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        浸漬法制備高選擇性1-丁烯齊聚催化劑

        2016-08-12 01:00:49肖林久陳家歡盛永剛李文澤王金豹
        關(guān)鍵詞:催化作用硫酸鐵齊聚

        肖林久, 陳家歡, 盛永剛, 李文澤, 王金豹

        (沈陽(yáng)化工大學(xué) 應(yīng)用化學(xué)學(xué)院 遼寧省稀土化學(xué)及重點(diǎn)應(yīng)用實(shí)驗(yàn)室, 遼寧 沈陽(yáng) 110142)

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        肖林久, 陳家歡, 盛永剛, 李文澤, 王金豹

        (沈陽(yáng)化工大學(xué) 應(yīng)用化學(xué)學(xué)院 遼寧省稀土化學(xué)及重點(diǎn)應(yīng)用實(shí)驗(yàn)室, 遼寧 沈陽(yáng) 110142)

        摘要:通過(guò)分步浸漬法制備/γ-Al2O3催化劑,并用于催化1-丁烯齊聚反應(yīng),考察了催化劑制備條件和反應(yīng)條件對(duì)催化性能的影響,并與Fe2(SO4)3/γ-Al2O3催化劑進(jìn)行性能比較。結(jié)果表明,在0.96 MPa、60℃、液時(shí)空速為5 h-1的反應(yīng)條件下,采用Fe負(fù)載量為負(fù)載量為1.2 mmol/g(γ-Al2O3)的/γ-Al2O3 催化劑,1-丁烯齊聚反應(yīng)的轉(zhuǎn)化率達(dá)到68.0%,二聚物選擇性為95.0%。α-Fe2O3是催化1-丁烯齊聚反應(yīng)的活性組分,并能提高二聚體選擇性;此外,α-Fe2O3晶相與的相互作用對(duì)其催化1-丁烯齊聚反應(yīng)的活性有重要影響,γ-Al2O3與的相互作用也對(duì)催化活性有一定的影響。Fe負(fù)載量為6%的/γ-Al2O3催化活性最高,此時(shí)NH3-TPD結(jié)果顯示,催化劑只存在較弱的酸中心和適中的酸量。

        關(guān)鍵詞:1-丁烯齊聚; 催化劑;; 硫酸鐵

        1 實(shí)驗(yàn)部分

        1.1原料和試劑

        γ-Al2O3(Al2O3質(zhì)量分?jǐn)?shù)98%,比表面積227.41 m2/g,平均孔徑5.08 nm),濟(jì)南魯淮商貿(mào)有限公司產(chǎn)品;Fe(NO3)3·9H2O、(NH4)2SO4,分析純,天津市大茂化工試劑廠產(chǎn)品;Fe2(SO4)3,分析純,天津市耀華化工廠產(chǎn)品。

        1.2催化劑的制備

        將載體γ-Al2O3研磨、篩分,選用粒徑20~40目部分。將稱量的Fe(NO3)3溶于一定量的去離子水中,待溶解后快速加入定量的γ-Al2O3,使其浸漬均勻,超聲波下充分震蕩1 h,放置120℃下烘干,然后移至馬福爐中500℃焙燒1 h,取出冷卻至室溫,制得Fe負(fù)載量(質(zhì)量分?jǐn)?shù),以下同)分別為2%、4%、6%、8%、10%的Fe2O3/γ-Al2O3催化劑。

        1.2.2Fe2(SO4)3/γ-Al2O3的制備

        將載體γ-Al2O3研磨、篩分,選用粒徑20~40目部分。將稱量的Fe2(SO4)3溶于一定量的去離子水中,待溶解后快速加入定量的γ-Al2O3,使其浸漬均勻,超聲波下充分震蕩1 h,放置120℃下烘干,然后移至馬福爐中500℃焙燒3 h,取出冷卻至室溫,制得Fe擔(dān)載量為6%的Fe2(SO4)3/γ-Al2O3催化劑。

        1.3反應(yīng)裝置和流程

        采用高壓微型固定床連續(xù)流動(dòng)的不銹鋼反應(yīng)器(內(nèi)徑8 mm,長(zhǎng)70 mm)進(jìn)行1-丁烯齊聚反應(yīng)。采用北京東方儀器廠產(chǎn)SB-2型雙柱塞微量泵將反應(yīng)原料從反應(yīng)器底部送入反應(yīng)床層。反應(yīng)溫度控制在40~200℃范圍,由背壓調(diào)壓器控制反應(yīng)壓力在0.8~1.8 MPa范圍。反應(yīng)產(chǎn)物從背壓閥流出后,經(jīng)六通閥進(jìn)入氣相色譜完成在線分析,隨時(shí)監(jiān)測(cè)反應(yīng)狀況。

        1.4聚合產(chǎn)物分析

        采用北京北分瑞利分析儀器公司3420A型氣相色譜儀和面積歸一化法分析液體產(chǎn)物和尾氣組成。色譜儀配有30 m HJ.624毛細(xì)管柱和FID檢測(cè)器;氣化溫度240℃,柱溫220℃,檢測(cè)器溫度250℃;由色譜分析工作站處理數(shù)據(jù)。根據(jù)分析結(jié)果計(jì)算1-丁烯轉(zhuǎn)化率和液體產(chǎn)物各組分的選擇性。

        1.5負(fù)載量計(jì)算方法

        (1)

        (2)

        2 結(jié)果與討論

        2.1.1表面分散狀態(tài)

        圖1 不同焙燒溫度下負(fù)載Fe2O3得到的的XRD譜Fig.1 XRD patterns of Fe2O3·different calcination temperatures ●Fe2(SO4)3;■α-Fe2O3;▲γ-Al2O3;★Fe2O3

        2.1.2催化劑的酸性

        圖2 不同F(xiàn)e負(fù)載量的的 NH3-TPD曲線Fig.with different Fe loadings

        w(Fe)/%: (1) 2; (2) 4; (3) 6; (4) 10; (4) 12

        2.2.1負(fù)載Fe2O3焙燒溫度的影響

        圖3 負(fù)載Fe2O3的焙燒溫度對(duì)所得催化劑催化1-丁烯齊聚反應(yīng)轉(zhuǎn)化率的影響Fig.3 Effect of calcination temperature for loading Fe2O3 of/γ-Al2O3 catalyst on oligomerization conversion of 1-butene over the catalyst

        2.2.2Fe負(fù)載量的影響

        圖4 Fe負(fù)載量對(duì)催化劑催化 1-丁烯齊聚反應(yīng)的影響Fig.catalyst on oligomerization of 1-butene at different temperatures

        (a)x; (b)s(Dimers); (c)s(Trimers)

        圖負(fù)載量對(duì)催化劑催化1-丁烯齊聚反應(yīng)的影響Fig.catalyst on oligomerization of 1-buteneT=60℃; p=0.96 MPa; LHSV=5 h-1; w(Fe)=6% (1) x; (2) s(Dimers); (3) s(Trimers)

        圖6 不同反應(yīng)溫度下Fe負(fù)載量為6%的Fe2(SO4)3/γ-Al2O3催化劑催化1-丁烯齊聚反應(yīng)的轉(zhuǎn)化率Fig.6 Conversion of 1-butene oligomerization vs reaction temperatures over Fe2(SO4)3/γ-Al2O3catalyst with 6% Fe loadingp=1.2 MPa; LHSV=1 h-1

        2.4.1反應(yīng)溫度的影響

        圖7 反應(yīng)溫度對(duì)催化劑催化 1-丁烯齊聚反應(yīng)的影響Fig.7 Effects of reaction temperature on oligomerization of

        (1)x; (2)s(Dimers); (3)s(Trimers)

        2.4.2反應(yīng)壓力的影響

        圖8 反應(yīng)壓力對(duì)催化劑催化 1-丁烯齊聚反應(yīng)的影響Fig.8 Effects of reaction pressure on oligomerization of

        (1)x; (2)s(Dimers); (3)s(Trimers)

        2.4.3液時(shí)空速的影響

        圖9 反應(yīng)液時(shí)空速對(duì)催化劑催化 1-丁烯齊聚反應(yīng)的影響Fig.9 Effects of liquid hourly space velocity on oligomerization of 1-butene over

        (1)x; (2)s(Dimers); (3)s(Trimers)

        3 結(jié) 論

        參考文獻(xiàn)

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        [7] VILLEGAS J I, KUMAR N, HEIKKILT, et al. A study on the dimerization of 1-butene over Beta zeolite[J].Topics in Catalysis, 2007, 45(1): 187-190.

        [8] LAVRNOV A V, DUPLYAKIN V K. Butene oligomerization over phosphoric acid: Structural characterization of products[J].Kinetics and Catalysis, 2009, 50(2): 235-240.

        [9] 蔡天錫,曹殿學(xué),齊愛(ài)華,等.NiSO4/γ-Al2O3對(duì)低級(jí)烯烴齊聚反應(yīng)的催化作用[J].催化學(xué)報(bào),1994, 15(1): 23-27.(CAI Tianxi, CAO Dianxue, QI Aihua, et al. Catalytic behavior of NiSO4/γ-Al2O3in alkene oligometization[J].Chinese Journal of Catalysis, 1994, 15(1): 23-27.)

        [10] 嚴(yán)志宇,唐曉東,曹殿學(xué),等.負(fù)載型硫酸鐵對(duì)烯烴齊聚催化作用的研究ⅡFe2(SO4)2/γ-Al2O3對(duì)1-丁烯齊聚反應(yīng)[J].石油學(xué)報(bào)(石油加工),1997, 13(1): 13-17.(YAN Zhiyu, TANG Xiaodong, CAO Dianxue, et al. Studies on catalysis of olefin oligomerization on supported ferric sulfateⅡA study on the catalytic behavior of Fe2(SO4)2/γ-Al2O3for 1-butene oligomerization[J].Acta Petrolei Sinica(Petroleum Processing Section), 1997, 13(1): 13-17.)

        [11] 王麗,丁洪生,趙春明,等.[Emim]HSO4-FeCl3催化1-丁烯齊聚反應(yīng)研究[J].華工科技,2012, 20(1): 10-12.(WANG Li, DING Hongsheng, ZHAO Chunming, et al. Study on oligomerization of 1-butene catalyzed by ionic liquid[Emim]HSO4-FeCl3[J].Science & Technology in Chemical Inductry, 2012, 20(1): 10-12.)

        [12] RIAAN B, PRINSLOOB N M. Butene oligomerization over phosphoric acid: Structural characterization of products[J].Industrial & Engineer Chemistry Research, 2009, 48(22): 10156-10162.

        [13] 嚴(yán)志宇,曹殿學(xué),蔡天錫.負(fù)載型硫酸鐵對(duì)烯烴齊聚催化作用的研究Ⅳ不同方法制備的Fe2(SO4)2/γ-Al2O3的丙烯齊聚反應(yīng)的考察[J].石油學(xué)報(bào)(石油加工),1997, 13(2): 41-45.(YAN Zhiyu, CAO Dianxue, CAI Tianxi. Studies on olefins oligomerization catalyzed by supported ferric sulfate Ⅳ A study of propene oligomerization on Fe2(SO4)2/γ-Al2O3prepated by different procedures[J].Acta Petrolei Sinica(Petroleum Processing Section), 1997, 13(2): 41-45.)

        [14] ZBORIL R, MASHLAN M, PEDRIDIS D. Iron(Ⅲ) oxides from thermal processess-synthesis, structural and magnetic properties, moessbauer spectroscopy characterization, and applications[J].Chemistry of Materials, 2002, 14(3): 969-982.

        [15] 劉科偉,陳天朗.硫酸銨的熱分解[J].化學(xué)研究與應(yīng)用,2002, 14(6): 737-738.(LIU Kewei, CHEN Tianlang. Studies on the thermal decomposition of ammonium sulfate[J].Chemical Research and Application, 2002, 14(6): 737-738.)

        [16] 許越,夏海濤.催化劑設(shè)計(jì)與制備工藝[M].北京:化學(xué)工業(yè)出版社,2003: 27.

        [17] 劉冰.Al-TiO2系的機(jī)械力化學(xué)和固相反應(yīng)動(dòng)力學(xué)[D].濟(jì)南:山東大學(xué),2005.

        [18] 唐曉東,嚴(yán)志宇,曹殿學(xué),等.負(fù)載型硫酸鐵對(duì)烯烴齊聚催化作用的研究ⅠFe2(SO4)2/γ-Al2O3對(duì)丙烯齊聚反應(yīng)催化作用的考察[J].石油學(xué)報(bào)(石油加工),1996, 12(4): 36-43.(TANG Xiaodong, YAN Zhiyu, CAO Dianxue, et al. Studies on catalysis of olefin oligomerization on supported ferric sulfateⅠ A study on the catalytic behavior of Fe2(SO4)2/γ-Al2O3for propene oligomerization[J].Acta Petrolei Sinica(Petroleum Processing Section), 1996, 12(4): 36-43.)

        [19] CAI T X, ZHANG L Y, QI A H, et al. Propene oligomerization catalyst derived from nikel sulfate supported onγ-alumina[J].Catalysis Today, 1991, 69(1): 1-13.

        [20] ADRIEN B, PIERRE-ALAIN R B, LIONEL M, et al. Novel catalytic system for ethylene oligomerization: An iron(Ⅲ) complex with an anionicN,N,Nligand[J].Inorganic Chemicals and Reactions, 2011, 30(10): 2640-2642.

        [21] ROMAN R, THEODORUS DE B, PASCAL R, et al. Theoretical unraveling of selective 1-butene oligomerization catalyzed by iron- bis(arylimino)pyridine[J].Organometallics, 2009, 28(18): 5358-5367.

        [22] 唐曉東,嚴(yán)志宇,曹殿學(xué),等.負(fù)載型硫酸鐵對(duì)烯烴齊聚催化作用的研究Ⅲ Fe2(SO4)2/γ-Al2O3的表征[J].石油學(xué)報(bào)(石油加工), 1997, 13(1): 13-17.(TANG Xiaodong, YAN Zhiyu, CAO Dianxue, et al. Studies on catalysis of olefin oligomerization on supported ferric sulfate Ⅲ Characterization of Fe2(SO4)2/γ-Al2O3catalyst[J].Acta Petrolei Sinica (Petroleum Processing Section), 1997, 13(1): 13-17.)

        收稿日期:2015-05-18

        基金項(xiàng)目:遼寧省科技技術(shù)攻關(guān)項(xiàng)目(2011223006)資助

        文章編號(hào):1001-8719(2016)04-0695-08

        中圖分類號(hào):O643.32

        文獻(xiàn)標(biāo)識(shí)碼:A

        doi:10.3969/j.issn.1001-8719.2016.04.006

        XIAO Linjiu, CHEN Jiahuan, SHENG Yonggang, LI Wenze, WANG Jinbao

        (LiaoningProvince,KeyLaboratoryforRare-EarthChemistryandApplication,CollegeofAppliedChemistry,ShenyangUniversityofChemicalTechnology,Shenyang110142,China)

        Abstract:/γ-Al2O3 catalyst was prepared by step-impregnation method, and its catalytic performance for 1-butene oligomerization was studied and compared with Fe2(SO4)3/γ-Al2O3 catalyst. The influences of the preparation and reaction conditions on the catalytic activity of /γ-Al2O3 for 1-butene oligomerization were investigated. The results showed that, on the reaction condition of pressure of 0.96 MPa, reaction temperature of 60℃ and liquid hourly space velocity of 5 h-1, with the /γ-Al2O3 of 6% Fe loading and 1.2 mmol/g(γ-Al2O3) loading as catalyst, the conversion rate of 1-butene oligomerization reached 68.0% and the dimerization selectivity was 95.0%. α-Fe2O3 is an active component in catalytic 1-butene oligomerization and high dimerization selectivity can be obtained. In addition, the interaction between α-Fe2O3 crystal phase and had an important influence on the catalytic activity of /γ-Al2O3 in 1-butene oligomerization and the interaction between γ-Al2O3and also had some influence. Catalyst activity of /γ-Al2O3 was maximum with 6% Fe loading, and its NH3-TPD results showed there existed weak acid sites and only a moderate amount of acid.

        Key words:1-butene oligomerization; catalyst; /γ-Al2O3; ferric sulfate

        通訊聯(lián)系人: 肖林久,男,教授,博士,從事精細(xì)化工、稀土材料、催化等方面的研究;Tel:024-89381616;E-mail:x109@163.com

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