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RadTech
UV/EB Technology Conference & Expo 2008
May 4-7, 2008
Lakeside Center at McCormick Place
Chicago, Illinois - United States of America
CHEMISTRY
Evaluation of Structural
Effects for Some Alkoxy Monomers
in UV Curable Coatings
TaiYeon Lee, DSM Desotech
Abstract:
Alkoxy acrylate monomers are used as diluents in UV curable coatings
for a variety of applications. Acrylate monomers with, different structural
moieties such as ethylene oxide or propylene oxide, varying amount
(0 to 6 moles) of alkoxylation, the presence or absence of a phenyl
group, the presence and type of an alkyl group, were used to investigate
the effect of monomer structure on photopolymerization speed and mechanical
properties.
Highly
Weather Resistant Radiation Curable Monomers and Oligomers
for Exterior Applications
William Schaeffer, Sartomer Company
Abstract: The weathering resistance of an exterior coating
is one of the main properties required by the end-user. The backbone
structure of several monomers and oligomers has been investigated
and subjected to accelerated outdoor weathering testing (Q-Trac)and
correlated with actual Florida exposure. The performance of these
products has also been compared to a standard 2 component urethane
intended automotive topcoat applications. The physical properties
including yellowing resistance and gloss retention will be presented.
This ongoing study has shown that these acrylates, which are free
from light stabilizers, can withstand 3 years of Florida exposure
without gegradation. Since the testing was conducted in accordance
with automotive test standards, these products are suitable for
any application requiring superior outdoor durability.
Modern
use of vinyl ethers and vinyl amids in UV curable applications
Matthias Fies, BASF
Abstract: Over the last years vinyl ethers and vinyl amids
are used in growing number of UV curable industrial applications.
The usage of vinyl ethers and vinyl amids is up-dated. A performance
comparison of vinyl ethers and vinyl amids with UV-acrylates in
specific formulations emphasizes the unique properties of vinyl
ethers/vinyl amids in UV-curing. For special applications in UV
curable coatings and inks new vinyl ether and vinyl amids have been
developed and are presented. Finally the performance of newly developed
vinyl esters as reactive diluents are presented.
Photocured
Imprintable Networks
Justin Chan , University of Southern
Mississippi
Abstract: Coatings consisting of mixtures of multifunctional
thiols and enes were exposed to UV light sources serve a efficient
networks for molecular imprinting of small molecule. By rinsing
these films in appropriate solvents, these networks efficiently
scavenge small molecule impurities which are targeted by the network
structure. The scavenging efficiency is shown to be dependent upon
the chemical structures of the thiols and enes used to form the
background network. Applications for UV curing in advanced imprintable
networks are discussed.
Photopolymerizable
hybrid sol-gel: new opportunities for UV-cured coatings
Céline Croutxé-Barghorn,
Department of Photochemistry
Abstract: Photopolymerizable organic-inorganic sol-gel coatings
combine numerous advantages: good adhesion to substrates, abrasion
and chemical resistance. Owing to the possibility of controlling
the inorganic network density, sol-gel films can also form an effective
barrier layer. Crackability is limited by the presence of the organic
component. The present paper focuses on the new opportunities opened
by these materials in the UV-curing field in terms of photopolymerization
process and final coatings properties.
Preparation
and Properties of UV curable urethane modified acrylate oligomer
Fengqi Huang, Tianjin Tianjiao Chemical
Co.,Ltd
Abstract: Preparation and Properties of UV curable urethane
modified acrylate oligomer Fengqi Huang1 , Wenzhi Yu1, Jiaxi Wang1,2*
1. Tianjin Tianjiao Chemical Co.,Ltd, Tianjin 300400 2. Department
of Polymer Science and Engineering, Hebei University of Technology,
Tianjin 300130 Abstract: N,N-dihydroxyethyl acrylamide (DHEAA),
which is an acrylate functionalized diol, has been prepared by reaction
of diethylanol amine with methyl acrylate. UV curable urethane modified
acrylate oligomers have been synthesized by the reaction of a series
of diol, triol, DHEAA and HEMA with TDI or IPDI in two reaction
orders. The one is the TDI or IPDI reacted with HEMA first to give
acrylate group ending mono isocyanate, then the mixture reacted
with diol or triol to generated urethane modified oligomer with
two or three functional group acrylates. The other is the TDI or
IPDI reacted with diol , triol or DHEAA first to give oligomer,
then resulted solution reacted with HEMA to obtain the UV curable
product with more functional groups. The average molecular weight,
structure unit of oligomer and number of functional groups can be
tuned by adjusting of adding order, ratio of starting material and
the reaction condition. The UV curing property such as curing rate,
hardness of cured film, impact strength, flexibility and so on have
been determined. The relationship between the component and the
properties of cured film has been discussed.
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