CN114573848A - Texture structure for antibiosis and product - Google Patents

Texture structure for antibiosis and product Download PDF

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Publication number
CN114573848A
CN114573848A CN202011387659.9A CN202011387659A CN114573848A CN 114573848 A CN114573848 A CN 114573848A CN 202011387659 A CN202011387659 A CN 202011387659A CN 114573848 A CN114573848 A CN 114573848A
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China
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micro
nano
texture structure
antibodies
nano antibodies
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CN202011387659.9A
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Chinese (zh)
Inventor
杨广舟
官灏
蒋雨
亢红伟
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Shine Optoelectronics Kunshan Co Ltd
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Shine Optoelectronics Kunshan Co Ltd
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Priority to CN202011387659.9A priority Critical patent/CN114573848A/en
Publication of CN114573848A publication Critical patent/CN114573848A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14Paints containing biocides, e.g. fungicides, insecticides or pesticides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2327/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2327/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2475/04Polyurethanes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials For Medical Uses (AREA)

Abstract

The invention discloses an antibacterial texture structure which is characterized by comprising a plurality of micro-nano antibodies distributed randomly or regularly, wherein the plurality of micro-nano antibodies are of convex structures and/or concave structures, and the plurality of micro-nano antibodies have the same length. Can reduce and prevent the attachment of germs, viruses and other microorganisms; can inhibit the transmission of virus and bacteria; meanwhile, the method can inhibit the propagation of virus and bacteria and prevent the formation speed of a biological film, and has good bacteriostatic effect. The invention also discloses an article with the texture structure for resisting bacteria.

Description

Texture structure for antibiosis and product
Technical Field
The invention relates to a texture structure for antibiosis and a product.
Background
The surfaces of objects in the environment are often attached and deposited by microorganisms and grow on the surfaces of the objects to form sources of contamination or pathogens, thereby becoming a threat to human health. Currently, the surface of an object is mainly sterilized by chemical methods, such as by using a disinfectant, such as bleach or ammonia, to sterilize the surface of the object. However, the use of disinfectants can cause secondary contamination of the surface of the object, and the removal of disinfectants can also cause certain environmental pollution. In addition, some antibacterial materials are used for performing antibacterial treatment on the surface of an object through chemical action, and the antibacterial materials are mainly prepared by mixing antibacterial substances or antibacterial material coatings in the materials for sterilizing the surface of the object. However, the antibacterial material is easily attenuated during actual use, and easily falls off under an external environment such as high temperature and high humidity, thereby losing the antibacterial function.
Disclosure of Invention
Based on this, there is a need to provide a texture structure for antibacterial purpose to solve the above technical problems.
The technical scheme of the invention is as follows:
the texture structure for antibiosis comprises a plurality of micro-nano antibodies which are randomly or regularly distributed, wherein the plurality of micro-nano antibodies are of convex structures and/or concave structures, and the plurality of micro-nano antibodies have the same length.
In one embodiment, the length of the micro-nano antibody is as follows: w is less than or equal to 100 mu m.
In one embodiment, the width of the micro-nano antibody is as follows: d is more than 0 and less than or equal to 50 mu m.
In one embodiment, the depth/height of the micro-nano antibody is as follows: h is more than or equal to 0.5 mu m and less than or equal to 5 mu m.
In one embodiment, two adjacent micro-nano antibodies are arranged at intervals, and the interval distance is defined as s, wherein s is more than 0 and less than or equal to 10 mu m.
In one embodiment, the micro-nano antibody arrays are arranged, the micro-nano antibodies in the same row are arranged at equal intervals or at variable intervals, and the micro-nano antibodies in multiple rows are arranged at equal intervals or at variable intervals.
In one embodiment, the micro-nano antibodies are randomly distributed, and the distance between every two adjacent micro-nano antibodies is not more than 10 μm.
In one embodiment, the micro-nano antibodies are arranged in multiple rows, each micro-nano antibody defines a set point at the same position, and the set points of the micro-nano antibodies in the same row are located on a straight line or a curve.
In one embodiment, at least a portion of the micro-nano antibodies in the same row are rotated from the set point by the same or different angles.
In one embodiment, the micro-nano antibody is in a waist shape, a cylindrical shape or a conical shape, and the cross section of the micro-nano antibody is in a rectangular shape, a triangular shape, a trapezoidal shape or a segmental shape.
In one embodiment, the micro-nano antibody is a convex structure or a concave structure containing an antibacterial material.
In one embodiment, the micro-nano antibody is a convex structure or a concave structure containing nano silver ions or nano metal zinc oxide.
An article comprising a carrying surface and the above-described texture for antimicrobial use disposed on the carrying surface.
In one embodiment, the bearing surface is a flat surface or a non-flat surface.
In one embodiment, the product is a medical article, a cultural and sports article, a household article, a digital product, a household appliance, a mother and baby article, or a food appliance.
The invention has the beneficial effects that: the micro-nano antibodies have the same length, can reduce and prevent the attachment of germs, viruses and other microorganisms, can inhibit the transmission of the viruses and the bacteria, can inhibit the propagation of the viruses and the bacteria and prevent the formation speed of a biological film, and has good antibacterial effect.
Drawings
FIG. 1 is a perspective view of a texture structure for antimicrobial use in accordance with the present invention;
FIG. 2 is a schematic plan view of FIG. 1;
FIG. 3 is another perspective view of the texture for antimicrobial use of the present invention;
FIG. 4 is a schematic plan view of FIG. 3;
FIG. 5 is another perspective view of the texture feature for antimicrobial use of the present invention;
FIG. 6 is another schematic plan view of a texture feature for antimicrobial use in accordance with the present invention;
FIG. 7 is another schematic plan view of a texture feature for antimicrobial use in accordance with the present invention;
FIG. 8 is another schematic plan view of a texture feature for antimicrobial use in accordance with the present invention;
FIG. 9 is a schematic structural view of an article of the present invention;
FIG. 10 is another schematic structural view of an article of the present invention;
fig. 11 is another schematic construction of an article of the present invention.
Detailed Description
To facilitate an understanding of the invention, the invention will now be described more fully with reference to the accompanying drawings. Preferred embodiments of the present invention are shown in the drawings. However, the present invention may be embodied in many different forms and is not limited to the embodiments described below. Rather, these embodiments are provided so that this disclosure will be thorough and complete.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used herein in the description of the invention is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items.
The invention discloses an antibacterial texture structure which comprises a plurality of distributed micro-nano antibodies, wherein the plurality of micro-nano antibodies are of a convex structure and/or a concave structure, have the same length, can reduce and prevent the attachment of germs, viruses and other microorganisms, can inhibit the propagation of the viruses and bacteria, can inhibit the propagation of the viruses and the bacteria and prevent the formation speed of a biomembrane, and have a good antibacterial effect. When the texture structure is applied to the surface of an object, when a small amount of microorganisms are attached to the texture structure, the propagation, growth and reproduction of the microorganisms are inhibited due to the micro-nano antibodies, and the surfaces of microbial cells or viruses are damaged, so that the aims of physical antibiosis and virus resistance are fulfilled, and a stable antibacterial effect is achieved. The texture structure can be applied to the surface of various objects, including the outer surface and the inner surface, such as medical instruments, daily necessities, baby products, stationery, keyboards, mice, implants and the like, and the physical antibacterial property is stable and long-term, non-toxic and low in cost.
Specifically, the micro-nano antibody defines a length w, a width d, and a depth/height h. Length of the micro-nano antibody: w is less than or equal to 100 mu m; width of the micro-nano antibody: d is more than 0 and less than or equal to 50 mu m; depth/height of the micro-nano antibody: h is more than or equal to 0.5 mu m and less than or equal to 5 mu m; two adjacent micro-nano antibodies are arranged at intervals, and the interval distance is defined as s, wherein s is more than 0 and less than or equal to 10 mu m. The micro-nano antibody selected in the range can achieve a good and stable antibacterial effect, and is easy to form. For example, the plurality of micro-nano antibodies have the same length, the same width and the same height; the spacing distance between the periphery of one micro-nano antibody and other adjacent antibodies can be equal or unequal or variable, and the spacing range is 1 mu m or more and 6 mu m or less. For example, if one micro-nano antibody is obliquely arranged relative to another adjacent micro-nano antibody, the distance between the two micro-nano antibodies is considered to be variable distance, and the range of the narrowest part and the widest part of the variable distance is 1 μm ≦ s ≦ 6 μm. The dimension has deviation due to factors such as process error during specific forming, and all the dimension within 5% can be regarded as having the same length or width or depth or height. The s is a fixed value or an indeterminate value, for example, if one micro-nano antibody is arranged at an included angle relative to the other micro-nano antibody, the s between the two micro-nano antibodies is the indeterminate value, and the s is changed from small to large along with the extension of the included angle.
In one embodiment, the micro-nano antibody arrays are arranged, the micro-nano antibodies in the same line are arranged at equal intervals or variable intervals, and the micro-nano antibodies in multiple lines are arranged at equal intervals or variable intervals. When the plurality of micro-nano antibody arrays are arranged, the rows, the columns, the same rows and the same columns can be distributed at equal intervals, or can be distributed at unequal intervals, or can be distributed at equal intervals in the same rows randomly, or can be distributed at equal intervals in the columns randomly, or the like.
In one embodiment, the plurality of micro-nano antibodies can also be randomly distributed, and the distance between adjacent micro-nano antibodies is not more than 10 μm. That is, in the plurality of micro-nano antibodies, the maximum distance between two micro-nano antibodies needs to be not more than 10 μm, so that the physical antibacterial effect can be ensured. The random distribution of the plurality of micro-nano antibodies can be local random distribution, random distribution in one direction, random arrangement of a rotation angle, and the like; and when the antibodies are randomly distributed, the distance between adjacent micro-nano antibodies is not more than 10 mu m, so that the stable and reliable antibacterial effect is ensured.
In one embodiment, the micro-nano antibodies are arranged in a plurality of rows, each micro-nano antibody defines a set point at the same position, and the set points of the micro-nano antibodies in the same row are positioned on a straight line or a curve. Preferably, at least a part of the micro-nano antibodies in the same row are rotated from the set point by the same or different angles. When the rotation angle is different, the rotation angles in the same row can be distributed in an equal difference mode, for example, the rotation angles are sequentially rotated within the angle range of 30-120 degrees and with the difference of 0.5 degree.
Specifically, the micro-nano antibody is in a waist shape, a cylindrical shape or a conical shape, and the cross section of the micro-nano antibody is in a rectangular shape, a triangular shape, a trapezoidal shape or a segmental shape. The plurality of micro-nano antibodies have the same shape within a limited size range; or have various shapes within a limited size range, such as a kidney shape and a cylinder shape. For example, when the micro-nano antibody is in a waist-shaped structure, two ends of the micro-nano antibody are semicircular in overlooking angle, and the middle of the micro-nano antibody is rectangular; in the case of a three-dimensional angle, the top surface is a flat surface having a height of 3 μm and is arranged parallel to the bottom surface (bearing surface). For example, the micro-nano antibody is cylindrical, the section of the micro-nano antibody is a semicircle, the micro-nano antibody can also be a base with a certain height, and the base is further provided with a semicircle. The micro-nano antibody is defined as a top surface and peripheral side surfaces, the top surface is a flat surface or an arc surface or a wave surface, and the opposite side surfaces can be arranged in parallel or have included angles.
In one embodiment, the micro-nano antibody is a raised structure or a recessed structure containing an antibacterial material, and preferably, the antibacterial material includes a material having an antibacterial effect, such as nano silver ions or nano metal zinc oxide. Therefore, the texture structure has a sterilization effect, and has chemical sterilization and physical sterilization effects, so that a better antibacterial effect is realized.
The texture structure of the present invention can be formed by the following steps:
step 1: arranging a bearing body with a bearing surface;
step 2: coating an imprinting material on the bearing surface, imprinting by using a mold, and curing and demolding.
The mold is provided with a structure which is suitable for the micro-nano antibodies of the texture structure, the supporting body is made of PVC membrane materials, and the stamping materials are liquid or colloidal TPU materials. The micro-nano antibody with the texture structure disclosed by the invention has the same or basically the same size and shape, is beneficial to forming, impressing and demolding of a mold, is easier to form and has stable antibacterial effect.
Of course, it can be formed by other means, such as coating, injection molding, die casting, extrusion, etc.
The invention also discloses a product which comprises a bearing surface and the texture structure for resisting bacteria, which is arranged on the bearing surface. The bearing surface is a flat surface or a non-flat surface, such as a cup, a mouse, a mobile phone shell, a book wrapping film, a transfusion tube and the like. Preferably, the product is medical product, stationery product, household product, digital product, household appliance, mother and infant product, food product (including catering product, food package, food storage) and the like.
Hereinafter, the texture structure and the product for antibacterial of the present invention will be described by way of example with reference to the accompanying drawings.
Referring to fig. 1 and 2, the present invention discloses an antibacterial texture structure, which includes a plurality of micro-nano antibodies 1, wherein the micro-nano antibodies 1 are protrusion structures, the length of the micro-nano antibodies 1 is w, the width of the micro-nano antibodies is d, and the height of the micro-nano antibodies 1 is h. In other embodiments, at least one of the difference in length w, width d, and height h between any two micro-nano antibodies 1 is not more than 5%, and within the above size difference, the micro-nano antibodies are considered to have the same size, and have the advantages of stable antibacterial effect and easy molding. In the embodiment, the material of the micro-nano antibody contains nano silver ions, so that the micro-nano antibody has a sterilization effect and can realize chemical sterilization and physical sterilization at the same time.
Specifically, the micro-nano antibody 1 is a waist-shaped structure with the thickness of h, two ends of the micro-nano antibody are arc-shaped, and the micro-nano antibody comprises a top surface 11 and a peripheral side surface 12. The micro-nano antibodies 1 are regularly arrayed, and the micro-nano antibodies 1 in the same row and column are equidistantly arrayed. For example, the length w of the micro-nano antibody 1 is 46 μm, the width d is 6.5 μm, and the height h is 2 μm; the interval between adjacent micro-nano antibodies 1 in the same row is 1.5 mu m, and the interval between adjacent micro-nano antibodies 1 in the same column is 4.5 mu m. Therefore, the micro-nano antibody 1 has a good antibacterial effect and a stable antibacterial effect. And the micro-nano antibody 1 with the same size and shape is easy to demould when being formed, for example, demould is carried out after being stamped by a mould, so that the processing is easy, and the yield is high.
Referring to fig. 3 and 4, in another embodiment of the texture structure of the present invention, the texture structure has a plurality of micro-nano antibodies 2, the micro-nano antibodies 2 are a plurality of convex structures, and include a length w, a width d and a height h, and all the dimensions of the plurality of micro-nano antibodies 2 are the same. The method comprises the following steps that a plurality of micro-nano antibodies 2 are arranged in an array, the plurality of micro-nano antibodies 2 in the same row are arranged at unequal intervals, namely the interval s between two adjacent micro-nano antibodies 2 in the same row is randomly arranged, and s is more than or equal to 1 mu m and less than or equal to 6 mu m; and the rows are arranged at equal intervals in the row direction. In other embodiments, please refer to fig. 5, the texture structure has a plurality of micro-nano antibodies 3, and the micro-nano antibodies 3 are a plurality of concave structures including a length w, a width d, and a depth h. The micro-nano antibodies 2 and 3 can be of a convex structure or a concave structure, or have the convex structure or the concave structure at the same time, and have the same antibacterial effect no matter the convex structure or the concave structure.
Referring to fig. 6, in another embodiment of the texture structure of the present invention, the texture structure has a plurality of micro-nano antibodies 4, the plurality of micro-nano antibodies 4 have the same shape and size, the plurality of micro-nano antibodies 4 are arranged, the micro-nano antibodies 4 in each row are arranged at equal intervals, and the micro-nano antibodies 4 in adjacent rows are arranged in a staggered manner.
Referring to fig. 7, in another embodiment of the texture structure of the present invention, the texture structure has a plurality of micro-nano antibodies 5, the plurality of micro-nano antibodies 5 have the same shape and size, the plurality of micro-nano antibodies 5 are arranged, the center points of the micro-nano antibodies 5 in each row are equidistantly arranged, but the micro-nano antibodies 5 rotate at different angles with the center points as the origin.
Referring to fig. 8, in another embodiment of the texture structure of the present invention, the texture structure has a plurality of micro-nano antibodies 6, the plurality of micro-nano antibodies 6 have the same shape and size, the plurality of micro-nano antibodies are arranged in an array, each row is arranged in a circumferential manner, and each row is arranged in a concentric circle, the micro-nano antibodies 6 are in an arc shape extending along the circumference, and the micro-nano antibodies 6 are strip-shaped, and the long sides thereof extend along the circumference. In another embodiment, referring to fig. 9, the texture structure has a plurality of micro-nano antibodies 7, the plurality of micro-nano antibodies 7 are arranged in an array, each row is arranged in a circumference, and each row is arranged in a concentric circle, the micro-nano antibodies 7 are distributed along the circumference and extend in a radial shape along the diameter, because the circumference of each row is different, and the number of each row is also different. In conclusion, the micro-nano antibodies of the texture structure can be arranged into various shapes according to setting, and the shapes of the micro-nano antibodies can be adjusted according to factors such as a curved surface or an arc shape, so that flexible setting is realized.
The texture structure of the invention can be applied to the inner and outer surfaces of various articles to achieve the antibacterial effect of the articles. Referring to fig. 10, a product, in this embodiment, a cup 100, includes a supporting surface 101 and a texture structure disposed on the supporting surface 101. The bearing surface 101 is the outer surface of the cup. The texture structure comprises a plurality of micro-nano antibodies 8 arranged in an array, wherein the plurality of micro-nano antibodies 8 have the same shape and size, are waist-shaped structures arranged in a concave manner in the embodiment, extend along the circumference of the cup body 202 and are vertically arranged. The outer surface of the cup body of the cup 100 is provided with a texture structure, and therefore has a good antibacterial effect. For clearly showing the distribution of the micro-nano antibodies 8 on the bearing surface 101, the processing is particularly enlarged in fig. 9, in practice, the micro-nano antibodies 8 are invisible to naked eyes because the sizes thereof are in the nanometer level, fig. 9 is only a schematic diagram, and of course, other diagrams in the present application are enlarged schematic diagrams.
Referring to fig. 11, in another embodiment of the present invention, a mobile phone 200 includes a carrying surface 201 and a texture structure disposed on the carrying surface 201. The bearing surface 201 is an outer surface of the rear cover. The texture structure comprises a plurality of array micro-nano antibodies 9 arranged in an array, and the plurality of micro-nano antibodies 9 have the same shape and size. In the figure, the micro-nano antibodies 9 are cut off at the edge of the back cover due to the structure and only appear partially, and the plurality of micro-nano antibodies 9 are still considered to have the same size as a whole. The mobile phone 200 has a good antibacterial effect.
In order to make the aforementioned objects, features and advantages of the present invention comprehensible, embodiments accompanied with figures are described in detail. In the above description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Moreover, the technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.
The above-mentioned embodiments only express several embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the present invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention. Therefore, the protection scope of the present patent shall be subject to the appended claims.

Claims (13)

1. The texture structure for antibiosis is characterized by comprising a plurality of micro-nano antibodies which are randomly or regularly distributed, wherein the plurality of micro-nano antibodies are of convex structures and/or concave structures, and the plurality of micro-nano antibodies have the same length.
2. The texture structure for antibiosis according to claim 1, wherein the length of the micro-nano antibody is as follows: w is less than or equal to 100 mu m.
3. The texture structure for antibiosis according to claim 1, wherein the width of the micro-nano antibody is as follows: d is more than 0 and less than or equal to 50 mu m.
4. The texture structure for antibiosis according to claim 1, wherein the depth/height of the micro-nano antibody is as follows: h is more than or equal to 0.5 mu m and less than or equal to 5 mu m.
5. The antibacterial texture structure of claim 1, wherein two adjacent micro-nano antibodies are spaced apart, and the spacing distance is defined as s, wherein s is greater than 0 and less than or equal to 10 μm.
6. The texture structure for antibiosis according to claim 1, wherein the plurality of micro-nano antibodies are arranged in an array, the plurality of micro-nano antibodies in the same row are arranged at equal intervals or at variable intervals, and the plurality of rows are arranged at equal intervals or at variable intervals.
7. The antibacterial texture structure of claim 1, wherein the micro-nano antibodies are randomly distributed, and the distance between every two adjacent micro-nano antibodies is not greater than 10 μm.
8. The texture structure for antibiosis according to claim 1, wherein the micro-nano antibodies are arranged in a plurality of rows, each micro-nano antibody defines a set point at the same position, and the set points of the micro-nano antibodies in the same row are located on a straight line or a curved line.
9. The texture structure for antibiosis according to claim 8, wherein at least a part of the micro-nano antibodies in the same row are rotated from the set point by the same or different angles.
10. The antibacterial texture structure according to claim 1, wherein the micro-nano antibody is waist-shaped, cylindrical or conical, and the cross section of the micro-nano antibody is rectangular, triangular, trapezoidal or segmental.
11. The antibacterial texture structure of claim 1, wherein the micro-nano antibody is a raised structure or a recessed structure containing nano silver ions or nano metal zinc oxide.
12. An article comprising a carrying surface and the textured structure for inhibiting bacteria of any one of claims 1 to 11 disposed on the carrying surface, wherein the carrying surface is flat or non-flat.
13. The article of claim 12, wherein the article is a medical article, a sporting article, a household article, a digital product, a home appliance, a maternal and infant article, a food implement.
CN202011387659.9A 2020-12-01 2020-12-01 Texture structure for antibiosis and product Pending CN114573848A (en)

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