JPH05227939A - Tobacco filter - Google Patents
Tobacco filterInfo
- Publication number
- JPH05227939A JPH05227939A JP6103492A JP6103492A JPH05227939A JP H05227939 A JPH05227939 A JP H05227939A JP 6103492 A JP6103492 A JP 6103492A JP 6103492 A JP6103492 A JP 6103492A JP H05227939 A JPH05227939 A JP H05227939A
- Authority
- JP
- Japan
- Prior art keywords
- filter
- hydroxybutyric acid
- polyester compound
- cigarette
- aliphatic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 235000002637 Nicotiana tabacum Nutrition 0.000 title description 8
- 244000061176 Nicotiana tabacum Species 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 23
- 235000019504 cigarettes Nutrition 0.000 claims abstract description 21
- 229920003232 aliphatic polyester Polymers 0.000 claims abstract description 18
- 229920000728 polyester Polymers 0.000 claims abstract description 15
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- -1 poly(3-hydroxybutyric acid) Polymers 0.000 claims abstract description 9
- 244000005700 microbiome Species 0.000 claims abstract description 8
- 238000007142 ring opening reaction Methods 0.000 claims abstract description 5
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 claims description 22
- REKYPYSUBKSCAT-UHFFFAOYSA-N 3-hydroxypentanoic acid Chemical compound CCC(O)CC(O)=O REKYPYSUBKSCAT-UHFFFAOYSA-N 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 10
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 claims description 6
- 229940006015 4-hydroxybutyric acid Drugs 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 3
- 239000011148 porous material Substances 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 9
- 238000004804 winding Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 15
- 241000208125 Nicotiana Species 0.000 description 7
- 239000004793 Polystyrene Substances 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 230000000391 smoking effect Effects 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000013535 sea water Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000860832 Yoda Species 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229920006238 degradable plastic Polymers 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 238000001955 polymer synthesis method Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
- Biological Depolymerization Polymers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は,紙巻タバコ用のフィル
タ−に関する。FIELD OF THE INVENTION The present invention relates to a filter for a cigarette.
【0002】[0002]
【従来の技術】紙巻タバコは,以前はフィルタ−を取り
付けず単に,刻んだタバコ葉を紙で巻いただけの状態で
喫煙されていた。最近では,口にタバコ葉が付着するの
を防ぐ,粉塵やタ−ル分除去効果がある,等の理由によ
り,フィルタ−付きのものが好まれている。フィルタ−
の材質としては,主にセルロ−ストリアセテ−トやポリ
プロピレンが知られている。2. Description of the Related Art Cigarettes used to be smoked without a filter attached, simply by cutting the cut tobacco leaf onto paper. Recently, filters are preferred because they prevent tobacco from sticking to the mouth and have the effect of removing dust and tar. Filter-
Cellulose triacetate and polypropylene are mainly known as materials for the.
【0003】フィルタ−に関する改良としては,特開昭
59−106284において,破砕した植物繊維をフィ
ルタ−として用いる煙の浄化装置,或は特開昭62−1
71664においては,菌じん類の加工体を含むフィル
タ−の研究が報告されている。また,香気成分を含有さ
せたり,特開昭61−195680のごとく,水等の消
火に役立つ物質を内臓したタバコフィルタ−の研究も行
われている。As an improvement relating to the filter, Japanese Patent Laid-Open No. 59-106284 discloses a smoke purifying device using crushed plant fibers as a filter, or Japanese Patent Laid-Open No. 62-1.
In 71664, a study on a filter containing a processed product of fungi is reported. Further, studies have also been conducted on a cigarette filter containing a fragrance component or containing a substance useful for extinguishing fire such as water as disclosed in JP-A-61-195680.
【0004】[0004]
【発明が解決しようとする課題】現在使用されているタ
バコフィルタ−は,分解性を有していないため,環境中
に廃棄された場合に汚染源となる。特に,公園や,海,
山,川,等の自然環境におけるタバコの投げ捨てのため
に,せっかくの景観を台無しにする原因の1つとなって
いる。また,今後,生態系への影響も懸念される。Since the tobacco filters currently used are not degradable, they become a pollution source when they are discarded into the environment. Especially in the park, the sea,
It is one of the causes of ruining the scenery due to the dumping of cigarettes in the natural environment such as mountains and rivers. There is also concern about the impact on the ecosystem in the future.
【0005】上記の問題は,喫煙者のモラル向上が第一
であるが,補助的な方法として廃棄されたフィルタ−に
分解性を持たせることも必要な方策の一つと考えられ
る。分解性を有するフィルタ−としては,上記の特開昭
59−106284に開示された植物繊維をフィルタ−
として用いる煙の浄化装置や,特開昭62−17166
4に開示された菌じん類の加工体を含むフィルタ−等が
適用できる。しかし,これらの特許はタ−ル分の除去を
目的としたものであり,分解性の材料の他に非分解性の
プラスチック材料を使用しており,本発明の目的と異な
る。The above-mentioned problem is primarily to improve the morale of smokers, but it is considered that one of the measures required to make the discarded filter have degradability as an auxiliary method. As the filter having degradability, the plant fiber disclosed in the above-mentioned JP-A-59-106284 is used.
For purifying smoke used as a device, and Japanese Patent Application Laid-Open No. 62-17166
The filter and the like containing the processed product of fungus and dust disclosed in 4 can be applied. However, these patents are for the purpose of removing tar components, and use non-degradable plastic materials in addition to degradable materials, which is different from the object of the present invention.
【0006】植物繊維や,菌じん類は,親水性であり,
本発明の目的を達成するために,これらの材料だけで構
成したフィルタ−は喫煙時に付着する唾等の水分のため
に変形し役目をなさない。[0006] Plant fibers and fungi are hydrophilic,
In order to achieve the object of the present invention, a filter composed only of these materials is deformed and does not serve due to moisture such as saliva adhering during smoking.
【0007】[0007]
【課題を解決するための手段】本発明者らは,上記問題
の解決のために,分解性の材料のみよりなるタバコフィ
ルタ−について,種々検討の結果,生分解性を有する脂
肪族ポリエステル化合物を用いる方法に到達した。即
ち,本発明は, (1)微細な気孔を有する,生分解性の脂肪族ポリエス
テル化合物よりなる,紙巻きタバコの先端に取り付ける
フィルタ− (2)(1)に記載した生分解性を有する脂肪族ポリエ
ステル化合物が,ポリ(3−ヒドロキシ酪酸),3−ヒ
ドロキシ酪酸と3−ヒドロキシ吉草酸の共重合体,3−
ヒドロキシ酪酸と4−ヒドロキシ酪酸の共重合体,微生
物が生産するポリ3−ヒドロキシアルカノエート系の高
分子,脂肪族ラクトン化合物の開環重合体若しくはC2
〜C12の脂肪族2塩基酸とC2〜C12の脂肪族ジオ
−ルよりなるポリエステル又はこれらの改質物であるフ
ィルタ−を提供する。In order to solve the above problems, the inventors of the present invention have conducted various studies on a tobacco filter made of only a degradable material, and have found that an aliphatic polyester compound having biodegradability is selected. The method used has been reached. That is, the present invention provides (1) a filter made of a biodegradable aliphatic polyester compound having fine pores, which is attached to the tip of a cigarette, and (2) the biodegradable aliphatic compound described in (1). The polyester compound is poly (3-hydroxybutyric acid), a copolymer of 3-hydroxybutyric acid and 3-hydroxyvaleric acid, 3-
Copolymer of hydroxybutyric acid and 4-hydroxybutyric acid, poly-3-hydroxyalkanoate-based polymer produced by microorganism, ring-opening polymer of aliphatic lactone compound or C2
A polyester comprising a C2-C12 aliphatic dibasic acid and a C2-C12 aliphatic diol, or a filter obtained by modifying these polyesters is provided.
【0008】本発明に用いる脂肪族ポリエステル化合物
は,疎水性でありかつ,微生物による分解をうけるた
め,上記問題の解決のためには最適の材料である。ま
た,タ−ル分除去に関しても,タ−ルに対する親和性は
高く,従来品と遜色ない効果を有する。また,セルロ−
ストリアセテ−トが現在最もよく用いられる材料である
が,可燃性である。これに対し,本発明の脂肪族ポリエ
ステル化合物は,自己消火性である。Since the aliphatic polyester compound used in the present invention is hydrophobic and is subject to decomposition by microorganisms, it is an optimum material for solving the above problems. Also, regarding the removal of the tar component, it has a high affinity for the tar and has an effect comparable to the conventional product. In addition,
Striacitate is currently the most commonly used material, but it is flammable. On the other hand, the aliphatic polyester compound of the present invention is self-extinguishing.
【0009】本発明に用いる脂肪族ポリエステル化合物
のうち,微生物の生産するものは,繊維状態で,土壌
中,海水中,淡水中,において2〜4カ月で,生分解を
うけ形態をとどめなくなる。また,それ以外の化学的に
合成される脂肪族ポリエステル化合物は,3〜10カ月
で,生分解をうけ形態をとどめなくなる。これらは最終
的には,炭酸ガスと水にまで分解される。Among the aliphatic polyester compounds used in the present invention, those produced by microorganisms are biodegradable in the fibrous state in soil, seawater, and fresh water within 2 to 4 months, and do not remain in the form. In addition, other chemically synthesized aliphatic polyester compounds undergo biodegradation and do not remain in the form within 3 to 10 months. Eventually, these are decomposed into carbon dioxide and water.
【0010】次に本発明を詳細に説明する。本発明に用
いる脂肪族ポリエステル化合物としては,ポリ(3−ヒ
ドロキシ酪酸),3−ヒドロキシ酪酸と3−ヒドロキシ
吉草酸の共重合体,3−ヒドロキシ酪酸と4−ヒドロキ
シ酪酸の共重合体,微生物が生産するポリ3−ヒドロキ
シアルカノエート系の高分子が挙げられる。Next, the present invention will be described in detail. Examples of the aliphatic polyester compound used in the present invention include poly (3-hydroxybutyric acid), copolymers of 3-hydroxybutyric acid and 3-hydroxyvaleric acid, copolymers of 3-hydroxybutyric acid and 4-hydroxybutyric acid, and microorganisms. Examples include poly-3-hydroxyalkanoate-based polymers to be produced.
【0011】脂肪族ラクトン化合物の開環重合体(化学
合成によるポリエステル化合物)としては,ラクチド,
グリコリド,β−プロピオラクトン,γ−バレロラクト
ン,δ−バレロラクトン,ε−カプロラクトン等の開環
重合体や,共重合体があげられる。The ring-opening polymer of an aliphatic lactone compound (polyester compound obtained by chemical synthesis) includes lactide,
Examples thereof include ring-opening polymers such as glycolide, β-propiolactone, γ-valerolactone, δ-valerolactone and ε-caprolactone, and copolymers.
【0012】また,C2〜C12の脂肪族2塩基酸と,
C2〜C12の脂肪族ジオ−ルよりなるポリエステル
(化学合成によるポリエステル化合物)としては,アジ
ピン酸と1.4−ブタンジオ−ルよりなるポリエステ
ル,琥珀酸と1.4−ブタンジオ−ルよりなるポリエス
テル,琥珀酸と1.6−ヘキサンジオ−ルよりなるポリ
エステル,セバチン酸と1.4−ブタンジオ−ルよりな
るポリエステル等を上げることが出来る。Further, a C2-C12 aliphatic dibasic acid,
Examples of the C2-C12 aliphatic diol polyester (polyester compound by chemical synthesis) include adipic acid and 1.4-butanediol polyester, succinic acid and 1.4-butanediol polyester, A polyester made of succinic acid and 1.6-hexanediol, a polyester made of sebacic acid and 1.4-butanediol and the like can be used.
【0013】化学合成によるポリエステル化合物として
は,直鎖状のものが生分解性が良好であり好ましい。炭
素数が12を越えた脂肪族ポリエステル化合物はやや生
分解性が低下する。As the polyester compound obtained by chemical synthesis, a linear compound is preferable because of its good biodegradability. The aliphatic polyester compound having more than 12 carbon atoms has a slightly lowered biodegradability.
【0014】上記した脂肪族ポリエステル化合物は,た
がいに2種以上を共重合体として用いて改質することも
できる。また,一般によく知られた方法(例えば、星
野、依田;高分子合成実験法(東京化学同人社,発行
日:1962年11月10日)鎖長を延長し分子量を向上させた
り,機械的強度や,繊維としての性能を改善するため
に,ヘキサメチレンジイソシアネ−トやイソホロンジイ
ソシアネ−ト,トリレンジイソシアネ−ト等の,ジイソ
シアネ−ト化合物で改質することも可能である。The above-mentioned aliphatic polyester compounds can also be modified by using two or more kinds as a copolymer. In addition, generally well-known methods (for example, Hoshino, Yoda; Experimental Polymer Synthesis Method (Tokyo Kagaku Dojinsha, date of issue: November 10, 1962)) chain length can be extended to increase molecular weight, and mechanical strength can be improved. Alternatively, in order to improve the performance as a fiber, it is possible to modify with a diisocyanate compound such as hexamethylene diisocyanate, isophorone diisocyanate, tolylene diisocyanate or the like.
【0015】本発明で用いる脂肪族ポリエステル化合物
の分子量は,ゲルパ−ミエ−ションクロマトグラフによ
る方法でポリスチレン基準の数平均分子量が10000
〜2000000程度のものを用いるのがよい。融点は
50℃〜250℃,好ましくは60℃〜200℃程度の
ものがよい。With respect to the molecular weight of the aliphatic polyester compound used in the present invention, the number average molecular weight based on polystyrene is 10,000 by the method of gel permeation chromatography.
It is preferable to use a material of about 2,000,000. The melting point is 50 ° C to 250 ° C, preferably about 60 ° C to 200 ° C.
【0016】本発明で用いる脂肪族ポリエステル化合物
は,繊維状,毛状,綿状,フェルト状,スポンジ状とな
しタバコの径と同じ径に加工する。繊維の径は0.5〜
500μm,好ましくは,1〜100μm程度とするの
が好ましい。フィルタ−の長さは,特に制限はなく,3
〜30mm程度の通常と同じ長さでよい。タ−ル分の吸
着量を上げるために活性炭等を添加してもよい。また,
メント−ル類,ハッカ類,プロピレングリコ−ル等,天
然,人造の香気成分や,防かび剤等を添加することもで
きる。The aliphatic polyester compound used in the present invention is processed into fibrous, fluffy, cotton-like, felt-like, sponge-like and non-cigarette tobacco having the same diameter. Fiber diameter is 0.5 ~
The thickness is preferably 500 μm, preferably about 1 to 100 μm. The length of the filter is not particularly limited and may be 3
The length may be the same as usual, about 30 mm. Activated carbon or the like may be added to increase the adsorption amount of the tar component. Also,
It is also possible to add a natural or artificial fragrance component such as menthol, peppermint, propylene glycol, etc., or a fungicide.
【0017】フィルタ−の製造法として一例を上げる
と,繊維状や,毛状,綿状の,脂肪族ポリエステル化合
物は,紙や脂肪族のポリエステル化合物等の生分解性の
フィルムで巻き,束ねて束状とし,適当な長さに切断す
ると微細な気孔を有するフィルタ−を製造することがで
きる。この際の通気性は,束状となったフィルタ−の密
度に反比例するが,喫煙に差し支えない範囲なら制限は
ない。この密度は,0.1〜0.3程度が好ましい。こ
のようにして製造されたフィルタ−は,タバコの喫煙口
に固定され,生分解性フィルタ−付紙巻きタバコが出来
上がる。As an example of a method for manufacturing a filter, a fibrous, hairy, or cotton-like aliphatic polyester compound is wrapped with a biodegradable film such as paper or an aliphatic polyester compound and bundled. A filter having fine pores can be manufactured by forming a bundle and cutting it into an appropriate length. The air permeability at this time is inversely proportional to the density of the bundled filter, but there is no limitation as long as it does not interfere with smoking. This density is preferably about 0.1 to 0.3. The filter manufactured in this manner is fixed to the smoking mouth of the cigarette, and the cigarette with the biodegradable filter is completed.
【0018】[0018]
【実施例】次に実施例により説明する。 実施例1 微生物により製造されたポリ(3−ヒドロキシ酪酸)
(ゲルパーミエションクロマト法によるポリスチレン基
準の数平均分子量が300000のもの)を,約8%濃
度で溶解している1.2−ジクロロエタン溶液を,ノズ
ルを通してn−ヘキサン中に押しだし,繊維を作製し
た。繊維の径は5〜50μmであった。この繊維を薄い
紙で束ね外径7mmのフィルタ−を作製し10mmの長
さに切断した。このフィルタ−は0.062gであり密
度は約0.16であった。これと同じ径を有する紙巻き
タバコの先端に薄い紙で巻き付けた。このフィルタ−付
紙巻きタバコは,従来のものに比べ喫煙時の味に変化は
なかった。また,海水中に3カ月浸漬したところほぼ形
態が認められなくなった。EXAMPLES Next, examples will be described. Example 1 Poly (3-hydroxybutyric acid) produced by microorganisms
A 1.2-dichloroethane solution in which a polystyrene-based number average molecular weight by gel permeation chromatography was 300,000 was extruded through a nozzle into n-hexane to prepare fibers. did. The fiber diameter was 5 to 50 μm. The fibers were bundled with thin paper to prepare a filter having an outer diameter of 7 mm and cut into a length of 10 mm. The filter had a weight of 0.062 g and a density of about 0.16. A thin paper was wrapped around the tip of a cigarette having the same diameter. This filter-tipped cigarette had no change in taste during smoking compared to the conventional cigarette. Moreover, when immersed in seawater for 3 months, almost no morphology was observed.
【0019】実施例2 微生物により生産された3−ヒドロキシ酪酸と3−ヒド
ロキシ吉草酸の共重合体(3−ヒドロキシ吉草酸成分を
22モル%含有し、ゲルパーミエーションクロマトグラ
フ法によるポリスチレン基準の数平均分子量が4500
00のもの)を160℃にて溶融させ,ノズルを通して
空冷した部分に押しだし繊維を作製した。この繊維は,
外径10〜100μmでありこの繊維を薄い紙で束ね,
外径7mmのフィルタ−を作製し10mmの長さに切断
した。このフィルタ−は,0.070gであり,密度は
約0.18であった。これと同じ径を有する紙巻きタバ
コの先端に薄い紙で取り付けた。このフィルタ−付タバ
コは,従来のものに比べ,喫煙時の味に変化はなかっ
た。また,土壌中に4カ月埋めたところ,ほぼ形態をと
どめていなかった。Example 2 Copolymer of 3-hydroxybutyric acid and 3-hydroxyvaleric acid produced by a microorganism (containing 22 mol% of 3-hydroxyvaleric acid component, number of polystyrene standard by gel permeation chromatography) Average molecular weight is 4500
No. 00) was melted at 160 ° C. and extruded through a nozzle into an air-cooled portion to prepare a fiber. This fiber is
The outer diameter is 10 to 100 μm, and these fibers are bundled with thin paper,
A filter having an outer diameter of 7 mm was produced and cut into a length of 10 mm. The filter had a weight of 0.070 g and a density of about 0.18. A thin paper was attached to the tip of a cigarette having the same diameter. Compared with the conventional cigarettes, this filter-tipped cigarette had no change in the taste during smoking. In addition, when it was buried in soil for 4 months, it had almost no morphology.
【0020】実施例3 アジピン酸14.6g,1.4−ブタンジオ−ル9.2
g,DL−リンゴ酸0.3gをトルエン40ml中で,
メタンスルフォン酸0.05gを,触媒として反応させ
脂肪族ポリエステルを合成した。ここに,ヘキサメチレ
ンジイソシアネ−ト0.25mlを加えて反応させ,改
質ポリエステルを合成した。このポリエステルのゲルパ
−ミエ−ションクロマト法によるポリスチレン基準の数
平均分子量は34000であり,重量平均分子量は79
000であった。融点は67℃であった。これを実施例
2と同じ方法で溶融紡糸し,径10〜100mmの繊維
を作製した。同様に外径7mm長さ10mmのフィルタ
−を作製した。密度は約0.18であった。これを同じ
径を有する紙巻きタバコの先端に取り付けた。フィルタ
−付タバコは,従来のものと味の上で差がなかった。こ
のフィルタ−を海水中に7カ月浸漬したところ,形態が
認められなくなった。Example 3 Adipic acid 14.6 g, 1.4-butanediol 9.2
g, DL-malic acid 0.3 g in toluene 40 ml,
0.05 g of methanesulfonic acid was reacted as a catalyst to synthesize an aliphatic polyester. To this, 0.25 ml of hexamethylene diisocyanate was added and reacted to synthesize a modified polyester. This polyester has a polystyrene-based number average molecular weight of 34,000 and a weight average molecular weight of 79 by gel permeation chromatography.
It was 000. The melting point was 67 ° C. This was melt-spun in the same manner as in Example 2 to produce fibers having a diameter of 10 to 100 mm. Similarly, a filter having an outer diameter of 7 mm and a length of 10 mm was produced. The density was about 0.18. This was attached to the tip of a cigarette having the same diameter. The tobacco with filter did not differ in taste from the conventional one. When this filter was immersed in seawater for 7 months, no morphology was observed.
【0021】実施例4 ポリカプロラクトン(ダイセル社製;数平均分子量70
0000(カタログより))を100℃にて溶融し,ノ
ズルを通して空冷した部分に押し出し繊維を作製した。
この繊維は外径10〜100μmであり,実施例3と同
様に外径7mm長10mmのフィルターを作製した。密
度は約0.17であった。これを同じ径を有する紙巻き
タバコの先端に取り付けた。フィルター付のタバコは,
味の上で従来のものと差がなかった。このフィルターを
土壌中に10ケ月埋めたところ若干形態が残っていた
が,大半は分解消失していた。Example 4 Polycaprolactone (manufactured by Daicel; number average molecular weight: 70)
0000 (from catalog)) was melted at 100 ° C., and extruded fiber was produced through a nozzle into an air-cooled portion.
This fiber has an outer diameter of 10 to 100 μm, and a filter having an outer diameter of 7 mm and a length of 10 mm was prepared in the same manner as in Example 3. The density was about 0.17. This was attached to the tip of a cigarette having the same diameter. Tobacco with filter is
There was no difference in taste from the conventional one. When this filter was buried in soil for 10 months, some morphology remained, but most of it was decomposed and disappeared.
【0022】実施例5 実施例2と全く同様に3−ヒドロキシ酪酸と4−ヒドロ
キシ酪酸の共重合体(4−ヒドロキシ酪酸成分を9.5
モル%含有し,ゲルパーミエーションクロマト法によ
る,ポリスチレン基準の数平均分子量が320000の
もの)を用い外径7mm,長さ10mmのフィルターを
作製した。フィルターを構成する繊維は10〜100μ
mの外径を有しており,フイルターの密度約0.17で
あった。これを紙巻きタバコの先端に薄い紙で巻いて取
り付けたフィルター付タバコは,味の上で従来のものと
差がなかった。土壌中に4ケ月埋めたところほぼ形態を
とどめなかった。Example 5 A copolymer of 3-hydroxybutyric acid and 4-hydroxybutyric acid (the 4-hydroxybutyric acid component being 9.5
A filter having an outer diameter of 7 mm and a length of 10 mm was produced by using a polystyrene-based number average molecular weight of 320,000 according to gel permeation chromatography. The fibers that make up the filter are 10-100μ
It had an outer diameter of m and a filter density of about 0.17. The cigarette with a filter attached to the tip of the cigarette wrapped with a thin paper did not differ from the conventional one in terms of taste. When it was buried in the soil for 4 months, it remained almost in its original form.
【0023】[0023]
【発明の効果】自然環境中で分解し環境汚染の恐れのな
い紙巻きタバコ用のフィルターが得られた。EFFECT OF THE INVENTION A filter for a cigarette which decomposes in a natural environment and is free from environmental pollution is obtained.
Claims (2)
リエステル化合物よりなる,紙巻タバコの先端に取り付
けるフィルタ−1. A filter which is made of a biodegradable aliphatic polyester compound having fine pores and which is attached to the tip of a cigarette.
物が,ポリ(3−ヒドロキシ酪酸),3−ヒドロキシ酪
酸と3−ヒドロキシ吉草酸の共重合体,3−ヒドロキシ
酪酸と4−ヒドロキシ酪酸の共重合体,ポリ3−ヒドロ
キシアルカノエ−ト系の微生物が生産する高分子,脂肪
族ラクトン化合物の開環重合体若しくはC2〜C12の
脂肪族2塩基酸とC2〜C12の脂肪族ジオ−ルよりな
るポリエステル又はこれらの改質物である請求項1のフ
ィルタ−2. A biodegradable aliphatic polyester compound is poly (3-hydroxybutyric acid), a copolymer of 3-hydroxybutyric acid and 3-hydroxyvaleric acid, or a copolymer of 3-hydroxybutyric acid and 4-hydroxybutyric acid. Polymers, polymers produced by microorganisms of poly-3-hydroxyalkanoate type, ring-opening polymers of aliphatic lactone compounds, or C2-C12 aliphatic dibasic acids and C2-C12 aliphatic diols The filter according to claim 1, which is a polyester or a modified product thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6103492A JP2839409B2 (en) | 1992-02-18 | 1992-02-18 | Tobacco filter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6103492A JP2839409B2 (en) | 1992-02-18 | 1992-02-18 | Tobacco filter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05227939A true JPH05227939A (en) | 1993-09-07 |
| JP2839409B2 JP2839409B2 (en) | 1998-12-16 |
Family
ID=13159599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6103492A Expired - Lifetime JP2839409B2 (en) | 1992-02-18 | 1992-02-18 | Tobacco filter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2839409B2 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994016581A1 (en) * | 1993-01-19 | 1994-08-04 | Rothmans International Services Limited | Biodegradable tobacco smoke filters |
| EP0706766A2 (en) | 1994-09-22 | 1996-04-17 | Daicel Chemical Industries, Ltd. | A tobacco filter material and a method for producing the same |
| US5678577A (en) * | 1994-10-31 | 1997-10-21 | Daicel Chemical Industries, Ltd. | Tobacco filter material and a tobacco filter as produced using the same |
| US5823201A (en) * | 1995-05-31 | 1998-10-20 | Daicel Chemical Industries, Ltd. | Tobacco filters and a method of producing the same |
| US5863652A (en) * | 1994-10-21 | 1999-01-26 | Daicel Chemical Industries Ltd. | Tobacco smoke filter materials, fibrous cellulose esters, and production processes |
| WO2011063630A1 (en) * | 2009-11-30 | 2011-06-03 | 北京中科高意引擎技术有限公司 | Biodegradable fiber for cigarette and preparation method thereof |
| JP2023123591A (en) * | 2017-04-05 | 2023-09-05 | バイオ-テック ビオローギッシュ ナチューフェアパックンゲン ゲーエムベーハー ウント コンパニ カーゲー | biodegradable film |
-
1992
- 1992-02-18 JP JP6103492A patent/JP2839409B2/en not_active Expired - Lifetime
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5664586A (en) * | 1993-01-19 | 1997-09-09 | Rothmans International Services Limited | Tobacco smoke filters and filter rods therefor |
| EP0680265A1 (en) * | 1993-01-19 | 1995-11-08 | Rothmans International Ltd | BIODEGRADABLE CIGARETTE SMOKE FILTERS. |
| WO1994016581A1 (en) * | 1993-01-19 | 1994-08-04 | Rothmans International Services Limited | Biodegradable tobacco smoke filters |
| US5856006A (en) * | 1994-09-19 | 1999-01-05 | Daicel Chemical Industries, Ltd. | Tobacco filter material and a method for producing the same |
| EP0706766A2 (en) | 1994-09-22 | 1996-04-17 | Daicel Chemical Industries, Ltd. | A tobacco filter material and a method for producing the same |
| US6344239B1 (en) | 1994-09-22 | 2002-02-05 | Daicel Chemical Industries, Ltd. | Method for producing a tobacco filter material |
| US5863652A (en) * | 1994-10-21 | 1999-01-26 | Daicel Chemical Industries Ltd. | Tobacco smoke filter materials, fibrous cellulose esters, and production processes |
| US5678577A (en) * | 1994-10-31 | 1997-10-21 | Daicel Chemical Industries, Ltd. | Tobacco filter material and a tobacco filter as produced using the same |
| US5927287A (en) * | 1994-10-31 | 1999-07-27 | Daicel Chemical Industries, Ltd. | Tobacco filter material and a tobacco filter as produced using the same |
| US5823201A (en) * | 1995-05-31 | 1998-10-20 | Daicel Chemical Industries, Ltd. | Tobacco filters and a method of producing the same |
| US5979460A (en) * | 1995-05-31 | 1999-11-09 | Daicel Chemical Industries, Inc. | Method of producing tobacco filters |
| WO2011063630A1 (en) * | 2009-11-30 | 2011-06-03 | 北京中科高意引擎技术有限公司 | Biodegradable fiber for cigarette and preparation method thereof |
| JP2023123591A (en) * | 2017-04-05 | 2023-09-05 | バイオ-テック ビオローギッシュ ナチューフェアパックンゲン ゲーエムベーハー ウント コンパニ カーゲー | biodegradable film |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2839409B2 (en) | 1998-12-16 |
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