JPS6136129B2 - - Google Patents
Info
- Publication number
- JPS6136129B2 JPS6136129B2 JP5118780A JP5118780A JPS6136129B2 JP S6136129 B2 JPS6136129 B2 JP S6136129B2 JP 5118780 A JP5118780 A JP 5118780A JP 5118780 A JP5118780 A JP 5118780A JP S6136129 B2 JPS6136129 B2 JP S6136129B2
- Authority
- JP
- Japan
- Prior art keywords
- main core
- combustion
- resistant
- liquid fuel
- wick
- 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
Links
- 238000002485 combustion reaction Methods 0.000 claims description 23
- 239000011230 binding agent Substances 0.000 claims description 21
- 239000000446 fuel Substances 0.000 claims description 21
- 239000007788 liquid Substances 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 4
- 239000004917 carbon fiber Substances 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 239000003365 glass fiber Substances 0.000 claims description 4
- 239000003779 heat-resistant material Substances 0.000 claims description 4
- 239000000919 ceramic Substances 0.000 claims description 3
- 239000008119 colloidal silica Substances 0.000 claims description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 3
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 3
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 3
- 239000011118 polyvinyl acetate Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 description 11
- 229920000742 Cotton Polymers 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 238000009834 vaporization Methods 0.000 description 4
- 230000008016 vaporization Effects 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- -1 polypropylene Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 238000009958 sewing Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012210 heat-resistant fiber Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Wick-Type Burners And Burners With Porous Materials (AREA)
Description
【発明の詳細な説明】
本発明は石油ストーブ等に用いられる液体燃料
燃焼芯に関するもので、その目的は充分な燃料の
吸上げ、気化能力を有しつつ、柔軟、強靭で加工
性に富み、かつ耐熱性及び機械的強度に秀れた液
体燃料燃焼芯を提供することを目的とするもので
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a liquid fuel combustion wick used in kerosene stoves, etc., and its purpose is to have sufficient fuel suction and vaporization ability, as well as to be flexible, strong, and highly workable. Another object of the present invention is to provide a liquid fuel combustion wick that has excellent heat resistance and mechanical strength.
ポータブル石油ストーブ等、吸上げ気化式の液
体燃料燃焼器に用いられる液体燃料燃焼芯は従
来、ガラス繊維、炭素繊維等の耐熱性繊維に綿、
スフ等を混紡した編組体が多く用いられている
が、これらの材質よりなる液体燃料燃焼芯には次
の様な欠点がある。 Liquid fuel combustion wicks used in suction vaporization type liquid fuel combustors such as portable kerosene stoves have conventionally been made of heat-resistant fibers such as glass fibers and carbon fibers, cotton,
Braided bodies made of a blend of cotton wool and the like are often used, but liquid fuel combustion wicks made of these materials have the following drawbacks.
見かけ体積当りの燃料吸上げに有効な気孔密
度(以下気孔率)が40〜50%しかなく、燃料の
保有量が少い。従つて燃焼中に燃焼芯先端部は
高温になり、タール状物質の生成量が多くな
る。このタール状物質は燃料の吸上げを阻害し
たり、気化面を閉塞して燃料気化量を低下せし
め、燃焼状態を悪化させるために臭気、スス、
あるいは有毒な一酸化炭素を発生する様な不具
合を容易に招いていた。 The effective pore density (hereinafter referred to as porosity) for fuel uptake per apparent volume is only 40 to 50%, and the amount of fuel retained is small. Therefore, the tip of the combustion wick becomes hot during combustion, and a large amount of tar-like substances are produced. This tar-like substance obstructs fuel uptake, blocks the vaporization surface, reduces the amount of fuel vaporized, and worsens combustion conditions, causing odor, soot, and
Otherwise, it could easily lead to problems such as the generation of toxic carbon monoxide.
また上記タール状物質の蓄積によつて液体燃
料燃焼芯の厚さを増大せしめ、従つて液体燃料
燃焼芯の上下動作を不可能ならしめるため、消
火操作が不能となる様な危険な状態に至る場合
もあつた。 In addition, the accumulation of the tar-like substance increases the thickness of the liquid fuel combustion wick, making it impossible to move the liquid fuel combustion wick up and down, leading to a dangerous situation in which fire extinguishing operations are impossible. There were cases.
このタール状物質を除去するために、燃料供
給を停止して燃焼を継続させる、いわゆる空焼
きを行う方法が一般に用いられるが、ガラス繊
維、炭素繊維等と綿、スフ等との混紡体は300
〜400℃の耐熱性は有するものの、炭素質の多
いタール状物質を除去し得る500〜600℃以上の
高温には耐えられず溶融もしくは脆化してしま
う。従つて従来の液体燃料燃焼芯を使用した場
合、上記加熱脆化を防止するために高温空焼き
は成し得ず、充分なタール状物質の除去は行え
なかつた。 In order to remove this tar-like substance, a so-called dry firing method is generally used in which the fuel supply is stopped and combustion is continued.
Although it has heat resistance of up to 400°C, it cannot withstand high temperatures of 500 to 600°C or higher, which would remove carbon-rich tar-like substances, and it melts or becomes brittle. Therefore, when conventional liquid fuel combustion wicks are used, high-temperature dry firing cannot be performed to prevent the above-mentioned heating embrittlement, and tar-like substances cannot be removed sufficiently.
本考案は上記従来の欠点を解消するもので、以
下その一実施例について添付図面に基づき説明す
る。 The present invention solves the above-mentioned conventional drawbacks, and one embodiment thereof will be described below with reference to the accompanying drawings.
第1図に於て、1は主芯でシリカーアルミナ系
のセラミツクフアイバーを主材料としている。主
芯1の先端部1aはコロイダルシリカ、アルミナ
ゾル等の耐熱性無機結合剤を含有し、下方部1b
はポリ酢酸ビニル、ポリクロロプレン、ポリアク
リル酸エステル等の耐油性有機結合剤を含有して
いる。2は吸上げ芯で、綿、ポリプロピレン等の
布体もしくは紐状体よりなる。3は縫製糸で、主
芯1及び吸上げ芯2の要部を縫製している。4は
火まわり芯でシリカクロス、炭素繊維等の耐熱性
材料よりなり、主芯1に挾持されるか、もしくは
側面に装着されても良い。 In FIG. 1, numeral 1 denotes the main core, which is mainly made of silica-alumina ceramic fiber. The tip portion 1a of the main core 1 contains a heat-resistant inorganic binder such as colloidal silica or alumina sol, and the lower portion 1b
contains oil-resistant organic binders such as polyvinyl acetate, polychloroprene, and polyacrylic esters. Reference numeral 2 denotes a wicking core, which is made of cloth or string-like material such as cotton or polypropylene. Reference numeral 3 denotes a sewing thread, which is used to sew the main parts of the main core 1 and the suction core 2. A fire wick 4 is made of a heat-resistant material such as silica cloth or carbon fiber, and may be held between the main wick 1 or attached to the side.
上記構成に於て、主芯1は80〜90%の気孔率を
有して結合剤で結合成型することが可能であり、
従来のガラス繊維等の燃焼芯に比べ単位体積当り
の燃料含有量は、はるかに大きくなる。従つて燃
焼中に主芯1先端部が高温になり、タール状物質
が急速に生成、蓄積する現象は著しく抑制され
る。このため、タール状物質に起因する燃焼状態
の悪化、燃焼気化量の減衰、あるいは消火不能と
いつた不具合は回避され、長期間に渡つて安定し
た、かつ安全な燃焼を保つことができる。 In the above configuration, the main core 1 has a porosity of 80 to 90% and can be bonded and molded with a binder,
The fuel content per unit volume is much higher than that of conventional combustion wicks such as glass fiber. Therefore, the phenomenon in which the tip of the main core 1 becomes hot during combustion and tar-like substances are rapidly generated and accumulated is significantly suppressed. Therefore, problems such as deterioration of combustion conditions, attenuation of combustion vaporization amount, or inability to extinguish fire due to tar-like substances are avoided, and stable and safe combustion can be maintained over a long period of time.
ここで主芯1の下方部1bはシリカ−アルミナ
系の材質を耐油性有機結合剤で結合しており、柔
軟性に富み、かつ強靭であるため、切断、成型、
縫合等が自在にできる。即ち平板上でも円筒状で
も加工が容易にでき、また綿、ポリプロピレン等
の吸上芯2との縫合接続も可能である。また柔軟
であるため上記の如く吸上芯2と縫合しても、あ
るいは吸上芯を主芯1に重ねてテープ状のもので
貼付けても、その接触部における密着性は良く、
燃料の吸上げ性能を阻害されることはない。更に
強靭であるので、運搬、組立あるいは使用中の衝
撃にも充分耐え得る強度を有している。 Here, the lower part 1b of the main core 1 is made of silica-alumina material bonded with an oil-resistant organic binder, and is highly flexible and strong, so it can be cut, molded,
Sutures etc. can be done freely. That is, it can be easily processed into either a flat plate or a cylindrical shape, and can also be connected to the wick 2 made of cotton, polypropylene, etc. by sewing. In addition, since it is flexible, even if it is sewn with the wicking core 2 as described above, or even if the wicking core is overlapped with the main core 1 and pasted with a tape-like material, the adhesion at the contact area is good.
Fuel siphoning performance is not hindered. Furthermore, it is strong enough to withstand shocks during transportation, assembly, and use.
この有機結合剤はポリ酢酸ビニル、ポリクロロ
プレン、ポリアクリル酸エステル等の耐油性の有
機結合剤であれば使用可能であるが、これらの結
合剤は150〜200℃に連続的に加熱されると分解さ
れ、徐々に結合力を失い、特に空焼きを行うこと
によつて加熱される部分の上記有機結合剤は殆ん
ど分解除去され、主芯1は著しく脆化されるが、
ここで主芯1の先端部1aをコロイダルシリカ、
アルミナゾル等の耐熱性無機結合剤で結合させて
おけば、耐熱強度は1000℃以上にも増し、空焼き
を繰り返しても主芯1bの特性は何ら損われるこ
とはなく、長期間に渡つて安定した燃焼を維持す
ることができる。また燃焼中にタール状物質が主
芯1先端部1aの近傍に蓄積した時、該タール状
物質の加熱収縮が生じるが、これに伴つて主芯1
自体も収縮応力を受ける。主芯1全体が有機結合
剤のみで結合されている場合には上記収縮作用に
よつて先端部が湾曲し、主芯1の上下動作が不能
となる場合も生ずるが、ここで上記の如く先端部
1bを無機結合剤により機械的強度を増すことに
よつて収縮を防止する事ができる。 Any oil-resistant organic binder such as polyvinyl acetate, polychloroprene, or polyacrylic acid ester can be used as this organic binder, but when these binders are continuously heated to 150 to 200°C, The organic binder decomposes and gradually loses its binding strength, and most of the organic binder in the parts heated by dry firing is decomposed and removed, and the main core 1 becomes extremely brittle.
Here, the tip 1a of the main core 1 is made of colloidal silica,
If it is bonded with a heat-resistant inorganic binder such as alumina sol, the heat-resistant strength will increase to over 1000℃, and the characteristics of the main core 1b will not be impaired in any way even after repeated dry firing, making it stable for a long time. It is possible to maintain a certain amount of combustion. Further, when tar-like substances accumulate near the tip 1a of the main core 1 during combustion, heating shrinkage of the tar-like substances occurs, and along with this, the main core 1
itself is subject to shrinkage stress. If the entire main core 1 is bonded only with an organic binder, the tip may curve due to the above-mentioned shrinkage effect, and the main core 1 may become unable to move up and down. Shrinkage can be prevented by increasing the mechanical strength of the portion 1b with an inorganic binder.
この無機結合剤は、主芯1を成型加工した後に
先端部1aに含浸させることも可能であり、有機
結合剤で結合された主芯1の良加工性を損うもの
ではない。また主芯1の先端部1aは有機結合剤
と無機結合剤を併含していても、あるいは無機結
合剤を含浸した後に加熱して有機結合剤を分解除
去する等の方法により、無機結合剤のみを含有す
る様にしても良く、いずれも上記諸効果は充分満
足される。 This inorganic binder can also be impregnated into the tip portion 1a after the main core 1 is molded, and does not impair the good workability of the main core 1 bonded with the organic binder. In addition, even if the tip 1a of the main core 1 contains both an organic binder and an inorganic binder, or by impregnating the inorganic binder and then heating it to decompose and remove the organic binder, the inorganic binder can be removed. However, the above-mentioned effects are fully satisfied in either case.
また、主芯1はシリカ系、シリカ−アルミナ系
またはアルミナ系のセラミツクフアイバーを主材
としているが、これにガラス繊維、炭素繊維等の
耐熱性材質を混合することにより、これらが長繊
維物質であるために、強靭性を増大させることも
できる。あるいはこれら耐熱性材質からなる補助
芯、例えば第1図の如き火まわり芯4等を装着す
ることも良く、いずれも上記効果を損うこと無く
性能を助長するものである。 The main core 1 is mainly made of silica-based, silica-alumina-based, or alumina-based ceramic fiber, but by mixing heat-resistant materials such as glass fiber and carbon fiber with it, these can be made into long-fiber materials. It can also increase toughness. Alternatively, an auxiliary wick made of these heat-resistant materials, such as the fire wick 4 shown in FIG. 1, may be installed, and any of these will enhance the performance without impairing the above-mentioned effects.
更に、第2図に示す如く、主芯1の下部を直接
燃料中に含浸させて用いる場合も良く、綿、ポリ
プロピレン等の吸上芯2の有無は上記本発明の効
果に何ら支障をきたすものではない。 Furthermore, as shown in FIG. 2, the lower part of the main wick 1 may be directly impregnated with fuel, and the presence or absence of the wick 2 made of cotton, polypropylene, etc. does not interfere with the effects of the present invention. isn't it.
以上の様に本発明の液体燃料燃焼芯はタール状
物質の生成を抑えて、長期間に渡る安定かつ安全
な燃焼を可能とし、更に加工性に富み耐熱性、機
械的強度に秀れたもので、その価値は極めて大な
るものである。 As described above, the liquid fuel combustion wick of the present invention suppresses the generation of tar-like substances, enables stable and safe combustion over a long period of time, and has excellent processability, heat resistance, and mechanical strength. And its value is extremely great.
第1図は本発明の液体燃料燃焼芯の一実施例の
部分切断図、第2図は他の実施例の部分切断図で
ある。
1……主芯、2……吸上げ芯、3……縫製糸、
4……火まわり芯。
FIG. 1 is a partially cutaway view of one embodiment of the liquid fuel combustion wick of the present invention, and FIG. 2 is a partially cutaway view of another embodiment. 1... Main core, 2... Wicking core, 3... Sewing thread,
4... Fire wick.
Claims (1)
を主材料とし、先端部に少くともコロイダルシリ
カ等の耐熱性無機結合剤を含有し、他部には少く
ともポリ酢酸ビニル、ポリクロロプレン等の耐油
性有機結合剤を含有することを特徴とする液体燃
料燃焼芯。 2 セラミツクフアイバーにガラス繊維、炭素繊
維等の耐熱性材料を混合、もしくは装着してなる
特許請求の範囲第1項に記載の液体燃料燃焼芯。[Scope of Claims] 1 The main material is ceramic fiber such as silica-alumina, the tip part contains at least a heat-resistant inorganic binder such as colloidal silica, and the other part contains at least polyvinyl acetate, polychloroprene, etc. A liquid fuel combustion wick characterized by containing an oil-resistant organic binder. 2. The liquid fuel combustion wick according to claim 1, which is made of a ceramic fiber mixed with or attached with a heat-resistant material such as glass fiber or carbon fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5118780A JPS56146907A (en) | 1980-04-17 | 1980-04-17 | Liquid fuel combustion wick |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5118780A JPS56146907A (en) | 1980-04-17 | 1980-04-17 | Liquid fuel combustion wick |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56146907A JPS56146907A (en) | 1981-11-14 |
JPS6136129B2 true JPS6136129B2 (en) | 1986-08-16 |
Family
ID=12879856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5118780A Granted JPS56146907A (en) | 1980-04-17 | 1980-04-17 | Liquid fuel combustion wick |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56146907A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57169506A (en) * | 1981-04-13 | 1982-10-19 | Matsushita Electric Ind Co Ltd | Combustion wick |
JPS5831203A (en) * | 1981-08-19 | 1983-02-23 | Matsushita Electric Ind Co Ltd | Combustion wick |
JPS5880412A (en) * | 1981-11-09 | 1983-05-14 | Matsushita Electric Ind Co Ltd | Combustion wick |
JPS58106314A (en) * | 1981-12-18 | 1983-06-24 | Matsushita Electric Ind Co Ltd | Combustion wick |
JPS5913810A (en) * | 1982-07-14 | 1984-01-24 | Matsushita Electric Ind Co Ltd | Wick |
JPS59210206A (en) * | 1984-04-11 | 1984-11-28 | Matsushita Electric Ind Co Ltd | Liquid fuel burning equipment |
JPS60207A (en) * | 1984-05-23 | 1985-01-05 | Matsushita Electric Ind Co Ltd | Wick for petroleum burning appliance |
-
1980
- 1980-04-17 JP JP5118780A patent/JPS56146907A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS56146907A (en) | 1981-11-14 |
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