JPS6331682B2 - - Google Patents

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Publication number
JPS6331682B2
JPS6331682B2 JP55163628A JP16362880A JPS6331682B2 JP S6331682 B2 JPS6331682 B2 JP S6331682B2 JP 55163628 A JP55163628 A JP 55163628A JP 16362880 A JP16362880 A JP 16362880A JP S6331682 B2 JPS6331682 B2 JP S6331682B2
Authority
JP
Japan
Prior art keywords
fuel
fuel vaporization
combustion
main core
tar
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.)
Expired
Application number
JP55163628A
Other languages
Japanese (ja)
Other versions
JPS5787508A (en
Inventor
Kinichi Adachi
Toshio Utagawa
Yasushi Hirata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP16362880A priority Critical patent/JPS5787508A/en
Publication of JPS5787508A publication Critical patent/JPS5787508A/en
Publication of JPS6331682B2 publication Critical patent/JPS6331682B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は液体燃料用燃焼器に用いられる燃焼芯
に関するもので、その目的とするところは燃焼芯
の燃料気化部におけるタール状物質の生成蓄積を
抑え、長期間にわたつて安定した燃焼を維持し得
る燃焼芯を提供することにある。 液体燃料を燃焼芯の毛細管現象によつて吸い上
げ、燃料気化部の表面から液体燃料を気化させて
燃焼させる、いわゆる吸い上げ気化式の燃焼器
は、石油ストーブ、石油コンロ等に広く用いられ
ている。この種の燃焼器では、燃料気化部が、高
温でかつ酸素の介在する雰囲気に暴露されている
ために、燃焼中において燃料気化部に含有される
燃料の一部が酸化、重合反応等によつてタール状
物質となり、燃料気化部に蓄積される。特に燃料
中に微量の高沸点成分が混入したり(例えば灯油
中に機械油、軽油、サラダ油等が混入した場合)、
あるいは燃料成分の一部が変質(例えば灯油を長
期間高温、あるいは直射日光下に保存し、酸化
物、過酸化物、樹脂等が成生されている場合)し
たりしている場合等には、前記タール状物質の生
成、蓄積量が著しく増大する。 このタール状物質が燃料気化部に蓄積した時、
燃料気化部の表面あるいは内部の毛細管が閉塞さ
れ、燃料の吸上げや気化が阻害される。このため
燃料気化量が異常に低下し、燃焼室における空燃
比が崩れて臭気、ススや有害な一酸化炭素が大量
に発する様になる。また点火時には上記タール状
物質によつて燃料気化部の速かなる温度上昇、燃
料気化量の増加が妨げられ、安定燃焼に至るまで
に著しく長時間を要し、その間には不安定過渡燃
焼による臭気、スス、一酸化炭素等が大量に発生
していた。更にタール状物質が燃焼芯とこれを支
持する金属部とを固着させ、燃焼芯の機械的動作
を不可能ならしめ、燃焼芯を下げて消火操作を不
能とし、危険なものであつた。 本発明はこれら従来の欠点を解消するために、
タール状物質の生成蓄積を抑制するもので、以下
本発明の一実施例を添付図面と共に説明する。 第1図において、1は主芯で、シリカ―アルミ
ナ系のセラミツクフアイバー(シリカ:アルミナ
≒50:50、重量比)をシリカ系結合剤で結合させ
たものである。2は吸い上げ芯で、ポリプロピレ
ン布よりなり、主芯1に連接されている。3は燃
料気化部で、燃焼器(図示せず)に装着した時、
燃焼室に露出される部分である。燃料気化部3の
上方表面は被覆材4で覆われている。この被覆材
4は、無機顔料、無水珪酸、および水溶性有機結
着からなるもので、多孔性を失わないように燃料
気化部3の表面に塗布している。5は縫製糸、6
は接着テープである。 上記構成において、液体燃料は吸い上げ芯2か
ら主芯1へと吸い上げられ、燃料気化部3表面か
ら気化する。ここで燃料の流れについて詳述する
と、第2図に示す様になる。即ち、燃料fは主芯
1内を吸い上げられ、燃料気化部3表面から気化
する。一方燃料fの一部は燃料気化部3表面近
傍、特に高温にさらされる燃料気化部3先端の表
面近くで、温度と酸素の影響を受けタール状物質
tに変化する。また灯油の中に含まれている不純
成分(変質成分もしくはサラダ油等の高沸点成
分)も灯油等により芯上部に押し上げられ上部に
蓄積される。それが目詰りをおこし気化面積を減
少させて、発熱量を低化させる。ところが本実施
例のごとく被覆材4を設けると、初期からその部
分の気化量が少なくなり、この結果この燃料気化
部3の表面および内部の温度が高くなる。よつて
この部分に高沸点成分があつてもそれらの成分が
気化したり分解したりしやすくなる。また燃料気
化部3の内部は、直接空気にふれないため、灯油
の酸化も少なくなり、いわゆる重縮合による高分
子量のタール成分も出来にくくなる。 さらに詳しくこれらの原理を説明すると、灯油
をもちいる灯芯気化タイプの従来の燃焼芯の燃料
気化部3の温度は灯油の成分によつて限定され、
一般に市販されているJIS―号灯油を使用した場
合、同燃料気化部3(先端から2―3mm下)の温
度は160℃〜170℃である。しかしこれぐらいの温
度では、それら灯油中にごくわずか含まれている
不純成分(高沸点成分)を気化したり分解したり
することはできず、この結果これら高沸点成分が
内部に蓄積して気化量が落ちてくる。そしてこう
なつて始めて燃料気化部3の温度が上昇するので
あるがこの時にはすでに発熱量が落ちているた
め、排ガス特性が悪くなつたり、臭気が強くなつ
たりする。しかし本発明実施例のごとく燃料気化
部3を灯油の気化をおさえる目的で被覆材4で覆
うと発熱量が落ちなくても温度が上昇して高温に
なつているので、それら成分をも簡単に分解し、
タール成分が蓄積されにくい。なお被覆材4は耐
熱性(600〜700℃)を有するものであればどのよ
うな成分のものでも良いが、顔料の粒子はあまり
細かすぎても又あまり大きすぎても良くなく、燃
料気化部3の平均細孔よりやや細かい10μ〜100μ
程度が良い。またこの被覆材4を燃料気化部4に
塗布する場合に結合剤が必要であるが、この結合
剤は耐熱性で燃料気化部3との接着性にすぐれ、
また耐熱性も十分にあり、さらに燃料気化部4の
内部に浸透せず、また被覆材4の多孔性もある程
度そこなわないようにすることが必要である。本
発明では、これら結着剤と顔料との成分比に関す
るものであり、以下具体的な実施例によりその効
果を説明する。 次の様な各種灯芯を用意した。なお灯芯の基本
構成は、第1図に示した構成であり、主芯1のみ
をそれぞれ変えた。 〔1〕 ガラス・スフ混紡で形成した主芯1 〔2〕 ガラス・スフ混紡でありかつ先端露出部
にFeOを主成分とした黒色の顔料固形分100に
対しコロイダルシリカ固形分5、ポリビニルア
ルコール(品番PVA117)2の割合で混合した
被覆材4を上端から4mm設けた主芯1。 〔3〕 シリカアルミナ系セラミツク芯により形
成し、燃料気化部3は未処理の主芯。 〔4〕 〔3〕の主芯1で前述の被覆材4を上端
から3mmに塗工したもの。 以上4種類の主芯1を用意した。そして促進実
験のために、サラダ油0.1%混入した灯油を使用
し、ポータブル石油ストーブをもちいて連続燃焼
させた。結果を第1表に示した。
The present invention relates to a combustion wick used in a liquid fuel combustor, and its purpose is to suppress the generation and accumulation of tar-like substances in the fuel vaporization part of the combustion wick and maintain stable combustion over a long period of time. The purpose is to provide a combustion wick that can be obtained. BACKGROUND ART A so-called suction vaporization type combustor, which sucks up liquid fuel by the capillary action of a combustion wick, vaporizes the liquid fuel from the surface of a fuel vaporization part, and burns it, is widely used in oil stoves, oil stoves, and the like. In this type of combustor, the fuel vaporization section is exposed to a high temperature and oxygen-containing atmosphere, so some of the fuel contained in the fuel vaporization section undergoes oxidation, polymerization, etc. during combustion. This turns into a tar-like substance that accumulates in the fuel vaporization section. Especially when trace amounts of high-boiling components are mixed into the fuel (for example, when machine oil, light oil, salad oil, etc. are mixed into kerosene),
Or, if some of the fuel components have changed in quality (for example, if kerosene is stored at high temperatures or under direct sunlight for a long period of time, oxides, peroxides, resins, etc. are formed). , the amount of generation and accumulation of the tar-like substance increases significantly. When this tar-like substance accumulates in the fuel vaporization section,
The capillary tubes on the surface or inside the fuel vaporizing section are blocked, inhibiting fuel suction and vaporization. As a result, the amount of fuel vaporized is abnormally reduced, the air-fuel ratio in the combustion chamber is disrupted, and a large amount of odor, soot, and harmful carbon monoxide are emitted. In addition, at the time of ignition, the tar-like substance prevents a rapid temperature rise in the fuel vaporization section and an increase in the amount of fuel vaporization, and it takes an extremely long time to reach stable combustion. Large amounts of odor, soot, and carbon monoxide were being generated. Furthermore, the tar-like substance caused the wick to stick to the metal part that supported it, making it impossible to mechanically operate the wick, and lowering the wick and making it impossible to extinguish the fire, which was dangerous. In order to eliminate these conventional drawbacks, the present invention
This invention suppresses the generation and accumulation of tar-like substances, and one embodiment of the present invention will be described below with reference to the accompanying drawings. In FIG. 1, 1 is the main core, which is made by bonding silica-alumina ceramic fibers (silica:alumina≒50:50, weight ratio) with a silica-based binder. Reference numeral 2 denotes a suction core, which is made of polypropylene cloth and is connected to the main core 1. 3 is a fuel vaporization section, when installed in a combustor (not shown),
This is the part exposed to the combustion chamber. The upper surface of the fuel vaporization section 3 is covered with a covering material 4. This coating material 4 is made of an inorganic pigment, anhydrous silicic acid, and a water-soluble organic binder, and is applied to the surface of the fuel vaporization section 3 so as not to lose its porosity. 5 is sewing thread, 6
is adhesive tape. In the above configuration, liquid fuel is sucked up from the suction wick 2 to the main wick 1 and vaporized from the surface of the fuel vaporization section 3. Here, the flow of fuel will be explained in detail as shown in FIG. 2. That is, the fuel f is sucked up inside the main core 1 and vaporized from the surface of the fuel vaporization section 3. On the other hand, a portion of the fuel f changes into a tar-like substance t near the surface of the fuel vaporization section 3, particularly near the surface of the tip of the fuel vaporization section 3 which is exposed to high temperatures, under the influence of temperature and oxygen. In addition, impure components (altered components or high boiling point components such as salad oil) contained in kerosene are also pushed up to the top of the wick by the kerosene and accumulated there. This causes clogging and reduces the vaporization area, lowering the amount of heat generated. However, when the covering material 4 is provided as in this embodiment, the amount of vaporization in that portion decreases from the beginning, and as a result, the temperature on the surface and inside of the fuel vaporization section 3 becomes high. Therefore, even if there are high boiling point components in this area, these components will easily vaporize or decompose. Furthermore, since the inside of the fuel vaporization section 3 is not directly exposed to air, kerosene is less likely to be oxidized, and high molecular weight tar components due to so-called polycondensation are less likely to be formed. To explain these principles in more detail, the temperature of the fuel vaporization section 3 of a conventional combustion wick of the kerosene vaporization type that uses kerosene is limited by the components of the kerosene.
When commercially available JIS kerosene is used, the temperature of the fuel vaporizing section 3 (2-3 mm below the tip) is 160°C to 170°C. However, at this temperature, it is not possible to vaporize or decompose the very small amount of impurity components (high boiling point components) contained in kerosene, and as a result, these high boiling point components accumulate inside and become vaporized. The quantity is decreasing. Only then does the temperature of the fuel vaporization section 3 rise, but by this time the calorific value has already decreased, resulting in poor exhaust gas characteristics and strong odor. However, if the fuel vaporization section 3 is covered with the covering material 4 for the purpose of suppressing the vaporization of kerosene as in the embodiment of the present invention, the temperature will rise and reach a high temperature even if the calorific value does not decrease, so these components can be easily removed. Disassemble,
Tar components are less likely to accumulate. The coating material 4 may be made of any component as long as it has heat resistance (600 to 700 degrees Celsius), but the pigment particles should not be too fine or too large, and should not be used in the fuel vaporization section. 10μ to 100μ slightly finer than the average pore of 3.
Good condition. In addition, a binder is required when applying this coating material 4 to the fuel vaporization part 4, but this binder is heat resistant and has excellent adhesiveness to the fuel vaporization part 3.
It is also necessary to have sufficient heat resistance, not to penetrate into the interior of the fuel vaporization section 4, and not to damage the porosity of the covering material 4 to some extent. The present invention relates to the component ratio of these binders and pigments, and the effects thereof will be explained below using specific examples. We prepared the following types of lamp wicks. The basic configuration of the lamp wick is the configuration shown in FIG. 1, with only the main wick 1 being changed. [1] Main core 1 made of a glass/splash blend [2] Main core 1 made of a glass/splash blend, with a black pigment solid content of 100% containing FeO as the main component at the exposed tip part, colloidal silica solid content of 5%, polyvinyl alcohol ( Main core 1 with coating material 4 mixed at a ratio of 2 parts (product number PVA117) 4 mm from the top end. [3] The main core is formed from a silica-alumina ceramic core, and the fuel vaporization section 3 is an untreated main core. [4] The above-mentioned coating material 4 is applied to the main core 1 of [3] 3 mm from the top end. The above four types of main cores 1 were prepared. For acceleration experiments, kerosene mixed with 0.1% salad oil was used and continuously burned in a portable oil stove. The results are shown in Table 1.

【表】 第1表から明らかなように〔1〕,〔2〕の主芯
1では被覆材4を設けても設けなくても、3〜4
時間程度で主芯1の先端より5〜10mmの所にター
ルが出来、そのため灯油を吸い上げ性が不足して
燃焼量劣化をおこした。〔3〕,〔4〕の主芯1の
場合被覆材4を設けていない〔3〕のものは、約
10時間で20%カロリーダウンとなり、タールも主
芯1の内部、先端からやや下に蓄積していた。被
覆材4を設けた〔4〕のものは、30時間で20%カ
ロリーダウンし、主芯1の先端部付近表面にター
ルが析出していたが、内部に蓄積されたタールは
ほとんどなかつた。又30%カロリーダウンするま
で約80時間もかかり〔3〕の主芯1に比して約5
倍の寿命があつた。 次に上記〔3〕の主芯1を用意し、下記の第2
表に示す様な配合で各種主芯1を作り、燃焼特性
をこの第2表に示した。なおこの主芯1は有機結
着剤を使用したもので厚み3mmでかつフレキシブ
ルなものである。この有機結着剤は水に溶解しな
いもので撥水性があつた。
[Table] As is clear from Table 1, in the main core 1 of [1] and [2], 3 to 4
Tar was formed at a distance of 5 to 10 mm from the tip of the main core 1 in about an hour, and as a result, the ability to absorb kerosene was insufficient and the amount of combustion deteriorated. In the case of the main core 1 of [3] and [4], the one of [3] without the covering material 4 is approximately
Calories were reduced by 20% in 10 hours, and tar had accumulated inside main core 1, slightly below the tip. The product [4] provided with the coating material 4 had a calorie reduction of 20% in 30 hours, and although tar was deposited on the surface near the tip of the main core 1, almost no tar was accumulated inside. Also, it takes about 80 hours to reduce calories by 30% compared to main core 1 of [3].
It lasted twice as long. Next, prepare the main core 1 of [3] above, and
Various main cores 1 were made with the formulations shown in the table, and the combustion characteristics are shown in Table 2. The main core 1 is made of an organic binder, has a thickness of 3 mm, and is flexible. This organic binder did not dissolve in water and was water repellent.

【表】 なお第2図中、 A (無機顔料、無水珪酸、有機結着剤の固形分
比率を言う。) B (0.1%サラダ油混入灯油での連続燃焼時間
を言い、初期からの燃焼量が80%の時を20%ダ
ウン、70%の時を30%ダウンと言う。) C (FeO,MnO2を主成分とした黒色顔料で、
水のサスペンジヨン状態のものである。) D (20%コロイダルシリカ溶液で日産化学(株)ス
ノーテツクスC―20を使用した。) E (ポリビニルアルコールでクラレ(株)PVA117
を使用した。) 第2表の〔5〕,〔6〕からわかるように結着剤
である無水珪酸が無機顔料に対して2以下のもの
は結着性が悪いため20%燃焼量劣化までは他のも
のとかわらず、未処理の主芯より良い特性を示し
ているが、燃焼中に被覆材4がはがれ出し30%劣
化の時間も短くなるし又、一度燃焼を中断し、再
燃焼させた時は、性能は未処理のものと変らなく
なつてしまつた。また
[Table] In Figure 2, A (represents the solid content ratio of inorganic pigment, silicic anhydride, and organic binder) B (represents the continuous combustion time with kerosene mixed with 0.1% salad oil, and the amount of combustion from the initial stage) When it is 80%, it is said to be 20% down, and when it is 70%, it is said to be 30% down.) C (A black pigment whose main components are FeO, MnO2 ,
It is in a water suspension state. ) D (20% colloidal silica solution using Nissan Chemical Co., Ltd. Snotex C-20) E (Polyvinyl alcohol using Kuraray Co., Ltd. PVA117
It was used. ) As can be seen from [5] and [6] in Table 2, those in which the binder silicic anhydride is less than 2 to the inorganic pigment have poor binding properties, so other materials may be used until the combustion rate deteriorates by 20%. However, the coating material 4 peels off during combustion and the time for 30% deterioration is shorter, and when combustion is interrupted and reburned, , the performance was no different from that of the unprocessed version. Also

〔9〕の主芯1のごとく逆
に無水珪酸が顔料に対し10以上になると、主芯1
中に顔料、結着剤である無水珪酸が浸透して先端
付近の含油量が少くなるために、被覆材4を設け
た効果がほとんどなくなつてしまつた。また
〔14〕の主芯1で示す様に有機結着剤が5をこえ
たものはそれが燃焼中にタール成分に変わるため
被覆材4による効果がなかつた。また〔12〕の主
芯1のごとく顔料と有機結着剤のみを用いたのは
初期特性は良いが、一度空焼を行うと結着性がな
くなり、はがれ出してしまつた。 以上の説明から明らかなように被覆材4の効果
を発揮させるためには、無機顔料に対して適当な
結着剤が必要であり、かつその比は顔料100に対
し無水珪酸2〜10、有機結着剤が5以下が適当で
あつた。また無水珪酸としてその他水ガラス系の
ものがあるが、これは、熱を加えると割れ現象が
おき、効果的ではなかつた。有機結着剤はある程
度の量では、あつてもなくても燃焼量劣化に対し
ては影響ないが、被覆材4の安定性から見ると非
常に効果がある。しかし有機結着剤の量が多すぎ
ると、被覆材4は安定なものが出来るが、燃焼中
に有機結着剤がタール化して目詰りをおこし、燃
焼量劣化をおこしてしまう。 以上の様に本発明によればタール状物質の生成
蓄積を抑え、長期間に渡る安定燃焼を得ることが
できる。
On the other hand, when the silicic anhydride is 10 or more compared to the pigment, as in main core 1 of [9], main core 1
Pigment and silicic anhydride as a binder permeate into the tip and the oil content near the tip decreases, so that the effect of providing the covering material 4 is almost lost. Further, as shown in main core 1 of [14], when the organic binder exceeds 5, the coating material 4 has no effect because it turns into a tar component during combustion. Also, as in main core 1 of [12], the initial properties were good when using only a pigment and an organic binder, but once the dry firing was carried out, the binding property was lost and it began to peel off. As is clear from the above explanation, in order to exhibit the effect of the coating material 4, an appropriate binder is required for the inorganic pigment, and the ratio is 2 to 10 parts of silicic anhydride to 10 parts of pigment, and 2 to 10 parts of organic pigment. It was appropriate for the binder to be 5 or less. In addition, there are other water glass-based silicic acid anhydrides, but they crack when heated and are not effective. A certain amount of organic binder has no effect on the deterioration of the combustion amount even if it is not present, but it is very effective from the viewpoint of stability of the coating material 4. However, if the amount of the organic binder is too large, the coating material 4 can be made stable, but the organic binder turns into tar during combustion, causing clogging and deteriorating the amount of combustion. As described above, according to the present invention, generation and accumulation of tar-like substances can be suppressed and stable combustion can be achieved over a long period of time.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の一実施例にかかる燃焼芯の部
分断面図、第2図はその作用説明図である。 1……主芯、2……吸い上げ芯、3……燃料気
化部、4……被覆材、5……縫製糸、6……接着
テープ。
FIG. 1 is a partial sectional view of a combustion wick according to an embodiment of the present invention, and FIG. 2 is an explanatory view of its operation. DESCRIPTION OF SYMBOLS 1... Main core, 2... Suction core, 3... Fuel vaporization part, 4... Covering material, 5... Sewing thread, 6... Adhesive tape.

Claims (1)

【特許請求の範囲】[Claims] 1 燃料気化部がシリカアルミナ系セラミツク繊
維からなり、その燃料気化部表面の少なくとも一
部を、無機顔料、無水珪酸、および有機結着剤よ
り構成される被覆材で被覆し、その配合比率が無
機顔料100に対し無水珪酸2〜10、有機結着剤5
以下であることを特徴とする燃焼芯。
1. The fuel vaporization section is made of silica-alumina ceramic fiber, and at least a part of the surface of the fuel vaporization section is coated with a coating material composed of an inorganic pigment, anhydrous silicic acid, and an organic binder, and the blending ratio is inorganic. 2 to 10 parts of silicic anhydride and 5 parts of organic binder to 100 parts of pigment
A combustion wick characterized by:
JP16362880A 1980-11-19 1980-11-19 Combustion wick Granted JPS5787508A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16362880A JPS5787508A (en) 1980-11-19 1980-11-19 Combustion wick

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16362880A JPS5787508A (en) 1980-11-19 1980-11-19 Combustion wick

Publications (2)

Publication Number Publication Date
JPS5787508A JPS5787508A (en) 1982-06-01
JPS6331682B2 true JPS6331682B2 (en) 1988-06-24

Family

ID=15777537

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16362880A Granted JPS5787508A (en) 1980-11-19 1980-11-19 Combustion wick

Country Status (1)

Country Link
JP (1) JPS5787508A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4949074A (en) * 1972-06-01 1974-05-13
JPS54149945A (en) * 1978-05-16 1979-11-24 Matsushita Electric Ind Co Ltd Liquid fuel combustion device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4949074A (en) * 1972-06-01 1974-05-13
JPS54149945A (en) * 1978-05-16 1979-11-24 Matsushita Electric Ind Co Ltd Liquid fuel combustion device

Also Published As

Publication number Publication date
JPS5787508A (en) 1982-06-01

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