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Ditemukan 2 dokumen yang sesuai dengan query
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Rhadiathul Wahyuli
"Nanokomposit berbasis biopolimer yang mengalami adsorpsi ion logam pada permukaan bahan pendukung magnetik memiliki kemampuan katalitik lebih baik sehingga menarik untuk dikembangkan sebagai katalis dalam reaksi reduksi 4-nitrofenol. Nanokomposit NaAlg-CMC/Fe3O4 dan NaAlg-CMC/Fe3O4-Cu telah berhasil disintesis yang didukung dengan karakterisasi menggunakan FTIR, XRD dan SEM-EDS Mapping. NaAlg-CMC merupakan biopolimer yang bertindak sebagai support katalis dan dapat membentuk komposit dengan sifat yang baik saat digabungkan dengan Fe3O4. Nanokomposit NaAlg-CMC/Fe3O4 dapat digunakan sebagai adsorben yang baik dalam penghilangan ion Cu2+. Kondisi optimum diperoleh pada berat nanokomposit 50 mg, pH 5,5, rasio NaAlg-CMC/Fe3O4 2:1, waktu kontak 90 menit dengan persen penghilang 97,80% dan kapasitas adsorpsi 48,9018 mg/g. Isoterm adsorpsi ion Cu2+ mengikuti model isoterm adsorpsi Langmuir dengan R2 sebesar 0,9944. Nanokomposit NaAlg-CMC/Fe3O4-Cu dapat menjadi katalis yang baik dalam reduksi katalitik 4-nitrofenol dengan persen reduksi sebesar 92,95 pada berat katalis 45 mg dan waktu reaksi 11 menit. Studi kinetika reaksi reduksi 4-nitrofenol menjadi 4-aminofenol mengikuti kinetika reaksi orde pertama dengan persamaan v = 0,2592 menit-1 [4-NP]. Nanokomposit yang diperoleh dapat menjadi solusi untuk mengurangi logam berat dan polutan organik yang ramah lingkungan.

Biopolymer-based nanocomposite with adsorbed metal ions on the surface of magnetic support has better catalytic ability that is interest to be developed as a catalyst in the reduction of 4-nitrofenol. SA-CMC/Fe3O4 and SA-CMC/Fe3O4-Cu have been successfully synthesized and supported by characterization using FTIR, XRD and SEM-EDS Mapping. SA-CMC is a biopolymer-based composite as a supporting catalyst and able to form composites with good properties when combined with Fe3O4. SA-CMC/Fe3O4 nanocomposites can be used as good adsorbents of Cu2+ in wastewater. The optimum conditions were obtained by the adsorbent dosage 50 mg, pH 5.5, ratio of SA-CMC/Fe3O4 2:1, contact time 90 minutes with efficiency removal 97.80% and maximum adsorption capacity reached 48,9018 mg/g. The adsorption process of Cu2+ removal follows the Langmuir adsorption isotherm model. SA-CMC/Fe3O4-Cu nanocomposite can be a good catalyst in the reduction of 4-nitrophenol with percent of reduction 92.95% by amount of catalyst 45 mg and reaction time 11 minutes. Study kinetics of reduction 4-nitrophenol to 4-aminophenol follows pseudo-first-order reactions with equation v = 0,2592 min-1 [4-NP]. Nanocomposite can remove heavy metal and organic pollutant in wastewater that are environmentally friendly.
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Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2020
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UI - Skripsi Membership  Universitas Indonesia Library
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Lee D. Wilson
"The adsorption properties of surface-modified mesoporous silica materials containing ?-cyclodextrin (CD ICS) were studied using two types of gas phase adsorbates (N2 and CH3Cl), along with a dye molecule (p-nitrophenol; PNP) in an aqueous solution. The CD ICS materials possess an ordered silica mesostructure framework that depends on the type of surfactant template and the level of loading of ?-CD. Incremental variations in the uptake of gas phase adsorbates and PNP from an aqueous solution were observed, according to the composition of CD ICS materials. For materials with similar CD loading, the surface area (SA) and pore volume doubled, as the surfactant from dodecylamine to hexadecylamine was varied. The SA of the CD ICS materials decreased by ca. 1.5-fold as the CD loading varied from 2% to 6%. The sorption capacity (Qe; mmol/g) of PNP increased from 61% to 84% as the CD loading increased from 2% to 6% and as the alkyl chain length of the surfactant template varied from C12 to C16. The adsorption properties of CD ICS materials with CH3Cl in the gas phase and for PNP in aqueous solution adopt a multi-layer adsorption profile, as described by the BET isotherm model."
Depok: Faculty of Engineering, Universitas Indonesia, 2015
UI-IJTECH 6:4 (2015)
Artikel Jurnal  Universitas Indonesia Library