JP2020015696A - Chemical-agent-containing body - Google Patents

Chemical-agent-containing body Download PDF

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JP2020015696A
JP2020015696A JP2018140665A JP2018140665A JP2020015696A JP 2020015696 A JP2020015696 A JP 2020015696A JP 2018140665 A JP2018140665 A JP 2018140665A JP 2018140665 A JP2018140665 A JP 2018140665A JP 2020015696 A JP2020015696 A JP 2020015696A
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drug
shape
basic
design
containing body
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JP7137389B2 (en
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雅俊 並木
Masatoshi Namiki
雅俊 並木
恵莉菜 寺尾
Erina Terao
恵莉菜 寺尾
吉田 真也
Shinya Yoshida
真也 吉田
憲悟 ▲高▼畑
憲悟 ▲高▼畑
Kengo Takahata
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Earth Corp
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Earth Chemical Co Ltd
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Catching Or Destruction (AREA)

Abstract

To provide a chemical-agent-containing body that is able to suppress the occurrence of such problems as ignition at a plurality of points while improving the degree of freedom of expression in design.SOLUTION: The chemical-agent-containing body is made up of a single path that is wound from an end holding portion (11) near the center to an ignition point (12), comprising: a basic wound portion (13) around the center that is wound in a basic shape; bent portions (14) outside of the basic wound portion (13) that vary in curvature; and an ornamental design portion (15) that provides a design different from the basic shape by the bent portions (14).SELECTED DRAWING: Figure 1

Description

本発明は、薬剤含有体に関し、特に渦巻き形状に巻回された薬剤含有体に関する。   The present invention relates to a drug substance, and more particularly to a drug substance wound in a spiral shape.

従来から、薬剤を含有した薬剤含有体を燃焼させて蚊等の害虫を防除する線香等が用いられている。これらの通常の線香では、燃焼時の薬剤揮散量を一定にするために、薬剤含有体の幅を略一定にしている。また、燃焼時間の長時間化を図るためには薬剤含有体を長く成形する必要があるが、直線形状では長時間化に限界があるため渦巻き形状に巻回して成形することが一般的である。   BACKGROUND ART Conventionally, incense sticks and the like for controlling a pest such as a mosquito by burning a drug-containing substance containing a drug have been used. In these ordinary incense sticks, the width of the drug-containing body is made substantially constant in order to make the amount of the drug volatilized during combustion constant. Further, in order to prolong the burning time, it is necessary to form the drug-containing substance for a long time. However, in the case of a linear shape, there is a limit to the prolongation of the drug-containing substance, and therefore, it is common to form the drug-containing substance by winding it into a spiral shape. .

このような渦巻き形状の薬剤含有体では、平板状の薬剤含有体を渦巻き形状に打ち抜いて分離することにより、相補的な一組の渦巻き形状を成形することができる。相補的な渦巻き形状の薬剤含有体を分離すると、略一定幅に巻回された薬剤含有体と略一定幅に巻回された空隙が得られる(例えば、特許文献1等を参照)。   In such a spiral shaped drug-containing body, a complementary set of spiral shapes can be formed by punching and separating a flat drug-containing body into a spiral shape. When the complementary spiral-shaped drug-containing body is separated, a drug-containing body wound to a substantially constant width and a void wound to a substantially constant width are obtained (for example, see Patent Document 1).

上述した従来からの薬剤含有体では、燃焼時間の長時間化と省スペース化の観点から略円形の渦巻き形状が最も効率的であるといえる。しかし、略円形であるがゆえに意匠面での自由度は極端に低く、薬剤含有体そのもので意匠上の差別化や顧客訴求力を追求することが困難であった。一方で、薬剤含有体そのもので意匠上の表現を試みたものも提案されている(例えば、特許文献2等を参照)。しかし特許文献2では、分離前の相補的な渦巻き形状にインキ等で所定のデザインを印刷しており、分離して使用する際には意匠面での差異を十分に認識することは困難であった。   In the above-mentioned conventional drug-containing substance, it can be said that a substantially circular spiral shape is most efficient from the viewpoint of prolonging the burning time and saving space. However, because of the substantially circular shape, the degree of freedom in design is extremely low, and it has been difficult to pursue differentiation in design and appeal to customers with the drug-containing substance itself. On the other hand, there has also been proposed a drug-containing substance that attempts to express a design (for example, see Patent Document 2). However, in Patent Literature 2, a predetermined design is printed with ink or the like in a complementary spiral shape before separation, and it is difficult to sufficiently recognize a difference in a design when separated and used. Was.

実開平7−19301号公報Japanese Utility Model Laid-Open No. 7-19301 特開2005−330201号公報JP 2005-330201 A

また、これら特許文献1,2のような略円形の渦巻き形状ではなく、薬剤含有体の巻回形状や幅を変更して、薬剤含有体の形状そのもので意匠上の表現をすることが可能である。しかし、薬剤含有体の幅を変化させると燃焼時の薬剤揮散量を一定に保つことができず、蚊取り線香等の用途には不向きである。また、薬剤含有体が枝分かれするような形状で意匠表現をすると、燃焼時間や燃焼経路の再現性が乏しくなり実使用には向かない。また、相補的な一組の形状を打ち抜く加工では形成できず、面積あたりの薬剤含有体量を確保できずパッケージが大型化するという問題も発生する。   Also, instead of the substantially circular spiral shape as in Patent Documents 1 and 2, the wound shape and width of the drug-containing material can be changed, and the design itself can be expressed by the shape of the drug-containing material itself. is there. However, if the width of the drug-containing body is changed, the amount of the drug volatilized during combustion cannot be kept constant, and it is not suitable for applications such as mosquito coils. In addition, if the design expression is made in such a shape that the drug-containing substance branches, the reproducibility of the burning time and the burning path becomes poor, which is not suitable for actual use. In addition, it cannot be formed by punching out a set of complementary shapes, and there is a problem that the amount of drug-containing substance per area cannot be secured and the package becomes large.

さらに、薬剤含有体の幅を略一定に保ちながら、多数の角部やカーブを含ませて星型やハート型、文字形状等に成形して、多様な意匠形状を表現することもできる。しかし薬剤含有体は、数ヶ月から数年もの長期間に亘って保管しておく使用方法が想定され、特にパッケージを開封した状態で湿度のある空間に曝されて保管される可能性もある。このように良好ではない保管状況では、薬剤含有体が吸湿して伸縮する可能性がある。   Furthermore, while keeping the width of the drug-containing substance substantially constant, it can be formed into a star shape, a heart shape, a character shape, or the like by including a large number of corners or curves to express various design shapes. However, it is assumed that the drug-containing substance is used for a long period of several months to several years. In particular, there is a possibility that the drug-containing substance is exposed to a humid space with the package opened and stored. In such poor storage conditions, the drug-containing body may expand and contract due to moisture absorption.

従来の略円形の渦巻形状であれば、薬剤含有体が吸湿により伸縮しても、その伸縮方向は薬剤含有体の延伸方向であるため渦巻き形状が維持される。しかし、多数の角部やカーブを含ませて意匠を表現している場合には、吸湿による伸縮が一様ではなく、当初の意匠から変形する可能性がある。このような変形が生じると、意匠面での表現が維持できないだけではなく空隙が縮まって薬剤含有体同士が接触し、複数箇所が同時に燃焼する多点着火等の不具合が生じる可能性がある。   In the case of the conventional substantially circular spiral shape, even if the drug-containing body expands and contracts due to moisture absorption, the expansion and contraction direction is the stretching direction of the drug-containing body, so that the spiral shape is maintained. However, when a design is expressed by including a large number of corners and curves, the expansion and contraction due to moisture absorption is not uniform, and the original design may be deformed. When such deformation occurs, not only the expression on the design surface cannot be maintained, but also the gaps shrink and the drug-containing bodies come into contact with each other, which may cause a problem such as multi-point ignition in which a plurality of places are burned simultaneously.

本発明は、このような従来の問題に鑑みてなされたものであり、意匠上の表現自由度を向上させつつ、多点着火等の不具合発生を抑制することができる薬剤含有体を提供することを目的とする。   The present invention has been made in view of such conventional problems, and it is an object of the present invention to provide a drug-containing substance that can suppress the occurrence of problems such as multipoint ignition while improving the degree of freedom of expression in design. With the goal.

上記課題を解決するため、本発明の薬剤含有体は、中心近傍の終端保持部から着火点部まで一本の経路が巻回して形成された薬剤含有体であって、前記中心近傍は基本形状で巻かれた基本巻部であり、前記基本巻部よりも外部に曲率が変化する屈曲部を有し、前記屈曲部によって前記基本形状から逸脱する意匠部を備えることを特徴とする。   In order to solve the above problem, the drug-containing body of the present invention is a drug-containing body formed by winding a single path from the end holding portion near the center to the ignition point portion, and the vicinity of the center has a basic shape. It is a wound basic winding part, has a bent part whose curvature changes outside the basic winding part, and is provided with a design part deviating from the basic shape by the bent part.

これにより、中心近傍を基本巻部とし基本巻部より外部に意匠部を備えることで、吸湿等による伸縮での形状変化を抑制でき、意匠上の表現自由度を向上させつつ、多点着火等の不具合発生を抑制することができる。   This makes it possible to suppress the shape change due to expansion and contraction due to moisture absorption, etc. by providing a design part outside the basic winding part with the vicinity of the center as the basic winding part, while improving the freedom of expression on the design, multipoint ignition etc. Can be suppressed from occurring.

また本発明の一態様では、前記基本巻部は、略円形または略楕円形を基本とする渦巻き形状である。   In one embodiment of the present invention, the basic winding portion has a spiral shape based on a substantially circular or substantially elliptical shape.

本発明によれば、意匠上の表現自由度を向上させつつ、多点着火等の不具合発生を抑制することができる薬剤含有体を提供することができる。   Advantageous Effects of Invention According to the present invention, it is possible to provide a drug-containing substance that can suppress the occurrence of problems such as multipoint ignition while improving the degree of freedom of expression in design.

実施形態における一組の相補的な形状の薬剤含有体を分離した状態を示す模式平面図であり、図1(a)は一方の巻回形状を示し、図1(b)は他方の巻回形状を示している。FIG. 1A is a schematic plan view showing a state in which a pair of complementary drug-containing bodies in the embodiment is separated, FIG. 1A shows one winding shape, and FIG. 1B shows the other winding shape. The shape is shown. 基本形状として略円形の巻回形状を説明する模式図である。It is a schematic diagram explaining a substantially circular winding shape as a basic shape. 比較例1の燃焼過程を示す図面代用写真である。4 is a photograph as a drawing substitute showing a combustion process of Comparative Example 1. 比較例2の燃焼過程を示す図面代用写真である。6 is a photograph as a drawing showing a combustion process of Comparative Example 2. 実施例1の燃焼過程を示す図面代用写真である。5 is a photograph as a substitute of a drawing, showing a combustion process in Example 1. 実施例2の燃焼過程を示す図面代用写真である。9 is a photograph as a substitute of a drawing, showing a combustion process in Example 2. 比較例1,2で発生した多点着火の状態を示す図面代用写真である。9 is a photograph as a substitute of a drawing showing a state of multipoint ignition that occurred in Comparative Examples 1 and 2.

以下、本発明の実施の形態について、図面を参照して詳細に説明する。各図面に示される同一または同等の構成要素、部材、処理には、同一の符号を付すものとし、適宜重複した説明は省略する。図1は、本実施形態における一組の相補的な形状の薬剤含有体を分離した状態を示す模式平面図であり、図1(a)は一方の巻回形状を示し、図1(b)は他方の巻回形状を示している。   Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. The same or equivalent components, members, and processes shown in the drawings are denoted by the same reference numerals, and the repeated description will be omitted as appropriate. FIG. 1 is a schematic plan view showing a state in which a pair of complementary drug-containing bodies in the present embodiment is separated, and FIG. 1 (a) shows one winding shape, and FIG. 1 (b). Indicates the other winding shape.

図1(a)(b)に示したように、本実施形態の薬剤含有体は、中心近傍の端部である終端保持部11から最外周の端部である着火点部12まで、一本の経路が巻回された形状でありその幅は略一定とされている。また、中心近傍から所定の長さにわたっては、略円形状の基本形状で巻回された基本巻部13であり、基本巻部13よりも外部には、曲率が変化する屈曲部14が形成されている。屈曲部14が形成されていることで、薬剤含有体の経路は基本形状から逸脱して意匠部15を構成している。   As shown in FIGS. 1 (a) and 1 (b), the medicine-containing body of the present embodiment has a single piece from the end holding portion 11 which is the end near the center to the ignition point 12 which is the outermost end. The path is wound and has a substantially constant width. The basic winding portion 13 is wound in a substantially circular basic shape over a predetermined length from the vicinity of the center, and a bent portion 14 whose curvature changes is formed outside the basic winding portion 13. ing. Due to the formation of the bent portion 14, the path of the drug-containing body deviates from the basic shape and forms the design portion 15.

薬剤含有体の成分は特に限定されず、薬剤の成分と成形材料の成分を混合して乾燥させている。薬剤の成分としては、各種の殺虫、忌避成分等が挙げられる。例えば、除虫菊エキス、天然ピレトリン、プラレトリン、イミプロトリン、フタルスリン、アレスリン、トランスフルトリン、レスメトリン、フェノトリン、シフェノトリン、ペルメトリン、サイパーメスリン、エトフェンプロックス、シフルスリン、デルタメスリン、ビフェントリン、フェンバレレート、フェンプロパスリン、エムペンスリン、シラフルオフェン、メトフルトリン、プロフルトリン等のピレスロイド系化合物; フェニトロチオン、ダイアジノン、マラソン、ピリダフェンチオン、プロチオホス、ホキシム、クロルピリホス、ジクロルボス等の有機リン系化合物; カルバリル、プロポクスル、メソミル、チオジカルブ等のカーバメート系化合物; メトキサジアゾン等のオキサジアゾール系化合物; フィプロニル等のフェニルピラゾール系化合物; アミドフルメト等のスルホンアミド系化合物; ジノテフラン、イミダクロプリド等のネオニコチノイド系化合物; メトプレン、ハイドロプレン、ピリプロキシフェン等の昆虫成長制御化合物; クロルフェナピル等のピロール系化合物; ベンジルアルコール、ハッカ油等の殺虫性精油類; ディート、ジ−n−ブチルサクシネート、ヒドロキシアニソール、エチル− ブチルアセチルアミノプロピオネート、p−メンタン−3 , 8−ジオール、シトロネラ油、ユーカリ油、ゲラニウム油、月桃油、蚊連草等の忌避剤等を挙げることができる。   The components of the drug-containing body are not particularly limited, and the components of the drug and the components of the molding material are mixed and dried. The components of the drug include various insecticidal and repellent components. For example, pyrethrum extract, natural pyrethrin, pralethrin, imiprothrin, phthalthrin, allethrin, transfluthrin, resmethrin, phenothrin, cyfenothrin, permethrin, cypermethrin, etofenprox, cyfluthrin, deltamethrin, bifenthrin, fenvalerate, fenpropathrin, empenthrin, empenthrin Pyrethroid compounds such as silafluofen, methfluthrin, and profluthrin; organic phosphorus compounds such as fenitrothion, diazinon, marathon, pyridafenthion, prothiophos, foxime, chlorpyrifos, dichlorvos; carbamate compounds such as carbaryl, propoxur, mesomil, and thiodicarb; Diazole compounds; phenyl such as fipronil Lupyrazole compounds; Sulfonamide compounds such as amidoflumet; Neonicotinoid compounds such as dinotefuran and imidacloprid; Insect growth controlling compounds such as methoprene, hydroprene and pyriproxyfen; Pyrrole compounds such as chlorfenapyr; Essential insecticides such as diet, di-n-butyl succinate, hydroxyanisole, ethyl-butylacetylaminopropionate, p-menthane-3,8-diol, citronella oil, eucalyptus oil, geranium oil, moon peach Repellents such as oil and mosquito repellents can be mentioned.

また、成形材料の成分としては、例えば燃焼基材(支燃剤)等が挙げられる。燃焼基材(支燃剤)としては、例えば、木粉、茶葉粉、コーヒー豆殻の内皮粉末、トウモロコシの芯の粉末、スガ、ツガ、カシ、ヤシ、タケ、ココナッツ、ミカン等の木本類の粉末、コットン、ケナフ、亜麻等の繊維等が挙げられる。   Further, as a component of the molding material, for example, a combustion base material (combustion agent) and the like can be mentioned. Examples of the burning base material (supporting agent) include wood powder, tea leaf powder, coffee bean shell endothelial powder, corn core powder, suga, hemlock, oak, coconut, bamboo, coconut, tangerine, and other woody species. Fibers such as powder, cotton, kenaf, flax and the like can be mentioned.

終端保持部11は、薬剤含有体の中心近傍に位置する端部であり、外側から燃焼した場合に最後に燃焼する終端である。また、薬剤含有体を保持するための器具を挿入するための切れ目が中央に形成されていてもよく、切れ目を形成するために他の領域よりも幅広に形成されてもよい。また、図1(a)(b)では終端保持部11を略半円形状に成形した例を示しているが、形状は特に限定されない。   The end holding part 11 is an end located near the center of the medicine-containing body, and is the end that burns last when burned from the outside. Further, a cut for inserting a device for holding the drug-containing substance may be formed at the center, and may be formed wider than other regions to form a cut. Further, FIGS. 1A and 1B show an example in which the end holding portion 11 is formed in a substantially semicircular shape, but the shape is not particularly limited.

着火点部12は、薬剤含有体の最外周に位置する端部であり、薬剤含有体を燃焼させる際に着火する終端である。図1(a)(b)に示すように着火点部12は、着火させやすいように最先端が鋭角とされ、幅方向に対して斜めに切断した端面に成形されている。   The ignition point portion 12 is an end located at the outermost periphery of the drug-containing material, and is a terminal that ignites when the drug-containing material is burned. As shown in FIGS. 1 (a) and 1 (b), the ignition point portion 12 has an acute angle at the extreme end so as to be easily ignited, and is formed on an end face cut obliquely to the width direction.

基本巻部13は、基本形状で巻回された渦巻き形状の領域であり、終端保持部11から所定の長さにわたって連続して形成されている。基本巻部13の所定長さとしては、終端保持部11から着火点部12までの全長の少なくとも10%以上が好ましく、より好ましくは30%以上である。基本形状の設計手法については図2を用いて後述する。基本形状としては、略円形状でも略楕円形状でもよいが、吸湿による伸縮での変形を効果的に抑制するためには、略円形状が最も好ましい。   The basic winding portion 13 is a spiral-shaped region wound in the basic shape, and is formed continuously from the end holding portion 11 over a predetermined length. The predetermined length of the basic winding portion 13 is preferably at least 10% or more, more preferably 30% or more of the entire length from the end holding portion 11 to the ignition point portion 12. The design method of the basic shape will be described later with reference to FIG. Although the basic shape may be a substantially circular shape or a substantially elliptical shape, a substantially circular shape is most preferable in order to effectively suppress deformation due to expansion and contraction due to moisture absorption.

屈曲部14は、曲率が変化することで基本形状から逸脱する部分であり、基本巻部13よりも外側に設けられている。屈曲部14を複数設けることで、薬剤含有体の経路は基本巻部13が成している基本形状から逸脱して意匠部15を構成している。図1(a)(b)に示した例では、屈曲部14は外周方向に伸びる外方逸脱部14aと内周方向に伸びる内方逸脱部14bとを備えており、猫の耳を模した意匠を表現している。複数の屈曲部14にそれぞれ外方逸脱部14aと内方逸脱部14bを設けることで、意匠上の表現自由度が向上する。   The bending portion 14 is a portion that deviates from the basic shape due to a change in curvature, and is provided outside the basic winding portion 13. By providing a plurality of bent portions 14, the path of the medicine-containing body deviates from the basic shape of the basic winding portion 13 to form the design portion 15. In the example shown in FIGS. 1A and 1B, the bent portion 14 includes an outward deviation portion 14 a extending in an outer peripheral direction and an inward deviation portion 14 b extending in an inner peripheral direction, and imitates a cat's ear. It expresses a design. By providing the outward deviation portion 14a and the inward deviation portion 14b in each of the plurality of bent portions 14, the degree of freedom of expression in the design is improved.

図1(a)に示した例では、屈曲部14よりも外側に着火点部12が位置しているが、意匠部よりも外側に位置する薬剤含有体の経路は比較的短く、さらに意匠部15と略平行または外方に反っている。また図1(b)に示した例では、屈曲部14およびそれにより構成される意匠部15は、基本巻部13よりも外側かつ最外周に位置しており、着火点部12は基本巻部13の外側に位置している。これにより、薬剤含有体が吸湿により伸縮しても、変形により着火点部12が意匠部15に接触して多点着火することを抑制できる。   In the example shown in FIG. 1A, the ignition point portion 12 is located outside the bent portion 14, but the route of the medicine-containing substance located outside the design portion is relatively short, and the design portion 15 It is warped almost parallel or outward. In the example shown in FIG. 1B, the bent portion 14 and the design portion 15 formed by the bent portion 14 are located outside and outside the basic winding portion 13, and the ignition point portion 12 is Is located outside. Thereby, even if the medicine-containing body expands and contracts due to moisture absorption, it is possible to prevent the ignition point portion 12 from coming into contact with the design portion 15 due to deformation and causing multipoint ignition.

次に、図2を用いて基本形状の設計手法について説明する。図2は、基本形状として略円形の巻回形状を説明する模式図である。まず、基本半径の1倍、2倍、3倍・・・の同心円を描き、それぞれの0度位置、90度位置、180度位置、270度位置を順に結んで渦巻き状の曲線を描く。図中に実線で示した曲線が図1(a)に示した渦巻き形状の幅方向外側線になり、基本半径の幅を持たせた渦巻き形状を構成できる。また、図中に示した渦巻き形状を180度回転させたものが相補的な渦巻き形状となる。図2では、基本形状として円形の場合を示したが、基本形状として楕円の場合には、同心円に代えて楕円を用いる。なお、図2に示した図は基本形状の概念を模式的に示すものであり、厳密に幾何学的な定義をするものではなく、類似の形状であればよい。   Next, a design method of the basic shape will be described with reference to FIG. FIG. 2 is a schematic diagram illustrating a substantially circular winding shape as a basic shape. First, a concentric circle of 1, 2, 3,... Of the basic radius is drawn, and a spiral curve is drawn by connecting the 0-degree, 90-degree, 180-degree, and 270-degree positions in order. A curve shown by a solid line in the drawing becomes an outer line in the width direction of the spiral shape shown in FIG. 1A, and a spiral shape having a width of a basic radius can be formed. In addition, what is obtained by rotating the spiral shape shown in the figure by 180 degrees becomes a complementary spiral shape. FIG. 2 shows a case where the basic shape is a circle. However, when the basic shape is an ellipse, an ellipse is used instead of a concentric circle. It should be noted that the diagram shown in FIG. 2 schematically shows the concept of the basic shape, and does not strictly define a geometric shape, but may be any similar shape.

(比較例)
中心近傍から意匠部15を構成した薬剤含有体を複数パターン成形して、開封した状態で数日間保管し燃焼実験を行った。図3は、比較例1の燃焼過程を示す図面代用写真である。図4は、比較例2の燃焼過程を示す図面代用写真である。図3に示した比較例1と、図4に示した比較例2とは、平板状の薬剤含有体を打ち抜き加工して得た相補的な形状となっている。図3,4に示したように、比較例1,2はハート形状A、花弁形状、動物形状Aを模しており、中心近傍である終端保持部11の直近から屈曲部14が形成されており、略円形または略楕円形の基本巻部13が存在しない形状である。
(Comparative example)
A plurality of drug-containing bodies constituting the design portion 15 were molded from the vicinity of the center, and stored in an opened state for several days to perform a combustion experiment. FIG. 3 is a photograph substituted for a drawing showing a combustion process of Comparative Example 1. FIG. 4 is a drawing substitute photograph showing a combustion process of Comparative Example 2. Comparative Example 1 shown in FIG. 3 and Comparative Example 2 shown in FIG. 4 have complementary shapes obtained by stamping out a flat drug-containing substance. As shown in FIGS. 3 and 4, Comparative Examples 1 and 2 simulate a heart shape A, a petal shape, and an animal shape A, in which a bent portion 14 is formed immediately before the end holding portion 11 near the center. And a shape in which the substantially circular or substantially elliptical basic winding portion 13 does not exist.

図3,4において(a)で示した写真は着火前を示し、(b)〜(f)の写真は着火後の経時変化を順に示している。写真中で薬剤含有体が白く変化している部分は、燃焼した灰である。図3,4に示したように、比較例1,2では燃焼前から吸湿により薬剤含有体が伸縮して変形しており、最外周の経路が内側の経路と接触するものも生じている。   3 and 4, the photographs shown in (a) show the state before ignition, and the photographs in (b) to (f) show the time-dependent changes after ignition. The part of the photograph where the drug substance is turned white is burnt ash. As shown in FIGS. 3 and 4, in Comparative Examples 1 and 2, the drug-containing substance expands and contracts due to moisture absorption before combustion, and some of the outermost paths contact the inner paths.

図3(f)および図4(f)で×印を付したものは多点着火が生じた不良品であり、△印を付したものは薬剤含有体の変形により外周の経路が内周と接触しており、多点着火や立ち消えが生じる可能性のある不具合品である。図3,4に示したように、薬剤含有体の吸湿による変形は、保管状態や吸湿の状態によって変形量が異なるため、全ての比較例1,2で多点着火や立ち消えが生じるものではない。しかし、中心近傍から屈曲部14を形成して意匠部15を構成しているため、吸湿による変形量が大きいものも存在して多点着火や立ち消え等の不良が生じる可能性があることがわかった。   3 (f) and 4 (f), those marked with a cross are defective products in which multipoint ignition has occurred. This is a faulty product that is in contact and may cause multipoint ignition or extinguishing. As shown in FIGS. 3 and 4, the deformation of the medicine-containing body due to moisture absorption differs depending on the storage state and the state of moisture absorption, and thus, in all of Comparative Examples 1 and 2, multipoint ignition and extinguishing do not occur. . However, since the design portion 15 is formed by forming the bent portion 14 from the vicinity of the center, it is found that there is also a case where the deformation amount due to moisture absorption is large and defects such as multipoint ignition and extinguishing may occur. Was.

(実施例)
中心近傍には基本巻部13を形成し、基本巻部13よりも外側に屈曲部14および意匠部15を構成した薬剤含有体を複数パターン成形して、開封した状態で数日間保管し燃焼実験を行った。図5は、実施例1の燃焼過程を示す図面代用写真である。図6は、実施例2の燃焼過程を示す図面代用写真である。図5に示した実施例1と、図6に示した実施例2とは、平板状の薬剤含有体を打ち抜き加工して得た相補的な形状となっている。図5,6に示したように、実施例1,2は動物形状B、ハート形状B、動物形状Cを模しており、中心近傍である終端保持部11から所定の長さには略円形の基本形状である基本巻部13が形成された形状である。
(Example)
A basic wound portion 13 is formed in the vicinity of the center, and a plurality of drug-containing bodies comprising the bent portion 14 and the design portion 15 outside the basic wound portion 13 are formed into a plurality of patterns. Was done. FIG. 5 is a drawing-substitute photograph showing the combustion process of Example 1. FIG. 6 is a photograph as a drawing showing the combustion process of Example 2. Example 1 shown in FIG. 5 and Example 2 shown in FIG. 6 have complementary shapes obtained by stamping out a flat drug-containing substance. As shown in FIGS. 5 and 6, the first and second embodiments simulate an animal shape B, a heart shape B, and an animal shape C, and have a substantially circular shape with a predetermined length from the end holding portion 11 near the center. This is the shape in which the basic winding portion 13 which is the basic shape of the above is formed.

図5,6において(a)で示した写真は着火前を示し、(b)〜(f)の写真は着火後の経時変化を順に示している。写真中で薬剤含有体が白く変化している部分は、燃焼した灰である。図5,6に示したように、実施例1,2でも燃焼前から吸湿により薬剤含有体が伸縮して変形しているが、比較例1,2よりも変形量が小さく、最外周の経路は内側の経路と接触していない。   5 and 6, the photographs shown in (a) show the state before ignition, and the photographs in (b) to (f) show the time-dependent changes after ignition. The part of the photograph where the drug substance is turned white is burnt ash. As shown in FIGS. 5 and 6, even in Examples 1 and 2, the drug-containing material was expanded and contracted due to moisture absorption before combustion, but the deformation amount was smaller than Comparative Examples 1 and 2, and the outermost route. Is not in contact with the inner path.

図5(f)および図6(f)に示したように、実施例1,2では薬剤含有体の変形により外周の経路が内周と接触しておらず、基本巻部13に至るまで屈曲部14および意匠部15が燃焼しても、多点着火や立ち消えが生じていない。これにより、中心近傍には屈曲部14を設けず基本巻部13としているため、吸湿による変形量が小さくなり多点着火や立ち消え等の不良を抑制できることがわかる。   As shown in FIGS. 5 (f) and 6 (f), in Examples 1 and 2, the path of the outer periphery is not in contact with the inner periphery due to the deformation of the drug-containing substance, and is bent to the basic winding portion 13. Even when the part 14 and the design part 15 burn, no multipoint ignition or extinguishing occurs. Thus, since the bent portion 14 is not provided in the vicinity of the center and the basic winding portion 13 is formed, the amount of deformation due to moisture absorption is reduced, and it is possible to suppress defects such as multipoint ignition and extinguishing.

図7は、比較例1,2で発生した多点着火の状態を示す図面代用写真である。図7(a)〜(d)に示したように、着火点部12から経路に沿って燃焼が継続するが、変形量が大きく内側の経路と接触した部分では、外側の経路が燃焼するにともなって内側の経路に着火している。図7(c)に示したように、内側の経路に完全に着火してしまうと、多点着火で内側経路の燃焼は終端保持部11方向と着火点部12方向に進行する。このような多点着火が生じると、着火点部12から終端保持部11までの長さを燃焼する時間が確保できず、燃焼継続時間が短縮されてしまう。また、多点着火している期間は燃焼量が多いため、薬剤の揮散量が多くなってしまう。   FIG. 7 is a drawing substitute photograph showing the state of multipoint ignition that occurred in Comparative Examples 1 and 2. As shown in FIGS. 7A to 7D, combustion continues along the path from the ignition point portion 12, but in a portion where the amount of deformation is large and comes into contact with the inner path, the outer path burns. The inner path is ignited. As shown in FIG. 7C, when the inner path is completely ignited, the combustion of the inner path proceeds in the direction of the end holding section 11 and the direction of the ignition point section 12 by multipoint ignition. When such multipoint ignition occurs, the time required to burn the length from the ignition point portion 12 to the end holding portion 11 cannot be secured, and the combustion continuation time is shortened. In addition, since the amount of combustion is large during the period of multipoint ignition, the amount of chemical vaporization increases.

図7では多点着火の例を示したが、外側の経路と内側の経路が接触していると、外側の経路に対する酸素の供給や燃焼に必要な温度が不足して、外側経路の燃焼が終了してしまう立ち消えが生じる可能性もある。   FIG. 7 shows an example of multipoint ignition. However, if the outer path and the inner path are in contact with each other, the temperature required for supplying and burning oxygen to the outer path is insufficient, and the combustion of the outer path is not performed. There is also a possibility that the extinction will end.

したがって、本実施形態の薬剤含有体では、中心近傍を基本巻部13とし基本巻部13より外部に意匠部15を備えることで、吸湿等による伸縮での形状変化を抑制でき、意匠上の表現自由度を向上させつつ、多点着火や立ち消え等の不具合発生を抑制することができる。   Therefore, in the medicine-containing body of the present embodiment, by changing the vicinity of the center to the basic winding portion 13 and providing the design portion 15 outside the basic winding portion 13, the shape change due to expansion and contraction due to moisture absorption and the like can be suppressed, and the expression on the design While improving the degree of freedom, it is possible to suppress the occurrence of problems such as multipoint ignition and extinguishing.

本発明は上述した各実施形態に限定されるものではなく、請求項に示した範囲で種々の変更が可能であり、異なる実施形態にそれぞれ開示された技術的手段を適宜組み合わせて得られる実施形態についても本発明の技術的範囲に含まれる。   The present invention is not limited to the embodiments described above, and various modifications are possible within the scope shown in the claims, and embodiments obtained by appropriately combining technical means disclosed in different embodiments. Is also included in the technical scope of the present invention.

11…終端保持部
12…着火点部
13…基本巻部
14…屈曲部
14a…外方逸脱部
14b…内方逸脱部
15…意匠部
DESCRIPTION OF SYMBOLS 11 ... Terminal holding part 12 ... Ignition point part 13 ... Basic winding part 14 ... Bent part 14a ... Outward deviation part 14b ... Inward deviation part 15 ... Design part

Claims (2)

中心近傍の終端保持部から着火点部まで一本の経路が巻回して形成された薬剤含有体であって、
前記中心近傍は基本形状で巻かれた基本巻部であり、
前記基本巻部よりも外部に曲率が変化する屈曲部を有し、
前記屈曲部によって前記基本形状から逸脱する意匠部を備えることを特徴とする薬剤含有体。
A drug-containing body formed by winding one path from the end holding portion near the center to the ignition point portion,
The vicinity of the center is a basic winding portion wound in a basic shape,
It has a bending portion where the curvature changes outside the basic winding portion,
A drug substance comprising a design part deviating from the basic shape by the bent part.
請求項1に記載の薬剤含有体であって、
前記基本巻部は、略円形または略楕円形を基本とする渦巻き形状であることを特徴とする薬剤含有体。
The drug-containing body according to claim 1,
The medicine-containing body, wherein the basic winding portion has a spiral shape based on a substantially circular or substantially elliptical shape.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5289484U (en) * 1975-12-27 1977-07-04
JPS5328280U (en) * 1976-08-13 1978-03-10
JPS5961202U (en) * 1982-10-15 1984-04-21 佐野 勇 mosquito coil
JPS6251102U (en) * 1985-09-18 1987-03-30

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5289484U (en) * 1975-12-27 1977-07-04
JPS5328280U (en) * 1976-08-13 1978-03-10
JPS5961202U (en) * 1982-10-15 1984-04-21 佐野 勇 mosquito coil
JPS6251102U (en) * 1985-09-18 1987-03-30

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ナスカの地上絵の蚊取り線香;世界の七不思議が蚊取り線香に?|ミライノシテン, JPN6022006541, 25 June 2016 (2016-06-25), ISSN: 0004710323 *

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