Analytical Methods in Environmental Chemistry Journal <p>The Analytical Methods in Environmental Chemistry journal&nbsp;is a peer-reviewed journal devoted to all aspects and phases of analytical chemistry and chemical analysis. The Analytical Methods in Environmental Chemistry&nbsp;publishes articles of modern analytical chemistry, cover innovations in the analytical techniques by nanotechnology, new analytical methods in Environmental and occupational health. This includes fundamental aspects, instrumentation, new developments, innovative and novel methods and applications including environmental and clinical field. Traditional classical analytical methods such as spectrophotometry as well as established instrumentation methods such as atomic absorption spectrometry, gas chromatography, and <em>High-performance liquid chromatography</em> methods will be considered.</p> <p>&nbsp;</p> en-US <p>&nbsp;JOURNAL PUBLISHING AGREEMENT</p> <p>&nbsp;<strong>PLEASE PROVIDE US THE FOLLOWING INFORMATION,</strong></p> <p><strong>&nbsp;</strong>Article entitled:</p> <p>Corresponding author:</p> <p>To be published in the journal:</p> <p>&nbsp;<strong><u>Your Status </u></strong></p> <p><strong>&nbsp;</strong><strong>I am the sole author of the manuscript </strong></p> <ul> <li class="show">I am an Iranian government employee.</li> <li class="show">I am a European government employee</li> <li class="show">I am a Asian government</li> <li class="show">None of the above</li> </ul> <p>&nbsp;<strong>I am one author signing on behalf of all co-authors of the manuscript </strong></p> <ul> <li class="show">I am an Iranian government employee.</li> <li class="show">I am a European government employee</li> <li class="show">I am a Asian government</li> <li class="show">None of the above</li> </ul> <p>&nbsp;Please tick the above blanks (as appropriate), review the Journal Publishing Agreement, and then sign and date the document in black ink.</p> <p><strong>Published Journal Article: </strong>the author may share a link to the formal publication through the relevant DOI. Additionally theses and dissertations which contain embedded Published Journal Articles as part of the formal submission may be hosted publicly by the awarding institution with a link to the formal publication through the relevant DOI. Any other sharing of Published Journal Articles is by agreement with the publisher only.</p> <p>&nbsp;Signed: ______________________________________ Name printed: ___________________________________________</p> <p>&nbsp;Title and Company (if employer representative): _______________________Date: __________________________________</p> <p><a href="\protected\files\journals\FORMS\Copyright-Form.pdf" target="_blank" rel="noopener"><strong>DOWNLOAD COPYRIGHT FORM</strong></a></p> (Hamid Shirkhanloo) (Sahar Zargari) Wed, 30 Dec 2020 00:00:00 +0000 OJS 60 Zinc based metal–organic framework for nickel adsorption in water and wastewater samples by ultrasound assisted-dispersive-micro solid phase extraction coupled to electrothermal atomic absorption spectrometry <p>In this research, Zn<sub>2</sub>(BDC)<sub>2</sub>(DABCO) metal–organic framework (MOF) as a solid phase was used for separation and preconcentration toxic nickel ions (Ni) from water samples by ultrasound assisted-dispersive-micro solid phase extraction coupled to electrothermal atomic absorption spectrometry (USA-D-μ-SPE/ET-AAS). The MOF nanostructure was characterized by field emission-scanning electron microscope (FE-SEM) and transmission electron microscopey (TEM) for presentation of morphology and size of MOF synthesis. By procedure, 25 mg of Zn<sub>2</sub>(BDC)<sub>2</sub>(DABCO) as MOF adsorbent was added to 25 mL of water samples and then, Ni ions chemically adsorbed based on dative bonding of nitrogen in DABCO (1,4-diazabicyclo [2.2. 2]octane); N<sub>2</sub>(C<sub>2</sub>H<sub>4</sub>)<sub>3</sub>) at pH=8. The adsorbent was separated from liquid phase by syringe cellulose acetate filters (SCAF, 0.2 μm) and Ni ions back extracted from MOF adsorbent before determined by ET-AAS. &nbsp;The maximum recovery of MOF for nickel ions as a physically and chemically adsorption was obtained 34.6% and 98.8% at pH=3 and 8, respectively.</p> Negar Motakef kazemi, (*Corresponding Author) (Author) ##submission.copyrightStatement## Tue, 29 Dec 2020 00:00:00 +0000 Sulfamethizole functionalized graphene oxide for in-vitro separation and determination lead in blood serum of battery manufactories workers by syringe filter-dispersive- micro solid phase extraction <p>The toxic effect of lead (Pb) causes to anemia and iron deficiency in human body. So, the lead determination in blood/serum samples is very important. &nbsp;In this study, a novel adsorbent based on sulfamethizole functionalized on nanographene oxide (C<sub>3</sub>H<sub>10</sub>N<sub>4</sub>O<sub>2</sub>S<sub>2</sub>-NGO; SM-NGO) was used for extraction of Pb(II) from human blood, serum and plasma samples in<em> battery</em><em>&nbsp;</em>manufactories workers by SF-D-µ-SPE.&nbsp; By procedure, 25 mg of SM-NGO mixed with 10 mL of human blood/serum or plasma samples and aspirated by 10 mL of syringe tube. After sonication of samples for 5 min, the Pb ions adsorbed based on sulfur of SM-NGO adsorbent at pH=6 and the solid phase separated by syringe coupled to Millex-FG hydrophobic PTFE membrane (0.2 µm). Then, the lead ions were back-extracted from SM-NGO/PTFE by elution phase with 0.5 mL of nitric acid solution (0.5 M). Finally, the concentrations of Pb(II) ions were determined by AT-FAAS.&nbsp;</p> Abhijit De, (*Corresponding Author), S. Mojtaba Mostafavi (Author) ##submission.copyrightStatement## Tue, 29 Dec 2020 00:00:00 +0000 Adsorption methodology: Synthesis of Nano-structured nitrogen-doped porous carbon adsorbents for perchloroethylene vapor adsorption <p>The perchloroethylene (PCE, tetrachloroethylene), as a representative of chlorinated ethylenes and volatile organic compounds (VOCs), can be easily transported and remain in the atmosphere due to its volatility and stability properties. As a result, there is a crucial need to reduce this pollution to the extent permitted by international standards. The concentration of PCE determined with Gas chromatography–mass spectrometry analyzer (GC-MS). Activated nanocarbons (ACs) doped with nitrogen functional groups were prepared using the walnut shell as a precursor to evaluate their adsorption capacity for PCE vapors. Several techniques, including scanning electron microscopy (SEM), N<sub>2</sub> adsorption-desorption, and the Fourier transforms infrared spectrometry (FTIR), were applied to characterize the physical-chemical properties of the ACs. It is found that the PCE adsorption considerably increased on the nitrogen-doped ACs (KNCWS) due to their structural and surface charge properties. By conducting kinetic study, the pseudo-first-order model matched well with experimental data.</p> Mohammad Ghasemi Kahangi, Ali Morad Rashidi, (*Corresponding Author), Mohammad Samipoorgiri (Author) ##submission.copyrightStatement## Wed, 30 Dec 2020 00:00:00 +0000 Solid phase microextraction of organochlorine pesticides in water using MWCNTs-doped polypyrrole coated on steel fiber <p>The analysis of organochlorine pesticides (OCPs) residues has received an increasing attention in the last decades. Solid-phase microextration (SPME) is a convenient and fast analytical method, which has been widely used for the determination of volatile and semivolatile organic compounds in aqueous samples. The multiwalled carbon nanotubes/polypyrrole composite coating was used for the SPME of OCPs in water samples. The effects of various parameters on the efficiency of SPME process such as extraction time, extraction temperature, ionic strength, desorption time, and desorption temperature were studied. Under optimized conditions, the detection limits for the OCPs varied between 0.051 and 0.39 pg mL<sup>-1</sup>, the inter-day and intra-day relative standard deviations for various OCPs using a single fiber were 6.5-11.5% and 3.6-11.5, respectively. The linear ranges varied between 0.001 and 1 ng mL<sup>-1</sup>. The method was successfully applied to the analysis of ground water samples with the recoveries from 86 to 110%.</p> Hamideh asadollahzadeh, (*Corresponding Author), Ebrahim Noroozian (Author) ##submission.copyrightStatement## Tue, 29 Dec 2020 00:00:00 +0000 Dispersive solid phase extraction using graphitic carbon nitride microparticles for the determination of trace amounts of lead in water samples <p>In this work, ultrasound-assisted dispersive micro-solid phase extraction (USA-D-µSPE) technique using graphitized carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) is proposed for the preconcentration of low level of lead in aqueous samples. In this method, microparticles of graphitized carbon nitride sorbent were dispersed in the samples using ultrasonic bath and Pb(II) ions were directly adsorbed on the surface of g-C<sub>3</sub>N<sub>4</sub> particles. After adsorption and desorption of lead ions from g-C<sub>3</sub>N<sub>4</sub> particles, the Pb concentration was determined by the inductively coupled plasma-&nbsp;optical emission spectroscopy&nbsp;(ICP-OES). The main advantages of this method are high speed, simplicity and cheapness. The effects of pH, sorbent amount, eluent type and time on the recovery of the analyte were investigated. Under the optimized conditions and preconcentration of 10 mL of sample, the detection limit of 1.24 μg L<sup>-1</sup> was obtained. The results were validated by standard reference materials (NIST, SRM) and spiking of real samples by USA-D-µSPE procedure.&nbsp;</p> Ehsan Zolfonoun, (*Corresponding Author) (Author) ##submission.copyrightStatement## Wed, 30 Dec 2020 00:00:00 +0000 Determination and investigation of heavy metal concentrations in sediments of the Persian Gulf coasts and evaluation of their potential environmental risk <p>&nbsp;The contamination of coastal sediments with toxic heavy metals caused to a serious concern due to their environmental consequences. The aim of this study was to determine the concentration of heavy metals such as lead (Pb), copper (Cu), nickel(Ni) and manganese (Mn) in the sediments of the Persian Gulf coast in Kangan and Siraf ports in Bushehr province. In this regard, the sampling was performed in 10 stations with different uses in two depths of 0-5 and 5-20 cm along the coast of the Persian Gulf. The concentration of heavy metals was measured after drying, acid digestion and microwave by using flame atomic absorption spectrometry (F-AAS). The results showed that the average concentrations of Mn(II), Ni(II), Cu(II) and Pb(II) was measured 121.47, 11.51, 11.59 and 5.30 in surface sediments, and 131.59, 10.81, 12.56 and 4.88 µg g<sup>-1</sup> in deep sediments. All analysis validated by electrothermal atomic absorption spectrometry (ET-AAS).</p> Hoda Allami, Afsaneh Afzali, (*Corresponding Author), Rouhollah Mirzaei (Author) ##submission.copyrightStatement## Wed, 30 Dec 2020 00:00:00 +0000 Separation of aniline from water and wastewater samples based on activated carbon nanoparticles and dispersive solid phase extraction procedure <p>The water, wastewater and air are the main sources of aniline in environment. Aniline has a toxic effect in the human body and environment and so, must be determined by novel techniques. In this study, the activated carbon with microwave heating methods (MHM-ACNPs) were used for extraction aniline from waters by dispersive ionic liquid solid phase extraction procedure (D-IL-SPE) and compared to the activated carbon (AC). For this purpose, the mixture of acetone, ionic liquid and 30 mg of MHM-ACNPs/AC added to 100 mL of water samples at pH=8. After sonication for 10 min, the benzene ring in aniline as electron acceptor was chemically adsorbed on carboxylic groups of MHM-ACNPs as electron donors (MHM-ACNPs-COO<sup>─</sup>……C<sub>6</sub>H<sub>5</sub>-NH<sub>2</sub>) and then, the adsorbent was collected by IL phase in bottom of conical centrifuging tube. Finally, the aniline was released from MHM-ACNPs in remained solution by changing pH and the concentration of aniline determined by GC-FID.</p> Saeed Fakhraie, (*Corresponding Author), Morteza Mehdipour Rabouri, Ahmad Salarifar (Author) ##submission.copyrightStatement## Tue, 29 Dec 2020 00:00:00 +0000