TECHNICAL FIELD
[0001] The present disclosure relates to the field of paper for use in a sack, such as a
cement sack.
BACKGROUND
[0002] During filling and storage of powdery material, such as cement, paper sacks are required
to meet high standards.
[0003] Firstly, the paper sacks need to hold a considerable material weight, i.e. have high
tensile strength. For this purpose, kraft paper is a suitable sack wall material.
The sacks typically have two or more walls, i.e. layers of paper material, to further
strengthen the sack construction. A wall layer of a sack is often referred to as a
ply. Production of ply material (i.e. sack paper) is for example disclosed in
WO 99/02772.
[0004] Secondly, a material such as cement is sensitive to moisture contamination during
storage. Hence, the contents of sacks often require protection against atmospheric
water vapor that may penetrate the sack plies. Such protection is typically achieved
by a moisture barrier incorporated as an intermediate layer in the sack, i.e. between
two plies. The moisture barrier is typically a plastic film ("free film"), e.g. of
polyethylene (PE), that is impermeable to water vapour. The free film may also improve
resistance to grease and prevent contamination by microorganisms.
[0005] Thirdly, the paper sack should vent air during filling. In detail, the air that accompanies
the powdered material shall efficiently vent from the sack since the filling machines
that delivers the material run at high throughput rates. The venting capacity of the
sack is often the factor limiting for the filling rate. Efficient venting also prevents
that air is trapped in the sack and causes under-weight packs, sack rupture and problems
when sacks are stacked for transportation.
[0006] During the filling process, the only way for air to escape from the interior of the
sack is in many sack constructions through the walls of the sack. Kraft paper of high
porosity is often used in the walls to facilitate air permeability. However, an increased
porosity of the paper normally results in a decrease in the overall strength. In particular,
the strength may be significantly reduced if holes must be made in the paper material
to achieve sufficient air permeability. Furthermore, the use of a free film may reduce
deaeration during filling, since most such films are impermeable to air. Therefore,
the free film layers have been provided with slits or openings to facilitate deaeration.
[0007] In
WO 2016/001029, the free film is replaced by two coating layers provided on the outer paper ply:
first a pre-coating layer and then a moisture barrier coating layer. In the examples
disclosed in this document, the moisture barrier layer is formed from latex and hyper-platy
clay. The two-layer coating structure of
WO 2016/001029 not only provides a barrier against moisture/water vapour, but it also facilitates
disintegration of the sack in a cement mixer.
SUMMARY
[0008] The hyper-platy clay used in
WO 2016/001029 is expensive and may be complicated to handle in the paper mill.
[0009] Accordingly, an objective of the present disclosure is to provide a barrier concept
of reduced cost that still runs well in a coating station and provides sufficient
protection against water vapour. While it is not necessary that this coating concept
facilitates disintegration in a cement mixer, it should allow for recycling of the
coated paper according to industry standards.
[0010] There is thus provided a coated paper comprising a kraft paper substrate, a precoating
layer provided on the kraft paper substrate and a water vapour barrier coating layer
provided on the pre-coating layer, wherein the grammage according to ISO 536:2019
of the coated paper is 65-155 g/m
2, the pre-coating layer comprises inorganic filler and binder in a dry weight ratio
of between 100:25 and 100:5 and the water vapour barrier coating layer comprises clay
pigment and styrene-butadiene co-polymer (SBR) binder in a dry weight ratio between
100:30 and 100:80, wherein the particle size distribution (% < 2 µm) of said clay
pigment is above 90 and the shape factor of said clay pigment is below 20, such as
below 10.
BRIEF DESCRIPTION OF THE FIGURES
[0011]
Fig 1 shows a sack according to the present disclosure configured to allow "top deaeration".
Fig 2 shows the sack of Fig 1 provided with a top patch for reinforcement.
DETAILED DESCRIPTION
[0012] As a first aspect of the present disclosure, there is provided a coated paper comprising
a kraft paper substrate, a precoating layer provided on the kraft paper substrate
and a water vapour barrier coating layer provided on the pre-coating layer.
[0013] The kraft paper substrate (also referred to as base paper) is preferably formed from
a pulp comprising at least 75% by dry weight of virgin fibres. These virgin fibres
are typically softwood fibres.
[0014] The kraft paper substrate may be bleached or unbleached.
[0015] For sufficient strength when used in a sack, the geometric tensile energy absorption
(TEA) index of the coated paper is preferably at least 2.0 J/g. In the present disclosure,
TEA is measured according to ISO 1924-3:2005. The TEA index is obtained by dividing
the TEA value by the grammage. The geometric TEA index is the geometric mean of the
TEA index in the machine direction and the TEA index in the cross direction.
[0016] The grammage of the coated paper is 65-155 g/m
2. Preferably it is 65-135 g/m
2, such as 75-115 g/m
2. In the present disclosure, grammage is measured according to ISO 536:2019.
[0017] The coat weight of the pre-coating layer is preferably 4-20 g/m
2, such as 4-12 g/m
2, such as 5-10 g/m
2 and the coat weight of the water vapour barrier coating layer is preferably 4-20
g/m
2, such as 4-12 g/m
2, such as 5-10 g/m
2.
[0018] Accordingly, the grammage of the kraft paper substrate is typically 50-140 g/m
2 and preferably 50-120 g/m
2, such as 60-100 g/m
2.
[0019] The Cobb 60s value of both sides of the kraft paper substrate may be below 40 g/m
2, such as below 35 g/m
2. Accordingly, the Cobb 60s value of the side the coated paper that is not provided
with the pre-coating and the barrier coating is preferably below 40 g/m
2, such as below 35 g/m
2. The Cobb 60s values of the present disclosure are measured according to ISO 535:2014.
To obtain lower Cobb 60s values, hydrophobic size, such as AKD, ASA and/or rosin size
may be added in the wet end during production of the kraft paper substrate.
[0020] In one embodiment, the kraft paper substrate comprises a wet strength agent. However,
the amount of the wet strength agent should be controlled such that the coated paper
is still recyclable.
[0021] The pre-coating layer comprises inorganic filler and binder in a dry weight ratio
of between 100:25 and 100:5, preferably between 100:20 and 100:8, and more preferably
between 100:16 and 100:8. In one embodiment, the dry weight ratio is between 100:16
and 100:10. The binder of the pre-coating layer may for example be a styrene-butadiene
co-polymer (SBR). The SBR is typically provided in the form of a latex when the coating
composition is prepared and coated onto the kraft paper substrate. The inorganic filler
of the pre-coating layer is preferably a relatively coarse pigment, such as a pigment
having a particle size distribution (% < 2 µm) below 70. In a particularly preferred
embodiment, the inorganic filler is a calcium carbonate pigment having a particle
size distribution (% < 2 µm) below 70. The person of skill in the art of pigments
for paper coating layers is familiar with particle size distribution values expressed
as the percentage of particles having a size below 2 µm. As an example, this type
of values is frequently found on data sheets for pigment products.
[0022] The water vapour barrier coating layer comprises clay pigment and styrene-butadiene
co-polymer (SBR) binder in a dry weight ratio between 100:30 and 100:80, wherein the
particle size distribution (% < 2 µm) of said clay pigment is above 90, preferably
above 95. The SBR is typically provided in the form of a latex when the water vapour
barrier coating composition is prepared and coated onto the pre-coating layer.
[0023] Further, the shape factor of the clay pigment of the water vapour barrier coating
layer is preferably below 20, more preferably below 10.
[0024] The dry weight ratio of clay pigment to SBR binder in the water vapour barrier layer
is preferably between 100:40 and 100:70, more preferably between 100:40 and 100:60.
[0025] As a second aspect of the present disclosure, there is provided a sack comprising
a ply formed from the coated paper of the first aspect. The sack is preferably a sack
for a hydraulic binder, such as cement. The contents of the sack is typically used
in mortar or tile fix.
[0026] In one embodiment, the sack comprises at least two plies and the ply formed from
the coated paper of the first aspect is an outer ply. Such a sack may comprise an
inner ply formed from a kraft paper having a Gurley permeance (also referred to as
Gurley value or air permeance) of 2-10 s, such as 4-8 s, such as 4-7 s, such as 5-6
s. In the present disclosure, Gurley permeance is measured according to ISO 5636-5:2013.
[0027] The kraft paper of the inner ply typically has a grammage of 60-90 g/m
2, preferably 60-85 g/m
2, such as 60-80 g/m
2.
[0028] The coated paper of the sack typically has a grammage of 75-105 g/m
2, such as 75-95 g/m
2. Accordingly, the paper substrate of the coated paper of the sack typically has a
grammage of 60-90 g/m
2, such as 60-80 g/m
2.
[0029] As understood by the skilled person, there typically is no free film in the sack.
[0030] The sack is typically configured to allow air to escape from an interspace between
the inner paper ply and the outer paper ply during filling of the sack.
[0031] This is facilitated by the permeability of the inner paper ply of the sack, which
allows air to pass from the inside of the sack to the interspace between the inner
paper ply and the outer paper ply. Such a sack is also configured to allow air to
escape from the interspace between the inner paper ply and the outer paper ply (to
the ambient air) during filling of the sack.
[0032] Preferably, the sack design is such that air can escape from the interspace between
the inner paper ply and the outer paper ply through a top end of the sack during filling
of the sack.
[0033] For example, a top end of the sack may be formed by folding and gluing the plies
such that a portion of the top end is not sealed and air can escape from the interspace
through the non-sealed portion during filling of the sack. Such an embodiment is further
discussed below with reference to figures 1 and 2.
[0034] The sack of the present disclosure is preferably a valve sack. Valve sacks are well
known to the skilled person. A valve sack is provided with a valve through which it
may be filled. Such a valve is normally provided at a folded top end of the sack.
A valve is further discussed below with reference to figures 1 and 2.
[0035] Figure 1 illustrates an embodiment of a multi-ply sack 100 having a top end 111 and
a bottom end 112. The sack comprises an inner paper ply 101 and an outer paper ply
102. To create a water vapour barrier, the paper of the outer ply 102 is coated as
described above. To facilitate deaeration, the Gurley permeance of the inner paper
ply 101 is 10 s or less.
[0036] The sack 100 is configured to allow air to escape (the air escape is illustrated
by the arrow 103) from an interspace between the inner paper ply 101 and the outer
paper ply 102 through the top end 111 of the sack 100 during filling of the sack 100.
Such a deaeration is achieved by a non-sealed portion 104 forming an opening between
the inner paper ply 101 and the outer paper ply 102 at the top end 111. The non-sealed
portion 104 may be flanked by sealed portions 105, i.e. portions in which the outer
paper ply 102 is sealed (preferably glued) to the inner paper ply 101. For a 25 kg
sack 100 having a width of 400-420 mm, the width of the non-sealed portion may for
example be 150-160 mm and for a 35 kg having a width of 440-460 mm, the width of the
non-sealed portion may be 190-200 mm.
[0037] The top end 111 of the sack 100 of figure 1 further has a filling valve 106 into
which a filling spout may be inserted. The arrow 107 illustrates how the filling spout
is inserted into the valve 106. A ceiling of the valve 106 is reinforced by a valve
reinforcement 108, which preferably is composed of paper. Because of the reinforcement
provided by the valve reinforcement 108, the sack 100 can hang on the filling spout
during filling without breaking. When fully opened, the opening of the valve 106 may
be approximatively diamond-shaped.
[0038] Figure 2 illustrates the sack 100 of figure 1 onto which a top patch 201 has been
applied. The top patch reinforces top end 111 of the sack 100. A slit 202 in the top
patch 201 ensures that the air still can escape through the non-sealed portion 104
during filling. The slit 202 is thus substantially aligned with the non-sealed portion
104. Further, the width of the slit 202 is preferably approximately the same as the
width of the non-sealed portion 104. Again, the escape of air from the interspace
between the inner paper ply 101 and the outer paper ply 102 through the top end 111
of the sack 100 is illustrated by the arrow 103.
EXAMPLES
[0039] In this examples section, "parts" means parts by dry weight. All base papers used
in the examples section are formed from pulps in which all cellulose fibres are virgin
softwood fibres.
Reference trial 1
[0040] A bleached sack kraft paper having a grammage of 70 g/m
2, a Cobb 60s value of 30 g/m
2, a Gurley value of 16 s and an MD stretchability of about 2.3 % was used as the base
paper.
Coating the top side (but not the wire side)
[0041] The top side of the base paper was blade coated with a pre-coating composition comprising
100 parts of Hydrocarb 60 (a relatively coarse calcium carbonate pigment commercialized
by OMYA), 13.5 parts of Ligos P 1217 (an SBR binder commercialized by TRINSEO), 0.62
parts of Finnfix 10 (a CMC rheology modifier commercialized by Nouryon), 0.01 parts
of an anti-foaming agent, 0.001 parts of colour and 0.07 parts of NaOH. The (dry)
coat weight of the pre-coating was 8 g/m
2.
[0042] After drying, the precoated side was blade coated with a coating composition comprising
100 parts of a 50/50 mixture of Hydragloss 90 (an ultra-fine (% < 2 µm = 96-100) clay
pigment commercialized by KaMin) and Hydrocarb 95 (an ultra-fine calcium carbonate
pigment commercialized by OMYA), 13 parts of Ligos P 1217, 0.65 parts of Finnfix 10,
0.01 parts of an anti-foaming agent and 0.07 parts of NaOH. The (dry) coat weight
of this coating was 7 g/m
2.
[0043] After drying, the double-coated base paper was calendered in a soft nip calender
at a temperature of 140°C using a line load of 160 kN/m.
Coating the wire side (but not the top side)
[0044] The wire side of the base paper was coated and calendered in the same way as the
top side.
Results
[0045] The WVTR of the coated papers was measured at 23°C/50% RH and at 38°C/90% RH. The
results are presented in table 1 below.
Table 1. WVTR values (g/m
2day) obtained in reference trial 1.
Sample |
WVTR (23°C/50% RH) |
WVTR (38°C/90% RH) |
Double-coated top side |
507 |
3760 |
Double-coated wire side |
541 |
4081 |
Reference trial 2
[0046] A coated paper was produced on several occasions over a production period of about
one year. In this production, a bleached sack kraft paper having a grammage of 80
g/m
2, a Cobb 60s value of about 80 g/m
2 and an MD stretchability of 6% was used as the base paper.
Coating the wire side (but not the top side)
[0047] The wire side of the base paper was blade coated with a pre-coating composition comprising
100 parts of Hydrocarb 60 (a relatively coarse calcium carbonate pigment commercialized
by OMYA), 13.5 parts of Litex P6115 (an SBR binder commercialized by Eka Synthomer),
0.62 parts of Finnfix 10 (a CMC rheology modifier commercialized by Nouryon), 0.024
parts of an anti-foaming agent and 0.097 parts of NaOH. The (dry) coat weight of the
pre-coating was 8 g/m
2.
[0048] After drying, the precoated side was blade coated with a barrier coating composition
comprising 100 parts of Barrisurf LX (a high aspect ratio (shape factor = 60) clay
pigment commercialized by IMERYS), 50 parts of Litex P6115, 0.6 parts of Rheocoat
27 (a rheology modifier commercialized by ARKEMA) and 0.13 parts of NaOH. The (dry)
coat weight of the barrier coating was 7 g/m
2.
[0049] After drying, the double-coated base paper was calendered in a soft nip calender
at a temperature of 80°C using a line load of 70 kN/m.
Results
[0050] The WVTR of the coated papers was measured at 38°C/90% RH. The average result from
the whole production period is presented in table 2 below. Before calculating the
average result, outliers (suspiciously high values) were deleted.
Inventive trial 1
[0051] The same base paper as in reference trial 2 was used.
Coating the wire side (but not the top side)
[0052] The wire side of the base paper was blade coated with a pre-coating in the same way
as in reference trial 2.
[0053] After drying, the precoated side was blade coated with a barrier coating composition
comprising 100 parts of Hydragloss 90, 50 parts of Litex P6115, 0.16 parts of Rheocoat
27 and 0.13 parts of NaOH. As in reference trial 2, the (dry) coat weight of the barrier
coating was 7 g/m
2.
[0054] After drying, the double-coated base paper was calendered in a soft nip calender
at a temperature of 80°C using a line load of 70 kN/m.
Results
[0055] The WVTR of the coated paper was measured at 38°C/90% RH. The result (an average
value) is presented in table 2 below.
Inventive trial 2
[0056] A coated paper was produced on several occasions over a period of about nine months.
The same base paper as in reference trial 2 and was used.
Coating the wire side (but not the top side)
[0057] The wire side of the base paper was blade coated with a pre-coating composition comprising
100 parts of Hydrocarb 60 (a relatively coarse calcium carbonate pigment commercialized
by OMYA), 9 parts of Ligos P1217, 0.16 parts of Rheocoat 27 and 0.13 parts of NaOH.
The (dry) coat weight of the pre-coating was 8 g/m
2.
[0058] After drying, the precoated side was blade coated with a barrier coating composition
comprising 100 parts of Hydragloss 90, 50 parts of Ligos P 1217, 0.16 parts of Rheocoat
27 and 0.13 parts of NaOH. As in reference trial 2, the (dry) coat weight of the barrier
coating was 7 g/m
2.
[0059] After drying, the double-coated base paper was calendered in a soft nip calender
at a temperature of 80°C using a line load of 70 kN/m.
Results
[0060] The WVTR of the coated paper was measured at 38°C/90% RH. The average result from
the whole production period is presented in table 2 below.
Table 2. WVTR values (g/m
2day) obtained in reference trial 2, inventive trial 1 and inventive trial 2.
Sample |
WVTR (38°C/90% RH) |
Reference trial 2 |
1116 |
Inventive trial 1 |
1124 |
Inventive trial 2 |
1174 |
[0061] Barrisurf LX (used in reference trial 2) is an expensive hyper-platy clay pigment
specifically designed to improve the water vapour barrier properties of coatings of
fibre-based substrates. Surprisingly, table 2 shows that the relatively inexpensive
clay pigment Hydragloss 90 that was used in inventive trials 1 and 2 provided WVTR
values on par with that for Barrisurf when used together with a SBR binder on top
of a pre-coating. A comparison to the data in table 1 shows that the WVTR values at
38°C/90% RH for inventive trials 1 and 2 are much lower than that for reference trial
1.
Inventive trial 3
[0062] In this trial, four different base papers were used:
- (i) a bleached sack kraft paper produced in BillerudKorsnäs' Karlsborg mill and having
a grammage of 70 g/m2, a Cobb 60s value of 30 g/m2, a Gurley value of 15 s and an MD stretchability of 6%;
- (ii) an unbleached sack kraft paper produced in BillerudKorsnäs' Skärblacka mill and
having a grammage of 70 g/m2, a Cobb 60s value of 30 g/m2, a Gurley value of 10 s and an MD stretchability of 6%;
- (iii) a bleached sack kraft paper produced in BillerudKorsnäs' Pietarsaari mill and
having a grammage of 75 g/m2, a Cobb 60s value of 21 g/m2, a Gurley value of 18 s and an MD stretchability of 6%; and
- (iv) an unbleached sack kraft paper produced in BillerudKorsnäs' Pietarsaari mill
and having a grammage of about 70 g/m2, a Cobb 60s value of about 23 g/m2, a Gurley value of about 19 s and an MD stretchability of 6.7%.
[0063] Base papers (iii) and (iv) comprised wet strength agent. Further, these base papers
comprised more AKD than (i) and (ii), which is reflected by lower Cobb values.
[0064] Inventive trial 3 was carried out in three rounds.
Coating the smoothest side
[0065] The smoothest side of each of the base papers (i)-(iv) was blade coated with a pre-coating
composition comprising 100 parts of Hydrocarb 60, 13.5 parts of Ligos P1217, 0.62
parts of Finnfix 10 and 0.07 parts of NaOH. The (dry) coat weight of the pre-coating
was 8 g/m
2.
[0066] After drying, the precoated side was blade coated with a barrier coating composition
comprising 100 parts of HG90, 50 parts of Ligos P1217, 0.16 parts of Rheocoat 27 and
0.13 parts of NaOH. The (dry) coat weight of the barrier coating was 7 g/m
2.
[0067] After drying, the double-coated base paper was calendered in a soft nip calender
at a temperature of 80°C using a line load of 70 kN/m.
Results
[0068] The WVTR of the coated papers was measured at 23°C/50% RH and at 38°C/90% RH. The
results are presented in table 3 below.
Table 3. Average WVTR values (g/m
2day) obtained in inventive trial 3.
Round |
Base paper |
WVTR (23°C/50% RH) |
WVTR (38°C/90% RH) |
1 |
(i) |
36 |
789 |
1 |
(iv) |
N/A |
662 |
1 |
(iii) |
34 |
699 |
2 |
(i) |
45 |
862 |
3 |
(i) |
62 |
940 |
3 |
(ii) |
59 |
866 |
[0069] Notably, the coated papers of inventive trial 3 exhibit much better water vapour
barrier properties than those of the coated paper of reference trial 1. Further, the
WVTR values at 38°C/90% RH are lower in inventive trial 3 than in reference trial
2.
[0070] The inventors further note that HG90 (i.e. a clay pigment having particle size distribution
(% < 2 µm) of 96-100 and a shape factor below 20) was uncomplicated to handle in full-scale
operation and did not cause any particular runnability problems.
[0071] It is also notable that the friction properties are satisfactory. Friction is needed
in most processes of conversion of the paper to a sack.
[0072] Further, the recyclability of coated papers produced according to inventive trial
3 was tested in a BillerudKorsnäs laboratory according to the standard method PTS-RH:021/97
Category II. The results are shown in table 4 below.
Table 4. Recyclability of the double-coated base papers of inventive trial 3.
Base paper |
(i) |
(ii) |
(iii) |
(iv) |
Disintegrat-ability |
Total reject |
0.08% |
0.64% |
0.38% |
0.98% |
Recyclability percentage |
99.92% |
99.36% |
99.62% |
99.02% |
Sheet formation |
Adhesive impurities |
None |
None |
None |
None |
(from accept) |
Optical inhomogeneities |
None |
None |
None |
None |
Overall recyclability rating |
Recyclable |
Recyclable |
Recyclable |
Recyclable |
[0073] Notably, also the base papers of lower cobb values (i.e. (iii) and (iv)) were recyclable
[0074] Finally, the recyclability of coated base papers (i) and (ii) produced according
to inventive trial 3 was tested by an external laboratory (PROPAKMA, Germany) according
to the standard method PTS-RH 021:2012. Both coated papers were found to be recyclable
according to the standard. Details of the test results are shown in table 5 below.
Table 5. Recyclability of the double-coated base papers (i) and (ii) of inventive
trial 3 according to PTS-RH 021:2012.
Base paper |
(i) |
(ii) |
Parameter |
Result |
Assessment (per parameter) |
Result |
Assessment (per parameter) |
Loose or easy to remove material |
None |
Recyclable |
None |
Recyclable |
Sheet adhesion test (from total stock) |
Negative |
|
Negative |
|
Residue of defibration test |
0% |
Recyclable |
0% |
Recyclable |
Sheet adhesion test (from screened stock) |
Negative |
Recyclable |
Negative |
Recyclable |
Visual assessment of screened stock |
Dirt specks |
Recyclable |
Dirt specks |
Recyclable |
1. A coated paper comprising a kraft paper substrate, a precoating layer provided on
the kraft paper substrate and a water vapour barrier coating layer provided on the
pre-coating layer, wherein the grammage according to ISO 536:2019 of the coated paper
is 65-155 g/m2, the pre-coating layer comprises inorganic filler and binder in a dry weight ratio
of between 100:25 and 100:5 and the water vapour barrier coating layer comprises clay
pigment and styrene-butadiene co-polymer (SBR) binder in a dry weight ratio between
100:30 and 100:80, wherein the particle size distribution (% < 2 µm) of said clay
pigment is above 90 and the shape factor of said clay pigment is below 20, such as
below 10.
2. The coated paper of claim 1, wherein the grammage according to ISO 536:2019 of the
kraft paper substrate is 50-140 g/m2, such as 50-120 g/m2, such as 60-100 g/m2.
3. The coated paper of claim 1 or 2, wherein the grammage according to ISO 536:2019 of
the coated paper is 65-135 g/m2, such as 75-115 g/m2.
4. The coated paper of any one of the preceding claims, wherein the coat weight of the
pre-coating layer is 4-20 g/m2, preferably 4-12 g/m2, such as 5-10 g/m2.
5. The coated paper of any one of the preceding claims, wherein the coat weight of the
water vapour barrier coating layer is 4-20 g/m2, preferably 4-12 g/m2, such as 5-10 g/m2.
6. The coated paper of any one of the preceding claims, wherein the dry weight ratio
of inorganic filler to binder in the pre-coating layer is between 100:20 and 100:8,
such as between 100:16 and 100:8.
7. The coated paper of any one of the preceding claims, wherein the dry weight ratio
of clay pigment to SBR binder in the water vapour barrier layer is between 100:40
and 100:70, such as between 100:40 and 100:60.
8. The coated paper of any one of the preceding claims, wherein the particle size distribution
(% < 2 µm) of said clay pigment is above 95.
9. A sack comprising a ply formed from the coated paper of any one of the preceding claims.
10. The sack of claim 9, wherein the sack comprises at least two plies and the ply formed
from the coated paper is an outer ply.
11. The sack of claim 10, wherein the sack comprises an inner ply formed from a kraft
paper having a Gurley permeance measured according to ISO 5636-5:2013 of 2-10 s, such
as, such as 4-8 s, such as 4-7 s, such as 5-6 s.
12. The sack of claim 11, wherein the kraft paper of the inner ply has a grammage according
to ISO 536:2019 of 60-90 g/m2, such as 60-80 g/m2.
13. The sack of any one of claims 10-12, wherein the coated paper has a grammage according
to ISO 536:2019 of 75-105 g/m2, such as 75-95 g/m2.
14. The sack of any one of claims 10-13, wherein the paper substrate of the coated paper
has a grammage according to ISO 536:2019 of 60-90 g/m2, such as 60-80 g/m2.