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NEO Chemical Seminar 2007 Toine Dinnissen / March 27th 2007 Page 1 Why Diluents ? That’s Why !!!!!!

Why Diluents ?

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Why Diluents ?. That’s Why !!!!!!. Why Diluents ??. High processing viscosities of unmodified liquid epoxy resin systems Impregnating and wetting properties are favourably influenced by reducing the viscosity Larger filler amounts may be used cheaper formulation - PowerPoint PPT Presentation

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Page 1: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 1

Why Diluents ?

That’s Why !!!!!!

Page 2: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 2

Why Diluents ??

• High processing viscosities of unmodified liquid epoxy resin systems

• Impregnating and wetting properties are favourably influenced by reducing the viscosity

• Larger filler amounts may be used– cheaper formulation– reduce the possible development of heat and shrinkage upon cure

• Possible Disadvantages;– May sweat out of the binder system

• Reduced flexibility– Influence the properties of the binder system

• Hardness• Rate of cure• Adhesion, Intercoat adhesion• Chemical resistance

Page 3: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 3

• Alcohols– Benzylalcohol– Furfurylalcohol– Nonyl phenol– Acceleration effect

• Phthalates– Dibutylphthalate

• Hydrocarbon Resins– Necirez-products– Epodil-L

• Pine-oil

Non-Reactive Diluents

OH

CH2-OH

Page 4: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 4

Reactive Diluents

• Polypropylene glycol diepoxides– D.E.R.™ 732P liquid epoxy resin– D.E.R. 736P liquid epoxy resin

™ Trademark of The Dow Chemical Company

O

O=

O

O

C

O

• Alcoholglycidylethers & esters [ mono- or multi-functional ]– EMS [ Grilonit ]– Prümmer [ Polypox ]– Resolution [ Heloxy, Cardura E-10]– Air Products [ Epodil ]– Etc…

Page 5: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 5

Reactive Diluents

EEW[g/eq]

HyCl[%]

Viscosity@ 25 °C [mPa.s]

Density@ 25°C [g/cm3]

Polypox R 3 1,4-Butanediol Diglycidylether 130 - 145 max. 0.2 12 - 22 1.10 - 1.12Polypox R 6 o-Cresyl Glycidylether 175 - 190 max. 0.3 5 - 10 1.07 - 1.09Polypox R 7 p-tert.-Butyl-Phenyl Glycidylether 220 - 240 max. 0.3 10 - 30 1.02 - 1.04Polypox R 9 Polyglycerine-3-Glycidylether 160 - 180 max. 1.0 1100 - 1360 1.21 - 1.25Polypox R 11 Cyclohexanedimethanol Diglycidylether 165 - 185 max. 1.0 60 - 90 1.08 - 1.11Polypox R 12 Glycerine Triglycidylether 140 - 150 max. 0.6 160 - 200 1.21 - 1.23Polypox R 14 Neopentylglycol Diglycidylether 150 - 160 max. 0.2 15 - 25 1.07 - 1.09Polypox R 16 Pentaerythrit Tetraglycidylether 156 - 170 max. 1.5 900 - 1200 1.23 - 1.25Polypox R 17 2-Ethyl-Hexyl Glycidylether 210 - 230 max. 0.3 2 - 4 0.89 - 0.91Polypox R 18 1,6-Hexanediol Diglycidylether 140 - 161 max. 0.2 15 - 25 1.06 - 1.08Polypox R 19 Polypropyleneglycol Diglycidylether 313 - 345 max. 0.3 40 - 90 1.02 - 1.06Polypox R 20 Trimethylolpropane Triglycidylether 140 - 150 max. 0.8 120 - 180 1.15 - 1.19Polypox R 24 C12-C14 Glycidylether 270 - 313 max. 0.1 5 - 10 0.88 - 0.91

Page 6: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 6

Viscosity Cutting Powder

100

1000

10000

0 5 10 15 20

2-EH GE = R 17

C12-C14 AGE = R 24

p-tert. BP GE = R 7

BDDGE, o-CGE, HDDGE = R 3, 6, 18

Page 7: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 7

General Observations

• The addition of reactive diluents might have the following effects:

– reduced viscosity,– changed surface tension [ wetting, air-release etc. ],– changed reactivity, especially for the mono-functional

reactive diluents,– changed solvent resistance,– changed physical strength,– changed linear coefficient of expansion,– changed flexibility / impact resistance,– changed abrasion resistance– ......

Page 8: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 8

Reactive Diluents used by Dow

o-Cresyl Glycidyl etherC12 - C14 alkyl Glycidyl ether

Hexane diol di Glycidyl ether

Compromise between Environmental, Hygiene & Safety aspects and performance.

Page 9: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 9

o-Cresyl Glycidyl ether

O

CH3

O

Typical properties

EEW 180 g/eqViscosity 7 mPa.s @ 25 °C

Page 10: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 10

Hexane Diol Di Glycidyl ether

OO

O O

Typical properties

EEW 142 g/eq

Viscosity 14 mPa.s @ 25 °C

Total Chlorine ca 4 wt%

Page 11: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 11

C12 - C14 Alkyl Glycidyl Ether

OO

N = 11-13

CH2 CH3

Typical properties

EEW 280 g/eq

Viscosity 7 mPa.s @ 25 °C

Total Chlorine ca 3 wt%

Remark : FDA approved for food contact applications

Page 12: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 12

Viscosity Cutting Power

100

1000

10000

0 5 10 15 20 25

Content in D.E.R.™ 331™ epoxy resin [ wt% ]

Vis

cosi

ty [

mP

a.s

]

o-Cresyl GE

Hexane Diol DGE

C12-C14 Alkyl GE

™ Trademark of The Dow Chemical Company

Page 13: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 13

Influence on the chemical resistance

Inorganic acids

Organic acids

Caustic Solvents

o-Cresyl GE Good Good Good Poor

C12 - C14 Alkyl GE

Good Poor Good Poor

Hexane Diol DGE

Poor Poor Good Good

Page 14: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 14

Chemical Resistance

D.E.R.™321 Dist. Water

10 wt% HCl

10 wt% NaOH

10 wt% HAc

Xylene

Gasoline

+ 1.3

+ 1.1

+ 1.1

+ 1.4

+ 1.4

- 0.1

+ 2.1

+ 1.7

+ 1.7

+ 5.4

+ 9.8

0

+ 1.2

+ 1.1

+ 1.0

+ 20

+ 4.9

+ 0.2

+ 2.5

+ 6.5

+ 2.0

Destroyed

Destroyed

+ 23

Aromatic IPD-adduct DETA-adduct Polyamide

D.E.R.™330 Dist. Water

10 wt% HCl

10 wt% NaOH

10 wt% HAc

Xylene

Gasoline

+ 1.4

+ 1.1

+ 1.1

+ 1.3

+ 0.1

+ 0.1

+ 1.4

+ 1.3

+ 1.0

+ 5.1

+ 0.1

0

™ Trademark of The Dow Chemical Company

Page 15: Why Diluents ?

NEO Chemical Seminar 2007

Toine Dinnissen / March 27th 2007 Page 15

Enough Chemistry !