CN112900110B - Preparation method of core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection - Google Patents

Preparation method of core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection Download PDF

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CN112900110B
CN112900110B CN202110170755.6A CN202110170755A CN112900110B CN 112900110 B CN112900110 B CN 112900110B CN 202110170755 A CN202110170755 A CN 202110170755A CN 112900110 B CN112900110 B CN 112900110B
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coating
tungsten
shell structure
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CN112900110A (en
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姚理荣
夏勇
杨涛
孙通
潘刚伟
徐思峻
季涛
高强
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Nantong University
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/14Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0061Organic fillers or organic fibrous fillers, e.g. ground leather waste, wood bark, cork powder, vegetable flour; Other organic compounding ingredients; Post-treatment with organic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0063Inorganic compounding ingredients, e.g. metals, carbon fibres, Na2CO3, metal layers; Post-treatment with inorganic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2209/00Properties of the materials
    • D06N2209/16Properties of the materials having other properties

Abstract

Hair brushThe invention relates to a preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection, which comprises the following steps: preparing a dopamine salt solution, adding a buffer solution to adjust the pH value, then adding tungsten powder, stirring, filtering, washing and drying to obtain W @ PDA; adding the obtained W @ PDA into gadolinium nitrate solution, stirring, filtering, and calcining at high temperature to obtain W @ Gd with core-shell structure2O3Powder; mixing W @ Gd2O3Adding the powder into dimethylacetamide, adding a certain amount of polyurethane resin adhesive, uniformly stirring, coating the fabric, and drying. The invention firstly prepares W @ PDA, because PDA has extraordinary adhesiveness on the surfaces of different substances, after tungsten is coated, the surface of PDA also contains a large amount of polar groups such as phenolic hydroxyl, amido and the like, which are complexing Gd+Provides rich active sites, and forms a nitrogen-doped carbon layer after high-temperature calcination. Compared with a single metal physical blending mode, the core-shell structure can play a role in cooperative protection in the aspect of radiation protection, and can eliminate a protection weak area and effectively absorb secondary radiation generated by radiation. The PU resin coating fabric has excellent wearability and mechanical property, and W @ Gd2O3The powder has good dispersibility in PU resin, so that the final protective performance of the coating fabric is more excellent.

Description

Preparation method of core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection
Technical Field
The invention relates to the field of preparation of radiation-proof materials, in particular to a preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X and gamma ray protection.
Background
The development of nuclear technology brings convenience to people and simultaneously generates a lot of radiation hazards, and the light, flexible and excellent-protection-performance textile for radiation protection is a hot spot of current research. The radiation protection material is mainly divided into a lead material and a lead-free material. Lead is mainly lead, and although the protective effect is good, the lead has toxicity, poor strength and large low-energy X-ray scattering. The lead-free material mainly comprises a composite material prepared from rare earth elements and heavy metal compounds such as tin, tungsten, bismuth and the like, and has excellent protection effect, light weight and safety.
In recent years, micro-nano core-shell materials with special structures attract wide attention of people. The composite particles with different core-shell microstructures have unique physicochemical properties, so that the composite particles have wide application prospects in various fields such as optics, electronics, catalysis, biology, radiation and the like. In the aspect of radiation protection, compared with a single metal physical blending mode, the radiation protection material with the core-shell structure can realize synergistic protection, eliminate a protection weak area and effectively absorb secondary radiation generated by radiation. The preparation method of the core-shell structure mainly comprises a template method, a precipitation method, a hydrothermal synthesis method, a spray drying method, a layer-by-layer self-assembly technology and the like. Li et al prepared gadolinium oxide hollow spheres with controllable shell thickness by using silicon dioxide as a template and adopting a homogeneous precipitation method. However, these methods have disadvantages of many steps and long time, so that it is necessary to specify an effective and simple method to overcome these disadvantages. Mussel secreted adhesion protein has strong adhesion capability, which inspires that the task group of Messer Smith at the northwest university in the United states in 2007 finds that Dopamine (DA) can be oxidized and self-polymerized into polydopamine on the surface of any material under the weak base condition simulating seawater. The polymerization condition is simple and controllable, and the product has excellent adhesiveness, hydrophilicity, stability and biocompatibility. Meanwhile, a large number of phenolic hydroxyl and amino active groups exist on the polydopamine, so that abundant active sites are provided for the complexation of metal ions.
Disclosure of Invention
The invention aims to overcome the defects in the prior art and provide a preparation method of a tungsten/gadolinium oxide PU coating fabric with a core-shell structure.
The purpose of the invention can be realized by the following technical scheme:
the invention provides a preparation method of a tungsten/gadolinium oxide PU coating fabric with a core-shell structure for X, gamma ray protection, which comprises the following steps:
(1) preparing a dopamine salt solution, adding a buffer solution to adjust the pH value, then adding tungsten powder, stirring, filtering, washing and drying to obtain W @ PDA;
(2) adding the W @ PDA obtained in the step (1) into a gadolinium nitrate solution, stirring, filtering, and calcining at high temperature to obtain W @ Gd of a core-shell structure2O3And (3) powder.
(3) Enabling the core-shell structure W @ Gd obtained in the step (2)2O3And adding the powder into dimethylacetamide for dispersion, adding a certain amount of polyurethane resin, uniformly stirring, coating the fabric, and drying.
According to the invention, the concentration of the prepared dopamine salt solution in the step (1) is controlled to be 1.5-2.5 g/L. Mainly because when the DA concentration is lower than 1.5g/L, only a small amount of PDA particles are deposited on the surface of W, and when the DA concentration is 1.5-2.5g/L, a PDA film is formed on the surface of W powder. When the concentration of DA is higher than 2.5g/L, larger PDA particles are formed on the surface of W powder through self-polymerization due to the fact that the concentration of DA is too high, and the subsequent adsorption of gadolinium ions is not facilitated.
It is noted that after the dopamine salt solution is prepared in step (1), a tris buffer solution is added into the system to adjust the pH value of the solution to 8.5, because dopamine can be polymerized into polydopamine by itself under the condition of weak alkali and oxygen, and the polydopamine on the surfaces of different substances has extraordinary surface activity and adhesiveness, and can provide a platform for secondary functionalization of materials.
Further, the stirring in the step (1) needs to be carried out for 18-24 hours under an electric stirrer.
In addition, for the washing in step (1), washing with water and ethanol is required 2 to 3 times, respectively.
The specific conditions for the drying in step (1) are not particularly limited as long as the object of drying the sample can be achieved.
According to the invention, the concentration of the gadolinium nitrate solution in the step (2) should be controlled to be 0.3-0.5M/L. Because when Gd is present+At a concentration of 0.02M/L, the surface of W is coated with a small amount of sparse nano-dotted Gd2O3And (3) granules. When Gd is present+Gd on the W surface increased to 0.1M/L2O3The nanoparticles become larger and larger due to Gd+Increased concentration of Gd2O3The nanoparticles combine with each other to form larger Gd2O3And (3) granules. When Gd is present+Gd on the W surface increased to 0.2M/L2O3The nanoparticles become larger and more dense. With Gd+Gd increased in concentration to 0.3M/L, W surface2O3The nanoparticles are combined with each other to form W @ Gd of a core-shell structure2O3. Continued increase in Gd+Gd on the W surface at a concentration of 0.4M/L2O3Nanoparticles compared to Gd+The concentration of 0.3M/L did not change much, due to poly-dopamine on the W surface to Gd+Chelating agents for Gd+Saturation has been reached at a concentration of 0.3M/L.
Further, the stirring in the step (2) is not particularly limited, and only magnetic stirring is needed for a certain time.
In addition, the high-temperature calcination in the step (2) needs to be carried out for 2-3h under the conditions of 800-1000 ℃ in a muffle furnace, and the temperature rise is 2-4 ℃/min. In order to avoid the formation of impurities during the reaction, the calcination in step (2) of the present invention is performed in a protective gas, wherein the protective gas includes nitrogen or an inert gas, and the inert gas may be argon, helium, etc., and the present invention is not particularly limited in this respect.
According to the invention, the ultrasonic dispersion is carried out for 30-60min by adding into dimethyl acetamide in the step (3).
It is noted that, for adding a certain amount of polyurethane resin adhesive in the step (3), the powder content in the coating material is controlled to be 60 wt%.
Further, the coating in step (3) is performed by using a mini-coater.
In addition, the drying in the step (3) is drying for 1-2h at the temperature of 60-80 ℃.
As a preferred technical scheme, the preparation method of the tungsten/gadolinium oxide PU coating fabric with the core-shell structure comprises the following steps:
(1) preparing 1.5g/L-2.5g/L dopamine salt solution, adding tris buffer solution to adjust the pH value to 8-9, then adding tungsten powder cleaned by ethanol, stirring for 18-24h by using an electric stirrer, filtering and separating, washing for 2-3 times by using deionized water and ethanol respectively, and drying to obtain W @ PDA;
(2) adding the W @ PDA obtained in the step (1) into gadolinium nitrate solution with the concentration of 0.3-0.5M/L, magnetically stirring for a certain time, filtering, separating, drying, introducing nitrogen into the prepared sample at the temperature of 800-2O3And (3) powder.
(3) Enabling the core-shell structure W @ Gd obtained in the step (2)2O3Adding the powder into dimethylacetamide, performing ultrasonic dispersion for 30-60min, adding a certain amount of polyurethane resin adhesive, controlling the content of the powder in the coating to be 60wt%, stirring for 2-3h by using an electric stirrer, coating the coating on a small-sized coating machine, and finally drying for 1-2h at the temperature of 60-80 ℃.
The core-shell structure W @ Gd prepared by adopting the preferred technical scheme2O3Compared with tungsten and gadolinium oxide blended powder, the core-shell structure can play a synergistic protection role in radiation protection, and secondary radiation generated by radiation is effectively absorbed while a protection weak area is eliminated.
Compared with the prior art, the invention at least has the following beneficial effects:
according to the invention, dopamine is firstly utilized to be self-polymerized into poly-dopamine under the condition of weak base and oxygen, and the poly-dopamine has extraordinary adhesion on the surfaces of different substances, so that tungsten can be successfully coated, and W @ PDA is obtained.
The PDA surface contains a large amount of polar groups such as phenolic hydroxyl, amido and the like, provides rich active sites for complexing various metal ions,can effectively neutralize Gd in gadolinium nitrate solution+Chelation was performed. After high-temperature calcination, the PDA forms a nitrogen-doped carbon layer attached to the surface of tungsten and reacts with Gd+Conversion of chelating W @ PDA to W @ Gd2O3
Drawings
FIG. 1 is a scanning electron microscope image of the core-shell tungsten/gadolinium oxide powder prepared in example 1.
Detailed Description
To better illustrate the invention and to facilitate the understanding of the technical solutions thereof, typical but non-limiting examples of the invention are as follows:
example 1
The embodiment provides a preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection, which comprises the following steps:
(1) preparing a dopamine salt solution with the concentration of 2g/L, adding a tris buffer solution to adjust the pH value of the solution to 8.5, then adding tungsten powder cleaned by ethanol, stirring for 24 hours by using an electric stirrer, filtering and separating, washing for 2 times by using deionized water and ethanol respectively, and drying for 5 hours at 80 ℃ to obtain W @ PDA;
(2) adding the W @ PDA obtained in the step (1) into a gadolinium nitrate solution with the concentration of 0.3M/L, magnetically stirring for 2 hours, filtering and separating, drying for 5 hours at 80 ℃, introducing nitrogen into the prepared sample at 800 ℃ and calcining at high temperature for 2 hours (the heating rate is 2 ℃/min), and finally obtaining the W @ Gd core-shell structure2O3And (3) powder.
(3) Enabling the core-shell structure W @ Gd obtained in the step (2)2O3Adding the powder into dimethylacetamide, performing ultrasonic dispersion for 30min, adding a certain amount of polyurethane resin adhesive, controlling the content of the powder in the coating to be 60wt%, stirring for 2h by using an electric stirrer, coating the fabric on a small-sized coating machine, and finally drying for 2h at 60 ℃.
W @ Gd prepared in this example2O3The powder was SEM-scanned, and the photograph is shown in FIG. 1, in which it was found that a PDA film was formed on the surface of the W powder.
Example 2
The embodiment provides a preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection, which comprises the following steps:
(1) preparing 1.5g/L dopamine salt solution, adding tris buffer solution to adjust the pH value of the solution to 8, then adding tungsten powder cleaned by ethanol, stirring for 20 hours by using an electric stirrer, filtering and separating, washing for 3 times by using deionized water and ethanol respectively, and drying for 8 hours at 60 ℃ to obtain W @ PDA;
(2) adding the W @ PDA obtained in the step (1) into a gadolinium nitrate solution with the concentration of 0.35M/L, magnetically stirring for 3 hours, filtering and separating, drying for 8 hours at 60 ℃, introducing nitrogen into the prepared sample at 900 ℃ and calcining for 2.5 hours at high temperature (the heating rate is 3 ℃/min), and finally obtaining the W @ Gd of the core-shell structure2O3And (3) powder.
(3) Enabling the core-shell structure W @ Gd obtained in the step (2)2O3Adding the powder into dimethylacetamide, performing ultrasonic dispersion for 40min, adding a certain amount of polyurethane resin adhesive, controlling the content of the powder in the coating to be 60wt%, stirring for 2.5h by using an electric stirrer, coating the fabric on a small-sized coating machine, and finally drying for 1.5h at 70 ℃.
Example 3
The embodiment provides a preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection, which comprises the following steps:
(1) preparing a dopamine salt solution with the concentration of 2.5g/L, adding a tris buffer solution to adjust the pH value of the solution to 9, then adding tungsten powder cleaned by ethanol, stirring for 18 hours by using an electric stirrer, filtering and separating, washing for 2 times by using deionized water and ethanol respectively, and drying for 6 hours at 70 ℃ to obtain W @ PDA;
(2) adding the W @ PDA obtained in the step (1) into a gadolinium nitrate solution with the concentration of 0.4M/L, magnetically stirring for 2.5h, filtering and separating, drying for 6h at 70 ℃, introducing nitrogen into the prepared sample at 1000 ℃ and calcining at high temperature for 3h (the heating rate is 4 ℃/min), and finally obtaining the W @ Gd of the core-shell structure2O3And (3) powder.
(3) Enabling the core-shell structure W @ Gd obtained in the step (2)2O3Adding the powder into dimethylacetamide, performing ultrasonic dispersion for 50min, adding a certain amount of polyurethane resin adhesive, controlling the content of the powder in the coating to be 60wt%, stirring for 3h by using an electric stirrer, coating the fabric on a small-sized coating machine, and finally drying for 1h at 80 ℃.
The embodiments described above are intended to facilitate the understanding and use of the invention by those skilled in the art. It will be readily apparent to those skilled in the art that various modifications to these embodiments may be made, and the generic principles described herein may be applied to other embodiments without the use of the inventive faculty. Therefore, the present invention is not limited to the above embodiments, and those skilled in the art should make improvements and modifications within the scope of the present invention based on the disclosure of the present invention.

Claims (15)

1. A preparation method of a core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection is characterized by comprising the following steps:
(1) preparing dopamine salt solution, adding buffer solution to adjust the pH value, then adding tungsten powder, stirring, filtering, washing and drying to obtain W @ PDA:
(2) adding the W @ PDA obtained in the step (1) into a gadolinium nitrate solution, stirring, filtering, and calcining at high temperature to obtain W @ Gd of a core-shell structure2O3Powder;
(3) enabling the core-shell structure W @ Gd obtained in the step (2)2O3And adding the powder into dimethylacetamide for dispersion, adding a certain amount of polyurethane resin adhesive, uniformly stirring, coating the fabric, and drying.
2. The preparation method of the core-shell structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein the buffer is added in step (1) to adjust the pH value, the buffer is tris, and the pH value is 8-9.
3. The preparation method of the shell fabric with the tungsten/gadolinium oxide PU coating layer in the core-shell structure according to claim 1, wherein the tungsten powder in the step (1) is tungsten powder cleaned by ethanol.
4. The preparation method of the shell fabric with the core-shell structure tungsten/gadolinium oxide PU coating according to claim 1, wherein the stirring in the step (1) is performed by an electric stirrer for 18-24 h.
5. The preparation method of the shell fabric with the tungsten/gadolinium oxide PU coating layer in the core-shell structure according to claim 1, wherein the washing in the step (1) is washing with deionized water and ethanol for 2-3 times respectively.
6. The preparation method of the shell fabric with the tungsten/gadolinium oxide PU coating layer in the core-shell structure according to claim 1, wherein the concentration of the dopamine salt solution in the step (1) is 1.5g/L-2.5 g/L.
7. The preparation method of the core-shell structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein in the step (2), the high-temperature calcination temperature is 800-1000 ℃, the time is 2-3h, and the heating rate is 2-4 ℃/min.
8. The preparation method of the shell-core structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein the calcination in the step (2) is performed in a protective gas, and the protective gas is nitrogen or inert gas.
9. The preparation method of the core-shell structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein the concentration of the gadolinium nitrate solution in the step (2) is 0.3-0.5M/L.
10. The preparation method of the shell fabric with the core-shell structure tungsten/gadolinium oxide PU coating, according to claim 1, wherein the step (3) of adding the shell fabric into dimethylacetamide is performed for dispersion for 30-60min by using ultrasound.
11. The preparation method of the core-shell structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein a certain amount of polyurethane resin adhesive is added in the step (3), and the content of powder in the coating is controlled to be 60 wt%.
12. The preparation method of the shell fabric with the core-shell structure tungsten/gadolinium oxide PU coating according to claim 1, wherein the stirring in the step (3) is mechanical stirring for 2-3 h.
13. The preparation method of the core-shell structure tungsten/gadolinium oxide PU coating fabric according to claim 1, wherein the coating in the step (3) is performed by using a mini-coater.
14. The preparation method of the shell fabric with the tungsten/gadolinium oxide PU coating layer in the core-shell structure according to claim 1, wherein the drying in the step (3) is performed for 1-2h at 60-80 ℃.
15. The preparation method of the shell fabric with the core-shell structure tungsten/gadolinium oxide PU coating, according to any one of claims 1 to 13, wherein the method comprises the following steps:
(1) preparing 1.5g/L-2.5g/L dopamine salt solution, adding tris buffer solution to adjust the pH value to 8-9, then adding tungsten powder cleaned by ethanol, stirring for 18-24h by using an electric stirrer, filtering and separating, washing for 2-3 times by using deionized water and ethanol respectively, and drying to obtain W @ PDA:
(2) adding the W @ PDA obtained in the step (1) into gadolinium nitrate solution with the concentration of 0.3-0.5M/L, magnetically stirring for a certain time, filtering, separating, drying, introducing nitrogen into the prepared sample at the temperature of 800-2O3Powder;
(3) enabling the core-shell structure W @ Gd obtained in the step (2)2O3Adding the powder into dimethyl acetamide to be dispersed by ultrasonic 30And (3) adding a certain amount of polyurethane resin adhesive after-60 min, controlling the content of powder in the coating to be 60wt%, stirring for 2-3h by using an electric stirrer, coating the fabric on a small-sized coating machine, and finally drying for 1-2h at the temperature of 60-80 ℃.
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CN112900110B (en) * 2021-02-08 2021-11-30 南通大学 Preparation method of core-shell structure tungsten/gadolinium oxide PU coating fabric for X, gamma ray protection
CN112831855B (en) * 2021-02-08 2022-05-31 南通大学 Preparation method of core-shell structure tungsten/gadolinium oxide functional fiber for X, gamma ray protection
CN112831078B (en) * 2021-02-08 2022-08-16 南通大学 Preparation method of core-shell structure tungsten/gadolinium oxide PVC (polyvinyl chloride) calendered material for X and gamma ray protection
CN112846173A (en) * 2021-02-08 2021-05-28 南通大学 Preparation method of core-shell structure tungsten/gadolinium oxide powder for X, gamma ray protection
CN115478430B (en) * 2022-08-26 2023-10-31 东华大学 Nuclear protection nanofiber aerogel with bionic structure and preparation method thereof
CN115787289B (en) * 2022-10-11 2023-10-10 无锡市圣华盾医疗科技有限公司 Light nuclear radiation protection fabric and preparation process thereof
CN116180259B (en) * 2022-12-22 2024-01-30 南京航空航天大学 In-situ preparation method of gadolinium-containing carbon nano composite fiber for neutron shielding

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