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CN106753192B - A kind of polysulfide sealant with room temperature self-healing and high elongation - Google Patents

A kind of polysulfide sealant with room temperature self-healing and high elongation Download PDF

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CN106753192B
CN106753192B CN201710027383.5A CN201710027383A CN106753192B CN 106753192 B CN106753192 B CN 106753192B CN 201710027383 A CN201710027383 A CN 201710027383A CN 106753192 B CN106753192 B CN 106753192B
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CN106753192A (en
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全一武
高文通
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Nanjing University
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J181/00Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur, with or without nitrogen, oxygen, or carbon only; Adhesives based on polysulfones; Adhesives based on derivatives of such polymers
    • C09J181/04Polysulfides
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/14Polysulfides
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/08Macromolecular additives
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

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Abstract

一种具有室温自修复性、高伸长率的聚硫密封胶,组成为100重量份端巯基液体聚硫橡胶,数均分子量2500~7000,5~15重量份环氧树脂,2~8重量份芳香族环氧缩水甘油醚改性的液体聚硫齐聚物,0.05~5重量份2,4,6‑三(二甲氨基甲基)苯酚;固化条件:混合均匀,室温固化14天或50℃固化2天或75℃固化1天;聚硫密封胶固化后拉伸强度为0.5~1MPa,拉断伸长率为350~800%;断开的密封胶在室温下相互接触,自修复12~72小时,拉伸强度为0.45~0.95MPa,拉断伸长率为320~720%,密封胶具有室温自修复性及室温重加工回收性能。

Figure 201710027383

A polysulfide sealant with room temperature self-healing properties and high elongation, comprising 100 parts by weight of terminal mercapto group liquid polysulfide rubber, number average molecular weight of 2500-7000, 5-15 parts by weight of epoxy resin, 2-8 parts by weight Parts of aromatic epoxy glycidyl ether-modified liquid polysulfide oligomer, 0.05 to 5 parts by weight of 2,4,6-tris(dimethylaminomethyl)phenol; curing conditions: mix well, cure at room temperature for 14 days or Cured at 50℃ for 2 days or 75℃ for 1 day; the tensile strength of the polysulfide sealant after curing is 0.5-1MPa, and the elongation at break is 350-800%; the broken sealant is in contact with each other at room temperature and self-healing For 12 to 72 hours, the tensile strength is 0.45 to 0.95 MPa, and the elongation at break is 320 to 720%. The sealant has room temperature self-healing properties and room temperature reprocessing and recycling properties.

Figure 201710027383

Description

Polysulfide sealant with room-temperature self-repairability and high elongation
Technical Field
The invention relates to a polysulfide sealant with room temperature self-repairability and high elongation, belonging to the technical field of sealants.
Background
The sealant prepared by taking polysulfide rubber as a main base material has good elasticity, water resistance, oxidation resistance, ultraviolet radiation resistance, chemical corrosion resistance and other properties, and is widely applied to the aspects of sealing buildings, oil tanks and the like. The polysulfide sealant material inevitably generates microcracks and local damage inside and outside the polysulfide sealant material due to the influence of external environment and mechanical fatigue in the long-term use process, the tiny defects are difficult to detect and repair, stress concentration points are easy to form, the overall mechanical property is reduced, and the service life is shortened. Therefore, the polysulfide sealant with self-repairing performance is developed, the maintenance and rework operation can be simplified, the material use is prolonged, and the resources are saved. The literature (Macromolecules, 2011, 44 (8): 2536-2541) reports that epoxy-terminated polysulfide resin is reacted with pentaerythritol tetra-3-mercaptopropionate to prepare a polymer with self-repairing properties, the tensile strength and the elongation at break of which are respectively 0.5MPa and 70 percent; the disconnected samples are mutually contacted at the temperature of 60 ℃ and are self-repaired for 30-60 minutes, the tensile strength is 0.35-0.45 MPa, and the elongation at break of the material is 45-65%. The literature (Chemistry of Materials, 2014, 26 (6): 2038-; the disconnected sample is repaired at room temperature for 12-24 hours under the catalysis of tri-n-butylphosphine, the tensile strength is 0.16-0.21 MPa, and the elongation at break is 66-100%. However, the elongation at break of the self-repairing polysulfide polymer material prepared by the method is less than 120 percent and is lower than that of the general polysulfide sealant, so the self-repairing polysulfide polymer material is not suitable to be used as the sealant.
Disclosure of Invention
The invention relates to a polysulfide sealant with room temperature self-repairability and high elongation.
The invention comprises the following components: 100 parts by weight of thiol-terminated liquid polysulfide rubber with a number average molecular weight of 2500-7000; 5-15 parts by weight of epoxy resin, wherein the epoxy resin is one or a mixture of aromatic or alicyclic epoxy resin; 2-8 parts by weight of an aromatic epoxy glycidyl ether modified liquid polysulfide oligomer; 0.05-5 parts by weight of 2, 4, 6-tris (dimethylaminomethyl) phenol (DMP-30) accelerator. Curing conditions are as follows: mixing, and curing at room temperature for 14 days, or at 50 deg.C for 2 days, or at 75 deg.C for 1 day. The sealant has the main properties: the tensile strength is 0.5-1 MPa, and the elongation at break is 350-800%; the disconnected sealants are contacted with each other at room temperature for 12-72 hours, and self-repairing of material performance can be realized, wherein the tensile strength is 0.45-0.95 MPa, the elongation at break is 320-720%, and the self-repairing rate reaches 80-97% (the self-repairing rate refers to the ratio of the tensile strength or the elongation at break after repairing to the tensile strength or the elongation at break of the material before cutting).
Wherein the liquid polysulfide oligomer modified by aromatic epoxy glycidyl ether is synthesized as follows: 100 parts by weight of terminal mercapto group liquid polysulfide rubber, 1000-5000 parts by weight of number average molecular weight, adding 5-20 parts by weight of aromatic epoxy glycidyl ether, uniformly stirring, reacting at 60-80 ℃ for more than 24 hours under the protection of nitrogen, monitoring reactant 2250cm by infrared spectroscopy-1When the content of the sulfydryl is reduced to be less than 0.5 percent or the strength of the sulfydryl absorption peak is not changed any more, stopping heating, and cooling to obtain the liquid polysulfide oligomer modified by the aromatic epoxy glycidyl ether. The aromatic glycidyl ether is preferably one or a mixture of several of the following compounds.
Figure GDA0002328360590000021
The room temperature self-repairability principle and the advantages of the polysulfide sealant of the invention are as follows: (1) the room temperature self-repairability of the polysulfide sealant is realized by adding the aromatic epoxy glycidyl ether modified liquid polysulfide oligomer. The main chain of the modified liquid polysulfide oligomer is polysulfide resin which is the same as the main material of the sealant; the end capping agent is aromatic epoxy glycidyl ether and is well compatible with curing agent epoxy resin. After the modified liquid polysulfide oligomer is added, the modified liquid polysulfide oligomer is easy to diffuse in a polysulfide sealant crosslinking network, so that the creep property of a sealant system chain segment is enhanced, the contact exchange probability of disulfide bonds between chain segments of a material section is improved, the formation of a new chain segment of the polysulfide network is facilitated, new crosslinking points are added, the room temperature self-repairability is improved, and the self-repairing rate reaches 80-97%. (2) The tensile elongation of the polysulfide sealant is 350-800%, and compared with the reported polysulfide polymer with self-repairing property, the polysulfide sealant has higher tensile elongation; the tensile elongation of the sealant can be regulated and controlled by changing the addition amount of the liquid polysulfide oligomer, and the application requirements of different occasions are met. (3) The polysulfide sealant of the invention also has room temperature processability: and (3) small fragments of the sealant with the diameter of less than 0.5cm can be remolded into a film at the die pressing temperature of 5-10 MPa for 12-72 hours, so that the reprocessing and recycling of the material are realized. (4) The polysulfide sealant has the advantages of easily obtained raw materials, simple synthesis and mild reaction conditions, and has good application prospect in the preparation of self-repairing materials and recycled materials.
Drawings
FIG. 1 is a schematic view showing that the incision on the surface of the polysulfide sealant of the present invention is placed at room temperature, and the incision gradually disappears and heals.
The polysulfide sealant broken in the attached figure 2 is contacted with each other at room temperature for 48 hours to self-repair, and then is stretched and deformed.
FIG. 3 shows that the small fragment polysulfide sealant forms a film at the die pressure of 5MPa and the room temperature for 36 hours, and the reprocessing and recovery are realized.
DETAILED DESCRIPTION OF EMBODIMENT (S) OF INVENTION
Example 1
Preparing a polysulfide sealant: 100 parts of end mercapto liquid polysulfide rubber, 4000 parts of number average molecular weight, 8.5 parts of bisphenol F type epoxy resin, 5 parts of benzyl epoxy glycidyl ether modified liquid polysulfide oligomer and 1 part of DMP-30 accelerator. Curing conditions are as follows: curing at 75 ℃ for 1 day.
Synthesizing a liquid polysulfide oligomer modified by benzyl epoxy glycidyl ether: 100 parts by weight of terminal mercapto group liquid polysulfide rubber, the number average molecular weight is 4000, 8.2 parts by weight of benzyl epoxy glycidyl ether is added, the mixture is uniformly stirred, the mixture reacts for 36 hours at 70 ℃ under the protection of nitrogen, and the reactant is monitored by an infrared spectroscopy at 2250cm-1And (4) reducing the content of sulfydryl to be less than 0.5%, and cooling to obtain the liquid polysulfide oligomer modified by the benzyl epoxy glycidyl ether.
The mechanical properties of the sample are as follows: tensile strength of 0.65MPa and elongation at break of 498%. Self-repairing performance: the cut samples are contacted with each other at room temperature for 24 hours, and after self-repairing, the tensile strength of the cut samples is 0.63MPa (the self-repairing rate is 96.9 percent), and the tensile elongation is 461 percent (the self-repairing rate is 92.6 percent).
Example 2
Preparing a polysulfide sealant: 100 parts of mercapto-terminated liquid polysulfide rubber, 4000 parts of number average molecular weight, 7.3 parts of bisphenol A type epoxy resin, 2 parts of cyclohexane-1, 2-dicarboxylic acid diglycidyl ester, 6 parts of phenyl epoxy glycidyl ether modified liquid polysulfide oligomer and 1.5 parts of DMP-30 accelerator. Curing conditions are as follows: curing at 50 ℃ for 2 days.
Synthesizing a liquid polysulfide oligomer modified by phenyl epoxy glycidyl ether: 100 parts by weight of end-mercapto liquid polysulfide rubber, the number average molecular weight is 1000, 16.4 parts by weight of phenyl epoxy glycidyl ether is added, the mixture is uniformly stirred, the mixture reacts for 24 hours at 80 ℃ under the protection of nitrogen, the absorption peak intensity of the mercapto group of the reactant is monitored by infrared spectroscopy to be not changed any more, and the liquid polysulfide oligomer modified by the phenyl epoxy glycidyl ether is obtained by cooling.
The mechanical properties of the sample are as follows: tensile strength of 0.51MPa and elongation at break of 747 percent. Self-repairing performance: the cut samples are contacted with each other at room temperature for 48 hours, and after self-repairing, the tensile strength of the cut samples is 0.49MPa (the self-repairing rate is 96.1 percent), and the elongation at break is 668 percent (the self-repairing rate is 89.4 percent).
Example 3
Preparing a polysulfide sealant: 50 parts of end-mercapto liquid polysulfide rubber, 2500 parts of number average molecular weight, 50 parts of end-mercapto liquid polysulfide rubber, 4000 parts of number average molecular weight, 5 parts of bisphenol A type epoxy resin, 6 parts of bisphenol F type epoxy resin, 3 parts of o-tolyl epoxy glycidyl ether modified liquid polysulfide oligomer and 2 parts of DMP-30 accelerator. Curing conditions are as follows: curing at room temperature for 14 days.
Synthesizing o-tolyl epoxy glycidyl ether modified liquid polysulfide oligomer: 100 parts by weight of end-mercapto liquid polysulfide rubber, the number average molecular weight of which is 4000, 7.5 parts by weight of o-tolyl epoxy glycidyl ether is added, the mixture is uniformly stirred at room temperature and reacts for 48 hours at 60 ℃ under the protection of nitrogen, and the reactant is monitored by an infrared spectroscopy at 2250cm-1Reducing the content of sulfydryl to below 0.5 percent, and cooling to obtain the o-tolyl epoxy glycidyl ether modified liquid polysulfide oligomer.
The mechanical properties of the sample are as follows: tensile strength of 0.71MPa and elongation at break of 437%. Self-repairing performance: the cut samples are contacted with each other at room temperature for 72 hours, and after self-repairing, the tensile strength of the cut samples is 0.64MPa (the self-repairing rate is 90.1 percent), and the tensile elongation is 364 percent (the self-repairing rate is 83.2 percent).

Claims (1)

1. A polysulfide sealant with room temperature self-repairability and high elongation comprises the following components: 100 parts by weight of thiol-terminated liquid polysulfide rubber, 2500-7000 parts by number average molecular weight, 5-15 parts by weight of epoxy resin, 0.05-5 parts by weight of 2, 4, 6-tris (dimethylaminomethyl) phenol, and is characterized by also comprising 2-8 parts by weight of aromatic epoxy glycidyl ether modified liquid polysulfide oligomer; curing conditions are as follows: mixing, and curing at room temperature for 14 days, or at 50 deg.C for 2 days, or at 75 deg.C for 1 day.
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CN108690178B (en) * 2018-05-30 2020-10-16 南京大学 Preparation method of polysulfide polyurea with self-repairing function
CN109081919A (en) * 2018-07-13 2018-12-25 安徽工业大学 A method of addition reaction is clicked based on sulfydryl-alkene and prepares self-repair material
CN109180938A (en) * 2018-08-31 2019-01-11 王雪峰 A kind of preparation method of shock resistance high-adhesion polysulfide rubber
EP4010398A1 (en) * 2019-08-06 2022-06-15 PPG Industries Ohio Inc. Adhesive compositions
CN110982464B (en) * 2019-11-22 2021-11-23 南京工程学院 Toughening epoxy adhesive capable of being reprocessed and recycled and curing method
CN113292926B (en) * 2021-04-28 2021-11-30 常州大学 Water-based self-repairing epoxy anticorrosive paint and preparation method thereof
CN116355565B (en) * 2023-01-17 2025-04-08 九江福莱克斯有限公司 Low dielectric adhesive with self-repairing function and preparation method and application thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101096544A (en) * 2006-06-30 2008-01-02 天津市振东涂料有限公司 Method for preparing liquid polysulfide prepolymer block modified epoxide resin protective coating
CN101434825A (en) * 2008-12-12 2009-05-20 河南永丽化工有限公司 Bicomponent terminal mercapto polyurethane mildewproof sealant and preparation thereof
CN104448314A (en) * 2014-12-08 2015-03-25 郑州中原应用技术研究开发有限公司 Epoxy group end-capped polysulfide polymer, preparation method and application thereof and room temperature fast-curing epoxy resin adhesive containing epoxy group end-capped polysulfide polymer

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1040045A (en) * 1987-12-28 1990-02-28 国家建筑材料工业局.秦皇岛玻璃研究院 The double glazing polysulfide epoxy sealing glue
US7553908B1 (en) * 2003-01-30 2009-06-30 Prc Desoto International, Inc. Preformed compositions in shaped form comprising polymer blends
CN101831270B (en) * 2010-05-27 2012-06-13 南京大学 Polysulfide sealant with low compressed permanent deformation
CN102702540B (en) * 2012-06-06 2013-09-11 南京大学 Plastification method for polysulfide sealant
CN103555264B (en) * 2013-10-11 2014-11-26 中国航空工业集团公司北京航空材料研究院 High peeling strength polysulfide sealant and sealing method
CN103865472B (en) * 2014-03-12 2015-12-30 浙江兴宇汽车零部件有限公司 A kind of flame-proof environmental protection polysulfide sealant and production method thereof
CN105400483B (en) * 2015-12-15 2018-12-04 锦西化工研究院有限公司 A kind of preparation method of polysulfide rubber electric insulation sealant

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101096544A (en) * 2006-06-30 2008-01-02 天津市振东涂料有限公司 Method for preparing liquid polysulfide prepolymer block modified epoxide resin protective coating
CN101434825A (en) * 2008-12-12 2009-05-20 河南永丽化工有限公司 Bicomponent terminal mercapto polyurethane mildewproof sealant and preparation thereof
CN104448314A (en) * 2014-12-08 2015-03-25 郑州中原应用技术研究开发有限公司 Epoxy group end-capped polysulfide polymer, preparation method and application thereof and room temperature fast-curing epoxy resin adhesive containing epoxy group end-capped polysulfide polymer

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