K. Narayan Prabhu

Bio: K. Narayan Prabhu is an academic researcher from National Institute of Technology, Karnataka. The author has contributed to research in topics: Heat transfer & Heat flux. The author has an hindex of 20, co-authored 103 publications receiving 1732 citations. Previous affiliations of K. Narayan Prabhu include Council of Scientific and Industrial Research.

Modification of eutectic silicon in Al-Si alloys

Abstract: The mechanical properties of Al–Si alloys are strongly related to the size, shape and distribution of eutectic silicon present in the microstructure In order to improve mechanical properties, these alloys are generally subjected to modification melt treatment, which transforms the acicular silicon morphology to fibrous one resulting in a noticeable improvement in elongation and strength. Improper melt treatment procedures, fading and poisoning of modifiers often result in the structure which is far from the desired one. Hence it is essential to assess the effectiveness of melt treatment before pouring. A much investigated reliable thermal analysis technique is generally used for this purpose. The deviation from the standard curve in thermal analysis helps in assessing the level of refinement of the Si structure. In the present review an attempt is made to discuss various aspects of modification, including mechanism, interaction of defects and non-destructive assessment by thermal analysis.

Review of Microstructure Evolution in Hypereutectic Al–Si Alloys and its Effect on Wear Properties

Abstract: Al–Si alloys with silicon content more than 13 % are termed as hypereutectic alloys. In recent years, these alloys have drawn the attention of researchers due to their ability to replace cast iron parts in the transportation industry. The properties of the hypereutectic alloy are greatly dependent on the morphology, size and distribution of primary silicon crystals in the alloy. Mechanical properties of the hypereutectic Al–Si alloy can be improved by the simultaneous refinement and modification of the primary and eutectic silicon and by controlling the solidification parameters. In this paper, the effect of solidification rate and melt treatment on the evolution of microstructure in hypereutectic Al–Si alloys are reviewed. Different types of primary silicon morphology and the conditions for its nucleation and growth are explained. The paper discusses the effect of refinement/modification treatments on the microstructure and properties of the hypereutectic Al-Si alloy. The importance and effect of processing variables and phosphorus refinement on the silicon morphology and wear properties of the alloy is highlighted.

Heat flux transients at the casting/chill interface during solidification of aluminum base alloys

Abstract: Heat flow at the metal/chill interface of bar-type castings of aluminum base alloys was modeled as a function of thermophysical properties of the chill material and its thickness. Experimental setup for casting square bars of Al-13.2 pct Si eutectic and Al-3 pet Cu-4.5 pct Si long freezing range alloys with chill at one end exposed to ambient conditions was fabricated. Experiments were carried out for different metal/chill combinations with and without coatings. The thermal history at nodal locations in the chill obtained during the experiments was used to estimate the interface heat flux by solving a one-dimensional Fourier heat conduction equation inversely. Using the data on transient heat flux q, the heat flow at the casting/chill interface was modeled in two steps: (1) The peak in the heat flux curve qmax was modeled as a power function of the ratio of the chill thickness d to its thermal diffusivity a, and (2) the factor (q/qmax) X α0.05 was also modeled as a power function of the time after the solidification set in. The model was validated for Cu-10 pct Sn -2 pct Zn alloy chill and Al-13.2 pct Si and Al-3 pct Cu-4.5 pct Si as the casting alloys. The heat flux values estimated using the model were used as one of the boundary conditions for solidification simulation of the test casting. The experimental and simulated temperature distributions inside the casting were found to be in good agreement.

The Design and Analysis of Experiments

Abstract: THE DESIGN AND ANALYSIS OF EXPERIMENTS. By Oscar Kempthorne. New York, John Wiley and Sons, Inc., 1952. 631 pp. $8.50. This book by a teacher of statistics (as well as a consultant for \"experimenters\") is a comprehensive study of the philosophical background for the statistical design of experiment. It is necessary to have some facility with algebraic notation and manipulation to be able to use the volume intelligently. The problems are presented from the theoretical point of view, without such practical examples as would be helpful for those not acquainted with mathematics. The mathematical justification for the techniques is given. As a somewhat advanced treatment of the design and analysis of experiments, this volume will be interesting and helpful for many who approach statistics theoretically as well as practically. With emphasis on the \"why,\" and with description given broadly, the author relates the subject matter to the general theory of statistics and to the general problem of experimental inference. MARGARET J. ROBERTSON

Handbook of Chemistry and Physics

Abstract: There is a special reason for reviewing this book at this time: it is the 50th edition of a compendium that is known and used frequently in most chemical and physical laboratories in many parts of the world. Surely, a publication that has been published for 56 years, withstanding the vagaries of science in this century, must have had something to offer. There is another reason: while the book is a standard fixture in most chemical and physical laboratories, including those in medical centers, it is not as frequently seen in the laboratories of physician's offices (those either in solo or group practice). I believe that the Handbook can be useful in those laboratories. One of the reasons, among others, is that the various basic items of information it offers may be helpful in new tests, either physical or chemical, which are continuously being published. The basic information may relate

Artificial Molecular Machines

Abstract: The widespread use of molecular machines in biology has long suggested that great rewards could come from bridging the gap between synthetic molecular systems and the machines of the macroscopic world. In the last two decades, it has proved possible to design synthetic molecular systems with architectures where triggered large amplitude positional changes of submolecular components occur. Perhaps the best way to appreciate the technological potential of controlled molecular-level motion is to recognize that nanomotors and molecular-level machines lie at the heart of every significant biological process. Over billions of years of evolution, nature has not repeatedly chosen this solution for performing complex tasks without good reason. When mankind learns how to build artificial structures that can control and exploit molecular level motion and interface their effects directly with other molecular-level substructures and the outside world, it will potentially impact on every aspect of functional molecule and materials design. An improved understanding of physics and biology will surely follow. The first steps on the long path to the invention of artificial molecular machines were arguably taken in 1827 when the Scottish botanist Robert Brown observed the haphazard motion of tiny particles under his microscope.1,2 The explanation for Brownian motion, that it is caused by bombardment of the particles by molecules as a consequence of the kinetic theory of matter, was later provided by Einstein, followed by experimental verification by Perrin.3,4 The random thermal motion of molecules and its implications for the laws of thermodynamics in turn inspired Gedankenexperiments (“thought experiments”) that explored the interplay (and apparent paradoxes) of Brownian motion and the Second Law of Thermodynamics. Richard Feynman’s famous 1959 lecture “There’s plenty of room at the bottom” outlined some of the promise that manmade molecular machines might hold.5,6 However, Feynman’s talk came at a time before chemists had the necessary synthetic and analytical tools to make molecular machines. While interest among synthetic chemists began to grow in the 1970s and 1980s, progress accelerated in the 1990s, particularly with the invention of methods to make mechanically interlocked molecular systems (catenanes and rotaxanes) and control and switch the relative positions of their components.7−24 Here, we review triggered large-amplitude motions in molecular structures and the changes in properties these can produce. We concentrate on conformational and configurational changes in wholly covalently bonded molecules and on catenanes and rotaxanes in which switching is brought about by various stimuli (light, electrochemistry, pH, heat, solvent polarity, cation or anion binding, allosteric effects, temperature, reversible covalent bond formation, etc.). Finally, we discuss the latest generations of sophisticated synthetic molecular machine systems in which the controlled motion of subcomponents is used to perform complex tasks, paving the way to applications and the realization of a new era of “molecular nanotechnology”. 1.1. The Language Used To Describe Molecular Machines Terminology needs to be properly and appropriately defined and these meanings used consistently to effectively convey scientific concepts. Nowhere is the need for accurate scientific language more apparent than in the field of molecular machines. Much of the terminology used to describe molecular-level machines has its origins in observations made by biologists and physicists, and their findings and descriptions have often been misinterpreted and misunderstood by chemists. In 2007 we formalized definitions of some common terms used in the field (e.g., “machine”, “switch”, “motor”, “ratchet”, etc.) so that chemists could use them in a manner consistent with the meanings understood by biologists and physicists who study molecular-level machines.14 The word “machine” implies a mechanical movement that accomplishes a useful task. This Review concentrates on systems where a stimulus triggers the controlled, relatively large amplitude (or directional) motion of one molecular or submolecular component relative to another that can potentially result in a net task being performed. Molecular machines can be further categorized into various classes such as “motors” and “switches” whose behavior differs significantly.14 For example, in a rotaxane-based “switch”, the change in position of a macrocycle on the thread of the rotaxane influences the system only as a function of state. Returning the components of a molecular switch to their original position undoes any work done, and so a switch cannot be used repetitively and progressively to do work. A “motor”, on the other hand, influences a system as a function of trajectory, meaning that when the components of a molecular motor return to their original positions, for example, after a 360° directional rotation, any work that has been done is not undone unless the motor is subsequently rotated by 360° in the reverse direction. This difference in behavior is significant; no “switch-based” molecular machine can be used to progressively perform work in the way that biological motors can, such as those from the kinesin, myosin, and dynein superfamilies, unless the switch is part of a larger ratchet mechanism.14

Contact Angle and Wetting Properties

Abstract: This chapter highlights a variety of techniques that are commonly used to measure contact angles, including the conventional telescope-goniometer method, the Wilhelmy balance method, and the more recently developed drop-shape analysis methods. The various applications and limitations of these techniques are described. Notably, studies of ultrasmall droplets on solid surfaces allow wetting theories to be tested down to the nanometer scale, bringing new insight to contact angle phenomena and wetting behavior.