Charges on the surfaces of two chlorites

Clay Minerals ◽  
1981 ◽  
Vol 16 (4) ◽  
pp. 347-359 ◽  
Author(s):  
Angela A. Jones
Keyword(s):  
Surface Charge ◽  
Surface Area ◽  
Negative Charge ◽  
Total Surface Area ◽  
Acid System ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Ph Dependent ◽  
Positively Charged

AbstractTwo chlorites, sheridanite and clinochlore, have been examined to determine their surface charge characteristics. In order to increase their surface area and to produce a measurable surface charge, the chlorites were treated with 10−3m, 10−2m, and 10−1m HCl in 10−2m MgCl2 solutions. These treatments are shown not to alter the crystallinity of the chlorites and to produce a small pH-dependent negative charge which is not directly related to the total surface area. The clinochlore, (Si6.13Al1.84)(Al1.53FeIII0.53FeII0.18Mg9.52)O20(OH)16, is more readily attacked by the acids than the sheridanite, (Si5.43Al2.55)(Al2.90FeII0.05Mg8.86)O20(OH)16, and also produces material with greater surface area and pH-dependent, negative, surface charge. It is concluded that: (i) isomorphous substitutions in the lattice are not reflected in a permanent surface charge; (ii) the observed surface charge arises not only at the edges of the particles but also at points where the chlorite is predisposed to attack by acids; (iii) in the chlorite-acid system used, anions—probably mainly silicate—block positively charged sites.

Transport of Particle-Laden Fluids Through Fixed-Valve Micropumps

1999 ◽  
Author(s):  
Ling-Sheng Jang ◽  
Christopher J. Morris ◽  
Nigel R. Sharma ◽  
Ron L. Bardell ◽  
Fred K. Forster
Keyword(s):  
Surface Charge ◽  
Surface Area ◽  
Flow Rate ◽  
Pure Water ◽  
Maximum Flow ◽  
Total Surface Area ◽  
Maximum Flow Rate ◽  
Number Density ◽  
Polystyrene Microspheres ◽  
Negative Surface

Abstract Micropumps designed for the flow-rate range of 100–1000μl/min have been developed by a number of research groups. However, little data is available regarding the ability of various designs to directly transport liquids containing particles such as cells, microspheres utilized for bead chemistry, or contaminants. In this study the ability of pumps with no-moving-parts valves (NMPV) to transport particles was investigated. The results showed that a NMPV micropump was able to directly pump suspensions of polystyrene microspheres from 3.1 to 20.3μm in diameter. The pump functioned without clogging at microsphere number densities as high as 9000 particles/μl of suspension, which corresponded to over 90,000 particles per second passing through the pump at a flow rate of 600μl/min. Performance with polystyrene microspheres was the same as pure water up to the point of cavitation. Microspheres manufactured with negative surface charge cavitated less readily that other microspheres studied that were manufactured without surface charge. However, cavitation did not appear to be a function of microsphere size, total surface area or number density. Thus pumping polystyrene microspheres was found to be more affected by surface effects than by size, surface area or number density within the range of parameters considered. In the case of charged microspheres, the maximum flow rate was reduced by 30% compared to pure water whereas for uncharged microspheres the maximum flow rate was reduced by approximately 80%.

scholarly journals Enforced expression of phosphatidylinositol 4-phosphate 5-kinase homolog alters PtdIns(4,5)P2 distribution and the localization of small G-proteins

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Yanbo Yang ◽  
Miriam Park ◽  
Masashi Maekawa ◽  
Gregory D. Fairn
Keyword(s):  
Plasma Membrane ◽  
Surface Charge ◽  
Electrostatic Interactions ◽  
Negative Charge ◽  
Anionic Charge ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Polybasic Domains ◽  
Phosphatidylinositol 4 ◽  
Hydrolysis Of

Abstract The generation of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) by phosphatidylinositol 4-phosphate 5-kinases (PIP5Ks) is essential for many functions including control of the cytoskeleton, signal transduction, and endocytosis. Due to its presence in the plasma membrane and anionic charge, PtdIns(4,5)P2, together with phosphatidylserine, provide the inner leaflet of the plasma membrane with a negative surface charge. This negative charge helps to define the identity of the plasma membrane, as it serves to recruit or regulate a multitude of peripheral and membrane proteins that contain polybasic domains or patches. Here, we determine that the phosphatidylinositol 4-phosphate 5-kinase homolog (PIPKH) alters the subcellular distribution of PtdIns(4,5)P2 by re-localizing the three PIP5Ks to endomembranes. We find a redistribution of the PIP5K family members to endomembrane structures upon PIPKH overexpression that is accompanied by accumulation of PtdIns(4,5)P2 and phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3). PIP5Ks are targeted to membranes in part due to electrostatic interactions; however, the interaction between PIPKH and PIP5K is maintained following hydrolysis of PtdIns(4,5)P2. Expression of PIPKH did not impair bulk endocytosis as monitored by FM4-64 uptake but did result in clustering of FM4-64 positive endosomes. Finally, we demonstrate that accumulation of polyphosphoinositides increases the negative surface charge of endosomes and in turn, leads to relocalization of surface charge probes as well as the polycationic proteins K-Ras and Rac1.

scholarly journals Environmental-Friendly Modifications of Zeolite to Increase Its Sorption and Anion Exchange Properties, Physicochemical Studies of the Modified Materials

Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3213 ◽  
Author(s):  
Jolanta Cieśla ◽  
Wojciech Franus ◽  
Małgorzata Franus ◽  
Karolina Kedziora ◽  
Justyna Gluszczyk ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Charge ◽  
Surface Area ◽  
Specific Surface Area ◽  
Isoelectric Point ◽  
Water Vapor Adsorption ◽  
Water Binding ◽  
Zeolite Surface ◽  
Negative Surface ◽  
Negative Surface Charge

Zeolites, naturally possessing a high negative surface charge and large specific surface, are used in agriculture as cationic fertilizers, water holders, heavy metals, and organic pollutants sorbents. Since some nutrients occur in anionic forms, there is a need to modify the zeolite surface to hold anions. In this study, hydrogen (hydrochloric acid), iron (Fe2+ and Fe3+), and aluminum cations as well as the influence of sodium hydroxide modifiers on the specific surface area, water vapor, adsorption energy, fractal dimension, mesopore volumes and radii, electrokinetic (zeta) potential, and isoelectric point were investigated. The use of alkali solution did not affect the zeolite properties significantly, whereas hydrogen, iron, and treatments with aluminum cations resulted in an increase in the specific surface area, mesopore volumes, and radii, and a decrease in the water-binding forces. Aluminum cations were the most effective in recharging the zeolite surface from negative to positive, shifting the isoelectric point toward the highest values. Calcination enlarged the negative surface charge and mesopore radius, and diminished the surface area and mesopore volume. The modified zeolites are promising carriers of anionic nutrients, large surface area sorbents, and suppliers of water for plant roots in soil.

scholarly journals Enforced expression of phosphatidylinositol 4-phosphate 5-kinase homolog (PIPKH) alters phosphatidylinositol 4,5-bisphosphate distribution and the localization of small G-proteins

2018 ◽  
Author(s):  
Yanbo Yang ◽  
Miriam Park ◽  
Gregory D. Fairn
Keyword(s):  
Plasma Membrane ◽  
Surface Charge ◽  
G Proteins ◽  
Negative Charge ◽  
Anionic Charge ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Polybasic Domains ◽  
Phosphatidylinositol 4 ◽  
Small G Proteins

AbstractThe generation of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) by phosphatidylinositol 4-phosphate 5-kinases (PIP5Ks) is essential for many of the functions including the control of cytoskeleton, signal transduction and endocytosis. Additionally, due to its presence in the plasma membrane and its anionic charge PtdIns(4,5)P2, together with phosphatidylserine, imbue the inner leaflet of the plasma membrane with a negative surface charge. This negative charge helps to define the identity of the plasma membrane as serves to recruit or regulate a multitude of proteins that contain polybasic domains or patches. Here we determine that the phosphatidylinositol 4-phosphate 5-kinase homolog (PIPKH) alters the subcellular distribution of PtdIns(4,5)P2 by re-localizing the PIP5Ks to endomembranes. Consistently, we find a redistribution of the PIP5K family members to endomembrane structures upon PIPKH overexpression that is accompanied by an accumulation of PtdIns(4,5)P2 and phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3), which further influences the distribution of endosomes and lysosomes. Additionally, we demonstrate that the accumulation of polyphosphoinositides increases their negative surface charge that in turn leads to the relocalization of surface charge probes as well as the polycationic proteins K-Ras and Rac1.

Surface charge and extracellular polymer of sludge in the anaerobic degradation process

1996 ◽  
Vol 34 (5-6) ◽  
pp. 309-316 ◽  
Author(s):  
X. S. Jia ◽  
Herbert H. P. Fang ◽  
H. Furumai
Keyword(s):  
Surface Charge ◽  
Growth Phase ◽  
Anaerobic Degradation ◽  
Degradation Process ◽  
Anaerobic Sludge ◽  
Batch Experiments ◽  
High Substrate Concentration ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Extracellular Polymer

Changes of surface charge and extracellular polymer (ECP) content were investigated in batch experiments for three anaerobic sludges, each of which had been enriched at 35°C and pH 639-7.3 for more than 40 batches using propionate, butyrate and glucose, individually, as the sole substrate. Results showed that both ECP and the negative surface charge were dependent on the growth phase of microorganisms. They increased at the beginning of all batches when the microorganisms were in the prolific-growth phase, having high substrate concentration and food-to-microorganisms ratio. Both later gradually returned to their initial levels when the microorganisms were in the declined-growth phase, as the substrate became depleted. The negative surface charge increased linearly with the total-ECP content in all series with slopes of 0.0187, 0.0212 and 0.0157 meq/mg-total-ECP for sludge degrading propionate, butyrate and glucose, respectively. The change of surface charge for the first two sludges was mainly due to the increase of proteinaceous fraction of ECP; but, for glucose-degrading sludge, that could be due to the increases of both proteinaceous and carbohydrate fractions of ECP. The negative-charged nature of anaerobic sludge implies that cations should be able to promote granulation of anaerobic sludge.

scholarly journals Nanoemulsions for the Encapsulation of Hydrophobic Actives

Cosmetics ◽  
2021 ◽  
Vol 8 (2) ◽  
pp. 45
Author(s):  
Eduardo Guzmán ◽  
Laura Fernández-Peña ◽  
Lorenzo Rossi ◽  
Mathieu Bouvier ◽  
Francisco Ortega ◽  
...  
Keyword(s):  
Surface Charge ◽  
Long Term Stability ◽  
Promising Tool ◽  
Oil In Water ◽  
Nanometric Range ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Highly Hydrophobic ◽  
Technological Interest

This work analyzes the dispersion of two highly hydrophobic actives, (9Z)-N-(1,3-dihydroxyoctadecan-2-yl)octadec-9-enamide (ceramidelike molecule) and 2,6-diamino-4-(piperidin-1-yl)pyrimidine 1-oxide (minoxidil), using oil-in-water nanoemulsions with the aim of preparing stable and safe aqueous-based formulations that can be exploited for enhancing the penetration of active compounds through cosmetic substrates. Stable nanoemulsions with a droplet size in the nanometric range (around 200 nm) and a negative surface charge were prepared. It was possible to prepare formulations containing up to 2 w/w% of ceramide-like molecules and more than 10 w/w% of minoxidil incorporated within the oil droplets. This emulsions evidenced a good long-term stability, without any apparent modification for several weeks. Despite the fact that this work is limited to optimize the incorporation of the actives within the nanoemulsion-like formulations, it demonstrated that nanoemulsions should be considered as a very promising tool for enhancing the distribution and availability of hydrophobic molecules with technological interest.

SURFACE-CHARGE-ENABLED PHOTOLYTIC HYDROGEN GENERATION IN V2O5·H2O/Au NANOCONJUGATES

MRS Advances ◽  
2016 ◽  
Vol 1 (46) ◽  
pp. 3121-3126
Author(s):  
Sunith Varghese ◽  
Charuksha Walgama ◽  
Mark Wilkins ◽  
Sadagopan Krishnan ◽  
Kaan Kalkan
Keyword(s):  
Surface Charge ◽  
Hydrogen Generation ◽  
Hydrogen Reduction ◽  
Energy Levels ◽  
Sol Gel ◽  
Band Edge ◽  
Conduction Band Edge ◽  
Current Voltage ◽  
Negative Surface ◽  
Negative Surface Charge

ABSTRACTThe present work investigates sol-gel synthesized vanadium oxyhydrate (V2O5·H2O) nanowires decorated with Au nanoparticles as potential photolytic H2 generators. As determined by UV photoelectron and optical spectroscopies, the conduction band edge of V2O5·H2O lies 0.6 eV below standard H+ reduction potential, implying no H2 can be generated. On the contrary, as measured by gas chromatography, our nanoconjugates yield reproducible light-to-hydrogen conversion efficiency of 5.3%, for the first hour of photolysis under 470 nm excitation. To explain the observed hydrogen reduction, we have hypothesized the vanadia electron energy levels are raised by some negative surface charge. With the objective of validating this hypothesis, we have performed cyclic current-voltage measurements. The derived conduction and valence band edge energies are not only consistent with the optical band gaps, but also validate the hypothesized energy increase by 1.6 eV, respectively. The negative surface charge is also corroborated by the ζ-potential. Based on the measured pH of 2.4, we attribute the negative surface charge to Lewis acid nature of the nanowires, establishing dative bonding with OH−. The present work establishes the importance of surface charge in photoelectrochemical reactions, where it can be instrumental and enabling in photolytic fuel production.

Effect of arsenate on adsorption of Zn(II) by three variable charge soils

Soil Research ◽  
2007 ◽  
Vol 45 (6) ◽  
pp. 465 ◽  
Author(s):  
Jing Liang ◽  
Ren-kou Xu ◽  
Diwakar Tiwari ◽  
An-zhen Zhao
Keyword(s):  
Zeta Potential ◽  
Surface Charge ◽  
Iron Oxides ◽  
Initial Concentration ◽  
Variable Charge ◽  
Study Results ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Enhanced Adsorption ◽  
Variable Charge Soils

The effect of arsenate on adsorption of Zn(II) in 3 variable charge soils (Hyper-Rhodic Ferralsol, Rhodic Ferralsol, and Haplic Acrisol) and the desorption of pre-adsorbed Zn(II) in the presence of arsenate were investigated in this study. Results showed that the presence of arsenate led to an increase in both the adsorption and desorption of Zn(II) in these variable charge soils. It was also suggested that the enhanced Zn(II) adsorption by arsenate was mainly due to the increase in negative surface charge of the soils induced by the specific adsorption of arsenate, and the increase in electrostatically adsorbed Zn(II) was responsible for the increase in the desorption of Zn(II). The effect of arsenate on Zn(II) adsorption primarily depends on the initial concentration of arsenate and Zn(II), the system pH, and the nature of soils. The enhanced adsorption of Zn(II) increased with the increase in the initial concentration of arsenate and the amount of arsenate adsorbed by the soils. The presence of arsenate decreased the zeta potential of soil suspensions and soil IEP and thus shifted the adsorption edge of Zn(II) to a lower pH region. The effect of arsenate on Zn(II) adsorption in these 3 soils followed the order Hyper-Rhodic Ferralsol > Rhodic Ferralsol > Haplic Acrisol, which was consistent to the contents of iron oxides in these soils and the amount of arsenate adsorbed by the soils.

Sign in / Sign up

Export Citation Format

Share Document