scholarly journals Spodumene Flotation Mechanism

Minerals ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 372 ◽  
Author(s):  
Lev Filippov ◽  
Saeed Farrokhpay ◽  
Lichau Lyo ◽  
Inna Filippova
Keyword(s):  
Zeta Potential ◽  
Surface Charge ◽  
Sodium Oleate ◽  
Calcium Ions ◽  
Mineral Surface ◽  
Flotation Recovery ◽  
Optimum Ph ◽  
Flotation Performance ◽  
Spodumene Flotation

Fine and coarse fractions of spodumene were obtained from a pegmatite ore and their flotation was investigated under different conditions. In particular, the optimum pH and collector dosage were studied. It was found that the best flotation performance occurs at pH 10 using 250 mg/L of sodium oleate. It was also observed that upon the addition of CaCl2, spodumene flotation recovery increases to about 90%. In addition, poor floatability was found for spodumene when Na2CO3 was used as a pH regulator (compared to NaOH).The zeta potential data confirmed the adsorption of oleate on the spodumene surface. It was found that activation of spodumene by calcium ions makes the surface charge less negative due to the adsorption of Ca2+ on the surface. The crystallographic properties of spodumene were analyzed. The adsorption of sodium oleate was attributed to the chemisorption of oleate to the exposed Al and Si sites generated after breakage of the Al–O and Si–O bonds on the mineral surface. It was observed that the {110} planes are the most favorable for the adsorption of oleate. The {110} plane is the weakest plane, and spodumene has the highest tendency to cleave along this plane. The XRD data revealed that fine spodumene particles have more {110} planes than the coarser fraction, which may explain why the former has better floatability.

scholarly journals Adsorption of 2-(Hexadecanoylamino)Acetic Acid Onto the Surface of Smithsonite: Mechanism and Flotation Performance

2018 ◽  
Author(s):  
Bin Luo ◽  
Junbo Liu ◽  
Quanjun Liu ◽  
Chao Song ◽  
Li Yu ◽  
...  
Keyword(s):  
Zinc Oxide ◽  
Acetic Acid ◽  
Organic Carbon ◽  
Zeta Potential ◽  
Sulfide Mineral ◽  
Flotation Recovery ◽  
Wide Ph Range ◽  
Flotation Performance ◽  
Ph Range ◽  
Important Objective

Zinc is mostly extracted from zinc oxide and sulfide minerals, and this process involves flotation as a key step. While it is easier to float the sulfide mineral, its consumption and depletion has led to an increased reliance on zinc oxide minerals, including smithsonite; hence the development of efficient ways of collecting smithsonite by flotation is an important objective. Herein, we describe the use of 2-(hexadecanoylamino)acetic acid (HAA), a novel surfactant, as a collector during smithsonite flotation. The mechanism and flotation performance of HAA during smithsonite flotation were investigated by total organic carbon (TOC) content studies, zeta potential measurements, FTIR spectroscopy, and XPS analyses, combined with micro-flotation experiments. The flotation results revealed that HAA is an excellent collector in pulp over a wide pH range (9–12) and at a relatively low concentration (2 × 10‒4 mol/L), at which a recovery of close to 90% of the smithsonite mineral was obtained. TOC-content studies reveal that the good flotation recovery is ascribable to large amounts of collector molecule adsorbed on the smithsonite surface, while zeta potential measurements show that the HAA is chemically adsorbed onto the smithsonite. FTIR and XPS analyses reveal that the HAA-collector molecules adsorb onto the smithsonite surface as zinc-HAA complexes involving carboxylate moieties and Zn sites on the smithsonite surface in alkaline solution.

scholarly journals Separation of Oxidized Pyrrhotite from Fine Fraction Serpentine

Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 472 ◽  
Author(s):  
Jian Zhou ◽  
Yiping Lu ◽  
Guozhi Mao
Keyword(s):  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Nickel Sulfide ◽  
Fine Fraction ◽  
Oxidation Products ◽  
Hydroxyl Groups ◽  
Mineral Surface ◽  
X Ray ◽  
Flotation Recovery ◽  
Sulfide Ore

Abstract: The valuable minerals in copper-nickel sulfide ore can easily be oxidized, leading to the reduction of their flotation recovery and a difficulty in separating them from gangue. In order to solve the problem, the reaction mechanism of the octanohydroxamic acid (OHA) on oxidized pyrrhotite was revealed through micro-flotation, adsorption tests, zeta potential measurements, and X-ray photoelectron spectroscopy (XPS) analysis. The results show that this is a feasible way to find a suitable collector that can directly react to oxidation products on the surface of pyrrhotite. OHA can efficiently reclaim oxidized pyrrhotite and achieve the selective separation of a pyrrhotite-serpentine mixture in a weak alkaline environment. The adsorption tests, zeta potential measurements, and XPS analyses show that OHA can interact with an oxidized pyrrhotite surface, and the interaction between OHA and serpentine is very weak. The XPS analyses indicate that the OHA collector can chelate with Fe(OH)3 on the surface of oxidized pyrrhotite and form an “O, O” five-ring chelate. At the same time, the OHA collector may compete with the hydroxyl groups of hydrophilic substances on the mineral surface to produce hydrophobic products and reduce the hydrophilic substances on the mineral surface.

scholarly journals Dispersive evaluation and surface chemistry of advanced, multifunctional silica/lignin hybrid biomaterials

2013 ◽  
Vol 11 (11) ◽  
pp. 1860-1873 ◽  
Author(s):  
Magdalena Nowacka ◽  
Łukasz Klapiszewski ◽  
Małgorzata Norman ◽  
Teofil Jesionowski
Keyword(s):  
Zeta Potential ◽  
Surface Charge ◽  
Electrochemical Sensors ◽  
Relevant Information ◽  
Structural Features ◽  
Kraft Lignin ◽  
Morphological Properties ◽  
Wide Range ◽  
Hybrid Biomaterials

AbstractAdvanced silica/lignin hybrid biomaterials were obtained using hydrated or fumed silicas (Aerosil®200) and Kraft lignin as precursors, which is a cheap and biodegradable natural polymer. To extend the possible range of applications, the silicas were first modified with N-2-(aminoethyl)-3-aminopropyltrimethoxsysilane, and then with Kraft lignin, which had been oxidized with sodium periodate. The SiO2/lignin hybrids and precursors were characterised by means of determination of their physicochemical and dispersive-morphological properties. The effectiveness of silica binding to lignin was verified by FT-IR spectroscopy. The zeta potential value provides relevant information regarding interactions between colloid particles. Measurement of the zeta potential values enabled an indirect assessment of stability for the studied hybrid systems. Determination of zeta potential and density of surface charge also permitted the quantitative analysis of changes in surface charge, and indirectly confirmed the effectiveness of the proposed method for synthesis of SiO2/lignin hybrid materials. A particularly attractive feature for practical use is their stability, especially electrokinetic stability. It is expected that silica/lignin hybrids will find a wide range of applications (polymer fillers, biosorbents, electrochemical sensors), as they combine the unique properties of silica with the specific structural features of lignin. This makes these hybrids biomaterials advanced and multifunctional.

CHARACTERIZATION OF A SURFACE-CHARGE MODULATION ELECTROFLUIDIC TRANSISTOR BY HYDRODYNAMIC MEASUREMENTS

2012 ◽  
Vol 11 (04) ◽  
pp. 1240021
Author(s):  
GUILLAUME LAFFITE ◽  
XU ZHENG ◽  
LOUIS RENAUD ◽  
FRANÇOIS BESSUEILLE ◽  
ELISABETH CHARLAIX ◽  
...  
Keyword(s):  
Experimental Study ◽  
Zeta Potential ◽  
Surface Charge ◽  
Gate Voltage ◽  
Silica Surface ◽  
Insulating Layer ◽  
Charge Regulation ◽  
Charge Modulation ◽  
Gating Effect

We present an experimental study on the electrofluidic transistor in this paper. A novel and easy way to integrate the transistor into a microchannel is developed. The performances of the insulating layer, especially the leakage current under gate voltage, are carefully characterized. The change of surface charge on silica surface by gate polarization is measured, however, by measuring the streaming current, the gating effect on zeta potential has not been observed. This result should imply new assumption in the understanding of the charge regulation in the electrical double layer under gate polarization.

scholarly journals Synthesis, and Characterization, and Evaluation of Cellular Effects of the FOL-PEG-g-PEI-GAL Nanoparticles as a Potential Non-Viral Vector for Gene Delivery

2010 ◽  
Vol 2010 ◽  
pp. 1-10 ◽  
Author(s):  
S. Ghiamkazemi ◽  
A. Amanzadeh ◽  
R. Dinarvand ◽  
M. Rafiee-Tehrani ◽  
M. Amini
Keyword(s):  
Gene Delivery ◽  
Zeta Potential ◽  
Surface Charge ◽  
Cell Line ◽  
Graft Copolymer ◽  
Viral Vector ◽  
Transfection Efficiency ◽  
High Surface ◽  
Liver Cells ◽  
Dna Complexes

In this manuscript, we synthesized the potential non viral vector for gene delivery with proper transfection efficiency and low cytotoxicity. Polyethylenimine (PEI) is a well-known cationic polymer which has high positive surface charge for condensing plasmid DNA. However; it is highly cytotoxic in many cell lines because of the high surface charge, non-biodegradability and non-biocompatibility. To enhance PEI biodegradability, the graft copolymer “PEG-g-PEI” was synthesized. To target cancer liver cells, two targeting ligands folic acid and galactose (lactobionic acid) which are over expressed on human hepatocyte carcinoma were attached to graft copolymer and “FOL-PEG-g-PEI-GAL” copolymer was synthesized. Composition of this grafted copolymer was characterized using1H-NMR and FTIR spectra. The molecular weight and zeta potential of this copolymer was compared to PEI. The particle size and zeta potential of FOL-PEG-g-PEI-GAL/DNA complexes at various N/P ratio were measured using dynamic light scattering (DLS). Cytotoxicity of the copolymer was also studied in cultured HepG2 human hepatoblastoma cell line. The FOL-PEG-g-PEI-GAL/DNA complexes at various N/P ratios exhibited no cytotoxicity in HepG2 cell line compared to PEI 25K as a control. The novel copolymer showed enhanced biodegradability in physiological conditions in compared with PEI and targeted cultured HepG2 cells. More importantly, significant transfection efficiency was exhibited in cancer liver cells. Together, our results showed that “FOL-PEG-g-PEI-GAL” nanoparticals could be considered as a useful non-viral vector for targeted gene delivery.

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.

Synthesis of Modified Chitosan with Thiamine Hydrochloride as the Adsorbent for Calcium (II) Ion Removal

2019 ◽  
Vol 798 ◽  
pp. 397-403
Author(s):  
Ratana Sananmuang
Keyword(s):  
Calcium Ions ◽  
Water Hardness ◽  
Batch Adsorption ◽  
Thiamine Hydrochloride ◽  
Modified Chitosan ◽  
Ion Removal ◽  
Effective Removal ◽  
Optimum Ph ◽  
Langmuir Isotherm Model ◽  
Nmr Techniques

Water quality is very important to food processing industry. Water hardness caused by calcium ions in water can affect the properties of food including aroma, texture, flavor and appearance. Chitosan has amino functional groups that can remove metal ions from aqueous solution. However, chitosan can give more effective removal of calcium ions if it is modified with functionalized substance such as thiamine hydrochloride. therefore, the objectives of this study were to synthesize the modified chitosan with thiamine hydrochloride (MCTH) and to determine its efficiency for removal of calcium ion in solution. Chitosan was prepared from crab shells and modified with thiamine hydrochloride at 30 °C. The morphology of both crab-shell chitosan (CSC) and MCTH was characterized by SEM, FTIR and NMR techniques. Batch adsorption experiments were conducted as a function of pH, contacted time and initial concentration of calcium (II) ions. The desorption of calcium(II) ion from both adsorbents was also investigated. The concentration of calcium in solution was measured by FAAS technique. The results indicated that the optimum pH for adsorption was 6.0 for both CSC and MCTH. The adsorption capacity for MCTH (48.31 mg g-1) was greater than that of CSC (1.52 mg g-1). The isotherm showed that the adsorption process of calcium (II) ions onto MCTH was fitted to Langmuir isotherm model. Calcium desorption from MCTH was lower than that of CSC.

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