Water-soluble wool lubricating oil, preparation method thereof and application of water-soluble wool lubricating oil in improvement of textile performance

By preparing water-soluble and crude oil-based products, the problem of moth repellents and antibacterial agents being insoluble in water was solved, enabling uniform addition during the spinning process, improving yarn performance and moth repellency, and reducing enterprise costs.

CN121496748APending Publication Date: 2026-02-10安徽远琦新材料科技有限公司
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Patent Information

Application Number
CN202511825494.1
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-12-05
Publication Date
2026-02-10

AI Technical Summary

Technical Problem

In existing technologies, mothproofing agents and antibacterial agents are insoluble in water, resulting in uneven application during the wool-making process. This affects spinning, yarn strength, and fiber spinnability. Furthermore, traditional dyeing processes are complex, affecting color fastness and hand feel, and increasing enterprise costs.

Method used

It uses water-soluble crude oil and contains components such as polyethylene glycol laurate, sorbitan laurate, polyoxyethylene polyoxypropylene block copolymer, isothiazolinone, and castor oil polyoxyethylene ether. During the preparation process, auxiliary agents such as deionized water are added to ensure uniform dispersion and dissolution, providing antibacterial and mothproof functions.

Benefits of technology

It effectively inhibits Staphylococcus aureus and Candida albicans during the spinning process, achieving excellent mothproofing performance, improving yarn strength and spinnability, meeting the requirements of spinning permeability, lubrication and antistatic properties, and reducing costs.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention belongs to the field of textile auxiliaries, and provides water-soluble wool lubricating oil, a preparation method thereof and application of the water-soluble wool lubricating oil to improvement of textile performance. The water-soluble wool lubricating oil is prepared from the following components: polyethylene glycol laurate, sorbitol laurate, a polyoxyethylene polyoxypropylene block copolymer, isothiazolinone, castor oil polyoxyethylene ether and an auxiliary agent. The water-soluble wool lubricating oil provided by the invention further comprises one or more of flavonoids extracted from natural plants, 3-(trimethoxysilyl) propyl dimethyl octadecyl amine chloride and pyrethroid. The wool lubricating oil provided by the invention has mothproof, antibacterial and enzyme-proof effects on textiles. The technical problems that a traditional mothproof agent, a traditional antibacterial agent and a traditional enzyme-proof agent in the domestic wool spinning industry are insoluble in water, uneven in wool blending and poor in effect, spinning is affected, and even the strength of yarn, the spinnability of fiber and the yield are affected can be effectively solved.
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Description

Technical Field

[0001] This invention belongs to the field of textile auxiliaries, specifically relating to a water-soluble oil and its preparation method and its application in improving the performance of textiles. Background Technology

[0002] Cashmere and wool fabrics are highly susceptible to damage from moths during storage and production. For a long time, to reduce moth damage to wool fabrics, people have commonly used sublimable chemicals such as camphor and naphthalene during production and storage, utilizing their volatile toxic gases to inhibit moth growth and infestation. Camphor balls containing dichlorobenzene and naphthalene are classified as pesticides and are generally used for moth control on industrial or agricultural products; they are not suitable for household items. These moth repellents have a short-lasting effect, are not washable, have a strong odor, are highly toxic, and pose certain health risks, including potential carcinogenicity.

[0003] Moth repellents are agents used to prevent, repel, or control wood-boring pests (such as the black-faced bark beetle, the yellow-faced bark beetle, the clothes moth, and the bagworm moth) that damage fur, fiber products, books, and paintings. An ideal moth repellent should meet the following criteria: high lethality against all types of wood-boring insects; non-toxic or with very low toxicity; safe for humans; moderate volatility; and not cause discoloration or deterioration of packaging materials in contact with clothing.

[0004] Dextromethorphan insecticides are a class of synthetic insecticides with chemical structures similar to natural pyrethrin. Pyrethroid moth repellents are all non-water-soluble, and currently, they mainly rely on the adsorption of protein fibers.

[0005] Currently, the domestic wool textile industry commonly suffers from mildew, insect infestation, and bacterial growth in cashmere and wool raw materials, yarns, and finished products. Traditionally, a single mothproofing agent is added during the dyeing process, which is complex and affects colorfastness and hand feel. After dyeing, cashmere and wool fibers undergo various post-treatments to ensure the fiber's hand feel and various fastness indicators. This process washes away a significant portion of the mothproofing agent, resulting in waste and affecting subsequent mothproofing effectiveness. Adding antibacterial auxiliaries during dyeing presents similar problems. Furthermore, adding excessive auxiliaries during the pre-spinning dyeing process negatively impacts the dyeing process. Additionally, antibacterial and mothproofing agents added during dyeing are generally expensive and wasteful, placing a heavy cost burden on enterprises and hindering their price competitiveness. Since most mothproofing and antibacterial agents are insoluble in water, adding them directly during wool blending results in uneven blending, poor effectiveness, and affects spinning, even impacting yarn strength, fiber spinnability, and yield. Summary of the Invention

[0006] Technical problem solved: In view of the above-mentioned technical problems, the present invention provides a water-soluble wool oil and its preparation method and its application in improving the performance of textiles. It can effectively solve the technical problems in the current domestic wool textile industry where traditional mothproofing agents, antibacterial agents and anti-enzyme agents are insoluble in water and are directly added during the wool mixing process, which will cause uneven wool mixing, poor effect, affect spinning, and even affect the strength of yarn, the spinnability of fibers and the yield.

[0007] In a first aspect, the present invention provides a water-soluble form and crude oil, employing the following technical solution: A water-soluble crude oil, and the crude oil components include: polyethylene glycol laurate, sorbitan laurate, polyoxyethylene polyoxypropylene block copolymer, isothiazolinone, castor oil polyoxyethylene ether, and auxiliaries; said auxiliaries are selected from one or two of deionized water or softened water.

[0008] Preferably, the water-soluble and crude oil components further include one or more of isothiazolinone, natural plant-derived flavonoids, 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and pyrethroids.

[0009] The wool-spun oil provided by this invention is mainly used for protein loose fibers such as cashmere and wool. It is an antibacterial and anti-moth functional oil added during the spinning process. Its main function is to add two functions to the wool-spun oil while maintaining the basic properties of the original wool-spun oil: 1) Antibacterial function: When this type of yarn with lint is used in the spinning process, it has a good inhibitory effect on Staphylococcus aureus and Candida albicans, which meets the standard requirements of the absorption method in Appendix D.7 of FZ / T 73023~2006 and has antibacterial properties.

[0010] 2) Mothproof function: When this type of yarn with wool oil is used in the spinning process, the mothproof performance reaches Grade 1A in GB / T 29776~2013, which has excellent mothproof performance.

[0011] Preferably, the water-soluble and crude oil components have the following mass fractions: 30-35% polyethylene glycol laurate, 15-25% sorbitol laurate, 16-27% polyoxyethylene-polyoxypropylene block copolymer, 0-10% isothiazolinone, 2-13% castor oil polyoxyethylene ether, and 5-20% auxiliaries.

[0012] Preferably, the mass fractions of the water-soluble and crude oil components are: 0-8% natural plant-derived flavonoids, 0-5% 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and 0-10% pyrethroids.

[0013] Secondly, the present invention provides a method for preparing water-soluble crude oil, employing the following technical solution: A method for preparing water-soluble crude oil includes the following steps: Step 1: Add the base oil agent in the preset proportion to the reaction vessel, start stirring, and mix evenly at room temperature to form a homogeneous oil phase; Step 2: Add the functional oil while continuously stirring; then slowly heat to the specified temperature and stir at a constant temperature to ensure that the functional components react and blend fully. Step 3: Cool the material to room temperature, and slowly add the auxiliary agent while stirring at a uniform speed to fully dilute and hydrate it, ensuring that the homogeneous oil phase system is completely stable; Step 4: Take samples of the blended product for testing. After passing the test, filter the product and then fill it in the correct quantity.

[0014] Preferably, a method for preparing a water-soluble crude oil includes, specifically, a base oil agent comprising: polyethylene glycol laurate, sorbitan laurate, polyoxyethylene-polyoxypropylene block copolymer, isothiazolinone, and castor oil polyoxyethylene ether; the functional oil agent comprising: one or more of natural plant-derived flavonoids, 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and pyrethroids; and the auxiliary agent being deionized water or softened water.

[0015] Preferably, in a method for preparing water-soluble crude oil, specifically, in steps 1 to 3, the stirring time is 15 to 60 minutes, the stirring speed is 30 to 50 rpm, and the mass fraction of the auxiliary agent is 5 to 20%.

[0016] Preferably, in a method for preparing water-soluble crude oil, specifically, in step 2, the specified temperature is 45°C.

[0017] Preferably, in a method for preparing a water-soluble crude oil, specifically, the conditions for complete stability of the homogeneous oil phase system in step 3 include: the system temperature is room temperature and the system pH value is 6.0~7.0.

[0018] Thirdly, the present invention provides the application of water-soluble and crude oils in improving the properties of textiles.

[0019] Beneficial effects:

[0020] 1. The water-soluble wool oil provided by the present invention selects auxiliary agents with antibacterial and anti-moth functions that are beneficial to spinning and wool addition during its preparation process, and uses special emulsifiers and surfactants to make it uniformly dispersed and dissolved in the wool oil system.

[0021] 2. The raw materials selected in the preparation process of the water-soluble and crude oil provided by this invention, as well as the control of the production process, are required to ensure that the prepared crude oil does not affect or helps the cohesion, permeability, antistatic properties, lubricity, and moisture regain of the yarn required in the cashmere and wool spinning process.

[0022] 3. Compared with existing yarn-making oils on the market, the water-soluble yarn-making oil provided by this invention can meet the general usage conditions of spinning, such as: good penetrating and wetting properties, certain fiber bundling and cohesion, certain antistatic properties, certain lubrication to facilitate fiber combing, and certain moisture regain of the yarn. While meeting general usage conditions, it also imparts antibacterial and moth-proof effects, filling a gap in the industry and solving a key industry problem. Detailed Implementation

[0023] The technical solution of the present invention will be described in detail below with reference to the embodiments. Example 1

[0024] The components of the water-soluble and crude oil provided in this embodiment are mass fractions.

[0025] This embodiment provides a water-soluble crude oil, specifically, the crude oil includes Deli Textile FC-620MP crude oil.

[0026] The components of three formulations of Deli Textile FC-620MP and crude oil: Formula a: Polyethylene glycol laurate: 30%; Sorbitol laurate: 17%; Isothiazolinone: 6%; Polyoxyethylene-polyoxypropylene block copolymer: 16%; 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride: 4%; Castor oil polyoxyethylene ether: 6%; Natural plant-derived flavonoids: 2%; Pyrethroids: 3%; Deionized water: 16%.

[0027] Formula b: Polyethylene glycol laurate: 35%; Sorbitol laurate: 21%; Isothiazolinone: 4%; Polyoxyethylene-polyoxypropylene block copolymer: 21%; 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride: 3%; Castor oil polyoxyethylene ether: 4%; Natural plant-derived flavonoids: 3%; Pyrethroids: 4%; Deionized water: 5%.

[0028] Formula c: Polyethylene glycol laurate: 32%; Sorbitol laurate: 23%; Isothiazolinone: 2.5%; Polyoxyethylene-polyoxypropylene block copolymer: 20%; 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride: 2%; Castor oil polyoxyethylene ether: 8%; Natural plant-derived flavonoids: 2%; Pyrethroids: 5%; Deionized water: 5.5%.

[0029] Isothiazolinone, natural plant-derived flavonoids, and 3-(trimethoxysilyl)propyldimethyloctadecylamine chloride have antibacterial effects; pyrethroids have a moth-proofing effect. Example 2

[0030] The components of the water-soluble and crude oil provided in this embodiment are mass fractions.

[0031] This embodiment provides the process specifications for Hedeli Textile FC-620MP and crude oil, taking component c of formulation 1 in Example 1 as an example, as follows: Deli Textile FC-620MP Water-Soluble and Crude Oil Production Process Specifications Step 1: Production Preparation and Confirmation Equipment status confirmation: Confirm that the reactor and pipelines are clean, all valves are in the required state according to the process, and the bottom discharge valve is closed.

[0032] Document and material confirmation: Review all production process sheets and raw material lists, and prepare the raw materials that have been verified to be correct to the feeding area.

[0033] Safety preparation: Operators should wear appropriate personal protective equipment as required.

[0034] Step 2: Oil Mixing Add 32% polyethylene glycol laurate and 23% sorbitol laurate sequentially into the reactor. Start stirring and stir at 30 rpm for 20 minutes to ensure the base oil is mixed evenly.

[0035] Step 3: Add the first set of oils While stirring, add 2.5% isothiazolinone and 20% polyoxyethylene-polyoxypropylene block copolymer sequentially. Maintain a speed of 30 rpm and continue stirring for 15 minutes to ensure uniform dispersion of the materials.

[0036] Step 4: Add the second set of oils. While stirring, add 2% 3-(trimethoxysilyl)propyldimethyloctadecylamine chloride and 8% castor oil polyoxyethylene ether in sequence.

[0037] Increase the stirring speed to 40 rpm and continue stirring for 15 minutes.

[0038] Step 5: Add the third group of oils and heat up to react. Add 2% natural plant-derived flavonoids and 5% pyrethroids while stirring. Slowly raise the temperature to 45°C and increase the stirring speed to medium-50 rpm, then continue stirring for 40 minutes.

[0039] Step 6: Add deionized water Stop heating and allow the material to cool naturally.

[0040] While maintaining a constant speed of 50 rpm, add deionized water, pausing for 30 seconds after every 15 seconds of addition. The total amount of deionized water added should be 5.5%. After all the deionized water has been added, continue stirring for 40 minutes to complete the final hydration and setting of the product.

[0041] Step 7: Product Completion Products are sampled and inspected, with the following indicators: solid content, appearance, pH value, and viscosity value. Only products that pass the inspection can be released.

[0042] The product is filtered before being filled and packaged.

[0043] Example 3: Mothproofing performance test of Deli Textile FC-620MP and wool oil The test data in this embodiment was provided by Shanghai Textile Group Testing Standards Co., Ltd.

[0044] According to the preparation method of Example 2, the components were prepared using formula a to obtain Deli Textile FC-620MP and wool oil samples, which were then sent to Shanghai Textile Group Testing and Standards Co., Ltd. for mothproofing performance testing.

[0045] According to the test results, the surface damage assessment of Deli Textile FC-620MP and wool oil test samples was Grade 1, and the assessment of moth-eaten holes was Grade A. Therefore, the Deli Textile FC-620MP and wool oil samples in this embodiment meet the Grade 1A requirements of GB / T 29776~2013 "Determination of Mothproof Performance of Textiles", confirming their excellent mothproof performance.

[0046] Example 4: Antibacterial performance test of Deli Textile FC-620MP and crude oil The test data in this embodiment was provided by Zhonglian Inspection (Fujian) Testing Service Co., Ltd. According to the preparation method in Example 2, Deli Textile FC-620MP and crude oil were prepared using formula a. The antibacterial rate of the obtained samples was determined by Zhonglian Testing (Fujian) Testing Service Co., Ltd., and the test results are as follows: Table 1 Results of antibacterial rate determination

[0047] As shown in Table 1, the Deli Textile FC-620MP and wool oil in this embodiment meet the standard requirements in Appendix D.7 Absorption Method of FZ / T 73023~2006 Antibacterial Knitted Fabrics Standard, indicating that they have excellent antibacterial properties.

[0048] Example 5: Water-soluble and crude oils used in wool and cashmere textiles This embodiment uses formula b from Example 1 and the preparation method from Example 2 to obtain the spinning process sheet for Delifang FC-620MP for wool and cashmere textiles, as detailed below: 1. Spinning raw materials and functional auxiliaries Main raw material: 100% pure white cashmere fiber, batch number: YQC252260001.

[0049] Functional additives: Wool oil: Deli Textile FC-620MP wool oil was prepared using the preparation methods of formulation b in Example 1 and Example 2. Its main function is to provide excellent lubrication, softness and cohesion properties for cashmere fibers.

[0050] Antistatic agent: FNE type antistatic agent is used to eliminate static electricity generated by fiber friction during spinning, ensuring smooth process.

[0051] Application: The target product is 26 / 2Nm (metric count) light blue pure cashmere yarn.

[0052] 2. Spinning process design and specific implementation parameters This embodiment introduces a composite auxiliary agent system consisting of a specific ratio of wool oil and an antistatic agent into the traditional spinning and wool processing steps. Specific spinning process parameters are listed in Table 2 according to the process sequence.

[0053] Table 2 Spinning Process Sheet for Coarse Wool Mills

[0054] Among them, the amount of Deli Textile FC-620MP type and wool oil added is 3.5% owf, and the amount of FNE type antistatic agent added is 0.5% owf; owf refers to the percentage of the mass of Deli Textile FC-620MP type and wool oil or the mass of FNE type antistatic agent to the dry weight of the fiber.

[0055] 3. Verification of process effects and analysis of yarn performance Samples of 26 / 2 Nm pure cashmere yarn produced according to the above process were taken for testing. The finished yarn was subjected to physical performance testing according to national standards. The core data of the yarn quality inspection report are shown in Table 3.

[0056] Table 3 Yarn Inspection Report

[0057] This embodiment uses a spinning auxiliary system of Deli Textile FC-620MP type and wool oil and FNE type antistatic agent for spinning treatment. The resulting pure cashmere yarn exhibits excellent physical properties and appearance quality. Test data shows that the actual yarn strength reaches 254.3 CN, higher than the design value, with a strength variation coefficient of 3.45%; the yarn evenness CV% is 8.21%, the twist deviation rate is only 0.91%, and the count deviation rate is approximately -0.36%. The yarn also meets or exceeds the expected indicators in terms of breaking elongation and detail control.

[0058] The inspection report shows that both the physical indicators and the appearance of the woven fabric meet the superior grade standard of FZ / T 71006-2020 "Cashmere Knitting Yarn", and the overall evaluation result is "excellent". The above quantifiable results reflect that the Delifang FC-620MP type yarn and yarn oil prepared using formula b in Example 1 and the preparation method in Example 2 of this invention have good permeability, lubricity, and antistatic properties during the spinning process, effectively improving the spinnability of the fiber and ensuring the overall excellent performance of the yarn's mechanical properties and appearance quality.

[0059] The above embodiments are merely illustrative of the technical concept of the present invention and should not be construed as limiting the scope of protection of the present invention. Any modifications made to the technical solutions based on the technical concept proposed in this invention shall fall within the scope of protection of this invention.

Claims

1. A water-soluble crude oil, characterized in that, The crude oil components include: polyethylene glycol laurate, sorbitol laurate, polyoxyethylene polyoxypropylene block copolymer, isothiazolinone, castor oil polyoxyethylene ether, and auxiliary agents; the auxiliary agents are selected from one or both of deionized water or softened water.

2. The water-soluble crude oil according to claim 1, characterized in that, The crude oil also includes one or more of the following: natural plant-derived flavonoids, 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and pyrethroids.

3. The water-soluble crude oil according to claim 1, characterized in that, The mass fractions of the crude oil components are: 30-35% polyethylene glycol laurate, 15-25% sorbitol laurate, 16-27% polyoxyethylene polyoxypropylene block copolymer, 0-10% isothiazolinone, 2-13% castor oil polyoxyethylene ether, and 5-20% auxiliary agents.

4. The water-soluble crude oil according to claim 1, characterized in that, The mass fractions of the components in the crude oil are: 0-8% natural plant-derived flavonoids, 0-5% 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and 0-10% pyrethroids.

5. A method for preparing water-soluble crude oil as described in any one of claims 1 to 4, characterized in that, Includes the following steps: Step 1: Add the base oil agent in the preset proportion to the reaction vessel, start stirring, and mix evenly at room temperature to form a homogeneous oil phase; Step 2: Add the functional oil while continuously stirring; then slowly heat to the specified temperature and stir at a constant temperature to ensure that the functional components react and blend fully. Step 3: Cool the material to room temperature, and slowly add the auxiliary agent while stirring at a uniform speed to fully dilute and hydrate it, ensuring that the homogeneous oil phase system is completely stable; Step 4: Take samples of the blended product for testing. After passing the test, filter the product and then fill it in the correct quantity.

6. The preparation method according to claim 5, characterized in that, The base oil includes: polyethylene glycol laurate, sorbitan laurate, polyoxyethylene polyoxypropylene block copolymer, isothiazolinone, and castor oil polyoxyethylene ether; the functional oil includes: one or more of natural plant-derived flavonoids, 3-(trimethoxysilyl)propyl dimethyl octadecylamine chloride, and pyrethroids; the auxiliary agent is deionized water or softened water.

7. The preparation method according to claim 5, characterized in that, In steps 1 to 3, the stirring time is 15 to 60 minutes and the stirring speed is 30 to 50 rpm; the mass fraction of the auxiliary agent is 5 to 20%.

8. The preparation method according to claim 5, characterized in that, In step 2, the specified temperature is 45℃.

9. The preparation method according to claim 5, characterized in that, In step 3, the conditions for the homogeneous oil phase system to be completely stable include: the system temperature is room temperature and the system pH value is 6.0~7.

0.

10. The use of a water-soluble crude oil as described in any one of claims 1 to 5 in improving the properties of textiles.