sio2
در نشریات گروه مهندسی شیمی، نفت و پلیمر-
In present study, two components of Ag/SiO2 nanocomposite were prepared by the Sonochemical method and then the PET/cotton fabric treated with Ag/SiO2 nanoparticles (Ag/SiO2 NPs) by Pad-Dry method. The treated fabric dyed at the optimum condition with direct dyes. The influence of the Ag/SiO2 nanocomposite on the performance of PET/cotton fabric was investigated by the use of X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscope (SEM), electron dispersive X-ray spectroscope (EDX) and reflectance spectrophotometer (RS). TEM images of Ag/SiO2 showed the particles size were 30-70 nm. SEM results of Ag/SiO2 nanocomposite powders show that nanoscale particles are well formed, also SEM micrograph of treated fabrics indicated that the nanoparticles were well dispersed on the surface of sample. EDX results showed the presence of nanoparticles increased on the surface of samples with increase concentration of colloid solution nanoparticles. The antibacterial properties were determined by reduction growth of a Gram-negative bacterium E. coli and a Gram-positive bacterium Staphylococcus aureus. Photo-catalytic activities of the coated PET/cotton fabric were evaluated through the degradation of methylene blue under UV irradiation.
Keywords: Antibacterial, Sonochemical Method, PET, Cotton, Nano Ag, Sio2, Dyeability -
In the present study, a one-dimensional unsteady-state model is developed to investigate an industrial Acheson reactor for producing SiC. The mechanisms of the SiO2 melting and converting to SiC are investigated using the experimental data of previous works. Additionally, the obtained models are utilized in the developed mathematical model. The finite difference method is used for the simulation of the developed model. The accuracy of the presented model is validated by empirical data. The complete discussions of the reaction progress, melting process, variations of the bed, and also the temperature inside the bed are presented. Attending to the importance of the existing competition between the melting of SiO2 and converting to SiC, these mechanisms are investigated using the presented data in previous relevant studies and the obtained models are utilized in the developed mathematical model. The model predictions show that the final produced cylinder of SiC at the center line of the reactor occupies 8.05% of the reactor diameter and has 8.16% weight loss during the production process.Keywords: Modeling, Acheson, SiO2, Carbon, SiC
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مطالعه و ساخت نانو کاتالیست مس و بررسی عملکرد آن در واکنش اکسیداسیون مونواکسید کربن به دی اکسید کربن
هدف مهم در این پژوهش، اکسیداسیون مونواکسید کربن به دی اکسید کربن، در حضور کاتالیست مس است. این گاز بی بو، به خاطر سمی بودن، لازم است به گونه ای حذف شود. از روش های حذف این گاز می توان از اکسایش به دی اکسید کربن و هیدروژناسیون نام برد. در حال حاضر روش دوم برای محققین به عنوان یک کلید تکنولوژی، برای تولید سوخت های پاک و مواد شیمیایی جالب و جذاب است. کاتالیست مس، به دلیل ارزان بودن و فعالیت مناسب در واکنش اکسیداسیون مونواکسید کربن، انتخاب شد. در این تحقیق، اثر پایه های مختلف بر روی گزینش محصول و میزان تبدیل خوراک، بررسی شد. در این پایان نامه، ابتدا نانو اکسیدهای مس، به روش هم رسوبی و میکرو امولسیون، تهیه و سپس کاتالیست نهایی، از طریق تلقیح مرطوب (مس روی پایه های مختلف) به دست آمد. کاتالیست های ساخته شده ازلحاظ خصوصیات فیزیکی و شیمیایی، ارزیابی و در شرایط عملیاتی معین از دما (o</sup>C 400-100)، فشار (atm 1)، نسبت حجمی خوراک (O2</sub>/CO/H2</sub>/N2</sub>=2/2/5/91) و فلوی گاز GHSV=1.5-6 nl.h-1.gCat-1 در سیستم راکتوری بستر ثابت، آزمون شد. نتایج آزمون راکتوری نشان می دهد که نانوکاتالیست مس با پایه ی TiO2</sub>، دارای میزان تبدیل مونواکسید کربن و گزینش پذیری بالاتری است. افزایش ارتقاء دهنده ی لانتان به ساختار کاتالیست، باعث افزایش میزان تبدیل مونواکسید کربن و گزینش پذیری دی اکسید کربن می شود.
کلید واژگان: کاتالیست نانو ساختار مس، پایه ها، آلومینا، تیتانیا، سیلیکا، ارتقادهنده لانتان، اکسیداسیون مونواکسید کربنThe main purpose of this study is the oxidation of carbon monoxide to carbon dioxide in the presence of copper catalyst. This odorless gas needs to be removed somehow because it is toxic. Oxidation methods include carbon dioxide oxidation and hydrogenation. At present, the second method is interesting for researchers as a key technology to produce clean fuels and chemicals. Copper catalyst was selected because of its cheapness and suitable activity in the carbon monoxide oxidation reaction. In this study, the effect of different bases on product selectivity and feed conversion rate was investigated. In this dissertation, first copper nanoxides were prepared by co-precipitation and microemulsion method and then the final catalyst was obtained by wet inoculation (copper on different bases). Catalysts are evaluated in terms of physical and chemical properties, and in certain operating conditions of temperature (100-400 °C), pressure (1 atm), feed volume ratio (O2</sub> / CO / H2</sub> / N2</sub> = 2/2/5/91 and GHSV= 1.5-6 nl.h-1.gCat-1 valley fixed bed reactor system was tested. The results of the reactor test show that TiO2</sub>-based copper nanocatalyst has a higher rate of carbon monoxide conversion and selectivity. Increasing the lanthanum enhancer to the catalyst structure increases the conversion rate of carbon monoxide and the selectivity of carbon dioxide.
Keywords: Copper nanoparticles, Support, Al2O3, TiO2, SiO2, La Promoter, CO oxidation -
فرضیه:
با وجود کاربرد گسترده غشاهای نانوفیلتری در فرایند اسمز مستقیم (FO)، پدیده قطبش غلظت درونی همچنان از مهم ترین چالش های این فرایند است. روش های مختلفی به منظور کاهش اثر این پدیده نامطلوب پیشنهاد شده است که یکی از آن ها بارگذاری نانوذرات آب دوست در ساختار غشاست. در این پژوهش، از نانوذرات SiO2/ZIF-8 برای بهبود ساختار و عملکرد غشاهای پلی اترسولفونی (PES) در فرایند اسمز مستقیم استفاده شده است.
روش هاابتدا، غشای پلی اتر سولفون با روش وارونگی فاز تهیه شد. در مرحله بعد، نانوذرات ZIF-8 و SiO2/ZIF-8 به عنوان پرکننده در دمای محیط سنتز شدند. غشاهای کامپوزیتی لایه نازک به عنوان لایه رویی برای فرایند اسمز مستقیم با روش پلیمرشدن بین سطحی و از واکنش میان دو مونومر واکنش پذیر آلی (TMC) و آبی (MPD) به دست آمدند. در نهایت، برای ارزیابی نانوذرات و غشاهای ساخته شده، آزمون های اندازه گیری زاویه تماس، طیف نمایی زیرقرمز تبدیل فوریه (FTIR)، میکروسکوبی الکترونی پویشی نشر میدانی (FE-SEM)، پراش سنجی پرتو X و اندازه گیری مقدار تخلخل غشا به کار گرفته شدند. همچنین، عملکرد غشاهای ساخته شده پایه و کامپوزیتی (غشایی که حداقل از دو ماده مختلف تشکیل شده است) و نانوکامپوزیتی لایه نازک با فرایندهای اسمز مستقیم و معکوس بررسی شد.
یافته هانتایج حاکی از وجود مقدار کمی SiO2/ZIF-8 در غشاست که سبب افزایش آب دوستی و تخلخل آن شده و شار و پس زنی فرایند FO را نیز بهبود داده است. شار آب غشای اسمز مستقیم لایه نازک نانوکامپوزیتی به طور چشمگیری از 15.23L/m2.hبه 25.13L/m2.h افزایش یافت، زمانی که از محلول 10 میلی مولار و 2 مولار NaCl، به ترتیب به عنوان محلول خوراک (FS) و محلول اسمزی (DS) استفاده شد. بهبود شار آب اسمز مستقیم را می توان به کمترشدن مولفه ساختاری غشا (S) در زیرلایه اصلاح شده PES و کاهش قطبش غلظت درونی نسبت داد.
کلید واژگان: اسمز مستقیم، غشای پلیمری پلی اترسولفون، آب دوستی، تخلخل، نانوذره SiO2، ZIF-8Hypothesis:
Despite the wide application of nanofiltration (NF) membranes in forward osmosis (FO) process, one of the most important challenges of this process is the internal concentration polarization (ICP) phenomenon. Different methods have been investigated to reduce the effect of this undesirable phenomenon and it is suggested that one of these methods is loading of hydrophilic nanoparticles in the membrane structure. In this study, SiO2/ZIF-8 nanoparticles were used to improve the structure and performance of polyethersulfone membranes (PES) in FO process.
MethodsAt first, polyethersulfone membrane was synthesized by phase inversion method. In the next step, ZIF-8 and SiO2/ZIF-8 nanoparticles as filler were synthesized at room temperature. Thin film composite membranes were prepared by the interfacial polymerization (IP) of two reactive organic (TMC) and aqueous (MPD) monomers. Finally, the produced membranes and nanocomposite were characterized by contact angle, FTIR spectroscopy, X-ray diffractometry (XRD), field emission scanning electron microscopy (FESEM), and porosity measurements. Also, the performance of all membranes composed of at least two different components was investigated using reverse and forward osmosisi processes.
FindingThe outcomes demonstrated that the presence of a small amount of SiO2/ZIF-8 nanoparticle in the membrane led to an increase in the membrane hydrophilicity and porosity, and also improved the water flux and rejection of the FO. The water flux of TFN FO membrane was reported to increase remarkably from 15.23 to 25.13 L/m2.h when 10 mM NaCl and 2 M NaCl salt were utilized as feed solution (FS) and draw solution (DS), respectively. The improvement in FO water flux was ascribed to the lower S parameter of modified PES sublayer and the reduction of internal concentration polarization (ICP).
Keywords: forward osmosis, polyethersulfone polymeric membrane, hydrophilicity, porosity, SiO2, ZIF-8 nanoparticle -
This paper describes the changes in TiO2/SiO2 nanolayers properties induced by Ultraviolet- visible spectroscopy (UV) irradiation in terms of hydrophilicity/photocatalycity. The TiO2/SiO2 nano particles were synthesized by the sol-gel method and deposited on soda-lime glass by dip-coating. X-ray diffraction (XRD) of the TiO2 particles showed that the nano-particles were crystallized in anatase crystal structure with a crystallite size of ~12 nm. The morphology and surface roughness of TiO2 nanolayer were observed by scanning electron microscope (SEM) and atomic force microscopy (AFM) analysis. The surface roughness (Ra) for TiO2/Glass and TiO2/SiO2 was measured ~ 5 and 19 nm, respectively. The hardness of nanolayers on the glass was evaluated and scratch thickness for 1000 g sinker was measured ~150 nm. The self-cleaning properties were tested in dry condition (RH<15%) under UV irradiation by evaluating the oleic acid photodegradation and monitoring the hydrophilic properties of the surface with a contact angle measurement. The result showed that contact angle of the layer decreases from 77 to 42° after 25 h UV irradiation. Fourier-transform infrared spectroscopy- Attenuated total reflectance (FTIR-ATR) showed the elimination of C=O bonds of oleic acid on the surface after UV light irradiation. Water droplet contact angle measurement on TiO2 nano-layer exhibited a less hydrophilicity after UV irradiation and the contact angle changed from 15 to 40°, which may be due to the low atmospheric humidity. Adding SiO2 nanoparticles increases roughness of the nano-layer, from 5 to 19 nm, without a significant effect on the photodegradation rate of oleic acid.Keywords: Nano-layers, TiO2, SiO2, Photocatalysis, Hydrophilicity
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SiO2-supported silyl chromate catalyst is an important industrial catalyst for production of high grade HDPE pipe materials. The control of the short chain branch (SCB) distribution using this catalyst system is still a great challenge. In this work, ethylene and 1-hexene copolymers were synthesized using SiO2 supported silyl chromate catalyst combined with triisobutylaluminium (TIBA), triethylaluminium (TEA) and mixed TIBA/TEA at molar ratio 1:1 (TIBA/TEA/1:1) as three different Al-alkyl co-catalysts.The temperature rising elution fractionation (TREF) and successive self-nucleation and annealing (SSA, by DSC) methods were combined to analyze the short chain branch distribution (SCBD) of these ethylene/1-hexene copolymers. The resultsshowedthat different types of co-catalyst had a great influence on SCBD of ethylene/1-hexene copolymers. The copolymer produced with TIBA showed better SCBD than the copolymer produced with TEA, and the copolymer produced with TIBA/ TEA/1:1 showed a SCBD in between those with TIBA and TEA.Keywords: ethylene, 1, hexene copolymerization, Al, alkyl co, catalyst, polymerization kinetics, SiO2, supported silyl chromate catalyst, short chain branch distribution
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tiO2-SiO2 photocatalytic nanostructure film on windshield was prepared via sol–gel dip-coating method for self-cleaning purposes. TiO2 films were prepared on automotive glass pre-coated with a SiO2 layer by a dip-coating method followed by annealing at 500 °C for 30 min. The films were characterized using X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM, FE-SEM) techniques. The TiO2-SiO2 films were transparent, uniform and crack-free and the temperature was best chosen. XRD shows that SiO2 precoated layer comparatively prevent rare elements ions diffusion from substrate to avoid unfavorable compounds. The results illustrate the crystalline anatase as main phase for films annealed at 500 °C with average crystallite size of 22-26 nm, which was preferable due to much higher photocatalytic activity of anatase compared to rutile phase. The FE-SEM surface morphology results indicate that the particle size was 22 nm, whereas some pores observed in the coatings which were due to un-perfect solvent evaporation.Keywords: SiO2, TiO2 film, Sol, gel, Surface morphology
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