JPS6333608B2 - - Google Patents
Info
- Publication number
- JPS6333608B2 JPS6333608B2 JP56129950A JP12995081A JPS6333608B2 JP S6333608 B2 JPS6333608 B2 JP S6333608B2 JP 56129950 A JP56129950 A JP 56129950A JP 12995081 A JP12995081 A JP 12995081A JP S6333608 B2 JPS6333608 B2 JP S6333608B2
- Authority
- JP
- Japan
- Prior art keywords
- fuel
- surfactant
- paint
- vaporization section
- fuel vaporization
- 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
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23D—BURNERS
- F23D3/00—Burners using capillary action
- F23D3/02—Wick burners
- F23D3/08—Wick burners characterised by shape, construction, or material, of wick
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
Description
【発明の詳細な説明】
本発明は液体燃料用燃焼器に用いられる燃焼芯
の製造法に関するもので、その目的は燃焼芯の燃
料気化部におけるタール状物質の生成蓄積を抑
え、長期間安定な燃焼を維持し得る燃焼芯を提供
することにある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing 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 to provide stable combustion for a long period of time. The object of the present invention is to provide a combustion wick that can maintain combustion.
液体燃料を燃焼芯の毛細管現象によつて吸い上
げ、この燃焼芯の気化室内に露出している先端部
分、即ち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という現象
が容易に生じていた。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た時に生ずる酸化物、
過酸化物、樹脂等)している場合等には、前記タ
ール状物質の生成、蓄積は著しく増大する。 A so-called siphon-vaporization type combustor sucks up liquid fuel by the capillary action of the combustion wick, and vaporizes and burns the liquid fuel from the tip of the combustion wick exposed in the vaporization chamber, that is, the surface of the fuel vaporization section. is widely used in oil stoves, oil stoves, etc. 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 is exposed to oxidation, polymerization, etc. during combustion. The phenomenon of turning into a tar-like substance and accumulating it in the fuel vaporizer easily occurred. In particular, if 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 are deteriorated (for example, if kerosene is left at high temperatures for a long period of time or exposed to direct sunlight), Oxides produced when stored under
peroxide, resin, etc.), the generation and accumulation of the tar-like substance increases significantly.
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、それに伴い発熱量が
著しく低下し、燃焼室における空燃比を崩して臭
気、ススや有毒な一酸化炭素を多発する様な不具
合を生じていた。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、安定燃焼に至るに著し
く長時間を有し、その間不安定過渡燃焼による臭
気、スス、一酸化炭素等の発生を増大させてい
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、燃焼芯を下げての消火操作
を不可能とする様な危険な状態もあつた。 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, and accordingly the amount of heat generated is significantly reduced, causing problems such as the air-fuel ratio in the combustion chamber being disrupted and the generation of odor, soot, and toxic carbon monoxide. Furthermore, 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. , and increased the generation of carbon monoxide, etc. Furthermore, there were dangerous situations in which the tar-like substance adhered to the wick and the metal parts that supported it, making it impossible to extinguish the fire by lowering the wick.
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。 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.
第1図において、1は主芯で、シリカ−アルミ
ナ系のセラミツク繊維(シリカ:アルミナ≒50:
50、重量比)を、有機バインダーの一例として用
いたポリアクリル酸エステルを加えて形成したも
のである。2は吸上げ芯で、ポリプロピレン布よ
りなり、主芯1に連接されている。3は主芯1上
部に形成した燃料気化部で、燃焼器に装着した
時、燃焼室に露出される部分である。燃料気化部
3には、無機顔料、無水ケイ酸及び界面活性剤か
ら成る塗料を含浸させてあり、この界面活性剤の
塗料に占める割合は0.2〜5%である。4は縫製
糸、5は接着テープである。 In Figure 1, 1 is the main core, which is a silica-alumina ceramic fiber (silica: alumina≒50:
50, weight ratio) and polyacrylic ester used as an example of an organic binder. 2 is a wicking core made of polypropylene cloth and connected to the main core 1. Reference numeral 3 denotes a fuel vaporization section formed on the upper part of the main core 1, which is exposed to the combustion chamber when installed in a combustor. The fuel vaporization section 3 is impregnated with a paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant, and the ratio of this surfactant to the paint is 0.2 to 5%. 4 is a sewing thread, and 5 is an adhesive tape.
上記構成において、液体燃料は吸上げ芯2から
主芯1へと吸上げられ、燃料気化部3表面から気
化する。ここで本実施例の効果を燃料の流れとと
もに、従来例、および塗料に占める界面活性剤の
割合と比較して詳述する。 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 effects of this example will be explained in detail in comparison with the flow of fuel, the conventional example, and the proportion of surfactant in the paint.
第2図は従来のセラミツク繊維のみからなる燃
料気化部3、第3図は燃料気化部3に、無機顔
料、無水ケイ酸及び界面活性剤から成る塗料を含
浸させたもので、界面活性剤の塗料に占める割合
を0.1%としたもので、第4図は燃料気化部3に、
前記塗料を含浸させたもので、界面活性剤の塗料
に占める割合を1%としたもの、第5図は燃料気
化部3に、前記塗料を含浸させたもので、界面活
性剤の塗料に占める割合を10%としたものであ
り、おのおのその断面を示す。 Figure 2 shows a conventional fuel vaporizer 3 made only of ceramic fibers, and Figure 3 shows a fuel vaporizer 3 impregnated with a paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant. The percentage in the paint is 0.1%, and Figure 4 shows the fuel vaporization section 3.
Figure 5 shows the fuel vaporization section 3 impregnated with the paint, with the surfactant accounting for 1% of the paint. The percentage is set at 10%, and each cross section is shown.
即ち、燃料F(実線矢印)は主芯1内を吸上げ
られ、燃料気化部3表面から気化する。このとき
従来例においては、第2図に示すように、燃料F
は燃料気化部3先端より多量に気化する。しかし
燃料中の微量の高沸点成分や変質成分は容易に気
化しない。このため、この先端に高沸点成分や変
質成分が蓄積し、温度と酸素の影響を受けタール
状物質T(白抜き矢印)に変化し、蓄積した。ま
た、第3図に示すように、界面活性剤の塗料に占
める割合を0.1%とした場合、塗料は、少量の有
機バインダーを含んだシリカ−アルミナ系セラミ
ツク繊維には、浸透しにくく、燃料気化部3表面
に、多量に吸着し易い。このため、燃料気化部3
表面の気孔径は小となりすぎ、気化量は著しく減
少する。このことにより、発熱量が著しく減少
し、気孔もタール成分で閉塞され易い状態となる
不具合が生じた。ところが、第4図に示すよう
に、界面活性剤の塗料に占める割合を1%とした
場合、塗料は、セラミツク繊維にある程度は浸透
するため、燃料気化部3表面の気孔径は小さくな
りすぎず、また気化量も減少するが、著しく発熱
量が減少することはない。このため、気化部3表
面の気孔径がある程度小となるため、毛細管現象
により、高温となつている気化部3表面にまで燃
料が吸上げられ易くなり、これとともに、燃料中
の高沸点成分や変質成分が高温となつている気化
部3表面にまで析出し易くなることや、燃料気化
部3において気化量の減少に伴う、熱量の蓄積に
よる燃料中の微量の高沸点成分や変質成分の熱分
解は、スムーズに進行し、タール状物質等の蓄積
は生じない。さらに、塗料中の無機顔料や無水ケ
イ酸は、一種の酸化触媒であり、その触媒作用に
よつて、この熱分解作用は促進される。しかし、
第5図に示すように界面活性剤の塗料に占める割
合を10%とした場合、塗料は、セラミツク繊維に
浸透しすぎるため、燃料気化部3表面の気孔径が
小となるだけでなく燃料気化部3内部の気孔径も
小となるため、燃料Fは、気化部表面への供給不
足となり、気化部内部でのタール蓄積もし易くな
る。さらに、界面活性剤の量が大となるため、界
面活性剤それ自身がタールの成因となる不具合も
顕著となる。 That is, fuel F (solid arrow) is sucked up within the main core 1 and vaporized from the surface of the fuel vaporization section 3. At this time, in the conventional example, as shown in FIG.
is vaporized in a larger amount than at the tip of the fuel vaporizing section 3. However, trace amounts of high-boiling components and degraded components in the fuel do not easily vaporize. For this reason, high boiling point components and altered components were accumulated at this tip, changed into a tar-like substance T (white arrow) under the influence of temperature and oxygen, and accumulated. Furthermore, as shown in Figure 3, when the proportion of surfactant in the paint is 0.1%, the paint is difficult to penetrate into the silica-alumina ceramic fibers that contain a small amount of organic binder, and the paint is difficult to penetrate into the silica-alumina ceramic fibers that contain a small amount of organic binder. A large amount is easily adsorbed on the surface of part 3. For this reason, the fuel vaporization section 3
The pore size on the surface becomes too small and the amount of vaporization decreases significantly. This caused a problem in that the calorific value decreased significantly and the pores were also likely to be clogged with tar components. However, as shown in Fig. 4, when the proportion of the surfactant in the paint is 1%, the paint penetrates into the ceramic fibers to some extent, so the pore size on the surface of the fuel vaporization part 3 does not become too small. , the amount of vaporization also decreases, but the amount of heat generated does not decrease significantly. For this reason, the pore diameter on the surface of the vaporization section 3 becomes small to some extent, making it easier for the fuel to be sucked up to the high temperature surface of the vaporization section 3 due to capillary action. It is easy for the altered components to precipitate even on the surface of the vaporization section 3, which is at a high temperature, and the heat of trace amounts of high boiling point components and altered components in the fuel due to the accumulation of heat as the amount of vaporization decreases in the fuel vaporization section 3. Decomposition proceeds smoothly and no accumulation of tar-like substances occurs. Furthermore, inorganic pigments and silicic anhydride in paints are a type of oxidation catalyst, and their catalytic action accelerates this thermal decomposition action. but,
As shown in Figure 5, when the proportion of the surfactant in the paint is 10%, the paint penetrates into the ceramic fibers too much, which not only reduces the pore size on the surface of the fuel vaporization section 3, but also reduces the amount of fuel vaporization. Since the pore diameter inside the portion 3 is also small, the fuel F is insufficiently supplied to the surface of the vaporization portion, and tar is likely to accumulate inside the vaporization portion. Furthermore, since the amount of surfactant is large, the problem that the surfactant itself causes tar becomes significant.
ちなみに吸上げ気化方式の石油燃焼器を用いて
燃焼させたときの結果を示すと第6図のようにな
る。燃料は白灯油にサラダ油を0.1容量%混合さ
せたものを用い、燃焼芯は以下の4種を用いた。 Incidentally, Figure 6 shows the results of combustion using a suction vaporization type oil combustor. The fuel used was a mixture of white kerosene and salad oil at 0.1% by volume, and the following four types of combustion wicks were used.
(1) 燃料気化部3をシリカ−アルミナ系セラミツ
ク繊維で形成し、未処理のもの。(1) The fuel vaporization section 3 is made of silica-alumina ceramic fiber and is untreated.
(2) 上記(1)の燃料気化部3に、無機顔料、無水ケ
イ酸及び界面活性剤からなる塗料を含浸させた
もので、界面活性剤の塗料に占める割合を0.1
%としたもの。(2) The fuel vaporization section 3 of (1) above is impregnated with a paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant, and the ratio of the surfactant to the paint is 0.1.
%.
(3) 上記(1)に(2)と同じ塗料を含浸させたもので、
界面活性剤の塗料に占める割合を1%としたも
の。(3) The above (1) is impregnated with the same paint as (2),
The percentage of surfactant in the paint is 1%.
(4) 上記(1)に(2)の塗料を含浸させたもので、界面
活性剤の塗料に占める割合を10%としたもの。(4) The above (1) is impregnated with the paint described in (2), with the proportion of surfactant in the paint being 10%.
この4種を比較すると、第6図に示すように、
界面活性剤の割合を1%としたもの(3)は、未処理
のもの(1)、界面活性剤の割合を0.1%としたもの
(2)、界面活性剤の割合を10%としたもの(4)に比べ
て発熱量の低下が著しく減少している。 Comparing these four types, as shown in Figure 6,
The one with a surfactant ratio of 1% (3) is the untreated one (1), and the one with a surfactant ratio of 0.1%.
(2), the decrease in calorific value is significantly reduced compared to (4) where the proportion of surfactant is 10%.
また、界面活性剤の塗料に占める割合によつ
て、発熱量の低下に与える影響を比較すると、第
7図に示すように、界面活性剤の割合が0.2〜5
%のときにおいて発熱量の維持特性が著しく良い
ことがわかる。 In addition, when comparing the effect on the reduction of calorific value depending on the proportion of surfactant in the paint, as shown in Figure 7, the proportion of surfactant is 0.2 to 5.
%, it can be seen that the calorific value maintenance characteristics are extremely good.
以上の様に本発明の燃焼芯の製造法は、セラミ
ツク繊維よりなる燃料気化部に、無機顔料、無水
ケイ酸及び界面活性剤から成る塗料を含浸させ、
かつ界面活性剤の塗料に占める割合を0.2〜5%
とすることによつて、タール状物質の生成、蓄積
を抑え、長時間にわたつて安定燃焼が得られる。 As described above, the method for producing a combustion wick of the present invention involves impregnating a fuel vaporization part made of ceramic fiber with a paint made of an inorganic pigment, anhydrous silicic acid, and a surfactant.
And the proportion of surfactant in the paint is 0.2 to 5%.
By doing so, the generation and accumulation of tar-like substances can be suppressed, and stable combustion can be obtained over a long period of time.
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〜第5図は燃焼芯の作用説明
図、第6図、第7図はその特性図である。
1……主芯、2……吸上げ芯、3……燃料気化
部。
FIG. 1 is a partial sectional view of a combustion wick according to an embodiment of the present invention, FIGS. 2 to 5 are diagrams for explaining the operation of the combustion wick, and FIGS. 6 and 7 are characteristic diagrams thereof. 1... Main core, 2... Suction wick, 3... Fuel vaporization section.
Claims (1)
えて多孔体の燃料気化部を形成し、この燃料気化
部表面の気孔径を小とするように燃料気化部の少
なくとも一部に、無機顔料、無水ケイ酸及び界面
活性剤から成る塗料で、かつ前記界面活性剤の塗
料に占める割合を0.2〜5%とした塗料を含浸さ
せ、前記燃料気化部内に浸透させた燃焼芯の製造
法。1 A small amount of organic binder is added to ceramic fibers to form a porous fuel vaporization section, and at least a portion of the fuel vaporization section is coated with inorganic pigments and silicic anhydride to reduce the pore size on the surface of the fuel vaporization section. A method for manufacturing a combustion wick, which is impregnated with a paint consisting of a surfactant and a surfactant, and in which the surfactant accounts for 0.2 to 5% of the paint, and permeates into the fuel vaporization section.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56129950A JPS5831203A (en) | 1981-08-19 | 1981-08-19 | Manufacturing method of combustion wick |
| US06/366,168 US4421477A (en) | 1981-04-13 | 1982-04-07 | Combustion wick |
| CA000400701A CA1196565A (en) | 1981-04-13 | 1982-04-08 | Combustion wick |
| EP82103050A EP0062910B1 (en) | 1981-04-13 | 1982-04-08 | Combustion wick |
| DE8282103050T DE3264865D1 (en) | 1981-04-13 | 1982-04-08 | Combustion wick |
| KR1019820001561A KR830010341A (en) | 1981-04-13 | 1982-04-09 | Combustion wick |
| AU82539/82A AU536532B2 (en) | 1981-04-13 | 1982-04-13 | Wick for burner |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56129950A JPS5831203A (en) | 1981-08-19 | 1981-08-19 | Manufacturing method of combustion wick |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5831203A JPS5831203A (en) | 1983-02-23 |
| JPS6333608B2 true JPS6333608B2 (en) | 1988-07-06 |
Family
ID=15022439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56129950A Granted JPS5831203A (en) | 1981-04-13 | 1981-08-19 | Manufacturing method of combustion wick |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5831203A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4966707A (en) * | 1986-05-13 | 1990-10-30 | Celanese Corporation | Liquid/liquid extractions with microporous membranes |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56146907A (en) * | 1980-04-17 | 1981-11-14 | Matsushita Electric Ind Co Ltd | Liquid fuel combustion wick |
| JPS6136129A (en) * | 1984-07-30 | 1986-02-20 | Sumitomo Electric Ind Ltd | Manufacturing method of glass base material for optical fiber |
-
1981
- 1981-08-19 JP JP56129950A patent/JPS5831203A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5831203A (en) | 1983-02-23 |
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