Synthesis and properties of novel self-crosslinked cationic fluorinated acrylic latex prepared with novel emulsified system

2016 ◽  
Vol 45 (4) ◽  
pp. 259-264
Author(s):  
Wen Li ◽  
Zhongbin Bao ◽  
Lijun Chen ◽  
Dongshun Deng
Keyword(s):  
Particle Size ◽  
Gemini Surfactants ◽  
Average Particle Size ◽  
Water Soluble ◽  
Average Particle ◽  
Mixed Surfactants ◽  
The Novel ◽  
Content Type ◽  
Acrylic Latex ◽  
Emulsion Polymerisation

Purpose At present, the conventional method of preparing cationic fluorinated acrylic latex is to emulsify copolymerised monomers with cationic surfactants. However, there has been a wide concern about using Gemini surfactants to prepare cationic polymer latex to improve its properties. The purpose of this paper was to focus on the synthesis of novel self-crosslinked cationic fluorinated acrylic latex (SCFAL), during which the copolymerised monomers were initiated with a water soluble azo initiator and emulsified with mixed surfactants of Gemini emulsifier and alkyl polyglycoside (APG). Design/methodology/approach The novel SCFAL was prepared successfully by the semi-continuous seeded emulsion polymerisation of butyl acrylate, methyl methacrylate, hexafluorobutyl methacrylate (HFMA) and hydroxy propyl methacrylate (HPMA) in aqueous medium. Findings The conversion is the maximum and the coagulation percentage the minimum when the amounts of emulsifier and initiator are 8 and 0.6 per cent, respectively. The average particle size of the latex is significantly reduced with the increase of the amount of emulsifiers used. However, the average particle size of the latex is increased with the increase of the amount of HPMA. The particle size of the latex is of a unimodal distribution, which means that the particle size was reasonably uniform. Contact angle is increased with the increase of the amount of the HFMA. Practical implications The novel SCFAL can be widely used as significant components in the field of coatings, leather, textile, paper, adhesives and so on. Originality/value SCFAL, which was emulsified with novel mixed surfactants of Gemini surfactant and APG, has been prepared successfully. Influences of amount of initiator, emulsifier, HPMA and HFMA on emulsion polymerisation and/or properties of novel latex are investigated in detail.

Synthesis and Characterization of Water-Soluble Monolayer-Protected Gold Nanoparticles

2011 ◽  
Vol 415-417 ◽  
pp. 617-620 ◽  
Author(s):  
Yan Su ◽  
Ying Yun Lin ◽  
Yu Li Fu ◽  
Fan Qian ◽  
Xiu Pei Yang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Gold Nanoparticles ◽  
Average Particle Size ◽  
Water Soluble ◽  
Synthesis And Characterization ◽  
Average Particle ◽  
Transmission Electron

Water-soluble gold nanoparticles (AuNPs) were prepared using 2-mercapto-4-methyl-5- thiazoleacetic acid (MMTA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The AuNPs product was analyzed by transmission electron microscopy (TEM), UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy (FTIR). The TEM image shows that the particles were well-dispersed and their average particle size is about 5 nm. The UV-vis absorption and FTIR spectra confirm that the MMTA-AuNPs was stabilized by the carboxylate ions present on the surface of the AuNPs.

Synthesis of Nanostructured Magnetic Mixed-Oxide Ferrite Powders by Using A Novel Chemical Method

2002 ◽  
Vol 720 ◽  
Author(s):  
N N Ghosh
Keyword(s):  
Particle Size ◽  
Mixed Oxide ◽  
Chemical Method ◽  
Average Particle Size ◽  
Cost Effective ◽  
Water Soluble ◽  
Average Particle ◽  
Chemical Route ◽  
Water Soluble Polymer ◽  
Different Temperatures

AbstractIn the present investigation, an attempt has been made to establish a new chemical route for synthesis of the nanostructured mixed oxide ferrite powders. By using this chemical method a variety of ferrite powders having spinel structure and doped with Co, Ni, Mn, Zn etc has been prepared. In this method nitrate salts of the different metals were used as starting materials. The aqueous solutions of the metal nitrates were mixed according to the molar ration of the compositions. Then the mixtures were mixed with an aqueous solution of water soluble polymer (polyvinyl alcohol). This mixture after drying yield fluffy brown powders. These powders were then calcined at different temperatures ranging from 400 °C to 700 °C. Nanostructured powders were obtained from the thermal decomposition of the brown powders. The powders, prepared by calcinations at different temperatures, were characterized by using X-Ray diffraction analysis, IR spectroscopy, TGA/DTA, and TEM. It was observed that the average particle size of the powders are in nanometer scale with a narrow size distribution. The average particle size of the powders was increased with the increase of calcinations temperature.This chemical method has proved to provide a convenient process for the preparation of nanostructured ceramic powders at comparatively low temperatures and offers the potential of being a simple and cost-effective route.

scholarly journals Modeling of Miniemulsion Polymerization of Styrene with Macro-RAFT Agents to Theoretically Compare Slow Fragmentation, Ideal Exchange and Cross-Termination Cases

Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 320 ◽  
Author(s):  
Dries Devlaminck ◽  
Paul Van Steenberge ◽  
Marie-Françoise Reyniers ◽  
Dagmar D’hooge
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Miniemulsion Polymerization ◽  
Monomer Conversion ◽  
Water Soluble ◽  
Explicit Calculation ◽  
Average Particle ◽  
Intermediate Radical ◽  
Raft Agent ◽  
The Impact

A 5-dimensional Smith-Ewart based model is developed to understand differences for reversible addition-fragmentation chain transfer (RAFT) miniemulsion polymerization with theoretical agents mimicking cases of slow fragmentation, cross-termination, and ideal exchange while accounting for chain length and monomer conversion dependencies due to diffusional limitations. The focus is on styrene as a monomer, a water soluble initiator, and a macro-RAFT agent to avoid exit/entry of the RAFT leaving group radical. It is shown that with a too low RAFT fragmentation rate coefficient it is generally not afforded to consider zero-one kinetics (for the related intermediate radical type) and that with significant RAFT cross-termination the dead polymer product is dominantly originating from the RAFT intermediate radical. To allow the identification of the nature of the RAFT retardation it is recommended to experimentally investigate in the future the impact of the average particle size (dp) on both the monomer conversion profile and the average polymer properties for a sufficiently broad dp range, ideally including the bulk limit. With decreasing particle size both a slow RAFT fragmentation and a fast RAFT cross-termination result in a stronger segregation and thus rate acceleration. The particle size dependency is different, allowing further differentiation based on the variation of the dispersity and end-group functionality. Significant RAFT cross-termination is specifically associated with a strong dispersity increase at higher average particle sizes. Only with an ideal exchange it is afforded in the modeling to avoid the explicit calculation of the RAFT intermediate concentration evolution.

scholarly journals INVESTIGATION ON DISSOLUTION PATTERN AND MATHEMATICAL MODELING OF DRUG RELEASE OF QUERCETIN BY COMPLEXATION WITH CYCLODEXTRIN NANOSPONGES

2019 ◽  
pp. 260-264
Author(s):  
SOBITHARANI P ◽  
ANANDAM S ◽  
MOHAN VARMA M ◽  
VIJAYA RATNA J ◽  
SHAILAJA P
Keyword(s):  
Particle Size ◽  
Drug Release ◽  
Average Particle Size ◽  
Particle Size Analysis ◽  
Water Soluble ◽  
Size Analysis ◽  
Average Particle ◽  
Scattering Method ◽  
Release Pattern ◽  
Cyclodextrin Nanosponges

Objective: The main objective of this study was to investigate the release pattern of a poorly water-soluble drug quercetin (QU) by fabricating its cyclodextrin nanosponges. Methods: Characterization of the original QU powder and QU-loaded nanosponges was carried out by the Fourier-transformed infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), and dissolution tester. The drug release pattern was subjected to various kinetic models. Results: FTIR studies confirmed the formation of inclusion complex of drug. The particle size analysis revealed that the average particle size measured by laser light scattering method is around 400–420 nm with low polydispersity index. The particle size distribution is unimodal and having a narrow range. A sufficiently high zeta potential indicates that the complexes would be stable and the tendency to agglomerate would be miniscule. TEM image revealed the porous nature of nanosponges. The dissolution of the QU nanosponges was significantly higher compared with the pure drug. Conclusion: From the kinetic study, it is apparent that the regression coefficient value closer to unity in case of Korsmeyer-Peppas model indicates that the drug release exponentially to the elapsed time. n value obtained from the Korsmeyer-Peppas plots, i.e., 0.9911 indicating non-Fickian (anomalous) transport ; thus, it projected that delivered its active ingredient by coupled diffusion and erosion.

Preparation and characterisation of modified VAc-VeoVa10 latex

2019 ◽  
Vol 48 (3) ◽  
pp. 210-215 ◽  
Author(s):  
Yilu Gong ◽  
Tantan Shao ◽  
Xiuming Wang ◽  
Xin Zhang ◽  
Zhijuan Sun ◽  
...  
Keyword(s):  
Vinyl Ester ◽  
Water Repellency ◽  
Latex Film ◽  
Mixed Surfactants ◽  
The Novel ◽  
Mass Ratio ◽  
Optimum Conditions ◽  
Content Type ◽  
Emulsion Polymerisation ◽  
Silicon Materials

Purpose Fluorine and silicon materials have received the keen attention of many researchers because of their water repellency and low surface free energy. The purpose this study was to prepare vinyl acetate (VAc)-vinyl ester of neodecanoic acid (VeoVa 10) copolymer latex modified with fluorine and silicone monomer, which is emulsified with the novel surfactants of disodium laureth sulfosuccinate (MES) and octylphenol polyoxyethylene ether (OP-10). Design/methodology/approach A series of modified latices containing fluorine-silicon have been prepared by semi-continuous seeded emulsion polymerisation of mixed monomers of VAc, VeoVa10, hexafluorobutylmethacrylate (HFMA) and vinyltriethoxysilane (VTES) and emulsified by novel surfactants of MES and OP-10. Findings The optimum conditions for preparing the modified latex is as follows: the amount of the surfactant was 4.0 Wt.% and the mass ratio of the anionic and nonionic surfactant was 3:1; the dosage of initiator was 0.4 Wt.% and the mass ratio of the main monomer was 3:1; and the amounts of VTES and HFMA were 2.0 and 6.0 Wt.%, respectively. In comparison with the conventional latex, the hydrophobicity of latex film was improved further. Originality/value The modified p (VAC-VeoVa) latex is prepared via semi-continuous seeded emulsion polymerisation, which is emulsified with the novel mixed surfactants of MES and OP-10. There are two main innovations. One is that the novel p (VAC-VeoVa) latex containing fluorine-silicon is prepared successfully. The other is that the emulsifier is composed of the novel mixed surfactants of MES and OP-10.

Slurry erosion performance study of HVFS sprayed Ni-20Al2O3 and Ni-15Al2O3-5TiO2 coatings under hydro accelerated conditions

2018 ◽  
Vol 70 (4) ◽  
pp. 805-817 ◽  
Author(s):  
Rajeev Kumar ◽  
Sanjeev Bhandari ◽  
Atul Goyal ◽  
Yogesh Kumar Singla
Keyword(s):  
Particle Size ◽  
Rotational Speed ◽  
Average Particle Size ◽  
Synergetic Effect ◽  
Average Particle ◽  
Flame Spray ◽  
Slurry Erosion ◽  
Content Type ◽  
Slurry Concentration ◽  
Ca6nm Steel

Purpose This paper aims to cover all the aspects of development, investigation and analysis phases to evaluate the slurry erosion performance of test coatings. The powders having composition of Ni-20Al2O3 and Ni-15Al2O3-5TiO2 were deposited on CA6NM grade turbine steel by using high velocity flame spray (HVFS) technique. The characterization of the coatings was done with the help of SEM/EDS and XRD techniques. Various properties such as micro-hardness and bonding strength of the coatings were also evaluated. Thereafter, these coatings were subjected to an indigenously developed high speed slurry erosion tester at different levels of rotational speed, erodent particle size and slurry concentration. The effect of these parameters on the erosion behavior of coatings was also evaluated. The slurry erosion tests and SEM of the eroded surfaces revealed remarkable improvement in slurry erosion resistance of Ni-15Al2O3-5TiO2 coating in comparison with Ni-20Al2O3 coating. Design/methodology/approach Two different compositions of HVFS coating were developed onto CA6NM steel. Subsequently, these coatings were evaluated by means of mechanical and microstructural characterization. Further, slurry erosion testing was done to analyze the erosive wear behavior of developed coatings. Findings The coatings were successfully developed by HVFS process. Cross-sectional microscopic analysis of sprayed coatings revealed a continuous and defect-free contact between substrate and coating. Ni-15Al2O3-5TiO2 coating showed higher value of bond strength in comparison with Ni-20Al2O3 coating. Under all the testing conditions, Ni-15Al2O3-5TiO2 coatings showed higher resistance to slurry erosion in comparison with Ni-20Al2O3 coatings. Rotational speed, average particle size of erodent and slurry concentration were found to have proportional effect on specific mass loss of coatings. The mixed behavior (brittle as well as ductile) of the material removal mechanism was observed for the coatings. Originality/value From the literature review, it was found that researchers have documented the various studies on Ni-Al2O3, Ni-TiO2 and Al2O3-TiO2 coatings. No one has ascertained the synergetic effect of Alumina and Titania on the slurry erosion performance of Nickel-based coating. In view of this, the authors have developed Ni-Al2O3 and Ni-Al2O3-TiO2 coatings, and an attempt has been made to compare their mechanical, microstructural and slurry erosion characteristics.

scholarly journals Formulation and Evaluation of Nanosuspension as an Alternative Approach for Solubility Enhancement of Simvastatin

2021 ◽  
Vol 71 (1) ◽  
Author(s):  
Mohini E. Shinde ◽  
Mitesh P. Sonawane ◽  
Avish D. Maru
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Entrapment Efficiency ◽  
Water Soluble ◽  
Average Particle ◽  
Particle Size Reduction ◽  
Drug Effectiveness ◽  
Saturation Solubility ◽  
Drug Content ◽  
Poorly Water Soluble

Solubility is an essential factor for drug effectiveness. Simvastatin is poorly water-soluble drug and its bioavailability is very low. Nanosuspension is one of those approach which can tremendously enhance the effective surface area of drug particles by reducing the particle size and there by increases the rate of dissolution and hence improve bioavailability. The main purpose of the present investigation was to increase the saturation solubility of simvastatin by preparation of nanosuspension. Nanosuspension of simvastatin were prepared by nanoprecipitation method using hydroxypropyl cellulose as stabilizer and sodium lauryl sulphate as surfactant. Prepared nanosuspension was evaluated for its particle size, total drug content, entrapment efficiency and saturation solubility study. On the basis of the evaluation, the best batch F8 formulation demonstrated highest drug content and entrapment efficiency with average particle size of 0.004µm. The saturation solubility studies show the solubility of the prepared nanosuspension has increased as compared to the pure drug due to the particle size reduction. The nanosuspension of simvastatin could be successfully prepared and can be concluded that the nanosuspension formulation is a promising approach to enhance the solubility. The nanoprecipitation is a simple and effective method to produce nano sized particles of poorly water-soluble drugs with enhance solubility.

scholarly journals Impact of Enzymatic Hydrolysis and Microfluidization on the Techno-Functionality of Oat Bran in Suspension and Acid Milk Gel Models

Foods ◽  
2022 ◽  
Vol 11 (2) ◽  
pp. 228
Author(s):  
Natalia Rosa-Sibakov ◽  
Maria Julia de Oliveira Carvalho ◽  
Martina Lille ◽  
Emilia Nordlund
Keyword(s):  
Particle Size ◽  
Colloidal Stability ◽  
Average Particle Size ◽  
High Viscosity ◽  
Water Soluble ◽  
Water Retention Capacity ◽  
Average Particle ◽  
Dry Matter Content ◽  
Retention Capacity ◽  
Oat Bran

Oat bran is a nutritionally rich ingredient, but it is underutilized in semi-moist and liquid foods due to technological issues such as high viscosity and sliminess. The aim of this work was to improve the technological properties of oat bran concentrate (OBC) in high-moisture food applications by enzymatic and mechanical treatments. OBC was hydrolyzed with β-glucanase (OBC-Hyd) and the water-soluble fraction (OBC-Sol) was separated. OBC, OBC-Hyd and OBC-Sol were further microfluidized at 5% dry matter content. Enzymatic treatment and microfluidization of OBC reduced the molecular weight (Mw) of β-glucan from 2748 kDa to 893 and 350 kDa, respectively, as well as the average particle size of OBC (3.4 and 35 times, respectively). Both treatments increased the extractability of the soluble compounds from the OBC samples (up to 80%) and affected their water retention capacity. OBC in suspension had very high viscosity (969 mPa·s) when heated, which decreased after both enzyme and microfluidization treatments. The colloidal stability of the OBC in suspension was improved, especially after microfluidization. The addition of OBC samples to acid milk gels decreased syneresis, improved the water holding capacity and softened the texture. The changes in the suspension and gel characteristics were linked with reduced β-glucan Mw and OBC particle size.

scholarly journals THE KINETICS OF THE COMBINED PROCESSES OF DISPERSION AND EXTRACTION OF HUMIC AND FULVIC ACIDS FROM PEAT AND VERMICOMPOST IN THE ROTOR-STATOR DEVICE

2019 ◽  
pp. 261-269
Author(s):  
Maksim Aleksandrovich Promtov ◽  
Andrey Yur'yevich Stepanov
Keyword(s):  
Particle Size ◽  
Solid Phase ◽  
Average Particle Size ◽  
Effective Diffusion ◽  
Fulvic Acids ◽  
Extraction Process ◽  
Solid Particles ◽  
Water Soluble ◽  
Combined Processes ◽  
Average Particle

Was conducted an experimental study of dispersion of solid particles, extraction of humic acids (HA) and fullview acids (FA) in suspensions of peat and vermicompost with repeated mechanical and hydrodynamic treatment in a rotor-stator device (RSD). According to reduce the average particle size and increase the concentration of HA and FA in suspensions of peat and vermicompost on the number of cycles in the RSD have an exponential character. The average particle size in suspensions of peat and vermicompost decreases from average size of 1 mm to 30 µm at 40 times the treatment of the suspension in the RSD. The intensity of the mass transfer of target substances from the solid phase to the liquid phase is due to an increase in the contact area of the phases, the value of which depends not only on the surface area of the solid particles, but significantly increases due to the opening of new pores and capillaries during particle grinding. The concentration of water-soluble HA in 25% peat suspension reaches 20 g/l, the concentration of FA – 6 g/l. The concentration of water-soluble HA in 25% vermicompost suspension reaches 12 g/l. Extractable substances on the surface of the particle and in the pores close to the surface, pass into the solution mainly during the first 10 treatment cycles. Effective diffusion coefficients and empirical coefficients of the kinetic equation for the extraction process of HA and FA in peat and vermicompost suspensions during their processing in RSD were determined.

Optimum formulation derivation for the ultimate packing fraction using monodispersed particle sizes when optimizing suspension viscosities

2019 ◽  
Vol 48 (1) ◽  
pp. 45-56
Author(s):  
Richard D. Sudduth
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Packing Fraction ◽  
Size Ratio ◽  
Average Particle ◽  
Particle Sizes ◽  
Monodisperse Particle ◽  
Content Type ◽  
Particle Size Ratio ◽  
Minimum Number

Purpose The importance of maximizing the particle packing fraction in a suspension by maximizing average particle size ratio of D5/D1 has been adequately shown to be important as previously reported in the literature. This study aims to extend that analysis to include the best formulation approach to maximize the packing fraction with a minimum number of monodisperse particle sizes. Design/methodology/approach An existing model previously developed by this author was modified theoretically to optimize the ratio used between consecutive monodisperse particle sizes. This process was found to apply to a broad range of particle configurations and applications. In addition, five different approaches for maximizing average particle size ratio D̅5/D̅1 were addressed for blending several different particle size distributions. Maximizing average particle size ratio D̅5/D̅1 has been found to result in an optimization of the packing fraction. Several new concepts were also introduced in the process of maximizing the packing fraction for these different approaches. Findings The critical part of the analysis to maximize the packing fraction with a minimum number of particles was the theoretical optimization of the ratio used between consecutive monodisperse particle sizes. This analysis was also found to be effectively independent of the maximum starting particle size. This study also clarified the recent incorrect claim in the literature that Furnas in 1931 was the first to generate the maximum theoretical packing fraction possible for n different particles that was actually originally developed in conjunction with the Sudduth generalized viscosity equation. In addition, the Furnas generated equation was also shown to give significantly different results from the Sudduth generated equation. Research limitations/implications Experimental data involving monodisperse particles of different blends with a minimum number of particle sizes that are truly monodisperse are often extremely difficult to obtain. However, the theoretical general concepts can still be applicable. Practical implications The expanded model presented in this article provides practical guidelines for blending pigments using a minimum number of monodisperse particle sizes that can yield much higher ratios of the particle size averages D̅5/D̅1 and thus potentially achieve significantly improved properties such as viscosity. Originality/value The model presented in this article provides the first apparent guidelines to control the blending of pigments in coatings by the optimization of the ratio used between consecutive monodisperse particle sizes. This analysis was also found to be effectively independent of the maximum starting particle size.

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