scholarly journals Defluorination of Polytetrafluoroethylene Surface by Hydrogen Plasma

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2855
Author(s):  
Alenka Vesel ◽  
Dane Lojen ◽  
Rok Zaplotnik ◽  
Gregor Primc ◽  
Miran Mozetič ◽  
...  
Keyword(s):  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
Treatment Time ◽  
Synergistic Effects ◽  
Surface Film ◽  
Hydrogen Plasma ◽  
Contact Angles ◽  
Hydrogen Atoms ◽  
Tof Sims ◽  
Discharge Parameters

Defluorination of polytetrafluoroethylene (PTFE) surface film is a suitable technique for tailoring its surface properties. The influence of discharge parameters on the surface chemistry was investigated systematically using radio-frequency inductively coupled H2 plasma sustained in the E- and H-modes at various powers, pressures and treatment times. The surface finish was probed by X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The measurements of water contact angles (WCA) showed increased wettability of the pristine PTFE; however, they did not reveal remarkable modification in the surface chemistry of the samples treated at various discharge parameters. By contrast, the combination of XPS and ToF-SIMS, however, revealed important differences in the surface chemistry between the E- and H-modes. A well-expressed minimum in the fluorine to carbon ratio F/C as low as 0.2 was observed at the treatment time as short as 1 s when plasma was in the H-mode. More gradual surface chemistry was observed when plasma was in the E-mode, and the minimal achievable F/C ratio was about 0.6. The results were explained by the synergistic effects of hydrogen atoms and vacuum ultraviolet radiation.

Zinc immobilization by zerovalent Fe: surface chemistry and mineralogy of reaction products

2003 ◽  
Vol 67 (6) ◽  
pp. 1285-1298 ◽  
Author(s):  
R. B. Herbert
Keyword(s):  
Oxygen Consumption ◽  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
Solid Phase ◽  
Surface Film ◽  
Column Experiment ◽  
Green Rust ◽  
Reaction Products ◽  
Solution Ph ◽  
X Ray

AbstractIn bioreactor systems for the treatment of metal-contaminated water, pretreatment with zerovalent Fe can be exploited for oxygen consumption and H2 production. In this study, a column experiment is used to investigate the changes in surface chemistry and solid phase products that result from the reaction of a Zn-sulphate-lactate solution with zerovalent Fe filings. The results of this study indicate that zerovalent Fe is very effective in immobilizing dissolved Zn with a porewater residence time of 1.3 –3.1 days. A combination of X-ray diffractometry, X-ray photoelectron spectroscopy, and mineral equilibria calculations indicates that Zn precipitates as Zn(OH)2 and zincite at pH 9 –10. At pH ≈6, Zn primarily adsorbs to abundant ferric oxyhydroxides, although incorporation in green rust is also considered. During the course of the experiment, the surface mineralogy changes from magnetitelepidocrocite- goethite to green rust-akaganéite-goethite. The results suggest that the zerovalent Fe surface becomes passivated by a surface film of ferric oxyhydroxides, green rust and organic material, so that the rate of electron transfer and proton consuming reactions (i.e. oxygen consumption, H2 generation) declines, resulting in a decrease in solution pH.

scholarly journals Recent Advances in Surface Activation of Polytetrafluoroethylene (PTFE) by Gaseous Plasma Treatments

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2295 ◽  
Author(s):  
Gregor Primc
Keyword(s):  
Surface Finish ◽  
Photoelectron Spectroscopy ◽  
Surface Film ◽  
Bond Scission ◽  
Chemical Inertness ◽  
Gaseous Plasma ◽  
Hydrophobic Recovery ◽  
Hydrophilic Character ◽  
Discharge Parameters ◽  
Deep Ultraviolet

Fluorinated polymers are renowned for their chemical inertness and thus poor wettability and adhesion of various coatings. Apart from chemical methods employing somewhat toxic primers, gaseous plasma treatment is a popular method for the modification of surface properties. Different authors have used different plasmas, and the resultant surface finish spans between super-hydrophobic and super-hydrophilic character. Some authors also reported the hydrophobic recovery. The review of recent papers is presented and discussed. Correlations between plasma and/or discharge parameters and the surface finish are drawn and the most important conclusions are summarized. The concentration of oxygen in the surface film as probed by X-ray photoelectron spectroscopy is inversely dependent on the concentration of oxygen in gaseous plasma. The predominant mechanism leading to hydrophilic surface finish is bond scission by deep ultraviolet radiation rather than functionalization with reactive oxygen species.

The Study of SiC Surface Cleaning by Hydrogen Plasma

2013 ◽  
Vol 473 ◽  
pp. 61-64
Author(s):  
Su Hua Chen
Keyword(s):  
Plasma Treatment ◽  
Photoelectron Spectroscopy ◽  
Treatment Time ◽  
Hydrogen Plasma ◽  
Surface Cleaning ◽  
Plasma System ◽  
Xps Spectra ◽  
X Ray ◽  
Surface Oxides ◽  
Before And After

The SiC surfaces were cleaned by the hydrogen plasma with ECRPEMOCVD plasma system at low temperature of 200°C, after the traditional wet cleaning. The surfaces were investigated by RHEED and X-ray Photoelectron Spectroscopy before and after hydrogen plasma treatment. The RHEED imagines showed that the SiC surfaces by hydrogen plasma treatment were more flatter than the SiC surfaces by the traditional wet cleaning, and we found the result that more treatment time, more flatter. The XPS spectra examinations indicated that the surface oxides reduced obviously and the C/C-H compounds on the SiC surface were removed by hydrogen plasma treatment, so the antioxidant ability of the SiC surface was improved.

Surface Chemistry of Nanocrystalline Cerium Oxide

1994 ◽  
Vol 351 ◽  
Author(s):  
Andreas Tschöpe ◽  
J.Y. Ying ◽  
K. Amonlirdviman ◽  
M. L. Trudeau
Keyword(s):  
Surface Chemistry ◽  
Cerium Oxide ◽  
Photoelectron Spectroscopy ◽  
Synergistic Effects ◽  
Oxygen Deficiency ◽  
High Surface ◽  
Reaction Chamber ◽  
Surface Reactivity ◽  
Promoting Effect ◽  
Reduction And Oxidation

ABSTRACTNanocrystalline cerium oxide was synthesized by magnetron sputtering of a metallic target, followed by controlled post-oxidation. The resulting cerium oxide clusters were <10 nm in size, and highly non-stoichiometric in nature. The oxygen deficiency of such materials was associated with the unusual catalytic activity in oxidation and redox reactions. This paper compares the surface chemistry of nanocrystalline CeO2−x with stoichiometric CeO2. It further explores the promoting effect of Cu-doping on surface reduction and oxidation.The oxidation states of metal cations were examined with X-ray photoelectron spectroscopy after various oxidizing and reducing heat treatments in a connected reaction chamber. Isothermal pulsed reduction and oxidation of the samples were investigated by thermogravimetric analysis. Reduction properties of the different materials are discussed in terms of their microstructure, oxygen deficiency and chemical composition. These studies will help to understand the importance of bulk defects and synergistic effects in multicomponent and multiphase materials for high surface reactivity.

scholarly journals Effect of sizing agent on interfacial properties of carbon fiber-reinforced PMMA composite

2021 ◽  
Vol 30 ◽  
pp. 2633366X2097865
Author(s):  
Li Jian
Keyword(s):  
Shear Strength ◽  
Surface Treatment ◽  
Photoelectron Spectroscopy ◽  
Resin Composite ◽  
Contact Angles ◽  
Static Contact ◽  
Before And After ◽  
C Value ◽  
Interlayer Shear Strength ◽  
Pmma Resin

The surface treatment of carbon fibers (CFs) was carried out using a self-synthesized sizing agent. The effects of sizing agent on the surface of CFs and the interface properties of CF/polymethyl methacrylate (PMMA) composites were mainly studied. Scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and static contact angle were used to compare and study the CFs before and after the surface treatment, including surface morphology, surface chemical element composition, and wettability of the surface. The influence of sizing agent on the mechanical properties of CF/PMMA resin composite interface was investigated. The results show that after sizing treatment, the CF surface O/C value increased by 35.1% and the contact angles of CF and resin decreased by 16.2%. The interfacial shear strength and interlayer shear strength increased by 12.6%.

scholarly journals Surface Chemical Heterogeneity of Low Rank Coal Characterized by Micro-FTIR and Its Correlation with Hydrophobicity

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 239
Author(s):  
Wei Wang ◽  
Long Liang ◽  
Yaoli Peng ◽  
Maria Holuszko
Keyword(s):  
Surface Chemistry ◽  
Functional Group ◽  
Group Composition ◽  
Contact Angles ◽  
Low Rank ◽  
Surface Chemical ◽  
Carbonyl Groups ◽  
Low Rank Coal ◽  
Different Types ◽  
Aliphatic Carbon

Micro-Fourier transform infrared (micro-FTIR) spectroscopy was used to correlate the surface chemistry of low rank coal with hydrophobicity. Six square areas without mineral impurities on low rank coal surfaces were selected as testing areas. A specially-designed methodology was applied to conduct micro-FTIR measurements and contact angle tests on the same testing area. A series of semi-quantitative functional group ratios derived from micro-FTIR spectra were correlated with contact angles, and the determination coefficients of linear regression were calculated and compared in order to identify the structure of the functional group ratios. Finally, two semi-quantitative ratios composed of aliphatic carbon hydrogen, aromatic carbon hydrogen and two different types of carbonyl groups were proposed as indicators of low rank coal hydrophobicity. This work provided a rapid way to predict low rank coal hydrophobicity through its functional group composition and helped us understand the hydrophobicity heterogeneity of low rank coal from the perspective of its surface chemistry.

scholarly journals Investigation into the color stripping of the pigment printed cotton fabric using the ozone assisted process: A study on the decolorization and characterization

2021 ◽  
Vol 16 ◽  
pp. 155892502199275
Author(s):  
Ajinkya Powar ◽  
Anne Perwuelz ◽  
Nemeshwaree Behary ◽  
Le vinh Hoang ◽  
Thierry Aussenac ◽  
...  
Keyword(s):  
Cotton Fabric ◽  
Photoelectron Spectroscopy ◽  
Treatment Time ◽  
Pilot Scale ◽  
Chemical Recycling ◽  
X Ray ◽  
Cellulosic Fibers ◽  
Dyeing Process ◽  
Cellulosic Textiles ◽  
Ozonation Process

Color stripping is one of the most convenient ways to rectify the various shade faults occurred during printing or dyeing process of textiles. But, the conventional chemical assisted process poses serious risk of the environmental pollution. Secondly, the chemical recycling of the cellulosic fibers may be disrupted due to the presence of the impurities like colorants, finishes, and the additives in the discarded textiles. So, there is a need to study ways to remove such impurities from the discarded cellulosic textiles in a sustainable manner. This work examines the decolorization of the pigment prints on cellulosic fabrics at pilot scale using an ozone-assisted process. The effect of varying pH, ozone concentration and the treatment time on the decolorization of the pigment prints was optimized using the response surface methodology technique. The effects of ozonation process parameters on the mechanical properties of cellulosic cotton fabric were measured. Decolorization of pigment printed samples was studied with respect to the surface effects by a scanning electron microscopy (SEM), and the chemical removal effects of ozonation treatment were studied using X-ray photoelectron spectroscopy. The possible mechanism regarding the action of ozone for the decolorization is discussed.

scholarly journals P4VP Modified Zwitterionic Polymer for the Preparation of Antifouling Functionalized Surfaces

Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 706 ◽  
Author(s):  
Chaoqun Wu ◽  
Yudan Zhou ◽  
Haitao Wang ◽  
Jianhua Hu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Cell Attachment ◽  
Raft Polymerization ◽  
Polymer Brush ◽  
Contact Angles ◽  
Polymerization Process ◽  
Water Contact ◽  
Zwitterionic Polymers ◽  
Ito Glass ◽  
Zwitterionic Polymer

Zwitterionic polymers are suitable for replacing poly(ethylene glycol) (PEG) polymers because of their better antifouling properties, but zwitterionic polymers have poor mechanical properties, strong water absorption, and their homopolymers should not be used directly. To solve these problems, a reversible-addition fragmentation chain transfer (RAFT) polymerization process was used to prepare copolymers comprised of zwitterionic side chains that were attached to an ITO glass substrate using spin-casting. The presence of 4-vinylpyridine (4VP) and zwitterion chains on these polymer-coated ITO surfaces was confirmed using 1H NMR, FTIR, and GPC analyses, with successful surface functionalization confirmed using water contact angle, X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) studies. Changes in water contact angles and C/O ratios (XPS) analysis demonstrated that the functionalization of these polymers with β-propiolactone resulted in hydrophilic mixed 4VP/zwitterionic polymers. Protein adsorption and cell attachment assays were used to optimize the ratio of the zwitterionic component to maximize the antifouling properties of the polymer brush surface. This work demonstrated that the antifouling surface coatings could be readily prepared using a “P4VP-modified” method, that is, the functionality of P4VP to modify the prepared zwitterionic polymer. We believe these materials are likely to be useful for the preparation of biomaterials for biosensing and diagnostic applications.

Application of principal component analysis and tof-sims to mineral recognition, surface chemistry and separation by flotation

2006 ◽  
Vol 70 (18) ◽  
pp. A597 ◽  
Author(s):  
Roger St. C. Smart ◽  
Brian Hart ◽  
Mark Biesinger ◽  
James Francis ◽  
Tesfaye Negeri
Keyword(s):  
Principal Component Analysis ◽  
Surface Chemistry ◽  
Principal Component ◽  
Component Analysis ◽  
Tof Sims

scholarly journals A Novel Synthetic UV-Curable Fluorinated Siloxane Resin for Low Surface Energy Coating

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 979 ◽  
Author(s):  
Chunfang Zhu ◽  
Haitao Yang ◽  
Hongbo Liang ◽  
Zhengyue Wang ◽  
Jun Dong ◽  
...  
Keyword(s):  
Surface Energy ◽  
Photoelectron Spectroscopy ◽  
Contact Angles ◽  
Proton Nuclear Magnetic Resonance ◽  
Energy Materials ◽  
Uv Curable ◽  
X Ray ◽  
Low Surface Energy ◽  
Low Concentrations ◽  
Siloxane Polymers

Low surface energy materials have attracted much attention due to their properties and various applications. In this work, we synthesized and characterized a series of ultraviolet (UV)-curable fluorinated siloxane polymers with various fluorinated acrylates—hexafluorobutyl acrylate, dodecafluoroheptyl acrylate, and trifluorooctyl methacrylate—grafted onto a hydrogen-containing poly(dimethylsiloxane) backbone. The structures of the fluorinated siloxane polymers were measured and confirmed by proton nuclear magnetic resonance and Fourier transform infrared spectroscopy. Then the polymers were used as surface modifiers of UV-curable commercial polyurethane (DR-U356) at different concentrations (1, 2, 3, 4, 5, and 10 wt %). Among three formulations of these fluorinated siloxane polymers modified with DR-U356, hydrophobic states (91°, 92°, and 98°) were obtained at low concentrations (1 wt %). The DR-U356 resin is only in the hydrophilic state at 59.41°. The fluorine and siloxane element contents were investigated by X-ray photoelectron spectroscopy and the results indicated that the fluorinated and siloxane elements were liable to migrate to the surface of resins. The results of the friction recovering assays showed that the recorded contact angles of the series of fluorinated siloxane resins were higher than the original values after the friction-annealing progressing.

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