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Calcium-based solid base catalyst, preparation method thereof, and application of catalyst in preparation of biodiesel

A solid base catalyst, calcium-based technology, used in molecular sieve catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of high economic cost, poor stability, easy deactivation, etc., and achieve high catalytic activity and stability. Good sex, easy separation effect

Pending Publication Date: 2020-01-10
SHANDONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] The inventors of the present disclosure have found through comprehensive research that when calcium-based catalysts are used for biodiesel synthesis, generally the reaction conditions are relatively mild and the yield of biodiesel is high, but there are usually disadvantages such as easy deactivation, poor stability and high economic cost.

Method used

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  • Calcium-based solid base catalyst, preparation method thereof, and application of catalyst in preparation of biodiesel
  • Calcium-based solid base catalyst, preparation method thereof, and application of catalyst in preparation of biodiesel

Examples

Experimental program
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Effect test

Embodiment 1

[0045] 35.7mmol Ca(NO 3 ) 2 4H 2 O, 7.7mmol Sr(NO 3 ) 2 4H 2 O and 39.3mmol Al(NO 3 ) 3 9H 2 O is dissolved in deionized water, stirred evenly to obtain a salt solution, which will contain 307.1mmol CO(NH 2 ) 2 The solution was mixed with the saline solution and stirred for 30 minutes. The obtained mixed solution was transferred to an autoclave with a capacity of 100 mL, heated to 120° C. for 12 h to form a precipitate. After natural cooling at room temperature, the resultant was dried overnight at 105°C. The dried sample was activated by calcining at 850°C for 4 hours in a muffle furnace to obtain a catalyst named 0.4Sr-Ca-1Al, where 0.4 represents the mass ratio of SrO and CaO, and 1 represents Al 2 o 3 With the mass ratio of CaO, the structural characterization diagram of the catalyst is shown in Figure 1~2 shown.

[0046] figure 1 Among them, compared with the Ca-1Al catalyst, the crystal phase of the 0.4Sr-Ca-1Al catalyst changed after adding Sr, and a new...

Embodiment 2

[0050] 35.7mmol Ca(NO 3 ) 2 4H 2 O, 7.7mmol Sr(NO 3 ) 2 4H 2 O was dissolved in deionized water, to which 2 g of ZrO 2 Stir well, will contain 130.2mmol CO(NH 2 ) 2 The solution was mixed with the saline solution and stirred for 30 minutes. The obtained mixed solution was transferred to an autoclave with a capacity of 100 mL, heated to 120° C. for 12 h to form a precipitate. After natural cooling at room temperature, the resultant was dried overnight at 105°C. The dried sample was activated by calcining at 850°C for 4 h in a muffle furnace to obtain a catalyst named 0.4Sr-Ca-1Zn, where 0.4 represents the mass ratio of SrO to CaO, and 1 represents the mass ratio of ZrO to CaO.

[0051] 10.5 g of methanol, 20 g of palm oil, and 1.5 g of catalyst (7.5% of the mass of palm oil) were added into a three-necked flask, and condensed and refluxed for 3 h at a temperature of 64° C. in a microwave reactor. The catalyst was separated from the reaction product by a centrifuge at ...

Embodiment 3

[0053] 35.7mmol Ca(NO 3 ) 2 4H 2 O, 11.6mmol Sr(NO 3 ) 2 4H 2 O and 39.3mmol Al(NO 3 ) 3 9H 2 O is dissolved in deionized water, and stirred evenly to obtain a salt solution, which will contain 318.8mmol CO(NH 2 ) 2 The solution was mixed with the saline solution and stirred for 30 minutes. The obtained mixed solution was transferred to an autoclave with a capacity of 100 mL, heated to 110° C. for 12 h to form a precipitate. After natural cooling at room temperature, the resultant was dried overnight at 105°C. The dried sample was activated by calcining at 850°C for 4 hours in a muffle furnace to obtain a catalyst named 0.6Sr-Ca-1Al, where 0.6 represents the mass ratio of SrO to CaO, and 1 represents Al 2 o 3 The mass ratio to CaO.

[0054] 10.5 g of methanol, 20 g of palm oil, and 1.5 g of catalyst (7.5% of the mass of palm oil) were added into a three-necked flask, and condensed and refluxed for 3 h at a temperature of 64° C. in a microwave reactor. The catalys...

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Abstract

The invention provides a calcium-based solid base catalyst, a preparation method thereof, and an application of the catalyst in the preparation of biodiesel. The preparation method comprises the following steps: dissolving a calcium salt, a strontium salt and a carrier or a carrier precursor in water, adding urea, carrying out a hydrothermal reaction to obtain a precipitate, and calcining the precipitate to obtain the calcium-based solid base catalyst, wherein the carrier is zirconium oxide or an MCM-41 molecular sieve, and the carrier precursor is an aluminum salt or a zinc salt. The catalystprepared in the invention has the advantages of high catalytic performance, reusability and low production cost.

Description

technical field [0001] The disclosure belongs to the technical field of catalyst preparation, and relates to a calcium-based solid base catalyst, a preparation method and its application in the preparation of biodiesel. Background technique [0002] The statements herein merely provide background information related to the present disclosure and may not necessarily constitute prior art. [0003] Energy shortages, as well as the greenhouse effect and environmental pollution caused by the use of fossil energy, have prompted countries to continuously develop renewable clean energy. Biodiesel is an important renewable clean energy, which has the advantages of high flash point, good lubricity and no harmful substances such as sulfur and aromatics. Biodiesel is a mixture of fatty acid methyl esters obtained by catalytic or non-catalytic reactions of a wide range of biological resources such as vegetable oils, animal fats, and waste oils with short-chain alcohols (mainly methanol ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/02B01J29/70C10G3/00
CPCB01J23/02B01J29/7038C10G3/44C10G2400/04Y02E50/10Y02P30/20
Inventor 牛胜利张玉娇韩奎华路春美李英杰齐建荟王永征
Owner SHANDONG UNIV