BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a system for making paper to be used as cover sheets
for gypsum wallboard, and more particularly refers to a polymer system for use in
making such paper and to a novel method for applying the system.
Description of the Prior Art
[0002] Gypsum wallboard is conventionally fabricated by depositing an aqueous slurry between
two paper cover sheets, setting the slurry and drying the finished product. In the
past, paper for utilization as paper cover sheets was prepared by utilizing an acid
size, alum and rosin. This sizing system was satisfactory and produced suitable paper
for cover sheets. It was subsequently found, however, that when a neutral size material
was utilized together with a cationic starch, a paper having greater strength was
produced. However, when the system was utilized with waste paper furnish, it was found
that contaminated material was deposited on the paper-making machine.
SUMMARY OF THE INVENTION
[0003] It is an object of the present invention to provide a paper suitable for use in the
production of gypsum wallboard having great strength.
[0004] It is a further object to provide a paper of the type described which is produced
by using a neutral sizing material.
[0005] It is still further an object to provide a paper suitable for use in making gypsum
wallboard with waste paper furnish which does not result in deposition of contaminants
in the paper-making machine.
[0006] It is an additional object to provide such a paper in which some or all of the expensive
cationic starch commonly utilized is eliminated.
[0007] These and other objects, advantages and functions of the invention will be apparent
on reference to the specification.
[0008] According to the invention, paper suitable for use in the production of gypsum wallboard
is prepared from waste paper furnish and utilizing a neutral size such as an alkenyl
succinic anhydride by eliminating a portion or all of the cationic starch conventionally
used with such neutral sizes by incorporating into the pulp furnish slurry one or
more cationic polymers at particularly selected places of the paper-making apparatus.
Through the use of the present system and process excellent paper is provided and
contamination of the paper-making machine is avoided.
[0009] Waste paper such as waste news, sections, mixed waste or old corrugated paper conventionally
contain contaminants such as wax, asphalt, hotmelt glues and adhesives. When pulp
furnish prepared from these materials is utilized to form paper, they often deposit
at various places of the paper-making machine and cause contamination that must be
periodically removed. This results in an added expense to the paper- making process.
Moreover, the cationic starch conventionally used together with alkenyl succinic anhydride
neutral sizes is quite expensive and a considerable reduction in cost could be achieved
if the use of these materials was reduced or discontinued completely.
[0010] The alkenyl succinic anhydride neutral size conventionally used for sizing gypsum
wallboard paper is disclosed in U.S. Patent No. 3,102,064, which also discloses the
use of a cationic starch as a retention aid. The general formula of the material is
as follows:

wherein R is selected from the group consisting of dimethylene and trimethylene radicals,
and wherein R' is a hydrophobic group containing more than 5 carbon atoms selected
from the group consisting of alkyl, alkenyl, aralkyl and aralkenyl groups.
[0011] Newslined paper is paper that is put on the back face of the gypsum wallboard which
is mounted on the inside of the wall in contact with the supporting frame members.
Consequently, it need not have the high grade surface required on the facing side
of the wallboard. Newslined paper is typically comprised of low grade materials which
are unsuitable for paper which is applied to the face of the wallboard. The low grade
constituents are old corrugated container stock which contains many plastics, hotmelt
adhesives, wax and other contaminants which may cause bleed-through and are unsuitable
for the outer or front face of the wallbaord. The newslined is also comprised of sections
which are highly coated, thereby creating contamination problems. Newslined can also
be inserts cut out of newspapers that are highly coated or printed with rotogravure.
[0012] A substantial cost savings may be accomplished by replacing all or part of the cationic
starch. According to the invention the replacement is made by adding a cationic polymer.
Basically the cationic density of the material relates to a number of reactive groups
on a given length of a molecule. The greater the number, the greater is the cationic
density and the greater will be the cationic charge on the retention aid molecule,
and this will increase what is known as its coagulating effect. In the present invention
the preferred cationic polymer a material of low cationic charge density is preferred.
This means that the frequency of cationic charges on a molecule is lower and, therefore,
it has a lower overall charge density. The material used in connection with a high
molecular weight molecule creates flocculating conditions, where the cationic charge
causes the molecule to be attracted to anionic groups. However, the process does not
require a very high charge density in order to accomplish the present purpose, but
the process depends more on the length of the molecule, and under these conditions
the effect which is achieved is flocculation. The cationic charge density is given
herein in terms of mole percent.
[0013] The present invention may be practiced in either one of two embodiments. In the first
embodiment a high molecular weight cationic polymer having a low charge density is
introduced into the paper-making process at the discharge of the fan pumps in highly
dilute form (for example 0.1% concentration). A portion of the cationic starch solution
conventionally utilized as a retention aid is eliminated, and only the primary starch
or the starch going through the emulsifier for the purpose of providing a cationic
charge to retain the neutral size is utilized. By inserting the retention aid polymer
only at the discharge of the fan pumps, contamination of the paper-making apparatus
is avoided. Additionally a savings in the cost of the eliminated cationic starch is
realized.
[0014] In a second embodiment of the invention, the two polymer system, in addition to adding
a high molecular weight low charge cationic polymer to the discharges of the fan pumps,
the entire cationic starch addition is replaced with a primary solution of the same
high molecular weight low charge density cationic polymer applied through the emulsifier,
and an additional dilute solution of a low molecular weight, high charged density
cationic polymer is applied to the machine chest. This results in a substantial savings
by eliminating the expensive cationic starch, and results in a clean operating paper-making
machine system. Because contamination is avoided, it is not necessary to use a liner
stock system sometimes utilized to keep the top press rolls from becoming filled with
contaminants. The use of the second polymer, a low molecular weight high charge density
cationic polymer coagulant in the machine chest provides cations to counter the anionic
trash present in the slurry.
[0015] Although the following discussion is not intended to be limiting in any manner, it
is believed that what happens with regard to the addition of second polymer to the
machine chest is that the strong coagulating power of the polymer causes contaminant
particles to coagulate and agglomerate into large particles with eventually considerably
reduced tackiness. These larger particles are better retained in the forming web and
hence are carried away in the sheet rather than becoming deposited on the paper machine
surfaces. It is believed to be fortuitous that the coagulating action occurs in the
machine chest, because here the tile surfaces of the machine chest are far less prone
to have contaminant plate-out than the rubber coverings of the press rolls, the wire
mesh of the cylinders or the fabric of the press felts.
[0016] It is believed that in the single cationic polymer system excellent performance is
accomplished because the high molecular weight low cationic charge polymer introduced
at the discharges of the fan pumps ties the contaminant particles into the forming
web without causing them to plate-out on the paper machine equipment. In this bridging
type action where the charge density of the polymer is not great, increasing molecular
weight of the polymer (more bridging) in close proximity to the forming cylinders
(after the fan pumps) is important in tying the contaminants into the forming web
without causing them to coagulate and plate-out.
[0017] The following examples are provided to illustrate general paper-making processes,
and including prior process as well as improved processes of the present invention,.
They are provided for illustrative purposes and are not intended to be limiting in
any manner.
EXAMPLE 1
GENERAL PROCESS FOR MAKING PAPER FOR GYPSUM WALLBOARD USE
[0018] A blend of varying ratios of hard and soft stocks, such as old corrugated stock and
sections, respectively, on newslined paper, is pulped, cleaned and refined, and then
discharged into a 25,000 gallon tile-lined machine chest. A low molecular weight,
high charge density cationic coagulant polymer is added to the paper stock in the
machine chest, where applicable, at the rate of about 0.15 to 0.45 dry lb. of polymer
per ton of paper. This coagulant serves to coagglomerate fine contaminant particles
into larger, more readily retained particles at a point where the agglomeration would
not cause plating out of the contaminant on the paper machine surfaces. The resulting
stock called "machine furnish" is then pumped at 3-1/2% oven dry consistency to the
fan pump inlets of the forming section of the paper machine where the furnish is divided
into 7 separate flows corresponding to their introduction to 7 separate fan pumps.
[0019] A neutral size emulsion, comprising an ASA (alkenyl succinic anhydride) size emulsified
in either a cationic starch or a cationic polymer solution, is added to the machine
furnish in the thick stock down legs just prior to entering the inlet piping to the
fan pumps. The function of the cationic starch or the cationic polymer is to cause
the size to adhere to the anionically-charged cellulose fibers of the machine furnish
in order to provide sizing after subsequent heat curing. The ASA size is added at
rates varying between 2.5 and 5.5 dry lb/ton of paper depending on sizing propensity
of the furnish and effectiveness of size retention on the paper machine. The flows
of machine furnish mixed with size emulsion is diluted to approximately 0.5 to 1.5%
consistency with recycled white water from the paper machine, and are then pumped
by the fan pumps to the continuously moving forming cylinders of the paper machine.
According to the invention, into the discharges of the fan pumps a high high molecular
weight, low charge density cationic flocculant polymer is pumped at the rate of 0.40
to 1.35 dry lb/ton of paper for use as a retention aid. The retention aid is mixed
with the dilute machine furnish by means of turbulence created by elbows in the approach
piping from the discharges of the fan pumps to the forming cylinders. The retention
aid serves to improve the retention of cellulose fines and agglomerated contaminant
particles which, if poorly retained in the sheet, could become embedded in paper machine
surfaces such as carrying and press felts, forming wires and press roll covers.
[0020] The machine furnish is formed on the forming cylinders into separate plies which
are joined together on a continuously moving carrying felt. The water drained through
the wire covers of the cylinders is caused to flow back to the separate fan pumps
for dilution of the pulp. A seven ply sheet is formed at 23-25% solids consistency
and is carried on continuously moving felts through the press section of the paper
machine, where the solids content of the sheet is increased to 40-45%. The sheet by
itself is then passed into the dryer section where it is dried to 1.0-2.5% moisture
content on continuously turning drying cylinders loaded to a minimum steam pressure
of 25 psig for proper curing of the ASA size.
[0021] The dried sheet of paper, after leaving the dryer section, passes through a wet calender
stack where water is applied to both faces of the sheet for finish by water addition
to the rolls at the calender stack via water boxes attached to the calender stack
rolls. The sheet of paper then passes through a following dry calender stack where
the caliper or thickness uniformity is improved. After leaving the dry stack the sheet
of paper is wound into a set of paper on a reel. Later the set is slit and wound on
a winder into separate rolls for later conversion to gypsum board.
[0022] When the type of paper produced or the furnish conditions make it necessary, a parallel
stock system to the filler stock system, called the liner system is run to provide
a two-ply liner on top of the filler stock. Two of the afore-mentioned cylinders are
utilized for this purpose. The filler portion of the paper, as a result, consits of
five plies. Where the contaminant level in the paper stock furnish causes a high level
of contaminant deposition on the paper machine press rolls and carrying and press
felts, the liner system is run utilizing paper stock from clean, cut-up rolls of paper.
The liner so formed alleviates the press roll deposition problem and allows continued
operation of the paper machine. Without this modification, the press rolls would soon
be covered with sticky contaminant causing picking of the sheet and eventual sheet
breaks.
[0023] The problems encountered with contaminant deposition as described , above are very
typical and frequent while a cationic starch is being added through the ASA size emulsifier
and no retention aid is being utilized in the fan pump discharges, and no coagulant
is being added to the machine chest. For this reason, under the above conditions the
liner system is utilized continuously. Applying the retention aid after the fan pumps,
according to the invention eliminates the deposit problem, as will be discussed below,
and permits a significant reduction in the rate of total cationic starch usage.
[0024] When the high molecular weight, low charge density flocculant polymer is added through
the emulsifier in place of the remaining cationic starch, the paper machine deposits
again begin to occur. Adding the low molecular weight high charge density cationic
coagulant polymer to the machine chest, as in the two polymer embodiment, helps to
alleviate the contaminant deposition when the cationic starch is completely replaced
with the flocculant, as is discussed below. When either the one polymer system method
or the two polymer system method are run, the liner system is not required.
[0025] The following example illustrates a process where no retention aid polymer was used,
as in prior art processes.
EXAMPLE 2
PAPER PRODUCED WITHOUT ADDITION OF POLYMER AFTER FAN PUMPS (PRIOR ART)
[0026] Paper was produced without the addition of any cationic polymer after the fan pumps
and had the composition shown below in Table I. The cationic starch solution was pumped
through the emulsifier with the ASA size, and was mixed with additional starch solution
after the emulsifier. The dilute ASA size emulsion was then pumped to the thick stock
lines to the fan pump inlets. Under these process conditions and with the resulting
contaminated condition of the furnish a total of 12.5 lb/ton of cationic starch and
5.0 lb/ton of ASA size were required to provide adequate paper sizing, and the liner
system had to be run utilizing cut up clean rolls of the same approximate fiber composition
as run in the filler stock.
[0027]

EXAMPLE 3
PAPER PRODUCED WITH ONE CATIONIC POLYMER RETENTION AID ADDED AFTER FAN PUMPS
[0028] Paper was prepared by the use of one cationic polymer retention aid applied immediately
after the fan pumps and had the composition shown in Table II below. In this example,
the cationic starch solution added to the ASA-starch emulsion after the emulsifier
was shut off and was replaced with clarified process water. A high molecular weight,
low charge density cationic polymer was added at the rate of 0.5 dry lb/ton paper
to the discharge of the fan pumps pumping dilute machine furnish to the forming cylinders.
The results of this mode of paper manufacture were that cationic starch usage, was
decreased by 9.0 lb/ton or 72% of the usage of Example 2 above. The neutral sizing
rate was reduced by 0.5 lb/ton or 10% of Example 2's usage and use of the liner system
with its attendant electrical power consumption was eliminated. The paper machine
press rolls remained clean with no assistance from the liner system.
[0029]

[0030] The following Example 4 illustrates the preparation of a two polymer system using
newslined paper according to a further embodiment of the invention.
EXAMPLE 4
TWO POLYMER SYSTEM NEWSLINED PAPER
[0031] Paper produced with the two cationic polymers had the composition illustrated in
Table III below. In this example, in addition to the polymer added to the fan pump
discharge as in Example 3 above, 0.25 dry lb/ton of a low molecular weight, high charge
density cationic coagulant polymer was added to the filler system machine chest. Initially,
the primary purpose of the coagulant addition was to trap anionic trash which consumed
a disproportionate share of the cationic size emulsion and reduced the efficiency
of sizing. It was discovered that its effect on coagulating furnish contaminant particles
was beneficial. This discovery permitted using the afore-mentioned high molecular
weight low charge density cationic flocculant polymer in place of the cationic starch
in the ASA size emulsifier. It was found that earlier replacement of the cationic
starch by this polymer without prior addition of the coagulant into the machine chests
caused deposition of contaminant on the paper machine.
[0032] In this example all of the remaining cationic starch utilized in the one polymer
system was replaced with only 0.15 lb/ton of the polymer flocculant, thus saving an
additional 3.5 lb/ton of cationic starch. As in the one polymer system, the high molecular
weight, low charge density cationic flocculant was added to the fan pump discharges.
The beneficial results of this mode of operation was in the elimination of the use
of the expensive cationic starch while still avoiding contaminant deposition. Additionally,
a further reduction in ASA sizing rate of 0.5 lb/ton was obtained. Use of the liner
system with its significant electrical consumption was also eliminated.

[0033] The following examples illustrate the preparation of the various ingredients used
in the present invention.
EXAMPLE 5
PREPARATION OF CATIONIC STARCH - ASA EMULSION
[0034] A pregelled powdered or flaked cationic potato starch was wetted out with fresh water
in a hopper-type eductor and was discharged into an agitated mixing tank where full
solubility of the the starch was achieved over 30-60 minutes, and the starch solution
concentration was adjusted to 3%. The completed batch of starch solution was transferred
to the holding tank and was pumped at a rate of 3.5 to 4.0 dry lb/ton of paper through
a turbine pump size emulsifier, where it served as the size emulsifying medium. An
oily ASA (alkenyl succinic anhydride) sizing agent was added at a rate of 3.5 to 5.0
lb/ton of paper to the starch solution just prior to the emulsifier. After emulsification,
the solids content of the emulsion was 6.0% including starch solids.
[0035] The thick-size starch emulsion flowed to the inlet of an eductor where the emulsion
was diluted with clarified water at a rate sufficient to lower the solids content
of the emulsion to 0.35% solids. The dilute emulsion was then metered through orifices
and was then injected into the thick paper machine stock slurry just prior to its
entry into the suction of the fan pumps. Subsequently, the thick stock was mixed and
diluted with white water drainings from the forming cylinders in the fan pumps.
EXAMPLE 6
PREPARaTION OF RETENTION AID POLYMER OF INVENTION
[0036] The high molecular weight low charge density cationic emulsion polymer, designated
hereinas polymer "A", consisting of 28-31% polymer solids, 40-43% water and 23-26%
hydrocarbon oil was inverted to a 1-3% solids aqueous solution in agitated mixing
and holding tanks. The polymer solids consisted of a copolymerization product of acrylamide
monomer and cationic trimethyl ammonium chloride methacrylate where the cationic charge
density of 7.5 mol percent was provided by quaternary amide groups attached to the
polymer. The mean average molecular weight of the polymer was 2,000,000. Wetting out
of the polymer was accomplished in hopper-type eductors with fresh water.
[0037] The moderately dilute aqueous polymer solution was pumped through a rotameter and
thence to a mixing eductor with a variable speed, non- pulsing type constant displacement
gear pump. Mill clarified water was used as the motivating fluid in the eductor to
raise the dilute polymer line pressure to approximately 60 psig pressure and to lower
the polymer solids concentration to approximately 0.1% solids.
[0038] For addition to paper, the dilute polymer was metered at the rate of 0.40 to 1.35
dry lb/ ton into the dilute paper machine stock slurry just before the forming cylinders
at the discharges of the forming cylinder fan pumps. The metering was accomplished
through orifices, and introduction of the polymer into the dilute machine stock slurry
was done through inlet quills set into the fan pumps discharge piping.
[0039] The dilute polymer was mixed with the dilute machine stock slurry in the turbulence
that occurs after each bend in the piping before the machine stock reaches the forming
cylinders. The dilute machine stock slurry was then formed by drainage through the
forming cylinder wires into plies which were co-joined onto a carrying felt. The joined
plies were transferred as a web onto another carrying felt, and the web was then pressed
between press rolls and contacted by several hot dryer rolls in a dryer section to
remove all but the last 2-5% of the moisture from the web.
[0040] The sheet was run between steel rolls to provide smoothness and uniform thickness.
The paper was wound on a reel and was later slit and rewound on a reel into rolls
that were shipped to the market or to the converting stage for making gypsum board.
[0041] The following example illustrates the preparation and use of the additional materials
for the two polymer system.
EXAMPLE #7
PREPARATION OF CATIONIC POLYMER COAGULANT FOR TWO POLYMER SYSTEM
[0042] A cationic quaternary amine polymer, designated herein as polymer "B", of very high
charge density of 100 mol percent and a low mean average molecular weight of approximately
200,000 was added at the rate of 0.15-0.45 dry lb/ton of paper to the machine chest
dilute at 10% of the as-received concentration. This polymer was added to the machine
chest and utilized to neutralize colloidal anionic furnish components that would have
consumed disproportionate amounts of cationically charged size. The polymer served
to coagulate dispersed contaminant particles in the machine chest. If such coagulation
were to have occurred on the paper machine proper, substantial deposits of contaminants
would have been prone to occur on the paper machine components such as the top press
rolls, cylinder wires and press felts.
EXAMPLE 8
PREPARATION OF CATIONIC - SIZE EMULSION FOR TWO POLYMER SYSTEM
[0043] Emulsion polymer, termed "A" in Example 6 related to the one polymer system, was
adjusted to a 0.18% solids content solution directly by wetting the polymer with fresh
water in a hopper eductor followed by strong agitation in a mix tank. The dilute polymer
was transferred to a holding tank and was then pumped through a variable speed gear
pump to a turbine pump size emulsifier at a rate of 0.10-0.15 dry lb/ton of paper
where it served as the size emulsifier medium. An oily ASA (alkenyl succinic anhydride)
sizing agent was added to the polymer solution at a rate of 2.5-5.0 lb/ton just prior
to the emulsifier. After emulsification the solids content of the emulsion was 6.2%
including polymer solids.
[0044] The thick size-polymer emulsion flowed to the inlet of an eductor where the emulsion
was mixed with a volume of clarified process water equal in volume to 30 times the
volume of the emulsion, thus providing a dilute emulsion of 0.19% solids concentration.
This dilute emulsion under approximately 60 psig pressure was metered to the thick
stock slurry lines ahead of the forming cylinder fan pumps through orifices. The dilute
emulsion was added to the thick stock slurry through injection quills set into the
thick stock slurry lines. The thick stock slurry was diluted with recycled white water
drainage from the forming cylinders and then was pumped to the forming cylinders as
dilute machine stock slurry.
EXAMPLE 9
PREPARATION AND USE OF RETENTION AID POLYMER This polymer was formed and introduced
in the same manner as in Example 6 above.
EXAMPLE 10
STARCH - SIZE EMULSIFYING SYSTEM
[0045] A pregelled powdered or flaked cationic potato starch was wetted out with fresh water
in a hopper type eductor and was discharged into an agitated mixing tank where full
solubilization of the starch was permitted to occur over 30-60 minutes, and the starch
solution concentration was adjusted to 3%. The completed batch of starch solution
was transferred to the holding tank and was pumped with a centrifugal pump to a turbine
pump emulsifier at a rate of 2.5-5.0 lb/ton. ASA size as previously discussed was
added at a rate of 4.5 to 5.5 lb/ton to the starch solution before emulsification
in the starch solution as emulsifying medium.
[0046] The size emulsion concentration leaving the emulsifier was 6%. The size emulsion
was mixed with a continuous flow of more starch solution equal to a rate of 6 to 11.5
dry lb/ton of starch in an eductor to provide a dilute emulsion solids concentration
of 4%. The dilute size emulsion was then metered to separate forming cylinders through
separate rotameters for each forming cylinder. The starch-size emulsion then flowed
to injection quills in the thick stock lines to the fan pump suctions where it was
added to the thick stock. The sheet of paper was then formed as described above.
DESCRIPTION OF MATERIALS USED IN THE PRESENT INVENTION
IN BOTH THE ONE POLYMER AND TWO POLYMER EMBODIMENTS
[0047] The retention aid polymer added to the discharge of the fan pumps according to the
invention is a copolymerization product of acrylamide monomer and cationic trimethyl
ammonium chloride methacrylate. The material has a cationic charge density of 7.5
mol percent. Materials having a mean average molecular weight of from 2,000,000 to
4,000,000 may be utilized. The structure of the polymer is as follows:

[0048] The formula product above is furnished commercially by the manufacturer Dow Chemical
Company, Midland, Michigan in the following form:
28-31% Polymer Solids
40-43% Water
23-26% Hydrocarbon Oil
[0049] Other materials that may be utilized are Betz 1260 or 1264 which are copolymers of
a quaternary amine and acrylamide with a mean average molecular weight of 5 x 10
6. The polymer has a cationic charge density of 20 mol percent. The amine provides
the cationicity.
[0050] 1260 is a dry material and 1264 is an emulsion polymer of 30% active polymer solids
content.
[0051] Another material which may be utilized is Hercules Reten 210 which is an acrylamide/quaternary
ammonium salt monomer copolymerization product which has a molecular weight in the
range of 9-10 x 10
6, a cationic charge density 7.5 Mol percent, and is supplied as a dry powder.
[0052] With respect to the two polymer system embodiment, the cationic polymer coagulant
is a cationic quaternary amine polymer of 200,000 mean average moleculer weight and
100 Mol percent charge density. It is supplied at low solids in solution under the
trademark Nalco 7625, and supplied by Nalco Chemical Co., Oak Brook, Illinois.
[0053] Alternatively a Dow coagulant under the trademark Polymeric PC Copolymer formed of
acrylamide and cationic monomer 50/50 by weight, can be used. The cationic monomer
is a quaternary methyl ammonium chloride salt with the monomer part cyclic in structure.
The cationic charge density is 7 mol percent, the range of molecular weight is 1.0-1.5
x 10
6. It is supplied as an 8% aqueous solution.
[0054] Still another coagulant which may be used is sold under the trademark Quaker 3015
and has a basic structure of polyamino/amide with a molecular weight range of from
200,000-300,000 and a cationic charge density of 50 mol percent. It is supplied as
a liquid solution containing 38X solids.
[0055] The gypsum board paper produced above utilizing the two-polymer system processes
was subjected to a number of quality control tests to make sure that it met minimum
standards required for proper conversion to wallboard. Table IV below provides test
data obtained by testing wallboard produced by using the paper produced by the methods
described above. In the table, tests of both manila and newslined gypsum board paper
met the indicated standards per test. The sizing or water resistance of both papers
as indicated by the saturations and cobb water resistance tests was good. Sheet strength
in terms of ply bond and tensile strength were also good. The manila paper tested
above was made up of 2 plies of a flyleaf liner stock applied to 5 plies of a filler
stock consisting of box plant kraft cuttings and waste news. The newslined paper was
made up of 7 plies of a blend of old corrugated container stock and waste stock.
[0056] The gypsum board papers described above were converted into gypsum board on a conventional
board line where stucco slurry was spread onto the inside face of the manila where
the flyleaf topliner was face down. a forming roll or forming plate on a continuously
moving forming belt. The board when fully set was cut into 8 foot lengths, inverted
and conveyed to a drying kiln where it was dried by forced convection drying. The
board after leaving the drying kiln was inspected and tested, and then made into bundles
and shipped.
[0057] Gypsum board produced as discussed above must meet a variety of quality tests in
order to reach the market. The covering papers must bond well to the gypsum board
core, and the board must possess adequate transverse strengths. The dry bond test
is conducted by first drying the finished board for one hour at 110°F in a forced
convection oven, and then subjecting the board to a force sufficient to break the
bond between the paper and the board core. The applied force or weight at failure
is the measure of bond strength. The bond failure is designated as the percentage
of the tested board surface that becomes exposed or has no fiber covering after the
bond has been broken. In reference to Table IV it is apparent that both manila and
newslined paper bonded well to the gypsum core because the bond strengths fall within
the desired range and the bond failure test shows zero bond failure for both papers.
[0058] Transverse strength tests were conducted by first conditioning the finished board
for 16 hours in a 70°F and 50% relative humidity environment, and then applying a
downward force in the center of the specimen supported at its opposing outer edges.
The face positioned downward is the face which is tested. Force applied at failure
is the measurement of transverse strength.
[0059] Referring to Table IV it is evident that the gypsum board met both machine-direction
and across-direction minimum transverse strength standards on the sides faced with
the manila and newslined paper.
[0060] The various paper and board tests indicate that the polymer-treated paper, as produced
in the two-polymer system processes, makes acceptable gypsum board. Additionally,
it permits the elimination of expensive cationic starch.

[0061] The method of the present invention offers several advantages over prior art methods
utilizing a neutral size for making paper suitable for gypsum wallboard. In the one-polymer
method, a high molecular weight low charge density retention aid polymer is added
immediately after the fan pumps instead of at a prior position. This results in the
prevention of the deposition of contaminants on the cylinder wires, press and carrying
felts and for press rolls of the paper-making machine. Additionally, it permits a
reduction in the use of a cationic starch retention aid, a material which is considerably
more expensive on a total use basis than the polymers utilized. In the two-polymer
method, a high molecular low charge density polymer of the same type is added immediately
after the fan pumps, obtaining the benefits described with regard to the one-polymer
method.
[0062] Additionally, a small amount of the same polymer is introduced into the emulsifier,
thereby completely replacing the use of the cationic starch. Additionally, a low molecular
weight high charge density polymer is added to the machine chest in order to further
cause agglomeration of contaminant products present in the slurry. As a result of
the use of the two-polymer system, contamination is avoided and the use of the cationic
starch is completely eliminated. Additionally, because the apparatus is maintained
in clean condition and the resulting paper is clean, a paper liner need not be applied
to the surfaces of the paper.
[0063] It is to be understood that the invention is not to be limited to the exact details
of operation or materials described, as obvious modifications and equilvalents will
be apparent to one skilled in the art.
1. In a process for producing paper in a paper-making apparatus suitable for use in
the production of gypsum wallboard, the process comprising preparing a pulp slurry,
introducing a neutral size material and a cationic retention material into the slurry,
passing the slurry through a plurality of fan pumps and forming and drying the paper,
the improvement which comprises the step of introducing a high molecular weight low
cationic charge density retention aid polymer into the slurry immediately at the discharge
situs of the fan pumps, whereby any contaminants present in this slurry are retained
therein and do not deposit out on the walls of the paper-making apparatus.
2. A process according to Claim 1, when said neutral size material has the structural
formula:

wherein R is-selected from the group consisting of dimethylene and trimethylene radicals,
and wherein R' is a hydrophobic group containing more than 5 carbon atoms selected
from the group consisting of alkyl, alkenyl, aralkyl and aralkenyl groups.
3. A process according to Claim 2, wherein said cationic retention material is a cationic
starch.
4. A process according to Claim 2, wherein said high molecular weight low cationic
charge density retention aid polymer is a copolymerization product of acrylamide monomer
and cationic trimethyl ammonium chloride methacrylate, having a mean average molecular
weight of from about 2,000,000 to about 4,000,000, and a cationic charge density of
7.5 mol percent.
5. A process according to Claim 4, wherein said high molecular weight low charge density
polymer is added in an amount of from 0.40-1.35.
6. A process according to Claim 1, wherein said cationic starch for the neutral size
is added in an amount of 2.5-4.0 dry lb./ton.
7. A process according to Claim 1, which additionally comprises passing said slurry
into a machine chest, wherein a low molecular weight high cationic charge density
polymer coagulant is introduced in said machine chest.
8. A process according to Claim 7, wherein additionally a portion of said high molecular
weight low cationic charge density polymer is introduced into an emulsifier and then
into said aqueous slurry to replace said cationic starch as a retention aid.
9. A process according to Claim 7, wherein said low molecular weight high density
cationic charge polymer is a cationic quaternary amine polymer having a mean average
molecular weight of about 200,000 and a charge density of about 100 mol percent.
10. A process according to Claim 9, wherein said cationic coagulant polymer added
to said machine chest in the amount of about 0.15-0.45 dry lb./ton.