cover
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 : -
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 796 Documents
Textile Wastewater Treatment Using Polypyrrole/Polyphenol Oxidase Membranes Anceu Murniati; Nadia Annisa Fajriana; Gilang Adi Nugraha; Restu Muchammad Ibrahim; Arie Hardian; Buchari Buchari; Suryo Gandasasmita; Zeily Nurachman
Jurnal Kimia Sains dan Aplikasi Vol 27, No 2 (2024): Volume 27 Issue 2 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.2.83-90

Abstract

Polypyrrole (PPy) is widely regarded as a useful electrode material because it has the advantages of low cost, high electrical conductivity, and thermal stability. This study aimed to synthesize PPy membranes using polyphenol oxidase (PPO) isolated from white oyster mushrooms as a biocatalyst for processing textile wastewater. The membranes were produced through the electropolymerization of pyrrole (Py) using the electrodeposition method. The raw materials comprised 0.05 M Py and crude PPO white oyster mushroom extract at 35% v/v in citrate buffer pH = 6.8. The electrolysis process was performed at 6.00 V and 1.063–1.142 A using 16.57-48.97% immobilized PPO in PPy, PPO activity of 1.640–4.160 U, and 0.35 mM phenol as a substrate. The results showed that the use of the membrane in textile wastewater with a discontinuous flow caused a decrease of pH by 14.86%, phenol by 6.80%, Chemical Oxygen Demand (COD) by 81.30%, Biological Oxygen Demand (BOD) by 78.25%, and Total Suspended Solids (TSS) by 20.65%. Meanwhile, using the sample with a continuous flow caused a decrease of pH by 23.97%, phenol by 26.09%, COD by 88.50%, BOD by 78.00%, and TSS by 65.70%. The physical performance of membrane application to textile wastewater with discontinuous (flow rate = 48.19–51.50 L/h, flux = 3191.6–3387.5 L.m-2.h-1, and permeability = 319.2–338.7 Lm-2.h-1.bar) and continuous flow (flow rate = 48.19 L/h, flux = 3191.6 Lm-2.h-1, and permeability = 319.2 Lm-2.h-1.bar) was also assessed in this study. The Scanning Electron Microscopy (SEM) image was used to assess the morphology of the membrane before and after its application.
Effects of Temperature, Molecular Weight, and Non-Solvent Variation on the Physical Properties of PVDF Membranes Prepared through Immersion Precipitation Resa Wulandari; Edi Pramono; Sun Theo Constan Lotebulo Ndruru; Abu Masykur; Sayekti Wahyuningsih; Aditya Muhammad Fadhilah; Ellya Syaharani; Elva Yoga Saputra; Mayzy Vanesia Insani
Jurnal Kimia Sains dan Aplikasi Vol 27, No 1 (2024): Volume 27 Issue 1 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.1.35-44

Abstract

Research on porous membrane technology is proliferating, especially in the process of fabrication of membranes. Different methods in membrane fabrication can affect the physical and chemical properties of the produced membrane. This study aims to investigate the influence of temperature, molecular weight, and non-solvent type on the physical-chemical properties of PVDF membranes. The membrane was produced by the immersion precipitation method with varying PVDF molecular weights of 64 kDa, 352 kDa (Solef 1010), 534 kDa, and 573 kDa (Solef 1015); non-solvent variations of alcohol (methanol, ethanol, isopropyl alcohol, and butanol); and drying temperature variations of 40, 50, and 60°C. The produced membranes were analyzed using ATR-FTIR, XRD, TGA, DSC, and SEM, and their wettability properties were evaluated using water contact angles. The optimal drying temperature for membrane production was 60°C. The ATR-FTIR data showed that molecular weight impacted membrane structure, where PVDF MW 534 kDa membrane had the highest percentage of β phase (77.47%). Non-solvent changes also affected membrane structure; PVDF Solef 1010 with non-solvent isopropyl alcohol had the highest percentage of β phase (67.45%). This is supported by the XRD diffractogram that displayed peaks at 2θ values between 20.24° and 20.66°, indicating the presence of a phase β PVDF. The thermal analysis exhibited three stages of degradation for Solef 1010 with ethanol non-solvent and two for the other seven membranes. The degradation temperature increases with the increase in molecular weight and the difference in non-solvents. The highest thermal stability membrane was PVDF Solef 1010 with isopropyl alcohol non-solvent (430°C). SEM images showed the membrane with non-solvent isopropyl alcohol, displaying a dense sponge-like morphology. The wettability of membranes is affected by molecular weight and non-solvent type. The membrane with isopropyl alcohol non-solvent obtained the smallest contact angle (54.77°) and indicated the most wettability membrane.
Optimization of Chitosan-Carboxymethyl Chitosan Membrane Modification with PVA to Increase Creatinine and Urea Permeation Efficiency Riska Nurfirda Annisa; Retno Ariadi Lusiana; Gunawan Gunawan; Hasan Muhtar
Jurnal Kimia Sains dan Aplikasi Vol 27, No 4 (2024): Volume 27 Issue 4 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.4.189-196

Abstract

Polyvinyl alcohol (PVA) modified chitosan-carboxymethyl chitosan (CMC) membrane has been successfully fabricated and used as a dialysis membrane. This research aims to examine the manufacturing process, characterization, and dialysis performance of CMC and PVA-modified chitosan membranes. The membrane used the phase inversion method in acetic acid solvent with 5 CS:CMC: PVA dope compositions. Based on FTIR data, the modification process did not produce new spectra. Furthermore, the interaction produces a membrane with higher physical characteristics in terms of porosity, swelling, water uptake, hydrophilicity, and pH resistance values, which increase by 1.5–115%. Meanwhile, chitosan modification makes the membrane structure different from the original, requiring a longer degradation time. The modification also increased the permeation ability of urea by 17–65% and creatinine permeation by 20–62%. Membranes have the ability to be used more than once.
Isolation of Phenolic Acids from Land Kale (Ipomoea reptans Poir) and Antioxidant Activity Enny Fachriyah; Sofiana Nur Aziiza; Ismiyarto Ismiyarto; Purbowatiningrum Ria Sarjono; Dwi Hudiyanti; Sumariyah Sumariyah
Jurnal Kimia Sains dan Aplikasi Vol 27, No 1 (2024): Volume 27 Issue 1 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.1.1-7

Abstract

Land kale or Ipomoea reptans Poir is widely consumed by Indonesian people. Land kale plants can be used as natural antioxidants because they contain polyphenolic compounds, one of which is phenolic acid. This research was carried out to determine the antioxidant activity and isolate phenolic acid compounds contained in land kale plants (Ipomoea reptans Poir). The sample used was an ethanol extract of land kale. The total phenolics were determined using the Folin-Ciocalteu method. Phenolic acids were isolated using alkaline hydrolysis and acid hydrolysis and without hydrolysis methods. Separation of isolates was carried out using the TLC method. The structure was identified using UV-Vis spectrophotometry and LC-MS/MS. Antioxidant activity was measured using the DPPH method. The total phenolics of land kale ethanol extract were 71.2420 ± 0.0791 mg/g GAE. TLC showed that the HB, HA, and TH fractions contained caffeic acid and ferulic acid compounds. Separation of the (HB) fraction produced three isolates: B2 with a yellow color, B3 with a slightly yellowish color, and B4 which is colorless. Isolate B2 was identified as potentially containing caffeic acid, while isolate B3 was indicated to potentially contain ferulic acid through analysis using a UV-Vis spectrophotometer. Isolate B4 was thought to have a hydroxybenzoic acid framework after being determined using LC-MS/MS. The ethanol extract of land kale has strong antioxidant activity because it produces an IC50 value of 94.83 mg/L.
The Characteristics of Urease Enzyme of Green Bean Seeds (Vigna radiata L.) and Its Activity as An Antifungal Against Candida albicans Niken Istikhari Muslihah; Zusfahair Zusfahair; Dian Riana Ningsih; Fajar Nuradha
Jurnal Kimia Sains dan Aplikasi Vol 27, No 3 (2024): Volume 27 Issue 3 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.3.145-150

Abstract

Urease is an enzyme responsible for catalyzing the hydrolysis reaction of urea into CO2 and NH3. The urease isolated in this study came from green bean seeds. The urease enzyme was then tested for its antifungal activity against Candida albicans. The research aims to extract and characterize the urease enzyme from green bean seeds and explore its potential use as an antifungal agent. Green bean seeds were smoothed with a mortar and pestle, followed by homogenization using a stirrer and cold centrifugation. The crude extract of the urease enzyme was assessed for its activity through the Nessler method and measured by employing a UV-Vis spectrophotometer at a wavelength of 500 nm. The well-diffusion method was conducted to determine the antifungal activity of rough enzyme extracts against C. albicans. Positive controls were 100% ketoconazole, and negative controls used a pH buffer of 7. The characterization of the urease enzyme from green bean seeds revealed the optimum urease activity at a concentration of 0.25 M, pH level of 7, and an incubation temperature of 35°C with a value of 32.115 U/mL. Maximum reaction rate (Vmax) and Michaelis-Menten constant value (KM) were obtained at 56.497 U/mL and 0.215 M, respectively. Antifungal tests of C. albicans resulted in strong inhibitory activity at a concentration of 100% crude urease extract of 12 mm inhibition zone. The inhibitory concentration value grows at least 0.5% by 0.25 mm and positive control of 19.802 mm.
Production, Quality Test, and Activity Evaluation of Methanol Extract and Nanoparticles from Pluchea indica (L.) Leaves as Additives in Natural Soap against Propionibacterium acnes Arsya Cahya Saputra; Elang Seta Wiratama; Fiyola Mayangsari; Via Divinka Oktafinantyas; Sri Handayani
Jurnal Kimia Sains dan Aplikasi Vol 27, No 2 (2024): Volume 27 Issue 2 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.2.91-100

Abstract

Pluchea indica (L.) leaves, both in the form of extracts and silver nanoparticles, are known to exhibit antibacterial activity, but they have not been widely utilized in the health sector, especially in dermatology. This study aims to determine the quality test and antibacterial evaluation of natural soap formulated with methanol extract and nanoparticles of Pluchea indica (L.) leaves against Propionibacterium acnes. The synthesis of silver nanoparticles (AgNPs) was conducted using the reduction method, with AgNO3 as a precursor and methanol extract of Pluchea indica (L.) leaves serving as a reducing agent or bioreductor. Natural soap was produced through the cold process method, with a curing period of 3 to 4 weeks. Natural soap, derived from herbal ingredients, was made by combining NaOH, essential oils, and additives such as methanol extract and silver nanoparticles from Pluchea indica (L.) leaves. Quality tests were performed to assess moisture content (MC), fatty acid content, and pH levels. Antibacterial activity was assessed utilizing the well-diffusion method, with various sample concentrations ranging from 1.0 g/mL to 0.0625 g/mL. The quality test results for all soap samples met the Indonesian National Standard (SNI) requirements for acidity, free fatty acids, and moisture content. The bar soap without additives exhibited antibacterial activity, with a maximum inhibition zone of 14.26 mm (at 0.25 g/mL) after 15 hours. Natural soap with methanol extract of Pluchea indica (L.) leaf demonstrated an inhibition zone of 11.49 mm (at 0.0625 g/mL) after 15 hours, while nanoparticle soap exhibited an inhibition zone of 12.77 mm (at 0.25 g/mL) after 12 hours. In summary, all soap samples showed antibacterial activity, indicating the potential of Pluchea indica (L.) leaves as effective antibacterial agents.
Metabolite Formation of Pesticide Isoprocarb in Coffee Beans During Short-Term Storage and Condition Rosaria Nainggolan; Asep Saefumillah; Endang Saefudin; Yanwar Pratama Putra
Jurnal Kimia Sains dan Aplikasi Vol 27, No 2 (2024): Volume 27 Issue 2 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.2.45-52

Abstract

Isoprocarb (IPC) is one of the most important carbamate pesticides for white flea control in coffee plants. The prevalence of isoprocarb pesticide residues in coffee, i.e., green coffee beans, is a cause for concern. Green coffee beans were intentionally contaminated with isoprocarb at concentrations >0.01 mg/kg, which was investigated in this research. Quantitative analysis of isoprocarb with the QuEChERS method and qualitative analysis for metabolite formation was characterized using UV-Vis, FTIR, 1H-NMR, GC-MS, and LC-QTOF-MS. Based on the data, the metabolite formed is o-cumenol through the hydrolysis reaction of o-aryl carbamate with the enzyme carboxylesterase. o-cumenol or 2- isopropylphenol as a phenol derivative. To verify the existence of metabolite analytes that are believed to be there in coffee tainted with isoprocarb, more reliable analytical techniques utilizing analytical standards must be developed. Isoprocarb concentrations decreased along the storage time, especially in unsterilized conditions. As a toxic compound, a quantitative structural activity relationship study (QSAR) was initially carried out through a software application for estimating toxicity (TEST) provided by the US Environmental Protection Agency (EPA). For additional information, based on the LC50 and LD50 data confirmed from the TEST application, it was concluded that isoprocarb is more toxic than o-cumenol.
Synthesis and Characterization of Fluorapatite-Copper(II) Oxide with Sol-Gel Method as an Antibacterial Biomaterial Manasye Erlangga; Charlena Charlena; Irma Herawati Suparto
Jurnal Kimia Sains dan Aplikasi Vol 27, No 4 (2024): Volume 27 Issue 4 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.4.174-181

Abstract

One of the calcium phosphate compounds that can be used as an antibacterial material for coating dental implants is fluorapatite (FAp). This research aims to synthesize FAp at three different sintering temperatures (600, 800, and 1000°C), copper(II) oxide (CuO), and fluorapatite-copper(II) oxide (FAp-CuO) using the sol-gel method, and test the antibacterial properties of the synthesized products. The sol-gel technique proved successful in synthesizing FAp, with optimal results observed at a sintering temperature of 1000°C, achieving a crystallinity level of 90%. Analyses conducted using X-ray diffractometer, Fourier-transform infrared spectrometer, and scanning electron microscope-energy dispersive X-ray spectrometer revealed FAp as the dominating phase, exhibiting Ca/P and P/F ratios of 1.84 and 4.67, respectively. In FAp-CuO, replacing Ca2+ with Cu2+ ions lowered the average crystallite size, crystallinity, and Ca/P ratio. FAp, CuO, and FAp-CuO all displayed antibacterial activities against S. aureus and E. coli, with FAp-CuO having the maximum average inhibitory zone diameters of 0.243 and 1.397 mm, respectively.
Application of Acid Activated Ouw’s Natural Clay (ONC) on Adsorption of Methylene Blue Dye Catherina Manukpadang Bijang; Yustinus Thobias Male; Shielda Natalia Joris; Chrismenda Kartini Wattimena
Jurnal Kimia Sains dan Aplikasi Vol 27, No 3 (2024): Volume 27 Issue 3 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.3.121-127

Abstract

The application of natural clay as an adsorbent has been widely used. This is supported by the porous surface texture of the clay. However, some treatments are needed to remove impurities in natural clay before using it as an adsorbent. The common effort is to activate it with acid. This research studied the effect of hydrochloric acid concentration on the adsorption capacity of methylene blue dye. The concentrations of hydrochloric acid used were 2, 3, and 4 M. Characterization was carried out with IR, XRD, and SEM-EDX spectroscopy to see the differences in ONC characters before and after adding hydrochloric acid. The characterization results showed that ONC contained montmorillonite and quartz, and an increase in base distance was directly proportional to the increase in the concentration of hydrochloric acid used. High concentrations of hydrochloric acid caused excessive dealumination and deionization. The dealumination process was supported by IR data where there was a shift in wavenumber in the Al-O stretching vibration region from 796 cm–1 to 794 cm–1; the sharper the vibration in the Si-O region (488-468 cm–1); there was also an increase in the Si/Al ratio of pure ONC from 1.7497 to 2.2970 for 3 M ONC-HCl. The concentration of hydrochloric acid did not significantly affect the capacity of ONC as an adsorbent for methylene blue. The adsorption capacity of pure ONC obtained was 4.97215 mg/g, while for ONC-HCl 3 M was 4.97746 mg/g.
Impact of Fermentation on Hyptolide and Phytochemical Composition of Hyptis pectinata (L.) Poit Arie Adhi Nugraha; Lanni Rahma Aulia; Meiny Suzery; Agustina L. N. Aminin
Jurnal Kimia Sains dan Aplikasi Vol 27, No 1 (2024): Volume 27 Issue 1 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.1.8-13

Abstract

Solid State Fermentation has been employed for the biotransformation of the herbal plant Hyptis pectinata (L.) Poit is widely distributed in tropical regions of Brazil and is also present in Indonesia. The plant has been used to treat anti-inflammatory, anti-cancer, bacterial infection, and wound healing. This study aims to investigate the effects of using a solid-state fermentation method to ferment the leaves of Hyptis pectinata (L.) Poit towards the composition of phytochemicals and hyptolides. This study was carried out in several stages, including fermentation of Aspergillus niger leaves, sample extraction with methanol, determination of total phenolic and total triterpenoid content, phytochemical screening, and analysis of hyptolide using HPLC. The research results showed the growth of Aspergillus niger on the leaves of Hyptis pectinata (L.) Poit got into the logarithmic phase at 36 hours. Triterpenes and phenolics were present in the phytochemical profile, while alkaloids, tannins, and flavonoids were absent. The total phenolic and triterpenoid content increased by 33.68% and 17.78% respectively. HPLC analysis showed a decrease in hyptolide content in the fermented product. These results indicate the potential of fermented Hyptis pectinata (L.) Poit as an additional cancer therapy.

Filter by Year

1998 2025


Filter By Issues
All Issue Vol 28, No 8 (2025): Volume 28 Issue 8 Year 2025 Vol 28, No 7 (2025): Volume 28 Issue 7 Year 2025 Vol 28, No 6 (2025): Volume 28 Issue 6 Year 2025 Vol 28, No 5 (2025): Volume 28 Issue 5 Year 2025 Vol 28, No 4 (2025): Volume 28 Issue 4 Year 2025 Vol 28, No 3 (2025): Volume 28 Issue 3 Year 2025 Vol 28, No 2 (2025): Volume 28 Issue 2 Year 2025 Vol 28, No 1 (2025): Volume 28 Issue 1 Year 2025 Vol 27, No 12 (2024): Volume 27 Issue 12 Year 2024 Vol 27, No 11 (2024): Volume 27 Issue 11 Year 2024 Vol 27, No 10 (2024): Volume 27 Issue 10 Year 2024 Vol 27, No 9 (2024): Volume 27 Issue 9 Year 2024 Vol 27, No 8 (2024): Volume 27 Issue 8 Year 2024 Vol 27, No 7 (2024): Volume 27 Issue 7 Year 2024 Vol 27, No 6 (2024): Volume 27 Issue 6 Year 2024 Vol 27, No 5 (2024): Volume 27 Issue 5 Year 2024 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