Relevant bibliographies by topics / Dissoluion

Academic literature on the topic 'Dissoluion'

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Published: 30 May 2022
Last updated: 31 May 2022

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Journal articles on the topic "Dissoluion"

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Bech-Nielsen, G., and J. C. Reeve. "The Anodic Dissolution of Iron XII. Recent Findings Supplementing the Information about the Kinetics of the Dissoluion Reactions." Key Engineering Materials 20-28 (January 1991): 239–48. http://dx.doi.org/10.4028/www.scientific.net/kem.20-28.239.

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BRUYAKA, OLGA P. "ALLIANCE PARTNER DIVERSITY AND BIOTECH FIRMS' EXIT: DIFFERING EFFECTS ON DISSOLUION VS. DIVESTMENT." Academy of Management Proceedings 2008, no. 1 (August 2008): 1–6. http://dx.doi.org/10.5465/ambpp.2008.33622325.

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Suter, D., C. Siffert, B. Sulzberger, and W. Stumm. "Catalytic dissoluion of iron(III)(hydr)oxides by oxalic acid in the presence of Fe(II)." Naturwissenschaften 75, no. 11 (November 1988): 571–73. http://dx.doi.org/10.1007/bf00377723.

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Truesdale, Victor W. "Tidying up the environment: A journey from exponential curves to hydrodynamics in environmental batch dissolutions." Pure and Applied Chemistry 83, no. 5 (February 21, 2011): 1113–28. http://dx.doi.org/10.1351/pac-con-10-08-13.

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This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left-over, and those in the middle ground where saturation is approached or attained, but where much of the solid originally added dissolves. The equations that describe these conditions are discussed, alongside sample results that validate their use with test substances, for example, salts, sucrose, silica gel, and gypsum. The equations are then shown to be consistent with the hydrodynamic approach to dissolution. Finally, further work with middle-ground dissolutions of gypsum lead to a mechanism for the back-reaction, which involves the CaSO40 ion-pair. After comparison with existing studies of calcium carbonate dissolution, it is argued that this is a universal mechanism for salt dissolutions. The work improves batch dissolution as a technique to the point where it can be used synergistically with chemo-stat and rotating disc approaches. Suggestions are made for greater standardization in dissolution conditions, especially in environmental work where the data collected has to have global consistency.
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Kawanishi, Sakiko, Hiroyuki Shibata, and Takeshi Yoshikawa. "Contribution of Dislocations in SiC Seed Crystals on the Melt-Back Process in SiC Solution Growth." Materials 15, no. 5 (February 27, 2022): 1796. http://dx.doi.org/10.3390/ma15051796.

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The melt-back process has a significant effect on the quality of solution-grown SiC crystals. However, the phenomena surrounding the SiC dissolution into the molten alloy during the melt-back process have not been clarified. In this study, the behavior of 4H-SiC dissolution into molten alloy was investigated by using high-temperature in situ observation and subsequent KOH etching, and the effects of different doping conditions and crystal polarity were studied. Local dissolutions with hexagonal pyramid-shape originating from threading screw dislocation (TSD) were observed on the C face of n-type SiC with light nitrogen doping. Our analysis of their behavior revealed that the process was governed by the spiral dissolution. In addition to the dissolution at TSD, local dissolutions at threading-edge dislocations were observed on the Si face of the same crystal. The shape of the local dissolution at the dislocation was significantly affected by the doping conditions and the polarity of the SiC crystal. This local dissolution may occur during the melt-back process, suggesting that it is important to promote the dissolution while maintaining a smooth interface through the selection of the seed crystal and by keeping the degree of interface undersaturation small.
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Gupta, V. Rama Mohan, Srikanth K, Sree Giri Prasad, B, G. Naveen Kumar Reddy, and Sudheer B. "Formulation and Evaluation of Directly Compressible Agglomerates of Celecoxib." International Journal of Pharmaceutical Sciences and Nanotechnology 3, no. 4 (February 28, 2011): 1193–204. http://dx.doi.org/10.37285/ijpsn.2010.3.4.4.

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Prepared spherical crystals of Celecoxib to increase the compressible properties, dissolution rate and bioavailability, using hydrophilic polymers such as PEG-4000, sod.CMC, sod.alginate and PVP K-30. All the formulations were characterized for micromeritic properties, Drug loading, solubility, in vitro drug release and mean dissolutiom time (MDT). New formulations showed higher dissolution rates and less MDT values than the pure celecoxib. Among all, the crystals prepared with 10 % w/v PVP K-30 exhibited maximum dissolution rate (2.95±0.23%) and very less MDT values (18.50 ± 4.01 min). Hence it was considered as optimized formulation.
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Kim, Tae Hwan, Soyoung Shin, Seok Won Jeong, Jong Bong Lee, and Beom Soo Shin. "Physiologically Relevant In Vitro-In Vivo Correlation (IVIVC) Approach for Sildenafil with Site-Dependent Dissolution." Pharmaceutics 11, no. 6 (June 1, 2019): 251. http://dx.doi.org/10.3390/pharmaceutics11060251.

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This study aimed to establish a physiologically relevant in vitro-in vivo correlation (IVIVC) model reflecting site-dependent dissolution kinetics for sildenafil based on population-pharmacokinetic (POP-PK) modeling. An immediate release (IR, 20 mg) and three sustained release (SR, 60 mg) sildenafil tablets were prepared by wet granulation method. In vitro dissolutions were determined by the paddle method at pH 1.2, 4.5, and 6.8 media. The in vivo pharmacokinetics were assessed after oral administration of the prepared IR and SR formulations to Beagle dogs (n = 12). The dissolution of sildenafil from SR formulations was incomplete at pH 6.8, which was not observed at pH 1.2 and pH 4.5. The relative bioavailability was reduced with the decrease of the dissolution rate. Moreover, secondary peaks were observed in the plasma concentration-time curves, which may result from site-dependent dissolution. Thus, a POP-PK model was developed to reflect the site-dependent dissolution by separately describing the dissolution and absorption processes, which allowed for estimation of the in vivo dissolution of sildenafil. Finally, an IVIVC was established and validated by correlating the in vitro and in vivo dissolution rates. The present approach may be applied to establish IVIVC for various drugs with complex dissolution kinetics for the development of new formulations.
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Nasaruddin, Indo Yama. "Efficiency and Effectiveness of Disclosure of Cooperation with Online." Esensi: Jurnal Bisnis dan Manajemen 10, no. 1 (December 24, 2020): 95–108. http://dx.doi.org/10.15408/ess.v10i1.17826.

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This research measures the efficiency and effectiveness of the dissolution of cooperatives conducted online. To see the efficiency and effectiveness of using cooperative dissolution performance variables, utilization of online services, performance in online services and interest in utilizing online services for cooperatives in cooperative dissolution activities. The analysis technique used is descriptive analysis by looking at the percentage of answers from respondents. The object of this research is cooperatives that are listed as cooperatives which are dissolved in the area of East Java Province and Yogyakarta Special Region as regions that have many cooperative dissolutions. The results showed that the performance of the dissolution of cooperatives in the Special Region of Yogyakarta and East Java Province was an average of 3.53 in the predicate of moderate capacity. Utilization of online services is quite high. The performance of online services obtained the average results of respondents' answers of 4.09 are in the predicate of high capacity. Interest in the need for cooperative online services as an alternative to cooperative dissolution systems in the Special Region of Yogyakarta and East Java Province is high.
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Lasaga, Antonio C., and Andreas Lüttge. "Mineralogical approaches to fundamental crystal dissolution kinetics - Dissolution of an A3B structure." European Journal of Mineralogy 16, no. 5 (October 18, 2004): 713–29. http://dx.doi.org/10.1127/0935-1221/2004/0016-0713.

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Baihaqi, Ahmad Ichsan, Dyah Utami Cahyaning Rahayu, and E. Budianto. "Effect of Drug Loading Method on Drug Dissolution Mechanism of Amoxicillin Trihydrate Encapsulated in Chitosan-Poly(N-Vinylpyrrolidone) Full-IPN Hydrogel as a Floating Drug Delivery System Matrix." Materials Science Forum 964 (July 2019): 251–56. http://dx.doi.org/10.4028/www.scientific.net/msf.964.251.

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Amoxicillin trihydrate suits to be encapsulated into a modified matrix to increase its bioavailability. In this study, the effect of drug loading methods on drug dissolution mechanism from chitosan-poly(N-vinylpyrrolidone) hydrogel with CaCO3 as the effervescent agent has been studied. It was found that the encapsulation efficiency of in situ and post loading methods were 93% and 75%, respectively. The dissolution values were 94% and 98%, respectively for in situ and post loading. The dissolution test data was incorporated into zero-order, first-order, Higuchi and Korsmeyer-Peppas models to evaluate the kinetic and the mechanism of the drug dissolutions. The in situ loading method fits well to first-order model (R2 = 0.9772), while the post loading method fits well to Higuchi model (R2 = 0.9880). Based on Korsmeyer-Peppas model, the dissolution mechanism of in situ loading was Fickian diffusion (n = 0.4024), while post loading was a combination of diffusion and erosion (n = 0.5532). From the SEM images, it showed that the surface and cross-sectional of the post loading method hydrogel formed pores and pore channels, both before and after the dissolution test. Meanwhile, on the surface and the cross-sectional of in situ loading method hydrogel had pores and pore channels only after dissolution test.
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Dissertations / Theses on the topic "Dissoluion"

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Портюх, Крістіна Валеріївна. "Цех з виробництва паперу для простирадл з целюлози у системі Публічного акціонерного товариства «Кохавинська паперова фабрика» з розробленням технологічного потоку." Bachelor's thesis, КПІ ім. Ігоря Сікорського, 2019. https://ela.kpi.ua/handle/123456789/29114.

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Дипломний проект: стор.85 , рис.3 , табл.11 , першоджерел 11, додатків 1. Метою дипломного проекту було розроблення технологічного потоку з виробництва паперу для простирадл з целюлози на основі Публічного акціонерного товариства «Каховинська паперова фабрика». Наведено стандарти та сертифікати якості на сировину, хімікати та готову продукцію. Розроблено та описано технологічну схему з виробництва паперу для простирадл. Розраховано матеріальний баланс води та волокна, а також тепловий баланс контактно-конвективного методу сушіння, для виробництва 1 т продукції. Проведено розрахунок та вибір основного обладнання. Описано об’ємно-планувальне і конструктивне рішення будівлі цеху. Наведені заходи щодо охорони навколишнього середовища.
Diploma project: pag. 85, draw. 3, 11 tables, primary sources 11, addition 1 The purpose of the diploma project was to develop a technological flow for the production of paper for a sheet on the basis of the Public Joint Stock Company "Kakhovinsky Paper Mill". The standards and quality certificates for raw materials, chemicals and finished products are given. A technological scheme for the production of sheet metal sheets has been developed and described. The material balance of water and fiber has been calculated, as well as the thermal balance of contact-convection drying method, for the production of 1 ton of product. The calculation and selection of basic equipment has been carried out. The volume-planning and constructive decision of the building of the shop is given. The measures on environmental protection are given.
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Frisby, Brandi N. "Communicative facework in marital dissolution and post-dissolution processes." Morgantown, W. Va. : [West Virginia University Libraries], 2010. http://hdl.handle.net/10450/11241.

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Thesis (Ph. D.)--West Virginia University, 2010.
Title from document title page. Document formatted into pages; contains viii, 159 p. Includes abstract. Includes bibliographical references (p. 108-125).
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Hougaard, Sunesen Vibeke. "Biorelevant dissolution media to simulate in vivo dissolution of poorly soluble drugs /." Cph. : The Danish University of Pharmaceutical Sciences, 2003. http://www.dfuni.dk/phd/defences/vibekehougaardsunesen.htm.

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Cordara, Théo. "Effet de la présence de produits de fission sur les mécanismes de dissolution de composés modèles à base de dioxyde d'uranium." Thesis, Montpellier, 2017. http://www.theses.fr/2017MONTT176/document.

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L’étape de dissolution des combustibles nucléaires usés, réalisée en milieu nitrique concentré, est complexe notamment du fait de leur complexité chimique et microstructurale à l’issue de leur passage en réacteur. Ainsi, la présence de produits de fission (PF) localisés au sein des différentes phases cristallines constitutives du combustible usé peut en impacter la vitesse de dissolution. Dans ce cadre, trois systèmes représentatifs du matériau combustible initial UO2, de UO2 contenant des PF dissous au sein de la phase fluorine ou formant de précipités métalliques ont été obtenus par conversion de précurseurs préparés par voie humide (oxalate, hydroxyde). Pour chaque système, des pastilles denses et de microstructures proches de celle retrouvée au sein du combustible usé ont été préparées à l’issue d’une étape de mise en forme suivie d’un traitement thermique à haute température.L’étude multiparamétrique de la dissolution (approche macroscopique) conduite dans plusieurs solutions d’acide nitrique et à diverses températures a souligné l’impact important joué par la composition chimique sur la durabilité chimique des échantillons. Ainsi, l’incorporation d’éléments lanthanide a conduit à une augmentation de la vitesse de dissolution par rapport à l’échantillon UO2 de référence, laquelle est demeurée largement inférieure à celle relevée en présence d’éléments platinoïde. Par ailleurs, les effets de l’acidité et de la température du milieu sur la vitesse de dissolution ont été examinés et des modifications significatives dans le mécanisme de dissolution prépondérant ont été suggérées pour des concentrations d’acide nitrique supérieures à 0,5 mol.L-1.Pour les trois systèmes sélectionnés, l’évolution de l’interface solide/solution a également été suivie en cours de dissolution à travers une étude operando, réalisée par Microscopie Electronique à Balayage en mode Environnemental (approche microscopique). En présence d’éléments lanthanide ou à proximité des éléments platinoïde métalliques, ce suivi a démontré l’existence de zones de dissolution préférentielles dont les joints de grains et les jonctions triples. Le couplage des résultats obtenus à travers ces deux approches a permis de fournir des données complémentaires en vue d’une meilleure compréhension des mécanismes de dissolution mis en jeu en présence des différents PF considérés
The dissolution of spent nuclear fuels, performed in concentrated nitric acid solution, is a complex process due to some chemical and microstructural heterogeneities. As instance, the presence of Fission Products (FP) in various phases constitutive of spent nuclear fuels can affect the chemical durability of the materials. In this context, three systems of interest representing fresh UO2 used as reference material, and UO2 doped with FP products dissolved in the fluorite structure (lanthanide elements) or incorporated as metallic precipitates (platinoids) were prepared by oxalic or hydroxide precipitation. Dense pellets with microstructure representative for spent nuclear fuel were prepared through sintering step at high temperature.The multiparametric study of the dissolution (macroscopic approach) was developed by varying independently several parameters. While incorporation of lanthanide elements induced a significant increase of the normalized dissolution rates, it remained lower compared to that observed for platinoids. Moreover, increase of nitric acid concentration or temperature led to the decrease of the chemical durability of the prepared materials. Additionally, significant modification of the preponderant mechanism of dissolution occurred for nitric acid concentration higher than 0.5 mol.L-1.For the three selected systems, the monitoring of the evolving solid/solution interface (microscopic approach) was performed operando by Environmental Scanning Electron Microscopy. Compared to pure UO2, the presence of FP (lanthanide elements or metallic platinoids) induced preferential dissolution of grain boundaries and triple junctions. Coupling the results obtained from micro- and macroscopic approaches led to complementary data of strong interest in order to improve the understanding of the role of FP during the dissolution of UO2
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Moore, Christopher Michael. "Dissolution Caves of Mississippi." MSSTATE, 2006. http://sun.library.msstate.edu/ETD-db/theses/available/etd-04132006-090433/.

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The purpose of this project was to distinguish between the karst and pseudokarst caves throughout Mississippi, create an inventory and survey of representative caves and karst features, identify the geology of the rocks hosting the caves, and produce a GIS-based digital karst map. The State of Mississippi is not known for its karst features, yet there are three distinct limestone units that contain dissolution caves: 1) Paleozoic (Mississippian) Tuscumbia Formation limestone; 2) Mesozoic carbonate units; and 3) Cenozoic limestone, Marianna Formation. There are a total of 44 caves known within the state based on past documentation, however the caves listed are not always differentiated between karst or pseudokarst features. This study located and mapped 20 caves, of which 18 were karst caves from eight counties and two were pseudokarst caves from two counties. Four of these caves were newly discovered karst caves, increasing the state total to 48; however two separate karst caves were connected, which makes the final state total 47 caves. Of the remaining 28 caves not surveyed, 11 were pseudokarst caves from eight counties and were not studied because the focus was on dissolutional karst caves. The remaining 17 missing karst caves either had been destroyed, access permission could not be obtained, or the caves could not be located. No active caving organizations exist in Mississippi to preserve cave location data or the caves themselves. Mining, deforestation, and other land use procedures have altered the landscape, resulting in concealment of some caves, and completely or partially destroying other caves.
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Feder, Jens. "Diffusion, dissolution and dispersion." Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-184715.

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Allen, Ansgar. "The dissolution of meritocracy." Thesis, University of Sheffield, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540602.

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Chen, Y. "Granule dissolution and disintegration." Thesis, University of Cambridge, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597529.

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The increasing use of granular materials in the chemical, petrochemical, food and pharmaceutical industries, both as intermediate and as end products, gives rise to the need for a better understanding of granule dissolution and disintegration (GDD). However, little is understood about the physical principles controlling the release of active ingredients from granules, a crucial knowledge for the design of product structure in order to optimise product performance. The aim of this work is to bring a scientific approach to the study of GDD in a systematic way. which has not been addressed hitherto. The work here is to highlight the testing of these hypotheses and provide insight into GDD mechanisms. The scientific concern in this thesis is to attempt to reveal the unique behaviour of GDD that is different from homogeneous material dissolution. Unlike homogeneous material dissolution, which depends mainly on the chemical properties of the solute and solvent, GDD is more complicated because the heterogeneous system involves mixed insoluble particles and soluble binder. Further complexity lies in the fact that various physical properties such as granule size, primary particle size, binder-solid ratio and internal pore structure play in influencing GDD behaviour. This thesis reports experiments and theoretical analysis of such GDD behaviour. Four hypotheses - reaction-limited consumption of binder, transport limit for binder removal, transport limit for particle removal and additional Hmit for particle and binder removal - were proposed to cover all of the possible GDD mechanisms. Theories were developed and experiments were set up to test the theory and give explanation of various limiting cases of GDD. A bimodal population balance model was developed. Furthermore, a dynamic shrinking-shell and core model was proposed to clarify GDD mechanisms. The analysis, which has its origin in comparing binder and particle transport coefficients, enables prediction of whether particle or binder transport will hmit GDD process. This evolved into a Sherwood number analysis, which provides a direct physical account of the controlling step. Based on a non-synchronous binder and particle transport analysis, a shrinking shell and core model was proposed to highlight that binder transport may be limited by internal particle shell build-up in the granule. A dynamic model was then developed to provide quantitative analysis of the binder Sherwood number, which was tested by experiment. A rigorous deduction of the model provided a clear physical meaning of the parameters in the equations. To demonstrate the theory and test hypotheses, an ionic binder, zeolite-NaLAS was used in high shear granulation, low shear granulation, fluidised bed granulation and spray drying granulation to provide a range of granule structures and to allow investigation of GDD by both PSD and electrical conductivity. Granules were characterised using mercury porosimetry, sieving, bulk density, particle size analyser and SEM to provide information concerning their various properties, such as binder content, internal pore structure and volume fraction, granule size and primary particle size distribution, as well as surface morphology and granule internal structure. Two main methodologies were adopted to investigate GDD behaviour including a): monitoring electrical conductivity and granule diameter simultaneously for a single granule; b) monitoring the evolution of the PSD by laser light scattering. Those results were analysed to support the theory. In general, the phenomena in GDD are quite different from the general cases of dissolution.
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Cha, Minsu. "Mineral dissolution in sediments." Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/50144.

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Mineral dissolution is an inherent chemo-hydro-mechanical coupled diagenetic process in sediments. This ubiquitous geological phenomenon affects all properties in sediments, however, its engineering impact remains largely unknown. This research centers on the effects of mineral dissolution on sediment behavior with emphasis on dissolution modes in nature and their engineering implications. Five different dissolution modes are identified: homogeneous, pressure-dependent, and localized dissolution, and the dissolution of shallow and deep dissolvable inclusions. The consequences of each dissolution mode are investigated through experiments and discrete element methods. While each dissolution mode triggers unique consequences, it is observed that in all cases 1) significant displacement takes places during dissolution, 2) there is a pronounced effect of internal friction and the extent of dissolution on the evolution of the sediment, 3) the sediment has higher compressibility and exhibits a more contractive tendency after dissolution, 4) a porous honeycomb-shaped internal fabric develops accompanied by contact force concentration along dissolved inclusions, and 5) horizontal stress reduction takes place during dissolution and shear localization may develop under zero lateral strain conditions. Mineral dissolution has important engineering implications, from soil characterization to slope stability and shallow foundations. Pre- and post-dissolution CPT studies show that dissolution decreases the tip resistance proportional to the extent of dissolution. Dissolution in sloping ground induces global settlement as the prevailing deformation pattern, and prominent lateral movements near the slope surface; sudden undrained shear failure may take place during otherwise quasi-static dissolution. While footings experience larger settlements during post-dissolution loading, subsequent dissolution beneath a previously loaded footing causes displacements that are greater than the sum of dissolution-induced and load-induced settlements.
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Feder, Jens. "Diffusion, dissolution and dispersion." Diffusion fundamentals 16 (2011) 19, S. 1, 2011. https://ul.qucosa.de/id/qucosa%3A13748.

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Books on the topic "Dissoluion"

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Sansom, C. J. Dissolution. New York: Viking, 2003.

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Tarrant, Newell. Dissolution. Coral Springs, FL: Llumina Press, 2004.

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Byers, Richard Lee. Dissolution. Renton, WA: Wizards of the Coast, 2002.

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Dissolution. London: Macmillan, 2003.

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Byers, Richard Lee. Dissolution. Renton, WA: Wizards of the Coast, 2003.

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Dissolution. [S.l: s.n.], 1990.

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Tarrant, Newell. Dissolution. Coral Springs, FL: Llumina Press, 2004.

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Dissolution. London: Pan Books, 2004.

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Dissolution. Leicester: W. F. Howes, 2003.

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Roubaud, Jacques. La dissolution. Caen: Nous, 2008.

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Book chapters on the topic "Dissoluion"

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Culshaw, Martin, and Anthony H. Cooper. "Dissolution." In Encyclopedia of Earth Sciences Series, 233–35. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-73568-9_93.

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Read, Christopher. "Dissolution." In The Making and Breaking of the Soviet System, 198–224. London: Macmillan Education UK, 2001. http://dx.doi.org/10.1007/978-0-230-62918-9_10.

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Culshaw, M. G., and A. H. Cooper. "Dissolution." In Selective Neck Dissection for Oral Cancer, 1–3. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-12127-7_93-1.

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Betts, Raymond F. "Dissolution." In France and Decolonisation 1900–1960, 78–93. London: Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-27933-3_7.

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Tiwary, A. K., Bharti Sapra, and Subheet Jain. "Dissolution." In Preclinical Development Handbook, 483–544. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470249031.ch15.

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Rohrer, Ingo. "Introduction." In Cohesion and Dissolution, 13–19. Wiesbaden: Springer Fachmedien Wiesbaden, 2013. http://dx.doi.org/10.1007/978-3-658-04360-5_1.

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Rohrer, Ingo. "Identifying with the Punk and Hardcore Scene." In Cohesion and Dissolution, 167–83. Wiesbaden: Springer Fachmedien Wiesbaden, 2013. http://dx.doi.org/10.1007/978-3-658-04360-5_10.

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Rohrer, Ingo. "Forming and Performing Communitas." In Cohesion and Dissolution, 185–203. Wiesbaden: Springer Fachmedien Wiesbaden, 2013. http://dx.doi.org/10.1007/978-3-658-04360-5_11.

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Rohrer, Ingo. "Three Spheres of Friendship." In Cohesion and Dissolution, 205–48. Wiesbaden: Springer Fachmedien Wiesbaden, 2013. http://dx.doi.org/10.1007/978-3-658-04360-5_12.

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Rohrer, Ingo. "The Impact of Social Differences on the Scene." In Cohesion and Dissolution, 249–66. Wiesbaden: Springer Fachmedien Wiesbaden, 2013. http://dx.doi.org/10.1007/978-3-658-04360-5_13.

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Conference papers on the topic "Dissoluion"

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Shih, Hsiao-Yi, Tung-Feng Yeh, Arnost Reiser, Ralph R. Dammel, Hans-Joachim Merrem, and Georg Pawlowski. "Percolation view of novolak dissolution: 3. dissolution inhibition." In SPIE's 1994 Symposium on Microlithography, edited by Omkaram Nalamasu. SPIE, 1994. http://dx.doi.org/10.1117/12.175366.

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Yeh, Tung-Feng, Hsiao-Yi Shih, and Arnost Reiser. "Percolation view of novolak dissolution and dissolution inhibition." In Micro - DL Tentative, edited by Anthony E. Novembre. SPIE, 1992. http://dx.doi.org/10.1117/12.59731.

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Putra, Narendra Kurnia, Suprijanto, Janivita Sudirham, and Saleh Wikarsa. "Simulation of tablet dissolution rate on virtual USP dissolution apparatus." In 2015 4th International Conference on Instrumentation, Communications, Information Technology, and Biomedical Engineering (ICICI-BME). IEEE, 2015. http://dx.doi.org/10.1109/icici-bme.2015.7401386.

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Faur, Maria, Mircea Faur, M. Goradia, and S. Bailey. "Anodic dissolution of InP." In International Conference on Indium Phosphide and Related Materials. IEEE, 1990. http://dx.doi.org/10.1109/iciprm.1990.203025.

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Jiang, Min, Richard Southern, Safa Tharib, and Jian Jun Zhang. "Energy-Based Dissolution Simulation." In 2013 International Conference on Computer-Aided Design and Computer Graphics (CAD/Graphics). IEEE, 2013. http://dx.doi.org/10.1109/cadgraphics.2013.69.

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Rahim, Mohd Amirul Rafiq Abu, Siti Aishah Mohd Shafie, Az’lina Abdul Hadi, Nornadiah Mohd Razali, and Nur Niswah Naslina Azid @ Maarof. "Determinants of marriage dissolution." In THE 22ND NATIONAL SYMPOSIUM ON MATHEMATICAL SCIENCES (SKSM22): Strengthening Research and Collaboration of Mathematical Sciences in Malaysia. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4932505.

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Chen, K. Rex, George M. Jordhamo, and Wayne M. Moreau. "Dissolution behavior of novolak resins." In SPIE's 1996 International Symposium on Microlithography, edited by Roderick R. Kunz. SPIE, 1996. http://dx.doi.org/10.1117/12.241854.

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Chauhan, Siddharth, Mark Somervell, Michael Carcasi, Steven Scheer, Roger T. Bonnecaze, Chris Mack, and C. Grant Willson. "Particle generation during photoresist dissolution." In SPIE Advanced Lithography, edited by Robert D. Allen. SPIE, 2010. http://dx.doi.org/10.1117/12.848424.

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Jiang, Li, Suzanne Stewart, and Jonathan Abbott. "Downhole Mineral Scale Dissolution Booster." In Offshore Technology Conference. OTC, 2022. http://dx.doi.org/10.4043/32069-ms.

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Abstract Mineral scale formation in the wellbore represents a widespread and serious threat to flow assurance and ultimately to well productivity. Scale formation is generally attributable to the incompatibility between reservoir and injection waters and the main mineral scale types include carbonate, sulfate and sulfide salts of divalent cations. Currently available scale dissolvers for the latter two types are often based on chelating ligand chemistry, restricted by a kinetically sluggish process of displacing the cations plus near static scale-fluid interface at the scale surface area in downhole scenarios. We wish to report two newly generated material developments aimed at accelerating downhole scale dissolution treatment performance by using either or both: Discrete surfactants able to encapsulate entrained gases in the form of micro- and nano-bubbles that migrate in the fluid body along the pressure differential.Gas generating reactions catalyzed by freshly produced divalent cations at the scale-fluid interface. It has been demonstrated through systematic, lab-based proof of concept tests that these minor additives can promote interfacial mass transfer of both reactant and products as such that some of the current physical and engineering challenges of downhole mineral scale treatment can be circumvented, resulting in remarkably enhanced scale dissolution rates. Further increase of scale dissolution rates can also be achieved by the inclusion of a genuinely sustainable biosurfactant which, at certain concentration range, can effectively remove any hydrocarbon coatings that might have saturated the mineral scale surface, hence eliminate the often-hazardous organic solvent based preflush. In addition to the aforementioned example, it is believed that the methodology reported in this manuscript can also be applicable to enhance other chemistry oriented downhole treatments where mechanic agitation is not viable.
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Jiang, Li, Suzanne Stewart, and Jonathan Abbott. "Downhole Mineral Scale Dissolution Booster." In Offshore Technology Conference. OTC, 2022. http://dx.doi.org/10.4043/32069-ms.

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Abstract:
Abstract Mineral scale formation in the wellbore represents a widespread and serious threat to flow assurance and ultimately to well productivity. Scale formation is generally attributable to the incompatibility between reservoir and injection waters and the main mineral scale types include carbonate, sulfate and sulfide salts of divalent cations. Currently available scale dissolvers for the latter two types are often based on chelating ligand chemistry, restricted by a kinetically sluggish process of displacing the cations plus near static scale-fluid interface at the scale surface area in downhole scenarios. We wish to report two newly generated material developments aimed at accelerating downhole scale dissolution treatment performance by using either or both: Discrete surfactants able to encapsulate entrained gases in the form of micro- and nano-bubbles that migrate in the fluid body along the pressure differential.Gas generating reactions catalyzed by freshly produced divalent cations at the scale-fluid interface. It has been demonstrated through systematic, lab-based proof of concept tests that these minor additives can promote interfacial mass transfer of both reactant and products as such that some of the current physical and engineering challenges of downhole mineral scale treatment can be circumvented, resulting in remarkably enhanced scale dissolution rates. Further increase of scale dissolution rates can also be achieved by the inclusion of a genuinely sustainable biosurfactant which, at certain concentration range, can effectively remove any hydrocarbon coatings that might have saturated the mineral scale surface, hence eliminate the often-hazardous organic solvent based preflush. In addition to the aforementioned example, it is believed that the methodology reported in this manuscript can also be applicable to enhance other chemistry oriented downhole treatments where mechanic agitation is not viable.
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Reports on the topic "Dissoluion"

1

Gray, J. H. Plutonium oxide dissolution. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/6689883.

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Gray, J. H. Plutonium oxide dissolution. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10131176.

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Knight, R. C., R. F. Creed, G. K. Patello, G. W. Hollenberg, M. F. Buehler, S. M. O`Rourke, A. Visnapuu, and D. F. McLaughlin. Calcination/dissolution residue treatment. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/80974.

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Martino, C. J. Saltcake Dissolution Simulant Tests. Office of Scientific and Technical Information (OSTI), February 2003. http://dx.doi.org/10.2172/808204.

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Brewer, K. N., R. S. Herbst, and T. J. Tranter. Dissolution of two NWCF calcines: Extent of dissolution and characterization of undissolved solids. Office of Scientific and Technical Information (OSTI), January 1995. http://dx.doi.org/10.2172/152645.

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Batcheller, Thomas Aquinas. Dissolution Kinetics of Alumina Calcine. Office of Scientific and Technical Information (OSTI), September 2001. http://dx.doi.org/10.2172/910675.

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Tkac, P., G. F. Vandegrift, and J. Harvey. Dissolution of Sintered Mo Disks. Office of Scientific and Technical Information (OSTI), October 2013. http://dx.doi.org/10.2172/1132238.

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Vienna, J. D., D. L. Alexander, and Hong Li. Plutonium dioxide dissolution in glass. Office of Scientific and Technical Information (OSTI), September 1996. http://dx.doi.org/10.2172/416955.

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Kessinger, G. F. Dissolution of Dresden Reactor Fuel. Office of Scientific and Technical Information (OSTI), November 2002. http://dx.doi.org/10.2172/804066.

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Martino, C. J. Tank 31H Saltcake Dissolution Tests. Office of Scientific and Technical Information (OSTI), April 2003. http://dx.doi.org/10.2172/809651.

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