What Is 2-Hydroxyethyl Acrylate (2-HEA) and How Is It Used in Polymer Chemistry?

2025-08-08 13:33

Technical Introduction

2-Hydroxyethyl Acrylate (2-HEA) is a colorless to pale yellow liquid monomer featuring both an acrylate group and a hydroxyl functional group. The acrylate moiety enables rapid free-radical polymerization, while the hydroxyl group allows for further chemical reactions such as crosslinking, grafting, or modification. This dual functionality makes 2-HEA a versatile monomer widely used in the synthesis of hydrophilic polymers, coatings, adhesives, and hydrogels. It imparts improved flexibility, adhesion, and water compatibility to polymer systems.

Applications

  • UV and Thermal Curable Coatings: Enhances adhesion, hardness, and flexibility.

  • Adhesives and Sealants: Improves bonding strength and moisture resistance.

  • Hydrogels: Used in biomedical applications such as contact lenses and wound dressings.

  • Textile Finishing: Adds hydrophilicity and improves fabric softness.

  • Waterborne Polymers: Acts as a hydrophilic monomer for emulsion polymerization.

  • 3D Printing Resins: Provides reactive sites for photocurable formulations.

Advantages

  • Dual Reactivity: Polymerizable acrylate and reactive hydroxyl group for crosslinking.

  • Improved Hydrophilicity: Enhances water absorption and compatibility.

  • Fast Polymerization: Enables efficient curing under UV or thermal initiators.

  • Versatile Co-Polymerization: Compatible with a wide range of monomers.

  • Enhanced Adhesion: Hydroxyl groups promote bonding to various substrates.

Specifications (Typical Parameters)

ParameterDescriptionTypical Value
AppearancePhysical stateClear to pale yellow liquid
PurityContent of 2-HEA≥ 99%
Hydroxyl ValueHydroxyl content250 - 270 mg KOH/g
Acid ValueFree acid content≤ 0.05 mg KOH/g
Viscosity (25°C)Flow property15 - 30 mPa·s
Density (25°C)Mass per volume1.07 - 1.09 g/cm³
Refractive IndexOptical property1.44 - 1.46

FAQ

Q1: What polymerization methods are suitable for 2-HEA?
A: Free radical polymerization under UV or thermal initiation is common, often as a co-monomer.

Q2: Does 2-HEA improve water compatibility in polymers?
A: Yes, the hydroxyl group enhances hydrophilicity and water absorption.

Q3: Can 2-HEA be used in biomedical materials?
A: Yes, it is widely used in hydrogels for contact lenses and wound dressings.

Q4: How should 2-HEA be handled safely?
A: Use protective gloves, goggles, and adequate ventilation to avoid skin contact and inhalation.

Q5: Is 2-HEA compatible with waterborne polymer systems?
A: Yes, it is often used in emulsion and dispersion polymerizations.

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