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Method for preparing gamma-aluminium oxide (Al2O3) framework material by using erythromycin fungus dreg produced by fermentation method as core-shell material

A technology of erythromycin residues and skeleton materials, which is applied in the field of recycling of waste pharmaceutical residues, can solve problems such as inactivation, environmental protection, and waste of resources, and achieve low production costs, resource conservation, and no secondary pollution Effect

Active Publication Date: 2013-01-02
四川金本科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

For decades, people have tried to utilize erythromycin residue as a resource, but all previous research work has focused on using the protein rich in the residue (18-22%wt) as animal feed or anaerobic fermentation of the residue Produce methane combustible gas; therefore, a common problem remains unresolved, that is the problem of erythromycin drug residues and Streptomyces rubrum anti-phage inactivation
However, many manufacturers still use the "dangerous goods landfill" method to dispose of the fungus residue, which not only fails to fundamentally solve the environmental protection problem, but also causes a huge waste of resources.

Method used

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  • Method for preparing gamma-aluminium oxide (Al2O3) framework material by using erythromycin fungus dreg produced by fermentation method as core-shell material
  • Method for preparing gamma-aluminium oxide (Al2O3) framework material by using erythromycin fungus dreg produced by fermentation method as core-shell material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] Example 1 see figure 1 , a production of erythromycin residue by fermentation as core-shell material to prepare γ-Al 2 o 3 The method of skeleton material, is characterized in that: use deionized water to extract erythromycin and amino acid from erythromycin slag produced by fermentation method, then press filter, and carry out syneresis on the slag after pressure filtration at 150°C Treatment (distillation) for 2 hours, followed by solid phase transformation treatment (thermal decomposition) at 680°C for 4 hours, to obtain γ-Al 2 o 3 Skeleton material.

[0016] γ-Al prepared by this example 2 o 3 Skeleton material with a pore size of 0.9nm and a specific surface area of ​​198m 2 / g.

Embodiment 2

[0017] Example 2 see figure 2 , a production of erythromycin residue by fermentation as core-shell material to prepare γ-Al 2 o 3 The method of skeleton material, is characterized in that: use distilled water to extract erythromycin and amino acid from the erythromycin slag produced by fermentation method, then carry out pressure filtration under 5MP pressure, carry out pressure filtration at 190 ℃ to the slag after pressure filtration Syneresis treatment (distillation) for 3 hours, followed by solid phase transformation treatment (thermal decomposition) at 780°C for 5 hours to obtain γ-Al 2 o 3 Skeleton material.

[0018] γ-Al prepared by this example 2 o 3 Skeleton material with a pore size of 1.3nm and a specific surface area of ​​200m 2 / g.

[0019] In order to comprehensively utilize the erythromycin residue produced by the fermentation method of this example, the erythromycin and amino acids can also be extracted and separated from the filtrate after the above-...

Embodiment 3

[0020] Example 3 see figure 2 , a production of erythromycin residue by fermentation as core-shell material to prepare γ-Al 2 o 3 The method of skeleton material, is characterized in that: use deionized water to extract erythromycin and amino acid from the erythromycin residue produced by fermentation method, then carry out press filtration under 50MP pressure, and filter the press-filtered bacteria at 200°C The slag was subjected to syneresis treatment (distillation) for 4 hours, and then solid phase transformation treatment (thermal decomposition) at 800°C for 6 hours to obtain γ-Al 2 o 3 Skeleton material.

[0021] γ-Al prepared by this example 2 o 3 Framework material with a pore size of 1.4nm and a specific surface area of ​​205m 2 / g.

[0022] In order to comprehensively utilize the erythromycin residue produced by the fermentation method of this example, the erythromycin and amino acids can be extracted and separated from the filtrate after the above-mentioned...

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Abstract

The invention discloses a method for preparing a gamma-aluminium oxide (Al2O3) framework material by using erythromycin fungus dreg which is produced by a fermentation method as a core-shell material. The method is characterized by comprising the following steps of: extracting erythromycin and an amino acid from the erythromycin fungus dreg which is produced by the fermentation method by using deionized water or distilled water; carrying out pressure filtration; carrying out syneresis treatment on the fungus dreg which is subjected to the pressure filtration for 2 to 4 hours at the temperature of 150 to 200 DEG C; and then carrying out solid-phase transition for 4 to 6 hours at the temperature of 650 to 800 DEG C to obtain the gamma-Al2O3 framework material. In the method, a residue culture medium and a mycelium in the erythromycin fungus dreg which is produced by the fermentation method serve as the core-shell material, and a metal aluminium ion source which is provided by a flocculating agent in the fungus dreg is utilized fully, so that resources are saved, production cost is low, the porous gamma-Al2O3 framework material with high chemical activity is produced, a good economicbenefit is brought, and the problem of little erythromycin residue in the fungus dreg is also solved. Moreover, the method is environment-friendly and secondary pollution is avoided.

Description

technical field [0001] The invention belongs to the field of recovery and utilization of waste pharmaceutical residues, and in particular relates to a method for preparing γ-Al by using fermentation method to produce erythromycin residues as core-shell materials. 2 o 3 Skeleton method. Background technique [0002] In the process of producing erythromycin raw material medicine by fermentation method in my country, the separation of fungus residue is first to use flocculant to make mycelium and residual medium produce flocculation phenomenon, so as to facilitate the subsequent pressure filtration and essence liquid and its erythromycin prime extract. This industry involves 17 manufacturers, large and small, from east to west, north, south, and north, most of which use polyaluminum trichloride as a flocculant, and the added metal aluminum ion content is as high as 8%wt; this industry in my country uses trichloride every year Aluminum chloride is used as a flocculant, and the ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01F7/30
Inventor 韩志范高继轩王利娅杨舒涵
Owner 四川金本科技有限公司
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