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عضویت

جستجوی مقالات مرتبط با کلیدواژه « degradation » در نشریات گروه « پزشکی »

  • Zihao Lu, Shuwen Li, Rui Wei, Wenwen Li, Yuqian Huang, Tingting Yang, Meng Yan *
    Objective (s)

    Quercetin is a plant flavonoid known for its pharmacological activities, such as antioxidant, anti-inflammatory, and anti-cancer properties. However, there is limited information available regarding its potential toxicities. A previous study showed that quercetin can inhibit human ether-a-go-related gene (hERG, also named KCNH2) currents, which may lead to long QT syndrome, torsade de pointes (TdP), and even sudden cardiac death. This study aimed to investigate the effects of quercetin on hERG and its potential mechanism.

    Materials and Methods

    hERG currents and action potential duration (APD) were assessed using the patch clamp technique. Molecular docking was employed to elucidate the binding sites between quercetin and hERG. Transfection of wild-type or mutant plasmids was used to verify the results of molecular docking. Western blot was performed to determine the expression levels of hERG, transcription factor SP1, molecular chaperones HSP70 and HSP90, phosphorylated E3 ubiquitin ligase p-Nedd4-2, serum- and glucocorticoid-inducible kinase (SGK1), and phosphatidylinositol 3-kinase (PI3K). Immunoprecipitation was conducted to evaluate hERG ubiquitination.

    Results

    Quercetin acutely blocked hERG current by binding to F656 amino acid residue, subsequently accelerating channel inactivation. Long-term incubation of quercetin accelerates Nedd4-2-mediated ubiquitination degradation of hERG channels by inhibiting the PI3K/SGK1 signaling pathway. Moreover, the APD of human induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs) is significantly prolonged by 30 μM quercetin.

    Conclusion

    Quercetin has a potential risk of proarrhythmia, which provided useful information for the usage and development of quercetin as a medication.

    Keywords: Degradation, KCNH2, Long QT Syndrome, Nedd4, Ubiquitination}
  • Ehsan Beigi Baktash, Negar Motakef-Kazemi, Sepideh Hamedi
    Objective (s)

    In this work, silver nanoparticles (Ag NPs) were synthesized by green tea plant extract as an easy, cost-effective, environmentally friendly, and reliable synthesis. The silver nanocomposite with different amounts of starch (0.5, 1, 1.5 g) were prepared. Then, the methylene blue (MB) dye degradation and the antibacterial activity of the nanocomposite were evaluated as an environmental challenge.

    Methods

    The samples were characterized using scanning electron microscope (SEM) for observation size and morphology, energy dispersive X-ray analysis (EDX) for determination elemental analysis, Fourier transform infrared spectroscopy (FTIR) for investigation functional groups, and X-ray diffraction analysis (XRD) for confirmation crystalline structure.  The catalytic properties of the synthesized samples were studied in MB degradation. 

    Results

    The maximum degradation (more than 90%) was related to Ag NP with 0.5 g of starch. The antibacterial activity of Ag NPs and nanocomposites was investigated against Staphylococcus aureus (S. aureus) as Gram-positive and Pseudomonas aeruginosa (P. aeruginosa) as Gram-negative bacteria. The samples indicated inhibitory activity with suitable inhibition zone and were more effective against S. aureus as compared to P. aeruginosa. 

    Conclusions

    In general, the green synthesis of Ag NP-starch has good catalytic potential in MB degradation in an aqueous medium in a short time with high efficiency.

    Keywords: Antibacterial activity, Degradation, Green synthesis, MB, Ag NPs, Starch}
  • Anosheh ZargarKharazi Emad Hosseini, Amir Shafaat, MohammadHoseinFathi
    Background

    Metal screws are commonly used for fracture fixations. However, the high modulus of elasticity relative to bones and releasing metallic ions by the metal screw needed a second surgery to remove the implant after the healing period. Furthermore, the removal of metal screws following the healing of the bone is a serious problem that can lead to refracture due to the presence of holes in the screw. Bioresorbable screws can overcome most of the problems associated with metallic screws which motivated research on manufacturing nonmetallic screws.

    Methods

    In this study, three‑layer poly L‑lactic acid/bioactive glass composite screws were manufactured according to functionally graded material theory, by the forging process. All of the physical and chemical parameters in the manufacturing stages from making composite layers to the forging process were optimized to obtain suitable mechanical properties and durability off the screw in load‑bearing positions.

    Results

    The tri‑layer composite screw with unidirectional, ±20° angled, and random fibers orientation from core to shell shows a flexural load of 661.5 ± 20.3 (N) with a decrease about 31% after 4‑week degradation. Furthermore, its pull‑out force was 1.8 ± 0.1 (N) which is considerably more than the degradable polymeric screws. Moreover, the integrity of the composite screws was maintained during the degradation process.

    Conclusions

    By optimizing the manufacturing process and composition of the composite and crystallinity, mechanical properties (flexural, torsion, and pull‑out) were improved and making it a perfect candidate for load‑bearing applications in orthopedic implants. Improving the fiber/matrix interface through the use of a coupling agent was also considered to preserve the initial mechanical properties. The manufactured screw is sufficiently robust enough to replace metals for orthopedic load‑bearing applications.

    Keywords: Composite screw, degradation, flexural strength, forging, mechanical property}
  • Parishan Mohammed, Kambiz Seyyedi *
    Background
    Aniline-based organic nanocomposites have a significant performance as photocatalysts in the advanced oxidation process (AOP).
    Methods
    In this study, polyaniline-tin dioxide (PA/SnO2) nanocomposite was prepared using an ultrasonic process. Next, its efficiency as a photocatalyst in the removal of Cefixime antibiotic pollutant from contaminated waters in a tubular photo reactor was investigated. The experiments were designed by the response surface methodology (RSM) via Minitab software, in such a way that the effects of various parameters on the process are investigated. The effect of different parameters such as reaction time, solution pH, flow rate, antibiotic concentration and hydrogen peroxide concentration on the removal efficiency was investigated.
    Results
    According to the results, the following optimal conditions were obtained: time of 120 min, pH of 8.69, hydrogen peroxide concentration of 4.22 mM, flow rate of 1.25 L/min and initial antibiotic concentration of 22.92 mg/L. Under the above-mentioned optimal conditions, the efficiency of Cefixime removal was more than 72.24%.
    Conclusion
    The present study confirms the usability of the PA/SnO2 nanocomposite as a novel and effective photocatalyst for photocatalytic degradation of Cefixime antibiotic in contaminated water under UV light.
    Keywords: degradation, Cefixime antibiotic, Photocatalytic Process, Polyaniline PA, SnO2 nanocomposite, tubular photo reactor, optimization, RSM}
  • Rajni Lasyal *, Shakunj Rajput
    In this study, the degradation of azo-dye acid orange 10 has been investigated using Polyvinylpyrrolidone and Brij-35 stabilized iridium oxide nanoclusters as catalysts. Simple chemical reduction method was used to synthesize the above-mentioned nanoclusters. The characteristics of the nanocatalysts were determined by UV-visible spectrophotometer, TEM and XRD. The kinetic study has been carried out at λmax of reaction mixture i.e. 479 nm spectrophotometrically. The degradation follows first order kinetics with respect to oxidant and catalyst concentration while order is one at lower substrate concentration tending towards zero at higher concentration. The degradation kinetics has been supported by the derived rate law. The results showed that Polyvinylpyrrolidone stabilized iridium oxide nanoclusters outperformed Brij-35 stabilized iridium oxide nanoclusters, exhibiting the fastest degradation rate. The progress of the degradation process was monitored by UV-vis spectroscopy. Using Polyvinylpyrrolidone stabilized iridium oxide nanoclusters as a catalyst is a very promising approach for the remediation of acid orange 10 due to the fast degradation rate and high degradation efficiency. In addition, Polyvinylpyrrolidone stabilized iridium oxide nanoclusters can be easily recovered and recycled for three consecutive cycles. It can be inferred from this study that catalytic oxidation methods are active and environment-friendly for the remediation of dyes.
    Keywords: Degradation, Kinetics, Rate law, Acid orange10}
  • Pedram Javidi, Nazanin Bashardoust, Aye Shekarbaghani
    Background

    Different studies about the effects of mouthwashes on force reduction by elastomeric chains are reported in the literature. Hence, this review was done for the assessment of force degradation in the elastomeric chains in different mouthwash compositions. This study helps to improve the clinical performance of elastomeric chains used in orthodontics, reducing force degradation, and finally assisting clinicians in choosing better and more efficient methods for their treatments.

    Materials and Methods

    In this review article, an extensive search was performed in the electronic databases of Cochrane Library, Web of Science, PubMed, and Scopus from the year 1990–2020. No language restriction was considered and manually investigated the reference lists of all articles related to the title. Out of 450 obtained articles, 14 in vitro studies were chosen based on the inclusion criteria, and their quality was assessed using modified CONSORT. This systematic review was limited and written based on the Preferred Reporting Items for Systematic Reviews and Meta‑Analyses protocol.

    Results

    Based on the results achieved, mouthwashes containing alcohol caused considerable force degradation in the elastomeric chains compared to the alcohol‑free ones and mouthwashes with fluoride caused lesser force degradation compared to other types.

    Keywords: Degradation, elastomeric, environment, mouthwash}
  • Maryam Dolatabadi, Akram Ghorbanian, Saeid Ahmadzadeh*
    Introduction

    Perchloroethylene (PCE) is one of the most well-known chlorinated organic compounds recently detected in aqueous environments. The presence of PCE in aquatic ecosystems has caused many health problems and environmental challenges. Therefore, its removal and treatment from aqueous environments are essential.

    Materials and Methods

    The electro-Fenton (EF) process was carried out in a cylindrical reactor containing 250 mL contaminated water with PCE. The effects of parameters, including solution pH (3-12), current density (2-10 mA cm-2), H2O2 concentration (20-70 µL H2O2 per 250 mL sample.), PCE concentration (5-50 mg L-1), and electrolysis time (1-15 min) on PCE degradation were investigated. The kinetics and radical’s scavenger of the EF process were examined to detect the exact mechanism of PCE degradation.

    Results

    The degradation of the PCE of 98.1% was obtained in the optimum condition, including solution pH of 5, the current density of 8 mA cm-2, H2O2 concentration of 50 µL per 250 mL sample, PCE concentration of 15 mg L-1, and electrolysis time of 10 min. The kinetics studies of the EF process indicated that the obtained results were in satisfactory agreement with the first-order model (R2 = 0.9858, Kapp = 0.2822). Also, the addition of ethanol and tertiary butanol caused an inhibiting effect.

    Conclusion

    The EF process was effectively applied to degrade PCE from polluted water as an efficient technique.  The obtained results indicated that the generation of •OH throughout the EF process was the key mechanism that controlled the EF process.

    Keywords: Aqueous Solution, Degradation, Electro-Fenton Process, Hydroxyl Radical, Perchloroethylene}
  • Mona Nabizad, Ahmad Dadvand Koohi *, Zahra Erfanipour

    In this study, alginate, magnetite, and hydroxyapatite were used to fabricate alginate-hydroxyapatite (Alg-Hap), alginate-Fe3O4 (Alg-Fe3O4), and alginate-magnetic hydroxyapatite (Alg-mHap) using ferric chloride (III) crosslinker to remove cefixime from an aqueous solution. FTIR, SEM, VSM, BET, and XRD tests were used to determine the functional groups, morphology, magnetization behavior, surface area, and crystallinity of catalysts, respectively. The optimal pH for the Fenton reaction was determined to be 3.3 for Alg-Hap and Alg-Fe3O4 catalysts and 4 for Alg-mHap catalysts. Increases in the concentration of hydrogen peroxide (1 to 3 mM) and the amount of catalyst (50 to 90 gr/L) increased the percentage of degradation to approximately 8% and 6%, respectively. The degradation efficiency of cefixime by using Alg-mHap as the best catalyst in the Fenton process was achieved 91%, at optimum condition (pH of 4, catalyst amount of 90 gr/L, initial cefixime concentration of 5 mg/L, H2O2 concentration of 3 mM within 90 min). Moreover, the second-order kinetic equation fits the experimental data for cefixime degradation for all three catalysts. Furthermore, not only did the catalysts display a negligible iron leaching (0.92 mg/L for Alg-mHap) but also after three consecutive cycles, the catalysts indicated long-term stability. Comparison between synthesized catalysts and other methods proved its effectiveness.

    Keywords: Alginate, Heterogeneous catalysts, Fenton, Degradation, Mechanism}
  • Seyed Jamshid Moosavi, Abdolrahim Pazira, Tayebeh Tabatabaie *, Neematollah Jaafarzadeh, Sahand Jorf

    According to the results obtained thus far, ozone/magnetic copper ferrite nanoparticles (CuFe2O4 MNPs)/potassium hydrogen monopersulfate (KMPS) is capable of totally degrading 20 mg/L diazinon (DZN) with 6 mg/L ozone, 0.6 g/L KMPS, and 0.1 g/L MNPs at pH = 7 in 20 min. The experiments showed that the concentrations of KMPS and MNPs were more effective than ozone on the system efficiency. Moreover, high concentrations of KMPS and MNPs were not very effective in DZN degradation. Furthermore, the degradation efficiencies of diazinon at pHs 3, 4, 5, 6, 7, 8, 9, and 10 were 94%, 95.35%, 97.45%, 98.15%, 99.2%, 99.3%, 99.3%, and 100%, respectively. The pH of the solution was effective on the system so that in the range of 7 - 10, the system had high efficiency. Even within the range of 3 - 6, the pH had not been so plummeted, resulting in a high percentage of DZN degradation. Besides, MNPs could be utilized in the system for up to five cycles without any loss of catalytic activity. The degradation efficiency of diazinon was 99.2% in the first use and 92.1% in the fifth use. Also, the process efficiency was assessed in four real environments showing that agricultural drainage and urban wastewater with the degradation percentages of 79.1% and 77.3%, respectively, were better treated than the urban and river water with the percentages of 93% and 88.4%, respectively. With the determination of active agents in the reaction using the scavenging agents, it was recognized that sulfate radicals, hydroxyl radicals, superoxide, and singlet oxygen contributed to DZN degradation. By the way, ozone was advantageous to both singlet oxygen and superoxide in the degradation of diazinon.

    Keywords: Advanced Oxidation Processes, Magnetic Nanoparticles, Degradation, Diazinon}
  • Asghar Sadeghabadi, Seyed Khatiboleslam Sadrnezhaad *, Azadeh Asefnejad, Nahid Hassanzadeh Nemati
    Objective (s)

    Bioresorbable scaffolds have been advocated as the new generation in interventional cardiology because they could provide temporary scaffolds and then disappear with resorption. Although, the available stents in clinical trials exhibited biosafety, efficacy, no death, and no apparent thrombosis, Mg-substrate degradation on drug release has not been investigated.

    Materials and Methods

    Therefore, more research has been needed to legitimize the replacement of current stents with Mg-based stents. UV-Vis spectrophotometer, scanning electron microscope (SEM), X-ray diffraction (XRD), pH measurement, H₂ evolution, and corrosion tests determined the change in hybrid properties and drug release rate. 

    Results

    The effect of Mg degradation on drug release from poly-L-lactide (PLLA) specimen was much higher than that of the L605/PLLA sample. Hydrogen evolution caused by magnesium degradation compelled everolimus out without significant PLLA decomposition during the first 100 days, while formation of Mg(OH)2 caused the PLLA to deform and crack. 

    Conclusion

    A combined mechanism of lattice/hole diffusion-dissolution governed the release of everolimus with the activation energies of 5.409 kJ/mol and 4.936 kJ/mol for the first 24 hr and diffusion coefficients 6.06×10-10 and 3.64×10-11cm2/s for the 50th to 100th days. Prolonged suppression of hyperplasia within the smooth muscle cells by hybrid stent insertion could bring about the cessation of restenosis.

    Keywords: Coronary Stent, Degradation, Diffusion, Drug Delivery, Nano-hybrid}
  • Farhad Mahmoodi, Reza Jalilzadeh Yengejeh, Farhang Tirgir *, Mehraban Sadeghi
    Background

    The 1-Naphthol, one of the derivatives of naphthalene, is the most significant industrial chemical that is widely used in the production of dyes, pharmaceuticals, and biochemical processes.

    Methods

    In the present study, N, S-doped TiO2 thin film immobilized on silica sulfuric acid (SSA) glass microspheres (MS) was investigated as a novel high efficient photocatalyst. The N, S-doped TiO2 immobilized on SSA was fabricated using a simple modified sol–gel process. Its photocatalytic activities were then assessed using 1-naphthol solution in the presence of visible light. The physico-chemical properties of photocatalyst were characterized using energy-dispersive X-ray (EDX), scanning electron microscope (SEM) images and X-ray diffraction (XRD) pattern.

    Results

    According to the obtained results, the optimal pH, time, concentration, and removal efficiency of 1-naphthol for N, S-doped TiO2 /SSA was 5, 50 minutes, 25mg/l and 92.12%.

    Conclusion

    The present study confirms the usability of the immobilized N, S-doped TiO2 on SSA glass MS as a novel, effective, and efficient technique for treatment of wastewater containing 1-naphthol under visible light.

    Keywords: Water Pollution, TiO2, photo catalytic, degradation, 1-Naphthol}
  • Haneef Ur Rehman, *, AbdulHameed Baloch, Muhammad Asif Nawaz

    Pectinase or pectinolyticenzyme is a complex enzyme with different catalytic units including polygalacturonase, pectin esterase and pectin lyase to degrade pectin polymers into different end products. The pectinase with degrading capability of pectin can be utilized in various industrial applications, such as clarification of fruits and vegetable juices, degumming of plant bast fibers, textile industries for removing non-cellulosic impurities, papermaking industries, wine clarification, coffee and tea fermentation, wastewater treatment, as well as, it is also used for the isolation of protoplasm in plant science research. Pectin derived oligosaccharides (POS) produced by pectinase are considered as prebiotic molecules. However, the low operational stability in harsh industrial conditions confines the utilization of pectinase in industrial processes. Immobilization is the technique, which not only enhanced the stability of pectinase, but also, made the enzyme reusable for continuous industrial processes. The current review shares information about the pectinase and how the immobilization technology can enhance the industrial application of pectinase. Furthermore, various supports such as sodium alginate, agar-agar, polyacrylamide, aminated silica gel, nanocomposite microspheres, silica coated chitosan, nylon-6, porous glass etc. have been tested for the immobilization of pectinase through different methods, including entrapment, binding to a support and enzyme crosslinking.

    Keywords: Degradation, Enzyme, Immobilization, Pectin, Pectinase}
  • Mahdieh Chegeni *, Mozhgan Mehri, Mehdi Hosseini
    The MoS2/S-doped graphitic carbon nitride (MoS2/S-g-C3N4) was synthesized by a simple method and applied for methylene blue (MB) removal as an organic pollutant. The structure of MoS2/S-doped graphitic carbon nitride was characterized using FTIR, XRD, SEM, TGA and BET techniques. The accomplishment of MoS2/S-doped graphitic carbon nitride as an adsorbent was investigated to removal of MB from aqueous solution. The various parameters were studied such as: pH, initial MB concentration, adsorbent dose, temperature and time. The best findings were obtained at pH=8, 8 ppm MB concentration, 0.05 g MoS2/S-g-C3N4, 30 min and 22 ˚C. The Langmuir isotherm model was adopted with the obtained data. The kinetic studies were showed that the adsorption of methylene blue can be well described by the second-order equation. Maximum adsorption was calculated as 166 mg/g. The degradation of MB was studied by MoS2/S-doped graphitic carbon nitride under Light Emmition Diode (LED). Results showed that the MoS2/S-doped graphitic carbon nitride can enhance photocatalytic activity compared to pure g-C3N4 and MoS2/g-C3N4. The findings confirmed that the MoS2/S-doped graphitic carbon nitride can be applied as an efficient, low-cost adsorbent, and photocatalyst to remove of cationic dyes such as methylene blue.
    Keywords: MoS2, S-doped graphitic carbon nitride, Adsorption, Methylene blue, Degradation}
  • MuhammadShamim Al Mamun *, Md. Israil Hossain, Jannatul Naime, Palash Dhar

    Comparing to the chemical and physical techniques, biosynthesis of nanoparticles is being facilitated due to its nontoxic and economically feasible availability. In this present study, plant-mediated silver nanoparticles (AgNPs) were synthesized using the fruit extract of Sonneratia apetala from the silver nitrate (AgNO3) solution. Among different physiological conditions, effect of reaction time was investigated during the AgNPs synthesis. Surface Plasmon Resonance (SPR) characterization was conducted for verifying the nanoparticles size and morphology. A distinct band centered around 400-480 nm in the UV-Visible spectroscopy represented the formation of AgNPs. FTIR spectroscopy revealed that –OH group may play important role for the reduction of Ag+ to AgNPs. XRD revels the face-centered cubic geometry of AgNPs. AFM image analysis helped to find out the shape of the synthesized AgNPs is sphereical. The efficiency of AgNPs as a promising catalyst through electron transfer in the degradation of methyl orange and methyl red was investigated. This catalytic activity of AgNPs can be used to synthesis different chemical intermediates and organic transformations.

    Keywords: Nanosilver, Green synthesis, Surface plasmon, resonance, Catalytic activity, Degradation, Sonneratia apetala}
  • رمضانعلی دیانتی تیلکی*، مرتضی قلعه نوئی، معصومه اسلامی فر
    سابقه و هدف

    پیل سوختی میکروبی در زمره تکنولوژی های مبتنی بر توسعه پایدار قرار دارد که می تواند هم زمان برای حذف بسیاری از آلاینده ها و تولید الکتریسیته مورد استفاده قرار گیرد. هدف از این تحقیق تعیین میزان حذف فنل در غلظت های زیاد در پیل سوختی میکروبی بود.

    مواد و روش ها

     یک پیل سوختی میکروبی دو محفظه ای مجهز به غشاء تبادل گر پروتون نفیونی و آند و کاتد از جنس پارچه کربنی ساخته شد و در انکوباتور دمای 30 درجه سانتی گراد به مدت 12 هفته به صورت جریان منقطع مورد بهره برداری قرار گرفت. آند در محفظه بی هوازی حاوی محیط کشت حداقل (ترکیبات معدنی) قرار گرفت و فنل به عنوان تنها منبع کربن در غلظت های 50 تا 1000 میلی گرم بر لیتر به آن اضافه شد. بذر باکتریایی تجزیه کننده فنل که از تصفیه خانه فاضلاب پالایشگاه نفت تهران تامین و به فنل آداپته شد و در محفظه آند بی هوازی پیل میکروبی استفاده شد. کاتد در محفظه هوازی حاوی بافر فسفات قرار گرفت. غلظت فنل باقیمانده در زمان های مختلف به وسیله دستگاه HPLC اندازه گیری شد.

    یافته ها

    حداکثر حذف فنل طی 24 ساعت اولیه هر مرحله از آزمایش اتفاق می افتاد. فنل در غلظت های تا ppm 800 طی 96 ساعت به طور کامل حذف شد. اما زمان لازم برای حذف کامل ppm 1000 فنل 120 ساعت بود.

    استنتاج

    با استفاده از لجن تصفیه خانه فاضلاب پالایشگاه نفت خو یافته به فنل در پیل سوختی میکروبی، حذف فنل تا غلظت ppm 1000 امکان پذیر شد.

    کلید واژگان: پیل سوختی میکروبی, تجزیه, فنل, لجن, پالایشگاه نفت}
    RamazanAli Dianati Tilaki*, Morteza Ghalenoei, Masoumeh Eslamifar
    Background and purpose

    Microbial fuel cell is one of the sustainable development technologies that can be used simultaneously for removal of many pollutants and generate electricity. The aim of this study was to determine the removal rate of high concentrations of phenol in a microbial fuel cell.

    Materials and methods

    A dual chamber microbial fuel cell having Nafion proton exchange membrane and carbon cloth as anode and cathode was fabricated and operated in batch mode in incubator at 30°C for 12 weeks. Anode was put in anaerobic chamber containing minimum growth medium and phenol (50-1000ppm) was added as the sole carbon source. Phenol degrading bacterial seed that was supplied by wastewater treatment plant of Tehran Petroleum Refinery was adapted to phenol and used in anaerobic anode chamber. Cathode was put in aerobic chamber containing phosphate buffer. Concentration of remained phenol in different times was analyzed by HPLC method.

    Results

    Maximum amount of phenol degradation occurred in the first 24h of each run. Phenol concentrations up to 800 ppm were completely removed during 96 h, but time to complete removal of 1000 ppm phenol was 120h.

    Conclusion

    By using sludge from wastewater treatment plant of oil refinery adapted to phenol in a microbial fuel cell, it is possible to remove 1000 ppm phenol.

    Keywords: microbial fuel cell, degradation, phenol, sludge, oil refinery}
  • Kadali Jagadeesh, Nowduri Annapurna*
    Background

    The combination of chlorthalidone and benidipine was used to manage hypertension. The mixture of chlorthalidone and benidipine in tablet dosage form has not been previously determined by any method. A stability indicating HPLC method was developed for the simultaneous determination of benidipine and chlorthalidone in bulk and tablets.

    Methods

    Chromatographic separation was accomplished in a reverse phase system using an isocratic elution with a mobile phase composed of methanol-0.1M dipotassium hydrogen phosphate buffer (40:60, v/v), at 1 ml/min flow rate. The photodiode array (PDA) detector set at 260 nm was used to detect and quantify benidipine and chlorthalidone. Benidipine and chlorthalidone tablet samples were subjected to degradation under acid, neutral, alkali, thermal, photo and oxidative. The proposed method was effectively adapted to quantify benidipine and chlorthalidone in the combined tablet formulation.

    Results

    The elution times for benidipine and chlorthalidone were approximately 4.573 min and 6.422 min, respectively. The method was validated within a concentration range of 2 - 6 μg/ml (R2 = 0.9997) for benidipine and 6.25 - 18.75 μg/ml (R2 = 0.9998) for chlorthalidone. Adequate results were obtained for precision (RSD% = 0.106% for benidipine and RSD% = 0.031% for chlorthalidone) and accuracy (99.95 - 100.25 % mean recovery for benidipine and 99.60 - 99.63% mean recovery for chlorthalidone). Robustness has also been found to be acceptable. During the degradation study, interference was not noticed in the analysis of studied drugs.

    Conclusion

    The findings demonstrated that the method could be useful for determination of the selected drug combination in routine analysis.

    Keywords: Benidipine, Chlorthalidone, Degradation, Tablets, HPLC-Analysis}
  • Amir Hossein Baghaie *, Aminollah Aghilizefreei

    In this study, we investigate the problems and obstacles of implementing the risk-based auditing in Iran. We set four hypotheses and used questionnaire containing 45 questions to collect the required data. The questionnaires were distributed between Iranian certified public accountants who were partners or directors of audit firms and audit organizations member of Iranian certified public accountant institute. To determine the validity of the research questionnaire limited number of questionnaires distributed between small sample of respondents and their views taken into account. The Cronbach’s alpha test is used to measure reliability of the questionnaire. The results of this study indicated that, lack of the theoretical foundations and regulations of risk-based auditing in Iran, structure and function of auditors and audit firms and factors related to the clients are the obstacles and limitations on implementation of risk-based auditing in Iran Then the most important factors prioritized using fuzzy hierarchy analysis. For this reason, a questionnaire was developed with 16 factors from approved hypotheses. Results revealed that related factors with the auditors and unfamiliarity of auditors with IT and lack of educational resources were the most important obstacles and limitations on implementation of the risk-based auditing in Iran.

    Keywords: Salicylic acid, Pseudomonas putida, Phenanthrene, Degradation}
  • Abdolmotaleb Seid Mohammadi, Mina Bahrami, Sana Omari, Fateme Asadi*

    In the present study, magnesium oxide/granular activated carbon (MgO/GAC) composite as a catalyst was synthesized using the sol-gel method and its catalytic potential was investigated in the presence of ultraviolet (UV) irradiation for the removal of cephalexin (CLX) in a batch mode reactor. Then, the characterization of the MgO/GAC composite was determined by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Next, the effect of operational parameters was evaluated, including the pH of the solution (3-11), the dosage of composite (1-6 g/L), initial CLX concentration (20-100 mg/L), and contact time (10-60 minutes). The maximum CLX degradation with an initial concentration of 20 mg/L was as high as 98% at pH=3, 4 g/L of MgO/GAC composite with UV irradiation within 60-minute contact time. In addition, the removal process of CLX could be described by the pseudofirst-order kinetic. Further, the chemical oxygen demand (COD) and total organic carbon (TOC) removal rate were 78% and, 62.3% in optimum conditions, respectively. The results indicated that the UV/MgO/GAC hybrid photocatalytic process can be considered as an efficient alternative for treating the wastewater containing CLX.

    Keywords: Degradation, Ultraviolet, Cephalexin, Magnesium oxide, Granular activated carbon}
  • Khadijeh Darabi, Abooalfazl Azhdarpoor *, Mansoureh Dehghani
    Background
    Carbamazepine is a pharmaceutical compound used as an anticonvulsant for epilepsy and can enter the environment by inappropriate treatment of hospital wastewater. Therefore, the present study aimed to investigate the removal of carbamazepine from the aquatic environment, using the ozonation process.
    Methods
    This is an experimental study in which certain concentrations of carbamazepine were removed, using the ozonation process. The effect of such factors as pH (3-11), carbamazepine concentration (5-15 ppm), ozone dose (200-400 mg/hr), and reaction time (15-180 seconds) on the removal efficiency was studied. Data analysis was performed to measure carbamazepine, using the High-Performance Liquid Chromatography (HPLC).
    Results
    The results showed that the carbamazepine removal efficacy at pHs of 5, 7, and 11 was 81%, 66%, and 21%, respectively at 15 ppm, the reaction time of 30 seconds, and the ozone dose of 200 mg/hr, respectively. Also, at the dose of 200 and 400 mg/hr injectable ozone at pHs of  5 and 7, removal efficiency was 81%, 66%, 97%, and 78%, respectively.
    Conclusion
    According to the results, at pH=5, reaction time of 30 seconds, the carbamazepine concentration of 15 ppm, injectable ozone dose of 200 mg/h, a removal efficiency of 81% was obtained. The ozonation process can react directly or indirectly with the drug contaminant in very low concentrations in aqueous solutions due to its high oxidation power, leading to its destruction or elimination, which may indicate that the ozonation method may be used as an effective method to remove carbamazepine and other similar contaminants.
    Keywords: Carbamazepine, Aquatic Environment, Ozone, Degradation}
  • مجید کرمانی، علی اسرافیلی، رقیه پیری، سیده نسترن اسدزاده *
    مقدمه و هدف
    کلروفنل از جمله آلاینده های سمی و خطرناک در پساب و فاضلاب های صنعتی می باشد که حذف آن از فاضلاب صنعتی و آب زیرزمینی ضروری است. در این ارتباط، مطالعه حاضر با هدف بررسی کارایی میزان تجزیه پذیری 4-کلروفنل با استفاده از فرایند UV/H2O2 انجام شد.
    روش کار
    در مطالعه حاضر اثر متغیرها شامل: غلظت اولیه آلاینده، زمان تماس، pH و غلظت H2O2 بر حذف 4-کلروفنل در مقیاس آزمایشگاهی مورد بررسی قرار گرفت و غلظت 4-کلروفنل باقی مانده با استفاده از دستگاه UV/Visible در طول موج 280 نانومتر اندازه گیری شد. علاوه بر این، میزان معدنی سازی در شرایط بهینه از طریق سنجش میزان حذف TOC)Total Organic Carbon) مطابق با روش 5310B استاندارد اندازه گیری گردید. مدل های سینتکی فرایند نیز مورد بررسی قرار گرفت.
    یافته ها
    در این مطالعه بازده بهینه حذف 4-کلروفنل توسط فرایند UV/H2O2 در غلظت پراکسید هیدروژن 580 میلی گرم بر لیتر، pH= 3 ، غلظت اولیه 4-کلروفنل 380 میلی گرم بر لیتر و حضور اشعه UV با طول موج 254 نانومتر در زمان تماس 30 دقیقه معادل 92 / 84 درصد به دست آمد. علاوه بر این، در شرایط بهینه 69 / 84 درصد از کل کربن آلی حذف گردید. شایان ذکر است که داده ها از مدل سینتیکی درجه اول کاذب تبعیت داشتند.
    نتیجه گیری
    با توجه به افزایش استفاده از اشعه فرابنفش در فرایندهای تصفیه آب و بازده قابل قبول فرایند UV/H2O2 برای حذف آلاینده 4-کلروفنل، پس از آنالیزهای سود- هزینه، استفاده از این روش برای حذف -4 کلروفنل پیشنهاد می شود. بر مبنای نتایج، فرایند UV/H2O2 با درنظرداشتن اهداف تصفیه و استانداردهای موجود جهت تخلیه پساب می تواند به عنوان پس تصفیه و یا تصفیه نهایی پساب به کار گرفته شود.
    کلید واژگان: تجزیه, رادیکال هیدروکسیل, 4-کلروفنل, معدنی سازی}
    Majid Kermani, Ali Esrafili, Roghaye Piri, Nastaran Asadzadeh Seyedeh *
    Introduction and purpose: Chlorophenol is known as one of the toxic and dangerous pollutants in industrial wastewaters that’s a essential to it’s removal from industrial wastewaters and ground waters. The aim of this study was to investigate the efficiency of 4-Chlorophenol (4-CP) degradation using Ultraviolet/Hydrogen Peroxide process (UV/H2O2).
    Methods
    The variables of the present study included initial concentration of pollutant, contact time, pH, and H2O2 concentration on 4-Chlorophenol removal on a laboratory scale. The concentration of residual 4-Chlorophenol was determined using UV/Visible at a wavelength of 280nm. In addition, the amount of mineralization in optimal conditions was evaluated using the measurement of total organic carbon (TOC) removal range according to the standard method 5310- B. Synthetic models of the process were also investigated.
    Results
    The optimum removal efficiency of 4-CP by UV/H2O2 process regarding the concentration of hydrogen peroxide was 580 mg/L. pH of 3 and initial 4-CP concentration was obtained as 380 mg/L, and the presence of UV rays with a wavelength of 254 nm during 30m contact was 84.92% . In addition, 84.69% of the TOC was removed under the optimal condition. Moreover ,it was found that the data followed the first-order synthetic models.
    Conclusion
    Considering the growing use of UV radiation in water treatment processes and the considerable efficiency of UV/ H2O2 process in removing 4-CP, this method can be proposed for the elimination of 4-CP after performing cost-benefit analyses. It can be concluded that with regard to purification goals and standards for wastewater treatment, UV/ H2O2 process can be used as a pre or final treatment.
    Keywords: Degradation, Hydroxyl radicals, 4-Chlorophenol, Mineralization, UV-H2O2 process}
نکته
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