scholarly journals Epoxidation of Podocarpus Falcatus Oil by Sulphuric Acid Catalyst: Process Optimization and Physio-chemical Characterization

2021 ◽  
Vol 9 (4) ◽  
pp. 84
Author(s):  
Yigezu Mekonnen
Author(s):  
Deni Mustika ◽  
Torowati Torowati ◽  
Arbi Dimyati ◽  
Sudirman Sudirman ◽  
Adel Fisli ◽  
...  

PURIFICATION OF INDONESIAN NATURAL GRAPHITE AS CANDIDATE FOR NUCLEAR FUEL MATRIX BY ACID LEACHING METHOD: CHEMICAL CHARACTERIZATION. Graphite matrix in Pebble Bed Reactor (PBR) – High Temperature Gas Cooled Reactor (HTGR) has an important role as heat transfer medium, neutron moderator and structural material to protect fuel. Thus, graphite matrix must fulfill chemical and physical characteristics for PBR-HTGR fuel. Indonesia has graphite sources in several regions that can potentially be purified. This research aimed to purify Indonesian natural graphite by several variation of acids and to perform chemical characterizations. Natural graphite from flotation process was purified by several variations of acid, i. e., hydrofluoric acid (HF), sulphuric acid + nitric acid (H2SO4 + HNO3) and hydrofluoric acid + hydrochloric acid + sulphuric acid (HF + HCl + H2SO4) and subsequently followed by chemical characterizations such as purity level, ash content, and boron quivalent. The highest purity was obtained in the purification process by HF with carbon content up to 99.52%; this purity level fulfills the specification of nuclear graphite (>99%). Ash content analysis shows a value in compliance with the specification requirement, i.e., < 100 ppm, and boron equivalent value also fulfills the specification value of < 1 ppm. It can be concluded from this study that the graphite purified by acid leaching with HF can be used as fuel matrix candidate but is qualified as low quality. Futher research is required to produce high quality nuclear graphite, particularly research in the minimization of the impurity by evaporation at temperatures over 950 oC to by far lower the ash content.Keywords:  Indonesian natural graphite, purification, nuclear fuel matrix, acid leaching, chemical characterization.


2010 ◽  
Vol 6 (3) ◽  
pp. 286-291 ◽  
Author(s):  
M. Farid Rahman ◽  
Elvina Dhiaul Iftitah

The synthesis of 1,3-dimethyl-6,7-dimethoxy-3,4-dihydroisoquinoline from methyleugenol with application of Ritter reaction for directly cyclization was presented. This research was carried out in 2 steps : (1) Determination of intermediate stability that undergo in the reaction by using hyperchem version 6 with AM 1 semi empirical method, and (2) Synthesis of dihydroisoquinoline from methyleugenol and acetonitrile with acid catalyst (H2SO4) in the laboratory. The result of AM 1 calculation found that generally, the intermediate encourage the formation dihydroisoquinoline product, had low energy were compared with the intermediate in other product. Therefore, the dihydroisoquinoline product was easily formed. The result of experimental laboratory found that dihydroisoquinoline could be synthesed from methyleugenol and acetonitrile in the presence sulphuric acid under reflux in 74,92% yields. In despite, the minor product was formed with amount 6,74%. While the reaction at room temperature gave dihydroisoquinoline in poor yield about 11,42%.   Keywords: stability of intermediate, dihydroisoquinoline, Ritter reaction


2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Jumat Salimon ◽  
Neeranjini Nallathamby ◽  
Nadia Salih ◽  
Bashar Mudhaffar Abdullah

A study was conveyed to produce estolide ester using ricinoleic acid as the backbone. The ricinoleic acid reacted with saturated fatty acid from C8–C18. These reactions were conducted under vacuum at 60°C for 24 h without solvent. The reaction used acid catalyst, sulphuric acid. The new saturate ricinoleic estolide esters show superior low-temperature properties (−52 ± 0.08°C) and high flash point (>300°C). The yield of the neat estolide esters ranged from 52% to 96%. The viscosity range was 51 ± 0.08 to 86 ± 0.01 cp. These new saturated estolide esters were also compared with saturated branched estolide esters.


RSC Advances ◽  
2020 ◽  
Vol 10 (53) ◽  
pp. 31824-31837
Author(s):  
Triana Kusumaningsih ◽  
Wahyu Eko Prasetyo ◽  
Maulidan Firdaus

A greatly improved procedure for the synthesis of antibiotic 2,4-diacetylphloroglucinol has been developed via a newly advanced synthetic method.


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