scholarly journals Study of UV Stability and Physical Properties of Jute/Soy Flour Green Nanocomposites

2018 ◽  
Vol 2 (1) ◽  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Mechanical Tests ◽  
Soy Flour ◽  
Morphological Properties ◽  
Gravimetric Analysis ◽  
Transmission Electron ◽  
Strong Interfacial Interaction ◽  
The Matrix ◽  
Ft Ir

Glutaraldehyde cross-linked jute fabric and soy flour was used to develop green nanocomposites via solution-induced intercalation method. The effect of TiO2 alone (TNP) and TiO2 in combination with nanoclay on the properties of the nanocomposites was studied. Fourier transfer infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray diffractrometry (XRD), and transmission electron microscopy (TEM) were used to examine the structural and morphological properties. They clearly revealed that both TNP and nanoclay were successfully loaded into the composite. The thermal and mechanical properties were determined using thermo gravimetric analysis (TGA), and mechanical tests, respectively. The study discloses noteworthy changes in the observed properties of the composites with inclusion of nanoparticles. Furthermore, in comparison to the unfilled composites, nanoparticles filled ones were found to exhibit much improved UV-resistance, flame retarding properties, and dimensional stability. The study revealed a strong interfacial interaction between the filler and the matrix within the prepared green nanocomposites.

Effect of Synthesis Temperature on Particles Size and Morphology of Zirconium Oxide Nanoparticle

2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Zirconium Oxide ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Crystallite Sizes ◽  
Ft Ir

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.

Biosynthesis and Characterization of Copper Nanoparticles Using a Bioflocculant Extracted from Alcaligenis faecalis HCB2

2019 ◽  
Vol 11 (11) ◽  
pp. 1064-1070 ◽  
Author(s):  
Nkosinathi G. Dlamini ◽  
Albertus K. Basson ◽  
V. S. R. Rajasekhar Pullabhotla
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Copper Nanoparticles ◽  
Average Particle Size ◽  
Thermo Gravimetric Analysis ◽  
Average Particle ◽  
Gravimetric Analysis ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir

Bioflocculant from Alcaligenis faecalis HCB2 was used in the eco-friendly synthesis of the copper nanoparticles. Nanoparticles were characterized using a scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-visible spectroscopy, thermo gravimetric analysis (TGA) and Fourier Transform Infrared Spectroscopy (FT-IR). The transmission electron microscopy images showed close to spherical shapes with an average particle size of ∼53 nm. Energy-dispersive X-ray spectroscopy analysis confirmed the presence of the Cu nanopartilces and also the other elements such as O, C, P, Ca, Cl, Na, K, Mg, and S originated from the bioflocculant. FT-IR results showed the presence of the –OH and –NH2 groups, aliphatic bonds, amide and Cu–O bonds. Powder X-ray diffraction peaks confirmed the presence of (111) and (220) planes of fcc structure at 2 of 33° and 47° respectively with no other impurity peaks.

scholarly journals Study on the Photodegradation Stability of Poly(butylene Succinate-co-butylene Adipate)/TiO2 Nanocomposites

2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Lihai Cai ◽  
Zhiguo Qi ◽  
Jun Xu ◽  
Baohua Guo ◽  
Zhongyao Huang
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Chain Scission ◽  
High Energy ◽  
Mechanical Tests ◽  
Scanning Calorimetry ◽  
Butylene Succinate ◽  
Transmission Electron ◽  
The Matrix ◽  
Ft Ir

A poly(butylene succinate-co-butylene adipate)/TiO2 (PBSA/TiO2) nanocomposite was prepared by a melt-blending process. The effect of TiO2 nanoparticles on the photodegradation behaviors of the nanocomposite was investigated by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FT-IR), field-emission scanning electron microscopy (FE-SEM), rheological measurements, and mechanical tests. TEM images of the PBSA/TiO2 revealed that the TiO2 nanoparticles were well dispersed in the matrix without obvious aggregation. The FT-IR results indicated that the TiO2 nanoparticles can block high-energy ultraviolet (UV) light and reduce the degradation of the PBSA matrix. The viscosity analysis results indicated that the TiO2 nanoparticles inhibited the chain scission of PBSA matrix under irradiation. In addition, the surface of the PBSA/TiO2 films and their mechanical properties change less than that of untreated PBSA films during the photoaging process. The obtained results imply that the TiO2 nanoparticles can be considered as an efficient photodegradation-resistant additive to PBSA for reducing photodegradation.

scholarly journals Influence of different functionalization methods of multi-walled carbon nanotubes on the properties of poly(L-lactide) based nanocomposites

2019 ◽  
Vol 73 (3) ◽  
pp. 183-196 ◽  
Author(s):  
Nevena Vukic ◽  
Ivan Ristic ◽  
Milena Marinovic-Cincovic ◽  
Radmila Radicevic ◽  
Branka Pilic ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Multi Walled Carbon Nanotubes ◽  
Ft Ir ◽  
Walled Carbon Nanotubes ◽  
Functionalized Mwcnts

This paper presents influence of the type of carbon nanotube functionalization on properties of poly(L-lactide) (PLLA) based nanocomposite materials. For this purpose surface modifications of multi-walled carbon nanotubes (MWCNTs) were performed by chemical and irradiation techniques, while thermo gravimetric analysis, UV-Visible and Fourier-transform infrared (FT-IR) spectroscopies confirmed successful covalent functionalization. Series of PLLA bionanocom-posites with different contents of functionalized MWCNTs (0.7; 1.6; 2.1 wt%), were synthesized via ring-opening solution polymerisation of L-lactide. FT-IR analysis confirmed that grafting of L-lactide, under controlled condition, is possible to perform starting from the surface of functionalized MWCNTs. From differential scanning calorimetry results it was concluded that even low contents of chemically and irradiation functionalized MWCNTs had a significant effect on thermal properties of the prepared nanocomposites, raising the values of melting and glass transition temperatures. Thermogravimetric analysis (TGA) has shown that the degradation onset temperature for composites with chemically functionalized MWCNTs, was much higher than that for the neat poly(L-lactide) sample and composites with irradiation functionalized MWCNTs. Morphology studies by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicated that poly(L-lactide) covered surfaces and separated functionalized MWCNTs. Good dispersion of carbon nanotubes in polymer matrix enabled conductivity of synthesized materials, as determined by conductivity tests.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.

scholarly journals An Efficient and Novel Ammonia Sensor Based on Polypyrrole/Tin Oxide/MWCNT Nanocomposite

2020 ◽  
Vol 32 (6) ◽  
pp. 1505-1510
Author(s):  
Ahmad Husain ◽  
Mohd Urooj Shariq ◽  
Anees Ahmad
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Charge Carriers ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Ammonia Sensing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

In present study, the synthesis and characterization of a novel polypyrrole (PPy)/tin oxide (SnO2)/MWCNT nanocomposite along with pristine polypyrrole is reported. These materials have been studied for their structural and morphological properties by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. PPy/SnO2/MWCNT nanocomposite has been converted into a pellet-shaped sensor, and its ammonia sensing studies were carried out by calculating the variation in the DC electrical conductivity at different concentration of ammonia ranging from 10 to 1500 ppm. The sensing response of the sensor was determined at 1500, 1000, 500, 200, 100 and 10 ppm and found to be 70.4, 66.1, 62.2, 55.4, 50.8 and 39.7%, respectively The sensor showed a complete reversibility at lower concentrations along with excellent selectivity and stability. Finally, a sensing mechanism was also proposed involving polarons (charge carriers) of polypyrrole and lone pairs of ammonia molecules

Preparation and characterization emulsion of PANI-TiO2 nanocomposite and its application as anticorrosive coating

2015 ◽  
Vol 35 (6) ◽  
pp. 597-603 ◽  
Author(s):  
Mohsen Khademian ◽  
Hossein Eisazadeh
Keyword(s):  
Electron Microscopy ◽  
Colloidal Particles ◽  
Aqueous Media ◽  
Corrosion Current ◽  
Ammonium Persulfate ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
The Matrix ◽  
Definition Of

Abstract Emulsion nanoparticles of polyaniline (PANI) were synthesized in the aqueous media by using hydroxylpropylcellulose (HPC) as a stabilizer and ammonium persulfate as an oxidant in the presence of TiO2 with nanometer size. New poly(vinyl acetate) (PVAc) coating over carbon steel was prepared by addition of emulsion nanoparticles in different concentrations (1%, 2% and 1.5%) in PVAc as the major matrix. The Tafel plot records were used for the definition of potential and corrosion current (Icorr). Nanoparticles were characterized and compared by X-ray diffraction (XRD), thermal gravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). By adding TiO2, the thermal stability of the nanocomposite increased. A small size of colloidal particles prevented the precipitation of conducting polymer particles and led to better dispersion of nanocomposites in the matrix of the PVAc binder; therefore, the paint was homogeneous and anticorrosion properties of the coating increased. According to the results, 1.5% of PANI-TiO2 nanocomposite in PVAc has a much lower Icorr in NaCl aqueous solution and 2% of PANI-TiO2 nanocomposite in PVAc has the best corrosion protection in HCl.

scholarly journals Synthesis of zirconia-based solid acid nanoparticles for fuel cell application

2016 ◽  
Vol 27 (2) ◽  
pp. 60 ◽  
Author(s):  
Rudzani A Sigwadi ◽  
Sipho E Mavundla ◽  
Nosipho Moloto ◽  
Touhami Mokrani
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Acid Sites ◽  
Precipitation Method ◽  
Zro2 Nanoparticles ◽  
Gravimetric Analysis ◽  
Ambient Temperatures ◽  
Fuel Cell Application ◽  
Transmission Electron ◽  
Zirconia Nanoparticles

Zirconia nanoparticles were prepared by the precipitation and ageing methods. The precipitation method was performed by adding ammonium solution to the aqueous solution of zirconium chloride at room temperature. The ageing method was performed by leaving the precipitate formed in the mother liquor in the glass beaker for 48 hours at ambient temperatures. The nanoparticles from both methods were further sulphated and phosphated to increase their acid sites. The materials prepared were characterised by X-ray diffraction (XRD), thermo-gravimetric analysis (TGA), Brunauer-EmmettTeller (BET), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) methods. The XRD results showed that the nanoparticles prepared by the precipitation method contained mixed phases of tetragonal and monoclinic phases, whereas the nanoparticles prepared by ageing method had only tetragonal phase. The TEM results showed that phosphated and sulphated zirconia nanoparticles obtained from the ageing method had a smaller particle size (10–12 nm) than the nanoparticles of approximately 25–30 nm prepared by precipitation only. The BET results showed that the ZrO2 nanoparticles surface area increased from 32 to 72 m2/g when aged.

scholarly journals Structural, Thermal, Morphological, Adsorption and Catalytic Properties of Poly(BPDAH-co-ODA/PPDA)-Ag/V2O5 Nanocomposites

2019 ◽  
Vol 15 (1) ◽  
pp. 155-174
Author(s):  
Govindharajan Sribala ◽  
Balakrishnan Meenarathi ◽  
Ramasamy Anbarasan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
1H Nmr ◽  
Catalytic Reduction ◽  
Aromatic Proton ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Ft Ir ◽  
Scanning Electron

Thermally stable polyimides (PIs) were prepared by condensation technique at 160 ºC for 5 hours in N-methylpyrrolidone (NMP) medium under N2 atmosphere both in the presence and absence of metal (Ag) and metaloxide (MO) (V2O5) nanoparticles (NPs). The synthesized polymers are characterized by Fourier Transform Infra Red (FT-IR) spectroscopy, 1H Nuclear Magnetic Resonance (1H NMR) spectroscopy, Differential Scanning Calorimetry (DSC), Thermal Gravimetric Analysis (TGA), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Field Emission Scanning Electron Microscopy with Energy Dispersive X-Ray (FE-SEM and EDX). The FT-IR spectrum showed a peak at 1786 cm-1 corresponding to the C=O stretching of dianhydride. The aromatic proton signals appeared between 6.7 and 7.5 ppm in the 1H-NMR spectrum of the resultant PIs. The oxydianiline (ODA) based PI with Ag NP loaded system exhibited the highest Tg value. The apparent rate constant values for the adsorption and catalytic reduction of p-nitrophenol (PNP), Cr6+ and rhodamine 6G (R6G) dye were determined with the help of UV-visible spectrophotometer. Among the catalysts, the system loaded with V2O5 NP has higher kapp values. The experimental results are critically analyzed and compared with the previously available literature values. Copyright © 2020 BCREC Group. All rights reserved 

Preparation and Characterization of Poly(Dimethyl Diallyl Ammonium Chloride)/Modified SiO2 Spherical Brushes

2015 ◽  
Vol 731 ◽  
pp. 569-572 ◽  
Author(s):  
Na Su ◽  
Zheng Min Cao
Keyword(s):  
Electron Microscopy ◽  
Ammonium Chloride ◽  
Thermo Gravimetric Analysis ◽  
Gel Permeation Chromatography ◽  
Gravimetric Analysis ◽  
Polyelectrolyte Brushes ◽  
Transmission Electron ◽  
Spherical Polyelectrolyte Brushes ◽  
Trimethoxy Silane

Novel cationic spherical polyelectrolyte brushes (CSPB) consisting of γ-methacryloxypropyl trimethoxy-silane (KH-570) modified SiO2cores and poly (Dimethyl diallyl ammonium chloride) (PDMDAAC) brushes were prepared by conventional free radical polymerization. The resulting CSPB were characterized by Fourier transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM), Scanning electron microscopy (SEM), and Thermo-gravimetric analysis (TGA). After cleaving the polyelectrolyte chains from the anchoring surface, the molecular weight of brushes was 1.824×103gmol-1from Gel Permeation Chromatography (GPC) measurements.

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