Nature of mixed iron and aluminium gels as affected by Fe/Al molar ratio, pH and citrate

Clay Minerals ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 511-519 ◽  
Author(s):  
A. Violante ◽  
C. Colombo ◽  
G. Cinquegrani ◽  
P. Adamo ◽  
P. Violante

AbstractThe nature and mineralogy of mixed Al and Fe(III) gels (initial Fe/Al molar ratios (Ri) of 1.0 and 2.5) formed at pH values ranging from 4.0 to 10.0, both in the presence and absence of citric acid (citrate/Fe + AI molar ratio (Rcit) of 0.01 and 0.1) and aged for a long period at room temperature and at 50°C have been studied. The complexes showed considerable differences in the mineralogy of the precipitation products. The samples formed at Ri = 1.0 contained ferrihydrite at pH 4.0, ferrihydrite + gibbsite at pH 5.0-7.0, and hematite + Al(OH)3polymorphs + ferrihydrite at pH 9.0-10.0. The samples formed at Ri = 2.5 had greater quantities of poorly crystallized ferrihydrite. Large amounts of Fe+Al (25-82%) were solubilized from the samples aged for 60 days at 50°C by ammonium oxalate. The addition of increasing concentrations of citrate to the gel suspensions containing equimolar amounts of Fe and AI strongly inhibited the formation of Al(OH)3polymorphs both at pH 5.0 or 8.5 by promoting the formation of short-range ordered materials. Citrate added initially to Fe-Al solutions (R*cit = 0.1) completely inhibited formation of crystals even after 135 days at 50°C.

2021 ◽  
Author(s):  
Ahmed Hamdy El-Kady ◽  
Zheng Chai ◽  
Hisham A. Nasr-El-Din

Abstract Aminopolycarboxylate-based chelants are used to control iron precipitation during acidizing operations by interacting directly with the iron, resulting in water-soluble complexes. This paper highlights that, in order to improve the effectiveness of iron control during acidizing operations, the type and the concentration of the chelants should be based on the formation properties and the well characteristics by comparing the cheltors’ performance as iron-control agents at different temperatures and pH environments with different levels of iron concentrations and chelant to iron molar ratios in acid (HCl). This study also addresses the interactions between the tested iron-control additives and acid, as well as the performance of the chelants in carbonate cores. Laboratory experiments were conducted to investigate the performance of nitrilotriacetic acid (NTA), glutamic acid, N, N-diacetic acid (GLDA), diethylenetriaminepentaacetic acid (DTPA), ethylenediamine-tetraacetic acid (EDTA), and hydroxyethylethylenediaminetriacetic acid (HEDTA) as iron control additives in 5 wt% HCl at pH values 0 to 4.5 to simulate carbonate acidizing at temperatures of 70 to 300°F, and initial iron concentrations of 2000 ppm. The performance of NTA and EDTA was also compared at higher initial iron concentration (4000 ppm). This work also quantified the effects of acid additives such as corrosion inhibitor and non-ionic surfactant on the chelation performance. Coreflood experiments using carbonate cores in acid with chelant helped determine its influence on permeability. Testing chelant-to-acid molar ratios of 1:1, 1.1:1, 1.2:1, 1.3:1, 1.4:1, 1.5:1, and 2:1 relative to iron concentration yielded optimal values. Additional tests monitored iron precipitation in solution using an inductively coupled argon plasma (ICAP) emission spectroscopy. Precipitates were filtered and analyzed using X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS). Without chelant, at 70°F and 2000 ppm initial iron concentration, precipitation began at pH 1.45 and completed by pH 2.42. At 150 and 210°F, iron precipitated at pH 0.68 and 0.3 and completed by pH 1.3 and 1, respectively. At 70°F, NTA showed a minimum of 98% chelation at pH 4.3; however, its performance declined at 150°F to 74% chelation at pH 4.24, and at 210°F to 53% chelation at pH 4.0. Although DTPA dissolves completely in live acid, precipitations occurred at partially spent acid. At pH 0.15, SEM-EDS showed that the precipitate contains as much as 13 wt% iron. Thus, DTPA is not a suitable iron-control agent. HEDTA showed a 90% chelation at 210°F and pH 4.8. GLDA's performance declined to less than 50% at 150°F. At higher iron concentrations of 4000 ppm, Na3NTA kept all iron in solution in a 5 wt% HCl up to pH 4.0 at 70°F and its performance declined to a minimum of 97% at pH 4.7 at same temperature. At 150°F, and 210°F, Na3NTA started to gradually decline at pH values greater than 3.9, and 3.5, respectively. The minimum chelation reached by NTA was 91% at pH 4.4, at 150°F, and 73% at pH 4 at 210°F. Upon comparing the NTA's results at high iron concentrations to the popular EDTA, Na4EDTA at 1-to-1 mole ratio with iron exceeded its maximum solubility in 5 wt% HCl and precipitated in the original solution. For NTA, a molar ratio of 1.4:1 is optimal at 70 and 150°F, showing chelation performance of 95% and 94%, respectively, while a molar ratio of 1.5:1 is optimal at 210°F, showing a chelation performance of 87%. This study's results improve field operations by identifying NTA and HEDTA as having the best iron-control chelation performance of the five additives tested, thus reducing guesswork and streamlining production. The work also provided recommendations for choosing the best type of iron-control agent based on solubility and coreflood analysis. The results can be used to design more efficient acidizing fluids. This work won second place in the Masters division of the 2020 Gulf Coast Regional Student Paper Contest, April 2020.


2014 ◽  
Vol 12 (4) ◽  
pp. 722-726 ◽  
Author(s):  
Sandra Isabel Escobar-Megchún ◽  
Hugo Alejandro Nájera-Aguilar ◽  
Magaly González-Hilerio ◽  
Javier Gutiérrez-Jiménez ◽  
Rubén Fernando Gutiérrez-Hernández ◽  
...  

This study relates to a method for evaluating the degradation efficiency of Ascaris lumbricoides eggs through a Fenton reaction, using hydrogen peroxide (H2O2) at 100, 250, and 500 mg/L, ferrous sulfate (FeSO4) at 458 mg/L Fe2+ and pH values of 3, 4.5, and 6. The experiments were conducted according to a 32 experimental design, with 1:1, 3:1, and 5:1 (H2O2/Fe2+) molar ratios. The oxidation and flocculation stages were performed at 130 rpm during 2 hours and at 25–30 rpm during 20 min, respectively. As a result of the Fenton reaction, an average of 91.2% Ascaris lumbricoides egg degradation was achieved at pH 6 using a 500 mg/L dose of H2O2 and a 3:1 (H2O2/Fe2+) molar ratio. Thus, this process is an alternative for eliminating parasites that are resistant to conventional disinfection processes and significantly reduces the human health hazard they represent.


MRS Advances ◽  
2017 ◽  
Vol 2 (61) ◽  
pp. 3851-3857 ◽  
Author(s):  
Jorge López-Cuevas ◽  
Juan C. Rendón-Angeles ◽  
José L. Rodríguez-Galicia ◽  
Carlos A. Gutiérrez-Chavarría

ABSTRACTHydroxyapatite [HAp, Ca5(PO4)3(OH)] was synthesized by chemical precipitation, using H3PO4 and Ca(OH)2 as chemical precursors. The precursors were slowly mixed in suitable proportions aiming to obtain Ca/P molar ratios of 1.5, 1.67 or 2.0 in the reacting suspension. This was followed by 21.5 h of aging. Both reaction and aging stages were carried out under an atmosphere of still ambient air and under continuous stirring, either at room temperature, 60 or 90 °C. The precipitates were characterized by ICP-AES and XRD. The results suggested that the most suitable Ca/P molar ratio for the production of pure phase HAp is Ca/P = 1.67, as long as the initial Ca(OH)2 particle size and/or the suspension pH are carefully controlled, especially when the synthesis is carried out above room temperature.


2020 ◽  
Vol 845 ◽  
pp. 21-26
Author(s):  
Narunchara Phurahong ◽  
Nantana Jiratumnukul

Nanocellulose fibers (NCF) is a renewable biodegradable polymer in nature. It has extensively interest as a reinforcement material in nanocomposites due to its nanoscale advantages. However, the efficiency of NCF dispersion in polymer matrix has limitation due to its self-agglomeration.The objective of this research was to prepare surface-modified NCF using three different acids; succinic anhydride, phthalic anhydride and citric acid. The molar ratios of acid to anhydroglucose units in NCF used in this work were 6:1, 8:1 and 10:1. The effects of acid types and molar ratios toward physical properties were studied. The results showed that succinic anhydride-modified NCF provided the highest DS range from 0.46-0.86. Dispersion of succinic anhydride-modified NCF provided good stability in water for 30 days. The succinic anhydride-modified NCF of 1:6 molar ratio is suitable for emulsion coating application.


1975 ◽  
Vol 30 (7-8) ◽  
pp. 575-581 ◽  
Author(s):  
Josef A. Veith ◽  
Günther Wiese

Mixtures of citric acid (H3Ci) and Fe(NO3)3 with variable molar ratios (H3Ci/Fe(NO3)3 from 0 to 2.55) were titrated with NaOH. The change in pH and the occurring inflection points were registered with a potentiograph (Fig. 1). For each inflection point (I.P.) the existing H3Ci/Fe(NO3)3 molar ratio was plotted against the NaOH/Fe(NO3)3 molar ratio which existed at the corresponding inflection point (at most three I.P. for each titration curve). The coefficients ej, fj and gj for each dehydratedFe-Ci-complex [Fefj(OH)gj-3ejCicj](gj-3fj)⁻ with j = 1, 2, . . . ,could be calculated from the points of intersection (Pj) in the x-y-diagram (Fig. 2). Thus, the following three Fe-Ci-complexes were calculated:From the 1st I.P. [Fe10(OH)18Ci5]3- with its maximum at pH ≃ 4.3.From the 2nd I.P. [Fe5(OH)9Ci4]6- with its maximum at pH ≃ 8.0.From the 3rd I.P. [Fe4(OH)11Ci]2- with its maximum at pH ≃ 10.1.The range of their existence as functions of H3Ci/Fe(NO3)3 ratios (Fig. 3 and 4) and pH (Fig. 4) is discussed.


2009 ◽  
Vol 7 (3) ◽  
pp. 423-428 ◽  
Author(s):  
Melda Altikatoglu ◽  
Candan Arioz ◽  
Yeliz Basaran ◽  
Huriye Kuzu

AbstractStabilization of Horseradish Peroxidase (HRP; EC 1.11.1.7) against temperature and pH via the formation of the conjugates obtained by multipoint covalent bonding of dextran aldehyde (DA) to the enzyme were studied. Hence, three different molar weighted dextrans (17.5 kD, 75 kD, 188 kD) were covalently bonded to purified enzyme with different molar ratios (nHRP/nDA 20/1, 10/1, 1/1, 1/5, 1/10, 1/15, 1/20). The thermal stabilities of the obtained conjugates were evaluated with the activities determined at different temperatures (25, 30, 35, 40, 50, 60, 70, 80°C) applying 60 minutes incubation time. Conjugates formed were characterized by gel-permeation chromatography (GPC) and fluorescence techniques. The conjugate synthesized using dextran 75 kDa with nHRP/nDA 1/10 molar ratio showed better thermal stability than other conjugates and purified enzyme at pH 7. This conjugate also has wider activity pH range than purified enzyme. In addition, mentioned conjugate at pH 7 had very long storage lifetime compared to purified enzyme at +4°C and room temperature; which is considered a favorable feature for usage in practice.


2017 ◽  
Vol 13 (2) ◽  
pp. 4671-4677 ◽  
Author(s):  
A. M. Abdelghany ◽  
A.H. Oraby ◽  
Awatif A Hindi ◽  
Doaa M El-Nagar ◽  
Fathia S Alhakami

Bimetallic nanoparticles of silver (Ag) and gold (Au) were synthesized at room temperature using Curcumin. Reduction process of silver and gold ions with different molar ratios leads to production of different nanostructures including alloys and core-shells. Produced nanoparticles were characterized simultaneously with FTIR, UV/vis. spectroscopy, transmission electron microscopy (TEM), and Energy-dispersive X-ray (EDAX). UV/vis. optical absorption spectra of as synthesized nanoparticles reveals presence of surface palsmon resonance (SPR) of both silver at (425 nm) and gold at (540 nm) with small shift and broadness of gold band after mixing with resucing and capping agent in natural extract which suggest presence of bimetallic nano structure (Au/Ag). FTIR and EDAX data approve the presence of bimetallic nano structure combined with curcumin extract. TEM micrographs shows that silver and gold can be synthesized separately in the form of nano particles using curcumin extract. Synthesis of gold nano particles in presence of silver effectively enhance and control formation of bi-metallic structure.


Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michika Sawada ◽  
Kandi Sridhar ◽  
Yasuharu Kanda ◽  
Shinya Yamanaka

AbstractWe report a synthesis strategy for pure hydroxyapatite (HAp) using an amorphous calcium carbonate (ACC) colloid as the starting source. Room-temperature phosphorylation and subsequent calcination produce pure HAp via intermediate amorphous calcium phosphate (ACP). The pre-calcined sample undergoes a competitive transformation from ACC to ACP and crystalline calcium carbonate. The water content, ACC concentration, Ca/P molar ratio, and pH during the phosphorylation reaction play crucial roles in the final phase of the crystalline phosphate compound. Pure HAp is formed after ACP is transformed from ACC at a low concentration (1 wt%) of ACC colloid (1.71 < Ca/P < 1.88), whereas Ca/P = 1.51 leads to pure β-tricalcium phosphate. The ACP phases are precursors for calcium phosphate compounds and may determine the final crystalline phase.


Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1573
Author(s):  
Aljaž Škrjanc ◽  
Ciara Byrne ◽  
Nataša Zabukovec Logar

The use of green solvents as an alternative to dimethylformamide (DMF) in the synthesis of zeolitic imidazolate framework-90 (ZIF-90) was investigated. Two biobased aprotic dipolar solvents CyreneTM and γ-valerolactone (GVL) proved to successfully replace DMF in the synthesis at room temperature with a high product yield. While the CyreneTM—based product shows reduced porosity after activation, the use of GVL resulted in materials with preserved crystallinity and porosity after activation, without prior solvent exchange and a short treatment at 200 °C. The primary particles of 30 nm to 60 nm in all products further form agglomerates of different size and interparticle mesoporosity, depending on the type and molar ratios of solvents used.


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