ORIGINAL_ARTICLE
Comparison of chelating ability of dipeptide (histidine-β-alanine) and (tetrakis(4-sulfonatophenyl)porphyrin) (TPPS4) for in vitro removal of toxic metals
Peptides are one of the best candidates for drug development due to their high specificity and low toxicity and porphyrins are significant macromolecules in biological systems with important roles. In this works ynthesis of dipeptide (histidine-β-alanine) was done by solid-phase peptide synthesis method (SPPS) and tetrakis(4-sulfonatophenyl)porphyrin (TPPS4) was synthesized by Adler method. The molecular structure of the dipeptide and porphyrin was defined by using different methods such as UV-Vis, FT-IR, 1H NMR and LC-Mass spectrometry for dipeptide. Kinetics study and comparison of the chelating ability of dipeptide (histidine-β-alanine) and TPPS4 was investigated for removing of metal ions Al3+, Cu2+, Hg2+ and Pb2+ in vitro.
https://icc.journals.pnu.ac.ir/article_3053_b5964a6f1294bb6d51912d5a0a20d5ff.pdf
2018-01-01
1
7
Dipeptide
solid-phase peptide synthesis
tetrakis(4-sulfonatophenyl)porphyrin
chelating ability
Rahmatollah
Rahimi
rahmatollah.rahimi@gmail.com
1
Iran University of Science & Technology
LEAD_AUTHOR
Maryam
Khosravi
khosravi_m@iust.ac.ir
2
Iran University of Science and Technology
AUTHOR
Mahboubeh
Rabbani
m_rabani@iust.ac.ir
3
Iran University of Science and Technology
AUTHOR
Ebrahim
Safavi
dr.safavi@yahoo.com
4
Member of the World Society of the Anti-Aging Medicine and International Hormone Society. Niavaran, 11977634461, Tehran, Iran.
AUTHOR
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22
ORIGINAL_ARTICLE
Preconcentration of acrylamide with dispersive liquid-liquid microextraction based on solidification of floating organic drop prior to determination by HPLC
A novel, rapid, simple and sensitive dispersive liquid-liquid microextraction method based on the solidification of floating organic drop (DLLME-SFO) combined with high performance liquid chromatography-ultra violet detection (HPLC-UV) was used to determine acrylamide in potato chips. The derivation of the acrylamide happened in the presence of KBr, KBrO3, H2SO4. Based on studies, 1-undecanol was selected as the extraction solvent. The factors affecting the extraction efficiency of DLLME-SFO such as the volume of the extraction solvent, kind and volume of the disperser solvent, effect of concentration of KBr, KBrO3, H2SO4 and time of centrifuge, time of derivative and extraction time were investigated and the optimal extraction conditions were estimated. Under the optimum conditions (extraction solvent: 150µl 1-undecanol;disperser solvent:1000 µl acetone; concentration of KBr, KBrO3:10 ppb; concentration of H2SO4 0.001 mol/l; extraction time: 3min), calibration curve is linear in the range of 0.5-15 ppb and correlation of determination (R2) is 0.993.The method was successfully applied for the determination of acrylamide in the actual potato chips.
https://icc.journals.pnu.ac.ir/article_3066_d733a17be9128de1045a7cefaf757907.pdf
2018-01-01
8
18
Acrylamide
DLLME-SFO
HPLC
1-undecanol
Shaghayegh
Mohebi
sh_mohebi86@yahoo.com
1
Department of Chemistry, Yadegar-e-Imam Khomeini (RAH) Branch, Islamic Azad University, Tehran Iran
AUTHOR
Ali
Mazloomifar
mazloomifar@yahoo.com
2
Department of Chemistry, Yadegar-e-Imam Khomeini (RAH) Branch, Islamic Azad University, Tehran Iran
LEAD_AUTHOR
[1] Y. Yamini, M. Ghanbarian, A. Esrafili, N. Yazdanfar, M. Moradi, Intern.J. Environ. Anal. Chem., 2012, 92, 1493-1505.
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ORIGINAL_ARTICLE
MWCNT incorporated silica aerogel prepared by ambient pressure drying: A recyclable catalyst for multicomponent synthesis of benzylpyrazolyl coumarin at room temperature
Multiwalled Carbon Nanotube (MWCNT) reinforced silica aerogel was synthesized in a very simple and cost effective sol - gel method. The process was followed by ambient pressure drying, and then the aerogel material was characterized by XRD, BET, SEM, EDX and FT-IR. 2.3 x 10-3 wt% MWCNTs were successfully incorporated in sodium silicate based silica aerogel. This metal-free nanocomposite catalyzed a four component organic reaction among 4-hydroxy coumarin, benzaldehyde, phenyl hydrazine, and ethyl acetoacetate for synthesizing medicinally important benzylpyrazolyl coumarin at room temperature. The MWCNT/silica aerogel composite material having easy accessible active sites and high catalytic activity was easily recovered and reused. The aerogel composite when impregnated with ceria offered very efficient and selective reaction methodology.
https://icc.journals.pnu.ac.ir/article_4216_9bbcaa7adf7e3f74e71d899454dfbaa7.pdf
2018-01-01
19
29
MWCNT/Silica aerogel
ambient pressure drying
MWCNT/Silica aerogel heterogeneous catalysis
multicomponent reaction
benzylpyrazolyl coumarin
Isak Rajjak
Shaikh
isak@india.com
1
School of Chemical Sciences, Swami Ramanand Teerth Marathwada University (SRTMU), Vishnupuri, Nanded – 431 606 (Maharashtra) India
LEAD_AUTHOR
Noor Mahmad Nabisaheb
Maldar
maldar_nn@rediffmail.com
2
Solapur University, Solapur (Maharashtra) India
AUTHOR
Caroline Sunyong
Lee
cslee@hanyang.ac.kr
3
Hanyang University ERICA campus, 5th Engineering Building, 55 Hanyangdaehak-ro, Sangrok-gu Ansan-si, Gyeonggi-do 426-791, South Korea
AUTHOR
Rajendra Charandeo
Pawar
rcpawar@hanyang.ac.kr
4
Hanyang University ERICA campus, 5th Engineering Building, 55 Hanyangdaehak-ro, Sangrok-gu Ansan-si, Gyeonggi-do 426-791, South Korea
AUTHOR
Hyung-Ho
Park
techchemtech@gmail.com
5
Department of Materials Science and Engineering, Yonsei University, Seodaemun-gu, Seoul 120-749, Republic of Korea
AUTHOR
Uzma Khwaja-Husain
Bangi
uzma.phys@gmail.com
6
School of Physical Sciences, Solapur University, Solapur city (Maharashtra) India
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ORIGINAL_ARTICLE
A spectroscopic study on Calf thymus DNA binding properties of nickel (II) complex with imidazole derivatives of 1,10-phenanthroline ligand
In this study, a nickel (II) complex with 1,10-phenanthroline based ligand, [Ni(FIP)2](OAC)2 (1) with FIP = 2-(Furan-2-yl)-1H-Imidazole[4,5-f][1,10] phenanthroline as ligand was synthesized and characterized by spectroscopic methods and elemental analysis. The interaction of [Ni(FIP)2](OAC)2 (1) with calf-thymus DNA (ct-DNA) was studied by UV-vis absorption, fluorescence spectroscopies and viscosity measurements in 20 mM Tris/HCl buffer solution, pH 7.0 at 25 °C. The complex (1) interacts with ct-DNA with an intrinsic binding constant of 1.11 ×105 M-1. Furthermore, the thermodynamic studies suggested that the interaction processes were endothermic disfavored (ΔH >0) and entropy favored (ΔS >0). The viscosity studies showed no considerable increasing changes in the viscosity of ct-DNA with increasing of the complex (1) concentration. Therefore, the [Ni(FIP)2](OAC)2 complex bind to ct-DNA via hydrophobic interaction as the main forces acting during the binding processes and the mode of binding is groove binding which was illustrated by hyperchromism in the UV-vis absorption band of [Ni(FIP)2](OAC)2 (1) with addition of ct-DNA and the decreasing of ethidium bromide (EB)-ct-DNA complex fluorescence in the presence of different concentrations of [Ni(FIP)2](OAC)2 complex and the unchanged viscosity of ct-DNA.
https://icc.journals.pnu.ac.ir/article_3068_4e97d4f72c676267c5bf87f8dfe75ab3.pdf
2018-01-01
30
38
Nickel complex
imidazole derivatives
DNA binding
Alireza
Amini khouzani
alireza_amini@yahoo.com
1
payame noor university
AUTHOR
Nasrin
Sohrabi
nsohrabi@gmail.com
2
Payame Noor University
AUTHOR
Nahid
Rasouli
n.rasooli55@yahoo.com
3
Payame Noor University
LEAD_AUTHOR
Mahboube
Eslami Moghadam
mah-eslami@yahoo.com
4
Chemistry & Chemical Engineering Research Center of Iran, Tehran, Iran.
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35
ORIGINAL_ARTICLE
MgCaFe-layered double hydroxide (LDH) for congo red dye removal in aqueous solution
In this work, the ability of the MgCaFe- Layered double hydroxide (LDH) for congo red (CR) dye removal in aqueous solution was investigated. Various parameters such as initial dye concentrations, temperature, adsorbent dosage, pH effect and agitation rate were examined and optimal conditions (10 mgL-1 of the dye concentration, 25 °C of temperature, 0.5 gL-1 of the adsorbent dosage, pH~7 and 450 rpm of agitation rate) were obtained. Moreover, the reusability of the adsorbent was investigated and promising result was obtained. Furthermore, the result showed the adsorption data on optimal condition was found to follow the pseudo- second order kinetic model with a high degree of correlation coefficient. Summary, this research illustrated that the MgCaFe-LDH can be used as efficient adsorbent for removing anionic dye in waste water.
https://icc.journals.pnu.ac.ir/article_3094_b47793c6890292abdb6c640097c60465.pdf
2018-01-01
39
48
Congo red
removal
MgCaFe-LDH
Zeynab
Soltani
zeynabsoltani85@gmail.com
1
Payame Noor University
AUTHOR
Hossein
Salavati
hosseinsalavati@pnu.ac.ir
2
Payame Noor University
AUTHOR
Maryam
Movahedi
maria_movahedi@yahoo.com
3
Payame Noor University
LEAD_AUTHOR
Zahra
Sadeghi
za.sadeghi@gmail.com
4
Payame Noor Universiti
AUTHOR
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23
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[25] C. Muthukumaran, V.M. Sivakumar, M. Thirumarimurugan, J. Taiwan Institute Chem. Engin., 2016, 63, 354-362.
25
ORIGINAL_ARTICLE
Synthesis of HA nanoparticles in the presence of anionic and cationic polyelectrolyte
Nanosized hydroxyapatite (HA) powders have been synthesized by an inverse microemulsion system using cyclohexane, an anionic surfactant and aqueous solutions of calcium nitrate tetrahydrate and biammonium hydrogen phosphate in the presence of anionic and caionic polyelectrolyte with the inducement of ultrasound irradiation. Prepared HA in presence of anionic polyelectrolyte has a different morphology from samples which are synthesized in presence of cationic polyelectrolyte. Cationic polyelectrolyte (poly diallyl dimethyl ammonium chloride PDADMAC) leads to formation of needle-like HA (10nm in diameter and 100nm in length). Formation of HA at room temperature was confirmed by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Size and morphology of the HA samples were characterized using transmission electron microscopy (TEM).
https://icc.journals.pnu.ac.ir/article_3193_cceb6b5ecae2b3494ff68eb259b746b5.pdf
2018-01-01
49
54
Hydroxyapatite
inverse microemulsion
nanoparticles
polyelectrolyte
Polyelectrolyte–modified microemulsion
Kobra
Akhavan Saravani
kobra.akhavan@gmail.com
1
islamic azad university rasht branch
LEAD_AUTHOR
[1] Y. Sun, G. Guo, D. Tao, Z. Wang, J. Phys. Chem. Sol., 2007, 68, 373-377.
1
[2] A.I. Iorgo, D. Berger, L. Alexandrescu, B.S. Vasile, Chalco. Letters., 2013, 12, 525- 531.
2
[3] W. Pon-on, S. Meejoo, I.M. Tang, Mat. Chem. Phys., 2008, 112, 453-460.
3
[4] G.C. Koumoulidis, A.T. Katsoulidis, A.K. Ladavos, J. Col. Inter. scien., 2003, 259, 254–260.
4
[5] P. Sharma, S. Singh, H.S. Virk, J. Nanosci. Nanotechnol., 2010, 6, 236-243.
5
[6] J. Arensds, J. Chistoffersen, M.R. Chistoffersen, H. Eckert, J. Cryst. Grow., 1987, 84, 515-532.
6
[7] S. Singh, P. Bhardwaj, V. Singh, S. Aggar-wal, U.K. Mandal, J. Colloid and Interface Sci., 2008, 319, 322-329.
7
[8] M.A. Malik, M.Y. Wani, M.A. Hashim, Arab. J. Chem., 2012, 5, 397-417.
8
[9] M. Dios, F. Barroso, J. Colloid Interface Sci., 2009, 333, 741-748.
9
[10] D. Sarkar, S. Tikku, V. Thapar, R.S. Srinivasa, K. C. Khilar, Coll. Sur. A: Physicochem. Eng.Aspects., 2011, 381, 123-129.
10
[11] W. Meier, Langmuir., 1996, 12, 1188-1192.
11
[12] A.M. Bellocq, Langmuir., 1998, 14, 3730-3739.
12
[13] B. Jakobs, T. Sottmann, R. Strey, J. Allgaier, L. Willner, D. Richter., Langmuir, 1999, 15,6707-6711.
13
[14] J. Kotez, J. Bahnemann, G. Lucase, B. Tiersch, S. Kosmella, Coll. Sur. A: Physicochem. Eng. Aspects., 2004, 250, 423-430.
14
[15] J. Kotez, J. Baier, S. Kosmella, Colloid. Polym. Sci., 2007, 285, 1719-1726.
15
[16] G.K. Lim, J. Wang, S.C. Ng, L.M. Gan, Mater. Lett., 1996, 28, 431-436.
16
[17] S. Mollazadeh, J. Javadpour, A. Khavandi, Cera. Int., 2007, 33, 1579-1583.
17
[18] Y. Wang, JingDi Chen., KunWei, ShuHua Zhang, XiDong Wang, Mate. Lett., 2006, 60, 3227-3231.
18
[19] A. Sinha, A. Guha, Mater. Sci. Eng., 2008, 29, 1330-1333.
19
ORIGINAL_ARTICLE
Phase transfer catalyzed reaction of disodium salt of 1,3-dihydroxybenzene with propargyl bromide in solid-liquid biphasic condition
The present work describes, the reaction between disodium salt of 1,3-dihydroxybenzene (in situ formation) and propargyl bromide was carried out in a solid-liquid biphasic phase transfer catalytic system at 50°C. Higher selectivity of the bis-derivative (1,3-bis(prop-2-ynyloxy)benzene) was obtained under solid-liquid PTC condion. The conversion of propargyl bromide of more than 99% was achieved in the presence of tetra-n-butylammonium bromide (TBAB) as catalyst. From the experimental evidence there is no mono-dervative observed. Experiments were conducted to increase the conversion of propargyl bromide such as, stirring speed, various PTCs, temperature, various solvents and amount of TBAB loading. All the experiments were conducted to obey pseudo-first order rate law. Apparent activation energy was also determined from the Arrhenius plot.
https://icc.journals.pnu.ac.ir/article_4007_e7e7715cc8eeec667cdd778d5a067d50.pdf
2018-01-01
55
61
Phase transfer catalyst
1,3-dihydroxybenzene
1,3-bis(prop-2-ynyloxy)benzene
solid-liquid reaction
Venugopal
Rajendran
1967sssr@gmail.com
1
Department of Chemistry, Pachaiyappa’s College for Men, 631 501, Kanchipuram, Tamil Nadu, India.
LEAD_AUTHOR
Varathan
Selvaraj
selvarajptc@gmail.com
2
Department of Chemistry, Pachaiyappa’s College for Men, 631 501, Kanchipuram, Tamil Nadu, India.
AUTHOR
Pachaiyappan
Abimannan
abimannan01@gmail.com
3
Department of Chemistry, Pachaiyappa’s College for Men, 631 501, Kanchipuram, Tamil Nadu, India.
AUTHOR
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ORIGINAL_ARTICLE
ZrOCl2.8H2O@nano SiO2: a green and recyclable catalyst for the synthesis of benzimidazoles
ZrOCl2.8H2O@nano SiO2 has been synthesized for the first time via a simple procedure and characterized by SEM (scanning electron microscopy), FT-IR, and EDX (energy-dispersive X-ray) techniques. The efficiency of the prepared nanostructure has been explored for the synthesis of benzimidazoles via the condensation reaction of orthoesters and diamines at 60 °C under solvent-free conditions. The successful synthesis of benzoxazole has also been explored through the condensation of orthoesters with 2-aminophenol in water media at room temperature. The recovery and reusability of the nanocatalyst has also been examined via 4 runs without activity loss. Partial short reaction times, high yields of products, mild reaction conditions in the absence of any hazardous solvent, and reusability of the nanocatalyst are noteworthy advantages of this method.
https://icc.journals.pnu.ac.ir/article_3282_4680761253214fbbbe6b1d7076f77c03.pdf
2018-01-01
62
69
Benzimidazoles
benzoxazole
green chemistry
ZrOCl2.8H2O
ZrOCl2.8H2O@nano SiO2
orthoester,
Kobra
Nikoofar
kobranikoofar@yahoo.com
1
chemistry department, faculty of physics and chemistry, alzahra university, vanak, Tehran, .Iran
LEAD_AUTHOR
Shekoufe
Moazzez Dizgarani
nikoofar.chem@gmail.com
2
chemistry department, faculty of physics and chemistry, alzahra university, Tehran, Iran
AUTHOR
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48
ORIGINAL_ARTICLE
Brassica oleraceae, a versatile plant for green synthesis of silver nanoparticles
In the present paper, silver nanoparticles (AgNPs) were synthesized using the Brassica oleraceae fruit extract under the simple and eco-friendly conditions. The reaction between silver nitrate, as metal source, and aqueous extract of Brassica oleraceae fruit, as reductant agent, produced AgNPs in high yield. The formation of AgNPs was confirmed by means of UV-Vis spectroscopy and scanning electron microscopy (SEM) was used for characterization of morphology and size of silver nanoparticle products. The investigation of diverse reaction parameters revealed that reductant concentrations, reaction pH, mixing ratio of the reactants and interaction time affected the size and morphology of synthesized AgNPs. AgNPs with 32.74 nm size and amorphous, based on SEM images, were produced within 24 h interaction period. AgNPs also showed a good antibacterial activity against Escherichia coli.
https://icc.journals.pnu.ac.ir/article_3301_691e12402c9d87cffce42a56b127bb96.pdf
2018-01-01
70
77
Green synthesis
Silver nanoparticles
brassica oleraceae
antibacterial activity
scanning electron microscopy (SEM)
Gholamhassan
Imanzadeh
imanzad2000@yahoo.com
1
Department of Chemistry, College of Basic Science, University of Mohaghegh Ardabili 56199-11367, Ardabil, Iran
LEAD_AUTHOR
Raha
Hadi
danna_411@yahoo.com
2
Department of Organic and Biochemistry, Faculty of Chemistry, University of Tabriz 51666-16471, Tabriz, Iran
AUTHOR
[1] S. Prashanth, I. Menaka, R. Muthezhilan, N.K. Sharma, Int. J. Eng. Sci. Technol, 2011, 3, 6235-5250.
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ORIGINAL_ARTICLE
Two new Schiff base complexes; synthesis, characterization, NMR, IR and mass study of a number of [1+1] Cd(II) complexes
In this paper we report the synthesis and characterization of two new binuclear Cd(II) macrocyclic Schiff base complexes [CdL23pydfp(NO3)], (1), and [CdL33pydfp(NO3)], (2). [1+1] cyclocondensation of L23py = N-(2-pyridylmethyl)-N-(3-aminpropyl)-1,3-diaminoethane and L33py = N-(3-pyridylmethyl)-N-(3-aminpropyl)-1,3-diaminopropane and 2,6-diformyl-4-methylphenol, dfp, in the presence of Cd(NO3)2.4H2O in equimolar ratios gave two new macrocylclic complexes. Resulting complexes were characterized by NMR, IR, mass spectroscopy and elemental analysis. Spectroscopy studying results show in spite the nitrogen and oxygen atoms of macrocyclic ligand with N4O donor set, one nitrate molecule (with two donor oxygen atoms) is coordinated to the Cd(II) center in each complex. So, the cadmium center is seven coordinated.
https://icc.journals.pnu.ac.ir/article_3344_da0be632a29228dde83eeb77316530b9.pdf
2018-01-01
78
86
Macrocyclic
Schiff base
cadmium
ligand
Reza
Golbedaghi
golbedaghi82@gmail.com
1
Department of Chemistry, Payame Noor University (PNU), Iran
LEAD_AUTHOR
Alirza
Salehi
2
Department of Industrial Engineering, Payame Noor University, P.O. BOX 19395-4697 Tehran, Iran
AUTHOR
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43
ORIGINAL_ARTICLE
Nickel ferrite as a recyclable nanocatalyst for synthesis of novel highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives
Highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives were synthesized by four-component reaction of aromatic aldehydes, malononitrile, ethyl acetoacetate and various phenylhydrazine, using nickel ferrite as a recyclable nanocatalyst by a grinding method under solvent-free and thermal conditions. The reaction has the advantages of good yields, less pollution, ease of separation of the desired products, and of being environment friendly. A possible mechanism for this reaction was proposed. Highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives were synthesized by four-component reaction of aromatic aldehydes, malononitrile, ethyl acetoacetate and various phenylhydrazine, using nickel ferrite as a recyclable nanocatalyst by a grinding method under solvent-free and thermal conditions. The reaction has the advantages of good yields, less pollution, ease of separation of the desired products, and of being environment friendly. A possible mechanism for this reaction was proposed.
https://icc.journals.pnu.ac.ir/article_3606_5512dc4806a36d3b660236fac750c904.pdf
2018-01-01
87
96
1
4-Dihydropyrano[2
3-c]pyrazoles
one-pot synthesis
four component reaction
nickel-ferrite nanoparticles nanocatalyst
Mohammad Reza
Poor Heravi
mrheravi@yahoo.com
1
Department of Chemistry, Payame Noor University, Abhar, Iran
LEAD_AUTHOR
Naheed
Morsalie
a_heravi@pnu.ac.ir
2
aDepartment of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, IRAN
AUTHOR
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ORIGINAL_ARTICLE
Fe2V4O13 assisted hetero-Fenton mineralization of methyl orange under UV-A light irradiation
Fe2V4O13 is prepared and characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), UV-diffuse reflectance spectroscopy (UV-DRS), high resolution scanning electron microscopy (HR-SEM) using energy dispersive X-ray spectroscopy (EDX) analysis. The hetero-Fenton catalyst can be used to mineralize Methyl Orange (MO) under UV-A light. The mineralization rate is influenced by hydrogen peroxide (H2O2) concentration, pH, and catalyst loading. The reusability of Fe2V4O13 is analyzed by five successive runs. At the maximum of 95% of degradation is observed in all five cycles. Therefore, the Fe2V4O13 catalyst is found to be reusable. The mineralization is confirmed by chemical oxygen demand (COD) measurements. Mechanism of the heterophoto-Fenton process is also proposed.Keywords: Fe2V4O13; Methyl Orange; wastewater treatment; hetero-Fenton reaction; photocatalysis
https://icc.journals.pnu.ac.ir/article_4356_4b3fed604dab04e3c00b31bf031e2038.pdf
2018-01-01
97
108
Fe2V4O13
methyl orange
wastewater treatment
hetero-Fenton reaction
photocatalysis
Kaliyamoorthy
Gowthami
1
Department of Chemistry, Annamalai University, Annamalainagar 608 002, Tamil Nadu, India
AUTHOR
Palusamy
Suppuraj
2
Department of Chemistry, Annamalai University, Annamalainagar 608 002, Tamil Nadu, India
AUTHOR
Ganesamoorthy
Thirunarayanan
3
Department of Chemistry, Annamalai University, Annamalainagar 608 002, Tamil Nadu, India
AUTHOR
Balu
Krishnakumar
4
Department of Chemistry, University of Coimbra, Coimbra 3004-535, Portugal
AUTHOR
Abílio José Fraga do Nascimento
Sobral
5
Department of Chemistry, University of Coimbra, Coimbra 3004-535, Portugal
AUTHOR
Meenakshisundaram
Swaminathan
chemres50@gmail.com
6
Nanomaterials Laboratory, International Research Centre, Kalasalingam University, Krishnan Koil 626 126, Tamil Nadu, India
AUTHOR
Inbasekaran
Muthuvel
profmuthuvelchem@yahoo.com
7
Annamalaiuniversity
LEAD_AUTHOR
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