Method for preparing lactic acid through catalyzing glycerol by supported copper catalyst

A technology for catalyzing glycerin and copper catalysts, which is applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problem of high reaction temperature and pressure requirements, glycerin reaction concentration, etc. Low temperature, long reaction time and other problems, to achieve the effect of low reaction temperature, good industrial prospects, and fast reaction rate

Inactive Publication Date: 2014-09-17
JIANGSU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004]Glycerin is a by-product in the production of biodiesel. For every ten tons of biodiesel produced, one ton of glycerin is produced. With the increase of biodiesel production year by year, glycerin The output is also very large, using glycerin to produce a series of chemicals and chemical intermediates, with the characteristics of renewable and zero carbon dioxide emissions, and glycerin is rich in active hydroxyl groups, which can be easily replaced to synthesize special chemicals, so glycerin's Development and utilization have great prospects; recent studies have found that the use of glycerol to prepare lactic acid not only develops new uses of glycerin, but also provides a sustainable source of raw materials for lactic acid; it ...

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Weigh 4.58 g of sodium hydroxide (Sinopharm Chemical Reagent Co., Ltd.) and 0.46 g of 5% Cu / MgO into a 400 mL autoclave, then weigh 9.20 g of glycerin (Sinopharm Chemical Reagent Co., Ltd.) with 100 The mL volumetric flask was fixed to volume, added to the reaction kettle, ventilated with nitrogen gas, then sealed well, heated to 230 °C, timed, and reacted for 2 hours.

[0021] At the end of the reaction, take 20 mL of the reaction solution and acidify it with hydrochloric acid until the pH is 2~3, measure the volume after acidification, transfer 1 mL with a pipette and dilute to 25 mL with deionized water, and perform high performance liquid chromatography detection. Measure the production of lactic acid; pipette 1 mL of the acidified sample and 20 μL of n-butanol for gas chromatography analysis; the analysis shows that the conversion rate of glycerol is 87%, and the selectivity of lactic acid is 78%.

[0022] Reaction conditions: glycerol concentration: 1.0 M; NaOH / gl...

Embodiment 2

[0024] Weigh 4.58 g sodium hydroxide (Sinopharm Chemical Reagent Co., Ltd.) and 0.46 g 20% ​​Cu / ZrO 2 , together into a 400 mL autoclave, then weighed 9.20 g of glycerin (Sinopharm Chemical Reagent Co., Ltd.) with a 100 mL volumetric flask for constant volume, added it to the autoclave, ventilated it with nitrogen gas, and then sealed it well , after heating to 220°C, timed and reacted for 2 hours.

[0025] At the end of the reaction, take 20 mL of the reaction solution and acidify it with hydrochloric acid until the pH is 2~3, measure the volume after acidification, transfer 1 mL with a pipette and dilute to 25 mL with deionized water, and perform high performance liquid chromatography detection. The production of lactic acid was measured; then 20 μL of 1 mL acidified sample was pipetted for gas chromatography analysis; the analysis showed that the conversion rate of glycerol was 80% and the selectivity of lactic acid was 70%.

[0026] Reaction conditions: Glycerol concentra...

Embodiment 3

[0028] Weigh 4.58 g sodium hydroxide (Sinopharm Chemical Reagent Co., Ltd.) and 0.46 g 20% ​​Cu / TiO 2 , together into a 400 mL autoclave, then weighed 9.20 g of glycerin (Sinopharm Chemical Reagent Co., Ltd.) with a 100 mL volumetric flask for constant volume, added it to the autoclave, ventilated it with nitrogen gas, and then sealed it well , after heating to 220°C, timed and reacted for 2 hours.

[0029] At the end of the reaction, take 20 mL of the reaction solution and acidify it with hydrochloric acid until the pH is 2~3, measure the volume after acidification, transfer 1 mL with a pipette and dilute to 25 mL with deionized water, and perform high performance liquid chromatography detection. The production of lactic acid was measured; 20 μL of 1 mL acidified sample was pipetted with a pipette for gas chromatography analysis; the analysis showed that the conversion rate of glycerol was 76%, and the selectivity of lactic acid was 78%.

[0030] Reaction conditions: Glycero...

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Abstract

The invention relates to the technical field of lactic acid preparation and particularly relates to a method for preparing lactic acid through catalyzing glycerol by a supported copper catalyst. According to the method, the selectivity of lactic acid can reach 70-90%, and the conversion ratio of glycerol can reach 72-100%. The method is characterized in that reaction is carried out on glycerol which serves as a raw material in a high-pressure reactor under anaerobic and alkali source provided alkaline conditions in the presence of supported copper oxide which serves as a catalyst, thereby obtaining lactic acid, wherein a support of the supported copper oxide catalyst contains metal oxides, including MgO, ZrO2, TiO2, CeO2 and ZnO, activated charcoal or hydroxyapatite; the supported copper catalyst is easy to prepare, low in cost and relatively long in service life. The method has the advantages that the reaction temperature and reaction pressure are low, the catalyst activity is high, the selectivity is good, the reaction rate is high, and the process flow is safe and environmental-friendly and the like, so that the industrial prospect is good.

Description

technical field [0001] The invention relates to the technical field of lactic acid preparation, in particular to a method for preparing lactic acid from glycerin catalyzed by a supported copper catalyst. Background technique [0002] Lactic acid, the chemical system is named 2-hydroxypropanoic acid (2-Hydroxypropanoic acid). Since the carbon atom at the alpha position of the carboxyl group in the lactic acid molecule is an asymmetric carbon atom, lactic acid has two kinds of optical activity: left-handed (L-type) and The dextrorotatory (D-type) enantiomer; lactic acid was first discovered in yoghurt by Scheele in 1850, hence the name of lactic acid; lactic acid is one of the three recognized organic acids in the world, widely present in the human body, animals and The metabolism of microorganisms also exists in all aspects of people's lives. [0003] Lactic acid is an organic acid with a wide range of uses, mainly used in the food and pharmaceutical industries. In the brewi...

Claims

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Application Information

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IPC IPC(8): C07C51/02C07C51/16C07C59/08B01J23/72B01J23/83B01J23/80B01J27/18
CPCB01J23/002B01J23/72B01J23/80B01J23/83B01J27/1817C07C51/02C07C51/16C07C59/08
Inventor 张长华尹海旭殷恒波沈灵沁冯永海王爱丽鲁华胜
Owner JIANGSU UNIV
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