PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL

Alcohol compound, 2-ethylhexanol (2-EH), is widely used as raw material for producing plasticizers, additives in soaps, coatings, surfactants, and so on. One of the reactions in the 2-EH synthesis process is the catalytic hydrogenation of 2-ethyl-2-hexenal (or Ethyl Propyl Acrolein/EPA) into 2-EH. C...

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Main Author: Adinda Inka P, Bernadeta
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/48449
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:48449
spelling id-itb.:484492020-06-29T11:48:45ZPENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL Adinda Inka P, Bernadeta Indonesia Final Project 2-ethylhexanol, hydrogenation, catalyst, nickel, promoter INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/48449 Alcohol compound, 2-ethylhexanol (2-EH), is widely used as raw material for producing plasticizers, additives in soaps, coatings, surfactants, and so on. One of the reactions in the 2-EH synthesis process is the catalytic hydrogenation of 2-ethyl-2-hexenal (or Ethyl Propyl Acrolein/EPA) into 2-EH. Currently, PT. Petro Oxo Nusantara is the only 2-EH producer in Indonesia. However, the hydrogenation catalyst used is still imported. Therefore, this research was conducted to obtain the recipe for EPA hydrogenation catalyst to 2-EH with the same or higher quality than those of commercial catalyst. Thus, Indonesia can independently meet the needs of the catalyst without relying on imports. In this research, Ni metal is used as the main active phase of the catalyst and AlOOH-SiO2 is used as support with a mass ratio of AlOOH:SiO2 of 2:1. The catalyst is synthesized through three main stages, which are precipitation of Ni(OH)2 to produce NiO, sol-gel process to synthesize supported NiO, and impregnation process to add promoters. This research is carried out by varying the precipitating agent between NaOH and NH4OH, varying mass ratio of NiO:support between 50:48 and 48:50, as well as varying the promoter using Cu (0.5-6%-w) and K (0.5-1%-w) metals. The synthesized catalyst was then tested using a fixed bed reactor under the operating conditions of 120oC, 30 bar, and LHSV of 2,2 h-1 for 8 hours, with sampling done every 1 hour. Samples were analyzed using Gas Chromatography (GC) with an FID detector and RTX-5 column. The crystallinity of the catalysts from the variation of precipitating agents were also analyzed using X-Ray Diffraction (XRD). Based on the study, the use of NH4OH as a precipitating agent resulted in better catalyst performance than those of NaOH. The NiO:support mass ratio of 50:48 provides better performance so that the support reduction as the increase of promoter is carried out on the synthesis of other catalysts. Meanwhile, 0.5%-w K promoted catalysts provide better results and stability than commercial catalysts with the average EPA conversion of 94% and average 2-EH selectivity of 96%. 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 Alcohol compound, 2-ethylhexanol (2-EH), is widely used as raw material for producing plasticizers, additives in soaps, coatings, surfactants, and so on. One of the reactions in the 2-EH synthesis process is the catalytic hydrogenation of 2-ethyl-2-hexenal (or Ethyl Propyl Acrolein/EPA) into 2-EH. Currently, PT. Petro Oxo Nusantara is the only 2-EH producer in Indonesia. However, the hydrogenation catalyst used is still imported. Therefore, this research was conducted to obtain the recipe for EPA hydrogenation catalyst to 2-EH with the same or higher quality than those of commercial catalyst. Thus, Indonesia can independently meet the needs of the catalyst without relying on imports. In this research, Ni metal is used as the main active phase of the catalyst and AlOOH-SiO2 is used as support with a mass ratio of AlOOH:SiO2 of 2:1. The catalyst is synthesized through three main stages, which are precipitation of Ni(OH)2 to produce NiO, sol-gel process to synthesize supported NiO, and impregnation process to add promoters. This research is carried out by varying the precipitating agent between NaOH and NH4OH, varying mass ratio of NiO:support between 50:48 and 48:50, as well as varying the promoter using Cu (0.5-6%-w) and K (0.5-1%-w) metals. The synthesized catalyst was then tested using a fixed bed reactor under the operating conditions of 120oC, 30 bar, and LHSV of 2,2 h-1 for 8 hours, with sampling done every 1 hour. Samples were analyzed using Gas Chromatography (GC) with an FID detector and RTX-5 column. The crystallinity of the catalysts from the variation of precipitating agents were also analyzed using X-Ray Diffraction (XRD). Based on the study, the use of NH4OH as a precipitating agent resulted in better catalyst performance than those of NaOH. The NiO:support mass ratio of 50:48 provides better performance so that the support reduction as the increase of promoter is carried out on the synthesis of other catalysts. Meanwhile, 0.5%-w K promoted catalysts provide better results and stability than commercial catalysts with the average EPA conversion of 94% and average 2-EH selectivity of 96%.
format Final Project
author Adinda Inka P, Bernadeta
spellingShingle Adinda Inka P, Bernadeta
PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
author_facet Adinda Inka P, Bernadeta
author_sort Adinda Inka P, Bernadeta
title PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
title_short PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
title_full PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
title_fullStr PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
title_full_unstemmed PENGEMBANGAN KATALIS BERBASIS NIKEL UNTUK HIDROGENASI 2-ETIL-2-HEKSENAL
title_sort pengembangan katalis berbasis nikel untuk hidrogenasi 2-etil-2-heksenal
url https://digilib.itb.ac.id/gdl/view/48449
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