Yen Ping Tan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Yen Ping Tan has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
Abdul Halim Abdullah
Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Serdang, Malaysia
1 shared publication- Abdul Halim Abdullah
Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Serdang, Malaysia
1 shared publication - Aloysius Akaangee Pam
Chemistry Department, Federal University Lokoja, Lokoja, Nigeria
1 shared publication - Alvin Lim Teik Zheng
Department of Applied Chemistry, Faculty of Engineering, Kyushu Institute of Technology, Fukuoka, Japan
1 shared publication - Azidah Abdul Kadir
Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia
1 shared publication - Ernee Noryana Muhamad
Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Serdang 43400 UPM, Selangor, Malaysia
1 shared publication
Latest Publications
- Open Access
Efficient and Stable Rice Husk Bioderived Silica Supported Cu2S-FeS for One Pot Esterification and Transesterification of a Malaysian Palm Fatty Acid Distillate
A novel heterogeneous catalyst composite (CuS-FeS/SiO2) derived from rice husk silica was engineered following pyrolysis, chemical precipitation, and chemical redox technique. The resulting catalyst was applied to the conversion of palm fatty acid distillate to biodiesel. The presence of CuS and FeS on the catalyst was verified using X-ray diffraction and Fourier transform infrared spectroscopy, nitrogen physisorption, scanning electron microscopy (FESEM) with energy dispersive X-ray (EDS) spectroscopy, and temperature-programmed desorption of NH3 (TPD-NH3), inductively coupled plasma-atomic emission spectrometry (ICP-AES), and TGA; a specific surface area of approximately 40 m2·g−1 was identified. The impact of independent variables, i.e., reaction temperature, reaction duration, methanol:oil ratio and catalyst concentration were evaluated with respect to the efficacy of the esterification reaction. The greatest efficiency of 98% with a high productivity rate of 2639.92 µmol·g−1·min−1 with k of 4.03 × 10−6 mole·S−1 was achieved with the following parameters: temperature, 70 °C; duration, 180 min; catalyst loading, 2 wt.%; and methanol to oil ratio, 15:1. The CuS-FeS/SiO2 catalyst showed relatively high stability indicated by its ability to be reused up to five times.
Open AccessEfficient and Stable Rice Husk Bioderived Silica Supported Cu2S-FeS for One Pot Esterification and Transesterification of a Malaysian Palm Fatty Acid Distillate
A novel heterogeneous catalyst composite (CuS-FeS/SiO2) derived from rice husk silica was engineered following pyrolysis, chemical precipitation, and chemical redox technique. The resulting catalyst was applied to the conversion of palm fatty acid distillate to biodiesel. The presence of CuS and FeS on the catalyst was verified using X-ray diffraction and Fourier transform infrared spectroscopy, nitrogen physisorption, scanning electron microscopy (FESEM) with energy dispersive X-ray (EDS) spectroscopy, and temperature-programmed desorption of NH3 (TPD-NH3), inductively coupled plasma-atomic emission spectrometry (ICP-AES), and TGA; a specific surface area of approximately 40 m2·g−1 was identified. The impact of independent variables, i.e., reaction temperature, reaction duration, methanol:oil ratio and catalyst concentration were evaluated with respect to the efficacy of the esterification reaction. The greatest efficiency of 98% with a high productivity rate of 2639.92 µmol·g−1·min−1 with k of 4.03 × 10−6 mole·S−1 was achieved with the following parameters: temperature, 70 °C; duration, 180 min; catalyst loading, 2 wt.%; and methanol to oil ratio, 15:1. The CuS-FeS/SiO2 catalyst showed relatively high stability indicated by its ability to be reused up to five times.
- Open Access
- 21 May 2021
- Published by Springer Nature in Applied Water Science
- Vol. 11 (6) , 1-15
Pb(II) removal in water via adsorption onto deep eutectic solvent fabricated activated carbon
In our current work, we have established a novel approach in the synthesis of a new adsorbent by using choline chloride and urea (DES)/orthophosphoric acid (H3PO4) as our activating agent and palm kernel shell (PKS) as our precursor. The resulting activated carbon (DES/H3PO4-6002:3) was used to adsorb Pb(II) from aqueous solution. Characterization of DES-H3PO4-6002:3 by nitrogen adsorption/desorption isotherm measurements, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) demonstrated good micropores structure and high surface area that makes DES/H3PO4-600 2:3 a suitable alternative for liquid phase adsorption. The fundamental batch experiment of DES/H3PO4-600 2:3 was investigated by different parameters (such as concentration, pH, temperature and absorbent dose). The results obtained indicated that Langmuir model and pseudo-second-order equation best fit the data, indicating that the adsorption was controlled by chemical reaction and monolayer uptake. In addition, the fabrication of DES/H3PO4 AC exhibits good potential for Pb(II) ions uptake, including its high adsorption capacity (97.1 mg/g) and good recyclability. The future potential of this works lies in the identification of alternatives to environmental benign synthesis AC and reuse of Pb(II) ion–laden biosorbent after heavy metal uptake.
- 21 May 2021
- Published by Springer Nature in Applied Water Science
- Vol. 11 (6) , 1-15
Open AccessPb(II) removal in water via adsorption onto deep eutectic solvent fabricated activated carbon
In our current work, we have established a novel approach in the synthesis of a new adsorbent by using choline chloride and urea (DES)/orthophosphoric acid (H3PO4) as our activating agent and palm kernel shell (PKS) as our precursor. The resulting activated carbon (DES/H3PO4-6002:3) was used to adsorb Pb(II) from aqueous solution. Characterization of DES-H3PO4-6002:3 by nitrogen adsorption/desorption isotherm measurements, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) demonstrated good micropores structure and high surface area that makes DES/H3PO4-600 2:3 a suitable alternative for liquid phase adsorption. The fundamental batch experiment of DES/H3PO4-600 2:3 was investigated by different parameters (such as concentration, pH, temperature and absorbent dose). The results obtained indicated that Langmuir model and pseudo-second-order equation best fit the data, indicating that the adsorption was controlled by chemical reaction and monolayer uptake. In addition, the fabrication of DES/H3PO4 AC exhibits good potential for Pb(II) ions uptake, including its high adsorption capacity (97.1 mg/g) and good recyclability. The future potential of this works lies in the identification of alternatives to environmental benign synthesis AC and reuse of Pb(II) ion–laden biosorbent after heavy metal uptake.