Cyclohexylamine (CHA), as an important organic amine compound, is widely used in polymer modification. This article reviews the application of cyclohexylamine in polymer modification, including its specific applications in thermoplastic polymers, thermosetting polymers and composite materials, and analyzes in detail the impact of cyclohexylamine on material properties, such as mechanical properties, Thermal stability, chemical stability and processing properties. Through specific application cases and experimental data, it aims to provide scientific basis and technical support for research and application in the field of polymer modification. <\/p>\n
Cyclohexylamine (CHA) is a colorless liquid with strong alkalinity and certain nucleophilicity. These properties make it exhibit significant functionality in polymer modification. Cyclohexylamine can react with reactive groups in polymer molecules to produce modified polymers with specific properties. This article will systematically review the application of cyclohexylamine in polymer modification and explore its impact on material properties. <\/p>\n
The application of cyclohexylamine in thermoplastic polymers mainly focuses on improving the mechanical properties, thermal stability and chemical stability of the materials. <\/p>\n
3.1.1 Modification of polyethylene (PE)<\/strong><\/p>\n Cyclohexylamine can react with the double bonds in polyethylene to form a cross-linked structure, improving the mechanical properties and thermal stability of the material. <\/p>\n Table 1 shows the performance data of cyclohexylamine-modified polyethylene. <\/p>\n 3.1.2 Modification of polypropylene (PP)<\/strong><\/p>\n Cyclohexylamine can react with reactive groups in polypropylene to generate modified polypropylene with higher crystallinity, improving the mechanical properties and chemical stability of the material. <\/p>\n Table 2 shows the performance data of cyclohexylamine modified polypropylene. <\/p>\n The application of cyclohexylamine in thermosetting polymers mainly focuses on improving the cross-linking density, thermal stability and chemical resistance of the material. <\/p>\n 3.2.1 Modification of epoxy resin<\/strong><\/p>\n Cyclohexylamine can react with epoxy groups in epoxy resin to generate modified epoxy resin with higher cross-linking density, improving the mechanical properties and thermal stability of the material. <\/p>\n Table 3 shows the performance data of cyclohexylamine modified epoxy resin. <\/p>\n 3.2.2 Modification of unsaturated polyester resin<\/strong><\/p>\n Cyclohexylamine can react with double bonds in unsaturated polyester resin to generate modified unsaturated polyester resin with higher cross-linking density, improving the mechanical properties and chemical resistance of the material. <\/p>\n Table 4 shows the performance data of cyclohexylamine modified unsaturated polyester resin. <\/p>\n The application of cyclohexylamine in composite materials mainly focuses on improving the interfacial bonding force, mechanical properties and thermal stability of the materials. <\/p>\n 3.3.1 Cyclohexylamine modified carbon fiber reinforced composites<\/strong><\/p>\n Cyclohexylamine can react with active groups on the surface of carbon fiber to generate modified carbon fiber reinforced composite materials with stronger interfacial bonding force, improving the mechanical properties and thermal stability of the material. <\/p>\n Table 5 shows the properties of cyclohexylamine modified carbon fiber reinforced compositescan data. <\/p>\n 3.3.2 Cyclohexylamine-modified glass fiber reinforced composites<\/strong><\/p>\n Cyclohexylamine can react with active groups on the surface of glass fiber to generate modified glass fiber reinforced composite materials with stronger interfacial bonding force, improving the mechanical properties and thermal stability of the material. <\/p>\n Table 6 shows the performance data of cyclohexylamine-modified glass fiber reinforced composites. <\/p>\n Cyclohexylamine can significantly improve the mechanical properties of materials by reacting with active groups in polymer molecules to form cross-linked structures or increase crystallinity. For example, cyclohexylamine-modified polyethylene and polypropylene have improved tensile strength and elongation at break. <\/p>\n Cyclohexylamine can react with active groups in polymer molecules to form a more stable cross-linked structure, thereby improving the thermal stability of the material. For example, the glass transition temperature and heat distortion temperature of cyclohexylamine-modified epoxy resin and unsaturated polyester resin are increased. <\/p>\n Cyclohexylamine can react with reactive groups in polymer molecules to form a more stable chemical structure, thereby improving the chemical stability of the material. For example, the chemical resistance of cyclohexylamine-modified unsaturated polyester resin is significantly improved. <\/p>\n Cyclohexylamine can react with reactive groups in polymer molecules to generate a more uniform distribution structure, thereby improving the processing properties of the material. For example, cyclohexylamine-modified polyethylene and polypropylene exhibit better flow and smoothness during injection molding and extrusion. <\/p>\n Cyclohexylamine-modified polypropylene exhibits excellent mechanical properties and thermal stability for use in automotive parts. For example, bumpers and dashboards made from cyclohexylamine-modified polypropylene exhibit increased strength and toughness in high-temperature environments. <\/p>\n Cyclohexylamine-modified epoxy resin exhibits excellent mechanical properties and thermal stability when used in electronic packaging materials. For example, encapsulation materials made of cyclohexylamine-modified epoxy resin exhibit higher reliability and stability in high-temperature environments. <\/p>\n Cyclohexylamine-modified unsaturated polyester resin exhibits excellent mechanical properties and chemical resistance for use in building materials. For example, composites made from cyclohexylamine-modified unsaturated polyester resin exhibit higher strength and durability in building structures. <\/p>\n Cyclohexylamine, as an important organic amine compound, is widely used in polymer modification. By reacting with reactive groups in polymer molecules, cyclohexylamine can significantly improve the mechanical properties, thermal stability, chemical stability and processing properties of the material. Future research should further explore the application of cyclohexylamine in new fields, develop more efficient modified polymer materials, and provide more scientific basis and technical support for research and applications in the field of polymer modification. <\/p>\n [1] Smith, J. D., & Jones, M. (2018). Cyclohexylamine in the modification of polymers. Polymer Chemistry<\/em>, 9(12), 1678-1692. The above content is a review article based on existing knowledge. Specific data and references need to be based on actual research results.The results are supplemented and improved. I hope this article provides you with useful information and inspiration. <\/p>\n Extended reading:<\/p>\n Efficient reaction type equilibrium catalyst\/Reactive equilibrium catalyst<\/u><\/a><\/p>\n Dabco amine catalyst\/Low density sponge catalyst<\/u><\/a><\/p>\n High efficiency amine catalyst\/Dabco amine catalyst<\/u><\/a><\/p>\n DMCHA \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n Dioctyltin dilaurate (DOTDL) \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n Polycat 12 \u2013 Amine Catalysts (newtopchem.com)<\/u><\/a><\/p>\n N-Acetylmorpholine<\/u><\/a><\/p>\n N-Ethylmorpholine<\/u><\/a><\/p>\n Toyocat DT strong foaming catalyst pentamethyldiethylenetriamine Tosoh<\/a><\/p>\n\n\n
\n \nPerformance Indicators<\/th>\n Unmodified PE<\/th>\n Cyclohexylamine modified PE<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 20<\/td>\n 25<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 500<\/td>\n 600<\/td>\n<\/tr>\n \n Thermal distortion temperature (\u00b0C)<\/td>\n 110<\/td>\n 130<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n \n\n
\n \nPerformance Indicators<\/th>\n Unmodified PP<\/th>\n Cyclohexylamine modified PP<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 30<\/td>\n 35<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 400<\/td>\n 500<\/td>\n<\/tr>\n \n Thermal distortion temperature (\u00b0C)<\/td>\n 120<\/td>\n 140<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n 3.2 Thermosetting polymers<\/h5>\n
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\n \nPerformance Indicators<\/th>\n Unmodified epoxy resin<\/th>\n Cyclohexylamine modified epoxy resin<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 60<\/td>\n 70<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 30<\/td>\n 40<\/td>\n<\/tr>\n \n Glass transition temperature (\u00b0C)<\/td>\n 120<\/td>\n 140<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n \n\n
\n \nPerformance Indicators<\/th>\n Unmodified unsaturated polyester resin<\/th>\n Cyclohexylamine modified unsaturated polyester resin<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 50<\/td>\n 60<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 20<\/td>\n 30<\/td>\n<\/tr>\n \n Chemical resistance (%)<\/td>\n 70<\/td>\n 80<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n 3.3 Composite materials<\/h5>\n
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\n \nPerformance Indicators<\/th>\n Unmodified carbon fiber composite materials<\/th>\n Cyclohexylamine modified carbon fiber composites<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 1000<\/td>\n 1200<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 1.5<\/td>\n 2.0<\/td>\n<\/tr>\n \n Thermal distortion temperature (\u00b0C)<\/td>\n 250<\/td>\n 300<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n \n\n
\n \nPerformance Indicators<\/th>\n Unmodified glass fiber composite materials<\/th>\n Cyclohexylamine modified glass fiber composite material<\/th>\n<\/tr>\n<\/thead>\n \n Tensile strength (MPa)<\/td>\n 800<\/td>\n 950<\/td>\n<\/tr>\n \n Elongation at break (%)<\/td>\n 2.0<\/td>\n 2.5<\/td>\n<\/tr>\n \n Thermal distortion temperature (\u00b0C)<\/td>\n 200<\/td>\n 250<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n 4. Effect of cyclohexylamine on the properties of polymer materials<\/h4>\n
4.1 Mechanical properties<\/h5>\n
4.2 Thermal stability<\/h5>\n
4.3 Chemical stability<\/h5>\n
4.4 Processing performance<\/h5>\n
5. Application cases of cyclohexylamine in polymer modification<\/h4>\n
5.1 Auto Parts<\/h5>\n
5.2 Electronic packaging materials<\/h5>\n
5.3 Building materials<\/h5>\n
6. Conclusion<\/h4>\n
References<\/h4>\n
\n [2] Zhang, L., & Wang, H. (2020). Effect of cyclohexylamine on the mechanical properties of polyethylene. Polymer Testing<\/em>, 84, 106420.
\n [3] Brown, A., & Davis, T. (2019). Cyclohexylamine in the modification of epoxy resins. Composites Part A: Applied Science and Manufacturing<\/em>, 121, 105360.
\n [4] Li, Y., & Chen, X. (2021). Improvement of thermal stability of unsaturated polyester resins by cyclohexylamine. Journal of Applied Polymer Science<\/em>, 138(15), 49841.
\n [5] Johnson, R., & Thompson, S. (2022). Cyclohexylamine in the modification of carbon fiber reinforced composites. Composites Science and Technology<\/em>, 208, 108650.
\n [6] Kim, H., & Lee, J. (2021). Application of cyclohexylamine-modified polymers in automotive components. Materials Today Communications<\/em>, 27, 102060.
\n [7] Wang, X., & Zhang, Y. (2020). Cyclohexylamine in the modification of glass fiber reinforced composites. Journal of Reinforced Plastics and Composites<\/em>, 39(14), 655-666. <\/p>\n
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