High Performance Near-Infrared (NIR) Photoinitiating Systems Operating under Low Light Intensity and in the Presence of Oxygen - Aix-Marseille Université Access content directly
Journal Articles Macromolecules Year : 2018

High Performance Near-Infrared (NIR) Photoinitiating Systems Operating under Low Light Intensity and in the Presence of Oxygen

Abstract

Photopolymerization under near-infrared (NIR) light is challenging due to the low energy of the absorbed photon but, if successful, presents significant advantages. For example, this lower energy wavelength is safer than UV light that is currently the standard photocuring light source. Also, NIR allows for a deeper light penetration within the material and therefore resulting in a more complete curing of thicker materials containing fillers for access to composites. In this study, we report the use of three component systems for the NIR photopolymerization of methacrylates: (1) a dye used as a photosensitizer in the NIR range, (2) an iodonium salt as a photoinitiator for the free radical polymerization of the (meth)acrylates, and (3) a phosphine to prevent polymerization inhibition due to the oxygen and to regenerate the dye upon irradiation. Several NIR-absorbing dyes such as a cyanine borate and a silicon phthalocyanine are presented and studied. Systems usi ng borate dyes resulted in methacrylate monomer conversion over 80% in air. We report three types of irradiation system: low-power LED at 660 and 780 nm as well as a higher power laser diode at 785 nm. The excellent performance reported in this work is due to the crucial role of the added phosphine.
No file

Dates and versions

hal-02091851 , version 1 (06-04-2019)

Identifiers

Cite

A. H. Bonardi, F. Dumur, T. M. Grant, G. Noirbent, D. Gigmes, et al.. High Performance Near-Infrared (NIR) Photoinitiating Systems Operating under Low Light Intensity and in the Presence of Oxygen. Macromolecules, 2018, 51 (4), pp.1314--1324. ⟨10.1021/acs.macromol.8b00051⟩. ⟨hal-02091851⟩
112 View
0 Download

Altmetric

Share

Gmail Mastodon Facebook X LinkedIn More