Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article A Phenomenological Kinetic Flotation Model: Intrinsic Floatability Profiling for Batch and Continuous Flotation Systems(Springer Heidelberg, 2026) Polat, Hürriyet; Polat, Mehmet; Kobas, Muammer; Polat, Hurriyet; 04.01. Department of Chemistry; 04. Faculty of Science; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyThis study presents a mechanistic flotation kinetics model that unifies the description of mineral particle floatability in both batch and continuous systems. Building on a physically explicit interpretation of bubble-particle interactions, the model introduces the concept of intrinsic floatability, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\upphi }_{\text{P},\text{ij}}<^>{\text{s}}$$\end{document}, defined as the size-and composition-dependent probability that a particle within a bubble's sweep volume reports to the froth. A central feature of the framework is that \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\upphi }_{\text{P},\text{ij}}<^>{\text{s}}$$\end{document} is decoupled from system-level rate-determining factors, such as bubble-particle encounter frequency, transport limits, and bubble surface crowding-that otherwise confound attempts to extract floatability distributions from kinetic data. This separation is achieved through three explicit, time-dependent parameters: the encounter rate kappa(t), the limiting flotation rate mu(t), and the bubble saturation factor chi(t). Together, these parameters isolate intrinsic particle behavior from external constraints. The model naturally reduces to the classical first-order rate law in dilute pulps, while in concentrated suspensions it predicts systematic deviations, approaching zero-order kinetics as bubble surfaces saturate. Importantly, the same formulation applies seamlessly to batch tests and multi-stage continuous circuits, enabling a consistent theoretical framework across scales and ore types. Requiring only standard flotation data and known system parameters, the model is practical for both laboratory coal flotation studies and industrial non-coal applications. Validation using batch coal data and continuous plant-scale copper flotation results demonstrates its robustness and broad relevance.Article Comparative Stability of Synthetic and Natural Polymeric Micelles in Physiological Environments: Implications for Drug Delivery(MDPI, 2025) Polat, Hürriyet; Polat, Mehmet; Polat, Mehmet; Koss, Kyle M.; Polat, Onur K.; 04.01. Department of Chemistry; 04. Faculty of Science; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyPolymeric micelles are widely studied as nanocarriers for hydrophobic drugs, yet their structural stability under physiological conditions remains a major limitation. This review provides a comparative evaluation of synthetic and natural polymeric micelles with a focus on their stability under dilution and in protein-rich environments. The discussion integrates thermodynamic and kinetic factors governing micelle integrity and examines how molecular composition, hydrophobic segment length, and core-shell modifications influence disintegration behavior. While synthetic micelles commonly collapse below their critical micelle concentration during intravenous administration, natural polymeric micelles, such as those derived from chitosan, alginate, or heparin, exhibit improved resistance to dilution but remain vulnerable to protein-induced destabilization. Strategies such as core or shell cross-linking, surface functionalization, and natural polymer coatings are reviewed as promising approaches to enhance circulation stability and controlled drug release. The work provides a framework for designing micellar systems with balanced biocompatibility, biodegradability, and robustness suitable for clinical drug-delivery applications.Article Citation - WoS: 3Citation - Scopus: 3Development of Xylan-Coated Acid-Resistant Micellar Drug Carriers for Colon-Targeted Oral Delivery(Taylor & Francis As, 2024) Zeybek, Nuket; Büyükkileci, Ali Oğuz; Polat, Hurriyet; Polat, Hürriyet; Gulec, Sukru; Güleç, Şükrü; Buyukkileci, Ali Oguz; 03.08. Department of Food Engineering; 04.01. Department of Chemistry; 03. Faculty of Engineering; 04. Faculty of Science; 01. Izmir Institute of TechnologyOral delivery of hydrophobic drugs from the stomach through the colon has some requirements: (1) an acid-resistant carrier (2) a colon-specific drug release mechanism; and (3) an enhanced bioavailability. In this study, curcumin-loaded polymeric micelles with a xylan-based composite coating were designed and developed. For this purpose, a new synthesis method was used to precipitate xylan by concurrent chitosan polymerization at different xylan/chitosan ratios using a negatively charged crosslinking agent, TPP. The study was to provide the stability of the coated micellar structures in the stomach (low pH conditions) and their degradation in the colon (a natural environment of bacteria) to release the drug. It was observed that the coating successfully prevented early drug release up to 85%, depending on the fraction of xylan in the coating. The nanocarriers that first passed through the stomach conditions were incubated with a xylanolytic colonic bacterium (Bacteroides ovatus) to determine the bacterium-related release mechanism, which was around 27%. This shows the colon-specific release expectation of coated nanocarriers in the colon environment, with an additional benefit due to the degradation of xylan and an improvement in the colon environment by prebiotic activity.