride
JP5368883B2 (ja) * 2009-05-29 2013-12-18 住友化学株式会社 塩素製造用触媒の賦活方法および塩素の製造方法
JP2010274216A (ja) * 2009-05-29 2010-12-09 Sumitomo Chemical Co Ltd 塩素製造用触媒の賦活方法および塩素の製造方法
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Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2451870A (en) * 1942-09-04 1948-10-19 Standard Oil Dev Co Chlorine manufacture
US2602021A (en) * 1948-06-30 1952-07-01 Kellogg M W Co Catalytic production of chlorine
US3006732A (en) * 1958-01-09 1961-10-31 Inst Francais Du Petrole Chlorine production
US3198750A (en) * 1962-12-26 1965-08-03 Standard Oil Co Mixed antimony oxide-uranium oxide oxidation catalyst
US3308151A (en) * 1965-01-11 1967-03-07 Standard Oil Co Process for the oxidation of olefinammonia mixtures to unsaturated nitriles
US3694376A (en) * 1969-07-12 1972-09-26 Gerhard E Kabisch Oxidation-reduction regeneration of noble metal catalysts used in hydrogen peroxide production
US4107280A (en) * 1977-08-01 1978-08-15 Battelle Memorial Institute Oxidation of hydrogen halides to elemental halogens with catalytic molten salt mixtures
US4738948A (en) * 1986-07-02 1988-04-19 Exxon Research And Engineering Company Cobalt-ruthenium catalysts for Fischer-Tropsch synthesis and process for their preparation
US5084264A (en) * 1989-12-12 1992-01-28 Battelle Memorial Institute Process for oxidation of hydrogen halides to elemental halogens
US5093292A (en) * 1989-11-22 1992-03-03 Mitsui Toatsu Chemicals, Incorporated Chromium oxide catalyst impregnation regeneration method
US5154911A (en) * 1989-11-02 1992-10-13 University Of Southern California Efficient method for the chemical production of chlorine and the separation of hydrogen chloride from complex mixtures
US5837636A (en) * 1995-10-20 1998-11-17 Uop Llc Method for reducing chloride emissions from a catalyst regeneration process
US5908607A (en) * 1996-08-08 1999-06-01 Sumitomo Chemical Co., Ltd. Process for producing chlorine
US20020028173A1 (en) * 1998-02-16 2002-03-07 Takuo Hibi Process for producing chlorine
US6475943B1 (en) * 1995-11-08 2002-11-05 Shell Oil Company Catalyst activation process
US20060263290A1 (en) * 2003-08-08 2006-11-23 Basf Aktiengesellschaft Method for the production of chlorine

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4729981A (en) * 1981-10-13 1988-03-08 Shell Internationale Research Maatschappij B.V. ROR-activated catalyst for synthesis gas conversion
US4925819A (en) * 1983-11-10 1990-05-15 Exxon Research & Engineering Company Method of regenerating a deactivated catalyst
JPS61275104A (ja) 1985-05-28 1986-12-05 Mitsui Toatsu Chem Inc 塩素の製造方法
JPS61136902A (ja) 1984-12-03 1986-06-24 Mitsui Toatsu Chem Inc 塩素の製造方法
JPH0615402B2 (ja) 1985-11-14 1994-03-02 三井東圧化学株式会社 塩素の製造方法
JPS62256930A (ja) * 1986-04-28 1987-11-09 Tanaka Kikinzoku Kogyo Kk ルテニウムを回収する方法
JPS62270405A (ja) 1986-05-19 1987-11-24 Mitsui Toatsu Chem Inc 塩素の製造方法
JP2602828B2 (ja) * 1987-04-14 1997-04-23 富士写真フイルム株式会社 スチルカメラ付きビデオカメラ
JP3284879B2 (ja) 1995-05-18 2002-05-20 住友化学工業株式会社 塩素の製造方法
DE19533659A1 (de) * 1995-09-12 1997-03-13 Basf Ag Verfahren zur Herstellung von Chlor aus Chlorwasserstoff
JPH10338502A (ja) 1996-10-31 1998-12-22 Sumitomo Chem Co Ltd 塩素の製造方法
JP3870596B2 (ja) 1998-02-16 2007-01-17 住友化学株式会社 塩素の製造方法
JP4081591B2 (ja) 1999-07-12 2008-04-30 住友化学株式会社 塩素の製造方法
JP3775179B2 (ja) 1999-08-05 2006-05-17 住友化学株式会社 担持酸化ルテニウム触媒の製造方法及び塩素の製造方法
JP4069619B2 (ja) * 2001-01-29 2008-04-02 住友化学株式会社 担持酸化ルテニウム触媒および塩素の製造方法
US6800579B2 (en) * 2002-01-29 2004-10-05 Exxonmobil Research And Engineering Company Catalyst regeneration
DE10244996A1 (de) * 2002-09-26 2004-04-01 Basf Ag Katalysator für die katalytische Chlorwasserstoff-Oxidation
JP2005289800A (ja) * 2004-03-22 2005-10-20 Sumitomo Chemical Co Ltd 塩素の製造方法
JP2006219325A (ja) * 2005-02-09 2006-08-24 Sumitomo Chemical Co Ltd 酸化アルミニウム−酸化チタン混合成形体の製造方法
JP4438771B2 (ja) * 2005-06-13 2010-03-24 住友化学株式会社 酸化用触媒の製造方法、塩素の製造方法、並びに一酸化炭素及び/又は不飽和炭化水素の酸化方法
JP4367381B2 (ja) 2005-06-29 2009-11-18 住友化学株式会社 塩素製造用触媒の賦活方法及び塩素の製造方法
JP4479716B2 (ja) * 2005-11-30 2010-06-09 住友化学株式会社 担持ルテニウムの再生方法および塩素の製造方法
DE102005061954A1 (de) * 2005-12-23 2007-07-05 Basf Ag Verfahren zur Wiedergewinnung von Ruthenium aus gebrauchten Rutheniumoxid-haltigen Katalysatoren

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2451870A (en) * 1942-09-04 1948-10-19 Standard Oil Dev Co Chlorine manufacture
US2602021A (en) * 1948-06-30 1952-07-01 Kellogg M W Co Catalytic production of chlorine
US3006732A (en) * 1958-01-09 1961-10-31 Inst Francais Du Petrole Chlorine production
US3198750A (en) * 1962-12-26 1965-08-03 Standard Oil Co Mixed antimony oxide-uranium oxide oxidation catalyst
US3308151A (en) * 1965-01-11 1967-03-07 Standard Oil Co Process for the oxidation of olefinammonia mixtures to unsaturated nitriles
US3694376A (en) * 1969-07-12 1972-09-26 Gerhard E Kabisch Oxidation-reduction regeneration of noble metal catalysts used in hydrogen peroxide production
US4107280A (en) * 1977-08-01 1978-08-15 Battelle Memorial Institute Oxidation of hydrogen halides to elemental halogens with catalytic molten salt mixtures
US4738948A (en) * 1986-07-02 1988-04-19 Exxon Research And Engineering Company Cobalt-ruthenium catalysts for Fischer-Tropsch synthesis and process for their preparation
US5154911A (en) * 1989-11-02 1992-10-13 University Of Southern California Efficient method for the chemical production of chlorine and the separation of hydrogen chloride from complex mixtures
US5093292A (en) * 1989-11-22 1992-03-03 Mitsui Toatsu Chemicals, Incorporated Chromium oxide catalyst impregnation regeneration method
US5084264A (en) * 1989-12-12 1992-01-28 Battelle Memorial Institute Process for oxidation of hydrogen halides to elemental halogens
US5837636A (en) * 1995-10-20 1998-11-17 Uop Llc Method for reducing chloride emissions from a catalyst regeneration process
US6475943B1 (en) * 1995-11-08 2002-11-05 Shell Oil Company Catalyst activation process
US5908607A (en) * 1996-08-08 1999-06-01 Sumitomo Chemical Co., Ltd. Process for producing chlorine
US20020028173A1 (en) * 1998-02-16 2002-03-07 Takuo Hibi Process for producing chlorine
US20060263290A1 (en) * 2003-08-08 2006-11-23 Basf Aktiengesellschaft Method for the production of chlorine

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120087855A1 (en) * 2009-06-10 2012-04-12 Basf Se Process for the oxidation of hydrogen chloride over a catalyst having a low surface roughness
US20130207055A1 (en) * 2010-09-10 2013-08-15 Toagosei Co., Ltd. Additive for molding of ceramic material
US9056800B2 (en) * 2010-09-10 2015-06-16 Toagosei., Ltd. Additive for molding of ceramic material

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