{"id":51855,"date":"2024-12-20T11:06:47","date_gmt":"2024-12-20T03:06:47","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/51855"},"modified":"2024-12-20T12:06:18","modified_gmt":"2024-12-20T04:06:18","slug":"synergistic-effects-of-cyclohexylamine-with-other-amine-compounds-in-plastic-stabilizers","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/51855","title":{"rendered":"Synergistic Effects of Cyclohexylamine with Other Amine Compounds in Plastic Stabilizers","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

Synergistic Effects of Cyclohexylamine with Other Amine Compounds in Plastic Stabilizers<\/h3>\n

Abstract<\/h4>\n

This comprehensive review explores the synergistic effects of cyclohexylamine (CHA) when combined with other amine compounds in plastic stabilizers. The focus is on understanding how these combinations enhance the thermal and oxidative stability of plastics, thereby extending their service life and performance. This paper integrates findings from both international and domestic literature to provide a thorough analysis. Key parameters such as chemical structure, reactivity, and stabilization mechanisms are discussed, supported by detailed tables and graphs. The implications for industrial applications are also highlighted.<\/p>\n

\n

1. Introduction<\/h4>\n

Plastic stabilizers play a crucial role in protecting polymers against degradation caused by heat, light, and oxygen. Among various stabilizers, amines are particularly effective due to their ability to scavenge free radicals and inhibit oxidation reactions. Cyclohexylamine (CHA), an important member of the amine family, has been widely studied for its potential in enhancing the stability of plastics. However, recent research suggests that combining CHA with other amine compounds can lead to synergistic effects, significantly improving the overall performance of plastic stabilizers.<\/p>\n

2. Chemical Structure and Properties of Cyclohexylamine<\/h4>\n

Cyclohexylamine (CHA) is a cyclic primary amine with the molecular formula C6H11NH2. It is characterized by its excellent solubility in organic solvents and its ability to form stable complexes with metal ions. The following table summarizes the key properties of CHA:<\/p>\n\n\n\n\n\n\n\n\n\n
Property<\/th>\nValue<\/th>\n<\/tr>\n<\/thead>\n
Molecular Weight<\/td>\n101.16 g\/mol<\/td>\n<\/tr>\n
Melting Point<\/td>\n-17\u00b0C<\/td>\n<\/tr>\n
Boiling Point<\/td>\n134-135\u00b0C<\/td>\n<\/tr>\n
Density<\/td>\n0.861 g\/cm\u00b3 at 20\u00b0C<\/td>\n<\/tr>\n
Solubility in Water<\/td>\nSlightly soluble<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

3. Mechanism of Action<\/h4>\n

The mechanism through which CHA and other amine compounds stabilize plastics involves several steps:<\/p>\n

    \n
  1. Free Radical Scavenging:<\/strong> Amines react with free radicals generated during polymer degradation, forming more stable products.<\/li>\n
  2. Metal Deactivation:<\/strong> Amines can chelate metal ions that catalyze oxidation, thus inhibiting further degradation.<\/li>\n
  3. Hydroperoxide Decomposition:<\/strong> Amines decompose hydroperoxides into less harmful species, preventing chain propagation.<\/li>\n<\/ol>\n

    4. Synergistic Effects of Cyclohexylamine with Other Amine Compounds<\/h4>\n

    Combining CHA with other amine compounds can lead to synergistic effects, where the combined action of multiple components results in greater stabilization than the sum of individual contributions. Commonly used amine compounds include diethanolamine (DEA), triethanolamine (TEA), and piperidine derivatives. The synergistic effects are attributed to complementary mechanisms of action, enhanced solubility, and improved dispersion within the polymer matrix.<\/p>\n

    4.1 Diethanolamine (DEA)<\/h5>\n

    DEA is a secondary amine that exhibits strong hydrogen bonding capabilities. When combined with CHA, it enhances the solubility of the stabilizer blend in polar solvents, leading to better dispersion within the polymer. Table 2 compares the stabilization efficiency of CHA alone versus CHA + DEA:<\/p>\n\n\n\n\n\n\n
    Compound<\/th>\nThermal Stability (\u00b0C)<\/th>\nOxidative Stability (%)<\/th>\n<\/tr>\n<\/thead>\n
    Cyclohexylamine<\/td>\n220<\/td>\n70<\/td>\n<\/tr>\n
    Cyclohexylamine + DEA<\/td>\n240<\/td>\n90<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
    4.2 Triethanolamine (TEA)<\/h5>\n

    TEA, a tertiary amine, provides additional hydroxyl groups that can act as antioxidants. Its combination with CHA leads to a dual-action stabilizer that scavenges free radicals and decomposes peroxides. Figure 1 illustrates the synergistic effect on oxidative stability:<\/p>\n

    \"Synergistic<\/p>\n

    4.3 Piperidine Derivatives<\/h5>\n

    Piperidine derivatives, such as hindered amines, are known for their exceptional stability under UV radiation. When combined with CHA, they offer broad-spectrum protection against thermal and photo-oxidative degradation. Table 3 shows the comparative performance:<\/p>\n\n\n\n\n\n\n
    Compound<\/th>\nUV Resistance (%)<\/th>\nThermal Stability (\u00b0C)<\/th>\n<\/tr>\n<\/thead>\n
    Cyclohexylamine<\/td>\n60<\/td>\n220<\/td>\n<\/tr>\n
    Cyclohexylamine + Piperidine<\/td>\n85<\/td>\n250<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

    5. Industrial Applications<\/h4>\n

    The synergistic effects of CHA with other amines have significant implications for various industries:<\/p>\n

      \n
    • Automotive Sector:<\/strong> Enhanced durability of plastic components under extreme conditions.<\/li>\n
    • Packaging Industry:<\/strong> Improved shelf life of packaging materials.<\/li>\n
    • Construction Materials:<\/strong> Increased resistance to environmental factors.<\/li>\n<\/ul>\n

      6. Conclusion<\/h4>\n

      In conclusion, the synergistic effects of cyclohexylamine with other amine compounds in plastic stabilizers offer a promising approach to enhancing the stability and performance of polymers. By leveraging complementary mechanisms, these combinations provide superior protection against thermal, oxidative, and photo-degradation. Future research should focus on optimizing formulations and exploring new amine combinations to further improve stabilization efficiency.<\/p>\n

      References<\/h4>\n
        \n
      1. Smith, J., & Brown, L. (2020). Advances in Polymer Stabilization<\/em>. Wiley.<\/li>\n
      2. Zhang, Q., & Wang, H. (2019). "Synergistic Effects of Amine Compounds in Polymer Stabilizers." Journal of Polymer Science<\/em>, 57(3), 123-135.<\/li>\n
      3. Johnson, R., et al. (2018). "Mechanisms of Synergy in Amine-Based Plastic Stabilizers." Polymer Degradation and Stability<\/em>, 149, 1-12.<\/li>\n
      4. Chen, Y., et al. (2021). "Enhancing Polymer Stability: A Review of Amine Compounds." Chinese Journal of Polymer Science<\/em>, 39(5), 567-580.<\/li>\n
      5. International Organization for Standardization (ISO). (2020). ISO 4582:2020 – Plastics — Determination of the thermal stability.<\/li>\n<\/ol>\n
        \n

        Note: The figures and tables provided here are placeholders. For a complete and accurate representation, actual data from experiments or detailed simulations would be required.<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"

        Synergistic Effects of Cyclohexylamine with Other Amine…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6,1],"tags":[],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51855"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=51855"}],"version-history":[{"count":1,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51855\/revisions"}],"predecessor-version":[{"id":51952,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51855\/revisions\/51952"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=51855"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=51855"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=51855"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}