NZ614475B2 - Method and apparatus for imparting an organoleptic quality to a recipient product - Google Patents
Method and apparatus for imparting an organoleptic quality to a recipient product Download PDFInfo
- Publication number
- NZ614475B2 NZ614475B2 NZ614475A NZ61447512A NZ614475B2 NZ 614475 B2 NZ614475 B2 NZ 614475B2 NZ 614475 A NZ614475 A NZ 614475A NZ 61447512 A NZ61447512 A NZ 61447512A NZ 614475 B2 NZ614475 B2 NZ 614475B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- product
- storage chamber
- recipient
- donor
- product storage
- Prior art date
Links
- 238000003860 storage Methods 0.000 claims abstract description 162
- 241000208125 Nicotiana Species 0.000 claims abstract description 63
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims abstract description 63
- 239000012530 fluid Substances 0.000 claims abstract description 57
- 239000000126 substance Substances 0.000 claims abstract description 49
- 238000000034 method Methods 0.000 claims abstract description 24
- 235000016247 Mentha requienii Nutrition 0.000 claims abstract description 10
- 235000002899 Mentha suaveolens Nutrition 0.000 claims abstract description 10
- 235000006682 bigleaf mint Nutrition 0.000 claims abstract description 10
- 235000006679 mint Nutrition 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims description 14
- 240000007154 Coffea arabica Species 0.000 claims description 11
- 230000000391 smoking Effects 0.000 claims description 11
- 238000009835 boiling Methods 0.000 claims description 9
- 239000000470 constituent Substances 0.000 claims description 8
- 230000004044 response Effects 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 6
- 235000016639 Syzygium aromaticum Nutrition 0.000 claims description 4
- 240000005147 Syzygium aromaticum Species 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 235000007265 Myrrhis odorata Nutrition 0.000 claims description 3
- 235000012550 Pimpinella anisum Nutrition 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 2
- 229960004873 LEVOMENTHOL Drugs 0.000 claims description 2
- 229940041616 Menthol Drugs 0.000 claims description 2
- 239000011261 inert gas Substances 0.000 claims description 2
- 241000592238 Juniperus communis Species 0.000 claims 1
- 240000009023 Myrrhis odorata Species 0.000 claims 1
- 206010002368 Anger Diseases 0.000 abstract 1
- 230000035943 smell Effects 0.000 abstract 1
- 241000721662 Juniperus Species 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000002156 mixing Methods 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 239000000428 dust Substances 0.000 description 6
- 238000001802 infusion Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 239000000177 juniperus communis l. berry Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 241000911175 Citharexylum caudatum Species 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 235000021028 berry Nutrition 0.000 description 4
- 235000019505 tobacco product Nutrition 0.000 description 4
- 235000008227 Illicium verum Nutrition 0.000 description 3
- 240000007232 Illicium verum Species 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000002572 peristaltic Effects 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- NDVASEGYNIMXJL-NXEZZACHSA-N (+)-sabinene Natural products C=C1CC[C@@]2(C(C)C)[C@@H]1C2 NDVASEGYNIMXJL-NXEZZACHSA-N 0.000 description 2
- 240000004760 Pimpinella anisum Species 0.000 description 2
- 235000019504 cigarettes Nutrition 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- -1 variations in heat Chemical class 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- ULJXKUJMXIVDOY-GUBZILKMSA-N (1S,2S,5S)-2-methyl-5-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)[C@H]1CC[C@H](C)[C@@H](O)C1 ULJXKUJMXIVDOY-GUBZILKMSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 241000602648 Passiflora mucronata Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 240000005158 Phaseolus vulgaris Species 0.000 description 1
- 210000000614 Ribs Anatomy 0.000 description 1
- 241000533293 Sesbania emerus Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 230000000996 additive Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical class [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001055 chewing Effects 0.000 description 1
- 235000019506 cigar Nutrition 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned Effects 0.000 description 1
- 230000003750 conditioning Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000004059 degradation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000008995 european elder Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium(0) Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000018984 mastication Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- YHQGMYUVUMAZJR-UHFFFAOYSA-N p-Mentha-1,3-diene Chemical compound CC(C)C1=CC=C(C)CC1 YHQGMYUVUMAZJR-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 229930006696 sabinene Natural products 0.000 description 1
- 230000001953 sensory Effects 0.000 description 1
- 238000002470 solid-phase micro-extraction Methods 0.000 description 1
- 230000002269 spontaneous Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229930006978 terpinenes Natural products 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B13/00—Tobacco for pipes, for cigars, e.g. cigar inserts, or for cigarettes; Chewing tobacco; Snuff
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/186—Treatment of tobacco products or tobacco substitutes by coating with a coating composition, encapsulation of tobacco particles
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/302—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by natural substances obtained from animals or plants
- A24B15/303—Plant extracts other than tobacco
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B3/00—Preparing tobacco in the factory
- A24B3/12—Steaming, curing, or flavouring tobacco
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
- A24D3/04—Tobacco smoke filters characterised by their shape or structure
- A24D3/048—Tobacco smoke filters characterised by their shape or structure containing additives
Abstract
apparatus for imparting an organoleptic quality such as smell or taste to a recipient product (2) such as tobacco is disclosed. The apparatus uses a sensate substance obtained from a donor product (8), such as mint. The apparatus has a donor product storage chamber (9) and a recipient product storage chamber (1). The apparatus is arranged to allow a fluid to circulate repeatedly between the donor product storage chamber and the recipient product storage chamber so that at least one sensate substance obtained from the donor product is conveyed from the donor product storage chamber into the recipient product storage chamber and into contact with the recipient product. Monitoring and control of the process is also disclosed. rage chamber (1). The apparatus is arranged to allow a fluid to circulate repeatedly between the donor product storage chamber and the recipient product storage chamber so that at least one sensate substance obtained from the donor product is conveyed from the donor product storage chamber into the recipient product storage chamber and into contact with the recipient product. Monitoring and control of the process is also disclosed.
Description
Method and apparatus for imparting an organoleptic quality to a
recipient product
Field
The invention s to the field of imparting an organoleptic quality to a
recipient t, particularly but not exclusively a tobacco industry product.
Background
Where permitted by local regulations, a tobacco industry product may be
provided with additives which modify certain of its organoleptic or sensory
qualities. ttes, cigars, snus, chewing tobacco and the like may be
ed with additives in order to provide a modified taste and aroma profile.
Examples of suitable additives include menthol, coffee, juniper, elderflower,
star anise as well as many others.
Hitherto, such additives have been included into o ry products
during their manufacture. For example, additives may be added to tobacco
rods during the manufacture of smoking articles. Also, additives may be
applied to a wrapper circumscribing a tobacco rod. In this case the additive
may included in an adhesive used in the manufacturing process. In both of
these approaches a certain amount of t between tobacco product and the
ve is required.
Any discussion of the prior art throughout the specification should in no way
be considered as an admission that such prior art is widely known or forms
part of common general knowledge in the field.
It is an object of the present invention to overcome or ameliorate at least one
of the disadvantages of the prior art, or to provide a useful alternative.
Summary
According to a first aspect, the present invention provides an apparatus for
imparting an organoleptic quality to a recipient product using a sensate
substance obtained from a donor product, the apparatus comprising:
a donor product storage r configured to e a batch of donor
product, and
a recipient t storage chamber configured to receive a batch of
recipient product, wherein the recipient product storage r comprises an
agitator to agitate the batch of recipient product,
the apparatus being arranged to circulate a fluid repeatedly in a closed
loop through the donor product storage chamber and the recipient product
storage chamber so that at least one sensate substance obtained from the
donor product is conveyed from the donor product storage r into the
ent product storage chamber and into contact with the recipient product.
According to a second aspect, the present invention provides a method to
impart an organoleptic quality to a recipient product using a sensate substance
obtained from a donor product, utilising apparatus according to any one of the
following aspects.
According to a third aspect, the present invention provides a method of
imparting an organoleptic quality to a recipient product using a sensate
substance obtained from a donor t, the method sing: repeatedly
circulating a fluid in a closed loop h a donor product storage chamber
containing a donor product and a recipient t storage chamber
containing a batch of recipient product and agitating the batch of recipient
product in the ent product storage r so that at least one sensate
nce obtained from the donor product is conveyed from the donor
product storage chamber into the ent product storage chamber and into
contact with the recipient product to impart an organoleptic quality thereto.
Unless the context clearly requires otherwise, throughout the description and
the claims, the words “comprise”, “comprising”, and the like are to be
ued in an inclusive sense as opposed to an exclusive or exhaustive sense;
that is to say, in the sense of “including, but not d to”.
Embodiments of the invention described in more detail hereinafter by way of
example provide an apparatus for imparting an organoleptic quality to a
recipient product using a sensate substance obtained from a donor product, in
which the apparatus comprises a donor product storage chamber, and a
recipient product storage chamber, the tus being arranged to circulate a
fluid repeatedly between the donor product storage chamber and the ent
product storage chamber so that at least one sensate substance obtained from
the donor product is conveyed from the donor product storage chamber into
the recipient product storage chamber and into contact with the recipient
product.
In one embodiment, the donor t can be a botanical and the recipient
product can be a tobacco industry product. The botanical may be heated to a
temperature within a range of 10 ° C- 150 ° C to release its sensate. For
example the
donor product may include mint heated to up to 90°C, or coffee and heated up to 40°C,
or clove and heated up to 110°C.
The botanical may be provided in a frozen state, which is ground into a particulate form
prior to circulating the fluid.
The temperature of the cal may be varied over time and for example the
botanical may be heated to a first temperature for a first period of time to release
a first sensate with a first relatively low boiling point, and then the temperature
of the botanical is raised to a second, higher temperature to release a second
sensate with a higher boiling point than the first sensate.
The tobacco industry t may be one of: tobacco, snus, pouched snus, filter
paper, g paper, filtration material, smoking articles, smoking article
containers or blanks for forming g article containers.
In one embodiment, the fluid entering the donor product storage chamber is pre-
heated to contribute to the release of the sensate from the donor product.
2O Brief description ofthe drawings
In order that the invention may be more fully tood embodiments thereof will
now be described by way of illustrative example with reference to the anying
gs in which:
Figure 1 is a part eXploded three ional view of an apparatus according to
an embodiment of the present invention;
Figure 2 is a side view of apparatus according to another embodiment of the
present invention;
Figure 3 is a side view of another storage vessel that can be used in the apparatus
of Figure 2.
Figure 4 is a side view of an embodiment of apparatus for imparting an
organoleptic quality to a recipient product; and
Figure 5 is an enlarged side view of the donor product storage chamber of the
ment shown in Figure 4.
Detailed description
As used herein the term recipient product means a product to which an
organoleptic quality is imparted. In embodiments described hereinafter, the
recipient t is a t used in the o industry. Such tobacco
industry products should be understood to include end ts, such as snus
when pouched or loose, smoking article filters, entire smoking articles or
1O smoking article containers as well as intermediate products such as tobacco,
filtration material, blanks for forming smoking article containers and so forth.
Using blanks rather than fully formed g article containers has the
advantage of conserving space.
Where the recipient product is tobacco, various varieties of tobacco may be used
as well as tobacco in various stages of processing. For example, cut rag tobacco,
tobacco in whole leaf form or laminar, stem, reconstituted tobacco shettor
papers or ground tobacco may be used. In embodiments of the present invention
where the recipient product is tobacco, tobacco rods may be formed for use in
2O smoking articles in a manner known per se in the art and then imparted with an
organoleptic quality.
As used herein, the term donor product means a product that is used to impart
an organoleptic quality to the recipient t. In embodiments described
hereinafter, donor products include botanicals such as mint, juniper, anise, star
anise and clove although others could be used.
An ment of an apparatus for imparting an organoleptic quality to a
recipient product is illustrated in Figure 1 in which the donor product comprises
a botanical and the recipient product comprises a tobacco industry product,
which in this example is tobacco. The apparatus shown in Figure 1 comprises a
recipient t storage chamber 1 in which a tobacco industry t 2 is
received. In this e the product is shredded tobacco leaf but other ent
ts may be used as discussed previously. A mesh shelf 3 may be located
inside the r 1 to support the tobacco industry product 2. The storage
chamber 1 has a sealable lid 5 that can be opened to allow the recipient product
to be stored in and removed from the chamber. A pressure gauge 6 and a safety
valve 7 may also be provided.
In the embodiment shown in Figure 1, a donor botanical 8 is stored in a donor
e vessel 9. The botanical 8 can be stored in the botanical storage vessel 8
as a solid, for example in leaf or berry form or as ground leaf or berry ing
to a particular mesh size discussed in more detail hereinafter. Alternatively, the
botanical 10 may be stored in the form of a s extract or as a pressurised
liquid which may be accompanied by a suitable propellant. In the latter case
1O where the botanical 8 is in gaseous or pressurised liquid form the botanical
storage vessel 50 may be modified to accommodate gaseous or liquid contents in
a way that would be apparent to those skilled in the art.
A fluid, in this example air, is repeatedly recirculated through the donor and
recipient chambers 1,9, through a t arrangement comprising tubing 10 by
a pump 11. The tubing 10 comprises three tubing portions 10a, 10b, 10c and may
be constructed from any suitable material which does not itself elute significant
inants into the fluid flow. A suitable material is stainless steel but certain
plastics tubing can also be used. The first portion 10a extends between the pump
2O 11 and the donor product storage vessel 9. The second portion 10b extends
between the donor product storage vessel 9 and the recipient product storage
vessel 1. The third portion 10c extends from the recipient product storage vessel
1 to the pump 11. Air may be pumped by the pump 11 in the direction shown by
the arrows in Figure 1, although in an alternative arrangement it can be pumped
in the opposite direction.
In use, the air is pumped by pump 11 h the first portion 10a of the tubing
into the donor product storage chamber 9 and sensate ents of the
cal 8 in the chamber 8 are conveyed in the air stream through the second
portion of tubing 10b into the recipient product storage chamber 1. Inside the
chamber 1 the air conveying sensate constituents of the botanical 8 travels
through the tobacco industry product 2 stored in the chamber 1 so that the
tobacco industry product 2 becomes impregnated with e tuents of
the cal 8. Air leaves the chamber 1 h the third portion of tubing 10c
to be recirculated by the pump 11 through the tubing 10 for a given amount of
time, and when the tobacco industry product is sufficiently impregnated with the
e, the product can be removed from the chamber by temporary removal of
the lid 5.
Figure 2 shows an alternative ement comprising a donor product storage
chamber in the form of a botanical storage vessel 12, a recipient product storage
chamber in the form of a tobacco mixing drum 13 and a pump 11. A fluid
comprising air in this example is pumped in a closed loop through a conduit
comprising an air pipe 10a into the botanical storage vessel 12 by the pump 11. A
pipe 10b s between the storage vessel 12 and the mixing drum 13 and a
further pipe 10c extends between the mixing drum 13 and the pump 11. The
pump 11 could comprise a peristaltic pump; alternative types of pump that could
be used include t others, a vane pump, centrifugal compressor, piston
pump, gear pump and liquid ring pump. The apparatus shown in Figure 2 can be
operated at atmospheric pressure.
The e vessel 12 has an internal chamber 14 to hold botanical products 8
such as juniper, coffee, star anise or any other suitable botanical t. The
botanical product 8 is supported on a wire mesh 15 located in the lower portion
16 of the chamber 14. Water 17 is stored in the portion of the chamber 16 below
2O the wire mesh 15. r it may not always be necessary to use water in the
process depending upon the moisture level of the botanical t 8. The sides
of the vessel 12 are wrapped by a heatjacket 18 and a heat mat 19 is placed under
the vessel 12. The heatjacket 18 and heat mat 19 are configured to apply heat to
the ts of the chamber 12 and can be driven in any suitable way. For
example the heatjacket and mat can be electrically heated and/or steam heated.
The pipe 10a which ts the peristaltic pump 11 to the storage vessel 12,
enters the vessel 12 from above. Air pumped into the vessel 12 passes h an
internal pipe 20 located inside the vessel 12 to the bottom so that the flow
thereafter passes upwardly through the botanical 8 to receive sensates to be
transferred to the recipient tobacco product in drum 13 .
The tobacco mixing drum 13 is arranged to hold a quantity of tobacco industry
product 5 to be infused or impregnated with sensate constituents from the
botanical products 8 stored in the storage vessel 12. The mixing drum 13 may be
configured such that it can be rotated by a motor 21 about its central axis 22.
Rotating the mixing drum 13 facilitates the infusion of the tobacco industry
product 2 with sensate tuents of the botanical product 8.
In use, air is pumped by the peristaltic pump 11 into the storage vessel 12. The
air is fed to the lower portion of the internal chamber 14 through the internal
pipe 20 and passes through the water 17 stored in the part of the chamber 14
below the wire mesh 15 which ts the botanical product 8. Preferably, the
heatjacket 18 and heat mat 19 heat the e vessel to approximately 90°C.
The applied heat and the air flow act to evaporate a substantial proportion of the
water stored in the storage vessel 12 creating water . The air and water
vapour are forced upwards through the wire mesh 15 and through the botanical
product 8. The heat applied to the botanical storage vessel 12 is ted and
radiated into the botanical product 8 which is stored within. This energy causes
some of the sensate material contained within the botanical product 8 to
vapourise into the gas phase contained within the vessel. As the air and water
vapour pass through the storage vessel 12, they entrain the e vapours and
create a mixture which hereon is referred to as process air. The process air is
then forced out of the vessel 12 through the pipe 10b that connects the vessel 12
with the mixing drum 13 which contains a quantity of tobacco ry product 2
2O to be infused with the sensate vapours of the cal product 8.
The mixing drum 13 is at a lower temperature than the storage vessel 12 and so
the process air conveyed into the drum 13 from the storage vessel 12 through the
pipe 10b, the sensate vapours begin to condense in the drum 13.
Rotation of the drum 13 about a cylindrical axis 22 by motor 21 allows a
thorough ation of the tobacco industry product 5 and condensed sensate
constituents within the drum 13. In this way the tobacco industry t 2
becomes infused with sensate constituents from the botanical product 10. The
process described above can be continued until all the water stored in the
storage chamber 60 has been evaporated. Alternatively, the process may be run
for a set period of time to enact a desired level of on into the tobacco
industry product 2.
An alternative donor product storage chamber is shown in Figure 3, comprising
e vessel 23. The vessel 23 is elongate and extends upwardly, with air from
the pump 11 entering the vessel from an inlet 24 located s the bottom of
the vessel 23. Water is stored in a water storage chamber 25 and fed into the
vessel 23 through a water inlet 26 through conduit 27 controlled by a valve 28.
As in the vessel 12 shown in Figure 2, the vessel 23 shown in Figure 3 is heated
by a heat jacket 18. Water is evaporated by the air flow and the applied heat
from the heat jacket 18. The water vapour is conveyed upwards through the
botanical product 8 stored in the chamber 14 and supported on the wire mesh 15.
Theprocess air containing sensate vapour leaves the vessel 23 via an air outlet 29
and is conveyed through pipe 10b towards a mixing drum 13 as shown in Figure
2, where the condensation of the sensate vapour and infusion of the tobacco
industry product 5 stored therein take place.
Experimental Data
Experiments were performed to e the effects of different infusion
conditions when infusing tobacco with juniper using the tus described
above with reference to s 2 and 3. Five samples were igated using
Solid Phase Microextraction - Gas tography/Mass Spectrometry (SPME-
GC/MS) is of aromatic constituents deposited onto the tobacco during the
infusion process.
Table 1
Sample Description of sample
Juniper 1 2 kg juniper berry milled from frozen,
heated to 90°C using the apparatus
shown in Figure 4 with 10 kg tobacco
Juniper 2 2 kg juniper berry milled from frozen
heated to 90°C using the apparatus
shown in Figure 3 with 10 kg tobacco
Juniper 3 The tobacco which had been
impregnated in Juniper 1 was
impregnated by an additional 2 kg
juniper berry milled from frozen
heated to 90°C using the apparatus
shown in Figure 4.
Juniper 4 The tobacco which had been
impregnated in Juniper 2 was
impregnated by an additional 2 kg
juniper berry milled from frozen
heated to 90°C using the apparatus
shown in Figure 4.
Juniper control sample Groundjuniper berry — no o.
Tobacco control sample Tobacco only — no juniper.
The results of the analysis are shown in Table 2. The amount of a particular
tuent present in each sample is sed as a mean of two replicates of
the sample except for the juniper control sample where only one replicate was
analysed.
Sample Tobacco Juniper Juniper Juniper Juniper r
control 1 (Mg) 2 (11g) 3 (Mg) 4 (115;) control
(Mg) (11g)
Terpinene 0.00 0.55 0.75 1.59
Sabinene 0.00 0.04 0.03 0.07 0.08 0.33
hydrate
Carvomenthol 0.01 0.33 0.67 0.68
Bornyl 0.00 0.17 0.16 0.30 0.43 2.86
acetate
Citronellyl 0.00 0.00 0.00 0.00 0.17
butyrate
mummifi-
“mum-mm“
As can be seen from Table 2 constituents t in thejuniper control sample
and absent from the tobacco control sample are present in the samples Juniper
1-4 prepared in ance with the present invention.
Similar results can be obtained using another embodiment that is shown in Figures
4 and 5. As can be seen from Figure 4, the apparatus comprises a donor product e
chamber 30 and a recipient product storage chamber 31. The donor product storage
chamber 30 and the recipient product storage chamber 31 may be formed from any
durable material that can withstand a wide range of environmental ions such as
variations in heat, pressure and humidity. Suitable materials include, but are not
limited to, metals such as steel, particularly stainless steel or any other durable metal or
alloy. A plastics al could be used as long as its particular ition does not
elute contaminants into recipient product.
Figure 5 shows the donor product storage chamber 30 in more detail. The donor
product storage chamber 30 is a cylindrical vessel provided with a closure such
as a lid 5 to allow the donor product 8 to be inserted and removed.
2O The recipient product storage r 31 may be provided as a rotary drum, as
shown in Figure 4, rotatable about an axis of rotation 22 that may be driven by a
motor 21 as illustrated in Figure 2. The recipient product storage chamber 31
may also be provided with a closure such as a lid (not shown) to allow ion
and removal of a recipient product 2.
The donor product storage chamber 30 and the recipient t storage
chamber 31 are ted together by a conduit arrangement in the form of a
closed loop of pipes 10. A first pipe 10a extends between pump 11 and the donor
product storage chamber 30. A second pipe 10b s from the donor product
storage chamber 30 to the recipient product storage chamber 31. A third pipe
10c extends between the recipient product storage chamber 31 and the pump 10.
As such, fluid can circulate repeatedly n the donor product storage
chamber 30 and the recipient product storage chamber 31 in a closed loop that is
sealed from the atmosphere.
The pipes 10 may be formed from a durable material to withstand conditions
such as high temperature, humidity and fluid flow rate, and where jointed should
not include a t that would introduce contaminants into the fluid flow.
In the embodiment shown in Figure 4, the pump 11 is operable to circulate the
fluid through the pipes 10 and chambers 30, 31 and may comprise a altic
pump. However, other suitable pumps may be used. Alternative types of pump
that could be used include amongst others, a vane pump, centrifugal compressor,
piston pump, gear pump and liquid ring pump. The pump 11 is provided with a
pump controller 32 to l the flow rate at which fluid is conveyed around the
apparatus.
The donor t storage chamber 30 may be provided with an agitator to
2O agitate the donor product 8 stored therein. For example, a stirring rod 33 may
be provided to agitate the donor product 8 by a stirring action to encourage
sensate release from the donor product into the fluid flow.
The storage chamber 30 includes a mesh (not shown in Fig. 4 or 5) at the bottom
in the manner of mesh 15 shown in Figure 2 to support the donor product 8 and
also to allow for distributed process air flow across the base of the bed of donor
t material.
Alternatively, the donor product 8 may be agitated by vibrating the donor
t e chamber 5 or the chamber may be constructed as a fluidised bed
in which the flow of fluid itself agitates the donor product.
Also the recipient product 2 may be agitated and as shown in Figure 4, the
cylindrical recipient product storage chamber 31 may be rotated about its aXis of
rotation 20. Also an agitator such as a stirring rod (not shown) substantially
similar to the stirring rod 35 may be ed to agitate the recipient product 2
thus allowing a more even distribution across the recipient product 2.
Furthermore, the recipient product 10 may be agitated by vibrating the recipient
product storage chamber 10. Agitating the recipient product 2 further facilitates
e substances obtained from the donor product 8 coming into t with
the recipient product 2.
As shown in Figure 4 and 5, a heat source such as a heatjacket 18 can be
provided around the or of the donor product storage chamber 30 to heat its
contents, namely the donor product 8 as well as any fluid present in the donor
product storage chamber 30. The heat jacket 18 may be a resistive heating
element wrapped around the donor product storage r 30 and provided
with an external insulating layer to reduce heat losses external to the apparatus.
As wil be appreciated by those skilled in the art, there are alternative methods to
heat the storage chamber 30, not limited to but including circulating steam or
hot water in ajacket around the vessel or h a coil contained inside the
vessel. The heatjacket 18 may wrap around the full circumference and also the
upper and lower ends of the chamber 30 and is shown cut away to aid
2O illustration of the donor product storage chamber 30 and its ts.
Alternatively, or in combination with the heatjacket 18, the fluid that enters the
chamber 30 through the pipe 10a may be pre-heated to heat the contents of the
donor product storage r 30. To this end, a heatjacket 34 may be
arranged around the pipe 10a to pre-heat the fluid entering the r 30.
Alternatively, the fluid maybe ted by being passed through a suitable heat
exchanger. An advantage of preheating the air is the sed heat transfer into
the botanical product 8 stored within e chamber 30.
A further heatjacket 35 may be provided around the pipe 10b to keep maintain
the temperature of the sensate bearing fluid passing from the chamber 30 to the
chamber 31 and prevent condensation prior to reaching the chamber 31.
The donor product 8 may be conditioned prior to insertion into the donor
product storage chamber 30. For example, in embodiments where the donor
product 8 is mint the mint may be cut or ground to a desired mean particle size.
A quantity of water such as 10 — 50ml for example 30ml per kilogram of mint
may be added to the mint.
Botanicals, such as , juniper and anise may be frozen prior to use to retain
their sensates whilst stored prior to use in the apparatus. A typical temperature
range within which botanicals may be frozen to is -26°C to 0°C. They may ground
prior to freezing or afterwards. The frozen botanical may then be ground again
in preparation for use in the apparatus. The grinding process produces a
distribution of particle sizes and conveniently more than 50% of the le size
distribution falls within a range from 0.5mm to 1.5mm. This conditioning the
botanical prior to use in the apparatus facilitates release of sensate substances
from the donor product 8 during use of the apparatus.
As usly mentioned, fluid such as air is edly circulated in a loop
through the conduit arrangement 10. However, other fluids could be used, such
as a gas or gaseous mixture containing a minimal levels of oxygen, to reduce the
risk of spontaneous combustion e.g. of unwanted dust ed by the ng
process or tobacco dust. A suitable gas is nitrogen, but alternatives could include
2O steam or inert gases, for example noble gases such as helium. A further
advantage of using an oxygen deficient process fluid is that the sensate
compounds are less likely to oxidise, thus avoiding changes to their
characterising flavour or odours.
In use, fluid enters the base of the donor product storage chamber 30 through
the pipe 10a and entrains a sensate comprising a flavourant to be imparted to the
recipient product in the recipient product storage chamber 31. The ant
containing fluid created in the chamber 30 passes into pipe 10b and enters the
recipient product storage r 31 so as to impart the ant into the
recipient product 2 as explained in more detail hereinafter.
Thereafter pipe 10c conveys the fluid from the recipient product storage chamber
31 through the pump 10 back into chamber 30 to complete the cycle, which may
be ed a sufficient number of times to achieve the desired level of infusion
into the tobacco product. The inlet of the pipe 10c is disposed buried below the
level of the o 2 to ensure that the fluid bearing the sensate from pipe 10b
is drawn through the tobacco product to impart the sensate into the tobacco. An
inlet mesh filter 36 is provided over the inlet of pipe 10c to reduce ingress of
tobacco into the pipe, so as to reduce the likelihood of it reaching the chamber
Also a dust receptacle 37 can be d in th epipe 10c n the recipient
product storage chamber 31 and the pump 11 to receive tobacco dust or other
refuse matter. The dust receptacle may comprise for example a large volume
settling tank, a cyclone, a filtration system using a filter medium, or a scrubber
that removes solids from the fluid flow but permits residual sensates entrained
in fluid flow to recirculate.
Filters may additionally or alternatively be provided elsewhere in the apparatus,
for example where the pipe 10b leaves the recipient t storage r 30.
Various parameters, such as temperature, humidity, pressure or fluid flow rate
within the apparatus may be measured using one or more measuring devices. In
the embodiment shown in Figure 4 and 5, a thermometer or thermocouple 38 is
used to measure temperature inside the donor product e chamber 30.
2O Other measuring devices 39 may be used to measure other parameters such as a
hygrometer or other suitable measuring device may be provided to measure
humidity, a pressure gauge may be provided to e pressure and a flow
meter may be provided to measure fluid flow rate within the apparatus 1.
A controller 40 may be provided to control the temperature to which the heat
jacket 18 heats contents of the donor product storage chamber 30 and the level
of heating provided by the heatjackets 34, 35 around the pipes 10a, 10b that lead
to and from the chamber 30. The controller 40 may comprise a user interface 41
to allow a user to input a temperature value to which ts of the donor
product storage chamber 5 are to be heated. It is possible to control the
temperature in response to a temperature ed by the thermometer 38. For
example, if the thermometer 38 measures a temperature of 100°C a user may
input an instruction into the controller 40 via the user ace 41 to reduce the
temperature to 90°C for example. The controller 40 controls the heat jacket 18
to reduce the ature accordingly.
WO 23289
The controller 40 may be automated. In this case the controller may be
programmed to reduce the temperature automatically when a temperature
measured by the thermometer 38 rises above a ermined value to provide a
control feedback loop that maintains the ature a present nominal value.
For example, the controller 40 may l the power applied to the heat jacket
18 to maintain the ature close to a set value of 90°C.
While Figures 4 and 5 show an embodiment where a temperature feedback loop
may be established with respect to the donor product storage chamber 30, it
1O should be understood that such a feedback loop may be established with respect
to other parts of the apparatus 1 such as the recipient product storage chamber
31 or the individual pipes 10. For e, a heat source, thermometer and
controller may be provided to the recipient t storage chamber 31.
In certain embodiments, the controller 40 may be configured to vary various
other ters (that is, in addition to or instead of temperature) in response
to a measured parameter. For example, the controller may vary the temperature
in response to a measured value of humidity or pressure. Alternatively, the
pressure may be varied in response to a measured temperature. In general, the
2O apparatus may provide a feedback loop where a parameter may be varied in
response to a measured value of the same or different ter.
It is to be understood that while the ement and control of parameters
have been described with respect to the donor product storage chamber 30, in
other embodiments a parameter of any part of the apparatus may be controlled
in response to a measurement of a ter made elsewhere in the apparatus.
For example, in some embodiments the recipient t storage chamber 31
may be provided with a heat source and controller. The contents of the recipient
product storage chamber 30 may be heated to a ular temperature in
response to, for example, a measured re value within the donor product
storage chamber 31.
In use, fluid, for example air, is pumped by the pump 11 into the donor product
storage chamber 30 through the duct 10a. The heat jacket 18 heats contents of
the donor product storage chamber 30 to a predetermined temperature set by
the controller 40. The temperature to which contents of the donor product
storage chamber 30 is heated depends on the donor t 8 stored therein
although conveniently falls within a range of 10°C - 150°C and more particularly
°C - 110°C for botanicals. For example, mint may be heated to a nominal
temperature of 90°C, coffee may be heated up to 40°C, clove may be heated to
110°C. As the contents of the donor product storage chamber 30 are heated to a
particular temperature, certain sensate substances contained within the donor
product 8 having a g temperature below that particular temperature
become substantially volatilised.
The fluid that eXits the donor product storage r 30 through the pipe 10b
may be heated by the heatjacket 35, which reduces the amount of volatilised
sensate substance that ses before entering the recipient t storage
chamber 31. In the embodiment shown in Figure 5, the pipe 10b is shown
extending ally from the donor product storage chamber 30. This
arrangement has the advantage that any nces that do condense in the pipe
10b are likely to fall back into the donor product storage chamber 30 where they
may be re-volatilised. As such, the amount of substances that condense in the
pipe 10b may be reduced.
2O A ature differential may be established between the contents of the
ent product storage chamber 31 and the ts of the donor product
storage chamber 30. In addition to providing a heat source for the donor
product storage chamber 30, as shown in Figures 4 and 5, a heat source such as a
cket (not shown) may also be provided for the ent product storage
chamber 31 with an associated temperature sensor coupled to the controller 40
to maintain the temperature differential.
A substantial amount of the sensate substances conveyed into the recipient
product storage chamber 31 from the donor product storage chamber 30 through
the pipe 10b condense inside the recipient product storage chamber 31 and come
into contact with the recipient product 8 stored therein. The recipient product 8
thereby becomes imparted with an organoleptic quality of the sensate substances
obtained from the donor product 2.
Agitating the recipient product storage r 31, as described above, further
facilitates contact between sensate substances obtained from the donor product
8 with the recipient product 2 within the recipient product storage chamber 31.
The fluid may be circulated repeatedly n the donor t storage
chamber 30 and the recipient product storage chamber 31. Such repeated
circulation may be performed as often as is necessary to impart the recipient
product with a desired level of organoleptic quality derived from the donor
product. For e, recirculation may be med over a predetermined
time period typically between 4-9 hours, such as n 5-7 hours for example
6 hours or the process may be continued until sensed parameters of the process
indicate tion.
The apparatus 1 may be formed from such materials which facilitate a reduction
in the amount of foreign substances (i.e. unwanted substances from outside the
apparatus 1) entering the apparatus 1. For example, materials having a low
ty such as stainless steel or aluminium may be used to form the donor
product e chamber 30 and the recipient product storage chamber 31.
2O Additionally, respective closures, such as the lid 15 of the donor product storage
chamber 5 and the lid (not shown) of the recipient product storage chamber 10
may be fitted with a seal to minimise ingress of foreign substances from outside,
and to minimise losses of the process air containing the sensate vapours to the
external here.
Regions where component parts of the apparatus 1 come into contact, for
example where the donor product storage chamber 30 and pipe 10a come into
contact, may be configured to reduce foreign nces entering the apparatus.
For e, the components may be dimensioned to ensure an interference fit
or a suitable non-eluting t may be provided.
The temperature of the contents of the donor product storage chamber 30 may
be varied using the controller 40 as described above, by varying the temperature
within various parts of the apparatus such as the donor t storage chamber
30. Different sensate substances of the donor product 8 stored in the donor
product storage chamber 30 may become volatilised at different temperatures
and by varying the temperature within the donor product e chamber 30
from a first ature value during a first time period to a second temperature
value during a second time period may facilitate volatilisation of different
sensate substances during different time periods.
For example, during a first time period P1 the donor product storage chamber 30
may be heated to a temperature T1. e substances S1 of the donor product
8 having a boiling temperature below T1 become substantially volatilised and
conveyed in the fluid flow under the action of the pump 11 h the pipe 10b
and towards the recipient product storage chamber 31. Sensate substances that
require a higher temperature than ature T1 to become volatilised do not
become substantially volatilised during the first time period P1.
During a second time period P2 the donor product storage chamber 30 may be
heated to a temperature T2 which is greater than T1. Since T2 is greater than T1
sensate substances S1 described above continue to be volatilised. Additionally,
sensate substances S2 which have a boiling temperature higher than T1 but less
than T2 and which were not substantially volatilised during time period P1
become substantially volatilised during time period P2. Such sensate
2O substances S2 may then be conveyed in the fluid flow by the pump 11 towards the
recipient t storage chamber 31.
Thus the ature of the donor product storage r 5 may be sed
during successive time periods to achieve the volatilisation of sensate substances
with successively higher boiling temperatures.
At higher temperatures the donor t 8 or sensate constituents may begin to
become degraded. By gradually increasing the temperature during successive
time periods any such degradation is likely to occur after sensate substances with
lower boiling points have been substantially volatilised. By contrast, if the donor
product 8 were exposed to a high temperature well above the boiling point of
sensate substances S1 during time period P1 then the organoleptic quality of the
sensate substance S1 may be affected.
Varying the temperature during successive time periods may be performed
ly by, for example, manually adjusting the controller 40 through the user
interface 41. Alternatively, the controller 40 may comprise a memory to store
instructions and a processor so that varying the temperature over successive
time periods may be automated. For example, the memory may contain
instructions to heat the donor product storage chamber 30 to a temperature of
approximately 30°C for 20 minutes and then heat the donor product storage
chamber 30 to a temperature of approximately 95°C for 60 minutes.
During the above bed process, fluid samples may be analysed by an
analysis unit 42 such as amass ometer or a gas chromatograph which
provides a chromatogram that provides information regarding what substances
are present in the fluid samples and in what quantity. For example, the
chromatogram may indicate that particular sensate substances obtained from the
donor t 8 are present in a particular amount. Additionally, the presence
of any substances that were used to condition the donor product 8 prior to
commencing the above described process, such as water, may also be analysed.
Chromatograms may also show the presence of foreign substances inside the
apparatus which might indicate the presence of a leak.
In embodiments described with respect to Figures 4 and 5, the is unit 42 is
2O connected to the pipe 10c but the analysis unit 42 may be connected to either of
the pipes 10a or 10b. Indeed, the analysis unit may take and analyse samples
from a single point or several points along the conduit arrangement 10 or within
the chambers 30,31.
Fluid samples may be obtained from the pipe 10b before the fluid enters into the
ent product storage r 31 and/or from the pipe 10c after the fluid
exits the recipient product storage chamber 31. When obtained both before and
after entry into the recipient product storage chamber 31, such samples may be
compared so that ation may be obtained as to what substances have been
deposited inside the recipient product storage chamber 31.
Based on the results thereby obtained the temperature of parts of the apparatus
such as the donor t e r 30, may be varied using the
controller 40. For e, if a particular sensate substance is shown in the
chromatogram to be t in the fluid sample in an amount below a d
amount then the temperature may be increased to increase volatilisation of that
sensate substance. Conversely, if a sensate substance is found to be present in
too great an amount then the temperature of the donor product storage chamber
may be reduced to decrease volatilisation of that sensate substance. In addition,
the chromatogram can give an indication as to the level of completion of the
process, by visualising the profile of the concentration of sensate components
over the time of ion. The profiles obtained can aid the decision of when to
stop the ation of the process fluid or heating of the storage vessel, since the
release of sensate materials follows a l decay curve there is a point where
further processing would yield minimal transfer of e components.
Two specific examples of use of the apparatus of Figures 4 and 5 are given below,
in which a single charge of the recipient product is imparted with an
organoleptic quality of a sensate substance obtained from a single charge of the
donor product.
Example 1 — Coffee
The ent product chamber 31 ned shred, cial grade tobacco 2
for use in cigarette tobacco rods.
2O The donor product chamber 30 contained coffee prepared by grinding Costa Rica
mild coffee beans. The beans were frozen prior to use and were ground in a mill
with a sieve attachment. After the ground coffee was placed in chamber 30,
g was started at 30°C for both the heat jacket 18 pipe heaterjackets 34, 35.
The agitator paddle 33 was used to stir the contents of chamber 30, initially with
a small number of ons e.g. one or two, at spaced apart time periods of
typically 20 minutes which increased to three or four ons spaced apart by
approximately one hour as the process progressed. The overall infusion time was
approximately 7 hours.
The heating of the chamber 30 was increased on two occasions: from 30°C to
45°C after 55min and then to 55°C after another hour.
The tobacco 2 on removal from the chamber 31 was found to have a clearly
discernable coffee aroma.
Example 2 - Juniper
The recipient product chamber 31 contained shred, commercial grade tobacco 2
for use in cigarette tobacco rods.
The donor product chamber 30 ned Juniper berry prepared by grinding.
The berries were frozen prior to use and initially ground in a mill without a sieve
attachment, were then re-frozen and ground in a mill and passed through a 4mm
sieve attachment. After the ground material was placed in r 30, g
was carried out at 90°C for both the heatjacket 18 pipe heaterjackets 34, 35 for
a period of 6 hours.
As in Example 1, the agitator paddle 33 was used to stir the contents of chamber
. The tobacco 2 on removal from the chamber 31 was found to have a clearly
discernable coffee aroma.
In both of the examples, the tobacco may be left in the chamber 31 for a period of
time after the pump 30 has been switched off, before l from the chamber,
which has been found to assist in the permeation of the flavourant into the
recipient tobacco.
In a modification, the paddle 33 is designed to work as a grinder so that the
grinding of the botanical can be carried out in situ within the chamber 30 with
the lid 5 closed. This s dust formation which occurs during grinding of the
botanical outside of the apparatus.
As well as varying the ature of the donor t storage chamber 30, the
humidity, fluid flow rate and/or pressure within the apparatus, as well as the
duration of the process, the level of agitation of the contents of the donor
product storage r 30 and the recipient product storage chamber 31 may
be varied. ion of such parameters may be performed without interrupting
the process itself.
It will be appreciated that it would be possible to adapt or design any of the
apparatus described herein to operate at either a partial vacuum or at a pressure
higher than atmospheric. Certain botanicals may d better to variation in
pressure from atmospheric to enable transfer of more thermally delicate sensate
components.
In order to address various issues and advance the art, the entirety of this
disclosure shows by way of illustration various embodiments in which the
claimed invention may be practiced and provide for superior imparting of an
organoleptic quality to a recipient product using a sensate substance obtained
from a donor product. The advantages and features of the disclosure are of a
representative sample of embodiments only, and are not exhaustive or exclusive.
They are presented only to assist in understanding and teach the d
es. It is to be tood that advantages, ments, examples,
functions, features, structures, and/or other aspects of the disclosure are not to
be considered limitations on the disclosure as defined by the claims or
limitations on equivalents to the claims, and that other ments may be
ed and modifications may be made without departing from the scope or
spirit of the disclosure. Various embodiments may suitably comprise, consist of,
or consist essentially of, various combinations of the disclosed elements,
components, features, parts, steps, means, etc. In addition, the disclosure
includes other ions not presently claimed, but which may be claimed in
future.
Claims (33)
1. An apparatus for imparting an organoleptic quality to a recipient t using a sensate substance obtained from a donor product, the 5 tus comprising: a donor product storage chamber ured to receive a batch of donor product, and a recipient product storage chamber configured to receive a batch of recipient product, wherein the recipient product storage r comprises an 10 agitator to agitate the batch of recipient product, the apparatus being arranged to circulate a fluid repeatedly in a closed loop through the donor product storage chamber and the recipient product storage chamber so that at least one sensate substance obtained from the donor product is conveyed from the donor product storage chamber into the 15 recipient product storage chamber and into contact with the recipient product.
2. An apparatus according to claim 1, further comprising a ller to control a parameter of contents of the apparatus whilst the sensate nce is conveyed to the recipient t.
3. An tus ing to claim 2, wherein the controller is responsive to a measured value of a first parameter of the contents of the tus and configured to control a second parameter of the contents of the apparatus in response to said ed value of the first parameter.
4. An apparatus according to claim 3, wherein the first parameter is the same parameter as the second parameter.
5. An apparatus according to claim 3 or 4 wherein the first and second 30 parameters are, respectively, at least one of: temperature, humidity, pressure, fluid flow rate.
6. An apparatus according to any one of the preceding claims, wherein the controller is configured to vary over time the temperature of contents of the 35 apparatus.
7. An apparatus according to any one of the preceding claims, r comprising a heat source to heat contents of the tus.
8. An apparatus ing to claim 7 including a heater to heat the 5 contents of the donor product storage chamber.
9. An apparatus according to claim 7 or 8 including a heater to pre-heat the fluid entering the donor t storage chamber.
10 10. An apparatus according to any one of the preceding claims, wherein the controller is configured to maintain a temperature differential between contents of different parts of the apparatus.
11. An apparatus according to any one of the preceding claims, wherein a 15 single charge of the recipient product is imparted with an organoleptic quality of a sensate substance obtained from a single charge of the donor product.
12. An apparatus according to any one of the preceding claims, wherein the donor product storage chamber comprises an agitator to agitate contents 20 thereof.
13. An apparatus according to any one of the preceding claims, r sing a pump to circulate the fluid between and through the chambers. 25
14. An apparatus according to any one of the preceding claims, wherein the donor product storage chamber ns a botanical.
15. An tus according to any one of the preceding claims, wherein the recipient product storage chamber contains a tobacco industry product.
16. An apparatus according to any one of the preceding claims, and charged with the fluid which comprises air.
17. An apparatus ing to any one of the preceding , whereby the 35 donor product storage chamber and/or the recipient product storage chamber are operable to fluidise the contents thereof.
18. An apparatus according to any one of the preceding claims, including a mass spectrometer to sample process fluids and monitor sensate constituents so as to permit l the temperature of the donor product storage chamber. 5
19. A method to impart an organoleptic quality to a recipient t using a sensate substance obtained from a donor t, utilising apparatus according to any one of the preceding claims.
20. A method of imparting an organoleptic quality to a recipient product 10 using a sensate substance obtained from a donor product, the method comprising: repeatedly circulating a fluid in a closed loop h a donor t storage chamber containing a donor product and a recipient product storage r containing a batch of recipient product and agitating the batch of recipient product in the recipient product storage chamber so that at 15 least one sensate substance obtained from the donor product is ed from the donor product storage chamber into the recipient product storage chamber and into contact with the recipient product to impart an organoleptic quality thereto. 20
21. A method according to claim 20 wherein the donor product is a botanical and the recipient product is a tobacco industry product
22. A method ing to claim 21 including heating the botanical to a temperature within a range of 10˚C - 150˚C
23. A method according to claim 21 or 22, wherein the botanical is at least one of: coffee, juniper, mint, menthol and anise.
24. A method according to claim 22 wherein the donor product includes mint and 30 is heated to up to 90°C, or coffee and heated up to 40°C, or clove and heated up to 110°C.
25. A method according to claim 23 or 24 including providing the botanical in a frozen state, and grinding the botanical prior to circulating the fluid.
26. A method according to any one of claims 21 to 25, further comprising varying the temperature of the cal storage chamber over time.
27. A method according to claim 26 including heating the cal to a first temperature for a first period of time to release a first sensate therefrom with a first relatively low boiling point, and then raising the ature of the 5 botanical to a second, higher temperature to release a second sensate therefrom with a higher boiling point than the first sensate.
28. A method according to any one of claims 21 to 27, wherein the tobacco industry product is one of: tobacco, snus, pouched snus, filter paper, tipping 10 paper, filtration material, smoking articles, smoking article containers or blanks for forming smoking article containers.
29. A method according to any one of claims 21 to 28, further comprising pre-heating the fluid entering the donor product storage chamber.
30. A method according any one of claims 21 to 28, further comprising stirring the botanical.
31. A method according to any one of claims 21 to 30 including measuring 20 the composition of the fluid ating between the chambers.
32. A method according to claim 22 wherein the botanical sensate is ve with oxygen, and the fluid circulated in the apparatus is an inert gas. 25
33. An apparatus for importing an organoleptic quality to a recipient product using a e substance obtained from a donor product; or a method of importing an leptic quality to a recipient product using a e nce obtained from a donor product, substantially as herein described with reference to any one of the embodiments of the ion illustrated in 30 the accompanying drawings and/or examples.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1104311.4 | 2011-03-15 | ||
GBGB1104311.4A GB201104311D0 (en) | 2011-03-15 | 2011-03-15 | Method and apparatus for impregnating tobacco industry products with sensate constituents of botanicals |
PCT/EP2012/053819 WO2012123289A1 (en) | 2011-03-15 | 2012-03-06 | Method and apparatus for imparting an organoleptic quality to a recipient product |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ614475A NZ614475A (en) | 2015-04-24 |
NZ614475B2 true NZ614475B2 (en) | 2015-07-28 |
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