Preparation method of plant antibacterial health care fabric containing fruit vitamins

By microencapsulating and processing the compound vitamin plant essential oil onto textiles, the problem of insufficient versatility of existing fabrics is solved, and the multifunctional effects of antibacterial, ultraviolet, moisture-absorbing and moisturizing and negative oxygen ions are achieved.

CN113789662BActive Publication Date: 2025-04-01NANTONG TISHA TEXTILE CO LTD
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Patent Information

Application Number
CN202111042306.X
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2021-09-07
Publication Date
2025-04-01
Estimated Expiration
2041-09-07

AI Technical Summary

Technical Problem

Existing textile fabrics lack versatility, especially in terms of antibacterial, UV-proof and moisture-absorbing and moisturizing, it is difficult to meet the needs of modern people for health care fabrics.

Method used

A plant antibacterial health care fabric containing fruit vitamins is prepared by microencapsulating compound vitamin plant essential oil and processing the microcapsules onto textiles or nonwovens using a padding process. This fabric not only has antibacterial and ultraviolet-proof functions, but also can absorb moisture and moisturize the skin and release negative oxygen ions.

Benefits of technology

It realizes the antibacterial, ultraviolet, moisture absorption and moisturizing and negative oxygen ion release functions of the fabric, improving the health and versatility of the fabric.

✦ Generated by Eureka AI based on patent content.

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Patent Text Reader

Abstract

The invention microencapsulates the compound vitamin plant essential oil so that the vitamin and plant essential oil components are retained to the maximum extent. The prepared microcapsules have high embedding rate, low water content, good solubility and lasting fragrance. Then, the microcapsules are processed onto textiles or non-woven fabrics by a padding process. The preparation method of the invention can obtain fruit vitamin fabrics with antibacterial health care effects. The preparation process is repeatedly tested to obtain an optimal core-to-wall ratio of 3, a reaction temperature of 55°C and a reaction time of 20 minutes. Finally, a novel plant antibacterial health care fabric containing fruit vitamins is prepared, which has the characteristics of antibacterial, UV protection, moisture absorption and skin moisturizing, and release of negative oxygen ions.
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Description

Technical Field

[0001] The invention belongs to the technical field of functional fabrics, and in particular relates to a plant antibacterial health care fabric containing fruit vitamins and a preparation method thereof. Background Art

[0002] With the improvement of people's living standards and the increase of sub-healthy groups, textiles with health functions are sought after by more and more people, and the market space is gradually expanding; at the same time, the organic combination of medical, cosmetics and textile industries conforms to the development of the times and responds to the country's call to encourage innovation.

[0003] Skin care finishing, the concept of which comes from the application of cosmetics, is a high-tech technology developed by Bayer of Japan that integrates fiber, biology and environmental protection. It uses the finishing process of textiles to give fabrics the same moisturizing, conditioning, moisturizing and other special functions as cosmetics.

[0004] In the current era of rapid social and economic development, the original single and monotonous textiles can no longer adapt to the development of the times and people's needs. In addition to the requirements for warmth, breathability, comfort and other wearing performance, textile fabrics also require antibacterial and UV-proof health care fabrics. Therefore, it is necessary to develop new multifunctional textile materials and preparation technologies to meet the consumption requirements of modern people. Summary of the invention

[0005] The purpose of this section is to summarize some aspects of embodiments of the present invention and briefly introduce some preferred embodiments. Some simplifications or omissions may be made in this section and the specification abstract and the invention title of this application to avoid blurring the purpose of this section, the specification abstract and the invention title, and such simplifications or omissions cannot be used to limit the scope of the present invention.

[0006] In view of the above problems and the problems existing in the prior art, the present invention is proposed.

[0007] Therefore, in view of the above-mentioned deficiencies in the prior art, according to one aspect of the present invention, the present invention provides the following technical solution: a method for preparing a plant antibacterial health care fabric containing fruit vitamins, comprising:

[0008] The compound essential oil solution is mixed with the fruit vitamin crude oil, and stirred evenly at room temperature to prepare a compound vitamin essential oil solution; the compound vitamin essential oil solution is mixed with an emulsifier, gum arabic, and deionized water to form a uniform emulsion, and then a gelatin solution is added and the pH value is adjusted to 4-4.5, and shear emulsification is performed to obtain a reaction solution;

[0009] The temperature of the reaction solution was adjusted to 10°C, a cross-linking agent was added, and the pH value was adjusted to 9.0. After stirring, the solution was allowed to stand until the microcapsules were completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain a microcapsule product;

[0010] Slowly add the microcapsule solution into the emulsion containing adhesive, softener and hydrophilic silicone oil, and continue stirring for 15 minutes after adding to prepare the finishing solution;

[0011] The padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is sent into the padding machine for extrusion and padding, which is repeated twice, and the microcapsules are processed onto the textile or non-woven fabric to obtain the plant antibacterial health care fabric containing fruit vitamins.

[0012] As a preferred scheme of the preparation method of the plant antibacterial health care fabric containing fruit vitamins according to the present invention, wherein: the mass fraction of the compound essential oil solution is 10-30%, and the solution includes camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil, and the mass ratio is 1:1:1:1:1; the fruit vitamin crude oil is one or more natural vitamin extracts from fruits such as apples, grapes, and lemons.

[0013] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the compound essential oil solution is mixed with the fruit vitamin crude oil, wherein the compound essential oil solution accounts for 80 to 90 parts and the fruit vitamin crude oil accounts for 10 to 20 parts.

[0014] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins according to the present invention, the core material compound vitamin essential oil solution is mixed with an emulsifier, gum arabic, and deionized water, and the content of each component is: 3 to 6 parts of the compound vitamin essential oil solution, 7 parts of the emulsifier, 2 parts of gum arabic, and 85 to 88 parts of deionized water.

[0015] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the added gelatin solution is a deionized water solution of 2% gelatin added in a mass ratio of 1:1 to the uniform emulsion.

[0016] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the shear emulsification comprises:

[0017] Shear at a constant temperature of 45-65°C for 10-30 min and a stirring rate of 1500 rpm.

[0018] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the cross-linking agent includes but is not limited to an aqueous solution of glutaraldehyde with a mass fraction of 25%, and the added amount is 20g of 25% glutaraldehyde aqueous solution per 1L of reaction solution.

[0019] As a preferred scheme of the preparation method of the plant antibacterial health care fabric containing fruit vitamins described in the present invention, wherein: the mass fraction of the microcapsule solution is 20-40%; the adhesive includes but is not limited to one or more of acrylate-butadiene elastomer copolymers and acrylonitrile copolymer adhesives; the softener includes but is not limited to pyridine quaternary ammonium salt derivative reactive softeners.

[0020] As a preferred embodiment of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the finishing liquid comprises:

[0021] Adhesive 20-30g / L, pyridine quaternary ammonium salt derivative reactive softener 15g / L, hydrophilic silicone oil 10g / L, microcapsule emulsion 30g / L.

[0022] As a preferred solution of the method for preparing the plant antibacterial health care fabric containing fruit vitamins of the present invention, the process conditions of the padding are: the liquid volume is 70% and the vehicle speed is 60 m / min.

[0023] Beneficial effects of the present invention:

[0024] The present invention microencapsulates the compound vitamin plant essential oil so that the vitamins and plant essential oil components are retained to the maximum extent. The prepared microcapsules have high embedding rate, low water content, good solubility and lasting fragrance retention. The microcapsules are then processed onto textiles or non-woven fabrics through a padding process to finally produce a new type of plant antibacterial health care fabric containing fruit vitamins that has the characteristics of antibacterial, UV protection, moisture absorption and skin moisturizing, and releasing negative oxygen ions.

[0025] The preparation methods of the present invention can obtain fruit vitamin fabrics with antibacterial health care effects, and the preparation process is repeatedly tested to obtain the optimal reaction conditions: the core-to-wall ratio is 3, the reaction temperature is 55° C., and the reaction time is 20 min. DETAILED DESCRIPTION

[0026] In order to make the above-mentioned objects, features and advantages of the present invention more obvious and easy to understand, the specific implementation methods of the present invention are described in detail below in conjunction with specific embodiments.

[0027] In the following description, many specific details are set forth to facilitate a full understanding of the present invention, but the present invention may also be implemented in other ways different from those described herein, and those skilled in the art may make similar generalizations without violating the connotation of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed below.

[0028] Secondly, the term "one embodiment" or "embodiment" as used herein refers to a specific feature, structure, or characteristic that may be included in at least one implementation of the present invention. The term "in one embodiment" that appears in different places in this specification does not necessarily refer to the same embodiment, nor does it refer to a separate or selective embodiment that is mutually exclusive with other embodiments.

[0029] The present invention adopts a compound essential oil solution mixed with a fruit vitamin crude oil as a core material, and a gum arabic and gelatin solution as a wall material to prepare a microcapsule product, and processes the microcapsule product onto a textile or non-woven fabric to obtain a plant antibacterial health care fabric containing fruit vitamins. In order to prevent the premature electrostatic effect between part of the gum arabic and the gelatin, the core material is first mixed with the gum arabic, and then the wall material gelatin is added.

[0030] The C13-15 branched fatty alcohol polyoxyethylene ether used in the embodiment of the present invention was purchased from Yangzi Petrochemical-BASF Co., Ltd.; the acrylate-butadiene elastomer binary copolymer used was purchased from Shanghai Textile Science Research Institute and is a low-temperature adhesive; the pyridinium quaternary ammonium salt derivative reactive softener used was purchased from Zhejiang Chuanhua Co., Ltd. and is softener TF-406; the hydrophilic silicone oil used was purchased from Zhejiang Chuanhua Co., Ltd. and is numbered TF-4918F; the acrylonitrile copolymer used was purchased from Shanghai Yuhui Chemical Co., Ltd. and is an adhesive JJS; the emulsifier used was purchased from Changzhou Meisheng Biomaterials Co., Ltd. and is an MS-1 emulsifier.

[0031] The present invention takes fruit vitamin E crude oil as an example.

[0032] Unless otherwise specified, other raw materials used in the present invention are commonly available on the market.

[0033] Embodiment 1:

[0034] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0035] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 4:7:2:87, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring conditions, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0036] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0037] (4) Accurately weighing an acrylate-butadiene elastomer binary copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule solution with a mass fraction of 30%; slowly adding the microcapsule solution to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0038] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0039] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0040] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0041] Embodiment 2:

[0042] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 90:10, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0043] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 6:7:2:85, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring conditions, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0044] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0045] (4) Accurately weighing an acrylate-butadiene elastomer copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0046] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0047] (5) A padding process is adopted, the finishing liquid is added into a padding machine, and then the fabric is sent into the padding machine for extrusion and rolling, which is repeated twice to treat the microcapsules onto the textile or non-woven fabric, pre-bake at 80° C. for 60 seconds, and bake at 150° C. for 3 minutes, and finally obtain a plant antibacterial health care fabric containing fruit vitamins.

[0048] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0049] Embodiment 3:

[0050] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 80:20, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0051] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 3:7:2:88, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0052] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0053] The process dosage of the curing agent is: 25% glutaraldehyde 20g / L.

[0054] (4) Accurately weighing an acrylate-butadiene elastomer copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0055] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0056] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0057] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0058] Embodiment 4:

[0059] The effect of reaction temperature of 45℃ and reaction time of 30min on the experimental product:

[0060] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0061] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 4:7:2:87, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring conditions, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 45°C for 30 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0062] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0063] (4) Accurately weighing an acrylate-butadiene elastomer copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0064] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0065] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0066] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0067] Embodiment 5:

[0068] The effect of reaction temperature of 65℃ and reaction time of 10min on the experimental product:

[0069] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0070] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 4:7:2:87, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 65°C for 10 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0071] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0072] (4) Accurately weighing an acrylate-butadiene elastomer copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0073] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0074] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0075] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0076] Comparative Example 1:

[0077] Experimental steps for using only single gum arabic as wall material:

[0078] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0079] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water are mixed in a mass fraction ratio of 4:7:2:83, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a dispersed emulsion; accurately weighed gum arabic and dissolved in deionized water to prepare a gum arabic solution with a mass fraction of 2%; the gum arabic solution is added to the dispersed emulsion under stirring at a mass ratio of 1:1, and after mixing evenly, the pH value is adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0080] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed until neutral, filtered and vacuum dried to obtain a microcapsule product.

[0081] (4) Accurately weighing an acrylate-butadiene elastomer copolymer adhesive, a pyridine quaternary ammonium salt derivative reactive softener, and a hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, the softener, and the hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0082] The dosage of each component in the finishing liquid is: 20g / L of acrylate-butadiene elastomer copolymer adhesive, 15g / L of pyridine quaternary ammonium salt derivative reactive softener, 10g / L of hydrophilic silicone oil, and 30g / L of 30% microcapsule emulsion.

[0083] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0084] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0085] Comparative Example 2:

[0086] Adhesive: Experimental steps for using acrylonitrile copolymer adhesive:

[0087] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0088] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water were mixed in a mass fraction ratio of 4:7:2:87, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weighed gelatin was dissolved in deionized water to prepare a gelatin solution with a mass fraction of 2%; the gelatin solution was added to the uniform emulsion in a mass ratio of 1:1 under stirring, and after the mixture was evenly mixed, the pH value was adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0089] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0090] (4) Accurately weighing acrylonitrile copolymer adhesive, pyridine quaternary ammonium salt derivative reactive softener, and hydrophilic silicone oil, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive, softener, and hydrophilic silicone oil under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0091] The dosage of each component in the finishing liquid is: 30 g / L acrylonitrile copolymer adhesive, 15 g / L pyridine quaternary ammonium salt derivative reactive softener, 10 g / L hydrophilic silicone oil, and 30 g / L 30% microcapsule emulsion.

[0092] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0093] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0094] Comparative Example 3:

[0095] Experimental steps for preparing products without adding hydrophilic silicone oil:

[0096] (1) Accurately weigh camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil in a mass ratio of 1:1:1:1:1, dissolve them in C13-15 branched chain fatty alcohol polyoxyethylene ether to prepare a compound essential oil solution with a mass fraction of 20%, and set aside; mix the compound essential oil solution with fruit vitamin E crude oil in a mass fraction ratio of 85:15, stir evenly at room temperature, and prepare a compound vitamin E essential oil solution.

[0097] (2) The compound vitamin E essential oil solution, emulsifier, gum arabic and deionized water are mixed in a mass fraction ratio of 4:7:2:87, stirred evenly at 150 rpm for 5 min at 45°C, and then emulsified at a shear rate of 1500 rpm for 10 min to obtain a uniform emulsion; accurately weigh gelatin and dissolve it in deionized water to prepare a gelatin solution with a mass fraction of 2%; under stirring, the gelatin solution is added to the uniform emulsion in a mass ratio of 1:1, and after mixing evenly, the pH value is adjusted to 4, and stirred at a constant temperature of 55°C for 20 min at a stirring rate of 1500 rpm to obtain a reaction solution.

[0098] (3) After the constant temperature stirring is completed, the temperature of the reaction solution is slowly adjusted to 10° C., 20 g of 25% glutaraldehyde aqueous solution is added to each 1 L of the reaction solution for cross-linking and curing, and the pH value is adjusted to 9.0. After stirring, the solution is allowed to stand until the microcapsules are completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain the microcapsule product.

[0099] (4) Accurately weighing an acrylate-butadiene elastomer binary copolymer adhesive and a pyridinium quaternary ammonium salt derivative reactive softener, adding deionized water and stirring to form a uniform emulsion; accurately weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule emulsion with a mass fraction of 30%; slowly adding the microcapsule emulsion to the emulsion containing the adhesive and the softener under stirring conditions, and continuing to stir for 15 minutes after the addition to prepare a finishing liquid.

[0100] The dosage of each component in the finishing liquid is: 20 g / L of acrylate-butadiene elastomer binary copolymer adhesive, 15 g / L of pyridine quaternary ammonium salt derivative reactive softener, and 30 g / L of 30% microcapsule emulsion.

[0101] (5) A padding process is adopted, the finishing liquid is added into the padding machine, and the fabric is then sent into the padding machine for extrusion and rolling, which is repeated twice to process the microcapsules onto the textile or non-woven fabric, and the fabric is pre-baked at 80°C for 60s and baked at 150°C for 3min, thereby finally obtaining a plant antibacterial health care fabric containing fruit vitamins.

[0102] The process conditions of padding are: liquid volume 70%, vehicle speed 60m / min.

[0103] Example 9

[0104] The mass fractions of the core material and the wall material used in Examples 1 to 3 are calculated according to the following formula.

[0105] Core material mass fraction (Wt%) = (A + B) × n ÷ 2 × 100%

[0106] Where A = mass fraction of vitamin crude oil in compound vitamin essential oil solution;

[0107] B = mass fraction of plant essential oil in compound vitamin essential oil solution;

[0108] n = fraction of compound vitamin E essential oil solution added.

[0109] The mass fraction of the wall material is the sum of the mass fractions of gum arabic and gelatin.

[0110] Table 1 Different core-to-wall ratios of plant antibacterial health care fabrics prepared in Examples 1 to 3

[0111]

[0112] (Note: The mass fraction of the core material and wall material is the mass fraction of the reaction solution)

[0113] The performance of the plant antibacterial health care fabrics containing fruit vitamins prepared in Examples 1 to 5 and Comparative Examples 1 to 3 was tested, and the testing method was as follows:

[0114] (1) The test method for the antibacterial performance of health care fabrics is as follows: refer to "GB / T 20944.2-2007 Evaluation of antibacterial properties of textiles Part 3 Oscillation method" to quantitatively test the antibacterial properties of fabrics.

[0115] (2) The test method for vitamin E content in health care fabrics is as follows: Referring to GB 5009.82-2016 National Food Safety Standard Determination of Vitamins A, D and E in Foods, the vitamin E in the sample is extracted and concentrated with an organic solvent, separated using a high performance liquid chromatography amide column or a silica gel column, detected using a fluorescence detector, and quantified using the external standard method.

[0116] (3) The test method for the moisture absorption performance of health care fabrics is as follows: refer to "GB / T 21655.1-2008 Evaluation of moisture absorption and quick-drying properties of textiles Part 1: One-way combined test method" to test the moisture absorption of fabrics. The water absorption rate and droplet diffusion time are used to characterize the fabric's ability to absorb liquid sweat; the water evaporation rate and moisture permeability are used to characterize the fabric's ability to retain moisture.

[0117] (4) The test method for the negative oxygen ion generation of health care fabrics is as follows: Referring to "GB / T 30128-2013 Test and Evaluation of Negative Ion Generation of Textiles", the fabric sample is installed on the upper and lower friction disks in a test chamber of a certain volume, and rubbed under specified conditions. An air ion meter is used to test the number of negative ions generated per unit volume when the fabric samples rub against each other.

[0118] (5) With reference to GB / T 18830-2009 Evaluation of UV protection performance of textiles, the UV protection performance of fabrics was tested using UV-2000 fabric sun protection index analyzer, which was characterized by the UPF value. The test specimens were kept dry and relaxed, the test light source was the solar luminescence spectrum EN 13758, the temperature was (20±2)℃, and the humidity was (65±2)%.

[0119] After testing, the experimental data obtained are shown in Tables 1 to 6.

[0120] Table 2 Experimental results of antibacterial rate of nursing fabrics obtained in the embodiments of the present invention

[0121]

[0122] Table 3 Experimental results of antibacterial rate of nursing fabrics obtained in the present invention after washing

[0123]

[0124]

[0125]

[0126] Table 4 Experimental results of vitamin E content in nursing fabrics prepared in the embodiments of the present invention

[0127]

[0128] Table 5 Experimental results of moisture absorption performance of nursing fabrics of the present invention

[0129]

[0130] Table 6 Experimental results of negative oxygen ion generation of nursing fabrics of the present invention

[0131]

[0132]

[0133] Table 7 Experimental results of UV protection performance of nursing fabrics of the present invention

[0134]

[0135] After testing, the antibacterial rate of the fabric against three bacteria is shown in Table 2, and the antibacterial rate of the fabric after washing is shown in Table 3. The prepared fabric has antibacterial properties against Staphylococcus aureus, Escherichia coli, and Candida albicans, and the antibacterial property can reach more than 96%. The fabric was washed and tested. It can be seen from Table 2 that the antibacterial effect can reach about 70% after washing 15 times, and it still has a good antibacterial effect. After washing 20 times, the antibacterial effect can still reach more than 60%.

[0136] As can be seen from Table 4, there is abundant vitamin E in the fabric, which means that the fruit vitamin E crude oil added in the preparation of the core material can be well preserved in the fabric microcapsules, making the fabric have skin-friendly, moisture-absorbing, anti-oxidation and other care functions.

[0137] It can be seen from Table 5 that the care fabrics prepared by the present invention have excellent hygroscopicity and good water retention capacity, and the care fabric prepared in Example 1 has a higher water absorption rate of 344%, a lower evaporation rate, and has a better water storage capacity.

[0138] Table 6 shows that the fabric has the function of negative ion emission. The plant antibacterial health care fabric containing fruit vitamins continuously releases plant essential oils with negative ion release function when in contact with air, water vapor and other media. When water molecules in the air, other molecules or moisture on the surface of the skin enter the negative ion electric field space (generally spherical with a radius of 10 to 15 μm), they are immediately ionized by the permanent electrode to produce OH - and H + . Due to H + Move very fast (H + The moving speed is OH - 1 to 8 times of the original mass), quickly moves to the negative electrode of the permanent electrode, absorbs an electron and becomes H2, which escapes into the air, while OH - It forms H3O2 with other water molecules - Negative ions. This change will continue as long as the air humidity is not zero, and will not produce toxic substances to cause other side effects. That is, it has health functions such as purifying the air, improving sleep and regulating blood pressure.

[0139] As shown in Table 7, the care fabrics prepared in Examples 1 to 5 all meet the national standards for UV protection, and the plant antibacterial health care fabrics containing fruit vitamins continuously release plant essential oils and fruit vitamins with UV protection when in contact with air, water vapor and other media. This fabric has a certain UV protection function.

[0140] In summary, the preparation methods of the present invention can obtain fruit vitamin fabrics with antibacterial health care effects, and the preparation process is repeatedly tested to obtain the optimal core-to-wall ratio of 3, the reaction temperature of 55°C, and the reaction time of 20 min.

[0141] The present invention microencapsulates the compound vitamin plant essential oil so that the vitamins and plant essential oil components are retained to the maximum extent. The prepared microcapsules have high embedding rate, low water content, good solubility and lasting fragrance retention. The microcapsules are then processed onto textiles or non-woven fabrics through a padding process to finally produce a new type of plant antibacterial health care fabric containing fruit vitamins that has the characteristics of antibacterial, UV protection, moisture absorption and skin moisturizing, and releasing negative oxygen ions.

[0142] The preparation method of the present invention can obtain fruit vitamin fabrics with antibacterial health care effects, and the preparation process is repeatedly tested to obtain the best core-to-wall ratio of 3, the reaction temperature of 55° C., and the reaction time of 20 min.

[0143] It should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention rather than to limit it. Although the present invention has been described in detail with reference to the preferred embodiments, those skilled in the art should understand that the technical solutions of the present invention may be modified or replaced by equivalents without departing from the spirit and scope of the technical solutions of the present invention, which should all be included in the scope of the claims of the present invention.

Claims

1. A method for preparing a plant antibacterial health care fabric containing fruit vitamins, characterized in that: include, The compound essential oil solution and the fruit vitamin crude oil are mixed at a mass fraction ratio of 85:15, and stirred evenly at room temperature to prepare a compound vitamin essential oil solution; the compound vitamin essential oil solution is mixed with an emulsifier, gum arabic, and deionized water to form a uniform emulsion, and then the gelatin solution is added and the pH value is adjusted to 4-4.5 to obtain a reaction solution by shear emulsification; The temperature of the reaction solution was adjusted to 10°C, a cross-linking agent was added, and the pH value was adjusted to 9.

0. After stirring, the solution was allowed to stand until the microcapsules were completely precipitated, filtered, washed with deionized water until neutral, filtered and vacuum dried to obtain a microcapsule product; Weighing an adhesive, a softener, and a hydrophilic silicone oil, adding deionized water, and mixing and stirring to form a uniform emulsion; weighing the prepared microcapsules and dispersing them in deionized water to prepare a microcapsule solution; Slowly add the microcapsule solution into the emulsion containing adhesive, softener and hydrophilic silicone oil, and continue stirring for 15 minutes after adding to prepare the finishing solution; The padding process is adopted, the finishing liquid is added to the padding machine, and the fabric is sent into the padding machine for extrusion and padding, which is repeated twice to process the microcapsules onto the textile or non-woven fabric to obtain the plant antibacterial health care fabric containing fruit vitamins; The mass fraction of the compound essential oil solution is 10-30%, and the compound essential oil solution comprises camellia oil, camphor oil, prickly ash oil, maca oil, and isatis root oil, and the mass ratio is 1:1:1:1:1; the fruit vitamin crude oil is fruit vitamin E crude oil; The shear emulsification is performed at a constant temperature of 55°C for 20 minutes with a stirring rate of 1500 rpm; The compound vitamin essential oil solution is mixed with an emulsifier, gum arabic, and deionized water in a mass fraction ratio of 4:7:2:87; The cross-linking agent is an aqueous solution of glutaraldehyde with a mass fraction of 25%, and the addition amount is 20 g of 25% glutaraldehyde aqueous solution per 1L of reaction solution; The added gelatin solution is a deionized water solution with a mass fraction of 2% gelatin added at a mass ratio of 1:1 to the uniform emulsion; The mass fraction of the microcapsule solution is 20-40%; the adhesive is an acrylate-butadiene elastomer binary copolymer; the softener is a pyridine quaternary ammonium salt derivative reactive softener; The finishing liquid comprises 20-30 g / L of an adhesive, 15 g / L of a quaternary pyridine ammonium salt derivative reactive softener, 10 g / L of a hydrophilic silicone oil, and 30 g / L of a microcapsule solution.

2. The method for preparing a plant antibacterial health care fabric containing fruit vitamins as claimed in claim 1, characterized in that: The process conditions of the padding are: liquid volume 70%, vehicle speed 60m / min.

Citation Information

Patent Citations

  • Processing method of skin protecting cloth

    CN101709552A