Effect of Grinding Aids on the Fracture Energy of Mica

2011 ◽  
Vol 402 ◽  
pp. 503-509
Author(s):  
Ze Hong Wang ◽  
Fu Jia Yu ◽  
Shan Cai ◽  
Shan Zhi Deng ◽  
Roger Horn
Keyword(s):  
Sodium Chloride ◽  
Fracture Energy ◽  
Sodium Citrate ◽  
Ph Value ◽  
Sodium Tripolyphosphate ◽  
Experimental System ◽  
Ammonium Bromide ◽  
Solution Ph ◽  
Grinding Aids ◽  
Slurry Rheology

An extension of the classical Obriemoff experiments has been set up to measure the fracture energy of mica. This experimental system will be entirely independent of slurry rheology. CTAB (Cetyl Trimethyl Ammonium Bromide), sodium tripolyphosphate, sodium hexametaphosphate, and tri-sodium citrate are used as grinding aids in this study and the fracture energy has been measured for mica in air, water, and water with the addition of various concentrations of these grinding aids. The results show that the fracture energy of mica in water is about half of what it is in air. Grinding aids are shown to reduce the fracture energy of mica, but not dramatically. Addition of grinding aids reduces the fracture energy by a further 10-20%, with tri-sodium citrate appearing to be the most effective. For each grinding aid there appears to be an optimal concentration, typically around 10 mmol. An experiment is also done with sodium chloride at a range of concentrations to investigate the mechanism of these grinding aids, but no reduction in fracture energy (compared to water) was observed, hence the molecular-level mechanism of action of these grinding aids remains unclear. The effect of solution pH values on the fracture energy are also investigated using tri-sodium citrate and sodium chloride. The results show that the solution pH value may effect on the fracture energy of mica. So, in practice, both concentration and pH value of solution are important for getting better grinding results.

scholarly journals Influence Of Marination On Salmonella Spp. Growth In Broiler Breast Fillets

2015 ◽  
Vol 65 (3) ◽  
pp. 417-428 ◽  
Author(s):  
Baltić Tatjana ◽  
Baltić Ž. Milan ◽  
Mišić Dušan ◽  
Ivanović Jelena ◽  
Janjić Jelena ◽  
...  
Keyword(s):  
Significant Influence ◽  
Sodium Citrate ◽  
Ph Value ◽  
Sodium Tripolyphosphate ◽  
Salt Content ◽  
Lag Phase ◽  
Table Salt ◽  
Salmonella Spp ◽  
Broiler Meat ◽  
Broiler Breast

AbstractThe aim of this study was to investigate the influence of marination, on the growth ofSalmonellaspp. in contaminated broiler breast fillets during storage. In the conducted study, broiler breast fillets were inoculated with a cocktail of differentSalmonellastrains and afterwards marinated in different solutions of table salt, sodium tripolyphosphate and/or sodium citrate. The total count ofSalmonellaspp. was examined on the 0, 3rd, 6thand 9thday of storage. Broiler breast fillets salted in 6% solution of table salt were used as the control. Proximate composition and salt content, pH value and awvalue, were determined as the meat quality parameters and parameters which can affect environmental conditions for bacterial growth, as well. Compared to initial contamination,Salmonellaspp. count in marinated and salted fillets did not change significantly (p<0.001) until the 3rdand 6thday of storage, respectively, but it increased significantly on the 9thday of storage. Marination of broiler breast fillets in different solutions of table salt, sodium tripolyphosphate and/or sodium citrate had a significant influence(p<0.05; p<0.01) on pH and awvalue, moisture, ash and salt content in marinated broiler meat, but there was no significant influence (p>0.05) on protein and fat content in broiler meat. According to the results obtained it can be concluded that marination of broiler breast fillets in solutions containing table salt, sodium trpolyphosphate and/or citrate, in some way, can prolongate the lag phase ofSalmonellaspp. growth, where sodium citrate is more effective than sodium tripolyphosphate.

Adsorption of Bisphenol-A by HDTMA Modified Clinoptilolite

2011 ◽  
Vol 71-78 ◽  
pp. 717-721
Author(s):  
Hong Yu Wang ◽  
Hang Li Zhang ◽  
Qian Zhao ◽  
Hui Fei Huang
Keyword(s):  
Bisphenol A ◽  
Rate Constant ◽  
Absorption Rate ◽  
Ph Value ◽  
Freundlich Isotherm ◽  
Ammonium Bromide ◽  
Solution Ph ◽  
Kinetics Of Adsorption ◽  
Modified Clinoptilolite ◽  
Kinetics Of

The adsorption of bisphenol-A (BPA) by hexadecyl trimethyl ammonium bromide (HDTMA) modified clinoptilolite was presented. In this paper, the equilibrium adsorption of BPA by HDTMA modified clinoptilolite was described by Freundlich isotherm with a correlation coefficient's square (R2) of 0.988. The kinetics of adsorption was defined by second-order kinetics with a rate constant (Kv) of 1.98 g/mg/h. The absorption rate was fast, and the liquid solid equilibrium was accomplished within 180 minutes. The effects of initial solution pH, and reaction temperatures had been estimated, showing that the adsorption was enhanced gradually by increasing pH value.

Controlled and uncontrolled physicochemical quality indicators of 0.9 % sodium chloride of various manufacturers

2020 ◽  
pp. 6-11
Author(s):  
Anton Kasatkin ◽  
Anna Nigmatullina ◽  
Mikhail Kopytov
Keyword(s):  
Sodium Chloride ◽  
Quality Indicators ◽  
Clinical Studies ◽  
Laboratory Tests ◽  
Ph Value ◽  
Chemical Parameters ◽  
Pharmacokinetics And Pharmacodynamics ◽  
Physicochemical Quality ◽  
Physico Chemical

The article presents the results of studies of osmolality and pH of 0,9 % sodium chloride of various manufacturers. To obtain data on the pH value, the data used in the passports are used, and the indicators of its osmolality are de- termined using laboratory tests. 0,9 % sodium chloride from different manufacturers has different pH and osmolality. Knowing the actual values of physico-chemical parameters can increase the accuracy of the results of future clinical studies, which compare the pharmacokinetics and pharmacodynamics of modern plasma-substituting solutions and a solution of 0,9 % sodium chloride.

Effect of pH and NH4NO3 as a Spray Additive on Penetration of NAA Through Isolated Tomato Fruit Cuticle

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 550a-550 ◽  
Author(s):  
Royal G. Fader ◽  
Martin J. Bukovac
Keyword(s):  
Direct Measurement ◽  
Sodium Citrate ◽  
Tomato Fruit ◽  
Initial Slope ◽  
Control Effect ◽  
Solution Ph ◽  
Ph Change ◽  
Effect Of Ph ◽  
Spray Droplets ◽  
Partition Behavior

We have reported that NH4NO3 (AN, 8 mM, pH 4.2), applied as simulated spray droplets, enhanced penetration of 14C-NAA through isolated leaf and fruit cuticles. One explanation for this response is that AN depresses NAA (pKa= 4.2) dissociation, increasing the nondissociated moiety, which penetrates more readily than the anion (NAA'). Direct measurement of AN (concn. 0-800 mM) effect on NAA (215 μM) dissociation as indexed by change in solution pH revealed no significant effect, with a pH change from 4.19 to 4.05. This change is not sufficient to account for the observed enhancement. When 14C-NAA, buffered (20 mM sodium citrate) at pH 3.2, 4.2, 5.2, 6.2, was partitioned against chloroform, there was a marked increase in NAA partitioning into chloroform as pH was decreased. AN (8 mM) did not alter this partition behavior, also indicating no effect on NAA dissociation. However, in cuticle penetration studies, using a finite dose system with 14C-NAA buffered at pH 3.2, 4.2, 5.2, 6.2, and in the presence and absence of 8 mM AN, there was no marked or consistent pH or AN (-70 to + 232 % of no AN control) effect on penetration as indexed by initial slope (4-12 h) or penetration after 120 h. The possible effects of AN and buffer on penetration of 14C-NAA from the droplet deposit will be discussed.

scholarly journals Chitosan Nanocarrier Entrapping Hydrophilic Drugs as Advanced Polymeric System for Dual Pharmaceutical and Cosmeceutical Application: A Comprehensive Analysis Using Box-Behnken Design

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 677
Author(s):  
Sara A. Abosabaa ◽  
Aliaa N. ElMeshad ◽  
Mona G. Arafa
Keyword(s):  
Particle Size ◽  
Sodium Tripolyphosphate ◽  
Chitosan Nanoparticles ◽  
Optimization Procedure ◽  
Entrapment Efficiency ◽  
Chitosan Solution ◽  
Polydispersity Index ◽  
Successful Implementation ◽  
Solution Ph ◽  
Box Behnken Design

The objective of the present research is to propose chitosan as a nanocarrier for caffeine—a commonly used drug in combating cellulite. Being a hydrophilic drug, caffeine suffers from insufficient topical penetration upon application on the skin. Chitosan nanoparticles loaded with caffeine were prepared via the ionic gelation technique and optimized according to a Box–Behnken design. The effect of (A) chitosan concentration, (B) chitosan solution pH, and (C) chitosan to sodium tripolyphosphate mass ratio on (Y1) entrapment efficiency percent, (Y2) particle size, (Y3) polydispersity index, and (Y4) zeta potential were studied. Subsequently, the desired constraints on responses were applied, and validation of the optimization procedure was confirmed by the parameters exhibited by the optimal formulation. A caffeine entrapment efficiency percent of 17.25 ± 1.48%, a particle size of 173.03 ± 4.32 nm, a polydispersity index of 0.278 ± 0.01, and a surface charge of 41.7 ± 3.0 mV were attained. Microscopical evaluation using transmission electron microscope revealed a typical spherical nature of the nanoparticles arranged in a network with a further confirmation of the formation of particles in the nano range. The results proved the successful implementation of the Box–Behnken design for optimization of chitosan-based nanoparticles in the field of advanced polymeric systems for pharmaceutical and cosmeceutical applications.

scholarly journals Separation of Radionuclides from a Rare Earth-Containing Solution by Zeolite Adsorption

Minerals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 20
Author(s):  
Deniz Talan ◽  
Qingqing Huang
Keyword(s):  
Rare Earth ◽  
Rare Earths ◽  
Contact Time ◽  
Separation Efficiency ◽  
Ph Value ◽  
Solid Phase ◽  
Separation Performance ◽  
Solution Ph ◽  
Zeolite Sample ◽  
Alternative Sources

The increasing industrial demand for rare earths requires new or alternative sources to be found. Within this context, there have been studies validating the technical feasibility of coal and coal byproducts as alternative sources for rare earth elements. Nonetheless, radioactive materials, such as thorium and uranium, are frequently seen in the rare earths’ mineralization, and causes environmental and health concerns. Consequently, there exists an urgent need to remove these radionuclides in order to produce high purity rare earths to diversify the supply chain, as well as maintain an environmentally-favorable extraction process for the surroundings. In this study, an experimental design was generated to examine the effect of zeolite particle size, feed solution pH, zeolite amount, and contact time of solid and aqueous phases on the removal of thorium and uranium from the solution. The best separation performance was achieved using 2.50 g of 12-µm zeolite sample at a pH value of 3 with a contact time of 2 h. Under these conditions, the adsorption recovery of rare earths, thorium, and uranium into the solid phase was found to be 20.43 wt%, 99.20 wt%, and 89.60 wt%, respectively. The Freundlich adsorption isotherm was determined to be the best-fit model, and the adsorption mechanism of rare earths and thorium was identified as multilayer physisorption. Further, the separation efficiency was assessed using the response surface methodology based on the development of a statistically significant model.

Synthesis and Application of Itaconic Acid Water-Coke Slurry Dispersant

2017 ◽  
Vol 896 ◽  
pp. 167-174 ◽  
Author(s):  
Zhi Yuan Yang ◽  
Zhuo Yue Meng ◽  
Zhi Hua Li ◽  
Si Tong Wang
Keyword(s):  
Surface Tension ◽  
Polyethylene Glycol ◽  
Itaconic Acid ◽  
High Performance ◽  
Ph Value ◽  
Raw Materials ◽  
Esterification Reaction ◽  
Solution Ph ◽  
Powder Surface ◽  
Coke Powder

Polyethylene glycol (PEG-200) and itaconic acid (IA) were used as raw materials to compound macromer through esterification reaction. A new type of specialized water-coke slurry dispersant was synthesized by copolymerization of microware, sodium methallyl sulfonate (SMAS) and maleic anhydride (MA). The experiment showed that the concentration of slurry could be reached to 63% with the dosage of 0.2%, and the apparent viscosity was 1140.3 mPa∙s. Through the analysis of the infrared, the dispersant was confirmed to have polyethylene glycol branched chain and hydrophilic functional groups such as carboxyl or sulfonic group. When the concentration of dispersant was 30 g/L, the surface tension of water could be decreased from 72.70 mN/m to 45.50 mN/m. Furthermore, when the solution pH value was 9, the Zeta potential of semi-coke powder surface could also be decreased from-13.38 mV to-25 mV with the addition of dispersant. Thus, this dispersant could increase electronegativity of semi-coke powder surface, enhance steric-hindrance effect and prevent the phenomenon of powder flocculation and gather. Meantime, it also could reinforce the semi-coke hydrophilic by reducing the surface tension of water effectively. And then, the high performance water-coke slurry could be obtained.

Synthesis and Characterization of CdSe Nanoparticles with Cadmium Precursor Variation in Colloidal Synthesis

2014 ◽  
Vol 976 ◽  
pp. 52-58 ◽  
Author(s):  
Janeth Sarmiento Arellano ◽  
Enrique Rosendo ◽  
Román Romano ◽  
Gabriela Nieto ◽  
Tomás Díaz ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Ph Value ◽  
Sodium Tripolyphosphate ◽  
Compositional Analysis ◽  
Cadmium Acetate ◽  
Cdse Nanoparticles ◽  
Molar Concentration ◽  
Colloidal Synthesis ◽  
Cadmium Nitrate ◽  
X Ray

A comparative study of the synthesis of cadmium selenide (CdSe) nanoparticles (NPs) using different cadmium precursors such as, cadmium nitrate (Cd (NO3)2·4H2O), cadmium acetate ((CH3COO)2Cd·2H2O) and cadmium chloride (CdCl2·2.5H2O) is presented in this work. The method used to obtain the CdSe NPs was the colloidal synthesis at low temperature and atmospheric pressure. The Cd2+ ions were obtained in aqueous solution at room temperature, the surfactant used in the process was an aqueous solution of sodium hydroxide (NaOH), penta-sodium tripolyphosphate and H2O named commonly extran, which not only helps to stabilize the NPs, but also allows adjusting the pH of the solution. Se2- ions were obtained with sodium borohydride (NaBH4) as reductant at 75 oC. The by-products from the reaction were eliminated through a cleaning process with hydrochloric acid (HCl). Molar concentration of Cd:Se was varied from 3:1 to 1:3 and the pH value was varied between 8 and 11. The obtained samples were characterized by X-ray diffraction (XRD), it was seen that the obtained NPs present cubic centered face structure. The crystallite size from the powder was calculated using the Debye-Scherrer equation and was found between 3.3 nm and 5.6 nm, the variation in size depends on the molar concentration of cadmium and selenium. Morphological study was done using scanning electron microscopy (SEM) and compositional analysis was done by energy dispersive x-ray analysis (EDAX).

scholarly journals CO2 mineralization by olivine at hydrothermal conditions

2014 ◽  
Vol 78 (6) ◽  
pp. 1473-1477
Author(s):  
Jan Přikryl ◽  
Andri Stefánsson
Keyword(s):  
Ph Value ◽  
Hydrothermal Conditions ◽  
Solution Ph ◽  
Rock Interaction ◽  
Carbonate Formation ◽  
Effects Of Temperature ◽  
Co2 Mineralization ◽  
Geochemical Reaction ◽  
Insight Into ◽  
Water Rock Interaction

The interaction of CO2-rich water with olivine was studied using geochemical reaction modelling in order to gain insight into the effects of temperature, acid supply (CO2) and extent of reaction on the secondary mineralogy, water chemistry and mass transfer. Olivine (Fo93) was dissolved at 150 and 250ºC and pCO2 of 2 and 20 bar in a closed system and an open system with secondary minerals allowed to precipitate. The progressive water–rock interaction resulted in increased solution pH, with gradual carbonate formation starting at pH 5 and various Mg-OH and Mg-Si minerals becoming dominant at pH>8. The major factor determining olivine alteration is the pH of the water. In turn, the pH value is determined by acid supply, reaction progress and temperature.

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