Supported metallic oxide catalyst for assisting microwave denitration and preparation method and using method thereof

A technology of oxides and catalysts, which is applied in the field of flue gas denitrification and purification, can solve the problems of low activity of metal oxide components, high loading capacity, and high reaction temperature, and achieve high catalytic decomposition efficiency, good microwave absorption capacity, and specific surface area big effect

Active Publication Date: 2015-12-23
CHONGQING UNIVERSITY OF SCIENCE AND TECHNOLOGY +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But the disadvantage is that the reaction temperature is still relatively high, and the decomposition efficiency is relatively low.
The existing catalytic decomposition method of nitrogen oxides under microwave conditions generally uses ZSM molecular sieve as the carrier. Although it can achieve a certain denitrification efficiency, the preparation process of the carrier is complicated, the hydrothermal stability of the carrier is poor, and the activity of the metal oxide components is low. Many disadvantages such as not high, especially the high loading of active components, even as high as 70%. Excessive loading will lead to a decrease in the specific surface area of ​​the catalyst, and second, it will easily cause catalyst components to agglomerate and deactivate. The metal oxide actually increases the temperature of the local reaction hot spot by enhancing the microwave absorption capacity, and does not really reflect the catalytic effect of the catalyst.

Method used

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preparation example Construction

[0024] The preparation method of the supported metal oxide catalyst for assisting microwave denitrification in this embodiment comprises the following steps:

[0025] The metal salt solution is loaded on the carbonaceous support by the impregnation method or the co-precipitation method, and the catalyst is obtained by drying and roasting. The metal salt is a soluble salt such as nitrate, acetate or hydrochloride; the above methods are all based on Metal salts of Cu, Ni, Ce, Mn, Fe, La, etc. are active component precursors, and impregnation or co-precipitation methods are existing methods. The key point is to prepare specific carbonaceous supports and oxides with this Invented products with catalytic properties.

[0026] The method for using the supported metal oxide catalyst for assisting microwave denitrification in this embodiment includes the following steps:

[0027] The catalyst is placed in a microwave field to form a reaction bed, and the nitrogen oxide gas is passed t...

Embodiment 1

[0031] Activated carbon was impregnated with a certain concentration of Cu(NO 3 ) 2 In the aqueous solution, the immersion time is more than 12h, then dried and roasted to obtain Cu 2 O / activated carbon catalyst, where Cu 2 The mass fraction of O is 5%; the Cu 2 The O / activated carbon catalyst is placed in a microwave reactor, the microwave frequency is 600MHz, and the bed temperature is set at 180°C. The microwave output power of the microwave reactor is automatically adjusted by the temperature controller according to the set temperature. The mixed gas containing NO concentration of 500ppm is mixed at a space velocity of 1000h -1 into the microwave reactor under microwave and activated carbon loaded Cu 2 The catalytic decomposition reaction is carried out under the synergistic effect of O, and the decomposition rate of NO is over 96% after testing by an online gas analyzer.

Embodiment 2

[0033] Activated carbon was impregnated with a certain concentration of Cu(NO 3 ) 2 and Ce(NO 3 ) 3 In the aqueous solution, the immersion time is more than 13h, then dried and roasted to obtain Cu 2 O-CeO 2 / activated carbon catalyst, Cu 2 The mass fraction of O is 5%, CeO 2 The mass fraction is 2%. Will Cu 2 O-CeO 2 / The activated carbon catalyst is placed in a microwave reactor, the microwave frequency is 2450MHz, and the bed temperature is set at 300°C. The microwave reactor automatically adjusts the microwave output power by the temperature controller according to the set temperature. The mixed gas containing NO concentration of 500ppm is mixed at a space velocity of 4000h -1 Under the conditions, enter the microwave reactor, and carry out the catalytic decomposition reaction under the synergistic effect of microwave and activated carbon-supported catalyst. After the online gas analyzer test, the NO decomposition rate is over 98%.

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Abstract

The invention discloses a supported metallic oxide catalyst for assisting microwave denitration and a preparation method and a using method thereof. The catalyst is the supported catalyst using carbon as a carrier and using a metallic oxide as an active ingredient. The carrier of the catalyst is carbon-based, is convenient to obtain, large in specific surface area and capable of playing a very good dispersing role on the active ingredient of the catalyst, and the phenomenon of ingredient agglomeration is not produced. The metallic oxide is high in activity, and required supporting amount is small. The carbon-supported metallic oxide has very good microwave absorbing ability, can well play the synergistic effect of microwaves and the catalyst, the catalytic decomposition efficiency of nitrogen oxide is high, the NO decomposition rate can be above 98%, and the catalytic decomposition temperature is low and the loss of the carbon carrier is low by means of the method.

Description

technical field [0001] The invention relates to the technical field of flue gas denitration and purification, in particular to a supported metal oxide catalyst for assisting microwave denitrification, a preparation method and a use method thereof. Background technique [0002] Nitrogen oxides (NOx) are important air pollutants, which mainly come from the combustion of fossil fuels and vehicle exhaust. The excessive emission of nitrogen oxides causes environmental problems such as acid rain, photochemical smog, enhanced greenhouse effect, and ozone layer destruction. Nitrogen oxides are not only the most harmful environmental pollution but also the most difficult to deal with. In the prior art, the harmless removal of NOx can be realized in two ways according to the steady state of N: (1) using oxides to first oxidize NO into NO 2 , and then converted into nitrate or nitric acid; (2) reducing NOx to N which is non-toxic to the environment 2 . The former is transformed int...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/72B01J23/83B01J23/755B01J23/34B01D53/56B01D53/86
Inventor 王金波张汉威秦瑞香唐宇星
Owner CHONGQING UNIVERSITY OF SCIENCE AND TECHNOLOGY
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