cover
Article Per Year (5 Year)
All
Home Page
OAI Link
Editorial Team
Contact
Reviewer
Google Scholar
Contact Name
Adi Darmawan
Contact Email
adidarmawan@live.undip.ac.id
Phone
-
Journal Mail Official
jksa@live.undip.ac.id
Editorial Address
-
Location
Kota semarang,
Jawa tengah
INDONESIA
JURNAL KIMIA SAINS DAN APLIKASI
Published by Universitas Diponegoro
ISSN : 14108917     EISSN : 25979914     DOI : -
Core Subject : Science, Engineering,
Chemical Engineering, Chemistry & Bioengineering Chemistry Engineering
urnal Kimia Sains dan Aplikasi (p-ISSN: 1410-8917) and e-ISSN: 2597-9914) is published by Department of Chemistry, Diponegoro University. This journal is published four times per year and publishes research, review and short communication in field of Chemistry.
Arjuna Subject : -
Articles 5 Documents
 1 
Search results for , issue "Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022" : 5 Documents clear
Synthesis of Magnetic Chitosan Composite Beads as an Adsorbent for Removal of Organic Matter from Peat Water Uul Warosatul Ambiya; Nurlina Nurlina; Gusrizal Gusrizal
Jurnal Kimia Sains dan Aplikasi Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.25.9.338-345

Abstract

Groundwater in peatlands has the potential to be utilized as a water source, but its high organic matter content presents challenges. This study aimed to improve the quality of peat water through the adsorption of organic matter using chitosan magnetic beads composite adsorbent. Magnetic chitosan beads (KMB) composite was synthesized by mixing chitosan, acetic acid, and a mixture of Fe2+/Fe3+ solution with a mole ratio of 1:2. This mixture was then dropped into a sodium hydroxide solution. In addition to KMB, magnetic composite beads containing glutaraldehyde crosslinking agent (KMBG) were also synthesized. The results of composites analysis using a Fourier transform infrared (FTIR) spectrophotometer showed typical Fe-O absorption bands at 582 cm-1 and 578 cm-1 for KMB and KMBG. The typical C=N absorption band for glutaraldehyde in KMBG appeared at 1631 cm-1. X-ray diffraction (XRD) analysis revealed the characteristic peaks of Fe3O4 for KMB and KMBG at 2θ = 30.2°, 35.5°, 43.2°, 57.0°, and 62.8° with an amorphous structure. The adsorption of organic matter was performed by varying the pH (2, 3, 4, and 5) of peat water and the mass of the adsorbent (50, 70, 100, 200, and 300 mg). The optimum adsorption occurred at pH 2 with an absorbent mass of 0.1 g KMB and 0.07 g KMBG. Applying KMB on peat water reduces turbidity, color, and absorbance at a wavelength of 254 nm (Aλ=254), which is better than using KMBG. These three parameters’ efficiency percentages were 44%, 78%, and 74% for KMB and 17%, 30%, and 59% for KMBG.
Fabrication of Cellulose Nanocrystal (CNCs) Based Biosorbent From Oil Palm Trunks Through Acid Hydrolysis With Sonication Assisted and Adsorption Kinetic Study Pra Cipta Buana Wahyu Mustika; Mega Mustikaningrum
Jurnal Kimia Sains dan Aplikasi Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.25.9.307-315

Abstract

Developing cellulose nanocrystal (CNCs) preparation techniques is a challenge confronted by many researchers. The advantages of property remain the reason for research to be developed. To deal with this issue, it is essential to conduct research related to process optimization, particularly in the hydrolysis process, which is the primary step in forming CNCs. In this study, the effect of sonication-assisted hydrolysis time was investigated. XRD characterization showed that the CNCs formed where the first group with specific peaks indicated. The crystallinity of CNCs decreased with increasing sonication duration, indicating that sonication-assisted hydrolysis was nonselective. The crystallinity of CNCs obtained for 15, 30, and 45 min was 61.6, 55.0, and 48.4 %, respectively. For sonication duration variations of 15, 30, and 45 min, the hydration diameter of CNCs was nearly identical at 42.35 ± 27.10, 42.99 ± 29.46, and 42.63 ± 29.49 nm, respectively. Similarly, the removal of methylene blue can be achieved using CNCs bio-adsorbent. The results of percent removal of methylene blue under sonication treatment of 15, 30, and 45 min of sonication were 73.34; 73.62; 72.86 %, respectively. The adsorption rate of CNCs follows the pseudo-second-order kinetic model, with the adsorption values under sonication treatment of 15, 30, and 45 min were 0.075 ± 0.008; 0.166 ± 0.013; 0.078 ± 0.005 g mg-1 min-1, respectively.
Synthesis of Cardanol-Based Acetaldehyde Novolac Resin from Cashew Nut Shell Liquid (CNSL) Surya Dewi Marliyana; Sayekti Wahyuningsih; Nisa Nur Hayati
Jurnal Kimia Sains dan Aplikasi Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.25.9.316-321

Abstract

Polymers are currently in the limelight. Phenolic resin is one of the polymer products obtained from the polymerization process, either from natural or synthetic sources. One of the natural compounds that can be applied to polymers is cardanol. This study aimed to synthesize cardanol-based acetaldehyde novolac resin from Cashew Nut Shell Liquid (CNSL). Isolation of cardanol from CNSL was done by liquid-liquid extraction method with acetone and purified by gravity column chromatography in a mixture of n-hexane and ethyl acetate in a ratio of 9:1. HPLC analysis showed that cardanol compounds had aliphatic chains with different levels of saturation and the yield was 18.48%. The cardanol-acetaldehyde novolac resin was synthesized through a condensation polymerization reaction with a cardanol-acetaldehyde mole ratio (1:0.5), using HCl as a catalyst. FTIR and 1H-NMR analysis were employed to identify the novolac resin structure. The product was a brownish-orange solid with a yield of 12.80 mg (40%) and followed ortho-ortho substitution. Cardanol is one of the natural phenol sources that might be utilized to manufacture novolac resins.
Enhanced SOFC Cathode Performance Through Surface Modification of NdBa0.5Sr0.5Co2O5+δ Nanoparticles Adi Subardi
Jurnal Kimia Sains dan Aplikasi Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.25.9.322-328

Abstract

The cathode materials fabrication with outstanding performance and stability at intermediate temperatures of 600–800℃ is required for the prospective mass production of solid oxide fuel cells (SOFCs). Infiltration is a potential method because it has proven successful in fabrication and cell performance enhancement. This study mainly focuses on the electrical conductivity and long-term reliability of cathode symmetric cells NdBa0.5Sr0.5Co2O5+δ (NBSC) fabricated by traditional solid-state reaction techniques. The electrical conductivity value of the cathode is in the range of 174–278 S.cm-1. Impedance analysis showed that the infiltration of 0.5M SDC on the NBSC cathode surface dramatically reduced the polarization resistance (Rp) between layers (cathode-electrolyte) from 3.32 Ω.cm2 to 1.82 Ω.cm2 at 600℃ or decreased by 45 % compared to NBSC cathode without 0.5M SDC infiltration. The enhanced stability of NBSC cathode specimens with 0.5M SDC infiltration (NBSC+0.5 M SDC) under SOFC operating conditions proves that samples with infiltration extend their lifetime. Compared to the NBSC cathode, the NBSC+0.5 M SDC cathode has better long-term stability with a lower RP value of 2.35 Ω.cm2. In the OPP range of 0.214-0.0027 atm at 800℃, the relatively tiny Rp value of the symmetrical cell is between 0.030 Ω.cm2 and 0.039 Ω.cm2, below the 0.15 Ω.cm2 suitable performance limit for solid oxide fuel cells.
Preparation of Biosorbent from Kapok Fruit Peel (Ceiba pentandra) for Adsorption of Lead Waste Eddy Heraldy; Novia Purnamawati; Yuniawan Hidayat; Khoirina Dwi Noegrahaningtyas; Idul Fitri Nurcahyo
Jurnal Kimia Sains dan Aplikasi Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.25.9.329-337

Abstract

The preparation of biosorbent from kapok fruit peel (KBK) for lead (Pb(II)) removal was conducted mechanically by expanding the surface of the biosorbent and activating KBK with the addition of 1 M HCl for 20 minutes. The effect of activation on increasing the number of active groups and the number of pores in the biosorbent was proven by Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). The FTIR data showed a shift and an increase in wavenumber intensities of active adsorbent groups such as -OH and -C=O. The SEM data revealed that the morphology of the adsorbent increased in the number of pores that appeared rough and irregular. The Pb(II) adsorption treatment used a batch method at pH 2–5, contact time of 0–120 minutes, and adsorbate concentration of 10–50 ppm. The adsorption of Pb(II) ions reached optimum conditions at pH 4 and a contact time of 60 minutes, with an adsorption capacity of 6.9522 mg/g and an adsorption rate of 98.71%. Adsorption data showed that Pb(II) ions uptake to KBK biosorbent followed the Langmuir isotherm model equation and pseudo-second-order kinetic model. The adsorption capacity of activated KBK is greater than that of non-activated KBK.

Page 1 of 1 | Total Record : 5

 1 

Filter by Year

2022 2022


Reset
Filter By Issues
All Issue Vol 27, No 4 (2024): Volume 27 Issue 4 Year 2024 Vol 27, No 3 (2024): Volume 27 Issue 3 Year 2024 Vol 27, No 2 (2024): Volume 27 Issue 2 Year 2024 Vol 27, No 1 (2024): Volume 27 Issue 1 Year 2024 Vol 26, No 12 (2023): Volume 26 Issue 12 Year 2023 Vol 26, No 11 (2023): Volume 26 Issue 11 Year 2023 Vol 26, No 10 (2023): Volume 26 Issue 10 Year 2023 Vol 26, No 9 (2023): Volume 26 Issue 9 Year 2023 Vol 26, No 8 (2023): Volume 26 Issue 8 Year 2023 Vol 26, No 7 (2023): Volume 26 Issue 7 Year 2023 Vol 26, No 6 (2023): Volume 26 Issue 6 Year 2023 Vol 26, No 5 (2023): Volume 26 Issue 5 Year 2023 Vol 26, No 4 (2023): Volume 26 Issue 4 Year 2023 Vol 26, No 3 (2023): Volume 26 Issue 3 Year 2023 Vol 26, No 2 (2023): Volume 26 Issue 2 Year 2023 Vol 26, No 1 (2023): Volume 26 Issue 1 Year 2023 Vol 25, No 12 (2022): Volume 25 Issue 12 Year 2022 Vol 25, No 11 (2022): Volume 25 Issue 11 Year 2022 Vol 25, No 10 (2022): Volume 25 Issue 10 Year 2022 Vol 25, No 9 (2022): Volume 25 Issue 9 Year 2022 Vol 25, No 8 (2022): Volume 25 Issue 8 Year 2022 Vol 25, No 7 (2022): Volume 25 Issue 7 Year 2022 Vol 25, No 6 (2022): Volume 25 Issue 6 Year 2022 Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022 Vol 25, No 4 (2022): Volume 25 Issue 4 Year 2022 Vol 25, No 3 (2022): Volume 25 Issue 3 Year 2022 Vol 25, No 2 (2022): Volume 25 Issue 2 Year 2022 Vol 25, No 1 (2022): Volume 25 Issue 1 Year 2022 Vol 24, No 7 (2021): Volume 24 Issue 7 Year 2021 Vol 24, No 6 (2021): Volume 24 Issue 6 Year 2021 Vol 24, No 5 (2021): Volume 24 Issue 5 Year 2021 Vol 24, No 4 (2021): Volume 24 Issue 4 Year 2021 Vol 24, No 3 (2021): Volume 24 Issue 3 Year 2021 Vol 24, No 2 (2021): Volume 24 Issue 2 Year 2021 Vol 24, No 1 (2021): Volume 24 Issue 1 Year 2021 Vol 23, No 12 (2020): Volume 23 Issue 12 Year 2020 Vol 23, No 11 (2020): Volume 23 Issue 11 Year 2020 Vol 23, No 10 (2020): Volume 23 Issue 10 Year 2020 Vol 23, No 9 (2020): Volume 23 Issue 9 Year 2020 Vol 23, No 8 (2020): Volume 23 Issue 8 Year 2020 Vol 23, No 7 (2020): Volume 23 Issue 7 Year 2020 Vol 23, No 6 (2020): Volume 23 Issue 6 Year 2020 Vol 23, No 5 (2020): Volume 23 Issue 5 Year 2020 Vol 23, No 4 (2020): Volume 23 Issue 4 Year 2020 Vol 23, No 3 (2020): Volume 23 Issue 3 Year 2020 Vol 23, No 2 (2020): Volume 23 Issue 2 Year 2020 Vol 23, No 1 (2020): Volume 23 Issue 1 Year 2020 Vol 22, No 6 (2019): Volume 22 Issue 6 Year 2019 Vol 22, No 5 (2019): Volume 22 Issue 5 Year 2019 Vol 22, No 4 (2019): Volume 22 Issue 4 Year 2019 Vol 22, No 3 (2019): Volume 22 Issue 3 Year 2019 Vol 22, No 2 (2019): Volume 22 Issue 2 Year 2019 Vol 22, No 1 (2019): volume 22 Issue 1 Year 2019 Vol 21, No 4 (2018): volume 21 Issue 4 Year 2018 Vol 21, No 3 (2018): Volume 21 Issue 3 Year 2018 Vol 21, No 2 (2018): Volume 21 Issue 2 Year 2018 Vol 21, No 1 (2018): Volume 21 Issue 1 Year 2018 Vol 20, No 3 (2017): Volume 20 Issue 3 Year 2017 Vol 20, No 2 (2017): Volume 20 Issue 2 Year 2017 Vol 20, No 1 (2017): Volume 20 Issue 1 Year 2017 Vol 19, No 3 (2016): Volume 19 Issue 3 Year 2016 Vol 19, No 2 (2016): Volume 19 Issue 2 Year 2016 Vol 19, No 1 (2016): Volume 19 Issue 1 Year 2016 Vol 18, No 3 (2015): Volume 18 Issue 3 Year 2015 Vol 18, No 2 (2015): Volume 18 Issue 2 Year 2015 Vol 18, No 1 (2015): Volume 18 Issue 1 Year 2015 Vol 17, No 3 (2014): Volume 17 Issue 3 Year 2014 Vol 17, No 2 (2014): Volume 17 Issue 2 Year 2014 Vol 17, No 1 (2014): Volume 17 Issue 1 Year 2014 Vol 16, No 3 (2013): Volume 16 Issue 3 Year 2013 Vol 16, No 2 (2013): Volume 16 Issue 2 Year 2013 Vol 16, No 1 (2013): Volume 16 Issue 1 Year 2013 Vol 15, No 3 (2012): Volume 15 Issue 3 Year 2012 Vol 15, No 2 (2012): Volume 15 Issue 2 Year 2012 Vol 15, No 1 (2012): Volume 15 Issue 1 Year 2012 Vol 14, No 3 (2011): Volume 14 Issue 3 Year 2011 Vol 14, No 2 (2011): Volume 14 Issue 2 Year 2011 Vol 14, No 1 (2011): Volume 14 issue 1 Year 2011 Vol 13, No 3 (2010): Volume 13 Issue 3 Year 2010 Vol 13, No 2 (2010): Volume 13 Issue 2 Year 2010 Vol 13, No 1 (2010): Volume 13 Issue 1 Year 2010 Vol 12, No 3 (2009): Volume 12 Issue 3 Year 2009 Vol 12, No 2 (2009): Volume 12 Issue 2 Year 2009 Vol 12, No 1 (2009): Volume 12 Issue 1 Year 2009 Vol 11, No 3 (2008): Volume 11 Issue 3 Year 2008 Vol 11, No 2 (2008): Volume 11 Issue 2 Year 2008 Vol 11, No 1 (2008): Volume 11 Issue 1 Year 2008 Vol 10, No 3 (2007): Volume 10 Issue 3 Year 2007 Vol 10, No 2 (2007): Volume 10 Issue 2 Year 2007 Vol 10, No 1 (2007): Volume 10 Issue 1 Year 2007 Vol 9, No 3 (2006): Volume 9 Issue 3 Year 2006 Vol 9, No 2 (2006): Volume 9 Issue 2 Year 2006 Vol 9, No 1 (2006): Volume 9 Issue 1 Year 2006 Vol 8, No 3 (2005): Volume 8 Issue 3 Year 2005 Vol 8, No 2 (2005): Volume 8 Issue 2 Year 2005 Vol 8, No 1 (2005): Volume 8 Issue 1 Year 2005 Vol 7, No 3 (2004): Volume 7 Issue 3 Year 2004 Vol 7, No 2 (2004): Volume 7 Issue 2 Year 2004 Vol 7, No 1 (2004): Volume 7 Issue 1 Year 2004 Vol 6, No 3 (2003): Volume 6 Issue 3 Year 2003 Vol 6, No 2 (2003): Volume 6 Issue 2 Year 2003 Vol 6, No 1 (2003): Volume 6 Issue 1 Year 2003 Vol 5, No 3 (2002): Volume 5 Issue 3 Year 2002 Vol 5, No 2 (2002): Volume 5 Issue 2 Year 2002 Vol 5, No 1 (2002): Volume 5 Issue 1 Year 2002 Vol 3, No 3 (2000): Volume 3 Issue 3 Year 2000 Vol 3, No 2 (2000): Volume 3 Issue 2 Year 2000 Vol 3, No 1 (2000): Volume 3 Issue 1 Year 2000 Vol 2, No 4 (1999): Volume 2 Issue 4 Year 1999 Vol 2, No 3 (1999): Volume 2 Issue 3 Year 1999 Vol 2, No 2 (1999): Volume 2 Issue 2 Year 1999 Vol 2, No 1 (1999): Volume 2 Issue 1 Year 1999 Vol 1, No 1 (1998): Volume 1 Issue 1 Year 1998 More Issue