Professional Documents
Culture Documents
UC-669B UCAR Solution Vinyl Resins For Coatings
UC-669B UCAR Solution Vinyl Resins For Coatings
Solution
Vinyl Resins
for Coatings
U
Contents
UCAR® Solution Vinyl Resins for Coatings|1
Typical Properties Table|2
Applications Table|4
General Characteristics Table|4
FDA Status|5
Product Safety|31
Further Information|31
Emergency Service|32
Return to Contents
Recoatable
Typically dry by evaporation. Hydroxyl-modified vinyls
can be cured by crosslinking.
1
Return to Contents
Reactive Functionality
Type — — — carboxyl carboxyl carboxyl
Acid No. — — — 10 10 19
Hydroxyl Value — — — — — —
Epoxy Equivalent Wt — — — — — —
Average Molecular Wt, Mn* 44,000 27,000 22,000 27,000 19,000 15,000
2
Return to Contents
UCARMAG® Binder
VERR-40 VAGH VAGD VAGF VAGC VROH 527 569
82 90 90 81 81 81 82 85
9 4 4 4 4 4 4 13
9b,c 6d 6d 15e 15e 15e 14a,e 2k
— — — — — — — —
— 76 76 59 63 66 59 —
1600g — — — — — —
67 79 77 70 65 65 72 72
40c 20 25 20 30 30 20 20
— 50/50 50/50 50/50 50/50 25/75 50/50 50/50
1000 350 400 171 184 340 170 500
3
Return to Contents
Applications
table 2
VYNS-3 ■ ■ ■ ■ ■ ■
VYHH ■ ■ ■ ■ ■ ■
VYHD ■ ■ ■ ■
VMCH ■ ■ ■ ■ ■
VMCC ■ ■ ■ ■ ■
VMCA ■ ■ ■ ■ ■
VERR-40 ■
VAGH ■ ■ ■ ■ ■ ■ ■
VAGD ■ ■ ■ ■ ■
VAGF ■ ■ ■ ■ ■ ■ ■
VAGC ■ ■ ■ ■ ■ ■
VROH ■ ■ ■ ■
UCARMAG®
Binder
527 ■
569 ■
*VERR-40 is a solution
4
Return to Contents
FDA Status
The UCAR® Solution Vinyl Resins listed below are cited in the
following regulations1 of the United States Food and Drug
Administration (FDA) for use in food-contact applications, such
as can, paper, film, and foil coatings, and coatings for closures.
21CFR 175.300 Components of resinous and polymeric coatings VYHD, VYHH, VYNS-3,
to be applied as continuous films to food-contact VMCA, VMCC, VMCH,
surfaces of articles intended for use in processing, VAGD, VAGH, VERR-40
manufacturing, packing, producing, heating,
packaging, holding, or transporting food.
21CFR 176.170 Components of the food-contact surface of paper VYHD, VYHH, VYNS-3,
and paperboard used to package aqueous and VMCA, VMCC, VMCH,
fatty foods. VAGD, VAGH
21CFR 176.180 Components of paper and paperboard in contact VYHD, VYHH, VYNS-3,
with dry food. VMCA, VMCC, VMCH,
VAGD, VAGH, VERR-40
21CFR 177.1210 Components of closures with sealing gaskets VYHD, VYHH, VYNS-3,
for food containers. VMCA, VMCC, VMCH,
VAGD, VAGH, VERR-40
(1) Since government regulations are subject to revision, it is the user’s responsibility to refer to the Code of Federal Regulations
or the Federal Register to determine current regulatory status.
5
Return to Contents
VYHH
A high molecular weight resin having a composition of
approximately 86 percent vinyl chloride and 14 percent
vinyl acetate. VYHH offers a desirable balance of chemical
resistance, solubility, film strength, and thermoplasticity.
VYHH is usually dissolved in a relatively strong
solvent/diluent combination, such as ketone solvent/
aromatic diluent (50/50 percent by weight). With this
system, a solids content of 20 to 22 percent can be
achieved. Marine and maintenance coatings, ink and
overlacquers for vinyl substrates, strippable coatings,
and masonry and metal coatings are among the principal
applications for UCAR Solution Vinyl Resin VYHH.
6
Return to Contents
Carboxyl-Modified
Vinyl Chloride/Vinyl Acetate Copolymers
The carboxyl-modified vinyl chloride/vinyl acetate When dissolved in a suitable solvent system, such as a
copolymers are made specifically for the formulation of 50 percent ketone/50 percent aromatic hydrocarbon,
coatings having excellent adhesion to various substrates, resin solutions of 23 to 25 percent solids can be achieved.
especially metals, cellulosics, and certain plastics. VMCC is often used in the same applications as VMCH.
However, because of its better solubility, it also finds
VMCH use as an adhesion promoter for vinyl organosols in
A high molecular weight resin containing approximately can coatings.
86 percent vinyl chloride, 13 percent vinyl acetate, and
1 percent maleic acid. UCAR® Solution Vinyl Resin VMCH VMCA
is usually dissolved in relatively strong solvent/diluent A low molecular weight resin containing approximately
combinations, such as 50 percent ketone/50 percent 81 percent vinyl chloride, 17 percent vinyl acetate, and
aromatic hydrocarbon, to produce solutions of 20 to 22 2 percent maleic acid. UCAR Solution Vinyl Resin VMCA
percent solids. UCAR Solution Vinyl Resin VMCH is used is characterized by a high degree of solubility in solvent
primarily for air-dry finishes, such as maintenance, systems having a high aromatic hydrocarbon content.
marine, and metal coatings. VMCH is often used to When dissolved in a suitable solvent/diluent combination,
make heat-sealable packaging coatings. such as 25 percent ketone/75 percent aromatic hydro-
carbon, resin solutions of 30 percent solids can be
VMCC achieved. VMCA yields the good balance of solubility
A medium molecular weight resin containing approxi- and viscosity properties needed for high-build, air-dry
mately 83 percent vinyl chloride, 16 percent vinyl acetate, maintenance finishes. VMCA can also be used in coatings
and 1 percent maleic acid. UCAR Solution Vinyl Resin and adhesives applications where higher solids are
VMCC is more soluble than VMCH in ketones, esters, and desirable.
other solvents used to dissolve vinyl resins. VMCC also has
a higher tolerance for aromatic hydrocarbon diluents.
Epoxy-Modified
Vinyl Chloride/Vinyl Acetate Copolymers
VERR-40
A low molecular weight epoxy-modified copolymer
available only as a solution at 40 percent solids in
MEK/toluene (3/2 by weight). VERR-40 can be blended
with carboxyl-modified vinyls (VMCH, VMCC, and VMCA)
to provide an all-vinyl reactive coating system that,
when cured by baking, yields coatings with enhanced
toughness, flexibility, and solvent resistance.
7
Return to Contents
Hydroxyl-Modified
Vinyl Chloride/Vinyl Acetate Copolymers
UCAR® Hydroxyl-Modified Vinyl Chloride/Vinyl Acetate with a hydroxyl content of approximately 2.3 percent.
Copolymers are manufactured using two different processes. The lower molecular weight provides improved solubility
VAGH and VAGD are polymers made in a two-step process and permits the formulation of solutions containing
that yields vinyl alcohol in the backbone. The other higher solids.
hydroxyl-modified resins are produced by a one-step
polymerization process similar to that used to make the
copolymer and carboxy-functional solution polymerized ■ DIRECTLY-POLYMERIZED RESINS
resins described above.
Hydroxyl-modified vinyl chloride/vinyl acetate copolymers
VAGF
are noted particularly for compatibility with other film-
A high molecular weight copolymer comprised of vinyl
forming resins, such as alkyds, urethane elastomers,
chloride, vinyl acetate, and a hydroxyalkyl acrylate. The vinyl
isocyanate resins, epoxy polymers, and urea and melamine
chloride portion is about 81 percent with the hydroxyl content
resins. Hydroxyl-modified vinyls are, therefore, often
at 1.8 percent. The solution viscosity and other properties of
formulated with these and other film-forming materials
VAGF strongly resemble those of VAGH. VAGF can be used for
to improve coating properties, such as adhesion, flexibility,
a wide range of coatings applications, including industrial
toughness, hardness, and chemical resistance. Hydroxyl-
maintenance and marine finishes, paper coatings, general
modified resins are often used to impart snap-dry properties
metal finishes, and as a binder in magnetic tape.
to a coating. The hydroxyl functionality permits crosslinking
reactions for thermoset coating systems that exhibit
VAGC
outstanding chemical and water resistance. Coatings based
A medium molecular weight copolymer comprised of vinyl
on these resins also have good adhesion to wash primers,
chloride, vinyl acetate, and a hydroxyalkyl acrylate. The
metals, wood, and many plastic substrates.
vinyl chloride portion is about 81 percent with the hydroxyl
content at 1.9 percent. The solution viscosity and other
properties of VAGC are very similar to those of VAGD.
■ HYDROLYZED RESINS
VAGC finds commercial application in clear and pigmented
coatings for metal, wood, paper, concrete, masonry, films,
VAGH foils, fabrics, and leather.
A high molecular weight, partially-hydrolyzed vinyl chlo-
ride/vinyl acetate resin having a composition of approxi- VROH
mately 90 percent vinyl chloride, 4 percent vinyl acetate, A low molecular weight terpolymer comprised of vinyl
with a hydroxyl content of approximately 2.3 percent. UCAR chloride, vinyl acetate, and a hydroxyalkyl acrylate. The
Solution Vinyl Resin VAGH can be dissolved in relatively vinyl chloride portion is approximately 81 percent, and the
strong solvent/diluent combinations, such as 50 percent hydroxyl content is approximately 2 percent. High tolerance
ketone/50 percent aromatic hydrocarbon, to produce resin for alcohols and aliphatic diluents broadens the usefulness
solutions of 20 percent solids. VAGH can be used for a of VROH. UCAR Solution Vinyl Resin VROH can be dissolved
wide range of coatings applications, including industrial in solvent/diluent combinations, such as 25 percent
maintenance and marine finishes, wood finishes, paper ketone/75 percent aromatic hydrocarbon, to produce resin
coatings, metal decorative and container coatings, and solutions of 30 percent solids. Also, 35 percent resin solutions
as a binder in magnetic tape. can be prepared with VROH using Rule 66-type exempt
solvent systems (for the wood coatings industry) containing
VAGD as much as 30 percent by volume butanol. UCAR Solution
A medium molecular weight, partially-hydrolyzed vinyl Vinyl Resin VROH can be used in a wide variety of clear
chloride/vinyl acetate resin having a composition of approxi- and pigmented coatings for metal, wood, paper, film, foil,
mately 90 percent vinyl chloride, 4 percent vinyl acetate, and fabric.
8
Return to Contents
Solutions
Several criteria must be weighed in choosing solvents In general, ketones are the most suitable solvents
and diluents for UCAR Solution Vinyl Resins: for vinyl resins. Compared to other solvents, ketones
■ Solvent Strength yield higher resin concentrations without gelling and
■ Volatility lower solution viscosities at equivalent solids content.
■ Toxicity Because of their solvency, they tolerate greater dilution
■ Odor with economical hydrocarbon diluents and exhibit
■ Cost better storage stability. Figure 1 compares the solvent
■ Flammability strength of different ketones for VYHD.
■ Type of Application Esters are useful in applications where minimal
attack on the substrate is desirable (as with coatings on
UCAR Solution Vinyl Resins are readily dissolved plastics). Because of their low solvency for vinyls, they
into clear solutions at room temperature by ketones, should be used in combination with other active solvents.
nitroparaffins, esters, and chlorinated hydrocarbons. Urethane-grade esters are preferred for minimum
viscosity and optimum viscosity stability. Figure 2 compares
the solvent strength of different esters for VYHD.
9
Return to Contents
10,000
8,000
6,000
Isophorone
5,000
4,000
Cyclohexanone
3,000
Methyl Isobutyl Ketone
2,000
1,000 Acetone
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
10
Return to Contents
figure 2
10,000
8,000
6,000
Methyl PROPASOL® Acetate
5,000
4,000
Isopropyl Acetate
3,000
Butyl Acetate
2,000
Ethyl Acetate
1,000
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 5 10 15 20 25 30 35
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
11
Return to Contents
table 4
Acetone 84 88
Methyl Ethyl Ketone 86 130
Methyl Propyl Ketone 124 212
Methyl Isobutyl Ketone 230 360
Methyl Isoamyl Ketone 304 504
Methyl n-Amyl Ketone 316 684
Cyclohexanone 672 360
Isophorone 930 484
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
Diluents lower coating costs, alter the evaporation rates, Optimum formulation stability and the lowest
and provide other important coating characteristics. solution viscosities are obtained when the solvent system
Typical diluents for use with UCAR® Solution Vinyl Resins contains only active solvents. As the proportion of diluent
include aromatic hydrocarbons, such as toluene and increases, the stability declines. Figures 3 to 5 compare
xylene. Aliphatic hydrocarbons, such as mineral spirits, the solution viscosity of UCAR Solution Vinyl Resins
VM&P naphtha, and heptane, can also be used. These versus solids content in methyl ethyl ketone and in
aliphatic hydrocarbons are less effective than aromatic a methyl isobutyl ketone/toluene (50/50) blend.
hydrocarbons and should be used at levels not Formulating at excessively high solids or with weak
exceeding 10 percent of the solvent blend. solvent mixtures can result in solutions having unstable
Ketones tolerate greater amounts of aromatic viscosities and can even lead to the formation of gel
diluents than do the ester solvents. Table 4 compares structures. As the molecular weight of the vinyl resin
the viscosity of VYHH in ketones with the viscosity in decreases, however, the diluent level can be increased
ketone/diluent mixtures. while maintaining the same level of viscosity.
12
Return to Contents
figure 3
10,000
8,000
6,000
5,000
4,000
VYNS-3
3,000
VYHH
2,000
VYHD
1,000
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
13
Return to Contents
10,000
8,000
6,000
5,000
4,000
VYNS-3
3,000
VYHH
2,000
VYHD
1,000
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
14
Return to Contents
figure 4
10,000
8,000
6,000
VAGH
5,000
4,000
VAGF
3,000
VAGD
2,000
VAGC
1,000 VROH
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
15
Return to Contents
10,000
8,000
6,000
VAGH
5,000
4,000
VAGF
3,000
VAGD
2,000
VAGC
1,000 VROH
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
16
Return to Contents
figure 5
10,000
8,000
6,000
5,000
4,000
3,000
VMCH
2,000
VMCC
1,000 VMCA
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
17
Return to Contents
10,000
8,000
6,000
5,000
4,000
3,000
VMCH
2,000
VMCC
1,000 VMCA
Viscosity at 25ºC, cP
800
600
500
400
300
200
100
80
60
50
40
30
20
10
0 10 20 30 40 50
NOTE: Viscosity was determined using a Brookfield viscometer model RVT, running at 50 or 100 rpm with spindles
#2 through #5, selected as appropriate for the solution being tested.
18
Return to Contents
figure 6
Cooled
Viscosity
Room Temperature
Heated
0 1 2 3 4 5
Time (weeks)
■ VISCOSITY BEHAVIOR
Another equilibrium condition that affects solution
Viscosity behavior of vinyl solutions is influenced by resin viscosity is the memory effect. It is noted in vinyl solutions
concentration, active solvent used, ratio of solvent to that have been subjected to increases or decreases in
diluent, and solution temperature. temperature and is characterized by a significant lag in
Viscosity changes in vinyl solutions are the result the rate at which a vinyl solution returns to equilibrium
of different equilibrium effects that occur during the viscosity after a temperature change. For example, a vinyl
preparation and storage of resin solutions. The formation solution that has been heated will maintain an abnormally
of a slight degree of micro-crystallinity among adjacent low viscosity for extended periods after it has returned to
polymer molecules in solution is responsible for the its initial temperature. This viscosity change is caused by
observed viscosity increase. differences in the degree of microcrystallinity of the solution
The time required to reach equilibrium viscosity at various temperatures. As the temperature increases, the
for vinyl resin solutions is influenced by resin molecular degree of microcrystalline regions that exist in the solution
weight, solids content, solvent strength, processing time, decreases and the viscosity decreases. The memory effect
and temperature. Vinyl resin solutions usually increase is illustrated in Figure 6.
in viscosity with time. The extent of the total increase can Formulators must be aware of both these effects and
range from a minor viscosity drift to a major change, such the time required to reach equilibrium conditions, so that
as gelation. Vinyl solutions that have gelled because of viscosity stability problems, resulting from the preparation
excessive solids content or a solvent mix that is too weak of solutions at incorrect solids levels or solvent blends,
can be restored to fluidity by proper thinning and mixing. are avoided.
19
Return to Contents
20
Return to Contents
table 5
. Relative
Evaporation Weight Flash Point,
Rate Solubility per gallon Distillation Closed
Solvents (BuAc=100) with VYHHa,b at 20ºC, lb Range, ºC Cup, ºF
Fast Evaporating
Acetone 1160 S 6.59 56-57 0
Ethyl Acetate, 99% 615 S 7.51 76-78 30
Methyl Ethyl Ketone 570 S 6.71 78-81 24
Isopropyl Acetate, 99% 500 S-G 7.26 86-90 42
Propyl Acetate 275 S 7.39 99-103 58
Medium Evaporating
Methyl Isobutyl Ketone 165 S 6.67 114-117 61
Isobutyl Acetate, Urethane Grade 145 S 7.25 112-117 62
Butyl Acetate, Urethane Grade 100 S 7.34 124-129 84
Slow Evaporating
Amyl Acetate, Primary 42 S 7.29 140-150 101
Cyclohexanone 23 S 7.89 156 111
Methyl PROPASOL® Acetate 34 S 8.09 146 114
Diisobutyl Ketone 18 S-G 6.72 163-173 120
Diacetone Alcohol 14 S 7.82 145-172 133
Isophorone 3 S 7.67 210-218 179
21
Return to Contents
Clear vinyl coatings can be modified with plasticizers, The optimum level of plasticizer for a formulation
heat and light stabilizers, and other materials for specific will depend upon the specific resin used and the perfor-
performance properties. Before incorporating any modifier mance property required by the application. To obtain
in the formulation, understand clearly how the modifier equivalent degrees of flexibility, higher molecular weight
meets the demands of the application. Do not use clear resins require more plasticizer than lower molecular
vinyl coatings for applications that involve long-term weight resins. Proportions of 10 to 25 parts plasticizer
exposure to ultraviolet light. per 100 parts of resin are typically used.
Table 6 provides a list of plasticizers having good
Plasticizers compatibility with UCAR Solution Vinyl Resins.
The addition of a plasticizer in the coating formulation
will enhance flexibility and help to minimize solvent Heat Stabilizers
retention in the film. The typical phthalate, adipate, As with all vinyl resins, UCAR Solution Vinyl Resins
citrate, epoxy, and phosphate plasticizers are compatible are degraded upon prolonged exposure to heat. The
with UCAR® Solution Vinyl Resins. In general, compatibility degradation products include hydrogen chloride, which
decreases as the hydrocarbon nature of the plasticizer accelerates further resin degradation and leads to the
increases. Polymeric plasticizers are less efficient than development of unsaturated polymer structures that can
monomeric plasticizers. be easily oxidized. The result is embrittlement, loss of
Other factors to consider in selecting plasticizers flexibility, and discoloration of the vinyl film. To minimize
include solubility, volatility, the effect on outdoor durability, the degradation of vinyl films, add suitable heat stabilizers.
the need for low-temperature flexibility, and suitability Baking at temperatures above 248ºF (120ºC) for more
for contact with food. Certain citrates, epoxies, and than five minutes will usually require a thermal
phthalates are permitted under FDA regulations. stabilizer to avoid degradation of the film. The use of
Monomeric plasticizers are most commonly used, a tin mercaptide stabilizer (1 percent*) in combination
although the polymeric plasticizers are used to provide with a liquid epoxy resin, such as ERL-4221, or diglycidyl
special film characteristics, such as low extractability ether of bisphenol A resin (3 to 5 percent*) gives the
or migration. Phosphate plasticizers are generally not best results.
recommended for outdoor exposure because of poor Do not use barium, cadmium, or zinc stabilizers with
light stability. the carboxyl-modified vinyl resins; they tend to react with
When a bake cycle is required, the volatility of the the carboxyl groups. Zinc stabilizers also tend to develop
plasticizer is particularly important. The plasticizer may color quickly, especially in low plasticizer systems. Iron
volatilize sufficiently to lower the concentration below and zinc surfaces can accelerate decomposition and
what was originally intended for the dried or cured discoloration.
formulation.
22
Return to Contents
Light Stabilizers
table 6
Type Product
An adequate quantity of a hiding pigment will screen out
incident radiation and prove the best light stabilizer for Phthalate Diisooctyl Phthalate
pigmented vinyl coatings. Do not use unpigmented vinyl Diisodecyl Phthalate
coatings outdoors. Where only limited ultraviolet light Butyl Benzyl Phthalate
exposure will be encountered, clear films should be formu- Butyl 2-Ethylhexyl Phthalate
lated with a light stabilizer system to prevent discoloration.
2-Ethylhexyl Isodecyl Phthalate
The best light stabilizer system includes an ultraviolet light
absorber (substituted benzophenones), a hindered amine Citrate Acetyl Tributyl Citrate
light stabilizer (HALS), and UNION CARBIDE ERL-4221, Acetyl Triethyl Citrate
a cycloaliphatic epoxy resin.
Tributyl Citrate
A typical system would be comprised of the following:
Phosphate Tri(2-ethylhexyl) Phosphate
Ingredients %* Triphenyl Phosphate
UV Absorber1 1 Tributyl Phosphate
HALS2 2
ERL-42213 3 Epoxy FLEXOL® Plasticizer EPO
(Epoxidized soybean oil)
* on weight of vinyl resin
(1) UV Absorber - “Uvinul” D-5O (BASF), “Tinuvin” 327 FLEXOL® Plasticizer EP-8
or 328 (Ciba Geigy) or equivalent.
(2) HALS - “Tinuvin” 292 (Ciba Geigy) or equivalent. (2-Ethylhexyl epoxy tallate)
(3) Cycloaliphatic Epoxide (Union Carbide).
FLEXOL® Plasticizer LOE
In all cases, choose stabilizers carefully and test them (Epoxidized linseed oil)
under actual use conditions. Consult suppliers of stabilizers
Polymeric Adipic Acid Polyester
for specific recommendations.
Azelaic Acid Polyester
Sebacic Acid Polyester
Blown Castor Oil
Blown Soybean Oil
Blown Linseed Oil
23
Return to Contents
Pigments are selected for hiding power, ultraviolet The use of extender pigments or fillers will help
protection, purity, and ease of wetting. Although most improve the economics of the formulation. They will
commercially-available pigments are suitable for use also help prevent sagging of thick wet films on vertical
with UCAR® Solution Vinyl Resins, there are some general surfaces, will help control gloss (flatting) at low levels,
constraints. Additionally, there are specific constraints that and will permit greater film thickness per coat. Talcs,
apply to UCAR Carboxyl-Modified Solution Vinyl Resins. clays, barytes, and silicas may be used as extender
Do not use natural iron oxide pigments with any pigments. If they are used, they will contribute little to
UCAR Solution Vinyl Resin. These pigments contain trace ultraviolet absorption. A sufficient quantity of ultraviolet-
impurities that can gel the coating or cause discoloration light-absorbing prime pigment must be included in
or excessive chalking of the film. Do not use iron- the formulation.
containing pigments, such as Prussian blue or the so- Table 7 provides a listing of pigment types and
called “chrome greens” (blends of Prussian blue and lead loadings typically recommended for UCAR Vinyl
chromate). Chromium oxide green, however, performs Copolymer and Hydroxyl-Modified Vinyl Resins.
well with UCAR Solution Vinyl Resins. Formulation with UCAR Carboxyl-Modified
When an iron oxide pigment is desired, use synthetic Vinyl Resins VMCH, VMCC, and VMCA involves special
iron oxides; they perform well with UCAR Solution Vinyl considerations. The carboxyl groups of these products are
Resins. With coatings containing synthetic iron oxides, randomly spaced along the polymer chain and will react
use a heat stabilizer, particularly when bake temperatures with basic materials to form irreversible gels or increased
may reach 248ºF (120ºC). consistency of pigment-vinyl combinations. Do not use
Gold bronze metallic pigments are powdered alloys basic pigments, extenders, or fillers with UCAR Carboxyl-
of copper and zinc. They tend to react with vinyl, causing Modified Vinyl Resins. Particularly, avoid lead-containing
color development and gellation. When used to make pigments (red lead, chrome yellow, chrome orange), zinc
gold inks, the powder is stirred into the ink vehicle shortly dust or zinc oxide, strontium-containing pigments, and
before use, and quantities sufficient for the job at hand calcium carbonate. Do not even use small amounts of
are prepared. these basic materials in pigment blends. With minor
There is a minimum amount of pigment that must proportions of basic pigments, viscosity aberrations may
be used to impart opacity to ultraviolet light. For example, not be predictable; some batches may have a normal
about 65 parts of titanium dioxide (TiO2) per 100 parts of viscosity and others will gel. Table 8 lists pigments typically
vinyl resin is the minimum amount that should be used. used with UCAR Carboxyl-Modified Vinyl Resins.
To obtain maximum hiding power in thin films, about
125 parts TiO2 per 100 parts of vinyl resin is a practical
maximum concentration. Exceeding this level can cause
excessive chalking. If color pigments are desired, they
can generally be substituted for TiO2 at an equal volume
replacement. There are exceptions; ultra-fine particle
size pigments, for example, are used at much lower
concentrations.
24
Return to Contents
table 7
Pigment 100 Parts Resin Pigment 100 Parts Resin
RED MAROON
Pigment Scarlet —* Thioindigo Types —
Permanent Red 2B Alizarine Types —
(Non-Resinated Calcium, Barium BON Types —
or Strontium Lakes of 2-B Acid — Perylene Maroon —
BON Reds —
Pyrazolone Reds — BROWN
Indanthrene Reds — Iron Oxide, Synthetic Types 55 to 100
Quinacridone Reds —
Perylene Scarlet — BLACK
Pyranthrone Scarlet — Carbon Black 5 to 7
Perylene Vermillion — Furnace Black 5 to 7
Iron Oxide, Synthetic Types 55 to 100 Lampblack 5 to 7
Iron Oxide, Synthetic Types 55 to 100
YELLOW
Nickel-Titanium Yellow — WHITE
Indanthrene Types — Antimony Oxide —
Benzidines — Titanium Dioxide 75 to 125
Nickel Azo Types — Zinc Oxide —
Flavanthrone —
Anthrapyrimidine — VIOLET
Pyratex Yellows — Carbazole —
Iron Oxide, Synthetic Types 55 to 100 Carbozole Dioxane —
ORANGE METALLIC
Vat Orange — Aluminum Pastes (65%),
Dianisidine Orange — Leafing or Non-Leafing 60 to 85
Benzidine Orange —
Anthanthrone — BLUE
Phthalocyanine Blue —
GREEN
Phthalocyanine Green 15 to 25
25
Return to Contents
Pigment 100 Parts Resin carboxyl-modified vinyl, the water molecule may form
a bridge between the polymer’s carboxyl group and the
Aluminum Powder 35 to 50 pigment surface. Silica and alumina hydrate are prone
Titanium Dioxide 75 to 125 to bridging or hydrogen bonding. Since most chloride-
Phthalocyanine Green process TiO2 pigments have silica, zinc oxide, or alumina
treatments, they can develop hydrogen bonding.
(Non-Resinated) 15 to 30
Hydrogen bonding manifests itself as viscosity instability.
Phthalocyanine Blue The viscosity may increase slowly over a period of several
(Non-Resinated) 15 to 30 months or it may increase rapidly in a few days or weeks.
Carbon Black 7 If the water content reaches two percent based on the
Iron Blue Chalks badly weight of carboxyl-modified vinyl, the paint may even gel.
Commercial-grade materials typically limit water
Iron Oxide Yellow, Synthetica 60 to 125
content adequately and should introduce no serious
Iron Oxide Red, Synthetica 60 to 125 viscosity instability. If water does contaminate the
Iron Oxide Black, Synthetica 60 to 125 formulation, it may come from the solvents or be
Iron Oxide Brown, Synthetica 60 to 125 introduced through poor storage practices.
Ultramarine Blue Chalks & fades Organic acids, mineral acids, and certain acid-esters
will reverse bridging from excessive moisture. Organic
Zinc Phosphate 75
acids (such as citric, maleic, or malonic) or mineral acids
Talc Use as filler (such as phosphoric) are all effective at concentrations
Clay or extender of one-fourth to one percent, based on the weight of
Barytes pigments the carboxyl-modified vinyl resin.
To restore a gelled paint to fluidity, first prepare a
Silica
solution of the acid or acid-ester in acetone or other
compatible solvent. Then, slowly add the solution to the
(a) Natural oxides are not satisfactory. Synthetic oxides are satisfactory gelled paint with agitation. Acid treatment of the coating
in either air-dried or baked coatings.
may, however, affect adhesion and reduce gloss.
A small amount of acid or acid-ester can also prevent
or minimize viscosity excursions during paint manufacture.
As with the restoration of gelled paints, this treatment
may also affect adhesion and reduce gloss.
The best way to control viscosity aberrations from
water content is to prevent water from entering the
formulation.
26
Return to Contents
Pigments can be easily dispersed into vinyl coatings Where maximum gloss is desired, add pigments in either
with conventional equipment, such as a pebble mill, vinyl pigment chip or vinyl pigment paste form. For faster
sand grinder, and high-speed stirrers. To prevent iron dispersion, incorporate wetting agents in the formulation.
contamination, do not use steel ball mills for pigment Soya licithin or “Nuosperse” 657 (Creanova, Inc.) have
dispersion. The most common technique is to dissolve been extensively tested and are effective wetting agents,
the vinyl resin in the appropriate solvents. The vinyl when used in concentrations of one to five percent,
solution is then blended with the plasticizers, stabilizers, based on pigment weight. Other suppliers such as Byk
grinding aid, and pigments. For higher gloss coatings, Chemie offer additives useful for pigment dispersion.
predisperse the pigment in plasticizer, thinner, and
grinding aid before adding to the vinyl resin solution.
27
Return to Contents
a
Compatibility of UCAR® Hydroxyl-Modified Vinyl Resins with Other Resins
Vinyl/Modifier Ratiob
table 9
Alkyds (non-drying)c
“Beckosol” 12-021, coconut, short oil, PA content - 47% C C C C C C
Alkyds (drying)c
“Beckosol” 11-035, soya, medium oil, PA content - 35% C I C I H I
“Beckosol” 12-005, soya, short oil, PA content - 42% C C C C C C
“Beckosol” 11-070,
linseed/soya, medium oil, PA content - 31% C I C I H I
“Beckosol” 12-054,
tall oil fatty acids, short oil, PA content - 41% C C C C C C
Urea-Formaldehyde Resins d
“Beetle” 55 (methylated resin) I I I I I I
“Beetle” 60 (methylated resin) I I I I I I
“Beetle” 65 (methylated resin) I I I I I I
“Beetle” 80 (butylated resin) C C C C C C
Hexamethoxymethylmelamine d
“Cymel” 303 C C C C C C
Melamine-Formaldehyde Resins d
“Cymel” 350 C C C C C C
“Cymel” 370 (methylated resin) C C C C C C
“Cymel” 225-10 (rapid-cure resin) H I H I H I
Urethane Prepolymerse
“Mondur” CB-60, aromatic polyisocyanate C C C C C C
“Desmondur” N-75, aliphatic polyisocyanate C C C C C C
“Mondur” HC, polyisocyanate copolymer C C C C C C
Key:
C = Compatible (a) 5-mil (125 microns) wet drawdowns on glass; coatings dried 20 min at 140°F (60ºC) prior to rating
H = Haze in film, but coating uniform (b) Solids basis
I = Incompatible (c) Reichhold
PA = Phthalic Anhydride (d) Cytec Industries
(e) Bayer
28
Return to Contents
Adhesion
For good adhesion, surfaces must be free of rust, grease, needed. Baking finishes can be cured with heated air,
oil, dirt, and other contamination. Common techniques infrared radiation, or by heating the metal surface on
for cleaning surfaces include solvent wash, vapor which the coating is applied. Control temperature care-
degreasing, chemical treatment, and brush cleaning. fully to avoid overbaking the coating. Maintain proper
For maximum adhesion, use a phosphate treatment ventilation and uniform temperature distribution.
or a vinyl butyral wash primer before applying the vinyl UCAR® Hydroxyl-Modified Solution Vinyl Resins
coating. Where vinyl butyral primers are used, the next adhere well to many types of finishes and are quite
coat must be based predominantly on hydroxyl-modified useful in applications where coatings based on the
resins (VAGF, VAGC, VAGH, or VAGD). unmodified vinyl resins will not adhere. UCAR Carboxyl-
Maximum adhesion of vinyl coatings is usually Modified Solution Vinyl Resins adhere to clean metal
obtained at bake temperatures high enough to drive and to air-dry or baked topcoats or primers. Table 10
out traces of residual solvents. Over porous surfaces, such compares the air-dry adhesion of coatings based on the
as concrete and cloth, mechanical adhesion should be three basic types of UCAR Solution Vinyl Resins.
sufficient for good performance; baking is not generally
29
Return to Contents
30
Return to Contents
Product Safety
When considering the use of any Union Carbide products Union Carbide requests that the customer read,
in a particular application, you should review our latest understand, and comply with the information contained
Material Safety Data Sheets and ensure that the use you in this publication and the current Material Safety Data
intend can be accomplished safely. For Material Safety Sheet(s). The customer should furnish the information
Data Sheets and other product safety information, in this publication to its employees, contractors, and
contact the Union Carbide sales office nearest you. Before customers, or any other users of the product(s), and
handling any other products mentioned in the text, you request that they do the same.
should obtain available product safety information and
take necessary steps to ensure safety of use.
No chemical should be used as or in a food, drug,
medical device, or cosmetic, or in a product or process
in which it may contact a food, drug, medical device, or
cosmetic, until the user has determined the suitability
and legality of the use. Since government regulations
and use conditions are subject to change, it is the user’s
responsibility to determine that this information is
appropriate and suitable under current, applicable
laws and regulations.
Further Information
For information on prices, delivery, and technical service,
phone 1-800-568-4000. For product information on safe
handling, ask for the latest Material Safety Data Sheet
(MSDS).
31
Return to Contents
Emergency Service
Continental Europe, Ireland, Phone BIG (Geel-Belgium) Phone CHEMTREC (United States):
Middle East, North and Central Africa (32)(0) 14 58-45-45 (703) 527-3887 (collect)
Latin America, Asia/Pacific, South Africa Phone United States: Phone CHEMTREC (Unites States):
and any other location worldwide (304) 744-3487 (collect) (703) 527-3887 (collect)
At sea, radio U.S. Coast Guard, who can directly contact Union Carbide HELP…
(800) 822-4357 (toll-free) or CHEMTREC… (800) 424-9300 (toll-free).
DO NOT WAIT! Phone if in doubt! You will be referred to a specialist for advice.
32
U
Union Carbide Corporation UC-669B
39 Old Ridgebury Road P8-8429
Danbury, CT 06817-0001 10/98 –3M
Printed in U.S.A.