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کاربرد نانوذرات مغناطیسی هیدروکسی‌آپاتیت در حذف Cd2+ از محیط های آبی | ||
| محیط شناسی | ||
| مقاله 14، دوره 40، شماره 3، آذر 1393، صفحه 739-750 اصل مقاله (674.94 K) | ||
| نوع مقاله: مقاله پژوهشی | ||
| شناسه دیجیتال (DOI): 10.22059/jes.2014.52217 | ||
| نویسندگان | ||
| ایرج کاظمی نژاد1؛ ثنا احمدی زاده* 2؛ علی اکبر بابایی3 | ||
| 1دانشیار، گروه فیزیک، دانشگاه شهید چمران اهواز | ||
| 2کارشناس ارشد، گروه فیزیک، دانشگاه شهید چمران اهواز | ||
| 3مرکز تحقیقات فناوری های زیست‌محیطی، دانشگاه علوم پزشکی جندی شاپور اهواز | ||
| چکیده | ||
| در این تحقیق نانوذرات مغناطیسی هیدروکسی‌آپاتیت به روش هم‌رسوبی ساخته شدند. نانوذرات ساخته‌شده با استفاده از دستگاه‌های الگوی پراش پرتو ایکس (XRD)، میکروسکوپ الکترونی روبشی گسیل میدانی (FESEM)، اسپکتروفوتومتری تبدیل فوریۀ مادون قرمز (FT-IR) و مغناطیس‌سنج نمونۀ ارتعاشی (VSM) مشخصه‌یابی شدند. الگوی پراش پرتو ایکس نمونه‌ها ساختار هگزاگونال هیدروکسی‌آپاتیت و تتراگونال مگمایت را تأیید کرد. نتایج میکروسکوپ الکترونی روبشی گسیل میدانی، نانوذرات تقریباً کروی‌شکل را نشان داد. میانگین اندازۀ نانوذرات 2±19 نانومتر بود. تبدیل فوریۀ مادون قرمز نشان‌دهندۀ تشکیل پیوندهای مورد انتظار بود. منحنی پسماند نانوذرات نشان داد که میزان نیروی وادارندگی نانوذرات تقریباً صفر است و نانوذرات خاصیت ابرپارامغناطیس از خود نشان می‌دهند. در نهایت نانوذرات تهیه‌شده به‌منزلۀ جاذب برای حذف یون‌های کادمیوم از محیط‌های آبی به کار گرفته شدند. در آزمایش‌های ناپیوستۀ جذب یون‌های کادمیوم اثر عواملی مانند: pH، مقدار جاذب، زمان تعادل و غلظت اولیۀ یون‌های کادمیوم بررسی شدند. در گسترۀ PH 5 تا 7، زمان تماس 30 دقیقه، مقدار جاذب 1/0 گرم و غلظت اولیۀ 10 تا 20 میلی‌گرم بر لیتر میزان جذب حداکثر بود. فرایند جذب از مدل هم‌دمای لانگمویر تبعیت کرد و بیشینۀ ظرفیت جذب یون‌های کادمیوم mg/g746/84 به دست آمد. نتایج آزمایش‌های مربوط به جذب یون‌های کادمیوم نشان داد که نانوذرات مغناطیسی هیدروکسی‌آپاتیت دارای درصد حذف بالا و زمان تعادل کوتاه (30 دقیقه) بودند و می‌توانند به‌منزلۀ روشی کارآمد در حذف یون‌های کادمیوم از محیط‌های آبی استفاده شوند. | ||
| کلیدواژه‌ها | ||
| روش هم‌رسوبی؛ کادمیوم؛ محیط‌های آبی؛ نانوذرات مغناطیسی؛ هیدروکسی‌آپاتیت | ||
| عنوان مقاله [English] | ||
| Application of Magnetic Hydroxyapatite Nanoparticles for Removal of Cd2 + from Aqueous Solutions | ||
| نویسندگان [English] | ||
| Iraj Kazeminezhad1؛ Sana Ahmadizadeh2؛ Ali akbar Babaie3 | ||
| 1Associate professor Physics Department, Faculty of Science, Shahid Chamran University, Ahvaz, Iran | ||
| 2MSc., Physics, Shahid Chamran University, Ahvaz, Iran | ||
| 3Assistant Professor, Environmental Technologies Research Center, Jundishapur University of Medical Sciences, Ahvaz, Iran | ||
| چکیده [English] | ||
| Introduction Environmental pollution by heavy metals is one of the most commonly-encountered problems in many areas in which biological controls have not been implemented. As these metals are non-biodegradable, they remain in the nature for a long time, and through deep percolation into underground water they can cause degradation of ecosystems. The uptake of these elements by plants and their inclusion in the chain of human and animal food is a great risk for the environment and the human being health. Due to non-biodegradable property of Cadmium and some other toxic heavy metals, these metals remain in the environment for a long time. Cadmium is one of the most toxic heavy metals and it has been reported to cause renal dysfunction, hyper-tension, lung insufficiency, bone lesions, cancer, and etc. The principal industrial sources of Cd in the environment are electroplating, smelting, alloy manufacturing, pigments, plastic, battery, mining and refining processes. In the recent years there have been some reports on the use of inorganic absorbents for separating and removing heavy metals from aqueous solutions. Due to the availability, cost-effectiveness, stability against oxidation and reduction conditions and the possibility of recycling, inorganic adsorbents are economically viable. Traditional inorganic adsorbents with a low surface area lose their ability to absorb. Thus, making high capacity adsorbents for fast and easy removal of contaminants is a necessary step. One of the outstanding characteristics of fast-emerging nanotechnology studies is the high surface area to volume ratio of nanomaterials. Because of these outstanding features and other unique properties, nanoparticles may have potential to absorb pollutants from contaminated environments. So far, many technologies to remove heavy metals from aqueous solutions including chemical precipitation, ion exchange, membrane technologies, electrodialysis, and biosorption have been developed. Many of these methods have disadvantages such as high cost of operation, the high sludge, and secondary contamination. Nanoparticles with extremely small size and high ratio of surface-area to volume, provide better kinetics for the adsorption of metal ions from aqueous solutions. Hydroxyapatite as one of the major components of bones and teeth are widely used in biomedical and dental applications, drug delivery, and waste water remediation because of biocompatibility, low solubility, ion exchange and high sorption capacity of heavy metals. Magnetic separation technology as an efficient, fast and economical method for separating magnetic materials has been widely used in textile, biology, and environmental protection. In this study, magnetic hydroxyapatite nanoparticles were synthesized by co-precipitation method. The nanoparticles were characterized by x-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared spectroscopy (FT-IR), Vibrating Sample Magnetometer (VSM). Finally, the produced nanoparticles were used as adsorbents for the removal of cadmium ions from aqueous solutions. In batch experiments, the effects of pH, evaluation time and initial concentration of Cd2+ ions on adsorption were investigated. Materials and Methods FeCl2·4H2O, FeCl3·6H2O, NH4OH (25%), Ca (NO3) 2·4H2O and (NH4)2HPO4 were purchased from Merck. All the solutions for the metal adsorption experiments were prepared using their nitrate salts. The amount of FeCl2·4H2O (1.85 mmol) and FeCl3·6H2O (3.7 mmol) was dissolved in 30mL of deoxygenated water under nitrogen atmosphere at room temperature, and then 10mL of NH4OH solution was added to the resulting solution under vigorous mechanical stirring (300 rpm). A black precipitate was produced instantly. After 15 min, up to 50mL of Ca(NO3)2·4H2O (33.7 mmol) and 50mL of (NH4)2HPO4 (20 mmol) solutions whose pH were all adjusted to 11 were drop wise added, simultaneously to the obtained precipitate solution for 30 min with mechanical stirring. The resulting puce suspension was heated at 110 ◦C for 2 h and then the mixture was cooled to room temperature and aged for 24 h without stirring. The obtained precipitate was separated by a magnet, washed repeatedly with deionized water till neutrality, dried in the drying oven at 110◦C, and grinded with mortar. The final products were the prepared magnetic hydroxyapatite nanoparticles adsorbents. The adsorption behavior of the magnetic hydroxyapatite nanoparticles for Cd2+ions was investigated by means of the batch experiments at 24±1°C. A known amount of magnetic hydroxyapatite nanoparticles was mixed with 50 mL of the corresponding Cd2+ solution over a period of time on a shaker at 150rpm. After that, the aqueous phase was separated by magnetic decantation; the concentration of Cd2+ in the solution was determined by using an atomic absorption spectrometer. In order to determine the optimum of pH, 0.05g of magnetic hydroxyapatite nanoparticles were added to 8 flask containing cadmium and under different pH conditions, the removal efficiency of cadmiumions by the adsorbent was detected. To evaluate the optimum dosage of magnetic hydroxyapatite nanoparticles adsorbent, 3–10 mg of freshly prepared magnetic hydroxyapatite nanoparticles was added to 50.0mL of aqueous solution containing 50.0mg/L Cd2+. The results showed that increasing the amount of adsorbent, the adsorption efficiency of Cd2+ due to increased absorption of available sites, has increased the effect of contact time on the adsorption of Cd2+ by magnetic hydroxyapatite nanoparticles (pH of the solution: 5.5, amount of adsorbent: 0.1g, Cd2+ concentration 50 ppm; temperature: 25±1°C). Sorption isotherms were obtained by equilibrating magnetic hydroxyapatite nanoparticles with metal solutions of different initial concentrations: 10-300 mg/l for 30 min. After separation, the final concentrations of metal in the solutions were measured. The adsorption capacity was calculated according to the following equation: qe = (C0 − Ce)V/m The removal efficiency of lead ions was calculated by the difference of lead ion concentrations in aqueous solution using the equation expressed as follows: R% = (C0 – Ce)/C0× 100 Where, qe (mg/g) is the amount of lead ions adsorbed onto the unit amount of the adsorbent, C0 (mg/L) is the initial lead ion concentration, Ce (mg/L) is the final or equilibrium lead ion concentration, V (L) is the volume of the solution, and m (g) is the adsorbent weight in dry form. The Langmuir and Freundlich models were used to describe the relationship between the absorbed amount of Cd2+ and its equilibrium concentration in solution. To determine whether the Cd2+ adsorption process by magnetic hydroxyapatite nanoparticles is favorable or unfavorable for the Langmuir type adsorption process, the isotherm shape can be classified by a term “RL”. RL values are ranged from 0 to 1 and indicate favorable adsorption, while RL >1, RL =1,and RL =0 indicate unfavorable, linear, and irreversible adsorption isotherms. Phase composition of the samples were characterized using a X-ray diffractmeter (XRD, Model pw-18/40, Philips, Germany) with CuKα (λ = 1.5418 Å) incident radiation over the 2θ range of 10–80◦ at room temperature with a step size of 0.02◦. The morphology of particles was investigated by scanning electron microscopy (SEM, Model VEGAII, XMU, Tescan, Czech Republic). To study the chemical structure of samples, Fourier Transform Infrared spectroscopy (FTIR, Model: EQUINOX55, Bruker, Germany) was used. For this, the samples prepared from 1:80 magnetic hydroxyapatite nanoparticles -KBr mixtures (by weight) were compacted into pellet form and then scanned from 4000 to 400 cm−1. The magnetization measurements were performed at room temperature using vibrating magnetometer. The concentration of Cd2+ in the solution was determined by using an atomic absorption spectrometer (Analytic jena- verio6). Conclusions In this study, magnetic hydroxyapatite nanoparticles were synthesized by co- precipitation method, and the adsorption potential of nanoparticles for the removal of Cd2+ from aqueous solutions was investigated. The experimental results confirm that this adsorbent has the potential application for removal of Cd2+ from aqueous solution. The nanoparticles were characterized by x-ray diffraction, Field emission scanning electron microscopy, FTIR, and vibrating sample magnetometer. The effect of contact time, initial metal ions concentrations, pH, adsorbent dosage was discussed. The XRD patterns of samples confirm the hexagonal structure of hydroxyapatite and tetragonal structure of maghemite. This pattern indicates that the diffraction peaks are in agreement with the standard card (0566-074-01 ICSD) of hydroxyapatite and (0566-013-01 ICSD) of the tetragonal of maghemite. FESEM image of the nanoparticles showed almost spherical shape. The average size of nanoparticles was 19±2.FTIR spectroscopyreveals expected bondsformation. Magnetic properties of nanoparticles prepared at room temperature were studied in the range of 10000 ± Oe. Hysteresis curves of nanoparticles showed that the saturation magnetization and coercivity of the nanoparticles was 2.8 emu/g and 0 Oe, respectively. The nanoparticles indicate super-paramagnetic behavior. The super-paramagnetic property of the magnetic hydroxyapatite nanoparticles is critical for their application in industrial catalysis, environmental protection, biomedical and bioengineering field, which prevents them from aggregation and enables them to re-disperse rapidly when the magnetic field is removed. Finally, the produced nanoparticles were used as adsorbents for the removal of Cd2+ from aqueous solutions. In batch experiments, the effects of pH, evaluation time, adsorbent dosage and initial concentration of Cd2+ ions on adsorption were investigated. The highest removal efficiency of Cd2+ was in the range pH = 5-7. The removal efficiency increases with time in the first 30 min. Then, the adsorption curve reached equilibrium after this time. Removal efficiency increased as the adsorbent dosage was raised. When a dosage of 0.1 g was used, the removal efficiency reached 96%, indicating that the composite adsorbent magnetic hydroxyapatite nanoparticles showed strong affinity to Cd2+. The adsorption was relatively fast and the equilibrium was established within 30 min to be considered the adsorption isotherm data could be well described by Longmuir equation. The RL values in this study were in the range from 0.045 to 0.488 which indicated the favorable adsorption between Cd2+ and magnetic hydroxyapatite nanoparticles sorbent. Maximum adsorption capacities of Cd2+ were 84.746 mg/g. The results of adsorption experiments indicated that magnetic hydroxyapatite nanoparticles have high adsorption efficiency with short reaction time (30 min) and can be very effective to remove Cd2+ ions from aqueous solution. The most prominent advantage of prepared magnetic hydroxyapatite nanoparticles adsorbents with super-paramagnetism and adsorption capacities was the separation convenience from aqueous solutions. | ||
| کلیدواژه‌ها [English] | ||
| aqueous solutions, Cadmium, co-precipitation method, Hydroxyapatite, Magnetic nanoparticles | ||
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