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    Journal of Applied Chemical Research ( Scientific )
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  • About the journal

    Journal of Applied Chemical Research

    Standard Abbreviation Title: JACR

    Publication Date:
    Quarterly

    Publishing language:
    English

    Average arbitration time:
    3 month

    Acceptance rate: 5
    0%

    Impact factor Based on Index of Islamic World Citation Database:
    0.058

    Quality Based on Index of Islamic World Citation Database:
    Q4

    Ministry of Science Assessment Score:
    B

    Journal Status:
    Free Access to Articles

    Reviewing Type:
    Peer Review Single Blind

     

    Journal of Applied Chemical Research (JACR)(Journal of Applied Chemistry, JAC, before) is electronically published as quarterly by Islamic Azad University, Karaj branch. Copyright is reserved by the University. JACR is indexed by Ministry of Science, Research and Technology and Islamic World Science Citation Center (ISC).

    Aims and Scope

    JACR is a journal covering all fields of applied chemistry. JACR welcomes high quality original papers in English dealing with experimental and applied research related to all branches of chemistry .These includes the fields of analytical, inorganic, organic, physical, medicinal, biological and applied chemistry area. Review articles discussing specific areas of chemistry of current chemical importance are also published. You are kindly invited to submit your manuscript to this Journal. All contributions in the form of Original Research and Review Articles will be peer reviewed and published free of charge after acceptance.

     

    Policies:

    Submission of a manuscript implies that:

    1) The work described has not been published before (except in the form of an abstract or as part of a published lecture, review, or thesis).

    2) It is not under consideration for publication elsewhere.

    3) Its publication has been approved by all coauthors, if any, as well as by the responsible authorities at the institute where the work has been carried out.

    4) Authors agree to automatic transfer of the copyright to the publisher, if and when their manuscript is accepted for publication.

    5) The manuscript will not be published elsewhere.

     

    Special Attention:

    Journal of Applied Chemical Research (JACR) uses authentication software and valid databases to verify the authenticity of submitted manuscripts. Therefore, if the proof of scientific theft is proved, the paper is declared invalid and this will be reported to the competent legal authorities.

    COPE:

    “This journal is following of Committee on Publication Ethics (COPE) and complies with the highest ethical standards in accordance with ethical laws”.

     


    Recent Articles

    • Open Access Article

      1 - An Investigation of the Charge Effects on the Uptake and Release Capacity of Mesoporous Silica Nanoparticles as Vehicles for Short Oligonucleotides
      Rafatosadat Badihi Ali Mahmoudi Mohammad Reza Sazegar Khodadad Nazari
      Issue 1 , Vol. 18 , Winter 2024
      An easy and cost-effective sol-gel procedure is described for the synthesis and co-modification of mesoporous silica nanoparticles (MSNs) with various metal ions and positive-charge inducing polymers including PEI and PEG, for the construction of a reliable gene deliver More
      An easy and cost-effective sol-gel procedure is described for the synthesis and co-modification of mesoporous silica nanoparticles (MSNs) with various metal ions and positive-charge inducing polymers including PEI and PEG, for the construction of a reliable gene delivery vehicle. All of the samples (denoted as PEI-MSN, M-MSN, PEI-M-MSN, and PEG-PEI-MSN, where, M= Fe2+, Fe3+, Co2+, Zn2+, Al3+), were unambiguously characterized by conventional techniques including FTIR, XRD, SEM, and BET. The adsorption capacity of siRNA was found to be more related to the zeta potential of the samples than their specific surface areas. The best adsorption result was obtained by using PEI-Fe(III)-MSN (48.8 µg of siRNA per mg of support). The release of siRNA from PEIFe(III)-MSN, was also good (91.5%), but a burst release profile was observed. Interestingly, when a layer of PEG was used as a co-modifier, a sustained release profile was achieved, and meanwhile, the released amount of siRNA was improved (93.2%). The whole combination showed noconsiderable cytotoxicity according to the MTT test. Manuscript profile

    • Open Access Article

      2 - Investigation of the Potential of Adsorption and Drug Delivery Application of the Duloxetine Antipsychotic by using its Molecular Imprinted Polymer
      Seyyedeh Fatemeh Hoseini chehreghani Parviz Aberoomand Azar Maryam Shekarchi Bahram Daraei
      Issue 1 , Vol. 18 , Winter 2024
      The synthesis and application of a molecular imprinted polymer (MIP) as a carrier for drug delivery of Duloxetine (DUL) antipsychotic was investigated. Mimicking the natural receptors of DUL drug by synthesizing its MIP would lead to formation of some special active sit More
      The synthesis and application of a molecular imprinted polymer (MIP) as a carrier for drug delivery of Duloxetine (DUL) antipsychotic was investigated. Mimicking the natural receptors of DUL drug by synthesizing its MIP would lead to formation of some special active sites, which make able the MIP to accept only this special medicinal compound. Therefore, this MIP, which has been templated by DUL, could selectively absorb the molecules of DUL from the mediums in certain conditions and could release those chemical species in another place with different conditions. This MIP with its artificial receptors could be applied as a carrier for drug delivery applications and sustained released tablets. In order to synthesize this MIP based carrier, the precipitation polymerization method was applied. Also, methacrylic acid (MAA; as the functional monomer), 2,2-azobisissobutyronitrile (AIBN; as the initiator), and ethylene glycol dimethacrylate (EGDMA;as the cross-linker), were applied to obtain this sorbent. Moreover, the release kinetics of the drug was investigated by HPLC system, which was shown to be fitted with the Higuchi expressionpattern at least at 5.8, and 6.8 pHs. Finally, the results revealed that the synthesized MIP is able to be used in formulation of the sustained released tablets. Manuscript profile

    • Open Access Article

      3 - Fabrication of Graphene Oxide Nanocomposite Based on Poly(3-hydroxybutyrate)-Chitosan as a Useful Drug Carrier
      Seyed Mohammadjafar Mousavi Mirzaagha Babazadeh Mahboob Nemati Moosa Esʼhaghi
      Issue 1 , Vol. 18 , Winter 2024
      This research work describes a simple, eco-friendly, and facile method to synthesize a novel graphene oxide (GO) nanocomposite based on poly(3-hydroxybutyrate)-chitosan (PHB-CS) grafted to poly(methyl methacrylate-block-(poly(ethylene glycol) methacrylate-random-2-(dime More
      This research work describes a simple, eco-friendly, and facile method to synthesize a novel graphene oxide (GO) nanocomposite based on poly(3-hydroxybutyrate)-chitosan (PHB-CS) grafted to poly(methyl methacrylate-block-(poly(ethylene glycol) methacrylate-random-2-(dimethyl amino)ethyl methacrylate)) copolymer. The obtained nanocomposite was designated as GO/PHB-CS-gP(MMA-b-(PEGMA-ran-DMAEMA)) and investigated as a drug delivery system. The synthesized products were characterized by FTIR, 1HNMR, scanning electron microscopy (SEM), dynamic light scattering (DLS) and thermogravimetric analysis (TGA). Doxorubicin (DOX) as an anticancer drug was loaded on the synthesized GO nanocomposite and the drug encapsulation efficiency was calculated about 76.4%. The release profiles indicated that the resulting GO nanocomposite has a pH-responsive behavior under physiological conditions due to the hydrogen bonding interaction between PHB-CS-g-P(MMA-b-(PEGMA-ran-DMAEMA)) and GO. The release property of DOX from GO nanocomposite exhibited a slow sustained release, and suggested that the GO/PHB-CS-gP(MMA-b-(PEGMA-ran-DMAEMA)) nanocomposite could be an appropriate candidate as a useful nanocarrier for the release of DOX in controlled drug delivery systems for treatment of cancer cells. Manuscript profile

    • Open Access Article

      4 - Preparation, Structural and Magnetic Behavior of Sr(AlCr)xFe(12-2x) O19 Hexagonal Ferrites
      Mahboobeh Alimoradi Mohammad Yousefi Babak Sadeghi Mostafa M.Amini Alireza Abbasi
      Issue 1 , Vol. 18 , Winter 2024
      In this investigation, strontium hexaferrite nanocomposites co-doped with aluminum and chromium were prepared Sr(AlCr)xFe(12-2x)O19 with x different amounts (x= 0, 0.2, 0.4, 0.6 and 0.8), were synthesized. The magnetic nanocomposites have been prepared by simple sol-gel More
      In this investigation, strontium hexaferrite nanocomposites co-doped with aluminum and chromium were prepared Sr(AlCr)xFe(12-2x)O19 with x different amounts (x= 0, 0.2, 0.4, 0.6 and 0.8), were synthesized. The magnetic nanocomposites have been prepared by simple sol-gel auto-combustion method. The morphology and structure of nano-samples were determined by FTIR, XRD and FESEM . The results of the XRD pattern confirmed P63/mmc space group and the single phase of the synthesized samples. The crystal size of the prepared samples decreases with increasing Al and Cr.The magnetic properties of these compounds are determined by the VSM. Magnetic properties (Mr, Ms and Hc) were measured. The result showed that Mr and Ms decrease with the increase of Al and Cr. Manuscript profile

    • Open Access Article

      5 - Ultrasonic Assisted Liquid Phase Microextraction of Pb2+ Based on Deep Eutectic Solvent Followed by Electrothermal Atomic Absorption Spectrometry
      Marjan Shahinfar Zahra Ahmadabadi Naseer Mohammed Ali Mohammed Muna Mahboubeh Masrournia
      Issue 1 , Vol. 18 , Winter 2024
      This study presents an efficient, rapid, green, and low-cost method for preconcentrating trace levels of Pb2+ using ultrasonic-assisted liquid-phase microextraction (UA-LPME) followed by electrothermal atomic absorption spectrometry. We used sulfanilamide as a complexin More
      This study presents an efficient, rapid, green, and low-cost method for preconcentrating trace levels of Pb2+ using ultrasonic-assisted liquid-phase microextraction (UA-LPME) followed by electrothermal atomic absorption spectrometry. We used sulfanilamide as a complexing agent to form a hydrophobic complex with Pb2+, and a mixture of choline chloride-phenol as an extraction solvent. We investigated and optimized several parameters affecting the analyte's extraction recovery, including pH of the sample solution, concentration of the complexing agent, mole ratio of choline chloride phenol, volume of extraction solvent, volume of tetrahydrophoran (as an aprotic solvent), and ultrasonic time. Under the optimized conditions, we found that the proposed method has a linear range of 0.5-10 µg L-1 Pb2+ and a limit of detection of 0.16 µg L-1 Pb2+ (n=6). The proposed method's accuracy was verified using certified reference material-trace metals in drinking water (CRM-TMDW) samples. We also successfully used the proposed method to determine trace levels of Pb2+ in different water samples. In conclusion, our study offers an effective UA-LPMEbased method for preconcentrating trace levels of Pb2+ that can be applied to environmental monitoring and analysis. Manuscript profile

    • Open Access Article

      6 - Removal of Benzyl Paraben from Wastewater Using Zeolitic Imidazolate-67 Modified by Fe3O4 Nanoparticles with Response Surface Methodology
      Mohammad Pourmohammad Arezoo Ghadi Ali Aghababai Beni
      Issue 1 , Vol. 18 , Winter 2024
      The applicability of Zeolitic Imidazolate-67, Modified by Fe3O4 Nanoparticles, was studied for the removal of benzyl paraben from wastewater by adsorption method studied using response surface methodology (RSM). For the adsorption characterization of the adsorbent used More
      The applicability of Zeolitic Imidazolate-67, Modified by Fe3O4 Nanoparticles, was studied for the removal of benzyl paraben from wastewater by adsorption method studied using response surface methodology (RSM). For the adsorption characterization of the adsorbent used in benzyl paraben adsorption, BET, FTIR, XRD, and SEM analyses were performed. The impacts of variables including initial benzyl paraben concentration (X1), pH (X2), adsorbent dosage (X3), and sonication time (X4) came under scrutiny using response surface methodology (RSM). The values of 10 mg L-1, 0.03 g, 7.0, and 4.0 min were considered as the ideal values for benzyl paraben concentration, adsorbent, pH, and contact time, respectively. Adsorption equilibrium and kinetic data were fitted with the Langmuir monolayer isotherm model and pseudo-second-order kinetics (R2: 0.999) with maximum adsorption capacity (92.0 mgg-1), respectively. The predicted values were in agreement with experimental values obtained for the components of the mixture. The values at the optimized process conditions indicated a commercially viable route for optimal removal of dyes from wastewater. Manuscript profile

    • Open Access Article

      7 - Ultrasonic assisted liquid phase microextraction of Pb2+ based on deep eutectic solvent followed by electrothermal atomic absorption spectrometry
      Marjan Shahinfar Mahboubeh Masrournia Zahra  Ahmadabadi Naseer Mohammed Ali Mohammed Muna
      Issue 1 , Vol. 18 , Winter 2024
      This study presents an efficient, rapid, green, and low-cost method for preconcentrating trace levels of Pb2+ using ultrasonic-assisted liquid-phase microextraction (UA-LPME) followed by electrothermal atomic absorption spectrometry. We used sulfanilamide as a complexin More
      This study presents an efficient, rapid, green, and low-cost method for preconcentrating trace levels of Pb2+ using ultrasonic-assisted liquid-phase microextraction (UA-LPME) followed by electrothermal atomic absorption spectrometry. We used sulfanilamide as a complexing agent to form a hydrophobic complex with Pb2+, and a mixture of choline chloride-phenol as an extraction solvent. We investigated and optimized several parameters affecting the analyte's extraction recovery, including pH of the sample solution, concentration of the complexing agent, mole ratio of choline chloride phenol, volume of extraction solvent, volume of tetrahydrophoran (as an aprotic solvent), and ultrasonic time. Under the optimized conditions, we found that the proposed method has a linear range of 0.5-10 µg L-1 Pb2+ and a limit of detection of 0.16 µg L-1 Pb2+ (n=6). The proposed method's accuracy was verified using certified reference material-trace metals in drinking water (CRM-TMDW) samples. We also successfully used the proposed method to determine trace levels of Pb2+ in different water samples. In conclusion, our study offers an effective UA-LPME-based method for preconcentrating trace levels of Pb2+ that can be applied to environmental monitoring and analysis. Manuscript profile
    Most Viewed Articles

    • Open Access Article

      1 - One-pot Synthesis of 2-amino-4H-chromene Derivatives as Potential Antimicrobial Agents using DABCO-CuCl Complex as an Effective Catalyst
      Bita Baghernejad Samaneh Koosha
      Issue 3 , Vol. 14 , Summer 2020
      A new and efficient synthesis of 2-amino-4H-chromene derivativeswhich have remarkable pharmacological properties is developed by one-pot three-component efficient reaction between aldehydes, malononitrile, andα or β-naphthol in MeOH as solvent using DABCO-CuC More
      A new and efficient synthesis of 2-amino-4H-chromene derivativeswhich have remarkable pharmacological properties is developed by one-pot three-component efficient reaction between aldehydes, malononitrile, andα or β-naphthol in MeOH as solvent using DABCO-CuCl complex as an effective catalyst at room temperature. The structures of synthesized compounds were characterized by techniques of IR,1H-NMR, Mass and elemental analysis. This method provides an efficient improved pathway for the synthesis of chromenes in the terms of excellent yields, short reaction times and reusability catalyst. Manuscript profile

    • Open Access Article

      2 - Removal of C.I. Acid red 1 (AR1) dye pollutant from contaminated waters by adsorption method using sunflower seed shells and pine cone as agro waste materials
      Samira Alizadeh Kambiz Seyyedi
      Issue 4 , Vol. 13 , Autumn 2019
      Dyes are widely used in various industries, since theirdirect discharge to nature can cause many biological and environmental problems. Some of these dyes are toxic, carcinogenic and can cause skin and eye irritation. There are various dye removal techniques, but Adsorp More
      Dyes are widely used in various industries, since theirdirect discharge to nature can cause many biological and environmental problems. Some of these dyes are toxic, carcinogenic and can cause skin and eye irritation. There are various dye removal techniques, but Adsorption found to be very effective and cheap method among the all available dye removal methods. The purpose of this study was to investigate the adsorption of C.I. Acid Red 1 (AR1)dye pollutant to sunflower seed shells (SSS) and pine cones(PC) as agro waste materials, to find out the optimalconditions formajor operational parameters such as contact time, adsorbent dosage, initial dye concentration and pH. The results showed that the optimal conditions for decolorization of the solution containing 40 mg/L AR1,by SSS and PC adsorbentswith removal efficiency of 84.2% and 74.47%, respectively, were obtained at100 min of contact time and pH= 2 at room temperature.Optimal value of adsorbent dosage for SSS and PC was determined 2.6 and 3.2 g/L, respectively.The physicochemical properties of the adsorbent were studied using various descriptive techniques such as FTIR, SEM, and BET.The adsorption process of both adsorbents was best fitted to Freundlich modeland followed pseudo-second-order rate kinetics. Manuscript profile

    • Open Access Article

      3 - Biosynthesis of Ag Nanoparticles at Ziziphus Jujuba Kernel Substrate using Tilia platyphyllos Extract: Catalytic Activity for Reduction of Organic Dyes
      Bahar Khodadadi Mohammad Sabeti Omulbanin Norozi
      Issue 1 , Vol. 15 , Winter 2021
      For the first time the extract of the plant of Tilia platyphyllos was used to green synthesis of Ag nanoparticles (NPs) supported on Ziziphus jujuba kernel as an environmentally benign support. Ag NPs/ Ziziphus jujuba kernelas an effective catalyst was prepared through More
      For the first time the extract of the plant of Tilia platyphyllos was used to green synthesis of Ag nanoparticles (NPs) supported on Ziziphus jujuba kernel as an environmentally benign support. Ag NPs/ Ziziphus jujuba kernelas an effective catalyst was prepared through reduction of Ag+ions using Tilia platyphyllos extractas the reducing and capping agent and Ag NPs immobilization on Ziziphus jujuba kernel surface in the absence of any stabilizer or surfactant. According to FT-IR analysis, the hydroxyl groups of phenolics in Tilia platyphyllos extract as bioreductant agents are directly responsible for the reduction of Ag+ions and formation of Ag NPs. The as-prepared catalyst was characterized by Fourier transform infrared (FT-IR) and UV-Vis spectroscopy, field emission scanning electron microscopy (FESEM) equipped with an energy dispersive X-ray spectroscopy (EDS), Elemental mapping, X-ray diffraction analysis (XRD) and transmittance electron microscopy (TEM). The synthesized catalyst was used in the reduction of Congo Red (CR), and Methyl Orange (MO) at room temperature.The Ag NPs/Ziziphus jujuba kernel showed excellent catalytic activity in the reduction of these organic dyes. In addition, it was found that Ag NPs/Ziziphus jujuba kernelcan be recovered and reused several times without significant loss of catalytic activity. Manuscript profile

    • Open Access Article

      4 - Synthesis and Molecular Docking studies of Some Tetrahydroimidazo[1,2-a] pyridine Derivatives as Potent α-Glucosidase Inhibitors
      Mohammad R. Asghariganjeh Ali A. Mohammadi Elham Tahanpesar Ayeh Rayatzadeh Somayeh Makarem
      Issue 1 , Vol. 15 , Winter 2021
      KAl(SO4)2.12H2O is found to efficiently and heterogeneously catalyze the one-pot three-component reaction of 2-(nitromethylene)imidazolidine, malononitrile and aldehydes under mild conditions to afford the corresponding tetrahydroimidazo[1,2-a]pyridine in good yields an More
      KAl(SO4)2.12H2O is found to efficiently and heterogeneously catalyze the one-pot three-component reaction of 2-(nitromethylene)imidazolidine, malononitrile and aldehydes under mild conditions to afford the corresponding tetrahydroimidazo[1,2-a]pyridine in good yields and short reaction times. Docking study of some compounds in the active site of α-glucosidase demonstrated that these compounds interacted with important active site residues with low binding energy in comparison to standard inhibitor acarbose. Manuscript profile

    • Open Access Article

      5 - Solvent Effect on the Molecular Structure, Chemical Reactivity and Spectroscopy Properties of Z-Ligustilide: A Main Active Component of Multitude Umbelliferae Medicinal Plants
      Mahmoud Osanloo Reza Ghiasi
      Issue 3 , Vol. 11 , Summer 2017
      In this investigation, the structural, electronic properties, 13C and 1H NMR parameters and firsthyperpolarizability of Z-Ligustilide were explored. As well, the solvent effect on structural parameters, frontier orbital energies, electronic transitions, and 13C and 1H N More
      In this investigation, the structural, electronic properties, 13C and 1H NMR parameters and firsthyperpolarizability of Z-Ligustilide were explored. As well, the solvent effect on structural parameters, frontier orbital energies, electronic transitions, and 13C and 1H NMR parameters was illustrated based on Polarizable Continuum Model (PCM).These consequences specify that the polarity of solvents participates on the structures and spectroscopic properties of Z-Ligustilide.NBO analysis was used to examining of the hybridation of atoms, atomic charges and their second order stabilization energy within the molecule. Manuscript profile

    • Open Access Article

      6 - Inhibition of Mild Steel Corrosion in Sulfuric Acid Solution by 2-Hydropyrimidine-2-Thione Derivative
      Laya Nejati Moghadam Effat Jamalizadeh Zahra Hassani Amir Hossein Jafari
      Issue 4 , Vol. 12 , Autumn 2018
      The corrosion inhibition potential and efficacy of 2-hydropyrimidine-2-thione derivative on mildsteel in 0.5 M sulfuric acid solution was investigated using electrochemical polarization and FTIRspectroscopic techniques. In addition, docking studies were carried out as t More
      The corrosion inhibition potential and efficacy of 2-hydropyrimidine-2-thione derivative on mildsteel in 0.5 M sulfuric acid solution was investigated using electrochemical polarization and FTIRspectroscopic techniques. In addition, docking studies were carried out as theoretical investigationof adsorption inhibitor on iron surface. The results of polarization studies indicate the exceptionallystrong efficiency of this compound as an inhibitor in H2SO4 solution. The electrochemical studies toelucidate the mechanism indicated adsorption obeying the Langmuir isotherm to be the main modeof action. The FTIR results indicated the presence of inhibitor molecules to formation protectivelayer on the surface of mild steel. Theoretical findings show that the most stable states ofcompound/iron system are via the molecular sites containing S atoms, ester groups and aromaticrings. Manuscript profile

    • Open Access Article

      7 - Sodium Bismuthate: An Efficient Catalyst for the One-pot Synthesis of Biologically Active Spiro[4H-pyran] Derivativesunder Solvent-free Conditions
      Farzaneh Mohamadpour Malek Taher Maghsoodlou Reza Heydari Mojtaba Lashkari
      Issue 3 , Vol. 11 , Summer 2017
      An efficient sodium bismuthate (NaBiO3) synthesis of biologically active spiro[4H-pyran]derivatives has been accomplished via one-pot three-condensation of isatin/acenaphthequinone, malononitrile and different reagents including 1,3-dicrbonyl compounds, α-naphthol More
      An efficient sodium bismuthate (NaBiO3) synthesis of biologically active spiro[4H-pyran]derivatives has been accomplished via one-pot three-condensation of isatin/acenaphthequinone, malononitrile and different reagents including 1,3-dicrbonyl compounds, α-naphthol and 4-hydroxycumarin under solvent-free conditions. The notable advantages of the present procedure are: eco-friendly, environmentally benign nature,low-cost and non-toxic catalyst, simplicity of operation with no necessity of chromatographicpurification steps, short reaction times, good to high yields and solvent-free conditions. Manuscript profile

    • Open Access Article

      8 - Prediction of the Trace Amounts of Atomoxetine in Biological Samples using optimized solvent bar microextraction technique coupled with HPLC-UV
      Nasim Faridi Nahid Ghasemi Mahnaz Qomi Majid Ramezani
      Issue 4 , Vol. 13 , Autumn 2019
      Atomoxetine, an attention-deficit/hyperactivity disorder (ADHD) agent , has severe adverse effects, which even causes suicidal ideation in patients and when combined with other drugs such as monoamine oxidase inhibitors or in patients with cardiovascular disorders or ph More
      Atomoxetine, an attention-deficit/hyperactivity disorder (ADHD) agent , has severe adverse effects, which even causes suicidal ideation in patients and when combined with other drugs such as monoamine oxidase inhibitors or in patients with cardiovascular disorders or pheochromocytoma, it can be fatal. In order to monitor the trough level of the drug, sensitive analytical methods are in demand.Therefore, for detection of trace levels of this drug, the trend solvent bar microextraction method coupled with HPLC-UV were implemented. Application of pH gradient of 10.3 and 3.0 (donor and acceptor phase, respectively) enabled preconcentration and microextraction of the target analyte. The results were modeled using Artificial Neural Network (ANN) successfully.The optimum results were obtained with a stirring rate of 365 rpm and salt addition by 15.1% at 25°C after 26 min. The limit of detection and quantification were 7.0 ng mL-1and 20 ng mL-1, respectively. It offered good linearity range of 20-5000 ng mL-1 with a coefficient of estimation higher than 0.9972 and a preconcentration factor of 112. The relative standard deviations of analysis were 4.6% within a day (n=3) and 6.2% between days (n=9).Overall, this method can be employed for several purposes such as for dosage adjustment in ADHD patients, clean validation in the pharmaceutical industry, and for trace determination in forensics. Manuscript profile

    • Open Access Article

      9 - Fabrication of Graphene–LaMnO3 Sensor for Simultaneous Electrochemical Determination of Dopamine and Uric Acid
      Sedigheh Akbari Shohreh Jahani Mohammad Mehdi Foroughi Hadi Hassani Nadiki
      Issue 4 , Vol. 14 , Autumn 2021
      Dopamine (DA) and uric acid (UA) are two of important bimolecular widely circulated in body blood. Therefore, development of simple and rapid methods for simultaneous determination of them in routine analysis has a great significance for many researchers. Therefore, for More
      Dopamine (DA) and uric acid (UA) are two of important bimolecular widely circulated in body blood. Therefore, development of simple and rapid methods for simultaneous determination of them in routine analysis has a great significance for many researchers. Therefore, for the first time, nanocomposite of graphene (Gr)LaMnO3has been utilized to fabricate the new electro-chemical sensor for simultaneously determining DA and UA via immobilizing Gr-LaMnO3 on the glassy carbon electrode(GCE). Because of the very god catalytic activities, greater electrical conductivity as well as higher surface area of the Gr-LaMnO3, DA and UA with two clearly described peaks have been simultaneously determined at the Gr-LaMnO3 modified electrode. Relative to peaks at the bare GCE, oxidation currents of DA and UA notably enhanced. Moreover, the catalytic peak current linearly depended on concentration of DA and UA in a range of 0.33 – 283.3 and 0.33 –283.3 μM with 0.040 and 0.051 μAμM-1sensitivity. In addition, limit of detection (LOD) for DA and UA equaled 0.03 and 0.045 μM and diffusion coefficient for DA and UA diffusion at the modified electrode has been computed as 1.71×10−5 and 1.38×10−5 cm2s−1, respectively. It has been found that our electrode could have a successful application for detecting DA and UA in real samples. Thus, this condition demonstrated that the Gr-LaMnO3 nanocomposite displays good analytical performances to detect DA and UA. Manuscript profile

    • Open Access Article

      10 - Sol-gel Synthesis and Characterization of Zinc Oxide Nanoparticles Using Black Tea Extract
      Saeid Taghavi Fardood Ali Ramazani Sang Woo Joo
      Issue 4 , Vol. 11 , Autumn 2017
      The use of plant extract is generating the interest of researchers toward cost effective,nontoxic, economic viability and eco-friendly green synthesis of nanoparticles. In the presentwork, zinc oxide (ZnO) nanoparticles were synthesized using black tea extract and zinc More
      The use of plant extract is generating the interest of researchers toward cost effective,nontoxic, economic viability and eco-friendly green synthesis of nanoparticles. In the presentwork, zinc oxide (ZnO) nanoparticles were synthesized using black tea extract and zinc nitrateas the zinc source by the sol-gel method. The synthesized ZnO nanoparticles werecharacterized by powder X-ray diffraction (XRD), UV-visible spectroscopy and FourierTransform Infrared Spectroscopy (FTIR). The average crystallite size of ZnO nanoparticleswas calculated using Scherrer formula. The X-ray powder diffraction (XRD) analysisrevealed the formation of wurtzite hexagonal phase ZnO with average particle size of 32 nm. Manuscript profile
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    Islamic Azad University, Karaj branch
    Director-in-Charge
    Bita Mohtat (Faculty member)
    Editor-in-Chief
    Abbas Ahmadi (Faculty member)
    Executive Manager
    Ali Mahmoudi (Faculty member)
    Editorial Board
    Reza Ghiasi,Prof., (Department of Chemistry, Faculty of Science, East Tehran Branch, Islamic Azad University, Tehran, Iran) Elham Keshmirizadeh, ssociate Prof., (Department of Chemistry, Faculty of Science, Karaj Branch, Islamic Azad University, Karaj, Iran) Mohsen Khalili, Prof., (Neurophysiology Research Center, Shahed University, Tehran, Iran) Mehrdad Roghani, Prof., (Neurophysiology Research Center, Shahed University, Tehran, Iran) Dr.Mahmoud Sharifimoghadam, Prof., (Department of Chemistry, Kharazmi University.) Dr.Mohsen Daneshtalab, Prof., (Medicinal Chemistry and Pharmacognosy, School of Pharmacy, University of Memorial, Canada (Honorary member).) Dr.Masayuki Sato, Prof., (School of Pharmaceutical Sciences University of Shizuka (Honorary member).) Dr.R.K.Agarwall, Prof., (Department of Chemistry, Singh University, India.) Dr.Khodadad Nazari, Associate Prof., (Research Institute of Petroleum Industry.) Dr.Surendra Prasad, Prof., (Department of Biological and Chemical Sciences, Thechnology and Environment, South Pacific (USP) University,Surva, fiji.)
    Print ISSN: 2008-3815
    Online ISSN:2008-3823

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