scholarly journals The Use of Inorganic Packing Materials during Methane Biofiltration

2010 ◽  
Vol 2010 ◽  
pp. 1-8 ◽  
Author(s):  
Josiane Nikiema ◽  
Michèle Heitz
Keyword(s):  
Particle Size ◽  
Gas Phase ◽  
Average Particle Size ◽  
High Specific Surface Area ◽  
Packing Material ◽  
Average Particle ◽  
Packing Materials ◽  
Clay Particles ◽  
Good Surface ◽  
Methane Elimination

The objective behind this study is to select a suitable inorganic packing material for methane biofiltration. Three packing materials are to be compared: two rock materials (average particles' sizes: 2 and 5 mm) and one porous clay particles (average particle size of 7 mm). The main parameter used to assess the efficiency of the packing material is the methane elimination capacity. The study reveals that the rock material having an average particle size around 2 mm is to be preferred. This result is probably due to its high specific surface area and to its good surface properties as compared to the other 2 tested porous materials. The influence of the nonirrigation with the nutrient solution of the biofilter is also investigated. It has been found that nonirrigation of biofilter causes the biofilter performance to decrease significantly (e.g., 45% decrease in 1 week) even with the humidification of the gas phase prior to its introduction into the biofilter.

Gas-phase particle size distributions and lead loss during spray pyrolysis of (Bi,Pb)–Sr–Ca–Cu–O

1995 ◽  
Vol 10 (7) ◽  
pp. 1644-1652 ◽  
Author(s):  
Abhijit S. Gurav ◽  
Toivo T. Kodas ◽  
Jorma Joutsensaari ◽  
Esko I. Kauppincn ◽  
Riitta Zilliacus
Keyword(s):  
Particle Size ◽  
Spray Pyrolysis ◽  
Gas Phase ◽  
Phase Particle ◽  
Average Particle Size ◽  
Particle Diameter ◽  
Processing Temperature ◽  
Average Particle ◽  
Size Distributions ◽  
Particle Size Distributions

Gas-phase particle size distributions and lead loss were measured during formation of (Bi,Pb)-Sr-Ca-Cu-O and pure PbO particles by spray pyrolysis at different temperatures. A differential mobility analyzer (DMA) in conjunction with a condensation particle counter (CPC) was used to monitor the gas-phase particle size distributions, and a Berner-type low-pressure impactor was used to obtain mass size distributions and size-classified samples for chemical analysis. For (Bi,Pb)-Sr-Ca-Cu-O, as the processing temperature was raised from 200 to 700 °C, the number average particle size decreased due to metal nitrate decomposition, intraparticle reactions forming mixed-metal oxides and particle densification. The geometric number mean particle diameter was 0.12 μm at 200 °C and reduced to 0.08 and 0.07 μm, respectively, at 700 and 900 °C. When the reactor temperature was raised from 700 and 800 °C to 900 °C, a large number (∼107 no./cm3) of new ultrafine particles were formed from PbO vapor released from the particles and the reactor walls. Particles made at temperatures up to 700 °C maintained their initial stoichiometry over the whole range of particle sizes monitorcd; however, those made at 800 °C and above were heavily depleted in lead in the size range 0.5–5.0 μm. The evaporative losses of lead oxide from (Bi,Pb)-Sr-Ca-Cu-O particles were compared with the losses from PbO particles to gain insight into the pathways involved in lead loss and the role of intraparticle processes in controlling it.

Fabrication of Nanosized Alumina Powders by a Simple Polymer Solution Route

2006 ◽  
Vol 6 (11) ◽  
pp. 3633-3636
Author(s):  
Sang-Jin Lee ◽  
Sung-Yong Chun ◽  
Choong-Hyo Lee ◽  
Young-Soo Yoon
Keyword(s):  
Particle Size ◽  
Polymer Solution ◽  
Gas Adsorption ◽  
Average Particle Size ◽  
High Specific Surface Area ◽  
Milling Process ◽  
Degree Of Polymerization ◽  
Average Particle ◽  
Porous Microstructure ◽  
Solution Route

Nanosized alumina (Al2O3) powders had been successfully fabricated by a simple polymer solution route employing polyvinyl alcohol (PVA) as an organic carrier. The fabricated alumina powders had an average particle size of 6.1 nm with a high specific surface area of 99.5 m2/g. As well, the alumina powders were fully crystallized to α phase at a relatively low temperature of 1000 °C. The PVA polymer contributed to a soft and porous microstructure of the calcined alumina powders, and ball-milling process with the porous powders was effective in making nanosized alumina powders. In addition, the content and degree of polymerization of the PVA affected the development of crystallization and powder properties. In this study, the simple polymer technique and milling process for the fabrication of nanosized alumina powders are introduced, and the effects of PVA on the property of the synthesized alumina powders are observed. For the study, the characterizations of the synthesized powders are conducted by using XRD, TEM, particle size analyzer, and nitrogen gas adsorption.

scholarly journals Characterizations of Ag Nanoparticles Prepared by Different Reducing Agents

2018 ◽  
Vol 2 (1) ◽  
Keyword(s):  
Particle Size ◽  
Ag Nanoparticles ◽  
Leaf Extract ◽  
Average Particle Size ◽  
Particle Morphology ◽  
Reducing Agents ◽  
Average Particle ◽  
Good Surface ◽  
Reducing Ability ◽  
Granular Particle

Pure Ag nanoparticles were successfully prepared by using KBH4 , ascorbic acid, and holly leaf extract as reducing agents. The prepared Ag nanoparticles were characterized by various techniques to understand their chemical and physical properties. All the Ag nanoparticles showed granular particle morphology with a nano-scale size of 16.1- 29.2 nm and three visible photoluminescence peaks. By comparison, KBH4 showed sufficient high reducing ability and so resulted in a rapid formation of Ag nanoparticles, largest average particle size, and highest crystallinity. In contrary, holly leaf extract leads to the slowest formation of Ag nanoparticles, smallest average particle size, and lowest crystallinity. The Ag nanoparticles prepared with the KBH4 and holly leaf extract showed the highest and lowest photocatalytic activities, respectively. The crystallinity plays a more important role in photocatalytic activity rather than average particle size. Moreover, some hydroxyls existed on the surface of the Ag nanoparticles exists, indicating a good surface hydrophilicity. Small amounts of the impurities coming from the reducing agent residues acting as a capping layer were found on the surface of the Ag nanoparticles.

Characterization of nano- and microparticles in Swiss waters and their role in potable water production

2006 ◽  
Vol 6 (1) ◽  
pp. 21-29
Author(s):  
W. Pronk ◽  
B. Sinnet ◽  
S. Meylan ◽  
M. Boller
Keyword(s):  
Particle Size ◽  
Membrane Fouling ◽  
Average Particle Size ◽  
Average Particle ◽  
Clay Particles ◽  
Particle Count ◽  
High Particle ◽  
Large Numbers ◽  
High Precipitation ◽  
Membrane Treatment

Particles in lake water samples originating from the Swiss lakes of Zurich and Constance were analysed, showing an exponential increase of particle number with decreasing particle size down to the detection limit (350 nm). Investigation of nanoparticles in Lake Zurich by microscopic methods showed that relatively large numbers of clay particles are present with different Al/Si composition and sizes. The small-sized clay particles (ca. 80 nm) tend to build aggregates with a size of 500–1,000 nm. In karstic spring water, the particle count and size distribution is strongly dependent on the precipitation rate. At high precipitation rates, channel flow occurs in the subsoil, leading to high particle counts among the whole size range and a larger average particle size. In membrane treatment by microfiltration and ultrafiltration this leads to membrane fouling due to pore blocking and cake formation, the latter being associated with the presence of organic compounds.

Determination of grinding parameters of fenugreek seed

1970 ◽  
Vol 26 (1) ◽  
pp. 16 ◽  
Author(s):  
S Balasubramanian ◽  
Rajkumar Rajkumar ◽  
K K Singh
Keyword(s):  
Particle Size ◽  
Energy Consumption ◽  
Moisture Content ◽  
Specific Energy ◽  
Feed Rate ◽  
Average Particle Size ◽  
Specific Energy Consumption ◽  
Average Particle ◽  
Fenugreek Seeds ◽  
Fenugreek Seed

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.  

Formulating SLN and NLC as Innovative Drug Delivery Systems for Non-Invasive Routes of Drug Administration

2020 ◽  
Vol 27 (22) ◽  
pp. 3623-3656 ◽  
Author(s):  
Bruno Fonseca-Santos ◽  
Patrícia Bento Silva ◽  
Roberta Balansin Rigon ◽  
Mariana Rillo Sato ◽  
Marlus Chorilli
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Drug Release ◽  
Drug Loading ◽  
Average Particle Size ◽  
Delivery Systems ◽  
Average Particle ◽  
Minor Importance ◽  
Routes Of Administration ◽  
Non Invasive

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.

Azithromycin nanosuspension preparation using evaporative precipitation into aqueous solution (EPAS) method and its comparative dissolution study

2020 ◽  
Vol 17 ◽  
Author(s):  
Mohammad Hossain Shariare ◽  
Tonmoy Kumar Mondal ◽  
Hani Alothaid ◽  
Md. Didaruzzaman Sohel ◽  
MD Wadud ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Dissolution Rate ◽  
Average Particle Size ◽  
Scale Up ◽  
Average Particle ◽  
Total Drug ◽  
Residual Solvent ◽  
Dissolution Study ◽  
Drug Content

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.

scholarly journals Evaluation of the Effects of Filler Fineness on the Properties of an Epoxy Asphalt Mixture

Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 2003
Author(s):  
Wei Xu ◽  
Jintao Wei ◽  
Zhengxiong Chen ◽  
Feng Wang ◽  
Jian Zhao
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Asphalt Mixture ◽  
Average Particle ◽  
Fine Dust ◽  
Bonding Structure ◽  
Epoxy Asphalt ◽  
Mineral Powder ◽  
Marshall Stability ◽  
Mixture Sample

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.

scholarly journals Surface Activity of Humic Acid and Its Sub-Fractions from Forest Soil

2021 ◽  
Vol 13 (15) ◽  
pp. 8122
Author(s):  
Shijie Tian ◽  
Weiqiang Tan ◽  
Xinyuan Wang ◽  
Tingting Li ◽  
Fanhao Song ◽  
...  
Keyword(s):  
Surface Tension ◽  
Particle Size ◽  
Humic Acid ◽  
Forest Soil ◽  
Surface Activity ◽  
Self Assembly ◽  
Average Particle Size ◽  
Gaussian Model ◽  
Exponential Model ◽  
Average Particle

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.

Microstructure Characterization of Ag Nanoparticles Prepared by Hydrothermal Method

2012 ◽  
Vol 476-478 ◽  
pp. 1138-1141
Author(s):  
Zhi Qiang Wei ◽  
Qiang Wei ◽  
Li Gang Liu ◽  
Hua Yang ◽  
Xiao Juan Wu
Keyword(s):  
Crystal Structure ◽  
Particle Size ◽  
Hydrothermal Method ◽  
Ag Nanoparticles ◽  
Average Particle Size ◽  
Average Particle ◽  
Face Centered Cubic ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Face Centered

Ag nanoparticles were successfully synthesized by hydrothermal method under the polyol system combined with traces of sodium chloride, Silver nitrate(AgNO3) and polyvinylpyrrolidone (PVP) acted as the silver source and dispersant respectively. The samples by this process were characterized via X-ray powder diffraction (XRD), Brunauer–Emmett–Teller (BET) adsorption equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED) to determine the chemical composition, particle size, crystal structure and morphology. The experiment results indicate that the crystal structure of the samples is face centered cubic (FCC) structure as same as the bulk materials, The specific surface area is 24 m2/g, the particle size distribution ranging from10 to 50 nm, with an average particle size about 26 nm obtained by TEM and confirmed by XRD and BET results.

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