scholarly journals Improved Adhesion of Nonfluorinated ZnO Nanotriangle Superhydrophobic Layer on Glass Surface by Spray-Coating Method

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Norfatehah Basiron ◽  
Srimala Sreekantan ◽  
Khairul Arifah Saharudin ◽  
Zainal Arifin Ahmad ◽  
Vignesh Kumaravel

In this present work, a superhydrophobic glass surface comprising zinc oxide nanotriangles (ZnO-nt) and nontoxic silylating agent was developed via a cost-effective spray-coating technology. ZnO-nt was synthesized by a hydrothermal method. Poly(dimethylsiloxane) (PDMS) and dimethyldiethoxysilane (DMDEOS) were used as nontoxic (nonfluoro) silylating agents. The morphology and crystallinity of ZnO-nt were studied using X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques. ZnO-nt with polymeric silane (PDMS) exhibited maximum wettability as compared to nonpolymeric silane (DMDEOS). The water contact angle (WCA), sliding angle (SA), and surface roughness of ZnO-nt/PDMS-coated glass substrate under UV treatment were 165 ± 1°, 3 ± 1°, and 791 nm, respectively. The WCA of ZnO-nt/PDMS was higher (165°) than that of commercial ZnO/PDMS (ZnO-C/PDMS). ZnO-nt/PDMS was strongly attached to the glass substrate with good stability and adhesion. The reasons for improved hydrophobicity, adhesion, and mechanism of hierarchical microstructure formation on the glass substrate were explained in detail. PDMS was attached to the glass substrate via hydrogen bonds from solvated zinc acetate.

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1506
Author(s):  
Xiang Liu ◽  
Kai Chen ◽  
Dekun Zhang ◽  
Zhiguang Guo

Herein, a low cost, durable, and stable conductive superhydrophobic composite coating (CSC coating) was fabricated on a Q345 steel surface by simple double-layer spray coating. The water contact angle (WCA) of the CSC coating was 160° and the sliding angle (SA) was 3°. In addition to its excellent conductivity (3.10 × 103 Ω), the fabricated composite coating had good durability and wear resistance. After 10 sand-washing cycles, the CSC coating surface still exhibited stable superhydrophobicity (149° WCA, 9.5° SA). At 200 g pressure, the surface of the optimized CSC coating still maintained fine superhydrophobicity (150° WCA, 9.2° SA) and conductivity (1.86 × 104 Ω) after 10 abrasion cycles. In addition, it also exhibited fine adhesion (0.307 MPa) between the composite coating and the substrate. This functional superhydrophobic surface can be applied in specialty fields with harsh conditions such as coal mining and petrochemical activities. This new coating may also expand the application fields of superhydrophobic surfaces and have broad practical application prospects.


2011 ◽  
Vol 356-360 ◽  
pp. 423-429
Author(s):  
Meng Ye ◽  
Jin Huang ◽  
Rui Chen ◽  
Qi Zhuang He

An elevated arsenic (As) content in groundwater imposes a great threat to people worldwide. Thus, developing new and cost-effective methods to remove As from groundwater and drinking water becomes a priority. Using Zero-Valent iron (ZVI) to remove As from water is a proven technology. In this study, ZVI modified SBA-15 mesoporous silicamolecular sieves (ZVI-SBA-15), was prepared, characterized, and used for removing arsenic from water. Wet impregnation, drying, and calcination steps led to iron inclusion within the mesopores. Iron oxide was reduced to ZVI by NaBH4, and the ZVI modified SBA-15 was obtained. Fourier-transform infrared spectroscopy confirmed the preparation process of the nitrate to oxide forms. The structure of the materials was confirmed by Powder X-ray diffraction. Its data indicated that the structure of ZVI-SBA-15 retained the host SBA-15 structure. Brunauer-Emmett-Teller analysis revealed a decrease in surface area and pore size, indicating ZVI-SBA-15 coating on the inner surfaces. Transmission electron micrographs also confirmed that modified SBA-15 retained the structure of the parent SBA-15 silica.It has a high uptake capability(more than 90 pecent) make it potentially attractive absorbent for the removal of arsenic from water.


2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
Dhiraj A. Jamdade ◽  
Dishantsingh Rajpali ◽  
Komal A. Joshi ◽  
Rohini Kitture ◽  
Anuja S. Kulkarni ◽  
...  

Rapid, eco-friendly, and cost-effective one-pot synthesis of copper nanoparticles is reported here using medicinal plants like Gnidia glauca and Plumbago zeylanica. Aqueous extracts of flower, leaf, and stem of G. glauca and leaves of P. zeylanica were prepared which could effectively reduce Cu2+ ions to CuNPs within 5 h at 100°C which were further characterized using UV-visible spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, energy dispersive spectroscopy, dynamic light scattering, X-ray diffraction, and Fourier-transform infrared spectroscopy. Further, the CuNPs were checked for antidiabetic activity using porcine pancreatic α-amylase and α-glucosidase inhibition followed by evaluation of mechanism using circular dichroism spectroscopy. CuNPs were found to be predominantly spherical in nature with a diameter ranging from 1 to 5 nm. The phenolics and flavonoids in the extracts might play a critical role in the synthesis and stabilization process. Significant change in the peak at ∼1095 cm−1 corresponding to C-O-C bond in ether was observed. CuNPs could inhibit porcine pancreatic α-amylase up to 30% to 50%, while they exhibited a more significant inhibition of α-glucosidase from 70% to 88%. The mechanism of enzyme inhibition was attributed due to the conformational change owing to drastic alteration of secondary structure by CuNPs. This is the first study of its kind that provides a strong scientific rationale that phytogenic CuNPs synthesized using G. glauca and P. zeylanica can be considered to develop candidate antidiabetic nanomedicine.


Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1803 ◽  
Author(s):  
Kanthasamy Raagulan ◽  
Ramanaskanda Braveenth ◽  
Hee Jang ◽  
Yun Seon Lee ◽  
Cheol-Min Yang ◽  
...  

MXene and graphene based thin, flexible and low-density composite were prepared by cost effective spray coating and solvent casting method. The fabricated composite was characterized using Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray (EDX). The prepared composites showed hydrophobic nature with higher contact angle of 126°, −43 mN·m−1 wetting energy, −116 mN·m−1 spreading Coefficient and 30 mN·m−1 lowest work of adhesion. The composites displayed excellent conductivity of 13.68 S·cm−1 with 3.1 Ω·sq−1 lowest sheet resistance. All the composites showed an outstanding thermal stability and constrain highest weight lost until 400 °C. The MXene-graphene foam exhibited excellent EMI shielding of 53.8 dB (99.999%) with reflection of 13.10 dB and absorption of 43.38 dB in 8–12.4 GHz. The single coated carbon fabric displayed outstanding absolute shielding effectiveness of 35,369.82 dB·cm2·g−1. The above results lead perspective applications such as aeronautics, radars, air travels, mobile phones, handy electronics and military applications.


Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2585 ◽  
Author(s):  
Ravi Mani Tripathi ◽  
Dohee Ahn ◽  
Yeong Mok Kim ◽  
Sang J. Chung

Recent developments in the area of nanotechnology have focused on the development of nanomaterials with catalytic activities. The enzyme mimics, nanozymes, work efficiently in extreme pH and temperature conditions, and exhibit resistance to protease digestion, in contrast to enzymes. We developed an environment-friendly, cost-effective, and facile biological method for the synthesis of ZnO-Pd nanosheets. This is the first biosynthesis of ZnO-Pd nanosheets. The synthesized nanosheets were characterized by UV–visible spectroscopy, X-ray diffraction (XRD), scanning electron microscopy, transmission electron microscopy, and energy-dispersive X-ray. The d-spacing (inter-atomic spacing) of the palladium nanoparticles in the ZnO sheets was found to be 0.22 nm, which corresponds to the (111) plane. The XRD pattern revealed that the 2θ values of 21.8°, 33.3°, 47.7°, and 56.2° corresponded with the crystal planes of (100), (002), (112), and (201), respectively. The nanosheets were validated to possess peroxidase mimetic activity, which oxidized the 3,3′,5,5′-tetramethylbenzidine (TMB) substrate in the presence of H2O2. After 20 min of incubation time, the colorless TMB substrate oxidized into a dark-blue-colored one and a strong peak was observed at 650 nm. The initial velocities of Pd-ZnO-catalyzed TMB oxidation by H2O2 were analyzed by Michaelis–Menten and Lineweaver–Burk plots, resulting in 64 × 10−6 M, 8.72 × 10−9 Msec−1, and 8.72 × 10−4 sec−1 of KM, Vmax, and kcat, respectively.


2009 ◽  
Vol 79-82 ◽  
pp. 581-584 ◽  
Author(s):  
Li Ang Song ◽  
Li Xin Cao ◽  
Ge Su ◽  
Wei Liu ◽  
Hui Liu ◽  
...  

Titanium based nanotubes (8-12nm outer diameter and 4-6nm inner diameter) were successfully fabricated by a simple and cost-effective hydrothermal method. The nanotube-like amorphous phases TNT(Na) and TNT(H) were obtained with different post treatment. The samples were characterized by means of high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), selected area electron diffraction (SAED), energy dispersive X-ray spectrum (EDS) and UV-Vis diffuse reflectance spectroscopy (DRS). The photocatalytic activities of the nanotubes were evaluated using photo-oxidation of methyl orange.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
B. Sadeghi ◽  
R. Sarraf-Mamoory ◽  
H. R. Shahverdi

LiMn2O4spinel cathode materials have been successfully synthesized by solid-state reaction. Surface of these particles was modified by nanostructured LiFePO4via sol gel dip coating method. Synthesized products were characterized by thermally analyzed thermogravimetric and differential thermal analysis (TG/DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX). The results of electrochemical tests showed that the charge/discharge capacities improved and charge retention of battery enhanced. This improved electrochemical performance is caused by LiFePO4phosphate layer on surfaces of LiMn2O4cathode particles.


NANO ◽  
2017 ◽  
Vol 12 (10) ◽  
pp. 1750120 ◽  
Author(s):  
M. Gurubhaskar ◽  
Narayana Thota ◽  
M. Raghavender ◽  
Y. P. Venkata Subbaiah ◽  
G. Hema Chandra ◽  
...  

In this paper, we employed a simple and cost-effective thioglycolic acid (TGA) free hydrothermal method, based on thiourea hydrolysis of stannous chloride dihydrate [SnCl2.2H2O] at 160[Formula: see text]C–190[Formula: see text]C for 6[Formula: see text]h, for the synthesis of SnS nanoparticles. The effect of hydrothermal autoclave reaction temperature on various properties of SnS nanoparticles have been examined at length using X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy attached with EDAX (FE-SEM), transmission electron microscopy (TEM) and ultraviolet-visible (UV-Vis) spectroscopy. The results suggest that the crystallization of orthorhombic SnS nanoparticles, with size varying from 3[Formula: see text]nm to 5[Formula: see text]nm, formed at R[Formula: see text]C. Further, the formation of SnS phase was confirmed by an IR Sn-S characteristic bands around 2350[Formula: see text]cm[Formula: see text], 1041[Formula: see text]cm[Formula: see text] and 570[Formula: see text]cm[Formula: see text], and four distinguished Raman peaks at 95[Formula: see text]cm[Formula: see text], 160[Formula: see text]cm[Formula: see text], 189[Formula: see text]cm[Formula: see text] and 220[Formula: see text]cm[Formula: see text]. The mechanism for the formation of SnS nanoparticles have been proposed and discussed. The SnS nanoparticles have exhibited reaction temperature dependent morphological features like nanoflowers, nanoflakes, spherical nanoparticles and nanogranules. The absorbance studies indicated both strong direct and weak indirect allowed transitions for SnS nanoparticles and the associated band gaps were found to be 1.5[Formula: see text]eV and 1.19[Formula: see text]eV, respectively. The dual band gap combination of SnS would favor strong direct absorption of carriers and improved minority carrier life time due to indirect nature, which means the grown particles are suitable for ideal absorber material for solar cell applications.


2013 ◽  
Vol 16 (1) ◽  
pp. 92-100
Author(s):  
Chien Mau Dang ◽  
Dam Duy Le ◽  
Tam Thi Thanh Nguyen ◽  
Dung Thi My Dang

In this study, we have successfully synthesized Fe3+ doped SiO2/TiO2 thin films on glass substrates using the sol-gel dip-coating method. After synthesizing, the samples were annealed at 5000C in the air for 1 hour. The characteristics and optical properties of Fe3+ doped SiO2/TiO2 films were then investigated by X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-vis) and Fourier transform infrared spectroscopy (FT-IR). An antifogging ability of the glass substrates coated with the fabricated film is investigated and explained by a water contact angle under visible-light. The analyzed results also show that the crystalline phase of TiO2 thin films comprised only the anatase TiO2, but the crystalline size decreased from 8.8 to 5.9 nm. We also observed that the absorption edge of Fe3+- doped SiO2/TiO2 thin films shifted towards longer wavelengths (i.e. red shifted) from 371.7nm to 409.2 nm when the Fe3+-doped concentration increased from 0 to 1 % mol.


MRS Advances ◽  
2018 ◽  
Vol 3 (14) ◽  
pp. 733-739 ◽  
Author(s):  
Seyma Dadı ◽  
Yemliha Altıntas ◽  
Emre Beskazak ◽  
Evren Mutlugun

ABSTRACTWe propose and demonstrate the photoluminescence enhancement of CsPbBr3 perovskite quantum dot films in the presence of Au nanoparticles. Embedded into a polymer matrix, Au nanoparticle- quantum dot film assemble prepared by an easy spin coating method enabled the photoluminescence enhancement of perovskite quantum dot films up to 78%. The properties of the synthesized perovskite QDs and gold nanoparticles have been analysed using high resolution transmission electron microscopy, X-ray diffraction, energy dispersive X- ray spectroscopy, UV-Vis absorption spectrophotometer, steady state and time-resolved photoluminescence spectrometer.


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