Patent Application
20150292152
The present invention relates to a method for preparing a black liquor obtained by treating a tobacco raw material. The present invention also relates to a method for preparing a flavor component-containing liquid obtained by treating the black liquor.
A black liquor generally refers to a black or brown liquid obtained by a digesting treatment in a pulp production process. Herein, the digesting treatment is a treatment for obtaining pulp by heating a pulp raw material with a chemical solution. The obtained pulp is industrially utilized as a raw material for paper, a sheet or the like.
The digesting treatment is performed by various methods. Examples of the methods include a kraft pulping process using a mixed solution of sodium hydroxide and sodium sulfate; a soda pulping process using an aqueous sodium hydroxide solution; an acid sulfite pulping process using bisulfite and sulfite gas; and a neutral sulfite pulping process using sodium hydroxide and bisulfite. The digesting treatment is generally performed under severe conditions, which makes it difficult to control the reaction. Therefore, the digesting treatment is not performed in order to obtain an intended specific compound. When wood pulp is industrially obtained, the black liquor obtained by the digesting treatment is often disposed of in the present circumstances.
On the other hand, in the tobacco industry, a sheet tobacco produced using a tobacco fiber as a raw material has been known. For example, the sheet tobacco is obtained by stirring a short midrib or a fine powder of a tobacco raw material in warm water of about 60° C., thereafter separating the resultant product into an extracted liquid and a residue (that is, a tobacco fiber), and making a sheet from the obtained tobacco fiber. A technique of appropriately adding a flavor preferable for a tobacco to the sheet tobacco has been known. As such a technique, for example, a flavor component-containing extract obtained at the time of extracting a tobacco fiber from a tobacco raw material is generally added to the sheet tobacco.
Examples of flavor components preferable for a tobacco include vanillin. A method of oxidizing a black liquor which is obtained at the time of producing sulfite pulp, under an alkaline condition has been known as a method for preparing vanillin (Patent Documents 1 to 3).
Patent Document 1: U.S. Pat. No. 2,516,827
Patent Document 2: U.S. Pat. No. 2,576,752
Patent Document 3: U.S. Pat. No. 2,576,753
If the method for preparing vanillin is applied to a tobacco raw material containing lignin, a black liquor containing vanillin is expected to be obtained. Further, if the black liquor thus obtained is added to a tobacco fiber, a sheet tobacco having a good flavor is expected to be obtained. On the other hand, the method for preparing vanillin using the acid sulfite pulping process, in which sulfur dioxide is used as a chemical agent, is known. Similarly, a method using a neutral sulfite pulping process, in which sodium sulfide is used as a chemical agent, is also known. However, if the tobacco raw material or the tobacco extracted liquid are treated with a compound containing sulfur, the treatment may impair the smoking taste of the tobacco, which is not preferable. Additionally, since the acid sulfite pulping process is a multistage operation that involves performing heating two or more times, the acid sulfite pulping process is problematic as regards the complexity of the treatment equipment required.
Therefore, an object of the present invention is to provide a method for preparing a black liquor by which a flavor component-containing black liquor can be obtained with fewer treating processes without impairing the smoking taste of a tobacco. Another object of the present invention is to provide a method for preparing a flavor component-containing liquid obtained by treating the black liquor.
According to a first aspect according to the present invention, there is provided a method for preparing a black liquor, the method comprising digesting a tobacco raw material under an alkaline condition to obtain the black liquor.
According to a second aspect according to the present invention, there is provided a method for preparing a flavor component-containing liquid, the method comprising: digesting a tobacco raw material under an alkaline condition; separating a product obtained by the digesting into a black liquor and a tobacco fiber; and desalinating the black liquor to obtain the flavor component-containing liquid.
The present invention can provide a method for preparing a black liquor by which a flavor component-containing black liquor can be obtained with fewer treating processes. The present invention can also provide a method for preparing a flavor component-containing liquid obtained by treating the black liquor.
Hereinafter, an embodiment of the present invention will be described in detail.
First, a method for preparing a black liquor according to an aspect of the present invention will be described with reference to
A tobacco raw material derived from a plant of the genus Nicotiana can be appropriately used as the tobacco raw material (A). A tobacco raw material containing a large amount of tobacco midrib, stalk, and root is preferably used. This is because the tobacco midrib, stalk, and root contain a larger amount of lignin as a raw material of vanillin than that contained in tobacco leaf (a leaf portion excluding the tobacco midrib).
The digesting treatment (S1) is performed by heating the tobacco raw material (A) in a chemical solution. In the present invention, the digesting treatment (S1) is performed under an alkaline condition. As long as the condition is alkaline, the extent of alkalinity is not limited. The digesting treatment (S1) is preferably performed under a strong alkaline condition. For example, the alkaline condition is made by using an alkaline solution as a chemical solution for the digesting treatment. The concentration of the chemical solution can be appropriately adjusted so that the chemical solution has a pH suitable for the digesting treatment. In the case of using the alkaline solution, the solution can be used in a concentration of, for example, 0.01 normality or more, and preferably 0.1 normality or more (hereinafter, ‘normality’ is also expressed as N). Although the upper limit of the concentration is not particularly limited, the alkaline solution can be used in a concentration of, for example, 0.1 to 2 normality.
In order to make the alkaline condition suitable for the digesting treatment, an alkaline solution having preferably a pH of 12 or more, and more preferably a pH of 13 or more, is used. Although the upper limit of the pH is not particularly limited, an alkaline solution having, for example, a pH of 12 to 14.3, and preferably a pH of 13 to 14.3, can be used. Examples of the alkaline solution to be preferably used include an NaOH aqueous solution, a KOH aqueous solution, a K2CO3 aqueous solution, an Na2CO3 aqueous solution, and an NaHCO3 aqueous solution. The chemical solution is particularly preferably a strong base aqueous solution of 0.1 normality or more. A vanillin production amount tends to be increased when the pH of the chemical solution is increased.
The used amount of the chemical solution varies depending on the pH of the chemical solution to be used. The used amount is not particularly limited as long as the tobacco raw material is sufficiently digested. For example, a ratio of the mass (g) of the tobacco raw material to the used amount (mL) of the chemical solution is preferably 1:2 to 1:100, more preferably 1:3 to 1:100, still more preferably 1:3 to 1:50, yet still more preferably 1:5 to 1:50, and particularly preferably 1:10 to 1:50.
From the results of
In general, a digesting treatment is performed at 120 to 180° C. Also in the present invention, the digesting treatment can be performed at the above temperature, more preferably 130 to 180° C., and particularly preferably 150 to 180° C. The amount of the flavor component in the black liquor tends to be increased as the temperature of the digesting treatment is increased within the above range. The reaction time of the digesting treatment is not particularly limited as long as the tobacco raw material is sufficiently digested in the reaction time. The reaction time varies depending on the pH of the chemical solution to be used. For example, the reaction time is preferably about 5 minutes to 6 hours, more preferably 30 minutes to 6 hours, and particularly preferably 1 hour to 6 hours. When the reaction time is set to 1 hour or more, the vanillin production amount tends to be stably increased. The vanillin production amount tends to be increased when the digesting treatment is performed for a longer period of time within the above range.
The digesting treatment is preferably performed in an oxygen atmosphere. A black liquor having a larger amount of flavor component can be obtained in a shorter time by performing the digesting treatment in the oxygen atmosphere. Specifically, air in a container containing the tobacco raw material and the chemical solution for the digesting treatment is replaced with oxygen to fill the container with oxygen, and the container is heated. The container is filled with oxygen so that the gage pressure in the container is preferably 0.05 to 1.0 MPa, more preferably 0.1 to 0.7 MPa, and particularly preferably 0.1 to 0.4 MPa.
Examples of a method for making a high oxygen atmosphere state include, but are not limited to, a method of injecting only oxygen into a container under pressure, and a method of injecting air into a container under pressure. When the air is injected under pressure, the air is injected under pressure so that the gage pressure in the container is preferably 0.25 to 5 MPa, more preferably 0.5 to 3.5 MPa, and particularly preferably 0.5 to 2.0 MPa.
A treatment after filling the container with oxygen can be performed in the same way as the above case where the oxygen filling is not performed.
After the digesting treatment, a step (S2) of separating the digesting product into the black liquor (B) and the tobacco fiber (C) can be performed by appropriately selecting a known separating method. Examples of the method include a screw press, a screen, and centrifugal dehydration.
Next, a method for preparing a flavor component-containing liquid according to another embodiment of the present invention will be described with reference to
The method for preparing a flavor component-containing liquid according to the present invention includes the following steps:
(i) digesting (S1) a tobacco raw material (A) under an alkaline condition;
(ii) separating (S2) a product obtained by the digesting into a black liquor (B) and a tobacco fiber (C);
and
After the digesting step under the alkaline condition (S1) or the subsequent separating step (S2), the digesting product (that is, the product after the digesting step and before the separating step) or the black liquor (B) may be optionally neutralized.
Herein, the desalinating means a step of removing a salt from the black liquor to separate the flavor component produced by the alkaline digesting and the salt from each other. Thereby, a flavor component-containing liquid containing no salt can be obtained.
Hereinafter, each of the above steps will be described in detail.
The steps of (i) and (ii) are as described above.
In the desalinating step (S3) of (iii), inorganic ions such as Na+ contained in the black liquor (B) or salts such as NaCl generated by neutralizing the black liquor (B) are removed to obtain a flavor component-containing liquid (D). Particularly, when a tobacco raw material is digested under a strong alkaline condition, the obtained black liquor (B) contains a large amount of inorganic ions (Na+ or the like) or salts (NaCl or the like). However, the inorganic ions or the salts adversely affect the smoking taste of a cigarette. Therefore, if the inorganic ions or the salts are removed from the black liquor to obtain the flavor component-containing liquid (D) of the present invention, and a tobacco filler produced by using the flavor component-containing liquid is applied to a cigarette, a flavor can be efficiently exhibited.
Examples of the desalinating step (S3) include a method using solvent extraction. Non-polar solvents such as ethyl acetate, hexane, and diethylether can be used as a solvent. In the method using the solvent extraction, first, a black liquor is neutralized. Herein, the neutralizing step is performed by adding an acid to the black liquor (B). Any acid can be used herein, as long as it can neutralize the black liquor (B). Examples of the acid include hydrochloric acid, sulfuric acid, and nitric acid. The pH of the black liquor (B) after the neutralizing step is preferably 7 or less, and more preferably 2.0 to 6.0. If the black liquor is neutralized, the black liquor can be efficiently desalinated by the solvent extraction.
Another example of the desalinating method includes a method using ion exchange. In this method, the black liquor (B) is desalinated by exchanging the inorganic ions in the black liquor (B) with hydrogen ions using a cation-exchange resin or the like. The pH of the flavor component-containing liquid (D) obtained by desalinating the black liquor (B) by the ion exchange is usually 7 or less.
Furthermore, the desalinating step (S3) can be performed by methods such as vacuum concentration and steam distillation. However, the method is not limited thereto.
As another desalinating method, a flavor component can be efficiently obtained by bringing a black liquor into contact with a synthetic adsorbent to make an intended flavor component contained in the black liquor adsorb to the synthetic adsorbent, removing the black liquor containing inorganic ions or salts, and making the flavor component desorb from the synthetic adsorbent using a suitable chemical agent. Herein, the synthetic adsorbent refers to a spherical cross-linked polymer prepared so as to have a porous structure by a special synthetic technique. Specifically, it refers to a product which is commercially available under the name of “synthetic adsorbent”. Since the synthetic adsorbent has no functional group, unlike an ion-exchange resin, the synthetic adsorbent has an advantage that it is chemically stable. Examples of the synthetic adsorbent used herein include a styrene-based synthetic adsorbent, an acrylic synthetic adsorbent, and a phenol-based synthetic adsorbent. Specific examples include, but are not limited to, Amberlite XAD (Organo Corporation) and Sepabeads (Mitsubishi Chemical Corporation).
The flavor component-containing liquid (D) obtained as described above contains a flavor component capable of improving the flavor of the cigarette. Examples of the flavor component include, but are not limited to, vanillin, syringaldehyde (also referred to as 4-hydroxy-3,5-dimethoxydibenzaldehyde), acetovanillone (also referred to as 4′-hydroxyl-3′-methoxyacetophenone), and acetosyringone (also referred to as 4′-hydroxy-3′,5′-dimethoxyacetophenone).
As described above, the flavor component-containing liquid (D) of the present invention is obtained through the desalinating step (S3). Therefore, even if the tobacco filler produced by using the flavor component-containing liquid of the present invention is applied to a cigarette, the tobacco filler does not adversely affect the smoking taste of the cigarette.
Next, a method for preparing a tobacco filler according to another embodiment of the present invention will be described with reference to
A method for preparing a tobacco filler according to the present invention includes applying the flavor component-containing liquid obtained as described above to a plant fiber or a formed product of the plant fiber. Examples of the plant fiber include a tobacco fiber. Furthermore, the plant fiber may be a fiber obtained from a plant other than a tobacco. The plant fiber may be obtained by mixing these fibers. Any plant fiber can be used without particular limitation as long as the plant fiber can be used to produce a tobacco filler. Hereinafter, a case where the tobacco fiber is used as the plant fiber will be described.
Specifically, addition (S5) of a flavor component-containing liquid (D) to a tobacco fiber (C) obtained by the digesting (S1) of a tobacco raw material (A) and the separating (S2) is performed. The tobacco fiber used herein may be a tobacco fiber (C) obtained from the same raw material in a process of preparing the flavor component-containing liquid (D) as described above, or may be a tobacco fiber obtained by another process.
The amount of the flavor component-containing liquid (D) added to the tobacco fiber can be appropriately set within a range where a desired flavor is obtained when the obtained tobacco filler is used for a cigarette.
The flavor component-containing liquid (D) may be concentrated to a predetermined concentration (for example, 5 to 10 times) via a concentration machine or the like, and then the concentrated flavor component-containing liquid (D) may be added to the tobacco fiber (C). When the concentrated liquid is used, the added amount of the concentrated liquid is preferably adjusted so that the amount of a flavor component contained in the tobacco fiber at the time of adding the concentrated liquid is the same as the amount of a flavor component contained in the tobacco fiber at the time of adding a non-concentrated flavor component-containing liquid in the above preferable amount.
The flavor component-containing liquid (D) can be added to the tobacco fiber (C) or the formed product of the tobacco fiber by a means appropriately selected from known addition methods. For example, the flavor component-containing liquid (D) can be added by means such as spraying, immersing, and coating.
After the flavor component-containing liquid (D) is added, a drying treatment (S6) is performed in a drier, and thereby a tobacco filler (E) according to the present invention adjusted to a predetermined moisture content is produced. A moisture content in the dried tobacco filler (E) is, for example, 5 to 15% by weight, and preferably 11 to 13% by weight.
The tobacco fiber (C) may be optionally formed into a predetermined shape (S4) before the flavor component-containing liquid (D) is added. When the tobacco fiber (C) is formed, the shape of the tobacco fiber is appropriately determined according to the intended shape of the tobacco filler. For example, a sheet tobacco can be produced by using the tobacco fiber (C) or the formed product of the tobacco fiber (C) as a base sheet tobacco. The shape of the tobacco fiber (C) may be, for example, a powdery shape or a shape molded by extrusion molding.
The sheet tobacco is produced by forming the tobacco fiber (C) into a sheet shape to produce a base sheet tobacco, and adding the flavor component-containing liquid (D) to the base sheet tobacco. The base sheet tobacco is produced by mixing a tobacco fiber obtained from a tobacco raw material with optionally a reinforcing agent and a binding agent in the presence of water or the like to form the tobacco fiber into a sheet shape, and drying the sheet. A moisturizing agent, a flavor, and a water resistant agent or the like in addition to the above flavor component-containing liquid can be appropriately added to the base sheet tobacco.
A fiberized product of pulp, or the like can be preferably used as the reinforcing agent. A carboxymethylcellulose sodium salt, methyl cellulose, ethyl cellulose, starch, sodium alginate, locust bean gum, and gum arabic or the like can be used as the binding agent.
However, the binding agent is not limited thereto.
Polyhydric alcohols such as glycerin and propylene glycol; a mixture of a polyhydric alcohol and corn syrup; and sugar alcohols such as sorbitol and maltitol; or the like can be used as the moisturizing agent. Furthermore, sugars and fruit extracts or the like can be used as the flavor.
For example, the base sheet tobacco can be produced by using a sheet tobacco producing apparatus disclosed in Jpn. Pat. Appln. KOKAI Publication No. 3-224472. The flavor component-containing liquid can be added to the base sheet tobacco by spray flavoring (electrostatic coating), roll coating, gravure coating, and a size press or the like. The addition rate of the flavor component to the sheet tobacco is about 30% when using the spray flavoring (electrostatic coating), and by contrast, is about 90% when using the roll coating or the gravure coating. Therefore, when using the roll coating or the gravure coating, the flavor and taste of the sheet tobacco can be enhanced by effectively using a small amount of the flavor component-containing liquid.
The obtained sheet tobacco is appropriately cut and used as a tobacco filler.
The present invention relates also to a tobacco filler obtained by the above method, and a tobacco product containing the tobacco filler. If the tobacco filler obtained by the above method is applied to a cigarette, a cigarette having excellent flavor and taste can be obtained. The obtained sheet tobacco can be used also as a material for cigarette manufacturing (for example, cigarette paper, a filter, wrapping paper, and a package). Furthermore, the obtained sheet tobacco can be used for tobacco products other than the cigarette, for example, tobacco products such as a pipe, a cigar, a cigarillo; noncombustible-type tobacco products; and smokeless tobacco products (for example, a snuff, and an oral tobacco).
The present invention can provide a black liquor according to a simpler method than a conventional method for preparing a black liquor (for example, an acid sulfite pulping process). That is, in the method of the present invention, a black liquor can be obtained by merely performing a one step reaction of subjecting a tobacco raw material to a digesting treatment under an alkaline condition. A method for preparing the black liquor according to the present invention also has a feature that it has a shorter heating time than that in the conventional method. The black liquor obtained by the method of the present invention contains the flavor component in an amount equal to or greater than, that of the black liquor obtained by the conventional method. In the present invention, a treatment using a chemical solution containing sulfur is not performed, unlike in the conventional method for preparing a black liquor, and thereby a cigarette having good smoking taste can be obtained when the black liquor obtained in the present invention is applied to a cigarette. Therefore, the present invention can provide a black liquor containing a flavor component in a shorter period of time with fewer treating processes.
Hereinafter, the present invention will be described in detail with reference to the Examples. However, the present invention are not limited thereto.
One g of roughly crushed pieces of flue-cured tobacco stalk or burley tobacco stalk, and 50 mL of a 2N NaOH aqueous solution were sealed in a pressure-resistant container, heated to 180° C. while being stirred, and then held in this state for 3 hours. Then, the heated product was cooled together with the container. A black liquor and a residue (that is, a tobacco fiber) were filtered with a glass filter, and separated and recovered. An amount of a flavor component contained in the black liquor was measured by GCMS, and the measured value was regarded as an amount of a flavor component produced from 1 g of a tobacco raw material.
The amount of the flavor component contained in the black liquor was measured by the following method.
An internal standard substance (p-BPA: 50 μg) was added to the black liquor, and the total amount was adjusted to 40 ml with pure water. Then, a 1 N HCl aqueous solution was added to the resultant solution to adjust a pH to 2±0.1. The total amount of the pH-adjusted black liquor was made to pass through a solid phase extraction column Oasis HLB 1 g/20 cc (manufactured by Waters) which had been previously conditioned in diethylether (20 ml) methanol (20 ml)→0.01 N HCl aqueous solution (20 ml) in this order. Then, diethylether was made to pass through the solid phase extraction column to obtain a recovery liquid. The obtained recovery liquid was concentrated at normal pressure, and then diluted with diethylether to a given volume to obtain an analysis sample. GCMS analysis of the obtained analysis sample was performed by the following method.
The GCMS analysis was performed by using an HP6890 GC system, a 5973N mass spectrometer, and a DB-FFAP column (30 m, 0.2 mm, 0.25 μm) (all manufactured by Agilent). Analysis conditions are shown in detail in the following Table A.
The results are shown in the following Table 1. Compounds listed as flavor components in Table 1 are considered to affect the smoking flavor and taste of a cigarette.
One g of roughly crushed pieces of burley tobacco stalk, and 50 mL of a 2N NaOH aqueous solution were sealed in a pressure-resistant container, heated to a predetermined temperature while being stirred, and then held in this state for a given length of time. A heating temperature was set to 130° C., 150° C., and 180° C., and a holding time was changed within a range of 5 to 320 minutes. The subsequent cooling process and separation recovery process were performed in the same way as Example 1. An amount of vanillin contained in a black liquor was measured by GCMS, and the measured value was regarded as an amount of vanillin produced from 1 g of a tobacco raw material. A weight of a separated residue was measured, and the measured value was regarded as a residue amount obtained from 1 g of a tobacco raw material. The results are shown in
One g of roughly crushed pieces of burley tobacco stalk, and 50 mL or 10 mL of a 2N NaOH aqueous solution were sealed in a pressure-resistant container, heated to 180° C. while being stirred, and then held in this state for a predetermined time. A holding time was changed within a range of 5 to 320 minutes. The subsequent cooling process and separation recovery process were performed in the same way as Example 1. An amount of vanillin contained in a black liquor and a weight of a separated residue were measured in the same way as Example 2. The results are shown in
From
One g of roughly crushed pieces of burley tobacco stalk, and 50 mL of an alkaline aqueous solution were sealed in a pressure-resistant container, heated to 180° C. while being stirred, and then held in this state for a predetermined time. A holding time was changed within a range of 5 to 320 minutes. A 2N NaOH (pH 14.3) aqueous solution, a 0.5N NaOH aqueous solution (pH 13.6), a 0.1N NaOH aqueous solution (pH 12.9), a 0.05N NaOH aqueous solution (pH 12.6), a 0.01N NaOH aqueous solution (pH 12.0), a 2N KOH aqueous solution (pH 14.3), a 0.1N KOH aqueous solution (pH 12.9), or 4 mol/kg of a K2CO3 aqueous solution (pH 12.5) was used as the alkaline aqueous solution. The subsequent cooling process and separation recovery process were performed in the same way as Example 1. Amounts of vanillin and syringaldehyde contained in a black liquor were measured by GCMS, and the measured values were regarded as amounts of vanillin and syringaldehyde produced from 1 g of a tobacco raw material. A weight of a separated residue was measured, and the measured value was regarded as a residue amount obtained from 1 g of a tobacco raw material. The results are shown in
From
Regarding samples A to D of black liquors shown below, a vanillin production amount was measured by GCMS. The results are shown in
The case where 1 g of roughly crushed pieces of burley tobacco stalk were used as a tobacco raw material in Example 1, was used as a sample A.
Roughly crushed pieces of burley tobacco stalk and a 2N NaOH aqueous solution were sealed at a solid-liquid ratio of 1:50 (50 mL of NaOH per 1 g of a tobacco raw material) (hereinafter, the same shall apply) in a pressure-resistant container, and then the container was filled with oxygen so that the gage pressure was set to 0.1 MPa. This was heated to 180° C. while being stirred, and then held in this state for 3 hours. The subsequent cooling process and separation recovery process were performed in the same way as Example 1.
Seven hundred g of roughly crushed pieces of burley tobacco stalk, 210 g of Na2SO3, 26.6 g of NaOH, 0.35 g of anthraquinone, and 2.1 L of water were sealed in a pressure-resistant container (solid-liquid ratio 1:3). This was heated to 179° C. while being stirred, and then held in this state for 6 hours. The subsequent cooling process and separation recovery process were performed in the same way as Example 1.
Five hundred g of roughly crushed pieces of burley tobacco stalk, and 2 L of a digesting chemical solution (9% by weight of SO2, 1.32% by weight of Ca(OH)2) were sealed in a pressure-resistant container (solid-liquid ratio 1:4). This was heated to 158° C., and then held in this state for 6 hours. Then, the heated product was cooled together with the container. A black liquor and a residue (that is, a tobacco fiber) were filtered with a glass filter, and separated and recovered. NaOH was added to the obtained black liquor so that the concentration of NaOH was set to 2 N. This was sealed in a pressure-resistant container, and heated at 180° C. for 3 hours. After cooling, the black liquor was recovered.
From
To 700 g of roughly crushed pieces of burley tobacco stalk, 2.1 L, 3.5 L, and 7 L of 2N NaOH aqueous solutions were added, to prepare samples so that solid-liquid ratios were set to 1:3, 1:5, and 1:10, respectively. These were sealed in a pressure-resistant container. Furthermore, air in the pressure-resistant container was replaced with oxygen at 0.4 MPa (gage pressure). The pressure-resistant container was heated to 150° C. while being stirred, and then held in this state for 3 hours. Then, the heated product was cooled together with the pressure-resistant container. A black liquor and a residue (that is, a tobacco fiber) were filtered with a glass filter, and separated and recovered. An amount of vanillin contained in the black liquor was measured by GCMS, and the measured value was regarded as a vanillin production amount from 1 g of a tobacco raw material. The results are shown in
Seven hundred g of roughly crushed pieces of burley tobacco stalk and 7 L of a 2N NaOH aqueous solution were sealed in a pressure-resistant container. Furthermore, air in the pressure-resistant container was replaced with oxygen at 0.1 MPa, 0.3 MPa, and 0.4 MPa (gage pressure). The pressure-resistant container was heated to 150° C. while being stirred, and then held in this state for 1 hour, 3 hours, and 6 hours. Then, the heated product was cooled together with the pressure-resistant container. A black liquor and a residue (that is, a tobacco fiber) were filtered with a glass filter, and separated and recovered. An amount of vanillin contained in the black liquor was measured by GCMS, and a vanillin production amount from 1 g of a tobacco raw material was calculated from the measured value. The results are shown in
Five g of roughly crushed pieces of burley tobacco stalk and 50 mL of a 2N NaOH aqueous solution were sealed in a pressure-resistant container. Furthermore, air was injected under pressure into the pressure-resistant container so that the pressure was set to 0.5 MPa (gage pressure). The pressure-resistant container was heated to 150° C. while being stirred, and then held in this state for 3 hours. Then, the heated product was cooled together with the pressure-resistant container. A black liquor and a residue (that is, a tobacco fiber) were filtered with a glass filter, and separated and recovered. As a comparison, a treatment was conducted in the same way as the above conditions except that air was not injected under pressure. An amount of vanillin contained in each black liquor was measured by GCMS, and a vanillin production amount from 1 g of a tobacco raw material was calculated from the measured value. The results are shown in
Hydrochloric acid was added to the black liquor obtained in Example 1, to neutralize the black liquor so that the pH was set to 7 or less. The neutralized black liquor and ethyl acetate of an amount equal to that of the black liquor were charged into a separating funnel, and sufficiently stirred. The resultant solution was left for a while, and then an organic layer was recovered. The organic layer was concentrated by using a rotary evaporator to remove ethyl acetate. An appropriate amount of ethanol was added to the obtained dried product to obtain a flavor component-containing liquid having a sweet flavor. A concentration of vanillin contained in the obtained flavor component-containing liquid was measured by GCMS, and a vanillin recovery rate from the original black liquor was calculated from the measured value. The results are shown in Table 3.
Hydrochloric acid was added to the black liquor obtained under a condition of a solid-liquid ratio 1:10 in Example 6, to neutralize the black liquor so that the pH was set to 7 or less. Four hundred and forty mL of the neutralized black liquor was made to pass through a column filled with 30 mL of a styrene-based synthetic adsorbent (Amberlite XAD4, Organo Corporation), and then pure water was made to pass through the column to wash the synthetic adsorbent. Furthermore, 240 mL of ethanol was made to pass through the column to recover the total amount. A concentration of vanillin contained in the recovered ethanol solution was measured by GCMS, and a vanillin recovery rate from the original black liquor was calculated from the measured value. The results are shown in Table 3.
The black liquor obtained in Example 1 was diluted 10 times with water, and the resultant solution was made to pass through a column filled with a cation-exchange resin (Amberlite IRC76, Organo Corporation). When the liquid passing through the column was recovered, and a pH of the recovered fraction was measured, the fraction had a pH of 2 to 6. From the pH value, it was found that Na+ ions contained in the black liquor were exchanged with H+ ions in the fraction. Further, when a concentration of vanillin contained in the fraction was measured by GCMS, the concentration was about the same as that of the black liquor which has not yet been made to pass through the column. A vanillin recovery rate from the original black liquor was calculated. The results are shown in Table 3.
A black liquor was desalted by vacuum concentration, and a change in an amount of vanillin in a black liquor were investigated as follows by using a model aqueous solution.
Twenty g of the model aqueous solution (2 mol/L NaCl, vanillin 0.221 g) was concentrated under reduced pressure at 50° C. by using an evaporator, to dry the model aqueous solution. The obtained dried product was dissolved in ethanol, and the resultant solution was filtered by using filter paper. A vanillin concentration of the obtained recovery liquid was measured by GCMS. A vanillin recovery rate was calculated by comparing the amount of vanillin contained in the recovery liquid after vacuum concentration with the amount of vanillin contained in the model aqueous solution before vacuum concentration. The results are shown in Tables 2 and 3.
The results of the above tests (Examples 8 to 12) are shown in the following Tables 2 and 3.
From Tables 2 and 3, it is found that the desalination of the black liquor by the synthetic adsorbent provides the highest vanillin recovery rate, and is very suitable as the desalinating method in the present invention. From Tables 2 and 3, it is found that desalinating methods other than the desalination by the synthetic adsorbent also provide a good vanillin recovery rate. Therefore, it can be said that the loss amount of vanillin caused by the desalination process is slight, and the desalinating process does not affect the effect of the present invention (that is, the preparation of the flavor component-containing liquid containing flavor components).
The flavor component-containing liquid obtained in Example 9 was spray-coated on a base sheet tobacco produced by using a tobacco fiber obtained from burley tobacco stalk, and dried. The dried sheet tobacco was cut to obtain a tobacco filler.
10% by weight of the tobacco filler obtained in Example 13 was blended with a shredded tobacco (90% by weight) to produce a hand-rolled cigarette. When the produced cigarette was smoked, a vanilla-like flavor and taste were felt.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-059045 | Mar 2013 | JP | national |
This application is a Continuation Application of PCT Application No. PCT/JP2014/057811, filed Mar. 20, 2014 and based upon and claiming the benefit of priority from Japanese Patent Application No. 2013-059045, filed Mar. 21, 2013, the entire contents of all of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2014/057811 | Mar 2014 | US |
| Child | 14750592 | US |
