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Activated carbon loaded CeO2-x catalyst and preparation method and application thereof

A technology of activated carbon and catalyst, which is applied in the field of activated carbon-loaded CeO2-x catalyst and its preparation, can solve the problems of large influence of pH on oxidation efficiency, consume a large amount of alkali, and decrease in deprotonation efficiency, so as to broaden the use of pH value range, good The effect of the degradation effect

Inactive Publication Date: 2019-08-13
HANGZHOU CHENGJIE ENVIRONMENTAL PROTECTION
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0007] However, the oxidation efficiency of the perozonation system is greatly affected by the pH of the reaction system. Under acidic conditions, H 2 o 2 The deprotonation efficiency decreases, resulting in insufficient treatment efficiency of perozonation for acidic wastewater
However, most of the industrial wastewater is acidic or strongly acidic, and when using H 2 o 2 / O 3 When the system is processed, a large amount of alkali needs to be used in advance to adjust the industrial wastewater to medium alkaline. On the one hand, the treatment process is increased, and on the other hand, a large amount of alkali needs to be consumed, which increases the cost of industrial wastewater treatment.

Method used

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  • Activated carbon loaded CeO2-x catalyst and preparation method and application thereof
  • Activated carbon loaded CeO2-x catalyst and preparation method and application thereof
  • Activated carbon loaded CeO2-x catalyst and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1~5

[0041] Activated carbon supported CeO 2-x The preparation method of catalyst comprises the following steps:

[0042] (1) The activated carbon was ultrasonically washed 3 times with double distilled water, then ultrasonically washed once with 30% ethanol, and then air-dried at 80°C for 12 hours;

[0043] (2) At 500°C, N 2 Under the atmosphere, the activated carbon after washing and drying was roasted for 4 hours in a tube furnace, and then cooled to room temperature for later use;

[0044] (3) adding 10 g of activated carbon carrier after roasting and cooling into 20 mL of a certain concentration of cerous nitrate solution and impregnating it for 6 h;

[0045] (4) Take out the impregnated solid with tweezers, put it into a glass watch glass, and air-dry it at 80°C for 12 hours;

[0046] (5) Transfer the dried impregnated solid into a tube furnace, at 500°C, N 2 Roasting under atmosphere for 4h (heating rate is 3°C·min -1 ), cooled naturally to room temperature to obtain ac...

Embodiment 6~11

[0053] The catalysts prepared in Comparative Example 1 and Examples 1-5 were applied to degrade acetic acid simulated wastewater.

[0054] Configure 250mL of acetic acid solution with a concentration of 100ppm as simulated wastewater, adjust its initial pH to 3, and add H to the simulated wastewater 2 o 2 Make its initial concentration 100mg·L -1 , Examples 6-11 add the catalysts prepared in Comparative Example 1 and Examples 1-5 to the simulated wastewater respectively, so that the catalyst concentration in the simulated wastewater is 4g L -1 , continue to feed ozone to react for 30min, and the dosage of ozone is 22.07mg·min -1 .

[0055] After the reaction, the residual concentration of acetic acid in the simulated wastewater was calculated respectively, and the removal rate of acetic acid was calculated. The results are shown in Table 1.

[0056] Catalyst impregnation concentration and acetic acid removal rate in the embodiment 6~11 of table 1

[0057] Detect...

Embodiment 12~14

[0060] Compared with Example 9, Examples 12-14 adjusted the initial pH of the simulated wastewater to 1, 5 and 7 respectively, and other reaction conditions and parameters were the same as Example 9.

[0061] After the reaction, the residual concentration of acetic acid in the simulated wastewater was calculated respectively, and the removal rate of acetic acid was calculated. The results are shown in Table 2.

[0062] The acetic acid removal rate in the embodiment 9 of table 2 and embodiment 12~14

[0063] Detection Indicator Example 12 Example 9 Example 13 Example 14 initial pH 1 3 5 7 Acetic acid removal rate (%) 20.25 65.88 70.2 99.7

[0064] It can be seen from Table 2 that AC-Ce / H 2 o 2 / O 3 The efficiency of the system decreases with the decrease of pH. Under the conditions of pH 3 and 5, AC-Ce / H 2 o 2 / O 3 The efficiency of the system is relatively close.

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Abstract

The invention discloses an activated carbon loaded CeO2-x catalyst and a preparation method thereof. The preparation method comprises the following steps that 1, activated carbon is washed and dried,then, calcinated under the atmosphere of inertia gas and cooled to room temperature for use; 2, the calcinated and cooled activated carbon is soaked with a CeO2-x precursor solution; the concentrationof the CeO2-x precursor solution is 0.5-10 g L<-1>; the mass volume ratio of the activated carbon to the CeO2-x precursor solution is 1g:1-5 mL; 3, after the soaked activated carbon is dried, calcination is performed under 400-600 DEG C under the inertia gas atmosphere, and cooling is performed to obtain the catalyst. The catalyst can effectively enlarge the pH value range of a H2O2 / O3 system, the H2O2 / O3 system has the good degrading effect under the acid condition, and the catalyst can be applied to catalyzing the H2O2 / O3 system to degrade acid wastewater.

Description

technical field [0001] The invention relates to the field of waste water treatment, in particular to an activated carbon loaded CeO 2-x Catalyst and its preparation method and application. Background technique [0002] With the development of industrial and agricultural production, more and more organic compounds are widely used in human production and life, accompanied by an increasing amount of wastewater containing a large number of refractory organic pollutants. This type of wastewater generally has the characteristics of high pollution concentration, high toxicity, and poor biodegradability. It has obvious carcinogenic, teratogenic, and mutagenic effects, which seriously threaten human health. Therefore, how to effectively treat this kind of refractory wastewater has become a difficult point and research hotspot in domestic and foreign water treatment work in recent years. The development of new, economical and effective refractory wastewater treatment technologies is ...

Claims

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Application Information

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IPC IPC(8): B01J23/10B01J37/08B01J37/02C02F1/72C02F1/78C02F101/34
CPCB01J23/10B01J37/0201B01J37/082C02F1/722C02F1/725C02F1/78C02F2101/34
Inventor 童少平丁亚磊朱显跃
Owner HANGZHOU CHENGJIE ENVIRONMENTAL PROTECTION