scholarly journals Research on the Adsorption Effects of Biomass by Microstructural Characterization and Intelligent Numerical Computation Method

2021 ◽  
Vol 2083 (3) ◽  
pp. 032073
Author(s):  
Yongli Zhang ◽  
Ruiting Li
Keyword(s):  
Ph Value ◽  
Orange Peel ◽  
Microstructural Characterization ◽  
Computation Method ◽  
Experimental Conditions ◽  
Adsorption Effect ◽  
Sodium Sulfide Solution ◽  
Simulated Wastewater ◽  
Sulfur Containing ◽  
Sulfide Solution

Abstract In this paper, sodium sulfide solution as a simulation of sulfur-containing wastewater, using orange peel as adsorbent, through the change of the absorbance of simulated wastewater to analyze the orange peel adsorbent on the treatment effect of simulated wastewater, to explore its optimal experimental conditions. The experimental results show that the adsorbent has a certain adsorption effect on the sulfur compounds in the sulfur-containing wastewater. With the change of the pH value of the adsorption environment, the adsorption rate has changed. The addition of different chemical modifiers in the water will affect the adsorption and effect of orange peel.

Insights into the mechanism of methylene blue removed by novel and classic biochars

2019 ◽  
Vol 79 (8) ◽  
pp. 1561-1570
Author(s):  
Wei Chen ◽  
Fengting Chen ◽  
Bin Ji ◽  
Lin Zhu ◽  
Hongjiao Song
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Ph Value ◽  
Low Cost ◽  
Underlying Mechanism ◽  
Maximum Adsorption Capacity ◽  
Experimental Conditions ◽  
Average Pore ◽  
Adsorption Effect ◽  
Magnolia Grandiflora

Abstract The adsorption behavior and the underlying mechanism of methylene blue (MB) sorption on biochars prepared from different feedstocks at 500 °C were evaluated. The biochar feedstocks included Magnolia grandiflora Linn. leaves biochar (MBC), pomelo (Citrus grandis) peel biochar (PBC) and badam shell biochar (BBC). The results of characterizing and analyzing the samples showed that different biochars had different effects on the adsorption of MB. It could be found that MBC had the best adsorption effect on MB due to its largest average pore diameter of 5.55 nm determined by Brunauer-Emmett-Teller analysis. Under the optimal conditions, the maximum adsorption capacities of BBC, PBC and MBC were 29.7, 85.15 and 99.3 mg/g, respectively. The results showed that the amount of adsorption was affected by the pH value. The maximum adsorption capacity of MBC was 46.99 mg/g when it was at pH of 3, whereas for the same experimental conditions the maximum adsorption capacity of BBC and PBC was 25.29 mg/g at pH of 11 and 36.08 mg/g at pH of 7, respectively. Therefore, MBC was found to be a most efficient low-cost adsorbentl for dye wastewater treatment compared with BBC and PBC, and it had the best removal effect under acidic conditions.

Evaluation of the Parameters of Orange Peel for the Adsorption of Furadan

2013 ◽  
Vol 864-867 ◽  
pp. 408-412
Author(s):  
Guang Fu Xu ◽  
Yi Yun Liu ◽  
Rui Xin Guo
Keyword(s):  
Ionic Strength ◽  
Ph Value ◽  
Low Cost ◽  
Orange Peel ◽  
Experimental Conditions ◽  
Second Stage ◽  
Initial Ph ◽  
Two Stages ◽  
Low Ionic Strength ◽  
Adsorbent Dose

In this study, orange peel was utilized as low-cost adsorbent to remove furadan from aqueous solution by adsorption. All the experiments were conducted at 30 °C to investigate the effects adsorbent dose, pH value and ionic strength on furadan adsorption and the optimal experimental conditions were ascertained. The percentage removal (%) increased with an increase in the initial adsorbent dose, whereas the value of qe (mg.g-1) decreased with an increase in the initial adsorbent dose .The curve of qe and removal percentage can be divided into two stages (first stage: adsorbent dose between 0.05 and 0.20 g; second stage: adsorbent dose between 0.25 and 0.35 g). The value of qe (mg.g-1) for OP increased as the pH increase, and reached the maximum at pH 7.81, then decreased as the pH continue increasing. The initial pH value of furadan solution should be controlled between 7.50 and 8.00. In addition, the value of qe decreased sharp as the initial Na+ concentration was increased from 0 to 2.5 ×10-3 mol.L-1, then, the value of qe was not significantly altered beyond the initial Na+ concentration 2.5×10-3 mol.L-1. Therefore in order to enhance adsorption efficiency of furadan by OP, the subsequent experiments were carried out in the low ionic strength of furadan solution.

scholarly journals Ultrasound-Enhanced Catalytic Ozonation Oxidation of Ammonia in Aqueous Solution

2019 ◽  
Vol 16 (12) ◽  
pp. 2139 ◽  
Author(s):  
Chen Liu ◽  
Yunnen Chen ◽  
Caiqing He ◽  
Ruoyu Yin ◽  
Jun Liu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Conversion Rate ◽  
Ammonia Oxidation ◽  
Ph Value ◽  
Ultrasonic Power ◽  
Operational Parameters ◽  
Experimental Conditions ◽  
Aquatic Life ◽  
Adsorption Effect ◽  
Ammonia Conversion

Excessive ammonia is a common pollutant in the wastewater, which can cause eutrophication, poison aquatic life, reduce water quality and even threaten human health. Ammonia in aqueous solution was converted using various systems, i.e., ozonation (O3), ultrasound (US), catalyst (SrO-Al2O3), ultrasonic ozonation (US/O3), ultrasound-enhanced SrO-Al2O3 (SrO-Al2O3/US), SrO-Al2O3 ozonation (SrO-Al2O3/O3) and ultrasound-enhanced SrO-Al2O3 ozonation (SrO-Al2O3/US/O3) under the same experimental conditions. The results indicated that the combined SrO-Al2O3/US/O3 process achieved the highest NH4+ conversion rate due to the synergistic effect between US, SrO-Al2O3 and O3. Additionally, the effect of different operational parameters on ammonia oxidation in SrO-Al2O3/O3 and SrO-Al2O3/US/O3 systems was evaluated. It was found that the ammonia conversion increased with the increase of pH value in both systems. The NH3(aq) is oxidized by both O3 and ·OH at high pH, whereas the NH4+ oxidation is only carried out through ·OH at low pH. Compared with the SrO-Al2O3/O3 system, the ammonia conversion was significantly increased, the reaction time was shortened, and the consumption of catalyst dosage and ozone were reduced in the SrO-Al2O3/US/O3 system. Moreover, reasonable control of ultrasonic power and duty cycle can further improve the ammonia conversion rate. Under the optimal conditions, the ammonia conversion and gaseous nitrogen yield reached 83.2% and 51.8%, respectively. The presence of tert-butanol, CO32−, HCO3−, and SO42− inhibited the ammonia oxidation in the SrO-Al2O3/US/O3 system. During ammonia conversion, SrO-Al2O3 catalyst not only has a certain adsorption effect on NH4+ but accelerates the O3 decomposition to ·OH.

Molecularly Imprinted Sensor for Ascorbic Acid Based on Gold Nanoparticles and Multiwalled Carbon Nanotubes

2020 ◽  
Vol 16 (7) ◽  
pp. 905-913
Author(s):  
Youyuan Peng ◽  
Qingshan Miao
Keyword(s):  
Carbon Nanotubes ◽  
Gold Nanoparticles ◽  
Ascorbic Acid ◽  
Multiwalled Carbon Nanotubes ◽  
Ph Value ◽  
Biological Fluids ◽  
Water Soluble ◽  
Multiwalled Carbon ◽  
Experimental Conditions ◽  
Molecularly Imprinted

Background: L-Ascorbic acid (AA) is a kind of water soluble vitamin, which is mainly present in fruits, vegetables and biological fluids. As a low cost antioxidant and effective scavenger of free radicals, AA may help to prevent diseases such as cancer and Parkinson’s disease. Owing to its role in the biological metabolism, AA has also been utilized for the therapy of mental illness, common cold and for improving the immunity. Therefore, it is very necessary and urgent to develop a simple, rapid and selective strategy for the detection of AA in various samples. Methods: The molecularly imprinted poly(o-phenylenediamine) (PoPD) film was prepared for the analysis of L-ascorbic acid (AA) on gold nanoparticles (AuNPs) - multiwalled carbon nanotubes (MWCNTs) modified glass carbon electrode (GCE) by electropolymerization of o-phenylenediamine (oPD) and AA. Experimental parameters including pH value of running buffer and scan rates were optimized. Scanning electron microscope (SEM), fourier-transform infrared (FTIR) spectra, cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were utilized for the characterization of the imprinted polymer film. Results: Under the selected experimental conditions, the DPV peak currents of AA exhibit two distinct linear responses ranging from 0.01 to 2 μmol L-1 and 2 to 100 μmol L-1 towards the concentrations of AA, and the detection limit was 2 nmol L-1 (S/N=3). Conclusion: The proposed electrochemical sensor possesses excellent selectivity for AA, along with good reproducibility and stability. The results obtained from the analysis of AA in real samples demonstrated the applicability of the proposed sensor to practical analysis.

scholarly journals Zeolite NaP1 Functionalization for the Sorption of Metal Complexes with Biodegradable N-(1,2-dicarboxyethyl)-D,L-aspartic Acid

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2518
Author(s):  
Dorota Kołodyńska ◽  
Yongming Ju ◽  
Małgorzata Franus ◽  
Wojciech Franus
Keyword(s):  
Experimental Data ◽  
Aspartic Acid ◽  
Ph Value ◽  
Complexing Agents ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Modified Zeolite ◽  
X Ray ◽  
Slow Release Fertilizers ◽  
Pseudo Second Order

The possibility of application of chitosan-modified zeolite as sorbent for Cu(II), Zn(II), Mn(II), and Fe(III) ions and their mixtures in the presence of N-(1,2-dicarboxyethyl)-D,L-aspartic acid, IDHA) under different experimental conditions were investigated. Chitosan-modified zeolite belongs to the group of biodegradable complexing agents used in fertilizer production. NaP1CS as a carrier forms a barrier to the spontaneous release of the fertilizer into soil. The obtained materials were characterized by Fourier transform infrared spectroscopy (FTIR); surface area determination (ASAP); scanning electron microscopy (SEM-EDS); X-ray fluorescence (XRF); X-ray diffraction (XRD); and carbon, hydrogen, and nitrogen (CHN), as well as thermogravimetric (TGA) methods. The concentrations of Cu(II), Zn(II), Mn(II), and Fe(III) complexes with IDHA varied from 5–20 mg/dm3 for Cu(II), 10–40 mg/dm3 for Fe(III), 20–80 mg/dm3 for Mn(II), and 10–40 mg/dm3 for Zn(II), respectively; pH value (3–6), time (1–120 min), and temperature (293–333 K) on the sorption efficiency were tested. The Langmuir, Freundlich, Dubinin–Radushkevich, and Temkin adsorption models were applied to describe experimental data. The pH 5 proved to be appropriate for adsorption. The pseudo-second order and Langmuir models were consistent with the experimental data. The thermodynamic parameters indicate that adsorption is spontaneous and endothermic. The highest desorption percentage was achieved using the HCl solution, therefore, proving that method can be used to design slow-release fertilizers.

scholarly journals Study on Chromaticity Removal from Mineral Processing Wastewater with Salicylic Hydroxamic Acid by Granular Activated Carbon Catalyzed Ozonation

Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 359
Author(s):  
Liping Zhang ◽  
Shengnian Wu ◽  
Nan Zhang ◽  
Ruihan Yao ◽  
Eryong Wu
Keyword(s):  
Activated Carbon ◽  
Reaction Time ◽  
Hydroxamic Acid ◽  
Ph Value ◽  
Oxygen Demand ◽  
Granular Activated Carbon ◽  
Mineral Processing ◽  
Ultraviolet Absorption Spectrum ◽  
Experimental Conditions ◽  
Removal Ratio

Salicylic hydroxamic acid is a novel flotation reagent used in mineral processing. However, it impacts the flotation wastewater leaving behind high chromaticity which limits its reuse and affects discharge for mining enterprises. This study researched ozonation catalyzed by the granular activated carbon (GAC) method to treat the chromaticity of the simulated mineral processing wastewater with salicylic hydroxamic acid. The effects of pH value, ozone (O3) concentration, GAC dosage, and reaction time on chromaticity and chemical oxygen demand (CODCr) removal were discussed. The results of individual ozonation experiments showed that the chromaticity removal ratio reached 79% and the effluent chromaticity exceeded the requirement of reuse and discharge when the optimal experimental conditions were pH value 3, ozone concentration 6 mg/L, and reaction time 40 min. The orthogonal experimental results of catalytic ozonation with GAC on chromaticity removal explained that the chromaticity removal ratio could reach 96.36% and the chromaticity of effluent was only 20 when the optimal level of experimental parameters was pH value 2.87, O3 concentration 6 mg/L, GAC dosage 0.06 g/L, reaction time 60 min respectively. The degradation pathway of salicylic hydroxamic acid by ozonation was also considered based on an analysis with ultraviolet absorption spectrum and high-performance liquid chromatography (HPLC).

scholarly journals Creep Behaviour and Microstructural Characterization of VAT 36 and VAT 32 Superalloys

Metals ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 877 ◽  
Author(s):  
Vagner Gobbi ◽  
Silvio Gobbi ◽  
Danieli Reis ◽  
Jorge Ferreira ◽  
José Araújo ◽  
...  
Keyword(s):  
Failure Analysis ◽  
Creep Resistance ◽  
High Performance ◽  
Creep Behaviour ◽  
Ductile Failure ◽  
Microstructural Characterization ◽  
Dislocation Slip ◽  
Creep Tests ◽  
Experimental Conditions ◽  
Wide Range

Superalloys are used primarily for the aerospace, automotive, and petrochemical industries. These applications require materials with high creep resistance. In this work, evaluation of creep resistance and microstructural characterization were carried out at two new nickel intermediate content alloys for application in aerospace industry and in high performance valves for automotive applications (alloys VAT 32 and VAT 36). The alloys are based on a high nickel chromium austenitic matrix with dispersion of intermetallic L12 and phases containing different (Nb,Ti)C carbides. Creep tests were performed at constant load, in the temperature range of 675–750 °C and stress range of 500–600 MPa. Microstructural characterization and failure analysis of fractured surfaces of crept samples were carried out with optical and scanning electron microscopy with EDS. Phases were identified by Rietveld refinement. The results showed that the superalloy VAT 32 has higher creep resistance than the VAT 36. The superior creep resistance of the alloy VAT 32 is related to its higher fraction of carbides (Nb,Ti)C and intermetallic L12 provided by the amount of carbon, titanium, and niobium in its chemical composition and subsequent heat treatment. During creep deformation these precipitates produce anchoring effect of grain boundaries, hindering relative slide between grains and therefore inhibiting crack formation. These volume defects act also as obstacles to dislocation slip and climb, decreasing the creep rate. Failure analysis of surface fractures of crept samples showed intergranular failure mechanism at crack origin for both alloys VAT 36 and VAT 32. Intergranular fracture involves nucleation, growth, and subsequent binding of voids. The final fractured portion showed transgranular ductile failure, with dimples of different shapes, generated by the formation and coalescence of microcavities with dissimilar shape and sizes. The occurrence of a given creep mechanism depends on the test conditions. At creep tests of VAT 32 and VAT 36, for lower stresses and higher temperature, possible dislocation climb over carbides and precipitates would prevail. For higher stresses and intermediate temperatures shear mechanisms involving stacking faults presumably occur over a wide range of experimental conditions.

Study on Decolorization of Wastewater Containing Acid Orange II by Adsorption on Expanded Graphite

2011 ◽  
Vol 183-185 ◽  
pp. 873-876
Author(s):  
Jun Jie Yue ◽  
Xing Long Jin ◽  
Zhao Hui Jin
Keyword(s):  
Ph Value ◽  
Expanded Graphite ◽  
Orange Ii ◽  
Dye Wastewater ◽  
Temperature Level ◽  
Initial Concentration ◽  
Acid Orange ◽  
Ph Values ◽  
Simulated Wastewater ◽  
Acid Orange Ii

In this paper, the adsorption and decolorization capability of expanded graphite (EG) on the simulated wastewater containing Acid Orange Ⅱwere studied. The experimental results show that the initial concentration of wastewater, the dosage of EG, the pH value and the temperature all have greater effects on the decolorization ratio of simulated Acid Orange Ⅱ wastewater. The dye- wastewater containing lower concentration(＜150 mg/L) of Acid Orange Ⅱ is more suitable to be treated by EG, and approximately 100 mg/L is the preferable concentration. The decolorization ratio increases with the increment of the dosage of EG and the temperature level, but the growth rate obviously decreases at the higher initial concentration. All the decolorization ratios under strong acidic (pH<5) and alkalic (pH>11) conditions are higher than that at the range of 5-11 pH values, the highest value even reaches over 94%, while the decolorization ratio under the latter conditions are only between 75% and 85%.

Light-induced change of the molecular charge in a spironaphthoxazine compound

1993 ◽  
Vol 71 (11) ◽  
pp. 1828-1833 ◽  
Author(s):  
Paul Rys ◽  
Ruth Weber ◽  
Qinglan Wu
Keyword(s):  
Flash Photolysis ◽  
Ph Value ◽  
Uv Light ◽  
Merocyanine Form ◽  
Acid Base ◽  
Experimental Conditions ◽  
Base Equilibrium ◽  
Acid Base Equilibrium ◽  
Molecular Charge ◽  
Spiro Form

To evaluate the experimental conditions for the light-induced change of the molecular charge, the dependence of the photochromic reaction behaviour of the indolino spiro naphthoxazine compound 1,3,3-trimethyl-spiro[2H-indol 2,3′-[3H]naphth[2,1-b]-[1,4]oxazine] on the pH value of the solution is investigated. In the absence of UV light an acid–base equilibrium between the spiro form and a protonated closed form is established. By irradiation under appropriate acidic conditions the spiro form can be transformed into an open cationic form through the merocyanine form. Between the two open forms an acid–base equilibrium is established. Except for the closed protonated form the structures are confirmed by mean of NMR. The kinetics of the thermal ring-closing reaction of both forms are investigated by flash photolysis. It is shown that the ring-closing reaction proceeds exclusively via the merocyanine form. The pK values determined for both equilibria give the pH range, in which the light-induced change of the molecular charge occurs.

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