Zeta potential of CO2-rich aqueous solutions in contact with intact sandstone sample at temperatures of 23°C and 40°C and pressures up to 10.0 MPa

Author(s):  
Miftah Hidayat ◽  
Mohammad Sarmadivaleh ◽  
Jos Derksen ◽  
David Vega-Maza ◽  
Stefan Iglauer ◽  
...  
2021 ◽  
pp. 58-62
Author(s):  
Dmitrii I. Belenkii ◽  
Dmitry V. Averkin ◽  
Dmitry V. Vishnevetskii ◽  
Svetlana D. Khizhnyak ◽  
Pavel M. Pakhomov

A comprehensive study to develop and create standard samples of the zeta potential unit of particles in a liquid in accordance with the requirements of GOST ISO 13099-2-2016 in the range of measured values from minus 150 mV to plus 150 mV was carried out. The existing standard samples of zeta potential in Russia and the world have been investigated; the analysis of the applicability of the starting materials and components for the creation of new standard samples has done. Samples based on modified polystyrene latex microspheres, bovine serum albumin and supramolecular systems based on aqueous solutions of L-cysteine, N-acetylcysteine, and silver acetate were considered as promising standard samples of the zeta potential of particles. All studies were carried out on equipment from the State Primary Standard of Dispersed Parameters of Aerosols, Suspensions and Powder Materials GET 163-2020 using the method of electrophoretic light scattering and measuring the pH value. It was found that polystyrene latex microspheres do not correspond to the requirements of the work in terms of developing a set of standard samples. Samples based on suspensions of bovine serum albumin do not correspond to the requirements of GOST ISO 13099-2-2016. Supramolecular systems based on aqueous solutions of L-cysteine, N-acetylcysteine, and silver acetate were proposed as standard samples. Such systems are characterized by the ability to modify the initial potential-determining layer of particles without changing their aggregate stability. Studies of the long-term stability of the developed standard samples of the zeta-potential unit of particles in a liquid have been carried out.


Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1109
Author(s):  
Manar Derhy ◽  
Yassine Taha ◽  
Rachid Hakkou ◽  
Mostafa Benzaazoua

The way to successfully upgrade a phosphate ore is based on the full understanding of its mineralogy, minerals surface properties, minerals distribution and liberation. The conception of a treatment process consists of choosing the proper operations with an adequate succession depending on the ore properties. Usually, froth flotation takes place in phosphate enrichment processes, since it is cheap, convenient, and well developed. Nevertheless, it is a complex technique as it depends on the mineral’s superficial properties in aqueous solutions. Aspects such as wettability, surface charge, zeta potential, and the solubility of minerals play a basic role in defining the flotation conditions. These aspects range from the reagents type and dosage to the pH of the pulp. Other variables namely particles size, froth stability, and bubbles size play critical roles during the treatment, as well. The overall aim is to control the selectivity and recovery of the process. The following review is an attempt to add to previous works gathering phosphate froth flotation data. In that sense, the relevant parameters of phosphate ores flotation are discussed while focusing on apatite, calcite, dolomite, and quartz as main constituent minerals.


Coatings ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 471 ◽  
Author(s):  
Huiying Cao ◽  
Baichao An ◽  
Yong Wang ◽  
Kun Zhou ◽  
Naiyan Lu

Nano/submicron particles can be activated by surfactants and aggregate at the air-water interface to generate and stabilize foams. Such systems have been applied extensively in the food, medicine, and cosmetic industries. Studying particle charging behavior in a particle/surfactant/water system is a fundamental way to understand the activation of the particle surface. This paper presents an investigation of the charging behavior of polystyrene (PS) particles dispersed in aqueous solutions of the surfactant sodium di-2-ethylhexylsulfosuccinate (AOT). The results showed that zeta potential of PS was related to the AOT concentration with two different concentration regions. Below the critical micelle concentration (CMC), the charging of PS particles was effected by AOT ions; while above the CMC, it came from both AOT ions and AOT micelles. This behavior was different from that observed for PS in aqueous salt solutions. Additionally, the particle concentration and size were found to affect the zeta potential differently in the two AOT concentration regions. By analyzing these results, the charging mechanism of the PS/AOT/water system was revealed to be preferential adsorption. In summary, the study disclosed the internal connection between the PS charging in aqueous AOT solution and the activation of PS particles, as well as their influence to foam formation and stability.


2018 ◽  
Vol 143 ◽  
pp. 129-135 ◽  
Author(s):  
Kejian Wei ◽  
Lin Chen ◽  
Yao Qu ◽  
Yifan Zhang ◽  
Xiaoyue Jin ◽  
...  

2019 ◽  
Vol 7 (2) ◽  
pp. 88-95
Author(s):  
Victor Maksin ◽  
Olga Kochkodan ◽  
Lidiya Kovshun

Adsorption of binary mixtures of sodium hexadecyl sulfate and oxyethylated octylphenols surfactants from aqueous solutions at activated carbon AG-3 was studied. It is found that the process of mixed adsorption depends on total surfactants concentration in the mixture, the ratio of components in the mixture and their surface activity. Adsorption data is confirmed by measurements of the zeta potential values of activated carbon particles in the surfactants mixtures.


2016 ◽  
Vol 23 (04) ◽  
pp. 1650023 ◽  
Author(s):  
LINGYUN LIU ◽  
FANFEI MIN ◽  
FANGQIN LU ◽  
MINGXU ZHANG ◽  
SHAOXIAN SONG

In this work, a novel method to determine the point of zero net proton charge (PZNPC) of colloidal kaolinite in aqueous solutions was presented through the measurement of zeta potential of the particles in various concentrations of NaCl solution and the mathematic regression of the zeta potential versus pH curves. This method is based on the observation that there are two common intersection points (CIP) in the two curves of zeta potential versus pH of colloidal kaolinite with a low and a high NaCl concentration. The observation might be attributed to that NaCl would compress the electric double layer of kaolinite particles and affect the efficiency of the protonation/deprotonation of the HD-faces. The experimental result showed that the PZNPC of kaolinite is 5.37.


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