scholarly journals Water-Resistant Surface Modification of Hydrophobic Polymers With Water-Soluble Surfactant Additives

2021 ◽  
Author(s):  
Colin Gibson ◽  
Matthew Litwinowicz ◽  
James Tellam ◽  
Rebecca Wellbourn ◽  
Maximilian W.A. Skoda ◽  
...  
Keyword(s):  
Surface Modification ◽  
Film Surface ◽  
Water Soluble ◽  
Surface Wetting ◽  
Force Microscopy ◽  
Depth Profiles ◽  
Hydrophobic Polymers ◽  
Hydrophilic Surfaces ◽  
Atomic Force ◽  
Tact Angle

Water-soluble nonionic surfactant, pentaethylene glycol monododecyl ether, C12E5, spontaneously blooms to the surface of spin-cast hydrophobic polyiso-prenes, generating hydrophilic surfaces. This system represents a simple model for hydrophilic chemical modification of rubbery polymers yet demonstrates surprisingly rich, complex and unexpected behaviour. The ver-tical depth profiles were quantified using neutron reflectometry (NR) and deuterated surfactant, and the surface properties were characterized using con-tact angle analysis and atomic force microscopy (AFM). Despite the low surface tension of the toluene solvent used in film preparation and the low surface en-ergy of the PI matrix, NR depth profiles revealed clear evidence of surfactant segregation. This surface layer was typically thicker than a monolayer, but incomplete, yet was remarkably stable with respect to dissolution, even when exposed to hundreds of thousands of times the volume of water required to dissolve all the surfactant on the surface. Despite the apparent resistance to removal from the surface, water exposure does alter the subsequent wettabil-ity of the surface, with a hydrophilic-to-hydrophobic transition occurring after rinsing. Complementary AFM images of these C12E5 / cis-PI films showed unexpected strand-like features on the surface of the film, which we attribute to a non-uniform lateral distribution of some of the surfactant. This surface structure becomes more evident after rinsing, and it appears that there are two distinct populations of surfactant on the PI film surface. We conclude that some of the bloomed surfactant exists as layers, which are relatively inert with respect to rinsing or surface modification, and some is laterally inhomogene-ous. This latter population is primarily responsible for surface wetting be-havior, but is not detected by specular NR.

scholarly journals Water-Resistant Surface Modification of Hydrophobic Polymers with Water-Soluble Surfactant Additives

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3407
Author(s):  
Colin P. Gibson ◽  
Matthew A. Litwinowicz ◽  
James P. Tellam ◽  
Rebecca J. L. Welbourn ◽  
Maximilian W. A. Skoda ◽  
...  
Keyword(s):  
Surface Modification ◽  
Film Surface ◽  
Water Soluble ◽  
Surface Wetting ◽  
Force Microscopy ◽  
Depth Profiles ◽  
Hydrophobic Polymers ◽  
Hydrophilic Surfaces ◽  
Low Surface Energy ◽  
Atomic Force

Water-soluble nonionic surfactant, pentaethylene glycol monododecyl ether, C12E5, spontaneously blooms to the surface of spin-cast hydrophobic polyisoprenes, generating hydrophilic surfaces. This system provides a simple model for hydrophilic chemical modification of rubbery polymers that demonstrates surprisingly rich, complex, and unexpected behaviour. The vertical depth profiles were quantified using neutron reflectometry (NR) using a novel procedure to account for undulations in the film thickness. Surface properties were characterized using contact angle analysis and atomic force microscopy (AFM). Despite the low surface tension of the toluene solvent used in film preparation and the low surface energy of the polyisoprene (PI) matrix, NR depth profiles revealed clear evidence of surfactant segregation. This surface layer was typically thicker than a monolayer, but incomplete, yet was remarkably stable with respect to dissolution, even when exposed to hundreds of thousands of times the volume of water required to dissolve all the surfactant on the surface. Despite the apparent resistance to removal from the surface, water exposure does alter the subsequent wettability of the surface, with a hydrophilic-to-hydrophobic transition occurring after rinsing. Complementary AFM images of these C12E5/cis-PI films showed unexpected strand-like features on the surface of the film, which we attribute to a non-uniform lateral distribution of some of the surfactant. This surface structure becomes more evident after rinsing, and it appears that there are two distinct populations of surfactant on the PI film surface. We conclude that some of the bloomed surfactant exists as layers, which are relatively inert with respect to rinsing or surface modification, and some is laterally inhomogeneous. This latter population is primarily responsible for surface wetting behaviour but is not detected by specular NR.

Self-assembly layer-by-layer fabrication using porphyrin dye anion and polycation

2009 ◽  
Vol 13 (07) ◽  
pp. 774-778 ◽  
Author(s):  
Byung-Soon Kim ◽  
Young-A Son
Keyword(s):  
Ultrathin Films ◽  
Self Assembly ◽  
Film Surface ◽  
Layer By Layer ◽  
Preparation Technique ◽  
Force Microscopy ◽  
Atomic Force ◽  
Diallyldimethylammonium Chloride ◽  
Afm Analysis ◽  
Progressive Growth

In this study, self-assembled alternating film using poly(diallyldimethylammonium chloride) (PDDAC) and meso-tetrakis(4-carboxyphenyl)porphyrin (MTCP) was prepared as a multilayer deposition on glass substrate. This preparation technique for dye deposition may provide new feasibilities to achieve the manufacture of ultrathin films for nanotechnology application. The deposition films were characterized by UV-vis spectrophotometer and Atomic Force Microscopy (AFM) analysis. The results of UV-vis spectra showed that the absorbance characteristic of the multilayer films linearly increased with an increased number of PDDAC and MTCP bilayers. AFM analysis showed the film surface was relatively uniform and the progressive growth of layers was determined.

scholarly journals The effect of replacing iron atoms instead of zinc of the quaternary compound CZTS

2021 ◽  
Vol 2114 (1) ◽  
pp. 012033
Author(s):  
Abubaker.S. Mohammed
Keyword(s):  
Full Width Half Maximum ◽  
Energy Gap ◽  
Film Surface ◽  
X Ray Diffraction ◽  
Quaternary Compound ◽  
Force Microscopy ◽  
Atomic Force ◽  
Coating Method ◽  
Degree Of Crystallization ◽  
High Degree

Abstract In this article, the quaternary compound Cu2MSnS4 was prepared in a simple and inexpensive approach, where M is the iron (Fe) and zinc (Zn) atoms by the spin coating method on a glass substrate at room temperature (RT), as a result of replacing Zn atoms by Fe. Quaternary Cu2ZnSnS4 (CZTS) and Cu2FeSrS4 (CFTS) structural and optical properties have been studied successfully. The material has been identified by X-ray diffraction, and it was discovered that CZTS has a polycrystalline Tetragonal (kesterite) structure, whereas CFTS has a Tetragonal (stannite) structure. A reduction in the full width half maximum (FWHM) of the preferred plane implies a high degree of crystallization. The structural properties of the film surface, such as grain size and roughness, were studied by Atomic force microscopy (AFM). The results explain an increase in nanoparticle size and surface roughness when Fe is substituted by Zn in the CZTS structure. The absorption coefficient values of all designed compounds in visible regions are greater than 104/cm, and the results show that the absorbance coefficient increases with Fe add. The CZTS films showed an energy gap of 1.88 eV, and this value became 1.69 eV with substituted Fe instead of Zn.

Scanning Tunneling Microscopy and Atomic Force Microscopy Investigation of Organic Tetracyanoquinodimethane Thin Films

1997 ◽  
Vol 12 (8) ◽  
pp. 1942-1945 ◽  
Author(s):  
H. J. Gao ◽  
H. X. Zhang ◽  
Z. Q. Xue ◽  
S. J. Pang
Keyword(s):  
Thin Films ◽  
Atomic Force Microscopy ◽  
Scanning Tunneling Microscopy ◽  
Pyrolytic Graphite ◽  
Film Surface ◽  
Scanning Tunneling ◽  
Tunneling Microscopy ◽  
Force Microscopy ◽  
Atomic Force ◽  
Microscopy Investigation

Scanning tunneling microscopy (STM) and atomic force microscopy (AFM) investigation of tetracyanoquinodimethane (TCNQ) and the related C60-TCNQ thin films is presented. Periodic molecular chains of the TCNQ on highly oriented pyrolytic graphite (HOPG) substrates were imaged, which demonstrated that the crystalline (001) plane was parallel to the substrate. For the C60-TCNQ thin films, we found that there were grains on the film surface. STM images within the grain revealed that the well-ordered rows and terraces, and the parallel rows in different grains were generally not in the same orientation. Moreover, the grain boundary was also observed. In addition, AFM was employed to modify the organic TCNQ film surface for the application of this type of materials to information recording and storage at the nanometer scale. The nanometer holes were successfully created on the TCNQ thin film by the AFM.

scholarly journals Superhydrophilic Coating with Antibacterial and Oil-Repellent Properties via NaIO4-Triggered Polydopamine/Sulfobetaine Methacrylate Polymerization

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2008
Author(s):  
Hsiu-Wen Chien ◽  
Hong-Yu Lin ◽  
Chau-Yi Tsai ◽  
Tai-Yu Chen ◽  
Wei-Nian Chen
Keyword(s):  
Surface Modification ◽  
Photoelectron Spectroscopy ◽  
Deposition Process ◽  
Water Contact ◽  
Water Separation ◽  
Force Microscopy ◽  
Atomic Force ◽  
Oil Water Separation ◽  
One Step ◽  
Oil Repellent

Superhydrophilic coatings have been widely used for the surface modification of membranes or biomedical devices owing to their excellent antifouling properties. However, simplifying the modification processes of such materials remains challenging. In this study, we developed a simple and rapid one-step co-deposition process using an oxidant trigger to fabricate superhydrophilic surfaces based on dopamine chemistry with sulfobetaine methacrylate (SBMA). We studied the effect of different oxidants and SBMA concentrations on surface modification in detail using UV–VIS spectrophotometry, dynamic light scattering, atomic force microscopy, X-ray photoelectron spectroscopy, and surface plasmon resonance. We found that NaIO4 could trigger the rate of polymerization and the optimum ratio of dopamine to SBMA is 1:25 by weight. This makes the surface superhydrophilic (water contact angle < 10°) and antifouling. The superhydrophilic coating, when introduced to polyester membranes, showed great potential for oil/water separation. Our study provides a complete description of the simple and fast preparation of superhydrophilic coatings for surface modification based on mussel-inspired chemistry.

scholarly journals Probing surface interactions of underwater oleophobic polyelectrolyte multilayers

2020 ◽  
Author(s):  
Kai Li ◽  
Wei Wang ◽  
Zhi-Peng Yu ◽  
Hang Jin ◽  
Yun-Tong Ge ◽  
...  
Keyword(s):  
Theoretical Calculations ◽  
Interaction Mechanism ◽  
Polyelectrolyte Multilayers ◽  
Layer By Layer ◽  
Surface Wetting ◽  
Force Microscopy ◽  
Atomic Force ◽  
Layer Deposition ◽  
Nacl Concentration ◽  
Force Curves

Abstract In the present work, the interaction mechanism of specific polyelectrolyte multilayers (PEMs), fabricated by layer-by-layer deposition of polydiallyldimethylammonium chloride (PDDA) and poly(sodium 4-styrenesulfonate) (PSS), is studied using atomic force microscopy. The underwater oil-repellency of PSS-capped PEMs was further explored by measuring the interaction forces between tetradecane droplets and PEMs-coated silica substrates under various salinities. The force curves were analyzed following the Stokes–Reynolds–Young–Laplace theoretical model. Desirable consistency was achieved between the experimental and theoretical calculations at low NaCl concentrations (0.1 mM and 1 mM); however, underestimation of the attractive force was found as the NaCl concentration increases to moderate (10 mM) and high (100 mM) levels. Discrepancy analyses and incorporated features toward a reduced surface charge density were considered based on the previous findings of the orientation of anionic benzenesulfonate moieties (Liu et al. in Angew Chem Int Ed 54(16):4851–4856, 2015. https://doi.org/10.1002/anie.201411992). Short-range steric hindrance interactions were further introduced to simulate “brush” effect stemming from nanoscale surface roughness. It is demonstrated in our work that the PSS-capped PEMs remains a stable underwater lipophobicity against high salinity, which renders it potential application in surface wetting modification and anti-fouling.

Review of Polymer Surface Modification Method

2016 ◽  
Vol 852 ◽  
pp. 626-631 ◽  
Author(s):  
Li Yuan Yu ◽  
Bo Zhu ◽  
Xun Cai ◽  
Yong Wei Wang ◽  
Rong Huan Han ◽  
...  
Keyword(s):  
Surface Modification ◽  
Polymer Surface ◽  
Processing Method ◽  
Surface Grafting ◽  
Atomic Force Microscopy Probe ◽  
Force Microscopy ◽  
Atomic Force ◽  
Irradiation Treatment ◽  
Modification Method ◽  
Polymer Surface Modification

This paper reviewed a variety of methods of polymer surface modification, which mainly includes Solution processing method, Plasma treatment，Surface grafting method，Irradiation treatment and method of Atomic force microscopy probe shock , and the specific polymer material combined with the modification method and its modification mechanism was introduced in detail.Polymer has very extensive application both in chemical fields and in daily life, but due to its poor surface hydrophilicity and wear resistance, the further application of polymer materials were limited. In order to improve its surface properties, modification are needed on the surface of the polymer. Polymer surface modification means to operate on the surface of polymer within the scope of nanometer level, and give some new properties on material surface, such as hydrophilicity, scratch resistance, under the premise of without affecting the material ontic properties.There are many methods of polymer surface modification. This paper reviewed Solution processing method, Plasma treatment，Surface grafting method，Irradiation treatment and method of Atomic force microscopy probe shock . Different methods of modification combined with specific materials are introduced as follow.

Nanoscale mapping of catalytic hotspots on Fe, N-modified HOPG by scanning electrochemical microscopy-atomic force microscopy

Nanoscale ◽  
2018 ◽  
Vol 10 (15) ◽  
pp. 6962-6970 ◽  
Author(s):  
Srikanth Kolagatla ◽  
Palaniappan Subramanian ◽  
Alex Schechter
Keyword(s):  
Atomic Force Microscopy ◽  
Surface Modification ◽  
High Resolution ◽  
Scanning Electrochemical Microscopy ◽  
Graphitic Carbon ◽  
Force Microscopy ◽  
Atomic Force ◽  
Electrochemical Microscopy

The scanning electrochemical microscopy-atomic force microscopy (SECM-AFM) technique is used to map catalytic currents post Fe and N surface modification of graphitic carbon with an ultra-high resolution of 50 nm.

scholarly journals Optimization of Anodization Parameters in Ti-30Ta Alloy

Metals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1059
Author(s):  
Patricia Capellato ◽  
Daniela Sachs ◽  
Lucas V. B. Vasconcelos ◽  
Miriam M. Melo ◽  
Gilbert Silva ◽  
...  
Keyword(s):  
Surface Modification ◽  
Biomedical Application ◽  
Anatase Phase ◽  
X Ray Diffraction ◽  
Bulk Alloy ◽  
Force Microscopy ◽  
Atomic Force ◽  
Anodization Process ◽  
Metallic Biomaterial ◽  
Cold Worked

The current metallic biomaterial still presents failures associated with the bulk alloy and the interface of material/human body. In previous studies, titanium alloy with tantalum showed the elastic modulus decrease in comparison with that of commercially pure (cp) titanium. In this study, surface modification on Ti-30Ta alloy was investigated. Titanium and tantalum were melted, homogenized, cold-worked by a rotary swaging process and solubilized. The anodization process was performed in electrolyte contained glycerol + NH4F 0.25% at 30 V using seven different durations—4 h, 5 h, 6 h, 7 h, 8 h, 9 h, and 10 h and annealed at 530 °C for 1 h. The surface topography was characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM) measurements, X-ray diffraction analysis (XRD), and contact angle. From the results, we conclude the time of anodization process influences the shape and morphology of the anodized layer. The 5 h-anodization process produced a smooth and porous surface. The 4-, 6-, 7-, 8-, 9-, and 10-h conditions showed nanotubes morphology. All surfaces are hydrophilic (<90°). Likewise, all the investigated conditions present anatase phase. So, this surface modification presents potential for biomedical application. However, more work needs to be done to better understand the influence of time on the anodization process.

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