Experiment table assembly for preparing protein nanofibers

By designing integrated experimental platform components and precisely controlling temperature, ultrasonic time, and airflow speed, the problem of inaccurate parameter control in the preparation of protein nanofibers in existing technologies has been solved, achieving high-quality and efficient nanofiber preparation.

CN223875068UActive Publication Date: 2026-02-06SHENZHEN JIAHONGSHUN IND CO LTD
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Patent Information

Application Number
CN202520425818.1
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2025-03-12
Publication Date
2026-02-06
Estimated Expiration
2035-03-12

AI Technical Summary

Technical Problem

Existing technologies lack integrated experimental platforms and fume hood systems, making it impossible to simultaneously meet the precise control of temperature, ultrasonic time, particle size, and airflow speed during the preparation of protein nanofibers, thus affecting the quality and preparation efficiency of nanofibers.

Method used

An experimental stage assembly was designed, comprising a functional housing component, a ceramic component, an ultrasonic particle size analyzer head, a gallium quantitative droplet component, an exhaust component, and a bottom support frame. Through precise control of the temperature control component, the ultrasonic particle size analyzer head, and the exhaust component, key parameters in the preparation process are ensured, thereby improving the quality and efficiency of nanofibers.

Benefits of technology

High-quality and efficient preparation of protein nanofibers has been achieved. In the production process, the nanofibers are finely ground into particles by heating and ultrasonication and then combined with metallic gallium to form a new material form, which improves the preparation quality and production efficiency.

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Abstract

The utility model discloses an experiment table assembly for protein nanofiber preparation, which comprises a functional box shell assembly, a ceramic assembly, an ultrasonic particle size analysis head, a gallium quantitative dripping assembly, an exhaust assembly, a bottom support frame body and a conveyor belt assembly, a temperature control group assembly is arranged in a first box body, and the temperature control group assembly comprises an exhaust hood and a temperature control end; an ultrasonic particle size analysis head and a gallium quantitative dripping assembly are arranged in the second box body; the air exhaust assembly comprises an air exhaust cabinet and an air speed display controller, and the air speed display controller is arranged in the air exhaust cabinet; by the adoption of the assembly, key parameters in the preparation process can be accurately controlled so as to improve the quality and the preparation efficiency of the protein nanofibers, the production technology comprises the steps that soybean products are cleaned, put into a container, heated to 90 DEG C, ultrasonically ground into particles and then combined with metal gallium, a new substance form is formed, the experiment purpose is achieved, and the production cost is reduced. The production efficiency is high while the preparation quality is improved.
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Description

TECHNICAL FIELD

[0001] The utility model relates to the experiment table technology especially, a kind of experimental table assembly for protein nanofiber preparation. BACKGROUND

[0002] Currently, in the field of biomaterial preparation, the preparation of protein nanofiber is a complex process, which requires precise control of multiple parameters, such as temperature, ultrasonic time, particle size and air flow speed. In the prior art, there is a lack of an integrated experiment table and fume hood system that can simultaneously meet these control requirements, thereby affecting the quality and preparation efficiency of protein nanofiber.

[0003] The patent document with application number "CN200810147127.0" discloses that when preparing plant protein stock solution, nanomaterials are added and fully matured in the reaction kettle. Under the action of a certain temperature, active agent or stirring, blending and copolymerization occur. Spinning stock solution is prepared, and colored or colorless plant protein nanofiber is spun out using a conventional wet spinning process of chemical fibers. The fiber density can be in the range of 0.7-7.0 dtex. Due to the addition of nanomaterials, the spun fiber is knitted or woven into cloth to make clothing, which has the functions of sterilization, bacteriostasis, health care, and longevity. The clothing made of the fiber has the functions of preventing ultraviolet rays and promoting microcirculation of blood, which can improve and assist in the treatment of various diseases and skin diseases. The raw material is abundant, the price is low, it is green and environmentally friendly, and it can be sustainably developed. The market prospect is immeasurable.

[0004] The patent document with application number "CN201410756416.6" discloses a nanofiber foam-based protein adsorption and separation device and a preparation method thereof. The nanofiber foam-based protein adsorption and separation device comprises a perforated protective cover, a nanofiber foam-based protein adsorption material is arranged in the perforated protective cover, a liquid collection capillary network is arranged in the nanofiber foam-based protein adsorption material, the liquid collection capillary network is connected to a main liquid delivery pipe, and the main liquid delivery pipe is connected to a liquid collection tank through a pump. The device has the advantages of simple preparation process, low production cost, convenient operation, strong expandability, fast mass transfer rate, fast adsorption rate, high adsorption capacity, high protein dissolution rate, good pressure resistance, and the like. The protein in the solution can be directly extracted and adsorbed onto the material, batch high-efficiency continuous separation and adsorption treatment of the protein-containing solution can be realized, and the device has a wide application prospect in the fields of biological pharmacy and the like.

[0005] The above patent documents combined with the prior art disclose that the existing experimental table assembly for protein nanofiber preparation has the following defects: SUMMARY

[0006] In order to overcome the prior art, the utility model provides a kind of experimental bench assembly for protein nanofiber preparation, solve the experimental bench assembly for protein nanofiber preparation problem.

[0007] The utility model discloses first aspect provides a kind of experimental bench assembly for protein nanofiber preparation, including function box shell body assembly, ceramic component, ultrasonic particle size analysis head, gallium quantitative drop-in component, exhaust component, bottom support frame body, conveyer belt component, the function box shell body assembly includes two box body assembly that link together, the conveyer belt component is set on the bottom support frame body, function box shell body assembly, gallium quantitative drop-in component, ultrasonic particle size analysis head, exhaust component are sequentially set on the conveyer belt component from left to right;Two the box body assembly is divided into first box body, second box body, temperature control group component is provided in the first box body, and the temperature control group component includes exhaust hood, temperature control end, ultrasonic particle size analysis head is provided in the second box body, and gallium quantitative drop-in component;The exhaust component includes exhaust cabinet, air velocity display controller, and air velocity display controller is set in the exhaust cabinet;The ceramic component is sequentially treated along the temperature control group component, ultrasonic particle size analysis head, gallium quantitative drop-in component, exhaust component along the conveyer belt component.

[0008] In the first aspect of the utility model, as a preferred embodiment, the first box body and the second box body are both provided with an exhaust hood.

[0009] In the first aspect of the utility model, as a preferred embodiment, the second box body is located between the first box body and the exhaust component.

[0010] In the first aspect of the utility model, as a preferred embodiment, the top of the exhaust component is provided with an exhaust fan.

[0011] In the first aspect of the utility model, as a preferred embodiment, the temperature control group component further includes a temperature sensor, and the temperature sensor is arranged in the first box body.

[0012] In the first aspect of the utility model, as a preferred embodiment, the exhaust component further includes an air velocity sensing probe, and the air velocity sensing probe is arranged in the exhaust cabinet.

[0013] In the first aspect of the utility model, as a preferred embodiment, the volume of the exhaust cabinet is greater than that of the first box body.

[0014] In the first aspect of the utility model, as a preferred embodiment, the exhaust cabinet and the first box body are both cuboids.

[0015] In the first aspect of the utility model, as a kind of preferred embodiment, the exhaust cabinet is equipped with several exhaust holes.

[0016] In the first aspect of the utility model, as a kind of preferred embodiment, the ceramic assembly includes ceramic container, backing plate assembly, the ceramic container is set on the backing plate assembly.

[0017] Compared with the prior art, the utility model has the beneficial effects that:

[0018] Two the box body assembly are divided into first box body, second box body, temperature control group component is provided in the first box body, and the temperature control group component includes exhaust hood, temperature control end, ultrasonic particle size analysis head is provided in the second box body, gallium quantitative drop-in component;The exhaust component includes exhaust cabinet, wind speed display controller, and the wind speed display controller is set in the exhaust cabinet;The ceramic assembly sequentially passes through temperature control group component, ultrasonic particle size analysis head, gallium quantitative drop-in component, exhaust component along the conveyer belt component and is handled.Using the component of the application, the system can accurately control the key parameters in preparation process to improve the quality and preparation efficiency of protein nanofiber, the production process is that soybean product is washed and placed in container, is combined with metal gallium after being finely divided into particles by heating to 90 degrees and ultrasonic, forms new material form, realizes experimental purpose, improves preparation quality while production efficiency is high. BRIEF DESCRIPTION OF DRAWINGS

[0019] Fig. 1 It is the structural diagram of the utility model;

[0020] Fig. 2 It is another structural diagram of the utility model.

[0021] In the drawing: 100, functional box shell assembly;101, box body assembly;200, ceramic assembly;201, ceramic container;202, backing plate assembly;10, temperature control group component;11, exhaust hood;12, temperature control end;13, temperature sensor;20, ultrasonic particle size analysis head;30, gallium quantitative drop-in component;40, exhaust component;41, exhaust cabinet;42, wind speed display controller;43, wind speed sensing probe;80, bottom support frame body;90, conveyer belt assembly. DETAILED DESCRIPTION

[0022] Hereinafter, the utility model will be further described in conjunction with the drawings and specific embodiments. It should be noted that the embodiments described below or technical features among them can be combined to form new embodiments without conflict. Unless otherwise specified, the materials and equipment used in the embodiments can be purchased from the market. The examples of the embodiments are shown in the drawings, wherein the same or similar reference signs represent the same or similar elements or elements with the same or similar functions throughout. The embodiments described below with reference to the drawings are exemplary and are only used to explain the present application and cannot be understood as a limitation on the present application.

[0023] In the description of the present application, it should be understood that the terms "upper", "lower", "front", "back", "vertical", "horizontal", "top", "bottom", "inner", "outer" and the like indicate the orientation or positional relationship shown in the drawings, and are only for the convenience of describing the present application and simplifying the description, and do not indicate or imply that the device or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore cannot be understood as a limitation on the present application. In the description of the present application, the meaning of "a plurality of" is two or more, unless otherwise specifically specified and limited.

[0024] In the description of the present application, it should be noted that unless otherwise explicitly specified and limited, the terms "connected", "communicated", "connected" should be understood in a broad sense, for example, it can be fixedly connected, or connected through an intermediate medium, or the internal connection of two elements or the interaction relationship between two elements. For those skilled in the art, the specific meaning of the above terms in the present application can be understood according to the specific circumstances.

[0025] The terms "first", "second", and the like in the specification and claims of the present application and the above drawings are used to distinguish similar objects, and do not necessarily describe a specific order or sequence. In addition, the terms "include" and "have" and any variations thereof are intended to cover non-exclusive inclusion, for example, a process, method, system, product or device including a series of steps or units does not necessarily limit to those clearly listed steps or units, but can include other steps or units not clearly listed or inherent to these processes, methods, products or devices.

[0026] As Figs. 1-2As shown, an experimental bench assembly for protein nanofiber preparation includes a functional box shell assembly 100, a ceramic assembly 200, an ultrasonic particle size analysis head 20, a gallium quantitative dropping assembly 30, an exhaust assembly 40, a bottom support frame body 80, and a conveyor belt assembly 90, the functional box shell assembly 100 includes two box assemblies 101 connected together, the conveyor belt assembly 90 is arranged on the bottom support frame body 80, and the functional box shell assembly 100, the gallium quantitative dropping assembly 30, the ultrasonic particle size analysis head 20, and the exhaust assembly 40 are sequentially arranged from left to right on the conveyor belt assembly 90; the two box assemblies 101 are divided into a first box and a second box, the temperature control group assembly 10 is arranged in the first box, the temperature control group assembly 10 includes an exhaust hood 11 and a temperature control end 12, and the ultrasonic particle size analysis head 20 and the gallium quantitative dropping assembly 30 are arranged in the second box; the exhaust assembly 40 includes an exhaust cabinet 41 and a wind speed display controller 42, and the wind speed display controller 42 is arranged in the exhaust cabinet 41; the ceramic assembly 200 sequentially passes through the temperature control group assembly 10, the ultrasonic particle size analysis head 20, the gallium quantitative dropping assembly 30, and the exhaust assembly 40 along the conveyor belt assembly 90 for processing. By using the assembly of the application, the key parameters in the preparation process can be accurately controlled to improve the quality and preparation efficiency of the protein nanofiber, the production process is that soybean products are washed, put into a container, heated to 90 degrees, finely ground into particles, combined with metal gallium to form a new material form, and the experimental purpose is achieved, and the preparation quality is improved while the production efficiency is high.

[0027] In the first aspect of the utility model, as a preferred embodiment, the first box and the second box are both provided with an exhaust hood 11. The second box is located between the first box and the exhaust assembly 40. The top of the exhaust assembly 40 is provided with an exhaust fan, which has good structural stability.

[0028] Specifically, the temperature control group assembly 10 can accurately control the temperature in the experimental bench and keep it at 90 DEG C to promote the full unfolding of the protein and the formation of nanofibers. The ultrasonic particle size analysis head 20 and the gallium quantitative dropping assembly 30 belong to ultrasonic control experimental assemblies, which can automatically adjust the ultrasonic time according to the paste state of the protein solution to ensure that the solution changes from paste to transparent state and avoid excessive ultrasonic.

[0029] Preferably, the application also includes a particle size control experimental bench module, which includes a particle sifter and a particle size analyzer and can screen and control the average particle size of gallium particles to be 400 nm to avoid rapid reaction and bubble generation caused by too small particles.

[0030] Specifically, the gallium quantitative dropping system is used for quantitative dropping control of gallium.

[0031] In the first aspect of the utility model, as a preferred embodiment, the temperature control assembly 10 further comprises a temperature sensor 13, which is arranged in the first box, thereby improving the accuracy.

[0032] In the first aspect of the utility model, as a preferred embodiment, the exhaust assembly 40 further comprises a wind speed sensing probe 43, which is arranged in the exhaust cabinet 41, thereby further improving the accuracy. The present application is suitable for biopharmaceutical, hospital, detection and other enterprises and institutions.

[0033] In summary, the present application has the following advantages:

[0034] 1. The corresponding equipment is customized according to the protein synthesis process, and the production flow operation is more smooth.

[0035] 2. Flexible installation, the equipment is a complete set of equipment, which can be moved and adjusted in position.

[0036] 3. Manual control of progress can be realized, and key parameters in the preparation process can be accurately controlled.

[0037] 4. The process can be adjusted, and the exhaust, control and other contents can be adjusted according to different experimental contents.

[0038] 5. Safe and effective.

[0039] In the first aspect of the utility model, as a preferred embodiment, the volume of the exhaust cabinet 41 is greater than that of the first box.

[0040] In the first aspect of the utility model, as a preferred embodiment, the exhaust cabinet 41 is provided with a plurality of exhaust holes. The ceramic assembly 200 comprises a ceramic container 201 and a backing plate assembly 202, and the ceramic container 201 is arranged on the backing plate assembly 202.

[0041] The above-mentioned embodiments are only preferred embodiments of the present application, and cannot be used to limit the scope of protection of the present application. Any non-essential changes and replacements made by those skilled in the art on the basis of the present application shall fall within the scope of protection of the present application.

Claims

1. An experimental setup for preparing protein nanofibers, characterized in that, The utility box shell assembly, the ceramic assembly, the ultrasonic particle size analysis head, the gallium quantitative dropping assembly, the exhaust assembly, the bottom support frame body, and the conveyor belt assembly are sequentially arranged from left to right on the conveyor belt assembly arranged on the bottom support frame body. The two box assemblies are divided into a first box and a second box. The temperature control assembly is arranged in the first box. The ceramic assembly sequentially passes through the temperature control assembly, the ultrasonic particle size analysis head, the gallium quantitative dropping assembly, and the exhaust assembly along the conveyor belt assembly for processing.

2. The benchtop assembly for protein nanofiber production of claim 1, wherein: The first box and the second box are both provided with an exhaust hood.

3. The benchtop assembly for protein nanofiber production of claim 2, wherein: The second box is located between the first box and the exhaust assembly.

4. The benchtop assembly for protein nanofiber production of claim 1, wherein: The top of the exhaust assembly is provided with an exhaust fan.

5. The benchtop assembly for protein nanofiber production of claim 1, wherein: The temperature control assembly further comprises a temperature sensor arranged in the first box.

6. The benchtop assembly for protein nanofiber production of claim 1, wherein: The exhaust assembly further comprises a wind speed sensing probe arranged in the exhaust cabinet.

7. The benchtop assembly for protein nanofiber production of claim 1, wherein: The volume of the exhaust cabinet is greater than that of the first box.

8. The benchtop assembly for protein nanofiber production of claim 1, wherein: The exhaust cabinet and the first box are both cuboids.

9. The benchtop assembly for protein nanofiber production of claim 1, wherein: The exhaust cabinet is provided with a plurality of exhaust holes.

10. The benchtop assembly for protein nanofiber production of claim 1, wherein: The ceramic assembly comprises a ceramic container and a cushion plate assembly. The ceramic container is arranged on the cushion plate assembly.

Citation Information

Patent Citations

  • Plant protein nanometer fibre and producing method thereof

    CN101338461A

  • A nanofiber foam-based protein adsorption and separation device and its preparation method

    CN104436754B