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HOME > Products > HYBRID MONOMERS : VEEA, VEEM
HYBRID MONOMERS : VEEA, VEEM

HYBRID MONOMERS
2- (2-Vinyloxyethoxy)ethyl (meth)acrylate (VEEA, VEEM)
- VEEA stands for acrylate, VEEM stands for methacrylate.

chemical structure

· not inhibited by moisture and bases
· many co-curable monomers
· no dark reaction
· not inhibited by oxygen
· good dilution
· good adhesion
· low skin irritating

Feature

· VEEA and VEEM have different kinds of polymerizable groups such as radical polymerizable (meth)acryloyl group and cationic polymerizable vinylether group installed in one molecule.
· Reactive Polymers having (meth)acryloyl group or vinylether group are obtained from VEEA, VEEM by selecting polymerization method.
· VEEA and VEEM show high performances in radiation curable formulations.
· VEEA and VEEM show high dilution performances.

Properties

  VEEA VEEM
CAS No. 86273-46-3 76392-22-8
Chemical formula C9H14O4 C10H16O4
Molecular weight 186.20 200.23
Appearance Colorless liquid Colorless liquid
Boiling point 115-116ºC/13.3 hPa 122-123ºC/13.3 hPa
Density 1.04 g/ml (15ºC) 1.03 g/ml (15ºC)
Viscosity 3.65 mPa· s 3.19 mPa· s
Solubility H2O:18 g/L (30ºC)
Organic solvent:soluble
H2O:2.2 g/L (30ºC)
Organic solvent:soluble

Application fields

· Coatings : Wood coating, Film coating, Hard coating, Optical disk coating, Optical fiber coating etc.
· Inks : Inkjet, Screen ink, Offset ink, Gravure ink etc.
· Photoresists : Dry film resist, Semiconductor resist, Photo polymer plate, Barrier rib for PDP etc.
· Adhesives : Adhesives for DVD etc.
· Others : Rapid prototyping etc.

Utilities
Utilities

Polymerization methods
chemical structure

Reactive diluent

· VEEA and VEEM are applicable to reactive diluent for heat, UV and EB curable formulations.
· VEEA and VEEM are curable in thin film, rapidly.

chemical structure

UV Curing performance of VEEA

Run No. 1 2 3
VEEA 100 - -
DEGDA - 100 53.53
DEGDV - - 46.47
Irgacure907 1 1 1
UV curing 0.1 J/cm2 - - --
performance (1) 0.2 J/cm2 - - --
0.3 J/cm2 ++ + --
0.4 J/cm2 ++ + --
0.5 J/cm2 ++ + --
UV curing 1 times ++ - --
performance (2) 2 times ++ - --
3 times ++ - --
4 times ++ - --
5 times ++ - --

UV curing
performance (1):
UV radiation device; PM25C-100 (Ushio Inc.) with 250 W ultrahigh-pressure mercury vapor lamp (dominant wavelength = 365 nm), Thickness; 300 µm, Surface tackiness; evaluated by finger touch (++ = loss of tack, -- = not cured)
UV curing
performance (2):
UV radiation device; UB031-5BM (EYEGRAPHICS Co., Ltd.) with 80 W high-pressure mercury vapor lamp, Thickness; 30 µm, Line speed; 14 m/min, Distance between lamp and substance; 10 cm, Radiation energy of one time; 125 mJ/cm2, Surface tackiness; evaluated by finger touch (++ is loss of tack, -- is not cured)

UV Curing performance of VEEA & VEEM as Reactive Diluent

Run No. 4 5 6 7 8 9
Unsaturated polyester resin 60 60 60 - - -
Bisphenolic epoxy resin - - - 60 60 60
VEEA 40 - - 40 - -
VEEM - 40 - - 40 -
DEGDA - - 40 - - 40
Irgacure907 1 1 1 1 1 1
Viscosity (mPa· s at 25ºC) 1102 1038 2670 295 289 855
UV curing 1 times + - - - - -
performance 2 times + - - ++ - ++
3 times ++ - - ++ - ++
4 times ++ + + ++ + ++
5 times ++ ++ + ++ ++ ++
7 times ++ ++ + ++ ++ ++
Pencil hardness (JIS K-5400) F HB B F F F
?Acetone resistance (100 times) ++ ++ ++ ++ ++ ++

UV curing performance: UV radiation device; UB031-5BM (EYEGRAPHICS Co., Ltd.) with 80W high-pressure mercury vapor lamp, Thickness; 30 µm, Line speed; 14 m/min, Distance between lamp and substance; 10 cm, Radiation energy of one time; 125 mJ/cm2, Surface tackiness; evaluated by finger touch (++ is loss of tack, -- is not cured)
Pencil hardness: evaluated after 10 times cured
Acetone resistance: evaluated after 10 times cured (++ = no change in gloss, -- = complete loss of gloss)

Reactive polymer having pendant vinylether group
Heat, UV, EB curable polymer
chemical structure

Reactive polymer having pendant (meth)acryloyl group
Heat, UV, EB curable polymer
chemical structure

Derivatives
Various kinds of acetal compounds are derived from VEEA and VEEM by additional reaction
These acetal compounds are easily decomposed by heating or addition of acid.
chemical structure

SAFETY DATA SHEET

PDFVEEA SAFETY [PDF]
PDFVEEM SAFETY [PDF]

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NIPPON SHOKUBAI CO., LTD.
E & I Materials Business Unit
Hibiya-Dai Bldg., 1-2-2, Uchisaiwaicho, Chiyoda-ku, Tokyo 100-0011, Japan
TEL:03-3506-7529 FAX:03-3506-7597
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