scholarly journals Pengaruh Kalsinasi Hidrotalsit Terhadap Aktivitas Katalitik Pada Reaksi Transesterifikasi Etil Asetat Menjadi Metil Asetat

2018 ◽  
Vol 1 (1) ◽  
pp. 26-37
Author(s):  
Imam Januar

This research is aim to study the optimum of time and calcination ffict on hydrotalcite in transesterification reaction in obtaining metyl ester. The reagen has been used in this reaclion were etyl acetat, methanol and hydrotalcite as catalyst. In the reaction was used various of times; 0,5, 1, 2, 3 hours and various catalysts; calcinated catalyst and non-calcinated catalyst. The caracterization of hydrotalcite has used XRD, BET and FTIR instrument.The result of GC intrepetation showed the decreasing of methanol concentration. The result caracterization hydrotalcite using XRD showed difractogram d= 7,60882; 3,79933 and 8,42876Å. These peaks have similiarity to the d of Mg/Al standar of hydrocalcite. BET intrepetation showed the specific surface area is 12,337 m2/g, averages of pores are 15,352 Å, volume of pores is 3,9 x 10-2 cm3/g. The result of FTIR showed the appearance of hydroxil group with the wavelength; 3450,40 cm-1 and 1635,38 cm-1, CO32- was 1366,66 cm-1  and 660,20 cm-1, MgO was 553,23 cm-1, Zn-O is 447,04 cm-1, these wavelengths showed the characteristic of hydrocalcite. Infrared intrepretation showed that the compound Mg-Zn-AlCO3.4H2O was hydrocalcite

Author(s):  
Yurii Melnyk ◽  
Stepan Melnyk ◽  
Halyna Mahorivska ◽  
Viktor Reutskyy

The physicochemical indicators of d-metal oxides (NiO, CuO, MnO, FeO, PbO, ZnO) which are heterogeneous catalysts for the transesterification process of sunflower oil triglycerides by ethanol and butan-1-ol have been determined. The available specific surface area, surface acidity and basicity, as well as the hydrogen potential change of the catalyst suspension in water were determined for the oxides. The available specific surface area of the oxides was determined by titration of their aqueous suspension with a solution of methylene blue with a predetermined concentration. The surface acidity and basicity of the catalysts were determined by back titration of samples treated with an aqueous solution of ammonia and acetic acid, respectively. It was found that all investigated d-metal oxides have a low specific surface area. The value of specific surface area is in the range of 0.6-1.5 m2/g. The surface acidity and basicity of the catalysts is 0.13-0.27 mmol/g and 0.019-0.066 mmol/g, respectively. It is shown that the change in the aqueous suspension hydrogen potential of the investigated catalysts relative to the distilled water pH is maximum for NiO and ZnO and it is 0.6-0.65, while for CuO this change is the smallest and it is only 0.3. The character of the pH change curves and the pH values of the oxides suspension in equilibrium condition indicate the presence of weak acid sites in the studied catalysts. The indicated catalysts characteristics are compared with the results obtained in the transesterification process of sunflower oil triglycerides by ethanol and butan-1-ol. It was found that there is a correlation between the surface acidity of catalyst and the reaction initial rate of triglycerides transesterification by ethanol and butan-1-ol. At the same time, such a correlation is absent for the surface basicity of the catalysts. This is consistent with the data on the catalysis of the triglyceride transesterification reaction only by strong major active sites. It is concluded that the transesterification reaction of sunflower oil triglycerides by ethanol and butan-1-ol occurs predominantly on the weak acid centers of the d-metal oxides.


Jurnal Kimia ◽  
2016 ◽  
Author(s):  
Ana Malia ◽  
Putu Suarya ◽  
Ida Ayu Raka Astiti Asih ◽  
I Made Wisnu Adhi Putra

The research of transesterification reaction catalyzed by CaO/natural zeolite has been carried out. This work was aimed to obtain the high yield of biodiesel. The supporting process of CaO on natural zeolite (CaO/ZAA) was done by using wet impregnation method and characterization of CaO/ZAA was performed using XRD, FTIR and the determination of specific surface area of natural zeolite as CaO supporter was performed by BET method. This research aims to study the influence of transesterification reaction which was executed by varying molar ratio of oil to methanol and reaction temperature. Analysis of functional groups and minerals using FTIR and XRD, respectively, showed no significant changes before and after the impregnation of CaO on natural zeolites. CaO supported on natural zeolite was undetected by FTIR. Instead, it was detected by the vibration of carbonate groups as the result of the CO2 absorption by CaO and the result of surface area analysis using BET method showed that the greater the size of natural zeolite, the smaller the specific surface area of catalyst. The result analysis using BET method showed that the spesific surface area of 200 mesh sized natural zeolite as CaO supporter was 9.993 m2/g. The simple gravimetric test revealed that  the amount of CaO supported on 200 mesh sized natural zeolite was 0.2155 g/g. It was concluded that CaO/ZAA 200 mesh was the most suitable catalyst which was then used in the production of biodiesel. The transesterification result showed that the highest biodiesel yield of 98.34% was gained at molar ratio of oil to methanol of 1:15 and at the temperature of 60 oC. The GC-MS analysis indicated that the main components of the biodiesel were methyl palmitate and methyl oleate.


2017 ◽  
Vol 68 (3) ◽  
pp. 483-486
Author(s):  
Constantin Sorin Ion ◽  
Mihaela Bombos ◽  
Gabriel Vasilievici ◽  
Dorin Bombos

Desulfurisation of atmospheric distillation gasoline and gas oil was performed by adsorption process on Fe/ bentonite. The adsorbent was characterized by determining the adsorption isotherms, specific surface area, pore volume and average pore diameter. Adsorption experiments of atmospheric distillation gasoline and gas oil were performed in continuous system at 280�320oC, 5 atm and volume hourly space velocities of 1�2 h-1. The efficiency of adsorption on Fe / bentonite was better at desulphurisation of gasoline versus gas oil.


Metals ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 345 ◽  
Author(s):  
Lianzan Yang ◽  
Yongyan Li ◽  
Zhifeng Wang ◽  
Weimin Zhao ◽  
Chunling Qin

High-entropy alloys (HEAs) present excellent mechanical properties. However, the exploitation of chemical properties of HEAs is far less than that of mechanical properties, which is mainly limited by the low specific surface area of HEAs synthesized by traditional methods. Thus, it is vital to develop new routes to fabricate HEAs with novel three-dimensional structures and a high specific surface area. Herein, we develop a facile approach to fabricate nanoporous noble metal quasi-HEA microspheres by melt-spinning and dealloying. The as-obtained nanoporous Cu30Au23Pt22Pd25 quasi-HEA microspheres present a hierarchical porous structure with a high specific surface area of 69.5 m2/g and a multiphase approximatively componential solid solution characteristic with a broad single-group face-centered cubic XRD pattern, which is different from the traditional single-phase or two-phase solid solution HEAs. To differentiate, these are named quasi-HEAs. The synthetic strategy proposed in this paper opens the door for the synthesis of porous quasi-HEAs related materials, and is expected to promote further applications of quasi-HEAs in various chemical fields.


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