JPS6016207A - Evaporating type liquid fuel combustion device - Google Patents
Evaporating type liquid fuel combustion deviceInfo
- Publication number
- JPS6016207A JPS6016207A JP58123828A JP12382883A JPS6016207A JP S6016207 A JPS6016207 A JP S6016207A JP 58123828 A JP58123828 A JP 58123828A JP 12382883 A JP12382883 A JP 12382883A JP S6016207 A JPS6016207 A JP S6016207A
- Authority
- JP
- Japan
- Prior art keywords
- liquid fuel
- film
- tar
- fuel combustion
- weight
- 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
- 238000002485 combustion reaction Methods 0.000 title claims abstract description 20
- 239000000446 fuel Substances 0.000 title claims abstract description 18
- 239000007788 liquid Substances 0.000 title claims abstract description 18
- 238000001704 evaporation Methods 0.000 title abstract 6
- 230000008016 vaporization Effects 0.000 claims abstract description 43
- 239000000463 material Substances 0.000 claims abstract description 26
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 25
- 239000003054 catalyst Substances 0.000 claims abstract description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 6
- 239000010439 graphite Substances 0.000 claims abstract description 6
- 239000003973 paint Substances 0.000 claims abstract description 6
- 239000010452 phosphate Substances 0.000 claims abstract description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 6
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 6
- LTPBRCUWZOMYOC-UHFFFAOYSA-N Beryllium oxide Chemical compound O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 claims abstract description 5
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 3
- 239000010936 titanium Substances 0.000 claims abstract description 3
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000009834 vaporization Methods 0.000 claims description 27
- 239000005416 organic matter Substances 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 9
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- -1 maxilum oxide Chemical compound 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 claims description 3
- 229910021536 Zeolite Inorganic materials 0.000 claims description 3
- 239000000378 calcium silicate Substances 0.000 claims description 3
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 3
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 3
- 238000001514 detection method Methods 0.000 claims description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 3
- 230000004907 flux Effects 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 3
- 239000010457 zeolite Substances 0.000 claims description 3
- INZDTEICWPZYJM-UHFFFAOYSA-N 1-(chloromethyl)-4-[4-(chloromethyl)phenyl]benzene Chemical compound C1=CC(CCl)=CC=C1C1=CC=C(CCl)C=C1 INZDTEICWPZYJM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052582 BN Inorganic materials 0.000 claims description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 229910052570 clay Inorganic materials 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 2
- MEOSMFUUJVIIKB-UHFFFAOYSA-N [W].[C] Chemical compound [W].[C] MEOSMFUUJVIIKB-UHFFFAOYSA-N 0.000 claims 1
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 6
- 239000011368 organic material Substances 0.000 abstract description 5
- 239000004568 cement Substances 0.000 abstract description 3
- 230000008020 evaporation Effects 0.000 abstract 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000395 magnesium oxide Substances 0.000 abstract 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 238000009825 accumulation Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000006200 vaporizer Substances 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000006864 oxidative decomposition reaction Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- 229910000680 Aluminized steel Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910021392 nanocarbon Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Evaporation-Type Combustion Burners (AREA)
- Spray-Type Burners (AREA)
- Catalysts (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は暖房器、調理器などに広く利用されている気化
式液体燃料燃焼装置に関するものであり、特にタールが
たい積すると011題になる気化室に関するものである
。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a vaporizing liquid fuel combustion device that is widely used in heaters, cookers, etc., and particularly relates to a vaporizing chamber that causes a 011 problem when tar accumulates. It is something.
従来例の構成とその問題点
従来装置の気化室は金属もしくは金属丘に耐熱性皮膜を
被覆したものであった。ところが従来の装置においてi
”x気化室内壁にタールがたい積し、着火、消火時に白
煙や臭気が発生する問題があった。Structure of the Conventional Example and Its Problems The vaporizing chamber of the conventional apparatus was made of metal or a metal hill coated with a heat-resistant film. However, in the conventional device, i
There was a problem with tar accumulating on the walls of the vaporization chamber, causing white smoke and odor when igniting and extinguishing the fire.
発明の目的
本発明はこのような従来の問題点を解決し、クールのた
い積の少ない気化室からなる気化式液体燃剥燃焼装置の
提供を目的とするものである。OBJECTS OF THE INVENTION It is an object of the present invention to solve these conventional problems and to provide a vaporizing type liquid burning and burning device that includes a vaporizing chamber with little accumulation of coolant.
発明の構成
この目的を達成するために本発明は、気化室内壁の全部
もしくは一部を高熱伝導性でかつ高ふく対性材料、有機
物分解触媒および耐熱性結合材よりなる有機物分解皮膜
で被覆し、膜部w4温度に保持する構成にすることによ
り、伝熱およびふ〈射の熱的作用1と共に触媒作用にょ
シタールのたい積金少なくするものである。Structure of the Invention In order to achieve this object, the present invention covers all or part of the wall of the vaporization chamber with an organic matter decomposition film made of a material with high thermal conductivity and high flux resistance, an organic matter decomposition catalyst, and a heat-resistant binder. By maintaining the temperature of the membrane portion W4, the thermal effects of heat transfer and radiation are reduced, as well as the accumulation of catalytic activity.
実施例の説明
本発明の気化室内壁皮膜の一つの主要成分は高熱伝導性
でかつ高ふく対性の微粉末け*1であり、炭素、黒鉛、
酸化ベリリウム、酸化マク7シウム、炭化ケイ素、バナ
ジウムカーパイ1−、タンクステンカーバイト、チタン
カーバイト、窒化ボロン、ジルコニウムポライドの群か
ら選んだ少なくとも1挿具11i15〜50重量%含有
することが必“なである。DESCRIPTION OF EMBODIMENTS One of the main components of the vaporization chamber wall coating of the present invention is a fine powder*1 with high thermal conductivity and high flux resistance, and contains carbon, graphite,
It may contain 15 to 50% by weight of at least one insert selected from the group of beryllium oxide, mak7ium oxide, silicon carbide, vanadium carbide, tank sten carbide, titanium carbide, boron nitride, and zirconium poride. It's a must.
また第二の主要成分は有機物分解触媒であり、チタン、
ジルコニウム、バナジウム、クロム、モリブデン、タン
グステン、マンガン、鉄、コバルト、ニッケル、銅、お
よび希土類の酸化物、元素状の白金Pよびパラジウム、
−活性白土、ゼオライト、ケイ酸カルシウム、アルミナ
セメント、炭1’l12カリウムの群から選んだ少なく
とも1神以1:ヲ、0.1〜15重量%含有することが
必要である。さらに第三の主要成分は耐熱性結合材で、
水溶性リン酸塩、水溶性ケイ酸塩、シリコン系塗料のl
!Yから選んだものを40〜80重量%含有することが
必要である。The second main component is an organic matter decomposition catalyst, including titanium,
Zirconium, vanadium, chromium, molybdenum, tungsten, manganese, iron, cobalt, nickel, copper, and rare earth oxides, elemental platinum P and palladium,
- It is necessary to contain 0.1 to 15% by weight of at least one selected from the group of activated clay, zeolite, calcium silicate, alumina cement, and potassium charcoal. Furthermore, the third main ingredient is a heat-resistant binder.
Water-soluble phosphate, water-soluble silicate, silicone paint l
! It is necessary to contain 40 to 80% by weight of one selected from Y.
第1図は本発明装置の原理を示すもので、液体燃料1を
空気2と共に噴出させ、加熱気化面3で気化し、混合カ
スをバーナーヘッド4で燃焼サセ火炎5を形成させるも
のである。FIG. 1 shows the principle of the apparatus of the present invention, in which liquid fuel 1 is ejected together with air 2, vaporized on a heating vaporization surface 3, and the mixed residue is formed into a combustion slag flame 5 in a burner head 4.
6ULアルミニウム、ステンレス、アルミニウム処理鋼
板などからなる金属気化筒であシ、7は気化筒加熱用電
気ヒータ、8は温度検出素子である。気化面3の温度は
検品素子8により検出しながら燃焼立ちに、シ時[は電
気ヒータ7により、定常燃焼時には/昏ナーヘッド4が
らの伝導熱、燃焼u1:ガスからの排熱回収により膜沸
騰温度に保持する。定常燃焼時には電気ヒータ7は補助
熱源として働く。6 is a metal vaporization cylinder made of UL aluminum, stainless steel, aluminum-treated steel plate, etc., 7 is an electric heater for heating the vaporization cylinder, and 8 is a temperature detection element. The temperature of the vaporization surface 3 is detected by the inspection element 8 at the beginning of combustion, by the electric heater 7 at the time of combustion, by the conduction heat from the stunner head 4 during steady combustion, and by the combustion u1: film boiling by recovering exhaust heat from the gas. Hold at temperature. During steady combustion, the electric heater 7 acts as an auxiliary heat source.
第2図ij:気化室の部分拡大図であり皮膜3は高熱伝
導性かつ高ふく射性材料9(×で表示)、有機物分解触
媒10(○で表示)および耐熱性結合材10(斜線で表
示)からなる。Figure 2 ij: This is a partially enlarged view of the vaporization chamber, and the coating 3 consists of a highly thermally conductive and highly radiation material 9 (indicated by x), an organic substance decomposition catalyst 10 (indicated by ○), and a heat-resistant binder 10 (indicated by diagonal lines). ).
このような気化室を有する装置で気化面温度を膜部1俺
温度に保持し、タールの原因となる不揮発成分12(Δ
で表示)を多く含む悪質な液体燃料1を気化させる場合
、皮膜中に高熱伝導慴でかつ高ふく対性オ料9が存在す
ると伝熱およびふ<q・lの熱的作用のため燃料中の揮
発成分は(萌めで短時間で気化し皮膜りでの滞留時間が
短くなりタールが少なくなる。また皮膜の熱伝導性が高
くなると液体燃料は膜部IIIを起し球状とな、って皮
膜り、ffi移動しながら気化するため不揮発成分のた
い積場所が拡大する。このため不揮発成分分解作用をイ
jする有機物分解触媒の負荷を軽減することになりター
ル生成を少なくする。In an apparatus having such a vaporization chamber, the temperature of the vaporization surface is maintained at the temperature of the membrane part 1, and the non-volatile component 12 (Δ
When vaporizing a bad liquid fuel 1 containing a large amount of gas (represented by Volatile components of (moe) vaporize in a short time, shorten the residence time in the film, and reduce the amount of tar.Also, when the thermal conductivity of the film increases, the liquid fuel raises the film part III and becomes spherical. Since the non-volatile components are vaporized while forming a film and moving, the area where non-volatile components accumulate increases.This reduces the load on the organic matter decomposition catalyst that inhibits the decomposition of non-volatile components, thereby reducing tar production.
もし皮膜中にアルミニウムのような高熱伝導性であって
も低ふく対性オ料が存在すると液(木燃才1は膜N1;
騰を起すが気化時間がしくl!J燃月の丙結GF N粗
大化が起り燃焼に悪影響をおよぼしη「捷しくない。Even if the film has high thermal conductivity such as aluminum, if there is a low-resistivity metal in the film, the liquid (Kinenzai 1 is film N1;
It causes vaporization, but the vaporization time is slow! J Mogetsu no Kyutsu GF N coarsening occurs and has a negative effect on combustion.
有機物分解触媒はタールの原因となる不揮光成分の酸化
分解、部分酸化分解、もしくはタラソギンクによりター
ル生成ケ少なくする。Organic matter decomposition catalysts reduce tar formation by oxidative decomposition, partial oxidative decomposition, or thalassoginking of non-volatile light components that cause tar.
耐熱性結合材は高熱伝導性でかつlf’?+ふく射j’
l F4 I+および有機物分解触媒を気化筒に接着す
るために必要な材料である。The heat-resistant bonding material has high thermal conductivity and lf'? +Fujija'
l F4 A material necessary for adhering I+ and the organic matter decomposition catalyst to the vaporization cylinder.
主材は水溶性リン酸塩、水溶性ケイ酸塩、シリコン系塗
料であるが、硬化の完全化、硬化時間の短設(j Aど
のため硬化材を使用したり、耐火性、耐油牲、耐水性な
どの皮膜性状を確保するため充填材を使用する。皮膜組
成としては高熱伝導性でかつ高ふく対性材料訃よび有機
物分解触媒の含有量は多いほど、耐熱性結合材の含有量
に少ないほどタール生成量は少なくなるが気化筒との密
着性、皮1関強度を確保するために40〜90重量%の
耐熱性結合オの添加が必要である。The main materials are water-soluble phosphate, water-soluble silicate, and silicone-based paints, but it is necessary to achieve complete curing and shorten the curing time (j A filler is used to ensure film properties such as water resistance.The film composition is a material with high thermal conductivity and high resistance to moisture, and the higher the content of organic decomposition catalyst, the higher the content of heat-resistant binder. The smaller the amount, the smaller the amount of tar produced, but it is necessary to add 40 to 90% by weight of the heat-resistant binder to ensure adhesion to the vaporizer cylinder and skin strength.
以FJ妻体例により説明する。This will be explained below using the example of FJ wife.
捷ず、従来例について説明する。For now, a conventional example will be explained.
(1)従来の耐熱性皮膜を被覆した装置に関し、充填は
としてフェライトを含むシリコン系耐熱性結合材?使月
jしたものである。その構造は第1図に示したのと同様
で、厚さ1.6朝のアルミ処理鋼板からなる内径40朋
、晶さ30喘の気化室内壁にと記耐熱性皮膜を厚さ30
μに被覆したものである。本実施例における皮膜の20
0℃に2けるふく対重は0.80、熱伝導率は約0.8
Kcat/mh ℃である。(1) Regarding devices coated with conventional heat-resistant films, is the filling a silicon-based heat-resistant binder containing ferrite? It's been a long time since I last used it. The structure is the same as that shown in Figure 1, and the inner diameter of the vaporization chamber is 40mm and the crystallinity is 30mm, which is made of aluminized steel plate with a thickness of 1.6mm, and a heat-resistant coating is coated on the wall of the vaporization chamber with a thickness of 3mm thick.
It is coated with μ. 20 of the film in this example
The weight per square meter at 0°C is 0.80, and the thermal conductivity is approximately 0.8.
Kcat/mh °C.
本装置においてヒータおよび燃焼熱により気化筒1m、
度を350℃とし、タールの原因となる不揮発成分を3
7.5ppm含む悪質な灯油を2.8tit苅r、空気
量5.3Nn?/Hrの割合で噴霧気化し、燃焼させな
がらたい積タール量の経時変化を測定すると第3図に示
す特性線1となった。1000時間で約300■のター
ルがたい積し15000時間では12以北のタールがた
い積する見込みとなり、点火、消火時に臭気、炭化水素
、−酸炭素排出紙が増加し燃焼器として望筐しくない結
果となる。In this device, a 1 m vaporizer cylinder is heated using a heater and combustion heat.
The temperature is 350℃, and the non-volatile components that cause tar are
2.8 tits of bad kerosene containing 7.5 ppm, air volume 5.3 Nn? When the tar was sprayed and vaporized at a rate of /Hr and the amount of accumulated tar was measured over time while being combusted, a characteristic line 1 shown in FIG. 3 was obtained. Approximately 300 cm of tar is expected to accumulate in 1000 hours, and it is expected that tar north of 12 will accumulate in 15,000 hours, resulting in an increase in odor, hydrocarbon, and acid carbon emissions during ignition and extinguishing, which is not a desirable result for a combustor. becomes.
この従来皮膜は熱伝導率が低いため灯油は衝突面近傍で
核沸騰気化しここにタールがたい積する問題点を示した
。Since this conventional coating has low thermal conductivity, kerosene vaporizes by nucleate boiling near the collision surface, causing tar to accumulate there.
次に、本発明の例について1jSj’、明する。Next, an example of the present invention will be explained.
(2) 上記(1)の例と同様の気化筒に焼成後の皮膜
組μの有機物分解皮膜を形成した。(2) An organic substance decomposition film of film group μ after firing was formed on the same vaporizing cylinder as in the example of (1) above.
ン酸アルミニウム、硬化材としてリン酸ナトリウム、充
填材としてアルミナより構成されたものである。It is composed of aluminum phosphate, sodium phosphate as a hardening agent, and alumina as a filler.
この皮膜の200t:に2けるふく対重は0.90 。The weight of this film over 200 tons is 0.90.
定すると第3図に示す特性線2となった。As a result, characteristic line 2 shown in FIG. 3 was obtained.
1000時間で約4.37ntのタールがたい積し、1
5000時間でも約6myと極めて少lくなる見込みで
ある。Approximately 4.37 nt of tar was accumulated in 1000 hours, and 1
Even after 5,000 hours, it is expected to be extremely small at about 6 my.
本実施例の皮膜は熱伝導率が高いため灯油は300℃以
上で膜沸騰を起し気化室底面全域で気化した。Since the film of this example had high thermal conductivity, kerosene caused film boiling at 300° C. or higher and was vaporized over the entire bottom surface of the vaporization chamber.
(3) 第4図お牛び第5図に示すようにたて形の気化
室において灯油衝突面は金属、他の面は上記(2)の例
と同じ皮膜で被覆し、F記(1)の例と同じ条件でたい
積タール量の経時変化全測定すると第3図に示す特性線
3となった。(3) As shown in Figure 4 and Figure 5, in a vertically shaped vaporizing chamber, the kerosene collision surface is covered with metal, and the other surfaces are coated with the same film as in the example in (2) above. ) When all changes over time in the amount of accumulated tar were measured under the same conditions as in the example (2), characteristic line 3 shown in FIG. 3 was obtained.
1000時間で約3゜2〜のタールが気化室底面にたい
積した。Approximately 3°2 of tar accumulated on the bottom of the vaporization chamber in 1000 hours.
(4上記(1)の例と同じ気化筒に焼成後の皮膜組成と
して酸化ベリリウム20重量%、有機物分解触媒として
アルミナセメン)10重量%、相半結合は70重量%か
らなる厚さ約30μのイ〕機物分解皮膜を形成した。本
実施例における←結合はは主材としてケイ酸ナトリウム
、充填伺としてシリカよシ構成されたものである。この
皮膜の200℃におけるふく対重は0.82、熱伝導率
は約10Kcal/mh’cである。、(1)の例と同
じ条件でたい憤タール量の経時変化を測定すると第3図
に示す特性線4となった。1000時間で約12Tn9
のタールが気化室底面にたい積した。(4) On the same vaporizer as in the example (1) above, the film composition after firing is 20% by weight of beryllium oxide, the organic matter decomposition catalyst is alumina cement), and the phase and semi-bonds are 70% by weight. B) A biodegradable film was formed. In this example, the bond is composed of sodium silicate as the main material and silica as the filling material. The weight of this film at 200° C. is 0.82, and the thermal conductivity is about 10 Kcal/mh'c. When the change in the amount of slag tar over time was measured under the same conditions as in example (1), characteristic line 4 shown in FIG. 3 was obtained. Approximately 12Tn9 in 1000 hours
of tar accumulated on the bottom of the vaporization chamber.
(5) 上記(1)の例と同じ気化筒に焼成後の皮膜組
成として黒鉛23重量%、曇弗結合財76.8重重%、
有機物分解触媒として062重量%の白金を担持した厚
さ約30μの有機物分解皮膜を形成した。(5) The same vaporizing cylinder as in the example (1) above has a film composition after firing of 23% by weight of graphite, 76.8% by weight of cloudy composite material,
An organic matter decomposition film having a thickness of about 30 μm was formed which supported 0.62% by weight of platinum as an organic matter decomposition catalyst.
本実施例に2ける世俗結合材は主1として第1す1ン酸
アルミニウム、硬化材としてリン酸ナトリウム、充填材
としてアルミナより構成されたものである。この皮膜の
200℃にPけるふく対重は0.81 、熱伝導率は約
7 Kcat/mh ’Cである。The conventional bonding material in Example 2 is mainly composed of aluminum monosulfate (1), sodium phosphate as a hardening agent, and alumina as a filler. The P ratio of this film at 200°C is 0.81, and the thermal conductivity is about 7 Kcat/mh'C.
(1)の例と同じ条件でたい積タール量の経時変化を測
定すると第3図に示す特性線5となった。When the change over time in the amount of accumulated tar was measured under the same conditions as in example (1), characteristic line 5 shown in FIG. 3 was obtained.
1000時間で約13mgのタールが気化室底面にたい
積した。Approximately 13 mg of tar accumulated on the bottom of the vaporization chamber in 1000 hours.
(61J二記(1)の例と同じ気化筒に焼成後の皮膜組
成として黒鉛23重量%、二酸化マンガン10重量%・
個喘危11合M67重量%からなる厚さ約30μのイJ
磯物分解皮膜を形成した。本実施例における一4結′合
材は主側として第1リン酸アルミニウム硬化材どしてリ
ン酸す1−リウム、充填側としてアルミナより構成され
たものである。この皮膜の200′Cにあ・けるふ〈対
車に0.83、熱伝導率は約8 Kca l/mh ’
Cである。(1)の例と同じ条件でたい積クール量の経
時変化を測定すると第3図に示す牛1性線6となった。(The same vaporizing tube as in the example in 61J 2 (1) has a film composition of 23% by weight of graphite, 10% by weight of manganese dioxide.
I J with a thickness of about 30μ made of 11 parts M67% by weight
A rock decomposition film was formed. The 14-bond material in this embodiment is composed of 1-lium phosphate such as a primary aluminum phosphate hardening material on the main side and alumina on the filling side. At 200'C, the thermal conductivity of this film is 0.83 to the car, and the thermal conductivity is approximately 8 Kcal/mh.
It is C. When the change in the amount of accumulated cool over time was measured under the same conditions as in example (1), the result was a cow sex line 6 shown in FIG.
1000時間で約40 mgのタールが気化室底面にだ
い槓した。Approximately 40 mg of tar was deposited on the bottom of the vaporization chamber in 1000 hours.
(7) 上記(1)の例と同じ気化簡尼焼成凌の皮股甜
成として黒鉛23重量%、ゼオライ) [Ca(Na+
K )a・Al−6s i 30072 :] 88重
量%活性白土[At2Si1痴29〕2痴情9〕2ホ結
合財67重量%からlる1!?さ約30μの有機物分解
皮膜を形成した。(7) 23% by weight of graphite, zeolite) [Ca(Na+
K ) a・Al-6s i 30072: ] 88% by weight activated clay [At2Si1 29] 2 9] 2 Ho combined goods 67% by weight 1! ? An organic matter decomposition film with a thickness of about 30 μm was formed.
本実施例における綱壽結合阿は主材として第1リン酸ア
ルミニウム、硬化はとしてリン酸す1−リウム、充填材
としてアルミナより構成されたものである。この皮膜の
200℃におけるふく対車は0.83、熱伝導率は約6
Kcat/mh ’Cである。The bonding material in this embodiment is composed of dibasic aluminum phosphate as the main material, 1-lium phosphate as the hardening material, and alumina as the filler. The resistance to vehicle of this film at 200℃ is 0.83, and the thermal conductivity is approximately 6.
Kcat/mh'C.
(1)の例と同じ条件でたい積タール1丁1の経11、
−変化を測定する第3図に示す特性線7となった。Under the same conditions as in the example (1), 1 piece of tar 1 piece 11,
- The characteristic line 7 shown in FIG. 3 was obtained for measuring the change.
1000時間で約5’;zmgのタールが気化室底面に
だい(貴した。Approximately 5 zmg of tar was deposited on the bottom of the vaporization chamber in 1000 hours.
(8) 上記(1)の例と同じ気化筒に焼成後の皮11
ツ見11成としてボウ素化ジルコン20重量%、二酸化
マンカン13重量%、44結合材67重量%からlるル
さ約30/lの有機物分解皮膜を形成した。本実施例に
おける構4結合f’:A’ Fi主材としてシリコン樹
脂、充填材としてフエライ1−より構成されたものであ
る。この皮膜の200℃にPけるふく則・キモは0゜8
1、熱伝導率は約6 Kc at/mh ’Cである。(8) The skin 11 after firing is placed in the same vaporizing cylinder as in the example of (1) above.
As Tsumi 11 composition, an organic matter decomposition film having a lurity of about 30/l was formed from 20% by weight of zirconate, 13% by weight of mankane dioxide, and 67% by weight of 44 binder. In this embodiment, the structure 4 bond f': A' Fi is composed of silicone resin as the main material and ferrite 1- as the filler. The basic rule and key point of this film at 200℃ is 0°8.
1. Thermal conductivity is approximately 6 Kcat/mh'C.
(1)の例と同じ条件でたい積タール量の杆時剥化を測
定すると第3図に示す特性線8となった。When the amount of accumulated tar was measured under the same conditions as in Example (1), the characteristic line 8 shown in FIG. 3 was obtained.
1000時間で約11C1yのクールが気化室底面にた
い積した。Approximately 11C1y of cool was accumulated on the bottom of the vaporization chamber in 1000 hours.
(9)上記(1)の例と同じ気化筒に焼成後の皮膜組成
として炭化けい素20重@%、けい酸カルシウム10重
量%、徊≠結合ナオ70重量%からなる有機゛物分解皮
膜を形成した。本実施例における牛喘結合同はケイ酸ナ
トリウムを主材としシリカを充填側とするものである。(9) In the same vaporizing cylinder as in the example (1) above, an organic material decomposition film consisting of 20% by weight of silicon carbide, 10% by weight of calcium silicate, and 70% by weight of free-bonded nanocarbons after firing was applied. Formed. In this embodiment, the bovine gastrointestinal bond is made of sodium silicate as the main material and filled with silica.
この皮膜の200℃におけるふく対車は0.80、熱伝
導率は約4 Kca7/mh℃である。This coating has a coefficient of resistance of 0.80 at 200°C and a thermal conductivity of approximately 4 Kca7/mh°C.
(1)の例と同じ条件でたい積クール量の経時変化を測
定すると第3図に示す特性線9となった。When the change in the amount of stored coolant over time was measured under the same conditions as in example (1), a characteristic line 9 shown in FIG. 3 was obtained.
1000時111Aで約140++yのタールが気化室
底面にたい積した。Approximately 140++y of tar was accumulated on the bottom of the vaporization chamber at 111A at 1000 hours.
発明の効果
以北のように本発明によれば、高熱伝導性でかつiv6
ふく射性材料、有機物分解触媒および耐熱性結合−より
なる有機物分解皮膜で被覆し気化面のる■度を膜/dl
i騰温度に保持する構成とすることにより、タールたい
積の極めて少ない気化式液体燃茎1燃焼装置が鍔ら几る
。According to the present invention, it has high thermal conductivity and iv6
Coated with an organic decomposition film consisting of a radiation material, an organic decomposition catalyst, and a heat-resistant bond, the vaporization surface is coated with a film/dl.
By maintaining the temperature at an elevated temperature, a vaporizing liquid fuel combustion device with extremely little tar accumulation can be created.
第1図a、bは本発明の気化式液体燃I1.ff6焼装
置の一実施例を示す1面図Pよび断面図、第21YIは
同装置に2ける気化室の部分拡大断面図+図、第3図は
燃焼時間とたい積タール量の関係を示す特性図、第4図
a、bは本発明の他の実施例の上面図および断面図、第
S図は同装置における気化室の部分拡大断面図である。
3・・・・・・Z化IJ11.7・・・・・・電気ヒー
タ、8・・・・・・ii’u’を度検出素子3、
代J、!11人の氏名 弁卯士 中 尾 敏 男 ほか
1名第1(il
第2図
第3図
ソγ ゾ9々シ@ A’i C%)
第4図Figures 1a and 1b show the vaporized liquid fuel I1 of the present invention. 1 side view P and a sectional view showing one embodiment of the FF6 burning device, 21st YI is a partial enlarged sectional view + figure of the vaporizing chamber in 2 of the same device, and 3rd figure is a characteristic showing the relationship between combustion time and accumulated tar amount 4A and 4B are a top view and a sectional view of another embodiment of the present invention, and FIG. 4 is a partially enlarged sectional view of the vaporizing chamber in the same apparatus. 3... Z conversion IJ11.7... Electric heater, 8... ii'u' as degree detection element 3, J,! Names of 11 people Ben Ushi Toshio Nakao and 1 other person 1st figure
Claims (1)
媒および耐熱性結合材よりなる有機物分解皮膜で被覆し
た気化面を膜沸騰温度に保持する構成とした気化式液体
燃料燃焼装置。 (2)有機物分解皮膜として高熱伝導性でかつ高ふく射
性材料15〜50重量%、有機物分解触媒0.1〜15
重量%、耐熱性結合材40〜80重量形よりなる特許請
求の範囲第1項記載の気化式液体燃料燃焼装置。 (3)高熱伝導性でかつ高ふく対性材料として、炭素、
黒鉛、酸化ベリリウム、酸化マクオシラム、炭化ケイ素
、バナジウムカー/くイト、タングステン力−ノくイ)
・、チタンカーバイト、窒化ボロン、ジルコニウムポラ
イドの群から選んだ少なくとも1種以北を含む特許請求
の約1ポ第2項記載の気化式液体燃料燃焼装置。 (41有機物分解触媒として、チタン、ジルコニウム、
バナジウム、クロム、モリブデン、タンツステン、マン
ガン、鉄、コバルト、ニッケル、銅、および希土類の酸
化物、元素状の白金およびパラジウム、活性白土、ゼオ
ライ1−、ケイ酸カルシウム、アルミナ七メントおよび
炭酸カリウムの1(工カら選んだ1種以に、を含む特許
請求の範囲第2項記載の気化式液体燃料燃焼装置fff
。 (5)耐熱性結合はとして、水溶性リン酸塩塗料、水溶
性ケイ酸塩塗料、シリコン系塗料の7iYよ!l1選ん
だ特許請求の範囲第2項記載の気化人液体燃才1燃焼装
置。 (6)電気ヒータ、温度検出素子により気化室2!+1
’を度ケ膜沸騰温度に保持する構成とした特1¥l請求
の9・h囲第1項記載の気化式液体燃料燃焼装置。[Claims] (1) A vaporization system having a structure in which a vaporization surface coated with an organic decomposition film made of a highly thermally conductive and highly fused material, an organic decomposition catalyst, and a heat-resistant binder is maintained at a film boiling temperature. Liquid fuel combustion equipment. (2) 15 to 50% by weight of a material with high thermal conductivity and high radiation properties as an organic matter decomposition film, and 0.1 to 15% by weight of an organic matter decomposition catalyst.
The vaporized liquid fuel combustion device according to claim 1, comprising 40 to 80% by weight of the heat-resistant binder. (3) As a material with high thermal conductivity and high flux resistance, carbon,
Graphite, beryllium oxide, maxilum oxide, silicon carbide, vanadium carbide, tungsten carbon)
The vaporized liquid fuel combustion device according to claim 1, which includes at least one selected from the group consisting of titanium carbide, boron nitride, and zirconium polide. (41 As an organic matter decomposition catalyst, titanium, zirconium,
oxides of vanadium, chromium, molybdenum, tungsten, manganese, iron, cobalt, nickel, copper, and rare earths, elemental platinum and palladium, activated clay, zeolite, calcium silicate, alumina heptamentum, and potassium carbonate. (The vaporized liquid fuel combustion device according to claim 2, which includes one or more types selected from the engineering field)
. (5) Heat-resistant bond is 7iY of water-soluble phosphate paint, water-soluble silicate paint, and silicone paint! 11. The vaporized liquid fuel 1 combustion device as claimed in claim 2. (6) Vaporization chamber 2 with electric heater and temperature detection element! +1
The vaporized liquid fuel combustion apparatus according to item 1 of subsection 9.h of claim 1, wherein the liquid fuel combustion apparatus is configured to maintain the liquid fuel at a film boiling temperature.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58123828A JPS6016207A (en) | 1983-07-07 | 1983-07-07 | Evaporating type liquid fuel combustion device |
US06/627,726 US4616993A (en) | 1983-07-07 | 1984-07-03 | Liquid fuel combustion apparatus |
CA000458296A CA1228529A (en) | 1983-07-07 | 1984-07-06 | Liquid fuel combustion apparatus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58123828A JPS6016207A (en) | 1983-07-07 | 1983-07-07 | Evaporating type liquid fuel combustion device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6016207A true JPS6016207A (en) | 1985-01-28 |
JPH0136001B2 JPH0136001B2 (en) | 1989-07-28 |
Family
ID=14870368
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58123828A Granted JPS6016207A (en) | 1983-07-07 | 1983-07-07 | Evaporating type liquid fuel combustion device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6016207A (en) |
-
1983
- 1983-07-07 JP JP58123828A patent/JPS6016207A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0136001B2 (en) | 1989-07-28 |
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