Embossed sheet comprising a ply of water-soluble material and method for manufacturing such a sheet

Information

  • Patent Grant
  • 8506756
  • Patent Number
    8,506,756
  • Date Filed
    Wednesday, March 4, 2009
    15 years ago
  • Date Issued
    Tuesday, August 13, 2013
    11 years ago
Abstract
The invention proposes an embossed sheet (10) comprising at least one ply (12) of tissue having an embossing pattern comprising at least one series of protuberances (18) formed projecting from one surface of the said ply (12) of tissue, and at least one ply joined to the said at least one ply (12) of tissue and located opposite the said surface of the ply (14) of water-soluble material,
Description

The invention proposes an embossed sheet comprising at least one ply of tissue and at least one ply of water-soluble material.


The invention proposes more particularly an embossed sheet comprising at least one ply of tissue having an embossing pattern comprising at least one series of protuberances formed and projecting from one surface of the said ply of tissue, and comprising at least one ply of water-soluble material.


The ply of water-soluble material is prepared so as to form a impermeable barrier to liquids, microorganisms such as bacteria and viruses contained in these liquids.


The function called “impermeable” of the barrier formed by the water-soluble ply consists here in temporarily preventing the liquids from passing through the said ply.


Thus, the use of a ply of water-soluble material, in combination with at least one ply of tissue, serves to obtain a product comprising, on the one hand, the absorbent properties of the tissue ply and, on the other, the waterproofness procured by the ply of water-soluble material.


These properties are particularly advantageous for the use of a paper product as a facial tissue or as bathroom tissue, because the bacteria and/or viruses cannot be transferred to the user's hand.


Moreover, when the paper product is used as bathroom tissue, each of the various plies constituting the paper product is suitable for being dispersed in the water, when the product is discarded into the toilet, without the risk of blocking the pipes.


Document GB-B-1 185 227 describes such a paper product, for which the ply of water-soluble material is prepared by hot extrusion and is hot bonded to the tissue plies discharged from the extruder, so that the tissue plies partly absorb the water-soluble material which has not yet hardened.


However, such a manufacturing method is relatively complicated to set up, and this document does not specifically describe the connection between the ply of water-soluble material and each ply of tissue.


It is the object of the invention to propose a paper product comprising a ply of water-soluble material which is joined to at least one ply of tissue so that the product has the usual properties of such a paper product.


For this purpose, the invention proposes an embossed sheet of the type described previously, characterized in that the ply of water-soluble material is joined to the said at least one ply of tissue at the summits of at least part of the protuberances.


According to other features of the sheet according to the invention, taken separately or in combination:

    • the ply of water-soluble material is joined to the said at least one ply of tissue by local dissolution of the ply of water-soluble material, at the summits of the said at least part of the protuberances, to which the ply of water-soluble material is joined;
    • the surface of the ply of water-soluble material is suitable for being dissolved for the joining of the ply of water-soluble material to the said at least one ply of tissue;
    • the ply of water-soluble material is suitable for being dissolved locally by a water-based liquid;
    • the liquid comprises water and an additive;
    • the liquid is water;
    • each of the said summits of the said at least part of the protuberances is suitable for being humidified before the joining of the ply of tissue to the ply of water-soluble material, to cause the partial dissolution of the ply of water-soluble material at the contact with the said summit of the said at least part of the protuberances;
    • the ply of water-soluble material is joined to the said at least one ply of tissue by adhesion of the water-soluble material to the said summits of the said at least part of the protuberances;
    • the sheet comprises at least two plies of tissue each having an embossing pattern which comprises at least one series of protuberances oriented inwardly from the sheet and the ply of water-soluble material is arranged between the said at least two plies of tissue and is joined to each of the said two plies at the summits of at least part of the protuberances of each of the said two plies of tissue;
    • the ply of water-soluble material is based on an at least partially hydrolysed polyvinyl alcohol;
    • the ply of water-soluble material is based on an at least 90% hydrolysed polyvinyl alcohol;
    • the thickness of the ply of water-soluble material is less than 25 μm;
    • the ply of water-soluble material is embossed and comprises at least one series of protuberances;
    • the ply of water-soluble material comprises perforations and/or micro-perforations.


It is a further object of the invention to propose a method for manufacturing an embossed sheet according to the invention, comprising at least one ply of tissue and at least one ply of water-soluble material,


characterized in that it consists in embossing at least one ply of tissue to form protuberances on one surface of the said at least one ply of tissue and then in joining the ply of water-soluble material to the summits of at least part of the protuberances of the said at least one ply of tissue.


According to other features of the method, taken separately or in combination:

    • the summits of the protuberances of the said at least part of the protuberances are coated with adhesive before the joining of the ply of water-soluble material to the said at least one ply of tissue;
    • the summits of the protuberances of the said at least part of the protuberances are humidified before the joining of the ply of water-soluble material to the summits of the protuberances to cause a local dissolution of the surface of the ply of water-soluble material upon its contact with the humidified summits;
    • the surface of the ply of water-soluble material located opposite the ply of tissue is humidified locally before the joining of the ply of water-soluble material to the said at least one ply of tissue;
    • the said surface of the ply of water-soluble material is humidified at the summits of the protuberances of the said at least one ply of tissue;
    • the ply of water-soluble material is embossed before its joining to the said at least one ply of tissue;
    • the ply of water-soluble material comprises perforations and/or micro-perforations which are produced before the embossing of the ply of water-soluble material;
    • the method is suitable for manufacturing a sheet which comprises at least one first and at least one second ply of tissue between which the ply of water-soluble material is arranged, and the ply of water-soluble material is joined simultaneously to the said at least one first ply of tissue and to the said at least one second ply of tissue during an operation for joining the plies.





Other features and advantages of the invention will appear from a reading of the detailed description that follows, for an understanding of which reference should be made to the appended figures in which:



FIG. 1 is a schematic representation of an embossed sheet according to the invention comprising two plies of tissue and an intermediate ply of water-soluble material;



FIG. 2 shows a section of the sheet shown in FIG. 1, showing the protuberances of the plies;



FIG. 3 shows a section of the sheet comprising a single ply of tissue and one ply of water-soluble material;



FIG. 4 shows a similar section to that of FIG. 2, showing an alternative embodiment of the invention, for which the ply of water-soluble material comprises protuberances;



FIG. 5 is a schematic representation of an installation for producing an embossed sheet according to the invention as shown in FIG. 3.






FIGS. 1, 2 and 3 show a paper product 10 such as an embossed sheet comprising a plurality of superimposed plies 12, 14.


The sheet 10 is, for example, a sheet of bathroom tissue or a disposable facial tissue.


In a first embodiment shown in FIGS. 1 and 2, the sheet 10 comprises two plies 12 of tissue and one ply 14 prepared from water-soluble material arranged between the two tissue plies 12.


In a second embodiment shown in FIG. 3, the sheet 10 comprises a ply 12 of tissue and a ply 14 prepared from water-soluble material.


It will be understood that the invention is not limited to these embodiments of the embossed sheet 10, which may comprise a larger number of plies 12 of tissue and/or a larger number of plies 14 of water-soluble material.


Furthermore, a ply 12 of tissue may comprise a group of plies joined together so as to behave like a single ply.


Each ply 12 of tissue is prepared in a conventional manner, for example by conventional wet pressing called CWP, and its basis weight is adapted to the use of the sheet, for example the basis weight of the tissue ply 12 is between 12 and 30 g/m2.


The ply 14 of water-soluble material is prepared from a material suitable for being dissolved after prolonged contact with water. It consists of a plastic, preferably a polyvinyl alcohol (PVA) which is a polyvinyl acetate (PVAc), that has been hydrolysed to become water-soluble.


A modification of the hydrolysis rate of the ply 14 of water-soluble material serves to modify the time required for the dissolution of the ply 14 of water-soluble material. Thus, it is possible to adjust this hydrolysis rate according to the desired properties of the sheet 10.


Preferably, the hydrolysis rate of the plastic is higher than ninety percent (90%).


Another property of the water-soluble material used to form the ply 14 further consists in that the material is non-porous and is suitable for forming a sealed barrier to liquids, before its dissolution.


Thus, the liquids and microorganisms such as bacteria and/or viruses applied to one surface of the sheet 10 cannot be transferred to the other surface of the sheet which is, for example, in contact with the user's hand, thereby serving to ensure a hygienic use of the sheet 10, in particular when the sheet 10 is used as a facial tissue or bathroom tissue, as previously mentioned.


The thickness of the ply 14 of water-soluble material is preferably lower than 25 μm.


Finally, according to an alternative embodiment of the embossed sheet 10, the ply 14 of water-soluble material comprises perforations and/or micro-perforations.


These perforations and/or micro-perforations serve in particular to increase the absorption rate of the sheet 10 and to improve its flexibility.


The sheet 10 is an embossed sheet, that is at least one of the plies 12, 14 comprises at least one embossing pattern.


According to a common definition, embossing is a mechanical operation of deformation which modifies the relief of a sheet.


According to the embodiments shown in FIGS. 1 to 3, each ply 12 of tissue comprises an embossing pattern 16 which extends over part of the surface of the ply 12 and which comprises a plurality of protuberances 18 oriented inwardly from the sheet 10.


Furthermore, according to these embodiments, the ply 14 of water-soluble material is flat, that is it does not comprise any embossing pattern.


According to the embodiment shown in FIG. 4, the ply 12 of tissue and the ply 14 of water-soluble material each comprise an embossing pattern composed of a plurality of protuberances 18, 20.


Here, each ply 12, 14 comprises a single embossing pattern and the relief of the protuberances caused by the embossing is identical for the two plies 12, 14. According to an alternative embodiment, at least one ply 12, 14 comprises a plurality of embossing patterns 16, forming for example a background pattern and a main pattern.


The height and density of the protuberances 18, 20 of a pattern 16 may be different from the height of the protuberances 18, 20 of the other pattern 16, thereby serving to procure for the sheet 10 desired properties of softness, absorption and flexibility.


Furthermore, here, the plies 12, 14 are joined together by a joining mode known by the designation points/points, that is, in such a way that the summits 18a, 20a of the protuberances of each of the plies 12, 14 are caused to coincide.


According to an alternative embodiment, not shown, the plies 12, 14 may be joined by the technique called “nested”, for which the protuberances are imbricated.


According to the invention, each ply 12 of tissue is joined to the ply 14 of water-soluble material at the summits 18a of at least part of the protuberances 18.


According to a first embodiment of the invention, the joining of each ply 12 of tissue to the ply 14 of water-soluble material is carried out by bonding all or part of the summits 18a of the protuberances 18 of each ply 12 of tissue to the opposite surface 14a of the ply 14 of water-soluble material.


Preferably, the bonding takes place by depositing adhesive on all or part of the summits 18a of the protuberances 18 before the plies 12, 14 are contacted with one another.


According to a preferred embodiment of the invention, the joining of each ply 12 of tissue to the ply 14 of water-soluble material is carried out by partial dissolution of the ply 14 of water-soluble material, at the summits 18a of the protuberances 18.


The partial dissolution of the ply 14 of water-soluble material is obtained by locally applying a water-based liquid to the ply 14 of water-soluble material.


The water-soluble material has the cohesion, or the behaviour, of a solid when it is dehydrated, and the cohesion of a viscous liquid when it is hydrated, that is when it is mixed with water.


When the summit 18a of a protuberance of the ply 12 of tissue is in contact with the partially dissolved zone of the ply 14 of water-soluble material, the summit 18a absorbs part of the dissolved water-soluble material. The tissue and the water-soluble material are thereby mixed.


Then, the two plies are joined together by pressing and then by natural or forced dehydration so that the contact zones between the plies 12, 14 become joining zones between the said plies following the cohesion thereby created.


According to a first embodiment, the product used to cause the partial dissolution of the water-soluble material is exclusively water, so that the ply 12 of tissue is joined to the ply 14 of water-soluble material exclusively by the quantity of water-soluble material that has been dissolved.


According to an alternative embodiment, the product used to cause the partial dissolution of the water-soluble material consists of a mixture of water and an additive such as adhesive, which serves to improve the joining of the ply 12 of tissue to the ply 14 of water-soluble material.


Furthermore, the quantity of liquid used to cause a local dissolution of the ply 14 of water-soluble material, is determined so that only the outer surface of the ply 14 of water-soluble material is dissolved, that is a central portion, in the thickness of the ply 14 of water-soluble material, is not dissolved. This serves in particular to preserve the impermeability function of the ply 14 of water-soluble material over its whole surface.


Such a feature of dissolution of the ply 14 of water-soluble material exclusively on the surface is preferably obtained by first humidifying the summits 18a of the protuberances 18, so that the quantity of liquid that dissolves the ply 14 of water-soluble material is limited, and the dissolution occurs when each ply 12 of tissue is placed in contact with the ply 14 of water-soluble material.


The ply 14 of water-soluble material is thereby placed in contact with the bonding liquid for a limited period of time.


When the ply 14 of water-soluble material is arranged between two plies 12 of tissue, as shown in FIGS. 1 and 2, each surface of the ply 14 of water-soluble material is joined to a ply 12 of tissue according to the invention, that is, the ply 14 of water-soluble material is joined to summits 18a of protuberances 18 of a ply 12 of tissue, which extends inwardly from the sheet 10, towards the ply 14 of water-soluble material.


By contrast, when the ply 14 of water-soluble material is joined to a single ply 12 of tissue, as shown in FIGS. 3 and 4, only one surface of the ply 14 of water-soluble material is joined to the ply 12 of tissue according to the invention, that is, the surface of the ply 14 of water-soluble material located opposite the ply 12 of tissue is joined to the summits 18a of all or part of the protuberances 18 of the said ply 12 of tissue.



FIG. 5 shows an installation for producing a sheet according to the invention.


This installation is constructed here in order to produce a sheet 10 comprising a single ply 12 of tissue which is embossed, and comprising a ply 14 of water-soluble material which is flat, as shown in FIG. 4.


The installation comprises an engraved embossing roller 22 of which the convex outer cylindrical surface 22a comprises a series of pins 24 formed in relief and of which the form or outer profile is identical to that which is to be obtained for each corresponding protuberance 18 of the ply 12 of tissue.


In a manner known per se, the ply 12 of tissue first passes between the first engraved roller 22 and an associated roller 26 to produce the embossing pattern of this ply 12. The associated roller 26 may have a rubber coating or similar, or optionally a rigid coating having a hardness lower than the hardness of the engraved roller 22.


The ply 12 of tissue then passes in front of the applicator roller 28 belonging to a coating unit 30, of known design, which deposits a bonding product on the summits 18a of the protuberances 18.


The coating unit 30 serves to deposit the bonding product on all the summits 18a of the protuberances 18, or on only part of the summits 18a of the protuberances 18, in particular on the summits 18a of the protuberances 18 which are the highest when the ply 12 of tissue comprises a plurality of embossing patterns 16 having different heights.


According to the invention, and as previously described, the bonding product may be adhesive, water or a mixture of water with a binder, and is referred to below by the term bonding product.


In a manner known per se, the coating installation 30 comprises an engraved roller 34, commonly called “anilox”, of which the cylindrical surface comprises cavities (not shown) which are suitable for being filled with bonding product, during the passage thereof in front of a tank 36 for then transferring the bonding product to the applicator roller 28.


The anilox 34 serves to transfer the bonding product in a predefined and controlled manner onto the applicator roller 28. This serves to limit the quantity of bonding product in motion.


The cavities of the anilox 34 are preferably such as to have a volume of between 3 and 40 cm3/m2.


The ply 14 of water-soluble material is then placed in contact with the ply 12 of tissue.


Then, the two plies 12 and 14 pass into a “nip” between the embossing roller 22 and a roller 32, called marrying roller, to associate the plies 12, 14 by the pressure of the marrying roller 32 against the embossing roller 22.


Thus, the method for manufacturing an embossed sheet 10 according to the invention via this installation comprises a first step of embossing of the ply 12 of tissue, to produce at least one embossing pattern 16 consisting of protuberances 18 on one surface of the said ply 12.


This embossing step is implemented by the cooperation of the engraved roller 22 with the associated roller 26.


This method also comprises a step of joining the ply 12 of tissue to the ply 14 of water-soluble material, here by cooperation of the engraved roller 22 with the marrying roller 32.


According to the invention, the step of embossing the ply 12 of tissue is implemented before the step of joining the ply 12 of tissue to the ply 14 of water-soluble material. Moreover, also according to the invention, the bonding step consists in joining the ply 12 of tissue to the ply 14 of water-soluble material at the summits 18a of the protuberances 18.


For this purpose, the coating installation 30 deposits the bonding product before the joining of the ply 12 of tissue to the ply 14 of water-soluble material.


Thus, when the bonding product is water-based, the ply 14 of water-soluble material is only locally dissolved when it is placed in contact with the ply 12 of tissue of which the summits 18a of the protuberances 18 have been humidified.


This serves to limit and control the extent of the dissolution of the ply 14 of water-soluble material, so as to avoid weakening its properties excessively, particularly the impermeability properties.


According to an alternative embodiment of the method of the invention, the bonding product is applied to the ply 14 of water-soluble material, before its joining to the ply 12 of tissue.


The installation is then modified accordingly, that is, the coating installation 30 is arranged to apply the bonding product directly to the ply 14 of water-soluble material.


When the ply 14 of water-soluble material passes opposite the ply 12 of tissue, the latter has been formed to have the properties previously mentioned, that is, the material has been partly hydrolysed.


Furthermore, in the case in which the ply 14 of water-soluble material comprises perforations or micro-perforations, they are generally produced before the ply 14 of water-soluble material reaches the installation as described previously.


Preferably, the micro-perforations in the context of the present invention have a density lower than 150/cm2 and their diameter is smaller than 1 mm.


Moreover, according to the embodiment of the embossed sheet 10 according to which the ply 14 of water-soluble material is also embossed, as shown in FIG. 4, the embossing is carried out before it is placed in contact with the ply 12 of tissue. For this purpose, the installation comprises an additional embossing unit (not shown).


The same applies for manufacturing the embossed sheet shown in FIG. 2, which comprises two plies 12 of tissue between which the ply 14 of water-soluble material is arranged.


The installation then comprises an engraved roller 22 and a coating unit 30 as described previously, associated with each ply 12 of tissue.


The ply 14 of water-soluble material is then placed opposite each of the two plies 12 of tissue, for it to be arranged between them.


Then, all the plies 12, 14 pass simultaneously in front of the matching roller 32 in order to associate the ply 14 of water-soluble material simultaneously with the two plies 12 of tissue.


The embossed sheet according to the invention thereby procures better temporary protection in comparison with a “conventional” sheet, that is one which does not comprise a ply of water-soluble material, and preserves conventional disintegration properties after use, that is, when it is discarded into the discharge lines of sanitary facilities.


The comparative table below shows the results of various measurements between a multi-ply sheet, for use as bathroom tissue, of which the design is called “conventional”, and which comprises three plies of tissue, and a multi-ply sheet according to the invention.


More precisely, the multi-ply sheet called “conventional three-ply paper” in the table comprises two outer plies of the CWP type and one central ply having a mechanical strength greater than that of the two outer plies.


The multi-ply sheet called “invention” in the table is manufactured according to the invention, and differs from the sheet called “conventional three-ply paper” only in terms of the central ply, which consists here of a ply of water-soluble material.

















Conventional





three-ply





bathroom





tissue
Invention







Thickness
As such
0.354 ± 0.006
0.524 ± 0.030


(mm)
In 12 plies
0.323 ± 0.003
0.491 ± 0.013


Absorption
Capacity
9.3
11.8



(g/g)





Time (s)
4
5


Disintegration
(s)
8
20 to 25


Strength
(N/m)




MD dry

199 ± 7 
>899


MD wet

  4.7 ± 0.7**
8.0 ± 1.1





  (12.9 ± 1.4)** 


CD dry

81 ± 5 
281 ± 10 


CD wet





MD elongation
%
19
25 to 73









It appears that all the measured parameters are improved, in particular the dry strength in the machine direction (MD), cross direction (CD), and the wet strength in the machine direction (MD) are improved. The elongation in the machine direction (MD) is also improved.


Moreover, the “disintegrability” function of the paper according to the invention is advantageously preserved.

Claims
  • 1. An embossed sheet, comprising: at least one ply of tissue, comprising an embossing pattern comprising a plurality of protuberances projecting from a surface of the at least one ply of tissue, the protuberances having summits; andat least one ply of water-soluble material joined to the at least one ply of tissue,wherein the at least one ply of water-soluble material is joined to the at least one ply of tissue via the summits of at least a portion of the protuberances,wherein the at least one ply of water-soluble material is joined to the at least one ply of tissue by partial dissolution of the at least one ply of water-soluble material, andwherein the at least one ply of water-soluble material comprises an at least 90% hydrolyzed polyvinyl alcohol.
  • 2. The embossed sheet of claim 1, wherein the at least one ply of water-soluble material is configured to be locally dissolved by a water-based liquid.
  • 3. The embossed sheet of claim 2, wherein the water-based liquid comprises water and an additive.
  • 4. The embossed sheet of claim 2, wherein the water-based liquid is water.
  • 5. The embossed sheet of claim 1, wherein the summits are configured to be humidified such that the humidified summits at least partially dissolve the at least one ply of water-soluble material upon contact.
  • 6. The embossed sheet of claim 1, wherein the at least one ply of water-soluble material is joined to the at least one ply of tissue by adhesion of the water-soluble material to the summits of at least a portion of the protuberances.
  • 7. The embossed sheet of claim 1, wherein the thickness of the at least one ply of water-soluble material is less than 25 μm.
  • 8. The embossed sheet of claim 1, wherein the ply of water-soluble material is embossed and comprises a plurality of protuberances.
  • 9. The embossed sheet of claim 1, wherein the ply of water-soluble material comprises perforations and/or micro-perforations.
  • 10. An embossed sheet comprising: at least two plies of embossed tissue, wherein each ply of tissue comprises a plurality of protuberances, and wherein the plurality of protuberances comprise summits; andat least one ply of water-soluble material arranged between the two plies of tissue and joined to the summits of at least a portion of the protuberances on each ply of tissue by partial dissolution of the at least one ply of water-soluble material, wherein the at least one ply of water-soluble material comprises an at least 90% hydrolyzed polyvinyl alcohol.
Priority Claims (1)
Number Date Country Kind
08 51455 Mar 2008 FR national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/FR2009/000231 3/4/2009 WO 00 9/2/2010
Publishing Document Publishing Date Country Kind
WO2009/115705 9/24/2009 WO A
US Referenced Citations (374)
Number Name Date Kind
1682346 Lorenz Aug 1928 A
2117256 Ration May 1938 A
2123982 Wiles Jul 1938 A
2142986 Arnold, Jr. Jan 1939 A
2546705 Strawinski Mar 1951 A
2755213 Hedstrom Jul 1956 A
2797168 Gimler Jun 1957 A
2897108 Harwood Jul 1959 A
2897109 Voigtman Jul 1959 A
2961367 Weisgerber et al. Nov 1960 A
3084092 Arlt, Jr. Apr 1963 A
3130111 Izumi Apr 1964 A
3212961 Weisgerber et al. Oct 1965 A
3261740 Wells Jul 1966 A
2824815 Downs et al. Feb 1968 A
3414459 Wells Dec 1968 A
3546716 Laumann Dec 1970 A
3554195 Murdoch Jan 1971 A
3607348 Wray Sep 1971 A
3612054 Matsuda et al. Oct 1971 A
3650882 Thomas Mar 1972 A
3654064 Laumann Apr 1972 A
3669822 Cowen Jun 1972 A
3673060 Murphy et al. Jun 1972 A
3684603 Ittins Aug 1972 A
3833937 Taylor Sep 1974 A
3867225 Nystrand Feb 1975 A
3868205 Thomas Feb 1975 A
3916447 Thompson Nov 1975 A
3925127 Yoshioka Dec 1975 A
3926700 Hopkins, Jr. et al. Dec 1975 A
3953638 Kemp Apr 1976 A
3960272 Hartbauer et al. Jun 1976 A
3978553 Honig Sep 1976 A
4018647 Wietsma Apr 1977 A
4071651 Hicklin et al. Jan 1978 A
4074959 Curry et al. Feb 1978 A
4075382 Chapman et al. Feb 1978 A
4100017 Flautt Jul 1978 A
4113911 LaFitte et al. Sep 1978 A
4117199 Gotoh et al. Sep 1978 A
4145464 McConnell et al. Mar 1979 A
4196245 Kitson et al. Apr 1980 A
4276339 Stoveken Jun 1981 A
4287251 King et al. Sep 1981 A
4288877 Klepfer Sep 1981 A
4302853 Mesek Dec 1981 A
4330888 Klepfer May 1982 A
4349610 Parker Sep 1982 A
4377615 Suzuki et al. Mar 1983 A
4447484 Slosberg et al. May 1984 A
4469735 Trokhan Sep 1984 A
4489118 Endres et al. Dec 1984 A
4537822 Nanri et al. Aug 1985 A
4559243 Passler et al. Dec 1985 A
4574021 Endres et al. Mar 1986 A
4601938 Deacon et al. Jul 1986 A
4610915 Crenshaw et al. Sep 1986 A
4618524 Groitzsch et al. Oct 1986 A
4637949 Manning et al. Jan 1987 A
4648876 Becker et al. Mar 1987 A
4657538 Becker et al. Apr 1987 A
4657946 Rende et al. Apr 1987 A
4660224 Ashcraft Apr 1987 A
4695422 Curro et al. Sep 1987 A
4786367 Bogart et al. Nov 1988 A
4788100 Janssen et al. Nov 1988 A
4789564 Kanner et al. Dec 1988 A
4806183 Williams Feb 1989 A
4816320 St. Cyr Mar 1989 A
4885202 Lloyd et al. Dec 1989 A
4924527 Hintermeyer May 1990 A
4927588 Schulz May 1990 A
4938515 Fazio Jul 1990 A
4950545 Walter et al. Aug 1990 A
4987632 Rowe et al. Jan 1991 A
5062158 Oka et al. Nov 1991 A
5093068 Schulz Mar 1992 A
5128182 Bunker et al. Jul 1992 A
5158523 Houk et al. Oct 1992 A
5167766 Honig et al. Dec 1992 A
5171808 Ryles et al. Dec 1992 A
5173351 Ruppel et al. Dec 1992 A
5180471 Sauer et al. Jan 1993 A
5196244 Beck Mar 1993 A
5223096 Phan et al. Jun 1993 A
5227242 Walter et al. Jul 1993 A
5252754 Bottorff Oct 1993 A
5260536 Peery Nov 1993 A
5397435 Ostendorf et al. Mar 1995 A
5399366 Geddes et al. Mar 1995 A
5407537 Malatesta et al. Apr 1995 A
5437766 Van Phan et al. Aug 1995 A
5437908 Demura et al. Aug 1995 A
5443889 Ruppel et al. Aug 1995 A
5449551 Taniguchi Sep 1995 A
5456968 Jones Oct 1995 A
5467936 Moody Nov 1995 A
5503919 Litchholt et al. Apr 1996 A
5514435 Suzuki et al. May 1996 A
5543202 Clark et al. Aug 1996 A
5550167 DesMarais Aug 1996 A
5552187 Green et al. Sep 1996 A
5552200 Gureff Sep 1996 A
5560945 Geddes et al. Oct 1996 A
5562805 Kamps et al. Oct 1996 A
5563179 Stone et al. Oct 1996 A
5571849 DeMarais Nov 1996 A
5578369 Nohr et al. Nov 1996 A
5582674 Patterson et al. Dec 1996 A
5585129 Geddes et al. Dec 1996 A
5595807 Gooding, Jr. et al. Jan 1997 A
5601871 Krzysik et al. Feb 1997 A
5601930 Mehta et al. Feb 1997 A
5609901 Geddes et al. Mar 1997 A
5614293 Krzysik et al. Mar 1997 A
5622734 Clark et al. Apr 1997 A
5635201 Fabo Jun 1997 A
5635279 Ma et al. Jun 1997 A
5650218 Krzysik et al. Jul 1997 A
5658639 Curro et al. Aug 1997 A
5665426 Krzysik et al. Sep 1997 A
5693406 Wegele et al. Dec 1997 A
5695487 Cohen et al. Dec 1997 A
5695608 Yagi et al. Dec 1997 A
5698291 Clark et al. Dec 1997 A
5716692 Warner et al. Feb 1998 A
5736223 Laurent Apr 1998 A
5766736 Baumuller Jun 1998 A
5792404 Cree et al. Aug 1998 A
5830558 Barnholtz Nov 1998 A
5849000 Anjur et al. Dec 1998 A
5851352 Vinson et al. Dec 1998 A
5858173 Propst, Jr. Jan 1999 A
5858554 Neal et al. Jan 1999 A
5864878 Mashrick Feb 1999 A
5882464 Theisgen et al. Mar 1999 A
5885697 Krzysik et al. Mar 1999 A
5904812 Salman et al. May 1999 A
5906711 Barnholtz May 1999 A
5919556 Barnholtz Jul 1999 A
5930836 Morris Aug 1999 A
5932316 Cree et al. Aug 1999 A
5968853 Kelly et al. Oct 1999 A
5990377 Chen et al. Nov 1999 A
6015935 LaVon et al. Jan 2000 A
6025049 Ouellette et al. Feb 2000 A
6027611 McFarland et al. Feb 2000 A
6030497 Watkins Feb 2000 A
6045900 Haffner et al. Apr 2000 A
6046378 Quincy, III et al. Apr 2000 A
6054020 Goulet et al. Apr 2000 A
6066379 Ma et al. May 2000 A
6074525 Richards Jun 2000 A
6107539 Palumbo et al. Aug 2000 A
6129972 McNeil et al. Oct 2000 A
6132803 Kelly et al. Oct 2000 A
6136422 Lichtenberg et al. Oct 2000 A
6149769 Mohammadi et al. Nov 2000 A
6159339 Hassler et al. Dec 2000 A
6162327 Batra et al. Dec 2000 A
6165585 Trokhan Dec 2000 A
6180052 Ouellette et al. Jan 2001 B1
6180214 Nissing et al. Jan 2001 B1
6182290 Morris Feb 2001 B1
6187141 Takeuchi et al. Feb 2001 B1
6187695 Krzysik et al. Feb 2001 B1
6203889 Quincy, III et al. Mar 2001 B1
6207734 Vinson et al. Mar 2001 B1
6221211 Hollenberg et al. Apr 2001 B1
6231948 Ouellette et al. May 2001 B1
6232521 Bewick-Sonntag et al. May 2001 B1
6238519 Jones et al. May 2001 B1
6267842 Ona et al. Jul 2001 B1
6270875 Nissing Aug 2001 B1
6277226 Schulz Aug 2001 B1
6286145 Welchel et al. Sep 2001 B1
6300409 Lau et al. Oct 2001 B2
6309731 Takeuchi et al. Oct 2001 B1
6328850 Phan et al. Dec 2001 B1
6332952 Hsu et al. Dec 2001 B1
6334220 Frye Jan 2002 B1
6372035 Juppo et al. Apr 2002 B1
6372064 Butterworth et al. Apr 2002 B1
6379497 Sandstrom Apr 2002 B1
6383960 Everett et al. May 2002 B1
6402871 Canary Jun 2002 B1
6403858 Quincy et al. Jun 2002 B1
6416624 Nielsen et al. Jul 2002 B1
6416628 Huang et al. Jul 2002 B1
6427240 Royal Aug 2002 B1
6436234 Chen et al. Aug 2002 B1
6439388 Lerner et al. Aug 2002 B1
6440268 Baggot et al. Aug 2002 B1
6444091 Ward et al. Sep 2002 B1
6454693 Harlacher et al. Sep 2002 B1
6454902 Chen Sep 2002 B1
6458243 Jones et al. Oct 2002 B1
6464829 Chen et al. Oct 2002 B1
6478927 Chen et al. Nov 2002 B1
6490731 Hyatt et al. Dec 2002 B1
6494990 Bazaj et al. Dec 2002 B2
6537407 Law et al. Mar 2003 B1
6544386 Krzysik et al. Apr 2003 B1
6548427 Shannon et al. Apr 2003 B1
6551691 Hoeft et al. Apr 2003 B1
6572722 Pratt Jun 2003 B1
6573203 McConnell et al. Jun 2003 B1
6576049 Dilts et al. Jun 2003 B1
6585859 Hangkansson Jul 2003 B1
6589634 Schultz et al. Jul 2003 B2
6599614 Roussel et al. Jul 2003 B1
6602387 Loughran et al. Aug 2003 B1
6607630 Bartman et al. Aug 2003 B2
6607636 Ross et al. Aug 2003 B2
6616806 Chen Sep 2003 B2
6635134 Lichtenberg et al. Oct 2003 B1
6649025 Mills et al. Nov 2003 B2
6656596 Gardner, Jr. Dec 2003 B1
6666952 Dilts et al. Dec 2003 B2
6673983 Graef Jan 2004 B1
6716312 Kehrer et al. Apr 2004 B2
6722606 Hanson et al. Apr 2004 B2
6723204 Van Handel et al. Apr 2004 B2
6727004 Goulet et al. Apr 2004 B2
6733608 Baggot et al. May 2004 B1
6733866 Muller May 2004 B2
6746558 Hoeft et al. Jun 2004 B2
6755928 Biagiotti Jun 2004 B1
6755938 Kehrer et al. Jun 2004 B2
6758923 Butterworth et al. Jul 2004 B2
6758943 McConnell et al. Jul 2004 B2
6773647 McGuire et al. Aug 2004 B2
6805766 Roussel et al. Oct 2004 B1
6811652 Hollmark Nov 2004 B2
6824649 Jewell et al. Nov 2004 B2
6827819 Dwiggins et al. Dec 2004 B2
6837972 Marsh Jan 2005 B2
6863107 Hein et al. Mar 2005 B2
6884494 Curro et al. Apr 2005 B1
6896766 Sarbo May 2005 B2
6896767 Wilhelm May 2005 B2
6896768 Dwiggins et al. May 2005 B2
6911573 Chen Jun 2005 B2
6913673 Baggot et al. Jul 2005 B2
6916403 Basler et al. Jul 2005 B2
6919111 Swoboda Jul 2005 B2
6924042 Von Paleske Aug 2005 B2
6936330 Fereshtehkhou et al. Aug 2005 B2
6939441 Nurminen et al. Sep 2005 B2
6949167 Shannon et al. Sep 2005 B2
6964725 Shannon et al. Nov 2005 B2
6992028 Thomaschefsky et al. Jan 2006 B2
7026037 Lefebvre Du Grosriez et al. Apr 2006 B2
7029546 Basler et al. Apr 2006 B2
7063766 Saarvali et al. Jun 2006 B2
7214633 Sun et al. May 2007 B2
7250448 Walchuk et al. Jul 2007 B2
7282273 Murphy et al. Oct 2007 B2
7300547 Luu et al. Nov 2007 B2
7381299 Shannon et al. Jun 2008 B2
7497923 Ward et al. Mar 2009 B2
7507781 Walchuk et al. Mar 2009 B2
7662257 Edwards et al. Feb 2010 B2
7666272 Williams et al. Feb 2010 B2
7666273 Williams et al. Feb 2010 B2
7794566 Edwards et al. Sep 2010 B2
7799169 Bhat et al. Sep 2010 B2
20010009180 Welch et al. Jul 2001 A1
20010051687 Bazaj et al. Dec 2001 A1
20020060000 Du Grosriez et al. May 2002 A1
20020088578 Jones et al. Jul 2002 A1
20020096280 Jones et al. Jul 2002 A1
20020096282 Leibler et al. Jul 2002 A1
20020103469 Chen et al. Aug 2002 A1
20020114933 Gould Aug 2002 A1
20020170649 Butterworth et al. Nov 2002 A1
20020195218 Chen Dec 2002 A1
20030008109 Basler et al. Jan 2003 A1
20030021952 Zink et al. Jan 2003 A1
20030021953 Graff Jan 2003 A1
20030026953 Muller Feb 2003 A1
20030045844 Taylor et al. Mar 2003 A1
20030056917 Jimenez Mar 2003 A1
20030070782 Proverb et al. Apr 2003 A1
20030075262 Ferdinand et al. Apr 2003 A1
20030075292 Kehrer et al. Apr 2003 A1
20030111196 Hu Jun 2003 A1
20030111198 Hu Jun 2003 A1
20030116292 Hollmark Jun 2003 A1
20030116294 Kehrer et al. Jun 2003 A1
20030119397 Von Paleske Jun 2003 A1
20030121628 Mills et al. Jul 2003 A1
20030121629 Hu Jul 2003 A1
20030121632 Nurminen et al. Jul 2003 A1
20030121633 Spence et al. Jul 2003 A1
20030127203 Hu Jul 2003 A1
20030129363 Hoeft et al. Jul 2003 A1
20030131960 McConnell et al. Jul 2003 A1
20030152724 Swoboda et al. Aug 2003 A1
20030188840 Van Handel Oct 2003 A1
20030192664 Kulick et al. Oct 2003 A1
20030201083 Marsh Oct 2003 A1
20030203195 Marsh Oct 2003 A1
20030205165 Thornton et al. Nov 2003 A1
20030205167 Dilts et al. Nov 2003 A1
20030215602 Andersson et al. Nov 2003 A1
20040003905 Hilbig Jan 2004 A1
20040009327 Saarvali et al. Jan 2004 A1
20040018369 Goulet et al. Jan 2004 A1
20040020614 Lindsay et al. Feb 2004 A1
20040038006 Biagiotti Feb 2004 A1
20040044320 Kainth et al. Mar 2004 A1
20040045685 Horner et al. Mar 2004 A1
20040048542 Thomaschefsky et al. Mar 2004 A1
20040055721 Hilbig Mar 2004 A1
20040060664 Lichtenberg et al. Apr 2004 A1
20040062916 Mansson Apr 2004 A1
20040089433 Propst et al. May 2004 A1
20040102528 Walchuk et al. May 2004 A1
20040118532 Sarbo et al. Jun 2004 A1
20040123963 Chen et al. Jul 2004 A1
20040140047 Sato et al. Jul 2004 A1
20040163783 Muller Aug 2004 A1
20040166290 Sembritzki et al. Aug 2004 A1
20040200590 Wilhelm Oct 2004 A1
20040206274 Kruckel Oct 2004 A1
20040206445 Butterworth et al. Oct 2004 A1
20040206467 Lindgren et al. Oct 2004 A1
20040221976 Williams et al. Nov 2004 A1
20040250969 Luu et al. Dec 2004 A1
20050034826 Hu Feb 2005 A1
20050034828 Graff et al. Feb 2005 A1
20050069679 Stelljes et al. Mar 2005 A1
20050069680 Stelljes et al. Mar 2005 A1
20050098281 Schulz et al. May 2005 A1
20050098286 Williams et al. May 2005 A1
20050103456 Hein et al. May 2005 A1
20050124704 Rasheed et al. Jun 2005 A1
20050155731 Martin et al. Jul 2005 A1
20050178515 Ryan et al. Aug 2005 A1
20050224200 Bouchard et al. Oct 2005 A1
20050230069 Hilbig Oct 2005 A1
20050241788 Baggot et al. Nov 2005 A1
20050247397 Kraus et al. Nov 2005 A1
20050251098 Wyss et al. Nov 2005 A1
20050257879 Fisher et al. Nov 2005 A1
20050263234 Shih Dec 2005 A1
20050274470 Shannon et al. Dec 2005 A1
20050276956 Zink et al. Dec 2005 A1
20050287340 Morelli et al. Dec 2005 A1
20060005916 Stelljes et al. Jan 2006 A1
20060013998 Stelljes Jan 2006 A1
20060037512 Pawlowska et al. Feb 2006 A1
20060042767 Bhat et al. Mar 2006 A1
20060062972 Lefebvre et al. Mar 2006 A1
20060070712 Runge et al. Apr 2006 A1
20060144541 Nickel et al. Jul 2006 A1
20060191656 Buzza et al. Aug 2006 A1
20060231224 Gelli et al. Oct 2006 A1
20060269706 Shannon et al. Nov 2006 A1
20060289136 Doherty et al. Dec 2006 A1
20060289137 Gelman et al. Dec 2006 A1
20070062658 Wiwi et al. Mar 2007 A1
20080003384 Murphy et al. Jan 2008 A1
20080044644 Luu et al. Feb 2008 A1
20080156449 Williams et al. Jul 2008 A1
20080248284 Williams et al. Oct 2008 A1
20080265222 Ozersky et al. Oct 2008 A1
20090162611 Ward et al. Jun 2009 A1
20100147473 Ward et al. Jun 2010 A1
20100212848 Hilbig et al. Aug 2010 A1
20100272965 Schinkoreit et al. Oct 2010 A1
20110020618 Brennan et al. Jan 2011 A1
Foreign Referenced Citations (26)
Number Date Country
10342201 Apr 2005 DE
0097036 Dec 1983 EP
0144658 Jun 1985 EP
0436170 Jul 1991 EP
0476976 Mar 1992 EP
1103522 May 2001 EP
1632604 Mar 2006 EP
2 075 452 Oct 1971 FR
2 321 389 Mar 1977 FR
2928383 Sep 2009 FR
1059746 Feb 1967 GB
1185227 Mar 1970 GB
2119709 Nov 1983 GB
2376436 Dec 2002 GB
2380447 Apr 2003 GB
2008272267 Nov 2008 JP
WO 9840207 Sep 1998 WO
WO 9842289 Oct 1998 WO
WO 0000698 Jan 2000 WO
WO 0015907 Mar 2000 WO
WO 0112902 Feb 2001 WO
WO 0114143 Mar 2001 WO
WO 0212622 Feb 2002 WO
WO 2004044320 May 2004 WO
WO 2006044117 Apr 2006 WO
WO 2010011646 Jan 2010 WO
Non-Patent Literature Citations (5)
Entry
Papermaking and Paperboard Making, Roland G. MacDonald & John N. Franklin, eds., 50-55 (2nd ed., 1970).
C. O. Au and I. Thorn in “Applications of Wet-End Paper Chemistry”, 1995, Blackie Academic & Professional and imprint of Chapman & Hall, First edition, pp. 102-119.
Hardell, Hanne-Lise et al., “A New Method for the Analysis of AKD Oligomers in Papermaking Systems,” 17 Nordic Pulp and Paper Research Journal 3, 340-345 (2002).
Written Opinion of the International Searching Authority that issued in PCT/FR2009/000231 on Aug. 29, 2006.
European Search Report for Application PCT/FR2009/000231.
Related Publications (1)
Number Date Country
20100326613 A1 Dec 2010 US