博碩士論文 89321036 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學工程與材料工程學系zh_TW
DC.creator蔡俊煌zh_TW
DC.creatorChun-Huang Tsaien_US
dc.date.accessioned2002-6-24T07:39:07Z
dc.date.available2002-6-24T07:39:07Z
dc.date.issued2002
dc.identifier.urihttp://ir.lib.ncu.edu.tw:444/thesis/view_etd.asp?URN=89321036
dc.contributor.department化學工程與材料工程學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract摘要 本研究以共沈澱法製備具有不同Mg/Al比例及不同Ni負載量的hydrotalcite先驅物Ni/HT(x),經高溫煅燒製得觸媒Ni/HTc(x)。利用X光繞射光譜(XRD)、全表面積測定 (BET) 、X-光電子光譜儀 (XPS) 、氫程溫脫附 (H2-TPD) 、氫程溫還原 (H2-TPR) 對觸媒的物理結構及表面性質做鑑定分析。藉由CH4/CO2重組反應測試,探討不同煅燒溫度、還原溫度、Mg/Al比例、Ni負載量及反應溫度之影響,並進行長時間反應穩定性測試,觀察上述之不同變因對觸媒壽命期之影響,並以程溫氫化反應(H2-TPSR)分析觸媒表面積碳,探討觸媒積碳阻抗的能力。 Ni/HTc(x)於800℃煅燒具有高表面積(125 m2/g以上),原觸媒先驅物Ni/HT(x)的hydrotalcite層狀結構經高溫煅燒瓦解形成Mg-Al-O共氧化物,隨著煅燒溫度上升,NiO與MgO逐漸形成固溶。Ni/HTc(x)觸媒不易還原,所需的還原溫度較傳統觸媒Ni/γ-Al2O3及Ni/SiO2高出釵h,且隨著煅燒溫度和Mg/Al比例的增加而增加,此外XPS表面組成分析發現Ni/(Mg+Al)莫耳比隨著煅燒溫度上升而下降,進一步證實NiO和MgO確實形成固溶,增加NiO-MgO之間的作用力。 CH4/CO2重組反應結果知CO2轉化率皆高於CH4轉化率,且CO/H2比值介於1.0~1.2之間。RWGS反應是主要的副反應,同時亦發生蒸氣重組反應,使CO/H2比值趨近於理論值1。CH4及CO2轉化率隨Ni負載量、還原及反應溫度上升而增加;隨煅燒溫度及Mg/Al比上升而減小。CH4/CO2重組反應結果以800℃煅燒,500℃還原,Mg/Al比3,8%Ni負載量,700℃反應溫度條件下的8%Ni/HTc(3)觸媒有較好的穩定性。8%Ni/HTc(3)與8%Ni/HTc(3)im(含浸法製備)、8%Ni/γ-Al2O3及8%Ni/SiO2觸媒進行CH4/CO2重組反應比較下,8%Ni/HTc(3)觸媒有最佳穩定性,H2-TPD計算得8%Ni/HTc(3)有最佳分散度,H2-TPSR亦發現8%Ni/HTc(3)觸媒有最佳的積碳阻抗。zh_TW
dc.description.abstractIn this study,we prepared different Mg/Al ratios and Ni loading precursor by coprecipitation method,and then calcined at high temperature to prepare Ni/HTc(x) catalysts. XRD 、BET、XPS、H2-TPR、H2-TPD were used to study the structure and surface properties. The effect of different calcination temperature、reducing temperature、Mg/Al ratios、Ni loading and reaction temperature was studied by CH4/CO2 reforming.H2-TPSR was used to study coking resistance of catalyst. Ni/HT(x) has the same structure with hydrotalcite,after calcined at high temperature,the layer stuucture was collased and became Mg-Al-O mixed-oxides,the surface also increased. As the calcined temperature increased NiO and MgO became solid solution. It is hard to reduce Ni/HTc(x) catalyst,and reducing temperature is higher than Ni/γ-Al2O3 and Ni/SiO2 catalyst. XPS found that Ni/(Mg+Al) ratio reduce as calcination temperature increase,furthre prove NiO and MgO were formed solid solution. In CH4/CO2 reformimg we found that 8%Ni/HTc(3) catalyst ,calcined at 800℃ ,reduced at 500℃ , Mg/Al ratio is 3,and 700℃ reaction temperature had the best stability than 8%Ni/γ-Al2O3,8%Ni/SiO2. H2-TPSR also found that 8%Ni/HTc(3) had best coking resistance.en_US
DC.subject合成氣zh_TW
DC.subject鎳鎂鋁氧觸媒zh_TW
DC.subject重組反應zh_TW
DC.subjectSurported Nickel Catalysten_US
DC.subjectMg/Al mixed oxideen_US
DC.subjectHydrotalciteen_US
DC.subjectSyngasen_US
DC.subjectCH4/CO2 reformingen_US
DC.titleNi/Mg-Al-O觸媒於CH4/CO2重組反應之研究zh_TW
dc.language.isozh-TWzh-TW
DC.titleCO2 Reforming of Methane on Ni/Mg-Al-O Catalysten_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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