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Electroanalytical Chemistry. Gary A. MabbottЧитать онлайн книгу.

Electroanalytical Chemistry - Gary A. Mabbott


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      In describing the fundamentals of electroanalytical methods, this book emphasizes conceptual models. An effort has been made to tie conceptual models of phenomena to basic mathematical relationships in order to provide a foundation to use in reasoning through new situations. Greater insight into electroanalytical phenomena is the intended result. As with other branches of science, new developments displace older techniques. A fundamental understanding of the phenomena upon which electroanalytical tools operate enables one to appreciate the basis for new techniques and related progress in the field. A conceptual understanding also provides a good starting point for learning about other areas of science and technology that involve electrochemical processes. Electrochemical principles play important roles in many natural phenomena and in modern technology [1]. Among these fields are the subjects of energy storage and conversion; biological processes such as cellular action potentials, tissue repair, and growth [2]; electrochemical synthesis; separation technology, nanoparticles, and materials processing in the electronics industry.

Attribute Makes possible
Sensitive Low detection limits
Small In vivo monitoring
Measurement in tiny volumes
Simple construction Implantable devices
Inexpensive Mass production
Use in poor communities
Simple operation On‐site operation
Health care monitoring
Remote sensing

      Before launching into the principles of electrochemistry, it is appropriate to say a word about the structure of this book. Chapter summaries appear at the beginning of each chapter in the form of an overview. Unlike reading a novel, here it is helpful for you to know the plot in advance. It helps you to know what to take away from the story. It is worthwhile to read the overview both before and after reading the other sections of the chapter. This book is aimed at students of instrumental analysis, but it is also intended to be a solid introduction to electroanalytical principles for any professional scientist. A lot of care has gone into explaining physical mechanisms and underlying concepts. Recent developments leading to new and interesting methods with better performance characteristics and a wide range of applications are described in most chapters. However, there is much more material than can be reasonably absorbed during a typical two‐to‐three‐week unit of a college instrumental analysis course. Therefore, in addition to summarizing the major ideas, these chapter briefings tell you what sections to read, if time is short.

      One volt equals one joule per coulomb of charge. The charge on a mole of electrons is 9.6485 x 104 C/mol. This number shows up in a lot of electrochemical relationships and is called the Faraday, F, after the nineteenth‐century scientist, Michael Faraday. Faraday established the relationship between charge, Q, transferred in an electrochemical reaction, such as the reduction of silver ions to silver metal, and the number of moles of reactant, N. This is Faraday's law: Q = nFN, where n is the number of moles of electrons transferred per mole of reactant. Another important concept is the free energy, ΔG, that drives an electrochemical reaction. The free energy of an electrochemical system is proportional to the voltage, E, and is a measurable quantity, ΔG = −nFE.

      Electrical current is the movement of charge and is analogous to current in a river. While a river's current is measured in the volume flow rate of the water, electrical current is measured in amperes. One ampere is equivalent to a coulomb of charge moving past a given point per second. Electrons carry charge in electrical circuits. Ions carry charge in solution. Although electrons are negatively charged, current is defined as though positive charges are moving in a circuit. The direction of the current, then, is defined as movement of charge from a higher potential to a lower potential.

      Electrochemical experiments are performed in containers called cells in which two or more electrodes connect the cell to an outside electrical circuit that allows one to measure the voltage and/or the current during the experiment. Potentiometric methods measure the voltage (that is, potential) between electrodes without the passage of a significant amount of current. No significant chemical changes occur in a properly performed potentiometric experiment. In Chapter 2, the Nernst equation that relates potential in a potentiometric experiment to the activity of an analyte is discussed. An activity is the effective


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