Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application

<p align="justify">Starch is used as a backbone molecule in the formation of graft copolymers with other polymers to be applied in Enhanced Oil Recovery (EOR). The advantages of using starch in polymerization reactions are due to its properties such as easily available natural polyme...

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Main Author: RAHMAWATI (NIM : 10513065), MIDRATHUL
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/28913
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:28913
spelling id-itb.:289132018-10-15T15:24:54ZSynthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application RAHMAWATI (NIM : 10513065), MIDRATHUL Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/28913 <p align="justify">Starch is used as a backbone molecule in the formation of graft copolymers with other polymers to be applied in Enhanced Oil Recovery (EOR). The advantages of using starch in polymerization reactions are due to its properties such as easily available natural polymers, inexpensive, and environmental-friendly. Starch-based copolymers are able to increase the viscosity of the water to increase the amount of oil into the reservoir. This research aims to study the variables that affect the polymerization reaction of cinnamic acid grafted with cassava starch to produce copolymers of starch-g-poly(cinnamic acid). The cinnamic acid polymerisation is carried out via radical polymerization using the cerium ammonium nitrate (CAN) as an initiator. The result of FTIR analysis on the resulting polymer shows the absorption peak of OH group which is sourced from starch at wavelength about 3500 cm-1 and the loss of C = C absorption peak alkena group at wave number 1610-1680 cm-1 because the cyclic acid double bond in cinnamic acid is substituted and forming a poly(cinnamic acid). The results of polymer analysis with NMR showed peaks in 4-5 ppm regions (RCH=CHR), 5.5-6.5 ppm (H aromatic) and 9.2-10 ppm regions showed peak shift (RCO2H). The viscosity test on the polymer carried out in room temperature to 75 oC indicates that the temperature rise results in a decrease in viscosity. The maximum viscosity obtained for the copolymer was 1.55 cP at room temperature (25 oC) for the use of 1% cerium ammonium nitrate (CAN) initiator and polymerization degree (DPn) 68. The polymer viscosity test is performed by adding NaOH solids 16% into the polymer solution to increase the solubility of the polymer. The polymer salinity test was performed by adding NaCl 10%. The highest polymer viscosity was obtaned 1.65 cP for room temperature.<p align="justify"> 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 <p align="justify">Starch is used as a backbone molecule in the formation of graft copolymers with other polymers to be applied in Enhanced Oil Recovery (EOR). The advantages of using starch in polymerization reactions are due to its properties such as easily available natural polymers, inexpensive, and environmental-friendly. Starch-based copolymers are able to increase the viscosity of the water to increase the amount of oil into the reservoir. This research aims to study the variables that affect the polymerization reaction of cinnamic acid grafted with cassava starch to produce copolymers of starch-g-poly(cinnamic acid). The cinnamic acid polymerisation is carried out via radical polymerization using the cerium ammonium nitrate (CAN) as an initiator. The result of FTIR analysis on the resulting polymer shows the absorption peak of OH group which is sourced from starch at wavelength about 3500 cm-1 and the loss of C = C absorption peak alkena group at wave number 1610-1680 cm-1 because the cyclic acid double bond in cinnamic acid is substituted and forming a poly(cinnamic acid). The results of polymer analysis with NMR showed peaks in 4-5 ppm regions (RCH=CHR), 5.5-6.5 ppm (H aromatic) and 9.2-10 ppm regions showed peak shift (RCO2H). The viscosity test on the polymer carried out in room temperature to 75 oC indicates that the temperature rise results in a decrease in viscosity. The maximum viscosity obtained for the copolymer was 1.55 cP at room temperature (25 oC) for the use of 1% cerium ammonium nitrate (CAN) initiator and polymerization degree (DPn) 68. The polymer viscosity test is performed by adding NaOH solids 16% into the polymer solution to increase the solubility of the polymer. The polymer salinity test was performed by adding NaCl 10%. The highest polymer viscosity was obtaned 1.65 cP for room temperature.<p align="justify">
format Final Project
author RAHMAWATI (NIM : 10513065), MIDRATHUL
spellingShingle RAHMAWATI (NIM : 10513065), MIDRATHUL
Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
author_facet RAHMAWATI (NIM : 10513065), MIDRATHUL
author_sort RAHMAWATI (NIM : 10513065), MIDRATHUL
title Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
title_short Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
title_full Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
title_fullStr Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
title_full_unstemmed Synthesis of Starch-g-poly(cinnamic acid) as a Potential Material for Enhanced Oil Recovery Application
title_sort synthesis of starch-g-poly(cinnamic acid) as a potential material for enhanced oil recovery application
url https://digilib.itb.ac.id/gdl/view/28913
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