Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of D-Glucosamine Hydrochloride

A technology of glucosamine hydrochloride and hydrochloric acid, which is applied in the field of glucosamine hydrochloride, can solve the problems that the volume concentration of hydrochloric acid and the hydrolysis reaction temperature cannot be too high at the same time, carbonization of citric acid waste residue, and prolonged reaction time, etc., to achieve production costs Low, pollution reduction, cost saving effect

Active Publication Date: 2011-08-31
NANTONG FOREIGN TRADE MEDICINES & HEALTH PRODUCTS CO LTD
View PDF4 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] First, glucosamine hydrochloride extracted from the shell of aquatic products is not suitable for many patients with allergic reactions to aquatic products;
[0006] Second, the purification process is complicated, and the product has a fishy smell and is unstable;
[0007] Third, affected by marine environmental pollution, glucosamine hydrochloride extracted from shrimp and crab shells is inevitably polluted by heavy metals
[0008] In order to solve the defects of the above-mentioned production method, before the present invention, some records related to the use of citric acid waste residue for the preparation of glucosamine hydrochloride invention patents are disclosed, such as patents such as CN200810088877.5 and CN200810238484.8, but these The inventors of the patent all have a misunderstanding in their understanding. They all believe that the volume concentration of hydrochloric acid and the hydrolysis reaction temperature should not be too high at the same time, especially the hydrolysis reaction temperature should not exceed 90°C, otherwise it will easily cause carbonization of citric acid waste residue, resulting in a loss of production low
In addition, when the reaction is carried out at a temperature lower than 90°C, the reaction time will be greatly prolonged. Generally, each reaction time needs to be more than 10 hours to fully react, but this greatly reduces the production capacity. efficiency

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] (1) Hydrolysis: 2000kg of hydrochloric acid with a mass concentration of 30% is pumped into the reaction kettle, steam is heated to 65°C, and 1000kg of citric acid waste residue is added, the steam is heated to 100°C, and the hydrolysis reaction is 2.5 hours;

[0027] (2) Suction filtration: put the above-mentioned hydrolyzed material into the suction filtration bucket and carry out suction filtration. The carbon residue after the suction filtration is rinsed twice with tap water, and then rinsed with 2% sodium hydroxide solution until neutral or Slightly acidic, collect and mix the suction and filtration mother liquor and rinsing water;

[0028] (3) Concentration: the above-mentioned mixed mother liquor is evaporated and concentrated, and when the weight of the feed liquid to be steamed is 80% of the original mixed mother liquor weight, the distillation is stopped, and the mother liquor after the distillation is transferred to a cooling tank for natural cooling to 30° C...

Embodiment 2

[0037] (1) Hydrolysis: 2250kg of hydrochloric acid with a mass concentration of 35% is pumped into the reactor, steam is heated to 60°C, and 1000kg of citric acid waste residue is added, the steam is heated to 105°C, and the hydrolysis reaction is performed for 5 hours;

[0038] (2) Suction filtration: the above-mentioned hydrolyzed material is put into the suction filtration bucket and carries out suction filtration, and the carbon residue after the suction filtration is rinsed 3 times with tap water, and then rinsing with a mass concentration of 3% ammonium hydroxide solution to neutral or Slightly acidic, collect and mix the suction and filtration mother liquor and rinsing water;

[0039] (3) Concentration: the above-mentioned mixed mother liquor is evaporated and concentrated, and when the weight of the feed liquid to be steamed is 80% of the original mixed mother liquor weight, the distillation is stopped, and the mother liquor after the distillation is transferred to a cool...

Embodiment 3

[0048] (1) Hydrolysis: 1800kg of hydrochloric acid with a mass concentration of 25% is pumped into the reactor, steam is heated to 70°C, and 1000kg of citric acid waste residue is added, the steam is heated to 95°C, and the hydrolysis reaction is performed for 2 hours;

[0049] (2) Suction filtration: the above-mentioned hydrolyzed material is put into suction filtration bucket and carries out suction filtration, and the carbon residue after the suction filtration is rinsed 2 times with tap water, and then is 1% sodium hydroxide solution rinsing to neutrality or Slightly acidic, collect and mix the suction and filtration mother liquor and rinsing water;

[0050] (3) Concentration: the above-mentioned mixed mother liquor is evaporated and concentrated, and when the weight of the feed liquid to be steamed is 80% of the original mixed mother liquor weight, the distillation is stopped, and the mother liquor after the distillation is transferred to a cooling tank for natural cooling...

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

No PUM Login to View More

Abstract

The invention discloses a preparation method of D-Glucosamine Hydrochloride, wherein citric acid waste residue, gained after production of the citric acid with a fermentation method, are used as raw material, and the D-Glucosamine Hydrochloride is prepared by the steps of hydrolysis, pumping filtration, concentration, etc. According to the invention, the citric acid waste residue is recycled, so that the waste residue pollution of the environment is mitigated; and the D-Glucosamine Hydrochloride produced with the citric acid waste residue as raw material is a D-Glucosamine Hydrochloride of vegetarian diet which has no fishlike smell, is not polluted by heavy metal, is safe and environmentally friendly, has a product purity up to 98-102% and accords with the quality standard of United States Pharmacopeia USP 32 edition. At the same time, because raw material resource is abundant, production resource has no restriction and production cost is low; further, cost in treatment of the environmental pollution is saved and relatively high circular economic gain is achieved; and more preferably, under the circumstance that technology prejudice in the technology field is overcome and simultaneously the product purity is guaranteed, output and production efficiency of the product are increased and time of the hydrolysis reaction is shortened.

Description

technical field [0001] The invention relates to the field of glucosamine hydrochloride, in particular to a method for preparing glucosamine hydrochloride from citric acid waste residue. Background technique [0002] Citric acid is a widely used organic acid. It can be used as a sour agent, thickener, and cleaning agent. It is widely used in food, beverage, pharmaceutical, chemical, detergent and other industries. Stimulated by exports, my country's domestic citric acid production increased from 380,000 tons in 2001 to 700,000 tons in 2005, and about 800,000 tons in 2006, with an average annual increase of 12.5%. 70% of the world. At present, in the process of producing citric acid by fermentation method in most enterprises, a large amount of citric acid waste residue is not comprehensively utilized, and is directly discharged. [0003] Glucosamine Hydrochloride, English D~Glucosamine Hydrochloride, molecular formula C 6 h 13 NO 5 ·HCl, white crystal, odorless, slightly s...

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
IPC IPC(8): C07H5/06C07H1/00C07H1/06
Inventor 白建国王德桂王健
Owner NANTONG FOREIGN TRADE MEDICINES & HEALTH PRODUCTS CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products