TECHNICAL FIELD
[0001] The present invention relates to a pouched product for oral use. The present invention
further relates to a method for manufacturing a pouched product for oral use.
BACKGROUND
[0002] A pouched product for oral use may be produced by measuring a portion of a filling
material, e.g. a smokeless tobacco composition, and enclosing the portion into a packaging
material forming a saliva-permeable pouch enclosing the filling material.
[0003] US 4,703,765 discloses a device and a method for packaging precise amounts of finely divided tobacco
products, such as snuff tobacco or the like, in a packaging material into which snuff
portions are injected via a fill tube. A flat web of packaging material is formed
into a tubular web around the fill tube by means of longitudinal heat-sealing. Downstream
from the fill tube, heat-sealing means are positioned for transverse sealing of the
packaging material, and also cutting means for severing the packaging material in
the area of the transverse seal to thus form discrete or individual portion packages.
[0004] A pouched product made in the device disclosed in
US 4,703,765 thus has a longitudinal seal, used to seal the flat web of packaging material in
a tubular shape and to hold it there, as well as two transverse seals at a respective
transverse edge of the pouched product.
[0005] Pouched products for oral use may alternatively be produced by placing portions of
a filling material, such as moist snuff, on a nonwoven web using a pouch packer machine
in accordance with the device disclosed in
US 6,135,120. This device comprises feeding means for feeding the tobacco material into pockets
formed in a rotary portioning wheel for portioning the material into portions, at
least one compression means for compressing the tobacco material portions, a unit
for advancing a packaging material, such as a nonwoven web, in synchrony with the
portions, at least one discharge means for discharging the portions from the pockets
to the packaging material, and a forming unit for forming individual portion-packages,
i.e. pouched products for oral use, from the discharged portions and the packaging
material. At the intended point of discharge of the portions to the packaging material,
the packaging material has the form of a tape. The compression means are arranged
to compress the portions in a direction which differs from the discharging and the
feeding directions. The compression is preferably effected in a direction perpendicular
to the discharging and the feeding directions. The compression may be effected in
the axial direction of the portioning wheel whereas the feeding and discharging may
be effected in the radial direction of the wheel.
[0006] Accordingly, also the pouched product made in the device disclosed in
US 6,135,120 has a longitudinal seal used to form the planar tape of packaging material into a
tubular web, as well as a two transverse seals at a respective transverse edge of
the pouched product.
[0007] Even if there exist a number of known methods for manufacturing pouched products
for oral use, as exemplified above, there is still a need to further improve the method,
and thus also the pouched product itself, in order to be able to provide a pouched
product for oral use, which is improved in relation to today's products, e.g. regarding
mouth feel, visual appearance and/or production cost. In particular, it is desirable
to provide a pouched product for oral use, which has a more conformable pouch than
previously known pouched products. There is further a need for a method being less
complex than prior art methods.
SUMMARY
[0008] The object of the present disclosure is to overcome or ameliorate at least one of
the disadvantages of the prior art, or to provide a useful alternative.
[0009] The object above is achieved by the subject-matter of the independent claims. Embodiments
are set forth in the appended dependent claims, in the following description and in
the drawings.
[0010] The present invention relates to a pouched product for oral use according to claim
1. The pouched product comprises a portion of a filling material and a pouch enclosing
the filling material. The pouch has a generally rectangular shape with a first pair
of opposing side edges and a second pair of opposing side edges. The pouch is formed
from a piece of packaging material, which is saliva-permeable and has a pair of opposing
side edges. The pouch comprises two seals only, each seal being located at or adjacent
to a corresponding one of the second pair of opposing side edges of the pouch. A first
edge portion of the piece of packaging material is arranged in an overlap with another
portion of the piece of packaging material, a major part of the overlapping portions
of the piece of packaging material being connected only by surface friction.
[0011] As an example, the pouched product may be a pouched nicotine containing product for
oral use, a pouched tobacco product for oral use and/or a pouched nicotine free product
for oral use.
[0012] The pouched product for oral use is normally sized and configured to fit comfortably
and discreetly in a user's mouth between the upper or lower gum and the lip. The pouched
product is placed as a whole in the mouth, i.e. not only the filling material but
also the enclosing pouch. The pouched product is not intended to be swallowed or eaten.
Instead, the pouch is removed from the mouth after the use and disposed of.
[0013] The pouch of the pouched product comprises only two seals, each seal being located
at or adjacent to a corresponding one of the second pair of opposing side edges of
the pouch. The seals are typically denoted transverse edge seals, since they are made
in a cross-machine direction of the apparatus for manufacturing the pouched product,
i.e. in the transverse direction of the pouched product. The seals may be made by
any method known to the skilled person, e.g. by means of heat-sealing and/or ultrasonic
welding. The seals preferably extend all the way out to the respective side edge,
but there may also be an interspace between the seals and the respective side edge
where the packaging material is un-sealed.
[0014] By the term "seal" as used herein is implied a permanent connection between elements
such as layers of a pouched product as disclosed herein. The seal is produced by actively
connecting the elements in a sealing operation, such as by heat-sealing, also called
thermal welding, ultrasonic welding, and/or by means of adhesive.
[0015] As used herein, the term "edge portion" of a piece of packaging material denotes
a portion of the piece of packaging material located at or adjacent to one edge of
the pair of opposing side edges of the piece of packaging material. The surface of
the edge portion may form up to 50% of the whole surface of the piece of packaging
material. It may for example form in the range of 2-50% or 5-45% or 10-40% or 20-30%
of the whole surface of the piece of packaging material.
[0016] In a major part, i.e. 50% or more, of the overlapping portions of the piece of packaging
material, the overlapping portions are connected to each other only by surface friction,
i.e. the overlapping portions are not connected by a seal. This implies that a major
part of the edge of the first edge portion is free, i.e. not sealed. A minor part,
i.e. less than 50%, preferably less than 30%, more preferably less than 10%, most
preferably less than 5%, of the overlapping portions of the piece of packaging material
may extend into and be included in the transverse edge seals of the pouch. The edge
of the first edge portion may then be perpendicular to the transverse edge seals of
the pouch or at an angle thereto deviating from 90°, as is further described herein.
[0017] The overlap between the portions is utilized to form a closed circumference of the
pouch as seen in a plane being parallel to the transverse edge seals of the pouch
and located somewhere between them, e.g. halfway. This plane thus forms a transverse
cross-sectional plane of the pouched product. Hence, for pouched products according
to the invention, the longitudinal seal or seals used in prior art products can be
dispensed with. This saves an operation step in manufacturing of the pouched products,
which makes manufacturing less complex. In addition, a seal made by welding or by
application of adhesive between layers of material may be perceived by a user as being
stiff and chafing against the mucous membranes in the oral cavity. By dispensing with
the longitudinally extending seal, it is possible to offer a pouched product having
a smoother and more uniform outer surface, as well as being more conformable to the
gums of the user.
[0018] The other portion of the piece of packaging material being overlapped by the first
edge portion may be a second edge portion and/or or any other portion of the piece
of packaging material.
[0019] The pouched product for oral use described herein may be dry, semi-dry or moist.
Generally, dry pouched products have a moisture content of less than 10 wt% and moist
pouched products have a moisture content of above 40 wt%. Semi-dry pouched products
have a moisture content between 10 wt% and 40 wt%.
[0020] The pouched product may be flavoured by mixing the flavour in the filling material
during manufacturing. Additionally or alternatively, the flavour may be added to the
pouched product after it has been manufactured.
[0021] By the term "tobacco" as used herein is meant any part, e.g., leaves, stems, and
stalks, of any member of the genus Nicotiana. The tobacco may be whole, shredded,
threshed, cut, ground, cured, aged, fermented, or treated otherwise, e.g. granulated
or encapsulated.
[0022] The term "tobacco material" is used herein for tobacco leaves or parts of leaves,
such as lamina and stem. The leaves and parts of leaves may be finely divided (disintegrated),
such as ground, cut, shredded or threshed, and the parts of leaves may be blended
in defined proportions in the tobacco material.
[0023] The filling material may comprise a finely divided tobacco material such as a ground
tobacco material or cut tobacco. In addition to the tobacco material, the filling
material may further comprise at least one of the following: water, salt (e.g. sodium
chloride, potassium chloride, magnesium chloride, and any combinations thereof), pH
adjuster, flavouring agent, cooling agent, heating agent, sweetening agent, colorant,
humectant (e.g. propylene glycol or glycerol), antioxidant, preservative (e.g. potassium
sorbate), binder, disintegration aid. In an example, the filling material comprises
or consists of finely divided tobacco material, salt such as sodium chloride, and
a pH adjuster.
[0024] For pouched products with no or low tobacco content, to which nicotine is added,
the nicotine of the filling material may be synthetic nicotine and/or nicotine extract
from tobacco plants. Further, the nicotine may be present in the form of nicotine
base and/or a nicotine salt. The nicotine salt may be free, i.e. it is mixed with
the other components of the pouched product without combining chemically with the
components. Additionally or alternatively, the nicotine salt may combine chemically
with one or more components of the filling material. For instance, the nicotine salt
may combine with alginate particles or cellulose.
[0025] As used herein, the term "moisture content" refers to the total amount of oven volatile
ingredients, such as water and other oven volatiles (e.g. propylene glycol) in the
preparation, composition or product referred to. The moisture content may be given
herein as percent by weight (wt%) of the total weight of the preparation, composition
or product referred to. If not stated otherwise, moisture content is herein given
in relation to the weight of the filling material.
[0026] The moisture content as referred to herein may be determined by using a method based
on literature references
Federal Register/ vol.74, no. 4/712-719/Wednesday, January 7, 2009/Notices "Total
moisture determination" and
AOAC (Association of Official Analytical Chemics), Official Methods of Analysis 966.02:
"Moisture in Tobacco" (1990), Fifth Edition, K. Helrich (ed). In this method, the moisture content is determined gravimetrically by taking 2.5±0.25
g sample and weighing the sample at ambient conditions, herein defined as being at
a temperature of 22°C and a relative humidity of 60%, before evaporation of moisture
and after completion of dehydration. Mettler Toledo's Moisture Analyzer HB43, a balance
with halogen heating technology, is used (instead of an oven and a balance as in the
mentioned literature references) in the values described herein. The sample is heated
to 105°C (instead of 99.5±0.5°C as in the mentioned literature references). The measurement
is stopped when the weight change is less than 1 mg during a 90 seconds time frame.
The moisture content as weight percent of the sample is then calculated automatically
by the Moisture Analyzer HB43.
[0027] Pouched products for oral use may or may not be post-moisturized after pouch formation.
Pouched products which are not post-moisturized are herein referred to as non-post-moisturized.
Post-moisturized pouched products may be produced by spraying water on the pouched
product before packaging the pouched products in user containers. Post-moisturized
pouches are sometimes referred to as "original" products. Non-post-moisturized pouched
products are sometimes referred to as "white" products and are by some consumers considered
to have a more appealing visual appearance. The moisture content of the final pouched
product comprising a moist or semi-dry snuff or snus product is normally within the
range of from 25 to 55 wt% based on the weight of the pouched product.
[0028] The saliva-permeable packaging material, which is used for the pouch, is typically
a nonwoven material, such as viscose. It may include a chemical binder. Nonwoven materials
are fabrics that are neither woven nor knitted. Methods for the manufacturing nonwoven
materials are commonly known in the art. The packaging material is typically provided
in a web-shaped or sheet-shaped format.
[0029] Pouched products for oral use are normally sized and configured to fit comfortably
and discreetly in a user's mouth between the upper or lower gum and the lip. In general,
pouched products for oral use have a generally rectangular shape as seen in a top
view, while being pillow-like when seen in a three-dimensional view. Some typical
shapes (length x width) of commercially available pouched products for oral use are,
for instance, 35 mm x 20 mm, 34/35 mm x 14 mm, 33/34 mm x 18 mm, 27/28 mm x 14 mm,
34 mm x 10 mm and 38 x 14 mm. Typical pouched products for oral use may have a maximum
length within the range of from 25 to 40 mm along the longitudinal direction of the
pouched product and a maximum width within the range of from 5 to 20 mm along the
transverse direction of the pouched product. The thickness ("height") of the pouched
product is normally within the range of from 2 to 8 mm. The total weight of commercially
available pouched products for oral use are typically within the range from about
0.3 to about 3.5 g, such as from about 0.5 to 1.7 g, per pouched product.
[0030] A user container typically contains in the range of 10-30 pouched products, such
as in the range of 20-25 pouched products. The pouched products may be placed randomly
in the user container or in a pattern, for instance as described in
WO 2012/069505 A1. The user container as disclosed herein is consumer package having a shape and a
size adapted for conveniently carrying the consumer package in a pocket or in a handbag
and may be used for packaging any known type of pouched product for oral use.
[0031] The term "tubular" as used herein refers to any cross-sectional shape; specifically,
it is not restricted to a circular tubular web. The piece of tubular web may e.g.
have a square, polygonal, elliptical or oval cross-sectional shape. However, the piece
of tubular web has a closed circumference, such that the piece of tubular web is able
to retain the filling material inside the piece of tubular web.
[0032] The overlap between the portions may have a width in the range of 3-40 mm, preferably
4-30 mm, more preferably 5-25 mm, most preferably 10-20 mm. The width of the overlap
is determined as the narrowest width of the overlap. The width of the overlap is typically
selected to be sufficiently wide to reduce, or preferably avoid, the risk of filling
material leaking out from the pouch.
[0033] The overlap may constitute in the range of 5%-100% of an exterior surface of the
pouch, preferably 10%-95%, more preferably 20%-90%, most preferably 25%-80%. There
may hence be surface portions of the pouch with no overlap. The exterior surface is
the total outer surface of the pouch. Hence, both outer sides of the rectangular pouched
product are included.
[0034] The part of the overlapping portions of the piece of packaging material connected
only by surface friction may constitute at least 50% of a surface area of the overlap,
preferably at least 70%, more preferably at least 90%, most preferably at least 95%.
As mentioned above, a minor part of the overlapping portions of the piece of packaging
material, i.e. less than 50%, preferably less than 30%, more preferably less than
10%, most preferably less than 5%, may extend into and be included in the transverse
edge seals of the pouch.
[0035] The piece of packaging material forming the pouch may comprise or be constituted
by at least one web-shaped piece of packaging material being helically wound thereby
forming adjacent revolutions, wherein the first edge portion of packaging material
in the overlap is an edge portion of one revolution and the other portion in the overlap
is an edge portion of an adjacent revolution. It is also feasible to use more than
one web-shaped piece of packaging material, e.g. two, with one of the web-shaped pieces
of packaging material being located inside the other. In that case, the two web-shaped
pieces of packaging material may be wound in the same helical manner or may be wound
in different ways.
[0036] If helically wound, an edge of the first edge portion may have an angle in the range
of 5°-85° in relation to an extension direction of the seals, i.e. the transverse
edge seals of the pouch, preferably in the range of 10°- 75°, more preferably in the
range of 15°- 65°, most preferably in the range of 20°- 50°.
[0037] As an alternative or a complement to the helically wound web-shaped piece of packaging
material, the pouch may comprise an edge of the first edge portion being arranged
perpendicularly, or substantially perpendicularly, to the two seals of the pouch.
Hence, the edge extends in a direction often referred to as a longitudinal direction
of the pouched product, since it coincides with a machine direction of the apparatus
for manufacturing the pouched product.
[0038] In that case, the piece of packaging material may comprise or be constituted by a
single sheet of packaging material formed such that opposite edge portions of the
sheet are arranged in the overlap. The sheet may be a cut piece of a web-shaped packaging
material. Thereby, the side edges of the web-shaped piece of packaging material may
be arranged such that they coincide with the two long side edges of the pouched product.
Hence, the width of the respective edge portions each forms about 1/3 of the width
of the web-shaped piece of packaging material, such that the overlap forms about half
the exterior surface of the pouch.
[0039] As an alternative to using a single sheet, the piece of packaging material may comprise
or be constituted by two sheets of the packaging material arranged such that they
at least partly overlap, one of the sheets being arranged inside the other sheet,
i.e. with an outer surface of the inner sheet facing an inner surface of the outer
sheet. As used herein, the outer surface of a pouch material is the surface facing
away from the filling material in the pouch and the inner surface of the pouch material
is the surface facing towards the filling material in the pouch. The overlap may then
constitute in the range of 90%-100% of an exterior surface of the pouch, preferably
95%-100%.
[0040] A degree of filling of the pouch by the portion of the filling material may be in
the range of 40%-100%, preferably in the range of 50%-90%, more preferably in the
range of 60%-80%. The filling material presses the packaging material of the pouch
outwards, which helps the pouch to keep its intended shape. Furthermore, the filling
material may thereby help to hold the overlapping portions in contact with each other
in the overlap. The degree of filling is measured by comparing the actual amount of
filling material enclosed in the pouch with the case when that pouch is maximally
filled with that filling material. Hence, the comparison is made for the actual pouch
with the actual filling material. 100% denotes that the pouch is maximally filled.
The measurement is made at set ambient conditions, with a temperature of 22°C and
a relative humidity of 60%. However, the overlap could be held by surface friction
also for a theoretical case with 0% filling material.
[0041] The packaging material may have a kinetic coefficient of friction of at least 0.03,
preferably at least 0.05, more preferably at least 0.07 as measured with ASTM D1894.
This level of the coefficient of friction has proven to give adequate surface friction
in the overlap.
[0042] The present invention also relates to a method for manufacturing a pouched product
for oral use. The method comprises:
- a) providing a saliva-permeable web-shaped packaging material, the web-shaped material
comprising a first edge portion and a second edge portion located at opposite side
edges of the web-shaped packaging material,
- b) forming a tubular web of the web-shaped packaging material by arranging the first
edge portion of the web-shaped packaging material in an overlap with another portion
of the web-shaped packaging material, the overlap being connected only by surface
friction, the tubular web extending in a longitudinal direction,
- c) providing the tubular web with a first transverse seal,
- d) supplying a portion of a filling material into the tubular web,
- e) providing the tubular web with a second transverse seal, thereby forming the pouched
product.
[0043] The pouched product which is produced by the method is typically the pouched product
for oral use as described herein. Hence, the pouched product for oral use as described
herein may be manufactured by the method as described herein. The details described
for herein for the pouched product for oral use are valid for the method as well.
Further, the effects and advantages described for the pouched product for oral use
are valid for the method as well and will not be described again.
[0044] The longitudinal direction of the pouched product typically corresponds to the machine
direction of an apparatus for manufacturing the pouched product for oral use. The
transverse direction typically corresponds to the cross-machine direction of the apparatus
for manufacturing the pouched product. Hence, the transverse seals formed in steps
c) and e) are perpendicular to, or at least substantially perpendicular to, the machine
direction of the apparatus for manufacturing the pouched product. The transverse seal
may be made by any method known to the skilled person, e.g. by means of heat-sealing
and/or ultrasonic welding.
[0045] When comparing the method according to the invention with prior art methods, it can
be seen that a step of longitudinal sealing has been omitted. This makes the method
less complex. Transvers sealing with heat-sealing is for example described in
US 4,703,
765. Ultrasonic sealing is for example described in
WO 2017093486 A1.
[0046] The method may further comprise:
f) separating the pouched product from a subsequent pouched product in or at the second
transverse seal.
[0048] Typically the separation is made within, preferably close to the centre, of the second
transverse seal. Thereby, the second transverse seal is split in two portions, typically
halves, wherein one portion forms a transverse edge seal of the pouched product and
the other portion forms a transverse edge seal of the subsequent product. Hence, step
e) will correspond to step c) when the subsequent pouched product for oral use is
manufactured.
[0049] Step b) may comprise winding the web-shaped packaging material in a helical manner
to form the tubular web, the edge portions of adjacent revolutions being arranged
in the overlap.
[0050] As an alternative, step b) may comprise arranging an edge of the first edge portion
in the longitudinal direction of the tubular web. This corresponds to the pouch comprising
an edge of the first edge portion arranged perpendicularly, or substantially perpendicularly,
to the two seals of the pouch.
[0051] In an embodiment,
step a) may comprise providing an additional saliva-permeable web-shaped packaging
material comprising two edge portions located at opposite edges of the additional
web-shaped packaging material, and
step b) may comprise forming a tubular web of the web-shaped packaging material by
arranging the web-shaped packaging material and the additional web-shaped packaging
material such that they at least partly overlap, the additional web-shaped packaging
material thereby being arranged inside the web-shaped packaging material.
[0052] This corresponds to a pouched product, in which the piece of packaging material comprises
or is constituted by two sheets of the packaging material arranged such that they
at least partly overlap, one of the sheets being arranged inside the other sheet.
The overlap may the constitute in the range of 90%-100% of an exterior surface of
the pouch, preferably 95%-100%.
BRIEF DESCRIPTION OF THE DRAWINGS
[0053] The present invention will hereinafter be further explained by means of non-limiting
examples with reference to the appended drawings wherein:
- Fig. 1a-b
- illustrate a pouched product for oral use according to prior art,
- Fig. 2a-c
- illustrate a pouched product for oral use according to a first embodiment of the invention,
- Fig. 3a-b
- illustrate helical winding,
- Fig. 4a-b
- illustrate a pouched product for oral use according to a second embodiment of the
invention,
- Fig. 5a-b
- illustrate a pouched product for oral use according to a third embodiment of the invention,
and
- Fig. 6
- illustrates a method for manufacturing a pouched product for oral use according to
the invention.
[0054] It should be noted that the appended drawings are not necessarily drawn to scale
and that the dimensions of some features of the present invention may have been exaggerated
for the sake of clarity. The drawings are schematic.
DETAILED DESCRIPTION
[0055] The invention will in the following be exemplified by embodiments. It should however
be realized that the embodiments are included in order to explain principles of the
invention and not to limit the scope of the invention, defined by the appended claims.
Details from two or more of the embodiments may be combined with each other.
[0056] Fig. 1a and 1b schematically illustrate a pouched product 101 for oral use according
to prior art, with Fig. 1a showing a top view and Fig. 1b showing a transverse cross-section
taken along the dashed line in Fig. 1a. The prior art product 101 has a rectangular
shape with a maximum length L
0 extending in a length direction, also referred to herein as a longitudinal direction,
and a maximum width W
0 extending in a width direction, also referred to herein as a transverse direction,
whereby the maximum length L
0 is greater than the maximum width W
0. The prior art pouched product 101 comprises a filling material 102 and a saliva-permeable
pouch 104 enclosing the filling material 102. The prior art product 101 comprises
two long side edges 103a, 103b and two short side edges 105a, 105b. The prior art
product 101 also has a maximum height H
0 extending in a height direction, being perpendicular to the length direction and
to the width direction, not seen in the top view of Fig. 1a, but indicated in Fig.
1b.
[0057] The prior art pouched product 101 comprises at least one seal 107 extending in the
length direction. Typically, and as illustrated in Fig. 1a, there is a single seal
107 extending in the length direction. This seal is often called a longitudinal seal,
since, when manufacturing the prior art product 101, this seal is made along the direction
of travel of the web forming the pouch 104. The longitudinal seal is often positioned
spaced apart from the long side edges 103a, 103b. Thereby it is often preferred to
position it at or close to the longitudinal centre-line, as is illustrated in Fig.
1a. The longitudinal seal 107 may be made by any method known to the skilled person,
e.g. by means of heat-sealing and/or ultrasonic welding. In a commonly used method,
the longitudinal seal 107 is formed as a fin seal, which is folded down upon the packaging
material, such that the pouch 104 locally comprises three plies of packaging material
on top of the filling material. See the cross-sectional view in Fig. 1b, where the
three plies on top of each other are illustrated in an exaggerated way to make the
three plies visible.
[0058] The prior art pouched product 101 further comprises two seals 109a, 109b extending
in the width direction. The two seals 109a, 109b seal the two short side edges 105a,
105b and thus form edge seals. These seals 109a, 109b are often called transverse
edge seals, since, when manufacturing the prior art product 101, these edge seals
are made transverse to the direction of travel of the web forming the pouch. In the
transverse seals, the packaging material forming the saliva-permeable pouch is double.
The transverse edge seals 109a, 109b may be made by any method known to the skilled
person, e.g. by means of heat-sealing and/or ultrasonic welding. Since the transverse
edge seals 109a, 109b are made after the longitudinal seal 107, i.e. downstream in
the manufacturing apparatus, the longitudinal seal 107 is included in the transverse
edge seals 109a, 109b, i.e. the longitudinal seal 107 forms part of the transverse
edge seals 109a, 109b. The longitudinal seal 107 may e.g. be welded into the transverse
edge seals 109a, 109b. There will then locally be four plies of packaging material
on top of each other.
[0059] Fig. 2a-c schematically illustrate a pouched product 201 for oral use according to
the invention, with Fig. 2a showing a top view, Fig. 2b showing a transverse cross-section
and Fig. 2c showing a longitudinal cross-section, with the cross-sections taken along
the dashed lines of Fig. 2a. The pouched product 201 comprises a filling material
202 and a saliva-permeable pouch 204 enclosing the filling material 202. The pouch
204 is formed by a web-shaped piece of packaging material being helically wound.
[0060] The pouched product 201 according to the invention has a rectangular shape and comprises
two long side edges 203a, 203b and two short side edges 205a, 205b. Similar to the
prior art pouched product 101, the pouched product 201 according to the invention
comprises two transverse seals but, contrary to prior art, it has no longitudinal
seal. The transverse seals form a first 209a and a second transverse edge seal 209b
sealing along the two short side edges 205a, 205b of the pouched product 201. The
transverse edge seals 209a, 209b preferably extend all the way out to the respective
short side edge 205a, 205b, but there may also be an interspace between the transverse
edge seal 209a, 209b and the short side edge 205a, 205b where the packaging material
is left un-sealed. The transverse seals 209a, 209b may be made by any method known
to the skilled person, e.g. by means of heat-sealing, and/or ultrasonic welding, with
ultrasonic welded seals shown in the illustrated embodiment.
[0061] The pouch 204 has a maximum length L extending in a length direction and a maximum
width W extending in a width direction, whereby the maximum length L is greater than
the maximum width W. The pouched product 201 also has a maximum height H extending
in a height direction, being perpendicular to the length direction and to the width
direction, not seen in the top view of Fig. 2a, but seen in the views of Fig. 2b and
2c. The maximum width W is measured at the short side edge 205a, 205b where the pouched
product 201 only has the height of twice the thickness of the packaging material.
[0062] The principle of helical winding is schematically illustrated with the help of Fig.
3a and 3b. A web-shaped piece 301 of packaging material has a narrowest width a and
a pair of opposing side edges, with a first side edge 311a and a second side edge
311b, see Fig. 3a. A first edge portion 313a and a second edge portion 313b of the
web-shaped piece 301 of packaging material are located at the edge of the respective
side edges. In the illustrative example of Fig. 3a and 3b, each edge portion 313a,
313b extends about 20% of the whole surface of the web-shaped piece 301 of packaging
material.
[0063] The web-shaped piece 301 of packaging material is helically wound, e.g. around a
tube 305 having a diameter d, see Fig. 3b, such that a tubular web 307 is formed.
The tube 305 may e.g. be a fill tube of an apparatus for manufacturing oral pouched
products. A centre axis A of the tube 305 extends in a longitudinal direction of the
tubular web 307. The tubular web 307 has a circumference being given by the outer
circumference of the tube 305, i.e. πd. The web-shaped piece 301 of packaging material
forms adjacent revolutions, which overlap with each other. Thereby, the first edge
portion of packaging material in the overlap is a first edge portion 313a of one revolution
and the other portion in the overlap is a second edge portion 313b of an adjacent
revolution. The width b of the overlap between adjacent revolutions is about to 20%
of the width a of the web-shaped piece 301 of packaging material in the illustrated
embodiment. Since there is an overlap of about 20% for both the preceding and the
subsequent revolutions, the total overlap in relation to the width a of the web-shaped
piece of packaging material is b+b, i.e. about 40%. An edge of the first edge portion
313a, i.e. the first side edge 311a of the web-shaped piece 301 of packaging material,
has an angle α in the range of 5°- 85° in relation to an extension direction of the
transverse edge seals to be made when forming the pouch, preferably in the range of
10°- 75°, more preferably in the range of 15°- 65°, most preferably in the range of
20°- 50°, in Fig. 3b illustrated as 40°.
[0064] In the embodiment of the pouched product for oral use illustrated in Fig. 2a-2c,
the overlap between adjacent revolutions is close to 50% of the width of the web-shaped
piece of packaging material. Since there is an overlap of close to 50% for both the
preceding and the subsequent revolutions, the total overlap in relation to the web-shaped
piece of packaging material is close to 100%. One of the side edges 211a of the web-shaped
piece of packaging material can be seen on the outside of the pouch 204, while the
other side edge 211b is located inside the pouch 204, see Fig. 2c. The first edge
portion 213a adjacent to the first side edge 211a overlaps with the second edge portion
213b of the adjacent revolution. The first side edge 211a has an angle α in the range
of 5°- 85° in relation to an extension direction of the transverse edge seals of the
pouch, preferably in the range of 10°- 75°, more preferably in the range of 15°- 65°,
most preferably in the range of 20°- 50°, see Fig. 2a wherein it is illustrated as
45°. The maximum width W of the pouched product 201 is half the circumference of the
tubular web, e.g. πd/2 if the tubular web of Fig. 3b is used.
[0065] The filling material 202 presses the packaging material of the pouch outwards, which
helps the pouch 204 to keep its intended shape. The filling material 202 may further
help to hold the overlapping portions 231a, 213b in contact with each other in the
overlap by expanding the pouch 204 from the inside. A degree of filling of the pouch
by the portion of the filling material may in the range of 40%-100%, preferably in
the range of 50%-90%, more preferably in the range of 60%-80%. However, the overlap
could be held by surface friction also for a theoretical case with 0% filling material.
[0066] The packaging material may be selected to have a kinetic coefficient of friction
of at least 0.03, preferably at least 0.05, more preferably at least 0.07 as measured
with ASTM D1894. This level of the coefficient of friction has proven to give adequate
surface friction to hold the overlapping portions in the overlap. Further, the width
of the overlap will influence the ability to hold the overlapping portions in the
overlap. Hence, it may be appropriate to use a material with a higher coefficient
of friction if the overlap is narrow as compared to a pouched product with a wider
overlap.
[0067] When comparing the pouched product 201 according to the invention and the prior art
pouched product 101, it can be seen that they may have similar generally rectangular
shapes. However, they differ from each other regarding the presence or absence of
the at least one longitudinal seal 107. They may also differ as regards size and/or
length to width ratio. They may also differ as regards the widths of the transverse
seals. Both Fig. 1a and Fig. 2a show a typical width for transverse edge seals made
with ultrasonic welding, which may have a width of less than 2 mm, preferably less
than 1 mm, more preferably less than 0.5 mm. If instead using the commonly known technology
of heat-sealing, the seal would typically be wider, e.g. in the range of 2-5 mm, which
can be seen for the longitudinal seal 107 of the prior art product 101.
[0068] In a filling material leakage test, a reference product made according to prior art,
looking like the prior art embodiment illustrated in Fig. 1a and 1b, was compared
to a sample product made according to the first embodiment of the invention illustrated
in Fig. 2a-2c. The reference product was ZYN Spearmint Mini Dry, which is a commercially
available product, having article no 7909. The reference product comprised a longitudinal
seal made by heat-sealing. Both the reference product and the sample product comprised
transverse edge seals made by ultrasonic welding.
[0069] The pouch of the sample product consisted of the same type of packaging material
as the pouch of the reference product. The packaging material of the sample product
was helically wound with an overlap of close to 50% for both the preceding and subsequent
revolution, see Fig. 2a-c. Further, the filling material, i.e. the content enclosed
by the pouch, being a granulate in this example, was of the same type for the sample
product as for the reference product. The degree of filling of the pouch by the portion
of the filling material was about 70% for both the reference product and the sample
product. The moisture content of the filling material was 1,57% for both the reference
product and the sample product.
[0070] The weight of both the reference product and the sample product was 0.40 g. It then
turned out that the reference product comprised in average 0.37 g filling material
per pouch and the sample product 0.33 g filling material per pouch.
[0071] Test procedure: The filling material leakage test was performed on a Retsch/ AS 200
control vibrating sieve with a mesh size of 1.7 mm. First 20 pouches of the reference
product were placed on the sieve and vibrated for 1 minute with an amplitude of 1
mm, then 20 pouches of the sample product were placed on the sieve and vibrated for
1 minute with an amplitude of 1 mm.
[0072] The weight of any filling material potentially having leaked out from the 20 pouches
was checked, but was, if any, for both the reference product and the sample product
below the detection limit of 0.01g of the scale.
[0073] Fig. 4a-b schematically illustrate a pouched product 401 for oral use according to
another embodiment of the invention, with Fig. 4a showing a top view and Fig. 4b a
transverse cross-section taken along the dashed line. The pouch 404 is formed by a
single sheet, the sheet being a cut-off portion of the web-shaped piece of packaging
material. Opposite edge portions 413a, 413b of the sheet are arranged in the overlap,
as can be seen in the cross-sectional view of Fig. 4b, with the first edge portion
being outside the second edge portion 413b. The pouch 404 comprises two transverse
edge seals 409a, 409b, but no longitudinal seal.
[0074] In the illustrated embodiment, the side edges 411a, 411b of the web-shaped piece
of packaging material are arranged such that they coincide with the two long side
edges 403a, 403b of the pouched product. Hence, the side edges 411a, 411b are perpendicular
to the transverse edge seals 409a, 409b. The widths of the respective edge portions
413a, 413b each forms about 1/3 of the width of the sheet, such that the overlap forms
about half the exterior surface of the pouch 404.
[0075] Fig. 5a-b schematically illustrate a pouched product 501 for oral use according to
another embodiment of the invention, with Fig. 5a showing a top view and Fig. 5b a
transverse cross-section taken along the dashed line. The pouch 504 is formed by a
first sheet 515 of packaging material and a second sheet 517 of packaging material
arranged such that they at least partly overlap, the second sheet 517 being arranged
inside the first sheet 515. The first sheet 515 comprises two edge portions 513a,
513b located at a respective side edge 511a, 511b of the sheet. The second sheet 517
comprises two edge portions 521a, 521b located at a respective side edge 519a, 519b
of the sheet. The pouch 504 further comprises two transverse edge seals 509a, 509b,
but no longitudinal seal.
[0076] In the illustrated embodiment, the width of each sheet 515, 517 is about as large
as the circumference of the pouch 504. The side edges 511a, 511b of the first sheet
515 are arranged such that they almost meet each other. Also the side edges 519a,
519b of the second sheet 517 are arranged such that they almost meet each other. Further,
the side edges 511a, 511b, 519a, 519b are perpendicular to the transverse edge seals
509a, 509b. The widths of the respective edge portions 513a, 513b; 521a, 521b each
forms about 50% of the width of the sheets 515, 517, such that the overlap forms about
100% of the exterior surface of the pouch 504.
[0077] Fig. 6 illustrates a method 601 for manufacturing a pouched product for oral use.
The pouched product of the method typically is the pouched product 201, 401, 501 for
oral use as described herein. Hence, the pouched product 201, 401, 501 for oral use
as described herein may be manufactured by the method 601 as described herein. The
details for the pouched product 201, 401, 501 for oral use, e.g. described in conjunction
with Fig. 2-5 are valid for the method as well.
[0078] The method 601 comprises:
- a) providing a saliva-permeable web-shaped packaging material 301, the web-shaped
material 301 comprising a first edge portion 313a and a second edge portion 313b located
at opposite side edges of the web-shaped packaging material 301,
- b) forming a tubular web 307 of the web-shaped packaging material 301 by arranging
the first edge portion 313a of the web-shaped packaging material 301 in an overlap
with another portion 313b of the web-shaped packaging material 301, the overlap being
connected only by surface friction, the tubular web 307 extending in a longitudinal
direction,
- c) providing the tubular web 307 with a first transverse seal,
- d) supplying a portion of a filling material 202 into the tubular web 307,
- e) providing the tubular web 307 with a second transverse seal, thereby forming the
pouched product.
[0079] The longitudinal direction of the pouched product 201, 401, 501 typically corresponds
to the machine direction of an apparatus for manufacturing the pouched product for
oral use, in Figure 3b illustrated by the longitudinal direction along the central
axis A of the tube 305. The transverse direction typically corresponds to the cross-machine
direction of the apparatus for manufacturing the pouched product. Hence, the transverse
seals formed in steps c) and e) are perpendicular to, or at least substantially perpendicular
to, the machine direction of the apparatus for manufacturing the pouched product.
The transverse seal may be made by any method known to the skilled person, e.g. by
means of heat-sealing and/or ultrasonic welding.
[0080] The method may further comprise:
f) separating the pouched product from a subsequent pouched product in or at the second
transverse seal.
[0081] Typically the separation is made within, preferably close to the centre, of the second
transverse seal. Thereby, the second transverse seal is split in two portions, typically
halves, wherein one portion forms a transverse edge seal 209b of the pouched product
and the other portion forms a transverse edge seal 209a of the subsequent product.
Hence, step e) will correspond to step c) when the subsequent pouched product for
oral use is manufactured.
[0082] Step b) may comprise winding the web-shaped packaging material 301 in a helical manner
to form the tubular web 307, the edge portions 313a, 313b of adjacent revolutions
being arranged in the overlap. Reference is thereby made to the helical winding shown
in Fig. 3a-3b and the text describing those figures. The resulting pouched product
may look like the pouched product 201 illustrated in Fig. 2a-c.
[0083] As an alternative, step b) may comprise arranging an edge 411a; 511a of the first
edge portion 413a; 513a in the longitudinal direction of the tubular web. The resulting
pouched product may look like the pouched products 401, 501 illustrated in Fig. 4a-5b.
The method step b) then corresponds to the pouch 404, 504 comprising an edge 411a,
511a of the first edge portion 413a, 513 being arranged perpendicularly to, or substantially
perpendicularly to, the two seals 409a, 409b; 509a, 509b of the pouch 404, 504.
[0084] In an embodiment,
step a) comprises providing an additional saliva-permeable web-shaped packaging material
comprising two edge portions 521a, 521b located at opposite edges 519a, 519b of the
additional web-shaped packaging material, and
step b) comprises forming a tubular web of the web-shaped packaging material by arranging
the web-shaped packaging material and the additional web-shaped packaging material
such that they at least partly overlap, the additional web-shaped packaging material
thereby being arranged inside the web-shaped packaging material.
[0085] This corresponds to a pouched product, in which the piece of packaging material comprises
or is constituted by two sheets of the packaging material arranged such that they
at least partly overlap, one of the sheets being arranged inside the other sheet.
The overlap may the constitute in the range of 90%-100% of an exterior surface of
the pouch, preferably 95%-100%.
[0086] An example of such a product is illustrated in Fig. 5a-b, wherein the saliva-permeable
web-shaped packaging material corresponds to the first sheet 515 and the additional
saliva-permeable web-shaped packaging material corresponds to the second sheet 517.
[0087] Further modifications of the invention within the scope of the appended claims are
feasible. As such, the present invention should not be considered as limited by the
embodiments and figures described herein. Rather, the full scope of the invention
should be determined by the appended claims, with reference to the description and
drawings.
1. A pouched product (201) for oral use,
the pouched product (201) comprising a portion of a filling material (202) and a pouch
(204) enclosing the filling material (202),
the pouch (204) having a generally rectangular shape with a first pair of opposing
side edges (203a, 203b) and a second pair of opposing side edges (205a, 205b), the
pouch (204) being formed from a piece of packaging material (301), the packaging material
(301) being saliva-permeable and having a pair of opposing side edges (311a, 311b),
characterized in that
the pouch (204) comprises two seals (209a, 209b) only, each seal (209a, 209b) being
located at or adjacent to a corresponding one of the second pair of opposing side
edges (205a, 205b) of the pouch (204), and
a first edge portion (213a) of the piece of packaging material is arranged in an overlap
with another portion (213b) of the piece of packaging material, a major part of the
overlapping portions (213a, 213b) of the piece of packaging material being connected
only by surface friction.
2. The pouched product (201) for oral use according to claim 1, wherein the overlap has
a width (b) in the range of 3-40 mm, preferably 4-30 mm, more preferably 5-25 mm,
most preferably 10-20 mm.
3. The pouched product (201) for oral use according to claim 1 or 2, wherein the overlap
constitutes in the range of 5%-100% of an exterior surface of the pouch (204), preferably
10%-95%, more preferably 20%-90%, most preferably 25%-80%.
4. The pouched product (201) for oral use according to any one of claims 1-3, wherein
the part of the overlapping portions of the piece of packaging material connected
only by surface friction constitutes at least 50% of a surface area of the overlap,
preferably at least 70%, more preferably at least 90%, most preferably at least 95%.
5. The pouched product (201) for oral use according to any one of claims 1-4, wherein
the piece of packaging material forming the pouch (204) comprises or is constituted
by at least one web-shaped piece of packaging material (301) being helically wound
thereby forming adjacent revolutions, wherein the first edge portion (213a) of packaging
material in the overlap is an edge portion of one revolution and the other portion
in the overlap is an edge portion (213b) of an adjacent revolution.
6. The pouched product (201) for oral use according to claim 5, wherein an edge (211a)
of the first edge portion (213a) has an angle (α) in the range of 5°- 85° in relation
to an extension direction of the seals (209a, 209b), preferably in the range of 10°-
75°, more preferably in the range of 15°- 65°, most preferably in the range of 20°-
50°.
7. The pouched product (201) for oral use according to any one of claims 1-4, wherein
an edge (221a) of the first edge portion (213a) is arranged perpendicularly, or substantially
perpendicularly to the two seals (209a, 209b) of the pouch (201).
8. The pouched product (401) for oral use according to any one of claims 1-4 or 7, wherein
the piece of packaging material comprises or is constituted by a single sheet formed
such that opposite edge portions (413a, 413b) of the sheet are arranged in the overlap.
9. The pouched product (501) for oral use according to any one of claims 1-4 or 7, wherein
the piece of packaging material comprises or is constituted by two sheets (515, 517)
of the packaging material arranged such that they at least partly overlap, one of
the sheets being arranged inside the other sheet.
10. The pouched product (201) for oral use according to any one of the preceding claims,
wherein a degree of filling of the pouch (204) by the portion of the filling material
(202) is in the range of 40%-100%, preferably in the range of 50%-90%, more preferably
in the range of 60%-80%.
11. The pouched product (201) for oral use according to any one of the preceding claims,
wherein the packaging material has a kinetic coefficient of friction of at least 0.03,
preferably at least 0.05, more preferably at least 0.07 as measured with ASTM D1894.
12. The pouched product (201) for oral use according to any one of the preceding claims,
wherein the pouched product (201) is a pouched nicotine containing product for oral
use, a pouched tobacco product for oral use and/or a pouched nicotine free product
for oral use.
13. A method (601) for manufacturing a pouched product (201) for oral use, the method
comprising:
a) providing a saliva-permeable web-shaped packaging material (301), the web-shaped
material (301) comprising a first edge portion (313a) and a second edge portion (313b)
located at opposite side edges of the web-shaped packaging material (301),
b) forming a tubular web (307) of the web-shaped packaging material by arranging the
first edge portion (313a) of the web-shaped packaging material in an overlap with
another portion (313b) of the web-shaped packaging material, the overlap being connected
only by surface friction, the tubular web (307) extending in a longitudinal direction
(A),
c) providing the tubular web (307) with a first transverse seal,
d) supplying a portion of a filling material (202) into the tubular web (307),
e) providing the tubular web (307) with a second transverse seal, thereby forming
the pouched product (201).
14. The method according to claim 13, wherein step b) comprises winding the web-shaped
packaging material (301) in a helical manner to form the tubular web (307), the edge
portions (313a, 313b) of adjacent revolutions being arranged in the overlap.
15. The method according to claim 13, wherein step b) comprises arranging an edge (411a,
511a) of the first edge portion (413a, 513a) in the longitudinal direction of the
tubular web.
16. The method according to any one of claims 13-15, wherein
step a) comprises providing an additional saliva-permeable web-shaped packaging material
comprising two edge portions (521a, 521b) located at opposite edges (519a, 519b) of
the additional web-shaped packaging material, and
step b) comprises forming a tubular web of the web-shaped packaging material by arranging
the web-shaped packaging material and the additional web-shaped packaging material
such that they at least partly overlap, the additional web-shaped packaging material
thereby being arranged inside the web-shaped packaging material.