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Artykuły w czasopismach na temat „Acidic Dissolution”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Asta, María P. Cama, and Patricia Acero. "Dissolution kinetics of marcasite at acidic pH." European Journal of Mineralogy 22, no. 1 (2010): 49–61. http://dx.doi.org/10.1127/0935-1221/2010/0022-1981.

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2

Descostes, M., P. Vitorge, and C. Beaucaire. "Pyrite dissolution in acidic media." Geochimica et Cosmochimica Acta 68, no. 22 (2004): 4559–69. http://dx.doi.org/10.1016/j.gca.2004.04.012.

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3

Chiriţă, Paul, and J. Donald Rimstidt. "Pyrrhotite dissolution in acidic media." Applied Geochemistry 41 (February 2014): 1–10. http://dx.doi.org/10.1016/j.apgeochem.2013.11.013.

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4

Elgersma, F., G. F. Kamst, G. J. Witkamp, and G. M. van Rosmalen. "Acidic dissolution of zinc ferrite." Hydrometallurgy 29, no. 1-3 (1992): 173–89. http://dx.doi.org/10.1016/0304-386x(92)90012-o.

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5

Acero, Patricia, Jordi Cama, and Carlos Ayora. "Sphalerite dissolution kinetics in acidic environment." Applied Geochemistry 22, no. 9 (2007): 1872–83. http://dx.doi.org/10.1016/j.apgeochem.2007.03.051.

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6

Ota, Kenichiro, Yuuki Koizumi, Shigenori Mitsushima, and Nobuyuki Kamiya. "Dissolution of Platinum in Acidic Media." ECS Transactions 3, no. 1 (2019): 619–24. http://dx.doi.org/10.1149/1.2356182.

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7

Mitsushima, Shigenori, Yuki Koizumi, Shunsuke Uzuka, and Ken-Ichiro Ota. "Dissolution of platinum in acidic media." Electrochimica Acta 54, no. 2 (2008): 455–60. http://dx.doi.org/10.1016/j.electacta.2008.07.052.

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8

Arinicheva, Yulia, Stefan Neumeier, Felix Brandt, Dirk Bosbach, and Guido Deissmann. "Dissolution kinetics of synthetic LaPO4-monazite in acidic media." MRS Advances 3, no. 21 (2018): 1133–37. http://dx.doi.org/10.1557/adv.2018.205.

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Single-phase monazite-type ceramics are discussed as waste forms for the safe disposal of surplus plutonium or separated minor actinides. To derive a fundamental understanding of the long-term stability of these materials under repository relevant conditions, the dissolution kinetics of synthetic lanthanum monazite (LaPO4) were studied in dynamic dissolution experiments in the temperature range from 50 to 90°C under acidic conditions. The surface area normalised dissolution rates increased with temperature from 3.2·10-5 g m-2 d-1 at 50°C to 1.8·10-4 g m-2 d-1 at 90°C. The apparent activation e

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9

Khawmee, K., A. Suddhiprakarn, I. Kheoruenromne, I. Bibi, and B. Singh. "Dissolution behaviour of soil kaolinites in acidic solutions." Clay Minerals 48, no. 3 (2013): 447–61. http://dx.doi.org/10.1180/claymin.2013.048.3.02.

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AbstractHighly weathered soils of the tropics and subtropics commonly have kaolinitedominated clay fractions. Under acidic conditions prevailing in these soils kaolinite dissolution occurs, contributing to the high levels of soluble Al in these soils. This study evaluates the dissolution behaviour of kaolinites from subsurface horizons of highly weathered soils from Thailand, along with a soil kaolinite from Western Australia (WA kaolinite) and Georgia kaolinite (KGa-2). Kaolinite-dominated clay fractions were isolated from soils by sedimentation and chemically treated to remove iron oxides. T

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10

Feng, Qicheng, Shuming Wen, Yijie Wang, Wenjuan Zhao, and Jian Liu. "Dissolution Kinetics of Cerussite in Acidic Sodium Chloride Solutions." Bulletin of the Korean Chemical Society 36, no. 4 (2015): 1100–1107. http://dx.doi.org/10.1002/bkcs.10203.

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The dissolution kinetics of cerussite in acidic sodium chloride solutions was investigated with respect to experimental variables such as particle size, stirring speed, sodium chloride concentration, hydrochloric acid concentration, and reaction temperature. Results show that leaching reagent concentration and reaction temperature have significant effects on the extraction of lead, whereas particle size and stirring speed have a relatively moderate effect on the leaching rate. The dissolution process followed the kinetic law of the shrinking core model, and a corresponding mixed control model

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11

Lalvani, S. B., B. A. DeNeve, and A. Weston. "Prevention of Pyrite Dissolution in Acidic Media." CORROSION 47, no. 1 (1991): 55–61. http://dx.doi.org/10.5006/1.3585220.

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12

TAKENOUCHI, Toshikazu, Unkai SATO, and Shin-ichi WAKABAYASHI. "Dissolution of Nickel by Acidic Electrolyzed Water." Journal of The Surface Finishing Society of Japan 57, no. 12 (2006): 907–11. http://dx.doi.org/10.4139/sfj.57.907.

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13

Kozhina, G. A., A. N. Ermakov, V. B. Fetisov, A. V. Fetisov, and K. Yu Shunyaev. "Electrochemical dissolution of Co3O4 in acidic solutions." Russian Journal of Electrochemistry 45, no. 10 (2009): 1170–75. http://dx.doi.org/10.1134/s1023193509100097.

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14

Dorozhkin, Surgey V. "Surface Transformations of Hydroxyapatite during Acidic Dissolution." Phosphorus, Sulfur, and Silicon and the Related Elements 147, no. 1 (1999): 73. http://dx.doi.org/10.1080/10426509908053517.

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15

Taxiarchou, M., D. Panias, I. Douni, I. Paspaliaris, and A. Kontopoulos. "Dissolution of hematite in acidic oxalate solutions." Hydrometallurgy 44, no. 3 (1997): 287–99. http://dx.doi.org/10.1016/s0304-386x(96)00075-8.

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16

Anik, Mustafa, and Tuba Cansizoglu. "Dissolution kinetics of WO3 in acidic solutions." Journal of Applied Electrochemistry 36, no. 5 (2006): 603–8. http://dx.doi.org/10.1007/s10800-006-9113-3.

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17

Luo, Qiuliang. "Copper Dissolution Behavior in Acidic Iodate Solutions." Langmuir 16, no. 11 (2000): 5154–58. http://dx.doi.org/10.1021/la991626+.

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18

Cherevko, Serhiy, Angel A. Topalov, Ioannis Katsounaros, and Karl J. J. Mayrhofer. "Electrochemical dissolution of gold in acidic medium." Electrochemistry Communications 28 (March 2013): 44–46. http://dx.doi.org/10.1016/j.elecom.2012.11.040.

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19

Mitsushima, Shigenori, Yuki Koizumi, Shunsuke Uzuka, and K. Ota. "Dissolution Mechanism of Platinum in Acidic Media." ECS Transactions 11, no. 1 (2019): 1195–201. http://dx.doi.org/10.1149/1.2781033.

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20

Constantin, Cristina A., and Paul Chiriţă. "Oxidative dissolution of pyrite in acidic media." Journal of Applied Electrochemistry 43, no. 7 (2013): 659–66. http://dx.doi.org/10.1007/s10800-013-0557-y.

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21

Chiriţă, Paul, and Michaël Descostes. "Anoxic dissolution of troilite in acidic media." Journal of Colloid and Interface Science 294, no. 2 (2006): 376–84. http://dx.doi.org/10.1016/j.jcis.2005.07.047.

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22

Couperthwaite, Sara J., Sujung Han, Talitha Santini, et al. "Bauxite residue neutralisation precipitate stability in acidic environments." Environmental Chemistry 10, no. 6 (2013): 455. http://dx.doi.org/10.1071/en13048.

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Environmental context Although land remediation programs for bauxite residues aim at vegetation coverage, the stability of compounds in the residues with acids produced by the vegetation has not been investigated. We show that, despite the instability of caustic components in the residues (negative effects on plant development), this instability actually assists in neutralising acidic soils. These results further affirm the suitability and sustainability of current land remediation programs for bauxite residues in terms of minimising acidic soil formation. Abstract This investigation used a co

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23

Yan, Changqi, Boyu Yuan, Zhenhui Li, Liang Li, and Chao Wang. "Digital Holographic Study of pH Effects on Anodic Dissolution of Copper in Aqueous Chloride Electrolytes." Metals 10, no. 4 (2020): 487. http://dx.doi.org/10.3390/met10040487.

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The anodic dissolution of copper in chloride electrolytes with different pH has been investigated by using polarization measurements and digital holography. In acidic and neutral NaCl solutions, the oxidation processes of copper are almost the same: copper firstly dissolves as cuprous ions, which then produces the CuCl salt layer. The dissolution rate in the acidic solution is a little higher than that in the neutral. However, the mechanism is quite different in the alkaline NaCl solution: copper turns passive easily due to the formation of a relatively stable Cu2O film which results in pittin

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24

Costa, Mayre Aparecida Borges da, Ana Lucia Vazquez Villa, Rita de Cássia da Silva Ascenção Barros, Eduardo Ricci-Júnior, and Elisabete Pereira dos Santos. "Development, characterization and evaluation of the dissolution profile of sulfasalazine suspensions." Brazilian Journal of Pharmaceutical Sciences 51, no. 2 (2015): 449–59. http://dx.doi.org/10.1590/s1984-82502015000200022.

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<p>This paper reports the development, characterization and <italic>in vitro</italic>dissolution behavior of sulfasalazine suspensions for treatment of chronic intestinal inflammatory diseases. Three formulations were developed, from powdered sulfasalazine obtained from different suppliers. The sulfasalazine was characterized regarding concentration, Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), X-Ray Diffraction (XRD), particle size distribution, polydispersion and solubility. The suspensions were developed and characterized regardi

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25

Devivaraprasad, Ruttala, Tathagata Kar, Arup Chakraborty, Ramesh Kumar Singh, and Manoj Neergat. "Reconstruction and dissolution of shape-controlled Pt nanoparticles in acidic electrolytes." Physical Chemistry Chemical Physics 18, no. 16 (2016): 11220–32. http://dx.doi.org/10.1039/c5cp07832f.

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26

Aleman, Ashton M., Colin Flynn Crago, Gaurav A. Kamat, et al. "Coupling Time-Resolved Mass Spectrometry Techniques to Unravel Cobalt Degradation Mechanisms in Acidic Media for Oxygen and Hydrogen Electrocatalysis." ECS Meeting Abstracts MA2024-02, no. 60 (2024): 4051. https://doi.org/10.1149/ma2024-02604051mtgabs.

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Cobalt plays a significant role within sustainable energy technologies, including but not limited to hydrogen fuel cells for transportation, lithium-ion batteries for electric vehicles and portable devices, and electrolyzers for renewable hydrogen production. For devices that contain a proton exchange membrane (PEM), such as proton exchange membrane fuel cells (PEMFCs) and proton exchange membrane water electrolyzers (PEMWEs), cobalt-based materials are commonly used to perform the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER), respectively. However, the PEM in these de

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27

Shangguan, Xiangdong, Yuandong Liu, Run Liu, et al. "Enhanced Chalcopyrite Dissolution in Acidic Culture Medium: The Impact of Arsenopyrite Presence." Minerals 14, no. 1 (2023): 50. http://dx.doi.org/10.3390/min14010050.

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Nowadays, research on promoting the dissolution of chalcopyrite is important. As a natural symbiotic mineral of chalcopyrite, arsenopyrite will have an impact on the dissolution of chalcopyrite. This paper shows the influence of arsenopyrite on the dissolution of chalcopyrite in an acidic culture medium. The leaching results showed that adding arsenopyrite increased the leaching concentration of copper by 332 mg/L. The residues showed a decrease in sulfur through X-ray diffraction analysis (XRD) and an increase in dissolution degree through scanning electron microscope (SEM). Electrochemical e

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28

YAMASHITA, Satoshi, Ken-ichi NAGATSUMA, Kyoshu HATA, and Sakichi GOTO. "Dissolution of Silver in Acidic Ammonium Thiocyanate Solution." Shigen-to-Sozai 107, no. 8 (1991): 562–68. http://dx.doi.org/10.2473/shigentosozai.107.562.

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29

Amrutha, M. S., F. Fasmin, P. Ilayaraja, S. Chandran, and R. Srinivasan. "Anodic Dissolution of Ti in Acidic Fluoride Media." ECS Transactions 72, no. 17 (2016): 75–90. http://dx.doi.org/10.1149/07217.0075ecst.

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30

Kau, P. M. H., D. W. Smith, and P. J. Binning. "THE DISSOLUTION OF KAOLIN BY ACIDIC FLUORIDE WASTES." Soil Science 162, no. 12 (1997): 896–911. http://dx.doi.org/10.1097/00010694-199712000-00005.

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31

Yokel, Robert A., Matthew L. Hancock, Eric A. Grulke, Jason M. Unrine, Alan K. Dozier, and Uschi M. Graham. "Carboxylic acids accelerate acidic environment-mediated nanoceria dissolution." Nanotoxicology 13, no. 4 (2019): 455–75. http://dx.doi.org/10.1080/17435390.2018.1553251.

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32

Simpson, Darren J., Thomas Bredow, Roger St C. Smart, and Andrea R. Gerson. "Mechanisms of acidic dissolution at the MgO() surface." Surface Science 516, no. 1-2 (2002): 134–46. http://dx.doi.org/10.1016/s0039-6028(02)01977-5.

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33

Healy, A. M., and O. I. Corrigan. "Dissolution and porosity of two-component acidic compacts." European Journal of Pharmaceutical Sciences 4 (September 1996): S186. http://dx.doi.org/10.1016/s0928-0987(97)86573-6.

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34

Bugajski, Jerzy, and Heinz Gamsj�ger. "Dissolution kinetics of MgO in aqueous, acidic media." Monatshefte f�r Chemie Chemical Monthly 117, no. 6-7 (1986): 763–72. http://dx.doi.org/10.1007/bf00810067.

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35

Okuyama, Masaru, Masahiro Kawakami, and Koin Ito. "Anodic dissolution of chromium in acidic sulphate solutions." Electrochimica Acta 30, no. 6 (1985): 757–65. http://dx.doi.org/10.1016/0013-4686(85)80124-9.

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36

Yang, Xiyun, Michael S. Moats, and Jan D. Miller. "Gold dissolution in acidic thiourea and thiocyanate solutions." Electrochimica Acta 55, no. 11 (2010): 3643–49. http://dx.doi.org/10.1016/j.electacta.2010.01.105.

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37

Acero, Patricia, Jordi Cama, and Carlos Ayora. "Rate law for galena dissolution in acidic environment." Chemical Geology 245, no. 3-4 (2007): 219–29. http://dx.doi.org/10.1016/j.chemgeo.2007.08.003.

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38

Alí, Salvador P., Miguel A. Blesa, Pedro J. Morando, and Alberto E. Regazzoni. "Reductive Dissolution of Hematite in Acidic Iodide Solutions." Langmuir 12, no. 20 (1996): 4934–39. http://dx.doi.org/10.1021/la960203u.

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39

Abd El Aal, E. E., W. Zakria, A. Diab, and S. M. Abd El Haleem. "Anodic Dissolution of Nickel in Acidic Chloride Solutions." Journal of Materials Engineering and Performance 12, no. 2 (2003): 172–78. http://dx.doi.org/10.1361/105994903770343312.

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40

Franke, M. D., W. R. Ernst, and A. S. Myerson. "Kinetics of dissolution of alumina in acidic solution." AIChE Journal 33, no. 2 (1987): 267–73. http://dx.doi.org/10.1002/aic.690330213.

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41

Sandbeck, Daniel J. S., Olaf Brummel, Karl J. J. Mayrhofer, Jörg Libuda, Ioannis Katsounaros, and Serhiy Cherevko. "Dissolution of Platinum Single Crystals in Acidic Medium." ChemPhysChem 20, no. 22 (2019): 2997–3003. http://dx.doi.org/10.1002/cphc.201900866.

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42

Bonomi, Chiara, Alexandra Alexandri, Johannes Vind, Angeliki Panagiotopoulou, Petros Tsakiridis, and Dimitrios Panias. "Scandium and Titanium Recovery from Bauxite Residue by Direct Leaching with a Brønsted Acidic Ionic Liquid." Metals 8, no. 10 (2018): 834. http://dx.doi.org/10.3390/met8100834.

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In this study, bauxite residue was directly leached using the Brønsted acidic ionic liquid 1-ethyl-3-methylimidazolium hydrogensulfate. Stirring rate, retention time, temperature, and pulp density have been studied in detail as the parameters that affect the leaching process. Their optimized combination has shown high recovery yields of Sc, nearly 80%, and Ti (90%), almost total dissolution of Fe, while Al and Na were partially extracted in the range of 30–40%. Si and rare earth element (REEs) dissolutions were found to be negligible, whereas Ca was dissolved and reprecipitated as CaSO4. The s

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43

Nyembwe, Kolela J., Elvis Fosso-Kankeu, Frans Waanders, and Martin Mkandawire. "Iron-Speciation Control of Chalcopyrite Dissolution from a Carbonatite Derived Concentrate with Acidic Ferric Sulphate Media." Minerals 11, no. 9 (2021): 963. http://dx.doi.org/10.3390/min11090963.

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The mechanisms involved in the dissolution of chalcopyrite from a carbonatite concentrate in a ferric sulphate solution at pH 1.0, 1.5 and 1.8, and temperatures 25 °C and 50 °C were investigated. Contrary to expectations and thermodynamic predictions according to which low pH would favour high Cu dissolution, the opposite was observed. The dissolution was also highly correlated to the temperature. CuFeS2 phase dissolution produced intermediate Cu rich phases: CuS, Cu2S and Cu5FeS4, which appeared to envelop CuFeS2. Thermodynamic prediction revealed CuS to be refractory and could hinder dissolu

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44

Narangarav, T., Sh Nyamdelger, G. Ariunaa, T. Azzaya, and G. Burmaa. "Dissolution behavior of copper concentrate in acidic media using nitrate ions." Mongolian Journal of Chemistry 15 (December 12, 2014): 79–84. http://dx.doi.org/10.5564/mjc.v15i0.328.

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This study was conducted to investigate the dissolution process of copper concentrate using sodium nitrate (NaNO3) in a sulfuric acid (H2SO4) medium under various controlling parameters, including dissolution temperature, time, particle size, solid/liquid (S/L) ratio and concentration of NaNO3 and H2SO4. The thermodynamic probability of mineral dissolution (CuFeS2, Cu2S, CuS, FeS2) reaction in the concentrate was estimated by standard Gibbs energy. The activation energy (Ea) for the dissolution of copper concentrate was calculated as 15.96kJ/mol. Batch experimental results show that about 89.9

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45

Zvimba, J. N., J. Mulopo, M. De Beer, L. Bologo, and M. Mashego. "The dissolution characteristics of calcium sulfide and utilization as a precipitation agent in acidic wastewater effluent treatment." Water Science and Technology 63, no. 12 (2011): 2860–66. http://dx.doi.org/10.2166/wst.2011.599.

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The dissolution characteristics of CaS in the presence of CO2 has been investigated by monitoring sulfide speciation, solution conductivity and pH during dissolution. The sulfide speciation associated with CaS dissolution was utilized for metal precipitation from acidic wastewater effluents. The mechanism involved in the dissolution process was observed to be pH-dependent, characterized by increased solution conductivity as the HS− species becomes dominant in solution in the form of the Ca(HS)2 complex. The replacement of HS− by CO32− in the Ca(HS)2 complex triggered CaCO3 precipitation and H2

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46

Tsuchiya, Hiroaki, Yo Iwasaki, Shouta Wakeya, and Masato Yamashita. "Effects of Metallic Cation on the Structure and Protectiveness of Corrosion Product Layers Formed on a Galvanized Steel." ECS Meeting Abstracts MA2025-01, no. 20 (2025): 1324. https://doi.org/10.1149/ma2025-01201324mtgabs.

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Carbon steel is widely used for various infrastructures as a structural material owing to its superior mechanical properties. However, it is prone to corrode during wet/dry cycles in atmospheric environments. Although zinc plating is often used as a typical countermeasure to suppress the atmospheric corrosion of carbon steel, the dissolution rate of zinc is strongly pH-dependent, in particular, the dissolution rate is extremely large in acidic environments. Therefore, the application of galvanized steel has been prevented in such environments. We recently reported that the atmospheric corrosio

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47

Chen, Wenjun, Jingyun Jiang, Xue Lan, Xinhui Zhao, Hongyu Mou, and Tiancheng Mu. "A strategy for the dissolution and separation of rare earth oxides by novel Brønsted acidic deep eutectic solvents." Green Chemistry 21, no. 17 (2019): 4748–56. http://dx.doi.org/10.1039/c9gc00944b.

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48

Widantha, Komang Widhi. "Immersion Behavior Study of Hydroxyapatite Scaffolds Derived from Bovine Sources In Acidic, Basic, and Neutral Solutions." Frontier Advances in Applied Science and Engineering 2, no. 1 (2024): 57–65. http://dx.doi.org/10.59535/faase.v2i1.296.

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This research investigates the effects of particle size and compaction pressure on the dissolution behavior of hydroxyapatite scaffolds synthesized from bovine bone in acidic neutral and basic solutions. Hydroxyapatite was extracted through a process involving cutting, cleaning, boiling, soaking in NaOH, sun drying, grinding into powder and calcination at 800°C. The powder was then sieved into two size fractions (75 and 150 microns) and compacted at pressures of 200, 250, and 300 MPa. The mass and dimensions of the scaffolds were measured to calculate porosity, followed by immersion in the res

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49

Abdul Kuddus, Syed, Afsana Alam, Abdullah Md. Sifat, et al. "Effect of Polymer Concentration on the Release of Naproxen from Enteric Coated Sustained Release Tablets." Journal of Biosciences and Experimental Pharmacology 1, no. 1 (2023): 70–90. https://doi.org/10.62624/jbep00.0005.

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Five different formulations of naproxen sodium core tablets were prepared using different amounts of Methocel K15M CR by direct compression method. From a particular formulation, 50 % of tablets were kept uncoated and enteric coating was applied to the remaining 50 % using cellulose acetate phthalate (6 % w/w). Dissolution, swelling and erosion tests of uncoated tablets were conducted 8 hours in phosphate buffer (pH 7.4). For enteric coated tablets, dissolution test was performed for first 2 hours in acidic medium (pH 1.2) then 8 hours in phosphate buffer (pH 7.4). Enteric coating was able to

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50

Stojanovski, Kevin, Valentin Briega Martos, Matej Zlatar, and Serhiy Cherevko. "A Comparative Study on Gold Dissolution in Broad pH Range from Acidic to Alkaline Media." ECS Meeting Abstracts MA2022-02, no. 56 (2022): 2155. http://dx.doi.org/10.1149/ma2022-02562155mtgabs.

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Gold is often employed in nanotechnology to develop biosensors and new drug delivery and cancer therapy strategies. Since these applications are used in physiological pH, understanding the stability of gold in a broader pH range including neutral values will provide an useful insight into how to expand the use of gold safely. By using buffer solutions with a constant concentration of phosphate species, electrochemical dissolution of gold in pH 1, 3, 5, 7, 9, 11 and 12.7 was investigated. The concentration of phosphate species was kept constant in order to minimize the possible effect of anion

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