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At COP26, countries representing 70 per cent of the global economy agreed to work together to cross the tipping points where clean technologies outcompete the fossils in each greenhouse-gas-emitting sector of the global economy. This could mark the start of a new era for climate change diplomacy. Success will need support from all sides.
At COP26, countries representing 70% of the global economy agreed to work together to cross the tipping points where clean technologies outcompete the fossils in each greenhouse gas emitting sector of the global economy. This could mark the start of a new era for climate change diplomacy. Success will need support from all sides.
Chapter 4 introduces the molecular diffusion concept and Fick’s Law to explain the mixing phenomena at a small-scale CV in the distributed models rather than the large CV of the well-mixed model. For this purpose, it begins with describing diffusion phenomena, then formulating Fick’s law and developing the diffusion equation. Subsequently, examining the random velocity of Brownian particles and their pure random walk, we articulate the probabilistic nature of the molecular diffusion process and the reason why Fick’s Law is an ensemble mean law. Next, analytical solutions to the diffusion equation for various types of inputs are introduced. The advection-dispersion equation (ADE) formulation then follows, which couples the effect of fluid motion at fluid continuum scale and random motion of fluid molecules at the molecular scale to quantify solute migration. Likewise, we present analytical solutions to the ADE for several input forms and discuss snapshots and breakthroughs for different input forms.
A common care location for seizure and epilepsy patients is the emergency department and inpatient setting. A thorough history to discern a specific diagnosis and localization guides testing and treatment decisions. These decisions include the need for additional imaging/laboratory testing and whether to start an antiseizure medicine (ASM). Electroencephalograms (EEGs) are often required with time length depending on clinical question. If an epilepsy diagnosis is certain without clear localization, one hour of testing is preferred. If the question (or diagnosis) is status epilepticus, 24-hour EEG is indicated. For patients with known epilepsy, ASM alteration can occur for seizures with appropriate compliance. If there is noncompliance, an ASM increase may not be required. The perioperative period requires ASM continuation, although the administration route may change. Patients with renal or hepatic impairment often necessitate dose adjustment. Specific situations like alcohol withdrawal seizures have accepted paradigms to follow and are discussed. Lastly, patients in epilepsy monitoring units (EMUs) are hospitalized for diagnostic reasons with management needs different than other epilepsy patients.
New product development processes need to be compliant to regulatory requirements, and this chapter highlights the salient processes and quality systems to put into place to achieve success. Project management is made simple with specific tools provided here. Customer feedback is channeled into specific product characteristics, and the right tools are shown in this chapter. The biopharma industry has statistics showing less than 10% of starting compounds succeed in reaching market approval, and this chapter explains what causes these failures. The key issues that have repeatedly caused failure during device and diagnostic product development are also pointed out. Ethical decisions have to be made during product development as shown in this chapter. Outsourcing is a real option due to the availability of many contract research and manufacturing organizations, and judicious use of this option is discussed in this chapter. Key milestones that reduce risk and show transition from early stage to preclinical prototype stages are reviewed here. Does the popular concept of minimum viable product in software development apply in biomedicine prototyping? Other similar questions that help the reader understand pitfalls and best practices are answered here.
This chapter lays the foundation for the study of the role of elections in non-democratic regimes. Using VDem data, the analysis in the chapter shows that while stability is the most common response to electoral autocracies, elections can produce change in a liberalizing or autocratizing direction. This introductory chapter describes this process of voter mobilization in Russia in 2011–2012 and in terms of the existing literature on autocratic stability. It creates the foundational framework for the empirical study that brings together important studies of autocratic elections, hybrid regime stability, and post-election protest. This foundation supports the central argument of the book: when controlled elections reveal information about the lack of regime accountability, voters protest at the ballot box and on the streets. Societal mobilization provides opportunities for opposition growth and forces regimes to respond to maintain stability. The final section of the chapter outlines the plan of the book and summarizes the arguments in each chapter.
The formal model presented in the chapter underscores that control over ballot access conveys a significant power advantage to autocratic incumbents. This control leaves electoral oppositions with few options. Yet, even with this power asymmetry, the model demonstrates that elections force autocrats to make strategic choices that reveal information about regime strengths and weaknesses. Banning strong opponents signals regime weakness. Committing fraud to secure victories signals that elections are not mechanisms of accountability. When opposition parties amplify this information, they can generate focal points to foster societal coordination, forcing the regime to respond with concessions or retribution. Depending on the size and structure of the mobilization, these changes can be sudden or incremental, generating uncertainty that has to be addressed in the inter-election period. Through this process, tightly controlled elections contested by weakly organized opposition parties can prompt regime shifts in a liberalizing or autocratic direction. The first part of the chapter presents the model discursively, and the second part formalizes the argument.
There is no second chance to improve the quality of life of a dying patient. Getting it right allows a good death and leads to an uncomplicated bereavement for the family. However, there is much more to palliative care prescribing than just instituting a syringe driver: this chapter provides important information on opioid use (including how to calculate breakthrough doses and converting oral morphine to subcutaneous formulations), antiemetics and other commonly used drugs in palliative care.
This chapter focusses on chromatographic processes for protein capture. The first part provides a detailed description of the mechanistic phenomena involved in protein capture, which can be regarded as a non-competitive binary system protein/impurity, where the protein of interest strongly interacts with the chromatographic medium. Several multi-column counter-current processes allowing the implementation of the sequence of operations necessary in protein capture (load, wash, recovery, regeneration) in a continuous manner are presented in the second part of the chapter. Two process design approaches for multi-column capture processes are provided: an empirical one, which allows to obtain a first guess of the operating conditions from breakthrough curves experiments, and a model-based one, which allows a more rigorous determination of the process variables. The model-based approach is used to compare the performance of multi-column and single-column processes.
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