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Spectra Group Limited H-Nu 535

Spectra Group Limited H-Nu 535 initiates both free-radical and cationic photopolymerization, using a different set of co-initiators depending on the polymerization process • Type II photinitiator: H-Nu 535 acts as a light harvester, followed by energy or electron transfer to a co-initiator molecule; produced reactive species activate photopolymerization • Commercial photoinitiator, non-toxic (LD50>2500 mg/kg).

Functions: Photoinitiator

CAS Number: 142189-38-6

End Uses: Radiation Curable Adhesive, Radiation Curable Coating, Radiation Curable Ink

Technical Data Sheet
  • TypeDocument Name
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Knowde Enhanced TDS

Identification & Functionality

CASE Ingredients Functions
Name
2,4,5,7-tetraiodo-3-hydroxy-6-fluorone
CAS No.
142189-38-6
Technologies

Features & Benefits

Labeling Claims
Advantages
  • High absorptivity, low concentrations are needed (0.01-0.15% by weight)
  • Cationic cured epoxides are not susceptible to oxygen inhibition and exhibit a tack free surface upon cure
  • Capable of significant depth of cure > 1 inch
  • Cure through UV opaque or pigmented substrates (e.g. Kapton)
  • Initiator bleaching (bright red to pale pink/no color) upon light interaction can act as cure indicator

Applications & Uses

Cure Method
Adhesive & Sealant Type
Ink & Toner Type
Examples of H-Nu 535 uses

SU-8 photoresist

  • Y. Lin, P.R. Hermann, and K.Darmawikarta, Appl. Phys. Lett. 86, 7, 071117 (2005)
  • J.H. Moon, S.-M. Yang, D.J. Pine, and W.-S. Chang, Appl. Phys. Lett. 85, 18, 4184 (2004)
  • D. Rodriguez Ponce, K Lozano, et al. J. Polym. Sci.: Part B: Polym. Phys. 48, 1, 47 (2010) 

Properties

Physical Form
Appearance
Red Powder
Typical Properties
ValueUnitsTest Method / Conditions
Absorbancemax. 535nmUV Visible spectroscopy
Melting Pointmin. 270°CMelting point Analysis
Molar Extinction Coefficient (535)91200nmUV Visible spectroscopy

Technical Details & Test Data

Wavelength

Spectra Group Limited H-Nu 535 - Wavelength

Applications Recommendations
  • Direct solubility of H-Nu 535 in resins can be difficult, pre-dissolution in one of the following resins/solvents before adding resin is recommended:
              Free-Radical Diluents                      Cationic Diluents
DMAA VMOX THFA HDDA HPMA IBOA Heloxy61 Heloxy62 EOXA1 ECC2 Eponex1510
S S,T0 I I I I I I I P,T0 S,T0

1% of H-Nu 535 in diluent is: S-soluble Tº-requires heat (60ºC for several hours) P-partially soluble I-insoluble

1 = 3-ethyl-3-hydroxymethyloxetane

2 = 3,4-epoxycyclohexylmethyl-3,4

Note: DMAA is an excellent solvent for H-Nu 535, but it cannot be used in cationic polymerization as it inhibits process.

  • The presence of any undissolved red particles is an indication of incomplete solubility. More heating (60℃) or stirring may help with incorporation, or pre-dissolution using different diluents is recommended.

Polymerization mechanisms
Free-Radical Cure (Acrylates)

  • H-Nu 535 concentration range spans from 0.05 to 0.2 wt.%, depending on a cure thickness. 0.05 wt% is recommended starting point for thick cure (>1mm) and 0.1wt% for thin cure.
  • Amine acrylates (AA) are needed as co-initiators at 5-10 wt.%. If amine use is counterindicated (acidic adhesion promoter, outgassing), as an alternative, another co-initiator, Borate V (0.5 wt.%) may provide similar cure response as typical amine co-initiators
  • H-Nu 254 iodonium salt is recommended for acceleration.

Spectra Group Limited H-Nu 535 - Applications Recommendations

Cationic Cure (Epoxides)

  • H-Nu 535 concentration range spans from 0.05 to 0.2 wt.%, with a good starting point at 0.1 wt.% based on solids.
  • H-Nu 254 iodonium salt is needed to achieve cure in epoxide resins (sulfonium salts will not work).
  • Accelerator AN-9,10-E can greatly enhance cure speed and sensitivity and is needed to achieve cure.
  • Amines or DMAA solvent cannot be used due to the superacid “poisoning” effect.
  • Caution & experimentation is required at higher temperatures as it can lead to thermal ground state polymerization. Additional stabilizers, depending on the  photopolymerization matrix can be used. As an example, 0.2 wt.% of PVP+BHT* mixture (1:1) can be added to glycidyl epoxide and 0.3 wt.% of PVP+BHT mixture (1:1) to cycloaliphatic epoxide.

Spectra Group Limited H-Nu 535 - Applications Recommendations - 1

Structure

Spectra Group Limited H-Nu 535 - Structure