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Patent 2145244 Summary

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Claims and Abstract availability

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(12) Patent: (11) CA 2145244
(54) English Title: PRESSURE BONDING ADHESIVE AND ADHESIVE COATED PRODUCT
(54) French Title: ADHESIF AUTOCOLLANT ET PRODUIT ENROBE DUDIT ADHESIF
Status: Expired and beyond the Period of Reversal
Bibliographic Data
(51) International Patent Classification (IPC):
  • C9J 7/38 (2018.01)
  • C9J 7/21 (2018.01)
(72) Inventors :
  • MEHTA, RAJENDRA (United States of America)
(73) Owners :
  • STANDARD REGISTER COMPANY (THE)
(71) Applicants :
  • STANDARD REGISTER COMPANY (THE) (United States of America)
(74) Agent: GOWLING WLG (CANADA) LLP
(74) Associate agent:
(45) Issued: 1998-08-04
(22) Filed Date: 1995-03-22
(41) Open to Public Inspection: 1996-09-23
Examination requested: 1995-07-24
Availability of licence: N/A
Dedicated to the Public: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data: None

Abstracts

English Abstract


A pressure bonding adhesive composition is provided for use
on cellulosic substrates which will not become tacky under high
temperatures, lose adhesive properties due to contact with silicone
oils, "block" when stacked prior to printing, or lose bond-forming
ability with age. Non-thermoplastic pigment particles and a
compound selected from the group consisting of a natural rubber
latex, a graft copolymer of natural rubber and acrylic monomer and
a blend of the natural rubber latex and the graft copolymer are
mixed together to form an adhesive with a glass transition
temperature in the range of -10 to -78°C and a green strength of
0.05 to 0.75 p.s.i.. The adhesive may also optionally contain a
chloroprene-methacrylic acid copolymer latex and a vinyl-
methacrylic acid copolymer latex.


French Abstract

Composition adhésive autocollante pour substrats cellulosiques, qui ne deviennent pas poisseux à haute température, ne perdent pas leurs propriétés adhésives par contact avec des huiles de silicone, ne forment pas de bloc lors de l'empilement avant l'impression, et enfin ne perdent pas leur capacité de former des liaisons en vieillissant. Des particules de pigment non thermoplastique et un composé choisi parmi un latex de caoutchouc naturel, un copolymère de greffe d'un caoutchouc naturel et d'un monomère acrylique, et un mélange du latex de caoutchouc naturel et du copolymère de greffe sont mélangés pour former un adhésif avec une température de transition vitreuse de -10 à -78 degrés C et une résistance initiale de 0,05 à 0,75 lb/po2. L'adhésif peut facultativement renfermer aussi un latex de copolymère de chloroprène-acide méthacrylique et un latex de copolymère de vinyle-acide méthacrylique.

Claims

Note: Claims are shown in the official language in which they were submitted.


-6-
Claims
1. An adhesive coated cellulosic substrate for use in producing
laser printed documents comprising:
a cellulosic substrate coated with an adhesive formed from
non-thermoplastic pigment particles, a compound selected from the
group consisting of a natural rubber latex, a graft copolymer of
natural rubber and acrylic monomer and a blend of said natural
rubber latex and said graft copolymer, and optionally one or more
compounds selected from the group consisting of chloroprene-
methacrylic acid copolymer latex and vinyl-methacrylic acid
copolymer latex, said adhesive having a glass transition
temperature in the range of from -10 to -78°C and a green strength
of 0.05 to 0.75 p.s.i..
2. The adhesive coated cellulosic substrate of claim 1 wherein
said non-thermoplastic pigment particles have a particle size of
1-40 microns and are present in the final adhesive in a solids
weight percent of 1 to 10%.
3. The adhesive coated cellulosic substrate of claim 2 wherein
said non-thermoplastic pigment particles are present in the final
adhesive in a solids weight percent of about 2%.
4. The adhesive coated cellulosic substrate of claim 1 wherein
said natural rubber late is present and is not chemically
modified.
5. The adhesive coated cellulosic substrate of claim 4 wherein
said graft copolymer is present and has an acrylic monomer content
of 30 to 50% by weight.
6. The adhesive coated cellulosic substrate of claim 5 wherein
said graft copolymer has a glass transition temperature of from
about -60 to -65°C.
7. The adhesive coated cellulosic substrate of claim 6 wherein
said acrylic monomer is selected from the group consisting of alkyl
acrylates and alkyl methacrylates.

-7-
8. The adhesive coated cellulosic substrate of claim 7 wherein
said acrylic monomer is selected from the group consisting of ethyl
acrylate, methyl methacrylate and ethyl methacrylate.
9. The adhesive coated cellulosic substrate of claim 1 wherein
said chloroprene-methacrylic acid copolymer latex is present and
said copolymer latex has a glass transition temperature of about
-45°C.
10. The adhesive coated cellulosic substrate of claim 1 wherein
said vinyl-methacrylic acid copolymer latex is present and has a
glass transition temperature in the range of from -14 to -25°C.
11. A pressure bonding adhesive for use on laser printed documents
comprising non-thermoplastic pigment particles, a compound selected
from the group consisting of a natural rubber latex, a graft
copolymer of natural rubber and acrylic monomer and a blend of said
natural rubber latex and said graft copolymer and optionally one
or more compounds selected from the group consisting of
chloroprene-methacrylic acid copolymer latex and a vinyl-
methacrylic acid copolymer latex, said adhesive having a glass
transition temperature in the range of -10 to -78°C and a green
strength of 0.05 to 0.75 p.s.i.
12. The pressure bonding adhesive of claim 11 wherein said non-
thermoplastic pigment particles have a particle size of 1-40
microns and are present in the final adhesive in a solids weight
percent of 1 to 10%.
13. The pressure bonding adhesive of claim 12 wherein said non-
thermoplastic pigment particles are present in the final adhesive
in a solids weight percent of about 2%.
14. The pressure bonding adhesive of claim 11 wherein said natural
rubber latex is present and is not chemically modified.
15. The pressure bonding adhesive claim 14 wherein said graft
copolymer is present and has an acrylic monomer content of 30 to
50% by weight.

-8-
16. The pressure bonding adhesive of claim 15 wherein said graft
copolymer has a glass transition temperature of from about -60 to
-65°C.
17. The pressure bonding adhesive of claim 16 wherein said acrylic
monomer is selected from the group consisting of alkyl acrylates
and alkyl methacrylates.
18. The pressure bonding adhesive of claim 17 wherein said acrylic
monomer is selected from the group consisting of ethyl acrylate,
methyl methacrylate and ethyl methacrylate.
19. The pressure bonding adhesive of claim 11 wherein a
chloroprene-methacrylic acid copolymer latex is present and said
copolymer latex has a glass transition temperature of about -45°C.
20. The pressure bonding adhesive of claim 11 wherein a vinyl-
methacrylic acid copolymer latex is present and said copolymer has
a glass transition temperature in the range of from -14 to -25°C.

Description

Note: Descriptions are shown in the official language in which they were submitted.


STD 501 PI ~ 452
PRESSURE BOI~ G ADHESIVE AND
ADXES~ VE COATED PRODUCT
Backqround of the InventiorL
This invention relate3 to a pressure bonding adhesive for u3e
5 on paper product3 which are subj ected to high temperature
condition3, and more particularly to an adhe8ive for use on
documents such as mailer forms produced by laser printing.
The use of ~lself" adhesives for use in mailer forms is well
known. In the past, heat ~;eal adhesives were u3ed on form3 which
10 were not 3ubj ected to heat and pre33ure until the f inal printed
form wa3 3ealed by applying heat to the adhe3ive. However, new
adhe3ive3 were required with the advent of la3er printer3, which
generally u3e heat and pres3ure - (fu3er roll3) for adhering toner
image3 to paper. The3e ad~le3ive3 need to form 3trong bond3 under
pre33ure alone and be able to with3tand fu3er roll temperature3 of
up to 232 C without becoming tacky .
Much effort ha3 been made to adapt "3elf" adhe3ive3 3uch a3
natural rubber latex coating3 to the need3 of la3er printer3.
The3e coating3 generally are adherent with other coating3 of the
3ame material but are not adherent toward other surfaces. The
pre33ure 3eal3 made after printing in la3er printer3 u3ing 3uch
"3elf" adhe3ive3 have not been entirely 3ati3factory for 3everal
rea30n3. Fir3t, 3uch adhe3ive3 have adhered to the fu3er roll3,
cau3ing fouling or jamming. Second, 3ilicone oil3 which are
commonly applied to fu3er roll 3urfaces have tran3ferred to the
adhe3ive3, preventing formation of 3trong self-adhesive bonds.
Third, adhesive coated form3 are 3tored in 3tack3, pack3 or roll3
prior to printing and "blocking" often occur3, which cau3e3 the
adjacent pile3 to 3tick to~ether, thu3 preventing proper feeding.
Finally, 3uch prior adhe3ive coating3 103e bond-forming ability
with age.
Some ef forts have been made to correct these problems using
adhesives such as the one d:isclosed in U.S. patent 4,918,128. This
adhesive is composed of a graft polymerized natural rubber latex
with styrene and methyl methacrylate comonomers and a non-
thermopla3tic particulate solid.
Still, there remains a need in the art for a pressure bonding
adhesive which will not become tacky under high temperatures, lose

214~24~
--2--
adheeive properties due to contact with silicone oils, "block" when
stacked prior to printing, or lose bond-forming ability with age.
SummarY of the Invention
The present invention meets that need by providing a pressure
bonding adhesive for use on laser printed documents which combines
non-thermoplastic pigment particles and a compound selected from
the group consisting of a natural rubber latex, a ~[raf t copolymer
of natural rubber and acrylic monomer and a blend of the natural
rubber latex and the graf t copolymer . These compounds produce an
adhesive capable of withstanding the heat and pressure conditions
of the fuser rolls in sheet fed and web fed laser printers such as
the Xerox 4050, the SiemenE; 2140, the IBM 3800 and 3900 and still
form a secure bond under pressure alone.
The adhesive comprises non-thermoplastic pigment particles,
a compound selected from the group consisting of unmodified natural
rubber latex, a graf t copolymer of natural rubber and acrylic
monomer and a blend of the ~nmodified natural rubber latex and the
graft copolymer and optionally one or more compounds selected from
the group consisting of chloroprene-methacrylic acid copolymer
latex and a vinyl-methacry~ ic acid copolymer latex. The adhesive
has a glass transition tem~?erature (Tg) in the range of -10 to
-78C and a green strength of 0 . 05 to 0 . 75 p . s . i . .
In a preferred embodiment, the acrylic monomer used in the
graft copolymer is choseII from the group consisting of ethyl
acrylate, methyl methacrylate and ethyl methacrylate. In addition,
the graft copolymer contains the acrylic monomer in a weight
percent of 30 to 50% and has a glass transition temperature of from
about -60 to -65C. When present, the optional chloroprene-
methacrylic acid copolymer latex should have a glass transition
temperature of about -45C and be used in the adhesive in a weight
percent of from 10 to 40%. It is also desirable for the optional
vinyl-methacrylic acid copolymer latex when present to have a glass
transition temperature in the range of from -14 to -25C and be
used in the adhesive in a ~ieight percent of from 10 to 40%.
The natural rubber la~ex and the graft copolymer of natural
rubber and acrylic monomer of the present invention give the
adhesive the properties necessary for effective pressure bonding.
The graft copolymer also reduces tack, which prevents blocking.
The non-thermoplastic pigment also reduces surface tack to prevent

-
21~24~
-3
blocking and absorbs the s:ilicone oils ueed on fuser rolls. The
optional chluL ,~Lelle-methacrylic acid copolymer latex and vinyl-
methacrylic acid copolymer latex help to prevent premature drying
of the adhesive during the application of the adhesive to a
3ubstrate.
Accordingly, it is an obj ect of the present invention to
provide an adhesive which will not become tacky under high
temperatures, loee adhesive properties due to contact with silicone
oils, "block" when stacked prior to printing, or lose bond-forming
ability with age.
Brief Deecription of the D~awinqs
Fig. 1 illustrates a typical cellulosic substrate which has
been coated with a pressure bonding adhesive in accordance with the
present invention.
Detailed Deec~i~tion of the Preferred Embodimente
Fig. 1 illustrates a typical embodiment of the adhesive coated
product of the present invention. A single sheet of paper 10 is
used to make a mailer document 12. The adhesive is applied to the
mailer at lines 70, 72, 80 and 82.
The adhesive may be applied to any suitable cellulosic
substrate and plastic sub3trates, preferably those having porous
surfaces that would allow the adhesive to adhere securely such as
Tyvek polyolefins. In a preferred embodiment, the adhesive is
applied to the substrate to provide a thickness when dry of from
0.3 to 0 7 mil, and most preferably about 0.5 mil. The adhesive
may be used to form various mailer products or envelopes which
require adhesives.
In its preferred form, the adhesive of the present invention
comprises a blend of a non- thermoplastic pigment particle such as
silica which has a particle size of 1-40 microns, a natural rubber
latex which is not chemically modified, and a graft copolymer of
natural rubber and acrylic monomer, the monomer being selected from
the group consisting of ethyl acrylate, methyl methacrylate and
ethyl methacrylate. The adhesive also optionally contains a
chloroprene-methacrylic acid copolymer latex and a vinyl-
methacrylic acid copolymer latex. The required physical
characteristic~ of the final adhesive are a glass transition
temperature (Tg) in the range of -10 to -78C and a green strength
of 0.05 to 0.75 p.s.i

2~45~4
--4--
The non-thermoplastic filler pigment may be any convenient
organlc or inorganic hard-particle pigment such as, for example,
silica gel. It is used in a solids weight percent of 1 to 10%,
most preferably about 2~. The effect the pigment has on the dried
5 adheGive film is to reduce surface tack, which prevents blocking
and improves feeding of forms having the adhesive. It also absorbs
the silicone oils uæed on many printer fuser rolls.
The unmodif ied natural rubber latex is a natural product
obtained from rubber trees. It can be used in a solids weight
10 percent of 0 to 99~, and ntost preferably in an aqueous emulsion
, r nt~;n~ng about 559~ rubber solids. It is comprised mainly of cis
1,4-polyi#oprene (93-95 wt 96), moigture (0.3-1.0 wt ~), acetone
soluble residue (1 . 5-4 . 5 wt ~), proteins (2 . 0-3 . 0 wt ~), and ash
(0.2-0.5 wt ~). The nominal properties of a dried film of natural
15 rubber are a glass transition temperature of -72C, a dielectric
constant of 2 . 3 7 and a green strength of 0 . 72 p . 8 . i . .
The graft polymerized natural rubber latex is produced by
reacting the natural latex with an acrylic monomer. This result~
in random and block copolynterization of the acrylic monomer with
20 the natural rubber of pol~isoprene. This treatment provides a
dried film adhesive with increasing hardness, reducing tack and
blocking tendency, raises the glass transition temperature from
about -72C to about -60 to -65C, and decreases the bond strength
formed when two films are joined by pressure. At some ratios, the
25 resultant copolymer may sho~r two glass transition temperatures, one
due to the natural rubber alld one due to the added copolymer. The
graft copolymers used in the present invention contain from 30~ to
5096 of the acrylic comonomer based on the weight of the copolymer.
The latex is preferably used a~ an aqueous emulsion of about 589~
30 solids. However, the graft copolymer can be used in a solids
weight percent of from 0 to 999~.
The optional chloroprene-methacrylic acid copolymer latex
preferably has a glass tra~lsition temperature of about -45C and
is present in the adhesive in a weight percent of from 10 to 40~.
35 A satisfactory chloroprene-methacrylic acid copolymer for use in
the present invention is Neoprene 115 from du Pont, which is
supplied as a 45~6 solids content composition.
The optional vinyl-methacrylic acid copolyrner latex has a
glass transition temperature in the range of from -14 to -25C and

21~524~
,
--5--
is present in the adhesive in a weight percent of from 10 to 40%.
An example of a vinyl-methacrylic acid copolymer latex which can
be used in the present invention is Haloflex 320 from Zeneca
Resins, a division of ICI.
The final adhesive may also contain water, and lesser amounts
of ammonia, defoamer and dye. The water helps to prevent premature
drying and can be present in a weight percent of 1 to 10% in
addition to the water already present in the aqueous latex
emulsions. The ammonia helps to stabilize the rubber latex and
provide a basic pH. It carL be used in a weight percent of 0.1 to
1. 0% . The defoamer is used to prevent foaming of the adhesive in
use and during application. It can be used in a weight percent of
o to 0.2%. The dye is used for aesthetic reasons to make the
adhesive more visible to the user and can be any color. The dye
should be water-soluble and can be used in a weight percent of 0
to 0.2%.
In order that the invention may be more readily understood,
reference is made to the following example which is intended to
illustrate the invention, but not limit the scope thereof.
Exam~le 1
A pressure bonding adhesive composition was prepared in
accordance with the present invention by blending 75% (weight
percentage) unmodified natural rubber latex (55% solids), 17% of
a graft copolymer of natural rubber and methyl methacrylate (58%
solids), 5.1% water, 2% inorganic CabosiI silica pigment particles
from Cabot, 0.4% ammonia, 0.01% water soluble dye and 0.019~
defoamer The composition was applied by a Flexo Analox roll at
a thickness of from 0.25 to 0.5 mil to a cellulosic substrate and
then dried using a radio frequency dryer. The dried film adhesive
exhibited satisfactory stability under high temperatures and did
not lose adhesive properties due to contact with silicone oils,
~block" when stacked prior to printing, or lose bond-forming
ability with age.

Representative Drawing
A single figure which represents the drawing illustrating the invention.
Administrative Status

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Event History

Description Date
Inactive: IPC assigned 2018-10-16
Inactive: IPC removed 2018-10-16
Inactive: IPC removed 2018-10-16
Inactive: IPC removed 2018-10-16
Inactive: IPC removed 2018-10-16
Inactive: First IPC assigned 2018-10-16
Inactive: IPC assigned 2018-10-16
Inactive: IPC expired 2018-01-01
Inactive: IPC removed 2017-12-31
Time Limit for Reversal Expired 2015-03-23
Letter Sent 2014-03-24
Grant by Issuance 1998-08-04
Pre-grant 1998-03-30
Inactive: Final fee received 1998-03-30
Notice of Allowance is Issued 1998-01-22
Letter Sent 1998-01-22
4 1998-01-22
Notice of Allowance is Issued 1998-01-22
Inactive: Status info is complete as of Log entry date 1998-01-06
Inactive: Application prosecuted on TS as of Log entry date 1998-01-06
Inactive: Approved for allowance (AFA) 1997-12-05
Application Published (Open to Public Inspection) 1996-09-23
Request for Examination Requirements Determined Compliant 1995-07-24
All Requirements for Examination Determined Compliant 1995-07-24

Abandonment History

There is no abandonment history.

Maintenance Fee

The last payment was received on 1998-03-06

Note : If the full payment has not been received on or before the date indicated, a further fee may be required which may be one of the following

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  • the late payment fee; or
  • additional fee to reverse deemed expiry.

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Please refer to the CIPO Patent Fees web page to see all current fee amounts.

Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
STANDARD REGISTER COMPANY (THE)
Past Owners on Record
RAJENDRA MEHTA
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
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Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Claims 1996-09-22 3 112
Drawings 1996-09-22 1 32
Cover Page 1998-07-27 1 58
Cover Page 1996-10-17 1 15
Abstract 1996-09-22 1 22
Description 1996-09-22 5 282
Representative drawing 1998-02-18 1 29
Representative drawing 1998-07-27 1 12
Commissioner's Notice - Application Found Allowable 1998-01-21 1 165
Maintenance Fee Notice 2014-05-04 1 170
Correspondence 1998-03-29 1 37
Fees 1997-02-25 1 78
Prosecution correspondence 1995-03-21 13 577
Prosecution correspondence 1995-11-16 1 22
Prosecution correspondence 1995-11-16 1 53
Prosecution correspondence 1995-06-04 1 40
Courtesy - Office Letter 1995-05-03 2 61
Prosecution correspondence 1995-07-09 1 43