scholarly journals Flotation Behavior of Diatomite and Albite Using Dodecylamine as a Collector

Minerals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 371 ◽  
Author(s):  
Ying Gao ◽  
Yuexin Han ◽  
Wenbo Li
Keyword(s):  
Unit Area ◽  
Alkaline Ph ◽  
Force Microscopy ◽  
Atomic Force ◽  
Mineral Flotation ◽  
Alkaline Conditions ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Ph Range ◽  
First Time

The flotation behaviors of diatomite and albite using dodecylamine (DDA) as a collector were investigated and compared. The pure mineral flotation results indicate that the flotability difference between albite and diatomite is above 87% at pH 5.5 to 10.5. The recovery of albite improves with increasing DDA dosage at pH 5.5 to 10.5. In the same pH range, diatomite has weaker flotability than albite, particularly in alkaline pH pulp. Zeta potential measurements indicate that diatomite has a higher negative surface charge than albite at pH 7 to 12, DDA interacts strongly with albite and weakly with diatomite. Thus, DDA preferentially absorbs on albite surface rather than diatomite under alkaline conditions. Fourier transform infrared spectra (FTIR) indicate that the amount of DDA adsorbed to albite is greater than that adsorbed to diatomite, under the same conditions. The adsorption of DDA on the surface of diatomite is investigated by using atomic force microscopy (AFM) for the first time. The adsorption of the collector DDA on the surface of albite per unit area is greater than that on diatomite. This accounts for the lower recovery of diatomite than that of albite.

Atomic force microscopy of mica surface after ion replacement

1991 ◽  
Vol 49 ◽  
pp. 628-629 ◽  
Author(s):  
B. L. Dixon Northern ◽  
Y. L. Chen ◽  
J.N. Israelachvili ◽  
J.A.N. Zasadzinski
Keyword(s):  
Surface Charge ◽  
Isomorphous Substitution ◽  
Potassium Ions ◽  
Force Microscopy ◽  
Atomic Force ◽  
Multivalent Ions ◽  
Monovalent Ions ◽  
Muscovite Mica ◽  
Negative Surface ◽  
Negative Surface Charge

Atomic Force Microscope (AFM), is the newest, and potentially most powerful of the scanning probe microscopes. The (AFM) is capable of resolutions approaching atomic dimensions on ideal surfaces. One of the favorite such surfaces is that of mica. Muscovite mica has a platelike structure consisting of an octahedral alumina sheet sandwiched by two tetrahedral silicate sheets. As a result of this structure, mica cleaves readily along a plane leaving a molecularly smooth surface. Because of the isomorphous substitution of the tetravalent silicon by trivalent aluminium, mica has an excess negative surface charge.This negative surface charge of 2.1-1014 charges per cm2 is neutralized by an equal number of positive monovalent ions, mainly potassium ions. The ion-exchangable surface ions of mica, in aqueous solution, can be readily replaced by other monovalent or multivalent ions. This ion exchange alters the surface of the mica. We then follow these changes by imaging with the AFM in air.

scholarly journals High resolution nanoscale chemical analysis of bitumen surface microstructures

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ayse N. Koyun ◽  
Julia Zakel ◽  
Sven Kayser ◽  
Hartmut Stadler ◽  
Frank N. Keutsch ◽  
...  
Keyword(s):  
Secondary Ion Mass Spectrometry ◽  
Force Microscopy ◽  
Photo Oxidation ◽  
Atomic Force ◽  
Para Phase ◽  
Key Sites ◽  
Respective Surface ◽  
Surface Domains ◽  
Surface Microstructures ◽  
First Time

AbstractSurface microstructures of bitumen are key sites in atmospheric photo-oxidation leading to changes in the mechanical properties and finally resulting in cracking and rutting of the material. Investigations at the nanoscale remain challenging. Conventional combination of optical microscopy and spectroscopy cannot resolve the submicrostructures due to the Abbe restriction. For the first time, we report here respective surface domains, namely catana, peri and para phases, correlated to distinct molecules using combinations of atomic force microscopy with infrared spectroscopy and with correlative time of flight—secondary ion mass spectrometry. Chemical heterogeneities on the surface lead to selective oxidation due to their varying susceptibility to photo-oxidation. It was found, that highly oxidized compounds, are preferentially situated in the para phase, which are mainly asphaltenes, emphasising their high oxidizability. This is an impressive example how chemical visualization allows elucidation of the submicrostructures and explains their response to reactive oxygen species from the atmosphere.

Preparation and Characterization of Chitosan-Casein Phosphopeptides Biocomposite Coatings on the Medical Titanium Alloy

2011 ◽  
Vol 480-481 ◽  
pp. 1065-1069
Author(s):  
Bin Liu ◽  
Lin Wang ◽  
Yin Zhong Bu ◽  
Sheng Rong Yang ◽  
Jin Qing Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Attenuated Total Reflectance ◽  
Ti Alloy ◽  
Force Microscopy ◽  
Implant Materials ◽  
Atomic Force ◽  
Casein Phosphopeptides ◽  
Potential Applications ◽  
First Time

Titanium (Ti) and its alloys have been applied in orthopedics as one of the most popular biomedical metallic implant materials. In this work, to enhance the bioactivity, the surface of Ti alloy pre-modified by silane coupling agent and glutaraldehyde was covalently grafted with chitosan (CS) via biochemical multistep self-assembled method. Then, for the first time, the achieved surface was further immobilized with casein phosphopeptides (CPP), which are one group of bioactive peptides released from caseins in the digestive tract and can facilitate the calcium adsorption and usage, to form CS-CPP biocomposite coatings. The structure and composition of the fabricated coatings were characterized by X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and atomic force microscopy (AFM). As the experimental results indicated, multi-step assembly was successfully performed, and the CS and CPP were assembled onto the Ti alloy surface orderly. It is anticipated that the Ti alloys modified by CS-CPP biocomposite coatings will find potential applications as implant materials in biomedical fields.

scholarly journals Microwave Spectroscopic Detection of Human Hsp70 Protein on Annealed Gold Nanostructures on ITO Glass Strips

Biosensors ◽  
2018 ◽  
Vol 8 (4) ◽  
pp. 118
Author(s):  
Rodica Ionescu ◽  
Raphael Selon ◽  
Nicolas Pocholle ◽  
Lan Zhou ◽  
Anna Rumyantseva ◽  
...  
Keyword(s):  
Indium Tin Oxide ◽  
Stress Disorders ◽  
Force Microscopy ◽  
Glass Substrates ◽  
Conductive Glass ◽  
Hsp70 Protein ◽  
Atomic Force ◽  
Ito Glass ◽  
First Time ◽  
Human Heat Shock Protein

Conductive indium-tin oxide (ITO) and non-conductive glass substrates were successfully modified with embedded gold nanoparticles (AuNPs) formed by controlled thermal annealing at 550 °C for 8 h in a preselected oven. The authors characterized the formation of AuNPs using two microscopic techniques: scanning electron microscopy (SEM) and atomic force microscopy (AFM). The analytical performances of the nanostructured-glasses were compared regarding biosensing of Hsp70, an ATP-driven molecular chaperone. In this work, the human heat-shock protein (Hsp70), was chosen as a model biomarker of body stress disorders for microwave spectroscopic investigations. It was found that microwave screening at 4 GHz allowed for the first time the detection of 12 ng/µL/cm2 of Hsp70.

scholarly journals Marrying Medicine and Materials: Artemisinin (Qinghaosu) Particle is Soft Enough for Scratching Hard SiC Wafer in Water

2016 ◽  
Author(s):  
Yu-rong Zhu ◽  
Dan Zhang ◽  
Yang Gan ◽  
Fei-hu Zhang
Keyword(s):  
Pure Water ◽  
High Hardness ◽  
Underlying Mechanism ◽  
Molecular Solids ◽  
High Brightness ◽  
Force Microscopy ◽  
Atomic Force ◽  
Chemical Inertness ◽  
Sic Wafer ◽  
First Time

<p>Silicon carbide (SiC) single crystals, along with sapphire and silicon, are one of most important substrates for high-brightness LED fabrications. Owing to extremely high hardness (Mohs&rsquo; scale of 9.5) and chemical inertness, the polishing rate of SiC with conventional chemical mechanical polishing (CMP) methods is not high, and surface scratches are also inevitable because of using slurry containing hard abrasives such as silica particles. Here artemisinin (Qinghaosu) crystals, very soft molecular solids, were found, for the first time to the best of our knowledge, to effectively polish SiC wafers even in pure water as demonstrated by proof-of-concept scratching experiments using atomic force microscopy (AFM). The underlying mechanism is attributed to activated oxidation of SiC by mechanically released reactive &middot;OH free radicals from the endoperoxide bridges. The preliminary results reported here have important implications for developing novel alternative green and scratch-free polishing methods for hard-brittle substrates including SiC and others.</p>

Surface charge on kaolinites in aqueous suspension

Soil Research ◽  
1976 ◽  
Vol 14 (2) ◽  
pp. 197 ◽  
Author(s):  
MDA Bolland ◽  
AM Posner ◽  
JP Quirk
Keyword(s):  
Surface Charge ◽  
Positive Charge ◽  
Aqueous Suspension ◽  
Isomorphous Substitution ◽  
Ph Values ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Decreasing Ph ◽  
Ph Range ◽  
Exchange Technique

The surface charge of several natural kaolinites was measured in the pH range 3-10 using an exchange technique. The positive charge was found to increase with decreasing pH and sometimes to increase with increasing ionic strength; it occurred on the kaolinites at pH values as high as 9 and 10 and was particularly evident at high ionic strengths. The positive surface charge on kaolinites is thought to be due to exposed alumina such as is found on oxide surfaces. Aluminium was found to dissolve from kaolinite at pH values beiow about 6.5. Aluminium dissolution increased with decreasing pH and time. When the proportion of dissolved aluminium ions balancing negative surface charge was taken into account, the negative and net negative surface charge on kaolinite was concluded to be largely due to pH independent charge resulting from isomorphous substitution, together with some pH dependent charge due to exposed SiOH sites. If Na+ was the index cation, dissolved aluminium ions from the clay replaced some of the Na+ balancing the negative surface charge. However, when Cs+ was the index cation, less Cs+ balancing the negative surface charge on the clay was replaced by dissolved aluminium. As the concentration of either Na+ or Cs+ was increased, less dissolved aluminium replaced the index cation as a counteraction to the negative surface charge.

scholarly journals First identification of nanoparticles on thorax, abdomen and wings of the worker bee Apis dorsata Fabricius

2016 ◽  
Vol 60 (1) ◽  
pp. 87-96
Author(s):  
Atanu Bhattacharyya ◽  
Shashidhar Viraktamath ◽  
Fani Hatjina ◽  
Santanu Bhattacharyya ◽  
Bhaktibhavana Rajankar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Average Diameter ◽  
The Body ◽  
Apis Dorsata ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Calcium Phosphate Nanoparticles ◽  
First Time

Abstract The presence of nanoparticles on the body of the honeybee Apis dorsata Fabricius, was investigated for the first time to better understand the bee’s behaviour. These have been observed by using Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and confirmed by Atomic Force Microscopy (AFM). Our study clearly denotes that the Indian rock honey bee Apis dorsata possess calcium silicate and calcium phosphate nanoparticles on its body surface of 5-50 nm in diameter. In particular, the nanoparticles on the abdomen and thorax of A. dorsata have an average diameter of about 10 nanometers and they are smaller than those found on wings of the same bees which are about 20 nanometers. The nanoparticles found are different of the ones previously observed on honey bees or other insects. The origin and role of these natural nanoparticles on the body of the Indian rock bee need to be to be further investigated; more research in the subject might raise important aspects in relation to the conservation of these unique pollinators.

The application of atomic force microscopy in mineral flotation

2018 ◽  
Vol 256 ◽  
pp. 373-392 ◽  
Author(s):  
Yaowen Xing ◽  
Mengdi Xu ◽  
Xiahui Gui ◽  
Yijun Cao ◽  
Bent Babel ◽  
...  
Keyword(s):  
Atomic Force Microscopy ◽  
Force Microscopy ◽  
Atomic Force ◽  
Mineral Flotation

HETERO-GROWTH OF (100) ORIENTATED ZNO FILMS ON SILICON BY SS-CVD

2002 ◽  
Vol 16 (28n29) ◽  
pp. 4250-4254 ◽  
Author(s):  
JIAN-GUO LU ◽  
ZHI-ZHEN YE ◽  
HAN-HONG CHEN ◽  
JING-YUN HUANG ◽  
BING-HUI ZHAO
Keyword(s):  
Texture Coefficient ◽  
Zinc Acetate Dihydrate ◽  
Chemical Vapor ◽  
Zno Films ◽  
X Ray Diffraction ◽  
Lower Growth ◽  
Force Microscopy ◽  
Atomic Force ◽  
First Time ◽  
Lower Growth Temperature

ZnO films with (100) preferred orientation are reported for the first time. ZnO films were synthesized on Si(100) substrate by solid-source chemical vapor deposition (SS-CVD) using zinc acetate dihydrate (solid) as a precursor. The structural properties were investigated by X-ray diffraction and atomic force microscopy. Results show that a lower growth temperature and a higher deposition rate will facilitate the formation of (100) texture. The texture coefficient for (100) plane is 3.28.

On the way to supramolecular photochemistry at the single-molecule level

2006 ◽  
Vol 78 (12) ◽  
pp. 2247-2259 ◽  
Author(s):  
Christian Schäfer ◽  
Björn Decker ◽  
Matthias Letzel ◽  
Francesca Novara ◽  
Rainer Eckel ◽  
...  
Keyword(s):  
Single Molecule ◽  
Binding Pocket ◽  
Ion Cyclotron Resonance ◽  
Dynamic Force ◽  
Fticr Mass Spectrometry ◽  
Single Molecule Level ◽  
Force Microscopy ◽  
Atomic Force ◽  
Molecular Length ◽  
First Time

Two examples of artificial supramolecular host-guest systems derived from resorc[4]arenes (calix[n]arenes based on resorcinol) and ammonium ions as guests have been studied by atomic force microscopy (AFM). For the first time, real single-molecule events have been determined for this type of supramolecular complexes and off-rates as well as molecular parameters of single-molecule aggregates such as the depths of the binding pocket (molecular length parameter) could be measured by applying the methods of dynamic force spectroscopy. In addition, this technique was also applied to differentiate between the two states (open and closed) of a photoswitchable resorc[4]arene-anthracene tweezer. An investigation of the exchange rates of various complexes in the gas phase by means of Fourier transform ion cyclotron resonance (FTICR) mass spectrometry confirmed the results of the AFM study.

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