scholarly journals Biocompatible/Biodegradable Electrowetting on Dielectric Microfluidic Chips with Fluorinated CTA/PLGA

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1332 ◽  
Author(s):  
Kaidi Zhang ◽  
Lei Chao ◽  
Jia Zhou
Keyword(s):  
Contact Angle ◽  
Photoelectron Spectroscopy ◽  
Contact Angle Hysteresis ◽  
Cellulose Triacetate ◽  
Microfluidic Chips ◽  
Electrowetting On Dielectric ◽  
Force Microscopy ◽  
Atomic Force ◽  
Dielectric Devices ◽  
Contact Line Pinning

One of the major hurdles in the development of biocompatible/biodegradable EWOD (Electrowetting-on-dielectric) devices is the biocompatibility of the dielectric and hydrophobic layers. In this study, we address this problem by using reactive ion etching (RIE) to prepare a super-hydrophobic film combining fluorinated cellulose triacetate (CTA) and poly (lactic-co-glycolic acid) (PLGA). The contact angle (CA) of water droplets on the proposed material is about 160°. X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) characterizations indicate that a slight increase in the surface roughness and the formation of CFx (C-F or CF2) bonds are responsible for the super-hydrophobic nature of the film. Alternating Current (AC) static electrowetting and droplet transportation experiments evidence that contact angle hysteresis and contact line pinning are greatly reduced by impregnating the CTA/PLGA film with silicon oil. Therefore, this improved film could provide a biocompatible alternative to the typical Teflon® or Cytop® films as a dielectric and hydrophobic layer.

scholarly journals Inhibition mechanism of Ca 2+ , Mg 2+ and Fe 3+ in fine cassiterite flotation using octanohydroxamic acid

2018 ◽  
Vol 5 (8) ◽  
pp. 180158 ◽  
Author(s):  
Liuyi Ren ◽  
Hang Qiu ◽  
Wenqing Qin ◽  
Ming Zhang ◽  
Yubiao Li ◽  
...  
Keyword(s):  
Contact Angle ◽  
Photoelectron Spectroscopy ◽  
Chemical Properties ◽  
Solution Chemistry ◽  
Inhibition Mechanism ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Afm Imaging ◽  
Flotation Performance

The existence of metal ions should not be ignored in both hydrometallurgy and flotation. In this study, the effects of Ca 2+ , Mg 2+ and Fe 3+ on the flotation performance of cassiterite using octanohydroxamic acid (OHA) as the collector were investigated by micro-flotation tests, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, contact angle, zeta ( ζ ) potential measurements and atomic force microscopy (AFM) imaging. The results of the flotation and contact angle experiments showed that the addition of Ca 2+ , Mg 2+ and Fe 3+ significantly decreased both the recovery and contact angle of cassiterite with pH ranged from 6.0 to 12.0 in the presence of OHA collector. ζ- Potential measurements, solution chemistry analysis and FTIR measurements indicated that the flotation recovery of the cassiterite declined due to the CaOH + , MgOH + and Fe(OH) 3 sites on the cassiterite surface. XPS results indicated that the chemisorption of OHA and calcium ions on the cassiterite surface finally changed its chemical properties. The AFM images also revealed that new species Fe(OH) 3 of Fe 3+ formed and adsorbed on the cassiterite surface at pH 9.0. The adsorption of Fe(OH) 3 reduced the adsorption of OHA on the cassiterite surface, thus the hydrophobicity of cassiterite was deteriorated.

scholarly journals Surface Modification of Polyethersulfone (PES) with UV Photo-Oxidation

Technologies ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 36
Author(s):  
Ibrahim Cisse ◽  
Sarah Oakes ◽  
Shreen Sachdev ◽  
Marc Toro ◽  
Shin Lutondo ◽  
...  
Keyword(s):  
Surface Roughness ◽  
Contact Angle ◽  
Atomic Force Microscopy ◽  
Photoelectron Spectroscopy ◽  
Water Contact ◽  
X Ray ◽  
Force Microscopy ◽  
Photo Oxidation ◽  
Atomic Force ◽  
Modified Surfaces

Polyethersulfone (PES) films are widely employed in the construction of membranes where there is a desire to make the surface more hydrophilic. Therefore, UV photo-oxidation was studied in order to oxidize the surface of PES and increase hydrophilicity. UV photo-oxidation using low pressure mercury lamps emitting both 253.7 and 184.9 nm radiation were compared with only 253.7 nm photons. The modified surfaces were characterized using X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and water contact angle (WCA) measurements. Both sets of lamps gave similar results, showing an increase of the oxygen concentration up to a saturation level of ca. 29 at.% and a decrease in the WCA, i.e., an increase in hydrophilicity, down to ca. 40°. XPS detected a decrease of sp2 C-C aromatic group bonding and an increase in the formation of C-O, C=O, O=C-O, O=C-OH, O-(C=O)-O, and sulphonate and sulphate moieties. Since little change in surface roughness was observed by AFM, the oxidation of the surface caused the increase in hydrophilicity.

scholarly journals Nanoscale Morphology of Apatite Precipitated onto Synthetic Hydroxyapatite from Simulated Body Fluid

2005 ◽  
Vol 284-286 ◽  
pp. 497-500 ◽  
Author(s):  
Jennifer Vandiver ◽  
Nelesh Patel ◽  
William Bonfield ◽  
Christine Ortiz
Keyword(s):  
Contact Angle ◽  
Simulated Body Fluid ◽  
Photoelectron Spectroscopy ◽  
Body Fluid ◽  
Lateral Dimension ◽  
Force Microscopy ◽  
Angle Measurements ◽  
Atomic Force ◽  
Synthetic Hydroxyapatite ◽  
Individual Grains

Dense, polycrystalline, synthetic hydroxyapatite (HA) was incubated for 36 days in modified simulated body fluid (SBF) with increased HCO3 - and reduced Cl- ion concentrations (27 and 120 mM, respectively) closer to actual blood plasma than typical SBF. The resulting precipitated apatite layer was characterized by X-ray photoelectron spectroscopy (XPS) and contact angle measurements and found to be nonstoichiometric, calcium deficient (Ca/P~1.06), non-carbonate containing, and of intermediate hydrophilicity (advancing contact angle, qa=76.5±1.3°). The nanoscale surface topography of the SBF-incubated HA sample was imaged by tapping mode atomic force microscopy (TMAFM), observed to be ≤100 nm in thickness, and composed of three distinct morphologies. These topographically distinct regions were localized within individual grains and facets of the initial HA surface and included: hemispherical, globular structures (maximum lateral dimension, d=44.7±12.7 nm, peak-tovalley height, h=3.6±2.7 nm); elongated, needle-like structures (minimum lateral dimension, w=31.0±8.5 nm, d=104.4±31.1 nm, h=5.0±3.2 nm), and regions of larger, irregularly shaped structures that were relatively smooth (d=504.9±219.1 nm, h=104.0±51.7 nm).

scholarly journals UV Photo-Oxidation of Polybenzimidazole (PBI)

Technologies ◽  
2020 ◽  
Vol 8 (4) ◽  
pp. 52
Author(s):  
Devon Shedden ◽  
Kristen M. Atkinson ◽  
Ibrahim Cisse ◽  
Shin Lutondo ◽  
Tyshawn Roundtree ◽  
...  
Keyword(s):  
Contact Angle ◽  
Photoelectron Spectroscopy ◽  
Treatment Time ◽  
Aerospace Industry ◽  
Water Contact ◽  
X Ray ◽  
Force Microscopy ◽  
Photo Oxidation ◽  
Redox Flow Batteries ◽  
Atomic Force

Since polybenzimidazole (PBI) is often used in the aerospace industry, high-temperature fuel cells, and in redox flow batteries, this research investigated the surface modification of PBI film with 253.7 and 184.9 nm UV photo-oxidation. As observed by X-ray photoelectron spectroscopy (XPS), the oxygen concentration on the surface increased up to a saturation level of 20.2 ± 0.7 at %. With increasing treatment time, there were significant decreases in the concentrations of C-C sp2 and C=N groups and increases in the concentrations of C=O, O-C=O, O-(C=O)-O, C-N, and N-C=O containing moieties due to 253.7 nm photo-oxidation of the aromatic groups of PBI and reaction with ozone produced by 184. 9 nm photo-dissociation of oxygen. Because no significant changes in surface topography were detected by Atomic Force Microscopy (AFM) and SEM measurements, the observed decrease in the water contact angle down to ca. 44°, i.e., increase in hydrophilic, was due to the chemical changes on the surface.

Surface Modification of Polyvinylidenefluoride-Trifluoroethylene Film Using Argon Gas Plasma

2012 ◽  
Vol 626 ◽  
pp. 317-323 ◽  
Author(s):  
Rozana Mohd Dahan ◽  
Muhamad Naiman Sarip ◽  
Yap Seong Ling ◽  
Mohamad Hafiz Mohd Wahid ◽  
Adillah Nurashikin Arshad ◽  
...  
Keyword(s):  
Surface Roughness ◽  
Contact Angle ◽  
Photoelectron Spectroscopy ◽  
Argon Plasma ◽  
Water Contact ◽  
Force Microscopy ◽  
Atomic Force ◽  
Gas Plasma ◽  
Good Biocompatibility ◽  
Surface Modified

This study investigates the surface properties of plasma surface modified spin coated PVDF-TrFE (70/30) film using Atomic Force Microscopy (AFM), Water Contact Angle (WCA) and X-ray Photoelectron Spectroscopy (XPS). The surfaces of the spin coated PVDF-TrFE film were modified using 13.56 MHz rf Argon plasma. The exposure time of the charged particle PVDF-TrFE films were varied for 1, 3 and 5mins. Prior to modification, the average surface roughness obtained was 8.615nm, but upon modification, the surface roughness was found to increase to 12.466nm. The value of the contact angle of the modified film was reduced from 90o to 43o and the XPS analysis showed dehydrofluorination of PVDF-TrFE films surfaces. The improved in surface roughness and the increased in wettability of the modified film, resulted in good biocompatibility of the modified PVDF-TrFE thin films. This phenomenon has created interest in researchers for developing functional polymer used for applications in areas such are biomedical, bio-analytical assays, textile and even food industry.

Investigation of the Effect of Uv-Assisted Oxidation and Nitridation of Hafnium Metal Films

2003 ◽  
Vol 780 ◽  
Author(s):  
C. Essary ◽  
V. Craciun ◽  
J. M. Howard ◽  
R. K. Singh
Keyword(s):  
Uv Radiation ◽  
Photoelectron Spectroscopy ◽  
Grazing Angle ◽  
X Ray Diffraction ◽  
Metal Thin Films ◽  
X Ray ◽  
Force Microscopy ◽  
Si Substrates ◽  
Atomic Force ◽  
Silicon Interface

AbstractHf metal thin films were deposited on Si substrates using a pulsed laser deposition technique in vacuum and in ammonia ambients. The films were then oxidized at 400 °C in 300 Torr of O2. Half the samples were oxidized in the presence of ultraviolet (UV) radiation from a Hg lamp array. X-ray photoelectron spectroscopy, atomic force microscopy, and grazing angle X-ray diffraction were used to compare the crystallinity, roughness, and composition of the films. It has been found that UV radiation causes roughening of the films and also promotes crystallization at lower temperatures.Furthermore, increased silicon oxidation at the interface was noted with the UVirradiated samples and was shown to be in the form of a mixed layer using angle-resolved X-ray photoelectron spectroscopy. Incorporation of nitrogen into the film reduces the oxidation of the silicon interface.

scholarly journals Photocatalytic reduction of graphene oxide with cuprous oxide film under UV-vis irradiation

2020 ◽  
Vol 59 (1) ◽  
pp. 207-214 ◽  
Author(s):  
Yao Wang ◽  
Jianqing Feng ◽  
Lihua Jin ◽  
Chengshan Li
Keyword(s):  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Photocatalytic Reduction ◽  
Force Microscopy ◽  
Atomic Force ◽  
Reduced Graphene ◽  
Reduction Efficiency ◽  
Metal Organic ◽  
Reduction Effect

AbstractWe have grown Cu2O films by different routes including self-oxidation and metal-organic deposition (MOD). The reduction efficiency of Cu2O films on graphene oxide (GO) synthesized by modified Hummer’s method has been studied. Surface morphology and chemical state of as-prepared Cu2O film and GO sheets reduced at different conditions have also been investigated using atomic force microscopy (AFM) and x-ray photoelectron spectroscopy (XPS). Results show that self-oxidation Cu2O film is more effective on phtocatalytic reduction of GO than MOD-Cu2O film. Moreover, reduction effect of self-oxidation Cu2O film to GO is comparable to that of environmental-friendly reducing agent of vitamin C. The present results offer a potentially eco-friendly and low-cost approach for the manufacture of reduced graphene oxide (RGO) by photocatalytic reduction.

scholarly journals Interface Structures and Electronic States of Epitaxial Tetraazanaphthacene on Single-Crystal Pentacene

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1088
Author(s):  
Yuki Gunjo ◽  
Hajime Kamebuchi ◽  
Ryohei Tsuruta ◽  
Masaki Iwashita ◽  
Kana Takahashi ◽  
...  
Keyword(s):  
Single Crystal ◽  
Photoelectron Spectroscopy ◽  
Grazing Incidence ◽  
Force Microscopy ◽  
Interface Dipole ◽  
Atomic Force ◽  
Interfacial Structures ◽  
Donor And Acceptor ◽  
A Charge ◽  
Interface Structures

The structural and electronic properties of interfaces composed of donor and acceptor molecules play important roles in the development of organic opto-electronic devices. Epitaxial growth of organic semiconductor molecules offers a possibility to control the interfacial structures and to explore precise properties at the intermolecular contacts. 5,6,11,12-tetraazanaphthacene (TANC) is an acceptor molecule with a molecular structure similar to that of pentacene, a representative donor material, and thus, good compatibility with pentacene is expected. In this study, the physicochemical properties of the molecular interface between TANC and pentacene single crystal (PnSC) substrates were analyzed by atomic force microscopy, grazing-incidence X-ray diffraction (GIXD), and photoelectron spectroscopy. GIXD revealed that TANC molecules assemble into epitaxial overlayers of the (010) oriented crystallites by aligning an axis where the side edges of the molecules face each other along the [1¯10] direction of the PnSC. No apparent interface dipole was found, and the energy level offset between the highest occupied molecular orbitals of TANC and the PnSC was determined to be 1.75 eV, which led to a charge transfer gap width of 0.7 eV at the interface.

scholarly journals Silane-Coating Strategy for Titanium Functionalization Does Not Impair Osteogenesis In Vivo

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1814
Author(s):  
Plinio Mendes Senna ◽  
Carlos Fernando de Almeida Barros Mourão ◽  
Rafael Coutinho Mello-Machado ◽  
Kayvon Javid ◽  
Pietro Montemezzi ◽  
...  
Keyword(s):  
Bone Formation ◽  
Photoelectron Spectroscopy ◽  
Titanium Surface ◽  
Rabbit Model ◽  
Biologically Active ◽  
Force Microscopy ◽  
Atomic Force ◽  
Silane Coating ◽  
Titanium Screws

Silane-coating strategy has been used to bind biological compounds to the titanium surface, thereby making implant devices biologically active. However, it has not been determined if the presence of the silane coating itself is biocompatible to osseointegration. The aim of the present study was to evaluate if silane-coating affects bone formation on titanium using a rabbit model. For this, titanium screw implants (3.75 by 6 mm) were hydroxylated in a solution of H2SO4/30% H2O2 for 4 h before silane-coating with 3-aminopropyltriethoxysilane (APTES). A parallel set of titanium screws underwent only the hydroxylation process to present similar acid-etched topography as a control. The presence of the silane on the surface was checked by x-ray photoelectron spectroscopy (XPS), with scanning electron microscopy (SEM) and atomic force microscopy (AFM). A total of 40 titanium screws were implanted in the tibia of ten New Zealand rabbits in order to evaluate bone-to-implant contact (BIC) after 3 weeks and 6 weeks of healing. Silane-coated surface presented higher nitrogen content in the XPS analysis, while micro- and nano-topography of the surface remained unaffected. No difference between the groups was observed after 3 and 6 weeks of healing (p > 0.05, independent t-test), although an increase in BIC occurred over time. These results indicate that silanization of a titanium surface with APTES did not impair the bone formation, indicating that this can be a reliable tool to anchor osteogenic molecules on the surface of implant devices.

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