scholarly journals Characterizing the impact of pyrite addition on the efficiency of Fe0/H2O systems

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Rui Hu ◽  
Xuesong Cui ◽  
Minhui Xiao ◽  
Willis Gwenzi ◽  
Chicgoua Noubactep
Keyword(s):  
Methylene Blue ◽  
Methyl Orange ◽  
Ph Value ◽  
Batch Experiments ◽  
Ph Variation ◽  
Ph Values ◽  
Ph Shifting ◽  
Co Precipitation ◽  
The Impact

AbstractThe role of pyrite (FeS2) in the process of water treatment using metallic iron (Fe0) was investigated. FeS2 was used as a pH-shifting agent while methylene blue (MB) and methyl orange (MO) were used as an indicator of reactivity and model contaminant, respectively. The effect of the final pH value on the extent of MB discoloration was characterized using 5 g L−1 of a Fe0 specimen. pH variation was achieved by adding 0 to 30 g L−1 of FeS2. Quiescent batch experiments with Fe0/FeS2/sand systems (sand loading: 25 g L−1) and 20 mL of MB were performed for 41 days. Final pH values varied from 3.3 to 7.0. Results demonstrated that MB discoloration is only quantitative when the final pH value was larger than 4.5 and that adsorption and co-precipitation are the fundamental mechanisms of decontamination in Fe0/H2O systems. Such mechanisms are consistent with the effects of the pH value on the decontamination process.

scholarly journals Characterizing the impact of MnO2 addition on the efficiency of Fe0/H2O systems

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Viet Cao ◽  
Ghinwa Alyoussef ◽  
Nadège Gatcha-Bandjun ◽  
Willis Gwenzi ◽  
Chicgoua Noubactep
Keyword(s):  
Ph Value ◽  
Iron Corrosion ◽  
Dissolved Iron ◽  
Ph Values ◽  
Solid Iron ◽  
Initial Ph ◽  
Fixation Capacity ◽  
Co Precipitation ◽  
The Impact

AbstractThe role of manganese dioxide (MnO2) in the process of water treatment using metallic iron (Fe0/H2O) was investigated in quiescent batch experiments for t ≤ 60 d. MnO2 was used as an agent to control the availability of solid iron corrosion products (FeCPs) while methylene blue (MB) was an indicator of reactivity. The investigated systems were: (1) Fe0, (2) MnO2, (3) sand, (4) Fe0/sand, (5) Fe0/MnO2, and (6) Fe0/sand/MnO2. The experiments were performed in test tubes each containing 22.0 mL of MB (10 mg L−1) and the solid aggregates. The initial pH value was 8.2. Each system was characterized for the final concentration of H+, Fe, and MB. Results show no detectable level of dissolved iron after 47 days. Final pH values varied from 7.4 to 9.8. The MB discoloration efficiency varies from 40 to 80% as the MnO2 loading increases from 2.3 to 45 g L−1. MB discoloration is only quantitative when the operational fixation capacity of MnO2 for Fe2+ was exhausted. This corresponds to the event where adsorption and co-precipitation with FeCPs is intensive. Adsorption and co-precipitation are thus the fundamental mechanisms of decontamination in Fe0/H2O systems. Hybrid Fe0/MnO2 systems are potential candidates for the design of more sustainable Fe0 filters.

scholarly journals Bonding of Selected Hardwoods with PVAc Adhesive

2020 ◽  
Vol 11 (1) ◽  
pp. 67
Author(s):  
Ján Iždinský ◽  
Ladislav Reinprecht ◽  
Ján Sedliačik ◽  
Jozef Kúdela ◽  
Viera Kučerová
Keyword(s):  
Adhesion Strength ◽  
Cold Water ◽  
Ph Value ◽  
Water Extract ◽  
Solid Wood ◽  
Contact Angles ◽  
Water Contact ◽  
Ph Values ◽  
Positive Tendency ◽  
The Impact

The bonding of wood with assembly adhesives is crucial for manufacturing wood composites, such as solid wood panels, glulam, furniture parts, and sport and musical instruments. This work investigates 13 hardwoods—bangkirai, beech, black locust, bubinga, ipé, iroko, maçaranduba, meranti, oak, palisander, sapelli, wengé and zebrano—and analyzes the impact of their selected structural and physical characteristics (e.g., the density, cold water extract, pH value, roughness, and wettability) on the adhesion strength with the polyvinyl acetate (PVAc) adhesive Multibond SK8. The adhesion strength of the bonded hardwoods, determined by the standard EN 205, ranged in the dry state from 9.5 MPa to 17.2 MPa, from 0.6 MPa to 2.6 MPa in the wet state, and from 8.5 MPa to 19.2 MPa in the reconditioned state. The adhesion strength in the dry state of the bonded hardwoods was not influenced by their cold water extracts, pH values, or roughness parallel with the grain. On the contrary, the adhesion strength was significantly with positive tendency influenced by their higher densities, lower roughness parameters perpendicular to the grain, and lower water contact angles.

Adsorption of Organic Compounds on Refined Latvian Clay

2018 ◽  
Vol 788 ◽  
pp. 83-88
Author(s):  
Oskars Leščinskis ◽  
Ruta Švinka ◽  
Visvaldis Švinka
Keyword(s):  
Methyl Orange ◽  
Zeta Potential ◽  
Adsorption Capacity ◽  
Clay Minerals ◽  
Organic Compounds ◽  
Clay Mineral ◽  
Rhodamine B ◽  
Ph Value ◽  
Ftir Spectra ◽  
Ph Values

Clays are materials consisting of clay minerals and non-clay minerals. Clay mineral fraction is considered to be a nanofraction. Clay minerals can be used for water purification and treatment. Description and characterization of 3 different Latvian clay nanosized minerals from 3 different geological periods (clay Liepa from Devonian period, clay Vadakste from Triassic period and clay Apriki from Quaternary period) as well as their adsorption capacity concerning organic compounds such as methyl orange and rhodamine B are summarized. Nanosized clay mineral particles were obtained using sedimentation method. Particle size distribution, zeta potential and FTIR spectra is given. The adsorption tests of above mentioned organic compounds were carried out in water solutions at 3 different pH values. The adsorption values were determined by means of UV-spectrophotometric technique. Zeta potential values for clay minerals Apriki, Liepa and Vadakste are -40.9 mV, -49.6 mV and -43.0 mV, respectively. FTIR spectra show similar tendencies for all 3 clay minerals. The best adsorption capacity concerning methyl orange and rhodamine B were in solutions with a pH value of 2, whereas at neutral and alkaline pH values adsorption in 24 hours was not observed.

scholarly journals Study of photocatalytic activity of TiO2 fluorinated by thermal shock method for the degradation of different dyes

2015 ◽  
Vol 18 (2) ◽  
pp. 121-131
Author(s):  
Khoa Tien Le ◽  
Ngoc Chau Hoang ◽  
Tien Thuy Thai ◽  
Anh Trung Le ◽  
Thinh Nguyen Huu Pham ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Thermal Shock ◽  
Photocatalytic Oxidation ◽  
Organic Dyes ◽  
Cationic Dye ◽  
Solution Ph ◽  
Ph Values ◽  
Methylene Blue Cationic Dye

TiO2 P25 was fluorinated by thermal shock method in order to study the influence of thermal shock fluorination on the surface properties and the photocatalytic activity for the degradation of cationic and anionic organic dyes at different pH values. The surface charge of catalysts was characterized by the pHPZC measurement. The photocatalytic activity of catalysts was evaluated via the degradation of methylene blue (cationic dye) and methyl orange (anionic dye). The results showed that the thermal shock fluorination and the rise of solution pH can increase the surface negative charge of TiO2, which enhanced the adsorption of methylene blue and then improved the photocatalytic degradation of this cationic dye under UV and visible light. On the other hand, after the fluorination, the adsorption of methyl orange on TiO2 was strongly reduced, which limited the photocatalytic oxidation of this anion dye.

Catalytic Hydrolysis of Hydrogen Cyanide on Cu-Al Catalyst

2015 ◽  
Vol 1094 ◽  
pp. 15-19
Author(s):  
Lin Xia Yan ◽  
Sen Lin Tian ◽  
Qiu Lin Zhang
Keyword(s):  
Calcination Temperature ◽  
Hydrogen Cyanide ◽  
Influence Factor ◽  
Ph Value ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Cu Content ◽  
Co Precipitation ◽  
The Impact ◽  
Hydrolysis Of

Cu-Al catalysts were synthesized by the co-precipitation method to study hydrolysis of hydrogen cyanide. During the synthesis, the impact of Cu/Al molar ratio, pH value and calcination temperature was investigated and the best synthesis condition was found. The results indicate that the remove of hydrogen cyanide first increases and then decreases with increasing Cu/Al molar ratio, pH value and calcination temperature, which reaches the maxima and remains above 95% at 360 min when Cu/Al molar ratio is 2:1, pH value is approximately 8.0 and calcination temperature is 400°C around. The analysis of X-ray diffraction (XRD) shows that Cu content is the main influence factor at Cu/Al molar ratio below 2:1 whereas crystallinity of catalysts is the key factor at Cu/Al molar ratio above 2:1.

Oxidative Decolorization of Azo Dyes with Copper Phthalocyanine Supported Mg-Al Hydrotalcites

2016 ◽  
Vol 703 ◽  
pp. 306-310
Author(s):  
Min Hong Xu ◽  
Jian Li Ma ◽  
Meng Xia Qian ◽  
Hui Na Qin
Keyword(s):  
Molecular Structure ◽  
Methylene Blue ◽  
Methyl Orange ◽  
Azo Dyes ◽  
Acidic Solution ◽  
Copper Phthalocyanine ◽  
Ph Value ◽  
Influence Factors ◽  
Amido Black ◽  
Initial Ph

Oxidative decolorization of azo dyes with a heterogeneous catalyst copper phthalocyanine supported Mg-Al hydrotalcites was studied and the influence factors such as initial pH value, temperature, H2O2 and CuPc-LDHs/H2O2 system were discussed. The results indicated that acidic solution and high temperature were conducive to oxidative decoloration of methyl orange. CuPc-LDHs/H2O2 system showed excellent oxidative decoloration capacity to remove azo dyes. The effects of oxidative decolorization of azo dyes were related to the molecular structure and weight of azo dyes. Oxidative decoloration effects followed the order as congo red > amido black > methyl blue> methyl orange> methylene blue.

scholarly journals Role of Charge Regulation and Fluctuations in the Conformational and Mechanical Properties of Weak Flexible Polyelectrolytes

2019 ◽  
Author(s):  
Pablo M. Blanco ◽  
Sergio Madurga ◽  
Claudio F. Narambuena ◽  
Francesc Mas ◽  
Josep L. Garcés
Keyword(s):  
Mechanical Properties ◽  
Electrostatic Interactions ◽  
Ph Value ◽  
Persistence Length ◽  
Excluded Volume ◽  
Average Charge ◽  
Zero Force ◽  
Charge Regulation ◽  
Ph Values

This work addresses the role of charge regulation (CR) and the associated fluctuations in the conformational and mechanical properties of weak polyelectrolytes. Due to CR, changes in the pH-value modifies the average macromolecular charge and conformational equilibria. A second effect is that, for a given average charge per site, fluctuations can alter the intensity of the interactions by means of correlation between binding sites. We investigate both effects by means of Monte Carlo simulations at constant pH-value, so that the charge is a fluctuating quantity. Once the average charge per site is available, we turn off the fluctuations by assigning the same average charge to every site. A constant charge MC simulation is then performed. We make use of a model which accounts for the main fundamental aspects of a linear flexible polyelectrolyte i.e. proton binding, angle internal rotation, bond stretching and bending. Steric excluded volume and differentiated treatment for short-range and long-range interactions are also included in the model. It can be regarded as a kind of "minimal'' model in the sense that contains a minimum number of parameters but still preserving the atomistic detail. It is shown that, if fluctuations are activated, gauche state bond probabilities increase, and the persistence length decreases, so that the polymer becomes more folded. Macromolecular stretching is also analyzed in presence of CR (the charge depends on the applied force) and without CR (the charge is fixed to the value at zero force). The analysis of the low force scaling behavior concludes that Pincus exponent becomes pH-dependent. Both with and without CR, a transition from 1/2 at high pH-values (phantom chain) to 3/5 to low pH-values (Pincus regime), is observed. Finally, the intermediate force stretching regime is investigated. It is found that CR induces a moderate influence in the force-extension curves and persistence length (which in this force regime becomes force-dependent). It is thus concluded that the effect of CR on the stretching curves is mainly due to changes in the average charge at zero force. It is also found that, for the cases studied, the effect of steric excluded volume is almost irrelevant compared to electrostatic interactions.

scholarly journals Revisiting the fundamentals of p-nitrophenol analysis for its application in the quantification of lipases activity. A graphical update.

Uniciencia ◽  
2020 ◽  
Vol 34 (2) ◽  
pp. 31-43
Author(s):  
Randall Syedd-León ◽  
Manuel Sandoval-Barrantes ◽  
Humberto Trimiño-Vásquez ◽  
Luis Roberto Villegas-Peñaranda ◽  
Gerardo Rodríguez-Rodríguez
Keyword(s):  
Lipase Activity ◽  
Ph Value ◽  
Protonated Form ◽  
Spectrophotometric Analysis ◽  
Spectrophotometric Methods ◽  
Ph Values ◽  
Reaction Media ◽  
Activity Quantification

p-Nitrophenol (pNP) is a widely used compound for analytical determinations of several esterases (EC. 3.1.1.X), including lipases (E.C. 3.1.1.3). Most enzymatic measurements employ pNP derivatives such as esters, which are broken down by enzymatic hydrolysis, releasing pNP that is quantified by its absorbance at 410 nm. Although this type of methods was developed a few decades ago, the spectrophotometric analysis of pNP requires analytical measurements of pH and temperature to achieve reliable determinations. The aim of this paper is to offer a graphical update of how pH and temperature affect the p-nitrophenol absorbance at different wavelengths in lipase emulsified media, due to its relevance for the quantitative determination of lipase activity using spectrophotometric methods. To highlight the importance of each variable involved in this analysis, we dissolved pNP in emulsified media (for lipase activity quantification) at several pH values from 4.00 to 11.00, and measured its absorbance in a range of 270 nm – 500 nm and at several temperatures from 25°C to 50°C. The absorption patterns of pNP under the established conditions were graphed in 3D plots. The constructed 3D plots showed that, regardless of the temperature, below pH 6.00, pNP predominantly absorbs at 317 nm, due to the greater abundance of its protonated form, which is completely predominant at pH 3.50 and below. On the other hand, at pH 10.0 and above, the major absorption occurs at about 401 nm, confirming that the equilibrium is completely shifted to the pNP anionic form. These results also indicate that close to neutral pH value pNP, it displays a temperature dependence effect, increasing absorbance to 410 nm at higher temperatures. Due to many analytical determinations of enzymatic activities, the release of pNP is carried around pH 7.00. It is necessary to consider the determinant role of both pH and temperature over these measurements, how these variables must be strictly controlled, and how the calibration curves and blanks should take the reaction media pH and temperature into account.

The Role of Acetate in Denitrification and Biological Phosphate Removal in Modified Bardenpho Systems

1989 ◽  
Vol 21 (4-5) ◽  
pp. 375-385 ◽  
Author(s):  
C. T. Winter
Keyword(s):  
Sodium Acetate ◽  
Ph Value ◽  
Phosphate Removal ◽  
Organic Substances ◽  
Phosphate Release ◽  
Ph Values ◽  
Experimental Systems ◽  
Removal Capacity ◽  
Equivalent Sequence

The importance of easily biodegradable organic substances such as acetate and propionate in biological phosphate removal has been recognised by many researchers. Laboratory-scale studies on the performance of three-stage modified Bardenpho nutrient removal systems, fed with settled sewage supplemented with 0, 50, 100 and 200 mg/l sodium acetate respectively are described. Particular attention is given to the effects of these additions on biological phosphate release and uptake and also to the fate of parameters such as pH, calcium, potassium, ammonia and nitrate. Additional phosphate of 10 mg/l (as P) was initially introduced into the feed in order to burden the experimental systems beyond their normal phosphate removal capacity. This was increased to 20 mg/l and eventually to 40 mg/l of phosphate (as P). Increasing concentrations of sodium acetate resulted in distinct increases in pH values, increase in phosphate release in the anaerobic zones and significantly improved overall phosphate removal in the experimental units. The correlation of phosphate removal on acetate concentration was found to be 0.9886. In some instances the unit receiving 200 mg/l acetate removed up to an average of 30 mg/l of phosphate (as P), constituting an improvement of up to 200% compared with the unit receiving no acetate. The alternating release and uptake of phosphate was accompanied by an equivalent sequence for potassium and magnesium. The high pH value plus the disappearance of phosphate, ammonia and magnesium places doubt on a purely biological phosphate removal but could point at the crystallization of ammonium magnesium phosphate.

scholarly journals Role of Charge Regulation and Fluctuations in the Conformational and Mechanical Properties of Weak Flexible Polyelectrolytes

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1962 ◽  
Author(s):  
Pablo M. Blanco ◽  
Sergio Madurga ◽  
Claudio F. Narambuena ◽  
Francesc Mas ◽  
Josep L. Garcés
Keyword(s):  
Mechanical Properties ◽  
Electrostatic Interactions ◽  
Ph Value ◽  
Persistence Length ◽  
Excluded Volume ◽  
Average Charge ◽  
Zero Force ◽  
Charge Regulation ◽  
Ph Values

This work addresses the role of charge regulation (CR) and the associated fluctuations in the conformational and mechanical properties of weak polyelectrolytes. Due to CR, changes in the pH-value modifies the average macromolecular charge and conformational equilibria. A second effect is that, for a given average charge per site, fluctuations can alter the intensity of the interactions by means of correlation between binding sites. We investigate both effects by means of Monte Carlo simulations at constant pH-value, so that the charge is a fluctuating quantity. Once the average charge per site is available, we turn off the fluctuations by assigning the same average charge to every site. A constant charge MC simulation is then performed. We make use of a model which accounts for the main fundamental aspects of a linear flexible polyelectrolyte that is, proton binding, angle internal rotation, bond stretching and bending. Steric excluded volume and differentiated treatment for short-range and long-range interactions are also included. This model can be regarded as a kind of “minimal” in the sense that it contains a minimum number of parameters but still preserving the atomistic detail. It is shown that, if fluctuations are activated, gauche state bond probabilities increase and the persistence length decreases, so that the polymer becomes more folded. Macromolecular stretching is also analyzed in presence of CR (the charge depends on the applied force) and without CR (the charge is fixed to the value at zero force). The analysis of the low force scaling behavior concludes that Pincus exponent becomes pH-dependent. Both, with and without CR, a transition from 1/2 at high pH-values (phantom chain) to 3/5 at low pH-values (Pincus regime) is observed. Finally, the intermediate force stretching regime is investigated. It is found that CR induces a moderate influence in the force-extension curves and persistence length (which in this force regime becomes force-dependent). It is thus concluded that the effect of CR on the stretching curves is mainly due to the changes in the average charge at zero force. It is also found that, for the cases studied, the effect of steric excluded volume is almost irrelevant compared to electrostatic interactions.

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