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Slides extracted from a poster presented in the CECAM workshop held in Geneve in February 2015.
Slides cecam
Slides cecam
Mario Fernández Pendás
This study addresses some numerical aspects of the implementation of a low-order Boundary Element Method (BEM) for three-dimensional steady potential flow calculations on lifting surfaces with partial cavitation. The method is based on an integral equation for the velocity perturbation potential. The presence of a cavity on the lifting surface is modelled as a free boundary problem. A thin cavity is assumed so that the boundary conditions on the cavity may be partially linearised with respect to the wetted flow. This implies that the dynamic and kinematic boundary conditions are applied on the foil surface beneath the cavity. On the wetted surfaces only the kinematic boundary condition is applied. The problem is closed by suitable specification of cavity detachment and closure, and a Kutta condition at the lifting surface trailing edge. The study focuses on the efficiency improvement due to an alternative iterative procedure to solve the linear system of equations resulting from the formulation of the cavitating flow problem. Usually, the solution of the problem for a given cavitation number is to iterate on the cavity length. For each iteration step a new linear system of equations is solved for the unknown source strengths on the cavity and the unknown potentials on the wetted part. The solution is obtained for given potentials on the cavity, known from the dynamic boundary condition and for given sources on the wetted part, known from the kinematical boundary condition. This implies the solution of a large system of equations (at least one matrix inversion) for each iteration step on the cavity length. With the alternative procedure, a reduced system of equations is set only on the cavity panels for the unknown source strengths due to the cavity perturbation to the wetted flow. The solution of this system is iterated with the solution of the complete cavitating flow problem with known source strengths. The larger matrix for this problem is identical to the matrix of the wetted flow problem and needs only one inversion. Numerical studies were carried out for the MARIN S-Propeller and results compared with other methods [1]. The procedure converged for all cases to the solution of the original coupled system. A large reduction in computational time is achieved with the alternative procedure for the cavity potential flow solution.
A Numerical Study on the Application of BEM to Steady Cavitating Potential Fl...
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João Baltazar
Bioavailability (BA) studies play a major role in the drug development phase for both new drug products and their generic equivalents, and thus attract considerable attention globally. There are several approaches to assess BA and each regulatory authority has its own regulations/guidance for conducting BA studies before approving generic products for marketing in their country. Therefore, a thorough understanding is required of these BA concepts and basic regulatory considerations for conducting BA studies. This article briefly reviews the BA concepts, approaches, designs, and conducting and analysis of data obtained. INTRODUCTION • Bioavailability means the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action. For drug products that are not intended to be absorbed into the bloodstream, bioavailability may be assessed by measurements intended to reflect the rate and extent to which the active ingredient or active moiety becomes available at the site of action. • Results in 100% bioavailability as the absorption process is bypassed. • The absolute bioavailability of a drug, when administered by an extra vascular route is usually less than one (i.e. F<100%).> Oral > Rectal > Topical. A systematic approach to ensure bioavailability of pharmaceutical products: BIOAVAILABILITY It the degree to which, or the rate at which, a medication or other substance is absorbed or becomes available at the targeted place in the body. Bioavailability can be influenced by inactive ingredients (see Excipients) in the drug such as additives that prevent the medication from dissolving in the stomach. If a medication that is intended to be taken on an empty stomach is taken instead with food, this can also change the absorption rate and affect the bioavailability of the active ingredient BIO AVAILABILITY FRACTION (F): Bio available fraction it refers to the fraction of administered dose that enters the systemic circulation. *100
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Slides extracted from a poster presented in the CECAM workshop held in Geneve in February 2015.
Slides cecam
Slides cecam
Mario Fernández Pendás
This study addresses some numerical aspects of the implementation of a low-order Boundary Element Method (BEM) for three-dimensional steady potential flow calculations on lifting surfaces with partial cavitation. The method is based on an integral equation for the velocity perturbation potential. The presence of a cavity on the lifting surface is modelled as a free boundary problem. A thin cavity is assumed so that the boundary conditions on the cavity may be partially linearised with respect to the wetted flow. This implies that the dynamic and kinematic boundary conditions are applied on the foil surface beneath the cavity. On the wetted surfaces only the kinematic boundary condition is applied. The problem is closed by suitable specification of cavity detachment and closure, and a Kutta condition at the lifting surface trailing edge. The study focuses on the efficiency improvement due to an alternative iterative procedure to solve the linear system of equations resulting from the formulation of the cavitating flow problem. Usually, the solution of the problem for a given cavitation number is to iterate on the cavity length. For each iteration step a new linear system of equations is solved for the unknown source strengths on the cavity and the unknown potentials on the wetted part. The solution is obtained for given potentials on the cavity, known from the dynamic boundary condition and for given sources on the wetted part, known from the kinematical boundary condition. This implies the solution of a large system of equations (at least one matrix inversion) for each iteration step on the cavity length. With the alternative procedure, a reduced system of equations is set only on the cavity panels for the unknown source strengths due to the cavity perturbation to the wetted flow. The solution of this system is iterated with the solution of the complete cavitating flow problem with known source strengths. The larger matrix for this problem is identical to the matrix of the wetted flow problem and needs only one inversion. Numerical studies were carried out for the MARIN S-Propeller and results compared with other methods [1]. The procedure converged for all cases to the solution of the original coupled system. A large reduction in computational time is achieved with the alternative procedure for the cavity potential flow solution.
A Numerical Study on the Application of BEM to Steady Cavitating Potential Fl...
A Numerical Study on the Application of BEM to Steady Cavitating Potential Fl...
João Baltazar
Bioavailability (BA) studies play a major role in the drug development phase for both new drug products and their generic equivalents, and thus attract considerable attention globally. There are several approaches to assess BA and each regulatory authority has its own regulations/guidance for conducting BA studies before approving generic products for marketing in their country. Therefore, a thorough understanding is required of these BA concepts and basic regulatory considerations for conducting BA studies. This article briefly reviews the BA concepts, approaches, designs, and conducting and analysis of data obtained. INTRODUCTION • Bioavailability means the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action. For drug products that are not intended to be absorbed into the bloodstream, bioavailability may be assessed by measurements intended to reflect the rate and extent to which the active ingredient or active moiety becomes available at the site of action. • Results in 100% bioavailability as the absorption process is bypassed. • The absolute bioavailability of a drug, when administered by an extra vascular route is usually less than one (i.e. F<100%).> Oral > Rectal > Topical. A systematic approach to ensure bioavailability of pharmaceutical products: BIOAVAILABILITY It the degree to which, or the rate at which, a medication or other substance is absorbed or becomes available at the targeted place in the body. Bioavailability can be influenced by inactive ingredients (see Excipients) in the drug such as additives that prevent the medication from dissolving in the stomach. If a medication that is intended to be taken on an empty stomach is taken instead with food, this can also change the absorption rate and affect the bioavailability of the active ingredient BIO AVAILABILITY FRACTION (F): Bio available fraction it refers to the fraction of administered dose that enters the systemic circulation. *100
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