WO2023151174A1 - 一种环保型柔性导电聚氨酯及其制备方法 - Google Patents

一种环保型柔性导电聚氨酯及其制备方法 Download PDF

Info

Publication number
WO2023151174A1
WO2023151174A1 PCT/CN2022/086127 CN2022086127W WO2023151174A1 WO 2023151174 A1 WO2023151174 A1 WO 2023151174A1 CN 2022086127 W CN2022086127 W CN 2022086127W WO 2023151174 A1 WO2023151174 A1 WO 2023151174A1
Authority
WO
WIPO (PCT)
Prior art keywords
parts
component
flexible conductive
preparation
conductive polyurethane
Prior art date
Application number
PCT/CN2022/086127
Other languages
English (en)
French (fr)
Inventor
戚栋明
黄志超
田千俊
王琳
刘承海
Original Assignee
浙江理工大学绍兴柯桥研究院有限公司
浙江理工大学
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 浙江理工大学绍兴柯桥研究院有限公司, 浙江理工大学 filed Critical 浙江理工大学绍兴柯桥研究院有限公司
Priority to US17/739,176 priority Critical patent/US11987662B2/en
Publication of WO2023151174A1 publication Critical patent/WO2023151174A1/zh

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/08—Polyurethanes from polyethers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3897—Low-molecular-weight compounds having heteroatoms other than oxygen containing heteroatoms other than oxygen, halogens, nitrogen, sulfur, phosphorus or silicon
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/24—Electrically-conducting paints
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/001—Conductive additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/011—Nanostructured additives

Definitions

  • the invention relates to the field of preparation of flexible conductive materials, in particular to an environment-friendly flexible conductive polyurethane resin and a preparation method thereof.
  • Polyurethane resin is a general term for a class of polymer compounds with carbamate units on the main chain synthesized from isocyanate, polyol and small molecule chain extender.
  • Polyurethane resin can be made into polyurethane plastic, polyurethane fiber, polyurethane rubber and elastomer, polyurethane coating, polyurethane adhesive and polyurethane synthetic leather, etc. It is an ideal flexible material.
  • Polyurethane flexible conductive material is a new composite material with both conductivity and flexibility, which is widely used in wearable electronic devices, flexible sensors and electronic skin.
  • ordinary flexible conductive materials are damaged by friction, stretching, bending, and wrinkling during use, which in turn affects the conductivity and ultimately affects the normal function of the device. Therefore, introducing self-healing or self-healing functions into flexible conductive materials can improve the reliability of electrical conduction of polyurethane materials.
  • Traditional polyurethane flexible conductive materials are generally prepared by the solvent method. This method uses a large amount of toxic and harmful solvents, which not only causes environmental pollution in the production process, but also makes the end products not environmentally friendly, and even endangers the health of consumers.
  • solvent-free polyurethane with self-healing function is a method that can well solve the above problems.
  • the research hotspot of polyurethane self-healing function is intrinsic self-healing, which mainly realizes self-healing of materials by breaking and reorganizing chemical bonds.
  • Common intrinsic self-healing mechanisms include S-S bond, Diels-Alder reaction, hydrogen bond, etc.
  • the self-repair of polyurethane synthesized by disulfide bond and Diels-Alder reaction requires high temperature or strong ultraviolet light, which limits its application range.
  • Most of the technical solutions for synthesizing self-healing polyurethane in the literature require the introduction of solvents, which have low requirements for environmental protection.
  • the invention patent with the publication number CN111825872A uses a self-healing conductive film based on DA thermally reversible reaction of polyurethane loaded nano-silver wires, which has good repair performance.
  • it needs to be under high temperature conditions to achieve self-healing effect; in addition, the prepared polyurethane film needs to use organic solvents, which is not environmentally friendly; the cost of the loaded conductive silver nanowires is high and uneconomical, which seriously affects its application prospects .
  • the invention patent with the publication number CN110527120A makes a conductive self-healing polyurethane film by adding conductive fillers into the self-healing polyurethane resin.
  • a solvent needs to be added during its use, and the solvent needs to be removed at the end, which easily causes pollution problems.
  • fillers it is also difficult to control the polyurethane resin film with both excellent electrical conductivity and excellent mechanical properties, which affects its application prospects.
  • the present invention makes it dispersed in the polyurethane resin matrix to form a special continuous structure by introducing low-cost one-dimensional rod-shaped multi-walled carbon nanotubes and spherical high-conductivity carbon black, thereby achieving good electrical conductivity; Or under the condition of light, the double selenium structure that can drive the self-repairing reaction ensures the continuity of the structure of the conductive material, thereby improving the reliability of the conductivity; the present invention selects a solvent-free system for preparation to ensure the environmental protection of the preparation process and the end product; the present invention adopts The degree of microphase separation of the molecular structure of soft and hard segments can regulate the mechanical properties, hand feeling and softness of conductive polyurethane.
  • the invention provides a preparation method of environment-friendly flexible conductive polyurethane, comprising the following steps:
  • component A To prepare component A, heat one or more of polyol, diselenide glycol, and T-type chain extender to 50-130°C, then add high-conductivity carbon black and dispersant, and stir while ultrasonically , and then add a catalyst and a leveling agent to obtain a polymer containing terminal hydroxyl groups, that is, component A;
  • component B heat polyisocyanate or polyol to 50-130°C, add multi-walled carbon nanotubes and dispersant, stir while ultrasonicating, then add the remaining materials, and stir at high temperature to obtain an isocyanate-terminated prepolymer , which is component B;
  • the preparation component A in terms of parts by weight, there are 60-90 parts of polyols, 50-80 parts of diselenide glycol, 30-60 parts of T-type chain extenders, high 0.1-2 parts of conductive carbon black, 0.01-0.2 parts of dispersant, 0.1-1 part of catalyst and 0.1-1 part of leveling agent.
  • the preparation component B in the preparation component B, 100-250 parts by weight of polyisocyanate, 30-100 parts of polyol, 0.05-0.4 part of multi-walled carbon nanotube, 0-250 parts of dispersant 0.1 part.
  • the weight ratio of the component A to the component B is 1:1-1.1.
  • step S1 there is a dynamic diselenide bond in the molecular chain of diselenide, and the structure of the T-type chain extender is that there is a side chain on the molecular chain of diolamine, and the side chain is a bisamide group.
  • the polyisocyanate is one or more of isophorone diisocyanate, toluene diisocyanate, hexamethylene diisocyanate, and diphenylmethane diisocyanate
  • the polyol is polytetrahydrofuran ether diol , one or more of polyglycolide diol, polypropylene glycol, polycarbonate diol, polyethylene adipate diol, and the relative molecular mass of the polyol is 1000-2000.
  • the dispersant is one or more of N-methylpyrrolidone, sodium lauryl sulfate, and dodecylbenzenesulfonic acid
  • the catalyst is dibutyltin dilaurate or stannous octoate
  • the leveling agent is BYK-UV3510.
  • the high-conductivity carbon black is powdery and spherical, with a particle size of 20-100 nm and a specific surface area of 60-1000m2 ⁇ g -1
  • the multi-walled carbon nanotubes are rod-shaped or tubular, with a length of 0.5-40 ⁇ m, The diameter is 10-30nm.
  • the structure of the double selenide glycol is:
  • Described T type chain extender structure is:
  • An environment-friendly flexible conductive polyurethane prepared according to any one of the methods.
  • the present invention has the following advantages and beneficial effects:
  • the environment-friendly self-healing polyurethane flexible conductive film prepared by the present invention has good self-healing properties and electrical conductivity, simple repairing conditions, and good mechanical properties.
  • the conductive film prepared by the present invention is to introduce multi-walled carbon nanotubes and high-conductivity nano-carbon black into the polyurethane, and the two conductive fillers form a "go network" structure inside the polyurethane resin, and cooperate to realize conduction. Under the circumstances to achieve excellent conductive effect.
  • the polyurethane resin synthesized by the present invention uses diselenide bonds and hydrogen bonds as self-repairing, breaking and recombining chemical bonds, wherein the diselenide bonds can only be triggered under visible light conditions, and the hydrogen bonds can be triggered at room temperature.
  • the combination of the two The solution can achieve excellent self-healing effect under room temperature and light conditions, the required repair conditions are simple, and the application prospect is broad
  • the polyurethane synthesized by the present invention does not need to use a solvent, and also solves the problem of organic pollutant discharge in the production and use of solvent-based polyurethane.
  • Using multi-walled carbon nanotubes and carbon black as conductive fillers can achieve low addition, Both low cost and conductivity are effective.
  • the polyurethane synthesized by the present invention has good electrical conductivity, and the volume resistivity can reach 1.8 ⁇ 104 ⁇ cm.
  • the repair conditions are simple. It only needs to be exposed to light at room temperature for 12 hours.
  • the material is safe and reliable, and has broad application prospects.
  • Figure 1 shows the morphology and structure of SFPU before and after repair
  • Figure 2 is a schematic diagram of the formation of a conductive network inside the SFPU film.
  • component A According to parts by weight, 60-90 parts of polyol, 50-80 parts of diselenide glycol, 30-60 parts of T-type chain extender, 0.1-2 parts of high-conductivity carbon black part, 0-0.2 part of dispersant, 0.1-1 part of catalyst and 0.1-1 part of leveling agent. °C, then add high-conductivity carbon black and dispersant, stir while ultrasonic, and then add the remaining materials to obtain a polymer containing terminal hydroxyl groups, that is, component A;
  • component B in parts by weight, 100-250 parts of polyisocyanate, 30-100 parts of polyol, 0.05-0.4 part of multi-walled carbon nanotube, 0-0.1 part of dispersant, polyisocyanate Or heat the polyol to 50-130°C, add multi-walled carbon nanotubes and dispersant, stir while ultrasonicating, then add the remaining materials, stir at high temperature, and obtain an isocyanate-terminated prepolymer, which is component B;
  • each raw material is prepared according to the following ratio:
  • Component A raw materials 85 parts of polypropylene glycol, 30 parts of T-type chain extender, 80 parts of diselenium glycol, 1 part of dibutyltin dilaurate, 1 part of high conductivity carbon black, 0.1 part of dodecylbenzenesulfonic acid , 0.1 part of dibutyltin dilaurate, 0.1 part of leveling agent BYK-UV35100;
  • Component B raw materials 100 parts of isophorone diisocyanate, 75 parts of polypropylene glycol, 0.4 part of multi-walled carbon nanotubes, and 0.1 part of dodecylbenzenesulfonic acid.
  • material B to material A, react at 1500r/min for 5 minutes, put it into a mold, scrape coat it to form a film, put it in an oven at 100°C for 1 hour, and cure it to form a film to obtain an environmentally friendly flexible conductive polyurethane.
  • each raw material is prepared according to the following ratio:
  • Component A raw materials 45 parts of polytetrahydrofuran ether diol, 40 parts of polyglycolide diol,
  • T-type chain extender 60 parts of double selenium glycol, 0.1 part of dibutyltin dilaurate, 0.1 part of leveling agent BYK-UV35100, 1 part of high conductivity carbon black, 0.1 part of N-methylpyrrolidone;
  • Component B raw materials 78 parts of toluene diisocyanate, 40 parts of polytetrahydrofuran ether diol, 35 parts of polyglycolide diol, 0.3 part of multi-walled carbon nanotubes, 0.1 part of N-methylpyrrolidone;
  • material B to material A, react at 1500r/min for 10 minutes, put it into a mold, scrape coat it to form a film, put it in an oven at 100°C for 1 hour, and solidify it to form a film to obtain an environmentally friendly flexible conductive polyurethane.
  • each raw material is prepared according to the following ratio:
  • Component A raw materials 85 parts of polypropylene glycol, 45 parts of T-type chain extender, 65 parts of diselenium glycol, 0.1 part of dibutyltin dilaurate, 0.1 part of leveling agent BYK-UV35100, 2 parts of high conductivity carbon black ;
  • Component B raw materials 78 parts of toluene diisocyanate, 75 parts of polypropylene glycol, 0.2 parts of multi-walled carbon nanotubes;
  • each raw material is prepared according to the following ratio:
  • Component A raw materials 85 parts of polytetrahydrofuran ether glycol, 50 parts of T-type chain extender, 60 parts of diselenium glycol, 0.1 part of dibutyltin dilaurate, 0.1 parts of leveling agent BYK-UV35100, high conductivity carbon 2 copies of black;
  • Component B raw materials 100 parts of isophorone diisocyanate, 75 parts of polytetrahydrofuran ether glycol, 0.1 part of multi-walled carbon nanotubes;
  • Embodiment 1-4 test performance is as follows:
  • test properties of various conductive polyurethanes are shown in Table 2 (source of data).
  • Figure 1 of the description shows the optical microscope photos before and after the sample of the example was cut open with a knife and lighted at room temperature for 12 hours, and the repair effect is obvious.
  • Figure 2 is a schematic diagram of the thin film conductive network.
  • the polyurethane synthesized by the present invention has good conductivity, and the volume resistivity can reach 1.8 ⁇ 104 ⁇ cm.
  • the repair conditions are simple. It needs to be exposed to light at room temperature for 12 hours. After repairing, the performance is good, and the repairing efficiency can reach up to 90%, which can ensure the safety and reliability of conductive materials.
  • the self-healing conductive polyurethane synthesized by the present invention can achieve conductive effect and low percolation threshold under the condition of low addition amount, and the polyurethane prepared by this scheme does not need to use a solvent, is healthy and environmentally friendly, and has simple self-repairing conditions.
  • the environment-friendly self-healing polyurethane flexible conductive film prepared in the embodiment of the present invention has good self-healing properties and electrical conductivity, simple repair conditions, and good mechanical properties.
  • the conductive film is made by introducing multi-walled carbon nanotubes and high-conductivity nano-carbon black into polyurethane. , the two conductive fillers form a "go network" structure inside the polyurethane resin, synergistically achieve electrical conduction, and achieve excellent electrical conductivity with a small amount of addition; the synthesized polyurethane resin uses diselenide bonds and hydrogen bonds as self-repairing fracture recombination Chemical bonds, among which diselenide bonds can be triggered only under visible light conditions, and hydrogen bonds can be triggered under room temperature conditions.
  • the combination of the two can achieve excellent self-repair effects under room temperature and light conditions, and the required repair conditions are simple.
  • the application prospect is broad.
  • the synthesized polyurethane does not require the use of solvents, and also solves the problem of organic pollutant emission during the production and use of solvent-based polyurethane.
  • Using multi-walled carbon nanotubes and carbon black as conductive fillers can achieve the effects of low addition, low cost and conductivity.
  • the conductive polyurethane obtained by the technical solution provided by the present invention has a broader application prospect.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种环保型柔性导电聚氨酯及其制备方法，由组分A与组分B按照一定质量比通过双组分预聚物原位无溶剂共混聚合法制备而成，其中A组分由多元醇、T型扩链剂、双硒二元醇、高导炭黑、分散剂、催化剂、流平剂等组成；B组分由多异氰酸酯、多元醇、多壁碳纳米管、分散剂等组成。本发明聚氨酯具有可靠的导电功能，且损伤的导电聚氨酯材料在室温或光照条件下具有自恢复性能，可以通过调节软硬段分子的微相分离值HBI(0.5～3.0)，达到调控不同手感和不同机械性能，有机污染物排放量(VOCs)低于50mg/kg，绿色环保，具有很好的工业化应用前景。

Description

一种环保型柔性导电聚氨酯及其制备方法
相关申请的交叉引用
本公开要求在2022年02月14日提交中国专利局、申请号为202210134031.0、名称为“一种环保型柔性导电聚氨酯及其制备方法”的中国专利申请的优先权，其全部内容通过引用结合在本公开中。
技术领域
本发明涉及柔性导电材料制备领域，具体涉及的是一种环保型柔性导电聚氨酯树脂及其制备方法。
背景技术
聚氨酯树脂是以异氰酸酯、多元醇、小分子扩链剂为原料合成的主链上带有氨基甲酸酯基单元的一类高分子化合物的总称。聚氨酯树脂可制成聚氨酯塑料、聚氨酯纤维、聚氨酯橡胶及弹性体、聚氨酯涂料、聚氨酯粘合剂及聚氨酯合成革等，是一种非常理想的柔性材料。
聚氨酯柔性导电材料是一种导电性与柔性兼备的新型复合材料，广泛应用于可穿戴电子设备、柔性传感器和电子皮肤等领域。然而普通柔性导电材料在使用过程中摩擦、拉伸、弯曲、折皱作用使其产生破损，进而影响导电性能，最终影响设备正常功能。因此将自修复或者自愈合功能引入到柔性导电材料中可以提高聚氨酯材料导电的可靠性。
传统聚氨酯柔性导电材料一般采用溶剂法制备，这种方法使用大量有毒有害溶剂，不但造成生产加工过程的不环保，污染环境；而且使终端产品的不环保，甚至危及消费者身体健康。
针对上述问题，具有自修复功能的无溶剂型聚氨酯是一种能够很好解决上述问题的方法。当前，聚氨酯自修复功能研究热点是本征型自修复，主要以化学键的断裂重组来实现材料的自修复。常见的本征型自修复机理有S-S键、Diels-Alder反应、氢键等。二硫键、Diels-Alder反应合成的聚氨酯自修复需要高温或者在强紫外线的条件下才可实现，这限制了它的应用范围。文献中关于合成自修复聚氨酯的技术方案中，大多需要引入溶剂，环保性要求 低。
公开号为CN111825872A的发明专利通过基于DA热可逆反应的聚氨酯负载纳米银线的自修复型导电薄膜，修复性能良好。然而，其需要在高温条件下才能实现自修复效果；此外，制备的聚氨酯薄膜需要使用有机溶剂，不环保；负载的导电纳米银线成本高、不经济性，这些都严重影响了它的应用前景。
公开号为CN110527120A的发明专利通过在自修复聚氨酯树脂中加入导电填料制成导电自修复聚氨酯薄膜。然而，其使用过程中需要加入溶剂，最后需要除去溶剂，容易造成污染问题。加入填料，也难以调控出优良导电性与优良机械性能兼备的聚氨酯树脂薄膜，影响了其使用前景。
因此，将导电材料引入自修复聚氨酯体系中，还存在一些共性问题，通常是为了提高聚氨酯导电性，引入导电材料过多，这样必然会破坏聚氨酯原有的机械性能和修复性能，或者是利用成本很高的纳米银线、纳米银针等造成的不经济性。
发明内容
基于以上问题，本发明通过引入低成本的一维棒状多壁碳纳米管和球状高导炭黑，使其分散在聚氨酯树脂基体中形成特殊的连续结构，从而达到良好的导电性能；通过引入常温或者光照条件下就能驱动自修复反应的双硒结构保证导电材料结构的连续性，从而提高导电性能的可靠性；本发明选用无溶剂体系制备保证制备过程和终端产品的环保性；本发明采用软硬段分子结构微相分离程度可调控导电聚氨酯的机械性能、手感、柔软度等。
本发明提供了一种环保型柔性导电聚氨酯的制备方法，包括以下步骤：
S1、制备组分A，将多元醇、双硒二元醇、T型扩链剂中的一种或多种加热到50～130℃，再加入高导炭黑和分散剂，边超声边搅拌，再加入催化剂和流平剂，得到含端羟基聚合物，即组分A；
S2、制备组分B，将多异氰酸酯或多元醇加热到50～130℃，加入多壁碳纳米管和分散剂，边超声边搅拌，再加入剩余物料，高温搅拌，得到端异氰酸酯基预聚体，即为组分B；
S3、制备环保型柔性导电聚氨酯，将制备的组分A和组分B按照一定重 量比加入到反应釜中，以1500～2000r/min速率高速搅拌混合4～10min，然后在100℃～120℃熟化1～2h，得到环保型柔性导电聚氨酯。
优选的，所述步骤S1中，所述制备组分A中按照重量份数计，多元醇60～90份、双硒二元醇50～80份、T型扩链剂30～60份、高导炭黑0.1～2份、分散剂0.01～0.2份、催化剂0.1～1份和流平剂0.1～1份。
优选的，所述步骤S2中，所述制备组分B中按照重量份数计，多异氰酸酯100～250份、多元醇30～100份、多壁碳纳米管0.05～0.4份、分散剂0～0.1份。
优选的，所述步骤S3中，所述组分A和组分B重量比为1：1～1.1。
优选的，所述步骤S1中，双硒二元醇分子链中带动态二硒键，所述T型扩链剂结构为二元醇胺分子链上带一个侧链，侧链上为双酰胺基团。
优选的，所述多异氰酸酯为异佛尔酮二异氰酸酯、甲苯二异氰酸酯、六亚甲基二异氰酸酯、二苯基甲烷二异氰酸酯中的一种或者多种，所述多元醇为聚四氢呋喃醚二醇、聚乙内酯二醇、聚丙二醇、聚碳酸酯二醇、聚己二酸乙二醇酯二醇中的一种或多种，多元醇的相对分子质量为1000～2000。
优选的，所述分散剂为N-甲基吡咯烷酮、十二烷基硫酸钠、十二烷基苯磺酸中的一种或者多种，所述催化剂为二月桂酸二丁基锡或辛酸亚锡；流平剂为流平剂BYK-UV3510。
优选的，所述高导炭黑为粉状球形，粒径为20～100nm，比表面积60～1000㎡·g -1，所述多壁碳纳米管为棒状或管状，长度为0.5-40μm，直径为10-30nm。
优选的，所述双硒二元醇结构为：
Figure PCTCN2022086127-appb-000001
所述T型扩链剂结构为：
Figure PCTCN2022086127-appb-000002
一种环保型柔性导电聚氨酯，根据任一项所述的方法制备得到。
本发明相对于现有技术，具有如下的优点及有益效果：
1、本发明制备的环保型自修复聚氨酯柔性导电薄膜，具有良好自修复性和导电性，修复条件简单，机械性能良好。
2、本发明制备的导电薄膜是在聚氨酯中引入多壁碳纳米管和高导纳米炭黑，两种导电填料在聚氨酯树脂内部形成“围棋网络”状结构，协同实现导电，在加入量少的情况下实现优良的导电效果。
3、本发明合成的聚氨酯树脂以二硒键和氢键为自修复断裂重组化学键，其中二硒键只需要在可见光条件下就可以触发，氢键在室温条件下就可以触发，两者组合的方案在室温光照条件下可以实现优秀的自修复效果，所需修复条件简单，应用前景广泛
4、本发明所合成的聚氨酯，无需使用溶剂，也解决了溶剂型聚氨酯生产和使用过程中有机污染物排放问题，采用多壁碳纳米管和炭黑做为导电填料，可以实现低添加量、低成本和导电性兼备效果。
5、本发明合成的聚氨酯导电性好，体积电阻率可到1.8×104Ω·cm，修复条件简单，只需要在室温光照下12h，修复后性能好，修复效率最高可达90％，可以保证导电材料的安全可靠，广阔的应用前景。
上述说明仅是本公开技术方案的概述，为了能够更清楚了解本公开的技术手段，而可依照说明书的内容予以实施，并且为了让本公开的上述和其它目的、特征和优点能够更明显易懂，以下特举本公开的具体实施方式。
附图说明
为了更清楚地说明本公开实施例或相关技术中的技术方案，下面将对实施例或相关技术描述中所需要使用的附图作一简单地介绍，显而易见地，下面描述中的附图是本公开的一些实施例，对于本领域普通技术人员来讲，在不付出创造性劳动的前提下，还可以根据这些附图获得其他的附图。
图1为SFPU修复前后形貌结构；
图2为SFPU薄膜内部形成导电网络示意图。
具体实施例
需要说明的是，在不冲突的情况下，本发明中的实施例及实施例中的特 征可以相互组合。
下面将结合本发明的实施例中的附图，对本发明的实施例中的技术方案进行清楚、完整地描述，显然，所描述的实施例仅仅是本发明一部分实施例，而不是全部的实施例。基于本发明中的实施例，本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例，都属于本发明保护的范围。
具体实施方式步骤为：
(1)组分A的制备：按照重量份数计，将多元醇60～90份、双硒二元醇50～80份、T型扩链剂30～60份、高导炭黑0.1～2份、分散剂0～0.2份、催化剂0.1～1份和流平剂0.1～1份，将多元醇、双硒二元醇、T型扩链剂中的一种或多种加热到50～130℃，再加入高导炭黑和分散剂，边超声边搅拌，再加入剩余物料，得到含端羟基聚合物，即组分A；
(2)组分B的制备：按照重量份数计，将多异氰酸酯100～250份、多元醇30～100份、多壁碳纳米管0.05～0.4份、分散剂0～0.1份，将多异氰酸酯或多元醇加热到50～130℃，加入多壁碳纳米管和分散剂，边超声边搅拌，再加入剩余物料，高温搅拌，得到端异氰酸酯基预聚体，即为组分B；
(3)将制备的组分A和组分B按照1：1～1.1的重量比加入到反应釜中，以1500～2000r/min速率高速搅拌混合4～10min，然后在100℃～120℃熟化1～2h，得到环保型柔性导电聚氨酯。
实施例1
一种环保型柔性导电聚氨酯，按照以下配比准备各原料：
组分A原料：聚丙二醇85份，T型扩链剂30份，双硒二元醇80份，二月桂酸二丁基锡1份，高导炭黑1份，十二烷基苯磺酸0.1份，二月桂酸二丁基锡0.1份，流平剂BYK-UV35100.1份；
组分B原料：异佛尔酮二异氰酸酯100份、聚丙二醇75份、多壁碳纳米管0.4份、十二烷基苯磺酸0.1份。
然后，采用上述的方法，将100份异佛尔酮二异氰酸酯加热到80℃，加入0.4份多壁碳纳米管和0.1份十二烷基苯磺酸，高温条件下搅拌超声1h，降温后与75份聚丙二醇混合，高速搅拌20分钟制得B料。将85份聚丙二醇加热到90℃，加入1份高导炭黑和0.1份十二烷基苯磺酸，高温条件下搅拌超声1h，逐步加入30份T型扩链剂、80份双硒二元醇、0.1份二月桂酸二丁基 锡、0.1份流平剂BYK-UV3510，搅拌10分钟，制得组分A。
然后，将B料加入到A料中，在1500r/min反应5分钟，到入模具中，刮涂成膜，放入100℃烘箱中1h，固化成膜，即得到环保型柔性导电聚氨酯。
实施例2
一种环保型柔性导电聚氨酯，按照以下配比准备各原料：
组分A原料：聚四氢呋喃醚二醇45份，聚乙内酯二醇40份，
T型扩链剂40份，双硒二元醇60份，二月桂酸二丁基锡0.1份，流平剂BYK-UV35100.1份，高导炭黑1份，N-甲基吡咯烷酮0.1份；
组分B原料：甲苯二异氰酸酯78份，聚四氢呋喃醚二醇40份，聚乙内酯二醇35份，多壁碳纳米管0.3份，N-甲基吡咯烷酮0.1份；
将78份甲苯二异氰酸酯加热到100℃，加入0.3份多壁碳纳米管和0.1份N-甲基吡咯烷酮，高温条件下搅拌超声40分钟，降温后，与40份聚四氢呋喃醚二醇、35份聚乙内酯二醇混合，高速搅拌20分钟制得B料。将40份T型扩链剂加热到60℃,加入1份高导炭黑和0.1份N-甲基吡咯烷酮，在高温条件下超声搅拌1小时，降温冷却。将在45份聚四氢呋喃醚二醇与40份聚乙内酯二醇中逐步加入已处理的T型扩链剂、60份双硒二元醇、1份二月桂酸二丁基锡、0.1份流平剂，高速搅拌20分钟制得A料。
然后，将B料加入到A料中，在1500r/min反应10分钟，到入模具中，刮涂成膜，放入100℃烘箱中1h，固化成膜，即得到环保型柔性导电聚氨酯。
如附图1所示样品用刀割开，在室温光照12h修复前后光学显微镜照片，修复效果明显。
实施例3
一种环保型柔性导电聚氨酯，按照以下配比准备各原料：
组分A原料：聚丙二醇85份，T型扩链剂45份，双硒二元醇65份，二月桂酸二丁基锡0.1份，流平剂BYK-UV35100.1份，高导炭黑2份；
组分B原料：甲苯二异氰酸酯78份，聚丙二醇75份，多壁碳纳米管0.2份；
将78份甲苯二异氰酸酯加热到80℃，加入0.2份多壁碳纳米管，在高温条件下搅拌超声1.5小时，降温后再与75份聚丙二醇混合，高速搅拌20分钟制得B料。将在85份聚丙二醇加热到120℃，加入2份高导炭黑，高温条件 下超声搅拌1小时，降温后逐步加入45份T型扩链剂、65份双硒二元醇、0.1份二月桂酸二丁基锡、0.1份流平剂，制得A料。
将B料加入到A料中，在2000r/min搅拌反应5分钟，到入模具中，刮涂成膜，放入100℃烘箱中1.5h，固化成膜，即得到环保型柔性导电聚氨酯。
实施例4
一种环保型柔性导电聚氨酯，按照以下配比准备各原料：
组分A原料：聚四氢呋喃醚二醇85份，T型扩链剂50份，双硒二元醇60份，二月桂酸二丁基锡0.1份，流平剂BYK-UV35100.1份，高导炭黑2份；
组分B原料：异佛尔酮二异氰酸酯100份，聚四氢呋喃醚二醇75份，多壁碳纳米管0.1份；
将100份异佛尔酮二异氰酸酯加热到60℃，加入0.1份多壁碳纳米管，高温条件下超声搅拌30分钟，降温后与75份聚四氢呋喃醚二醇混合，高速搅拌15分钟制得B料。将85份聚四氢呋喃醚二醇加热到100℃，加入2份高导炭黑，高温条件下超声搅拌1小时，降温后再逐步加入50份T型扩链剂、60份双硒二元醇、0.1份二月桂酸二丁基锡、0.1份流平剂BYK-UV3510，制得A料。
将B料加入到A料中，在2000r/min搅拌反应8分钟，到入模具中，刮涂成膜，放入120℃烘箱中1h，固化成膜，即得到环保型柔性导电聚氨酯。
实施例1-4测试性能如下：
表1：
Figure PCTCN2022086127-appb-000003
由表1可以得到根据国标测试的多种性能数据。
对比例：
目前存在多种导电聚氨酯的测试性能见表2(数据出处)。
表2：
Figure PCTCN2022086127-appb-000004
[1]CN111825872A一种具有导电性的、热可逆性的自修复透明聚氨酯复合材料及其制备方法
[2]Xu Y,Yang Y,Yan D X,et al.Flexible and conductive polyurethane composites for electromagnetic shielding and printable circuit[J].Chemical Engineering Journal,2019,360:1427-1436.
[3]Al-Attabi N Y,Adhikari R,Cass P,et al.Silver nanowire as an efficient filler for high conductive polyurethane composites[J].Materials Science and Technology,2019,35(4):462-468.
[4]Andreoli E,Liao K S,Cricini A,et al.Carbon black instead of multiwall carbon nanotubes for achieving comparable high electrical conductivities in polyurethane-based coatings[J].Thin Solid Films,2014,550:558-563.
说明书附图1为实施例样品用刀割开，在室温光照12h修复前后光学显微镜照片，修复效果明显。图2为薄膜导电网络示意图。
通过将本发明制备的环保型柔性导电聚氨酯与目前采用其他方案制备的柔性导电聚氨酯进行性能对比可知本发明合成的聚氨酯导电性好，体积电阻率可到1.8×104Ω·cm，修复条件简单，只需要在室温光照下12h，修复后性能好，修复效率最高可达90％，可以保证导电材料的安全可靠。
本发明合成的自修复导电聚氨酯在低添加量的情况下即可实现导电效果，实现低渗流阈值，并且本方案制备的聚氨酯无需使用溶剂，健康环保，自修复条件简单。
本发明实施例制备的环保型自修复聚氨酯柔性导电薄膜，具有良好自修复性和导电性，修复条件简单，机械性能良好，导电薄膜是在聚氨酯中引入多壁碳纳米管和高导纳米炭黑，两种导电填料在聚氨酯树脂内部形成“围棋 网络”状结构，协同实现导电，在加入量少的情况下实现优良的导电效果；合成的聚氨酯树脂以二硒键和氢键为自修复断裂重组化学键，其中二硒键只需要在可见光条件下就可以触发，氢键在室温条件下就可以触发，两者组合的方案在室温光照条件下可以实现优秀的自修复效果，所需修复条件简单，应用前景广泛。同时，所合成的聚氨酯，无需使用溶剂，也解决了溶剂型聚氨酯生产和使用过程中有机污染物排放问题。采用多壁碳纳米管和炭黑做为导电填料，可以实现低添加量、低成本和导电性兼备效果。
综合评价来看，本发明提供的技术方案得到的导电聚氨酯具有更加广阔的应用前景。
最后应说明的是：以上所述仅为本发明的优选实施例而已，并不用于限制本发明，尽管参照前述实施例对本发明进行了详细的说明，对于本领域的技术人员来说，其依然可以对前述各实施例所记载的技术方案进行修改，或者对其中部分技术特征进行等同替换，凡在本发明的精神和原则之内，所作的任何修改、等同替换、改进等，均应包含在本发明的保护范围之内。

Claims (10)

  1. 一种环保型柔性导电聚氨酯的制备方法，其特征在于，包括以下步骤：
    S1、制备组分A，将多元醇、双硒二元醇、T型扩链剂中的一种或多种加热到50～130℃，再加入高导炭黑和分散剂，边超声边搅拌，再加入催化剂和流平剂，得到含端羟基聚合物，即组分A；
    S2、制备组分B，将多异氰酸酯或多元醇加热到50～130℃，加入多壁碳纳米管和分散剂，边超声边搅拌，再加入剩余物料，高温搅拌，得到端异氰酸酯基预聚体，即为组分B；
    S3、制备环保型柔性导电聚氨酯，将制备的组分A和组分B按照一定重量比加入到反应釜中，以1500～2000r/min速率高速搅拌混合4～10min，然后在100℃～120℃熟化1～2h，得到环保型柔性导电聚氨酯。
  2. 根据权利要求1所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于，所述步骤S1中，所述制备组分A中按照重量份数计，多元醇60～90份、双硒二元醇50～80份、T型扩链剂30～60份、高导炭黑0.1～2份、分散剂0.01～0.2份、催化剂0.1～1份和流平剂0.1～1份。
  3. 根据权利要求2所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述步骤S2中，所述制备组分B中按照重量份数计，多异氰酸酯100～250份、多元醇30～100份、多壁碳纳米管0.05～0.4份、分散剂0～0.1份。
  4. 根据权利要求1-3任一项所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述步骤S3中，所述组分A和组分B重量比为1：1～1.1。
  5. 根据权利要求4所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述步骤S1中，双硒二元醇分子链中带动态二硒键，所述T型扩链剂结构为二元醇胺分子链上带一个侧链，侧链上为双酰胺基团。
  6. 根据权利要求4所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述多异氰酸酯为异佛尔酮二异氰酸酯、甲苯二异氰酸酯、六亚甲 基二异氰酸酯、二苯基甲烷二异氰酸酯中的一种或者多种，所述多元醇为聚四氢呋喃醚二醇、聚乙内酯二醇、聚丙二醇、聚碳酸酯二醇、聚己二酸乙二醇酯二醇中的一种或多种，多元醇的相对分子质量为1000～2000。
  7. 根据权利要求5所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述分散剂为N-甲基吡咯烷酮、十二烷基硫酸钠、十二烷基苯磺酸中的一种或者多种，所述催化剂为二月桂酸二丁基锡或辛酸亚锡；所述流平剂为流平剂BYK-UV3510。
  8. 根据权利要求5-7任一项所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于，所述高导炭黑为粉状球形，粒径为20～100nm，比表面积60～1000㎡·g -1，所述多壁碳纳米管为棒状或管状，长度为0.5-40μm，直径为10-30nm。
  9. 根据权利要求5-7任一项所述的一种环保型柔性导电聚氨酯的制备方法，其特征在于：所述双硒二元醇结构为：
    Figure PCTCN2022086127-appb-100001
    所述T型扩链剂结构为：
    Figure PCTCN2022086127-appb-100002
  10. 一种环保型柔性导电聚氨酯，其特征在于：根据权利要求1-9任一项所述的方法制备得到。
PCT/CN2022/086127 2022-02-14 2022-04-11 一种环保型柔性导电聚氨酯及其制备方法 WO2023151174A1 (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US17/739,176 US11987662B2 (en) 2022-02-14 2022-05-09 Environmentally-friendly flexible conductive polyurethane (PU) and preparation method thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN202210134031.0 2022-02-14
CN202210134031.0A CN115286991A (zh) 2022-02-14 2022-02-14 一种环保型柔性导电聚氨酯及其制备方法

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/739,176 Continuation US11987662B2 (en) 2022-02-14 2022-05-09 Environmentally-friendly flexible conductive polyurethane (PU) and preparation method thereof

Publications (1)

Publication Number Publication Date
WO2023151174A1 true WO2023151174A1 (zh) 2023-08-17

Family

ID=83820978

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2022/086127 WO2023151174A1 (zh) 2022-02-14 2022-04-11 一种环保型柔性导电聚氨酯及其制备方法

Country Status (2)

Country Link
CN (1) CN115286991A (zh)
WO (1) WO2023151174A1 (zh)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102186927A (zh) * 2008-08-20 2011-09-14 拜尔材料科学股份公司 抗静电或导电聚氨酯，及其制备方法
CN109354877A (zh) * 2018-10-29 2019-02-19 西南大学 一种具有模量不匹配区域的柔性应变响应材料及其制备方法
CN110527120A (zh) * 2019-10-09 2019-12-03 南昌航空大学 一种高强度的柔性导电自修复薄膜的制作方法
CN111205631A (zh) * 2020-02-28 2020-05-29 青岛科技大学 一种通电加热自修复聚氨酯弹性体及其制备方法
CN113651938A (zh) * 2021-07-11 2021-11-16 浙江理工大学 一种无溶剂型自修复功能的聚氨酯及其制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102186927A (zh) * 2008-08-20 2011-09-14 拜尔材料科学股份公司 抗静电或导电聚氨酯，及其制备方法
CN109354877A (zh) * 2018-10-29 2019-02-19 西南大学 一种具有模量不匹配区域的柔性应变响应材料及其制备方法
CN110527120A (zh) * 2019-10-09 2019-12-03 南昌航空大学 一种高强度的柔性导电自修复薄膜的制作方法
CN111205631A (zh) * 2020-02-28 2020-05-29 青岛科技大学 一种通电加热自修复聚氨酯弹性体及其制备方法
CN113651938A (zh) * 2021-07-11 2021-11-16 浙江理工大学 一种无溶剂型自修复功能的聚氨酯及其制备方法

Also Published As

Publication number Publication date
CN115286991A (zh) 2022-11-04

Similar Documents

Publication Publication Date Title
Li et al. Biomimetic, recyclable, highly stretchable and self-healing conductors enabled by dual reversible bonds
Shokry et al. Synthesis and characterization of polyurethane based on hydroxyl terminated polybutadiene and reinforced by carbon nanotubes
WO2017194034A1 (zh) 三组分耐低温聚酯型聚氨酯弹性体及其制备方法
Qi et al. Bio-based, robust, shape memory, self-healing and recyclable elastomers based on a semi-interpenetrating dynamic network
WO2022041614A1 (zh) 一种微孔可修复tpu薄膜材料及其制备方法
CN109898342B (zh) 一种基于高回弹水性聚氨酯的耐刮擦合成革制备方法
CN105153394A (zh) 耐热性高阻尼聚氨酯弹性体及其制备方法
CN110885550B (zh) 一种有机硅改性热塑性聚氨酯弹性体及其制备方法
CN109181278B (zh) 聚氨酯/氟硅橡胶热塑性弹性体及其制备方法
Lv et al. Robust, healable and hydrophobically recoverable polydimethylsiloxane based supramolecular material with dual-activate hard segment
CN111393651A (zh) 一种自修复聚硅氧烷弹性体及其制备方法和应用
CN112646355A (zh) 一种高强耐磨的热塑性聚氨酯弹性体及其制备方法
WO2023151174A1 (zh) 一种环保型柔性导电聚氨酯及其制备方法
Wu et al. Preparation and characterization of thermoplastic starch mixed with waterborne polyurethane
Zhang et al. Polyurethane-polysiloxane copolymer compatibilized SiR/TPU TPV with comfortable human touch toward wearable devices
CN108440738B (zh) 一种高弹抗菌性聚氨酯及其制备方法和应用
JP4938513B2 (ja) ポリウレタン系エラストマー樹脂組成物およびその製造法
Yang et al. Carbon nanotubes grafted by polyurethane chains with dopamine-mediation to enhance the mechanical and damping properties of polyurethane elastomer
CN107488334B (zh) 一种复合热塑性弹性体及其制备方法
Gao et al. A stretch hardening self-assembly strategy inspired by natural rubber for degradable, recyclable and self-repairing polyurethane elastomers
US11987662B2 (en) Environmentally-friendly flexible conductive polyurethane (PU) and preparation method thereof
Zheng et al. Bioinspired Integrated Auxetic Elastomers Constructed by a Dual Dynamic Interfacial Healing Strategy
CN109265977A (zh) 一种运动场地面层材料及制备工艺
CN112239541A (zh) 一种具有高介电常数低模量高击穿场强的介电弹性体材料及其制备方法
CN110564134A (zh) 一种聚氨酯基复合丁腈橡胶介电弹性体的制备方法

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 22925535

Country of ref document: EP

Kind code of ref document: A1