EP2077731A2 - Cigarette components having encapsulated catalyst particles and methods of making and use thereof - Google Patents
Cigarette components having encapsulated catalyst particles and methods of making and use thereofInfo
- Publication number
- EP2077731A2 EP2077731A2 EP07713116A EP07713116A EP2077731A2 EP 2077731 A2 EP2077731 A2 EP 2077731A2 EP 07713116 A EP07713116 A EP 07713116A EP 07713116 A EP07713116 A EP 07713116A EP 2077731 A2 EP2077731 A2 EP 2077731A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- cigarette
- catalyst particles
- encapsulated
- tobacco
- volatile
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
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- 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
-
- 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
- A24B15/281—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
- A24B15/283—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by encapsulation of the chemical substances
-
- 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
-
- 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
-
- 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
- A24B15/281—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
- A24B15/282—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by indirect addition of the chemical substances, e.g. in the wrapper, in the case
-
- 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
- A24B15/285—Treatment of tobacco products or tobacco substitutes by chemical substances characterised by structural features, e.g. particle shape or size
- A24B15/286—Nanoparticles
-
- 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
- A24B15/287—Treatment of tobacco products or tobacco substitutes by chemical substances by inorganic substances only
-
- 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
- A24B15/287—Treatment of tobacco products or tobacco substitutes by chemical substances by inorganic substances only
- A24B15/288—Catalysts or catalytic material, e.g. included in the wrapping material
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES OF CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D1/00—Cigars; Cigarettes
- A24D1/02—Cigars; Cigarettes with special covers
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES OF CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D3/00—Tobacco smoke filters, e.g. filter tips or filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces of cigars or cigarettes
- A24D3/06—Use of materials for tobacco smoke filters
- A24D3/16—Use of materials for tobacco smoke filters of inorganic materials
Definitions
- Cigarettes produce both mainstream smoke during a puff and sidestream smoke during static burning. Constituents of both mainstream smoke and sidestream smoke are carbon monoxide (CO) and nitric oxide (NO) . The reduction of carbon monoxide and/or nitric oxide in smoke is desirable.
- CO carbon monoxide
- NO nitric oxide
- cigarettes and components of cigarettes comprising encapsulated catalyst particles capable of decreasing carbon monoxide and/or nitric oxide in mainstream tobacco smoke, wherein the encapsulated catalyst particles comprise catalyst particles that are at least partially coated with a volatile encapsulant .
- the catalyst particles are fully coated with the volatile encapsulant.
- the catalyst particles which can comprise nanoscale particles, preferably comprise an elemental metal, alloy, oxide and/or oxyhydroxide of at least one element selected from the group consisting of Mg, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Ag, Sn, Ce, Pr, La, Hf, Ta, W, Re, Os, Ir and Au.
- Preferred catalyst particles can decrease tobacco smoke constituents, e.g., catalyze the conversion of carbon monoxide to carbon dioxide and/or nitric oxide to nitrogen, oxidize carbon monoxide to carbon dioxide and reduce nitric oxide to nitrogen.
- the volatile encapsulant is preferably a wax, a water-soluble polymer or a water insoluble polymer.
- the volatile encapsulant can comprise a flavor-bearing compound such as menthol, a menthol derivative or a menthol precursor.
- Preferred volatile encapsulants have a volatilization temperature of between about 40 0 C and about 350 0 C or volatilize upon exposure to an atmosphere having a relative humidity of greater than about 5%.
- the volatile encapsulant comprises a first layer (e.g. , a flavor-bearing layer) in contact with the catalyst particles and a second layer formed over the first layer.
- the volatile encapsulant is adapted to volatilize ⁇ e.g., thermally or chemically degrade) during the smoking of a cigarette to expose an active surface of the catalyst particles .
- the encapsulated catalyst particles can be incorporated homogeneously or non-homogeneousIy along the tobacco rod of a cigarette.
- the encapsulated catalyst particles can be incorporated into the paper wrapper or filter of a cigarette.
- the encapsulated catalyst particles can be incorporated into the first (i.e., inner) layer of a multi-layer wrapper.
- the encapsulated catalyst particles can be distributed throughout the paper wrapper or printed on a surface of the paper wrapper.
- a cigarette can comprise a mixture of different encapsulated catalyst particles.
- a method of making a cigarette comprises (i) incorporating encapsulated catalyst particles in and/or on at least one of tobacco cut filler and a cigarette wrapper; (ii) providing the tobacco cut filler to a cigarette making machine to form a tobacco column,- and (iii) placing the cigarette wrapper around the tobacco column to form a tobacco rod of a cigarette; and (iv) optionally attaching the cigarette filter to the tobacco column using tipping paper.
- the encapsulated catalyst particles can be incorporated by spraying, dusting or immersion.
- encapsulated catalyst particles can be incorporated in cigarette paper by spraying or coating the encapsulated catalyst particles onto a wet base web, intermediate web or finished web.
- Figure l(a) shows an optical microscope image of as-received NANOCAT iron oxide catalyst particles.
- Figures 1 (b) and l(c) show optical microscope images of alginate encapsulated NANOCAT iron oxide in the form of particles and fibers, respectively.
- the encapsulated catalyst particles comprise a core of one or more catalyst particles and a volatile encapsulating layer (i.e., coating) formed around the core.
- a volatile encapsulating layer can be a protective layer for the catalyst particles at near-ambient temperatures (e.g., during cigarette storage and downstream of the combustion/pyrolysis zone in a lit cigarette) , but upon exposure to an elevated temperature, humidity or gas-phase constituents of cigarette smoke the volatile material can volatilize (e.g. , thermally or chemically degrade) to expose the underlying catalyst particles.
- Encapsulated catalyst particles can be incorporated into one or more components of a cigarette such as tobacco cut filler, cigarette paper and cigarette filter of the cigarette. In cigarettes comprising the encapsulated catalyst particles, the amount of carbon monoxide and/or nitric oxide in mainstream smoke can be reduced. Methods for providing cigarettes comprising encapsulated catalyst particles include encapsulation of the catalyst particles and incorporation of the encapsulated catalyst particles into one or more components used to form a cigarette .
- Catalyst particles can be incorporated into a cigarette in order to reduce the concentration in mainstream smoke and/or in sidestream smoke of one or more gas-phase constituents (e.g., CO or NO) .
- gas-phase constituents e.g., CO or NO
- semi-volatile or nonvolatile combustion products such as tar can form on the catalyst particles.
- encapsulated catalyst particles comprising a volatile coating that is formed directly on an exposed surface (e.g., a catalytic surface) of the catalyst particles.
- volatile is meant that the encapsulating layer preferably has a volatilization temperature that is less than the volatilization temperature of tar or other solid-phase byproducts of tobacco combustion/pyrolysis .
- the volatile coating Prior to smoking a cigarette comprising the encapsulated catalyst particles, the volatile coating preferably at least partially encapsulates, more preferably fully encapsulates, the catalyst particles. Preferred volatile coatings are volatilized during smoking of a cigarette.
- the volatile coating forms a protective layer upon which semi-volatile and non-volatile materials (e.g., tar) can deposit.
- Semi-volatile or nonvolatile materials can form and deposit on the volatile coating and not on the catalyst particles .
- the temperature reaches or exceeds the volatilization temperature of the encapsulant, the volatile coating - as well as any materials formed thereon - can be removed to expose an active surface of the catalyst particles.
- an active surface of the catalyst particles can be exposed under smoking conditions (i.e., in advance of the combustion zone) to catalyze and/or oxidize gaseous constituents of mainstream and/or sidestream smoke.
- Applicants have unexpectedly found that encapsulated catalyst particles that are incorporated into a cigarette have a higher catalytic efficiency during smoking of the cigarette than catalyst particles that are not encapsulated.
- a cigarette comprises encapsulated catalyst particles wherein during smoking of the cigarette the volatile encapsulant is volatilized at a distance of from about 0.1 mm to about 10 mm, preferably from about 0.5 mm to about 2 mm in advance of the charline.
- the "charline” is the line created in a cigarette paper wrapper at the edge of the combustion zone of the cigarette, produced during smoking of the cigarette.
- the encapsulating layer is formed from a volatile material that can thermally or chemically degrade.
- the encapsulant material can thermally degrade ⁇ e.g., melt, sublime or pyrolyze) upon exposure to a temperature above an ambient temperature, but below about 350 0 C, preferably below about 200 0 C to expose a surface of the catalyst particles to mainstream smoke, sidestreara smoke or both.
- Preferred encapsulant materials thermally degrade at a temperature between about 40 0 C and about 200 0 C.
- the encapsulant material can chemically degrade [e.g., dissolve) upon exposure to components of cigarette smoke that are generated during smoking.
- moisture in mainstream smoke can interact with the encapsulating layer to volatilize the encapsulant material and expose the catalyst particles .
- Preferred encapsulating layers chemically degrade upon exposure to mainstream smoke or sidestream smoke having a relative humidity of greater than about 5%, more preferably greater than about 20%.
- an active catalytic surface of particles that are incorporated into a cigarette can be exposed in advance of the combustion region of a cigarette.
- the volatile encapsulating layer can minimize physical interaction and chemical reaction between the catalyst particles and non-volatile or semi-volatile combustion and/or pyrolysis products (e.g., tar). For example, high temperature cracking of tar molecules via reaction with the catalyst particles can be minimized.
- the catalyst particles which comprise the core of the encapsulated catalyst particles, can comprise an elemental metal, alloy, oxide and/or an oxyhydroxide of at least one element selected from the group consisting of Mg, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Ag, Sn, Ce, Pr, La, Hf, Ta, W, Re, Os, Ir and Au.
- the catalyst particles preferably comprise nanoscale particles .
- nanoscale is meant that the catalyst particles have an average particle diameter of less than a micron.
- the nanoscale particles have an average particle size of less than about 100 nm, more preferably less than about 50 nm, and most preferably less than about 10 nm.
- Preferred catalyst particles comprise oxides and/or oxyhydroxides of iron.
- MACH I, Inc. King of Prussia, Pennsylvania, U.S.A. markets Fe 2 O 3 nanoscale particles under the trade names NANOCAT S Superfine Iron Oxide (SFIO) and NANOCAT ® Magnetic Iron Oxide.
- the NANOCAT ® Superfine Iron Oxide (SFIO) is amorphous ferric oxide in the - S - form of a free flowing powder, with a particle size of about 3 ran, a specific surface area of about 250 m 2 /g, and a bulk density of about 0.05 g/ml.
- the NANOCAT 0 Superfine Iron Oxide (SFIO) is synthesized by a vapor-phase process, which renders it substantially free of impurities that may be present in conventional catalysts, and is suitable for use in food, drugs, and cosmetics.
- the NANOCAT 0 Magnetic Iron Oxide is a free flowing powder with a particle size of about 25 nm and a surface area of about 40 m 2 /g.
- Further preferred catalyst particles comprise oxides and/or oxyhydroxides of manganese, copper or cerium.
- the encapsulant which forms a coating that encapsulates the catalyst particles, can comprise a wax, a water-soluble polymer, a water insoluble polymer or other material capable of volatilizing during the smoking of a cigarette to expose the underlying catalyst particles.
- Preferred encapsulating materials are non-toxic, easily coated onto catalyst particles, and stable [e.g., thermally and chemically stable) under typical cigarette storage conditions.
- a preferred encapsulant comprises one or more flavor-bearing compounds .
- the encapsulant can comprise a wax.
- Preferable waxes include thermomeltable materials having a melting temperature of from about 40 °C to about 350 0 C.
- Exemplary waxes include beeswax, coconut wax, candelilla wax, carnauba wax, montan wax, ouricury wax, paraffin wax, rice wax, or mixtures thereof.
- the encapsulant can comprise a water-soluble polymer.
- exemplary water-soluble polymers include polyvinyl alcohol, polyvinyl pyrrolidone, polyethylene oxides, water-soluble polyamides, water soluble polyesters, water soluble celluloses, acrylic acid polymers, or mixtures thereof.
- Natural and modified water-soluble polymers include starches, dextrins, gums, gelatins, pectin, alginates, gum arabic, or mixtures thereof.
- Alginates are salts of the long-chain, carbohydrate biopolymer alginic acid, and include sodium alginate, calcium alginate, potassium alginate, and propylene glycol alginate. Though alginic acid is insoluble in water, the salts are hydrocolloids (i.e., they bind or absorb water) and can be formed into a coating. Alginates are generally acid stable and heat resistant. Adjusting the concentration of calcium ions, which cause cross- linking, controls gel strength. Combining alginate with other gums, such as pectin, can increase the viscosity.
- Alginates can be dispersed in ambient temperature water, though the solubility is typically less as the water temperature decreases .
- Alginate concentrations above 2 wt.% can be dispersed using high shear mixing to eliminate clumps.
- High-speed mixers combine high flow with high shear to increase mixing efficiency.
- a preferred method of forming encapsulated catalyst particles comprising a calcium alginate coating is discussed below.
- the encapsulant can comprise a water-insoluble polymer.
- exemplary water-insoluble polymers include polyethylene, polypropylene, polyacrylates , polymethacrylates, polymethylmethacrylates, polyvinyl chloride, polyvinylidene chloride, polysaccharides, or mixtures thereof.
- the encapsulant can comprise a flavor-bearing compound.
- Preferred flavor compounds include menthol, menthol derivatives, and menthol precursors .
- Other suitable flavor compounds include synthetic and natural fragrances, essential oils, alcohols, aldehydes, esters, ethers, ketones, phenols, and mixtures thereof.
- the flavor compound can be an aromatic compound or a non-aromatic compound.
- Catalyst particles can be coated with one or more layers of the same or different volatile encapsulants . For example, multiple coating steps can be used to achieve the desired thickness and/or coverage of a desired encapsulant.
- catalyst particles can be coated with a first volatile coating, and then with a second volatile coating.
- the first volatile coating comprises a flavor-bearing compound.
- Suitable methods include providing the catalyst particles and forming at least one volatile encapsulating layer over the catalyst particles .
- the methods include gas phase techniques and liquid phase techniques.
- catalyst particles can be mixed with a liquid phase encapsulant [e.g., solution or neat liquid of a volatile compound) to form a mixture.
- a liquid phase encapsulant e.g., solution or neat liquid of a volatile compound
- the temperature and the amount of agitation can be controlled.
- catalyst particles and a solution of an encapsulant can be mixed at room temperature and ultrasonicated to form a homogeneous mixture .
- a catalyst particle-encapsulant mixture can be dried to form the encapsulated catalyst particles .
- the mixture can be aspirated to form an aerosol comprising catalyst particles coated with the encapsulant.
- the aerosolization temperature and dispensation rate can be controlled to form solid phase encapsulated catalyst particles (i.e., wherein the encapsulant layer dries to form a solid coating on the catalyst particles) .
- encapsulated catalyst particles comprising 50 wt. % NANOCAT ® iron oxide particles coated with gum arabic can be prepared by first mixing iron oxide particles ( ⁇ 1 g) with gum arabic ( ⁇ 1 g) in about 30 ml of de-ionized water under constant agitation to form a uniform suspension of the iron oxide particles.
- the suspension is aerosolized using a 0.5 mm nozzle at about 170 0 C whereby the water present in the mixture is evaporated and gum arabic-coated iron oxide particles are formed.
- the encapsulated catalyst' particles can be in the form of a powder, granulate or agglomerate.
- the encapsulated catalyst particles can be in the shape of spheres, spheroids, threads, fibrils, and the like.
- catalyst particles can be immersed in a liquid phase encapsulant or encapsulant precursor (e.g., solution or neat liquid of a volatile compound) to form a mixture wherein a coating is formed on the catalyst particles .
- a liquid phase encapsulant or encapsulant precursor e.g., solution or neat liquid of a volatile compound
- the temperature during the immersion can be controlled and the mixture can optionally be agitated (e.g., stirred).
- Catalyst particles and an encapsulant can be mixed at room temperature to form the coating .
- the coated catalyst particles can be dried and optionally processed further to form encapsulated catalyst particles . Further processing can comprise cross-linking the encapsulating polymer, such as via an ion exchange reaction.
- a method of forming alginate-encapsulated catalyst particles comprises immersing catalyst particles in a solution of an alginate salt to form coated catalyst particles, and then treating the coated catalyst particles to form a cross-linked polymeric alginate coating.
- encapsulated catalyst particles comprising 50 wt. % NANOCAT 0 iron oxide particles coated with calcium and/or sodium alginate can be prepared by first mixing iron oxide particles ( ⁇ 1 g) with a solution of sodium alginate (1 g of sodium alginate in 100 ml of de-ionized water) under constant agitation to form sodium alginate coated iron oxide particles.
- the mixture is preferably homogenized ⁇ e.g., for 30-130 seconds), allowed to sit in air (e.g., for 10-60 minutes), and then re-homogenized ⁇ e.g., for 30-130 seconds).
- the sodium alginate coating can be at least partially and preferably fully converted ⁇ e.g., polymerized) to a calcium alginate coating via an ion exchange reaction.
- a known volume of the sodium alginate coated iron oxide particles is preferably contacted with a solution comprising a multivalent cation.
- the solution can comprise an aqueous or a non-aqueous (e.g., alcoholic) solution.
- the solution comprises calcium chloride (e.g. , 0.1 M aqueous solution of calcium chloride) whereby Ca 2+ is exchanged for Na 1+ via an ion exchange reaction that forms a cross-linked volatile calcium alginate shell around the iron oxide particles.
- multivalent cation solutions suitable for forming a cross-linked encapsulating layer can comprise aluminum, manganese, iron, copper, zinc, strontium, silver and barium.
- the hardness of a cross-linked polymer encapsulant can be controlled by varying the degree of cross- linking.
- the amount of cross-linking is proportional to the reaction time (i.e., cure time) between the encapsulant and the multivalent cation solution.
- Other polymers that can be cross-linked via ion exchange include polysaccharides .
- a known volume of the sodium alginate coated iron oxide particles is dispersed drop-wise (e.g., through a syringe such as a 26.5 gauge needle) into a calcium chloride solution.
- the height and rate of dispensation can be controlled to control the size of the encapsulated particles.
- Excess calcium chloride solution can be removed (e.g. , filtered or decanted) after a pre-set cure time (e.gr., up to about 2 hours) and the calcium alginate-coated particles can be washed and dried.
- Encapsulated catalyst particles comprising at least about 10, 20, 30, 40, 50, 60, 70, 80 or 90 ⁇ 5 wt .
- % catalyst particles e.g., iron oxide particles
- Optical micrographs of iron oxide/calcium alginate samples are shown in Figure 1.
- Figure 1 (a) shows an optical micrograph of as- received NANOCAT ® iron oxide particles.
- Figure 1 (b) shows an optical micrograph of calcium alginate encapsulated iron oxide particles in the form of irregular and spherical particles.
- Figure l(c) shows an optical micrograph of calcium alginate encapsulated iron oxide particles in the form of fibrils.
- Additional methods for forming encapsulated catalyst particles include polymer-polymer incompatibility (wherein catalyst particles are coated via preferential adsorption of one polymer from a solution of incompatible polymers that are dissolved in a common solvent) ; fluidized-bed encapsulation and gas phase polymerization.
- Encapsulated micron sized catalyst particles can have an average particle size of from about 1 micron or less to about 1000 microns or more .
- the encapsulated catalyst particles can have an average particle size of 10, 20, 30, 40, 50, 60, 70, 80 or 90 microns + 5 microns up to about 100, 200, 300, 400, 500, 600, 700, 800 or 900 microns ⁇ 50 microns.
- the encapsulated catalyst particles can comprise individual particles or an agglomerate of coated catalyst particles .
- Preferred encapsulated catalyst particles have an average particle size of less than 1 micron.
- Submicron and nanoscale catalyst particles can be encapsulated to form encapsulated catalyst particles having an average particle size of 10, 20, 30, 40, 50, 60, 70, 80 or 90 nm ⁇ 5 nm up to about 100, 200, 300, 400, 500, 600, 700, 800 or 900 nm ⁇ 50 nm, depending on the average thickness of the encapsulant .
- the encapsulated catalyst particles are incorporated in at least one of tobacco cut filler, cigarette paper and cigarette filter that are used to form a cigarette.
- the catalyst particles By incorporating the catalyst particles into one or more components of a cigarette, the amount of carbon monoxide and/or nitric oxide in mainstream smoke during smoking can be reduced.
- a catalyst is capable of affecting the rate of a chemical reaction, e.g. , a catalyst can increase the rate of oxidation of carbon monoxide to carbon dioxide without participating as a reactant or product of the reaction.
- An oxidant is capable of oxidizing a reactant, e.g., by donating oxygen to the reactant, such that the oxidant itself is reduced.
- a reducing agent is capable of reducing a reactant, e.g., by receiving oxygen from the reactant, such that the reducing agent itself is oxidized.
- the temperature ranges from ambient to about 150 0 C.
- the major process in this zone is the condensation/filtration of the smoke components.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Nanotechnology (AREA)
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
- Manufacture Of Tobacco Products (AREA)
- Paper (AREA)
- Catalysts (AREA)
- Manufacturing Of Micro-Capsules (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SI200730717T SI2077731T1 (en) | 2006-01-17 | 2007-01-17 | Cigarette components having encapsulated catalyst particles and methods of making and use thereof |
| PL07713116T PL2077731T3 (en) | 2006-01-17 | 2007-01-17 | Cigarette components having encapsulated catalyst particles and methods of making and use thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75903606P | 2006-01-17 | 2006-01-17 | |
| PCT/IB2007/000576 WO2007083245A2 (en) | 2006-01-17 | 2007-01-17 | Cigarette components having encapsulated catalyst particles and methods of making and use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2077731A2 true EP2077731A2 (en) | 2009-07-15 |
| EP2077731B1 EP2077731B1 (en) | 2011-08-31 |
Family
ID=38255036
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07713116A Active EP2077731B1 (en) | 2006-01-17 | 2007-01-17 | Cigarette components having encapsulated catalyst particles and methods of making and use thereof |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20070246054A1 (en) |
| EP (1) | EP2077731B1 (en) |
| JP (1) | JP5562559B2 (en) |
| KR (1) | KR20080083349A (en) |
| CN (1) | CN101374429B (en) |
| AT (1) | ATE522153T1 (en) |
| AU (1) | AU2007206684B2 (en) |
| BR (1) | BRPI0706603A2 (en) |
| DK (1) | DK2077731T3 (en) |
| EA (1) | EA013588B1 (en) |
| ES (1) | ES2372702T3 (en) |
| MY (1) | MY143942A (en) |
| NO (1) | NO20083552L (en) |
| NZ (1) | NZ569666A (en) |
| PL (1) | PL2077731T3 (en) |
| PT (1) | PT2077731E (en) |
| SI (1) | SI2077731T1 (en) |
| UA (1) | UA93231C2 (en) |
| WO (1) | WO2007083245A2 (en) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007503829A (en) * | 2003-09-03 | 2007-03-01 | レシス アクティエボラーグ | Cigarette smoke filter |
| US7677254B2 (en) * | 2003-10-27 | 2010-03-16 | Philip Morris Usa Inc. | Reduction of carbon monoxide and nitric oxide in smoking articles using iron oxynitride |
| US8006703B2 (en) | 2003-10-27 | 2011-08-30 | Philip Morris Usa Inc. | In situ synthesis of composite nanoscale particles |
| US8051859B2 (en) | 2003-10-27 | 2011-11-08 | Philip Morris Usa Inc. | Formation and deposition of sputtered nanoscale particles in cigarette manufacture |
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- 2007-01-17 WO PCT/IB2007/000576 patent/WO2007083245A2/en not_active Ceased
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- 2007-01-17 DK DK07713116.7T patent/DK2077731T3/en active
- 2007-01-17 KR KR1020087019071A patent/KR20080083349A/en not_active Abandoned
- 2007-01-17 PT PT07713116T patent/PT2077731E/en unknown
- 2007-01-17 UA UAA200810462A patent/UA93231C2/en unknown
- 2007-01-17 US US11/653,856 patent/US20070246054A1/en not_active Abandoned
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2008
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| UA93231C2 (en) | 2011-01-25 |
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| CN101374429A (en) | 2009-02-25 |
| BRPI0706603A2 (en) | 2011-03-29 |
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| US20070246054A1 (en) | 2007-10-25 |
| ES2372702T3 (en) | 2012-01-25 |
| WO2007083245A2 (en) | 2007-07-26 |
| EA200870175A1 (en) | 2009-12-30 |
| JP2009523439A (en) | 2009-06-25 |
| DK2077731T3 (en) | 2011-10-31 |
| SI2077731T1 (en) | 2011-10-28 |
| MY143942A (en) | 2011-07-29 |
| HK1126937A1 (en) | 2009-09-18 |
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