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Addition of Calcined Na2B4O7 on the Synthesis of Li7La3Zr2O12 Imam Shofid Alaih; Sidiq Fathonah; Khoirina Dwi Nugrahaningtyas; Fitria Rahmawati
Jurnal Kimia Sains dan Aplikasi Vol 24, No 3 (2021): Volume 24 Issue 3 Year 2021
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (3899.233 KB) | DOI: 10.14710/jksa.24.3.77-84

Abstract

Li7La3Zr2O12 (LLZO) is a garnet-type electrolyte for all-solid-state lithium-ion batteries (ASSB). It has good chemical and electrochemical stability against lithium and a relatively high ionic conductivity. However, the ionic conductivity needs to be further increased to provide a high specific capacity of the ASSB. Element doping into LLZO is an effort to increase molecular defect, known to enhance the conductivity. This research studied the effect of the Na2B4O7 addition on the LLZO synthesis, producing LLZBO(A). The investigation aims to understand whether the sodium ions dope into the LLZO structure during synthesis, or it is only B ions to enter into the structure. Therefore, another synthesis with B2O3 of B precursor was conducted for comparison (LLZBO(B)). The precursors were mixed stoichiometrically by following the formula of Li7-xLa3-xZr2-xBxNaxO12 (LLZBO, x= 0.15; 0.20; 0.30). XRD analysis equipped with Le Bail refinement found that LLZBO(A) and LLZBO(B) mainly consist of cubic and tetragonal LLZO with a %mol of 69.06 – 69.84 %, and the main secondary phase is La2Zr2O7. The surface morphology of LLZBO(A) and LLZBO(B) is almost similar to the irregular form of large aggregates. The particles become more dispersed when 0.3 %mol dopant was submitted. Impedance analysis found a high ionic conductivity of LLZBAO(A)0.3 1.042x10-3 Scm-1.
Studi awal kestabilan struktur katalis logam transisi periode pertama berbasis HZSM-5 Khoirina Dwi Nugrahaningtyas; Syafira Nur Zalfa; Fitria Rahmawati; I.F. Nurcahyo; Yuniawan Hidayat
Jurnal Rekayasa Proses Vol 17, No 1 (2023)
Publisher : Departemen Teknik Kimia Fakultas Teknik Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/jrekpros.76449

Abstract

Katalis logam transisi periode pertama (Fe, Co, Ni, Cu, atau Zn) berbasis Hydrogen Zeolite Socony Mobil – 5 (HZSM-5) merupakan katalis yang menjanjikan untuk berbagai macam reaksi. Pada penelitian ini akan dipelajari keperiodikan aktivitas dan kestabilan struktur katalis tersebut pada reaksi cracking anisol. Uji katalitik dilakukan dengan menggunakan reaktor semi alir. Produk dari hasil proses cracking anisol dianalisis menggunakan kromatografi gas-spektra massa (GC-MS), kemudian karakter katalis bekas seperti kristalinitas dan komposisi fasa dianalisis menggunakan X-ray diffraction (XRD), sedangkan luas permukaan dan porositas dianalisis menggunakan surface area analyzer (SAA). Hasil penelitian menunjukkan bahwa tidak nampak kaitan antara sifat periodik unsur dengan aktivitas katalitiknya.  Karakter setiap katalis yang telah digunakan mengalami sedikit perubahan pada komposisi fasanya, terutama katalis Fe/HZSM-5 dan Co/HZSM-5, sedangkan luas permukaan dan porositasnya mengalami penurunan.
Studi awal kestabilan struktur katalis logam transisi periode pertama berbasis HZSM-5 Khoirina Dwi Nugrahaningtyas; Syafira Nur Zalfa; Fitria Rahmawati; I.F. Nurcahyo; Yuniawan Hidayat
Jurnal Rekayasa Proses Vol 17, No 1 (2023)
Publisher : Departemen Teknik Kimia Fakultas Teknik Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/jrekpros.76449

Abstract

Katalis logam transisi periode pertama (Fe, Co, Ni, Cu, atau Zn) berbasis Hydrogen Zeolite Socony Mobil – 5 (HZSM-5) merupakan katalis yang menjanjikan untuk berbagai macam reaksi. Pada penelitian ini akan dipelajari keperiodikan aktivitas dan kestabilan struktur katalis tersebut pada reaksi cracking anisol. Uji katalitik dilakukan dengan menggunakan reaktor semi alir. Produk dari hasil proses cracking anisol dianalisis menggunakan kromatografi gas-spektra massa (GC-MS), kemudian karakter katalis bekas seperti kristalinitas dan komposisi fasa dianalisis menggunakan X-ray diffraction (XRD), sedangkan luas permukaan dan porositas dianalisis menggunakan surface area analyzer (SAA). Hasil penelitian menunjukkan bahwa tidak nampak kaitan antara sifat periodik unsur dengan aktivitas katalitiknya.  Karakter setiap katalis yang telah digunakan mengalami sedikit perubahan pada komposisi fasanya, terutama katalis Fe/HZSM-5 dan Co/HZSM-5, sedangkan luas permukaan dan porositasnya mengalami penurunan.
Synthesis of Al-Y doped-lithium lanthanum zirconate and the effect of cold isostatic pressure to its electrical properties Fitria Rahmawati; Septia K Arifah; Yuniawan Hidayat
International Journal of Renewable Energy Development Vol 12, No 4 (2023): July 2023
Publisher : Center of Biomass & Renewable Energy, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/ijred.2023.53901

Abstract

This research aims to study the Al-Y dopant to Lithium Lanthanum Zirconate (LLZO) to the characteristics and electrical properties of the LLZO as solid electrolyte. The synthesis was conducted through solid state reaction with Al2O3 and Y2O3 as dopant precursors. X-ray diffraction analysis along with Le Bail refinement was done to understand their structure, and phase content inside. The result found that Al and Y doping increased the cubic phase from 49.58% to 84.91%. The Al-Y doped-LLZO (LLZAYO) powder was then treated by a various cold isostatic pressing, CIP of 0, 20, 30, and 40 MPa to understand the effect of cold isostatic pressure to the ionic conductivity and solid electrolyte performance of the material even without heat sintering treatment. The result found that the green pellet of LLZAYO) which was isostatically pressed by 40 MPa at room temperature provides (9.06 ±0.26) x10-6 Scm-1, about 8 times higher than the LLZO without doping, i.e., (1.25 ±0.01) x 10-6 Scm-1. All solid-state battery with the prepare LLZAYO CIP 40 as solid electrolyte shows reversible reaction of Li/Li+ redox accompanied with Al/Al3+ redox. The Al/Al3+ reaction seems to decrease the electronic resistance between LCO-LLZAYO CIP40-Li which causes the full cell performance to decrease. The initial specific charging capacity is 82 mAh/g, and the initial discharge was 83 mAh/g, confirming 101 % of Coulombic efficiency. The discharge capacity drops to 46 mAh/g at second cycle, leading to a decrease in Coulombic efficiency to 56 %.
Conversion of Wood Waste to be a Source of Alternative Liquid Fuel Using Low Temperature Pyrolysis Method Gesyth Mutiara Hikhmah Al Ichsan; Khoirina Dwi Nugrahaningtiyas; Dian Maruto Widjonarko; Fitria Rahmawati; Witri Wahyu Lestari
Jurnal Kimia Sains dan Aplikasi Vol 22, No 1 (2019): volume 22 Issue 1 Year 2019
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1837.269 KB) | DOI: 10.14710/jksa.22.1.7-10

Abstract

Conversion of wood waste into bio-oil with low temperature pyrolysis method has been successfully carried out using tubular transport reactors. Pyrolysis carried out at temperatures of 250-300°C without using N2 gas. Bio-oil purified by a fractionation distillation method to remove water and light fraction compounds. The materials obtained from different types of wood waste, namely: Randu wood (Ceiba pentandra), Sengon wood (Paraserianthes falcataria), Coconut wood (Cocos nucifera), Bangkirei wood (Shorea laevis Ridl), Kruing wood (Dipterocarpus) and Meranti wood (Shorea leprosula). Bio-oil products are analyzed for their properties and characteristics, namely the nature of density, acidity, high heat value (HHV), and elements contained in bio-oil such as carbon, nitrogen and sulfur content based on SNI procedures, while bio-oil chemical compositions are investigated using Gas Chromatography Mass Spectroscopy (GC-MS). The maximum yield of bio-oil products occurs at 300°C by 40%. Bio-oil purification by fractional distillation method can produce purity of 16-31% wt. The characterization results of the chemical content of bio-oil showed that bio-oil of methyl formate, 2,6-dimetoxy phenol, 1,2,3 trimethoxy benzene, levoglucosan, 2,4-hexadienedioic acid and 1,2- benzenediol.
Synthesis of Al-Y doped-lithium lanthanum zirconate and the effect of cold isostatic pressure to its electrical properties Fitria Rahmawati; Septia K Arifah; Yuniawan Hidayat
International Journal of Renewable Energy Development Vol 12, No 4 (2023): July 2023
Publisher : Center of Biomass & Renewable Energy, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/ijred.2023.53901

Abstract

This research aims to study the Al-Y dopant to Lithium Lanthanum Zirconate (LLZO) to the characteristics and electrical properties of the LLZO as solid electrolyte. The synthesis was conducted through solid state reaction with Al2O3 and Y2O3 as dopant precursors. X-ray diffraction analysis along with Le Bail refinement was done to understand their structure, and phase content inside. The result found that Al and Y doping increased the cubic phase from 49.58% to 84.91%. The Al-Y doped-LLZO (LLZAYO) powder was then treated by a various cold isostatic pressing, CIP of 0, 20, 30, and 40 MPa to understand the effect of cold isostatic pressure to the ionic conductivity and solid electrolyte performance of the material even without heat sintering treatment. The result found that the green pellet of LLZAYO) which was isostatically pressed by 40 MPa at room temperature provides (9.06 ±0.26) x10-6 Scm-1, about 8 times higher than the LLZO without doping, i.e., (1.25 ±0.01) x 10-6 Scm-1. All solid-state battery with the prepare LLZAYO CIP 40 as solid electrolyte shows reversible reaction of Li/Li+ redox accompanied with Al/Al3+ redox. The Al/Al3+ reaction seems to decrease the electronic resistance between LCO-LLZAYO CIP40-Li which causes the full cell performance to decrease. The initial specific charging capacity is 82 mAh/g, and the initial discharge was 83 mAh/g, confirming 101 % of Coulombic efficiency. The discharge capacity drops to 46 mAh/g at second cycle, leading to a decrease in Coulombic efficiency to 56 %.
Screen printed carbon electrode from coconut shell char for lead ions detection Kinkind Raras Heliani; Fitria Rahmawati; Agung Tri Wijayanta
International Journal of Renewable Energy Development Vol 13, No 1 (2024): January 2024
Publisher : Center of Biomass & Renewable Energy, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/ijred.2024.57679

Abstract

This research aimed to produce a screen-printed carbon electrode (SPCE) from an activated coconut shell carbon. As a raw material, coconut shell char provides renewability and is abundantly available in the market. Meanwhile, SPCE offers a simple electroanalytical electrode because the working, counter, and reference electrodes are in one piece. The coconut shell carbon was activated by steam at 700 oC for 1h, producing AC700 that was then characterized to ensure the result by following per under carbon as the main component, the phases, crystal structure, surface area, morphology, and elemental content. The result showed that the surface area of AC700 is 816 m2/g, and the surface structure is porous, as identified by SEM images. Impedance analysis followed by data fitting and conductivity calculation found a high conductivity of 8.68 x 10-2 Scm‑1. The produced-SPCE or SPAC700 was modified by ferrocene at various compositions of 10%; 20%; and 30% of mass. The SPAC700-Fc30 provided the best performance for lead analysis with a detection limit of 0.35 mM, a quantitation limit of 1.17 mM, and good reproducibility with a Repeatability Coefficient (RC) of 0.022. SPAC700-Fc30 showed good lead ions detection despite under 10% Cu2+ and 10% Co2+ interferences. The result confirmed the potential use of coconut shell char as the raw material for SPCE production.
The Optical Properties and Photo catalytic Activity of ZnS-TiO2/Graphite Under Ultra Violet and Visible Light Radiation Fitria Rahmawati; Rini Wulandari; Irvina M. Murni; Moedjijono Moedjijono
Bulletin of Chemical Reaction Engineering & Catalysis 2015: BCREC Volume 10 Issue 3 Year 2015 (December 2015)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.10.3.8598.294-303

Abstract

This paper discuss research about the optical properties and photo catalytic activity of TiO2 film on graphite substrate and its modification with ZnS. The optical properties investigated are the light response at various light wavelength and the gap energy (Eg). Meanwhile, the photocatalytic activity was studied from isopropanol degradation to determine the Quantum Yield, QY and kinetics of reaction. The results show that the TiO2 layer is consisted of rutile and anatase phases. Meanwhile, the ZnS peaks are at 2θ of 27.91o and 54.58o. The gap energy of TiO2/G consist of two band gap representing the band gap of rutile and anatase. The ZnS deposition shifted the band gap into single gap of 3.40 eV which is in between the gap energy of single TiO2 and single ZnS. The isopropanol degradation with TiO2/G photocatalyst under visible light radiation did not produce any new peaks representing product. Meanwhile, the photocatalytic process under 380 nm light produce new peaks representing the electronic transition of acetone. The isopropanol degradation with ZnS-TiO2/Graphite produced new peaks that indicates the photocataytic activity of ZnS-TiO2/Graphite whether under UV or visible light radiation. The siginificant role of ZnS also proven by the increase of QY values and the increase of rate constant, k. Copyright © 2015 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
The Photocatalytic Activity of SiO2-TiO2/Graphite and Its Composite with Silver and Silver oxide Fitria Rahmawati; Sayekti Wahyuningsih; Dian Irianti
Bulletin of Chemical Reaction Engineering & Catalysis 2014: BCREC Volume 9 Issue 1 Year 2014 (April 2014)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.9.1.5374.45-52

Abstract

This research study the mixed semiconductor of SiO2-TiO2 which was immobilized on graphite substrate and also studies the effect of surface modification on its mixed semiconductor. The surface modification was carried out by electrode position of Ag from 0.4 M of AgNO3 solution at various applied current. The electrode position was conducted for 30 minutes at 0.004; 0.008; 0.010; 0.012 and 0.014 A. In the electrode position cell, SiO2-TiO2/Graphite was used as cathode and a graphite rod was used as anode. The weight of deposited Ag was analyzed gravimetrically. The current efficiency of electrode position was calculated by comparing its experimental weight to its theoretical weight founded from calculation using Faraday’s equation for electrolytic cell. Meanwhile, the photo electrochemical testing was carried out to investigate the efficiency of induced photon to current conversion; it was measured as %IPCE (% Induced Photon to Current Efficiency). The crystallinity and crystal structure of the prepared materials were analyzed by X-ray diffraction and their surface morphology was analyzed by Scanning Electron Microscope (SEM). This research found that silver was deposited as silver metal, Ag and as silver oxide, AgO. The electrode position efficiency at applied current of 0.014 A is 92.30 % with diameter of cluster is 7 - 11.9 mm. It is founded that Ag and AgO deposition enhanced the efficiency of photon conversion into current up to 89.92 %. The optimum %IPCE value is at 28.6 % of Ag content. Ag-SiO2-TiO2/G has higher photo conversion than Ag-TiO2/G, shown by the %IPCE value at 300 nm is 83.25 % higher than Ag-TiO2/G. It indicates the significant role of silica network in photo excitation mechanisms in the composite material. © 2014 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0)
Carbon Waste Powder Prepared from Carbon Rod Waste of Zinc-Carbon Batteries for Methyl Orange Adsorption Fitria Rahmawati; Viona Natalia; Agung T. Wijayanta; Siti Rondiyah; Koji Nakabayashi; Jin Miyawaki
Bulletin of Chemical Reaction Engineering & Catalysis 2020: BCREC Volume 15 Issue 1 Year 2020 (April 2020)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.15.1.5148.66-73

Abstract

A research on the preparation of Carbon Waste Powder, CWP, was conducted and made from carbon rod waste which was extracted from used zinc-carbon batteries. This research was an effort to overcome environmental problem caused by battery waste by converting into adsorbent for methyl orange (MO) that frequently used by textile industries. The prepared powder was then analyzed to understand its characteristic peaks, crystallinity, and to compare the properties with other carbonaceous forms, i.e. a commercial Carbon Paper (CP), and a commercial meso- carbon micro-beads (MCMB). The analysis found that CWP is dominated by graphitic carbon. An adsorption experiment was then conducted to study their adsorption ability to methyl orange solution. The result found that those three carbonaceous materials have the ability to adsorb methyl orange with different activities. MCMB has the highest adsorption capacity of 0.197 mg.g-1. Meanwhile, CWP and CP show adsorption capacity of 0.066 mg.g-1 and 0.062 mg.g-1, respectively. Methyl orange adsorption on CWP and CP were under second order, which means the adsorption could be four times faster as the MO solution doubled. Moreover, the rate constant of MO adsorption on CWP is 8×10-4 min-1, which was higher than the rate constant of MO adsorption on CP. It confirmed that the CWP can be used as a promising adsorbent for dye waste water. Copyright © 2020 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
Co-Authors -, Patiha Abu Masykur Abu Masykur Agung T. Wijayanta Agung Tri Wijayanta AGUS PURWANTO Agustin Widyowati Alaih, Imam Shofid Andini W. Pratiwi Anggia Putri Gustami Arikasuci Fitonna Ridassepri Aryanthi, G. Ayu Aryunani ., Aryunani Aulia, Nabila Putri Bagus Swandito, Paulus Bintang Junita Siagian, Bintang Junita Byba Melda Suhita Chanif Mahdi Chintya Dewi, Chintya Dani G Syarif Dedi Rohendi Dhini A. Phasa Dian Irianti Dian Irianti Dian Maruto Widjonarko Dwi Aman Nur Romadhona Dwi Nugrahaningtyas, Khoirina Dyah Purwaningsih Eddy Heraldy Eddy Heraldy Eddy Heraldy Eddy Heraldy Eddy Heraldy Eddy Heraldy Edi Pramono Fadlulloh, Zaki Firanda Larasati Gesyth Mutiara Hikhmah Al Ichsan Handaka, Muhammad F. A. Heliani, Kinkind Raras I F Nurcahyo I F Nurcahyo, I F I. F. Nurcahyo I.F. Nurcahyo IF Nurcahyo Imam Shofid Alaih Indah Rizki Fitriani, Indah Rizki Irvina M. Murni Irvinna Mutiara Murni Istiqomah, Ana Ulfa Ita Permadani Ivandini Tribidasari Anggraningrum Jin Miyawaki Jun Nakamura Kardi, Soeparman Karima Apriany Khoirina Dwi Nugrahaningtiyas Khoirina Dwi Nugrahaningtyas Khoirina Dwi Nugrahaningtyas Khoirina Dwi Nugrahaningtyas Khoirina Dwi Nugrahaningtyas Khoirina Dwi Nugrahaningtyas Khoirina Nugrahaningtyas Kinkind Raras Heliani Koji Nakabayashi Larasati Larasati Lisa Agustina Nurlaila Mahsus, Mahsus Maisaroh, Ummi Mawasthi, Wanodya Anggit Moedjijono Moedjijono Mohamad Syafri Mudjijono Mudjijono Muhammad A. Munir Muhammad Farhan Muzayanha, Soraya U. Nilasary, Hanida Nugraheni, Putranty Widha Nur Aini NUR FADILAH Nurani Handayani Nurcahyo, I. F. Nurcahyo, I.F. Nursukatmo, Hartoto Oktaviano, Haryo S. Pamularsih A.W Paramartha, I Gusti Ayu Filia Patiha - Pranoto . Puspitasari, Noviana Putri, Denis Octareta Amelia Qurrotul'aini, Nisriina 'Abidah Raihan, Edo Ridwan, Qanita Rini Wulandari Rini Wulandari Rizki Nur Analita Rochmi I. Apriyani, Rochmi I. Rosalin, Azka W Saputri, Dini Deviana Sayekti Wahyuningsih Sayekti Wahyuningsih Sayekti Wahyuningsih Sentot B. Rahardjo, Sentot B. Septia K Arifah Shobikah, Nanik Shota Sato Sidiq Fathonah Siti Rondiyah Sofia, Iva Suciana Nur Cahyaningsih Syafira Nur Zalfa Syoni Soepriyanto Syulfi Faiz Taufiiq-Yap Yun Hin Trianingsih Eni Lestari Viona Natalia Viona Natalia W.W, Soegimin Wanodya Anggit Mawasthi Widiasih Wijayanta, Agung Tri Witri Wahyu Lestari Wulan Cahya Inayah Yuni, Prima Novia Yuniawan Hidayat Yuniawan Hidayat Yuniawan Hidayat Yuniawan Hidayat Yuniawan Hidayat Yuniawan Hidayat Zalfa, Syafira Nur