TWI379710B - Plasma assisted catalyst reformation apparatus and method - Google Patents

Plasma assisted catalyst reformation apparatus and method Download PDF

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TWI379710B
TWI379710B TW98120992A TW98120992A TWI379710B TW I379710 B TWI379710 B TW I379710B TW 98120992 A TW98120992 A TW 98120992A TW 98120992 A TW98120992 A TW 98120992A TW I379710 B TWI379710 B TW I379710B
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recombination
chamber
preheating
plasma
catalyst
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TW98120992A
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Chinese (zh)
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TW201100164A (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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1379710 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褒置與方法。 【先剷技術】 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 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=式 而轉換為氫氣燃料,而氫氣燃料是目前所認為較為環保^ 燃料之一。 傳統的觸媒重Μ裝置必須要先利用輔助燃燒 器先行加_絲,直·媒床達打作溫度後 ^ 熱後之故氫氣體與空氣進行部份氧化重組反細轉 氣、’並藉由部份氡化重組反應所產生的熱量以維持觸=床 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魔大且較為产 =構件,並仙於先行加_媒床,在使訂非常沒^ 另-種傳統的觸媒重組裝置是用於碳氫液體_且, ,要是利賴爐來加熱碳纽體與水㈣使其汽化 乳體’藉以加熱觸媒床而進行重組反應,故此觸媒重^ 置必須持續運作鋼爐來加熱碳氫㈣與水份。然而,、 加熱的效率過差,使得能量損耗較大,且鍋爐通常亦^ 1379710 積龐大且危險的構件。 此外,習知技藝另有提出電漿輔助觸媒重組裝置,利 用電漿反應器產生高壓高頻的交流電,藉以產生放電來加 熱碳氫氣體與空氣,藉以將電漿化之碳氫氣體與空氣加熱 觸媒床以使觸媒床達到工作溫度而產生重組反應。當觸媒 床的溫度到達上限值時,便可切斷電漿反應器電源,且當 觸媒床的溫度下降至下限值時,便重新恢復電漿反應器電 源。 • 另外,美國第6,702,991號專利、美國第6,804,950號 專利、美國第6,506,359號專利則是以前述習知技藝再稍加 改良。然而,無論是針對碳氫氣體或碳氩液體,均都需要 額外配置加熱器具以加熱觸媒床到達工作溫度,使得觸媒 重組裝置整體的體積非常龐大,且非常危險。再者,加熱 器具的加熱效率均不甚理想,且均在熱交換至觸媒床的過 程中浪費許多能量。 藝 【發明内容】 有鑑於此,本發明之目的是提供一種電漿輔助觸媒重 組裝置,將高溫重組反應器包覆在預熱器内,並利用再循 環管的配置以導引熱源,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。 6 為達上述或是其他㈣’本發明S出一種電装輔助觸 預孰!!裝置,包括進料器、電漿反應器、重組反應器以及 ,二,,其中重組反應器是連接電漿反應器。進料器具有 源而電聚反應器包括電®腔體、電聚電極與電褒電 〜早元,其中電漿腔體具有電漿腔入口與電漿 電元輕接電㈣體與電聚電極’以於 腔體、第二=】 ge)。重組反應器包括第—重組 重、、,腔體、再循環管、多孔板以及第一觸媒庆。 -重組腔開/,、而且腔八口、第-重組腔出口與第 一:腔體是位於第二重組腔體内,而第二重組腔體具; 組腔出口。再循環管是部份位於第一重組腔體内, 再循環管之一诚县嗝吐诊 版円,而 -m ^連接弟一重組腔開口,且再循環管之另 疋!由第一重組腔出口而穿出第二重組腔出口。 一=配置於第一重級腔體内,並鄰近第一重組腔入口。第 1媒床是配置於第—重組腔體與第二重組腔體内 二二括預熱腔體與預熱管,其中重組反應器是位於預熱: ^ θ且預熱腔體具有預熱腔入口與預熱腔出口’而預哉 二,置於韻腔體内’並環繞重組反應器,且預熱管之 端疋連接電漿腔入口’又預熱管之另一端是穿出預 入口以連接混合室。 ‘、、、 為達上述或是其他目的,本發明另提出—種電漿辅助 觸媒重組方法,包括下列步驟:提供壓電霧化單元將 液體與水份霧化;提供空氣;混合空氣以及霧化之碳氣液 體與水份,並將霧化之碳氫液體與水份氣化;提供電漿反 1379710 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 • 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,而沿再循環管邊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氫氣體進入混合室之流量。 瞻 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 1379710 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 • 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 •化之碳氫液體與水份於預熱管内形成氣化之碳氫液體與水 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。 1379710 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,以分別控制碳氫液體與水份之流量。 在本發明之一實施例申,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, • 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,藉此以縮小電漿輔助觸媒重組裝置的體積,並提高碳 氫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 B 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, 本發明之電漿輔助觸媒重組裝置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 1379710 程 到增加重組效率與熱源使用效率二:: 各個構件與其連接關係,接著再說明本發明 电.槳反應|§ 110包括 ^ „ 冤漿腔體112、電漿電極114與 電漿電源供應皁元116,甘士+故& 干u ib,其中電漿電源供 接電漿腔體112與電漿雷盔^丄 疋祸 电水電極114,藉由供應高壓高頻的交1379710 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. [First Shovel Technology] With the advancement of technology, the available energy is also diversified, and the petrochemical fuel or biofuel can be converted into hydrogen fuel, especially through catalyst recombination. In general, natural gas, alcohol, decane: butane and other hydrocarbon gases or hydrocarbon liquids can be converted to hydrogen fuel at high temperatures through the recombination of the catalyst, and hydrogen fuel is currently considered to be more environmentally friendly. ^ One of the fuels. The traditional catalyst heavy-duty device must first use the auxiliary burner to add _ silk first, and the direct-medium bed reaches the temperature. After the heat, the hydrogen gas and the air are partially oxidized and recombined. The auxiliary burner or electric heater is turned off by the heat generated by the partial deuteration recombination reaction to maintain the temperature of the contact = bed. However, auxiliary burners or electric heaters are usually large in size and relatively productive, and they are used in advances to add _ media beds, which are very difficult to make. Another traditional catalyst recombination device is used for hydrocarbon liquids. _ and, if the furnace is used to heat the carbon body and water (4) to vaporize the milk body to recombine by heating the catalyst bed, the catalyst must continue to operate the steel furnace to heat the hydrocarbon (4) and water. Share. However, the efficiency of heating is too low, resulting in a large energy loss, and the boiler is usually also a large and dangerous component. In addition, the prior art also proposes a plasma-assisted catalyst recombination device for generating a high-voltage high-frequency alternating current by using a plasma reactor, thereby generating a discharge to heat the hydrocarbon gas and the air, thereby pulverizing the hydrocarbon gas and the air. The catalyst bed is heated to bring the catalyst bed to operating temperature to produce a recombination reaction. When the temperature of the catalyst bed reaches the upper limit, the power to the plasma reactor can be cut off, and when the temperature of the catalyst bed drops to the lower limit, the plasma reactor power is restored. In addition, U.S. Patent No. 6,702,991, U.S. Patent No. 6,804,950, U.S. Patent No. 6,506,359, the disclosure of which is incorporated herein by reference. However, whether it is for hydrocarbon gas or carbon argon liquid, an additional heater is required to heat the catalyst bed to the operating temperature, making the overall volume of the catalyst recombination unit very bulky and very dangerous. Moreover, the heating efficiency of the heating means is not ideal, and both energy is wasted in the process of heat exchange to the catalyst bed. SUMMARY OF THE INVENTION In view of the above, an object of the present invention is to provide a plasma assisted catalyst recombination device, which comprises a high temperature recombination reactor coated in a preheater and configured by a recirculation pipe to guide a heat source. Effective use of heat sources and drastically reduce the size of the catalyst recombination unit. Further, another object of the present invention is to provide a plasma-assisted catalyst recombination method in which a hydrocarbon liquid is first atomized and then a hydrocarbon liquid is heated and vaporized. Since the atomized hydrocarbon liquid has a large surface area, the heating efficiency can be greatly improved. 6 in order to achieve the above or other (four) 'the invention S out of a electrical auxiliary touch pre-!! device, including the feeder, the plasma reactor, the recombination reactor and the second, wherein the recombination reactor is connected to the plasma reaction Device. The feeding device is active and the electropolymerization reactor comprises an electric cavity, an electric polyelectrode and an electric current to an early element, wherein the plasma cavity has a plasma chamber inlet and a plasma battery to be electrically connected (four) body and electropolymer The electrode 'is in the cavity, the second = ge). The recombination reactor includes a first-recombination weight, a chamber, a recirculation tube, a multiwell plate, and a first catalyst. - Recombination chamber opening /, and the cavity eight, the first - recombination chamber outlet and the first: the chamber is located in the second recombination chamber, and the second recombination chamber has; the chamber outlet. The recirculation pipe is partially located in the first recombination chamber, and one of the recirculation tubes is the one of the recirculation tubes, and the -m ^ is connected to the recombination chamber opening, and the recirculation tube is another one! The second recombination chamber outlet is passed through the first recombination chamber outlet. One = is disposed in the first heavy chamber and adjacent to the first recombination chamber inlet. The first media bed is disposed in the first recombination cavity and the second recombination cavity, the second preheating cavity and the preheating pipe, wherein the recombination reactor is located in the preheating: ^ θ and the preheating cavity has preheating The inlet of the chamber and the outlet of the preheating chamber are pre-twisted, placed in the cavity and surrounded by the recombination reactor, and the end of the preheating tube is connected to the inlet of the plasma chamber, and the other end of the preheating tube is pretreated. The entrance is to connect the mixing chamber. For the above or other purposes, the present invention further provides a plasma assisted catalyst recombination method comprising the steps of: providing a piezoelectric atomizing unit to atomize liquid and moisture; providing air; mixing air and Atomized carbon gas liquid and water, and vaporized atomized hydrocarbon liquid and water; providing plasma anti- 1379710 reactor to excite air and vaporized hydrocarbon liquid and water into 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 the high temperature reformed gas is suitable for heating the atomized hydrocarbon liquid and water to make the mist The hydrocarbon liquid is vaporized with 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 is recombined from the first catalyst chamber into the second recombination chamber to form a high temperature recombination gas, and the high temperature recombination is performed. 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 hydrocarbon gas. The flow into the mixing chamber. In one embodiment of the invention, the portion of the recirculation tube in the first recombination chamber is, for example, a coil. In one embodiment of the invention, the direction in which one end of the preheating tube is connected to the inlet of the 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 1379710 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 partitioning plate, and the third dividing plate is disposed in the preheating cavity to distinguish the preheating cavity into the first connected Preheating zone and 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, and 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 the 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 misty hydrocarbon liquid And the water forms a vaporized hydrocarbon liquid and water in the preheating pipe, and enters the plasma cavity along the preheating pipe to form a quasi-neutral mixed gas, and the quasi-neutral mixed gas enters the first recombination cavity. And recombining in the first catalyst bed to form a high-spiking reaction gas, and the high-temperature reaction gas is recombined from the first recombination chamber into the second recombination chamber to form a high-temperature recombination gas, a high-temperature recombination gas. The first recombination chamber opening enters the recirculation tube, 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 exits from the preheating chamber outlet Preheat the cavity. 1379710 In one 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 hydrocarbon 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 feeder has a fifth regulator, and the fifth regulator is connected to the preheat chamber opening to control 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 recombination of hydrocarbon gas 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 this 10 1379710 is to increase reorganization. Efficiency and heat source use efficiency 2:: The relationship between each component and its connection, and then the electric paddle reaction of the present invention|§ 110 includes ^ 冤 slurry cavity 112, plasma electrode 114 and plasma power supply soap element 116, Gans + 故 & dry u ib, where the plasma power supply is connected to the plasma chamber 112 and the plasma lightning helmet ^ 丄疋 electric water electrode 114, by supplying high voltage and high frequency

流電,可於電聚腔體112内產生電弧放電,以游離= 體112内的氣體(之後會再詳述此氣體為空氣、碳氮氣體或 氣化之碳氫液體等混合氣體)。 此外’電裝腔體112具有電聚腔入口 112a與電聚腔出 口 U2b’而前述之氣體便是由«腔人π 112a進入電黎 腔體112,並在被游離後從電漿腔出口 U2b離開電漿腔體 112,其中電漿反應器ι1〇是連接重組反應器12〇,而使離 開電漿腔體112後的氣體便會進入重組反應器12〇。 重組反應斋120包括第一重組腔體121、第二重組腔 體122、再循環管123、多孔板124以及第一觸媒床125, 其中第一重組腔體U1是位於第二重組腔體!22内,且第 一觸媒床125是配置於第一重組腔體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〗21與第二重組腔體 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12ι與第二重 組腔體122的形狀。 11 1379710 此外,第一重組腔體121具有相對之第一重組腔入口 Hla與第-重組腔出口 12lb,而第—重組腔人口 接電聚腔出口 mb,以使游離後之氣體可由第―重电腔^ = 2la進人第-重組腔人〇 121a内而與第一觸媒床⑵ 進仃重組反應。接著,氣體便由第—重組腔出口 121b進入 第二重組腔體122内而繼續與第—觸媒床125進行重組反 應0 、The galvanic current can generate an arc discharge in the electropolymerization chamber 112 to free the gas in the body 112 (this gas will be described later as a mixture of air, carbon nitrogen gas or vaporized hydrocarbon liquid). In addition, the 'electric cavity 112 has an electrical cavity inlet 112a and an electrical cavity outlet U2b', and the aforementioned gas enters the electrical cavity 112 from the cavity π 112a and exits the U2b from the plasma cavity after being freed. Leaving the plasma chamber 112, wherein the plasma reactor ι1 is connected to the recombination reactor 12, and the gas leaving the plasma chamber 112 enters the recombination reactor 12A. The recombination reaction 120 includes a first recombination chamber 121, a second recombination chamber 122, a recirculation tube 123, a perforated plate 124, and a first catalyst bed 125, wherein the first recombination chamber U1 is located in the second recombination chamber! 22, 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 both in the shape of a barrel, and the first recombination cavity 21 overlaps with the center line of the second recombination cavity 122 and is aligned with the plasma. The centerline of the cavity 112 is convenient for assembly operations. However, the present invention does not limit the shape of the first recombination cavity 12i and the second recombination cavity 122. 11 1379710 In addition, the first recombination chamber 121 has a first recombination chamber inlet Hla and a first recombination chamber outlet 12lb, and the first recombination chamber population is electrically connected to the outlet chamber mb, so that the free gas can be made by the first weight The electric cavity ^ = 2la enters the first-recombination chamber 〇121a and reacts with the first catalyst bed (2). Then, the gas enters the second recombination chamber 122 from the first recombination chamber outlet 121b to continue the recombination reaction with the first catalyst bed 125.

亦即依據氣體在第-觸媒床125的流向,可將第一觸 媒床125大致區分為位於第一重組腔體pi内鄰近一重組 腔入口 121a之重組反應如段、位於第一重組腔體κι與第 -重組腔體122交界處之重組反應中段,以及位於第二重 組腔體122内鄰近一重組腔入口 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 實質進行重組反應的過程並無不同。 為使氣體從第一重叙腔入口 i2la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 i21a。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124後,由於第一重組 腔體121與第二重組腔體122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(fl〇w_s上0it_.e4iGuit)或通路效應 (channeling effect)問題’而使氣體在流動的過程中接觸最 12 ⑸ 9710 ,少的觸媒。 々為解決上述缺點,本發明於第一重組腔體121再開設 第重組腔開口 12〗c,並於第二重組腔體122開設第二重 紐腔出口 122a,其中第一重組腔開.口 121(:可開設於第一觸 ,床125的重組反應後段區域,而第二重組腔出口 是 鄰近第一重組腔出口 121b,而可開設於第一觸媒床125的 重組反應中段區域。 承接上述,再循環管123是部分位於第一重組腔體121 内,而再循環管123之一端是連接第一重組腔開口 12卜, 且再循環管123之另一端是經由第一重組腔出口 Ulb而穿 出第二重組腔出口 122a。再循環管123於第一重組腔體121 内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的重组反應前段區域。 如此一來,氣體乃以較長的路徑通過第一觸媒床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 應=效率。此外,再循環管123於第一重組腔體121内的 • 部份可為盤管而呈現不規則的排列,藉以身生前述之 氣流短路問題。 請在參考圖ΙΑ〜1B,預熱器13〇包括預熱腔體132 與預熱管134,其甲重組反應器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123 ml出重組反應器12〇而進入預熱腔體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 1379710 口 132被收集利用。 此外,賴腔體132另具有預熱腔人口咖,而預孰 = 134是配置於預熱腔體132内,並環繞重組反應器η。。 =卜’預熱官134之-端是連接霞腔人口 112&,又預熱 官:34之另-端是穿出預熱腔入口 ma以連接進料器_ 之心合至142 °如此-來’氣體最初是在混合室⑷進行 =’而經由預熱管134進人電漿腔體112内進行游離反 應0That is, according to the flow direction of the gas in the first-catalyst bed 125, the first catalyst bed 125 can be roughly divided into a recombination reaction located in the first recombination cavity pi adjacent to a recombination chamber inlet 121a, such as a segment, located in the first recombination chamber. The middle portion of the recombination reaction at the junction of the body κι and the first-recombination cavity 122, and the rear portion of the recombination reaction located in the second recombination chamber 122 adjacent to a recombination chamber inlet 121& Of course, the division of the first catalyst bed 125 into three segments is for convenience only, and the process of substantially performing the recombination reaction is not different. In order to allow the gas to be evenly distributed after entering the first recombination chamber 121 from the first refill chamber inlet i2la, the present invention can dispose the perforated plate 124 within the first recombination chamber 121 and adjacent to the first recombination chamber inlet i21a. In this way, by the diffusion effect of the perforated plate 124, the gas can be uniformly passed through the perforated plate 124 to react with the first catalyst bed 125. In general, after the gas passes through the perforated plate 124, due to the geometric arrangement of the first recombination cavity 121 and the second recombination cavity 122, the gas still cannot pass the first catalyst bed 125 completely uniformly, but will be the shortest. The path passes through the first catalyst bed 125 to the first recombination chamber outlet 121b. These phenomena are often referred to as airflow shorts (0it_.e4iGuit on fl〇w_s) or channeling effect problems, which cause the gas to contact the most 12 (5) 9710, less catalyst during the flow. In order to solve the above disadvantages, the present invention reopens the first recombination cavity opening 12 〖c in the first recombination cavity 121, and opens the second re-nuclear cavity outlet 122a in the second recombination cavity 122, wherein the first recombination cavity opens. 121 (: can be opened in the first touch, the rear reaction region of the bed 125, and the second recombination chamber outlet is adjacent to the first recombination chamber outlet 121b, and can be opened in the middle portion of the recombination reaction of the first catalyst bed 125. In the above, the recirculation pipe 123 is partially located in the first recombination cavity 121, and one end of the recirculation pipe 123 is connected to the first recombination cavity opening 12, and the other end of the recirculation pipe 123 is via the first recombination cavity outlet U1b. The second recombination chamber outlet 122a is passed out. The portion of the recirculation tube 123 in the first recombination chamber 121 can be regarded as an obstacle to prevent the gas from passing through the recombination reaction front region of the first catalyst bed 125 in the shortest manner. As a result, the gas passes through the recombination reaction front region of the first catalyst bed 125 in a longer path, thereby contacting more catalyst to enhance the recombination reaction=efficiency. Further, the recirculation tube 123 is in the first reorganization. Cavity 121 The portion can be arranged in an irregular arrangement for the coil to thereby cause the short-circuit problem of the airflow described above. Referring to Figures ΙΑ1 to 1B, the preheater 13A includes a preheating chamber 132 and a preheating tube 134. The recombination reactor 120 is located in the preheating chamber 132, and the preheating chamber 132 has a preheating chamber outlet 132b. When the gas flows through the rear reaction region of the first catalyst bed 125, it passes through the first The chamber opening 121c is recombined and flows into the recirculation tube 123, and proceeds into the preheating chamber 132 along the recirculation tube 123 ml out of the recombination reactor 12, and the gas which finally completes the recombination reaction fills the entire preheating chamber. 132 is taken from the preheating chamber 13 1379710 port 132. In addition, the ray chamber 132 has a preheating chamber population, and the pre 孰 = 134 is disposed in the preheating chamber 132 and surrounds the recombination reactor η = Bu's preheating officer 134's - end is connected to the Xia cavity population 112 & and preheating officer: 34 the other end is through the preheating chamber inlet ma to connect the feeder _ heart to 142 ° So - the 'gas is initially in the mixing chamber (4) = ' while entering the plasma chamber via the preheating tube 134 112 free for reaction 0

附帶一提的是,再循環管123之另一端在穿出第二重 組腔出口 122a後,可配設在預熱腔體132内的任何位置, 而在本實施例中’再# ί哀管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輔助觸媒重組裝置1〇〇之各 個構件間複雜的配置之後以下將具體以曱烷之碳氫氣體 說明電漿辅助觸媒重組裝置100的操作流裎。不過本發明 並不限定碳氫氣體的種類’舉凡乙烷、丙烷、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組反應(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。 1379710 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 或完全氧化重組反應的關鍵條件便是調整碳氫氣體與空氣 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,若曱炫對空氣的比 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 • 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更可具有第一調節閥 145與第二調節閥146,而第一調節閥145與第二調節閥 146是連接混合室142,以分別控制空氣(未繪示)與甲烷(未 緣示)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 • 為20 : 1(亦即氧碳比為4.2 : 1)。 接著,空氣與曱烷便沿著預熱管134而進入電漿腔體 112’並藉由電漿腔體ip内的放電現象而活化。詳細而 '言’部份的空氣與曱烷會受到非熱電漿的高能量電子衝擊 而產生游離(I〇nizati〇n)、解離(Dissociati〇n)、激發 (Excitation)等等反應,進而形成含有離子(I〇n)、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 1379710 丁:王ft而釋放出大量的熱量以加熱第-觸媒床 125,猎以使卜觸媒床125中的觸媒溫度上升。儘管甲烧 ^全燃料可騎“大的熱量,但是此賴是發生在 工乳與代朗到第―觸媒床125之前的混合狀態,所以 f院所釋«賴量無法完全經錢相(缝的空氣與甲 烧)至固相(觸媒)的傳導而傳遞至第一觸媒床125。 ,得注意的是,本實施例是先將空氣與曱烷混合後再Incidentally, the other end of the recirculation pipe 123 may be disposed at any position within the preheating cavity 132 after passing through the second recombination chamber outlet 122a, and in the present embodiment, The other end of 123 is disposed adjacent to the preheating tube 134 adjacent to the plasma chamber 112 to heat the gas in the preheating tube 134. The operation flow of the plasma assisted catalyst recombination apparatus 100 will be specifically described below with the hydrocarbon gas of decane, after roughly explaining the complicated arrangement between the respective members of the plasma assisted catalyst recombination apparatus 1 of the present invention. However, the present invention is not limited to the type of hydrocarbon gas. It is also applicable to hydrocarbon gas such as ethane, propane or gas. In the process of recombination reaction with a catalyst, if the hydrocarbon gas can be reconstituted into the expected 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 and recombination 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. . 1379710 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 complete oxidation and recombination reaction is to adjust the hydrocarbon. The ratio of gas to air. In the case of methane, for example, 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 sputum to air is higher, the partial oxidative recombination reaction is easier. In this way, the present invention does not require any additional auxiliary heaters to directly burn the first catalyst bed 125 by completely burning the hydrocarbon gas in the aforementioned apparatus, 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 regulating valve 145 and a second regulating valve 146, and the first regulating valve 145 and the second regulating valve 146 are connected to the mixing chamber 142 to respectively control the air ( The flow rate of methane (not shown) entering the mixing chamber is shown. In the start-up phase (preheating) of the present 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 flow ratio of air to methane is 20 : 1 (that is, the oxygen to carbon ratio is 4.2: 1). Next, air and decane enter the plasma chamber 112' along the preheating tube 134 and are activated by the discharge phenomenon in the plasma chamber ip. In detail, the air and decane in the 'speaking' part are subjected to high-energy electron impact of non-thermal plasma to generate free (I〇nizati〇n), dissociation (Excitation), etc., and then form A quasi-neutral mixed gas containing ions (I〇n), electrons (Electron) and free radicals (not shown). The quasi-neutral mixed gas mentioned above enters the first recombination chamber 121 and releases a large amount of heat to heat the first catalyst bed 125, so as to catalyze the catalyst in the catalyst bed 125. The temperature rises. Although the full fuel can be used to ride a "large amount of heat, it depends on the mixed state of the working milk and the Dailang to the first catalyst bed 125, so the f-room can not completely pass the money phase ( The slit air and the burnt gas are transferred to the first catalyst bed 125 by conduction to the solid phase (catalyst). It should be noted that this embodiment first mixes the air with the decane.

導入第-觸媒$ 125。但若是將曱烧與空氣分別導入第一 觸媒床125後’再使空氣與曱燒混合燃燒的話,儘管第一 觸媒床125是由多孔性的觸媒所構成,但是多孔性的觸媒 仍會導致甲⑥與m其中混合不良,產生燃燒不完全的 問題。 ^ a—般來說,第一觸媒床125在重組反應前段、中段與 後段區域的溫度會呈遞減的狀態,而當重組反應前段區域 之第一觸媒床125的溫度超過底限值時,便可以開始調整 甲焼•與空氣的比例’以使甲烷可漸進式地調整為不完全燃 態。以甲烷為例,此底限值的溫度為550°C,而接著 可分別調整空氣與曱烷的流量比為11.9 : 1、14.76 : 1或 9·52 : 1(亦即氧碳比分別為為2 5 :卜3丨:!或2 :丨),以 減> 空氣而使甲烷進行一連串不同程度的不完全燃燒,而 將釋放出的大量熱量持續翹由氣相至固相的傳導而不斷加 熱第一觸媒床125。 此時由於重組反應前段區域的觸媒溫度已超過底限 5 5 〇 °C ’所以空氣中少部分未燃燒的氧分子會與曱烷分子4 觸媒表面上進行部分氧化重組,而由於此不完全燃燒是音 16 1379710 生在Am域之每個觸媒的表面上,所以此部分 所=放出的熱!會直接傳遞到每個單一觸媒 :且 反應前段區域的觸媒溫度會迅速升高。 吏件重組 田接著’經由第一觸媒床125間固相至固相的傳 上甲燒與空氣燃燒所釋出的熱量,便可加速第一觸:V 其他區域的升溫’而使第—觸媒床二:在床二 值=以上,但不超過極限值900〇C為原則。、 ,得注意的是’若是完全以甲烧與空氣進行完. 所產生的熱量加熱整個第一觸媒床125,而使 j 應TV中段與後段區域的溫度都到達底限 的時間才能^ 更多的甲院與空氣,並耗掉更長 第-媒床125的溫度上升而接近9歡時,亦即 女125在重組反應前段、中段與後段區域的溫度 大=達底限值繼以上時,便可再次調整空氣與甲炫 里:為9.52 : 1或8.57 : 1 (亦即氧碳比分別為為2 : 1 ί —入·^以進—步減少勉而使甲燒再進行不同程度的 媒:二溫ί釋放其所含較少的熱f以持續維持第-觸 由於第:觸媒床125在重組反應前段、中段與後段區 :皿度夕半已在工作溫度以上’所以空氣尹較多部份的 ,刀子與甲淀分子在第一觸媒床125中大部分的單一觸媒 2賴穩定的部份氧化重組,且其所釋出的熱量會直接 傳遞到母個早一觸媒以維持第—觸媒床125的溫度,而使 17 觸媒床125的溫度保持在55〇oc〜9〇〇°C之間。 ㊉亦即,在本發明之電漿辅助觸媒重組裝置1〇〇中,僅 i ^ 需額外設置耗費大量 ,預熱器,便可使第一觸媒床125迅速升高的工作溫 X,错此可使電漿辅助觸媒重組裝置1〇〇迅速且較省成本 、方式元成起機(預熱觸媒床)程序以達正常運作。 ^田70成起機程序後,以下將再敘述正常運作的流程。 月再參考圖1A〜1B,類似前述’首先調整第一調節閥145 與第二調節閥146而使空氣與甲烷以前述比例進入混合室 142進行混合,而空氣與曱烷的流量可比為9.52:丨或8.57: 1 (亦即氧碳比分別為為2 : 1或丨8 :丨)之欲進行非完全燃 燒的比例。 接著,空氣與甲烷會進入預熱管134進行加熱(此被餘 熱加溫的過程會在之後詳述),並順著預熱管134進入電漿 腔體112,並藉由電漿腔體U2内的放電現象進而形成含 有離子、電子與自由基的準中性混合氣體(未繪示)。在本 • 實施例中,預熱管134連接電漿腔入口 112a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漿腔體 112後會繞著電漿電極114產生渦漩流動,藉此使空氣與 甲烧更均勻地混合以被活化為準中性混舍氣體。 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 混合氣體中的游離甲烷分子與游離氧分子便會在重組反應 刖段區域的觸媒表面進行部份氧化重組(partial 〇xidati〇n Reforming)反應’逐漸產生一氧化碳、二氧化碳、氫氣與 18 1379710 .水份,此時這些一氧化碳、二氧化碳、氩氣、水份(氣態)、 不反應作用的氮、尚未反應的甲烷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’鬲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 氣體中尚未反應的曱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 〇xidati〇n • Reforming)反應,逐漸將尚未反應的甲烷分子與氧分子完 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之重組反應後段區域中的這些一 氧化碳、二氡化碳、氫氣、水份(氣態)、不反應作用的氮 便形成高溫重組氣體(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 鲁 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 混清。 接著,高溫重組氣體會從第一重組腔開口 12ic進入再 循環管123内。在前文的敘述中,再循環管123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’咼溫重組氣體可吸收第一觸媒床125之重組反應前段 19 區域中的熱量,並將熱量傳遞至笛 十丄 ❽主弟一觸媒床125之重組反 應中段區域,藉此可使第一觸棋戍^ ’綠床125的溫度分布均勻, 以進-步提升整體第-觸媒床125的反應效果。 高:重組氣體便沿著再循環管123進入預熱腔 =:二 132内之空氣與甲院,而在預熱管 之空氣與甲燒進入電聚腔體112後會較為容 , ^ ^ . 丰發明僅利用兩溫重組氣體的餘溫 Μ加熱空氣與甲院,而母需 ^ 可而另外设置外部加熱器,藉此可 降低建置成本’並縮傾置整體的尺寸。 在本實施例中,再循環管123之另-端穿出第二重组 腔出口咖後是配置在鄰近„腔體112的二熱^134附 =而使得剛離開重組反應器12G之高溫重組氣體可直接 ,、.、!·夬進入電聚腔體112 β之空氣與甲烧,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 ,體132内的部份例如是以雙層環繞的方式圍繞重組反應 f 120以達到吸收高溫重組氣體熱量以及重組反應器120 :卜傳遞熱里的車父佳效果,不過本發明並不限制預熱管134 以何^環繞重組反應nm。 辅二:重:ϊϊ :3〇是包覆重組反應器120’可娜 應器120 我置100的溫度分佈是從内部高溫的重組反 以楹θ杜向外逐漸降低至外圍中、低溫的預熱器130 ’藉 庫芎體的熱利用率’並可避免直接接觸高溫之重組反 應盗12〇的風險。 熱腔出口;3=1:显且富含氫氣的高溫重組氣體便會從預 D離開預熱腔體132,而輸送到下游的裝置, 20 丄⑽710 經進—步處理後以供應如燃料 途。 了 電池、内燃機等等之後續用 於第:Jf考® 1A〜1B’在本實施例中,再循環管123 弟重組腔體121内的形妝i 以障礙物的為早條不規_盤管,藉由 第-觸媒床12"5的番/十生混合氣體以最短的方式通過 限定段區域。不過’本發明並不 量為多::二= 量與形狀,而當再循環管123的數 重組腔開口 me。⑽體121亦需再開設對應之第一 更可;第:觸媒床125的重組效率,本發明 重組腔體121或是第二重組腔體122内設置分 方#,4 ·將再另舉實施例並配合圖錢明,而為求說明 ’目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浆輔助觸媒重組 裝置的剖面示意圖,並省略繪示第一觸媒床、再循環管與 第重組腔開口,而圖2B為圖2A之重組反應器沿AA連 線的剖面上視圖。請參考圖2A〜2b,本實施例之電聚辅助 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 220是配置於第一重組腔體12ι内,以使第一重組腔體m 區分出多個各自獨立的第一反應區域S1。 在本實拖例中’第—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si之 橫截面積僅有原本第一重組腔體121之橫截面積的四分之 21 1379710 一’亦即每個第一反應區域S1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 王發展的紊流(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 得以充分接觸此區域内的觸媒。亦即,本實施例之準中性 鲁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S1内的觸媒,而在觸媒表面進行反應,藉以完全利用 第—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 • 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 使第二重組腔體121區分出多個各自獨立的第二反應區域 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 I3〆Import the first catalyst $ 125. However, if the crucible and the air are separately introduced into the first catalyst bed 125 and then the air is mixed with the crucible, the first catalyst bed 125 is composed of a porous catalyst, but the porous catalyst It still causes poor mixing of the 6 and m, resulting in incomplete combustion. ^ a generally speaking, the temperature of the first catalyst bed 125 in the front, middle and rear regions of the recombination reaction is in a decreasing state, and when the temperature of the first catalyst bed 125 in the region before the recombination reaction exceeds the lower limit value Then, you can start to adjust the ratio of nails to air' so that methane can be gradually adjusted to incomplete combustion. Taking methane as an example, the temperature of the lower limit is 550 ° C, and then the flow ratio of air to decane can be adjusted to be 11.9 : 1, 14.76 : 1 or 9·52 : 1 respectively (that is, the oxygen to carbon ratio is For 2 5 : Bu 3丨:! or 2 :丨), to reduce the air to make a series of incomplete combustion of methane, and release a large amount of heat from the gas phase to the solid phase. The first catalyst bed 125 is continuously heated. At this time, since the catalyst temperature in the region before the recombination reaction has exceeded the limit of 5 5 〇 ° C ', a small portion of the unburned oxygen molecules in the air will undergo partial oxidation recombination with the surface of the decane molecule 4 catalyst, and since this is not Complete combustion is the sound of 16 1379710 born on the surface of each of the Am domains, so this part = the heat released! It is passed directly to each single catalyst: and the catalyst temperature in the front region of the reaction rises rapidly. The reorganization of the field will then accelerate the first touch: the temperature rise of the other areas of the V through the solid phase of the first catalyst bed to the solid phase of the fire and the combustion of the air. Catalyst bed 2: In the bed two values = above, but not exceeding the limit value of 900 〇 C as the principle. It should be noted that 'if it is completely burnt with air and the heat generated, the entire first catalyst bed 125 is heated, so that the temperature of the middle and rear sections of the TV should reach the bottom limit. A lot of hospitals and air, and the temperature of the longer medium-bed 125 rises close to 9 Huan, that is, the temperature of the female 125 in the front, middle and back regions of the recombination reaction is large = the bottom limit is above , you can adjust the air and the accompaniment again: 9.52 : 1 or 8.57 : 1 (that is, the oxygen-to-carbon ratio is 2: 1 ί - enter · ^ to advance - step to reduce 勉 and make the smoldering to different degrees The medium: two temperature ί release less heat f contained to maintain the first-touch due to: the catalyst bed 125 in the front, middle and back sections of the recombination reaction: the half of the dish has been above the working temperature 'so air In most parts of Yin, the knives and the Mt. molecules in the first catalyst bed 125 are mostly oxidized and recombined by the single catalyst 2, and the heat released is directly transmitted to the mother. The catalyst maintains the temperature of the first catalyst bed 125 while maintaining the temperature of the 17 catalyst bed 125 at 55. Between oc and 9 〇〇 ° C. In other words, in the plasma-assisted catalyst recombination device 1 of the present invention, only a large amount of extra heating is required, and the first catalyst can be used. The working temperature X of the bed 125 is rapidly increased, which may cause the plasma-assisted catalyst recombination device to be quickly and cost-effectively, and the method is to start the machine (preheating the catalyst bed) to achieve normal operation. After the 70% starting procedure, the normal operation flow will be described below. Referring again to FIGS. 1A to 1B, similarly to the foregoing, 'the first regulating valve 145 and the second regulating valve 146 are first adjusted to allow air and methane to enter the mixture in the aforementioned ratio. The chamber 142 is mixed, and the flow rate of air to decane is 9.52:丨 or 8.57:1 (that is, the ratio of oxygen to carbon is 2:1 or 丨8:丨, respectively) to the ratio of incomplete combustion. Air and methane will enter the preheating tube 134 for heating (this process of warming by residual heat will be detailed later), and enter the plasma chamber 112 along the preheating tube 134, and through the plasma chamber U2 The discharge phenomenon further forms a quasi-neutral mixed gas containing ions, electrons and radicals (not shown) In the present embodiment, the direction in which the preheating tube 134 is connected to the plasma chamber inlet 112a is, for example, offset from the center of the plasma chamber 112, so that air and nails are burned into the plasma chamber 112 and then generated around the plasma electrode 114. The vortex flows, thereby allowing the air to be more uniformly mixed with the smoldering to be activated as a quasi-neutral mixed gas. Then, the quasi-neutral mixed gas enters the first recombination chamber 121' and is in the first touch When the media bed 125 is higher than the working temperature, the free methane molecules and the free oxygen molecules in the quasi-neutral mixed gas will undergo partial oxidation recombination on the catalyst surface of the recombination reaction zone (partial 〇xidati〇n Reforming). The reaction 'gradually produces carbon monoxide, carbon dioxide, hydrogen and 18 1379710. Water, at this time these carbon monoxide, carbon dioxide, argon, water (gaseous), unreactive nitrogen, unreacted methane molecules and oxygen molecules in the first touch A high temperature reaction gas (not shown) is formed in the front region of the recombination reaction of the media bed 125. The above-mentioned 'hot temperature reaction gas will enter the second recombination cavity 122 from the first recombination chamber outlet 121b to continue the reaction. Similarly, the unreacted decane molecules and oxygen molecules in the high temperature reaction gas will be in the middle and the rear stage of the recombination reaction. The surface of the catalyst is partially oxidized and recombined (Partial 〇xidati〇n • Reforming), and the unreacted methane molecules and oxygen molecules are gradually converted into carbon monoxide, carbon dioxide, hydrogen and water (gaseous). Thus, the carbon monoxide, carbon dioxide, hydrogen, moisture (gaseous), and unreactive nitrogen in the post-recombination reaction zone of the first catalyst bed 125 form a high temperature reformed 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 concept of a partial oxidation recombination process, and the high-temperature reaction gas is only a general term for the concept of a partial oxidation recombination process and is familiar with the art and can be easily understood without being mixed. clear. Next, the high temperature reformed gas enters the recirculation pipe 123 from the first recombination chamber opening 12ic. In the foregoing description, the recirculation pipe 123 has a problem of avoiding 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 improve the recombination efficiency. And greatly reduce the volume of the recombination reactor 12 。. In addition, the 'tempering recombination gas can absorb the heat in the region of the first stage of the recombination reaction of the first catalyst bed 125, and transfer the heat to the middle portion of the recombination reaction of the flute tenth bed of the fleece bed 125. This allows the temperature distribution of the first touch chessboard 'green bed 125' to be uniform to further enhance the reaction effect of the overall first-catalyst bed 125. High: the recombination gas enters the preheating chamber along the recirculation pipe 123 =: the air in the second 132 and the courtyard, and the air in the preheating tube and the burning of the nail into the electropolymer cavity 112 will be more suitable, ^ ^ . Feng invention only uses the residual temperature of the two-temperature recombination gas to heat the air and the courtyard, and the mother needs to provide an external heater, thereby reducing the construction cost and shrinking the overall size. In the present embodiment, the other end of the recirculation pipe 123 passes through the second recombination chamber outlet and is disposed at a temperature adjacent to the "cavity 112" to cause the high temperature recombination gas just leaving the recombination reactor 12G. It is possible to directly enter the air and the smoldering of the electropolymerization chamber 112β, thereby maximizing the residual heat of the high-temperature recombination gas. Further, the preheating tube 134 is preheated, and the inside of the body 132 is preheated. For example, the recombination reaction f 120 is surrounded by a double-layered manner to achieve heat absorption of the high-temperature reformed gas and the effect of the regenerative reactor 120: the heat transfer is not limited to the preheating tube 134. Surrounding the recombination reaction nm. Auxiliary 2: Heavy: ϊϊ: 3〇 is coated with a recombination reactor 120' can be used in 120. The temperature distribution of I set 100 is from the internal high temperature recombination, and the 楹θ Du is gradually reduced to the periphery. The medium and low temperature preheater 130 'borrows the heat utilization rate of the corpus callosum' and avoids the risk of direct contact with high temperature recombination reactions. Hot chamber outlet; 3=1: high temperature recombination gas rich in hydrogen Will leave the preheating chamber 132 from the pre-D and transport it downstream The device, 20 丄 (10) 710 is processed after the step-by-step process to supply the fuel. The battery, the internal combustion engine, etc. are used for the following: Jf test® 1A~1B' In this embodiment, the recirculation pipe 123 recombination chamber The shape i in the body 121 is an irregularity_coil with the obstacle, and the mixed gas of the first-catalyst bed 12" 5 passes through the defined segment area in the shortest way. However, the present invention It is not excessive:: two = quantity and shape, and when the number of recirculation tubes 123 is recombination chamber opening me. (10) body 121 also needs to be opened corresponding to the first one; first: the recombination efficiency of the catalyst bed 125, The recombination cavity 121 of the present invention or the second recombination cavity 122 is provided with a partition #, 4 · will be further exemplified and cooperated with the diagram, and the same name is used for the purpose of explaining the same function. 2A is a schematic cross-sectional view of a plasma assisted catalyst recombination apparatus according to another embodiment of the present invention, and the first catalyst bed, the recirculation tube and the first recombination chamber opening are omitted, and FIG. 2B is FIG. 2A. A top view of the cross section of the recombination reactor along the AA line. Please refer to Figures 2A to 2b, this embodiment The electropolymerization assisted catalyst recombination apparatus 200 is similar to the aforementioned plasma assisted catalyst recombination apparatus 1 (shown in FIG. 1A). The only difference is that the recombination reactor 220 of the plasma assisted catalyst recombination apparatus 2 is more The first partitioning plate 226' is disposed in the first recombination cavity 12i, so that the first recombination cavity m distinguishes a plurality of independent first reaction zones S1. In the example, the first partition 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 si has only the cross section of the original first recombination cavity 121. 21 of the area is 1379710. That is, the equivalent diameter of each first reaction zone S1 is one-half of the equivalent diameter of the first recombination cavity 121, so the length of each first reaction zone S1 The ratio is twice the original length ratio of the first recombination cavity 121. When the airflow quickly passes through a relatively large area of the long diameter, it is easier to form a Fully-developed Turbulence. The different gas components in the turbulent 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 in full contact with the catalyst in this region. That is, the completely mixed gas component in the quasi-neutral Lu mixed gas of the present embodiment is more in contact with the catalyst in the first reaction zone S1, 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. 2C is a cross-sectional view 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 dividing plate 227' and the second dividing plate 227 is disposed in the second recombination cavity 122 to distinguish the second recombination cavity 121 from a plurality of independent stages. The second reaction zone S2 ° In the present embodiment, the number of the second partition plates 227 is, for example, eight, to divide the second recombination cavity 122 into eight symmetrical second reaction zones S2° similar to the foregoing, the second reaction The gas flow in the region S2 is liable to form a fully developed turbulent flow so that the completely mixed gas component in the high temperature reaction gas can more sufficiently contact the catalyst in the second reaction region S2 to enhance the reaction effect. Of course, the present invention does not limit the first partitioning plate 226 and the second partitioning plate 22 I3〆

, 2以的數量與形狀,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 <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辅助觸媒重組 姨蓼的剖面示意圖,並省略繪示第一觸媒床,而圖3B為圖 ^ A A盤狀預熱通道沿BB連線的剖面上視圖。請參考圖3 A 贷,本實施例之電漿辅助觸媒重組裝置300與前述之電 餐_助觸媒重組裝置100(如圖1A所示)相似,其差別僅在 ^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,而空氣與甲烷會從預熱管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 鳆腔體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 烷。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。 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,本實施例之電漿辅助觸媒 重級裝置400與前述之電漿輔助觸媒重組裝置100(如圖 23 1379710 所示)相似’其差別僅在於電漿輔助觸媒重组裝置400之預 熱器430更包括第三分隔板438,而第三分隔板438是配 置於預熱腔體132内,以將預熱腔體132區分為相連之第 一預熱區T1與第二預熱區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T2是位在第一預熱區T1的外 圍。 如此一來’從再循環管123進入預熱腔體132的高溫 重組氣體便會依序通過第一預熱區T1與第二預熱區T2, 而使高溫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 (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楽·輔助觸媒重組裝置以 使其亦能應用於破氫液體的重組反應。圖5A為依據本發 24 、 1379710 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 辅助觸媒重組裝置1〇〇(如圖1A所示)相似,其差別僅在於 電漿辅助觸媒重組裝置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 • 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。 φ 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 1379710 比例,而使碳氳液體逐漸改為進行部份燃燒。類似的程序 已在前述曱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,而碳氫液體亦 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 • 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。 • 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ΙΟμιη,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 1379710 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组腔體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 碳、氫氣、水伤(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,咼溫反應氣體會從第一重組腔出口 1211>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 反應的酒精分子與氧分子完全轉換為一氧化碳、二氧化 礙、氫氣與水份(氣態)。如此一來,在第一觸媒床125之 重組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高溫重組氣體(未繪 示)。 南溫重組氣體會從第一重組腔開口 12ic進入再循環 管123内,以沿著再循環管123進入預熱腔體132中以加 熱預熱管132内的空氣、霧化之酒精與霧化之水份,而在 預熱管132内被加熱之空氣與被氣化之酒精與水份在進入 電漿腔體112後會較為容易被激發活化。 類似前述,為求進一步提升高溫重組氣體中的氫氣含 里或疋降低咼温重組氣體中一氧化碳的含量,本實施例更 27 1379710 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。 請再參考圖5A〜5B’本實施例之電漿辅助觸媒重組裝 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,以將預熱腔體丨32區分 為相連之第一預熱區T1與第二預熱區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The number and shape of 2 are not limited to the shape of the first reaction zone SI or the second reaction zone S2. For example, the first divider 226a' is also 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 crucible according to another embodiment of the present invention, and the first catalyst bed is omitted, and FIG. 3B is a cross-sectional view of the disc-shaped preheating passage along the BB. View on the section. Referring to FIG. 3A, the plasma-assisted catalyst recombining device 300 of the present embodiment is similar to the aforementioned electric-meal-catalyst recombining device 100 (shown in FIG. 1A), and the difference is only in the plasma-assisted catalyst. The preheater 330 of the reconstitution device 300 further includes a disk-shaped pre-heating 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 112a. between. In response to the above, the disk-shaped preheating passage 336 has an air passage spirally surrounding the plasma chamber 112, and the air and methane will enter the disk-shaped preheating passage 336 from the preheating pipe 134, and follow the air passage in the disk-shaped preheating passage 336. The inner winding 'and finally 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 chamber 112 is also relatively high. By means of the design of the disk-shaped preheating passage 336, the heat in the plasma chamber 112 can be transferred outward along the disk-shaped preheating passage 336 to further heat the air in the disk-shaped preheating passage 336. Methane. 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. 4 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 re-leveling device 400 of the present embodiment is similar to the plasma assisted catalyst recombining device 100 (shown in FIG. 23 1379710). The difference is only in the plasma assisted catalyst recombining device. The preheater 430 of 400 further includes a third partitioning plate 438, and the third partitioning plate 438 is disposed in the preheating cavity 132 to distinguish the preheating cavity 132 into the connected first preheating zone T1 and a second 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 T2 is located The periphery of the first preheating zone T1. Thus, the high-temperature reformed gas entering the preheating chamber 132 from the recirculation pipe 123 sequentially passes through the first preheating zone T1 and the second preheating zone T2, thereby causing the high temperature reformed gas to transfer heat to the periphery. Generally, the high temperature reformed gas still has some carbon monoxide, and carbon monoxide is toxic to humans. Therefore, carbon monoxide selective oxidation (CO Preferential Oxidation) can be disposed in the first preheating zone T1 and the second preheating zone T2. The medium is used to convert carbon monoxide into carbon dioxide. Of course, the present invention does not limit 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 reconfigured 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 preheat the third partitioning plate 438 according to the foregoing. The 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. Hereinafter, the electro-hydraulic/assisted catalyst recombination apparatus will be slightly modified so that it can also be applied to the recombination reaction of the hydrogen-trapping liquid. 5A is a schematic 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, A schematic cross-sectional view of a three-catalyst 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 (flat average particle size smaller than ΙΟμιη) are fed to the mixing chamber 142 and mixed with 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. φ 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 the hydrocarbon liquid to be completely burned (completely oxidized and recombined) or not completely burned (incompletely oxidized and recombined). 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 1379710, and the carbon enthalpy liquid is gradually changed to partial combustion. A similar procedure has been described in detail in the start-up process of the aforementioned smoldering, and those skilled in the art can easily understand it, and will not be described again. In the present embodiment, the hydrocarbon liquid is exemplified by, for example, alcohol, but the present invention does not limit the type of the hydrocarbon liquid, and the hydrocarbon 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 into 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. • Next, the air, atomized alcohol and atomized water will enter the preheating tube 134 for heating, similar to the above, at this time, the preheating chamber 132 is filled with high temperature gas, and the atomized alcohol and atomized The water is heated to form a vaporized alcohol and vaporized water. It is worth noting that the average particle size of the fine mist droplets is smaller than ΙΟμιη, 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 piezoelectric atomization in this embodiment. 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 ions, electrons and free radicals are formed by the discharge phenomenon in the plasma chamber 112 26 1379710. Quasi-neutral mixed gas (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 reaction will be carried out on the surface of the catalyst in the front region of the recombination reaction, gradually producing carbon monoxide, carbon dioxide, hydrogen and water. At this time, these carbon monoxide, carbon dioxide, hydrogen, water damage (gaseous), unreactive nitrogen, have not yet The reacted 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 warming reaction gas will continue to react from the first recombination chamber outlet 1211 into the second recombination chamber 122. Similar to the above, the unreacted alcohol molecules and oxygen molecules in the high temperature reaction gas will be in the middle and rear stages of the recombination reaction. The surface of the catalyst is partially oxidized and recombined, and the unreacted alcohol molecules and oxygen molecules are gradually converted into carbon monoxide, oxidizing, hydrogen and water (gaseous). As a result, the carbon monoxide, carbon dioxide, hydrogen, water (gaseous), and unreacted nitrogen in the post-recombination reaction zone of the first catalyst bed 125 form a high temperature reformed gas (not shown). The south temperature reformed gas enters the recirculation tube 123 from the first recombination chamber opening 12ic to enter the preheating chamber 132 along the recirculation tube 123 to heat the air in the preheating tube 132, atomized alcohol and atomization. The moisture, and the heated air and the vaporized alcohol and water in the preheating tube 132 are more easily activated and activated after entering the plasma chamber 112. Similar to the foregoing, in order to further increase the content of hydrogen in the high-temperature reformed gas or reduce the content of carbon monoxide in the temperature-recombinant gas, in this embodiment, 27 1379710 may re-dispose the catalyst in the preheating chamber 132 to recombine the high-temperature recombination gas. Carry out the reaction. Referring to FIG. 5A to FIG. 5B respectively, 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 disposed in the preheating cavity 132. The preheating chamber 丨32 is divided into the first preheating zone T1 and the second preheating zone T2, wherein the preheating pipe 134 is along the first preheating zone T1 and the second preheating zone T2. Layer wrapping

圍繞重組反應器120,而第二預熱區Τ2是位在第一預熱區 Τ1的外圍。 此外,預熱器530更可包括第二觸媒床531、第三觸 媒床533與第四觸媒床535,而第二觸媒床531可位於第 :預=T1 ’且第三觸媒床533可位於第-預熱區T1與 ί 處’又第四觸媒床535可位於第二預熱Around the recombination reactor 120, the second preheating zone Τ2 is located at the periphery of the first preheating zone Τ1. In addition, the preheater 530 may further include a second catalyst bed 531, a third catalyst bed 533 and a fourth catalyst bed 535, and the second catalyst bed 531 may be located at: pre=T1' and the third catalyst The bed 533 can be located at the first preheating zone T1 and ί and the fourth catalyst bed 535 can be located in the second preheating

移觸媒而第ΓΙ’第二觸媒床531可具有高溫水氣轉 第四觸媒庆可具有低溫水氣轉移觸媒,且 Π可具有一氧化碳選择性氧化觸媒。 以以=三觸媒床床 高溫重組氣體中t C I31與第三觸媒床533中, ,轉移觸媒與低^的轉^7子與—氧化碳會在高溫水 :二生成氫氣與二氧 于降低一氡化碳含量。 乂杈间虱虱含量,並同 此外,^ t 氣轉移反應是放熱的過程,因此所釋放出的 28 1379710 熱量可進一步傳遞至預熱管134,以加熱預熱管134中的 空氣,並將霧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500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氧化碳濃度可降低到 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500的 建置成本。 • 當通過第二觸媒床531與第三觸媒床533後,高溫重 組氣體通常仍會殘留約2%(Vol.)濃度的一氧化碳,並逐漸 降低溫度而形成t溫重組氣體(未繪示)。在第四觸媒床535 中,中溫重組氣體中的殘留的一氧化碳分子與氧分子會在 一氧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。 當通過第四觸媒床535後,中溫重組氣體逐漸降低溫 B 度而形成低溫重組氣體,其中低溫重組氣體富含氫氣燃 料,且幾乎沒有殘留對人體有害的一氧化碳。最後,低溫 重組氣體便從預熱腔出口 132b離開預熱腔體132,而輸送 到下游的裝置作為燃料。 值得注意的是,前述所稱高溫重組氣體、中溫重組氣 體與低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、中溫或低溫重組氣體 僅是為方便說明將一氧化碳轉換為氫氣或是去除殘留一氧 化碳的概念的階段性名詞,而熟悉此項技藝當可輕易理解 29 而不致混淆。 山此外,一氧化碳亦是燃料的一種 蚊,亦可不需設置第二觸媒床531、 觸媒床535,而直接由預熱腔出口 氣體即可。The second catalyst bed 531 may have a high temperature water vapor shift. The fourth catalyst medium may have a low temperature water vapor transfer catalyst, and the niobium may have a carbon monoxide selective oxidation catalyst. In order to use a high-temperature reforming gas in a three-catalyst bed, t C I31 and a third catalyst bed 533, the transfer catalyst and the lower ^7 and the carbon monoxide will generate hydrogen in the high temperature water: Oxygen reduces the amount of carbon monoxide. The helium enthalpy content, and in addition, the gas transfer reaction is an exothermic process, so the released 28 1379710 heat can be further transferred to the preheating pipe 134 to heat the air in the preheating pipe 134 and The atomized alcohol and water are heated to form vaporized alcohol and moisture, thereby increasing the overall heat utilization rate of the plasma assisted catalyst recombination device 500. It should be noted that after the high-temperature water-gas conversion catalyst passing through the second catalyst bed 531, if the concentration of carbon monoxide in the high-temperature reformed gas can be reduced to 2% (Vol.), the third embodiment can also be omitted. The low temperature water gas conversion catalyst of the catalyst bed 533 is used to reduce the construction cost of the plasma auxiliary catalyst recombination device 500. • After passing through the second catalyst bed 531 and the third catalyst bed 533, the high temperature reformed gas usually still retains about 2% (Vol.) concentration of carbon monoxide, and gradually lowers the temperature to form a t-temperature reformed gas (not shown) ). In the fourth catalyst bed 535, residual carbon monoxide molecules and oxygen molecules in the intermediate temperature reformed gas are oxidatively recombined on the surface of the carbon monoxide selective oxidation catalyst to generate carbon dioxide and release heat to heat the preheating tube 134 to The overall heat utilization rate of the plasma assisted catalyst recombination device 500 is increased. After passing through the fourth catalyst bed 535, the intermediate temperature reformed gas gradually lowers the temperature B to form a low temperature reformed gas, wherein the low temperature reformed gas is rich in hydrogen fuel, and there is almost no residual carbon monoxide harmful to the human body. Finally, the cryogenic recombination gas exits the preheating chamber 132 from the preheating chamber outlet 132b and is delivered to the downstream unit as a fuel. It is worth noting that the aforementioned high temperature recombination gas, medium temperature recombination gas and low temperature recombination gas are only conceptual differences, and the present invention does not specifically distinguish the exact position where it is located. That is, high temperature, medium temperature or low temperature reformed gas is only a phased term for the concept of converting carbon monoxide to hydrogen or removing residual carbon monoxide, and familiarity with this technique can be easily understood without confusion. In addition, carbon monoxide is also a kind of mosquito of the fuel, and it is also possible to directly supply the gas from the preheating chamber without providing the second catalyst bed 531 and the catalyst bed 535.

氣化护’酉精而言,其亦是生質燃料的-種,進而可降低二 的排放的量。因為植物是從環境吸收碳原子後被製 酒精之類的生質_ ’所以燃燒酒精之類的生質燃料 僅^地球環境碳原子的循環,衫會增加祕线環境中 一礼:碳的總量’進而可達到環保的目標。In the case of gasification, it is also a type of biofuel, which in turn reduces the amount of emissions. Because plants are produced from the environment after the absorption of carbon atoms, such as alcohol, such as alcohol, so the burning of alcohol and other raw fuels only ^ the circulation of the earth's environmental carbon atoms, the shirt will increase the secret line environment: the total amount of carbon 'Therefore, the goal of environmental protection can be achieved.

右不欲去除一氧化 第二觸媒床533與第 132b處收集高溫重組 π再參考目5A〜5B,為提升中溫重組氣體在第四觸媒 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,一氧化破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54〇更可具有第五調節閥549, 而第五調節閥549是連接預熱腔開 口 132c以調節空氣的流 里’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 ^379710 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氫液體與水份, 以使霧化之碳氫液體與水份氣化。 綜上所述,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: • 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,而使碳氫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 • 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 1379710 四、 預熱器是包覆重組反應器,以使電漿辅助觸媒重 組裝置的溫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。 • 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 ϋ 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 1379710 【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之電漿辅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辅助觸媒重組 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。 • 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。 ^ 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 的流程示意圖。 【主要元件符號說明】 100、200、300、400、500 :電漿輔助觸媒重組裝置 33 1379710 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 • 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 :多扎板 125 :第一觸媒床 φ 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 1379710 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 S1 第一反應區域 S2 第二反應區域 T1 第一預熱區 T2 第二預熱區 S1- “S4 :步驟 35The right does not want to remove the oxidized second catalyst bed 533 and the 132b to collect the high temperature recombination π and refer to the heads 5A to 5B, in order to improve the reaction efficiency of the medium temperature reformed gas in the fourth catalyst 535 to completely remove the residual carbon monoxide, The preheating chamber 132 of the present embodiment further has a preheating chamber opening 132c so that air can enter the preheating chamber 132 from the preheating chamber opening 132c, so that oxygen molecules in the air can be selectively oxidized and oxidized. The surface of the medium is oxidatively recombined with residual carbon monoxide. Of course, the feeder 54 can further have a fifth regulating valve 549, and the fifth regulating valve 549 is connected to the preheating chamber opening 132c to regulate the flow of air. The person skilled in the art can easily understand that, Let me repeat. 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 to 30 ^ 379 710 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 into a high-temperature reaction gas by a recombination reactor, and then the high-temperature reaction gas is subjected to a high-temperature reaction gas. Recombination forms a high temperature reformed gas, wherein the high temperature reformed gas is adapted to heat the atomized hydrocarbon liquid and moisture to vaporize the atomized hydrocarbon liquid and moisture. In summary, the plasma assisted catalyst recombination apparatus and method of the present invention have at least the following advantages: 1. The recirculation pipe is configured to 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 reorganization The volume of the reactor is reduced to reduce manufacturing costs. In addition, when the high-temperature reformed gas flows into the recirculation pipe, the heat in the region before the recombination reaction can be carried to the middle portion of the recombination reaction to increase the temperature uniformity of the first catalyst bed, thereby further increasing the recombination efficiency. 2. The start-up procedure is completed by adjusting the flow rate of the hydrocarbon gas (or hydrocarbon liquid) to the air to cause the hydrocarbon gas to be completely combusted to heat the first catalyst bed, thereby allowing the first catalyst bed to reach the operating temperature. . Therefore, the present invention does not require any additional auxiliary heaters, thereby reducing the cost of construction, reducing the overall equipment volume, and avoiding the danger of providing an auxiliary heater. 3. By means of the preheating tube setting, the residual heat of the high temperature reformed gas can be utilized to heat the air in the preheating tube, the hydrocarbon gas, the atomized hydrocarbon liquid or the atomized water, etc., thereby enhancing the excitation activation. effect. Since it is not necessary 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 size of the device can be reduced. 31 1379710 The preheater is a coated 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, thereby improving the overall heat utilization. Rate and avoid the risk of direct contact with high temperature recombination reactors. 5. By the arrangement of the first partitioning plate and the second dividing plate, the gas can be fully developed turbulent flow to further improve the efficiency of catalytic recombination conversion. 6. By the arrangement of the disk-shaped preheating passage, the heat in the plasma chamber can be absorbed to prolong the life of the plasma reactor. • 7. Using the second catalyst bed, the third catalyst bed and the fourth catalyst bed to recombine with the high temperature reformed gas, in addition to increasing the hydrogen content and reducing the carbon monoxide content, the heat released by the recombination reaction can be simultaneously The gas in the preheating tube or the atomized liquid is heated to increase the overall heat utilization rate. 8. When alcohol is used as a hydrocarbon liquid to produce hydrogen fuel, it will not achieve an increase in the total amount of carbon dioxide in the earth's air environment, thereby achieving environmental protection goals. While the present invention has been described in its preferred embodiments, it is not intended to limit the invention, and the invention may be modified and modified without departing from the spirit and scope of the invention. The scope of the invention is defined by the scope of the appended claims. 32 1379710 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. • Figures 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, the third catalyst bed and the fourth catalyst bed removed from the plasma assisted catalyst recombination apparatus of Figure 5A. FIG. 6 is a schematic flow chart of a plasma assisted catalyst recombination method according to an embodiment of the invention. [Main component symbol description] 100, 200, 300, 400, 500: plasma assisted catalyst recombination device 33 1379710 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 • 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: multi-plate 125: first catalyst bed φ 130, 330, 430: preheater 132: preheating chamber. 132a Preheating chamber inlet 132b: preheating chamber outlet 132c: preheating chamber opening 134: preheating tube 140, 540: feeder 142: mixing chamber 145: first regulating valve 34 1379710 146: second regulating valve 226, 226a : first partition plate 227 : second partition plate 336 : disk-shaped preheating passage 438 , 538 : third partition plate 531 : second catalyst bed 533 : third catalyst bed 535 : fourth catalyst bed • 544: Piezoelectric atomization unit 547: third regulating valve 548: fourth regulating valve 549: fifth regulating valve S1 first reaction zone S2 second Shall preheating zone T2 T1 of the first area of the second preheating zone S1- "S4: Step 35

Claims (1)

1379710 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; • 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 • 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 σ ; 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 1379710 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,其中一空氣與一碳氫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 • 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氫氣體,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 ® 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 u/9710 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,並連接於義熱管之—端與該電㈣人口之間。 7. 如申請專利範圍第1項所述之電漿輔助觸媒重組裝 其中该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. 如巾靖專利範圍第7項所述之錢輔助觸媒重組裝 ,其中該第一分隔版為十字分隔板或井字分隔板。1379710 VII. Patent application scope: 1. A plasma auxiliary catalyst recombining device, comprising: a feeder having a mixing chamber; a plasma reactor comprising: a plasma chamber having a plasma 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; • a recombination reactor, connected 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 inlet is connected to the a 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 recirculation tube, a portion Located in the first recombination chamber, one end of the recirculation tube is connected to the first recombination chamber opening, and the other end of the recirculation tube is passed through the second recombination chamber outlet to pass through the second recombination a cavity σ; a porous plate, Disposed in the first recombination chamber and adjacent to the first recombination chamber inlet; a first catalyst bed disposed in the first recombination chamber and the second recombination chamber; a preheater comprising: a preheating chamber, wherein the recombination reactor is located in the preheating chamber 36 1379710, and the preheating chamber has a preheating chamber inlet and a preheating chamber outlet; and a preheating tube disposed at the The preheating chamber is surrounded by the recombination reactor, and 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 out of 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 hydrocarbon 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 hydrocarbon gas, and exit the preheating chamber from the preheating chamber outlet. 3. The plasma assisted catalyst reassembly apparatus according to 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 second regulating valve is 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 catalytic reassembly of the first embodiment of the invention is as follows: 37 u/9710 wherein the preheater further comprises a disk-shaped preheating passage disposed in the preheating chamber and connected to Between the end of the heat pipe and the population of the electricity (four). 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 money assisted catalyst reassembly according to item 7 of the patent scope of the towel, wherein the first partition is a cross partition or a cross-shaped partition. 9·如申4專利㈣帛1項所述之電漿輔助觸媒重組裝 ’其中該重組反應器更包括—第二分隔板,配置於該第 一重組腔體内。 ι〇.如申凊專利範圍第1項所述之電漿輔助觸媒重組裝 ’其中該預熱器更包括一第三分隔板,配置於該預熱腔 _内,以將該預熱腔體區分為相連之一第一預埶區盥一 一預熱區。 八 11. 如中凊專利1巳圍第1G項所述之電I輔助觸媒重組 1L其巾該賴管是沿該第―韻區能k預熱區雙 g长繞該重組反應器。 12. 如中凊專利圍第1()項所述之電漿辅助觸媒重組 ^ 其中該預熱⑨更包括—第二觸媒床、—第三觸媒床 ς —第四觸媒床,而該第二觸媒床位於該第—預熱區,且 =第了觸媒床位於該第一預熱區與該第二預熱區交界處, 該第四觸媒床位於該第二預熱區。 13·如申請專利範圍第12項所述之電漿輔助觸媒重組 :置,其中該第二觸媒床具有高溫水氣轉移觸媒,而第三 媒床具有低溫水氣轉移觸媒,且第四觸媒床具有一氧化 38 1379710 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,霧化之該碳氫液 體與該水份於該預熱管内形成氣化之該碳氫液體與該水 • 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 之碳氫液體與霧化之水份,且自預熱腔出口離開預熱腔體。 • 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項所述之電漿輔助觸媒重組 39 1379710 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碳氫液體與一水份霧化; 提供一空氣; # 混合該空氣以及霧化之該碳氫液體與該水份,並將霧 化之該碳氫液體與該水份氣化; 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 一高溫反應氣體,並將該高溫反應氣體進行重組形成一高 溫重組氣體,且該高溫重組氣體適於加熱霧化之該碳氫液 體與該水份,以使霧化之該碳氫液體與該水份氣化。 • 21.如申請專利範圍第20項所述之電漿輔助觸媒重組 方法,其中該碳氫液體為酒精或液化石油氣。 409. The plasma assisted catalyst reassembly according to claim 4 (4), wherein the recombination reactor further comprises a second partition plate disposed in the first recombination chamber. The plasma-assisted catalytic reassembly of the first aspect of the invention, wherein the preheater further comprises a third partition plate disposed in the preheating chamber to preheat the The cavity is divided into one of the first pre-twisting zones and one of the preheating zones. 8. 11. The electric I assisted catalyst recombination as described in the 1G item of Zhongyi Patent 1 1L. The lining of the lining is to rewind the recombination reactor along the first g-zone preheating zone. 12. The plasma-assisted catalyst recombination as described in paragraph 1 () of the Chinese patent, wherein the preheating 9 further comprises a second catalyst bed, a third catalyst bed ς - a fourth catalyst bed, The second catalyst bed is located in the first preheating zone, and the first catalyst bed is located at the boundary between the first preheating zone and the second preheating zone, and the fourth catalyst bed is located in the second preheating zone. Hot zone. 13. The plasma-assisted catalyst recombination according to claim 12, wherein the second catalyst bed has a high temperature water gas transfer catalyst, and the third medium bed has a low temperature water gas transfer catalyst, and The fourth catalyst bed has a oxidized 38 1379710 carbon selective oxidation catalyst. 14. The plasma assisted catalyst reassembly of claim 1, wherein the feeder further has a piezoelectric atomizing unit coupled 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 mix with air entering one of the mixing chambers and entering the preheating tube, atomizing the hydrocarbon liquid and the water in the preheating tube to form a vaporized hydrocarbon liquid and the water 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, atomized hydrocarbon liquid and atomized water in the preheating tube, and self preheating The chamber outlet exits the preheating chamber. 16. The plasma assisted catalyst recombination device of claim 15, wherein the hydrocarbon liquid is alcohol or liquefied petroleum gas. 17. The plasma assisted catalyst recombination 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 a regulating valve is connected to the mixing chamber to control a flow rate of air entering 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 The flow into the piezoelectric atomizing unit. 18. The plasma assisted catalyst recombination 39 1379710 device of claim 14, wherein the preheating chamber further has a preheating chamber opening to allow an air to enter the preheating from the preheating chamber opening. Inside the cavity. 19. The plasma assisted catalyst recombining device 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 atomizing unit to atomize a hydrocarbon liquid with one water; providing an air; # mixing the air and atomizing the hydrocarbon liquid with The water, and atomizing the atomized hydrocarbon liquid with the water; providing a plasma reactor to excite the air and the vaporized hydrocarbon liquid and the moisture 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 high temperature reformed gas is suitable for heating the atomized hydrocarbon liquid And the moisture to vaporize the atomized hydrocarbon liquid with the water. • 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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