CA2208640C - High density tissue and process of making - Google Patents

High density tissue and process of making Download PDF

Info

Publication number
CA2208640C
CA2208640C CA 2208640 CA2208640A CA2208640C CA 2208640 C CA2208640 C CA 2208640C CA 2208640 CA2208640 CA 2208640 CA 2208640 A CA2208640 A CA 2208640A CA 2208640 C CA2208640 C CA 2208640C
Authority
CA
Canada
Prior art keywords
tissue
sheet
micropeak
microns
web
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CA 2208640
Other languages
French (fr)
Other versions
CA2208640A1 (en
Inventor
Paul Thomas Weisman
Scott Thomas Loughran
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority claimed from PCT/US1996/000216 external-priority patent/WO1996021769A1/en
Publication of CA2208640A1 publication Critical patent/CA2208640A1/en
Application granted granted Critical
Publication of CA2208640C publication Critical patent/CA2208640C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Paper (AREA)

Abstract

A smooth, high density tissue. The tissue has a relatively low caliper, yet maintains visually discernible machine direction micropeaks at a suitable micropeak frequency.

Description

WO 96121769 PCTlL;S96i00216 HIGH DENSTTY TISSUE
AND PROCESS OF MAKING
to FIELD OF THE INVENTION
This invention relates to tissue and more particularly to high density tissue having a soft tactile sensation.
BACKGROUND OF THE BWENTIpN
15 Tissue is well lrnown in the art and a staple of everyday life. Tissue is commonly divided into two uses - toilet tissue and fi~cial tissue. Both require several attributes in order to be accepted by the consumer. One of the most important attributes is softness.
Softness is a subjective evaluation of the tactile sensation the user feels when zo handling or using the tissue. Softness cannot be directly measured. However relative softness values can be meastued in panel score units (PSU) according to he technique set forth in commonly assigned U.S. patent 5,534,425 i~~ pots 11, 1994 to Mackey et al., except that the samples are not allowed to be judged equally soft.
SoRness has been found to be 25 related to 1) the surfi~ce topography of the tissue, 2) the fladbility of the tissue, and 3 ) the slip-stick coeff cient of fiiction of the siuface of the tissue.
Several attempts have been made in the art to improve softness by increasing the flexibility of the tissue. For example, commonly assigned U.S. patent 4,191,609 isatred to Trokhan has proven to be a commaciaUy successful way to increase 3o flextb>vty through a bilsteraUy staggered arrutgement of low density regions.
However, it has been well recognized in the art that multi-density tissues, which provide very high and commercially succ~ful flexibility and softness, have an inherattly distinctive topography.
However, improving, and even maintaining, softness by providing a smoother 35 surfi<ce topography has proven to be elusive. The reason for this elusiveness is the trade-off between the smoother surface topography and increased density.
Typically densificstion increases fiber to fiber contacts, potentially causing bonding at the contact points. This negatively impacts flexibility and hence softness. This interdependent density/softness relationship has been referred to as virtually 4o axiomatic in commonly assigned U.S. patent 4,300,981 issued Nov. 17, 1981 to Carstens. The Carstens '981 patent also discusses the PSU softness measurement .

PC'T/L,'S96IOOZ 16 - _ This relationship is also stated in competitive European Patent Application 0 613 979 Al, published September 7, 1994, as increased void volume (i.e., decreased density) correlates with improved softness. Unfortunately, this trade-off has inimical effects for tissue products sought by the consumers.
1o Unexpectedly, applicants have found a way to decouple the prior art relationship between density and softness. Accordingly, it is now possible to improve the surbce topography of tissue without encountering the concomitant loss of sods that occurs in the prior art. Therefore, softness levels, previously unattainable at relatively high densities, are possible with the present invention. Also, 1s unexpectedly, absorbency is maintained at the highs. density. This is contrary to prior art beliefs, as illustrated by Europe p~~t p~pph~on 0 616 074 A1, which holds lower density resuh;s in more bulky and absorbent sheets.
Further unexpectedly, it has been found necessary to utilize a multidensity substrate to make tissue according to the present invention. This is unexpected 2o because multidensity tissue, particularly through air dried tissue, generally has a lass density than conventionally dried tissue having a uniform density throughout.
Thus, rather than using high density tissue as a starting point in the caJendering process, one must utilize relatively lower density tissues as the starting point.
BRIEF DESCRIPTION OF T~ DRAWINGS
All Figures are of tissue and are taken in the machine direction.
Figure 1 is a sectional view of tissue, showing how micropeak height, micropeak widths and the number of micropeaks per inch are measured.
Figure 2 is as optical microscope photomicrograph of through air dried tissue 3o according to the prior art having 20 % crepe.
Figure 3 is an optical microscope photomicrograph of tissue according to the praau irrvention.
Figure 4 is an optical microscope photomicrograph of competitive through air dried tissue which has been heavily calendered.
PC'T/US96i00216 SLfMMARY OF THE INYEN~ON
The invention comprises a sheet of tissue. The tissue is a macroscopically monoplanar multidensity through air dried cellulosic fibrous structure. The tissue has a smoothness with a physiological surface smoothness of less than or equal to about 600 microns, preferably less than or equal to about 550 microns, and more preferably 10 less than or equal to about 500 microns.
T~ ~~~ ~Y ~ ode from a through air dried substrate. The substrate may be dried to a moisture love! of about 1.9 to about 3.5 percent. The tissue may then be calendered at a ptGisure of about 200 to 2,000 psi, and 30 to 400 pli in the nip.
In accordance with one embodiment, the invention provides a sheet of tissue, IS wherein the tissue is a macroscopically monoplanar through air dried multidensity cellulosic fibrous structure having low density regions extending outwardly from the plane of the tissue, the tissue having two opposed faces, at least one of the faces having a smoothness less than or equal to about 600 microns and a micropeak m frequency of at least about 30 micropeaks per inch.
In accordance with a further embodiment, the invention provides a sheet of tissue, wherein the tissue is a macroscopically monoplanar through air dried multidensity cellulosic fibrous structure having low density regions extending outwardly from the plane of the tissue, the tissue having two opposed faces, one face of the tissue having a smoothness less than or equal to about 500 microns, the tissue having a bulk density of at least about 0.150 grams per cubic centimeter and a micropeak frequency of at least about 30 micropeaks per inch.
In accordance with a further embodiment, a process of making smooth tissue paper, the process comprises the steps o~
providing an aqueous dispersion of papermaking fibers;
providing a water pervious Fourdrinier wire;
forming an embryonic web of the papermaking fibers on the wire;

providing a through air drying belt;
transferring the web to the through air drying belt, wherein a first plurality of regions of the web are dedensified upon transfer;
blowing air through the web;
vo providing a Yankee drying drum;

3a transferring the web from the through air drying belt to the Yankee drying drum, whereby a second plurality of regions of the web are densified upon transfer;
drying the web on the Yankee drying drum to a mean moisture level of about 1.9 to 10.0 percent to yield a mufti-density tissue suitable for calendering;
providing two axially parallel rolls juxtaposed to form a nip therebetween, the nip being suitable for calendering the tissue; and calendering the tissue in the nip at the mean moisture level to provide the tissue with a smoothness less than or equal to about 600 microns and a micropeak frequency of at least about 30 micropeaks per inch.

The tissue according to the present invention comprises a macroscopically monoplanar cellulosic fibrous structure. The tissue is two dimensional, although not nay ~, By "~~pically monoplanar' it is meant that the tissue lies PM~p~y in a single plane, recogniring that undulations in s~uface topographies do exist on a micro scale. The tissue, therefore, has two opposed faces. The teen "cdlulosic" means the tissue comprises at least 50~x, cdluiosic fibers. The ceUulosic fibers may either be hardwood or so Rvvood, and processed as 1 thermomechanical, stoneground pulp, etc. all of which are weU known in the art and do not comprise part of the present inversion. The term "fibrous" refers to elements which are fibs like, having one major axis with a dimension significantly greater than the other two dimensions orthogonal thereto. The term sheet refers to a macroscopically monoplanar formation of ceUulosic fibers which is taken off the forming wire as a single lamina and which does not change in basis weight unless fiber's are added to or ranaved therefrom. It is to be recognized that two, or more ~, ~ ~~ined together - with either or both having been made according to the ptesem inv~ion.
The tissue of the present imrention is through air dried, and may be made according to either of commonly assigned U.S. patents 4,191,609 issued March 4, 1980 to Trokhan; 4,637,859 issued January 20, 1987 to Trokhan; or 5,334,289 issued August 2, 1994 issued to Trokhan et al.

'Through sir drying according to tl;e aforementioned patents produces a multidensity tissue. Multidensity, through air dried tissues generally have a lesser density than tissues conventionally dried using a press feh and comprising a single region of one density. Particularly, a multidensity tissue made according to the three aforementioned patents comprises two regions, a high density region and discrete protuberances. The protuberances are of particularly PCT.~.,'S96~00216 5 low density relative to the balance of the tissue. The high density regions may comprise discrete regions juxtaposed with the low density regions or may comprise an essentially continuous network.
The tissue preferably, but not nxessar~ly, is layered according to commonly assigned U.S. patent 3,994,771 issued to Morgan et al.
to The tissue according to the present invention has a smoothness with a Physiological surface sm~thnas (PSS) of less than or equal to 600 microns, prefecsbty less than or equal to 550 microns and more preferably less than or equal to 500 microns. The physiological s<u<ace smoothness is measured according to the 15 procedure set forth in the 1991 Imernsiional Paper Physics Conference, TAPPI Book 1, more particularly the article entitled "Methods for the Measurement of the Mahattical Properties of Tissue Papa" by Ampulsb et al. and found at page 19.
The specific procedure used is set forth at page 22, entitled "Physiological Surface Smoothneaa." However, the PSS value obtained by the method set forth in this 2o article are multiplied by 1,000, to account for the conversion from millimeters to microns.
Physiological s~ul~ce smoothr~ is also described in commonly assigned U.S. Patents 4,959,125 issued Sept. 25, 1990 to Spendel and 5,059,282 issued 2s October 22, 1991 to Ampulab et al.
For the smoothness measurement, a sample of the tissue is selected. The sample is xlected to avoid wrinkles, tears, perforations, or grow deviations from ~~Pto ~~P. The sample is conditioned at 71 to 75 degrees F and 48 3o to 52 pacmt relative humidity for at least two hours. The sample is placed on a ~°~ ~1~ ~d oally secured in place. The only deviation from the aform»oned procedure is that sixteen traces (tight forward, eight reverse) per supple arc utilised, ratha then the tvverttyr traces set forth in the aforementioned article. Each forward and reverse trace is tranaversdy offstt from the adjacent 3s forward and revere trace about one millimeta. All sateen traces are averaged from the same sample to yield the smoothness value for that sample.
Eitha face of the tisane may be selected for the smoothness measurement, provided aU traces are taken from the same face. If either face of the tissue meets any of the smoothness criteria set forth herein the entire sample of the tissue is 4o deemed to fall within that criterion. Preferably both faces of the tissue meet the above criteria.

W O 96!21769 PCT/US96100216 5 The tissue according to the present invention preferably has a relatively low caliper. Caliper is measured according to the following procedure, without r considering the micro-deviations from absolute planarity inherent to the mufti-density tissues made according to the aforementioned incorporated patents.
~ The tissue paper is preconditioned at 71° to 75°F and 48 to 52 percent relative to humidity for two hours prior to the caliper measurement. If the caliper of toilet tissue is being measured, 15 to 20 sheets are first removed and discarded. If the caliper of facial tissue is being measured, the sample is taken from near the center of the package. The sample is selected and then conditioned for an additional 15 minutes.
i5 Caliper is measured using a low load Thwing-Albert micrometer, Model 89-1'1, available from the Thwing-Albert Instrument Company of Philadelphia, Pennsylvania.
The micrometer loads the sample with a pressure of 95 grams per square inch using a 2.0 inch diameter presser foot and a 2.5 inch diameter support anvil. The micrometer has a measurement capability range of 0 to 0.0400 inches. Decorated regions, n ne~nf~ltl(111C PC~QP P~P.I'.tC Ptr nfti,P t1CC11P cffnWr~ hP wni~ur~
i~~neei~,ln __ r.-_.-~--~---, ..a. ~~~~~-, ~~~., v. v..v v.~svrv vaav~a~ vv ca~vauvV a t,IW7v7aVlr.
The caliper of tissue according to the present invention is preferably less than or equal to about 8.0 mils, more preferably less than or equal about 7.5 mils, and still more preferably less than or equal to about 7.0 mils. One skilled in the art will understand a mil~is equivalent to 0.001 inches.
25 The tissue according to the present invention preferably has a basis weight of about 7 to about 35 pounds per 3,000 square feet. Basis weight is measured according to the following procedure.
The tissue sample is selected as described above, and conditioned at 71° to 75°
F and 48 to 52 percent relative humidity for a minimum of 2 hours. A stack of six 3o sheets of tissue is placed on top of a cutting die. The die is square, having dimensions of 3.5 inches by 3.5 inches and may have soft polyurethane rubber within the square to ease removal of the sample from the die after cutting. The six sheets are cut using the die, and a suitable pressure plate cutter, such as a Thwing-Albert Alfa Hydraulic Pressure Sample Cutter, Model 240-10. A second set of six sheets is 35 also cut this way. The two six-sheet stacks are then combined into a 12 sheet stack and conditioned for at least 15 additional minutes at 71° to 75°F and 48 to 52 percent humidity.
The 12 ply samples are then weighed on a calibrated analytical balance having a resolution of at least 0:0001 grams. The balance is maintained in the same room in 4o which the samples were conditioned. A suitable balance is made by Sartorius Instrument Company, Model A200S.
s The basis weight, in units of pounds per 3,000 square feet, is calculated according to the following equation:
Weight of 12 ~lv sample (,~) x 3000 (453.6 grams/pound) x (12 plies) x (12.25 sq. in per ply/144 sq. in/sq. ft.) to The basis weight in units of pounds per 3,000 square feet for this 12 ply sample is more simply calculated using the following conversion equation:
Basis Weight (lb/3,000 ft2) = Weight of 12 ply pad (g) x 6.48 is The units of density used here are gams per cubic centimeter (g/cc). With these density units of g/cc, it may be convenient to also express the basis weight in units of grams per square centimeters. The following equation may be used to make this conversion:
20 Wei t of 12 ply pad (g) Basis Weight (g/cm2) = 948.4 The tissue according to the present invention preferably has a relatively high density. The density of the tissue is calculated by dividing its basis weight by its 25 caliper. Thus, density is measured on a macro-scale, considering the tissue sample as a whole, and without regard to the differences in densities between individual regions of the paper.
The tissue according to the present invention preferably has a density of at least about 0.130 grams per cubic centimeter, preferably at least about 0.140 grams per so cubic centimeter, more preferably at least about 0.150 grams per cubic centimeter, and still more preferably at least about 0.160 grams per cubic centimeter.
The tissue according to the present invention preferably has micropeaks occurring in the machine direction. A plurality of these micropeaks have a micropeak height of at least about 0.05 millimeters, preferably at least about 0.10 millimeters 3s and more preferably at least about 0.12 millimeters. Micropeak height is illustrated in Figure 1 as the amplitude of the tissue taken normal to the base plane of the tissue.
Micropeak height is measured as the distance from the base plane of the tissue to the top of the micropeak of the tissue. The measurements are made from digitized images, as described herein. Micropeak height is taken as the mean of 12 micropeak 4o height measurements per sample.
i Micropeak width is orthogonal to micropeak height and represents the lateral extent of the micropeak in the machine direction, as illustrated in Figure 1.
Micropeak width is measured at an elevation of coincident one-half of the micropeak height as the machine direction distance from the left outside edge of the micropeak to the right outside edge of the micropeak. The measurements are made from 1o digitized images, as described herein. lViicropeak width is taken as the mean of 15 micropeak width measurements per sample.
The tissue according to the present invention preferably has a micropeak frequency of about 30 to about 60 micropeaks per inch. Micropeak frequency is measured from digitized images. A digitized cross sectional image of about 40x is provided of the tissue. Typically, the image covers about 2.0 to 2.8 millimeters of machine direction tissue. A line is drawn on the digitized image coincident the mid-elevation, left outside edge of the left-hand micropeak in the image. The line is extended horizontally to the right to the same point on the right hand peak in the image. The length of this line is measured, using image analysis software, and the 2o number of full peaks occurring on this line are counted. The micropeak count per millimeter is obtained by dividing the integer number of micropeaks by the length of the digitized region: This procedure is repeated until five different tissue regions of the sample are measured this way. A micropeak per millimeter value is obtained for each region and the five values are averaged. This value is converted to micropeaks per inch by multiplying by 25.4. This value, in micropeaks per inch is the micropeak frequency for that sample. If the five part average has the specified micropeak frequency, the entire tissue is judged to meet the specified micropeak frequency.
Iv)icropeak height, micropeak width, and micropeak frequency are an artifact of the creping and through air drying processes, rather than being caused by or due to 3o any embossing process. Mlcropeak height, micropeak width, and micropeak frequency are measured according to the following procedure.
. The sample to be measured is stapled to a rigid frame measuring about 1.25 inches x 2.125 inches on the outside, and having a central cut out measuring 0.75 inches by 1.5 inches. The frame may be made from a common manila folder, as is sold by the Smead Corp. Hastings, Mumesota. The sample and frame are embedded in resin. MEH100 polymeric resin, available from the Hercules Company of Wilmington, Delaware has been found to work well. After the resin is cured, the sample is cross sectioned using a sliding knife microtome, so that the machine direction is viewed, as illustrated in Figure 1. Care must be taken that the 4o microtome intercepts the maximum height and width of the micropeak to be studied.
A model 860 microtome available from the American Optical Company of Buffalo, New York has been found to work well.
The cross sectioned samples of the tissue are then viewed on a Nikon stereomicroscope and digitized using JVC TK-885U CCD, or similar, camera, available from JVC Professional Products of Elmwood Park, New Jersey and a Data to Translation Quick Capture Frame grabber Board, made by Data Translation, Inc. of Marlboro, Massachusetts. The measurements are then made as described above using the Optimas Image Analysis software, available from Bioscan, Inc. of Edmunds, Washington and a 0.01 millimeter increment slide micrometer.
As illustrated by Figure 2, creped tissue according to the prior art shows a pattern of visually discernible micropeaks. This sample had approximately 20%
crepe.
As illustrated by Figure 3, tissue according to the present invention still retains micropeaks measurable as described above. Without being bound by theory, it is believed this topography contributes to the softness of the tissue according to the 2o present invention. This tissue is further described in Example 3 below.
As illustrated by Figure 4, a competitive through air dried tissue when calendered may have virtually no visually discernible topography.
The process for making a tissue according to the present invention comprises the following steps. First an aqueous dispersion of papermaking fibers and a foraminous forming surface, such as a Fourdrinier wire, are provided. The embryonic web is contacted with the Fourdrinier wire to form an embryonic web of papermaking fibers on the wire. Also a through air drying belt, such as is described above, is provided. The Fourdrinier wire and embryonic web are then transferred to the through air drying belt. During the transfer, a differential pressure is applied 3o through the through air drying belt. This differential pressure deflects regions of the tissue into the belt. These deflected regions are the low density regions discussed above, and are believed to be critical to making the tissue of the present invention -despite the fact that such low density regions are later calendered to a higher density.
A heated contact drying surface, such as a Yankee drying drum, is also provided. The web of cellulosic fibers is then brought into contact with the Yankee drying drum, and preferably impressed thereagainst. This impression further increases the local difference in density between the high and low density regions of the tissue. The tissue is then dried to the desired moisture level, as set forth below, on the Yankee drying drum. Generally, the appropriate moisture level may be about 0.3 to 0.4 percent higher than moisture levels for conventional calendering operations.
The tissue is foreshortened and removed from the Yankee drying drum using a doctor blade as is well known in the art and described in commonly assigned U.S.
Patent 4,919,756 issued April 24, 1990 to Sawdai.
It is recognized that the angle of the doctor blade relative to the Yankee drying drum may be adjusted, and that such adjustments may affect the Io micropeak height and/or the micropeak frequency of the tissue.
ARer drying, the tissue is calendered ai a mean moisture level between about 1.9 and 10.0 percent, pre>~ly ~,~ hut 1.9 and 3.5 percent, and more P~~IY ~~n about 2.5 and 3.0 percent. Relatively higher moisture levels provide greater densification at generally lower caliper pressures. However, as I5 moisture levels increase, moisture profiles on the paperntaiang ~~e ~e generally exaggerated. Additionally, as moisture ltvels increase, the ~~ Mmes stiffer, and hence has less softness, possibly due to hydrogen bonding, transfer of adhesive from the Yankee drying drum, etc.
qty inereasa of 50 to 100 percent are typical accord~g to the catendering 20 operation of the present invention. It is to be understood thu the calendering operation incrases the density of the tissue as a whole, and may or may not provide uniform percxntage density increases of all regions of the multidensity tissue.
The calendering is performed using two rolls juxtaposed to form a nip between the rolls. As will be recognized by one skilled in the art, calendering may be 25 performed using more than two rolls, with the rolls being arranged in pain to form multiple nips. It will be fiutha apparent to one skilled in the arc that the same roll may be used in more than one pair.
The rolls may be axially parallel. However, in order to accommodate the slender pr~ures desirable with the present invention, one of the rolls may be 3o abwned. The axis of tt~ other roll may be bent so that it conforms to the crown of the >5rst roll. Ahanatively, the axes of the rolls may be slightly skewed.
Either or both of the rolls forming the nip may be steel, rubber cooed, fabric P~ ~~ etc. Either or both rolls may be maintained at a temperature optimum for roll life, i.e., to prevent overheating of the roll, or at a temperature 35 which heats the substrate. One roll may be atanalty driven, the other may be fractionally driven by the first roll, so that slip is minimized.
The pairs of rolls are loaded together with a nip pressure of about 200 to 2,000 psi, and preferably with a nip pressure of about 400 to 800 psi. This loading provides a lineal nip pressure of 30 to 400 pli, and more preferably about 40 to 100 pli. One 4o skilled in the art will recognize that the nip width can be obtained by dividing the lineal nip pressure in pli by the nip pressure in psi (pli/psi).

5 It is recognized that calendering the tissue according to the present invention may likely yield an increase in opacity as well. Opacity increases of about 20% are possible with the present invention.
The merits ot~ and techniques for making, the present invention are illustrated to by the following nonlimiting examples. Each of the samples below represents a single ply, through air dried tissue. The softness measurements (in PSU) were made using Charmin brand toilet tissue, as currently marketed by The Procter &
Gamble Company of Cincinnati, Ohio, as the standard.

Kleenex Double Roll brand toilet tissue, manufactured by the Kimberly-Clark Corporation of Dallas, Texas was used for Example 1. The Kleenex Double Roll tissue of Example 1, was as commercially obtained, and had a caliper of 9.8 mils, and a density of grams 0.116 grams per cc. the tissue was calendered in a steel to steel 2o nip at a pressure of 614 psi and a lineal pressure of 38 pli. The resulting tissue had a Yankee side smoothness of 584 microns and a smoothness of 614 microns on the opposite face. The density 0.197 grams per cc. While his tissue had improved smoothness, as illustrated in Figure 4, it lacks the preferred micropeak height and frequency according to the present invention.

A single ply, through air dried toilet tissue according to the present invention was made on a pilot plant line. This tissue was dried on a five shed, Atlas weave fabric made according to commonly assigned U.S. Patent 4,239,065 issued to 3o Trokhan. The fabric had a warp count of 59 fibers per inch and a weft count of 44 fibers per inch. The tissue was dried to about 2.0 percent moisture on the Yankee, then immediately calendered in a rubber to steel nip at a pressure of about 95 psi and a lineal nip pressure of about 95 pli. The tissue was later calendered in a steel to steel nip at a pressure of about 600 psi and a lineal nip pressure of about 32 pli.
The tissue of Example 2 had a caliper of 6.6 mils, and a density of 0.164 grams per cc.
The resulting tissue had a Yankee side smoothness of 584 microns, a smoothness of microns on the opposite face, and a softness of 0.5 PSU.

WO 96!21769 PCT/US961002i6 A single ply, through air dried toilet tissue according to the present invention was made on a pilot plant line. This tissue was dried on a five shed, Atlas weave fabric made according to commonly assigned U.S. Patent 4,239,065 issued to Trokhan. The fabric had a warp count of 59 fibers per inch and a weft count of 1o fibers per inch. The tissue was dried to about 2.1 percent moisture on the Yankee, then immediately calendered in a rubber to steel nip at a pressure of about 10 psi and a lineal nip pressure of about 25 pli. The tissue was later calendered in a steel to rubber nip at a pressure of about 2,000 psi and a lineal nip pressure of about 310 pli.
The tissue of Example 3 had a caliper of 5.8 mils, and a density of 0.159 grams per 1s cc. The resulting tissue had a Yankee side smoothness of 534 microns, a smoothness of 490 microns on the opposite face, and a softness of 0.2 PSU. The tissue had a nlicropeak height of 0.14 millimeters and a micropeak frequency of 52 micropeaks per inch.
~n www,m ~ w vv iiAl~lYlC Lli 'f A single ply, through air dried toilet tissue according to the present invention was made on a pilot plant line. This tissue was dried on a five shed, Atlas weave fabric made according to commonly assigned U.S. Patent 4,239,065 issued to Trokhan. The fabric had a warp count of 59 fibers per inch and a weft count of 25 fibers per inch. The tissue was dried to about 2.1 percent moisture on the Yankee, then immediately calendered in a rubber to steel nip at a pressure of about 10 psi and a lineal nip pressure of about 25 pli. The tissue was then conditioned in a high relative humidity environment until its moisture level increased to 11 %. The tissue was then calendered in a steel to rubber nip at a pressure of about 2,000 psi and a 30 lineal nip pressure of about 310 pli. The tissue of Example 4 had a caliper of 5.5 mils, and a density of 0.171 grams per cc. The resulting tissue had a Yankee side smoothness of 436 microns, a smoothness of 443 microns on the opposite face, and a softness of 0.2 PSU. The tissue had a micropeak height of 0.12 millimeters and a micropeak frequency of 45 micropeaks per inch.
The results of Examples 1 to 4 are illustrated in Table I. For completeness, J
Table I also provides the basis weight, density, caliper, and peak frequency of each sample.

TABLE I
BASIS

SMOOTHNESS WEIGHT

YANKEE (POUNDS

SIDFJOPPOSITE PER 3,000, DENSTTY

EXAMPLE SOFTNESS SIDE SQUARE CALIPER (GRAMS ' NUMBER ~ (MICRONS FEET (MILS) PER CC) 1 NA 584/614 16.9 5.5 0.197 2 0.5 584/696 16.9 6.6 0.164 3 0.2 534/490 14.4 5.8 0.159 4 0.2 436/443 14.7 5.5 0.171 It will be apparent to one skilled in the art that the aforementioned parameters may be optimized as necessary. For example, it may be feasible to have a tissue of lesser smoothness, providing it has the proper density. In particular a tissue with a to smoothness less than or equal to about 550 microns, and having a density of at least about 0.140 grams per cubic centimeter may be feasible. Preferably both faces of such tissue have a smoothness of less than or equal to about 550 microns, although if either face meets this criterion the tissue is made according to the present invention.
The density of such tissue may preferentially be increased to 0.150 or to 0.160 grams is per cubic centimeter.
The softness of one face of the tissue may be less than or equal to about 550 microns, the softness of the other face may be less than or equal to about 500 microns. More preferably, the softness of both faces of the tissue may be less than or equal to about 550 microns, and more preferably less than or equal to about 20 microns.
All such variation are within the scope of the appended claims.

Claims (18)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A sheet of tissue, wherein said tissue is a macroscopically monoplanar through air dried multidensity cellulosic fibrous structure having low density regions extending outwardly from the plane of said tissue, said tissue having two opposed faces, at least one of said faces having a smoothness less than or equal to about 600 microns and a micropeak frequency of at least about 30 micropeaks per inch.
2. A sheet of tissue according to claim 1, said one of said faces of said tissue having a smoothness less than or equal to 550 microns.
3. A sheet of tissue according to claim 2, said one of said faces of said tissue having a smoothness less than or equal to 500 microns.
4. A sheet of tissue according to claim 1, said tissue having a bulk density of at least about 0.130 grams per cubic centimeter.
5. A sheet of tissue according to claim 4, said tissue having a bulk density of at least about 0.140 grams per cubic centimeter.
6. A sheet of tissue according to claim 5, wherein both said faces of said tissue have a smoothness of less than or equal to about 600 microns.
7. A sheet of tissue according to claim 4, said tissue having a caliper less than about 8.0 mils.
8. A sheet of tissue according to claim 7, said tissue having a caliper less than about 7.0 mils.
9. A sheet of tissue according to claim 1, said tissue having a machine direction micropeak height of at least about 0.05 millimeters.
10. A sheet of tissue according to claim 9, said tissue having a micropeak height of at least about 0.10 millimeters.
11. A sheet of tissue, wherein said tissue is a macroscopically monoplanar through air dried multidensity cellulosic fibrous structure having low density regions extending outwardly from the plane of said tissue, said tissue having two opposed faces, one said face of said tissue having a smoothness less than or equal to about 500 microns, said tissue having a bulk density of at least about 0.150 grams per cubic centimeter and a micropeak frequency of at least about 30 micropeaks per inch.
12. A sheet of tissue according to claim 11, said tissue having a bulk density of at least about 0.160 grams per cubic centimeter.
13. A sheet of tissue according to claim 11, wherein both said faces of said tissue have a smoothness of less than about 500 microns.
14. A process of making smooth tissue paper, said process comprising the steps of:
providing an aqueous dispersion of papermaking fibers;
providing a water pervious Fourdrinier wire;
forming an embryonic web of said papermaking fibers on said wire;
providing a through air drying belt;
transferring said web to said through air drying belt, wherein a first plurality of regions of said web are dedensified upon transfer;
blowing air through said web;
providing a Yankee drying drum;
transferring said web from said through air drying belt to said Yankee drying drum, whereby a second plurality of regions of said web are densified upon transfer;
drying said web on said Yankee drying drum to a mean moisture level of about 1.9 to 10.0 percent to yield a multi-density tissue suitable for calendering;
providing two axially parallel rolls juxtaposed to form a nip therebetween, said nip being suitable for calendering said tissue; and calendering said tissue in said nip at said mean moisture level to provide said tissue with a smoothness less than or equal to about 600 microns and a micropeak frequency of at least about 30 micropeaks per inch.
15. The process according to claim 1 wherein said tissue has an average micropeak height of at least about 0.10 millimeters.
16. The process according to claim 1 wherein said nip provides a pressure during said calendering of said tissue of about 20 to 2,000 psi.
17. The process according to claim 3 wherein said nip provides a lineal pressure during said calendering of said tissue web of about 30 to 400 pli.
18. A paper according to claim 1 wherein said tissue has a micropeak frequency of about 30 to about 60 micropeaks per inch.
CA 2208640 1995-01-10 1996-01-05 High density tissue and process of making Expired - Fee Related CA2208640C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US37071695A 1995-01-10 1995-01-10
US08/370,716 1995-01-10
PCT/US1996/000216 WO1996021769A1 (en) 1995-01-10 1996-01-05 High density tissue and process of making

Publications (2)

Publication Number Publication Date
CA2208640A1 CA2208640A1 (en) 1996-07-18
CA2208640C true CA2208640C (en) 2000-03-14

Family

ID=29552593

Family Applications (1)

Application Number Title Priority Date Filing Date
CA 2208640 Expired - Fee Related CA2208640C (en) 1995-01-10 1996-01-05 High density tissue and process of making

Country Status (1)

Country Link
CA (1) CA2208640C (en)

Also Published As

Publication number Publication date
CA2208640A1 (en) 1996-07-18

Similar Documents

Publication Publication Date Title
EP0805896B1 (en) High density tissue and process of making
AU710026B2 (en) Smooth, through air dried tissue and process of making
US6551453B2 (en) Smooth, through air dried tissue and process of making
US6821386B2 (en) Smooth, micropeak-containing through air dried tissue
EP0642614B1 (en) Paper towel with dual level diagonal infundibulate striae of slitted elongate hexagonal bosses
US20210321831A1 (en) Multi-ply resilient tissue products
CA2540659C (en) High bulk strong absorbent single-ply tissue-towel paper product
EP0741820B1 (en) Wet pressed paper web and method of making the same
CA2622899C (en) Tissue paper
US11795625B2 (en) Embossed multi-ply tissue products
KR102624012B1 (en) Embossed multi-ply tissue products
US20210310197A1 (en) Embossed multi-ply tissue products
CA2208640C (en) High density tissue and process of making
MXPA97005196A (en) High density hygienic paper and defibration process
MXPA97005195A (en) Hygienic paper smooth by drying with air and processing fabricac

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed

Effective date: 20160105