Surface Modification of Parylene C Film and Application

2013 ◽  
Vol 750-752 ◽  
pp. 1887-1890
Author(s):  
Li Sheng Zhang ◽  
Yuan Lin Zhou ◽  
Yang Guo ◽  
Ye Yang

In this article, we report the surface modification results of Parylene C Film by solution of sodium naphthalene complex and its application. In this work, the function group and the crystal structure of the film were characterized separately with Attenuated Total Reflection Fourier transformation infrared spectroscopy (ATR-FTIR) and X-ray diffraction (XRD).The result of test shows that the bond of carbon (C) and chlorine (Cl) is damaged; The crystalline of the film reduces, and the NaCl crystal exist on the film surface. The surface energy of the film is increased from 28.64mJ/m2 to 41.48mJ/m2, and the shearing tension of modified film was reached over 212.8kPa.The generalized analysis result indicated that nucleophilic reagent destructs the C-Cl bond on the benzene ring, the chlorine (Cl) atom on the benzene ring and the sodium ion in modified reagent forms the sodium chloride which adheres to the film surface.

2011 ◽  
Vol 287-290 ◽  
pp. 2314-2317
Author(s):  
Li Sheng Zhang ◽  
Yuan Lin Zhou ◽  
Ya Hui Sun ◽  
Hong Bo Bao

In this article,we report the results obtained from a study adopting solution of sodium naphthalene complex to modify the poly(chloro-p-xylylene)(parylene C) thin film.In this work,the function group and the crystal structure of the film before and after modifying are characterized separately with Attenuated Total Reflection Fourier transformation infrared spectroscopy(ATR- FTIR)and X-ray diffraction(XRD).The result of test shows that the bond of carbon(C) and chlorine(Cl) is damaged;The crystalline of the film reduces,and the NaCl crystal exist on the film surface.The surface energy of the film is increased from 28.64mJ/m2 to 41.48mJ/m2.The generalized analysis result indicated that nucleophilic reagent destructs the C-Cl bond on the benzene ring, the chlorine(Cl) atom on the benzene ring and the sodium ion in modified reagent forms the sodium chloride which adheres to the film surface.


Materials ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3191
Author(s):  
Arun Kumar Mukhopadhyay ◽  
Avishek Roy ◽  
Gourab Bhattacharjee ◽  
Sadhan Chandra Das ◽  
Abhijit Majumdar ◽  
...  

We report the surface stoichiometry of Tix-CuyNz thin film as a function of film depth. Films are deposited by high power impulse (HiPIMS) and DC magnetron sputtering (DCMS). The composition of Ti, Cu, and N in the deposited film is investigated by X-ray photoelectron spectroscopy (XPS). At a larger depth, the relative composition of Cu and Ti in the film is increased compared to the surface. The amount of adventitious carbon which is present on the film surface strongly decreases with film depth. Deposited films also contain a significant amount of oxygen whose origin is not fully clear. Grazing incidence X-ray diffraction (GIXD) shows a Cu3N phase on the surface, while transmission electron microscopy (TEM) indicates a polycrystalline structure and the presence of a Ti3CuN phase.


2012 ◽  
Vol 472-475 ◽  
pp. 1451-1454
Author(s):  
Xue Hui Wang ◽  
Wu Tang ◽  
Ji Jun Yang

The porous Cu film was deposited on soft PVDF substrate by magnetron sputtering at different sputtering pressure. The microstructure and electrical properties of Cu films were investigated as a function of sputtering pressure by X-ray diffraction XRD and Hall effect method. The results show that the surface morphology of Cu film is porous, and the XRD revealed that there are Cu diffraction peaks with highly textured having a Cu-(220) or a mixture of Cu-(111) and Cu-(220) at sputtering pressure 0.5 Pa. The electrical properties are also severely influenced by sputtering pressure, the resistivity of the porous Cu film is much larger than that fabricated on Si substrate. Furthermore, the resistivity increases simultaneously with the increasing of Cu film surface aperture, but the resistivity of Cu film still decreases with the increasing grain size. It can be concluded that the crystal structure is still the most important factor for the porous Cu film resistivity.


2015 ◽  
Vol 1125 ◽  
pp. 60-63
Author(s):  
Chutharat Paikaew ◽  
Juthamas Inthanont ◽  
Adisak Punyanut ◽  
Ekachai Hoonnivathana ◽  
Pichet Limsuwan ◽  
...  

The purpose of this research was to investigate physical properties, configuration and color of topaz. Topazes were irradiated with electron beam linear accelerator at different dose from 40 to 180 MGy. The color of topaz was analyzed by UV-vis and it was shown that the color of topaz was becoming strong color with increased electron beam dose. Crystal structure and function group of topaz were characterized by X- ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. The results showed that the topaz has orthorhombic structure and no other crystalline. After irradiated, topaz released OH indicating higher crystallinity of topaz and this was confirmed with the results of electron spin resonance (ESR). Electron beam dose response of topaz was investigated. ESR results showed that the Al3+ ion was substituted in Si4+ site and Ti3+ impurity in Al4+ site and this result corresponds to the results of FTIR. The experiment result indicated that electron beam could be making defect on crystal structure and color enhancement of topaz.


1992 ◽  
Vol 275 ◽  
Author(s):  
M. Shinn ◽  
B. -S. Hong ◽  
S. A. Barnett

ABSTRACTEpitaxial B1-structure TiN/NbN superlattices have been grown by reactive magnetron sputtering On MgO(001). X-ray diffraction and transmission electron microscopy (TEM) diffraction spectra exhibited up to nine orders of superlattice reflections, indicating that the superlattice interfaces were relatively sharp. TEM images also showed well-defined layers. The superlattice wavelength (∧) dependence of the superconducting transition temperature (Tc), critical Current density (Jc), and electrical resistivity (ρ) have been investigated. Tc values increased from 12 K to 17 K with increasing ∧. Jc in a magnetic field perpendicular to the film surface ranged from 104 to 106 A/cm2, increasing with increasing wavelength and decreasing with increasing applied magnetic field. Jc in a field parallel to the film surface was > 10 times higher, ≈ 107 A/cm2. The resistivity exhibited different ∧ dependencies in three different A ranges.


2020 ◽  
Vol 20 (9) ◽  
pp. 5671-5675
Author(s):  
Sang Chul Jung ◽  
Min Ki Kim ◽  
Young-Kwon Park ◽  
Ho Young Jung ◽  
Wang Geun Shim ◽  
...  

The catalytic oxidation of benzene and toluene (VOCs) was carried out in order to assess the properties and catalytic activities of spent vanadium-based catalyst and that modified with copper and manganese. The properties of the prepared catalysts were characterized by the Brunauer Emmett Teller (BET) surface area method as well as X-ray diffraction (XRD), Attenuated total reflection-Fourier transform infrared (ATR-FTIR), and Scanning electron microscopy-Energy dispersive X-ray (SEM-EDX) analyses. The experimental results showed that oxalic acid treatment significantly affected the activity of the spent vanadium-based catalyst, ultimately attributing to the removal of catalyst poison such as sulfur and the even redistribution of catalyst components. Moreover, the addition of copper or manganese to the spent vanadium base catalyst treated with oxalic acid (SVO) enhanced its catalytic activity.


2020 ◽  
Vol 1010 ◽  
pp. 526-531
Author(s):  
Asanah Radhi ◽  
Abdullah Othman ◽  
Muhammad Afif Aziz ◽  
Nik Raihan Nik Yusoff

Lignocellulosic materials are generally considered hydrophilic due to the high density of hydroxyl groups. The use of lignocellulosic materials in hydrophobic systems thus require surface modification. Therefore, in this study, cellulose (MCC) and sawdust (SD) have been pretreated with ionic liquid, 1-butyl-3-methylimidazolium chloride (BMIMCl) prior to surface modification with cationic surfactant, hexadecyl trimethylammonium bromide (CTAB). The effect of BMIMCl pretreatment prior to surface modification has been investigated. Crystallinity, functional group changes, morphology and thermal stability of the sawdust and cellulose upon BMIMCl pretreatment and surface modification have been studied using x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric Analysis (TGA). XRD results showed that the structure of lignocellulosic materials became more amorphous upon pretreatment with BMIMCl. FTIR results indicated that the modification of lignocellulosic is more efficient in BMIMCl-pretreated samples. Percentage of decomposition is higher for the BMIMCl-pretreated and CTAB modified samples.


2019 ◽  
Vol 796 ◽  
pp. 80-87
Author(s):  
Akinsanya Damilare Baruwa ◽  
Esther Titilayo Akinlabi ◽  
Oluseyi Philip Oladijo ◽  
Stephen Akinwale Akinlabi ◽  
Jeff Chinn

The aim of the research is to subject the three different silanes to chemical and electrochemical investigations in other to determine the most efficient organic compound. Three types of hydrophobic silanes [Tris (Trimethylsiloxy) silyethyl] dimethylchlorosilane (Alkyl); Tridecafloro-1,1,2,2-tetrahydrooctyltrichlorosilane (FOTS) and Henicosyl-1,1,2,2-tetrahydrododecyltricholrosilane (FDDTS) are presented and investigated. The three silanes are of different composition but are deposited at the same parameters and conditions. The chemical investigation was studied through (attenuated total reflection Fourier-transform infrared (ATR-FTIR) and x-ray diffraction (XRD), while the electrochemical study was conducted through EIS using natural seawater electrolyte at room temperature. From the investigation techniques, only electrochemical impedance results show that FDDTS performed better than both Alkyl and FOTS. The chemical analysis showed the presence of hydrophobic silane on all the coated samples, and no distinction can be drawn from associated peaks.


2014 ◽  
Vol 625 ◽  
pp. 651-656 ◽  
Author(s):  
Masashi Yoshida ◽  
Zhou Tao ◽  
Noah Utsumi

In this study, aluminum alloys were subjected to nitriding at 823 K for 0–18.0 ks using alumina and magnesium powders for improving their radiation performance. After nitriding, aluminum nitride films were formed on the aluminum substrate. The thickness of the formed films varied from 1.5 to 11 μm, and the color of the film surface was dark brown or black. The thickness of the aluminum nitride film increased with an increase in the treatment time. X-ray diffraction and electron probe microanalysis results showed that the film was composed of aluminum nitride, alumina, aluminum, and magnesium. Further, the film showed good adhesion at 0 ks.


1978 ◽  
Vol 31 (3) ◽  
pp. 555 ◽  
Author(s):  
GI Feutrill ◽  
CL Raston ◽  
AH White

The crystal structure of the title compound has been determined at 295 K by single-crystal X-ray diffraction methods and refined by least- squares techniques to a residual of 0.049 for 1046 'observed' reflections. Crystals are monoclinic, P21/c, a 11.584(6), b 5.449(7), c 15.273(8) Ǻ, β 92.44(4)°, Z4. The pair of quinol hydrogen atoms are both located on the one benzene ring as the title indicates.


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