Nanoscale Particles of Iron Aluminide and Iron Aluminum Carbide by the Reduction of Iron Salts
Background[0001]
The iron aluminum system forms a series of solid solutions from 0 to 52 atomic percent aluminum. At room temperature, alloys with less than 18.5 atomic percent (about 10 weight percent) aluminum are body-centered cubic solid solutions with a disordered structure. However, alloys with 18.5 to 35 atomic percent (about 10 to 18 weight percent) aluminum form a DO3 ordered structure, and alloys with greater than about 35 atomic percent (greater than about 18 weight percent) aluminum form
the cubic B2 ordered structure.
0002 Intermetallic iron aluminide alloys are of commercial interest because of their high tensile strength, low density, and excellent resistance at high temperatures to wear, corrosion and oxidation. According to commonly assigned Published U.S. Application No. 2002/0014453, nanoscale iron alimiinides are also attractive as filtration materials, for example, for the selective abatement of 1,3- butadiene. However, as disclosed by Haber et al. in Advanced Materials, 1996, 8, No. 2 (pp. 163-166) and in Chem. Mater., 2000, 12 (pp. 973-982), commercial application of aluminides has been limited because coarse-grained aluminides are
too brittle for many applications. As disclosed by Varin et al, in Intermetallics, 7 1999, (p. 917), particle size refinement, particularly to nanoscale (below 1 micron)
dimensions, has been predicted to improve physical properties of iron alumimde intermetallic alloys.
0003 As disclosed by Haber et al. in J. Aerosol Sci., Vol 29, No 5/6 (1998) (pp. 637-645), nanoscale particles have been made from metals, alloys, intermetallics and ceramics. U.S. Patent Nos. 5,580,655; 5,695,617; 5,770,022;
5,851,507; 5,879,715; 5,891,548; 5,962,132; 6,262,129 and 6,368,406, the disclosures of which are all hereby incorporated by reference, relate to the formation of nanoscale particles using a variety of techniques including chemical synthesis, gas-phase synthesis, deposition by ionized cluster beams, high speed milling and sol- gel routes. These methods suffer from numerous drawbacks, however, including agglomeration, impurities or broad particle size distribution. In J. Mater. Res. Vol.
11, No. 2 (1996) (pp. 439-448 and 449-457) Suryanarayana et al. disclose the formation of nanocrystalline copper powder via the reduction of CuCl in NaBH4.
0004 The most common method reported in the literature for the synthesis of intermetallic nanoparticles is mechanical ball milling. (See, for example, Jartych E., et al, J. Phys. Condens. Matter, 10:4929 (1998); Jartych E.5 et al, Nanostructured Materials, 12:927 (1999); and Amilis, X., et al. , Nanostructured Materials 12:801 (1999)). Commonly assigned U.S. Patent No. 6,368,406 discloses preparation of nanoscale FeAl by laser vaporization.
0005 Despite the developments to date, there is interest in improved and more efficient methods of making aluminide materials and/or materials effective in
reducing the amount of various constituents such as 1,3-butadiene in the mainstream smoke of a cigarette during smoking. Preferably, such methods and compositions should not involve expensive or time consuming manufacturing and/or processing steps.
0006 Disclosed is a simple, novel and high yield approach for synthesizing iron aluminide and/or iron aluminum carbide nanoparticles via the chemical reduction of iron salts with lithium aluminum hydride. The chemical reduction technique provides several advantages including the capacity to generate large quantities of nanoscale particles.
Summary
0007 A method of manufacturing intermetallic nanoscale particles comprising iron aluminide and/or iron aluminum carbide, comprises (a) preparing a mixture comprising a solvent, an iron salt and LiAlH4; and (b) heating the mixture to
form the intermetallic nanoscale particles.
0008 According to one embodiment, the solvent comprises toluene, 1,3,5-
trimethyl benzene, diethyl ether, tetrahydrofuran or mixtures thereof, and the iron salt comprises iron chloride. The UAIH4 can be added to the mixture to give an atomic ratio of Al:Fe of about 10 to 52%. Preferably, the step of preparing the
mixture is carried out at a temperature of from about 20EC to 100EC in an inert
atmosphere. According to another embodiment, the mixture of FeCl3 and LiAlH
can be refluxed in a non-aqueous solvent and an inert atmosphere for a period of about 1 to 48 hours.
0009 The mixture can be filtered prior to the step of heating and/or dried prior to the step of heating. Drying of the mixture can be carried out in vacuum or in
an inert atmosphere by heating the mixture to a temperature of from about 100EC to
250EC.
0010 The step of heating comprises heating the mixture, preferably in an
inert and/or reducing atmosphere, to a temperature of from about 400EC to 1200EC.
According to a preferred embodiment, the step of heating the mixture can be carried out in an atmosphere comprising hydrogen and argon. According to a further preferred embodiment the mixture can be heated at a heating rate of less than about
5EC/min. whereby the intermetallic nanoscale particles comprise greater than about
50% by volume iron aluminide. According to another preferred embodiment, the
mixture can be heated at a heating rate of greater than about 5EC/min. whereby the
intermetallic nanoscale particles comprise greater than about 50% by volume iron aluminum carbide.
0011 The nanoscale particles can comprise iron aluminide particles having an average particle size of from about 2 to 10 nm. Alternatively, the nanoscale particles can comprise iron aluminum carbide particles having an average particle
size of from about 30 to 100 nm. Preferably the nanoscale particles comprise
crystalline particles that are magnetic. According to a preferred embodiment, the
nanoscale particles have a B2 or DO3 ordered structure. The intermetallic nanoscale particles can be formed in an aluminum and oxygen-rich matrix such as an amorphous alumina phase.
0012 According to a further embodiment, a tobacco cut filler composition comprises tobacco and intermetallic nanoscale particles of iron aluminide and/or iron aluminum carbide in an alumina matrix capable of reducing the amount of 1,3- butadiene in mainstream smoke. Preferably the tobacco cut filler comprises the intermetallic nanoscale particles in an amount effective to remove at least about 10%, preferably at least about 15%, more preferably at least about 25% of the 1,3- butadiene in the mainstream smoke of a cigarette. Another embodiment provides a method of making a cigarette, comprising (i) adding iron aluminide and/or iron aluminum carbide nanoscale particles in an alumina matrix to tobacco cut filler, cigarette paper and/or a cigarette filter; (ii) providing the cut filler to a cigarette making machine to form a tobacco rod; (iii) placing a paper wrapper around the tobacco rod to form the cigarette; and (iv) optionally attaching a cigarette filter to the cigarette. A still further embodiment relates to a cigarette comprising cut filler, wherein the cut filler comprises tobacco and intermetallic nanoscale particles of iron aluminide and/or iron aluminum carbide in an alumina matrix.
Brief Description of the Drawings
0013 Figure 1 shows effects of heating on the presence of lithium chloride and iron aluminum carbide in precipitated colloids using THF as a solvent: (A) prior to
heating; (B) after heating at 300EC; (C) after heating at 550EC; and (D) after
heating at 875EC in argon.
0014 Figures 2A-C show SEM micrographs of the nanoscale particles
formed following heating of the initial colloidal mixture at (A) 300EC, and (B-C)
875EC in argon wherein Figures 2A and B are magnifications of l,500x and Figure
2C shows a portion of Figure 2B but with a magnification of 30,000x.
0015 Figures 3 A-B show EDX spectra from the nanoscale particles formed
after heating the colloidal mixture using THF as a solvent at (A) 300EC, and (B)
875EC in argon, respectively, showing presence and absence of chlorine.
0016 Figure 4A shows a TEM (magnification about 180,000x) and Figures 4B and 4C show site specific EDX analysis, respectively, of composite particles comprising nanoscale iron aluminum carbide in alumina after heating the colloidal
solution to 875EC in argon. Figure 4B shows data corresponding to the alumina
matrix surrounding the iron aluminum carbide particle and Figure 4C shows data corresponding to the iron aluminum carbide.
0017 Figure 5 shows a TEM image (magnification about 230,000x) of nanoscale iron aluminum carbide particles in a matrix comprising aluminum and oxygen.
0018 Figure 6 shows effects of heating on the presence of lithium chloride and iron aluminum carbide in precipitated colloids using diethyl ether as a solvent
(A) prior to heating; (B) after heating at 600EC, and (C) after heating at 750EC in
argon.
0019 Figures 7 A and 7B show the effects of solvent on the formation of iron aluminide and iron aluminum carbide.
0020 Figures 8 A and 8B show TEM and EDX analysis of particles
comprising nanoscale iron aluminide after heating to 750EC in argon.
0021 Figures 9 and 10 show TEM images of nanoscale iron aluminide particles in a matrix comprising aluminum and oxygen.
0022 Figures 11 A and 1 IB show the effect of heating rate on formation of iron aluminide and iron aluminum carbide.
Detailed Description of the Preferred Embodiments
0023 A method of manufacturing nanoscale iron aluminide and/or iron aluminum carbide intermetallic particles comprises preparing a mixture of solvent(s), a metal salt and LiAlH4, and heating the mixture to form the intermetallic nanoscale particles.
0024 By way of example, the mixture can be prepared by dissolving an iron salt
in a solvent or mixture of solvents and adding L1AIH4 to the mixture. The salt may
comprise anhydrous iron salts such as nitrates, sulfates and hydroxides. According
to a preferred embodiment, the iron salt is iron chloride. The step of preparing the
mixture can be performed at a temperature of from about 20EC to 100EC, e.g., from
about 60EC to 80EC. The solubility of the salt in the solvent can be increased by heating the temperature of the mixture to above room temperature during the step of preparing the mixture. The LiAlH4 serves both as a reducing agent and as a source of Al. LiAlH4 is commercially available as a powder or in solution with diethyl ether or tetrahydrofuran. As seen with reference to the equations below, the stoichiometry of the reactants can control which intermetallic phases are formed. Preferably, the LiAlH4 is added to the mixture to give an atomic ratio of Al:Fe of from about 10 to 52%, e.g., an Al:Fe ratio of 10:90, 15:85, 20:80, 25:75, 30:70, 35:65, 40:60, 45:55 or 50:50. When ethereal solvents are used, an excess of LiAlH4 can be added in order to compensate for aluminum that may complex with the solvent and form aluminum oxide during the heating step. The mixture of FeCl3 and LiAlHt can be refluxed in a non-aqueous solvent in an inert atmosphere for a period of about 1 to 48 hours, e.g., 2 to 8 to 16, 16 to 24 or 24 to 48 hours.
0025 Because LiAlH4 reacts violently with acidic protons (e.g. , H2O, MeOH), non-protic aromatic solvents such as toluene or 1,3,5-trimethyl benzene, or non- protic ethereal solvents such as diethyl ether (Et2O) or tetrahydrofuran (THF) are preferred. The solvents are preferably in an anhydrous form (e.g., greater than about 99.5% purity). Furthermore, due to the high level of reactivity of the hydride to
moisture, preferably the step of preparing the mixture is carried out in a dry, inert or
reducing atmosphere. The inert or reducing atmosphere can comprise, for example, helium, nitrogen, argon or mixtures thereof.
0026 Addition of LiAlH4 to the mixture causes reduction of the iron salt and the precipitation of black colloidal particles. Hydrogen gas is evolved according to the general equations:
2 FeCl3 + 3 LiAlH4 6 2 FeAl + A1C13 + 3 LiCl + 6 H2
3 FeCl3 + 3 LiAlH46 Fe3Al + 2 A1C13 + 3 LiCl + 6 H2
0027 Figure 1 shows an x-ray diffraction pattern for as-precipitated colloids prepared under nitrogen gas using THF as a solvent. The as-precipitated product is mainly amorphous. Referring to Figure 1, the crystalline peaks in curve A
correspond mainly to LiCl, while the broad reflection between about 40-44E (shown
by the arrow) corresponds to amorphous nanoscale phases. It is believed that the amorphous nanoscale phases comprise a highly homogeneous mixing of Fe- and Al- containing phases.
0028 Heating of the colloidal mixture to a temperature of from about 400EC to
1200EC drives the above reactions to completion and results in the formation of
nanoscale iron aluminide phases. The as-formed colloidal mixture can be directly
heated to form the intermetallic particles or the colloidal mixture can initially be converted to a dried powder by drying the colloidal mixture at a temperature up to
about 120EC in an inert or reducing atmosphere. For both the optional drying step
and the heating step, preferably the mixture is heated in an inert or reducing
atmosphere such as hydrogen, nitrogen, helium, argon or mixtures thereof. According to a preferred embodiment, the mixture can be heated in an atmosphere
comprising 5-10%) hydrogen in argon. At temperatures above about 550EC, the
LiCl is removed from the samples by sublimation. The resulting intermetallic nanoscale particles comprise iron aluminide (e.g., FeAl) and/or iron aluminum carbide (e.g., Fe3AlC0.5). The heating step is typically carried out for a period of about 10 hours, and the as-heated samples are preferably stored under nitrogen or another inert gas. It is believed that the as-precipitated colloids comprise a highly homogeneous, molecular-level mixing of Fe- and Al-containing phases that upon heating react to form crystalline nanoscale particles. As discussed below, the intermetallic nanoscale particles can crystallize in an amorphous alumina matrix wherein the amount of nanoscale particles can range from about 1 to 99%, 5 to 95%,
10 to 90%, 15 to 85%, 20 to 80%, 25 to 75%, 30 to 70%, 35 to 65%, 40 to 60%, or 45 to 55%. Prior to the step of heating, the mixture can be washed with solvents such as THF or diethyl ether and filtered. The presence of carbon in the nanoscale particles can increase the ductility, creep resistence and/or yield strength of articles made from the particles.
0029 Curves B-D in Figure 1 show x-ray diffraction patterns as a function of temperature for the sample discussed above in reference to curve A. After heating to
about 300EC in argon (curve B) the predominant crystalline phase is LiCl. Further
heating to about 550EC in argon (curve C) results in a black magnetic powder
having x-ray reflections consistent with nanoscale Fe and nanoscale iron aluminum
carbide (Fe3AlC05). Finally, after heating to about 875EC in argon (curve D), the sample comprises a black magnetic powder and the XRD pattern comprises reflections from intermetallic iron aluminide (e.g., B2 type FeAl) and iron aluminum carbide only.
0030 Figure 2 A shows an SEM image of the above curve B sample after heat
treatment to 300EC in argon. The sample comprises mainly irregularly shaped,
micron-sized aggregates. Figure 2B shows an SEM image of the curve D sample
after heat treatment to 875EC in argon and Figure 2C shows a higher magnification
of the portion of Figure 2B enclosed within the rectangular border. Referring to Figures 2B and 2C, the sample comprises individual nanoscale intermetallic particles dispersed on larger, micron-scale aggregates.
0031 Changes in chemical composition of samples after heating to 300EC and
875EC in argon are shown in Figures 3 A and 3B. Referring to Figure 3A, which
shows energy dispersive x-ray analysis (EDX), after heating to 300EC the sample
comprises mostly Cl, Fe and Al, while after heating to 875EC (Figure 3B) the
sample comprises mostly Fe and Al. TEM and site-specific EDX, shown in Figures
4A-4C reveal that after heating to 875EC in argon the samples comprise nanoscale
iron aluminum carbide (Fe3AlC0.5) crystallites 4 (Figure 4C) in an amorphous
alumina matrix 2 (Figure 4B). Figure 5 shows a TEM image of the nanoscale iron
aluminum carbide particles 4 in an alumina matrix 2. These particles, which were
derived from a THF-based reduction of FeCl3, are oval in shape and have an average particle size of from about 30 to 100 nm. The intermetallic nanoscale particles can have an average particle size less than about 100 nm, e.g., less than 90 nm, less than 80 nm, less than 70 nm, less than 60 nm, less than 50 nm, less than 40 nm, less than 35 nm, less than 30 nm, less than 25 nm, less than 20 nm, less than 15 nm, or less than 10 nm. After heating, samples made from the reduction of iron chloride in THF comprise nanoscale intermetallic iron aluminide and iron aluminum carbide particles in an amorphous alumina matrix. The intermetallic particles made using THF are predominately iron aluminum carbide.
0032 The choice of solvent can affect the composition of the intermetallic nanoscale particles. When diethyl ether (Et2O) is used as a solvent, similar results to those obtained for tetrahydrofuran (THF) are obtained. LiAlH4 is a soluble, strong reducing agent in both diethyl ether and tetrahydrofuran. Curves A-C of Figure 6 show the x-ray diffraction patterns as a function of temperature for FeCl3 reduced with LiAlH4 using Et2O as a solvent. After heating the precipitates in argon to
temperatures below about 550EC (curve A) the dominant reflections are from LiCl
and nanoscale Fe particles. As previously noted, when the samples are heated in
argon to temperatures above about 550EC, the LiCl is removed by sublimation and
the samples comprise a black magnetic powder. After heating to about 600EC
(curve B), the samples comprise crystalline Fe, FeAl and Fe3AlCo.5 phases. After
heating to about 750EC (curve C), the samples comprise a mixture of FeAl and
Fe3AlC0.5 phases only. The intermetallic nanoscale particles made using ethereal solvents are predominately iron aluminum carbide. Without wishing to be bound by
theory, it is believed that ethereal solvents such as diethyl ether and tetrahydrofuran
provide sources of carbon that can contribute to carbide formation. Furthermore,
intermetallic nanoscale particles made using ethereal solvents are embedded in an alumina matrix. The alumina matrix is believed to form from Al that combines with
oxygen that is abstracted from ethereal solvents in the presence of a strong reducing
agent.
0033 In contrast to ethereal solvents, when the non-protic solvent is
predominately toluene the major crystalline phase after heating to elevated
temperatures is iron aluminide (FeAl). Compared with ethereal solvents, the LiAlH4
is less soluble in aromatic solvents such as toluene and 1,3,5-trimethylbenzene. A
comparison of the resulting intermetallic crystalline phases is shown in Figures 7 A
and 7B, which show the diffraction patterns for two different samples heated in
argon to 750EC. For the sample shown in Figure 7A, the solvent used was diethyl
ether. In contrast, for the sample shown in Figure 7B, the solvent used was a 75/25
vol.% toluene/THF mixture. Other suitable mixture ratios include 20/80 vol.%,
30/70 vol.%, 40/60 vol.%, 50/50 vol.%, 60/40 vol. %, 70/30 vol.% and 80/20 vol.%.
The x-ray reflections from the sample where ether was the solvent, consistent with
the results discussed previously, are predominately Fe3AlC0.5, while the x-ray
reflections from the sample where a 75/25 vol.% toluene/THF mixture was the solvent are predominantly B2 type FeAl.
0034 For FeCl3 reduced with LiAlH4 using a 75/25 vol.% toluene/THF mixture as a solvent, TEM and EDX, shown in Figures 8A and 8B, respectively, reveal that
after heating to 750EC in argon the samples comprise nanoscale iron aluminide
(FeAl) particles 6. EDX (Figure 8B) shows that the sample comprises mostly O, Al and Fe. Figures 9-10 show TEM images of the nanoscale iron aluminide (FeAl) particles 6 in an amorphous alumina matrix 2. These nanoscale FeAl particles are oval in shape and have an average particle size of from about 2 to 10 nm.
0035 After heating, samples made from the reduction of iron chloride in a 75/25 vol.% toluene/THF mixture comprise predominately intermetallic iron aluminide particles in an alumina matrix. Furthermore, unlike ethereal solvents, which can strongly coordinate with Al and form alumina, aromatic solvents do not introduce a direct source of oxygen to the mixture. Therefore, as compared to ethereal solvents, less alumina can be formed using aromatic solvents. The presence of THF in the 75/25 vol.%) toluene/THF mixture is believed to contribute to the formation of the carbide phase and the alumina matrix.
0036 The heating rate can affect the composition of the intermetallic nanoscale particles when an ethereal solvent is used in the reduction of FeCl3. Using an
ethereal solvent, iron aluminum carbide (Fe3AlC0.5) comprises greater than 50% by volume of the intermetallic nanoscale particles when the sample is heated at a
heating rate of greater than about 5EC/min., while iron aluminide (FeAl) comprises greater than about 50%) by volume of the intermetallic nanoscale particles when the
sample is heated at a heating rate of less than about 5EC/min. This effect can be
seen in Figures 11 A-1 IB, which show XRD scans for two samples heated to 600EC
in argon. In Figure 11 A, the sample was ramped to temperature at lOEC/min. and comprises predominately the carbide phase, while in Figure 1 IB the sample was
ramped to temperature at 2EC/min. and comprises predominately iron aluminide.
0037 The effect of heating rate can be minimized by drying the mixture prior to the step of heating. Preferably, the mixture is dried in vacuum or in an inert
atmosphere at a temperature of from about 100EC to 250EC. Complete removal of
solvent prior to heating the colloids to elevated temperature (e.g., greater than about
400EC) can decrease the amount of carbide phase that forms. Furthermore, as
compared to ethereal solvents, when a non-ethereal solvent was used the heating rate had less effect on the composition of the final product.
0038 Because of their high surface area to volume ratio, the intermetallic
nanoscale particles can be used in catalysis applications. A preferred catalyst material comprises nanoscale iron aluminide particles and/or nanoscale iron aluminum carbide particles in an alumina matrix.
0039 One embodiment provides a tobacco cut filler composition comprising
tobacco and an effective amount of nanoscale iron aluminide and/or iron aluminum carbide particles in an alumina matrix for the removal of one or more gas
constituents such as 1,3-butadiene in the mainstream smoke of a cigarette. Another embodiment provides a cigarette comprising tobacco cut filler, wherein the cut filler comprises iron aluminide and/or iron aluminum nanoscale carbide particles in an alumina matrix for the removal of one or more gas constituents such as 1,3- butadiene from the mainstream smoke of the cigarette. While direct placement of the nanoscale particles in the tobacco cut filler is preferred, the nanoscale particles may be placed in the cigarette filter, or incorporated in the cigarette paper. The nanoscale particles can also be placed both in the tobacco cut filler and in other locations.
0040 The intermetallic nanoscale particles will preferably be distributed throughout the tobacco rod portion of a cigarette. By providing the particles throughout the tobacco rod, it is possible to reduce the amount of gas constituents such as 1,3-butadiene drawn through the cigarette. The intermetallic nanoscale particles may be provided along the length of a tobacco rod by distributing the particles on the leaf tobacco prior to cutting or incorporating them into the cut filler tobacco using any suitable method. The particles may be provided in the form of a powder or in the form of a dispersion. The intermetallic nanoscale particles in the form of a dry powder can be dusted on the cut filler tobacco. The particles may also be present in the form of a dispersion and sprayed on the cut filler tobacco.
Alternatively, the tobacco may be coated with a dispersion containing the particles. For instance, the particles may be added to the cut filler tobacco supplied to the
cigarette making machine or added to a tobacco column just prior to wrapping cigarette paper around the tobacco column.
0041 By distributing the nanoscale particles in the components of a cigarette, the amount of gas constituents such as 1,3-butadiene in mainstream smoke can be reduced, thereby also reducing the amount of 1,3-butadiene reaching the smoker and/or given off in second-hand smoke.
0042 By preparing nanoscale intermetallic particles in an alumina matrix the particles are easier to handle and easier to combine with tobacco cut filler than unsupported nanoscale particles. The alumina matrix can act as a separator, which inhibits agglomeration or sintering together of the nanoscale particles during combustion of the cut filler. Particle sintering may disadvantageously elongate the combustion zone during combustion of the tobacco cut filler, which can result in excess 1,3-butadiene production. Because the alumina matrix can minimize particle sintering it can minimize the loss of active surface area of the nanoscale intermetallic particles.
0043 In general, nanoscale intermetallic particles and an alumina matrix can be synthesized in any suitable ratio to give a desired loading of intermetallic particles in the matrix. For example, nanoscale iron aluminide particles can be synthesized via the LiAlH4 reduction of FeCl3 in THF to produce from about 0.1 to 90 wt.% nanoscale iron aluminide particles in an alumina matrix, e.g., about 1 to 90 wt.%,
about 5 to 80 wt.%, about 10 to 70 wt.%, about 20 to 60 wt.% or about 30 to 50
wt.%) nanoscale particles of nanoscale iron aluminide particles and about 99 to 10 wt.%), about 95 to 20 wt.%, about 90 to 30 wt.%, about 80 to 40 wt.% or about 70 to 50 wt.% alumina matrix, respectively. The amount of alumina that forms during the synthesis of the nanoscale intermetallic particles can be decreased by decreasing the amount of oxygen, e.g., ethereal solvent, present during the mixing and heating steps.
0044 "Smoking" of a cigarette means the heating or combustion of the cigarette to form smoke, which can be drawn through the cigarette. Generally, smoking of a cigarette involves lighting one end of the cigarette and, while the tobacco contained
therein undergoes a combustion reaction, drawing the cigarette smoke through the mouth end of the cigarette. The cigarette may also be smoked by other means. For example, the cigarette may be smoked by heating the cigarette and/or heating using electrical heater means, as described in commonly-assigned U.S. Patent Nos. 6,053,176; 5,934,289; 5,591,368 or 5,322,075.
0045 The term "mainstream" smoke refers to the mixture of gases passing down the tobacco rod and issuing through the filter end, i.e. the amount of smoke issuing
or drawn from the mouth end of a cigarette during smoking of the cigarette.
0046 The amount of the intermetallic nanoscale particles can be selected such that the amount of selected gas constituents (such as 1,3-butadiene) in mainstream smoke is reduced during smoking of a cigarette. Preferably, the amount of the intermetallic nanoscale particles will be an effective amount, e.g., from about a few
milligrams, for example, 5 mg/cigarette, to about 100 mg/cigarette or more, sufficient to reduce the amount of selected gas constituents (such as 1,3-butadiene) in the mainstream smoke by at least about 10%, preferably at least about 25%, more preferably at least about 50%.
0047 In cigarette manufacture, the tobacco is normally employed in the form of cut filler, i.e. in the form of shreds or strands cut into widths ranging from about 1/10 inch to about 1/20 inch or even 1/40 inch. The lengths of the strands range from between about 0.25 inches to about 3.0 inches. The cigarettes may further comprise one or more flavorants or other additives (e.g. burn additives, combustion modifying agents, coloring agents, binders, etc.) known in the art.
0048 Any suitable tobacco mixture may be used for the cut filler. Examples of suitable types of tobacco materials include flue-cured, Burley, Maryland or Oriental tobaccos, the rare or specialty tobaccos, and blends thereof. The tobacco material can be provided in the form of tobacco lamina, processed tobacco materials such as volume expanded or puffed tobacco, processed tobacco stems such as cut-rolled or cut-puffed stems, reconstituted tobacco materials, or blends thereof. The tobacco can also include tobacco substitutes.
0049 A further embodiment provides a method of making a cigarette, comprising (i) adding iron aluminide and/or iron aluminum carbide nanoscale
particles in an alumina matrix to a tobacco cut filler, cigarette paper and/or a
cigarette filter; (ii) providing the cut filler to a cigarette making machine to form a
tobacco column; (iii) placing a paper wrapper around the tobacco column to form a tobacco rod; and (iv) optionally attaching a cigarette filter to the tobacco rod.
0050 Techniques for cigarette manufacture are known in the art. Any conventional or modified cigarette making technique may be used to incorporate the intermetallic nanoscale particles. The resulting cigarettes can be manufactured to any known specifications using standard or modified cigarette making techniques and equipment. Typically, the cut filler composition is optionally combined with other cigarette additives, and provided to a cigarette making machine to produce a tobacco rod, which is then wrapped in cigarette paper, and optionally tipped with filters.
0051 Cigarettes may range from about 50 mm to about 120 mm in length. Generally, a regular cigarette is about 70 mm long, a "King Size" is about 85 mm long, a "Super King Size" is about 100 mm long, and a "Long" is usually about 120 mm in length. The circumference is typically from about 15 mm to about 30 mm in
circumference, and preferably around 25 mm. The tobacco packing density is typically between the range of about 100 mg/cm3 to about 300 mg/cm3, and preferably 150 mg/cm3 to about 275 mg/cm3.
0052 While the invention has been described with reference to preferred embodiments, it is to be understood that variations and modifications may be
resorted to as will be apparent to those skilled in the art. Such variations and
modifications are to be considered within the purview and scope of the invention as defined by the claims appended hereto.