scholarly journals Evaluation of rheological properties of mortar with TiO2 addition

2021 ◽  
Vol 21 (4) ◽  
pp. 7-21
Author(s):  
Sérgio Roberto Andrade Dantas ◽  
Francisco Jordão Nunes de Lima ◽  
Roberto Cesar de Oliveira Romano ◽  
Rafael Pileggi ◽  
Kai Loh
Keyword(s):  
Fine Particles ◽  
High Surface ◽  
High Surface Area ◽  
Squeeze Flow ◽  
Physical Parameters ◽  
Blind Test ◽  
Depth Analysis ◽  
Flow Table ◽  
Tio2 Addition ◽  
Rheological Indices

Abstract Adding TiO2 tocoating mortars is carried out to promote self-cleaning through photocatalytic activity. However, this addition influences the workability of the mortar and, consequently, the application stage as the TiO2 used can present a large number of fine particles and a high surface area, increasing the demand for mixing water, requiring consistency adjustments before coating. In this work, three mortars (two with the addition of different types of TiO2 and one reference) were developed on a laboratory scale to maintain similar workability, using the flow table test. The amount of kneading water was changed to maintain a spread of 220 ± 10 mm and the content of air-entrained was kept constant, around 25%. The mortars were evaluated using the squeeze flow method. Then, a blind test was performed to assess the mason sensitivity during handling and application of the coating, and all mortars were considered similar. However, the yield of the compositions with TiO2 addition was lower compared to the reference composition, making it possible to explain the results based on the physical parameters of the formulations and with a more in-depth analysis of the rheological indices obtained by the squeeze flow test.

scholarly journals Dissolution Enhancement of Gliclazide Using pH Change Approach in Presence of Twelve Stabilizers with Various Physico-Chemical Properties

2009 ◽  
Vol 12 (3) ◽  
pp. 250 ◽  
Author(s):  
Roya Talari ◽  
Ali Nokhodchi ◽  
Seyed Abolfazl Mostafavi ◽  
Jaleh Varshosaz
Keyword(s):  
Dissolution Rate ◽  
Fine Particles ◽  
High Surface ◽  
High Surface Area ◽  
Chemical Properties ◽  
High Energy ◽  
Dissolution Enhancement ◽  
Ph Change ◽  
Fast Dissolution

Purpose: The micronization using milling process to enhance dissolution rate is extremely inefficient due to a high energy input, and disruptions in the crystal lattice which can cause physical or chemical instability. Therefore, the aim of the present study is to use in situ micronization process through pH change method to produce micron-size gliclazide particles for fast dissolution hence better bioavailability. Methods: Gliclazide was recrystallized in presence of 12 different stabilizers and the effects of each stabilizer on micromeritic behaviors, morphology of microcrystals, dissolution rate and solid state of recrystallized drug particles were investigated. Results: The results showed that recrystallized samples showed faster dissolution rate than untreated gliclazide particles and the fastest dissolution rate was observed for the samples recrystallized in presence of PEG 1500. Some of the recrystallized drug samples in presence of stabilizers dissolved 100% within the first 5 min showing at least 10 times greater dissolution rate than the dissolution rate of untreated gliclazide powders. Micromeritic studies showed that in situ micronization technique via pH change method is able to produce smaller particle size with a high surface area. The results also showed that the type of stabilizer had significant impact on morphology of recrystallized drug particles. The untreated gliclazide is rod or rectangular shape, whereas the crystals produced in presence of stabilizers, depending on the type of stabilizer, were very fine particles with irregular, cubic, rectangular, granular and spherical/modular shape. The results showed that crystallization of gliclazide in presence of stabilizers reduced the crystallinity of the samples as confirmed by XRPD and DSC results. Conclusion: In situ micronization of gliclazide through pH change method can successfully be used to produce micron-sized drug particles to enhance dissolution rate.

Filler Aggregates and Their Effect on Reinforcement

1974 ◽  
Vol 47 (2) ◽  
pp. 411-433 ◽  
Author(s):  
A. I. Medalia
Keyword(s):  
Carbon Black ◽  
Fine Particles ◽  
High Surface ◽  
High Surface Area ◽  
Experimental Studies ◽  
Spherical Particles ◽  
Rubber Compound ◽  
Carbon Blacks ◽  
Reinforcing Fillers ◽  
Aggregate Nature

Abstract The most highly reinforcing fillers, namely carbon blacks and silicas, consist of aggregates of quasi-spherical particles fused together. In the absence of direct experimental studies with single-particle carbon blacks or silicas of high surface area, we cannot be sure if aggregated structure is essential for good reinforcement, or whether aggregation and fusion just happen to accompany the formation of fine particles at practical concentrations. In any case, there is no doubt that the aggregate nature of the filler plays a major role in determining the properties of the rubber compound. Here I would like to review what we know about filler aggregates, especially of carbon black, and suggest some mechanisms for their effects on rubber; and also indicate where our knowledge seems inadequate at the present time.

scholarly journals High Surface Area Ceria Nanoparticles via Hydrothermal Synthesis Experiment Design

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Stanislav Kurajica ◽  
Iva Minga ◽  
Martina Guliš ◽  
Vilko Mandić ◽  
Ivan Simčić
Keyword(s):  
Hydrothermal Synthesis ◽  
Surface Area ◽  
Fine Particles ◽  
High Surface ◽  
High Surface Area ◽  
Soot Oxidation ◽  
Nitrogen Adsorption ◽  
Synthesis Temperature ◽  
Oxidation Catalyst ◽  
Adsorption Desorption

Hydrothermal synthesis of CeO2was optimized on two reactant concentrations and synthesis temperature and duration, in order to achieve material having the greatest specific surface area (SSA). Taguchi method of experimental design was employed in evaluation of the relative importance of synthesis parameters. CeO2nanoparticles were characterized using X-ray diffraction, nitrogen adsorption-desorption isotherms, and scanning electron microscopy. Optimum conditions for obtaining particles with greater SSA were calculated according to Taguchi’s model “the-higher-the-better.” Synthesis temperature was found to be the only parameter significant for enabling nanoparticles with greater SSA. Mesoporous nanocrystalline ceria with SSA as great as 226 m2 g−1was achieved, which is unprecedented for the hydrothermally synthesized ceria. The reason for this achievement was found in temperature dependence of the diffusion coefficient which, when low, favors nucleation yielding with fine particles, while when high it favors crystal growth and formation of one-dimensional structures. The occurrence of 1D-structure in sample exhibiting the smallest SSA was confirmed. Very fine crystallites with crystallite size as low as 5.9 nm have been obtained being roughly inverse proportional to SSA. Selected samples were tested as catalyst for soot oxidation. Catalyst morphology turned out to be decisive factor for catalytic activity.

The synthesis and characterization of solid-state materials produced by high shear-hydrodynamic cavitation

1995 ◽  
Vol 10 (9) ◽  
pp. 2322-2335 ◽  
Author(s):  
W.R. Moser ◽  
B.J. Marshik ◽  
J. Kingsley ◽  
M. Lemberger ◽  
R. Willette ◽  
...  
Keyword(s):  
Solid State ◽  
Metal Oxides ◽  
Fine Particles ◽  
Continuous Process ◽  
High Surface ◽  
High Surface Area ◽  
Hydrodynamic Cavitation ◽  
Complex Metal Oxides ◽  
Solid State Materials

A new method for the synthesis of complex metal oxides, based on hydrodynamic cavitation, was used to prepare pure phase, nanostructured solid-state materials. The continuous process afforded a wide variety of metal oxides in grain sizes of 1-10 nm. Catalysts, ceramics, superconductors, piezoelectrics, and zeolites were prepared by cavitational synthesis. The method enabled the synthesis of fine particles of metals and metal oxides supported on high surface area supports such as silica, and the synthesis of fine particles of cubic zirconia without ion modification.

In Situ microscopy of the anodic etching of silicon

1995 ◽  
Vol 53 ◽  
pp. 232-233
Author(s):  
Frances M. Ross ◽  
Peter C. Searson
Keyword(s):  
Composite Structures ◽  
High Surface ◽  
High Surface Area ◽  
Chemical Properties ◽  
Selective Etching ◽  
Silicon On Insulator ◽  
Second Phase ◽  
Porous Layers ◽  
New Class ◽  
Porous Semiconductors

Porous semiconductors represent a relatively new class of materials formed by the selective etching of a single or polycrystalline substrate. Although porous silicon has received considerable attention due to its novel optical properties1, porous layers can be formed in other semiconductors such as GaAs and GaP. These materials are characterised by very high surface area and by electrical, optical and chemical properties that may differ considerably from bulk. The properties depend on the pore morphology, which can be controlled by adjusting the processing conditions and the dopant concentration. A number of novel structures can be fabricated using selective etching. For example, self-supporting membranes can be made by growing pores through a wafer, films with modulated pore structure can be fabricated by varying the applied potential during growth, composite structures can be prepared by depositing a second phase into the pores and silicon-on-insulator structures can be formed by oxidising a buried porous layer. In all these applications the ability to grow nanostructures controllably is critical.

Electron holography of catalysts

1995 ◽  
Vol 53 ◽  
pp. 416-417
Author(s):  
A. K. Datye ◽  
D. S. Kalakkad ◽  
L. F. Allard ◽  
E. Völkl
Keyword(s):  
Heterogeneous Catalysts ◽  
High Surface ◽  
High Surface Area ◽  
Atomic Scale ◽  
Nano Particles ◽  
Phase Image ◽  
Electron Holography ◽  
Specimen Thickness ◽  
Phase Information ◽  
Particle Structure

The active phase in heterogeneous catalysts consists of nanometer-sized metal or oxide particles dispersed within the tortuous pore structure of a high surface area matrix. Such catalysts are extensively used for controlling emissions from automobile exhausts or in industrial processes such as the refining of crude oil to produce gasoline. The morphology of these nano-particles is of great interest to catalytic chemists since it affects the activity and selectivity for a class of reactions known as structure-sensitive reactions. In this paper, we describe some of the challenges in the study of heterogeneous catalysts, and provide examples of how electron holography can help in extracting details of particle structure and morphology on an atomic scale.Conventional high-resolution TEM imaging methods permit the image intensity to be recorded, but the phase information in the complex image wave is lost. However, it is the phase information which is sensitive at the atomic scale to changes in specimen thickness and composition, and thus analysis of the phase image can yield important information on morphological details at the nanometer level.

Structure and composition of metal particles in Pt-Sn/Al2O3 bimetallic catalysts

1990 ◽  
Vol 48 (4) ◽  
pp. 278-279
Author(s):  
A. Sachdev ◽  
J. Schwank
Keyword(s):  
Bimetallic Catalysts ◽  
Bimetallic Catalyst ◽  
Size Structure ◽  
High Surface ◽  
High Surface Area ◽  
Metal Particles ◽  
Alloy Formation ◽  
Particle Size Range ◽  
Oxide Supports ◽  
Petroleum Fractions

Platinum - tin bimetallic catalysts have been primarily utilized in the chemical industry in the catalytic reforming of petroleum fractions. In this process the naphtha feedstock is converted to hydrocarbons with higher octane numbers and high anti-knock qualities. Most of these catalysts contain small metal particles or crystallites supported on high surface area insulating oxide supports. The determination of the structure and composition of these particles is crucial to the understanding of the catalytic behavior. In a bimetallic catalyst it is important to know how the two metals are distributed within the particle size range and in what way the addition of a second metal affects the size, structure and composition of the metal particles. An added complication in the Pt-Sn system is the possibility of alloy formation between the two elements for all atomic ratios.

Intercalation of First Row Transition Metals inside Covalent-Organic Frameworks (COF): a Strategy to Fine Tune the Electronic Properties of Porous Crystalline Materials

2018 ◽  
Author(s):  
Srimanta Pakhira ◽  
Jose Mendoza-Cortes
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Electronic Properties ◽  
High Surface ◽  
Electronic Devices ◽  
High Surface Area ◽  
Main Role ◽  
Covalent Organic Frameworks ◽  
Porous Network ◽  
Crystalline Materials

<div>Covalent organic frameworks (COFs) have emerged as an important class of nano-porous crystalline materials with many potential applications. They are intriguing platforms for the design of porous skeletons with special functionality at the molecular level. However, despite their extraordinary properties, it is difficult to control their electronic properties, thus hindering the potential implementation in electronic devices. A new form of nanoporous material, COFs intercalated with first row transition metal is proposed to address this fundamental drawback - the lack of electronic tunability. Using first-principles calculations, we have designed 31 new COF materials <i>in-silico</i> by intercalating all of the first row transition metals (TMs) with boroxine-linked and triazine-linked COFs: COF-TM-x (where TM=Sc-Zn and x=3-5). This is a significant addition considering that only 187 experimentally COFs structures has been reported and characterized so far. We have investigated their structure and electronic properties. Specifically, we predict that COF's band gap and density of states (DOSs) can be controlled by intercalating first row transition metal atoms (TM: Sc - Zn) and fine tuned by the concentration of TMs. We also found that the $d$-subshell electron density of the TMs plays the main role in determining the electronic properties of the COFs. Thus intercalated-COFs provide a new strategy to control the electronic properties of materials within a porous network. This work opens up new avenues for the design of TM-intercalated materials with promising future applications in nanoporous electronic devices, where a high surface area coupled with fine-tuned electronic properties are desired.</div>

Tenacious Mass Transfer Limitations Drive Catalytic Selectivity during Electrochemical Carbon Dioxide Reduction

2019 ◽  
Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Catalyst Layer ◽  
Active Surface ◽  
Active Surface Area ◽  
High Concentration ◽  
Copper Electrodes ◽  
Surface Enhanced ◽  
Local Current

<p>This study evaluated the performance of the commonly used strong buffer electrolytes, i.e. phosphate buffers, during CO<sub>2</sub> electroreduction in neutral pH conditions by using in-situ surface enhanced infrared absorption spectroscopy (SEIRAS). Unfortunately, the buffers break down a lot faster than anticipated which has serious implications on many studies in the literature such as selectivity and kinetic analysis of the electrocatalysts. Increasing electrolyte concentration, surprisingly, did not extend the potential window of the phosphate buffers due to dramatic increase in hydrogen evolution reaction. Even high concentration phosphate buffers (1 M) break down within the potentials (-1 V vs RHE) where hydrocarbons are formed on copper electrodes. We have extended the discussion to high surface area electrodes by evaluating electrodes composed of copper nanowires. We would like highlight that it is not possible to cope with high local current densities on these high surface area electrodes by using high buffer capacity solutions and the CO<sub>2</sub> electrocatalysts are needed to be evaluated by casting thin nanoparticle films onto inert substrates as commonly employed in fuel cell reactions and up to now scarcely employed in CO<sub>2</sub> electroreduction. In addition, we underscore that normalization of the electrocatalytic activity to the electrochemical active surface area is not the ultimate solution due to concentration gradient along the catalyst layer.This will “underestimate” the activity of high surface electrocatalyst and the degree of underestimation will depend on the thickness, porosity and morphology of the catalyst layer. </p> <p> </p>

Sign in / Sign up

Export Citation Format

Share Document