Note: Descriptions are shown in the official language in which they were submitted.
3~
It is generally well re~ognized by those skilled in the
art of printing that printing plates made from multiple lay-
ers having different hardness ~e.g., soft underlayments used
in combination with the harder materials commonly used as
printing surfaces) can result in improved print quality.
This is evident by the widespread use of foam backings for
printing plates.
Printing plates produced from photopolymerixable mate-
rials are also well known in the printing art. See, for
example, U.S. 2,760,863 to Plambeck. Attempts to combine
the advantages of photopolymerization platemaking with those
of soft backed plates led to the dèvelopment of plates made
from multiple layers of solid photopolymers as described in
U.S. 2,993,789 to Crawford; U.S. 3,157,505 to Notley; and
U.S. 3,990,897 to Zuerger et al. While these multilayer
solid plates have advantages, they nevertheless suffer from
several drawbacks. Frequently, adhesives are required to
join the solid photopolymer layers together, and, since the
soft base is not an integral part of the relief surface,
delamination of the base layer from the relief polymer is
likely. In addition, solid plates are subject to ware-
housing problems due to the different plate sizes and layer
thicknesses required by the printing industry. Also,
printing plates made from precast solid polymers are more
difficult to develop and washout than photopolymer plates
prepared from liquid resins. Solid plates are also subject
to deterioration on storage due to migration o~ components
and to distortions resulting from handling.
According to this invention/ a process for making a
printing plate having at least two distinct contiguous
layers comprises exposing to actinic light, through a
- , . . . .
photographic negative, a photopolymerizable element compris-
ing: a prin~ing layer of a liquid photopolymerizable compo-
sition comprising at least one addition polymerizable com-
pound having a normal boiling point above about 100C.~ a
molecular weight of less than about 1500 and at least one
ethylenically unsaturated group capable of forming a high
polymer by photoinitiated polymerization; at least one
unsaturated polymeric material which is soluble in said
addition polymerizable compound; at least one polymerization
inhibitor and a photoinitiator; and a base layer of a
different liquid photopolymerizable composition comprising
at least one addition polymerizable compound having a normal
boiling point above about 100C., a molecular weight of
less than about 1500 and at leas~ one ethylenically unsat-
urated group capable of forming a high polymer by photo-
initiated polymerization; at least one unsaturated polymeric
material which is soluble in said addition polymerizable
compound; at least one polymerization inhibitor; and an
amount of photoinitiator greater than that in said printiny
layer such that said base layer has a photopolymerization
rate about 1.5 to about 250 times that of said printing
layer, said printing layer and base layer compositions hav-
ing differing crosslinkability such that, upon exposure, the
layers have moduli differing by at least about 50 p.s.i.;
and removing unpolymerized portions of said layers.
It will be understood from the above that the moduli is
controlled by the crosslinkability of the different liquid
photopolymerizable compositions, while the differing amounts
of photoinitiator controls the shoulder angles of the photo-
polymer layers.
Preferably, the individual layers will be from about 1mil to about 250 mils thick, the most preferred range for
the layer used as the printing surface being generally from
about 4 mils to about 150 mils. Preferably, for convenient
removal of the unpolymerized parts of the laye~s, the photo-
polymerizable composition should be dispersible at a concen-
tration of from about 1% to about 40% by weight of a solvent
in which the polymerized resin is insoluble. Suitable
:: :
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3fi~
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solvents are water, aqueous base solutions or water-miscible
organic solvents.
The invention contemplates a printing plate made by the
above described process, in which the printing layer is
doctored over a supported photographic negative that is pro-
tected by a cover film and the base layer is covered by a
backing layerO
The photopolymerizable compositions used according to
this invention are of such a nature that adjacent layers re-
main distlnct entities after the curing process, yet bondtogether tightly enough (without the aid of an adhesive),
that the layers will not separate or fracture during the
printing process. The unsatura~ed polymeric component,
hereinafter referred to as the prepolymer, is chosen from
such chemical classes as polyesters, polyurethanes, poly-
ethers, polybutadienes and polyamides, the only restriction
being that the polymer be solubla in the addition polymer
izable compound. Dyes and inert ultraviolet absorbers are
often desirable additives to the compositions and waxes or
other additives may be added to the resins, if desired.
Suitable unsaturated polymeric compositions which can be
used as the prepolymers in the photopolymerizable composi-
tion include unsaturated polyesters produced from at least
one polyol and at least one unsaturated dicarboxylic acid,
its anhydride or its methyl or ethyl ester (see U.S. patent
3,858l510 to Kai et al); unsaturated polyester-polyether
block polyurethanes such as those described in U S. patent
3,960,572 to Ibata et al; unsaturated polyether-polyurethanes
such as those described in German 2,641,189; polyene-poly-
thiol compositions such as those described in U.S. patent3,661,575 to Ketley et al; and terminally unsaturated homo-
polymers and copolymers of butadiene, isoprene~ chloroprene,
styrene, isobutylene and ethylene in which the terminal un-
saturation is attached to the polymer through a combination
of at least two ether, thioether, ester, keto or amide
groups (see Belgian Patent 847,986).
In general, the unsaturated polymeric component may be
present in amounts from about 40~ to about 95% by weight.
-
Likewise, the addition polymerizable compound may be present
in amounts from about 2% to about 50% by weight.
Typical ethylenically unsaturated addition polymeriza-
tion compounds are acrylic acid, methacrylic acid, methyl
acrylate, ethyl acrylate, n-propyl acrylate, isopropyl
acrylate, n-hexyl acrylate, n-octyl acrylate, cyclohexyl
acrylate, allyl acrylate, glycidyl acrylate, styrene, vinyl
toluene, divinyl benzene, carboxys~yrene, diallyl phthalate,
triallyl cyanurate, vinyl acetate, acrylamide, methacryl-
amide, n-butyl acrylamide, N-methylol acrylamide, N-methylol
methacrylamide, N-methoxymethyl acrylamide, N-ethoxymethyl
acrylamide, N-ethoxymethyl methacrylamide, N-n-butoxymethyl
acrylamide, N,N'-methylene bis acrylamide, N,N'-methylene
bis methacrylamide, N,N'-trimethylene bis acrylamide, ~,N'-
hexamethylene bis acrylamide, methyl methacrylate, 2-
hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, lauryl
methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl
methacrylate, 3-chloro-2-hydroxypropyl acrylate, 4-hydroxy-
butyl acrylate, diethylene glycol monoacrylate, dipropylene
glycol monoacrylate, polyethylene glycol monoacrylate,
ethylene glycol diacrylate, tetraethylene glycol diacrylate,
propylene glycol dimethacrylate, diethylene glycol dimeth-
acrylate, triethylene glycol dimethacrylate, tetraethylene
glycol dimethacrylate, polyethylene glycol dimethacrylate,
trimethylolpropane triacrylate, 1,6-hexanediol dimethacryl-
ate, N-3-oxo-propyl acrylamide, N-3-oxobutyl acrylamide,
N-3~oxo-1-methylbutyl acrylamide, N-3-oxo-1-dibutyl-2-n-
propylheptyl acrylamide, etc.
The composition of each individual layer must be adjus-
ted so that the layers will have the desired relative hard~ness after curing. This may be accomplished by controlling
the amount of crosslinking which occurs during photopolymer-
ization, i.e., the more the polymerization product is cross-
linked, the harder it will be. There are several ways to
control crosslinking. ~he degree of unsaturation in the
prepolymer can be adjusted during its preparation to provide
the required number of crosslink sites. Likewise, the amoun~
of crosslinking can be controlled by selecting addition
-
--5--
polymerizable compounds (which act as the cross-linking
agent) which have varying degrees of unsaturation or by
adjusting the amount of addition polymerizable compound in
the photopolymerizable composition.
In general, the individual layers of the printing
plates of this invention should have moduli falling within
the range of about 50 p.soi. to about 80,000 p.s.i. In
addition, the modulus of the cured upper, i.e., printing,
layer polymer should be at least 50 p.s.i. higher (where a
hard printing layer/soft base plate is desired) or lower
(where a soft printing layer/hard base plate is desired)
than the modulus of the cured underlayer, i.e., base layer,
polymer.
In the description of this invention, modulus has been
used to describe differences in hardness. The Young's
moduli o this invention are determined by extending the
initial straight section o the stress-strain curve obtained
according to ASTM D-638 and dividing the slope of this load
over distance by the cross-~ectional area of the sample.
Samples are prepared from 40 mil thick plates cured with 20
seconds back exposure with GE F-20-T-12 BL fluorescent lamps
with an intensity of about 1.2 mwatts/cm.2 and a relief
exposure with a medium pressure 2 KW mercury arc lamp with
an intensity of about 8 mwatts/cm. for 270 seconds.
In some printing applications, such as printing on
rough stock like corrugated boxesl burlap, paper bags, etc.,
it is desirable to use a printing plate having a soft upper,
i.e., printing, layer and a harder underlayer. The sGfter
upper layer polymer generally carries more ink and thus
transfers more of it to the stock than do printing plates
having harder surfaces. The printing plate having the soft
printing surface generally prints with less "wiping" action
than the hard surface plate.
It is well recognized from photopolymerization theory
that the rate at which the liquid photopolymer resins used
in this invention will polymerize will depend on the initi-
ator level and type, the inhibitor level and type, the ultra-
violet absorber level and type and the overall resin layer
:,
-6- ~ 2 ri~
thickness. (See G. Odian, Principles o~ Polymerization,
McGraw Hill Book Co., N.Y., NY, 1970, p. 183.)
The photopolymerization rate also depends on the reac-
tivity and absorption spectrum of the resin, and correspond-
ingly the spectral energy distribution and intensity levelof the radia~ion source used for exposure. A reduction in
shoulder formation in the upper layer (giving a high shoulder
angle) is aided by absorbing less divergent or stray radia-
tion in the areas adjacent to the image areas and by use of a
resin which reacts more slowly to such divergent radiation.
Such lower light absorption is achieved by using a lower
concentration of photoinitiator or other light absorber in
the upper resin layer. For the same reason a higher level
of photoinitiator or other light absorber in the lower resin
layer will result in utilization of divergent light which
comes through (is not absorbed by) the upper resin or is re-
flected from the support sheet to cause formation of insol-
uble polymer over a broader area than that of the image open-
ing (thus giving a lower shoulder angle). It should, there-
fore, be stressed that, in this invention, the photospeed(i.e., polymerization rate) of the upper resin is slower
relative to the underlayer resin.
Acceptable initiators include benzoin; alpha-hydroxy-
methyl benzoin; 2,2-diethoxyacetophenone; haloalkylbenzo-
phenones; alpha, alpha, alpha~trichloroacetophenone; keto-
sulfides; 2-alkoxy-1,3-diphenyl-1,3-propanedione; alkyl
benzoin ethers; alpha, alpha-di-methoxyphenylacetophenone;
l-phenyl-1,2-propanedione-2,0-benzyl-oxime; S,S'-diphenyl-
thiocarbonate; and the like. The alkyl benzoin ethers and
alpha, alpha-dimethoxyphenylacetophenone are preferred
initiators. Ultraviolet absorbers or dyes include aceto-
phenone, benzophenone, thioxanthone, anthra~uinone,
fluorenone, benzotriazole, o-nitroaniline, and the like.
Preferred ultraviolet absorbers or dyes are benzophenone and
o-nitroaniline.
Thus, concurrent with the above compositional modifica-
tions used to achieve the desired moduli, the level of
initiator, inhibitor, and/or ultraviolet absorber should be
~ ...................... `, :' ~'
~ ~ . ,, ., . :' ~
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adjusted so that the upper resin layer (whether harder or
softer than the underlayer) has a slower photospeed relative
to the resin used as the underlayerO The response to ultra-
violet radiation of the resin used as the underlayer can be
about 1.5 to about 250 times that o the resin used as the
upper layer, preferably about 5 to about 20 times that of the
upper layer resin. The preferred manner of adjusting photo-
speed is by preadjusting the initiator level in the resin
used for each layer. For initiators such as alkyl benzoin
ethers or alpha, alpha-dime~hoxyphenylacetophenone about 0.1%
to about 1% by weight may be used in the upper (i.e. print-
ing) layer and about 0.5% to about 2.5% by weight may be used
in the underlayer. Preferably, about 0.3~ to about 0.5% ini-
tiator may be used in the upper layer and about 0.8% to about
1.5% in the underlayer.
The attached drawing illustrates the effect of the
above-described difference in photospeed. The Figure shows
a cross-sectional view of a portion of a printing plate made
according to this invention. By varying the photospeed bal-
ance between the resins used for the upper layer 3 and lowerlayer 2, printing plates can be made which have a shoulder
angle b for the entire depth of the upper layer, i.e., the
angle formed by the outside inclined edge of ~he upper layer
3 and the plane of the interface between the upper and lower
- 25 layers, which is at least 10 greater than the shoulder
angle a for the lower layer, i.e, the angle formed by the
; outside inclined edge of the lower layer 2 and the plane of
the interface between the lower layer 2 and the backing sheet
1, which plane is parallel to the plane of the interface be-
tween the upper and lower layers.
The shoulder angles of the upper layer may be about
lG to about 85 (preferably about 30 to about 60)
greater than the shoulder angles of the lower layer. This
is particularly advantageous in plates having hard upper
layers as this structure offers a balance between print
quality and plate durability which has not been demonstrated
with single layer printing plates. In addition, the more
open relief surface resulting fro~ the increased shoulder
.
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angles prevents plugging by ink, lint, etc., during the
printing process, thus requiring less press down-time for
cleaning. Layers of the resins formulated as described
above form, in a synchronous and harmonious fashion upon
exposure to ultraviolet light, printing plates having inte-
grated tailored relief elements and little or no failure due
to delamination at the layer-layer interface.
The pho~opolymerizable compositions may also contain at
least one polymerization inhibitor. Generally, the amount
of inhibitor may range from about 300 parts per million to
about 3000 parts per million, with about 1000 to about 2000
parts per million being preferred. Examples of useful polym-
erization inhibitors are di-tert-butyl p-cresol, hydroquinone
monomethyL-ether, pyrogallol, quinone, phenotbiazine and the
like. Di-tert-butyl p-cresol is particularly preferred.
To avoid excessive mixing yet allow proper flow of the
photopolymerizable compositions of each layer during the
plate-making process, the viscosity of the composition for
each layer should be between about 1000 cps. and about
60,000 cps. with about 5,000-30,000 cps. being preferred.
There is, however, no requirement that the compositions used
for each layer have the same viscosity as long as they fall
within the above range. In the examples described herein-
after, all of the photopolymerizable compositions have vis-
cosities within the above range.
Those plates having a hard upper layer and soft baselayer also demonstrate superior impression and wider screen
latitude. Normally, with a single layer polymer plate, as
impression is increased, the printing surfaces will distort
and the printed copy will be larger than the intended image
areas of the printing plate. However, with the hard upper
layer and soft base layer, the distortion due to impression
is absorbed by the softer base layer, since the base layer
is formulated and designed to compress before the harder
upper polymer. Since the softer base polymer does compress,
the harder upper polymer does not distort and the fidelity
of the printing image is maintained over a wide range of
impression. In addition, because of the tailored structure
.. ' :
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of the relief surface (due to the low initiator level) in
the harder upper layer, the relief images do not begin to
broaden until the softer base layer is highly compressed.
In normal plates prepared ~rom a single li~uid resin, the
images begin to broaden at the relief surface. Further, the
layered plates do not exhibit image growth as the plate
wears until the entire upper surface is worn away. Since
the depth of this upper layer can be easily adjusted with
the liquid system used in this invention, image growth due
to plate wear can be avoided.
The layered photopolymerizable printing plates of this
invention can easily be made on site in a printing plant by
doctoring the liquid photopolymerizable resin which will
ultimately be the upper or printing layer at the desired
thickness over a polymeric film covering (and thereby pro-
tecting) a negative. The second liquid resin which will
ultimately serve as the base layer is then doctored at the
proper thickness over the first resin while the first resin
still in a liquid state and the whole is covered with a
suitable support which may, if desired, contain an adhesive.
(Generally, it is desirable to use an ultraviolet transpar-
ent film as the support to make possible a secondary back
exposure which provides broader shoulder angles in the base
layer than can be achieved with opaque supports. These
broader shoulder angles provide stronger SUppoLt for the
relief surface.) It should be emphasized that both resin
layers remain liquid throughout the foregoing operations~
It is not until the liquid layers are exposed that they
solidify. Selected areas of the plate are exposed by sub-
jecting them to ultraviolet radiation through the negative.Unpolymerized resin is then removed from those areas which
were not fully exposed, i.e., those corresponding to the
darker portions of the negative.
The above description simply provides one manner in
which the printing plates of this invention can be made and
is not intended to limit the manner in which the described
plates can be prepared or the number of layers which can be
used.
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In the following examples all parts are by weight and
each of the described photopolymerizable compositions has a
viscosity between about 1,000 cps. and about 60,000 cps.
Exam~le 1
A Mylar bac~ing sheet approximately 4 mils thick is
coated with an adhesive solution containing a red dye as an
antihalation agent.
Four to six mils of a liquid polyester I resin composi-
tion prepared by dissolving 100 parts of polyester I (pre-
pared from 2 mole~ of diethylene glycol, 2 moles propylene
glycol, 2 moles adipic acid and 2 moles fumaric acid) in 45
parts triethylene glycol dimethacrylate, 15 parts N-3-oxo-
butylacrylamide, 0.038 part of di-tertiary butyl p-cresol,
0.02 part of the methyl ether of hydroquinone, and 0.5 part
lS benzoin isobutyl ether is doctored onto a 0.75 mil poly-
propylene film covering a line process negative. This poly-
ester I resin composition, when photocured, has a hardness
of 50D and a modulus of 52,503 lbs./in.2. Next, 7-9 mils
of a liquid polyester II resin composition prepared by dis-
solving 100 parts of a polyester prepared from 1 mole di-
ethylene glycol, 1 mole propylene glycol, 0.5 mole fumaric
acid, 0.5 mole phthalic anhydride, and 1 mole adipic acid in
50 parts styrene, 50 parts triethylene glycol dimethacrylate,
0.07 parts di-tert butyl p-cresol, 0.03 part methyl ether of
hydroquinone and 1.8 parts benzoin isobutyl ether is doctored
over the 4-6 mils of the still liquid polyester I composi-
tion. This polyester II resin composition, when photopoly-
merized, has a hardness of 67A and a modulus of 1260 lb./in.2
The above mentioned backing sheet is laid over the above
liquid resin layers and the whole is irradiated for ten sec-
onds through the backing sheet with GE F-20-T-12 BL fluores-
cent lamps (of intensity 1.2 mwatt/cm.2 as measured by an
Ultraviolet Back-Ray meter). The resin sandwich is then
irradiated through the negative for 80 seconds with a 2000
watt medium pressure mercury arc lamp (at an intensity of 7
mwatt/cm.2). After exposure, the polypropylene film is
s~ripped away and the unexposed polymer removed by spray
washing for 2 minutes with a 0.5% sodium hydroxide aqueous
,~e~/~ J~'~ ~t~ ~,oD~ ~te-~
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36~
solution and an additional 30 seconds wi~h water. The dry
plate is exposed for 10 minutes under a nitrogen blanket
with fluorescent lamps ~of 1.2 mwatt/cm.2 intensity).
The formed plate is 17 mils thick (including the backing
sheet) with a relief height of 12-13 mils, and a selected
shadow area had an etch depth of 0.0067 mm. while a similar
shadow area in a plate using only polyester II composition
alone had an etch dep~h of only 0.0025 mm. In addition, a
sharp relief image bonded to the base support corresponding
to the clear areas in the negative is formed. The angle of
a highlight element in the base layer is 58 with the
horizontal while the angle of this same highlight element
in the upper layer is 85 with the horizontal. The same
highlight element in a plate made of only polyester II com-
position has an angle of 50O The angle of the elementin the layered plate changes about 4 mils below the relief
surface.
The plate exhibits long press life and no image growth
is observed when 10 mils impression is applied or as the
plate wears. No plugging or low spots are observed, over-
all screen and tonal range held and printed with this plate
is extended over that of nonlayered plates and overall print
quality and appearance is better than that observed with
nonlayered printing plates.
Example_2
A laye~ed plate is prepared as described in Example 1
except that 8 mils of liquid polyester I composition is
doctored onto the polypropylene film followed by 10 mils of
liquid polyester I~ formulation. The plate is exposed for
20 seconds through the backing sheet and 80 seconds throughthe negative. The formed 22 mil thick plate is developed
in the washout solution described in Example 1 and has a
relief depth of 15 mils. The bottom portion of a relie~
element makes an angle of 3~ with the horizontal and the
upper portion has an angle of 78. The etch depth in a
shadow area is 0.015 mm. This plate possesses the overall
printing qualities exhibited b~ the plate described in
Example 1.
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Example 3
A layered plate is prepare~ as described in Example 1
except that 4-6 mils of a liquid polyurethane I resin formu-
lation is used as the upper layerO The polyurethane pre-
polymer for this resin is prepared reacting 26.1 g. of amixture of 2,4-toluene diisocyanate and 2,6-toluene diiso-
cyanate under nitrogen with 200 g. of polyethylene adipate
diol (molecular weight approximately 450) at 70C. with
stirring in the presence of dibutyltin dilaurate for 2 hours.
Then the resulting isocyanate terminated polyester urethane
is further reacted with 100 g. of polypropylene glycol diol
(molecular weight approximately 1000) at 70C. for 2 hours.
Then 300 g. of the resulting polyester-polyether urethane
block polymer were reacted with 25 g. o 2-hydroxypropyl
methacrylate containing 0.09 part of 2,6-di-t-butyl-p-
cresol as stabilizer at 70C. for 2 hours under an air
sparge. 70 parts of this prepolymer is then added to 12
parts of 2-hydroxypropyl methacrylate, 16 parts n-butyl
acrylamide, 2 parts acrylamide, 0.04 part di-tert butyl
p-cresol, 0.04 part hydroguinone methyl ether and 0.3 part
alpha, alpha-dimethoxyphenyl-acetophenone. This polyureth-
ane I resin composition, when photocured, has a hardness of
70A and a modulus of 920 lb./in.2. A 7-9 mil layer of
liquid polyester II composition in Example 1 is doctored
over a 4-6 mil layer of the still liquid polyurethane I
formulation and given a back exposure of 12 seconds and a
relief exposure of 120 seconds. The 17 mil plate with a 13
mil relief is developed as described in Example 1 and a
relief highlight element has an angle of 48 in the base
layer and 82 in the upper layer. The etch depth of a
shadow area is 0.0083 mm~ This plate has the overall print
quality advantages of the plate described in Example 1 with
the added advantages of better abrasion resistance of the
polyurethane composition polymer than when the polyester5 polymer composition is used on the relief surface.
Example 4
A layer of 5-8 mils of liquid polyurethane I composi-
tion described in Example 3 containing 0.5 part alpha,
': ' ., . , , ,:
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: : . ., , , , .
3~
~13-
alpha-dimethoxyphenylacetophenone instead of 0.3 part is
doctored over polypropylene film coveriny a test negative
containing a Bychrome screen tint. Over this, a 50-53 mil
layer of liquid polyurethane II formulation which is pre-
pared as described in Example 3 by adding 70 parts of apolyurethane prepolymer (prepared from 37.65 parts poly-
ethylene adipate diol, 34.97 parts polypropyleneglycol diol,
7.31 parts of 2,4-toluene diisocyanate and 2,6-toluene di-
isocyanate in an 80:20 mixture and capped with 17.75 parts
polyethylene glycol monomethacrylate having an average de-
gree of polymerization of 7) to 12 parts n-butyl acrylamide,
12 parts of 2-hydroxyethyl methacrylate, 2.0 parts acryl-
amide, 5.0 parts styrene, 0.05 part di-tert-butyl p cresol~
and 1.0 part benzoin isobutyl ether. The photocured polymer
from this resin has a hardness of 40A and a modulus of 220
lb./in.2. The plate is formed by exposing the liquid
resin layers through a backing sheet prepared as described
in Example 1 without the antihalation dye for 55 seconds
and through the negative for 180 seconds.
Example S
A layered plate is prepared by using the backing sheet
described in Example 1 without the red antihalation material
and by doctoring 5-8 mils of liquid polyurethane I composi-
tion described in Example 3 containing 0.1 part alpha,
alpha-dimethoxyphenylacetophenone instead of 0.3 part over
50-53 mils liquid polyurethane III composition which is pre-
pared by adding 76.52 parts of the prepolymer used for poly-
urethane II composition in Example 4 to 9.98 parts lauryl
methacrylate, 1.60 parts 2-hydroxyethyl methacrylate, 10.64
parts of polyethylene glycol dimethacrylate, 0.04 part di-
tert-butyl p-cresol, 0.04 part hydroquinone methyl ether and
1 part benzoin isobutyl ether. This polyurethane III resin
composition, when photocured, has a hardness of 22A and a
modulus of 150 lb./in.2. The plate is formed by exposing
through the backing sheet for 80 seconds and through the
Bychrome screen test negative for 180 seconds. The 62 mil
thick plate with 30 mils relief, tailored relief printing
elements and open etch depth is developed and post exposed
.
-14-
as described in Example 1.
Example 6
125 Mils of liquid polyure~hane IV formulation, which
yields a photocured polymer of 90A hardness and a modulus of
10,000 lbs./in.2 and is prepared by adding 70 parts of
the prepolymer used to prepare polyurethane I composition
described in Example 3 to 10 parts triethylene glycol
dimethacrylate, 16 parts n-butyl acrylamide, 4 parts methyl
methacrylate, 0.3 part hydroquinone methyl ether, 0.3 part
di-tert-butyl p-cresol, and 0O3 part alpha, alpha-dimethoxy-
phenacetophenone is doctored over a polyester film covering
a line process negative. A 125 mil layer of liquid poly-
urethane V composition, which yields a photocured polymer
having a hardness of 35A and a modulus of 171 and is pre-
lS pared by adding 70 parts of the prepolymer used to preparepolyurethane II composition described in Example 4 (except
that the prepolymer was capped with a polyethylene glycol
monomethacrylate having an average degree of polymerization
of 15 instead of 7) to 1~ parts 2-hydroxyethyl methacrylate,
12 parts n-butyl acrylamide, 2 parts acrylamide, 5 parts
styrene, 0.05 hydroquinone methyl ether, 0.05 part di-tert-
butyl p-cresol, and 0.3 part alpha, alpha-dimethoxyphenyl-
acetophenone, is doctored over the liquid polyurethane IV
formulation layer and the backing sheet described in
Example 1 without the red antihalation dye is applied. The
plate is hardened by exposing through the backing sheet for
2.5 minutes and through the negative for 7 minutes. The
~50 mil plate having 125 mil relief is developed as de-
scribed above and has strong tailored relief elements.
Example 7
~ ~ To 100 parts of a carboxyl terminated polybutadiene
(Hycar~CTB-2000X162 - B. F. Goodrich) are added 6.7 parts
of glycidyl methacrylate, 0.015 part phenothiazine, (0.0075
part nitrobenzene, 0.08% sodium methoxide) and 0.20 part di-
tert-butyl p-cresol. This mixture is heated under a stream
of air at 100C. until an acid number of 0.36 is obtained.
Eighty-eight parts of this prepolymer are added to 6 parts
1,6-hexanediol dimethacrylate, 6 parts lauryl methacrylate
.
,` ~ `
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,: ' ' : '
-15-
and 0.6 part alpha, alpha~diethoxyacetophenone which gives
`a photocured polymer having a hardness of 55A and a modulus
of 600 lb./in.2. A layer of 5-15 mils of this liquid
polybutadiene I resin composition is doctored over a poly-
`5 propylene film covering a line process negative and a 80-90
mil layer of liquid polyurethane II composition, which when
cured has a hardness of 40A and modulus of 220 lb./in., is
doctored over the polybutadiene I resin formulation. The
plate is hardened by exposing through the backing sheet of
Example 1 (containing no antihalation dye) for 2 minutes
and exposing through the negative for 5 minutes. The plate
is developed by spray washing with a warm (50C.) solution
of 1.0~ Bioterge~alpha olefin sulfonate detergent (Stepon
Chem. Co.) and post-exposed under a nitrogen blanket for 10
minutes. This 90-95 mil thick plate with 45 mils relief has
the overall printing qualities of the plates in the previous
examples, plus the advantage of being resistant to alcohol
inks and solvents.
Example 8
Four to five mils of liquid polyester I composit~on in
Example 1 is doctored over a film covering a Bychrome~screen
negative. Then 8-9 mils of a liquid photopolymer resin con~
taining 38.5 parts of the prepolymer used for polyester II
composition in ~xample 1 and 41.08 parts of the prepolymer
used to prepare polyurethane I composition in Example 3,
both dissolved in 16 parts n~butyl acrylamide, 12 parts 2-
hydroxyethyl methacrylate, 5 parts styrene, 2 parts acryl-
amide, 0.04 part di-tert-butyl p-cresol, 0.04 part methyl
ether of hydroquinone, 0.65 part benzoin isobutyl ether, and
0.55 part alpha, alpha-dimethoxyphenyiacetophenone (which
yields a polymer of hardness of 61A and 760 modulus when
photocured) is doctored over the polyester I resin composi-
tion layer. This plate is hardened by exposing through the
backing sheet described in Example 1 for 10 seconds and
through the negative for 80 seconds. The plate is developed
as described in Example 1 and has the tailored relief
elements characteristic of the plates described in this
invention.
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-16-
ExamPle 9
A 125 mil layer of liquid polyurethane III composition
described in Example 5 having a cured hardness of 22A and a
modulus of 150 lb./in.2 is doctored over a polypropylene
film covering a production type negative for printing corru-
gated boxes. A 125 mil layer of liquid polyurethane VI
composition, which yields a photocured polymer having a
hardness of 50A and modulus of 420 p.s.i. and is prepared
by adding 70 parts of the prepolymer used to prepare poly-
urethane II composition described in Example 4 to 12 partsn-butyl acrylamide, 6 parts 2-hydroxyethyl methacrylate, 6
parts tetraethylene glycol dimethacrylate, and 2 parts
styrene, 0.05 part hydroquinone methyl ether, 0.05 di-tert-
butyl p-cresol, and 0.3 part alpha, alpha-dimethoxyphenyl-
acetophenone, is doctored over the polyurethane III formula-
tion layer and a backing sheet described in Example 1 (with-
out the red antihalation dye) is applied. The plate is
cured by exposing through ~he backing sheet for 2.5 minutes
and through the negative for 5 minutes. The 250 mil plate
having 125 mil relief is developed as described above and
has strong tailored relief elements. This printing plate is
used to print corrugated boxes. Solid areas with this plate
have better ink coverage than plates printed with a 250 mil
plate of polyurethane III composition alone (i.e., not a two
layered plate).
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SUPPLEMENTARY DISCLOSURE
It has been found that acrylonitrile can be used
in the copolymer used to prepare the printing plate of the
present invention. The following example is illustrative of
such use of acrylonitrile.
Example 10
1313 g (0.745 equivalents, acid number 31.9) of a
carboxyl terminated copolymer of butadiene and acrylonitrile
containing 10% acrylonitrile, 77.8 g (0.48 equivalents) of the
digycidyl ether of Bisphenol A and 3.3 g of N,N-dimethylbenzylamine
are placed in a 2 litxe resin kettle equipped with a stirrer, a
thermometer, a gas inlet and outlet tubes. The reaction mixture
is maintained und~r a nitrogen atmosphere at 100C for 7 hours~
The acid number is 9.4. Dry air is sparged through the reaction
mixture for 20 minutes and a solution of 58.3 g of glycidyl
methacrylate, 3.9 g of butylated hydroxy toluene and 0.078 g of
phenothiazine is added. The kettle is maintained at 100C for
an additional hour and then cooled.
The product has an acid number of 2.7 and a Brookfield
viscosity of 700,000 cps at 25C.
A photosensitive composition is prepared by blending
256 g of the prepolymer (prepared in the manner described
above) with 8~ g of lauryl methacrylate, 64 g of 1,3-butylene
glycol dimethacrylate and 2.4 g of 2,2-dimethoxy-2-phenyl
acetophenone at 40C until a homogenous solution is obtained
(approximately 1 hour). After curing using ultraviolet
radiation, the resin has a tensile strength of 880 psi, an
elongation of 120%, a tensile modulus of 644 psi and a Shore A
hardness of 55. When a sample of this cured resin is immersed
- ~D17 -
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in a solution of 90% ethyl alcohol and 10% propyl acetate
j for 24 hours it increases only 13% in weight.
A layer of 5-15 mils of the liquid polybutadiene-
acrylonitrile based resin composition is doctored over a
polypropylene film covering a line process negative, and a
80-90 mil layer of liquid polyurethane II composition which
when cured has a hardness of 40A and a modulus of 220 lb/inch
is doctored over the polybutadiene I resin formulation. The
plate is hardened by exposing through the backing sheet of
Example I (containing no antihalation dye) for 2 minutes and
exposing through the negative for 5 minutes. The plate is
developed by spray washing with a warm (50C) solution 1.0%
Bioterge alpha-olefin sulfonate detergent (Stepon Chem. Co.)
and post-exposed under a nitrogen blanket for 10 minutes. The
90-95 mil thick plate with 45 mils relief has the overall
printing qualities of the platesin the previous examples plus
the advantage of being resistant to alcohol inks and solvents.
The plate shows exceptional resistance to delamination
(separation of the resin layers) on extended use of the printing
plate.
- SD18 -
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