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    H2O2穩(wěn)定性的密度泛函研究

    2018-06-01 00:58:08學(xué)
    泰山學(xué)院學(xué)報 2018年3期
    關(guān)鍵詞:鍵長雙氧水氣相

    程 學(xué) 禮

    (泰山學(xué)院 化學(xué)化工學(xué)院,山東 泰安 271000)

    1 前言

    雙氧水(H2O2)是一種清潔氧化劑而被廣泛用于造紙和化學(xué)合成[1],能夠參與多種氧化還原反應(yīng)[2-4].H2O2還常被用于有機(jī)污染物的降解[5-7],著名的芬頓反應(yīng)就是用H2O2和Fe2+的混合溶液氧化有機(jī)化合物,特別是難降解有機(jī)污染物[8-9].

    H2O2可以通過氫氣和氧氣直接反應(yīng)或氧氣電還原等方法低成本合成[10-11].然而,無論在氣相還是溶液中H2O2均不穩(wěn)定,易分解釋放氧氣(ΔH=-98.23 kJ/mol);H2O2對光照敏感,雙氧水在λ= 275-366nm下均可分解[12-13].在金屬陽離子、碘離子和金屬氧化物催化下,H2O2能夠快速分解[14-17].一般情況下,H2O2分解為2個羥基自由基參與反應(yīng),因此,O-O鍵長的變化在H2O2分解過程中將扮演重要角色.

    2 計(jì)算方法

    3 結(jié)果與討論

    3.1 基態(tài)結(jié)構(gòu)

    圖1 B3LYP和M06-2X方法結(jié)合得到的分子結(jié)構(gòu)(鍵長的單位是nm,括號內(nèi)為氣相鍵長)

    3.2 發(fā)射光譜

    表1 TD-M062X模擬得到的4種結(jié)構(gòu)發(fā)射光譜的最大發(fā)射波長λmax(振子強(qiáng)度f)和躍遷軌道(躍遷貢獻(xiàn)比). λmax以nm為單位.方括號內(nèi)數(shù)據(jù)為氣相數(shù)據(jù)

    3.3 激發(fā)態(tài)結(jié)構(gòu)

    圖2 T1態(tài)優(yōu)化結(jié)構(gòu)參數(shù)

    4 結(jié)論

    [參考文獻(xiàn)]

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    [2]Yin G.,Ni Y. Mechanism of the ClO2generation from the H2O2-HClO3reaction[J].Can.J.Chem.Eng.,2000,78(4):827-833.

    [3]Jena N. R.,Mishra P. C. Mechanisms of formation of 8-oxoguanine due to reactions of one and two OHradicals and the H2O2molecule with guanine: A quantum computational study[J].J.Phys.Chem.B,2005,109(29):14205-14218.

    [4]Das S., Bhattacharyya J.,Mukhopadhyay S. Mechanistic studies on oxidation of hydrogen peroxide by an oxo-bridged diiron complex in aqueous acidic media[J].Dalton Trans.,2008(46):6634-6640.

    [5]Gain S., Mishra R., Mukhopadhyay S., Banerjee R. Mechanistic studies on oxidation of hydrogen peroxide and hydrazine by a metal-bound superoxide[J].Inorg.Chim.Acta,2011(373):311-314.

    [6]朱承駐,秦艷,周元祥,董文博,侯惠奇.266 nm光照下水溶液中氯苯與H2O2的反應(yīng)機(jī)理研究 [J].化學(xué)學(xué)報,2007,65(5):451-458.

    [7]Merényi G, Lind J., Naumov S.,von Sonntag C. Reaction of ozone with hydrogen peroxide (peroxone process): A revision of current mechanistic concepts based on thermokinetic and quantum-chemical consideration[J].Environ.Sci.Technol.,2010,44(9):3505-3507.

    [8]Perez-Benito J.F. Iron(III)-hydrogen peroxide reaction: Kinetic evidence of a hydroxyl-mediated chainmechanism[J].J.Phys.Chem.A,2004,108(22):4853-4858.

    [9]Navalon S., Dhakshinamoorthy A., Alvaro M., Garcia H. Heterogeneous Fenton catalysts based on activatedcarbon and related materials[J].ChemSusChem,2011,4(12):1712-1730.

    [10]Zhao K., Su Y.,QuanX., Liu Y.,ChenS.,YuH. Enhanced H2O2production by selective electrochemical reduction of O2on fluorine-doped hierarchically porous carbon[J].J.Catal.,2018(357):118-126.

    [11]Wilson N.M.,Priyadarshini P.,Kunz S.,Flaherty D.W. Direct synthesis of H2O2on Pd and AuxPd1clusters: Understanding the effects of alloying Pd with Au[J].J.Catal.,2018(357):163-175.

    [12]Odochian L., Iancu L., Humelnicu I., Mocanu A.M., Baiceanu A. Contributions to the reaction mechanism of photochemicaldecomposition of hydrogen peroxide in aqueous solution[J]. Rev. Chim. (Bucharest),2011,62(10):1012-1016.

    [13]Nedrygailov I.I., Lee C., Moon S.Y., Lee H., Park J.Y. Hot electrons at solid liquid interfaces: A large chemoelectriceffect during the catalytic decomposition of hydrogen peroxide[J].Angew.Chem.Int. Ed.,2016,55(36):10859-10862.

    [14]Dalmázio I., Moura F.C. C., Ara jo M.H., Alves T.M. A., Lago R.M., de Lima G.F., Duarte H.A.,R.Augusti. The iodide-catalyzed decomposition of hydrogen peroxide: Mechanistic details of an oldreaction as revealed by electrospray ionization mass spectrometry monitoring[J].J. Braz. Chem. Soc., 2008,19(6):1105-1110.

    [15]Voloshin Y., Manganaro J., Lawal A. Kinetics and mechanism of decomposition of hydrogen peroxide over Pd/SiO2catalyst[J]. Ind. Eng. Chem. Res.,2008,47(21):8119-8125.

    [16]Do S.-H.,Batchelor B.,Lee H.-K.,Kong S.-H. Hydrogen peroxide decomposition on manganese oxide (pyrolusite): Kinetics, intermediates, and mechanism[J].Chemosphere,2009(75):8-12.

    [17]Zhao Y., Chen Z., Shen X., Zhang X. Kinetics and mechanisms of heterogeneous reaction of gaseoushydrogen peroxide on mineral oxide particles[J].Environ. Sci. Technol.,2011,45(8):3317-3324.

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    [21]Pedulla J. M., Vila F., Jordan K. D. Binding energy of the ring form of (H2O)6: Comparison of the predictions of conventional and localized-orbital MP2 calculations[J].J.Chem.Phys.,1996,105(24):11091-11099.

    [22]Pedulla J. M., Kim K., Jordan K. D. Theoretical study of the n-body interaction energies of the ring, cage and prism forms of (H2O)6[J].Chem.Phys.Lett.,1998(291):78-84.

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