Method for preparing lactate by catalyzing sugar

A lactic acid ester and catalyzed sugar technology, which is applied in the field of catalyzed sugar to prepare lactic acid ester, can solve problems such as the inability to realize large-scale production and application of lactic acid, atmospheric environmental pollution, large solid waste residue, etc., and is suitable for large-scale industrial production applications, Improve reaction efficiency, process safety and high efficiency

Active Publication Date: 2020-06-09
CHINA PETROLEUM & CHEM CORP +1
View PDF5 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The process has a long reaction route, high production cost and produces a large amount of solid waste, which makes it impossible to realize large-scale production and application of lactic acid at present.
The commonly used chemical synthesis methods are the lactonitrile method and the propionic acid method. The lactonitrile method uses acetaldehyde and highly toxic hydrocyanic acid as the reaction raw materials, and concentrated sulfuric acid as the catalyst. Therefore, the production process is seriously polluted and has potential safety hazards.
The propionic acid method uses toxic chlorine gas as a raw material, which not only requires high operational safety and airtightness, but also easily pollutes the atmospheric environment

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing lactate by catalyzing sugar

Examples

Experimental program
Comparison scheme
Effect test

Embodiment approach

[0051] According to the first embodiment, preferably the tin-titanium-silicon molecular sieve is at 460 cm in the FT-IR spectrum -1 、975cm -1 、800cm -1 and 1080cm -1 There is absorption nearby. Preferably, the tin-titanium-silicon molecular sieve has absorption at 200-300 nm in the UV-Vis spectrum, preferably at 200-260 nm.

[0052] According to the first embodiment, preferably the molar ratio of the tin element to the silicon element in the tin-titanium-silicon molecular sieve is 0.05-10:100, more preferably 0.1-5:100, particularly preferably 0.2-2:100. Preferably, the molar ratio of titanium element to silicon element in the tin-titanium-silicon molecular sieve is 0.05-10:100, more preferably 0.1-5:100, particularly preferably 0.5-4:100. Such proportions of tin, titanium and silicon can further optimize the catalytic activity of the tin-titanium-silicon molecular sieve of the present invention.

[0053] According to the first embodiment, it is preferred that the tin-tit...

preparation Embodiment 1

[0098] In this preparation example, a Sn-Ti-MFI-1 molecular sieve is prepared according to the method of Example 1 of the Chinese patent CN 105217645A specification, and the specific preparation method is as follows:

[0099] (1) At 25°C, stirring and contacting tetrapropylammonium hydroxide aqueous solution (concentration: 15% by weight) with tetrabutyl titanate and tin tetrachloride pentahydrate for 30 minutes to obtain a mixture;

[0100] (2) At 60°C, add silicon molecular sieve S-1 to the above mixture and stir for 0.5h to obtain the mixture (during this contact process, add water or not add water as required, if the feeding in step (1) can meet the requirement of water Feeding requirements, there is no need to add water, if it is not met, you can add water when the mixture containing tetrapropylammonium hydroxide, tetrabutyl titanate and tin chloride is stirred and contacted with silicon molecular sieve, or distill off water, and the rest The preparation examples are simi...

preparation Embodiment 2

[0104] This preparation example prepares the Sn-Ti-MFI-2 molecular sieve according to the method of the Chinese patent CN105217645A specification example 2, and the specific preparation method is as follows:

[0105] (1) At 25°C, stirring and contacting tetrapropylammonium hydroxide aqueous solution (concentration: 20% by weight) with tetrabutyl titanate and tin tetrachloride pentahydrate for 30 minutes to obtain a mixture;

[0106] (2) At 25°C, add silicon molecular sieve S-1 to the above mixture and stir for 0.5h to obtain the mixture; wherein, ensure that the molar ratio of each substance is: silicon source (silicon molecular sieve): alkali source template (four Propyl ammonium hydroxide): titanium source (tetrabutyl titanate): tin source (tin tetrachloride): water=100:15:2:0.1:200, wherein the silicon source is SiO 2 In terms of titanium source as TiO 2 Tin source is calculated as tin element;

[0107] (3) Transfer the above mixture into a sealed stainless steel reaction...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to view more

Abstract

The invention relates to a method for preparing lactate by catalyzing sugar. The method comprises the following steps: contacting sugar and alcohol with a catalyst in a reactor, and reacting to obtaina lactate-containing product, wherein the molar ratio of the sugar to the alcohol is 1:(50-900), the reaction temperature is 150-250 DEG C, the reaction time is 10-50 hours, the catalyst contains a tin-titanium-silicon molecular sieve, and the weight ratio of the sugar to the tin-titanium-silicon molecular sieve based on dry basis weight is 1:(1-6). The method provided by the invention has high sugar conversion rate and high lactate yield.

Description

technical field [0001] The invention relates to a method for catalyzing sugar to prepare lactate. Background technique [0002] Methyl lactate, hydroxycarboxylate compound, chemical formula C 4 h 8 o 3 , Colorless liquid, flammable, soluble in water, ethanol, organic solvents, irritating, density 1.09, boiling point 144.8°C, melting point -66.2°C. Methyl lactate is an important oxygen-containing organic chemical intermediate, which can be used as a high-boiling solvent, cleaning agent, synthetic raw material, etc., and is widely used in medicine, resin coatings, adhesives, cleaning agents, dry cleaning fluids, printing inks, cosmetics, tobacco and alcohol , beverages and other food industries. For example, it can be used as a solvent for nitrocellulose, cellulose acetate, cellulose acetate butyrate, cellulose acetate propionate and cellulose ether. When used as a solvent for nitrocellulose paint and paint, it can improve the whitening resistance and ductility of the pai...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07C67/00C07C69/68C07C45/60C07C49/17C07C45/00C07C45/51C07C45/52C07C49/185B01J29/89B01J35/10
CPCC07C67/00C07C45/60C07C45/00C07C45/51C07C45/52B01J29/89B01J35/1014B01J35/1019B01J35/1023B01J2229/18C07C69/68C07C49/17C07C49/185
Inventor 刘聿嘉赵毅夏长久彭欣欣林民罗一斌朱斌舒兴田
Owner CHINA PETROLEUM & CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap