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INDONESIA
Indonesian Journal of Chemistry
ISSN : 14119420     EISSN : 24601578     DOI : -
Indonesian Journal of Chemistry is an International, peer-reviewed, open access journal that publishes original research articles, review articles, as well as short communication in all areas of chemistry including applied chemistry. The journal is accredited by The Ministry of Research, Technology and Higher Education (RISTEKDIKTI) No : 21/E/KPT/2018 (in First Rank) and indexed in Scopus since 2012. Since 2018 (Volume 18), Indonesian Journal of Chemistry publish four issues (numbers) annually (February, May, August and November).
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Articles 25 Documents
Search results for , issue "Vol 25, No 5 (2025)" : 25 Documents clear
Accelerated Biodegradation of Waste Polyethylene Terephthalate (PET) Fiber by Recombinant Hydrophobin HGFI Fused with Ideonella sakaiensis PETase Puspitasari, Nathania; Liu, Chia Tzu; Lee, Cheng Kang
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.93092

Abstract

Nowadays, an efficient and environmentally friendly polyethylene terephthalate (PET) recycling method has gained greater attention, enabling a circular economy for polyesters. Since PET is a hydrophobic polymer, the enzyme's binding affinity to PET becomes a significant issue. Herein, the first strategy is introduced to enhance PET fiber hydrolysis by genetically fusing hydrolyzing enzymes such as cutinase and PETase to protein hydrophobin HGFI. HGFI, a surface-active protein from Grifola frondosa, was used to improve the rate of enzyme hydrolysis. Furthermore, cellulose binding domains (CBD) were employed as a solubility enhancer tag of PETase fusion due to the insoluble characteristics of HGFI and PETase. The fusion proteins (CBD-HGFI-PETase and HGFI-Cut_2) were constructed with a flexible linker, expressed in Escherichia coli, and then purified by chromatography. PETase fusion exhibited 2.5-fold higher concentrations of monomer products released than that of cutinase fusion after 5 days of hydrolysis. According to the results, the fusion of HGFI to PETase showed excellent performance for enhancing the binding affinity of the enzyme on PET fiber substrate due to the increasing number of self-assembled hydrophobin interactions that modified the PET surface to be more hydrophilic. Therefore, this study indicates that the construction of CBD-HGFI-PETase enzyme fusion could be used as a novel method for efficiently accelerating PET biodegradation.
Sustainable Synthesis of Bacterial Cellulose Nanocrystals from Glucomannan-Based Bacterial Cellulose Widjaja, Tri; Nurkhamidah, Siti; Ni’mah, Hikmatun; Wardhono, Endarto Yudo; Rohmah, Aisyah Alifatul Zahidah; Tirta, Anggi; Nailah, Rossesari; Sari, Citra Yulia
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.99360

Abstract

Bacterial cellulose (BC), derived from glucose fermentation, is a renewable material known for its abundant availability, quick production, cost-effectiveness, and eco-friendly characteristics. This study focuses on converting BC into BC nanocrystals (BCNC) via fermentation, hydrolysis using acid solutions, and ultrasonication. Glucomannan flour with concentrations of 50, 60, and 90% was fermented using Acetobacter xylinum for 10 days at pH 5 to produce BC. The BC was then hydrolyzed with HCl solutions at 1, 2, 3, 4, and 5 M concentrations, followed by sonication. The 90% glucomannan flour yielded the highest BC amount (22.61 g). BCNC hydrolyzed with 1 M HCl exhibited the highest crystallinity (86%) and an elongated rod-like morphology. In contrast, hydrolysis with 4 and 5 M HCl caused carbonization, reducing crystallinity to below 30%. Particle size analysis showed the largest particle size for BCNC-2 (549.4 nm) and the smallest for BCNC-5 (207.2 nm). This research highlights the potential of glucomannan as a resource to produce BCNC for sustainable materials for various applications.
Synthesis of Two Analogues of Xylapeptide A and Their Potency as New Antimicrobial Agent Maharani, Rani; Muchlis, Handi Nugraha; Hidayat, Ace Tatang; Al-Anshori, Jamaludin; Nurlelasari, Nurlelasari; Harneti, Desi; Mayanti, Tri; Farabi, Kindi; Supratman, Unang
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.100353

Abstract

Xylapeptide A, derived from the fungus Xylaria sp. x Sophora tonkinensis, exhibits potent and selective antimicrobial properties. Our research group has successfully synthesized xylapeptide A. In our recent work, two xylapeptide A analogues (An1 and An2) were synthesized using a combination of solid- and solution-phase synthesis methods. The linear precursors of An1 and An2 were synthesized on 2-CTC resin with the Fmoc strategy. The coupling reagents HBTU/HOBt and HATU/HOAt were employed. Subsequently, the linear precursor was cleaved from the resin using either 20% TFA or a TFE mixture, and then cyclized in solution phase with HBTU. The synthesized products were purified using semi-preparative RP-HPLC, giving the percent yields 16% for An1 and 12% for An2. Both compounds were then characterized by HR-ToF-MS, 1H- and 13C-NMR. The synthesized xylapeptide A and its analogues were evaluated against Bacillus cereus, Bacillus subtilis, Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Klebsiella pneumoniae, and Candida albicans. The result showed that An2, possessing arginine residue, exhibited higher activity compared to xylapeptide A and An1. This research suggests that xylapeptide A analogues hold great promise as novel antimicrobial agents.
Synthesis of Titanium Dioxide Nanoparticles for Removal of Pb2+, Cd2+ and Cr3+ from Wastewater Mansoor, Hadeel Salah; Salman, Taghried Ali; Dhahir, Saadiyah Ahmed
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.102753

Abstract

Water pollution is widely regarded as one of the most pressing global challenges, exacerbated by human progress in industrial, agricultural, and technological sectors. Wastewater often contains non-biodegradable heavy metals that accumulate in living organisms. This accumulation poses significant risks to both environmental ecosystems and human health. The structures and surface morphology were characterized by FTIR, UV-vis measurements, XRD, SEM, and AFM. TiO2 nanoparticles could remove heavy metal ions (Pb2+, Cd2+, and Cr3+) from two samples (laboratory samples and real samples from Babylon battery factory in Al-Waziriya, Baghdad/Iraq) and measured by AAS. The results indicated that the removal percentages of heavy metal ions by TiO2 nanoparticles from real sample ions were 91.32, 64.28 and 58.33% for Pb2+, Cd2+, and Cr3+, respectively. The optimum conditions for removal were 0.1 g of TiO2 nanoparticles, 10 ppm concentration of the pollutant ions, 75 min stirring time, a 100-rpm stirring rate, and a pH level of 7. The kinetic data were related to the pseudo-second-order (R2 = 0.9455), and the isotherm models were related to the Langmuir equation (R2 = 0.9769).
Modification of Chitosan using Fe3O4 and Glucose and Its Application for Phenol Removal Rizki, Widya Twiny; Lestari, Siti Marwah; Rahmah, Vindi Annisa; Dauli, Rd Rahmat
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.103140

Abstract

In this study, chitosan was modified with Fe3O4 and glucose to enhance its capacity and effectiveness in adsorbing phenol from organic waste. XRD analysis revealed distinct differences between unmodified chitosan and the Fe3O4/glucose-modified version, with the resulting nanocomposite showing a particle size of 17.21 nm. FTIR spectra exhibited new, sharper peaks at 531 and 544 cm−1, indicating interactions between chitosan and Fe3O4 via the nitrogen atom in the NH2 group. VSM characterization showed a saturation magnetization of 63.4 emu/g, confirming that the chitosan/Fe3O4/glucose nanocomposite is superparamagnetic. SEM analysis revealed an uneven, porous surface, while the morphology displayed dark Fe3O4 spots dispersed across a lighter chitosan matrix. The optimal adsorption condition was achieved at a contact time of 60 min, with an adsorption efficiency of 16.46%. In addition to reducing phenol content in wastewater, the modified nanocomposite also exhibited antibacterial activity against Staphylococcus aureus and Escherichia coli. This multifunctional material offers a promising solution for wastewater treatment, targeting both organic pollutants and pathogenic bacteria to help address water pollution challenges.
Innovative High-Speed Homogenizer Approach for Synthesizing PVDF-GO Membranes from Recycled Battery Graphite Febriasari, Arifina; Ferdiansyah, Ferry; Salsabila, Shafa Marwa; Ridwan, Muhammad; Mahardika, Muhammad Bagas Adhistya; Hilyati, Hilyati; Sudjarwo, Wisnu Arfian Anditya; Arlofa, Nina; Supriyadi, Supriyadi; Toca-Herrera, Jose Luis; Kartohardjono, Sutrasno
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.103909

Abstract

Effective waste management is essential for achieving a zero-waste environment, particularly in handling hazardous domestic waste like used dry cell batteries. This study explores a sustainable approach by recovering graphite from battery waste to synthesize graphene oxide (GO) for enhancing poly-vinylidene fluoride (PVDF) membranes. GO was synthesized using the Hummers method and a modified high-speed homogenization approach, then characterized via Raman spectroscopy and X-ray diffraction (XRD). The fabricated PVDF-GO membranes were further analyzed using SEM-EDS, AFM, water contact angle measurements, and bacterial rejection tests. Results confirmed successful GO synthesis and integration into the polymer matrix. GO incorporation improved hydrophilicity, reducing the water contact angle from 120° (pure PVDF) to 66° and 56° in PVDF/PVP-GO membranes via high-speed homogenization and conventional methods, respectively. The modified membranes exhibited a 5–6 times larger pore size than pure PVDF and achieved nearly 100% bacterial rejection. Additionally, PVDF/PVP-GO(h) showed a 91.76% faster production time efficiency than PVDF/PVP-GO(s).
Toxicity and α-Amylase Inhibitory Potential of Tagetes erecta Leaf Extract: In Vitro and In Silico Approaches Rasyid, Herlina; Soekamto, Nunuk Hariani; Musa, Bulkis; Siswanto, Siswanto; Labanni, Arniati; Suma, Artania Adnin Tri; Syahrir, Nur Hilal A; Bahrun, Bahrun; Badrawati, Kadek Susi; Yusuf, Mohammad Taufik
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.104489

Abstract

Tagetes erecta is one of traditional herbs with a variety of pharmacological actions. This study attempted to assess the toxicity and antidiabetic activity of T. erecta leaf extract. The extraction was carried out by maceration, then continued with phytochemical analysis. Toxicity of the extract was conducted using the brine shrimp lethality test. The antidiabetic activity was evaluated by α-amylase inhibitory using the 3,5-dinitrosalicylic acid method. The phytochemical of the most active extract was identified using GC-MS and subjected to bind the α-amylase (PDB ID: 2QV4) employing molecular docking. The LC50 values of n-hexane, EtOAc, and MeOH extracts were 33.41, 14.00, and 35.03 ppm, respectively, indicating high toxicity. The antidiabetic activity showed that EtOAc extract has the lowest IC50 value (1053.95 mg/L). Molecular docking analysis revealed the compounds 1–5 has range of binding energy at −4.07 to −4.83 kcal/mol. Acarbose as a positive control showed the lower binding energy at −5.03 kcal/mol, indicated more effective α-amylase inhibitory. This study revealed that T. erecta leaf extract has significant cytotoxic potential, which may warrant further exploration for anticancer applications. However, the relatively weak α-amylase inhibitory and lower binding affinity compared to acarbose imply limited utility as an antidiabetic agent.
Photocatalytic Deactivation of E. coli Bacteria by Copper(II) Oxide Doped-Titanium Dioxide Nanocomposite in Water Catchment Systems Kustomo, Kustomo; Wu, Xiaoli
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.104537

Abstract

This study investigates the synthesis and evaluation of CuO-doped TiO2 nanocomposites for photocatalytic deactivation of Escherichia coli in the water catchment systems. Nanocomposites with varying CuO concentrations (0.25, 0.50, and 0.85% w/w) doped into TiO2 were prepared via the co-precipitation method and characterized by FTIR, SEM-EDS, and UV-vis DRS. The incorporation of CuO into TiO2 resulted in a progressive reduction of band gap energy, with the 0.85% CuO-TiO2 sample exhibiting the lowest value. Photocatalytic testing demonstrated that the 0.85% CuO-TiO2 nanocomposite achieved a 99.23% reduction of E. coli, surpassing the performance of undoped TiO2. The enhanced activity is attributed to improved visible light absorption and more efficient charge separation due to the synergistic effect between CuO and TiO2. These results indicate that optimizing CuO doping in TiO2 nanocomposites can significantly enhance photocatalytic disinfection, offering a promising solution for water treatment applications.
Synthesis, Characterization, and Optical Properties Study of Poly(o-aminophenol)/MWCNT Composite Hussein, Hajar Ali; Mohammed, Mohammed Qasim; Al-Saymari, Furat Ahmed
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.104558

Abstract

In this paper, a functionalized multi-walled carbon nanotube (MWCNT) was prepared to be more active. Poly(o-aminophenol) was attached to MWCNT to create POAP:MWCNT nanocomposites using chemical polymerization. The polymerization process occurred in the acidic medium of hydrochloric acid and ammonium persulfate ((NH4)2S2O8) as an oxidizing reagent. The product nanocomposites were characterized via FTIR, XRD, SEM, and TGA. The effects of the addition on the structure, morphology, thermal, electrical, and optical properties of POAP and POAP:MWCNT were investigated. FTIR spectra revealed that carboxylic acid groups formed at the MWCNTs and the nanocomposite. As TGA confirmed, insertions of MWCNT within the polymer matrix led to apparent thermal amelioration. Furthermore, XRD spectra displayed the crystalline nature of POAP and nanocomposite materials. The SEM images of POAP:MWCNT show that the MWCNTs are dispersed within the structure of polymer chains, proving that the POAP:MWCNT composite was successfully prepared. The findings revealed that the electrical conductivity of poly(o-aminophenol) composite thin film was significantly enhanced by about 20000× due to doping by 1 wt.% MWCNT.
Temperature-Programmed Desorption of H2 from Mg-Ni/C for Hydrogen Storage Application Rudypratama, Billy; Nurfitrah, Aditya Eka; Ismoyojati, Rizki; Priyono, Bambang
Indonesian Journal of Chemistry Vol 25, No 5 (2025)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.104644

Abstract

Hydrogen is a flexible energy carrier with the potential to replace fossil fuels as a clean and renewable energy source. However, efficient storage systems under ambient conditions are essential for practical applications. This study investigates magnesium–nickel-based metal hydrides for hydrogen storage, enhanced with 20% graphite or additional nickel. The synthesized samples—MgNi2, MgNi2 + graphite 20%, Mg2Ni + graphite 20%, and Mg2Ni + Ni 1:1—were characterized using XRD, BET, SEM-EDX, and hydrogen temperature-programmed desorption (TPD). Crystallite sizes were found to be 132.125, 137.125, 77.168, and 92.335 nm, respectively. BET analysis revealed surface areas of 2.144, 1.664, 7.113, and 2.308 m2/g, corresponding pore volumes of 0.0038, 0.0031, 0.0137, and 0.0100 cm3/g. TPD results showed that Mg2Ni + graphite 20% had the fastest desorption rate (46 min), consistent with its highest surface area and pore volume. This sample also achieved the highest hydrogen adsorption capacity at 0.0615 mmol/g. These findings demonstrate that Mg-Ni hydrides, especially those modified with graphite, offer promising performance for hydrogen storage applications, particularly in systems requiring rapid desorption and efficient kinetics, such as fuel-cell electric vehicles. The results highlight the potential of tailored Mg-Ni composites for advanced hydrogen storage solutions.

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