TW201100164A - Plasma assisted catalyst reformation apparatus and method - Google Patents

Plasma assisted catalyst reformation apparatus and method Download PDF

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TW201100164A
TW201100164A TW98120992A TW98120992A TW201100164A TW 201100164 A TW201100164 A TW 201100164A TW 98120992 A TW98120992 A TW 98120992A TW 98120992 A TW98120992 A TW 98120992A TW 201100164 A TW201100164 A TW 201100164A
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recombination
chamber
preheating
plasma
catalyst
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TW98120992A
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Chinese (zh)
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TWI379710B (en
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Hung-Tsai Hu
Chao-Yuh Chen
Yu Chao
Shiaw-Huei Chen
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Iner Aec Executive Yuan
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Abstract

A plasma enhanced catalyst recombination apparatus including a feeder, a plasma reactor, a recombination reactor and a pre-heater is provided. A first recombination cavity of the recombination reactor is connected with a plasma cavity of the plasma reactor, and the recombination reactor is disposed inside a pre-heating cavity of the pre-heater. A pre-heating pipe of the pre-heater is connected between a mixing room of the feeder and the plasma cavity, and some portion of the pre-heating pipe is disposed inside the pre-heating cavity. The first recombination cavity is disposed inside a second recombination cavity of the recombination reactor. One end of a recirculation pipe of the recombination reactor is connected with a first recombination opening of the first recombination cavity and is disposed inside the first recombination cavity. Another end of the recirculation pipe is passes through a second recombination outlet of the second recombination cavity and is disposed inside the pre-heating cavity. Besides, a plasma enhanced catalyst recombination method is also provided.

Description

201100164 六、發明說明: 【發明所屬之技術領域】 本發明是有關於一種觸媒重組裝置與方法,且特別是 有關於一種電漿辅助觸媒重組裝置與方法。 【先前技術】 隨著科技的進步,可用能源也趨向多樣化的發展,而 特別是透過觸媒重組的方式可使石化燃料或生質燃料轉換 〇 成氫氣燃料。一般來說,天然瓦斯、酒精、曱烷、丁烷等 等碳氫氣體或碳氫液體可在高溫下,透過觸媒重組的方式 而轉換為氳氣燃料,而氫氣燃料是目前所認為較為環保的 燃料之一。 傳統的觸媒重組裝置必須要先利用輔助燃燒器或電熱 器先行加熱觸媒床,直到觸媒床達到工作溫度後才通入加 熱後之碳氫氣體與空氣進行部份氧化重組反應以轉換為氳 氣,並藉由部份氧化重組反應所產生的熱量以維持觸媒床 Q 的溫度,藉以關閉辅助燃燒器或電熱器。 然而,輔助燃燒器或電熱器通常為體積龐大且較為危 ' 險的構件,並僅用於先行加熱觸媒床,在使用上非常沒有 - 效率。 另一種傳統的觸媒重組裝置是用於碳氫液體的重組, 主要是利用鍋爐來加熱碳氫液體與水份而使其汽化成高溫 氣體,藉以加熱觸媒床而進行重組反應,故此觸媒重組裝 置必須持續運作鍋爐來加熱碳氫液體與水份。然而,鍋爐 加熱的效率過差,使得能量損耗較大,且鍋爐通常亦為體 201100164 積龐大且危險的構件。 =外,習知技藝另有提出電_助觸媒重組裝置,利 =電漿反絲產生高壓高頻的交流%,藉以產生放電來加 =^氣體與空氣,藉以將㈣化<碳氩氣體與空氣加熱 2床以使觸媒床達到卫作溫度而產生重組反應。當觸媒 :::度到達上限值時’便可切斷電聚反應器電源,且當 、的μ度下降至下限值時’便重新恢復電漿反應器電 Ο 另外,美國第632^號專利、美國第6,綱,95〇號 =、美國第6,506,359號專利則是以前述習知技藝再稍加 (。然而’無論是針對碳氫纽或錢㈣,均都 名外配置加熱H具以加熱觸媒床到達卫作溫度,使得觸 重㈣置整體的體積非常龐大,且非f危險。再者,加熱 益具的加減率均不甚理想,且均在滅換媒 ^ 程中浪費許多能量。 〇 【發明内容】 • 有鏗於此,本發明之目的是提供一種電漿辅助觸媒重 ,裝置,將高溫重組反應器包覆在預熱器内,並利用再循 %盲的配置以導引熱源,可有效利用熱源並大幅縮減觸媒 重組裝置的體積。 、 此外’本發明之另一目的是提供一種電漿輔助觸媒重 組方法,利用先對碳氫液體進行霧化後,再對碳氫液體加 熱進行汽化。由於霧化後的碳氫液體具有較大的表面積, 可大幅提升加熱的效率。 201100164 為達上述或是其他目的,本發明提出一種電漿輔助觸 媒重組裝置,包括進料器、電漿反應器、重組反應器以及 預熱益’其中重組反應器是連接電漿反應器。進料器具有 混合至’而電漿反應器包括電漿腔體、電漿電極與電漿電 源供應單元,其中電漿腔體具有電漿腔入口與電漿腔出 口將而電漿電源供應單元耦接電漿腔體與電漿電極,以於 Ο Ο s n生放t (disetoge)。重組反應器包括第一重組 弟一重組腔體、再循環管、多孔板以及第一觸媒床。 1看f組腔體具有第—重組腔人口、第—重組腔出口與第 組腔開口,而第一重組腔入口連接電漿腔出口。 ^腔體是位於第二重組腔體内,而第二重組腔體具有第 -重組腔出口。再循環管是第內 再循環管之—龄趁楚h a 腔體内’而 -端是姆“ 腔開口,且再循環管之另 :广第一重組腔出口而穿出第二重組腔出 孔 -第一重組腔體内’並鄰近第一重虹腔入口。第 Μ括^配置於第—重組腔體與第二重組腔體内。預孰 t 7腔體與賴管,其中重組反應以位於預孰腔 …内’且預熱腔體具有預熱腔人口與預熱腔出口 ^ 官是配置於預熱腔體内,並環繞重組反應器 予^ -端是連接電衆腔入口,又預熱管之另 入口以連接混合t。 腔 為達上述或是其他目的,本發明另提出一種 觸媒重組方法’包括下列步驟:提供壓電霧化單元將 空氣;混合空氣以及霧化之碳= 體與水伤,颇霧化之碳驗體與水錢化;提供電裝反 7 201100164 應器將空氣以及氣化之碳氫液體與水份激發為準中性混合 氣體;提供重組反應器將準中性混合氣體進行重組形成高 溫反應氣體,並將高溫反應氣體進行重組形成高溫重組氣 體,且高溫重組氣體適於加熱霧化之碳氫液體與水份,以 使霧化之碳氫液體與水份氣化。 在本發明之一實施例中,其中空氣與碳氫氣體是在混 合室混合,並沿預熱管進入電漿腔體而成為準中性混合氣 體,準中性混合氣體進入第一重組腔體内而在第一觸媒床 〇 中進行重組形成高溫反應氣體,高溫反應氣體自第一重組 腔出口進入第二重組腔體内而在第一觸媒床中進行重組形 成高溫重組氣體,高溫重組氣體自第一重組腔開口進入再 循環管,而沿再循環管進入預熱腔體中以加熱預熱管内之 空氣與碳氫氣體,且自預熱腔出口離開預熱腔體。 在本發明之一實施例中,上述之進料器更可具有第一 調節閥與第二調節閥,而第一調節閥與第二調節閥是連接 混合室,以分別控制空氣與碳氳氣體進入混合室之流量。 q 在本發明之一實施例中,上述之再循環管於第一重組 腔體内之部分例如為盤管。 * 在本發明之一實施例中,上述之預熱管之一端連接電 -漿腔入口的方向例如是偏離電漿腔體中心。 在本發明之一實施例中,上述之預熱器更可包括盤狀 預熱通道,配置於預熱腔體内,並連接於預熱管之一端與 電漿腔入口之間。 在本發明之一實施例中,上述之重組反應器更可包括 第一分隔板與第二分隔板,而第一分隔板是配置於第一重 8 201100164 組腔體内,且第二分隔板是配置於第二重組腔體内。第一 分隔版可為十字分隔板或井字分隔板。 ‘在本發明之一實施例中,上述之預熱器更可包括第三 ' 分隔板,而第三分隔板是配置於預熱腔體内,以將預熱腔 體區分為相連之第一預熱區與第二預熱區。此外,預熱管 是沿第一預熱區與第二預熱區雙層環繞重組反應器。另 外,預熱器更可包括第二觸媒床、第三觸媒床與第四觸媒 床,而第二觸媒床位於第一預熱區,且第三觸媒床位於第 0 一預熱區與第二預熱區交界處,又第四觸媒床位於第二預 熱區。第二觸媒床可具有高溫水氣轉換觸媒,而第三觸媒 床可具有低溫水氣轉換觸媒,且第四觸媒床可具有一氧化 碳選擇性氧化觸媒。 在本發明之一實施例中,上述之進料器更可具有壓電 霧化單元,且壓電霧化單元是連接混合室。碳氫液體與水 份是在壓電霧化單元中形成霧化之碳氫液體與水份而進入 混合室,以與進入混合室之空氣混合後進入預熱管内,霧 Q 化之碳氫液體與水份於預熱管内形成氣化之碳氳液體與水 份,並與空氣沿預熱管進入電漿腔體而成為準中性混合氣 ' 體,準中性混合氣體進入第一重組腔體内而在第一觸媒床 , 中進行重組形成高溢反應氣體,高溫反應氣體自第一重組 腔出口進入第二重組腔體内而在第一觸媒床中進行重組形 成高溫重組氣體,高溫重組氣體自第一重組腔開口進入再 循環管,而沿再循環管進入預熱腔體中以加熱預熱管内之 空氣、霧化之碳氫液體與霧化之水份,且自預熱腔出口離 開預熱腔體。 9 201100164 在本發明之一實施例中,上述之碳氫液體例如為酒精 或液化石油氣。 在本發明之一實施例中,上述之進料器更可具有第一 調節閥、第三調節閥與第四調節閥,而第一調節閥是連接 混合室以控制空氣流量,且第三調節閥與第四調節閥是連 接壓電霧化單元,以分別控制碳氳液體與水份之流量。 在本發明之一實施例中,上述之預熱腔體更具有預熱 腔開口,以使空氣自預熱腔開口進入預熱腔體内。此外, 0 進料器更具有第五調節閥,而第五調節閥是連接預熱腔開 口以控制空氣流量。 綜上所述,在本發明之電漿輔助觸媒重組裝置與方法 中,藉由再循環管的配置,可讓觸媒床的溫度均勻分佈且 使空氣與碳氫氣體得以均勻地流過多孔性的觸媒而充分利 用,藉此以縮小電漿辅助觸媒重組裝置的體積,並提高碳 氳氣體重組為氫氣的效率。 為讓本發明之上述和其他目的、特徵和優點能更明顯 Q 易懂,下文特舉較佳實施例,並配合所附圖式,作詳細說 明如下。 【實施方式】 圖1A為依據本發明一實施例之電漿輔助觸媒重組裝 置的剖面示意圖,而圖1B為圖1A之電漿輔助觸媒重組裝 置省略繪示第一觸媒床的剖面示意圖。請參考圖1A〜1B, 本發明之電漿辅助觸媒重組裝置1〇〇包括電漿反應器 110、重組反應器120、預熱器130以及進料器140,而這 10 201100164 些構件間錯綜複雜的連接方式便是本發明的精神,藉以達 到心加重組效率與熱源使用效率的目的。以下先分別介紹 各個構件與其連接關係,接著再說明本發明重組的詳細過 程0 電漿反應器110包括電漿腔體112、電漿電極114與 電漿電源供應單元116,其中電漿電源供應單元116是耦 接電漿腔體112與電漿電極114,藉由供應高壓高頻的交 流電,可於電漿腔體112内產生電弧放電,以游離電衆腔 Ο 體112内的氣體(之後會再詳述此氣體為空氣、碳氫氣體或 氣化之碳氫液體等混合氣體)。 此外’電漿腔體112具有電漿腔入口 112a與電聚腔出 口 112b’而前述之氣體便是由電漿腔入口 i12a進入電漿 腔體112,並在被游離後從電漿腔出口 U2b離開電聚腔體 112’其中電聚反應器no是連接重組反應器120,而使離 開電漿腔體112後的氣體便會進入重組反應器120。 重組反應器120包括第一重組腔體121、第二重組腔 Q 體122、再循環管I23、多孔板124以及第一觸媒床125, 其中第一重組腔體121是位於第二重組腔體122内,且第 ‘ 一觸媒床125是配置於苐一重組腔體121與第二重組腔體 , 122 内。 、 在本實施例令,第一重組腔體121與第二重組腔體122 的形狀均為圓桶狀,且第一重組腔體121與第二重纽腔體 122的中心線重疊並對齊電漿腔體112的中心線以方便組 裝運作’不過本發明並不限定第一重組腔體121與第二重 組腔體122的形狀。 201100164 ⑵m:重組腔體121具有相對之第-重組腔入口 ,、第重、,且腔出口 121b,而第一重袓胪入口 12 接電漿腔出口 112b,以# _ 工 連 σ & 乂使游離後之軋體可由第一重組腔入 口 121a進入第一舌鈿純 , 、m应虛杜腔入口 121a内而與第一觸媒床⑵ 第體 重組腔出σ 121b進入 f 一重、腔體122内而輯與第—觸媒床Π5進行重組反 應0 Ο201100164 VI. Description of the Invention: [Technical Field] The present invention relates to a catalyst recombination apparatus and method, and more particularly to a plasma assisted catalyst recombination apparatus and method. [Prior Art] With the advancement of technology, the available energy has also become more diversified, and in particular, the conversion of fossil fuel or biomass fuel into hydrogen fuel can be achieved through catalyst recombination. In general, natural gas, alcohol, decane, butane and other hydrocarbon gases or hydrocarbon liquids can be converted to helium fuel at high temperatures through recombination of the catalyst, which is currently considered to be more environmentally friendly. One of the fuels. The conventional catalyst recombination device must first use an auxiliary burner or an electric heater to heat the catalyst bed first, until the catalyst bed reaches the working temperature, and then the heated hydrogen sulfide gas and the air are subjected to partial oxidation recombination reaction to be converted into Helium, and the heat generated by the partial oxidation recombination reaction to maintain the temperature of the catalytic bed Q, thereby turning off the auxiliary burner or the electric heater. However, auxiliary burners or electric heaters are usually bulky and dangerous components and are only used to heat the catalyst bed first, and there is very little efficiency in use. Another conventional catalyst recombination device is used for the recombination of hydrocarbon liquids, mainly by using a boiler to heat a hydrocarbon liquid and water to vaporize it into a high temperature gas, thereby heating the catalyst bed for recombination reaction, so the catalyst The reconstitution unit must continue to operate the boiler to heat the hydrocarbon liquid and water. However, the efficiency of boiler heating is too low, resulting in a large energy loss, and the boiler is usually a large and dangerous component of the body 201100164. In addition, the conventional technique also proposes an electric-assisted catalyst recombination device, which generates a high-voltage high-frequency alternating current %, thereby generating a discharge to add a gas and air, thereby (4) < carbon argon. The gas and air are heated for 2 beds to cause the catalyst bed to reach the temperate temperature to produce a recombination reaction. When the catalyst::: degree reaches the upper limit value, 'the power of the electropolymer reactor can be cut off, and when the μ degree drops to the lower limit value, the plasma reactor power is restored. In addition, the US 632 The ^ patent, the US sixth, the outline, the 95 = =, the US 6,506, 359 patent is a little more than the aforementioned conventional skills. (However, whether it is for carbon hydride or money (four), all are equipped with heating H has the temperature of the heating catalyst bed to reach the temperature of the maintenance, so that the overall weight of the weight (4) is very large, and it is not dangerous. In addition, the addition and subtraction rate of the heating utility is not ideal, and both are in the process of extinguishing the medium. A lot of energy is wasted. 〇 [Summary] In view of this, the object of the present invention is to provide a plasma-assisted catalyst weight, device, and a high-temperature recombination reactor coated in a preheater, and The blind configuration to guide the heat source can effectively utilize the heat source and greatly reduce the volume of the catalyst recombination device. Further, another object of the present invention is to provide a plasma-assisted catalyst recombination method, which utilizes a mist for a hydrocarbon liquid first. After heating, the hydrocarbon liquid is heated and steamed. Since the atomized hydrocarbon liquid has a large surface area, the heating efficiency can be greatly improved. 201100164 For the above or other purposes, the present invention provides a plasma assisted catalyst recombining device, including a feeder and a plasma. a reactor, a recombination reactor, and a preheating reactor in which the recombination reactor is connected to a plasma reactor. The feeder has a mixing to 'the plasma reactor includes a plasma chamber, a plasma electrode, and a plasma power supply unit, The plasma chamber has a plasma chamber inlet and a plasma chamber outlet, and the plasma power supply unit is coupled to the plasma chamber and the plasma electrode, so as to generate a t (disetoge). The recombination reactor includes A recombination chamber, a recombination chamber, a recirculation tube, a perforated plate, and a first catalyst bed. 1 see that the f group cavity has a first-recombination cavity population, a first-recombination cavity outlet and a first group cavity opening, and the first recombination cavity The inlet is connected to the outlet of the plasma chamber. The cavity is located in the second recombination chamber, and the second recombination chamber has the outlet of the first recombination chamber. The recirculation tube is the inner recirculation tube--the age of the cavity 'And-end is the m' cavity Opening, and the recirculation tube is another: the first recombination chamber outlet passes through the second recombination chamber outlet-first recombination chamber and is adjacent to the first re-nuclear chamber inlet. a cavity and a second recombination cavity. Pre-t7 cavity and a sluice tube, wherein the recombination reaction is located in the pre-chamber cavity... and the preheating cavity has a preheating cavity population and a preheating cavity outlet. In the preheating chamber, and surrounding the recombination reactor, the end is connected to the entrance of the electric chamber, and the other inlet of the preheating tube is connected to the mixing t. The cavity is for the above or other purposes, and the invention further provides a touch The medium recombination method includes the following steps: providing a piezoelectric atomizing unit to supply air; mixing air and atomized carbon = body and water injury, relatively atomized carbon test body and water money; providing electric equipment counter 7 201100164 Exciting the air and the vaporized hydrocarbon liquid and water into a quasi-neutral mixed gas; providing a recombination reactor to recombine the quasi-neutral mixed gas to form a high temperature reaction gas, and recombining the high temperature reaction gas to form a high temperature reformed gas, and High temperature recombination gas suitable for heating fog The hydrocarbon liquid and water are used to vaporize the atomized hydrocarbon liquid and water. In an embodiment of the invention, the air and the hydrocarbon gas are mixed in the mixing chamber and enter the plasma chamber along the preheating tube to become a quasi-neutral mixed gas, and the quasi-neutral mixed gas enters the first recombination chamber. Internally, the first catalyst bed is recombined to form a high-temperature reaction gas, and the high-temperature reaction gas enters the second recombination chamber from the outlet of the first recombination chamber to be recombined in the first catalyst bed to form a high-temperature recombination gas, and the high-temperature recombination gas The gas enters the recirculation tube from the first recombination chamber opening and enters the preheating chamber along the recirculation tube to heat the air and hydrocarbon gas in the preheating tube and exit the preheating chamber from the preheating chamber outlet. In an embodiment of the invention, the feeder may further have a first regulating valve and a second regulating valve, and the first regulating valve and the second regulating valve are connected to the mixing chamber to respectively control air and carbon helium gas. The flow into the mixing chamber. q In one embodiment of the invention, the portion of the recirculation tube described above within the first recombination chamber is, for example, a coil. * In an embodiment of the invention, the direction in which one end of the preheating tube is connected to the inlet of the electro-plasma chamber is, for example, offset from the center of the plasma chamber. In an embodiment of the invention, the preheater may further include a disk-shaped preheating passage disposed in the preheating chamber and connected between one end of the preheating tube and the inlet of the plasma chamber. In an embodiment of the present invention, the recombination reactor may further include a first partition plate and a second partition plate, and the first partition plate is disposed in the first weight 8 201100164 group cavity, and the first The two partition plates are disposed in the second recombination chamber. The first divider can be a cross divider or a ticker. In an embodiment of the present invention, the preheater may further include a third 'dividing plate, and the third dividing plate is disposed in the preheating chamber to distinguish the preheating cavity into a connected one. The first preheating zone and the second preheating zone. Further, the preheating tube is a double-layered recombination reactor along the first preheating zone and the second preheating zone. In addition, the preheater may further include a second catalyst bed, a third catalyst bed and a fourth catalyst bed, wherein the second catalyst bed is located in the first preheating zone, and the third catalyst bed is located in the first preheating zone. At the junction of the hot zone and the second preheating zone, the fourth catalyst bed is located in the second preheating zone. The second catalyst bed may have a high temperature water gas shift catalyst, and the third catalyst bed may have a low temperature water gas shift catalyst, and the fourth catalyst bed may have a carbon monoxide selective oxidation catalyst. In an embodiment of the invention, the feeder is further provided with a piezoelectric atomizing unit, and the piezoelectric atomizing unit is connected to the mixing chamber. The hydrocarbon liquid and water are formed into a mixing chamber by forming an atomized hydrocarbon liquid and water in the piezoelectric atomizing unit, and are mixed with the air entering the mixing chamber to enter the preheating tube, and the mist-hydrogenated hydrocarbon liquid Forming a vaporized carbon crucible liquid and moisture with water in the preheating tube, and entering the plasma chamber along the preheating tube to form a quasi-neutral mixture, and the quasi-neutral mixed gas enters the first recombination chamber Recombining in the first catalyst bed to form a high-spiking reaction gas, and the high-temperature reaction gas is recombined in the first catalyst bed to form a high-temperature recombination gas from the outlet of the first recombination chamber into the second recombination chamber, The high temperature reformed gas enters the recirculation pipe from the opening of the first recombination chamber, and enters the preheating chamber along the recirculation tube to heat the air in the preheating tube, the atomized hydrocarbon liquid and the atomized water, and self preheating The chamber outlet exits the preheating chamber. 9 201100164 In an embodiment of the invention, the hydrocarbon liquid described above is, for example, alcohol or liquefied petroleum gas. In an embodiment of the invention, the feeder may further have a first regulating valve, a third regulating valve and a fourth regulating valve, and the first regulating valve is connected to the mixing chamber to control the air flow, and the third regulating The valve and the fourth regulating valve are connected to the piezoelectric atomizing unit to separately control the flow rate of the carbon dioxide liquid and the water. In an embodiment of the invention, the preheating chamber further has a preheating chamber opening to allow air to enter the preheating chamber from the preheating chamber opening. In addition, the 0 feeder has a fifth regulator valve, and the fifth regulator valve is connected to the preheat chamber opening to control the air flow. In summary, in the plasma assisted catalyst recombination apparatus and method of the present invention, by the arrangement of the recirculation pipe, the temperature of the catalyst bed can be uniformly distributed and the air and the hydrocarbon gas can be uniformly flowed through the porous The catalyst is fully utilized to reduce the volume of the plasma-assisted catalyst recombination device and to increase the efficiency of carbon monoxide gas recombination into hydrogen. The above and other objects, features, and advantages of the present invention will become more apparent from the understanding of the appended claims. 1A is a cross-sectional view of a plasma assisted catalyst recombination apparatus according to an embodiment of the present invention, and FIG. 1B is a cross-sectional view of the plasma assisted catalyst recombination apparatus of FIG. 1A, which is omitted from the first catalyst bed. . Referring to FIGS. 1A to 1B, the plasma assisted catalyst recombination apparatus 1 of the present invention includes a plasma reactor 110, a recombination reactor 120, a preheater 130, and a feeder 140, and these 10 201100164 components are complicated. The connection method is the spirit of the present invention, so as to achieve the purpose of heart recombination efficiency and heat source use efficiency. The following describes the respective components and their connection relationship, and then describes the detailed process of the reorganization of the present invention. The plasma reactor 110 includes a plasma chamber 112, a plasma electrode 114 and a plasma power supply unit 116, wherein the plasma power supply unit 116 is coupled between the plasma chamber 112 and the plasma electrode 114. By supplying high-voltage high-frequency alternating current, an arc discharge can be generated in the plasma chamber 112 to free the gas in the cavity 112 (afterwards) Further, this gas is a mixed gas such as air, hydrocarbon gas or vaporized hydrocarbon liquid). In addition, the plasma chamber 112 has a plasma chamber inlet 112a and an electropolymer chamber outlet 112b', and the aforementioned gas enters the plasma chamber 112 from the plasma chamber inlet i12a, and is discharged from the plasma chamber outlet U2b after being released. Leaving the electropolymerization chamber 112' wherein the electropolymerization reactor no is connected to the recombination reactor 120, and the gas leaving the plasma chamber 112 enters the recombination reactor 120. The recombination reactor 120 includes a first recombination chamber 121, a second recombination chamber Q body 122, a recirculation tube I23, a perforated plate 124, and a first catalyst bed 125, wherein the first recombination chamber 121 is located in the second recombination chamber 122, and the first catalyst bed 125 is disposed in the first recombination cavity 121 and the second recombination cavity 122. In this embodiment, the first recombination cavity 121 and the second recombination cavity 122 are all in the shape of a barrel, and the center lines of the first recombination cavity 121 and the second re-ball cavity 122 are overlapped and aligned. The centerline of the slurry cavity 112 is convenient for assembly operations. However, the present invention does not limit the shape of the first recombination cavity 121 and the second recombination cavity 122. 201100164 (2) m: the recombination cavity 121 has a relative first-recombination cavity inlet, a third weight, and a cavity outlet 121b, and the first heavy-duty inlet 12 is connected to the plasma chamber outlet 112b, with #_工连σ & The free rolling body can be made into the first tongue and groove pure from the first recombination chamber inlet 121a, and the m should be in the virtual chamber inlet 121a and the first catalyst bed (2) is recombined with the first unit bed σ 121b into the f-weight, cavity 122 internal and the first - catalyst bed Π 5 for recombination reaction 0 Ο

亦即依據氣體在第一觸媒床125的流向,可將第一觸 媒床125 A致區分為位於第-重組腔體m内鄰近-重組 腔入口 121a之重組反應前段、位於第一重組腔體κι與第 -重組腔體122交界處之重組反應巾段,以及位於第二重 組腔體122内鄰近一重址腔入口 121&之重組反應後段。當 然’將第一觸媒床125區分為三段僅是為求方便說明’而 貝貝進行重組反應的過程並無不同。 為使氣體從第一重組腔入口 12ia進入第一重組腔體 121後能均勻分佈,本發明可將多孔板124配置於第一重 組腔體121内’並鄰近第一重組腔入口 i2la。如此一來, 藉由多孔板124的擴散效果,可使氣體均勻通過多孔板124 而與第一觸媒床125進行反應。 一般來說’當氣體通過多孔板Π4後,由於第一重組 腔體121與第二重組腔體丨22的幾何配置方式,氣體仍無 法完全均勻地通過第一觸媒床125,而是會以最短的路徑 通過第一觸媒床125而到達第一重組腔出口 121b。上述現 象通常稱為氣流短路(flow-short-circuit)或通路效應 (channeling effect)問題,而使氣體在流動的過程中接觸最 12 201100164 少的觸媒。 為解決上述缺點,本發明於第一重組腔體I。再開設 第一重組腔開口 121C,並於第二重組腔體122開設 、、且腔出口 122a,其中第—重組腔開口 121c可開設於第一觸 媒床125的重組反應後段區域’而第二重組腔出口、12仏是 鄰近第一重組腔出口 121b,而可開設於第一觸媒床125 = 重組反應中段區域。That is, according to the flow direction of the gas in the first catalyst bed 125, the first catalyst bed 125 A can be divided into a recombination reaction front stage located in the first-recombination cavity m adjacent to the recombination chamber inlet 121a, and located in the first recombination chamber. The recombination reaction towel segment at the junction of the body κι and the first recombination cavity 122, and the recombination reaction segment located in the second recombination cavity 122 adjacent to a relocation chamber inlet 121& Of course, the process of dividing the first catalyst bed 125 into three sections is for convenience only, and Babe's process of recombination reaction is not different. In order to allow the gas to be evenly distributed from the first recombination chamber inlet 12ia into the first recombination chamber 121, the present invention can dispose the perforated plate 124 within the first recombination chamber 121 and adjacent to the first recombination chamber inlet i2la. As a result, the gas can be uniformly reacted with the first catalyst bed 125 through the porous plate 124 by the diffusion effect of the porous plate 124. Generally speaking, after the gas passes through the perforated plate 4, due to the geometric arrangement of the first recombination cavity 121 and the second recombination cavity 22, the gas still cannot pass the first catalyst bed 125 completely uniformly, but instead The shortest path passes through the first catalyst bed 125 to the first recombination chamber outlet 121b. These phenomena are often referred to as flow-short-circuit or channeling effects, which cause the gas to contact the most catalysts during the flow. In order to solve the above disadvantages, the present invention is in the first recombination chamber 1. The first recombination cavity opening 121C is opened, and the second recombination cavity 122 is opened, and the cavity outlet 122a, wherein the first recombination cavity opening 121c can be opened in the recombination reaction rear section area of the first catalyst bed 125 and the second The recombination chamber outlet, 12 仏 is adjacent to the first recombination chamber outlet 121b, and can be opened in the first catalyst bed 125 = recombination reaction mid-section region.

承接上述,再循環管123是部分位於第一重組腔體121 内而再循環官123之一端是連接第一重組腔開口 , 且循環官123之另一端是經由第一重組腔出口 121b而穿 出第二重組腔出口 122a。再循環管123於第一重組腔體121 ,的部份可視為是障礙物,以阻止氣體以最短的方式通過 第一觸媒床125的重組反應前段區域。 如此一來,氣體乃以較長的路徑通過第—觸媒床125 的重組反應前段區域,藉此接觸較多的觸媒以提升重組反 ,的效率。此外,再循環管123於第一重組腔體121内的 ,份可為盤管而呈現不規則的排列,藉以避免發生前述之 氣流短路問題。 請在參考圖ΙΑ〜1B,預熱器13〇包括預熱腔體Η〕 與預熱管134,其中重組反應器120是位於預熱腔體132 内’且預熱腔體132具有預熱腔出口 132b。當氣'體流經到 第一觸媒床125的重組反應後段區域後,便會經由第一重 組腔開口 121c而流進再循環管123,並順著再循環管Η] 流出重組反應器120而進入預熱腔體132内,且最終完成 重組反應的氣體便會充滿整個預熱腔體132而從預熱腔出 13 201100164 . 口 132被收集利用。 - 此外,預熱腔體132另具有預熱腔入口 132a,而預埶 • f 134是配置於預熱腔體1心,並環繞重組反應器120。 另外,預熱官134之一端是連接電漿腔入口 112a,又預熱 官134之另一端是穿出預熱腔入口 U2a以連接進料器14〇 之混合室142。如此一來,氣體最初是在混合室142進行 混合,而經由預熱管134進入電聚腔體112内進行游離反 應。 〇 Μ帶—提的是’再循環管123之另-端在穿出第二重 組腔出口 122a後,可配設在預熱腔體132内的任何位置, 而在本實施例t,再循環管123之另一端是配置在鄰近電 漿腔體112的預熱管134附近,藉以加熱預熱管134内的 氣體。 在大致說明本發明之電漿辅助觸媒重組裝置1〇〇之各 個構件間複雜的配置之後,以下將具體以甲烷之碳氫氣體 說明電漿輔助觸媒重組裝置100的操作流程。不過本發明 ❹ 並不限定破虱氣體的種類,舉凡乙燒、丙烧、瓦斯等等之 碳氫氣體亦可適用。 以觸媒進行重組反應的過程中,若需要碳氫氣體能重 組成預期的氫氣或一氧化碳,則觸媒的溫度必須高於工作 溫度,且碳氫氣體是要進行部份氧化重纽反應(不完全燃燒) 始能轉換為氫氣或一氧化碳。為使觸媒的溫度高於工作溫 度,本發明是先通入碳氫氣體進行完全氧化重組反應(完全 燃燒)’藉以釋放出大量的熱量至第一觸媒床125中以進行 預熱的過程。 14 201100164 、 當觸媒的溫度高於工作溫度後,便將碳氫氣體改為進 行部份氧化重組反應以產生氫氣,而碳氫氣體是進行部份 或元全氧化重組反應的關鍵條件便是調整破氫氣體與空氟 的比例。以甲烷為例,若甲烷對空氣的比例愈低’則較為 容易進行完全氧化重組反應,相反地,若甲嫁對空氣的比 例愈高’則較為容易進行部份氧化重組反應。 如此一來,本發明並不需要額外再增設任何的輔助加 熱器,便可直接以前述的設備將碳氫氣體完全燃燒而對第 〇 一觸媒床125進行加熱藉此.可降低建置成本、減少整體 設備體積並避免設置輔助加熱器所帶來的危險性。 請再參考圖1A〜1B’進料器140更可具有第一調節闕 145與第二調節閥146,而第一調節閥145與第二調節闕 146是連接混合室142’以分別控制空氣(未緣示)與甲烷(未 繪示)進入混合室之流量。在本實施例之起機(預熱)階段, 首先是打開第一調節閥145與第二調節閥146而使空氣與 曱烷進入混合室142進行混合,其中空氣與甲烷的流量比 ❹ 為20 : 1(亦即氧碳比為4.2 : 1)。 接著,空氣與甲烷便沿著預熱管134而進入電漿腔體 112,並藉由電漿腔體112内的放電現象而活化。詳細而 ' 言,部份的空氣與甲烷會受到非熱電漿的高能量電子衝擊 而產生游離(Ionization)、解離(Dissociation)、激發 (Excitation)等等反應,進而形成含有離子(Ion)、電子 (Electron)與自由基(Free Radical)的準中性混合氣體(未繪 示)。 前述之準中性混合氣體便會進入第一重組腔體121而 15 201100164 進打完全燃,而釋放出大量的熱量以加熱第一觸媒床 12^,藉以使第—觸媒床125巾的觸媒溫度上升。儘管甲烧 在π全燃燒時可釋放出最大的熱量’但是此燃燒是發生在 空氣與甲院接觸到第—觸媒床125之前的混合狀態,所以 甲院所釋放出的熱量無法完全經由氣相(職的线與曱 烷)至固相(觸媒)的傳導而傳遞至第一觸媒床125。 、值得注意的是’本實施例是先將空氣與曱烷混合後再 ΟIn response to the above, the recirculation tube 123 is partially located in the first recombination chamber 121 and one end of the recirculation officer 123 is connected to the first recombination chamber opening, and the other end of the circulation official 123 is pierced through the first recombination chamber outlet 121b. The second recombination chamber outlet 122a. The portion of the recirculation tube 123 in the first recombination chamber 121 can be considered an obstacle to prevent gas from passing through the recombination reaction front region of the first catalyst bed 125 in the shortest manner. In this way, the gas passes through the recombination reaction front region of the first catalyst bed 125 in a longer path, thereby contacting more catalyst to improve the efficiency of the recombination reaction. In addition, the portions of the recirculation tube 123 in the first recombination chamber 121 may be arranged in an irregular arrangement for the coil to avoid the aforementioned short-circuit problem of the air flow. Referring to FIGS. 1 to 1B, the preheater 13 includes a preheating chamber Η and a preheating tube 134, wherein the recombination reactor 120 is located in the preheating chamber 132 and the preheating chamber 132 has a preheating chamber. Exit 132b. When the gas flows through the rear reaction region of the first catalyst bed 125, it flows into the recirculation pipe 123 through the first recombination chamber opening 121c, and flows out of the recombination reactor 120 along the recirculation pipe. The gas entering the preheating chamber 132 and finally completing the recombination reaction will fill the entire preheating chamber 132 and exit the preheating chamber 13 201100164. The port 132 is collected and utilized. In addition, the preheating chamber 132 further has a preheating chamber inlet 132a, and the pre-flushing unit f 134 is disposed in the center of the preheating chamber 1 and surrounds the recombination reactor 120. Further, one end of the preheating 134 is connected to the plasma chamber inlet 112a, and the other end of the preheating 134 is a mixing chamber 142 which passes through the preheating chamber inlet U2a to connect the feeder 14'. As a result, the gas is initially mixed in the mixing chamber 142 and enters the electropolymerization chamber 112 via the preheating tube 134 for free reaction. The present invention is that the other end of the recirculation tube 123 can be disposed at any position within the preheating chamber 132 after passing through the second recombination chamber outlet 122a, and in this embodiment t, recirculation The other end of the tube 123 is disposed adjacent to the preheating tube 134 adjacent to the plasma chamber 112, thereby heating the gas in the preheating tube 134. After roughly explaining the complicated configuration between the respective members of the plasma assisted catalyst recombination apparatus 1 of the present invention, the operation flow of the plasma assisted catalyst recombination apparatus 100 will be specifically described below with the hydrocarbon gas of methane. However, the present invention does not limit the type of gas to be destroyed, and hydrocarbon gas such as ethylene, propylene, gas, etc. may also be used. In the process of recombination reaction with a catalyst, if hydrocarbon gas is required to recombine the desired hydrogen or carbon monoxide, the temperature of the catalyst must be higher than the working temperature, and the hydrocarbon gas is subjected to partial oxidation heavy reaction (incomplete Combustion) can be converted to hydrogen or carbon monoxide. In order to make the temperature of the catalyst higher than the working temperature, the present invention firstly introduces a hydrocarbon gas to perform a complete oxidation recombination reaction (complete combustion), thereby releasing a large amount of heat to the first catalyst bed 125 for preheating. . 14 201100164 、 When the temperature of the catalyst is higher than the working temperature, the hydrocarbon gas is changed to a partial oxidation recombination reaction to generate hydrogen, and the key condition for the hydrocarbon gas to undergo partial or partial total oxidation recombination reaction is Adjust the ratio of hydrogen-destroying gas to empty fluorine. In the case of methane, if the ratio of methane to air is lower, it is easier to carry out a complete oxidative recombination reaction. Conversely, if the ratio of a marry to air is higher, the partial oxidation recombination reaction is easier. In this way, the present invention does not require any additional auxiliary heaters, and the first catalyst bed 125 can be directly heated by the above-mentioned equipment to completely burn the hydrocarbon gas, thereby reducing the construction cost. Reduce the overall equipment volume and avoid the danger of setting up the auxiliary heater. Referring again to FIGS. 1A to 1B, the feeder 140 may further have a first regulator 145 and a second regulator 146, and the first regulator 145 and the second regulator 146 are coupled to the mixing chamber 142' to control the air ( The flow rate of entering the mixing chamber with methane (not shown). In the starting (preheating) phase of the embodiment, first, the first regulating valve 145 and the second regulating valve 146 are opened to mix air and decane into the mixing chamber 142, wherein the air to methane flow ratio ❹ is 20 : 1 (that is, the oxygen to carbon ratio is 4.2: 1). Then, air and methane enter the plasma chamber 112 along the preheating tube 134 and are activated by the discharge phenomenon in the plasma chamber 112. In detail, part of the air and methane will be subjected to high-energy electron impact of non-thermal plasma to cause Ionization, Dissociation, Excitation, etc., to form ions (Ion) and electrons. A quasi-neutral mixture of (Electron) and Free Radical (not shown). The aforementioned quasi-neutral mixed gas will enter the first recombination chamber 121 and 15 201100164 to fully burn, and release a large amount of heat to heat the first catalyst bed 12^, thereby making the first catalyst bed 125 The catalyst temperature rises. Although the fire can release the maximum heat when π is fully burned, the combustion occurs when the air is in contact with the first catalyst bed 125, so the heat released by the hospital cannot be completely passed through the gas. The phase (the line and the decane) is transferred to the first catalyst bed 125 by conduction to the solid phase (catalyst). It is worth noting that this embodiment first mixes air with decane and then Ο

導入第-觸媒$ 125。但若是將甲烧與空氣分別導入第一 觸媒床125後’再使空氣與曱炫混合燃燒的話,儘管第一 ,媒床125是由多孔性的觸媒所構成,但是多孔性的觸媒 =導致甲燒與空氣在其中混合不良,產线燒不完全 問題。 般來說’第—觸媒床125在重組反應前段、中段與 ,域的溫度會呈遞減的狀態,而當重組反應前段區域 曱俨床125的溫度超過底限值時,便可以開始調整 空氣的比例,以使甲烷可渐進式地調整為不完全燃 八先、。以甲烷為例,此底限值的溫度為550°C,而接著 "刀別調整空氣與甲燒的流量比為11.9 :卜14.76 : 1或 二1ί亦即氧碳比分別為為2·5:卜3.1:…:D,以 將二=氣而使曱烷進行一連串不同程度的不完全燃燒,而 拥 出的大量熱量持續經由氣相至固相的傳導而不斷加 熱苐一觸媒床125。 兄〇。(^時由於重組反應前段區域的觸媒溫度已超過底限值 C,所以空氣中少部分未燃燒的氧分子會與甲烷分子在 、表面上進行部分氧化重組,而由於此不完全燃燒是發 16 201100164 src每個觸媒的表面上,所以此部分氡化會έ 所釋放出的熱量會直接傳Κ匕重組 反應錢區域的觸媒温度會迅速媒’而使得重組 上曱::空二 其他區域的升溫,而便可加速Γ觸媒床125 值550。(:以上,彳..觸媒床125的溫度保持在底限 值得注土,但不超過極限值9〇〇°C為原則。 _ ΟImport the first catalyst $ 125. However, if the fired and air are introduced into the first catalyst bed 125, respectively, and then the air and the smoldering are mixed and burned, although the first, the medium bed 125 is composed of a porous catalyst, the porous catalyst = causing poor mixing of the burnt air and air, and the production line is not completely burnt. Generally speaking, the temperature of the first-stage, middle-stage and the middle of the recombination reaction is declining, and when the temperature of the trampoline 125 in the region before the recombination reaction exceeds the lower limit, the air can be adjusted. The ratio is such that methane can be progressively adjusted to be incompletely burned. Taking methane as an example, the temperature at the bottom limit is 550 ° C, and then the flow ratio of the air to the smoldering is 11.9: b. 14.76: 1 or 2 ί, that is, the oxygen to carbon ratio is 2· 5: Bu 3.1:...:D, in order to carry out a series of incomplete combustion of decane with two = gas, and the large amount of heat that is escaping continues to be heated through the gas phase to the solid phase to continuously heat the one-touch bed. 125. Brothers. (^) Since the catalyst temperature in the front region of the recombination reaction has exceeded the lower limit value C, a small portion of the unburned oxygen molecules in the air will partially oxidize and recombine with the methane molecules on the surface, and since this incomplete combustion is 16 201100164 src on the surface of each catalyst, so the heat released by this part will be directly transmitted. The temperature of the catalyst in the recombination reaction area will quickly mediate and make the reorganization of the upper:: empty two other The temperature rises in the area, and the value of the catalyst bed 125 is accelerated by 550. (: Above, the temperature of the catalyst bed 125 is kept at the bottom limit, but the limit is not exceeded by 9 〇〇 °C. _ Ο

所產生的熱i::整:c曱烷與空氣進行完全燃燒 Π5在重組反應;觸媒床125,而使第1媒床 值550。。以上::又與後段區域的溫度都到達底限 燃燒的話,則反與空氣的比例以進行部份 的時間才能_ 多的㈣與空氣,並耗掉更長 第4:::=25的溫度上升而接近,C時,亦即 、25在重組反應前段、中段與後段區域的 、=達底限值55G°C以上時,便可再次調整空氣與^ 里比為9.52·· 1或8.57: 1(亦即氧碳比分別為為2: i 5二·8: 1),以進一步減少空氣而使甲烷再進行不同程度的 不凡全燃燒,並釋放其所含較少的熱量以持續維持第一觸 媒床125的溫度。 由於第一觸媒床125在重組反應前段、中段與後段區 戌的溫度多半已在工作溫度以上,所以空氣中較多部份二 氧分子與甲烷分子在第一觸媒床125中大部分的單一觸媒 表面進行穩定的部份氧化重組,且其所釋出的熱量會直接 傳遞到每個單一觸媒以維持第一觸媒床125的溫度,而使 17 201100164 第一觸媒床125的溫度保持在5,c〜9⑽。c 亦即,在本發明之電漿輔助觸媒重組 需調整空氣與甲烧的流量比例,而益需額二气中,僅 燃料的預熱器’便可使第—觸媒床125迅速=置耗費大量 度’藉此可使電漿辅助觸媒重組裝置】 巧的工作溫 的方式完成起機(職_床)程細達=較省成本 Ο 〇 當完成起機程序後,以下將再敘述正作。 π再參考圖1A〜1B’類似前述,首轴整第 與第二調節閥146而使空氣與f炫以前 ^ :行混合’而空氣與甲燒的流量可比為9. 接著,空氣與甲齡進人職f 134進行加 熱加溫的過程會在之後詳述),並順著預熱管134進人電聚 :體m’並藉由電漿腔體112内的放電現象進而形成含 有離子、電子與自由㈣準巾性混合氣體(未㈣)。在本 實施例中,預熱管134連接電聚腔入口 U2a的方向例如是 偏離電漿腔體112中心,藉以使空氣與甲烧進入電聚腔體 112後會繞著㈣電極114產生雌流動,藉此使空氣與 曱烧更均勻地混合以被活化為準巾性混合氣體。 再來,準中性混合氣體便會進入第一重組腔體121 内’且在第-觸媒床125高於工作溫度的情況下,準中性 混合氣體巾的游離代分子與游離氧分子便會在重組反應 前段區域的觸媒表面進行部份氧化重組(partial 〇xidati〇n Reforming)反應,逐漸產生—氧化碳、二氧化碳、氫氣與 18 201100164 -水份,此時這些一氧化碳、二氧化礙、氫氣、水份(氣態)、 .不反應作用的氮、尚未反應的甲炫分子與氧分子在第一觸 .媒床125之重組反應前段區域便形成南溫反應氣體(未繪· 示)。 承接上述,高溫反應氣體會從第一重組腔出口 121b進 入該第二重組腔體122内繼續反應,類似前述,高溫反應 氣體中尚未反應的甲烷分子與氧分子會在重組反應中段、 後段區域的觸媒表面進行部份氧化重組(Partial Oxidation 〇 Reforming)反應,逐漸將尚未反應的曱烷分子與氧分子完 全轉換為一氧化碳、二氧化碳、氫氣與水份(氣態)。如此 一來,在第一觸媒床125之重詛反應後段區域中的這些一 氧化碳、二氧化碳、氫氣、水份(氣態)、不反應作用的氮 便形成南溫重組氣體(未繪示)。 值得注意的是,高溫反應氣體與高溫重組氣體僅是概 念上的分別,而本發明並未特意區分其所在的精確位置。 亦即高溫反應氣體僅是尚未完全進行部份氧化重組過程之 〇 概念總稱’而高溫反應氣體僅是已經完全進行部份氧化重 組過程之概念總稱,且熟悉此項技藝當可輕易理解而不致 混淆。 接著’尚溫重組氣體會從第一重組腔開口 121 c進入再 循環管123内。在前文的敘述中,再循環管丨23具有避免 •產生氣流短路的問題,而使準中性混合氣體在通過第一觸 媒床125之重組反應前段區域中可接觸最多的觸媒,以提 升重組效率並大幅減少重組反應器12〇的體積。除此之 外,高溫重組氣體可吸收第一觸媒床125之重組反應前段 201100164 • 區域中的熱量,並將熱量傳遞至第一觸媒床125之重组反 . 應、中段區域,藉此可使第—觸媒床U5的溫度分布均句, , 以進一步提升整體第一觸媒床125的反應效果。 再來,高溫重組氣體便沿著再循環管123進入預熱腔 體132中以加熱預熱管132内之空氣與甲烷,而在預&管 132内被加熱之空氣與甲烷進入電漿腔體112後會較為容 易被激發活化。亦即,本發明僅利用高溫重組氣體的餘溫 以加熱空氣與甲烷,而毋需另外設置外部加熱器,藉此$ 〇 降低建置成本,並縮小裝置整體的尺寸。 在本實施例令,再循環管123之另一端穿出第二重組 腔出口 122a後是配置在鄰近電漿腔體112的預熱管134附 近,而使得剛離開重組反應器120之高溫重組氣體可直接 加熱快進入電漿腔體Π2内之空氣與曱烷,藉此將高溫重 組氣體的餘熱發揮最大的效果。此外,預熱管134在預熱 腔體132内的部份例如是以雙層環繞的方式圍繞重組反應 器120’以達到吸收高溫重組氣體熱量以及重組反應器120 〇 向外傳遞熱量的較佳效果,不過本發明並不限制預熱管134 是以何方式環繞重組反應器120。 另外,預熱器130是包覆重組反應器120,可使電漿 辅助觸媒重組裝置100的溫度分佈是從内部高溫的重組反 應器120向外逐漸降低至外圍中、低溫的預熱器130,藉 以提昇整體的熱利用率,並可避免直接接觸高溫之重組反 應器120的風險。 最後,逐漸降溫且富含氫氣的高溫重組氣體便會從預 熱腔出口 132b離開預熱腔體132,而輸送到下游的裝置, 20 201100164 :=進V處理後以供應如燃料電池、内燃機等等之後續用 途0 j參考圖1Α〜1Β’在本實施例中,再循環管123 、^就組腔體121内的形狀為單條不規則的盤管,藉由 Sis白勺方式以阻止準中性混合氣體以最短的方式通過 弟—媒床125的重組反應前段區域。不過,本發明並不 :::循%官123的數量與形狀,而當再循環管123的數 ΟThe generated heat i:: whole: c-decane is completely burned with air Π5 in the recombination reaction; the catalyst bed 125, and the first media bed is 550. . Above:: If the temperature in the back section reaches the bottom limit, then the ratio of the air to the air will take part of the time to _ more (four) with the air, and consume a longer temperature of 4:::=25 When rising, it is close to, when C, that is, 25 in the front, middle and back regions of the recombination reaction, when the bottom limit is 55 G °C or more, the air and the ratio can be adjusted again to 9.52··1 or 8.57: 1 (that is, the ratio of oxygen to carbon is 2: i 5 2:8: 1), in order to further reduce the air and make the methane carry out different degrees of extraordinary total combustion, and release less heat contained in it to maintain the first The temperature of a catalyst bed 125. Since most of the temperature of the first catalyst bed 125 in the front, middle and rear sections of the recombination reaction is above the operating temperature, most of the oxygen molecules and methane molecules in the air are mostly in the first catalyst bed 125. The single catalyst surface undergoes stable partial oxidation recombination, and the heat released therefrom is directly transferred to each single catalyst to maintain the temperature of the first catalyst bed 125, so that 17 201100164 first catalyst bed 125 The temperature is maintained at 5, c~9 (10). c, that is, in the plasma-assisted catalyst recombination of the present invention, it is necessary to adjust the flow ratio of air to the burnt gas, and in the second gas, only the fuel preheater can make the first-catalyst bed 125 quickly = A large amount of consumption can be used to enable the plasma-assisted catalyst recombination device to complete the start-up (job_bed) process finer than the cost-saving Ο 完成 When the start-up procedure is completed, the following will be described again. Work. π Referring again to FIGS. 1A to 1B', similarly to the foregoing, the first axis is adjusted to the second and the second regulating valve 146 to mix the air with the f: the flow rate of the air and the fire is comparable to 9. Next, the air and the age of The process of heating and heating of the user f 134 will be described later in detail, and the electric heating is carried out along the preheating pipe 134: the body m' is formed by the discharge phenomenon in the plasma cavity 112, Electron and free (four) standard mixed gas (not (four)). In the present embodiment, the direction in which the preheating tube 134 is connected to the electrocavity chamber inlet U2a is, for example, offset from the center of the plasma chamber 112, so that air and nails are burned into the electropolymer chamber 112 to generate a female flow around the (four) electrode 114. Thereby, the air and the smoldering are more uniformly mixed to be activated into a scalloped mixed gas. Then, the quasi-neutral mixed gas enters the first recombination chamber 121' and the free generation molecule and the free oxygen molecule of the quasi-neutral mixed gas towel are in the case where the first-catalyst bed 125 is higher than the working temperature. Partial 〇xidati〇n Reforming reaction is carried out on the surface of the catalyst in the front part of the recombination reaction, and carbon monoxide, carbon dioxide, hydrogen and water are gradually produced. At this time, these carbon monoxide, oxidizing, Hydrogen, water (gaseous), unreacted nitrogen, unreacted formazan molecules and oxygen molecules form a south temperature reaction gas in the region before the recombination reaction of the first catalyst bed 125 (not shown). In response to the above, the high temperature reactive gas will enter the second recombination chamber 122 from the first recombination chamber outlet 121b to continue the reaction. Similarly, the unreacted methane molecules and oxygen molecules in the high temperature reaction gas will be in the middle and rear regions of the recombination reaction. The Partial Oxidation (Reforming) reaction is carried out on the surface of the catalyst to gradually convert the unreacted decane molecules and oxygen molecules into carbon monoxide, carbon dioxide, hydrogen and water (gaseous). As a result, the carbon monoxide, carbon dioxide, hydrogen, water (gaseous), and unreacted nitrogen in the rear region of the first catalyst bed 125 form a south temperature recombination gas (not shown). It is worth noting that the high temperature reaction gas and the high temperature reformed gas are only conceptual differences, and the present invention does not specifically distinguish the exact position where it is located. That is to say, the high-temperature reaction gas is only a general term for the partial oxidation recombination process, and the high-temperature reaction gas is only a general term for the partial oxidation recombination process, and it is easy to understand and not be confused when familiar with the technology. . Then, the still warming gas will enter the recirculation pipe 123 from the first recombination chamber opening 121c. In the foregoing description, the recirculation pipe 23 has a problem of avoiding the occurrence of a short circuit of the air flow, so that the quasi-neutral mixed gas can contact the most catalyst in the region before the recombination reaction through the first catalyst bed 125 to enhance Recombination efficiency and a significant reduction in the volume of the recombination reactor 12〇. In addition, the high temperature reformed gas can absorb the heat in the region of the first reaction bed 125 of the first catalyst bed 125 and transfer the heat to the recombination counter of the first catalyst bed 125. The temperature distribution of the first catalyst bed U5 is made uniform to further enhance the reaction effect of the entire first catalyst bed 125. Then, the high temperature reformed gas enters the preheating chamber 132 along the recirculation pipe 123 to heat the air and methane in the preheating tube 132, and the heated air and methane in the preamplifier tube 132 enter the plasma chamber. After body 112, it is easier to be activated and activated. That is, the present invention utilizes only the residual temperature of the high-temperature reformed gas to heat the air and methane without additionally providing an external heater, thereby reducing the construction cost and reducing the overall size of the apparatus. In this embodiment, the other end of the recirculation pipe 123 passes through the second recombination chamber outlet 122a and is disposed near the preheating tube 134 adjacent to the plasma chamber 112, so that the high temperature recombination gas just leaving the recombination reactor 120 The air and decane in the plasma chamber Π2 can be directly heated to maximize the residual heat of the high-temperature reformed gas. In addition, the portion of the preheating tube 134 in the preheating chamber 132 surrounds the recombination reactor 120', for example, in a double-layered manner to achieve heat absorption of the high temperature recombination gas and heat transfer to the recombination reactor 120. The effect, however, does not limit the manner in which the preheating tube 134 surrounds the recombination reactor 120. In addition, the preheater 130 is a coated recombination reactor 120, and the temperature distribution of the plasma assisted catalyst recombination device 100 can be gradually reduced from the internal high temperature recombination reactor 120 to the peripheral low temperature preheater 130. In order to improve the overall heat utilization rate, and avoid the risk of direct contact with the high temperature recombination reactor 120. Finally, the gradual cooling and hydrogen-rich high-temperature reformed gas will leave the preheating chamber 132 from the preheating chamber outlet 132b and be transported to the downstream device, 20 201100164 := after V treatment to supply fuel cells, internal combustion engines, etc. For the subsequent use 0 j, refer to FIG. 1Α~1Β' In the present embodiment, the recirculation pipes 123, ^ are in the shape of a single irregular coil in the cavity 121, and the Sis is used to prevent the quasi-middle. The mixed gas passes through the recombination reaction front region of the media bed 125 in the shortest manner. However, the present invention does not ::: follow the number and shape of the official 123, and when the number of the recirculation pipe 123 is Ο

::、、、條時’則第-重組腔體ΐ2ι亦需再開料應之第一 重組腔開口 121C。 為,一步再提升第一觸媒床125的重組效率,本發明 更可於第-重組腔體121或是第二重組腔體122内設置分 隔板’以下將再另舉實施例並配合圖*說明,而為求說明 方便’相同功能之構件仍沿用相同之名稱與標號。 圖2A為依據本發明另一實施例之電漿輔助觸媒重組 f置的剖面不意圖’並省略繪示第一觸媒床、再循環管與 第一重組腔開口,而圖2B為圖2八之重組反應器沿AA連 線的剖面上視圖。請參考圖2A〜2B,本實施例之電漿辅助 觸媒重組裝置200與前述之電漿輔助觸媒重組裝置1〇〇(如 圖1A所示)相似,其差別僅在於電漿輔助觸媒重組裝置2〇〇 之重組反應器220更包括第一分隔板226,而第一分隔板 226是配置於第一重組腔體121内,以使第一重組腔體121 區分出多個各自獨立的第一反應區域S1。 在本實施例中,第一分隔板226例如為十字分隔板以 形成4個第一反應區域S1,其中每個第一反應區域S1之 橫戴面積僅有原本第一重組腔體121之橫截面積的四分之 21 201100164 •一,亦即母個第一反應區域s 1之等效直徑為第一重組腔體 • 121之等效直徑的二分之一,因此每個第一反應區域S1之 • 『長徑比』是原本第一重組腔體121『長徑比』的兩倍。 當氣流快速通過長徑比較大的區域時,較容易形成完 全發展的紊流(Fully-developed Turbulence)。紊流狀態的氣 流中的不同氣體成分極容易達到完全混合,並以梯形的速 度分佈均勻地通過此區域,所以完全混合的不同氣體成份 付以充分接觸此區域内的觸媒。亦即,本實施例之準中性 〇 混合氣體中完全混合的氣體成份更得以充分接觸第一反應 區域si内的觸媒,而在觸媒表面進行反應,藉以完全利用 第一觸媒床125而提升反應效果。 附帶一提的是,為配合第一分隔板226分隔的效果, 再循環管123的數量可相同於第一反應區域S1的數量,以 使每個第一反應區域S1内均配設一條再循環管123,熟悉 此項技藝者當可輕易理解,於此便不再贅述。 圖2C為依據本發明另一實施例之重組反應器的剖面 〇 上視圖。類似前述,重組反應器220a更包括第二分隔板 227 ’而第二分隔板227是配置於第二重組腔體122内,以 使第一重組腔體121區分.出多個各自獨立的第·一反應區域 S2。在本實施例中,第二分隔板227的數量例如為8個, 以將第二重組腔體122區分為8個對稱之第二反應區域 S2。類似前述,第二反應區域S2中的氣流容易形成完全發 展的紊流,以使高溫反應氣體中完全混合的氣體成份更得 以充分接觸第二反應區域S2内的觸媒,而提升反應效果。 當然,本發明並不限定第一分隔板226與第二分隔板 22 201100164::, ,, and strips' then the first recombination chamber ΐ2ι also needs to be re-opened to the first recombination chamber opening 121C. In order to improve the recombination efficiency of the first catalyst bed 125 in one step, the present invention can further provide a partition plate in the first recombination cavity 121 or the second recombination cavity 122. *Description, and for the sake of explanation, the same name and label are still used for the same function. 2A is a cross-sectional view of a plasma assisted catalyst recombination f according to another embodiment of the present invention, and omits the first catalyst bed, the recirculation tube and the first recombination chamber opening, and FIG. 2B is FIG. A top view of the section of the eight-recombination reactor along the AA line. 2A to 2B, the plasma assisted catalyst recombination apparatus 200 of the present embodiment is similar to the plasma assisted catalyst recombination apparatus 1 (shown in FIG. 1A), and the difference is only in the plasma assisted catalyst. The recombination reactor 220 of the reconstitution device further includes a first partitioning plate 226, and the first partitioning plate 226 is disposed in the first recombination cavity 121 to distinguish the first recombination cavity 121 from the plurality of respective recombination chambers 121. Independent first reaction zone S1. In the present embodiment, the first partitioning plate 226 is, for example, a cross partition plate to form four first reaction regions S1, wherein the cross-sectional area of each of the first reaction regions S1 is only the original first recombination cavity 121. 21/24 of the cross-sectional area 201100164 • One, that is, the equivalent diameter of the first reaction zone s 1 of the parent is one-half of the equivalent diameter of the first recombination cavity • 121, so each first reaction In the area S1, the "length to diameter ratio" is twice the length ratio of the first recombination chamber 121. When the airflow quickly passes through a relatively large area of the long diameter, it is easier to form a fully developed turbulence (Fully-developed Turbulence). The different gas components in the turbulent state of the gas flow are extremely easy to achieve complete mixing and uniformly pass through this region at a trapezoidal velocity distribution, so that the completely mixed different gas components are sufficiently contacted with the catalyst in this region. That is, the completely mixed gas component in the quasi-neutral krypton mixed gas of the present embodiment is more in contact with the catalyst in the first reaction zone si, and reacts on the catalyst surface, thereby completely utilizing the first catalyst bed 125. And improve the reaction effect. Incidentally, in order to cooperate with the effect of separating the first partition plates 226, the number of the recirculation pipes 123 may be the same as the number of the first reaction regions S1, so that each of the first reaction regions S1 is provided with one more The circulation tube 123, which is familiar to those skilled in the art, can be easily understood, and will not be described again. Figure 2C is a top plan view of a cross-section of a recombination reactor in accordance with another embodiment of the present invention. Similar to the foregoing, the recombination reactor 220a further includes a second partitioning plate 227' and the second partitioning plate 227 is disposed in the second recombination cavity 122 to distinguish the first recombination cavities 121. The first reaction zone S2. In the present embodiment, the number of the second partitioning plates 227 is, for example, eight, to divide the second recombination cavity 122 into eight symmetrical second reaction regions S2. Similarly to the foregoing, the gas flow in the second reaction zone S2 easily forms a completely developed turbulent flow so that the completely mixed gas component in the high-temperature reaction gas is more sufficiently contacted with the catalyst in the second reaction zone S2 to enhance the reaction effect. Of course, the present invention does not limit the first dividing plate 226 and the second dividing plate 22 201100164

. 227的數量與形狀,亦不限定其所區分出第一反應區域SI 或第二反應區域S2的形狀。舉例來說,第一分隔板226a * • 亦可為井字分隔板而如圖2D之重組反應器220b所示。 圖3A為依據本發明另一實施例之電漿輔助觸媒重組 裝置的剖面示意圖,並省略繪示第一觸媒床,而圖3B為圖 3A之盤狀預熱通道沿BB連線的剖面上視圖。請參考圖3A 〜3B,本實施例之電漿辅助觸媒重組裝置300與前述之電 漿輔助觸媒重組裝置1〇〇(如圖1A所示)相似,其差別僅在 〇 於電漿輔助觸媒重組裝置300之預熱器330更包括盤狀預 熱通道336,而盤狀預熱通道336是配置於預熱腔體132 内,並連接於預熱管134之一端與電漿腔入口 112a之間。 承接上述,盤狀預熱通道336具有螺旋環繞電漿腔體 112的氣道,而空氣與曱烷會從預熱管134進入盤狀預熱 通道336後,順著盤狀預熱通道336中氣道向内繞行,而 最終經由電漿腔入口 112a進入電漿腔體112。 由於電漿腔體112内會產生高壓的放電現象,因此電 ❹ 漿腔體112的溫度亦相當高。藉由盤狀預熱通道336的設 計,便可使電漿腔體112中的熱量沿著盤狀預熱通道336 向外傳遞,以進一步加熱盤狀預熱通道336内的空氣與甲 烧。除此之外,藉由盤狀預熱通道336迅速吸收熱量,可 快速對電漿腔體112與電漿電極114進行降溫,進而可延 長電漿反應器110的壽命。The number and shape of the 227 are also not limited to the shape in which the first reaction region SI or the second reaction region S2 is distinguished. For example, the first divider 226a* can also be a tic-tray separator as shown in the recombination reactor 220b of Figure 2D. 3A is a cross-sectional view of a plasma assisted catalyst recombination apparatus according to another embodiment of the present invention, and the first catalyst bed is omitted, and FIG. 3B is a cross section of the disk-shaped preheating passage of FIG. 3A along the BB line. Top view. Referring to FIG. 3A to FIG. 3B, the plasma assisted catalyst recombining device 300 of the present embodiment is similar to the plasma assisted catalyst recombining device 1 (shown in FIG. 1A), and the difference is only in the case of plasma assisting. The preheater 330 of the catalyst recombining device 300 further includes a disk-shaped preheating passage 336, and the disc-shaped preheating passage 336 is disposed in the preheating chamber 132 and is connected to one end of the preheating tube 134 and the plasma chamber inlet. Between 112a. In response to the above, the disk-shaped preheating passage 336 has an air passage spirally surrounding the plasma chamber 112, and air and decane enter the disk-shaped preheating passage 336 from the preheating pipe 134, and follow the air passage in the disk-shaped preheating passage 336. It circulates inward and eventually enters the plasma chamber 112 via the plasma chamber inlet 112a. Since the high-voltage discharge phenomenon occurs in the plasma chamber 112, the temperature of the electric discharge chamber 112 is also relatively high. By the design of the disk-shaped preheating passage 336, heat in the plasma chamber 112 can be transferred outwardly along the disk-shaped preheating passage 336 to further heat the air and the combustible in the disk-shaped preheating passage 336. In addition, by rapidly absorbing heat by the disk-shaped preheating passage 336, the plasma chamber 112 and the plasma electrode 114 can be quickly cooled, thereby extending the life of the plasma reactor 110.

圖4為依據本發明另一實施例之電漿輔助觸媒重組裝 置的剖面示意圖。請參考圖4,本實施例之電漿輔助觸媒 重組裝置400與前述之電漿輔助觸媒重組裝置100(如圖1A 23 201100164 .所二)相似,其差別僅在於電漿輔助觸媒重組裝置400之預 ‘熱器430更包括第三分隔板438,而第三分隔板是配 .置於預熱腔n m内,以將預熱腔體132區分為相連之第 預,、.、區T1與弟一預熱區T2,其中預熱管134是沿第一 預熱區T1與第二預熱區T2而以雙層環繞的方式圍繞重組 反應器120,而第二預熱區Τ2是位在第一預熱區τι的外 圍。 ,此一來,從再循環管123進入預熱腔體132的高溫 重、’且氣體便會依序通過第-預熱區T1與第二預熱區T2, 而使冋/皿重組氣體向外圍傳遞熱量。通常來說,高溫重組 氣體仍會有部分的一氧化碳,而一氧化碳對於人類具有毒 性’因此可於第一預熱區T1與第二預熱區T2中配置一氧 化碳選擇性氧化(CO Preferential Oxidation)觸媒,藉以將一 氧化碳轉換為二氧化碳。當然,本發明並不限定在第一預 熱區T1與第二預熱區T2再配置何種觸媒,舉例來說,第 一預熱區T1與第二預熱區T2亦可再配置水氣轉移觸媒 〇 (water-gas_shifting)以將高溫重組氣體中的一氧化碳轉換為 二氧化碳。 值得注意的是,本發明並不限定第三分隔板438僅能 ' 將預熱腔體132區分為兩個區域,熟悉此項技藝者當可依 據前述而利用第三分隔板438將預熱腔體132區分為三個 以上的相連區域,惟其均仍屬本發明之範疇中。 在之前的敘述中,主要是以碳氫氣體為例,進行重組 反應的說明,以下將再稍加修改電漿辅助觸媒重組裝置以 使其亦能應用於碳氫液體的重組反應。圖5A為依據本發 24 201100164 明另一實施例之電漿輔助觸媒重組裝置的剖面示意圖,而 圖5B為圖5A之電漿辅助觸媒重組裝置移除第二觸媒床、 第三觸媒床與第四觸媒床的剖面示意圖。請參考圖5A〜 5B,本實施例之電漿輔助觸媒重組裝置500與前述之電漿 輔助觸媒重組裝置1〇〇(如圖1A所示)相似,其差別僅在於 電漿輔助觸媒重組裝置500之進料器540更具有壓電霧化 單元544,且壓電霧化單元544是連接混合室142,而壓電 霧化單元544是用於將碳氫液體與水份霧化成微細霧滴(平 〇 均粒徑小於ΙΟμιη)後送入混合室142與空氣進行混合。 如此一來,這些在空氣中的微細霧滴的行為幾乎可等 同氣體,而從預熱管134進入電漿腔體112進行放電活化。 詳細而言,進料器540乃具有第一調節閥145、第三調節 閥547與第四調節閥548,而第一調節閥145是連接混合 室142以控制空氣流量,且第三調節閥547與第四調節閥 548是連接壓電霧化單元544,以分別控制碳氫液體與水份 之流量。 Q 類似前述,適當調整碳氫液體與空氣之間的比例(或氧 碳比),可使碳氫液體進行完全燃燒(完全氧化重組)或是不 完全燃燒(不完全氧化重組)。在起機的階段中,本實施例 可先利用前述的方法先以曱烷(碳氫氣體)對第一觸媒床 125進行燃燒加熱至工作溫度後,再開始通入碳氫液體、 水份與空氣以進行碳氫液體的部份氧化重組。 當然,在其他實施例中,起機階段亦可先通入碳氫液 體與空氣,藉由適當的比例分配而使碳氫液體完全燃燒以 加熱第一觸媒床125,之後再漸進調整碳氫液體與空氣的 25 201100164 .比例,而使碳_氫液體逐漸改為進行部份燃燒。類似的程序 已在前述甲烧的起機過程中詳述,熟悉此項技藝者當可輕 易類推理解,於此便不再贅述。 在本實施例中,碳氫液體例如是以酒精為例進行說 明,不過本發明並不限制碳氫液體的種類,而碳氩液體亦 可為液化石油氣或丙醇。附帶一提的是,第三調節閥547 與第四調節閥548可再外接壓電幫浦或微小泵,藉以將酒 精與水份注入壓電霧化單元544。此外,本發明並不限定 Ο 壓電霧化單元544的數量,舉例而言,其他實施例亦可設 置兩個壓電霧化單元以分別將酒精與水份霧化後再送入混 合室142進行混合。 當第一觸媒床125已達到工作溫度而完成起機階段 後,接著便可進入正常運作的流程。請再參考圖5A〜5B, 首先調節第一調節閥145、第三調節閥547與第四調節閥 548,以將空氣、霧化之酒精與霧化之水份送入混合室142 混合。 〇 接著,空氣、霧化之酒精與霧化之水份會進入預熱管 134進行加熱,類似前述,此時預熱腔體132是充滿高溫 的氣體,而霧化之酒精與霧化之水份會被加熱而形成氣化 ' 之酒精與氣化之水份。值得注意的是,微細霧滴的平均粒 徑是小於1 Ομιη,所以這些微細霧滴具有相對較大的表面 積,而非常容易吸收熱量而氣化,此即為本實施例要先使 用壓電霧化單元544將酒精與水份霧化的原因之一。 當空氣、氣化之酒精與氣化之水份順著預熱管134進 入電漿腔體112後,會藉由電漿腔體112内的放電現象而 26 201100164 ο4 is a cross-sectional view showing a plasma assisted catalyst reassembly according to another embodiment of the present invention. Referring to FIG. 4, the plasma assisted catalyst recombining device 400 of the present embodiment is similar to the plasma assisted catalyst recombining device 100 (FIG. 1A 23 201100164.), and the difference lies only in the plasma assisted catalyst recombination. The pre-heater 430 of the device 400 further includes a third partition plate 438, and the third partition plate is disposed in the preheating chamber nm to distinguish the preheating cavity 132 into a connected pre-, a zone T1 and a preheating zone T2, wherein the preheating pipe 134 surrounds the recombination reactor 120 in a double-layered manner along the first preheating zone T1 and the second preheating zone T2, and the second preheating zone Τ2 is located at the periphery of the first preheating zone τι. In this way, the high temperature of the preheating chamber 132 from the recirculation pipe 123 is heavy, and the gas passes through the first preheating zone T1 and the second preheating zone T2 in sequence, thereby causing the reef gas to be reorganized. The heat is transferred from the periphery. Generally, high-temperature reformed gas still has some carbon monoxide, and carbon monoxide is toxic to humans. Therefore, CO Preferential Oxidation catalyst can be disposed in the first preheating zone T1 and the second preheating zone T2. In order to convert carbon monoxide into carbon dioxide. Of course, the present invention is not limited to which catalyst is disposed in the first preheating zone T1 and the second preheating zone T2. For example, the first preheating zone T1 and the second preheating zone T2 may be further configured with water. Water-gas shifting to convert carbon monoxide in a high temperature reformed gas to carbon dioxide. It should be noted that the present invention does not limit the third partitioning plate 438 to only 'divide the preheating cavity 132 into two regions. Those skilled in the art can use the third dividing plate 438 to advance according to the foregoing. The thermal cavity 132 is divided into three or more connected regions, all of which are still within the scope of the present invention. In the foregoing description, the description of the recombination reaction is mainly carried out by taking hydrocarbon gas as an example, and the plasma assisted catalyst recombination apparatus will be slightly modified as follows to enable it to be applied to the recombination reaction of a hydrocarbon liquid. 5A is a cross-sectional view of a plasma assisted catalyst recombination apparatus according to another embodiment of the present invention, and FIG. 5B is a plasma assisted catalyst recombination apparatus of FIG. 5A for removing a second catalyst bed and a third touch. A schematic cross-sectional view of a media bed and a fourth catalyst bed. Referring to FIGS. 5A-5B, the plasma assisted catalyst recombination apparatus 500 of the present embodiment is similar to the plasma assisted catalyst recombination apparatus 1 (shown in FIG. 1A), and the difference is only in the plasma assisted catalyst. The feeder 540 of the recombining device 500 further has a piezoelectric atomizing unit 544, and the piezoelectric atomizing unit 544 is connected to the mixing chamber 142, and the piezoelectric atomizing unit 544 is used for atomizing the hydrocarbon liquid and the water into fine particles. The mist droplets (the average particle size of the crucibles are smaller than ΙΟμιη) are sent to the mixing chamber 142 and mixed with the air. As a result, the fine droplets in the air behave almost equally, and enter the plasma chamber 112 from the preheating tube 134 for discharge activation. In detail, the feeder 540 has a first regulating valve 145, a third regulating valve 547 and a fourth regulating valve 548, and the first regulating valve 145 is connected to the mixing chamber 142 to control the air flow, and the third regulating valve 547 The piezoelectric atomizing unit 544 is connected to the fourth regulating valve 548 to control the flow rates of the hydrocarbon liquid and the water, respectively. Q Similar to the above, the ratio between the hydrocarbon liquid and the air (or the ratio of oxygen to carbon) can be appropriately adjusted to allow complete combustion (complete oxidation recombination) or incomplete combustion (incomplete oxidation recombination) of the hydrocarbon liquid. In the initial stage, in the embodiment, the first catalyst bed 125 is first burned to the working temperature by decane (hydrocarbon gas), and then the hydrocarbon liquid and water are introduced. Recombination with air for partial oxidation of the hydrocarbon liquid. Of course, in other embodiments, the hydrocarbon phase may be first introduced into the hydrocarbon liquid and air, and the hydrocarbon liquid is completely combusted to heat the first catalyst bed 125 by appropriate proportion distribution, and then the hydrocarbon is gradually adjusted. The ratio of liquid to air is 25 201100164 . The carbon-hydrogen liquid is gradually changed to partial combustion. A similar procedure has been described in detail during the start-up process of the above-mentioned artemisia, and those skilled in the art can easily understand it, and will not repeat them here. In the present embodiment, the hydrocarbon liquid is exemplified by, for example, alcohol, but the present invention does not limit the kind of the hydrocarbon liquid, and the carbon argon liquid may be liquefied petroleum gas or propanol. Incidentally, the third regulating valve 547 and the fourth regulating valve 548 may be externally connected with a piezoelectric pump or a micro pump to inject the alcohol and water into the piezoelectric atomizing unit 544. In addition, the present invention is not limited to the number of piezoelectric atomizing units 544. For example, other embodiments may also provide two piezoelectric atomizing units to atomize alcohol and water, respectively, and then send them to the mixing chamber 142. mixing. When the first catalyst bed 125 has reached the operating temperature and the start-up phase is completed, then the normal operation flow can be entered. Referring again to FIGS. 5A-5B, the first regulator valve 145, the third regulator valve 547, and the fourth regulator valve 548 are first adjusted to mix air, atomized alcohol, and atomized water into the mixing chamber 142. Then, the air, the atomized alcohol and the atomized water will enter the preheating tube 134 for heating, similar to the above, at this time, the preheating chamber 132 is filled with a high temperature gas, and the atomized alcohol and the atomized water The portion will be heated to form a vaporized alcohol and vaporized water. It is worth noting that the average particle diameter of the fine mist droplets is less than 1 Ομιη, so these fine mist droplets have a relatively large surface area, and are very easy to absorb heat and vaporize, which is the first use of the piezoelectric mist in this embodiment. The chemical unit 544 is one of the reasons for atomizing alcohol and moisture. When the air, the vaporized alcohol and the vaporized water enter the plasma chamber 112 along the preheating tube 134, the discharge phenomenon in the plasma chamber 112 is caused. 26 201100164

形成含有離子、電子與自由基的準中性混合氣體(未繪 示)。再來,準中性混合氣體便會進入第一重組腔體121内, 且在第一觸媒床125高於工作溫度的情況下,準中性混合 氣體中的游離酒精分子與游離氧分子便會在重組反應前段 區域的觸媒表面進行部份氧化重組反應,逐漸產生一氧化 碳、二氧化碳、氫氣與水份,此時這些一氧化碳、二氧化 奴、氫氣、水份(氣態)、不反應作用的氮、尚未反應的酒 精分子與氧分子在第一觸媒床125之重組反應前段區域便 形成高溫反應氣體(未繪示)。 承接上述,高溫反應氣體會從第一重組腔出口 121b進 ^該第二重組腔體122内繼續反應,類似前述,高溫反應 氣體中尚未反應的酒精分子與氧分子會在重組反應中段、 後段區域的觸媒表面進行部份氧化重組反應,逐漸將尚未 f應,酒精分子與氧分子完全轉換為一氧化碳、二氧化 奴、氫氣與水份(氣態)。如此一來,在第一觸媒床125之 重、,且反應後&區域中的這些一氧化碳、二氧化碳、氫氣、 水伤(氣態)、*反應作㈣氮便形成高溫重組氣體(未綠 示)。 高溫重組氣體會從第—重組關π 121e進入再循3 ^23 ? ’以沿著再循環管123進人預熱腔體132中〜 …預熱官132内的空氣、霧化之_與霧化之水份,而々 ::管132内被加熱之空氣與被氣化之酒精 電漿腔體112後會較為容易被激發活化。 退 類似祕,為求進-步提升高溫重城射的氨氣令 罝或是降低南溫重組氣體中一氧化碳的含量,本實施例更 27 201100164 可在預熱腔體132再配置觸媒以使高溫重組氣體再進行反 應0 請再參考圖5Α〜5Β’本實施例之電漿辅助觸媒重组裝 置500之預熱器530更包括第三分隔板538,而第三分隔 板538是配置於預熱腔體132内,以將預熱腔體132區= ^相連之第一預熱區τι與第二預熱區Τ2,其中預熱管134 是沿第-預熱區Τ1與第二預熱區Τ2而以雙層環繞的方式 ΟA quasi-neutral mixed gas containing ions, electrons and radicals is formed (not shown). Then, the quasi-neutral mixed gas enters the first recombination chamber 121, and when the first catalyst bed 125 is higher than the working temperature, the free alcohol molecules and the free oxygen molecules in the quasi-neutral mixed gas are Partial oxidative recombination reactions are carried out on the catalyst surface in the pre-reaction zone to gradually produce carbon monoxide, carbon dioxide, hydrogen and water. At this time, these carbon monoxide, sulphur dioxide, hydrogen, water (gaseous), unreactive nitrogen The unreacted alcohol molecules and oxygen molecules form a high temperature reaction gas (not shown) in the region before the recombination reaction of the first catalyst bed 125. In response to the above, the high temperature reaction gas will continue to react from the first recombination chamber outlet 121b into the second recombination chamber 122. Similarly, the unreacted alcohol molecules and oxygen molecules in the high temperature reaction gas will be in the middle and rear regions of the recombination reaction. The surface of the catalyst is partially oxidized and recombined, and the alcohol molecules and oxygen molecules are completely converted into carbon monoxide, sulphur dioxide, hydrogen and water (gaseous). In this way, the carbon monoxide, carbon dioxide, hydrogen, water damage (gaseous), and *reaction (4) nitrogen in the first catalyst bed 125 and the reaction & region form a high temperature reformed gas (not green) ). The high-temperature recombination gas will enter from the first-recombination off π 121e and then follow the 3^23?' to enter the preheating chamber 132 along the recirculation pipe 123. ...the air in the preheating officer 132, the atomization_and the fog The water is hydrated, and the heated air in the tube 132 and the vaporized alcohol plasma chamber 112 are more easily activated and activated. Reducing the similarity, in order to improve the ammonia gas emitted by the high-temperature heavy city or reduce the content of carbon monoxide in the south temperature recombination gas, this embodiment further 27 201100164 can re-dispose the catalyst in the preheating cavity 132 to make The high temperature reformed gas is further reacted. Referring again to FIG. 5A to 5B, the preheater 530 of the plasma assisted catalyst recombining device 500 of the present embodiment further includes a third partitioning plate 538, and the third dividing plate 538 is configured. In the preheating cavity 132, the first preheating zone τ1 and the second preheating zone Τ2 are connected to the preheating cavity 132=^, wherein the preheating pipe 134 is along the first preheating zone Τ1 and the second Preheating zone Τ2 and surrounded by double layersΟ

圍繞重組反應器12GH預熱區Τ2是位在第—預熱區 Τ1的外圍。 *''' 此外,預熱器530更可包括第二觸媒床53卜 媒床533與第四觸媒床奶,而第二觸媒床531可位;:第 一預熱區Τ1,且第三觸媒庆533^ 望-mm— h 可位於第—預熱區Τ1與 第四觸媒床535可位於第二預孰 =2據在本實施例中,第二觸媒床531可 轉 533可具有低溫水氣轉移觸媒ΐ 第四觸媒床535可具有—氧化碳選擇性氧化觸媒。 如此一來,從再循環管123進入預熱腔體η 重組氣體便會逐漸通過第一預埶區彻、、 、同/皿 531. T2 ^ 奶進行反應。在第二觸媒床531 j 51、第四觸媒床 ^ ^ L 蜩跺床531與第三觸媒床533中, -溫重組氣體中的汽化的水f分分子 t 氣轉移觸媒表面== 時降低—氧:碳含量氧W ’藉此以提高氫氣含量,並同 匕外水氣轉移反應是放熱的過程,因此所釋放出的 28 201100164 熱量可進一步傳遞至預熱管丨34,以加熱預熱管134申的 空氣,並將務化之酒精與水份加熱形成氣化之酒精與水 份,進而提升電漿辅助觸媒重組裝置5〇〇的整體熱利用率。 值得注意的是,在通過第二觸媒床531之高溫水氣轉 換觸媒後,若高溫重組氣體中的一氣化碳濃度可降低到 2%(Vol.)附近,本實施例亦可省略設置第三觸媒床533之 低溫水氣轉換觸媒,以降低電漿輔助觸媒重組裝置的 建置成本。 ΟThe preheating zone 围绕2 around the recombination reactor 12GH is located at the periphery of the first preheating zone Τ1. *''' In addition, the preheater 530 may further include a second catalyst bed 53 and a fourth catalyst bed milk, and the second catalyst bed 531 is positionable; the first preheating zone Τ1, and The third catalyst 543^望-mm-h can be located in the first preheating zone Τ1 and the fourth catalyst bed 535 can be located in the second pre- 孰=2. In this embodiment, the second catalyst bed 531 can be rotated. 533 may have a low temperature water vapor transfer catalyst. The fourth catalyst bed 535 may have a carbon oxide selective oxidation catalyst. As a result, the recombination gas entering the preheating chamber η from the recirculation pipe 123 gradually undergoes the reaction through the first pre-zone, the same, and the same dish 531. T2 ^ milk. In the second catalyst bed 531 j 51, the fourth catalyst bed ^ L 蜩跺 531 and the third catalyst bed 533, the vaporized water in the -temperature recombination gas f is the molecular weight of the gas transfer catalyst surface = = decrease in time - oxygen: carbon content oxygen W ' thereby increasing the hydrogen content, and the external water vapor transfer reaction is an exothermic process, so the released heat of 2011 201100164 can be further transferred to the preheating tube , 34 The air preheated by the preheating pipe 134 is heated, and the alcohol and water are heated to form vaporized alcohol and water, thereby improving the overall heat utilization rate of the plasma auxiliary catalyst recombining device 5〇〇. It should be noted that after the high-temperature moisture conversion catalyst through the second catalyst bed 531, if the concentration of a vaporized carbon in the high-temperature reformed gas can be reduced to around 2% (Vol.), the embodiment may also omit the setting. The low temperature water-gas conversion catalyst of the third catalyst bed 533 is used to reduce the construction cost of the plasma-assisted catalyst recombination device. Ο

富通過第二觸媒床別與第三觸媒床Μ3後,高溫重 氣體通常仍會殘留約2%(v〇1)濃度的_氧化碳,並逐漸 击低溫度而形成中溫重組氣體(未身示)。在第四觸媒床奶 一:中溫重組氣體中的殘留的-氧化碳分子與氧分子會在 乳化碳選擇性氧化觸媒表面上進行氧化重組,以生成二 氧化碳並釋放出熱量加熱預熱管134,以提升電漿輔助觸 媒重組裝置500的整體熱利用率。…聚輔助觸 度 4===: 料’且幾乎沒有殘留對人體有害::氧::體氫氣, 重組氣體便從預熱腔出口 132b 取後’低溫 到下游的裝置作為燃料。细離開預熱腔體132,而輸送 值得注意的是,前述戶斤餘^ 體與低溫重組氣體僅是概重組氣體、中溫重組氣 區分其所在的精確位置以r?本發明並未特意 為方便說明將-氧 厌的概念的階段性名詞,而熟悉此項技藝當可輕易= 29 201100164 . 而不致混淆。 此外,一氧化碳亦是燃料的一種。若不欲去除一氧化 碳,亦可不需設置第二觸媒床531、第三觸媒床533與第 四觸媒床535,而直接由預熱腔出口 132b處收集高溫重組 氣體即可。 以酒精而言,其亦是生質燃料的一種,進而可降低二 氧化碳的排放的量。因為植物是從環境吸收碳原子後被製 成如酒精之類的生質燃料,所以燃燒酒精之類的生質燃料 〇 僅是地球環境碳原子的循環,並不會增加地球空氣環境中 二氧化碳的總量,進而可達到環保的目標。 請再參考圖5A〜5B,為提升中溫重組氣體在第四觸媒 床535中的反應效率以完全去除殘留的一氧化碳,本實施 例之預熱腔體132更具有預熱腔開口 132c,以使空氣可從 預熱腔開口 132c進入預熱腔體132内,而使空氣中的氧分 子在一氧化碳選擇性氧化觸媒表面上與殘留的一氧化碳進 行氧化重組。當然,進料器540更可具有第五調節閥549, 〇 而第五調節閥549是連接預熱腔開口 132c以調節空氣的流 量,熟悉此項技藝者當可輕易理解,於此便不再贅述。 ' 儘管前文已同時詳述本發明之電漿輔助觸媒重組方 ' 法,但為使讀者更加清楚,以下將再配合圖示說明。圖6 為依據本發明一實施例之電漿輔助觸媒重組方法的流程示 意圖。請參考圖6,如步驟S61〜S64所示,首先提供壓電 霧化單元將碳氫液體與水份霧化,並提供空氣而於混合室 中混合空氣以及霧化之碳氫液體與水份。 承接上述,在預熱管中將霧化之碳氫液體與水份加熱 30 201100164 氣化,以形成氣化之碳氫液體與水份。接著以電漿反應器 將空氣以及氣化之碳氫液體與水份激發為準中性混合氣 體,然後以重組反應器將準中性混合氣體進行重組形成高 ( 溫反應氣體,再將高溫反應氣體進行重組形成高溫重組氣 體,其中高溫重組氣體適於加熱霧化之碳氬液體輿水份, 以使霧化之碳氫液體與水份氣化。 综上所述,本發明之電漿輔助觸媒重組裝置與方法至 少具有下列優點: 〇 一、再循環管的配置可避免氣流短路問題,以大幅提 升氣體與觸媒反應效率,進而可減少重組反應器的體積以 降低製作成本。此外,當高溫重組氣體流進再循環管時, 可將重組反應前段區域的熱量帶往重組反應中段區域,以 提升第一觸媒床的溫度均勻性,進而可再增加重組效率。 二、藉由調整碳氫氣體(或碳氫液體)對於空氣的流 量,而使碳氳氣體產生完全燃燒以加熱第一觸媒床,藉以 使第一觸媒床到達工作溫度而完成起機程序。因此本發明 〇 不需要額外再增設任何的辅助加熱器,藉此可降低建置成 本、減少整體設備體積並避免設置輔助加熱器所帶來的危 險性。 * 三、藉由預熱管的設置,可利用高溫重組氣體的餘熱 以加熱預熱管内之空氣、碳氫氣體、霧化之碳氫液體或是 霧化之水份等等,藉以提升激發活化的效果。由於不需要 設置外部加熱器以預熱空氣、碳氫氣體、霧化之碳氫液體 或是霧化之水份等等,藉此可降低建置成本,並縮小裝置 整體的尺寸 31 201100164 .四、預熱器是包覆重組反應器,以使電漿輔助觸媒重 組裝置的温度分佈是從内部高溫的重組反應器向外逐漸降 低至外圍中、低溫的預熱器,藉以提昇整體的熱利用率, 並可避免直接接觸高溫之重組反應器的風險。 五、 藉由第一分隔板與第二分隔板的設置,可使氣體 形成完全發展的紊流,以進一步提升觸媒重組轉換的效率。 六、 藉由盤狀預熱通道的設置,可吸收電漿腔體中的 熱量以延長電漿反應器的壽命。 〇 七、利用第二觸媒床、第三觸媒床與第四觸媒床再與 高溫重組氣體進行重組反應,除了可提升氫氣含量並減少 一氧化碳含量外,重組反應所釋放出的熱量可同時加熱預 熱管内的氣體或霧化之液體,藉以提升整體的熱使用率。 八、當酒精作為碳氫液體而使用製造氫氣燃料時,由 於不會增加地球空氣環境中二氧化碳的總量,進而可達到 環保的目標。 雖然本發明已以較佳實施例揭露如上,然其並非用以 Q 限定本發明,任何熟習此技藝者,在不脫離本發明之精神 和範圍内,當可作些許之更動與潤飾,因此本發明之保護 * 範圍當視後附之申請專利範圍所界定者為準。 32 201100164 【圖式簡單說明】 圖1A為依據本發明一實施例之電漿輔助觸媒重組裝 置的剖面示意圖。 圖1B為圖1A之電漿輔助觸媒重組裝置省略繪示第一 觸媒床的剖面示意圖。 圖2A為依據本發明另一實施例之電漿輔助觸媒重組 裝置的剖面示意圖。 圖2B為圖2A之重組反應器沿AA連線的剖面上視圖。 〇 圖2C〜2D為依據本發明另一實施例之兩種重組反應 器的剖面上視圖。 圖3A為依據本發明另一實施例之電漿辅助觸媒重組 裝置的剖面示意圖 圖3B為圖3A之盤狀預熱通道沿BB連線的剖面上視 圖。 圖4為依據本發明另一實施例之電漿輔助觸媒重組裝 置的剖面示意圖。 Q 圖5A為依據本發明另一實施例之電漿輔助觸媒重組 裝置的剖面示意圖。 ' 圖5B為圖5A之電漿輔助觸媒重組裝置移除第二觸媒 ' 床、第三觸媒床與第四觸媒床的剖面示意圖。 圖6為依據本發明一實施例之電漿輔助觸媒重組方法 的流程不意圖。 【主要元件符號說明】 100、200、300、400、500 :電漿輔助觸媒重組裝置 33 201100164 110 :電漿反應器 112 :電漿腔體 112a :電漿腔入口 112b :電漿腔出口 114 :電漿電極 116 :電漿電源供應單元 120、220、220a、220b :重組反應器 121 :第一重組腔體 O 121a:第一重組腔入口 121b :第一重組腔出口 121c :第一重組腔開口 122 :第二重組腔體 122a :第二重組腔出口 123:再循環管 124 :多孔板 125 :第一觸媒床 〇 130、330、430 :預熱器 132 :預熱腔體 132a :預熱腔入口 132b :預熱腔出口 132c :預熱腔開口 134 :預熱管 140、540 :進料器 142 :混合室 145 :第一調節閥 34 201100164After passing through the second catalyst bed and the third catalyst bed, the high temperature heavy gas usually still retains about 2% (v〇1) concentration of carbon monoxide, and gradually lowers the temperature to form a medium temperature reformed gas ( Not shown). In the fourth catalyst bed milk 1: residual - carbon oxide molecules and oxygen molecules in the medium temperature reformed gas will be oxidatively recombined on the surface of the emulsified carbon selective oxidation catalyst to generate carbon dioxide and release heat to heat the preheating tube 134 to increase the overall heat utilization rate of the plasma assisted catalyst recombination device 500. ...the poly-assistance 4===: material' and almost no residue is harmful to the human body:: oxygen:: body hydrogen, the recombination gas is taken from the preheating chamber outlet 132b, and the low-temperature to downstream device is used as fuel. Leaving the preheating chamber 132 finely, it is worth noting that the above-mentioned household body and the low-temperature recombination gas are only the exact recombination gas and the medium-temperature recombination gas to distinguish the exact position where they are located. It is convenient to explain the staged nouns of the concept of oxygen-oxygen, and it is easy to be familiar with this technique = 29 201100164 . Without confusion. In addition, carbon monoxide is also a type of fuel. If it is not desired to remove carbon monoxide, it is also possible to collect the high-temperature recombination gas directly from the preheating chamber outlet 132b without providing the second catalyst bed 531, the third catalyst bed 533 and the fourth catalyst bed 535. In the case of alcohol, it is also a type of biofuel, which in turn reduces the amount of carbon dioxide emissions. Because plants are made into biomass fuels such as alcohol after absorbing carbon atoms from the environment, biofuels such as burning alcohol are only the circulation of carbon atoms in the earth's environment, and do not increase the carbon dioxide in the earth's air environment. The total amount, in turn, can achieve the goal of environmental protection. Referring to FIG. 5A to FIG. 5B, in order to improve the reaction efficiency of the intermediate temperature reformed gas in the fourth catalyst bed 535 to completely remove the residual carbon monoxide, the preheating cavity 132 of the embodiment further has a preheating chamber opening 132c to Air can be introduced into the preheating chamber 132 from the preheating chamber opening 132c, and the oxygen molecules in the air are oxidatively recombined with the residual carbon monoxide on the surface of the carbon monoxide selective oxidation catalyst. Of course, the feeder 540 may further have a fifth regulating valve 549, and the fifth regulating valve 549 is connected to the preheating chamber opening 132c to adjust the flow rate of the air, which can be easily understood by those skilled in the art, and no longer Narration. Although the plasma-assisted catalyst recombination method of the present invention has been described in detail above, for the sake of clarity of the reader, the following description will be further illustrated. Figure 6 is a schematic flow diagram of a plasma assisted catalyst recombination method in accordance with an embodiment of the present invention. Referring to FIG. 6, as shown in steps S61-S64, a piezoelectric atomizing unit is first provided to atomize a hydrocarbon liquid and water, and air is supplied to mix air in the mixing chamber and atomize the hydrocarbon liquid and water. . In accordance with the above, the atomized hydrocarbon liquid and the water are heated in a preheating tube to form a vaporized hydrocarbon liquid and moisture. Then, the air and the vaporized hydrocarbon liquid and the water are excited into a quasi-neutral mixed gas by a plasma reactor, and then the quasi-neutral mixed gas is recombined by the recombination reactor to form a high (warming reaction gas, and then the high temperature reaction is performed). The gas is recombined to form a high temperature reformed gas, wherein the high temperature reformed gas is adapted to heat the atomized carbon argon liquid to vaporize the atomized hydrocarbon liquid and the water. In summary, the plasma assisted touch of the present invention The media recombination device and method have at least the following advantages: First, the recirculation pipe arrangement can avoid the problem of short circuit of the air flow, thereby greatly improving the reaction efficiency of the gas and the catalyst, thereby reducing the volume of the recombination reactor to reduce the manufacturing cost. When the high-temperature reformed gas flows into the recirculation pipe, the heat in the region before the recombination reaction can be taken to the middle portion of the recombination reaction to increase the temperature uniformity of the first catalyst bed, thereby further increasing the recombination efficiency. The flow of hydrogen gas (or hydrocarbon liquid) to the air, so that the carbon helium gas is completely burned to heat the first catalyst bed, thereby making the first The catalyst bed reaches the working temperature to complete the start-up procedure. Therefore, the present invention does not require any additional auxiliary heaters, thereby reducing the construction cost, reducing the overall equipment volume, and avoiding the danger of setting the auxiliary heater. 3. By means of the preheating tube setting, the residual heat of the high temperature recombination gas can be used to heat the air in the preheating tube, the hydrocarbon gas, the atomized hydrocarbon liquid or the atomized water, etc. Initiate the effect of activation. Since there is no need to provide an external heater to preheat air, hydrocarbon gas, atomized hydrocarbon liquid or atomized water, etc., the construction cost can be reduced, and the overall device can be reduced. Dimensions 31 201100164 . Fourth, the preheater is coated with a recombination reactor, so that the temperature distribution of the plasma assisted catalyst recombination device is gradually reduced from the internal high temperature recombination reactor to the peripheral medium and low temperature preheater. In order to improve the overall heat utilization rate, and avoid the risk of direct contact with the high temperature recombination reactor. 5. The gas shape can be formed by the arrangement of the first partition plate and the second partition plate. Fully developed turbulent flow to further improve the efficiency of catalyst recombination conversion. 6. By the arrangement of the disk-shaped preheating channel, the heat in the plasma chamber can be absorbed to prolong the life of the plasma reactor. The second catalyst bed, the third catalyst bed and the fourth catalyst bed are recombined with the high temperature reformed gas, and in addition to increasing the hydrogen content and reducing the carbon monoxide content, the heat released by the recombination reaction can simultaneously heat the preheating tube. Gas or atomized liquid to improve the overall heat utilization rate. 8. When alcohol is used as a hydrocarbon liquid to produce hydrogen fuel, it will not increase the total amount of carbon dioxide in the earth's air environment, thereby achieving environmental protection goals. Although the present invention has been described above by way of a preferred embodiment, it is not intended to limit the invention, and those skilled in the art can make some modifications and refinements without departing from the spirit and scope of the invention. The scope of protection of the present invention is defined by the scope of the appended claims. 32 201100164 BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1A is a schematic cross-sectional view showing a plasma assisted catalyst reassembly according to an embodiment of the present invention. 1B is a schematic cross-sectional view showing the first catalyst bed in the plasma assisted catalyst recombination apparatus of FIG. 1A. 2A is a schematic cross-sectional view of a plasma assisted catalyst recombination apparatus in accordance with another embodiment of the present invention. Figure 2B is a top plan view of the recombination reactor of Figure 2A taken along line AA. 2C to 2D are cross-sectional top views of two recombination reactors in accordance with another embodiment of the present invention. 3A is a cross-sectional view of a plasma-assisted catalyst recombination apparatus according to another embodiment of the present invention. FIG. 3B is a cross-sectional view of the disc-shaped preheating passage of FIG. 3A taken along line BB. 4 is a cross-sectional view showing a plasma assisted catalyst reassembly according to another embodiment of the present invention. Figure 5A is a cross-sectional view showing a plasma assisted catalyst recombination apparatus in accordance with another embodiment of the present invention. Figure 5B is a cross-sectional view showing the second catalyst 'bed, third catalyst bed and fourth catalyst bed removed from the plasma assisted catalyst recombination apparatus of Figure 5A. FIG. 6 is a schematic flow diagram of a plasma assisted catalyst recombination method according to an embodiment of the present invention. [Main component symbol description] 100, 200, 300, 400, 500: plasma assisted catalyst recombination device 33 201100164 110: plasma reactor 112: plasma chamber 112a: plasma chamber inlet 112b: plasma chamber outlet 114 : plasma electrode 116: plasma power supply unit 120, 220, 220a, 220b: recombination reactor 121: first recombination chamber O 121a: first recombination chamber inlet 121b: first recombination chamber outlet 121c: first recombination chamber Opening 122: second recombination chamber 122a: second recombination chamber outlet 123: recirculation tube 124: perforated plate 125: first catalyst bed 130, 330, 430: preheater 132: preheating chamber 132a: pre Hot chamber inlet 132b: preheating chamber outlet 132c: preheating chamber opening 134: preheating tube 140, 540: feeder 142: mixing chamber 145: first regulating valve 34 201100164

146 : 第二調節閥 226 > 226a :第一分隔板 227 : 第二分隔板 336 : 盤狀預熱通道 438、 538 :第三分隔板 531 : 第二觸媒床 533 : 第三觸媒床 535 : 第四觸媒床 544 : 壓電霧化單元 547 : 第三調節閥 548 : 第四調節閥 549 : 第五調節閥 SI : 第一反應區域 S2 : 第二反應區域 ΤΙ : 第一預熱區 Τ2 : 第二預熱區 S1〜 S4 :步驟 35146: second regulating valve 226 > 226a: first partitioning plate 227: second partitioning plate 336: disk-shaped preheating passage 438, 538: third partitioning plate 531: second catalyst bed 533: third Catalyst bed 535 : Fourth catalyst bed 544 : Piezoelectric atomization unit 547 : Third regulator valve 548 : Fourth regulator valve 549 : Fifth regulator valve SI : First reaction zone S2 : Second reaction zone ΤΙ : a preheating zone Τ2: second preheating zone S1~S4: step 35

Claims (1)

201100164 ,七、申請專利範圍: 1.一種電漿輔助觸媒重組裝置,包括: _ _ 一進料器,具有一混合室; 一電漿反應器,包括: 一電漿腔體,具有一電漿腔入口與一電漿腔出口; 一電漿電極; 一電漿電源供應單元,耦接該電漿腔體與該電漿 電極,以於該電漿腔體内產生放電; Ο 一重組反應器,連接該電漿反應器,該重組反應器包 括: 一第一重組腔體,具有一第一重組腔入口、一第 一重組腔出口與一第一重組腔開口,而該第一重組腔入口 連接該電漿腔出口; 一第二重組腔體,而該第一重組腔體是位於該第 二重組腔體内,且該第二重組腔體具有一第二重組腔出口; 一再循環管,部份位於該第一重組腔體内,而該 〇 再循環管之一端是連接該第一重組腔開口,且該再循環管 之另一端是經由該第一重組腔出口而穿出該第二重組腔出 π ; " 一多孔板,配置於該第一重組腔體内,並鄰近該 第一重組腔入口; 一第一觸媒床,配置於該第一重組腔體與該第二 重組腔體内; 一預熱器,包括: 一預熱腔體,而該重組反應器是位於該預熱腔體 36 201100164 .内,且該預熱腔體具有一預熱腔入口與一預熱腔出口;以 及 _ 一預熱管,配置於該預熱腔體内,並環繞該重組 反應器,而預熱管之一端是連接該電漿腔入口,且預熱管 之另一端是穿出該預熱腔入口以連接該混合室。 2. 如申請專利範圍第1項所述之電漿辅助觸媒重組裝 置,其中一空氣與一碳氳氣體是在該混合室混合,並沿該 預熱管進入該電漿腔體而成為一準中性混合氣體,該準中 〇 性混合氣體進入該第一重組腔體内而在該第一觸媒床中進 行重組形成一高溫反應氣體,該高溫反應氣體自該第一重 組腔出口進入該第二重組腔體内而在該第一觸媒床中進行 重組形成一高溫重組氣體,該高溫重組氣體自該第一重組 腔開口進入該再循環管,而沿該再循環管進入該預熱腔體 中以加熱該預熱管内之該空氣與該碳氳氣體,且自該預熱 腔出口離開該預熱腔體。 3. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 〇 置,其中該進料器更具有一第一調節閥與一第二調節閥, 而該第一調節閥與該第二調節閥是連接該混合室,以分別 ^ 控制一空氣與一碳氫氣體進入該混合室之流量。 ' 4.如申請專利範圍第1項所述之電漿輔助觸媒重組裝 置,其中該再循環管於該第一重組腔體内之部分為盤管。 5. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 置,其中該預熱管之一端連接該電漿腔入口的方向偏離該 電漿腔體中心。 6. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 37 201100164 -置,其中該預熱器更包括一盤狀預熱通道,配置於該預熱 > 腔體内,並連接於該預熱管之一端與該電漿腔入口之間。 . 7.如申請專利範圍第1項所述之電漿輔助觸媒重組裝 置,其中該重組反應器更包括一第一分隔板,配置於該第 一重組腔體内。 8. 如申請專利範圍第7項所述之電漿輔助觸媒重組裝 置,其中該第一分隔版為十字分隔板或井字分隔板。 9. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 〇 置,其中該重組反應器更包括一第二分隔板,配置於該第 二重組腔體内。 10. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 置,其中該預熱器更包括一第三分隔板,配置於該預熱腔 體内,以將該預熱腔體區分為相連之一第一預熱區與一第 二預熱區。 11. 如申請專利範圍第10項所述之電漿辅助觸媒重組 裝置,其中該預熱管是沿該第一預熱區與該第二預熱區雙 〇 層環繞該重組反應器。 12. 如申請專利範圍第10項所述之電漿輔助觸媒重組 裝置,其中該預熱器更包括一第二觸媒床、一第三觸媒床 ' 與一第四觸媒床,而該第二觸媒床位於該第一預熱區,且 該第三觸媒床位於該第一預熱區與該第二預熱區交界處, 又該第四觸媒床位於該第二預熱區。 13. 如申請專利範圍第12項所述之電漿辅助觸媒重組 裝置,其中該第二觸媒床具有高溫水氣轉移觸媒,而第三 觸媒床具有低溫水氣轉移觸媒,且第四觸媒床具有一氧化 38 201100164 . 碳選擇性氧化觸媒。 14. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 .置,其中該進料器更具有一壓電霧化單元,連接該混合室。 15. 如申請專利範圍第14項所述之電漿辅助觸媒重組 裝置,其中一碳氫液體與一水份是在壓電霧化單元中形成 霧化之該碳氫液體與該水份而進入該混合室,以與進入該 混合室之一空氣混合後進入該預熱管内,霧化之該碳氳液 體與該水份於該預熱管内形成氣化之該碳氫液體與該水 Ο 份,並與該空氣沿該預熱管進入該電漿腔體而成為一準中 性混合氣體,該準中性混合氣體進入該第一重組腔體内而 在該第一觸媒床中進行重組形成一高溫反應氣體,該高溫 反應氣體自該第一重組腔出口進入該第二重組腔體内而在 該第一觸媒床中進行重組形成一高溫重組氣體,該高溫重 組氣體自該第一重組腔開口進入該再循環管,而沿該再循 環管進入該預熱腔體中以加熱該預熱管内之該空氣、霧化 之碳氳液體與霧化之水份,且自預熱腔出口離開預熱腔體。 〇 16.如申請專利範圍第15項所述之電漿輔助觸媒重組 裝置,其中該碳氫液體為酒精或液化石油氣。 17. 如申請專利範圍第14項所述之電漿辅助觸媒重組 裝置,其中該進料器更具有一第一調節閥、一第三調節閥 與一第四調節閥,而該第一調節閥是連接該混合室以控制 一空氣進入該混合室之流量,且該第三調節閥與該第四調 節閥是連接該壓電霧化單元,以分別控制一碳氫液體與一 水份進入該壓電霧化單元之流量。 18. 如申請專利範圍第14項所述之電漿辅助觸媒重組 39 201100164 . 裝置,其中該預熱腔體更具有一預熱腔開口,以使一空氣 自該預熱腔開口進入該預熱腔體内。 , 19.如申請專利範圍第18項所述之電漿輔助觸媒重組 裝置,其中該進料器更具有一第五調節閥,而該第五調節 閥是連接該預熱腔開口以控制該空氣流量。 20.—種電漿輔助觸媒重組方法,包括: 提供一壓電霧化單元將一 ί炭氫液體與一水份霧化; 提供一空氣; 〇 混合該空氣以及霧化之該碳氫液體與該水份,並將霧 化之該碳氳液體與該水份氣化; 提供一電漿反應器將該空氣以及氣化之該碳氫液體與 該水份激發為一準中性混合氣體;以及 提供一重組反應器將該準中性混合氣體進行重組形成 一高温反應氣體,並將該高溫反應氣體進行重組形成一高 溫重組氣體,且該南溫重組氣體適於加熱霧化之該碳鼠液 體與該水份,以使霧化之該碳氫液體與該水份氣化。 〇 21.如申請專利範圍第20項所述之電漿辅助觸媒重組 方法,其中該碳氫液體為酒精或液化石油氣。 40201100164, VII, the scope of application for patents: 1. A plasma-assisted catalyst recombination device, comprising: _ _ a feeder having a mixing chamber; a plasma reactor comprising: a plasma chamber having an electric a slurry chamber inlet and a plasma chamber outlet; a plasma electrode; a plasma power supply unit coupled to the plasma chamber and the plasma electrode to generate a discharge in the plasma chamber; Connected to the plasma reactor, the recombination reactor comprises: a first recombination chamber having a first recombination chamber inlet, a first recombination chamber outlet and a first recombination chamber opening, and the first recombination chamber The inlet is connected to the plasma chamber outlet; a second recombination chamber, wherein the first recombination chamber is located in the second recombination chamber, and the second recombination chamber has a second recombination chamber outlet; a portion of the first recombination chamber is connected to the first recombination chamber, and the other end of the recirculation tube is pierced through the first recombination chamber outlet. Two recombination chambers out π ; &quot a porous plate disposed in the first recombination chamber adjacent to the first recombination chamber inlet; a first catalyst bed disposed in the first recombination chamber and the second recombination chamber; The preheater comprises: a preheating chamber, wherein the recombination reactor is located in the preheating chamber 36 201100164 . and the preheating chamber has a preheating chamber inlet and a preheating chamber outlet; a preheating tube disposed in the preheating chamber and surrounding the recombination reactor, wherein one end of the preheating tube is connected to the inlet of the plasma chamber, and the other end of the preheating tube is passed through the inlet of the preheating chamber To connect the mixing chamber. 2. The plasma assisted catalyst recombining device of claim 1, wherein an air and a carbon helium gas are mixed in the mixing chamber and enter the plasma chamber along the preheating tube to become a a quasi-neutral mixed gas entering the first recombination chamber and recombining in the first catalyst bed to form a high temperature reaction gas, the high temperature reaction gas entering from the outlet of the first recombination chamber The second recombination chamber is recombined in the first catalyst bed to form a high temperature recombination gas, and the high temperature recombination gas enters the recirculation tube from the first recombination chamber opening, and enters the pretreatment tube along the recirculation tube The hot chamber is configured to heat the air in the preheating tube and the carbon helium gas, and exit the preheating chamber from the preheating chamber outlet. 3. The plasma assisted catalyst reassembly device of claim 1, wherein the feeder further has a first regulating valve and a second regulating valve, and the first regulating valve and the first regulating valve The two regulating valves are connected to the mixing chamber to control the flow rate of an air and a hydrocarbon gas into the mixing chamber, respectively. 4. The plasma assisted catalyst reassembly according to claim 1, wherein the portion of the recirculation tube in the first recombination chamber is a coil. 5. The plasma-assisted catalyst reassembly according to claim 1, wherein a direction of one end of the preheating tube connected to the plasma chamber inlet is offset from a center of the plasma chamber. 6. The plasma-assisted catalyst reassembly according to claim 1, wherein the preheater further comprises a disk-shaped preheating passage disposed in the preheating chamber; Connected between one end of the preheating tube and the inlet of the plasma chamber. 7. The plasma assisted catalyst reassembly according to claim 1, wherein the recombination reactor further comprises a first partition plate disposed in the first recombination chamber. 8. The plasma assisted catalyst reassembly according to claim 7, wherein the first partition is a cross partition or a cross-shaped partition. 9. The plasma assisted catalyst reassembly apparatus of claim 1, wherein the recombination reactor further comprises a second separator disposed in the second recombination chamber. 10. The plasma assisted catalyst recombining device of claim 1, wherein the preheater further comprises a third partitioning plate disposed in the preheating chamber to preheat the cavity It is divided into one of the first preheating zone and the second preheating zone. 11. The plasma assisted catalyst recombination apparatus of claim 10, wherein the preheating tube surrounds the recombination reactor along the first preheating zone and the second preheating zone. 12. The plasma assisted catalyst recombination device of claim 10, wherein the preheater further comprises a second catalyst bed, a third catalyst bed' and a fourth catalyst bed, and The second catalyst bed is located at the first preheating zone, and the third catalyst bed is located at a boundary between the first preheating zone and the second preheating zone, and the fourth catalyst bed is located at the second preheating zone. Hot zone. 13. The plasma assisted catalyst recombination device of claim 12, wherein the second catalyst bed has a high temperature water vapor transfer catalyst, and the third catalyst bed has a low temperature water gas transfer catalyst, and The fourth catalyst bed has an oxidation 38 201100164 . Carbon selective oxidation catalyst. 14. The plasma assisted catalyst reassembly according to claim 1, wherein the feeder further has a piezoelectric atomizing unit connected to the mixing chamber. 15. The plasma assisted catalyst recombining device of claim 14, wherein a hydrocarbon liquid and a water are formed in the piezoelectric atomizing unit to atomize the hydrocarbon liquid and the water. Entering the mixing chamber to enter the preheating tube after being mixed with air entering one of the mixing chambers, atomizing the carbon enthalpy liquid and the water to form a vaporized hydrocarbon liquid and the leeches in the preheating tube And entering the plasma chamber along the preheating tube to form a quasi-neutral mixed gas, the quasi-neutral mixed gas entering the first recombination chamber and being carried out in the first catalyst bed Recombining to form a high temperature reaction gas from the outlet of the first recombination chamber into the second recombination chamber and recombining in the first catalyst bed to form a high temperature recombination gas, the high temperature recombination gas from the first a recombination chamber opening enters the recirculation tube, and enters the preheating chamber along the recirculation tube to heat the air, the atomized carbon crucible liquid and the atomized water in the preheating tube, and self preheating The chamber outlet exits the preheating chamber. The plasma assisted catalyst recombination device of claim 15, wherein the hydrocarbon liquid is alcohol or liquefied petroleum gas. 17. The plasma assisted catalyst recombining device of claim 14, wherein the feeder further has a first regulating valve, a third regulating valve and a fourth regulating valve, and the first regulating The valve is connected to the mixing chamber to control the flow of air into the mixing chamber, and the third regulating valve and the fourth regulating valve are connected to the piezoelectric atomizing unit to respectively control a hydrocarbon liquid and a water inlet. The flow rate of the piezoelectric atomizing unit. 18. The plasma assisted catalyst recombination 39 201100164 as claimed in claim 14, wherein the preheating chamber further has a preheating chamber opening to allow an air to enter the preheating chamber opening. Hot cavity inside. 19. The plasma assisted catalyst recombining apparatus of claim 18, wherein the feeder further has a fifth regulating valve, and the fifth regulating valve is connected to the preheating chamber opening to control the Air flow. 20. A plasma assisted catalyst recombination method comprising: providing a piezoelectric atomization unit to atomize a liquid of hydrogen and one water; providing an air; mixing the air and atomizing the hydrocarbon liquid And the water, and atomizing the carbonized liquid and the water; providing a plasma reactor to excite the air and the vaporized hydrocarbon liquid and the water into a quasi-neutral mixed gas And providing a recombination reactor to recombine the quasi-neutral mixed gas to form a high temperature reaction gas, and recombining the high temperature reaction gas to form a high temperature reformed gas, and the south temperature reformed gas is suitable for heating the atomized carbon The mouse liquid and the water are such that the atomized hydrocarbon liquid is vaporized with the water. 〇 21. The plasma assisted catalyst recombination method of claim 20, wherein the hydrocarbon liquid is alcohol or liquefied petroleum gas. 40
TW98120992A 2009-06-23 2009-06-23 Plasma assisted catalyst reformation apparatus and method TWI379710B (en)

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