Abstract
The biodiesel production from waste cooking oil in this data collection process was focused on the utilization of the heterogeneous catalyst of CaO/silica. The CaO was obtained from eggshell after preparation process and the silica was successfully extracted from peat clay using sodium hydroxide with various molarities. The CaO/silica catalyst was formed by the impregnation of the CaO catalyst on the support of silica. The FTIR, SEM and XRD characterization for the various formed catalysts were presented. The generated catalysts were further used for the production of biodiesel. The GCMS chromatogram with the type of methyl esters for each data was presented. The data presented here are related to the previous research article [1].
Keywords: Biodiesel, CaO, Silica, Peat clay, Waste cooking oil
Specifications Table
Subject | Chemical Engineering |
Specific subject area | Catalysis in Energy Process |
Type of data | Tables and Figure |
How data were acquired | SEM, FTIR, XRD and GCMS |
Data format | Raw and analyzed |
Experimental factors | The catalyst was characterized after activation (calcination) at 900 °C for 2 h. The transesterification reaction was conducted at the time range of 30–120 min and the temperature range of 30–60 °C. |
Experimental features | The heterogeneous catalyst was collected from impregnation of CaO on silica support. The silica was obtained from extraction of peat clay. |
Data source location | Lambung Mangkurat University, Banjarbaru, Indonesia |
Data accessibility | Data were available within the article |
Related research article | Meilana Dharma Putra, Chairul Irawan, Udiantoro, Yuli Ristianingsih and Iryanti Fatyasari Nata A cleaner process for biodiesel production from waste cooking oil using waste materials as a heterogeneous catalyst and its kinetic study Journal of Cleaner Production https://doi.org/10.1016/j.jclepro.2018.06.010 |
Value of the Data
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1. Data
Fig. 1 shows the FTIR characterization for three catalysts of CaO/silica. The similar observations were obtained for those catalysts; however, the strong peak was observed at 850 cm−1 and around 720 cm−1 for the type catalyst of CaO/silica (12.5%) due to Si–O interaction and CaO, respectively. Fig. 2 presents the XRD characterization for three catalysts of CaO/silica with the identical trends. The presence of CaCO3, CaO and silica was observed in the peak of around 30° [2], in the range of 34–44° [3] and about 27° [1], respectively. The similar observations were also shown for SEM characterization (with enlargement of 7000X) for the three types of CaO/silica catalysts as shown in Fig. 3. The important point of these finding is that the different concentrations of solvent for silica extraction lead to similar characteristic observations of the catalysts. Hence, the developed CaO/silica catalyst stands as a promising catalyst for biodiesel production. Fig. 4, Fig. 5, Fig. 6, Fig. 7, Fig. 8, Fig. 9, Fig. 10 show the chromatogram marks for various reaction condition. The components of methyl palmitate, methyl linoleate, elaidic acid and oleic acid were majorly observed as shown in Table 1. The composition of fatty acid was dominantly composed of the carbon chain of C16–C20 [4,5]. The different compositions of fatty acid resulted for various conditions are important for further development of this prospective work.
Fig. 1.
FTIR characterization for (a). CaO/silica (7.5%); (b). CaO/silica (10%) and (c). CaO/silica (12.5%).
Fig. 2.
XRD characterization for (a). CaO/silica (7.5%); (b). CaO/silica (10%) and (c). CaO/silica (12.5%).
Fig. 3.
SEM characterization for (a). CaO/silica (7.5%); (b). CaO/silica (10%) and (c). CaO/silica (12.5%).
Fig. 4.
Chromatogram result of sample for 15 min at 60 °C with 14 M ratio of methanol to biodiesel.
Fig. 5.
Chromatogram result of sample for 45 min at 60 °C with 14 M ratio of methanol to biodiesel.
Fig. 6.
Chromatogram result of sample for 60 min at 60 °C with 14 M ratio of methanol to biodiesel.
Fig. 7.
Chromatogram result of sample for 75 min at 60 °C with 14 M ratio of methanol to biodiesel.
Fig. 8.
Chromatogram result of sample for 90 min at 60 °C with 21 M ratio of methanol to biodiesel.
Fig. 9.
Chromatogram result of sample for 90 min at 60 °C with 17 M ratio of methanol to biodiesel.
Fig. 10.
Chromatogram result of sample for 90 min at 60 °C with 12 M ratio of methanol to biodiesel.
Table 1.
Type of fatty acid component in biodiesel products.
Condition | Component |
|||||
---|---|---|---|---|---|---|
Methyl palmitate | Palmitic acid | Methyl linoleate | Elaidic acid | Methyl stearate | Oleic acid | |
T = 60 °C; t = 15 min; ratio = 14 | 25.24 | 10.77 | 49.37 | 13.93 | ||
T = 60 °C; t = 45 min; ratio = 14 | 24.87 | 4.99 | 8.39 | 8.39 | 29.18 | |
T = 60 °C; t = 60 min; ratio = 14 | 28.04 | 7.88 | 8.22 | 35.90 | 2.58 | 16.98 |
T = 30 °C; t = 75 min; ratio = 14 | 29.54 | 0.43 | 8.71 | 38.79 | 22.23 | |
T = 60 °C; t = 90 min; ratio = 21 | 0.54 | 22.49 | 64.24 | 12.03 | ||
T = 60 °C; t = 90 min; ratio = 18 | 17.18 | 6.21 | 8.54 | 32.39 | 0.90 | 34.68 |
T = 60 °C; t = 90 min; ratio = 12 | 11.91 | 0.35 | 9.20 | 28.36 | 49.86 |
2. Experimental design, materials, and methods
The catalyst of CaO was obtained from eggshell after process of cleaning, sieving and calcination was conducted. Silica as support of catalyst was extracted from peat clay upon the preparation process of cleaning, crushing, sieving and calcination were conducted. The extraction process was carried out at 80 °C for 1 h using 60 mL NaOH with the variation of molarities of 1.86 N, 2.5 N and 3.12 N. These molarities corresponded to the sodium hydroxide concentration of 7.5%, 10% and 12.5%. The CaO catalyst was finally combined with the obtained silica resulted from the extraction as support using impregnation method [6]. The three types of catalyst were then namely CaO/silica (7.5%), CaO/silica (10%) and CaO/silica (12.5%). The catalyst was utilized in the transesterification process at various temperature and time to produce biodiesel. The waste cooking oil and methanol were used as raw material. The biodiesel component was analyzed using GCMS (2010S Shimadzu, Tokyo, Japan). The catalyst was characterized using FTIR, XRD and SEM with the detailed equipment described there [1].
Acknowledgments
The authors extend the appreciation to Ministry of Research, Technology and Higher Education, Republic of Indonesia that provided a Research Grant with contract No. 061/SP2H/LT/DRPM/2018 for the generous support and funding of this research.
Conflict of Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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