OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol

OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol

ABSTRACT: <br /> <br /> <br /> <br /> <br /> In this study, method of determining p-nitrophenol was developed by using oxidation peak from p-nitrophenol reduction product. This determination used carbon paste electrode. The electrode consist of graphite and paraffi...

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Main Author: (NIM 10500013), Rokhmaturrokhman
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/6704
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:6704
spelling id-itb.:67042017-09-27T11:42:32ZOXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol (NIM 10500013), Rokhmaturrokhman Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/6704 ABSTRACT: <br /> <br /> <br /> <br /> <br /> In this study, method of determining p-nitrophenol was developed by using oxidation peak from p-nitrophenol reduction product. This determination used carbon paste electrode. The electrode consist of graphite and paraffin with composition 7:3 by weight. This method used phosphat buffer solution with pH of 7.4. The method required 60 second reduction of p-nitrophenol at potential of -1000 mV to Ag/AgCl (naCl 3 M). The calibration plots of p-nitrophenol standards were linear in the range at 0,1-10 mM of p-nitrophenol with detection limit of 0,07 mM. Percent recovery of p-nitrophenol analysis was between 91.9percent-130.5percent. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description ABSTRACT: <br /> <br /> <br /> <br /> <br /> In this study, method of determining p-nitrophenol was developed by using oxidation peak from p-nitrophenol reduction product. This determination used carbon paste electrode. The electrode consist of graphite and paraffin with composition 7:3 by weight. This method used phosphat buffer solution with pH of 7.4. The method required 60 second reduction of p-nitrophenol at potential of -1000 mV to Ag/AgCl (naCl 3 M). The calibration plots of p-nitrophenol standards were linear in the range at 0,1-10 mM of p-nitrophenol with detection limit of 0,07 mM. Percent recovery of p-nitrophenol analysis was between 91.9percent-130.5percent.
format Final Project
author (NIM 10500013), Rokhmaturrokhman
spellingShingle (NIM 10500013), Rokhmaturrokhman
OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
author_facet (NIM 10500013), Rokhmaturrokhman
author_sort (NIM 10500013), Rokhmaturrokhman
title OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
title_short OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
title_full OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
title_fullStr OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
title_full_unstemmed OXIDATION PEAK OF p-nitrophenol REDUCTION PRODUCT FOR VOLTAMMETRIC ANALYSIS OF p-nitrophenol
title_sort oxidation peak of p-nitrophenol reduction product for voltammetric analysis of p-nitrophenol
url https://digilib.itb.ac.id/gdl/view/6704
_version_ 1820663953356750848

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