On the Electrochemical Properties of α-Li3FeF6 Prepared by Precipitation from Aqueous-Alcohol Based Solutions

2011 ◽  
Vol 1313 ◽  
Author(s):  
A. Basa ◽  
E. Gonzalo ◽  
A. Kuhn ◽  
F. García-Alvarado

ABSTRACTThe α-polymorph of Li3FeF6 has been prepared from aqueous-based solution by precipitation under different conditions to obtain small particles. Several alcohols have been used to vary the precipitation media. Among them 2-propanol has been found to provide particles of about 100 nm under controlled conditions of temperature and H2O: R-OH volume ratio. The average particle size of some of the as-prepared samples is smaller than that obtained for those samples obtained by precipitation in water. However, the expected enhancement of electrochemical performances does not occur for the as-prepared samples. Inserted amount of lithium into the cryolite structure of Li3FeF6 increases significantly only when composites of asprepared Li3FeF6 and carbon are milled mechanically. For example 12h milling is needed to reach 64 mAh/g (45% of theoretical capacity).

1996 ◽  
Vol 11 (5) ◽  
pp. 1199-1209 ◽  
Author(s):  
J. M. McHale ◽  
P. C. McIntyre ◽  
K. E. Sickafus ◽  
N. V. Coppa

An aqueous, all nitrate, solution-based preparation of BaTiO3 is reported here. Rapid freezing of a barium and titanyl nitrate solution, followed by low temperature sublimitation of the solvent, yielded a freeze-dried nitrate precursor which was thermally processed to produce BaTiO3. XRD revealed that 10 min at temperatures ≧600 °C resulted in the formation of phase pure nanocrystalline BaTiO3. TEM revealed that the material was uniform and nanocrystalline (10–15 nm). The high surface to volume ratio inherent in these small particles stabilized the cubic phase of BaTiO3 at room temperature. It was also found that the average particle size of the BaTiO3 produced was highly dependent upon calcination temperature and only slightly dependent upon annealing time. This result suggests a means of selection of particle size of the product through judicious choice of calcination temperature. The experimental details of the freeze-dried precursor preparation, thermal processing of the precursor, product formation, and product morphology are discussed.


1941 ◽  
Vol 14 (1) ◽  
pp. 98-112 ◽  
Author(s):  
D. Parkinson

Abstract The mechanism of filler reinforcement has not yet been fully explained, but there is general agreement that an important, probably the most important, factor is the enormous surface development between the rubber and filler due to the fine particle size of the filler. Explanations have been attempted to show how small particles can cause reinforcement, but a complete theory of the phenomenon which accounts for all the facts is still awaited. Particle size oj carbon blacks.—A knowledge of this property is important in an understanding of the mechanism of reinforcement by carbon black. Because of the difficulty of distinguishing between ultimate particles and compact aggregates, and because the particles themselves are too small to be resolved in an ordinary microscope, the usual microscopical methods of measurement are inapplicable. Ultramicroscopical methods have been used with some success, the results obtained by the method of Gehman and Morris being probably the most reliable. These authors quote an average particle size of 61µµ for a sample of a standard rubber gas black (Micronex). The figures given for P-33 black, Shawinigan acetylene black and Thermatomic black are 159µµ, 130µµ and 1120µµ, respectively.


2002 ◽  
Vol 57 (3-4) ◽  
pp. 154-158 ◽  
Author(s):  
C. Cannas ◽  
G. Concas ◽  
F. Congiu ◽  
A. Musinu ◽  
G. Piccaluga ◽  
...  

A series of Fe2O3-SiO2 nanocomposites (25 weight % of Fe2O3) has been prepared using a sol-gel method. Samples showing different features were obtained by varying the evaporation conditions acting on the surface / volume ratio of the starting sol. The samples were investigated using Mössbauer spectroscopy at low temperature. The Fe2O3 nanoparticles have been identified as maghemite ( γ-Fe2O3) particles. The samples show a superparamagnetic behavior with a blocking temperature that depends on the average particle size.


2014 ◽  
Vol 997 ◽  
pp. 312-316
Author(s):  
Xue Ming Zheng ◽  
Xiao Na Duan ◽  
Yang Yang Sun ◽  
Hui Jian Shang

At present, the methods of analysising the average particle size of silica sol are the intuitive analysis, such as analysising the size distribution and morphology of the particle by the laser particle size instrument and the transmission electron microscopy. But some of the small particles tend to be ignored. Using the classical chemical titration method and BET to auxiliary analysis can make the date more complete. Through the comprehensive analysis with the four methods, found that longer reaction time have the effect of purification of sol system.


2021 ◽  
Vol 2021 ◽  
pp. 1-18
Author(s):  
Pimsumon Jiamboonsri ◽  
Sompit Wanwong

The green synthesis of silver nanoparticles (AgNPs) has been attractive in biomedical applications due to its nontoxic and eco-friendly approach. This study presents the facile, rapid, and cost-effective synthesis of AgNPs by photoassisted chemical reduction using Riceberry (RB) rice extract as a reducing agent. The effects of reaction parameters including photoirradiation, irradiation time, the volume ratio of silver nitrate (AgNO3) to RB extract, and pH condition on the AgNP formation were also investigated. The characterization of AgNPs was determined by UV–visible spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier-transform infrared (FT-IR) spectroscopy. For antibacterial application, the synthesized AgNPs were studied by disc diffusion method against Escherichia coli and Staphylococcus aureus. The results indicated that light irradiation was an important factor to accelerate the formation of AgNPs. The synthesis parameters including volume of RB extract and pH condition significantly affected the particle size and crystallinity of AgNPs. The volume ratio of AgNO3 to RB extract 1 : 12.5 at pH 2.5 under photoirradiation was the successful condition to form nanometer-sized crystalline particles (average particle size of 59.48 ± 0.37   nm ) within 30 min with a rate constant of 0.210 min–1. The FT-IR measurement also suggested that the phytochemical constituents in RB extract were served as reducing and stabilizing agents for the synthesis of AgNPs. Additionally, the obtained AgNPs from various conditions demonstrated the antibacterial activity against both strains. Therefore, this study proposes an effective integration technique to synthesize AgNPs within a short time for antibacterial application.


1970 ◽  
Vol 26 (1) ◽  
pp. 16 ◽  
Author(s):  
S Balasubramanian ◽  
Rajkumar Rajkumar ◽  
K K Singh

Experiment to identify ambient grinding conditions and energy consumed was conducted for fenugreek. Fenugreek seeds at three moisture content (5.1%, 11.5% and 17.3%, d.b.) were ground using a micro pulverizer hammer mill with different grinding screen openings (0.5, 1.0 and 1.5 mm) and feed rate (8, 16 and 24 kg h-1) at 3000 rpm. Physical properties of fenugreek seeds were also determined. Specific energy consumptions were found to decrease from 204.67 to 23.09 kJ kg-1 for increasing levels of feed rate and grinder screen openings. On the other hand specific energy consumption increased with increasing moisture content. The highest specific energy consumption was recorded for 17.3% moisture content and 8 kg h-1 feed rate with 0.5 mm screen opening. Average particle size decreased from 1.06 to 0.39 mm with increase of moisture content and grinder screen opening. It has been observed that the average particle size was minimum at 0.5 mm screen opening and 8 kg h-1 feed rate at lower moisture content. Bond’s work index and Kick’s constant were found to increase from 8.97 to 950.92 kWh kg-1 and 0.932 to 78.851 kWh kg-1 with the increase of moisture content, feed rate and grinder screen opening, respectively. Size reduction ratio and grinding effectiveness of fenugreek seed were found to decrease from 4.11 to 1.61 and 0.0118 to 0.0018 with the increase of moisture content, feed rate and grinder screen opening, respectively. The loose and compact bulk densities varied from 219.2 to 719.4 kg m-3 and 137.3 to 736.2 kg m-3, respectively.  


2020 ◽  
Vol 27 (22) ◽  
pp. 3623-3656 ◽  
Author(s):  
Bruno Fonseca-Santos ◽  
Patrícia Bento Silva ◽  
Roberta Balansin Rigon ◽  
Mariana Rillo Sato ◽  
Marlus Chorilli

Colloidal carriers diverge depending on their composition, ability to incorporate drugs and applicability, but the common feature is the small average particle size. Among the carriers with the potential nanostructured drug delivery application there are SLN and NLC. These nanostructured systems consist of complex lipids and highly purified mixtures of glycerides having varying particle size. Also, these systems have shown physical stability, protection capacity of unstable drugs, release control ability, excellent tolerability, possibility of vectorization, and no reported production problems related to large-scale. Several production procedures can be applied to achieve high association efficiency between the bioactive and the carrier, depending on the physicochemical properties of both, as well as on the production procedure applied. The whole set of unique advantages such as enhanced drug loading capacity, prevention of drug expulsion, leads to more flexibility for modulation of drug release and makes Lipid-based nanocarriers (LNCs) versatile delivery system for various routes of administration. The route of administration has a significant impact on the therapeutic outcome of a drug. Thus, the non-invasive routes, which were of minor importance as parts of drug delivery in the past, have assumed added importance drugs, proteins, peptides and biopharmaceuticals drug delivery and these include nasal, buccal, vaginal and transdermal routes. The objective of this paper is to present the state of the art concerning the application of the lipid nanocarriers designated for non-invasive routes of administration. In this manner, this review presents an innovative technological platform to develop nanostructured delivery systems with great versatility of application in non-invasive routes of administration and targeting drug release.


2020 ◽  
Vol 17 ◽  
Author(s):  
Mohammad Hossain Shariare ◽  
Tonmoy Kumar Mondal ◽  
Hani Alothaid ◽  
Md. Didaruzzaman Sohel ◽  
MD Wadud ◽  
...  

Aim: EPAS (evaporative precipitation into aqueous solution) was used in the current studies to prepare azithromycin nanosuspensions and investigate the physicochemical characteristics for the nanosuspension batches with the aim of enhancing the dissolution rate of the nanopreparation to improve bioavailability. Methods: EPAS method used in this study for preparing azithromycin nanosuspension was achieved through developing an in-house instrumentation method. Particle size distribution was measured using Zetasizer Nano S without sample dilution. Dissolved azithromycin nanosuspensions were also compared with raw azithromycin powder and commercially available products. Total drug content of nanosuspension batches were measured using an Ultra-Performance Liquid Chromatography (UPLC) system with Photodiode Array (PDA) detector while residual solvent was measured using gas chromatography (GC). Results: The average particle size of azithromycin nanosuspension was 447.2 nm and total drug content was measured to be 97.81% upon recovery. Dissolution study data showed significant increase in dissolution rate for nanosuspension batch when compared to raw azithromycin and commercial version (microsuspension). The residual solvent found for azithromycin nanosuspension is 0.000098023 mg/ mL or 98.023 ppb. Conclusion: EPAS was successfully used to prepare azithromycin nanoparticles that exhibited significantly enhanced dissolution rate. Further studies are required to scale up the process and determine long term stability of the nanoparticles.


Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 2003
Author(s):  
Wei Xu ◽  
Jintao Wei ◽  
Zhengxiong Chen ◽  
Feng Wang ◽  
Jian Zhao

The type and fineness of a filler significantly affect the performance of an asphalt mixture. There is a lack of specific research on the effects of filler fineness and dust from aggregates on the properties of epoxy asphalt (EA) mixtures. The effects of aggregate dust and mineral powder on the properties of an EA mixture were evaluated. These filler were tested to determine their fineness, specific surface area and mineral composition. The effects of these fillers on the EA mastic sample and mixture were evaluated. The morphology of the EA mastic samples was analyzed using scanning electron microscopy (SEM). The effects of the fillers on the Marshall stability, tensile strength and fatigue performance of the EA mixture were evaluated. The dust from the aggregates exhibited an even particle size distribution, and its average particle size was approximately 20% of that of the mineral powder. The SEM microanalysis showed that the EA mastic sample containing relatively fine dust formed a tight and dense interfacial bonding structure with the aggregate. The EA mixture sample containing filler composed of dust from aggregate had a significantly higher strength and longer fatigue life than that of the EA sample containing filler composed of mineral powder.


2021 ◽  
Vol 13 (15) ◽  
pp. 8122
Author(s):  
Shijie Tian ◽  
Weiqiang Tan ◽  
Xinyuan Wang ◽  
Tingting Li ◽  
Fanhao Song ◽  
...  

Surface activity of humic acid (HA) and its six sub-fractions isolated from forest soil were characterized by surface tension measurements, dynamic light scattering, and laser doppler electrophoresis. The surface tension of HA and its sub-fractions reduced from 72.4 mN·m−1 to 36.8 mN·m−1 in exponential model with the increasing concentration from 0 to 2000 mg·L−1. The critical micelle concentration (CMC) and Z-average particle size ranged from 216–1024 mg·L−1 and 108.2–186.9 nm for HA and its sub-fractions, respectively. The CMC have related with alkyl C, O-alkyl C, aromatic C, and carbonyl C (p < 0.05), respectively, and could be predicted with the multiple linear regression equation of CMC, CMC = 18896 − 6.9 × C-296 × alkyl C-331 × aromatic C-17019 × H/C + 4054 × HB/HI (p < 0.05). The maximum particle size was 5000 nm after filtered by a membrane with pore size of 450 nm, indicating HA and its sub-fractions could progressed self-assembly at pH 6.86. The aggregate sizes of number-base particle size distributions were mainly in six clusters including 2 ± 1 nm, 5 ± 2 nm, 10 ± 3 nm, 21 ± 8 nm, 40 ± 10 nm, and >50 nm analyzed by Gaussian model that maybe due to the inconsistency of the components and structures of the HA sub-fractions, requiring further study. It is significance to explore the surface activity of HA and its sub-fractions, which is helpful to clarify the environmental behavior of HA.


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