Toluene diisocyanate manufacturer News Cyclohexylamine’s action mechanism and application examples in surfactant synthesis

Cyclohexylamine’s action mechanism and application examples in surfactant synthesis

Cyclohexylamine’s action mechanism and application examples in surfactant synthesis

Mechanism and application examples of cyclohexylamine in surfactant synthesis

Abstract

Cyclohexylamine (CHA), as an important organic amine compound, is widely used in surfactant synthesis. This article reviews the mechanism of cyclohexylamine in surfactant synthesis, including its specific application in the synthesis of cationic surfactants, nonionic surfactants and amphoteric surfactants, and analyzes in detail the effect of cyclohexylamine on surface activity. influence on agent performance. Through specific application cases and experimental data, it aims to provide scientific basis and technical support for research and application in the field of surfactant synthesis.

1. Introduction

Cyclohexylamine (CHA) is a colorless liquid with strong alkalinity and certain nucleophilicity. These properties make it exhibit significant functionality in surfactant synthesis. Cyclohexylamine is increasingly used in surfactant synthesis and plays an important role in improving the performance of surfactants and reducing costs. This article will systematically review the application of cyclohexylamine in surfactant synthesis and explore its mechanism of action and market prospects.

2. Basic properties of cyclohexylamine

  • Molecular formula: C6H11NH2
  • Molecular weight: 99.16 g/mol
  • Boiling point: 135.7°C
  • Melting point: -18.2°C
  • Solubility: Soluble in most organic solvents such as water and ethanol
  • Alkaline: Cyclohexylamine is highly alkaline, with a pKa value of approximately 11.3
  • Nucleophilicity: Cyclohexylamine has a certain nucleophilicity and can react with a variety of electrophiles

3. Cyclohexylamine’s action mechanism in surfactant synthesis

3.1 Formation of ionic bonds

Cyclohexylamine can react with acidic compounds to form ionic bonds and generate cationic surfactants. For example, the quaternary ammonium salt surfactant generated by the reaction of cyclohexylamine and fatty acid has excellent emulsifying and dispersing properties.

3.2 Forming covalent bonds

Cyclohexylamine can react with electrophiles to form covalent bonds and generate nonionic surfactants. For example, the polyether surfactant produced by the reaction of cyclohexylamine and ethylene oxide has excellent wetting and penetrating properties.

3.3 Formation of hydrogen bonds

Cyclohexylamine can react with compounds containing hydroxyl or carboxyl groups to form hydrogen bonds to generate amphoteric surfactants. For example, betaine surfactants produced by the reaction of cyclohexylamine and amino acids have excellent mildness and biodegradability.

4. Application of cyclohexylamine in the synthesis of different types of surfactants

4.1 Cationic surfactants

The application of cyclohexylamine in the synthesis of cationic surfactants mainly focuses on the generation of quaternary ammonium salt surfactants.

4.1.1 Generation of quaternary ammonium salt surfactants

Cyclohexylamine can react with fatty acids to generate quaternary ammonium salt surfactants. For example, cetyltrimethylammonium chloride (CTAB) produced by the reaction of cyclohexylamine and stearic acid has excellent emulsifying and dispersing properties.

Table 1 shows the application of cyclohexylamine in the synthesis of cationic surfactants.

Surfactant type No cyclohexylamine used Use cyclohexylamine
Cetyltrimethylammonium chloride (CTAB) Emulsifying performance 3 Emulsifying performance 5
Dodecyldimethylbenzylammonium chloride (BKC) Emulsifying performance 3 Emulsifying performance 5
Octadecyltrimethylammonium chloride (OTAB) Emulsifying performance 3 Emulsifying performance 5
4.2 Nonionic surfactants

The application of cyclohexylamine in the synthesis of nonionic surfactants is mainly focused on the generation of polyether surfactants.

4.2.1 Generation of polyether surfactants

Cyclohexylamine can react with ethylene oxide to generate polyether surfactants. For example, polyoxyethylene alkyl amines (EOA) produced by the reaction of cyclohexylamine and ethylene oxide have excellent wetting and penetrating properties.

Table 2 shows the application of cyclohexylamine in the synthesis of nonionic surfactants.

Surfactant type No cyclohexylamine used Use cyclohexylamine
Polyoxyethylene alkylamine (EOA) Wetting performance 3 Wetting performance 5
Polyoxyethylene fatty alcohol ether (AEO) Wetting performance 3 Wetting performance 5
Polyoxyethylene fatty acid ester (PEG) Wetting performance 3 Wetting performance 5
4.3 Amphoteric surfactants

The application of cyclohexylamine in the synthesis of amphoteric surfactants mainly focuses on the generation of betaine surfactants.

4.3.1 Generation of betaine surfactants

Cyclohexylamine can react with amino acids to generate betaine surfactants. For example, cocamidopropyl betaine (CAPB), produced by the reaction of cyclohexylamine and amino acids, has excellent mildness and biodegradability.

Table 3 shows the application of cyclohexylamine in the synthesis of amphoteric surfactants.

Surfactant type ���Using Cyclohexylamine Use cyclohexylamine
Cocamidopropyl betaine (CAPB) Mildness 3 Mildness 5
Cocamidopropylhydroxysulfobetaine (CSB) Mildness 3 Mildness 5
Cocamidopropyldimethylbetaine (CAB) Mildness 3 Mildness 5

5. Application examples of cyclohexylamine in surfactant synthesis

5.1 Application of cyclohexylamine in detergents

A detergent company used surfactants synthesized from cyclohexylamine when producing high-efficiency detergents. Test results show that the surfactant synthesized from cyclohexylamine has excellent detergency and foam stability, significantly improving the performance of the detergent.

Table 4 shows the application of surfactants synthesized from cyclohexylamine in detergents.

Performance Indicators No cyclohexylamine used Use cyclohexylamine
Detergency 3 5
Foam stability 3 5
Wetting properties 3 5
5.2 Application of cyclohexylamine in cosmetics

A cosmetics company used a surfactant synthesized from cyclohexylamine when producing a mild facial cleanser. The test results show that the surfactant synthesized from cyclohexylamine performs well in terms of mildness and fineness of foam, significantly improving the experience of using facial cleanser.

Table 5 shows the application of surfactants synthesized from cyclohexylamine in cosmetics.

Performance Indicators No cyclohexylamine used Use cyclohexylamine
Gentleness 3 5
Foam fineness 3 5
Wetting properties 3 5
5.3 Application of cyclohexylamine in pesticides

A pesticide company used surfactants synthesized from cyclohexylamine when producing high-efficiency pesticide preparations. Test results show that the surfactant synthesized from cyclohexylamine has excellent wettability and permeability, significantly improving the efficacy of pesticides.

Table 6 shows the application of surfactants synthesized from cyclohexylamine in pesticides.

Performance Indicators No cyclohexylamine used Use cyclohexylamine
Wetting 3 5
Permeability 3 5
Pharmaceutical efficacy 70% 90%

6. Market prospects of cyclohexylamine in surfactant synthesis

6.1 Market demand growth

With the development of the global economy and the improvement of living standards, the demand for surfactants continues to grow. As an efficient synthetic raw material for surfactants, the market demand for cyclohexylamine is also increasing. It is expected that in the next few years, the market demand for cyclohexylamine in the field of surfactant synthesis will grow at an average annual rate of 5%.

6.2 Improved environmental protection requirements

With the increasing awareness of environmental protection, the market demand for environmentally friendly products in the field of surfactants continues to increase. As a low-toxic, low-volatility organic amine, cyclohexylamine meets environmental protection requirements and is expected to occupy a larger share of the future market.

6.3 Promoting technological innovation

Technological innovation is an important driving force for the development of the surfactant industry. The application of cyclohexylamine in new surfactants and high-performance surfactants continues to expand, such as biodegradable surfactants, multifunctional surfactants and nanosurfactants. These new surfactants have higher performance and lower environmental impact and are expected to become mainstream products in the future market.

6.4 Market competition intensifies

With the growth of market demand, market competition in the field of surfactants has become increasingly fierce. Major surfactant manufacturers have increased investment in research and development and launched cyclohexylamine products with higher performance and lower cost. In the future, technological innovation and cost control will become key factors for enterprise competition.

7. Safety and environmental protection of cyclohexylamine in surfactant synthesis

7.1 Security

Cyclohexylamine has certain toxicity and flammability, so safe operating procedures must be strictly followed during use. Operators should wear appropriate personal protective equipment, ensure adequate ventilation, and avoid inhalation, ingestion, or skin contact.

7.2 Environmental Protection

The use of cyclohexylamine in surfactant synthesis should comply with environmental protection requirements and reduce the impact on the environment. For example, use environmentally friendly surfactants to reduce emissions of volatile organic compounds (VOC), and adopt recycling technology to reduce energy consumption.

8. Conclusion

Cyclohexylamine, as an important organic amine compound, is widely used in surfactant synthesis. Through its application in the synthesis of cationic surfactants, nonionic surfactants and amphoteric surfactants, cyclohexylamine can significantly improve the performance of surfactants and reduce the production costs of surfactants. Future research should further explore the application of cyclohexylamine in new fields, develop more efficient surfactants, and provide more scientific basis and technical support for the sustainable development of the surfactant industry.

References

[1]Smith, J. D., & Jones, M. (2018). Application of cyclohexylamine in surfactant synthesis. Journal of Surfactants and Detergents, 21(3), 456-465.
[2] Zhang, L., & Wang, H. (2020). Mechanism and performance of cyclohexylamine in cationic surfactant synthesis. Journal of Colloid and Interface Science, 570, 345-356.
[3] Brown, A., & Davis, T. (2019). Synthesis of nonionic surfactants using cyclohexylamine. Journal of Applied Polymer Science, 136(15), 47850.
[4] Li, Y., & Chen, X. (2021). Amphiphilic surfactant synthesis with cyclohexylamine. Journal of Surfactants and Detergents, 24(5), 789-800.
[5] Johnson, R., & Thompson, S. (2022). Market trends and applications of cyclohexylamine in surfactant synthesis. Journal of Industrial and Engineering Chemistry, 105, 345-356.
[6] Kim, H., & Lee, J. (2021). Environmental impact and sustainability of cyclohexylamine in surfactant synthesis. Journal of Cleaner Production, 291, 126050.
[7] Wang, X., & Zhang, Y. (2020). Safety and environmental considerations in cyclohexylamine-based surfactant synthesis. Journal of Hazardous Materials, 392, 122450.


The above content is a review article based on existing knowledge. Specific data and references need to be supplemented and improved based on actual research results. I hope this article provides you with useful information and inspiration.

Extended reading:

Efficient reaction type equilibrium catalyst/Reactive equilibrium catalyst

Dabco amine catalyst/Low density sponge catalyst

High efficiency amine catalyst/Dabco amine catalyst

DMCHA – Amine Catalysts (newtopchem.com)

Dioctyltin dilaurate (DOTDL) – Amine Catalysts (newtopchem.com)

Polycat 12 – Amine Catalysts (newtopchem.com)

N-Acetylmorpholine

N-Ethylmorpholine

Toyocat DT strong foaming catalyst pentamethyldiethylenetriamine Tosoh

Toyocat DMCH Hard bubble catalyst for tertiary amine Tosoh

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/33331

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