Paint & Coatings Industry August 2014
Paint & Coatings Industry August 2014
Paint & Coatings Industry August 2014
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www.pcimag.com
August 2014
VOLUME 30, NUMBER 8
Paint Coatings Industry
INSIDE
UV LED Curing
Equipment Directory
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Thomas E. Tom Gosz
PORTAGE, IN Sherwin-Williams Scien-
tist Thomas E. Tom Gosz of Portage,
IN, passed away June 30, 2014. He was
born October 2, 1960, in Kaukauna,
WI, the son of Clifford and Janice (Wit-
tmann) Gosz.
Gosz graduated from Michigan
Technological University in 1983.
He received a Masters Degree from
DePaul University in 1989. Gosz
worked as a scientist for the Sherwin-
Williams Co. for over 25 years and was
involved in the application of Sherwin-
Williams coatings to many of the wind
turbines seen along the highways.
OBITUARY
AUGUST 2014
|
W W W . P C I M A G . C O M 12
COMPANY NEWS
Bayer Receives Responsible Care Honor
PITTSBURGH Bayer Corp. has been named a 2014 Responsible
Care
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AUGUST 2014
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W W W . P C I M A G . C O M 14
COMPANY NEWS
demand throughout Asia for solutions targeted at the packaging,
coil, specialty finishes and powder coatings markets.
The extension will also double the number of people working in
R&D at Songjiang, to around 200, over the next couple of years.
When fully operational, the new laboratory will be Performance
Coatings second-largest research and development base after
Felling in the UK.
Located in the greater Shanghai area, the Songjiang site was
recently expanded to create one of AkzoNobels biggest resin
plants for performance coatings.
PPG Plans Facility Expansion in Brazil
PITTSBURGH PPG Industries recently announced an invest-
ment of about $40 million in its coatings manufacturing facility
located in Sumare, So Paulo, Brazil.
The expansion project will add a 65,000-square-foot plant for
on-site resin production. The resin will be used to manufacture
PPGs electrocoat products to meet growing demand among OEMs
and industrial coatings customers in the region. PPG anticipates
completion of the project in 2015 and expects to add more than 30
new positions at the facility.
ISO Certification for Custom Milling & Consulting
FLEETWOOD, PA Custom Milling & Consulting Inc. has been
granted ISO 9001:2008 Quality Management System Certifica-
tion for the manufacture and provision of its complete range of
products and services.
ISO 9001:2008 is an internationally recognized certification
that provides guidelines for the implementation of standard prac-
tices to ensure products meet regulatory and customer require-
ments. The certification covers design, development, production,
sales, marketing, and servicing of wet milling machinery, includ-
ing wet mill toll processing. Also, the design, development, manu-
facture and sale of colorants for the landscape industry.
PPG Reaches Agreement to Acquire Comex
PITTSBURGH PPG Industries has reached a definitive agreement
to acquire Consorcio Comex, S.A. de C.V. (Comex), an architectural
and industrial coatings company with headquarters in Mexico City,
Mexico. The transaction is valued at $2.3 billion and is subject to
regulatory approvals and customary closing conditions.
Comex manufactures coatings and related products in Mexico
and sells them in Mexico and Central America through approxi-
mately 3,600 stores that are independently owned and operated
by more than 700 concessionaires. Comex also sells its products
through regional retailers, wholesalers and direct sales to cus-
tomers. The company has approximately 3,900 employees, eight
manufacturing facilities and six distribution centers, and had
sales of approximately $1 billion in 2013. Comex is a privately
held company that was founded in 1952.
Charles E. Bunch, PPG Chairman and CEO, said that PPG plans
to fund the acquisition primarily using currently held cash and
short-term investments, but he indicated that the company may
fund a portion of the purchase price through the addition of debt.
Bunch added that excluding non-recurring acquisition-related
costs the deal will be immediately accretive to earnings, and that
the company anticipates acquisition-related synergies of 3-4% of
acquired sales will be achieved over a two-year period.
The companys North American architectural coatings busi-
ness has also reached a definitive agreement to acquire Mas-
terwork, an independent architectural paint distributor head-
quartered in Pittsburgh. The acquisition of Masterwork, which
operates a 13-store network throughout western Pennsylvania,
Ohio and New York, will expand PPGs company-owned stores
footprint in the region.
Perstorp Acquires Chemkos Penta Business
PERSTORP, Sweden Specialty chemicals company Perstorp
has acquired the pentaerythritol, penta and calcium formate
businesses from Chemko a.s. Strske, a chemicals producer
in Slovakia.
The sales agreement includes Chemko a.s. Strskes penta
and calcium formate businesses, related technology and certain
assets. It does not include the manufacturing plant in Strske,
Slovakia, any real estate or employees. The transaction is part of
Perstorps plan to increase polyol capacity.
The polyalcohol penta is used in applications including alkyd
resins, PVC stabilizers, synthetic lubricants, varnishes and other
products. Perstorp is now producing penta in three different pro-
duction plants in Germany, the United States and Sweden.
Saint Clair Systems Inc. Buys Norcross Corp.
WASHINGTON TOWNSHIP, MI Saint Clair Systems Inc., Wash-
ington Township, MI, has purchased the assets of Norcross Corp.,
a Massachusetts-based viscosity-control company. Saint Clair
Systems President C. Robert Gladstone believes the combination of
technology and experience shared by the two companies provides
additional opportunities to serve existing customers and a signifi-
cant opportunity to expand into new markets.
Gladstone also noted that Saint Clair Systems will benefit from
Norcross international sales network.
RPM Acquires Waterproofing
Products Manufacturer
MEDINA, OH RPM International Inc. announced that Viapol
Ltda., part of The Euclid Chemical Co. and RPMs Performance
Coatings Group, has acquired Betumat Quimica Ltda., a water-
proofing products manufacturer based in Candeias, Brazil.
Betumat offers a full line of waterproofing products, including
asphaltic membranes, cementitious grouts and modified asphalt
products, to professional contractors and builders primarily in
northern Brazil.
Datacolor Acquires Media Logic
LAWRENCEVILLE, NJ Datacolor AG announced the acquisi-
tion of Media Logic SNC, a software provider for the Italian and
European retail paint market. The acquisition includes Media
Logic SNCs distribution company. The privately held company is
headquartered in Reggio Emilia, Italy, and provides customized
software solutions focused on the industrial paint market. All
seven Media Logic employees, as well as the founder Corrado Iotti,
are joining the Datacolor team.
Media Logics software, Ymity, manages the entire process of
color communication for tinting systems, from measuring to mix-
ing color at points of sale in the retail market and at laboratories.
The software offers management of multiple dispensers and seam-
less data exchange between the paint manufacturer and paint
dealers, assuring the right paint color. The company also provides
a smartphone and tablet application that allows users to simulate
color choices for their home in 3D.
PAI NT & COATI NGS I NDUS TRY
15
C O MP A N Y N E WS
ALTANA Group Invests in Landa Digital Printing
WESEL, Germany/REHOVOT, Israel The specialty chemicals
group ALTANA and Landa Corp. have concluded an equity
financing agreement under which ALTANA will invest 100
million for a minority stake in Landa Digital Printing. Both
companies see the agreement not only as a financial invest-
ment, but also as a starting point for a long-term strategic part-
nership to bring digital printing solutions to the commercial,
packaging and publishing markets. Other units of the Landa
Group, including Landa Labs and Landa Ventures, are not
included in the transaction.
The proceeds will be used for completing the development of
Nanography, Landas water-based digital printing process, includ-
ing engineering and production ramp-up of Landa Nanographic
Printing Presses and building of manufacturing plants for
Landa NanoInk colorants.
ALTANA is expected to be an active partner, drawing on
print industry expertise gained from its BYK Additives &
Instruments, ECKART Effect Pigments, and ACTEGA Coatings
& Sealants divisions.
Protex International Buys
Chartwell International
PARIS Protex International, Paris, France, has acquired Chart-
well International Inc., Attleboro Falls, MA. Larry Cohen will
remain with the company as a consultant, and there are no
changes planned in the agent and distribution system that has
been set up by Chartwell.
The name Chartwell will continue to be used for the companys
adhesion promoter family.
Protex International is a diversified, privately held company with
sales to a range of end markets including specialty chemicals, coat-
ings, textile, electronics, water pretreatment, food and perfume.
Clariant and Ashland Complete
Sale of Joint Venture
MUTTENZ, Switzerland/COVINGTON, KY Clariant and Ash-
land Inc. have closed the previously announced sale of their joint
venture ASK Chemicals, headquartered in Hilden, Germany, to
investment funds affiliated with Rhne, a London and New York-
based private equity investment firm.
The divestment of our stake in ASK Chemicals is part of our
continuous active portfolio management to reallocate capital
towards our more profitable growth areas, said Hariolf Kott-
mann, CEO of Clariant.
ASK Chemicals is a leading foundry chemicals manufacturer
with a portfolio that encompasses a broad and innovative range
of foundry resources such as binders, coatings, feeders, filters and
release agents, as well as metallurgical products including inocu-
lants, inoculation wires and master alloys.
and Devoe
References
1
Townsin, R.L.; Byrne, D.; Svensen, T.E.; Milne, A. Trans
SNAME 89. 1981, 295-318.
2
Grigson, C.W.B. J. Ship Res. 1992, 36: 182-196.
3
Kempf, G. Trans INA. 1937, 79: 109- 119.
4
Schultz M.P.; Bendick, J.A.; Holm, E.R.; Hertel, W.M. Biofoul-
ing 2011, 27: 87- 98.
5
Townsin, R.L. Biofouling 2003, 19 (suppl.): 9- 16.
6
Holm, E.R.; Schultz, M.P.; Haslbeck, E.G.; Talbott, W.J.; Field,
A.J. Biofouling 2004, 20: 219- 226.
7
Granville, P.S. J. Fluids Eng. 1982, 104: 373- 377.
For more information, e-mail Dr. Klijnstra at Job.Klijnstra@endures.nl.
D
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a
g
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e
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(
%
)40
30
20
10
0
-10
Rotation Speed (RPM)
700 900 1100 1300 1500
n Coating I (FRC) n Coating II (FRC) n Coating III (SPC)
FIGURE 8 Test set-up for rotation aging of hull coatings applied onto
disks suitable for drag measurements.
AUGUST 2014
|
W W W . P C I M A G . C O M 24
D
eveloping a coating with improved dirt
pickup resistance continues to be an
important goal in the coatings indus-
try. Reasons for this include growth
in softer elastomeric wall and roof
coatings; demand for low-VOC formulations, which tra-
ditionally result in tackier coatings due to reduced glass
transition temperatures (Tgs); and the planned construc-
tion of high-rise commercial buildings, most notably in
Asia, which is driving the need for coatings that are easier
to clean and maintain.
One approach to improving dirt pickup resistance has
been to create a harder finish by raising the Tg of the
coating. There are, however, downsides to this approach.
First, it is nonviable in elastomeric applications, such as
elastomeric roof coatings that require elongation and flex-
ibility, since the increased Tg can decrease the flexibility of
the coating. Such a decrease in flexibility can lead to the
formation of cracks in the coating. Second, increasing the
Tg of a coating can require the use of coalescing solvents,
which typically have a high VOC content. The increased
VOC is in direct opposition to the need to decrease VOCs in
coatings due to government regulations.
Other approaches included using highly crosslinked
polymers, which try to provide a low-tack surface that
impedes dirt penetration. While this method can provide
an effective solution for automotive coating applications,
architectural and elastomeric coatings provide unique
challenges due to the need to retain elongation, making
crosslinked polymers a less viable approach.
A New Option
Multi-staged polymers represent fairly new technology
that involves a mixture of polymers with different Tg
ranges, resulting in a mix of hard and soft segments. This
technology, however, has yet to overcome many of the
same issues discussed above, specifically elongation prop-
erties. The aqueous binder composition of the multi-staged
polymers includes (a) polymer particles of average particle
diameter with a Tg of -30 C or lower, and (b) polymer
particles of average diameter with a Tg of 50 C, or higher,
where the average diameter ratio between particles of the
first polymer and particles of the second polymer must be
at least 4:1. To avoid sedimentation, the particle diameter
ratio between particles of the first polymer and particles of
the second polymer must be no greater than 6:1.
The first and second polymer particles both have a par-
ticle size distribution and an average molecular weight that
are each in a predetermined value range. The average par-
ticle diameter of the first polymer particle ranges from 0.33
to 0.60 micrometers; the average particle diameter of the
second polymer particle ranges from 0.06 to 0.09 microm-
eters. For the various embodiments, the first polymer
particle and the second polymer particle each have a high
average molecular weight and a polydispersity index (PDI)
of no greater than 1.11. Particle size ratio, high molecular
weight (MW) and narrow molecular weight distribution
are important to assure high dirt pickup resistance.
The combination of the average particle diameter and
particle diameter ratio of the first and second polymer
particles allows for a percolation threshold volume (Vp) to
be obtained when the aqueous coating composition has at
least 75 volume percent of the first polymer particle on a
dry basis of the aqueous coating composition. It is believed
that for the various embodiments, achieving the perco-
lation threshold volume for the particle diameter ratio
allows for the second polymer particles (the smaller of the
two particles) to preferentially percolate through the first
polymer particles to an outer surface of the elastomeric
coating where they can help to form a hard and rough
skin layer that improves dirt pickup resistance.
The first polymer particle and the second polymer
particle each include a hydrophobic branched monomer
in polymerized form; particles were synthesized by a free
radical polymerization process prepared with a hydropho-
bic branched monomer. For the various embodiments, the
hydrophobic branched monomer in the first polymer par-
ticle is a NEO monomer with a Tg of -40 C. For the second
polymer particle the hydrophobic branched monomer is a
NEO monomer with Tg of +70 C.
The aqueous binder composition does not require addi-
tional components, such as solvents and/or coalescents to
By Hugo De Notta, Ph.D., R&D Director | Multiquimica s.a., Santo Domingo, Dominican Republic
New
Elastomeric
Binder
with Dirt Pickup Resistance
PAI NT & COATI NGS I NDUS TRY
25
form a film. For the various embodiments, the elastomeric
binder formed can provide an elongation value of 850-
1000%, determined according to ASTM D2370. Likewise,
the elastomeric binder gives the possibility of formulating
elastomeric wall paints with a vapor transmission of 5
to 9 g/m
2
/day determined according to ASTM F1249 or
TAPPI 448, and a water absorption (after 96 h soaking in
tap water) of 9.0% or less. For the various embodiments,
the elastomeric coating formed with the aqueous coating
composition can provide a contact angle of at least 128
determined according to ASTM D7334.
The binder synthesized according to this technology also
shows high dirt pickup resistance, which is a consequence
of several technical facts such as the high reactivity of
the branched hydrophobic monomers used (which gives
a high-MW polymer with low polydispersity), the ratio of
particle size between the two binders, the low polydispersity
of each polymer to be blended, the relative binder composi-
tion, and the usage of a UV-reactive monomer to synthesize
the low-particle-size hard polymer. These properties allow
the formulation of elastomeric coatings that are particu-
larly well suited for use on masonry, concrete surfaces and
stone surfaces, among others.
As has been mentioned, the first and the second poly-
mer in the aqueous binder composition have an average
particle size distribution that is very narrow. In other
words, both polymers to be blended have very small poly-
dispersity (standard deviation of the average particle size
distribution). For example, the polydispersity for the first
polymer particle can be 5% or less, while the polydisper-
sity for the second polymer particle can be 7% or less.
As a result, the aqueous coating composition can have
essentially a bimodal particle size distribution, or a binary
mixture, of the first and second polymer particles.
The bimodal distribution and the particle diameter ratio
of the first and second polymer particles have an influence
on how the polymer particles segregate during the forma-
tion of the elastomeric coating. As appreciated, a system
of particles in motion (such as the first and second poly-
mer particles in the aqueous coating composition as the
elastomeric coating is forming) distributes itself through
a variety of mechanisms, including what is known as per-
colation. During percolation, different-sized particles of the
system can migrate in different directions depending upon
a number of different factors. These factors can include the
relative size and weight of the particles as well as the tem-
perature at which the percolation is occurring. As a result
of this migration, the different-sized particles can segregate
themselves to different parts of the elastomeric coating.
A Hard and Rough Layer
For the various embodiments, the particle diameter ratio
(with its bimodal distribution) and the weight average
molecular weight of the first and second polymer par-
ticles, among other things, are believed to affect the segre-
gation of the polymer particles as the elastomeric coating
forms. In particular, a Vp has been identified from these
parameters that provides a volume percentage of the sec-
ond polymer particle (the relatively smaller hard polymer
particle as compared to the first polymer particle) needed
to cause the second polymer particles to preferentially seg-
regate to an outer surface of the elastomeric coating dur-
ing the drying process. In this relative position, the second
polymer particles can help to form a hard and rough layer
that is hydrophobic and that helps to improve dirt pickup
resistance, while the first polymer particle helps to bal-
ance and control the elastomeric behavior of the elasto-
meric coating. For the various embodiments, the Vp can
be obtained with aqueous coating compositions having at
least 75 volume percent of the first polymer particle on a
dry basis of the aqueous coating composition; the remain-
ing volume percent of the aqueous coating composition
can be the second polymer particle.
There is not necessarily a complete segregation of the
first and second polymer particles as the elastomeric coat-
ing forms. For the various embodiments, the hard and
rough layer of the elastomeric coating can include a blend
of the first and second polymer particles. Such blends, how-
ever, will typically include a majority of the second polymer
particle when the volume percentage of the second polymer
particle is within the Vp. In other words, the Vp of the pres-
ent disclosure can be used to better ensure that the bimodal
system of the first and second polymer particles will pref-
erentially segregate so that the majority of the hard and
rough layer is formed with the second polymer particles. It
mostly depends on the particle size polydispersity.
Even more surprisingly, it has also been found that
when the volume percentage of the second polymer par-
ticle is within the percolation threshold volume, the aque-
ous coating composition does not require a coalescing
agent in order to form the elastomeric coating.
For the various embodiments, the morphological struc-
ture of the hard and rough layer also contributes to the elas-
tomeric coatings ability to provide dirt pickup resistance.
As illustrated in the following sections, the hard and rough
layer of the elastomeric coating includes a topography hav-
ing projections or bumps that provide for a rough surface.
One skilled in the art will appreciate that the presence of a
relatively high degree of surface roughness can provide for
at least two important contact effects between the rough
surface and materials that can come into contact with the
rough surface. First, the existence of a high degree of sur-
face roughness can provide for a very small contact area
between the surface and a contaminant (e.g., a particulate
or an aqueous liquid droplet) that can come into contact
with the surface. As such, adhesion between the contami-
nant and the surface can be minimized due to the minimal
contact area between the two. Second, the surface rough-
ness can facilitate the trapping of air beneath a portion of
the contaminant. For instance, when considering a liquid
droplet coming into contact with the rough surface, an air
Multi-staged polymers represent fairly
new technology that involves a mixture of
polymers with different Tg ranges, resulting
in a mix of hard and soft segments.
New Elastomeric Binder with Dirt Pickup Resistance
AUGUST 2014
|
W W W . P C I M A G . C O M 26
boundary layer can form between portions of the droplet
and the surface; this air boundary layer can increase the
contact angle between the droplet and the surface.
Although surface roughness can provide a surface with
some degree of hydrophobicity, hydrophobicity can be fur-
ther enhanced when combined with a surface chemistry
providing a low surface energy. The hard and rough layer of
the elastomeric coating also displays a low surface energy,
which, coupled with the rough surface, leads to a high
contact angle that resists wetting and adherence of dirt and
contaminants. Thus, when a solid particulate or a liquid
droplet, (e.g., a water droplet) contacts the coating, it can roll
down or slide off of the surface due to the combined effects of
surface roughness and low surface energy. Also, when con-
sidering a liquid droplet, as the droplet rolls down the surface
and encounters a solid particle on the surface, the particle
can adhere to the passing droplet and can simultaneously
be removed from the surface with the liquid, as adhesion
between the surface and the particle has been minimized.
Thus, the particle can preferentially adhere to the liquid and
be cleaned from the surface of the elastomeric coating.
It has been discovered that if a coalescing agent is used,
the resulting hard and rough layer structure is altered to
a smoother surface relative to the hard and rough surface
formed without the use of the coalescing agent. Therefore,
the use of coalescent aids is not recommended.
Forming the Polymer Particles
For the various embodiments, elastomeric coatings
formed with the aqueous coating composition of the pres-
ent disclosure can have contact angles of 128 minimum.
Known synthesis techniques have been used to control
the polymer particle size. Surfactant type and the polymer-
ization process, among other things, have a great influence
on the polymer particle size. The size and polydispersity of
the polymer particles have been controlled by the choice of
polymerization starting materials and conditions for the
first and second polymer, such as seed size and concentra-
tion, polymerization rate, catalyst or initiator concentra-
tion, reaction temperature, surfactant concentration, etc.
The first polymer and the second polymer can each be
prepared by an emulsion polymerization process using at
least one hydrophobic ethylenically unsaturated mono-
mer and several hydrophilic ones.
These hydrophilic functional monomers that are use-
ful in forming the first and second polymer particles can
include, but are not limited to, hydrophilic functional
monomers that contain ethylenically unsaturated double
bonds for free radical reaction with the hydrophobic ethyl-
enically unsaturated monomer or other monomers during
polymerization. Examples of such hydrophilic functional
monomers can include acrylic acid, methacrylic acid,
n-butyl acrylate, 2-ethylhexyl acrylate, methyl methacry-
late, acrylamide, and mixtures thereof.
Monomers used in forming the first polymer particle
can include mixtures of 2-ethylhexyl acrylate and/or
n-butyl acrylate, NEO monomer with Tg of -40 C, acrylic
or methacrylic acid, and/or acrylamide, and methyl meth-
acrylate that contains more than 40% by weight of NEO
monomer. The remaining monomer is mostly 2-ethyl-
hexyl acrylate, n-butyl acrylate or combination thereof.
Monomers used in forming the second polymer particle
can include mixtures of NEO monomer with Tg of +70 C
and several hydrophilic ones such as 2-ethylhexyl acry-
late and/or butyl acrylate, acrylic or methacrylic acid,
acrylamide and methyl methacrylate that contains more
than 40% by weight of NEO monomer, no more than 5%
by weight of methyl methacrylate, and less than 3% of
4-(2-acryloyloxyethoxy)-2-hydroxybenzophenone, with
the remaining monomer being 2-ethylhexyl acrylate,
n-butyl acrylate or a combination thereof.
Suitable polymerization conditions must be used. Typi-
cally, the reaction temperature is 70-80 C. The polymer-
ization can be conducted using polymerization initiators.
Suitable free radical polymerization initiators are known
to promote emulsion polymerization and can include
water-soluble oxidizing agents, such as organic perox-
ides (e.g., t-butyl hydroperoxide, cumene hydroperoxide,
etc.), inorganic oxidizing agents (e.g., hydrogen perox-
ide, potassium persulfate, sodium persulfate, ammonium
persulfate, etc.), and those initiators that are activated in
the water phase by a water-soluble reducing agent. Such
initiators are employed in an amount sufficient to cause
polymerization. The amount of such free radical initiators
used can be in the range of 0.05-0.20% by weight based
on the weight of all monomers present.
Redox initiators may be employed, especially when
polymerization is carried out at lower temperatures. For
example, reducing agents may be used in addition to
the persulfate and peroxide initiators mentioned above.
Typical reducing agents can include, but are not limited
to, alkali metal salts of hydrosulfites, sulfoxylates, thio-
sulfates, sulfites, bisulfites, etc. In general, the reducing
agents are used in the range of 0.01-0.20% by weight
based on the weight of all monomers present.
Various additives can be added before, during or after
polymerization. These include surfactants, reactive surfac-
tants, radical chelating agents, buffering agents, neutral-
izing agents, defoamers and polymeric stabilizers, among
others. Suitable surfactants can include, but are not limited
to, those having a low critical micelle concentration (CMC).
For the various embodiments, suitable surfactants have
a CMC of less than 0.009 g/100 g in 0.1 M NaCl at 25 C.
So, for the various embodiments the first polymer and the
second polymer include surfactant having a critical micelle
concentration of less than 0.009 g/100 g in 0.1 M NaCl at
25 C combined with reactive surfactants.
Examples of suitable surfactants can include alkyldi-
phenyloxide disulfonate, polyoxyethylene tridecyl ether
phosphate, ammonium salt, and polyoxyethylene alkyl-
phenyl ether ammonium sulfate. For the various embodi-
ments, the amount of the surfactant can be in the range of
0-2.8% by weight.
Study 1: Percolation Threshold
In this example, the percolation threshold volume, Vp,
as a function of the particle diameter ratio was studied.
As discussed earlier, the Vp provides a volume percent-
age of the second polymer particle (the relatively smaller,
hard polymer particle as compared to the first polymer
particle) needed to cause the second polymer particles to
preferentially segregate to an outer surface of the elas-
PAI NT & COATI NGS I NDUS TRY
27
tomeric coating during the drying process. The bimodal
distribution and the particle diameter ratio of the first and
second polymer particles have an influence on how the
polymer particles segregate during the formation of the
elastomeric polymer film. As shown in Figure 1, as the
particle diameter ratio increased, the Vp decreased. As a
result, a lower concentration of the second polymer par-
ticle (hard) is required to achieve the Vp. For the various
embodiments, improvements in the dirt pickup resistance
and other properties of the elastomeric coating are also
observed as the particle diameter ratio increases. Values
for the particle diameter ratio that provide for the Vp, as
well as dirt pickup resistance and elongation properties,
include those where the first average particle diameter
to the second average particle diameter have a particle
diameter ratio in the range of 4:1 to 6:1. Particle diameter
ratio values above 6:1 have been found to cause sedimen-
tation of the first polymer particle in the aqueous coating
composition over time.
From the data provided in Figure 1, aqueous coating
compositions of the first and second polymer particles
at percolation threshold volumes of 57% and 25% were
prepared. For the aqueous coating compositions with the
percolation threshold volumes of 57%, the first polymer
particle had a PDI of 1.09, a Tg of -40 C, high MW and an
average particle diameter of 0.1 micron. The second poly-
mer particle had a PDI of 1.08, a Tg of 50 C, high MW and
an average particle diameter of 0.09 micron. The volume
average particle diameters for the first and second polymer
particles allow for aqueous coating compositions having
particle diameter ratios of 1.11:1 to achieve the Vp of 57%.
In this case, due to the volume of hard polymer neces-
sary to achieve percolation, a non-elastomeric behavior
is expected. The volume average particle diameters of the
first and second particles are determined based on spheri-
cal geometry using diameter measurements from a Nano-
trac
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New Elastomeric Binder with Dirt Pickup Resistance
AUGUST 2014
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W W W . P C I M A G . C O M 30
Each of the aqueous coating compositions was formed in the
same manner as the previous studies. An elastomeric coating was
formed with each of the aqueous coating compositions by apply-
ing a 0.007 inch-thick coat of the aqueous coating composition to
a Leneta P121-10N chart. The aqueous coating composition was
allowed to dry at 25 C and a controlled relative humidity of 50%
for 24 h to form the elastomeric coating.
The residual tack of each coating was tested using a Rolling Ball
test method according to ASTM D3121. For the test of residual tack,
the distance in centimeters the ball rolls determines the presence of
residual tack, where distances less than 20 centimeters indicate a
coating with an unacceptable tack, and distances of 20 centimeters
or greater indicate a coating with an acceptable tack or no tack. A
TT-100 Rolling Ball Track Tester, which meets standards set by the
Pressure Sensitive Tape Council (PSTC-6) and the ASTM (ASTM
D3121) was used for testing tack of the film.
The film crack properties of each of the elastomeric coatings
were also tested and the presence of cracks determined by visual
observation according to ASTM D823.
The results for both the residual tack and the film crack proper-
ties are shown in Table 2.
As shown in Table 2, as the Tg of the second polymer particle
is increased, the elastomeric coating transitions from having a
residual tack (Tg of 40 C for the second polymer particle) to not
having a residual tack at Tg values of 70 C and greater. However,
if the Tg of the second polymer particle is increased to a value of
90 C or above, the elastomeric coating shows film crack.
Study 4: Soiling Test and Elongation
In this example, a soiling test was used to measure dirt pickup resis-
tance of elastomeric coatings formed with aqueous binder composi-
tions having different particle diameter ratios. In addition, elongation
of the elastomeric coatings formed with aqueous binder compositions
having different particle diameter ratios was measured.
Aqueous binder compositions of the first and second polymer
particles having particle diameter ratios of 3:1, 4:1 and 6:1 were
prepared. For this study, the first polymer particle had a PDI of
1.08, a Tg of -30 C, high MW, and average particle diameters of
either 0.27, 0.36 or 0.54. The second polymer particle had a PDI
of 1.08, a Tg of 70 C, high MW and an average particle diameter
of 0.09. The average particle diameters for the first and second
polymer particles allow for aqueous binder compositions having
particle diameter ratios of 3:1, 4:1 and 6:1 to achieve the Vp of
TABLE 2 Tack and film crack properties.
T
g
(C)
Second Polymer
Particle
T
g
(C)
First Polymer
Particle
Residual Tack Film Crack
40 -30 Yes No
45 -30 Yes No
70 -30 No No
90 -30 No Yes
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PAI NT & COATI NGS I NDUS TRY
31
28%, 25% and 16%, respectively. The average particle diameters
of the first and second particles were determined based on spheri-
cal geometry using diameter measurements from a Nanotrac
150 device, where the measurements were taken on a 1 weight
percent aqueous suspension of the particles in distilled water.
Each of the aqueous coating compositions was formed in the
same manner as in the previous examples. Allow the composition
to rest 24 hours before preparing the elastomeric coating.
For the soiling test, an elastomeric coating was formed with
each of the aqueous coating compositions by applying a 0.007
inch (7 mils)-thick coat of the aqueous coating composition to the
varnished side of a Leneta Form 2C opacity chart. The aqueous
coating composition was allowed to dry at 25 C and a controlled
relative humidity of 50% for 24 h to form the elastomeric coating.
An initial reflectance of each coating was measured and recorded
using a Technibrite Micro TB-1C (measurement angle of 45
using a 457 nm wavelength). The entire surface of the elastomeric
coating was soiled with a slurry of iron oxide in water (50% weight/
weight slurry of red iron oxide and water). To soil the elastomeric
coating, the slurry was applied using a brush at 25 C. The soiled
coating was placed in an oven (Blue M Industrial Oven) set to 60 C
for 8 h. The coating was allowed to cool to room temperature and
was then washed with high-pressure water (tap water at room
temperature) using an air pistol (Cane NT) working at a pressure of
40 PSI and at a distance of 20 to 30 cm from the soiled coating. The
coating was then dried at room temperature and humidity. This
soiling process was repeated a total of five times.
After the fifth soiling process, a final reflectance of the soiled
coating was measured using the Technibrite at the same setting
used to measure the initial reflectance. The initial reflectance of
the elastomeric coating and the final reflectance of the soiled coat-
ing were used to calculate a percent drop of reflectance using the
following equation:
% Drop of Reflectance = [(Initial reflectance) (Final Reflec-
tance) / Initial Reflectance] x 100
To test elongation of the elastomeric coatings, an elastomeric
coating was formed with each of the aqueous coating compositions
by forming a 1.2 mm-thick coating of the aqueous coating composi-
tion on a glass plate. The coating was allowed to dry at 25 C and a
controlled relative humidity of 50% for seven days to form the elas-
tomeric coating. The coating was removed from the glass plate, and
the elongation of the elastomeric coating was measured according
to ASTM D2370 using an Instron 1011.
Table 3 provides data on the percent drop in reflectance for the
soiled elastomeric coatings, where the larger the percent drop in
reflectance the lower the dirt pickup resistance. Table 3 also pro-
vides data on the elongation of the elastomeric coatings.
As can be seen, the aqueous coating composition having a par-
ticle diameter ratio of 6:1 provided a percent drop in reflectance and
an elongation that is superior to the aqueous coating composition
having a particle diameter ratio of 3:1. As discussed earlier, for the
given Tgs, the particle diameter ratio has an impact on the effi-
ciency of the percolation of the aqueous coating composition. It is
TABLE 3 Drop in reflectance and elongation.
Particle
Diameter Ratio
Drop in Reflectance (%) Elongation (%)
3:1 -20% 197
4:1 -16 % 884
6:1 -14% 1252
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New Elastomeric Binder with Dirt Pickup Resistance
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W W W . P C I M A G . C O M 32
believed that particle diameter ratios of less than 4:1 for the aqueous
coating composition percolate less efficiently, which results in less
of the second polymer particle in the skin layer of the elastomeric
coating as compared to ratios of 4:1 or 6:1. This less-efficient per-
colation results in more of the second polymer particle remaining
below the skin layer of the elastomeric coating, where it causes
an increase in the overall Tg of the elastomeric coating below the
skin layer. In addition, when more of the second polymer particle
is present below the skin layer, it may form hard polymer domains
that create discontinuities in the elastomeric coating below the skin
layer, leading to the negative effect on the elongation of the elasto-
meric coating as illustrated in Table 3.
Study 5: Blistering Resistance, Elongation, Dirt
Pickup Resistance and Porosity
In this example, the aqueous coating composition was used as a
binder in paint formulations with different pigment volume con-
centrations (PVCs). Elastomeric coatings formed with the paint
formulations were tested for blistering resistance, elongation, dirt
pickup resistance and porosity.
The aqueous coating composition of the first and second poly-
mer particles at a Vp of 25%, which corresponds to a particle
diameter ratio of 4:1, was prepared. For this example, the first
polymer particle had a PDI of 1.08, high MW, a volume average
particle diameter of 0.36 and a Tg value of -30 C. The second
polymer particle had a PDI of 1.08, high MW, a volume average
particle diameter of 0.09 microns and a Tg value of 70 C. Each of
the aqueous coating compositions was formed in the same man-
ner as in earlier studies. The aqueous binder composition had 60
weight % solids content.
The paint was formulated in two steps. In the first step, a grind
was prepared by adding to a 1 Kg glass beaker 44.00 weight %
water, 0.12 weight % defoamer, 0.40 weight % dispersing agent,
0.10 weight % non-ionic surfactant and 0.40 weight % HEC
ER-30,000 thickener, while mixing at low speed (no more than
20 RPM) with a COWLES mixer (Morehouse Cowles) for 10 min at
room temperature.
TABLE 4 Blister resistance, elongation, dirt pickup resistance
and porosity results.
Paint
Formulated
at PVC (%)
Blistering
Resistance*
Elongation
(%)
Drop in
Reflectance
(%)
Porosity
(ASTM
D3258)**
20 Poor 1120 -17 Very Low
42 Good 981 -15 Very Low
55 Good 584 -25
Medium-
High
* Blistering resistance: Poor means MD (Blister size 2); Good means F (Blister size
8) or less.
** Results are presented as the difference of reflectance of the untested coating
and that of the penetrated coating. For PVC equal to 20%, Very Low means a 3%
drop; for PVC equal to 42% Very Low means a 5% drop; and for PVC equal to 55%
Medium- High means a 27% drop.
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PAI NT & COATI NGS I NDUS TRY
33
To prepare the grind, 20.00 weight %
hydrophobic-modified titanium dioxide
pigment, 16.90 weight % high-purity sil-
ica produced from synthesized cristobalite
extender and 17.97 weight % hydrous
aluminum silicate treated extender were
stirred in at high speed (more than 50
RPM). After adding the last extender, agi-
tation was maintained at high speed for 1
h. Finally, 0.046 weight % OIT (fungicide)
and 0.064 weight % isothiazolinone blend
14% were added as bactericides.
In the second step, the letdown was pre-
pared at a speed of no more than 20 RPM
by adding the aqueous coating composi-
tion (used as the binder) to the grind to
obtain three different PVCs of 20%, 42%
and 55%. For a PVC of 20%, 40 weight
% grind was blended with 60 weight %
aqueous coating composition. For a PVC of
42%, 66 weight % grind was blended with
34 weight % aqueous coating composi-
tion. For a PVC of 55%, 76 weight % grind
was blended with 24 weight % aqueous
coating composition. The resulting paint
formulations were mixed an additional 10
min at 10 RPM. The pH was adjusted to 8
using ammonia or other base.
To test blistering resistance, a coating
was formed with each of the paint formu-
lations by forming a 1.2 mm-thick coating
of the aqueous coating composition on
a glass plate. The aqueous coating com-
position was allowed to dry at 25 C and
controlled relative humidity of 50% for
seven days to form the elastomeric coat-
ing. The coating was removed from the
glass plate and was cut into a 5 cm by 5 cm
test specimen. The specimen was placed
in a glass beaker filled with tap water and
allowed to soak at room temperature for
96 h. The specimen was removed from the
tap water, and the surface was dried with
a paper tissue. The blister resistance was
tested according to ASTM D714.
To test elongation, a coating was formed
with each of the paint formulations as dis-
cussed above for the blistering resistance
test. The elastomeric coating was removed
from the glass plate, and the elongation of
the elastomeric coatings prepared with
the different paint formulations was mea-
sured according to ASTM D2370 using an
Instron 1011.
Drop of reflectance for the elastomeric
coatings prepared with the paint formu-
lations using the soiling test discussed
above in Study 4 was also measured.
To test the porosity of the elastomeric
coatings formed from the paint formula-
tions, a coating was formed with each
of the paint formulations by applying a
0.007 inch (7 mils)-thick coat of the paint
formulation to a Leneta P121-10N chart.
The paint formulation was allowed to dry
at 25 C and controlled relative humidity of
50% for 24 h to form the elastomeric coat-
ing. The porosity of the elastomeric coat-
ings prepared from the paint formulations
was tested according to ASTM D3258.
Table 4 shows the results for blister
resistance, elongation, dirt pickup resis-
tance (as measured by drop in reflec-
tance), and porosity for coatings prepared
with the paint formulations.
As shown in Table 4, elastomeric coat-
ings prepared from the paint formulation
having a PVC of 20% have high elonga-
tion, very low porosity resulting in poor
New Elastomeric Binder with Dirt Pickup Resistance
AUGUST 2014
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W W W . P C I M A G . C O M 34
blister resistance and a 17% drop in reflectance after the
soiling test. Elastomeric coatings prepared from the 42%
PVC have a lower elongation as compared to the elasto-
meric coating prepared from the paint formulation having
a PVC of 20%, a 17% drop in reflectance after the soiling
test, very low porosity, but good blister resistance. It is
believed that PVC of 42% is very close to the critical PVC
for the paint formulation as prepared for this study
Study 6: Contact Angle and Dirt Pickup
Resistance with Different TiO
2
In this example, three paint formulations having a 42%
PVC, with different types of titanium dioxide, were pre-
pared. The elastomeric coatings formed from the paint
formulations were tested for contact angle and dirt pickup
resistance. The different types of titanium dioxide for use in
the paint formulations were a multipurpose rutile titanium
dioxide pigment manufactured by the chloride process with
93% TiO
2
(Titanium I), a rutile titanium dioxide pigment
designed to provide maximum hiding in high-quality,
high-PVC architectural coatings with 80% TiO
2
(Titanium
II), and a universal rutile titanium dioxide pigment, manu-
factured by the chloride process, that is designed to deliver
both high gloss and excellent durability in coatings with
93% TiO
2
(Titanium III). Each type of titanium dioxide had
surface treatment with amorphous silica and alumina at
different weight percentages. Of the three titanium diox-
ides, Titanium III had a hydrophobic surface treatment.
To test the contact angle, a coating was formed in the
same manner as above. Contact angles were measured
using a Dataphysics OCA 150 equipment according to
ASTM D7334 (Pendant drop method).
To test drop in reflectance, a drawdown of each paint
formulation was prepared by applying a 0.007 inch-thick
coat of the paint formulation to the varnished side of a
Leneta Form 2C opacity chart. Drop of reflectance was
measured using the soiling test discussed in Example 4.
Table 5 shows the results for the contact angle and the
drop of reflectance for the elastomeric coatings prepared
with the 42% PVC paint formulations having different
titanium dioxide.
As shown in Table 5, Titanium III gives the paint for-
mulation the lowest drop in reflectance and the highest
contact angle as compared to the other types of titanium
dioxides tested.
Study 7: Contact Angle and Dirt Pickup
Resistance with Different Extenders
In this example, two paint formulations having a 42%
PVC, with different combinations of extenders were pre-
pared. The elastomeric coatings formed from the paint
formulations were evaluated for contact angle and dirt
pickup resistance. The different types of extenders included
high-purity silica produced from synthesized cristobalite
extender, a hydrous aluminum silicate, treated extender,
platy talc and calcium carbonate. Cristobalite and alumi-
num silicate have a hydrophobic behavior. Platy talc is less
hydrophobic than cristobalite and calcium carbonate is a
hydrophilic calcium carbonate.
The paints were formulated as described in Example
5, where the first paint formulation included the follow-
ing combination of extenders: cristobalite and aluminum
silicate; a second paint formulation included the following
combination of extenders: talc and calcium carbonate. For
the second combination, the paint formulation included
16.90 weight % talc and 17.97 weight % calcium carbonate
To test drop in reflectance, a coating was formed with
each of the paint formulations by applying a 0.007 inch (7
mils)-thick coat of the paint formulation to the varnished
side of a Leneta Form 2C opacity chart. The paint formulation
was allowed to dry at 25 C and a controlled relative humid-
ity of 50% for 24 h to form the elastomeric coating. Drop of
reflectance for the elastomeric coatings prepared with the
paint formulations was measured using the soiling test.
To test the contact angle, a coating was formed with
each of the paint formulations by applying a 0.007 inch-
thick coat of the aqueous coating composition to a Leneta
P121-10N chart. The paint formulation was allowed to
dry at 25 C and controlled relative humidity of 50% for
24 h to form the elastomeric coating. Contact angles were
measured using a Dataphysics OCA 150 according to
ASTM D7334 (Pendant drop method).
Table 6 shows the results for the contact angle and the
drop of reflectance for the elastomeric coatings prepared
with the 42% PVC paint formulations using different com-
binations of extenders.
As shown in Table 6, the use of the first combination of
extenders (cristobalite and aluminum silicate) provided
for a more hydrophobic coating as compared to the second
combination of extenders (talc and calcium carbonate).
The lower drop in reflectance showed by the paint formu-
TABLE 7 Elongation, tensile strength, water absorption and vapor
transmission results.
Paint
Formulated
at 42% PVC
Elongation
(%)
Tensile [gram
(force)/mm
2
)
Water
Absorption (%)
Vapor Transm.
(gram/m
2 .
day)
Prototype 987 95 8.2 14.2
Competitor I
(-20 C)
981 92 12.3 11.3
Competitor II
(-30 C)
834 85 12.9 11.5
Competitor
IV (-40 C)
657 75 15.7 18.8
TABLE 6 Contact angle and drop in reflectance with different extenders.
42% PVC Paint Formulated
with Hydrophobic TiO
2
and the Following Extenders
Contact Angle ()
Drop in
Reflectance (%)
Cristobalite/aluminum silicate 148 -14
Talc/calcium carbonate 136 -21
TABLE 5 Contact angle and dirt pickup resistance with different TiO
2
.*
42% PVC Paint
Formulated With
Contact Angle () Drop in Reflectance (%)
Titanium I 137 -19
Titanium II 136 -18
Titanium III 146 -14
* Measured as drop in reflectance
PAI NT & COATI NGS I NDUS TRY
35
lated with the first combination of extenders also confirms
the higher dirt pickup resistance typically seen on rough,
hydrophobic surfaces.
Study 8: Elongation, Tensile Strength,
Water Absorption and Vapor Transmission
In this example, four paint formulations, each having a
42% PVC, were prepared. The first paint formulation used
the aqueous binder composition (prototype) as the binder
(prepared as described in Example 5). The second example
was the same paint formulation using a competitive poly-
mer (Tg of -20 C) as a binder. The third paint formulation
used another competitor as the binder (Tg of -30 C), and
the fourth paint formulation used a commercial polymer
with Tg of - 40 C as a binder. The coatings formed with
the paint formulations were tested for elongation, tensile
strength, water absorption and vapor transmission.
To test elongation, tensile strength, water absorption
and vapor transmission of the coatings, a 1.2 mm film
with each of the paint formulations was prepared. The
formulations were allowed to dry at 25 C and controlled
relative humidity of 50% for seven days to form the coat-
ing. For the elongation and tensile strength, the coating
was removed from the glass plate, and the elongation and
tensile strength were measured according to ASTM D2370
using an Instron 1011. Water absorption was measured,
as discussed herein, and vapor transmission according to
ASTM F1249. The results are shown in Table 7.
Study 9: Soiling Test
In this example, four paint formulations were prepared.
The first one had a 42% PVC using the same paint formula-
tion described in Example 5 and the prototype with ratio of
particle size 4:1 and 75%/25% blend as a binder. The second
paint formulation had a 42% PVC using the same paint for-
mulation described in Example 5 with the prototype binder
with particle size 4:1, but with the composition 81%/19% as
a binder. The third paint formulation had a 42% PVC using
the same paint formulation described in Example 5, where
Competitor II was the binder. The fourth paint formulation
had 42% PVC using the same paint formulation described
in Example 5, where Competitor III was the binder.
For the soiling test, drawdowns of each paint formula-
tion were made by applying a 0.007 inch-thick coat to
the varnished side of a Leneta Form 2C opacity chart. The
paint formulation was allowed to dry at 25 C and a con-
trolled relative humidity of 50% for 24 h.
Initial ref lectance of each coating was measured
using a Technibrite (measurement angle of 45 using
a 457 nm wavelength). Then the entire surface of the
coating was soiled with a slurry of iron oxide in water
(50% weight/weight slurry of red iron oxide and water)
using a brush at 25 C. The soiled coating was placed
in an oven set to 60 C for 8 h. The soiled coating was
allowed to cool to room temperature. Finally the coat-
ing was washed with high-pressure water (tap water at
room temperature) using an air pistol (Cane NT) work-
ing at a pressure of 40 PSI and at a distance of 20 to 30
cm from the soiled coating. The coating was allowed
to dry at room temperature and humidity. This soiling
process was repeated a total of five times.
Figure 4 provides images of the coatings after the
soiling test, where the ref lectance is measured in a
region of the soiled coatings that have been washed as
discussed above. For the images, the dark portions in
the region indicate the presence of soil on the coatings.
As can be seen, a visual comparative evaluation dem-
onstrates that the elastomeric coatings formulated with
the aqueous coating composition as the binder (the first
and second) provides superior dirt pickup resistance
as compared to the other two coatings (the third and
fourth paint formulations).
It is also easy to see that the second paint formulation
shows poorer performance than the first one. It is justified
by the fact that for this example the amount of hard polymer
present is lower than the one necessary to achieve percola-
tion for the particle size ratio 4:1
Study 10: Contact Angle
In this example, a paint formulation having 42% PVC,
using the prototype with particle size ratio 4:1 and with
composition of 75% soft polymer and 25% hard polymer,
was prepared. A drawdown was made by applying a 0.007
inch-thick coat of the paint formulation to a Lenexa P121-
10N chart. The paint formulation was allowed to dry at
25 C and controlled relative humidity of 50% for 24 h.
SL70 / HS30
Prototype Particle Size Ratio 4:1
Composition 25% Hard / 75% Soft
Prototype Particle Size Ratio 4:1
Composition 19% Hard / 81% Soft
Competitor II - 42% PVC Competitor III - 42% PVC
FIGURE 4 The coatings after the soiling test.
New Elastomeric Binder with Dirt Pickup Resistance
AUGUST 2014
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W W W . P C I M A G . C O M 36
Contact angle was measured using Data physics OCA 150 accord-
ing to ASTM D7334 (Pendant drop method).
The elastomeric coating produces a contact angle of 142.
Figure 5 shows a picture of a drop of water on the elastomeric
coating, whose shape indicates that the surface of the elastomeric
coating is hydrophobic.
Summary
This new binder, adequately formulated, gives coalescent-free elas-
tomeric wall paints and elastomeric roof coatings with elongation
values of 500 to 1,000% (according to ASTM D2370), high storage
modulus, which means good elongation retention within a wide
range of temperatures, a vapor transmission of 5 to 9 g/m
2
/day
determined according to ASTM F 1249, a water absorption lower
than 9.0% after soaking in tap water for 96 h, a minimum contact
angle of 138 and excellent dirt pickup resistance.
References
1. Kusy, R.P. Influence of Particle Size Ratio on the Continuity of Aggre-
gates, J. Appl. Phys. (1978), 48, 5301.
2. Bierwagen, G.P. Critical Pigment Volume Concentration (CPVC) as a
Transition Point in the Properties of Coatings, J. Coat. Tech. (1992),
64(806), 71.
3. Floyd, F.L.; Holsworth, R.M. CPVC as Point of Phase Inversion in
Latex Paints, J. Coat. Tech. (1992), 64(806), 65.
4. Eckersley, J.S.T.; Helmer, B.J. Mechanistic considerations of particle
size effects on film properties of hard/soft latex blends, JCT Journal of
Coatings Technology.
5. Dickie, R.A. Heterogeneous Polymer-Polymer Composites. I. Theory
of Viscoelastic Properties and Equivalent Mechanical Models, J. Appl.
Poly. Sci. (1973), 17, 45.
For more information, email hugo.denotta@multiquimica.com.
This paper was presented at the 2013 ABRAFATI International Coatings Congress in
Sao Paulo, Brazil.
FIGURE 5 Contact angle.
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products
1 . 8 0 0 . 5 3 1 . 7 1 0 6 | n e x e o s o l u t i o n s . c o m
C HE MI C A L S | P L A S T I C S | C OMP O S I T E S | E N V I R ONME N T A L S E R V I C E S
AUGUST 2014
|
W W W . P C I M A G . C O M 38
A
utomotive paints have to withstand a
lot whether it is dirt, road salt or UV
radiation. The coatings protect a cars
body against mechanical and environ-
mental influences, and also serve an
important optical purpose. Most of todays automotive
coatings are comprised of four paint layers. The topmost
layer the clearcoat, which is about 40 micrometers
thick is crucial to a cars visual presentation. For design
reasons, the clearcoat has to be transparent and shiny,
but also strong and flexible so it does not splinter when
impacted by foreign objects.
Modern polyurethane-based two-pack clearcoats are
remarkably resistant to chemical influences. Automo-
bile manufacturers are using clearcoats with improved
scratch resistance, particularly beginning with upper
midrange vehicles. This is done in an attempt to meet cus-
tomer demands, as well as reduce the cost of maintaining
vehicle fleets and leased vehicles for resale.
Over time, however, and with regular visits to the car
wash, brushes, as well as dust and dirt, leave behind visible
micro-scratches in these clearcoats. This is why a clearcoat
may lose its shine over the years. Even today, coatings that
are labeled as scratch-resistant and are formulated with
nanoparticles only start out as scratch-resistant. The prob-
lem is that the binding agent weathers over time, causing
particles on the surface of the clearcoat to be washed out by
brushes and cleaners, which means scratches will occur.
New Binder Technology
For over 30 years, scientific literature has shown that
silane-modified resins can significantly improve the prop-
erties of adhesives and coatings. But a key component of
these resins is difficult to produce in high yields on an
industrial scale, which has a noticeable impact on the
price. This is why the technology is currently limited to
niche applications, such as high-performance adhesives.
When it comes to automotive clearcoats, which are far
more price-sensitive, silane-modified resins had not even
been considered until now.
Evoniks Crosslinkers Business Line of the Coatings &
Additives Business Unit has developed a technology plat-
form that can be used to significantly improve the scratch
resistance of clearcoats. For developing this VESTANAT
Quartz Mirror
Substrate
Substrate
Glass
Window
SLM
Array
FIGURE 4 FireEdge UV LED light source.
Quartz Mirror
Substrate
Substrate
Glass
Window
SLM
Array
FIGURE 5 Scalability of the FireJet UV LED light source.
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Visit the unique European event
for coating professionnals in 2014!
Meet more than 150 exhibitors of your sector, experts in
raw materials, equipment, packaging
Learn more about Sustainable Development and New
Technologies in Coatings thanks to the 25 workshops of
the congress.
Request your badge!
on www.eurocoat-expo.com
Code : PCI
RAW MATERIALS
RESINS
PIGMENTS
MINERAL DILUENTS
ADJUVANTS
SOLVENTS
BIOBASED PRODUCTS
PRODUCTION AND
APPLICATION MATERIALS
DISPERSERS
CONTROL AND MEASURING
MIXERS
SHREDDERS
CHEMICAL PACKAGING
CODING AND LABELLING
LABORATORY MATERIALS
COLORIMETRY
PACKAGING
TRAINING AND TEACHING
SURFACE TREATMENTS
MATERIALS HANDLING
PRODUCTION ENGINEERING
International Exhibition & Congress
for the paint, printing ink, varnish, glue and adhesive industries
2 3 , 2 4 , 2 5
Sept ember
P a r i s E x p o
Porte de Versailles
F r a n c e
www.eurocoat-expo.com
An event co-organised by:
AUGUST 2014
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W W W . P C I M A G . C O M 52
PRODUCTS
Mixers
CHARLES ROSS & SON CO.
These 200-gallon double planetary mixers feature recipe controls
that transform the entire mixing/discharge/cleaning cycle into an
automated, simplified process with a high degree of repeatability.
The standard module allows users to write up to 10 recipes each
with 10 process sequences based on agitator speed, time, tempera-
ture and vacuum/pressure level set points. E-mail sales@mixers.com.
Wireless Access Point
DEFELSKO CORP.
The PosiTector Access Point feature allows users to directly con-
nect a smart device or Wi-Fi-enabled computer to a PosiTector
Advanced body without the need for Wi-Fi network access or a
mobile hotspot. The access point allows users to communicate
directly with the Advanced gage body using a web browser or
PosiSoft Mobile App. Visit www.defelsko.com/AccessPoint.
Walk-In Oven
THE GRIEVE CORP.
No. 941 is an electrically heated, 750 F walk-in oven currently used
for drying resin mixtures. Workspace dimensions measure 48W x
48D x 72H. 60KW are installed in Incoloy-sheathed tubular heat-
ing elements, while a 4200 CFM, 3-HP recirculating blower pro-
vides horizontal airflow. It features 6 insulated walls throughout
and Type 304 2B stainless steel interior with continuously welded
seams. E-mail sales@grievecorp.com.
Abrasion Tester
BYK-GARDNER USA
The new Gardner-scrub abrasion tester can be configured to com-
ply with most ASTM, ISO and DIN methods for wet scrub abrasion
and washability testing, or set up for custom applications. Features
include a touchscreen display, a compact design and the ability to
run custom tests. E-mail info.BYK.Gardner.USA@altana.com.
Fume Hoods
HEMCO CORP.
Perchloric acid hoods are engineered for the safe handling of
perchloric acids in laboratory procedures. Hoods come in 48, 60
and 72 widths and include a dedicated wash down and exhaust
system. Visit www.HEMCOcorp.com.
Viscometer
AUTOMATION PRODUCTS INC.
The Dynatrol CL-10DV viscometer features performance and lon-
gevity, a microprocessor for digital accuracy, and noise immunity
for harsh industrial environments. Call 800/231.2062.
GRINDING MEDIA
FOR ALL
MILLING
APPLICATIONS
Any density - any diameter - any composition
Zirconium Oxide, Glass, Steel, Steel Shot, Tungsten
Carbide, Alumina, Silicon Carbide, Silicon Nitride,
Ottawa Sand, Agate, Titanium Oxide, Flint Pebbles,
Rare Earth ZrO/CeO, Nickel, Plastics, etc.
Precision Glass Balls for ball bearings, check valves,
level gauges and low temperature
critical applications are also available
Small orders welcome.
www.glenmills.com
Large stocks - Competitive Prices - Attentive service.
Please phone for full information and prices.
Glen Mills Inc.
220 Delawanna Ave., Clifton, NJ 07014
Tel: (973) 777-0777 Fax: (973) 777-0070
PAI NT & COATI NGS I NDUS TRY
53
CLASSIFIEDS
Stainless IT Stainless ITT
The CONN Blades
Most Efficient & Aggressive Available
UHMW Poly
w w w . c o n n b l a d e . c o m
(814) 723-7980
EQUIPMENT CUSTOM MANUFACTURING EQUIPMENT
www.pcimag.com/PCIclassifieds
Its time to change
your Blade!
www.quickblades.net
sales@quickblades.net
2603592072
High Speed Dispersion
POSITIONS AVAILABLE
Sto Corp., ISO 9001 and 14001
certied world class manufacturer of
cladding and coating systems, offers
toll blending services for cement
based powders and water based
textured or smooth coatings.
Contact: Jerry Haller
jhaller@stocorp.com
or 678-429-2572
Mozel is an ISO 9001:2008 certifed contract
blending and flling company specializing
in polyisocyanates, solvents, and other
fammable or corrosive products. Mozel
ofers turnkey solutions and focuses on
adding value for its customers.
Let us put our expertise to work for you.
www.MozelChem.com (615)878-2199
tbarnwell@mozelchem.com
484-684-6986
sales@norstoneinc.com
www.grindingmediadepot.biz
www.bladedepot.biz
1-800-243-ROSS
www.DualShaftMixers.com
Scan to learn
more & get a
free quote.
Free Tag Reader:
http://gettag.mobi
DUAL SHAFT
MIXERS
New 50, 100 & 200 gal.
mixers in stock!
TOLL BLENDING
ISO-9001 certifed manufacturer with
nationwide network of plants seeks toll
blending inquiries: sand/cement blends,
latex or epoxy liquid packing, FFS form fll
& seal packaging, private label products.
Contact Dominic Di Cenzo
203.915.0279 or djdicenzo@cox.net
RECRUITMENT SERVICES
Specializing in paint/coatings industry. Seeking
passionate, high-impact professionals for nationwide
positions. Send your resume in confidence to:
Spencer M. Hermann
SEARCHLIGHT PARTNERS
28052 Camino Capistrano, Suite 209
Laguna Niguel, CA 92677
(949)429-8813 spencer@mrisearchlight.com
NANO Coating Sales Reps
Needed NOW!
Contact Greg at Ph: 858.220.1596
greg.ingles@appliedtechintl.com
www.appliedtechintl.com
AUGUST 2014
|
W W W . P C I M A G . C O M 54
CLASSIFIEDS
PUBL I S HI NG/ S AL ES S TAF F
Publisher/ Donna M. Campbell
East Coast Sales Tel: 610/650.4050 Fax: 248/502.1091
E-mail: campbelld@pcimag.com
Midwest/ Lisa Guldan
West Coast Sales Tel: 630/293.7261
E-mail: guldanl@pcimag.com
China Media Rep. Arlen Luo
Tel: 0086-10-88579899
E-mail: nsmchina@126.com
Europe Regional Uwe Riemeyer
Manager Tel: 49 (0)202-271690
E-mail: riemeyer@intermediapartners.de
Inside Sales Manager Andrea Kropp
Tel: 810/688.4847
E-mail: kroppa@pcimag.com
Production Manager Brian Biddle
Tel: 847/405.4104 Fax: 248/244.3915
E-mail: biddleb@bnpmedia.com
EDI TORI AL S TAF F
Editor Kristin Johansson
Tel: 248/641.0592 Fax: 248/502.2094
E-mail: kristin@pcimag.com
Technical Editor Darlene R. Brezinski, Ph.D.
E-mail: darpaint@aol.com
Associate Editor Karen Parker
Tel: 248/229.2681
E-mail: parkerpcimag@gmail.com
Art Director Clare L. Johnson
OPERATI ONS S TAF F
Single Copy Sales Ann Kalb
E-mail: kalbr@bnpmedia.com
Tel: 248/244.6499 Fax: 248/244.2925
Reprint Manager Jill L. DeVries
248/244.1726
E-mail: devriesj@bnpmedia.com
LIST RENTAL, POSTAL & E- MAIL CONTACTS
Sr. Account Manager Kevin Collopy
kevin.collopy@infogroup.com
Tel: 845/731.2684 Toll Free: 800/223.2194 Ext. 684
Sr. Account Manager Michael Costantino
michael.costantino@infogroup.com
Tel: 402/836.6266
For subscription information or service,
please contact Customer Service at:
Tel: 847/763.9534 or Fax: 847/763.9538
or e-mail PCI@halldata.com
Arkema Coating Resins . . . . . . . . . . . . 3
www.arkemacoatingresins.com/neocar
BASF Corporation . . . . . . . . . . . . . . . . . 7
www.basf.us/dpsolutions
BYK USA Inc. . . . . . . . . . . . . . . . . . . . . 43
www.byk.com
BioAmber. . . . . . . . . . . . . . . . . . . . . . . . . 9
http;//webinars.pcimag.com
www.bio-amber.com
Brenntag North America. . . . . . . . . . 17
www.brenntagnorthamerica.com
Brookfield Engineering
Laboratories . . . . . . . . . . . . . . . . . . . . . 10
www.brookfieldengineering.com
CHEMIR - A Division of Evans
Analytical Group . . . . . . . . . . . . . . . . . 10
www.eag.com
www.chemir.com
Classifier Milling Systems . . . . . . . . . 32
www.cms-can.com
CNNC Hua Yuan . . . . . . . . . . . . . . . . . 54
www.sinotio2.com
Coatings Trends & Technologies 46-47
www.coatingsconference.com
Conn and Co.. . . . . . . . . . . . . . . . . . . . . 28
www.connblade.com
Custom Milling & Consulting . . . . . 30
www.cmcmilling.com
DeFelsko Corp. . . . . . . . . . . . . . . . . . . . 15
www.defelsko.com
Dymax . . . . . . . . . . . . . . . . . . . . . . . . . . 41
www.dymax-oc.com
Elcometer . . . . . . . . . . . . . . . . . . . . . . . 18
www.elcometer.com
Emerald Performance Materials. . . . 13
www.emeraldmaterials.com
EMI . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
www.EMImills.com
Eurocoat Expo 2014 . . . . . . . . . . . . . . 51
www.eurocoat-expo.com
Glen Mills Inc.. . . . . . . . . . . . . . . . . . . . 52
www.glenmills.com
HERO . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
www.hero.ca
Heubach. . . . . . . . . . . . . . . . . . . . . . . . . . 2
www.heubach.com
Konica Minolta. . . . . . . . . . . . . . . . . . . 16
www.sensing.konicaminolta.us
Myers Engineering. . . . . . . . . . . . . . . . 36
www.myersmixer.com
Myriant Corporation. . . . . . . . . . . . . . 33
www.myriant.com
Nexeo Solutions, LLC. . . . . . . . . . . . . . 37
www.nexeosolutions.com
Palmer Holland . . . . . . . . . . . . . . . . . . 56
www.palmerholland.com
Parker Domnick Hunter. . . . . . . . . . . 43
www.parker.com/dhprocessipc
Particle Sizing Systems. . . . . . . . . . . . 43
www.pssnicomp.com
Paul N. Gardner Company, Inc. . . . . 52
www.gardco.com
The Pigment & Color
Science Forum 2014 . . . . . . . . . . . . . . 40
www.pigmentmarkets.com
Phoseon Technology. . . . . . . . . . . . . . 31
www.phoseon.com/PCI/
P.L. Thomas. . . . . . . . . . . . . . . . . . . . . . 54
www.plthomas.com
Powder Technologies Incorporated. . 55
www.powdertechusa.com
Q-Lab . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
www.q-lab.com/CRH
Ross, Charles and Son . . . . . . . . . . . . . 4
www.mixers.com
TecFiveUSA . . . . . . . . . . . . . . . . . . . . . . 43
www.tec5usa.com
UL Information & Insights. . . . . . . . . 29
www.ULProspector.com
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