scholarly journals Effects of Different Raw Materials in the Synthesis of Boehmite andγ- andα-Alumina

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Isabel Padilla ◽  
Sol López-Andrés ◽  
Aurora López-Delgado
Keyword(s):  
Crystallite Size ◽  
Surface Area ◽  
Aluminum Chloride ◽  
Raw Materials ◽  
Precipitation Method ◽  
Synthesis Process ◽  
Naoh Solution ◽  
Tg Studies ◽  
Metastable Alumina ◽  
Alumina Polymorphs

Two alumina polymorphs, the metaestableγ-Al2O3and the stableα-Al2O3, were obtained from thermal treatment of the precursorγ-AlOOH (boehmite). This precursor was prepared by a precipitation method employing different raw materials in order to study their effect on the synthesis process and several characteristics of the materials, such as the crystallite size, the thermal behavior, and the surface area. Aluminum chloride (AlCl3·6H2O) and an aluminum waste were used as the source of aluminum. A 1 M NaOH solution and a 1 M n-butylamine solution were used as alkalizing agents, due to their strong and weak alkaline characteristics, respectively. The XRD profiles of the boehmites obtained from waste show lower crystallinity than samples obtained from aluminum chloride. The content of water, from TG studies, was higher in the samples obtained from waste, which fit well with the smaller crystallite size. The use of n-butylamine as alkalizing agent favors the formation ofγ-alumina with higher surface area (177.2 cm2 g−1, for aluminum waste, and 159.4 cm2 g−1, for aluminum pure reagent). The temperature of transformation from gamma to alpha, from DTA results, is higher for samples obtained from the waste, and accordingly the presence of impurities in the waste stabilizes the metastable alumina phase.

scholarly journals Facile Synthesis of Spherical Flake-shaped CuO Nanostructure and Its Characterization towards Solar Cell Application

2021 ◽  
Vol 18 (18) ◽  
Author(s):  
Jemibha PAULDURAI ◽  
Ahila Mudisoodum PERUMAL ◽  
Dhanalakshmi JEYARAJA ◽  
Panimaya Valan Rakkini AMAL
Keyword(s):  
Solar Cell ◽  
Crystallite Size ◽  
Surface Area ◽  
Average Crystallite Size ◽  
Lattice Parameter ◽  
Peak Position ◽  
Cuo Nanoparticles ◽  
Precipitation Method ◽  
Solar Cell Application ◽  
Morphological Studies

The aim of this work is to synthesis CuO nanoparticles and investigates their eminent properties to identify their diverse application capability in the field of solar cells.  In this work, CuO nanoparticles were synthesized by precipitation method using Copper (II) nitrate and Copper (II) chloride. Surface effects due to defects, structural properties related through lattice parameter, and crystallite sizes of nanoparticles have been identified from XRD. The crystal plane and reflection peak position was calculated using Bragg’s law. It showed that CuO nanoparticles have a monoclinic structure, and that the average crystallite size of CuO nanoparticles was 28.82 nm. n-type semiconductor behavior had a direct band of Eg = 1.465(2) eV, analyzed from optical studies by DRS. The band gap of the sample was determined from the reflectance spectra using Kubelka-Munk (K-M) function. Elements present were found through absorption peak of FTIR. The blue shifts observed in FTIR spectra in CuO nanoparticles were compared with that of bulk CuO, and absorption band agreed with XRD results.  Morphological studies revealed the formation of spherical flake-shaped formation of CuO. It had a higher surface area and was well-suited to solar cell applications. HIGHLIGHTS The CuO nanoparticles were synthesized by precipitation method The average crystallite size of CuO nanoparticles obtained in the range of 28.82 nm Spherical flake-shaped nanostruture with higher surface area formed in this method Optical property of CuO (Eg = 1.465 eV) and good electron mobility make it a suitable solar cell absorber material GRAPHICAL ABSTRACT

scholarly journals Effect of Surfactant Type on Synthesis and Characteristics of Nanonickel Hydroxide

2021 ◽  
Vol 15 (2) ◽  
pp. 217
Author(s):  
Kevin Cleary Wanta ◽  
Stephen Lim ◽  
Ratna Frida Susanti ◽  
Gelar Panji Gemilar ◽  
Widi Astuti ◽  
...  
Keyword(s):  
Nickel Hydroxide ◽  
Sodium Dodecyl ◽  
Nickel Sulfate ◽  
Precursor Solution ◽  
Vital Role ◽  
Precipitation Method ◽  
Synthesis Process ◽  
Energy Storage Materials ◽  
Alkyl Benzene Sulfonate ◽  
Naoh Solution

Nickel hydroxide has a vital role in various applications, especially as a support material for energy storage materials. Nickel hydroxide can be synthesized through the hydroxide precipitation method. However, the product formed by this method may be large or more than 100 nm because the agglomeration step can occur easily. This present work aims to study the effect of surfactant types in the synthesis and characterization of nickel hydroxide nanoparticle. Nickel sulfate (NiSO4) solution was used as a precursor solution, while 5M sodium hydroxide (NaOH) solution was used as a precipitation agent. The surfactants studied were alkyl benzene sulfonate (ABS), sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), and polyvinylpyrrolidone (PVP). The nickel hydroxide synthesis process was carried out at 50 oC for 1 hour. The surfactant concentration used was at the critical micelle concentration (CMC), where the CMC for ABS, SDS, CTAB, and PVP were 0.01; 0.05; 3; and 0.5 %w/v, respectively. The synthesis of nickel hydroxide nanoparticle was carried out successfully precipitated almost 100% of Ni2+ ions. The product characterization that has been carried out shows that ABS surfactant produces the best nickel hydroxide nanoparticle product where the particle size is 3.12–4.47 nm.

Synthesis of yttria-stabilized zirconia nanoparticles by decomposition of metal nitrates coated on carbon powder

1996 ◽  
Vol 11 (9) ◽  
pp. 2318-2324 ◽  
Author(s):  
Shusheng Jiang ◽  
Gregory C. Stangle ◽  
Vasantha R. W. Amarakoon ◽  
Walter A. Schulze
Keyword(s):  
Carbon Black ◽  
Crystallite Size ◽  
Surface Area ◽  
Yttria Stabilized Zirconia ◽  
Synthesis Process ◽  
Carbon Powder ◽  
Stabilized Zirconia ◽  
Black Powder ◽  
Carbon Black Powder ◽  
Metal Nitrates

Weakly agglomerated nanoparticles of yttria-stabilized zirconia (YSZ) were synthesized by a novel process which involved the decomposition of metal nitrates that had been coated on ultrafine carbon black powder, after which the carbon black was gasified. The use of ultrafine, high-surface-area carbon black powder apparently allowed the nanocrystalline oxide particles to form and remain separate from each other, after which the carbon black was gasified at a somewhat higher temperature. As a result, the degree of agglomeration was shown to be relatively low. The average crystallite size and the specific surface area of the as-synthesized YSZ nanoparticles were 5−6 nm and 130 m2/g, respectively, for powder synthesized at 650 °C. The as-synthesized YSZ nanoparticles had a light brown color and were translucent, which differs distinctly from conventional YSZ particles which are typically white and opaque. The mechanism of the synthesis process was investigated, and indicated that the gasification temperature had a direct effect on the crystallite size of the as-synthesized YSZ nanoparticles. High-density and ultrafine-grained YSZ ceramic articles were prepared by fast-firing, using a dwell temperature of 1250 °C and a dwell time of two minutes or less.

scholarly journals Alkali-Hydrothermal Treatment of K-Rich Igneous Rocks for Their Direct Use as Potassic Fertilizers

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 140
Author(s):  
Aaron Mbissik ◽  
Abdellatif Elghali ◽  
Muhammad Ouabid ◽  
Otmane Raji ◽  
Jean-Louis Bodinier ◽  
...  
Keyword(s):  
Hydrothermal Treatment ◽  
Inductively Coupled Plasma ◽  
Structural Changes ◽  
Raw Materials ◽  
Hydrothermal Process ◽  
Atomic Emission ◽  
Igneous Rocks ◽  
Gravimetric Analysis ◽  
African Countries ◽  
Naoh Solution

Due to the increasing demand for conventional sources of potassium (K) and their inaccessibility by African countries, K-rich igneous rocks are increasingly studied as potential alternative sources. In this study, six potassic igneous rocks (syenites and trachytes) from the Tamazeght, Jbel Boho, Ait Saoun, and El Glo’a regions (Morocco) were sampled and characterized. Then they were hydrothermally treated to enhance their K release for potential use as potassic fertilizers. The raw materials are mainly formed by microcline (up to 74%), orthoclase (20–68%), albite (36–57%), biotite-muscovite (15–23%), and titanite, calcite, hematite, and apatite as accessory minerals. These samples were crushed and milled to reach a particle size <150 µm and mixed with 4 N NaOH solution in an autoclave. The liquid/solid (L/S) ratio was about 44 mL/50 g. The powders were allowed to react with the solution at 170 °C for 7 h. For all tests, NaOH reacted completely with the powders and no liquid was observed after the treatment. X-ray diffraction (XRD), thermal gravimetric analysis (TGA), infrared spectroscopy (IRTF), and scanning electron microscopy (SEM-EDS) were carried out on treated samples to characterize the mineralogical and structural changes due to the alkali-hydrothermal treatment. Indeed, the treated samples revealed the presence of sodic neoformed phases such as thermonatrite, sodalite, analcime, and cancrinite. The treated material was leached for a week using deionized water and the elements released were measured using inductively coupled plasma–atomic emission spectroscopy (ICP-AES). The hydrothermal process showed a strong effect on structure breakdown as well as on the release of K and other nutrients such as P, Fe, Si, Mg, and Ca. Therefore, the alkali-hydrothermal treatment allowed the release of 50.5 wt% K. Moreover, the release of Mg, Ca, Fe, P, K, and Si were significantly increased. Mg, Ca, Fe, P, K, and Si release within raw materials was about (0.5–3.6), (3.5–31.4), (0.01–0.4), (0.01–0.3), (20–55), and (4.6–8) mg/kg, respectively, whereas treated samples showed a higher release of these elements. Quantitatively, Mg, Ca, Fe, P, K, and Si releases were about (10–11.8), (60–70), (7–20), (1.2–15), (218–1278), and (1119–2759) mg/kg, respectively. Consequently, the treated igneous rocks (syenite and trachyte) could be directly used as potassic fertilizers that would also be a source of other nutrients.

Preparing high surface area porous carbon from biomass by carbonization in a molten salt medium

RSC Advances ◽  
2015 ◽  
Vol 5 (92) ◽  
pp. 75728-75734 ◽  
Author(s):  
Huishan Shang ◽  
Yanjie Lu ◽  
Feng Zhao ◽  
Cong Chao ◽  
Bing Zhang ◽  
...  
Keyword(s):  
Molten Salt ◽  
Surface Area ◽  
Porous Carbon ◽  
High Surface ◽  
High Surface Area ◽  
Molten Salt Synthesis ◽  
Synthesis Process ◽  
Salt Medium ◽  
Peanut Shells

Peanut shells were transformed into porous carbon with a high surface area through a simple ZnCl2-molten salt synthesis process.

TECHNOLOGICAL BASICS OF MOISTURE PRESERVATION DURING THE PRODUCTION AND STORAGE OF FLOUR CONFECTIONERY PRODUCTS

2021 ◽  
Author(s):  
Т.В. САВЕНКОВА ◽  
М.А. ТАЛЕЙСНИК ◽  
Н.А. ЩЕРБАКОВА ◽  
С.Ю. МИСТЕНЕВА ◽  
И.И. МИЗИНЧИКОВА
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Raw Materials ◽  
Malt Extract ◽  
Forming Process ◽  
Confectionery Products ◽  
Partial Concentration ◽  
Egg Powder ◽  
Two Stages

Описаны и теоретически обоснованы разработанные технологические приемы производства мучных кондитерских изделий при сохранении влаги на всех стадиях производства. В рамках исследования решали следующие задачи: увеличение удельной поверхности частиц дисперсной фазы эмульсии за счет моделирования рецептурного состава; дезагрегирование муки, повышение равномерности распределения дисперсионной среды (эмульсии) с образованием оболочек вокруг максимально возможного количества частиц муки различных фракций. Объектом для моделирования рецептурного состава было сахарное печенье. Установлено, что замена рецептурных компонентов с повышенной влажностью на сырье с высоким содержанием сухих веществ позволяет высвободить влагу и использовать новые виды сырья с повышенными нативными свойствами. Предложенные приемы подготовки сырьевых компонентов: снижение вязкости солодового экстракта, используемого для снижения количества сахара-песка, осмотическое набухание яичного порошка, пластикация жира со стабилизацией его структуры лецитином, инверсия сахарозы в условиях совмещения гидродинамического и акустического кавитационных воздействий при получении инвертного сиропа – обеспечивают благоприятные условия получения эмульсии с повышенной удельной поверхностью. Отличительной особенностью предлагаемой технологии является получение эмульсии в две стадии: приготовление суспензии без жира и собственно получение эмульсии. Раздельная подача сахара в два приема: 40–60% его рецептурного количества вносится на стадии приготовления суспензии, оставшаяся часть – при приготовлении эмульсии – и кавитационная обработка суспензии при температуре 36–38°С и частоте колебаний волновода 24 кГц позволяют повысить частичную концентрацию частиц сахара в 8–12 раз. При приготовлении эмульсии пластицированный жир и лецитин предварительно смешивают с оставшейся частью сахара-песка, а затем с суспензией. Дезагрегированную путем аэрации муку и эмульсию одновременно и параллельно подают в месильную машину для достижения их заданного соотношения до начала процесса тестообразования. Разработанный комплекс технологических приемов позволил создать технологический поток производства сахарного печенья с улучшенными показателями качества – намокаемостью до 230% (по классической технологии 180–200%), сниженной на 20% плотностью, повышенными пористостью и рассыпчатостью и сохраняющего до 92% влажности, что на 18% выше, чем в изделиях, полученных по классической технологии. The developed technological techniques for the production of flour confectionery products while maintaining moisture at all stages of production are described and theoretically justified. The following tasks were solved in the framework of the study: increasing the specific surface area of the particles of the dispersed phase of the emulsion by modeling the recipe composition; disaggregating flour, increasing the uniformity of the distribution of the dispersion medium (emulsion) with the formation of shells around the maximum possible number of flour particles of various fractions. The object for modeling the formulation composition was sugar cookies. It is established that the replacement of prescription components with high humidity with raw materials with a high content of dry substances allows you to release moisture and use new types of raw materials with increased native properties. The proposed methods of preparation of raw materials: reducing the viscosity of malt extract used to reduce the amount of granulated sugar, osmotic swelling of egg powder, fat plasticization with the stabilization of its structure with lecithin, sucrose inversion under conditions of combining hydrodynamic and acoustic cavitation effects in the production of invert syrup – provide favorable conditions for obtaining an emulsion with an increased specific surface area. The production of an emulsion in two stages is a distinctive feature of the proposed technology: the preparation of a suspension without fat and the actual production of the emulsion. Separate supply of sugar in two steps: 40–60% of its prescription amount is introduced at the stage of preparation of the suspension, the remaining part – during the preparation of the emulsion – and cavitation treatment of the suspension at a temperature of 36–38°С and the waveguide oscillation frequency of 24 kHz, it is possible to increase the partial concentration of sugar particles by 8–12 times. When preparing the emulsion, the plasticized fat and lecithin are pre-mixed with the remaining part of the granulated sugar, and then with the suspension. The aeration-disaggregated flour and emulsion are fed simultaneously and in parallel to the kneading machine to achieve their desired ratio before the dough-forming process begins. The developed complex of technological techniques allowed to create a technological flow for the production of sugar cookies with improved quality indicators – wetting up to 230% (according to the classical technology 180–200%), reduced density by 20%, increased porosity and friability, and preserving up to 92% humidity, which is 18% higher than in products obtained by the classical technology.

Photocatalytic Degradation of Synthetic Sulfur Pollutants in Petroleum Fractions under Different pH and Photocatalyst

2021 ◽  
Vol 02 (01) ◽  
Author(s):  
Mohamad Alif Hakimi Hamdan ◽  
◽  
Nur Hanis Hayati Hairom ◽  
Nurhafisza Zaiton ◽  
Zawati Harun ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Zno Nanoparticles ◽  
Low Cost ◽  
Industrial Effluents ◽  
Degradation Process ◽  
Vital Role ◽  
Petroleum Fraction ◽  
Precipitation Method ◽  
Synthesis Process ◽  
Petroleum Fractions

Thiophene is one of the sulfur compounds in the petroleum fraction that can be harmful to living things and lead to a critical effect on the ecosystem. Photocatalytic degradation is one of the promising methods in treating wastewater as it can mineralization of pollutants into carbon dioxide and water. Other than that, this method is non-toxic and relatively low cost. The production of hydroxyl radicals playing a vital role in the degradation of organic pollutants. It has been claimed that the usage of zinc oxide (ZnO) nanoparticles could give an excellent degradation process as this photocatalyst have high photosensitivity, low cost and chemically stable. However, the preparation method of ZnO nanoparticles will affect the agglomeration, particle size, shape and morphology of particles and lead to influence the photocatalytic activity in degrading thiophene. Therefore, this study focused on the effectiveness of ZnO nanoparticles in the presence of fibrous nanosilica (KCC-1) and polyethylene glycol (PEG) as the capping agent to degrade synthetic thiophene. ZnO/KCC-1 had been synthesized via the precipitation method and characterized by using Fourier Transform Infrared (FTIR). The chemical bond and nature of the photocatalyst from the FTIR results proved that the synthesis process to produce the ZnO/KCC-1 was succeed. The large surface area of KCC-1 increases the effectiveness of ZnO which is supported by the experimental data. Accordingly, the optimum condition for photocatalytic degradation of thiophene is under pH 7 by using ZnO/KCC-1 as photocatalyst. Hence, it is believed that this research could be implemented to remove the thiophene in petroleum fraction from the actual industrial effluents and this can preserve nature in the future.

The effects of solvent viscosity on the morphology and photocatalytic activity of BiOBr catalysts

2021 ◽  
Author(s):  
Fengjuan Ge ◽  
Jie Zhu ◽  
Yan Xu ◽  
Jing Li ◽  
Xueyang Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Surface Area ◽  
Rhodamine B ◽  
Synthesis Method ◽  
Degradation Process ◽  
High Viscosity ◽  
Precipitation Method ◽  
Glycerol Solution ◽  
Solvent Viscosity ◽  
Degradation Tests

BiOBr photocatalysts were prepared by changing the solvent and synthesis method. SEM, XRD and BET characterization shows that the sample prepared in high-viscosity solution by precipitation method has tremella-like microstructure, with smaller size and higher surface area. Among them, the BiOBr prepared in glycerol solution (GR-P) has the highest surface area of 113.8 m2⋅[Formula: see text]. XRD also indicates that the GR-P has much more exposed (110) facets than other samples. The Rhodamine B degradation tests show that the GR-P has the best activity on both deethylation and aromatic ring destruction steps, indicating that the exposed (110) facets promote the degradation process.

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