scholarly journals Preparation of Chitosan Coated Magnetic Hydroxyapatite Nanoparticles and Application for Adsorption of Reactive Blue 19 and Ni2+Ions

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Van Cuong Nguyen ◽  
Quoc Hue Pho
Keyword(s):  
Removal Efficiency ◽  
Weight Percent ◽  
Textile Dye ◽  
Gravimetric Analysis ◽  
Hydroxyapatite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Reactive Blue 19 ◽  
Adsorption Capacities ◽  
Initial Ph

An adsorbent called chitosan coated magnetic hydroxyapatite nanoparticles (CS-MHAP) was prepared with the purpose of improvement for the removal of Ni2+ions and textile dye by coprecipitation. Structure and properties of CS-MHAP were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM). Weight percent of chitosan was investigated by thermal gravimetric analysis (TGA). The prepared CS-MHAP presents a significant improvement on the removal efficiency of Ni2+ions and reactive blue 19 dye (RB19) in comparison with chitosan and magnetic hydroxyapatite nanoparticles. Moreover, the adsorption capacities were affected by several parameters such as contact time, initial concentration, adsorbent dosage, and initial pH. Interestingly, the prepared adsorbent could be easily recycled from an aqueous solution by an external magnet and reused for adsorption with high removal efficiency.

scholarly journals Synthesis of Hydroxyapatite Nanoparticles in Presence of a Linear Polysaccharide

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Humberto A. Monreal Romero ◽  
José Mora Ruacho ◽  
Carlos A. Martínez Pérez ◽  
Perla E. García Casillas
Keyword(s):  
Scanning Tunneling Microscope ◽  
Scanning Tunneling ◽  
Gravimetric Analysis ◽  
Hydroxyapatite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Peak Intensity ◽  
Bet Analysis ◽  
Ir Analysis ◽  
Natural Hydroxyapatite

Hydroxyapatite nanoparticles compounds were synthesized. Natural hydroxyapatite and a linear polysaccharide (1–3 linked   β-D galactopyranose and 1,4 linked 3,6 anhydro-α-L-galactopyranose) were used as a precursor in its formation. Our purpose was to produce nanoparticles in the presence of a linear polysaccharide with the use of a gelification method. The powder sample was evaluated by scanning tunneling microscope (STM), Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction pattern (XRD), differential thermal analysis (DTA), infrared (IR) analysis, and thermal gravimetric analysis (TGA). According to the results, it was found that these nanoparticles can successfully be synthesized using a polysaccharide in a solution. On the other hand, the XRD peak intensity corresponds to hydroxyapatite structure in the range of temperature of 810°C. The influence of the polysaccharide on the evolution of the nanoparticles has been demonstrated. This observation opens up new routes for the fabrication of nanoparticles using polysaccharides network. The synthesized nanoparticles have diameters ranging from 10 nm to 11 nm approximately. The elaboration conditions such as pH and concentration were optimized in this solution.

Effects of TETA or TEPA Loading on CO2 Adsorption Properties Using Pore-Expanded KIT-6 as Support

NANO ◽  
2018 ◽  
Vol 13 (04) ◽  
pp. 1850042 ◽  
Author(s):  
Jianwen Wei ◽  
Dejun Mei ◽  
Zhifeng Lin ◽  
Linlin Geng ◽  
Siqi Chen ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Maximum Adsorption Capacity ◽  
Gravimetric Analysis ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Structure Directing Agent ◽  
X Ray ◽  
Silica Source ◽  
Adsorption Capacities ◽  
Adsorption Desorption

Mesoporous silica pore-expanded KIT-6 was synthesized using tetraethoxysilane (TEOS) as the silica source, tri-block copolymer (P123) as a structure-directing agent and 1,3,5-trimethylbenzene (TMB) as swelling agents by a hydrothermal method. Then, pore-expanded KIT-6 (PE-KIT-6) was modified with different amounts of amines including triethylenetetramine (TETA) and tetraethylenepentamine (TEPA) by a post-synthetic impregnation method. The samples were characterized by small-angle X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N2 adsorption/desorption, elemental analysis and thermal gravimetric analysis (TGA). Experimental results revealed that the modifiers were introduced into the samples and the CO2 adsorption capacity increased first and then decreased with the increase of TETA/TEPA loadings. Under the same loadings of TETA/TEPA, the samples modified by TEPA exhibited better CO2 adsorption capacities than the samples modified by TETA because TEPA has one more amine group than TETA in the molecule. The results also indicated that the samples had good adsorption capacities at the loadings ranging from 30% to 35%. Among them, the sample modified by TEPA with the loading of 35% had the maximum adsorption capacity of 2.9[Formula: see text]mmol/g. After five cycles of adsorption/desorption, the adsorption capacity only dropped 4.59%, indicating that the adsorbent of PE-KIT-6 modified by TEPA has good cyclic stability.

Removal of a reactive dye from simulated textile wastewater by environmentally friendly oxidant calcium peroxide

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Behzat Balci ◽  
Nurevsan Aksoy ◽  
F. Elcin Erkurt ◽  
Fuat Budak ◽  
Mesut Basibuyuk ◽  
...  
Keyword(s):  
Removal Efficiency ◽  
Low Cost ◽  
Environmentally Friendly ◽  
Textile Wastewater ◽  
Textile Dye ◽  
Reactive Black 5 ◽  
X Ray Diffraction ◽  
Bending Vibration ◽  
Calcium Peroxide ◽  
X Ray

Abstract In the present study, calcium peroxide (CaO2) was used separately for potential application as an environmentally friendly and low-cost oxidant for the removal of a textile dye ‘Reactive Black 5’ (RB5) from simulated textile wastewater containing auxiliary chemicals of textile production. The specific morphology, elemental analysis, particle size distribution, specific surface area, identification of crystalline phases and surface functional groups of the synthesized CaO2 were investigated by scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), laser diffraction (LD), Brunaure–Emmett–Teller method (BET), X-ray diffraction (XRD) and Fourier transmission infrared (FTIR), respectively. X-ray Diffraction analysis confirmed the synthesized oxidant as CaO2 with the tetragonal crystalline structure. The signal corresponded to a bending vibration of O–Ca–O was detected in the fingerprint region of the FTIR spectroscopy. The effects of various independent parameters such as contact time, pH, initial RB5 concentration and CaO2 dosage on decolorization were investigated. The results of the study showed that pH, initial dye concentration and the CaO2 amounts have significant effects on removal of the RB5. The optimum pH was determined 7 for the removal of RB5 by CaO2. 2.0 g CaO2 was found to be sufficient for the removal of 300 mg/L RB5 with 96.93% removal efficiency. Also 82.8% chemical oxygen demand (COD) removal efficiency from simulated textile wastewater (STW) was obtained by 2.0 g CaO2. The results of the present study showed that the CaO2 can be used as an environmentally friendly and low-cost oxidant for effective removal of reactive textile dyes.

scholarly journals In-Situ High-Energy X-ray Diffraction Study of Austenite Decomposition During Rapid Cooling and Isothermal Holding in Two HSLA Steels

2021 ◽  
Vol 52 (5) ◽  
pp. 1812-1825
Author(s):  
Sen Lin ◽  
Ulrika Borggren ◽  
Andreas Stark ◽  
Annika Borgenstam ◽  
Wangzhong Mu ◽  
...  
Keyword(s):  
Isothermal Holding ◽  
Weight Percent ◽  
High Energy ◽  
Decomposition Kinetics ◽  
Bainitic Transformation ◽  
Austenite Decomposition ◽  
X Ray Diffraction ◽  
Rapid Cooling ◽  
X Ray

AbstractIn-situ high-energy X-ray diffraction experiments with high temporal resolution during rapid cooling (280 °C s−1) and isothermal heat treatments (at 450 °C, 500 °C, and 550 °C for 30 minutes) were performed to study austenite decomposition in two commercial high-strength low-alloy steels. The rapid phase transformations occurring in these types of steels are investigated for the first time in-situ, aiding a detailed analysis of the austenite decomposition kinetics. For the low hardenability steel with main composition Fe-0.08C-1.7Mn-0.403Si-0.303Cr in weight percent, austenite decomposition to polygonal ferrite and bainite occurs already during the initial cooling. However, for the high hardenability steel with main composition Fe-0.08C-1.79Mn-0.182Si-0.757Cr-0.094Mo in weight percent, the austenite decomposition kinetics is retarded, chiefly by the Mo addition, and therefore mainly bainitic transformation occurs during isothermal holding; the bainitic transformation rate at the isothermal holding is clearly enhanced by lowered temperature from 550 °C to 500 °C and 450 °C. During prolonged isothermal holding, carbide formation leads to decreased austenite carbon content and promotes continued bainitic ferrite formation. Moreover, at prolonged isothermal holding at higher temperatures some degenerate pearlite form.

scholarly journals Rapid four-component synthesis of dihydropyrano[2,3-c]pyrazoles using nano-eggshell/Ti(IV) as a highly compatible natural based catalyst

BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Arefeh Dehghani Tafti ◽  
Bi Bi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri ◽  
Naeimeh Salehi
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Reaction Times ◽  
Diffraction Field ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Work Up

AbstractNano-eggshell/Ti(IV) as a novel naturally based catalyst was prepared, characterized and applied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. The characterization of nano-eggshell/Ti(IV) was performed using Fourier Transform Infrared spectroscopy, X-ray Diffraction, Field Emission Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and Thermo Gravimetric Analysis. Dihydropyrano[2,3-c]pyrazoles were synthesized in the presence of nano-eggshell/Ti(IV) via a four component reaction of aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate at room temperature under solvent free conditions. The principal affairs of this procedure are mild condition, short reaction times, easy work-up, high yields, reusability of the catalyst and the absence of toxic organic solvents.

scholarly journals Ti/RuO2-IrO2-SnO2 Anode for Electrochemical Degradation of Pollutants in Pharmaceutical Wastewater: Optimization and Degradation Performances

2020 ◽  
Vol 13 (1) ◽  
pp. 126
Author(s):  
Guozhen Zhang ◽  
Xingxing Huang ◽  
Jinye Ma ◽  
Fuping Wu ◽  
Tianhong Zhou
Keyword(s):  
Removal Rate ◽  
Inorganic Compounds ◽  
Oxide Coating ◽  
X Ray Diffraction ◽  
Pharmaceutical Wastewater ◽  
High Concentration ◽  
Dimensionally Stable Anodes ◽  
X Ray ◽  
Initial Ph ◽  
Cod Removal Rate

Electrochemical oxidation technology is an effective technique to treat high-concentration wastewater, which can directly oxidize refractory pollutants into simple inorganic compounds such as H2O and CO2. In this work, two-dimensionally stable anodes, Ti/RuO2-IrO2-SnO2, have been developed in order to degrade organic pollutants from pharmaceutical wastewater. Characterization by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) showed that the oxide coating was successfully fabricated on the Ti plate surface. Electrocatalytic oxidation conditions of high concentration pharmaceutical wastewater was discussed and optimized, and the best results showed that the COD removal rate was 95.92% with the energy consumption was 58.09 kW·h/kgCOD under the electrode distance of 3 cm, current density of 8 mA/cm2, initial pH of 2, and air flow of 18 L/min.

Adsorption of the harmful hormone ethinyl estradiol inside hydrophobic cavities of CTA+ intercalated montmorillonite

2016 ◽  
Vol 74 (3) ◽  
pp. 663-671 ◽  
Author(s):  
A. E. Burgos ◽  
Tatiana A. Ribeiro-Santos ◽  
Rochel M. Lago
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
High Efficiency ◽  
Interlayer Space ◽  
Ethinyl Estradiol ◽  
Significant Loss ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrophobic Cavity ◽  
Adsorption Capacities ◽  
Derivative Thermogravimetry

Hydrophobic cavities produced by cetyltrimethylammonium cation (CTA+) exchanged and trapped in the interlayer space of montmorillonite were used to remove the harmful hormone contaminant ethinyl estradiol (EE2) from water. X-ray diffraction, thermogravimetry/derivative thermogravimetry, elemental analysis (carbon, hydrogen, nitrogen), Fourier transform infrared, scanning electron microscopy/energy dispersive spectroscopy, Brunauer–Emmett–Teller and contact angle analyses showed that the intercalation of 9, 16 and 34 wt% CTA+ in the montmorillonite resulted in the d001 expansion from 1.37 to 1.58, 2.09 and 2.18 nm, respectively. EE2 adsorption experiments showed that the original clay montmorillonite does not remove EE2 from water whereas the intercalated composites showed high efficiency with adsorption capacities of 4.3, 8.8 and 7.3 mg g−1 for M9CTA+, M16CTA+ and M34CTA+, respectively. Moreover, experiments with montmorillonite simply impregnated with cetyltrimethylammonium bromide showed that the intercalation of CTA+ to form the hydrophobic cavity is very important for the adsorption properties. Simple solvent extraction can be used to remove the adsorbed EE2 without significant loss of CTA+, which allows the recovery and reuse of the adsorbent for at least five times.

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.

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.

scholarly journals Carbonation Resistance of Surface Protective Materials Modified with Hybrid NanoSiO2

Coatings ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 269
Author(s):  
Kailun Xia ◽  
Yue Gu ◽  
Linhua Jiang ◽  
Mingzhi Guo ◽  
Lei Chen ◽  
...  
Keyword(s):  
Construction Material ◽  
Chemical Components ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Carbonation Depth ◽  
X Ray ◽  
Carbonation Resistance ◽  
Ideal Situation ◽  
Caco3 Content ◽  
Reference Samples

To date, reinforcement concrete is the main construction material worldwide. As the concentration of atmospheric CO2 is steadily increasing, carbonation of the reinforcement concrete becomes a pressing concern. In this study, novel surface protective materials (SPMs) modified with hybrid nanoSiO2 (HNS), fly ash, and slag were developed to reduce CO2 emissions and extend the service life of the reinforcement concrete. The carbonation depths were measured by phenolphthalein to reflect the carbonation resistance. X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FTIR), and thermal gravimetric analysis (TGA) were conducted to analyze the chemical components of the samples after carbonation. In addition, MIP was carried out to examine the microstructures of the samples prior to carbonation. Thermodynamic modeling was employed to calculate the changes in the phase assemblages of each blends in an ideal situation. The experimental results showed that the carbonation depth and CaCO3 content of the SPM modified with HNS decreased by 79.0% and 64.6% compared with the reference, respectively. The TGA results showed that after carbonation, the CaCO3 contents were 4.40% and 12.42% in the HNS modified samples and reference samples, respectively. MIP analysis demonstrated that the incorporation of HNS in SPM led to a 48.3% and 58.5% decrease in big pores and capillary pores, respectively. Overall, the SPMs modified with HNS in this study possessed better carbonation resistance and refined pore structures.

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