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    • 专利摘要:
    combustible heat source, smoke article, and combustible heat source production method. The present invention relates to a combustible heat source (4) for a smoking article (2) which comprises carbon and a binding agent. the binding agent includes a combination of three binding components: an organic polymeric binding material, a carboxylate burning salt and an inorganic non-combustible binding material. at least one non-combustible organic binder material comprises a sheet silicate material. preferably, the combustible heat source further comprises an ignition aid.
    公开号:BR112014033121B1
    申请号:R112014033121-9
    申请日:2013-07-03
    公开日:2021-07-20
    发明作者:Alexandre Malgat；Laurent Poget
    申请人:Philip Morris Products S.A.；
    IPC主号:
    专利说明:

    [0001] The present invention relates to a combustible heat source for a smoking article, the heat source comprising carbon and an improved binding agent including a combination of organic and inorganic binding materials. The invention further relates to a heated smoking article comprising such a combustible heat source and an aerosol forming substrate.
    [0002] A number of smoking articles in which tobacco is heated rather than burned have been proposed in the art. One purpose of such 'heated' tobacco articles is to reduce known harmful smoke constituents of the type produced by the combustion and pyrolytic degradation of tobacco in conventional cigarettes.
    [0003] In a known type of heated smoke article, an aerosol is generated by transferring heat from a combustible heat source to an aerosol forming substrate located downstream of the combustible heat source. During smoking, volatile compounds are released from the aerosol-forming substrate by heat transfer from the combustible heat source, and entrained in exhausted air through the smoking article. As the released compounds cool, they condense to form an aerosol that is inhaled by the user.
    [0004] For example, WO-A-2009/022232 discloses a smoking article comprising a combustible heat source, an aerosol forming substrate downstream of the combustible heat source, and a heat conduction element around and in contact with a rear portion of the combustible heat source and an adjacent front portion of the aerosol forming substrate. The heat conducting element in the smoke article of WO-A-2009/022232 helps to transfer the heat generated during combustion from the heat source to the aerosol forming substrate.
    [0005] Some carbon-based heat sources incorporate an organic binder, such as a cellulose derivative, to help improve the integrity of the heat source during production, processing and storage. However, organic binders are typically combustible at temperatures reached within the heat source during burning. As a result, organic binders were found to disintegrate during smoking of the heated smoking article, leading to a loss of heat source integrity.
    [0006] The disintegration of the organic binder can result in deformation of the heat source during and after burning, which can, in turn, cause cracking or breakdown of the heat source, or the release of ash from the burned heat source . Furthermore, during burning of the organic binder, gases are typically released, which create pressure within the heat source, further increasing the likelihood of cracking or breaking.
    [0007] It would be desirable to provide a combustible heat source for a heated smoking article that has improved integrity during and after smoking. It would be particularly desirable to provide such a combustible heat source which also has improved burning properties.
    [0008] According to the invention, there is provided a combustible heat source for a smoking article, the combustible heat source comprising carbon and a binding agent including at least one organic polymeric binder material, at least one burning salt of carboxylate, and at least one non-combustible organic binder material, wherein the at least one non-combustible inorganic binder material comprises a sheet silicate material.
    [0009] According to the invention, there is also provided a smoking article comprising a combustible heat source according to the invention, as defined above, and an aerosol forming substrate downstream of the combustible heat source.
    [00010] The invention further provides the use of a binding agent to improve the integrity of a carbon-containing combustible heat source for a smoking article, the binding agent comprising at least one organic polymeric binding material, at least one carboxylate burning salt, and at least one inorganic non-combustible binder material, wherein the at least one inorganic non-combustible binder material comprises a sheet silicate material.
    [00011] The invention further provides a method of producing a combustible heat source having improved integrity, the method comprising the steps of: combining one or more carbon-containing materials with a binding agent including at least one organic polymeric binder material at least one carboxylate burning salt, and at least one inorganic non-combustible binder material, wherein the at least one inorganic non-combustible binder material comprises a sheet silicate material; preforming the mixture of the one or more carbon-containing materials and the binding agent into an elongated rod; and drying the elongated rod.
    [00012] The combustible heat source of the invention can be an extruded heat source, formed by an extrusion process, as described in more detail below. Alternatively and preferably, the combustible heat source of the invention may be a pressed heat source, formed by a pressing process, as also described in more detail below. Pressed heat sources have been found to show the greatest improvement in integrity as a result of using a binding agent including the combination of three components defined above.
    [00013] The term "bonding agent" is used here to refer to the component of the combustible heat source that binds carbon and any other additives within the heat source together, such that a solid heat source can be formed that retains its structure.
    [00014] The term "carboxylate burning salt" is used to refer to a salt of a carboxylic acid, which is believed to modify the combustion of carbon. Preferably, the carboxylate burning salt comprises a monovalent, divalent, or trivalent cation, and a carboxylate anion at room temperature, in which the carboxylate anion burns when the combustible heat source is ignited. More preferably, the carboxylate burning salt is an alkali metal carboxylate burning salt comprising a monovalent alkali metal cation and a carboxylate anion at room temperature, in which the carboxylate anion burns when the combustible heat source is ignited. . Specific examples of carboxylate burning salts that may be included in the inventive combustible heat source binding agent include, but are not limited to, alkali metal acetates, alkali metal citrates, and alkali metal succinates.
    [00015] In certain embodiments, the binding agent may include a simple carboxylate burning salt. In other embodiments, the coupling agent can comprise a combination of two or more different carboxylate burning salts. The two or more different carboxylate burning salts can comprise different carboxylate anions. Alternatively or in addition, the two or more different carboxylate burning salts may comprise different cations. By way of example, the binding agent may comprise a mixture of an alkali metal citrate and an alkaline earth metal succinate.
    [00016] The term "non-combustible" is used herein to refer to an inorganic binder material that does not burn or decompose during ignition and burning of the combustible heat source of the invention. The inorganic non-combustible binding material is therefore stable at the temperatures to which the binding agent is subjected during burning of the combustible heat source, and will remain substantially intact during and after burning.
    [00017] The terms "upstream", "front", "downstream" and "rear" are used herein to describe the relative positions of components or component portions of smoke articles of the invention with respect to the direction of air withdrawn through of smoking articles during use.
    [00018] In the combustible heat source of the invention, carbon is combined with a binding agent formed from a specific new combination of inorganic and organic binding materials. In particular, an organic polymeric binder material, such as that used in prior art combustible heat sources, is combined with at least one carboxylate burning salt and at least one inorganic non-combustible binder material in which the at least one non-combustible binder material inorganic comprises a silicate sheet material. In the following description, the organic polymeric binder material, the carboxylate burning salt, and the inorganic non-combustible binder material are collectively referred to as the "binding components".
    [00019] The use of a binding agent including a specific combination of an organic polymeric binding material, a carboxylate burning salt, and an inorganic non-combustible binding material comprising a sheet silicate material, has been advantageously found to increase the integrity of the source of combustible heat during and after burning, compared to a heat source comprising only organic binding material. The combustible heat source of the invention exhibits reduced deformation due to burning, so that the occurrence of fractures, breakage or fragmentation of the heat source is reduced. Furthermore, the combustible heat source of the invention forms a more cohesive ash after burning so that particles or fragments of the ash are less likely to break down from the heat source. The appearance of gray is also found to be improved, with a more uniform consistency and a darker, more uniform color.
    [00020] The term "integrity" is used herein to refer to the ability of the combustible heat source of the invention to remain complete or intact. Any significant loss of combustible heat source integrity could result in cracking or breakdown of the heat source. Poor integrity of a combustible heat source can also be indicated by the generation of sparks or flames during ignition of the heat source.
    [00021] As described in more detail below, a quantitative measure of the integrity of a combustible heat source can be provided using an experimental test in which the probability of a portion of the combustible heat source within a heated smoke article decreases under conditions of controlled burning, known as "reduction", is measured. In particular, the test provides a direct comparison of the integrity of combustible heat sources including different binding agents. It has been found that the probability of decrease of a combustible heat source of the invention is reduced compared to the probability of decrease under the same conditions for a prior art combustible heat source including only organic binder material.
    [00022] The lower the probability of decay of a combustible heat source, the better the integrity of the combustible heat source is considered to be. Preferably, the probability of decrease of a combustible heat source of the invention is less than 20 percent, more preferably less than 10 percent, and most preferably close to 0 percent, under the experimental conditions described below.
    [00023] The improvement provided in the integrity of the fuel heat source as a result of using the specific combination of binding components defined above is greater than can be predicted based on the behavior of the individual binding components. In addition, the use of the combination of the three binder components has been shown to provide an unexpected improvement in the mechanical strength of the fuel heat source, as demonstrated by an increase in the compressive strength of the fuel heat source. The binding agent, therefore, surprisingly provides advantageous effects on the physical properties of the fuel heat source of the invention.
    [00024] It has also been advantageously found that the ratio of the three binding components of the binding agent of the fuel heat source of the invention can be adjusted so as to modify and improve the burning properties of the heat source. For example, the ratio of the binder components can be adapted to increase the firing temperature or the firing lifetime of the heat source compared to a heat source including only organic binder material.
    [00025] The use of a binding agent comprising the combination of three different binder components in the fuel heat source of the invention has also been advantageously shown to increase the rate of combustion propagation of carbon from the heat source from the front end to the end. of the heat source after ignition of the front end of the same. The propagation of carbon combustion through the combustible heat source is clearly shown by a change in color on the surface of the combustible heat source due to the downstream movement of a forward deflagration from the front end to the rear end of the combustible heat source . The faster propagation of carbon combustion through the combustible heat source after ignition advantageously reduces the time to first puff. As described in more detail below, the three different binding agent binding components each provide a different structure and function within the fuel heat source. Furthermore, the binding components each become different after burning from the combustible heat source. The combination of the different properties and behaviors of the binding components provides improved binding effects and, in particular, the surprising improvement in the integrity of the fuel heat source.
    [00026] The organic polymeric binder in the fuel heat source binding agent of the invention is typically formed from long, flexible organic polymers. Organic polymeric binder material is typically a good fuel that improves the burning qualities of the combustible heat source. As stated above, the organic polymeric binder material also helps to bind carbon during the production of the fuel heat source and prior to burning. However, the organic polymeric binder material burns upon ignition of the heat source and thus does not provide any significant binding effect during or after burning.
    [00027] The organic polymeric binder material can include any suitable organic polymeric binders that do not produce harmful by-products after heating or burning. The organic polymeric binder material may include a single type of organic polymer, or a combination of two of more different types of organic polymer. Preferably, the organic polymeric binder material comprises one or more cellulosic polymer materials. Suitable cellulosic polymer materials include, but are not limited to, cellulose, modified cellulose, methyl cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, and combinations thereof. In particularly preferred embodiments of the invention, the organic polymeric binder material comprises carboxymethyl cellulose (CMC). A suitable source of CMC for use in the invention is available from Phrikolat GmbH, Germany. Alternatively or in addition to the one or more cellulosic polymer materials, the organic polymeric binder material can comprise one or more non-cellulosic polymer materials, including, but not limited to, gums such as, for example, guar gum; wheat flour; starches; sugars; vegetable oils, and combinations thereof.
    [00028] Preferably, the binding agent includes between about 25 percent by weight and about 80 percent by weight of the organic polymeric binder material, more preferably, between about 30 percent by weight and about 75 percent by weight. weight of organic polymeric binder material.
    [00029] In contrast to organic polymeric binder material, the carboxylate burning salt in the combustible heat source binding agent of the invention typically comprises ions that are generally smaller in size to each other, larger molecules in the heat source. The carboxylate burning salt promotes combustion of the heat source. In addition, unlike the organic binder, the carboxylate burning salt has been found to retain a cohesive structure around the other molecules within the fuel heat source during and after burning, which helps to bind the heat source materials together. The carboxylate burning salt, therefore, improves the integrity of the combustible heat source during and after burning, and reduces the likelihood of deformation and breakdown of the heat source. Retaining the binding effect of the carboxylate firing salt after firing further improves the cohesion and appearance of the ash material.
    [00030] The inclusion of a carboxylate burning salt in the fuel heat source of the invention further provides improvement in the burning properties of the fuel heat source. In particular, the carboxylate burning salt can increase the burning time of the fuel heat source of the invention compared to fuel heat sources including only organic binder material. In addition, the promotion of combustion of the heat source by the carboxylate burning salt can enable a higher density combustible heat source to be used in a heated tobacco article. This enables a combustible heat source to be produced with a higher amount of carbon fuel for a heat source of a given size, which can additionally improve the burning time of the combustible heat source.
    [00031] Preferably, the carboxylate burning salt is a potassium or sodium salt of a carboxylic acid such as a citrate, acetate or succinate. In preferred embodiments, the carboxylate burning salt is an alkali metal citrate salt. In particularly preferred embodiments of the invention, the carboxylate burning salt is potassium citrate, more preferably, mono-potassium citrate.
    [00032] The nature of the cation and the nature of the anion selected for the carboxylate burning salt can both have an impact on the burning properties of the fuel heat source and, in particular, on the useful burn time, on the burning temperature, and at the initial temperature during ignition of the combustible heat source. The nature of the carboxylate burning salt and the amount of carboxylate burning salt incorporated in the binding agent can therefore be adjusted depending on the desired burning properties of the combustible heat source.
    [00033] Preferably, the binding agent comprises between about 5 percent by weight and about 50 percent by weight of the carboxylate burning salt, more preferably, between about 8 percent by weight and about 40 percent by weight of the carboxylate burning salt.
    [00034] The inorganic non-combustible binder material comprises a sheet silicate material.
    [00035] The inorganic binder material is preferably formed of a material with relatively large, flat and inflexible molecules. The inorganic binder material is non-combustible at the temperatures reached within the combustible heat source during burning, so the inorganic binder material is still present after ignition and burning of the heat source. The inorganic binder material, therefore, retains its binding properties, and will continue to bind the heat source materials together after the organic binder has been burned. At certain levels, the addition of an inorganic binder material can additionally increase the burning temperature of the fuel heat source so that the burning properties can be adjusted. In particular, the level of inorganic non-combustible binding material can be adjusted to increase the temperature of the heat source during ignition.
    [00036] The inorganic binder material can include any suitable inorganic binders that are inert and do not burn or decompose during combustion of the heat source. The inorganic non-combustible binder material may include a single type of inorganic binder, or a combination of two of more different types of inorganic binder. Suitable sheet silicate materials for inclusion in the inorganic non-combustible binder material include, but are not limited to, clays, micas, serpentinites, and combinations thereof. In particularly preferred embodiments, the inorganic non-combustible binder material comprises one or more clays. Other inorganic binders suitable for inclusion in the inorganic non-combustible binder material include, but are not limited to, alumina-silicate derivatives, alkali silicates, limestone derivatives, alkaline earth compounds and derivatives, aluminum compounds and derivatives, and combinations thereof.
    [00037] The term "clay" is used herein to refer to aluminum phyllosilicate materials formed from two dimensional sheets of silicate and aluminate ions, which form a distinct layered structure within the clay. Suitable clays for use in the combustible heat source binding agent of the invention include, but are not limited to, bentonite, montmorillonite and kaolinite. Suitable clays are available from Worlee-Chimie GmbH, Germany or Nanocor.
    [00038] Particularly preferably, the one or more clays used in the combustible heat source binding agent of the invention are exfoliated clays. The term "exfoliated clays" is used herein to refer to clays that support an exfoliation or delamination process, in which the separation between the layers of silicate and aluminate sheets is increased, in some cases by up to 20 times or more.
    [00039] The large flat structure of sheet silicate material, such as clays, is, in contrast to the long flexible molecules of the organic binder material and the small ions of the carboxylate burning salt. The combination of the binder molecules with these different structures has been found to be effective in providing binding properties, not only during the production and storage of the fuel heat source of the invention, but also during the afterburning.
    [00040] Preferably, the binding agent comprises between about 10 percent by weight and about 35 percent by weight of the inorganic non-combustible binding material, more preferably, between about 15 percent by weight and about 35 percent by weight. weight of inorganic non-combustible binding material.
    [00041] In particularly preferred embodiments of the invention, the combustible heat source comprises a binding agent comprising a combination of carboxymethyl cellulose as the organic binding material, potassium citrate as the carboxylate burning salt, and clay as the binding material inorganic non-combustible. In certain preferred embodiments, the binding agent comprises about 73 percent by weight of carboxymethyl cellulose as the organic binder material, about 17 percent by weight of potassium citrate as the carboxylate burning salt, and about 10 weight percent clay as the inorganic non-combustible binder material.
    [00042] This combination of bonding components has been found to show particularly effective bonding properties, and the resulting combustible heat sources retain integrity, with little or no visible deformation or cracking during or after firing. The ash that remains after combustion of the combustible heat source including this combination of binder components has also been found to have improved cohesion and appearance compared to prior art combustible heat sources including only organic binder material.
    [00043] The combustible heat sources of the invention preferably comprise between about 2 percent by weight and about 10 percent by weight of the binding agent including the three different binding components, more preferably between about 4 percent by weight and about 10 percent by weight of the binding agent, and more preferably, between about 5 percent by weight and about 9 percent by weight of the binding agent. In certain preferred embodiments, the combustible heat sources of the invention comprise about 8 percent by weight of the binding agent.
    [00044] The binding agent is preferably incorporated into the combustible heat source of the invention during production of the heat source. A combination of the three binding agent binding components can be incorporated into the heat source material in a single step during production, or the three binding components can be added in two or three separate steps.
    [00045] One or more binding agent binding components may be added to the other components of the combustible heat source in the form of a substantially dry solid powder. Alternatively, one or more of the binder components of the binding agent may be added to the other components of the fuel heat source in the form of a binder solution comprising the one or more binder components dissolved or suspended in a suitable solvent, such as water. Preferably, at least the carboxylate burning salt is added to the other components of the fuel heat source in the form of a solution. For example, where the carboxylate burning salt comprises potassium citrate, a solution of between 5% by weight and 10% by weight of potassium citrate in water can be used.
    [00046] Where one or more of the binder components of the binding agent are incorporated in the form of a binder solution, the pH of the binder solution is preferably adapted to a basic pH of at least pH 8, more preferably at least pH 10, and more preferably about pH 12. The natural pH of the solution will typically be acidic, and in such cases, the pH can readily be increased by the addition of a suitable alkali.
    [00047] The binding components and, in particular, the organic polymeric binding material are typically sensitive to changes in pH. This may be particularly true for a charged organic polymeric binder material, for which an increase in the pH of the binder solution can influence the charge on the binder molecules and therefore the molecular configuration and binding properties. It has been found that the use of a binder solution having a basic pH (pH 8 or above) improves the burning properties of the fuel heat source of the invention compared to a similar fuel heat source formed using an acidic binder solution. In particular, it has been found that the combustible heat source has an increased burn life so that the combustible heat source can continue to burn for a longer time.
    [00048] Furthermore, the use of a basic binder solution has been found to produce a fuel heat source of increased density and improves the integrity of the fuel heat source after burning, compared to a similar fuel heat source formed using a solution of acidic binder.
    [00049] The combustible heat sources of the invention are carbon-containing heat source comprising carbon as a fuel. Preferably, the combustible heat sources according to the invention have a carbon content of at least about 35 percent, more preferably, at least about 40 percent, more preferably, at least about 45 percent. dry weight of the combustible heat source.
    [00050] In some embodiments, the combustible heat source according to the invention is a carbon-based heat source. As used herein, the term "carbon-based heat source" is used to describe a heat source comprised primarily of carbon. Combustible carbon-based heat sources for use in smoking articles according to the invention have a carbon content of at least about 50 percent, preferably at least about 60 percent, more preferably, at least about 70 percent, more preferably, at least about 80 percent dry weight of the carbon-based fuel heat source.
    [00051] The combustible heat sources according to the invention may be formed from one or more suitable carbon-containing materials. Suitable carbon-containing materials are well known in the art, and include, but are not limited to, carbon powder.
    [00052] The combustible heat sources according to the invention preferably additionally comprise at least one ignition aid.
    [00053] As used herein, the term "ignition aid" denotes a material that releases one or both of energy and oxygen during ignition of the combustible heat source, where the rate of release of one or both of energy and oxygen by the material does not it is limited ambient oxygen diffusion. In other words, the rate of release of one or both of energy and oxygen by the material during ignition of the combustible heat source is largely independent of the rate at which ambient oxygen can reach the material. As used herein, the term "ignition aid" also denotes an elemental metal that releases energy during ignition of the combustible heat source, in which the ignition temperature of the elemental metal is below about 500°C, and the heat of combustion of the elemental metal is at least about 5 kJ/g.
    [00054] As used herein, the term "ignition aid" does not include carboxylate burning salts as defined above.
    [00055] Ignition aids suitable for use in the combustible heat source of the invention are known in the art.
    [00056] The combustible heat sources, according to the invention, can comprise one or more ignition aids consisting of a simple element or compound that releases energy after ignition of the combustible heat source. The release of energy by the one or more ignition aids after ignition of the combustible heat source directly causes a 'pulse' in temperature during an early stage of combustion of the combustible heat source.
    [00057] For example, in certain embodiments, the combustible heat sources according to the invention may comprise one or more energetic materials consisting of a simple element or compound that exothermically reacts with oxygen after ignition of the combustible heat sources. Examples of suitable energy materials include, but are not limited to, aluminum, iron, magnesium, and zirconia.
    [00058] Alternatively or in addition, the combustible heat sources according to the invention may comprise one or more ignition aids comprising two or more elements or compounds that react with each other to release energy after ignition of the combustible heat source.
    [00059] For example, in certain embodiments, combustible heat sources according to the invention may comprise one or more termites or termite compounds comprising a reducing agent, such as, for example, a metal, and an agent of oxidation, such as, for example, a metal oxide, which react with each other to release energy after ignition of the combustible heat sources. Examples of suitable metals include, but are not limited to, magnesium, and examples of suitable metal oxides include, but are not limited to, iron oxide (Fe2O3) and aluminum oxide (Al2O3)
    [00060] In other embodiments, the combustible heat sources, according to the invention, may comprise one or more ignition aids comprising other materials that support exothermic reactions after ignition of the combustible heat source. Examples of suitable metals include, but are not limited to, intermetallic and bimetallic materials, metal cerbetes, and metal hydrides.
    [00061] In preferred embodiments, the combustible heat sources, according to the invention, comprise at least one ignition aid that releases oxygen during ignition of the combustible heat source.
    [00062] In such embodiments, the release of oxygen by at least one ignition aid after ignition of the combustible heat source indirectly results in a 'boost' in temperature during an early stage of combustion of the combustible heat source by increasing the rate of combustion of the combustible heat source.
    [00063] For example, the combustible heat sources, according to the invention, can comprise one or more oxidizing agents that decompose to release oxygen after ignition of the combustible heat source. Combustible heat sources according to the invention may comprise organic oxidizing agents, inorganic oxidizing agents, or a combination thereof. Examples of suitable oxidizing agents include, but are not limited to: nitrates such as, for example, potassium nitrate, calcium nitrate, strontium nitrate, sodium nitrate, barium nitrate, lithium nitrate, aluminum nitrate, and iron nitrate; nitrites; other organic and inorganic nitro compounds; chlorates such as, for example, sodium chlorate and potassium chlorate; perchlorates such as, for example, sodium perchlorate; chlorites; bromates, such as, for example, sodium bromate and potassium bromate; perbromates; bromites; borates, such as, for example, sodium borate and potassium borate; ferrates, such as, for example, barium ferrate; ferrites; manganates, such as, for example, potassium manganate; permanganates, such as, for example, potassium permanganate; organic peroxides such as, for example, benzoyl peroxide and acetone; inorganic peroxides, such as, for example, hydrogen peroxide, strontium peroxide, magnesium peroxide, calcium peroxide, barium peroxide, zinc peroxide and lithium peroxide; superoxides, such as, for example, potassium superoxide and sodium superoxide; iodates; periodates; iodides; sulfates; sulfites; other sulfoxides; phosphates; phosphinates; phosphites; and phosphinites.
    [00064] Alternatively or in addition, the combustible heat sources according to the invention may comprise one or more sequestering or oxygen storage materials that release oxygen upon ignition of the combustible heat source. Combustible heat sources according to the invention may comprise sequestering or oxygen storage materials that store and release oxygen through encapsulation, physisorption, chemosorption, structural change, or a combination thereof. Examples of suitable oxygen scavenger or storage materials include, but are not limited to: metal surfaces, such as, for example, metallic silver or metallic gold surfaces; mixed metal oxides; molecular sieves; zeolites; metal-organic structures; covalent organic structures; spinels; and perovskites.
    [00065] The combustible heat sources, according to the invention, may comprise one or more ignition aids consisting of a simple element or compound that releases oxygen after ignition of the combustible heat source. Alternatively or in addition, combustible heat sources according to the invention may comprise one or more ignition aids comprising two or more elements or compounds which react with each other to release oxygen upon ignition of the combustible heat source.
    [00066] The combustible heat sources according to the invention may comprise one or more ignition aids that release both energy and oxygen after ignition of the combustible heat source. For example, combustible heat sources in accordance with the invention may comprise one or more oxidizing agents that decompose exothermically to release oxygen upon ignition of the combustible heat source.
    [00067] Alternatively, or in addition, the combustible heat sources according to the invention may comprise one or more first ignition aids that release energy after ignition of the combustible heat source, and one or more second ignition aids, which are different from the one or more first ignition aids, and which release oxygen upon ignition from the combustible heat source.
    [00068] In certain embodiments, combustible heat sources according to the invention may comprise at least one metal nitrate salt having a thermal decomposition temperature of less than about 600°C, more preferably less than about 400°C.
    [00069] Preferably, the at least one metal nitrate salt has a decomposition temperature of between about 150°C and about 600°C, more preferably between about 200°C and about 400°C.
    [00070] In such embodiments, when the combustible heat source is exposed to a lighter conventional yellow flame, or other means of ignition, the at least one metal nitrate salt decomposes to release oxygen and energy. This causes an initial rise in the temperature of the combustible heat source, and also assists in igniting the combustible heat source. After the decomposition of at least one metal nitrate salt, the combustible heat source continues to burn at a lower temperature.
    [00071] The inclusion of at least one metal nitrate salt advantageously results in ignition of the combustible heat source being initiated internally, and not only at a point on the surface thereof. In certain embodiments, the at least one metal nitrate salt is distributed substantially homogeneously throughout the fuel heat source.
    [00072] Preferably, the at least one metal nitrate salt is present in the combustible heat source in an amount of between about 20 percent and about 50 percent by dry weight of the combustible heat source.
    [00073] Preferably, the at least one metal nitrate salt is selected from the group consisting of potassium nitrate, sodium nitrate, calcium nitrate, strontium nitrate, barium nitrate, lithium nitrate, aluminum nitrate, and iron nitrate.
    [00074] In certain embodiments, combustible heat sources according to the invention may comprise at least two different metal nitrate salts.
    [00075] In one embodiment, the combustible heat sources, according to the invention, comprise potassium nitrate, calcium nitrate, and strontium nitrate. Preferably, potassium nitrate is present in an amount of between about 5 percent and about 15 percent dry weight of the fuel heat sources, calcium nitrate is present in an amount of between about 2 percent and about 10 percent dry weight of the fuel heat source, and the strontium nitrate is present in an amount of between about 15 percent by weight and about 25 percent dry weight of the fuel heat source.
    [00076] In other embodiments, the combustible heat sources according to the invention may comprise at least one peroxide or superoxide that actively envelops oxygen at a temperature of less than about 600°C, more preferably at a temperature of less than about 400°C.
    [00077] Preferably, the at least one peroxide or superoxide actively involves oxygen at a temperature of between about 150°C and about 600°C, more preferably between about 200°C and about 400°C, plus preferably, at a temperature of about 350°C.
    [00078] In use, when the combustible heat source is exposed to a lighter yellow flame, or other means of ignition, the at least one peroxide or superoxide decomposes to release oxygen. This causes an initial boost in the temperature of the combustible heat sources, and also assists in igniting the combustible heat sources. Following decomposition of the at least one peroxide or superoxide, the combustible heat source continues to burn at a lower temperature.
    [00079] Preferably, the at least one peroxide or superoxide is present in the combustible heat sources in an amount of between about 20 percent and about 50 percent by the dry weight of the combustible heat sources, more preferably in an amount of between about 30 percent and about 50 percent by the dry weight of the fuel heat source.
    [00080] Suitable peroxides and superoxides for inclusion in the fuel heat source, according to the invention, include, but are not limited to, calcium peroxide, strontium peroxide, magnesium peroxide, barium peroxide, lithium peroxide, zinc peroxide, potassium superoxide, and sodium superoxide.
    [00081] Preferably, the at least one peroxide is selected from the group consisting of calcium peroxide, strontium peroxide, magnesium peroxide, barium peroxide, and combinations thereof.
    [00082] Alternatively or in addition to the at least one ignition aid, the combustible heat sources according to the invention may comprise one or more other additives to improve the properties of the combustible heat sources. Suitable additives include, but are not limited to, additives to promote consolidation of the fuel heat source (eg, sintering aids), and additives to promote decomposition of one or more gases produced by combustion of the fuel heat source (eg. , catalysts such as CuO, Fe2O3 and Al2O3).
    [00083] The combustible heat sources according to the invention are preferably formed by mixing one or more carbon-containing materials with the binding agent and other additives, where included, and preforming the mixture into a form desired. The mixture of one or more materials containing carbon, bonding agent, and other optional additives, can be preformed into a desired shape using any suitable known ceramic forming methods, such as, for example, slip casting, extrusion, injection molding, compaction or mold pressing. In certain preferred embodiments, the blend is preformed into a desired shape by extrusion or pressing.
    [00084] Preferably, the mixture of one or more materials containing carbon, binding agent, and other additives, is preformed into an elongated rod. However, it will be appreciated that the mixture of one or more materials containing carbon, binding agent, and other additives, can be preformed into other desired shapes.
    [00085] After formation, particularly after extrusion, the elongated rod or other desired shape is preferably dried to reduce its moisture content and then pyrolyzed in a non-oxidizing atmosphere at a temperature sufficient to carbonize the binding agent and substantially eliminate any volatiles in the elongated rod or otherwise. The elongated rod or other desired shape is pyrolyzed, preferably in a nitrogen atmosphere at a temperature of between about 700°C and about 900°C.
    [00086] The combustible heat source preferably has a porosity of between about 20 percent and about 80 percent, more preferably, between about 20 percent and 60 percent. Even more preferably, the combustible heat source has a porosity of between about 50 percent and about 70 percent, more preferably between about 50 percent and about 60 percent, as measured by, for example, mercury porosimetry, or helium pycnometry. The required porosity can be readily achieved during the production of the combustible heat source using conventional methods and technology.
    [00087] Advantageously, the combustible heat sources according to the invention have a bulk density of between about 0.6 g/cm3 and about 1.0 g/cm3.
    [00088] Preferably, the combustible heat sources according to the invention have a mass of between about 300 mg and about 500 mg, more preferably between about 400 mg and about 450 mg.
    [00089] Preferably, the combustible heat sources according to the invention have a length of between about 5 mm and about 20 mm, more preferably between about 7 mm and about 15 mm, more preferably, of between about 11 mm and about 13 mm. As used herein, the term "length" denotes the maximum longitudinal dimension of elongated fuel heat sources in accordance with the invention between the upstream end and the downstream end thereof.
    [00090] Preferably, the combustible heat sources according to the invention have a diameter of between about 5 mm and about 10 mm, more preferably between about 7 mm and about 8 mm. As used herein, the term "diameter" denotes the maximum transverse dimension of elongated fuel heat sources in accordance with the invention.
    [00091] Preferably, the combustible heat sources according to the invention are of substantially uniform diameter. However, combustible heat sources according to the invention may alternatively be tapered so that the diameter of the rear portion of the combustible heat source is greater than the diameter of the rear portion of the front portion thereof. Particularly preferred are combustible heat sources which are substantially cylindrical. The combustible heat source may, for example, be a tapered cylinder or cylinder of substantially circular cross section, or a tapered cylinder or cylinder of substantially elliptical cross section.
    [00092] The combustible heat sources according to the invention can be "blind" combustible heat sources. As used herein, the term "blind combustible heat source" is used to denote a combustible heat source that does not contain any longitudinal airflow channels. As used herein, the term "longitudinal air flow channel" is used to denote a hole that passes through an inner portion of the fuel heat source, and extends along the length of the fuel heat source.
    [00093] Alternatively, the combustible heat sources according to the invention may comprise at least one longitudinal air flow channel. For example, combustible heat sources according to the invention may comprise one, two or three longitudinal air flow channels. In such embodiments, the combustible heat sources according to the invention preferably comprise a single longitudinal air flow channel, more preferably a substantially central single longitudinal air flow channel. The diameter of the single longitudinal airflow channel is preferably between about 1.5 mm and about 3 mm. The inner surface of the at least one longitudinal air flow channel of the fuel heat sources according to the invention can be partially or completely coated. Preferably, the coating covers the inner surface of all longitudinal airflow channels.
    [00094] Optionally, the combustible heat sources according to the invention may comprise one or more, preferably up to and including six, longitudinal grooves extending along part of or the entire periphery of the combustible heat sources. If desired, the combustible heat sources according to the invention can comprise one or more longitudinal grooves and at least one longitudinal air flow channel. Alternatively, the combustible heat sources according to the invention may be blunt combustible heat sources comprising one or more longitudinal slots.
    [00095] Preferably, at least a part of the combustible heat sources according to the invention is enclosed in a combustion resistant envelope. The term "combustion resistance" is used herein to refer to a casing that remains substantially intact throughout the combustion of the combustible heat source. The combustion resistant wrap is preferably wrapped around and in direct contact with at least a portion of the combustible heat source. Preferably, at least a rear or downstream portion of the combustible heat source is enveloped in the combustion resistant wrap. Preferably, at least a front or upstream portion of the combustible heat source is not enveloped in the combustion resistant envelope.
    [00096] The combustible heat sources, according to the invention, can be wrapped in a combustion resistant envelope that is heat conductor.
    [00097] In use in tobacco articles, according to the invention, the heat generated during combustion of the combustible heat sources, according to the invention, involved in a heat-conducting combustion-resistant wrapper, can be transferred by conduction to the aerosol forming substrate of the smoking articles via the heat conduction combustion resistant wrap.
    [00098] Alternatively or in addition, the combustible heat sources, according to the invention, may be enveloped in an oxygen-restricted combustion resistant envelope that restricts or prevents oxygen access to at least part of the combustible heat sources involved in the oxygen-restriction combustion resistant casing. For example, the combustible heat sources according to the invention can be encased in a substantially oxygen-impermeable combustion resistant envelope. In such embodiments, at least part of the combustible heat sources involved in the oxygen-restricting combustion resistant envelope substantially lacks access to oxygen and, therefore, does not burn.
    [00099] Preferably, the combustible heat sources, according to the invention, are enveloped in a combustion resistant casing that is both heat-conducting and oxygen-restricting.
    [000100] Combustion resistant wraps suitable for use in the invention include, but are not limited to: metal sheet wraps, such as, for example, aluminum foil wraps, steel sheet wraps, steel sheet wraps , and copper foil wraps; alloy foil wraps; graphite sheet wraps; fiberglass wraps; ceramic fiber wraps; and certain paper wrappers.
    [000101] In smoking articles according to the invention, preferably at least a rear portion of the fuel heat source, and at least a front portion of the aerosol forming substrate, are wrapped in the combustion resistant wrap as described above. Preferably, a front portion of the combustible heat source is not enveloped in the combustion resistant envelope. Preferably, a rear portion of the aerosol forming substrate is not enveloped in the burn resistant wrap.
    [000102] Preferably, the rear portion of the combustible heat source involved in the burn resistant wrap is between about 2 mm and about 8 mm in length, more preferably between about 3 mm and about 5 mm in length.
    [000103] Preferably, the front portion of the combustible heat source not involved in the burn resistant envelope is between about 4 mm and about 15 mm in length, more preferably between about 4 mm and about 8 mm in length.
    Preferably, the aerosol forming substrate has a length of between about 5 mm and about 20 mm, more preferably between about 8 mm and about 12 mm. Preferably, the front portion of the aerosol forming substrate involved in the burn resistant wrap is between about 2mm and about 10mm in length, more preferably between about 3mm and about 8mm in length, most preferably. probably between about 4 mm and about 6 mm in length. Preferably, the backside of the aerosol forming substrate not wrapped in the burn resistant wrap is between about 3 mm and about 10 mm in length. In other words, the aerosol forming substrate preferably extends between about 3 mm and about 10 mm downstream beyond the burn resistant wrap. More preferably, the aerosol forming substrate extends at least about 4 mm downstream beyond the burn resistant wrap.
    [000105] Smoke articles according to the invention may comprise a combustible heat source according to the invention and an aerosol forming substrate located immediately downstream of the combustible heat source. In such embodiments, the aerosol forming substrate can support the combustible heat source.
    [000106] Alternatively, smoking articles according to the invention may comprise a combustible heat source according to the invention, and an aerosol forming substrate located downstream of the combustible heat source, in which the substrate of aerosol formation is spaced apart from the combustible heat source.
    [000107] Preferably, smoking articles according to the invention comprise aerosol forming substrates comprising at least one aerosol former and a material capable of emitting volatile compounds in response to heating.
    [000108] The at least one aerosol former may be any suitable known compound or mixture of compounds which, in use, facilitate the formation of a dense and stable aerosol. The aerosol former is preferably resistant to thermal degradation at the operating temperature of the smoking article. Suitable aerosol formers are well known in the art, and include, for example, polyhydric alcohols, esters of polyhydric alcohols, such as glycerol mono-, di- or triacetate, and aliphatic esters of mono-, di- or polycarboxylic acids, such as , dimethyl dodecanedioate and dimethyl tetradecanedioate. Preferred aerosol formers for use in smoking articles in accordance with the invention are polyhydric alcohols or mixtures thereof, such as triethylene glycol, 1,3-butanediol and, more preferably, glycerin.
    [000109] Preferably, the material capable of emitting volatile compounds in response to heating is a load of plant-based material, more preferably, a load of homogenized plant-based material. For example, the aerosol forming substrate can comprise one or more plant-derived materials including, but not limited to: tobacco; tea, for example green tea; Mint; blond; eucalyptus; basil; saves; verbena; and tarragon. The herb material can comprise additives including, but not limited to, humectants, flavors, binders, and mixtures thereof. Preferably, the herb material consists essentially of tobacco material, more preferably, homogenized tobacco material.
    [000110] Smoking articles according to the invention may comprise an air flow directing element downstream of the aerosol forming substrate. The air flow directing element defines an air flow path through the smoking article. At least one air inlet is preferably provided between the downstream end of the aerosol forming substrate and a downstream end of the air flow directing element. The air flow directing element directs air from at least one inlet to the mouth end of the smoking article.
    [000111] The air flow directing element may comprise an open-end substantially air-impermeable cast body. In such embodiments, air withdrawn through the at least one air inlet is first withdrawn upstream along the outer portion of the open-end substantially air-impermeable cast body and then downstream through the interior of the substantially impermeable cast body. to open-end air.
    [000112] The smoking article according to the invention preferably further comprises an expansion chamber downstream of the aerosol forming substrate and, where present, downstream of the airflow directing element. The inclusion of an expansion chamber advantageously allows for additional cooling of the aerosol generated by heat transfer from the fuel heat source to the aerosol forming substrate. The expansion chamber also advantageously allows the overall length of smoking articles according to the invention to be adjusted to a desired value, for example to a length similar to that of conventional cigarettes, by an appropriate choice of chamber length. of expansion. Preferably, the expansion chamber is an elongated hollow tube.
    [000113] The fume articles according to the invention may also additionally comprise a nozzle downstream of the aerosol forming substrate and, where present, downstream of the airflow directing element and expansion chamber. The nozzle may, for example, comprise a filter made from cellulose acetate, paper, or other suitable known filtration materials. Preferably the nozzle is of low filtration efficiency, more preferably very low filtration efficiency. Alternatively or in addition, the mouthpiece may comprise one or more segments comprising absorbents, adsorbents, flavorings, and other aerosol modifiers and additives that are used in conventional cigarette filters, or combinations thereof.
    [000114] If desired, ventilation can be provided at a location downstream of the combustible heat source of smoking articles in accordance with the invention. For example, where present, ventilation may be provided at a location along the integral mouthpiece of smoking articles in accordance with the invention.
    [000115] Smoking articles according to the invention can be assembled using known methods and machinery.
    [000116] The invention will be further described, by way of example only, with reference to the accompanying drawings, in which: Figure 1 shows a schematic longitudinal cross-section of a smoking article according to the invention; and Figure 2 shows a graph of the temperature profile of a combustible heat source according to the invention produced in accordance with Example 1 below, and a comparative temperature profile of a prior art heat source.
    [000117] The smoke article 2 shown in Figure 1 has an overall length of 70 mm, a diameter of 7.9 mm, and comprises a combustible heat source 4 according to the invention, an aerosol forming substrate 6, an elongated expansion chamber 8, and a nozzle 10. As shown in Figure 1, the combustible heat source 4, aerosol forming substrate 6, elongated expansion chamber 8, and nozzle 10 are in bearing coaxial alignment and are packaged in an outer wrapper of 12 low air permeability cigarette paper.
    [000118] The combustible heat source 4 is 11 mm in length and 7.8 mm in diameter, and has a density of about 0.84 g/cm3. The combustible heat source 4 comprises a central air flow channel 16 of circular cross section extending longitudinally through the combustible heat source 4. A substantially air-impermeable heat resistant coating (not shown) having a thickness 80 microns, is provided on the inner surface of the central air flow channel 16, which is 2 mm in diameter.
    [000119] The aerosol forming substrate 6, which is 10 mm long, 7.8 mm in diameter, and has a density of about 0.8 g/cm3, is located immediately downstream of the combustible heat source 4 The aerosol forming substrate 6 comprises a cylindrical plug of homogenized tobacco material 18 comprising glycerin as an aerosol former and circumscribed by the filter plug wrap 20. The homogenized tobacco material 18 consists of longitudinally aligned strands of tobacco material extruded.
    [000120] A combustion resistant casing 22 consisting of an aluminum foil tube having a thickness of 20 microns, a length of 9 mm, and a diameter of 7.8 mm, surrounds and is in contact with a rear part 4b of the combustible heat source 4 4 mm long, and a supporting front part 6a of the aerosol forming substrate 6 5 mm long. As shown in Figure 1, a front portion of the fuel heat source 4 7 mm in length, and a rear portion of the aerosol forming substrate 6 5 mm in length, are not surrounded by the combustion resistant wrap 22.
    [000121] The elongated expansion chamber 8, which is 42 mm in length and 7.8 mm in diameter, is located downstream of the aerosol-forming substrate 6, and comprises a cylindrical cardboard open-end tube 24. The nozzle 10 of the smoking article 2, which is 7 mm in length and 7.8 mm in diameter, is located downstream of the expansion chamber 8, and comprises a circumscribed very low filtration efficiency cylindrical cellulose acetate trailer shutter 26 by filter plug wrap 28. Nozzle 10 can be circumscribed by filter paper (not shown).
    [000122] In use, the consumer turns on the combustible heat source 4 and then draws air through the central air flow channel 16 downstream towards the nozzle 10. The front part 6a of the aerosol forming substrate 6 is heated primarily by conduction through the non-combustion backing 4b supporting the fuel heat source 4 and the combustion resistant envelope 22. The withdrawn air is heated as it passes through the central air flow channel 16 and, then heats the aerosol forming substrate 6 by convection. Heating the aerosol forming substrate 6 releases volatile and semi-volatile compounds, including the aerosol former from the tobacco material 18, which are entrained in the heated exhaust air as it flows through the aerosol forming substrate. The heated air and entrained compounds pass downstream through expansion chamber 8, cool and condense, to form an aerosol which passes through the mouthpiece in the consumer's mouth at about room temperature.
    [000123] To produce the smoking article 2, a rectangular piece of the burn resistant wrap 22 is glued to the cigarette paper 12. The combustible heat source 4, the aerosol forming substrate shutter 6, and the expansion chamber 8, are properly aligned and positioned on the cigarette paper 12 with the burn resistant wrap 22 attached. The cigarette paper 12 with the burn-resistant wrap 22 attached is wrapped around the back 4b of the combustible heat source 4, the aerosol forming substrate 6, and the expansion chamber 8, and glued together. The nozzle 10 is attached to the open end of the expansion chamber using known filter combination technology.
    [000124] The combustible heat sources according to the invention can be produced according to Example 1 or Example 2 below. Example 1 describes a pressing process for producing a combustible heat source, and Example 2 describes an extrusion process. EXAMPLE 1 - Pressing
    [000125] Combustible heat sources, according to the invention, were prepared by mixing the components shown in Table 1 below to form a granular mixture.

    [000126] 800 mg of the mixture was introduced into the cylindrical mold cavity of a press mold using a funnel, and the mixture was pressed into the mold cavity using a manual press to obtain a cylindrical heat source having a length of 13 mm . The pressed heat source was removed from the mold cavity and then dried at about 100°C for about 1 hour, and conditioned at about 22°C, 30 percent relative humidity, for about 12 hours. The density of the heat source was between about 0.80 g/cm3 and about 0.85 g/cm3.
    [000127] The temperature of a combustible heat source 4 produced according to Example 1 during ignition and combustion of the combustible heat source 4 was measured using a thermocouple inserted in the intermediate part of the combustible heat source. The results are shown in Figure 2. To generate the profile shown in Figure 2, the upstream end of the combustible heat source was ignited using a conventional lighter yellow flame.
    [000128] For the purpose of comparison, the temperature of a prior art heat source, including only an organic binder material, was measured under similar experimental conditions. The prior art heat source was produced according to Example 1, but with the three binder components replaced by 15 grams of carboxymethyl cellulose. The density of the prior art heat source was about 0.84 g/cm3 . The results are also shown in Figure 2.
    [000129] As can be seen from Figure 2, the combustible heat source 4 of the invention, including the binding agent comprising a combination of organic and inorganic binding materials, achieves a higher firing temperature, and a longer firing life. longer than the prior art heat source, including only organic binder material. These results demonstrate an improvement in the burning properties provided through the use of the improved binding agent, including the specific combination of three binding components, as described above. In particular, these results demonstrate that the use of the improved binding agent, including the specific combination of three binding components, surprisingly results in the combustible heat source 4 of the invention having a longer burn life than the heat source of the art. above, even though the combustible heat source 4 of the invention comprises less combustible organic material than the prior art heat source.
    [000130] During ignition of a sample of combustible heat sources 4 produced according to Example 1, no sparks or flames were visible for any heat source. In contrast, during firing of a corresponding sample of prior art heat sources including only an organic binder material, sparks or flames were observed during firing by at least two-thirds of the heat sources in the sample. This provides a qualitative indication of the improved integrity of the inventive combustible heat sources, including the three binder components, compared to prior art heat sources including only the organic binder material.
    [000131] In order to more quantitatively demonstrate the improved integrity of the combustible heat source produced in accordance with Example 1, a "drop" test was conducted on a sample of 20 heated smoke articles incorporating one of the prepared combustible heat sources according to Example 1. A corresponding drop test was conducted on a sample of 20 heated smoke articles of the same construction, but including a prior art heat source, comprising only organic binder material.
    [000132] In each case, the combustible heat sources were first conditioned for 12 hours at 22°C and 50 percent relative humidity. Each heat source was then inserted into a heated smoke article, in which the same heated smoke article construction was used for all samples for the comparison proposal. For each smoking article tested, the smoking article was mounted on a retaining bar in a metal block. The assembled tobacco article was connected to a vacuum system for carrying out puffs by drawing air through the tobacco article, in which the vacuum system includes a vacuum pump capable of producing 177.8 mmHg during a puff, with a flow rate of 2 liters per minute.
    [000133] The combustible heat source was ignited using a lighter yellow flame. Each lit smoking article was then subjected to four fall cycles, each cycle comprising twenty drops into which the metal block on which the smoking article was mounted was dropped from a height of 3.81 cm. The fall cycles were actuated immediately after lighting, 3 minutes after lighting, 6 minutes after lighting, and 9 minutes after lighting. After each cycle, a two-second puff was taken on the smoking article.
    [000134] For each drop cycle, the number of drops was observed, in which a "drop" is made up of at least one-sixth the length of the combustible heat source falling from the smoke article. For the sample of 20 cigarettes, the percentage drop rate was calculated for each cycle by dividing the number of falls during that cycle by the total number of smoking articles, ie 20, and then multiplying this value by 100 .
    [000135] During the test conducted with the sample of 20 smoke articles incorporating combustible heat sources according to the invention produced in accordance with Example 1, a drop rate of 0 percent (0%) was observed for all fall cycles. No drop was observed during the full experimental test.
    [000136] During comparative tests conducted with the sample of 20 smoke articles incorporating prior art heat sources, including only an organic binder material, a drop rate of at least 20 percent was observed after the first cycle of fall conducted immediately after ignition, and a percentage fall of at least 40 percent was observed after the second fall cycle conducted 3 minutes after ignition. No drop was typically observed during drop cycles performed at 6 and 9 minutes after ignition. These results demonstrate that the integrity of prior art heat sources during burning is less than the integrity of the fuel heat sources of the invention. Prior art heat sources have been observed to become less prone to cracking and breakage during burning than the combustible heat source of the invention, incorporating the improved binding agent. EXAMPLE 2 - Extrusion
    [000137] The combustible heat sources according to the invention, having properties similar to those exhibited by the combustible heat sources prepared according to Example 1, were prepared as described below.
    [000138] The same components shown in Table 1 were first mixed in a high shear kneading mixer to form a granular mixture. Using a ram extruder, the granulated mixture was then extruded at a speed of 60 cm 3 /min through a mold having a circular cross-section central mold hole having a diameter of 8.7 mm, to form rods. cylindrical having a length of about 20 cm to about 22 cm, and a diameter of about 9.1 mm to about 9.2 mm.
    [000139] The cylindrical stems were dried at about 22°C, 45 percent relative humidity, for about 24 hours. After drying, the cylindrical rods were cut to form individual combustible heat sources having a length of about 13 mm and a diameter of about 7.8 mm. The individual combustible heat sources were then dried at about 100°C for about 1 hour, and conditioned at about 22°C, 30 percent relative humidity, for about 12 hours. The individual heat sources have a mass of about 800 mg.
    权利要求:
    Claims (15)
    [0001]
    1. Combustible heat source (4) for a smoke article (2), the combustible heat source (4) being characterized in that it comprises: carbon; and a binding agent including at least one organic polymeric binding material, at least one carboxylate burning salt, and at least one inorganic non-combustible binding material, wherein the at least one inorganic non-combustible binding material comprises a sheet silicate material.
    [0002]
    2. Fuel heat source (4) according to claim 1, characterized in that the at least one carboxylate burning salt includes one or more of: at least one alkali metal citrate salt; at least one alkali metal acetate salt; and at least one alkali metal succinate salt.
    [0003]
    3. Fuel heat source (4) according to claim 1 or 2, characterized in that the at least one carboxylate burning salt includes at least one alkali metal citrate salt.
    [0004]
    4. Fuel heat source (4), according to claim 1, 2 or 3, characterized in that the at least one organic polymeric binder material comprises a cellulosic material.
    [0005]
    5. Fuel heat source (4), according to any one of claims 1 to 4, characterized in that the at least one inorganic non-combustible binding material comprises one or more clays.
    [0006]
    6. Fuel heat source (4) according to any one of claims 1 to 5, characterized in that the binding agent comprises between 25 percent and 80 percent by weight of the organic polymeric binder material.
    [0007]
    7. Fuel heat source (4) according to any one of claims 1 to 6, characterized in that the binding agent comprises between 5 percent and 50 percent by weight of the carboxylate burning salt.
    [0008]
    8. Fuel heat source (4), according to any one of claims 1 to 7, characterized in that the binding agent comprises between 10 percent and 35 percent by weight of the inorganic non-combustible binding material.
    [0009]
    9. Fuel heat source (4), according to any one of claims 1 to 8, characterized in that it comprises between 2 percent and 10 percent by weight of the binding agent.
    [0010]
    10. Fuel heat source (4), according to any one of claims 1 to 9, characterized in that it additionally comprises at least one ignition aid.
    [0011]
    11. Fuel heat source (4) according to claim 10, characterized in that the at least one ignition aid comprises at least one peroxide or superoxide.
    [0012]
    12. Fuel heat source (4), according to any one of claims 1 to 11, characterized in that the fuel heat source is a pressed heat source, formed by a pressing process.
    [0013]
    13. Smoking article (2), characterized in that it comprises a combustible heat source (4) as defined in any one of claims 1 to 12 and an aerosol forming substrate (18) downstream of the combustible heat source .
    [0014]
    14. A smoking article (2) according to claim 13, characterized in that at least one rear portion of the combustible heat source (4b) and at least one front portion of the aerosol forming substrate (6a) are wrapped in a combustion resistant wrap (22).
    [0015]
    15. Method of production of the fuel heat source (4) as defined in any one of claims 1 to 12, the method being characterized in that it comprises the steps of: combining one or more carbon-containing materials with a binding agent including by at least one organic polymeric binder material, at least one carboxylate burning salt, and at least one inorganic non-combustible binder material, wherein the at least one inorganic non-combustible binder material comprises a sheet silicate material; preforming the mixture of the one or more carbon-containing materials and the binding agent into an elongated rod; and drying the elongated rod.
    类似技术:
    公开号 | 公开日 | 专利标题
    BR112014033121B1|2021-07-20|FUEL HEAT SOURCE, SMOKE ARTICLE, AND FUEL HEAT SOURCE PRODUCTION METHOD
    KR102047720B1|2019-11-25|Combustible heat source for a smoking article
    JP2019129838A|2019-08-08|Insulated heat source
    BR112014009377B1|2020-12-08|smoking article and fuel heat source with a rear barrier coating
    BR112014020679B1|2021-06-15|MULTI-LAYER FUEL HEAT SOURCE AND SMOKING ARTICLE
    NZ619159B2|2016-01-06|Combustible heat source for a smoking article
    同族专利:
    公开号 | 公开日
    AU2013285466B2|2016-11-10|
    UA114327C2|2017-05-25|
    EP2869721A1|2015-05-13|
    AR092024A1|2015-03-18|
    CN104519758B|2020-03-10|
    TW201408229A|2014-03-01|
    HK1204231A1|2015-11-13|
    PH12014502706A1|2015-02-02|
    RU2015103537A|2016-08-20|
    KR102220688B1|2021-03-03|
    CA2878143A1|2014-01-09|
    US20170198228A1|2017-07-13|
    IL236095A|2020-05-31|
    EP2869721B1|2019-12-04|
    ZA201408873B|2017-09-27|
    PH12014502706B1|2015-02-02|
    CN104519758A|2015-04-15|
    BR112014033121A2|2017-06-27|
    JP6275710B2|2018-02-07|
    MX371170B|2020-01-21|
    KR20150035606A|2015-04-06|
    IL236095D0|2015-01-29|
    MX2014015719A|2015-08-05|
    JP2015525565A|2015-09-07|
    US20150166916A1|2015-06-18|
    AU2013285466A1|2015-01-22|
    IN2014DN10411A|2015-08-14|
    MY171475A|2019-10-15|
    WO2014006078A1|2014-01-09|
    US10676687B2|2020-06-09|
    CA2878143C|2018-10-16|
    SG11201500023PA|2015-01-29|
    RU2635078C2|2017-11-08|
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    法律状态:
    2018-03-06| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-03-13| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-03-20| B06I| Publication of requirement cancelled [chapter 6.9 patent gazette]|Free format text: ANULADA A PUBLICACAO CODIGO 6.6.1 NA RPI NO 2462 DE 13/03/2018 POR TER SIDO INDEVIDA. |
    2019-10-01| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2021-03-16| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2021-05-18| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-07-20| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 03/07/2013, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    EP12174915|2012-07-04|
    EP12174915.4|2012-07-04|
    PCT/EP2013/064006|WO2014006078A1|2012-07-04|2013-07-03|Combustible heat source with improved binding agent|
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