Normal view MARC view ISBD view

Conversion of carbon dioxide to methanol over visible light responsive catalyst / Mariotte Anak Patrick Jebi

By:

Mariotte Patrick Jebi [author.]

Material type: Text

text
text

Media type:

unmediated
computer

Carrier type:

volume
computer disc

ISBN:

THE0000948(Local)

Subject(s):

Dissertation note: Project Paper (Bachelor of Chemical Engineering) -- Universiti Malaysia Pahang – 2017 Abstract: The significant increase of carbon dioxide contributed for the largest share of the world’s greenhouse gas emissions. There is a growing need to mitigate CO2 emissions. One of the strategies to mitigate CO2 emissions is using CO2 as a raw material in chemical processes. In the present study, a TiO2 loaded copper (II) oxide (CuO) photoelectrode was synthesized, characterized and studied for photoelectrocatalytic (PEC) reduction of carbon dioxide (CO2) into methanol under visible light (λ > 470 nm) irradiation. In this perspective, The material was constructed via sol-gel method from copper (II) nitrate, Cu(NO3)2.3H2O (99 %) and commercial Degussa P25 TiO2 as precursors. The photocatalysts were characterized by X-ray diffraction, UV-vis absorption specra, X-ray photoelectron spectroscopy (XPS), photoluminescence spectrophotometer, and mott schottky (MS). Linear sweep voltammetry (LSV) was employed to evaluate the effect of visible light (λ >400 nm) on the CO2 reduction reactions. The characterization results indicated that the band gap energy of the CuO-TiO2 catalyst from UV-Vis is 1.39 eV. The flat band potential calculated from the MS data as 0.83 V versus normal hydrogen electrode (NHE). The LSV the dark and under visible light irradiation further support the visible light-responsive photocatalytic activities CuO-TiO2 giving onset potential value from -0.20 V with current peak potential appearing at -0.35V (vs NHE) suggesting an increase in photocurrent and occurrence CO2 photoreduction reaction. The PEC performance of CuO-TiO2 photocatalyst showed an increased methanol yield of 20.1 μmol.L-1.cm-2 under visible light irradiation.

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

Holdings ( 2 )
Title notes ( 4 )

Holdings
Item type	Current library	Call number	Copy number	Status	Notes	Date due	Barcode
Final Year Report	UMPLIB GAMBANG	CD12434 (Browse shelf(Opens below))	1	Not for loan			T000000486
Final Year Report	UMPLIB GAMBANG	FKKSA .M37 2017 r Bc. (Browse shelf(Opens below))	1	Not for loan	PROSES TUKAR TAG RFID KEPADA UHF		0000122258

Faculty of Chemical & Natural Resources Engineering

Project Paper (Bachelor of Chemical Engineering) -- Universiti Malaysia Pahang – 2017

Includes bibliographical references

The significant increase of carbon dioxide contributed for the largest share of the world’s greenhouse gas emissions. There is a growing need to mitigate CO2 emissions. One of the strategies to mitigate CO2 emissions is using CO2 as a raw material in chemical processes. In the present study, a TiO2 loaded copper (II) oxide (CuO) photoelectrode was synthesized, characterized and studied for photoelectrocatalytic (PEC) reduction of carbon dioxide (CO2) into methanol under visible light (λ > 470 nm) irradiation. In this perspective, The material was constructed via sol-gel method from copper (II) nitrate, Cu(NO3)2.3H2O (99 %) and commercial Degussa P25 TiO2 as precursors. The photocatalysts were characterized by X-ray diffraction, UV-vis absorption specra, X-ray photoelectron spectroscopy (XPS), photoluminescence spectrophotometer, and mott schottky (MS). Linear sweep voltammetry (LSV) was employed to evaluate the effect of visible light (λ >400 nm) on the CO2 reduction reactions. The characterization results indicated that the band gap energy of the CuO-TiO2 catalyst from UV-Vis is 1.39 eV. The flat band potential calculated from the MS data as 0.83 V versus normal hydrogen electrode (NHE). The LSV the dark and under visible light irradiation further support the visible light-responsive photocatalytic activities CuO-TiO2 giving onset potential value from -0.20 V with current peak potential appearing at -0.35V (vs NHE) suggesting an increase in photocurrent and occurrence CO2 photoreduction reaction. The PEC performance of CuO-TiO2 photocatalyst showed an increased methanol yield of 20.1 μmol.L-1.cm-2 under visible light irradiation.