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جستجوی مقالات مرتبط با کلیدواژه « microwave » در نشریات گروه « شیمی »

تکرار جستجوی کلیدواژه « microwave » در نشریات گروه « علوم پایه »
  • Nasimeh Mahmoudinasab-Manoujan, FARID MOEINPOUR*, Fatemeh S. Mohseni-Shahri

    Efficient synthesis of naphthopyranopyrimidine derivatives using copper(II)/polyimide linked covalent organic frameworks (Cu(II)/PL-COF) has been achieved through a solvent-free and microwave-assisted method. This one-pot protocol combines β-naphthol, aromatic aldehydes, and N,N-dimethylbarbituric acid. The process offers various advantages, including safe operation, minimal pollution, fast product formation, and easy setup due to microwave irradiation and a lack of solvents. Additionally, the catalyst demonstrates high reusability, allowing for multiple repetitions of the reaction without experiencing any significant loss in activity.

    Keywords: Covalent organic frameworks, Naphthopyranopyrimidine, Solvent-free, Microwave}
  • Chahinez Benouis, Ferrahi Mohammed Issam, Rachid Meghabar, Bouras Brahim, Zennaki Mohammed el Amine, Zzerigui Hafida

    In this work, N-vinyl imidazole (NVI) and glycidyl methacrylate (GMA) were combined to create Poly(NVI-GMA). The synthesis of this novel cationic copolymer was initiated using high-temperature, ultraviolet (UV), and microwave radiation. The cationic level of Poly(NVI-GMA) was optimized during the copolymerization process. The ideal synthesis conditions included a 2% initiator concentration, equal proportions of NVI and GMA (50% (v/v) each), a polymerization duration of 4 minutes, and an acidic pH reaction media. UV-visible, FTIR, and 1H-NMR techniques were employed to examine the structure of the copolymer. To investigate the flocculation performance of the highly cationic Poly(NVI-GMA) in purifying water with high turbidity, several analyses, including Fourier transform infrared (FTIR), X-ray diffraction (XRD), and thermogravimetric (TGA) analyses, were conducted to study and summarize the flocculation mechanism. Experimental simulations utilizing maghnite as a coagulant yielded a transmittance of 96.9% in the supernatant with a concentration of 6 mg/L, a brief stirring duration of 20 minutes, an acidic pH, and a stirring speed of 200 rpm

    Keywords: N-vinyl imidazole, Microwave, Copolymerization, Turbidity, Maghnite}
  • مریم یلداگرد*
    در این مطالعه نانوکامپوزیت Pt-Co/PAA/GNP به دلیل رفع مشکل بازده و پایداری پایین الکترود کاتد پیل های سوختی پلیمری به واسطه استفاده از الکتروکاتالیست تجاری Pt/C در ترکیب لایه کاتالیست مجموعه الکترود و غشای پیل های سوختی توسعه یافت. برای این منظور  نخست گرافن اکسید به عنوان ماده نگهدارنده به روش اصلاح شده هامر و آفنمن سنتز شد. سپس گرافن اکسید با پلی آلیل آمین به روش پلمیریزاسیون به روش اتصال عرضی عامل دار شد. پس از آن الکتروکاتالیست آلیاژ پلاتین-کبالت توسط روش نوین سنتز پلی ال به کمک امواج مایکروویو بر روی ماده نگهدارنده پخش شد. اندازه گیری های طیف رامان ساختار گرافیتی صفحه های گرافن احیا شده را تایید نمود. نتیجه های طیف فروسرخ حضور پلی آلیل آمین را در ترکیب ماده نگهدارنده نشان داد. پس از بررسی ساختار و ترکیب الکتروکاتالیست های Pt-Co/PAA/GNP، Pt/PAA/GNP وPt/C توسط تفرق اشعه ایکس و میکروسکوپ الکترونی روبشی سرانجام کارایی الکترودها با روش های الکتروشیمیایی گوناگون از جمله منحنی های ولتامتری چرخه ای، ولتامتری روبش خطی در واکنش کاهش اکسیژن ارزیابی شدند. نتیجه های تفرق اشعه ایکس، اندازه میانگین ذره های آلیاژ پلاتین-کبالت پخش شده بر روی نگهدارنده را به تقریب 11 نانومتر نشان داد. تصویرهای میکروسکوپ الکترونی روبشی نشان داد که کاتالیست دو فلزی پلاتین-کبالت در اندازه نانو به طور موفقیت آمیزی روی نانوصفحه های گرافن اکسید عامل دار شده با پلی آلیل آمین پخش شده و این ذره ها در فیلم به صورت کروی هستند و به خوبی در سطح نگه دارنده توزیع شده اند. طبق اندازه گیری های الکتروشیمیایی مساحت سطح فعال الکتروشیمیایی 42/15 مترمربع بر میلی گرم پلاتین با بهره وری 62 درصد کاتالیست و جریان پیک فعالیت ویژه و جرمی به بزرگی 3345/26 و 7078/1 میلی آمپر بر میلی گرم پلاتین برای Pt-Co/PAA/GNP به دست آمد که قابل مقایسه با مقدارهای به دست آمده برای الکترود Pt/PAA/GNP و نمونه تجاری می باشد.
    کلید واژگان: نانوصفحه های گرافن, پلی آلیل آمین, نانوذره های پلاتین-کبالت, امواج مایکروویو, واکنش احیای اکسیژن, پیل سوختی پلیمری}
    Maryam Yaldagard *
    In this research nanocomposites of Pt-Co–Polyallylamine-Graphene Nanoplates (Pt-Co/PAA/GNPs) was developed to improve the oxygen reduction reaction activity and stability of commercial Pt/C electrocatalyst. For this purpose, first graphene oxide (GO) as a support material was synthesized according to hamer and affenman method. Then graphene oxide was functionalized with Polyallylamine through cross linking. After that Pt-Co as a catalyst was dispersed on the as prepared support by a novel process polyol synthesis method assisted by microwave. Raman spectroscopy measurements confirmed the graphitic structure of the produced reduced graphene oxide nanoplates. Fourier transform infrared spectroscopy results illustrate the presence of Polyallylamine in the composite. After investigation of the structure, morphology and composition of the prepared electrodes were characterized by X-ray diffraction, Field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy. the catalytic activities of prepared electrodes for the oxygen reduction reaction were evaluated through cyclic voltammetry and linear sweep voltammetry measurements in the oxygen reduction reaction. X-ray diffraction results showed that Pt-Co particles were dispersed on the support with mean particle size of about 11. FESEM images showed that the nanosized Pt- Co were successfully dispersed on functionalized graphene oxide nanoplates. The nanoparticles in the film were observed to be uniform spherical objects and well distributed. According to the electrochemical measurements, active electrochemical surface area of 15.42 m2Pt/mgPt with 62% catalyst utilization and the specific and mass activity peak currents as high as of 26.3345 and 1.7078 mA/mgPt was found for Pt-Co/PAA/GNP which is comparable with respect to the Pt/PAA/GNP electrode and commercial one.
    Keywords: graphene nanoplates, Polyallylamine, Pt-Co nanoparticles, Microwave, Oxygen reduction reaction, Proton exchange membrane fuel cell}
  • شهره جلالی، مجید بنی آدم، مرتضی مغربی*
    نانوکامپوزیت های نانولوله کربنی/ پلی استایرن به کمک پلیمریزاسیون در جا تحت تابش امواج مایکروویو سنتز شدند. به علت اینکه نانو لوله های کربنی جاذب مایکروویو هستند در اثر تابش مایکروویو گرم شدند و پلیمریزاسیون حرارتی خود به خودی استایرن بدون استفاده از آغازگر انجام شد. برای بررسی تاثیر امواج مایکروویو در پلیمریزاسیون، سنتز نانو کامپوزیت نانو لوله کربنی/پلی استایرن به کمک حرارت دهی نیز انجام شد. ریخت شناسی نمونه ها توسط میکروسکوپ الکترونی روبشی نشر میدانی و میکروسکوپ الکترونی عبوری مورد مطالعه قرار گرفت. مشخصه یابی نمونه ها به کمک آنالیز های طیف سنجی فروسرخ تبدیل فوریه، گرما سنج وزنی و رامان  انجام شد و رسانایی الکتریکی نمونه ها نیز بررسی گردید. نتیجه ها نشان دادند که استفاده از امواج مایکروویو می تواند باعث ایجاد یک لایه پلی استایرنی روی نانو لوله ها شود و نانو کامپوزیت حاصله دارای کلوخه های اندکی بود. علاوه بر این، با افزایش توان مایکروویو، ضخامت لایه پلیمری ایجاد شده روی نانولوله ها افزایش و رسانایی الکتریکی نانو کامپوزیت ها از 37/14 زیمنس بر متر برای نانوکامپوزیت سنتز شده با حرارت (صفر وات) به 17/7، 39/5 و 94/2 زیمنس بر متر به ترتیب برای نانوکامپوزیت سنتز شده با مایکروویو با قدرت300، 500 و 700 وات، کاهش یافت.
    کلید واژگان: نانو لوله کربنی, مایکروویو, پلیمریزاسیون, نانو کامپوزیت}
    Shohreh Jalali, Majid Baniadam, Morteza Maghrebi Maghrebi *
    Carbon nanotube/polystyrene nanocomposites were synthesized via microwave-assisted in-situ polymerization. Since carbon nanotubes can absorb microwave irradiation, they can form hot spots in the mixture, and the auto thermal polymerization of styrene monomers can be initiated from their surface without using any chemical initiator. In order to investigate the effectiveness of the microwave irradiation on the polymerization process, carbon nanotube/polystyrene nanocomposites were synthesized via heating. Samples were characterized by TEM, FESEM, FT-IR, TGA and Raman spectra, and the electrical conductivity of samples were also measured. The results showed that using microwave irradiation can result in forming a polymeric layer on carbon nanotubes, and the resultant nanocomposite had a few agglomerations. In addition, by increasing the power of microwave irradiation, the thickness of the polymeric layer increased and electrical conductivity decreased.
    Keywords: Carbon nanotubes, Microwave, polymerization, Nanocomposites}
  • Ali Afshar Ebrahimi *
    There is interest in minimizing or eliminating the dependency on the use of non-recyclable, expensive and homogeneous catalysts. This can be achieved by replacing them with more durable nanoheterogeneous catalysts, which offer high catalytic performance and easy recoverability. Designing highly active and stable heterogeneous catalysts for the selective hydrogenation of phenol is still a challenge. In this study, a novel type of Pt/γ-Al2 O3 nanocatalyst is elaborately designed and prepared using a clean and green colloid-Microwave assisted synthetic method. The obtained nanocatalyst was characterized using TEM and BET analysis. The results of TEM and chemisorption characterization results confirm that the confined nanocatalyst possesses stronger Pt-Al2O3 interaction, with an excellent monodispersity of Pt nanoparticle on the surface of solid support. The prepared nanocatalyst exhibited enhanced catalytic activity and stability for the hydrogenation of phenol to cyclohexanone compared to the unsupported nanocatalyst. Cyclohexanone is widely used in pesticides, coatings, dyes, lubricants, and other industries due to its low volatility and high solubility. At 1 MPa, 3 hours, and 80 °C, a selectivity of 92.6 % and complete conversion of phenol to cyclohexanone were achieved.
    Keywords: Pt, γ -Al2O3 nanocatalyst, colloid, Microwave, Hydrogenation, Phenol}
  • Masoud Moghimi, Masoud Honarvar *, Mehrdad Ghavami, Hossein Ahmadi Chenarbon

    Extensive research has begun on the production of naturally occurring red colorants as permitted food additives. The Betalain in Beetroot (Beta vulgaris) cells can be used to prepare a natural red color additive for food products. Betalains are more resistant to acidic conditions and high temperatures than other red pigments such as anthocyanins. However, the low stability of Betalain compared to synthetic colorants is considered a big challenge in its extraction, processing, and storage. Therefore, it is very important to use a suitable extraction method for it. In recent years, the use of supercritical carbon dioxide (scCO2) for isolation and extraction of natural products instead of conventional methods such as extraction with organic solvents has attracted interest because the final product may become contaminated with the solvents. In the same vein, this research evaluated the effects of microwave power (100-450 W), carbon dioxide flow rate (1-3 mL/min), temperature (30-70℃), and pressure (15-40 MPa) on extraction efficiency, 2,2-diphenyl-1-picrylhydrazyl, and the quantities of phenolic compounds extracted from Beetroot. The results suggested that temperature, pressure, flow rate, and microwave power significantly influenced the amounts of phenolic compounds, extraction efficiency, and antioxidant properties of the compounds extracted from Beetroot. Increases in temperature, pressure, microwave power, and carbon dioxide flow rate in the (50-60℃), (20-30 MPa), (300-400 W), and (1-2 mL/min) ranges, respectively, increased the quantities of phenolic compounds, ability to suppress free radicals and extraction efficiency as the response. However, increases beyond the mentioned ranges caused decreases in the response variables. Optimal extraction of Betalain from Beetroot using supercritical carbon dioxide and microwave pretreatment was achieved at a temperature of 45 °C, pressure of 27.5 MPa, CO2 flow rate of 2 mL/min, and microwave power of 300W.

    Keywords: Supercritical carbon dioxide, Beetroot, Betalain, Microwave, Antioxidant, RSM}
  • زهرا غیاثی فر، ندا ادیب پور*، اسکندر علی پور، فرزاد کبارفرد، محمدرضا شوشی زاده

    در این مطالعه، با هدف گسترش شیمی سبز، کاتالیزوری بر پایه هیدروکسیدهای لایه ای دوگانه (LDHs) متصل به هگزامتیلن-1و6-دی ایزوسیانات (HMDI) و اسید سیتریک (LDHs-g-HMDI-Citric acid) تهیه و با استفاده از تکنیک های مختلف FT-IR، XRD، EDX، SEM، TGA و DTG شناسایی گردید. فعالیت کاتالیستی این کاتالیزور هتروژن قابل بازیافت برای سنتز مشتقات جدید ایمیدو دی کربونیک دی آمید (بیورت) تحت شرایط مایکروویو مورد ارزیابی قرار گرفت. استفاده از روش مایکروویو منجر به استفاده ی بسیار اندک از حلال های آلی، کاهش زمان واکنش و افزایش راندمان محصولات گردید که در جهت توسعه شیمی سبز و حفاظت از محیط زیست محقق شد. همچنین این بیورت ها جهت بررسی فعالیت بازدارندگی بر تکثیر ویروس نقص ایمنی انسانی نوع 1 (HIV-1)، توسط کیت ELISA آنتی ژن p24 HIV-1 مورد ارزیابی قرار گرفته و سه مورد از آن ها (5b، 5c و 5f) فعالیت متوسطی روی ویروس HIV-1 با مقادیر IC50 در محدوده 1/55 تا 100 میکرومولار در مقایسه با آزیدوتیمیدین به عنوان داروی مرجع (11/0 IC50 = میکرومولار) نشان داد. در نهایت مطالعات داکینگ مولکولی جهت بررسی مکانیسم اثر ترکیبات بر آنزیم پروتیاز ویروس صورت گرفت، که نتایج کارهای عملی آزمایشگاهی و مطالعه داکینگ مولکولی تطابق خوبی را از خود نشان دادند.

    کلید واژگان: شیمی سبز, مایکروویو, هیدروکسیدهای لایه ای دوگانه, ایمیدو دی کربونیک دی آمید, اثر ضدایدز, داکینگ مولکولی}
    Zahra Ghiasifar, Neda Adib Pour *, Eskandar Ali Pour, Farzad Kobarfard, MohammadReza Shoushi Zadeh

    In this paper, to develop green chemistry, a catalyst based on layered double hydroxides (LDHs) attached by hexamethylene-1,6-diisocyanate (HMDI) and citric acid (LDH-g-HMDI-citric acid) were prepared and characterized by FT-IR, XRD, EDX, SEM, TGA, and DTG analytical methods. The catalytic activity of this recyclable heterogeneous catalyst was evaluated for the synthesis of new imidodicarbonate diamide derivatives (biuret) under microwave conditions. The use of the microwave method led to the use of organic solvents in small amounts, reduced reaction times, and increased yields of products, which was achieved for the development of green chemistry and environmental protection. These biurets were evaluated for inhibitory activity on human immunodeficiency virus type 1 (HIV-1) by HIV-1 p24 antigen ELISA kit and three of them (5b, 5c, and 5f) had moderate activity on HIV -1 virus with IC50 values in the range of 55.1 to 100 μM compared to azidothymidine as the reference drug (IC50 = 0.11 μM). Finally, to investigate the mechanism of the effect of biuret compounds on the virus protease enzyme, docking analysis studies were performed and the results of in vitro test and docking study were in good correlation.

    Keywords: Green chemistry, microwave, Layered double hydroxides, Imidodicarbonic diamide, Anti-AIDS effect, Molecular docking}
  • علی روستایی*، محمد مهدوی، رضا حداد
    نقاط کربنی، نانوذرات شبه کروی هستند که نسبت به دگرشکلهای کربن (نانولوله های کربنی، کربن فعال، گرافنها و فولرنها) رفتار متفاوتی نشان میدهند و دارای ویژگی های اپتوالکترونیکی جالب و قابل توجهی هستند. نقاط کربنی به علت داشتن عناصر بی ضرر در ساختارشان (دوست دار محیط زیست)، سمیت پایین، حساسیت بالا و پایدار، پاسخ دهی سریع و قیمت ارزان نسبت به دیگر نانوذرات کوانتومی، توجهات بسیاری را به خود جلب نموده است. شرایط و روش سنتزی نقاط کربنی نقش اساسی در کیفیت آن ها داشته و باعث بهبود خواص محصول نهایی خواهد شد. در این پژوهش برای اولین بار، نقاط کربنی اصلاح شده با گروه های عاملی فعال در یک مرحله با استفاده از روش ریزموج سنتز می گردند. نقاط کربنی سنتز شده توسط تکنیک های دستگاهی مورد ارزیابی و بررسی قرار گرفت و وجود گروه های نیتروژن و اکسیژنی در سطح و ساختار کربن دات سنتز شده تایید گردید. این ترکیب دارای جذب پهن در محدوده 200 تا حدود 500 می باشد و همچنین دارای نشر در تهیج های مختلف با طول موج های نشر متفاوت می باشد. طول موج تهیج 365 نانومتر دارای نشر قوی در طول موج حدود 436 نانومتر می باشد. اندازه نقاط کربنی سنتز شده حدود 20 نانومتر است.
    کلید واژگان: اصلاح سطح, سنتز ریزموج, فلورسانس, نقاط کربنی}
    Ali Roostaie *, Mohammad Mahdavi, Reza Haddad
    Carbon dots are spherical nanoparticles that behave differently from other carbon allotropes (carbon nanotubes, activated carbon, graphenes, and fullerenes) and have interesting and significant optoelectronic properties. Carbon dots have attracted a lot of attention due to their harmless elements in their structure (environmentally friendly), low toxicity, high and stable sensitivity, fast response and cheap price compared to other quantum nanoparticles.Conditions and synthetic methods of carbon dots have an essential role in their quality and will improve the properties of the final product. In this study, for the first time, modified carbon dots with active functional groups are synthesized in one step using the microwave method. The synthesized carbon dot was evaluated by instrumental techniques and the presence of nitrogen and oxygen groups in the surface and structure of the synthesized carbon dot was confirmed. The excitation wavelength of 365 nm has a strong emission in the wavelength of about 436 nm. The size of the synthesized carbon dot is about 20 nanometers. Using devices such as UV-Vis, scanning electron microscope (SEM) and transient electron microscopy (TEM), the presence of gold nanoparticles synthesized by red apple peel extract was investigated.The results show that gold nanoparticles prepared using red apple peel extract have a size of 13-20 nm, spherical morphology and good dispersion that are stable for a long time.
    Keywords: Carbon dot, Microwave, Surface modification, Fluorescence, component ratio}
  • مهدیه محسن پور، حمید عمادی*، حمید گلچوبیان
    امروزه سوخت بیودیزل به عنوان یکی از منابع اصلی برای جایگزینی سوخت های فسیلی در حال تولید و مصرف در سراسر دنیا است. در این پژوهش از روی اکسید دوپه شده با کبالت به عنوان نانوکاتالیزگر برای تولید بیودیزل از روغن سویا به روش تبادل استری استفاده شده است. در ابتدا نانوکاتالیزگرهای مورد استفاده با روش مایکروویو تهیه شدند و به وسیله ی روش‎های پراش اشعه ایکس (XRD)، میکروسکوپ الکترونی روبشی (SEM) و طیف بینی انرژی پخش اشعه ایکس (EDS) شناسایی گردیدند. در مرحله بعد کاتالیزگرهای تهیه شده در واکنش تولید بیودیزل از روغن سویا مورد استفاده قرار گرفتند. بیودیزل تولید شده با استفاده از طیف سنجی رزونانس مغناطیسی هسته (NMR) و کروماتوگرافی گازی -طیف نگار جرمی (GC-MS) شناسایی شده است. شرایط بهینه واکنش تولید بیودیزل با نانوکاتالیزگر روی اکسید دوپه شده با کبالت، در زمان 3 ساعت، دمایC 60، غلظت کاتالیزگر 3% وزنی و نسبت مولی روغن به متانول 1 به 41 به درصد تبدیل 98%منجر شد. در بخش دیگری از این پژوهش، از تابش مایکروویو با توان 250 وات به عنوان منبع تامین انرژی در واکنش تولید بیودیزل استفاده گردید که در حضور 4% وزنی کاتالیزگر و نسبت مولی روغن به متانول 1 به 20 منجر به درصد تبدیل 91% در 180 ثانیه شد.
    کلید واژگان: بیودیزل, ترانس استری شدن, مایکروویو, نانوکاتالیزگر}
    Mahdieh Mohsenpour, Hamid Emadi *, Hamid Golchoubian
    Today, biodiesel is being produced and consumed around the world as one of the main sources for replacing fossil fuels. In current research, cobalt doped zinc oxide was used as nanocatalyst to produce biodiesel from soybean oil by transesterification reaction. The nanocatalysts used were first prepared by microwave method and identified by X-ray diffraction (XRD), scanning electron microscopy (SEM) and x-ray energy dispersive spectroscopy (EDS). In the next step, the prepared catalysts were used in the reaction of biodiesel production from soybean oil. The produced biodiesel was characterized using nuclear magnetic resonance spectroscopy (NMR) and gas chromatography-mass spectroscopy (GC-MS). Optimal reaction conditions of biodiesel production with cobalt doped zinc oxide nanocatalyst obtained, at 3 h, temperature 60 ˚C, catalyst concentration 3% by weight, and molar ratio of oil to methanol 1 to 41 resulted in 98% efficiency. In another part of this research, microwave radiation with a power of 250 W was used as a source of energy in the biodiesel production reaction which in the presence of 4% by weight of catalyst and molar ratio of oil to methanol 1 to 20 resulted in 91% efficiency in 180 s.
    Keywords: Biodiesel, transesterification, microwave, nanocatalyst}
  • Shyamali Wijekoon, Chinthika Gunasekara, Lalinda Palliyaguru, Neluka Fernando, Pradeep Jayaweera, Upul Kumarasinghe *
    A simple, efficient, and environmentally benign green approach was developed for the synthesis of 3-alkenyl oxindole derivatives with effective antifungal properties. The targeted compounds (3a-3g) were synthesized by using Knoevenagel condensation with oxindole and substituted aromatic aldehydes in the solvent-free, microwave-assisted reaction conditions. Silica extracted from rice husk waste was functionalized with (3-aminopropyl) triethoxysilane (APTES) to use as an eco-friendly, reusable, and solvent-free reaction medium. The structures of the final products were confirmed by their melting points, IR, 1H-NMR, 13C-NMR, and elemental analysis. The desired products were isolated with 72-88% yields in 12 minutes. The in vitro antimicrobial activity against ATCC standard cultures of human pathogenic Candida species, clinical isolates of Candida albicans, and several Gram-positive and Gram-negative bacteria were investigated and reported. All the synthesized 3-alkenyl oxindole derivatives exhibited the selective antifungal properties with the minimum inhibitory concentration (MIC) values ranging from 2 µg/mL to 125 µg/mL against tested Candida species. The findings of this study emphasized that green synthesized 3-alkenyl oxindole derivatives can be considered as the potential lead compounds to develop the effective antifungals against human pathogenic Candida species.
    Keywords: Microwave, Assisted Solvent, Free 3, Alkenyl Oxindole Derivatives Amino Functionalized Silica Antifungal Activity}
  • Sajid Maksad Radhi *, Ban Hasan Taresh, Nesser Kadham Shareef, Luma Majeed Ahmed
    In this study, two different methods were described for the synthesis of 2-(aryl)-3-((2-oxo-2-(2-oxo-2H-chromen-3-yl)ethyl)amino)imidazolidin-4-one derivatives under microwave irradiation. The first method was step by step method. In step by step method, 3-(2-hydrazinylacetyl)-2H-chromen-2-one and aromatic aldehydes in 1 mL of absolute ethanol were irradiated with appropriate power within 3-10 min to obtain imine products. Then, the imine products were isolated and reacted with glycine to produce the 2-(aryl)-3-((2-oxo-2-(2-oxo-2H-chromen-3-yl)ethyl)amino)imidazolidin-4-one under microwave irradiation. In the one-pot method, the graphene oxide nanosheets were applied as heterogeneous catalysts. Hence, the graphene oxide nanosheets were synthesized based on Hummer’s method. The catalyst was characterized by field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, and X-ray diffraction (XRD) techniques. Then, 3-(2-hydrazinylacetyl)-2H-chromen-2-one, glycine, and aromatic aldehydes were irradiated using microwave irradiation in the presence of 0.5 mol% of graphene oxide nanosheets in ethanol. The prepared catalyst showed superior reusability for seven catalytic cycles. Our results showed that the one-pot method was better than the step by step method.
    Keywords: Graphene oxide, One-pot, imidazolidine, Microwave, Synthesis, catalyst}
  • Fazal- Rehman, Shahid Adeel *, Memoona Pervaiz, Aminoddin Haji, Wafa Haddar, Muhammad Hussaan, Nimra Amin, Ahlem Guesmi
    Green technologies in isolation and extraction of natural products have always been welcomed due to awareness about environmental standards for global health. The current research was performed to use microwave energy to extract natural dyes from lac insects and their application onto nylon fabric. For isolation of natural dye from lac insect in acidic and acidified methanolic media Mw irradiation for 3, 5, and 7 min. has been given and used to dye nylon fabric. Bio-mordants from herbal-based sources such as Acacia and Turmeric were also employed to develop new shades and to improve fastness properties in comparison with metallic salts of Al (Alum) and Fe (ferrous sulfate). The evidence from this study suggests an increase in color yield (K/S) with the use of 5 min. of microwave energy when acid solubilized extract of lac insect was used to dye onto nylon fabric. It has been demonstrated also that in the case of the pre-mordanting method, 5% of Acacia and 1% of Turmeric give the best fastness properties and the highest color yields.  It is concluded that Microwave energy has an excellent efficacy to isolate the colorant, whereas the addition of bio-mordants has made the process more sustainable and greener.
    Keywords: Acacia, Alum, Iron sulfate, Lac dye, Microwave, Nylon, Sustainability, Turmeric}
  • Indah Raya, Gunawan Widjaja, Kadda HACHEM, Rodin M.N., A. Ali Ahmed, Mustafa M. Kadhim, Yasser Mustafa, Zaid Mahmood, Surendar Aravindhan
    In this research, MnCo2O4/Co3O4 nanocomposites were prepared via simple and fast microwave method. The effect of irradiation power and irradiation type (continuous and non-continuous irradiation) on crystalline structure, purity, size and morphological properties of products were investigated via X-ray diffraction (XRD) analysis, energy dispersive spectroscopy (EDS), Transmission Electron Microscopy (TEM), FT-IR and Scanning Electron Microscopy (SEM) respectively. Results revealed that shape and morphological properties of MnCo2O4/Co3O4 nanocomposites can be affected via power and time of microwave irradiation. In the next step, prepared nanocomposites were applied for photodegradation of rhodamine B and methyl violet as organic pollutants. Findings demonstrated that MnCo2O4/Co3O4 nanocomposites can degrade rhodamine B and methyl violet via 58% and 61% efficiency.Transition-metal oxides based nanocomposites exhibit novel properties that significantly have different physical and chemical properties than those matrix material and the filler resulting [1-4]. In other hand, nanocomposites have a unique and attractive properties due to small size effect [5, 6]. Magnetic nanocomposites not only have unique size-dependent properties but also get benefits from interesting magnetic properties.
    Keywords: MnCo2O4, Co3O4, Nanocomposites, Photocatalysis, Microwave}
  • Ali Reza Maleki, Leila Nateghi *, Peyman Rajai

    Microwave energy is non-ionizing radiation that causes the molecule to move and is a good way to extract compounds from plant extracts. This study aimed to investigate the effect of three independent variables including solvent type (water and methanol 80%), time (3, 6, and 9 minutes), and microwave power (100, 200, and 300 watts) on the flavonoids, anthocyanins, antioxidant properties (IC50) of the Persian Golnar plant or Punica granatum var. pleniflora (PGP) extract. According to results, simultaneous optimization of extraction conditions with 95.609% desirability in 300-watt microwave power, 9 minutes, and use of methanol solvent the flavonoid content was 5.7597 mg /g, anthocyanin content was 4.7983 µmol/g, and IC50 value was 6.5063 mg/ml. The highest average of minimum inhibitory concentration and minimum Bactericidal concentration of PGP extract were 1250 and 5000 µg/ml, respectively against Clostridium perfringens and Escherichia coli, and the better antimicrobial effect was against Staphylococcus aureus with the highest diameter of zone of inhibition (11 mm) compared to Escherichia and Clostridium perfringens. According to the results of this study, microwave pretreatment with optimized conditions can be used to extract significant amounts of phenolic and antimicrobial compounds of PGP extract as a rich source of antioxidants with minimal damage to its effective compounds.

    Keywords: Anthocyanin, Antioxidant, Flavonoid, Microwave, Punica granatum var. pleniflora}
  • Susan Sarvarian, Mehdi Zamani *, Seied Ali Pourmousavi
    In this research, the controllable synthesis of carbon nanotubes (CNTs) functionalized with derivatives of diazonium salts containing -NO2 was carried out under mild and more efficient conditions (i.e. lower reaction temperature, shorter reaction time, assisting microwave and using radical scavenger) to study the morphology of these compounds before and after functionalization. For this purpose, the reactions of single-walled (SWCNT) and multi-walled (MWCNT) carbon nanotubes with 2-nitroaniline, 4-nitroaniline and 2,4-dinitroaniline in the presence of isoamyl nitrite as diazotization agent were performed at different conditions (i.e. solvent free, in dimethylformamide (DMF) solvent, thermal and microwave). The nitroaryl functionalized CNTs were characterized by X-ray diffraction (XRD) measurement, field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, ultraviolet-visible (UV-Vis) spectroscopy, energy dispersive X-ray (EDX) technique and elemental map analysis. The results clearly confirmed the successful controllable functionalization of CNTs by nitroaryl diazonium ions without any byproducts. The morphology of CNTs after functionalization is tubular. Functionalization of SWCNT by nitroaryl diazonium ions improves the crystallinity of starting material; while the crystallinity of MWCNT decreases with functionalization. The samples synthesized under microwave are more amorphous than samples synthesized under thermal conditions.
    Keywords: Carbon Nanotube, Diazonium, Thermal, Microwave, morphology, Radical scavenger}
  • لیلا کافی احمدی*، شاهین خادمی نیا، رژین اسمعیلی
    2-آمینو-H4- کرومن ها دسته مهمی از ترکیب های هتروسیکل می باشند که در شیمی آلی و پزشکی از اهمیت فراوانی برخوردارند. این ترکیبات دارای خواصی همچون خواص ضد سرطانی ، ضد باکتری ، ضد انعقادی و ضد توموری بوده و در تهیه مواد آرایشی ، بهداشتی و مواد رنگی کاربرد دارند. تاکنون روش های متنوعی برای سنتز این ترکیبات ارایه شده است که اکثر این روش ها معایبی نظیر استفاده از حلال های سمی و فرار، راندمان پایین، زمان واکنشی طولانی و عدم بازیافت کاتالیست را به همراه دارند. در این کار پژوهشی پیروکلر Sr2As2O7 به عنوان یک کاتالیست موثر در سنتز 2-آمینو-4Hکرومن ها از طریق واکنش سه جزیی و تک ظرفی آلدهیدهای آروماتیک، مالونونیتریل و بتا نفتول با استفاده از تابش مایکروویو به کار گرفته شده است. ابتدا این کاتالیست با استفاده از روش سولوترمال در حلال آب و اتانول به نسبت 1:1 همراه با اولتراسونیک، به آسانی تهیه شده و توسط تکنیک های PXRD ، FESEM و FTIR مورد شناسایی قرار گرفت. سپس قابلیت کاتالیستی این ترکیب در سنتز مشتقات 2-آمینو-4H کرومن مورد مطالعه قرار گرفت. برای انجام واکنش ابتدا شرایط واکنش نظیر، زمان انجام واکنش، نوع حلال و مقدار کاتالیست بهینه گردیده و واکنش ها تحت شرایط بهینه انجام شدند . مشخص گردید که شرایط بهینه 15 میلی گرم کاتالیست، حلال آب و 9- 6 دقیقه زمان انجام واکنش می باشد.
    کلید واژگان: 2-آمینو- 4H - کرومن ها, استرانسیوم پیرو آرسنات, مایکروویو}
    Leila Kafi-Ahmadi *, Shahin Khademinia, Rozhin Esmaeili
    2-Amino-4H-chromene compounds are belonged to an important heterocyclic groups that have extensive important in organic chemistry and medicine. The compounds have anti-cancer, anti-bacterial, anti-coagulation and anti-tumor properties and have applications to produce dye, make up and hygienic materials. Until know, several methods have been reported for the synthesis of the compounds. Most of them, suffers defects such as poisoning and volatile solvents, low yield, high length reaction time, and no reusability of used catalyst. In the present work, Sr2As2O7 pyrochlore material was used as a catalyst for the synthesis of 2-amino-4H-cromens derivatives using a three component one-pot synthesis method under microwave irradiation. The raw materials were aromatic aldehydes, malononitrile and beta-naphtol. Sr2As2O7 was synthesized by an ultrasonic assisted solvothermal method using H2O and C2H5OH solvents mixtures at the 1:1 volumetric ratio. The materials were characterized by PXRD, FESEM and FTIR techniques. Then, the catalytic performance of the synthesized nanomaterial was used for the synthesis of 2-amino-4H-chromene derivatives. To do the process, the reaction parameters such as reaction time, solvent type and catalyst amount were optimized and the reactions were performed under the conditions. It was found that the optimum conditions were 15 mg catalyst, H2O as solvent and 6-9 min reaction time.
    Keywords: 2-amino-4H-chromene derivatives, Strontium pyroarsenate, microwave}
  • H. Shahbazi Alavi *, J. Safaei Ghomi

    Bis (1(3-trimethoxysilylpropyl)-3-methyl-imidazolium) copper tetrachloride tethered to colloidal silica nanoparticles have been used as an efficient catalyst for the preparation of 2,4-diamino-6-arylpyrimidine-5-carbonitrile derivatives by the one-pot reaction of aromatic aldehydes, malononitrile, and guanidinehydrochlorideunder conventional heating, microwave and ultrasound irradiations. The catalyst was characterized by 1H NMR spectroscopy,dynamic light scattering (DLS), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and thermogravimetric analysis (TGA). The remarkable advantages of this methodology are easy work-up, short reaction times, high to excellent product yields, operational simplicity, low catalyst loading and use of ultrasonic irradiation as a valuable and powerful technology.

    Keywords: Pyrimidine, Heterogeneous catalyst, Ionic liquid, Colloidal silica nanoparticles, Microwave, ‎Ultrasound irradiation.‎}
  • Sylvia Devi Henam *, Farooq Ahmad Dar, Ashaq Hussian Sofi, Seemim Rubab, Shazia Parveen, Abdul Hamid Wani, Mohammad Ashraf Shah
    Microwave heating has been adopted as green approach for the synthesis of bohmite (AlO(OH)) and brucite (Mg(OH)2) nanoparticles (NPs) for antifungal activity. The synthesis of AlO(OH) and Mg(OH)2 NPs were carried out at 150 °C and the resulting NPs have an average diameter of 10-20 nm. The Mg(OH)2 and AlO(OH)  have trigonal and orthorhombic crystal structure, respectively. The antifungal activity of the synthesized NPs was assessed using the Penicillium Expansum (P. expansum) through agar well diffusion method. The Mg(OH)2 and AlO(OH) revealed comparable significant antifungal activities towards P. expansum. About 79% and 74% reduction in the growth of the fungus was obtained respectively of AlO(OH) and Mg(OH)2 as compared to the standard control haxahit. Nanomaterials bind on the surface of the fungi thereby preventing the normal activity of fungi and inhibit their growth, ultimately kill them. Reported NPs have significant potential to replace expensive nanomaterials in the field of antimicrobial studies.
    Keywords: Green synthesis, Microwave, Nanoparticles, Antifungal activity}
  • سوسن منصوری، محمدرضا فدوی اسلام*

    در این پژوهش نانوذرات نیم رسانای اکسیدقلع آلاییده با آهن با نسبت مولی آهن به قلع 0، 1، 2 و 3 درصد به روش مایکروویو سنتز شدند. ساختار بلوری، ریخت شناسی سطح، پیوندهای شیمیایی و ویژگی های نوری نمونه ها به وسیله پراش سنج پرتوایکس (XRD)، میکروسکوپ الکترونی روبشی اثر میدان (FESEM)، طیف سنج تبدیل فوریه فروسرخ (FTIR) و طیف سنجی (UV-vis) مطالعه شده است. آنالیز عنصرها به وسیله طیف سنجی پراکندگی انرژی پرتوایکس (EDAX) انجام شد. نتیجه های پراش پرتوایکس نشان داد که نمونه ها بس بلور بوده و دارای قله های ارجح مربوط به صفحات (110)، (101)، (200)، (211)، (220)، (002)، (310)، (112) و (301) فاز SnO 2 با ساختار چهارگوشه روتیل هستند. افزایش تراکم ناخالصی آهن از صفر به سه درصد، سبب کاهش اندازه متوسط نانوبلورک ها از 53 / 23 به nm 03 / 11، کاهش اندازه دانه ها از 37 به nm 28 و افزایش حجم سلول واحد از 61 / 70 به  40 / 71 و گاف نوری از 13 / 3 به eV 2 / 4 می شود. نتیجه های آنالیز FTIR پیوند SnO 2 را در نمونه ها تایید می کند. بررسی ویژگی های حس گری گاز اتانول به وسیله نمونه ها نشان داد که زمان پاسخ حس گرها در گستره 75 / 15 تا s 85 / 38 هست. حس گر ساخته شده با نانوذرات با تراکم یک درصد آهن شرایط بهینه حس گری را از خود نشان داد.

    کلید واژگان: نانوذرات اکسیدقلع, ناخالصی آهن, مایکروویو, حس گری گازی, اتانول}
    Soosan Mansoori, Mohammadreza Fadavieslam *

    In this study, iron-doped tin oxide semiconductor nanoparticles with an iron to tin mole ratio of 0, 1, 2 and 3% synthesized by microwave method. The crystal structure, surface morphology, chemical bonds, and optical properties of the samples were studied by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), infrared fourier transform spectroscopy (FTIR), and UV–Vis spectroscopy. Elements analysis was performed by EDAX. The X-ray diffraction results showed that the samples were polycrystalline, and have the preferred peaks of plates (110), (101), (200), (211), (220), (002), (310), (112), and (301) SnO2 phase with rutile rectangular structure. Increasing the iron impurity density from zero to three percent causes the reducing average size of nanocrystals from 23.53 to 11.03 nm, reducing grain size from 37 to 28 nm, and increasing unit cell volume from 70.61 to 71.40  and the optical band gap from 3.3 to 4.2 eV. The results of FTIR analysis confirm the SnO2 bond in the samples. Investigation of the sensing properties of ethanol gas by the samples showed that the response time of the sensors is in the range of 15.75 to 38.85 s. The sensor made with nanoparticles with a concentration of 1% iron exhibited optimum sensing conditions.

    Keywords: Tin Oxide Nanoparticles, Iron Impurity, Microwave, Gas sensor, Ethanol}
  • Taher Shahi, Ali Zonouzi, Babak Beheshti *, Morteza Almasi
    The present study attempts to investigate Solvent Extraction (SE), Ultrasonic Assisted Extraction (UAE), Microwave Assisted Extraction (MAE), and acid treatment lipid extraction (ATLE) methods for the extraction of oil from Dunaliella Sp. In doing so, the results showed that UAE, MAE, and ATLE led to an increase in lipid extraction compared to SE. The extracted lipid using MAE (with 17.83 % extraction efficiency) was significantly higher than UAE (14.5 %) and SE (9.16 %) methods. However, considering the energy aspects, ATLE method (17.06%) by omitting the algal biomass drying process and directly extracting lipid from wet biomass could be introduced as an effective method for lipid extraction and biodiesel production process from Dunaliella Sp cells. The fatty acid profile of extracted oil from different methods showed that the extraction method has not a significant effect on the fatty acid composition of the oil. Also, the produced biodiesel properties were according to ASTM standards.
    Keywords: microalgae, Oil extraction, Ultrasonic, Microwave, Acid treatment, Efficiency}
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