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> Hamid Shirkhanloo en-US Analytical Methods in Environmental Chemistry Journal 2645-5552 <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> Analysis of complexation between new bidentate bis-NHC ligand and some metal cations at different temperature <p>In this research, the determination and complexation process between 3,3'-(2,2'-(4-methyl-phenylenesulfonamido)bis(ethane-2,1-diyl))bis(1-benzyl-3H-benzo[d]imidazol-1-ium)dibromide with Ni<sup>2+</sup>, Zn<sup>2+</sup>, Pd<sup>2+</sup>, Ag<sup>+</sup>, and Hg<sup>2+</sup> cations in the binary mixture of methanol (MeOH) and water (H<sub>2</sub>O) at different temperatures (15, 25, 35 and 45ºC) were studied using a conductometric method. The results show that the stoichiometry of the complexes in all binary mixed solvents for Ni<sup>2+</sup>, Zn<sup>2+</sup>, and Pd<sup>2+</sup> were 1:1 (M:L), while in other cases 1:2 (M:L) and 2:1(M:L). The stability constants (log ) of complex formation have been determined by fitting molar conductivity curves using a computer program (GENPLOT). The obtained data shows that in the pure methanol solvent system, the stability order is Ni<sup>2+</sup>&lt; Pd<sup>2+</sup>&lt;Zn<sup>2+</sup>&lt;Hg<sup>2+</sup>&lt;Ag<sup>+</sup> and the complexation process seems more stable in pure methanol in most cases. The thermodynamic parameters were determined conductometrically. The complexes in all cases were found to be enthalpy destabilized but entropy stabilized. The experimental data was tested by using an artificial neural network (ANN) program and was in good agreement with the estimated data.</p> Nur Rahimah Said Majid Rezayi, Corresponding Author, Ninie Suhana Abdul Manan Amirhossein Sahebkar Yatimah Alias, Corresponding Author, ##submission.copyrightStatement## 2022-06-28 2022-06-28 5 02 5 23 10.24200/amecj.v5.i02.169 Adsorption of diazinon using Cd-MOF nanoparticles before determination by UV-Vis spectrometer: isotherm, kinetic and thermodynamic study <p>In this work, Cd MOF has been prepared using a hydrothermal method and characterized by the SEM, elemental mapping, XRD, EDS, and BET analysis. The diazinon stability has been investigated in various pH (4-8) and temperature (298<sup>o</sup>K – 323<sup>o</sup>K) using UV-Vis spectrometer in the range of 230 – 280 nm, at its main absorption peak at 247 nm. Adsorption behaviors of diazinon on the Cd MOF were considered in different conditions. UV-Vis spectroscopy was used to monitor the removal of diazinon using the Cd MOF. The adsorption capacity of 138 mg g<sup>-1</sup> was obtained. The effect of temperature (298 K -323 K), pH (4-8), adsorbent dose (1-7 mg), initial concentration (4-12 mg L<sup>-1</sup>), stirring speed (0-500 rpm), and adsorption kinetics were studied using batch rout. All the studied parameters have shown significant effects on the efficiency of removal of diazinon by the Cd MOF. The adsorption thermodynamic was investigated in the temperature range of 298 k to 323 K and it has shown the endothermic nature of adsorption of diazinon using prepared Cd MOF. The adsorption isotherm follows by the Langmuir isotherm model. It was demonstrated that synthesized adsorbent could be effectively used for the removal of diazinon from water.</p> Faeze Khakbaz Mohamad Mahani, Corresponding Author, Mehdi Yoosefian ##submission.copyrightStatement## 2022-06-29 2022-06-29 5 02 24 38 10.24200/amecj.v5.i02.175 Response surface modeling for the treatment of methylene blue from aqueous media using electro-Fenton process before determination by UV-VIS spectrometer: Kinetic and degradation mechanism <p>In the present study, response surface methodology was employed to investigate the effects of main variables, including the initial MB concentration, hydrogen peroxide dosage, current density, and electrolysis time on the removal efficiency of MB using the electro-Fenton (EF) process. The MB concentration determination by UV-VIS spectrometer<strong>.</strong> The EF process degrades the MB contaminant molecules by the highly oxidizing species of the <sup>•</sup>OH. A quadratic regression model was developed to predict the removal of MB, where the R<sup>2</sup> value was found to be 0.9970, which indicates the satisfactory accuracy of the proposed model. ANOVA analysis showed a non-significant lack of fit value (0.0840). Moreover, the predicted correlation coefficient values (R<sup>2</sup>=0.9915) were reasonably in agreement with the adjusted correlation coefficient value (R<sup>2</sup>=0.9958), demonstrating a highly significant model for MB dye removal. In addition, the obtained results showed 95.8% MB was removed in the optimum removal efficiency, including the initial MB concentration of 20 mg L<sup>-1</sup>, H<sub>2</sub>O<sub>2</sub> dosage of 400 μL, and the current density of 7.0 mA cm<sup>-2</sup>, and electrolysis time of 10 min which was agreed with the predicted removal efficiency of 98.3%. Electrical energy consumption was found to be 0.163 kWh m<sup>-3</sup>.</p> Sara Zahedi Ali Asadipour Maryam Dolatabadi Saeid Ahmadzadeh, Corresponding Author, ##submission.copyrightStatement## 2022-06-29 2022-06-29 5 02 39 50 10.24200/amecj.v5.i02.178 Application of pipette-tip solid-phase extraction technique for fast determination of levofloxacin from wastewater sample using cobalt metal-organic framework <p>In this research, a miniaturized solid-phase extraction method based on pipette tip solid-phase extraction (PT-SPE) was employed for the determination of levofloxacin. Cobalt metal-organic framework (CoMOF) was used as an adsorbent. Levofloxacin was determined using high-performance liquid chromatography and UV detection (HPLC-UV). &nbsp;Important parameters that influence the extraction efficiency (<em>i.e.</em> pH, amount of adsorbent, extraction time, volumes of sample, and eluting solvent) were tested and optimized. Results indicated that the proposed method was validated over the range of 0.70 - 150.0 µg L<sup>-1</sup>. The relative standard deviation (RSD%) was below 2.75% for the levofloxacin. The limit of detection (LOD) of this method is 0.041 µg L<sup>-1</sup>. The preconcentration factor (PF) was obtained at 200 and the analysis time was around 10 min that confirming the reliability and accuracy of this method for extraction of levofloxacin. The PT-SPE procedure based on CoMOF adsorbent was efficiently extracted for levofloxacin more than 95%. In a static system, the adsorption capacity of CoMOF adsorbent for levofloxacin was obtained at 156.7 mg g<sup>-</sup><sup>1</sup> (<em>n</em>=10). The validation of results was successfully obtained for levofloxacin values based on the spiking real samples before determination by the HPLC technique.</p> Mohammad Abbaszadehbezi Mohammad Reza Rezaei Kahkha Alireza Khammar Morteza Mehdipour Rabouri ##submission.copyrightStatement## 2022-06-30 2022-06-30 5 02 51 59 10.24200/amecj.v5.i02.185 Magnetic solid-phase extraction based on the Carbonized cotton fabric/zeolite imidazolate framework-71/Fe3O4/polythionine followed by atomic absorption spectrometry for cadmium monitoring in water, tomato and cabbage samples <p>Carbonized cotton fabric/zeolite imidazolate framework-71/Fe<sub>3</sub>O<sub>4</sub>/polythionine (CCF/ZIF-71/Fe<sub>3</sub>O<sub>4</sub>/PTh) was fabricated, characterized, and applied as efficient magnetic sorbent in magnetic solid-phase extraction (MSPE) of cadmium from water and food samples before determination by flame atomic absorption spectrometry (FAAS). This modification of carbonized cotton fabric led to making a great surface area and porosity, increase extraction efficiency, and acceptable selectivity. The characterization of this proposed sorbent was performed by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), and Fourier transform-infrared (FT-IR) spectroscopy analysis techniques. The impact of several analytical parameters including pH, sorbent dosage, time of extraction, desorption condition, chelating agent concentration, the amount of salt and effect of potentially interfering ions on the selectivity and extraction recoveries of cadmium, were evaluated and optimized. In this proposed methodology, the limit of detection (LOD), the limit of quantification (LOQ), and relative standard deviation (RSD, n = 3) were found to be 0.21 ng mL<sup>−1</sup>, 0.6 ng mL<sup>−1</sup> and lower than 3.0%, respectively. The validation and accuracy of the new advanced procedure were confirmed by applying the proposed procedure for certified reference materials (SRM1570A). Eventually, CCF/ZIF-71/Fe<sub>3</sub>O<sub>4</sub>/PTh can be utilized as a selective sorbent, for the rapid, accurate and sensitive determination of Cd (II)&nbsp; in the samples.</p> Yasaman Sanaei Mohsen Zeeb, Corresponding Author, Seyed Saied Homami Amirhossein Monzavi Zahra Khodadadi ##submission.copyrightStatement## 2022-06-29 2022-06-29 5 02 60 75 10.24200/amecj.v5.i02.186 Determination of mercury values in urine and air of chloralkali workers by copper nanoparticles functionalized in carboxylic carbon nanotubes and the effects of mercury exposure on oxidative stress <p>Mercury exposure can produce toxic organic compounds in the body. Also, mercury can potentially cause oxidative damage and cellular disorders. In this study, the determination of mercury values in urine and air of chloralkali workers based on copper nanoparticles functionalized in carboxylic carbon nanotubes (CuNPs@CNT-COOH) were obtained by cold vapor atomic absorption spectrometer (CV-AAS). The urine samples were determined by magnetic solid-phase extraction (MSPE) at pH 8.0. By measuring the mercury level in the air and the urine sample of workers, the level of oxidative stress (Malondialdehyde (MDA), Superoxide Dismutase (SOD) and Catalase (Cat)), Interleukin-6 (IL-6), and Tumor Necrosis Factor α (TNF-α) as the proinflammatory cytokines were measured in the subject group. The results revealed statistically significant differences in the mercury level of the urine samples in the case and control groups (p&lt;0.001). Similarly, the malondialdehyde (MDA) level was significantly different between the two research groups (p&lt;0.001). Catalase concentration was not significantly different in the two groups (p=0.059). The LOD and linear range for mercury determination in urine were achieved at 0.012 µg L<sup>−1 </sup>and 0.05-7.0 µg L<sup>−1</sup>, respectively. Workers’ exposure to mercury can significantly increase oxidative stress and inflammatory cell signaling molecules such as cytokines.</p> Ali Faghihi Zarandi Somayyeh Karami-Mohajeri Morteza Mehdipour Rabouri Abbas Mohammadhosseini- Heyran Zahed Ahmadi, Corresponding Author, ##submission.copyrightStatement## 2022-06-30 2022-06-30 5 02 76 89 10.24200/amecj.v5.i02.188 Design a continuous microfluidic flow cell for turbidimetric-flow injection technology: A new approach for routine analysis of active pharmaceutical formulations <p>In this study, a new flow injection analysis (FIA) based on a microfluidic flow cell (MFC) with a sample capacity of 40 µL is described. A Tungsten lamp directs light from a typical 2100P Portable Turbidimeter apparatus into a quartz flow cell through a round sidewall aperture of 2.0 mm and emerges through the identical aperture on the opposite side of the flow cell, where a photodiode array (light detector) detects the passing light. When compared to a traditional cuvette (25 mm x 60 mm round) with the same nominal route length, this technique improves sensitivity by around 4.0. This improvement is due to the use of a short, narrow internal diameter microfluid as the flow cell, which reduces physical dispersion. The designed flow cell has been evaluated by developing a turbidimetric method for the detection of promethazine in pure form or pharmaceutical dosages. The developed method is based on forming of a yellowish ion-pair association complex due to the reaction of promethazine and sodium tetraphenylborate (STPB) in an acidic medium. At the flow optimum conditions, the calibration curve (CC) and the LOD for promethazine were obtained 0.5-90 µg mL<sup>-1</sup> and 0.35 µg mL<sup>-1</sup>, respectively (R<sup>2</sup> = 0.9955).&nbsp;</p> Aktham N. Jasim, Corresponding Author, Nagham S. Turkey Hussein Fares Abd-Alrazack ##submission.copyrightStatement## 2022-06-29 2022-06-29 5 02 90 104 10.24200/amecj.v5.i02.184