Preparation and Characterization of Dabco (1,4-Diazabicyclo [2.2.2]octane) modified bentonite: Application for Congo red removal

被引:7
|
作者
Taher, Tarmizi [1 ]
Rohendi, Dedi [2 ]
Mohadi, Risfidian [2 ]
Lesbani, Aides [1 ,2 ]
机构
[1] Univ Sriwijaya, Program Pascasarjana, Environm Sci Study, Jl Padang Selasa 524, Bukit Besar, Palembang, Indonesia
[2] Univ Sriwijaya, Dept Chem, Fac Math & Nat Sci, Jl Raya Palembang Prabumulih,Km 32, Indralaya, Ogan Ilir, Indonesia
关键词
Natural bentonite; Dabco modified bentonite; Adsorption; Congo red; WASTEWATERS SIMULTANEOUS SORPTION; AQUEOUS-SOLUTION; ACTIVATED BENTONITE; ACID DYES; ADSORPTION; ESTERIFICATION; ISOTHERM; SURFACE; CLAY;
D O I
10.1088/1757-899X/299/1/012055
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Natural bentonite provided from Sarolangun deposit was modified with 1,4-Diazabicyclo [2.2.2]octane (Dabco) to form a new class of porous material. Prior further modification, the natural bentonite was cleaned up and activated by NaCl to remove the impurities and increase the bentonite nature. Dabco modified bentonite (Dabco-bent) was prepared by exchanging the inorganic cation placed in the interlayer space of the montmorillonite mineral structure with the 0.01 M Dabco(1+) at pH 6. The modified bentonite products were characterized using X-Ray powder diffraction and FT-IR to monitor the change of the bentonite crystallinity and function group due to the modification process. The XRD result confiuned that during the modification process, the d(001) of smectite peak at 2 theta around 6 degrees was shifted. After the modification, the d(001) reflection of the montmorillonite interlayer was shifted 0.36 degrees to the left indicating that the interlayer space of the montmorillonite has been expanded during the modification process. The FTIR spectra of Dabco modified bentonite exhibit no significantly different with the host bentonite. However, the presence of the new band at the wavenumber around 3000 and 2800 cm(-1) indicates that the Dabco molecule has been successfully inserted to the bentonite molecule. The Congo red adsorption experiment was perfouned onto Dabco-bent product by batch technique. The experiment data described that kinetic model for Congo red adsorption onto Dabco-bent was adequately followed the second- order kinetic model and well described by Freundlich adsorption isotherm model.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] PICOSECOND AND NANOSECOND STUDIES OF THE PHOTOREDUCTION OF BENZOPHENONE BY 1,4-DIAZABICYCLO[2.2.2]OCTANE - CHARACTERIZATION OF THE TRANSIENT
    DEVADOSS, C
    FESSENDEN, RW
    JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (11): : 4540 - 4549
  • [32] Efficient solvent- and metal-free Sonogashira protocol catalysed by 1,4-diazabicyclo(2.2.2) octane (DABCO)
    Luque, Rafael
    Macquarrie, Duncan J.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2009, 7 (08) : 1627 - 1632
  • [33] SYNTHESIS AND CHARACTERIZATION OF 1,4-DIAZABICYCLO[2.2.2] OCTANE AND PIPERIDINE ADDUCTS OF DIVALENT TIN HALIDES
    DEANS, RA
    GEANANGEL, RA
    INORGANICA CHIMICA ACTA-ARTICLES, 1980, 43 (02): : 159 - 163
  • [34] Synthesis, Antifungal Activity, and Biocompatibility of Novel 1,4-Diazabicyclo[2.2.2] Octane (DABCO) Compounds and DABCO-Containing Denture Base Resins
    Herman, Jenny L.
    Wang, Yapin
    Lilly, Elizabeth A.
    Lallier, Thomas E.
    Peters, Brian M.
    Hamdan, Suleiman
    Xu, Xiaoming
    Fidel, Paul L., Jr.
    Noverr, Mairi C.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2017, 61 (04)
  • [35] Self condensation of methyl acetopyruvate in the presence of 1,4-diazabicyclo[2.2.2]octane
    Lee, HJ
    Kim, TY
    Kim, JN
    SYNTHETIC COMMUNICATIONS, 1999, 29 (24) : 4375 - 4379
  • [36] Reverse sequence of transitions in prototypic relaxor 1,4-diazabicyclo[2.2.2]octane
    Nowicki, Waldemar
    Olejniczak, Anna
    Andrzejewski, Michal
    Katrusiak, Andrzej
    CRYSTENGCOMM, 2012, 14 (20) : 6428 - 6434
  • [37] Multiple Roles of 1,4-Diazabicyclo[2.2.2]octane in the Solvothermal Synthesis of Iodobismuthates
    Cai, Yunhe
    Chippindale, Ann M.
    Curry, Richard J.
    Vaqueiro, Paz
    INORGANIC CHEMISTRY, 2021, 60 (07) : 5333 - 5342
  • [38] HYDROXYALKYLATION OF METHYLVINYL KETONES AND ACRYLONITRILE IN THE PRESENCE OF 1,4-DIAZABICYCLO[2.2.2]OCTANE
    AMRI, H
    VILLIERAS, J
    TETRAHEDRON LETTERS, 1986, 27 (36) : 4307 - 4308
  • [39] 1,4-Diazabicyclo[2.2.2]octane Bis(sulfur dioxide) Adduct (DABSO)
    Martial, Ludovic
    SYNLETT, 2013, 24 (12) : 1595 - 1596
  • [40] QUENCHING OF TRIPLET BENZOPHENONE BY 1,4-DIAZABICYCLO[2.2.2]OCTANE IN ACETONITRILE REVISITED
    HASELBACH, E
    JACQUES, P
    PILLOUD, D
    SUPPAN, P
    VAUTHEY, E
    JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (19): : 7115 - 7117