scholarly journals Development of sedimentation resistant water-acrylic titanium dioxide dispersions

2021 ◽  
Vol 4 (6(112)) ◽  
pp. 51-59
Author(s):  
Antonina Dyuryagina ◽  
Aida Lutsenko

According to the results of the research, the effect of stabilization of dispersions of titanium dioxide in water-acrylic compositions was established. It was proved that in aqueous-acrylic suspensions at all variations of film-forming agent (from 0 to 5 g/dm3), the maximum of stabilizing activity of the surfactants under study is achieved at CSAS=0.25 g/dm3. The minimum deposition rate of titanium dioxide dispersions at a dosing of 0.25 g/dm3 of sodium polyacrylate was at the level of 0.097 10-3 g/s at any content of film-forming agent (Cff=0.5÷5 g/dm3) in suspensions. At the introduction of the same concentration (CSAS=0.25 g/dm3) of the polyether siloxane copolymer, a decrease in sedimentation rate to 0.053 10-3 g/s in suspensions with a limited acryl content (C≤1 g/dm3) was recorded. At an increase in the concentration of a film-forming agent (C>1 g/dm3) in suspensions, sedimentation stability decreased, which is proved by an increase in the sedimentation rate of TiO2 to 0.110∙10-3 g/s at Cff=5.0 g/dm3. It was found that in aqueous-acrylic suspensions with the film-forming content from 0.5 to 1 g/dm3, the minimum average diameter was 2.64÷3.1 μm CSAS=0.25 g/dm3. Further concentration of acryl (Cff=4÷5 g/dm3) at the same dosage of polyether siloxane copolymer was accompanied by an increase in the average particle size up to 4.30÷4.61 μm. The maximum of wedging activity of sodium polyacrylate (CSAS=0.25 g/dm3) corresponds to the same minimum of the average diameter (2–3 μm).

1986 ◽  
Vol 18 (1) ◽  
pp. 31-42 ◽  
Author(s):  
E. A. Shpirt ◽  
K. T. Alben

The particle size distribution at different bed depths of a fixed bed of granular activated carbon (GAC) has been monitored during 50 weeks of a pilot column run at the Waterford, New York potable water treatment plant. Initial backwashing resulted in significant stratification of GAC in the column: larger particles (average diameter 1.18 mm) settled in the bottom of the column (105 cm), and smaller particles (average diameter 0.97 mm) were concentrated near the top (24 cm), compared to samples of unstratified virgin Calgon F400 (average diameter 1.09 mm). During column loading and initial backwashing, more fines were created than were present in the virgin GAC (average 6.5% of GAC fines in the > 40 mesh fraction, compared to only 0.3% in the > 40 mesh fraction for virgin Calgon F400). After 50 weeks of service there was an overall trend toward a smaller average particle size (0.9 mm) with development of a more regular pattern of bed stratification (1.08 mm at the bottom and 0.75 mm at the top). These changes are attributed to breaking of large particles (12-20 mesh) and creation of intermediate size particles (20-30 and 30-40 mesh).


2016 ◽  
Vol 690 ◽  
pp. 236-239
Author(s):  
Oratai Jongprateep ◽  
Rachata Puranasamriddhi

High photocatalytic activity of nanoparticulate titanium dioxide has attracted worldwide attention. Synthesis techniques of the nanoparticles, however, often require high energy supply or costly initial reagents. Solution combustion technique is an energy-effective technique capable of synthesizing nanosized titanium powders. This research aimed at utilizing a less expensive initial reagent in synthesis of nanoparticulate titanium dioxide by the solution combustion technique. The research also examined effects of dissolving agents on chemical composition and particle sizes of the synthesized powders. A low-cost initial reagent, titanium dioxide with average particle size of 154 nanometers, was dissolved in sulfuric acid or dispersed in nitric acid prior to the combustion. Experimental results revealed that the pure anatase phase titanium dioxide was successfully obtained in powders prepared from both sulfuric acid and nitric acid. The average particle size of the powder prepared from sulfuric acid was 77 nanometers, while that of the powder prepared from nitric acid was 117 nanometers. The difference in particle sizes was attributed to solubility of the initial reagent in the acid. Complete solution of initial reagent in sulfuric acid was the main factor attributed to finer particle size.


2015 ◽  
Vol 33 (1) ◽  
pp. 18-24 ◽  
Author(s):  
T.K. Mandal

AbstractPbZr0:5Ti0:5O3 nanopowders (~27 nm) have been prepared by a controlled reconstructive thermal decomposition and crystallization from an amorphous polymeric precursor with polyvinyl alcohol (PVA) and sucrose at 400 to 700 °C in air. The Rietveld refinement of the XRD profiles which were recorded at room temperature for the PbZr0:5Ti0:5O3 powder prepared by a thermal treatment at 700 °C for 2 h, confirmed the P4mm tetragonal crystal structure of the as prepared PbZr0:5Ti0:5O3 nanopowders, with a = 0.4036 nm and c = 0.4147 nm. A hexagonal symmetry (R3c), with a = 0.5774 nm and c = 1.4212 nm, was also detected from Rietveld refinement analysis. Thus, tetragonal and hexagonal phases were found to coexist with the as prepared PbZr0:5Ti0:5O3 nanopowders. The average particle size (D) of the PbZr0:5Ti0:5O3 powders, estimated with the help of the specific surface area, measured by BET method, was 26.1 nm. Average D value, calculated by D2θ1/2 in the XRD peaks with the Debye-Scherrer relation was ~24 nm. TEM study made it possible to measure the particle size of PbZr0:5Ti0:5O3 powders with an average diameter of 27 nm.


2019 ◽  
Vol 7 (1) ◽  
pp. 51-60
Author(s):  
Paulina Taba ◽  
Nadya Yuli Parmitha ◽  
Syahruddin Kasim

Silver nanoparticles have been synthesized by the reduction method using salam leaf extract (Syzygium polyanthum) as a reducing agent. The silver nanoparticles produced were then tested for their activity as antioxidants. The formation of silver nanoparticles was carried out by adding the leaf extract into the solution of AgNO3 and homogenized using a magnetic stirrer. A UV-Vis spectrophotometer was used to confirm the formation of silver nanoparticles. Particle Size Analyzer (PSA), Scanning Electron Microscope (SEM), X-Ray Diffractometer (XRD) and Fourir Transform Infra Red (FTIR) spectrometers were used to characterize the nanoparticles produced before being tested for antioxidant activity. The results showed that the absorbance value increased with increasing reaction contact time. The maximum uptake was obtained at wavelengths of 432-446 nm using a UV-Vis spectrophotometer. The particle size was determined using a PSA with an average particle size distribution of 45.7 nm. The average diameter of silver nanoparticles was 10.06 – 13.97 nm and the silver nanoparticles had rod-shapes. Functional groups that play a role in the synthesis of nanoparticles were –OH, –C=O, and –C-O groups. Silver nanoparticles inhibited free radicals as antioxidants with the IC50 value of 582.7 ppm.


Author(s):  
Yu. M. Domnina ◽  
S. A. Kedik ◽  
V. V. Suslov ◽  
E. A. Shnyak ◽  
S. S. Kryukova

The work is dedicated to the production of polymer suspensions using ultrasonic dispergation in a flow mode. An apparatus was designed on the basis of a Russian flow ultrasonicator. The applicability of this apparatus for obtaining aqueous dispersions of polymeric micro- and nanoparticles by means of one-step emulsification followed by solvent extraction / evaporation was demonstrated. The influence of the process parameters on the characteristics of the obtained suspensions was studied. The particle size distribution and the average size of the resulting particles were evaluated by using Delsa Nano S, Beckman Coulter laser analyzer (USA). The dependence of the average diameter of the suspension particles on the stabilizer concentration and on the change of the phases feed rate was shown. When polyvinyl alcohol was used as a stabilizer in the concentration range 0.5-2%, the average particle size was 30-400 nm. The feed rates of the aqueous and organic phases affect the nature of the particle size distribution.


2019 ◽  
Vol 16 (4) ◽  
pp. 0910
Author(s):  
Fayyadh Et al.

In this research, titanium dioxide nanoparticles (TiO2 NPs) were prepared through the sol-gel process at an acidic medium (pH3).TiO2 nanoparticles were prepared from titanium trichloride (TiCl3) as a precursor with Ammonium hydroxide (NH4OH) with 1:3 ratio at 50 °C. The resulting gel was dried at 70 °C to obtain the Nanocrystalline powder. The powder from the drying process was treated thermally at temperatures 500 °C and 700 °C. The crystalline structure, surface morphology, and particle size were studied by using X-ray diffraction (XRD), Atomic Force Microscopy (AFM), and Scanning Electron Microscope (SEM). The results showed (anatase) phase of titanium dioxide with the average grain size of 110 nm at 500 °C calcination temperature, and (anatase- rutile) mixed phase of titanium dioxide with the average particle size of 118.1 nm at 700 °C calcination temperature. The anti-bacterial activity of the synthesis specimens was recorded through the Kirby-Bauer disc method (disc devotion method). The results displayed a pretty excellent antibacterial activity of TiO2 NPs to bacteria strains: Gram positive staphylococcus aureus, gram negative pseudomonas aeruginosa, and "gram negative escherichia coli. The sensitivity of the tested bacteria to TiO2 NPs depends on the oxidation state of the TiO2 NPs, particle size, volume, and the density of the unit cell. The small- average particle size of titanium dioxide particles showed high antibacterial activity against bacteria, while the larger- average particle size of titanium dioxide particles showed less antibacterial activity. The novelty of this production is the manufacturing of a novel kind of TiO2 NPs and achievement its best antibacterial activity.


2011 ◽  
Vol 347-353 ◽  
pp. 979-983
Author(s):  
Jing Zhi Jiang ◽  
Pei Ying Peng ◽  
Hai Ting Cui ◽  
Zhi Yi Li

ZrO2 nano-particles were successfully prepared by supercritical hydrolysis in two steps (hydrolysis and dehydration) and were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and laser particle-size analyzer. The influences of operation parameters, including operation pressure and temperature, CO2 total flow and ratio of CO2 branch flow, on the particles were investigated experimentally. The results show that average particle size increases with the increase of the operation temperature, while it decreases with the increase of the operation pressure and the CO2 total flow. The smallest particles with average diameter of 793nm can be prepared under the condition: operation temperature and pressure of 50°C and 8MPa, CO2 total flow of 30 standard cubic centimeter per Minute and ratio of CO2 branch flow of 3.


2011 ◽  
Vol 410 ◽  
pp. 228-231
Author(s):  
Wimonlak Sutapun ◽  
Yupaporn Ruksakulpiwat ◽  
Nitinat Suppakarn ◽  
Rachasit Jeencham ◽  
Ajcharaporn Aontee

In this work, PCC was prepared from chicken eggshell powder (ESP) by dissolving 100 g ESP in 1 M hydrochloric acid at room temperature. Under vigorous stirring, PCC was precipitated from the ESP-dissolved solution using 1 M sodium carbonate solution. The dried PESP (precipitated eggshell powder) was then characterized by particle size analyzer, X-ray diffractometer, Brunauer-Emmett-Teller surface analyzer and thermogravimetric analyzer. The particle shape of the PESP was revealed using scanning electron microscope. It was found that PESP was a binary mixer of calcite and vaterite. The particles were in cubic and spherical shape. In addition, PESP had a volume average diameter of 8.16 μm, D[V, 0.5] of 7.22 μm, D[V,0.9] of 16.57 μm, and the specific surface area of 4.38 m2/g. The average particle size was lower than and the specific surface area was higher than that of ESP. The decomposition process of PESP occured in a single step between 610 and 770 °C, with 44.43% weight loss.


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.


Sign in / Sign up

Export Citation Format

Share Document