Nanoscience and Nanotechnology Handbook ( ) ( ) ( ) ( ) ( )
Author H. Panda ISBN 9788178331263
Code ENI225 Format Paperback
Price: Rs 1675   1675 US$ 45   45
Pages: 608 Published 2010
Publisher Asia Pacific Business Press Inc.
Usually Ships within 5 days

Nanotechnology is the engineering of functional systems at the molecular scale. In its original sense, nanotechnology refers to the projected ability to construct items from the bottom up, using techniques and tools being developed today to make complete, high performance products. In this rising world of rapid technological developments, the role of state of art materials & composites is pivotal in frontier applications like aerospace, aviation, automobile, defense, electronics, chemical, biomedical, energy & nuclear sectors etc. with the advent of 21st century & initiation of Nanotechnology the atomic & molecular structures of materials is redefined. This shall result in new smart materials namely nanoparticles, powder, wires, rods, carbon nano tubes & so on. Nanotechnology is very diverse, ranging from novel extensions of conventional device physics, to completely new approaches based upon molecular self-assembly, to developing new materials with dimensions on the nanoscale, even to speculation on whether we can directly control matter on the atomic scale. Potential of nanotechnology to manipulate and program matter with atomic precision has invited the attention of scientists to explore innumerable applications of nanotechnology was an inspiration for the benefit of researchers, academicians and industries associated with this field. The global market for nanotechnology products is worth an estimated compound annual growth rate (CAGR) of 11.1% from 2010 to 2015.The largest segment of the market, made up of nanomaterials, is expected to increase at a 5 year CAGR of 14.7%.
This book basically deals with design of protein based nanomachines, metastabilities in nanocrystalline, nanoscale characterization of nanowires, thermopower measurements on nickel nanowires, a nanoporous tio2 electrode, nanoscale in investigation of ultrathin, silicone oxide thermal decomposition, cylindrical nanodot arrays, nanocrystalline silicon films, dispersion of carbon nanotubes, electrical conductivity study of nanocomposite films, magnetic properties of nanospheres, generation spectroscopy of nanoparticle monolayer, au nanoparticles on light emitting polymers, etc.

This handbook deals with the technology frontiers, its applications, the current & future challenges etc. This book will be an invaluable resource to all academicians, industrialists, scientists, upcoming entrepreneurs & technocrats. 

PREFACE
1. DESIGN OF PROTEIN BASED NANOMACHINES
Introduction
Renowned Nanomachines of the Biological Cell Confirm Engineering Principles and Inspire Nanomachine Design
De Novo Design of Diverse Elastic-Contractile Protein Machines
Hydrophobic and Elastic Consilient Mechanisms: Definitions
Hydrophobic Consilient Mechanism and the Inverse Temperature Transition
The Elastic Consilient Mechanism and the Nature of Near Ideal Elasticity
Coupled Hydrophobic and Elastic Consilient Mechanisms
Principal Thermodynamic Quantities Controlling Diverse Energy Conversions in Model Proteins
The Change in Gibbs Free Energy for Solubility, G(solubility) = H-TS
The Change in Gibbs Free Energy for a Phase Transition
The Change in Gibbs Free Energy for an Inverse Temperature Transition
Apolar-Polar Repulsive Gibbs Free Energy of Hydration, Gap
Calculations of the Entropic Elastic Force and Energy
Biologyâ€TMs Protein-based Nanomachines Confirm the Hydrophobic and Elastic Consilient Mechanisms
The Three Classes of Energy Conversion Within the Cell
Complex III of the Electron Transport Chain Within the Inner Mitochondrial Membrane
ATP Synthase of the Inner Mitochondrial Membrane
The Myosin II Motor of Muscle Contraction
Confirmation of the Hydrophobic and Elastic Consilient Mechanisms
Designing Protein-based Nanomachines Using the Hydrophobic and Elastic Consilient Mechanisms
Design of an AFM-Based Stress-Strain Nanomachine for the Detection of a Single Molecular Event
Use of the 3 kHz Mechanical Resonances in the Design of an AFM-Based Nanomachine for Detection of Interactions at Fixed Length
An Additional Opportunity in the Deciphering of Engineering Principles for the Design of Protein-Based Nanomachines
2. METASTABILITIES IN NANOCRYSTALLINE 
SILICON
Experimental Procedure
Results
Discussion
Conclusion
3. INTERACTION OF SULPHURIC ACID WITH 
GRAPHENE
Sulphuric Acid in Gas and Solid Phases
Sulphuric Acid on Graphene
Conclusions
4. NANOSCALE CHARACTERIZATION OF 
NANOWIRES
Experimental Methods
Nanowire Morphology, Periodicity and Diameter
Chemical Analysis of the CoPt/Pt Nanowires
Structural Analysis of the CoPt/Pt Nanowires
Discussion
Conclusions
5. THERMOPOWER MEASUREMENTS ON NICKEL
NANOWIRES
Experimental Details
Results and Discussion
Structural Characterization of the NWs
Initial Characterization of the Measurement Device
6. MULTI-WALLED CARBON NANOTUBE EMITTERS
EXPERIMENT
Fabrication of CNT Cathode
Experimental Structures
Current-Voltage Characteristics
Simulations
Simulated Structures
Predicted Iâ€"V Characteristics
Cathode Support Structure Geometry
Conclusion
7. VIBRATION OF A CARBON NANOTUBE
The Model for a CNT filled with a C-chain
Vibration of a CNT filled with a C-chain
Axisymmetric Radial Breathing Vibration (n = 0)
Coupled Vibration with n = 1
Vibration of Higher-order Modes (n > 2)
Conclusions
8. A NANOPOROUS TiO2 ELECTRODE
Experimental Details
Preparation of the ILSE Films
Characterization of the ILSE Films
Electrode and DSSC Fabrication Containing the ILSE
Electrode Characterization
Results and Discussion
Conclusions
9. FREEZING BEHAVIOUR OF AN NANOMETER-
SIZED Au DROPLET
Numerical Simulations
Results and Discussion
Conclusions
10. NANOSCALE IN INVESTIGATION OF ULTRATHIN
SILICONE OXIDE THERMAL DECOMPOSITION
Experimental Details
Results and Discussion
High Temperature STM in situ Observation of the Thermal Decomposition Process
Individual Void Growth Kinetics at the Initial Decomposition Stage
Decomposition Rate Variation and Rate Limiting Steps
Morphology Effects on the Decomposition Process
Conclusions
11. CARBON NANOTUBE FIELD-EFFECT
TRANSISTOR
Methodology
Results and Discussion
Conclusions
12. CYLINDRICAL NANODOT ARRAYS
System and Units
Theoretical Model
Vortex-core Magnetization
Total Energy Calculation
Results and Discussion
Conclusions
13. SUPERELASTICITY OF ENGINEERING
CERAMICS BY NANOTUBES
Experimental Details
Results and Discussion
Conclusion
14. POROUS ANODIC ALUMINA
Experimental Details
Results
Initial Specimens and Anodizing 
Film Morphology
Film Composition
Discussion
Conclusions
15. METAL NANOCLUSTERS IN GLASS
Experimental Procedure 
Results and Discussion
Ion-Beam Mixed Ag in Silica
Ion-Exchanged Ag in Soda Lime Glass 
Conclusion
16. LIGHT EMISSION FROM NANOCOMPOSITES
Experiments
Results and Discussion
Conclusion
17. NANOCRYSTALLINE SILICON FILMS
Experimental Details
Results
Optical Absorption Study
X-ray Diffraction Study
Infrared Absorption Study
Raman Study
Electron Microscopy
Discussion
Conclusion
18. CARBON NANOTUBES IN CHEMICAL VAPOUR
DEPOSITION
19. NANOSCALE DEEP INDENTATION
Simulation Methodology
Results and Discussion
Conclusion
20. REDUCTION OF NANOWIRES
Experimental Details
Results and Discussions
Summary and Conclusion
21. DISPERSION OF CARBON NANOTUBES
Experimental Details
Purification and Dispersion of MWCNTs
Preparation of Nanocomposite Films
Carbon Nanotube Dispersion Study in Solution and in Nanocomposite Films
Electrical Conductivity Measurement
Results and Discussion
MWCNT Dispersion in Solution
Nanocomposite Preparation and Carbon Nanotube Distribution in Composite Films
Electrical Conductivity Study of Nanocomposite Films
Conclusion
22. CREATION OF CARBON ONIONS AND COILS
Experimental Details
Result and Discussion
Conclusions
23. MAGNETIC PROPERTIES OF NANOSPHERES
Experimental Details
Results and Discussion
Conclusion
24. LUMINESCENCE OF CRYSTALS NANORODS
Experimental Section
Results and Discussion
Conclusions
25. NANONECKLACE MORPHOLOGY
Experimental Details
Growth of Cu-Pt Nanoparticles
Growth of Cu-Pt Nanonecklace Nanowires
Conclusions
26. OPTICAL PROPERTIES OF NANODOT ARRAYS
Experimental Details
Results and Discussion
Conclusions
27. GENERATION SPECTROSCOPY OF NANOPARTICLE MONOLAYER
Experimental Section
Materials
Synthesis of AuNPs
Synthesis of Dense AuNPs Monolayer
Dodecanethiol SAM Formation
Characterization
SFG Set-up
Results and Discussion
Conclusions
28. CHEMICAL DOPING WITH CARBON NANOTUBES
Experimental Details
Results and Discussion 
Summary
29. DIRECT-WRITE PROGRAMMING OF 
NANOSCALE DEMULTIPLEXER ARRAYS
30. POLY(N-ISOPROPYLACRYLAMIDE)
NANOPARTICLES
Introduction 
Experimental Details
PNIPAM-coated Fe3O4@SiO4@CdTe Nanoparticles and ZnPcS Loading
Biological Systems 
PL and Fluorescence Measurements
ZnPcS Released from the Nanoparticles in PBS Solution 
ZnPcS Released from the Nanoparticles in the CHO Cells 
Results and Discussion
ZnPcS Embedded in the PNIPAM of Nanoparticles 
Release of ZnPcS from the ZnPcSâ€"loaded Nanoparticles in PBS Solution
Release of ZnPcS from the ZnPcS-loaded Nanoparticles in CHO Cells
Release of ZnPcS from the ZnPcS-loaded Nanoparticles in Zebra Fish 
Movement of the Nanoparticles in Zebra Fish by the Magnetic Field Gradient 
Phthalocyanines and PDT
Conclusion
31. COBALT FERRITE NANOPARTICLES
Experimental Details
Sythesis
Characterization Methods
Results and Discussion
Fundamental Characteristics, Crystallite size Versus Coercivity and Remanence
Mossbauer Spectra and Distribution of Cations
Heating Efficiency from Calorimetric Measurements and ac 
Hysteresis Loops
Conclusions
32. Au NANOPARTICLES ON LIGHT-EMITTING POLYMERS
Experimental Section
Measurements
Device Fabrication and Characterization
Materials
Synthesis of PDOFT-bis-4-thiol
End-capping at AuNP onto PDOFT-bis-4-thiol (PDOFT-Au 10, PDOFT-Au15, PDOFT-Au 20 and PDOFT-Au 30)
Results and Discussion
Synthesis and Characterization
Photophysical Properties
Electroluminescent Properties and Current Density-Voltage-Luminescence (J-V-L) Characteristics of the PLED Devices
Conclusions
33. CARBON NANOSTRUCTURE BASED NANOCOMPOSITES
Experimental Details
Results and Discussion
Conclusions
34. Au NANOPARTICLE CHAINS
Experimental Results and Discussion
Sample Preparation and Measuring System
General Considerations on Dielectrophoresis 
Dielectrophoresis on Flat Substrates
Dielectrophoresis on V-groove-etched Substrates
Discussion of Results on Patterned Substrates, Electric Field Numerical Calculation
CONCLUSION
35. GOLD-SILICA NANOCOMPOSITES
36. NANOPINS BY CHEMICAL VAPOUR DEPOSITION
Experimental Section
Preparation
Characterization
Results and Discussion
Conclusions
37. OXIDATION RESISTANT METAL NANOPARTICLES
Experimental Details
Thermo-Gravimetric Studies
Particle Size Reduction
Synthesis and Coating of Metal Nanoparticles
Results and Discussion
Thermo-Gravimetric Analysis
Fluidized Bed Processing
Particle Size Reduction
Passivation of Metal Nanoparticles by in situ ALD
Conclusions 
38. MOLECULAR CARBON-ONIONS
Experimental Details
Discussion of Results
Conclusion
39. ATOMIC SCALE MANIPULATION
Tip-Surface Interaction
Experimental Response
Discussion and Conclusion
40. SILICONE NANOWIRES
Experimental Session
Results and Discussion
Conclusion
41. CARBON NANOFIBERS
Experimental Details
Results
Discussion and Conclusion
42. SINGLE-CRYSTALLINE NANOWIRES
Experiments
Results and Discussion
Conclusion
43. SILICONE OXIDE NANOSTRUCTURES
Experimental Details
Results and Discussion
Conclusion
44. A SQUARE TITANIUM NANOMESH
Experimental Details 
Results and Discussion
Conclusions
45. NANO-POROUS ANODIC ALUMINIUM OXIDE MEMBRANES
Experimental Details
Results and Discussion
Conclusions
46. Co NANOPARTICLES
Experimental Section
Materials
Synthesis and Assembly of Cobalt Nanoparticles
Characterization
Results and Discussion
Conclusions
47. ZERO-BIAS CONDUCTANCE OF GOLD MOLECULAR 
JUNCTION
Methodology
Results and Discussion
Conclusion
48. ALL-INKJET-PRINTED ELECTRONICS OF METAL NANOPARTICLES
Fabrication and Experimental Details
Nanoparticle Solution Preparation
Semi-conducting Polymer Preparation
Organic Field Effect Transistor Fabrication Process and Characterization (Inkjet Printing of Nanoparticle Solution, Polymer Dielectric Layer and Semi-conducting Polymer)
Results and Discussion
Nanoparticle Sintering Characterization
OFET Charactrization
Summary
49. TRIODE TYPE CARBON NANOTUBE FIELD EMITTER
Experimental Details
Results and Discussion
Conclusions
50. PROTEIN AND POLYMER IMMOBILIZED NANOPARTICLES FOR BIOMEDICAL APPLICATIONS
Methodology
Chemicals and Materials
Experimental Set-up
Analyses
Results and Discussion
Protein Estimation
Conjugation Studies
Magnetic Studies
Microscopy Studies
Cytotoxicity Studies
Leaching Studies
Hyperthermia Studies
Conclusion
51. 3D STRUCTURES OF NANOWIRES
Methods
Nanowire Growth
TEM Characterization
Image Simulations
Result
Crystal Structure
lmage Simulations
Discussion
Summary
52. SUPERIOR CONDUCTIVITY OF NANOPARTICLES
Experimental Details
Synthesis of Nanocomposites
Characterization
Results and Discussion
Conclusions
53. STRUCTURAL AND ELECTRONIC PROPERTIES OF ZnO 
NANOTUBES
Computational Method
Results and Discussion
Conclusions
54. SYNTHESIS OF NANOCRYSTALLINE CERAMIC POWDERS
Experimental Procedure
Results and Discussion 
Nanocrystalline CeO2 Powders Through Glycine-Nitrate and Citrate-Nitrate Combustion
Auto-Ignition Synthesis of Monophasic BaTi4O9 and Ba2Ti9O12 Powders
Combustion Synthesis of TbO2, and MTbO3 (M = Ba and Sr)
Conclusions
55. NANOCLUSTERS ON POLYMER SURFACES
Organization of Nanoparticles on the Polymer Matrices: Why?
Nanoclusters Organization on Polymers: How?
Electrostatic Organization
Covalent Organization
Vander-Waals Organization
Different Preparation Strategies
Nanocomposites Versus Surface Functionalisation
Selection of Polymers 
Selection of Clusters 
Metallic Nanoclusters
Semi-conducting Nanoclusters
Characterisation Techniques
Selected Applications
Catalytic Applications 
Photovoltaic Applications 
Biological Applications
Limiations of Cluster Organization on Polymers
Conclusion

 

Design of Protein Based Nanomachines

Introduction

Renowned Nanomachines of the Biological Cell Confirm Engineering Principles and Inspire Nanomachine Design

 

Definition of a Machine

 A combination of rigid or resistant bodies having definite motions and capable of performing useful work.

Proteins and protein based polymers constitute the resistant bodies of interest here. Proteins are polypeptides and protein based polymers are composed of repeating peptide sequences in which the repeating unit may be as small as a dipeptide or as large as hundreds of residues. The definite motions of protein arise from changing hydrophobic associations that result in deformations and relaxations of protein chain segments capable of performing mechanical work. The changing hydrophobic associations are also capable of performing a range of other forms of work most commonly chemical work.

A de novo design approach using elastic contractile model proteins gives rise to engineering principles

The approach to the elucidation of engineering principles required for the design of protein based nanomachines as reviewed in the following section began with a relatively simple repeating pentapeptide sequence from an extra cellular matrix protein. Then without recourse to an already known protein based machine de novo design involving stepwise introduction of compositional changes in elastic contractile model proteins resulted in the demonstration of diverse energy converting capacities. The approach of designing and characterizing elastic contractile model proteins allowed recognition of engineering principles that have now been used as demonstrated in the following section to describe the function of key intracellular protein machines. By this means engineering principles for design of protein based nanomachines have been developed and substantiated.

Nanomachines of living cell confirm engineering principles

Driving forces for cellular machines differ from those of man made macroscopic machines. The protein machines within the cell are of nanometer dimensions and require an aqueous milieu in which to function. These protein nanomachines are remarkable structures capable of operating at high efficiencies. In some cases they bear astonishing structural analogy to machines of the macroscopic world even though composed of very different rigid or resistant materials that operate by means of very different forces. The forces that dominate in protein based machines are not so familiar to the mechanical engineer. The forces of hydrophobic association/dissociation and those concerned with the extent of irreversible deformation of single protein chain segments replace gravitation and surface frictional loss of the macroscopic world. The interior of the living cell therefore provides the ultimate site for confirming model protein derived engineering principles for the design of protein based nanomachines.

The difficulty of determining engineering principles from cellular protein machines. The compositional complexity of the evolutionarily optimized protein nanomachine of the cell makes difficult a direct attack on elucidating the engineering principles. Rather a de novo design approach in which the energies and forces can be dissected by careful control of composition and selection of experimental method provides the opportunity one variable at a time to characterize the energies and forces involved in function. Elastic contractile model proteins capable of a phase transition unique to aqueous systems exhibit the properties essential for revealing the sought after engineering principles.

Engineering principles from designed elastic contractile model proteins confirmed by crystal structure in two key functional states of three vital cellular protein machines. Once a set of engineering principles is derived using elastic contractile model proteins these principles can be tested by detailed consideration of cellular protein machines for which crystal structural detail is available in critical functional states. In the present case the principles are remarkably demonstrated in Complex III of the electron transport chain of mitochondria that produces the proton gradient in the adenosine triphosphate (ATP) synthase of the inner mitochondrial membrane that uses the proton concentration gradient to produce nearly 90% of the ATP for an organism and in the myosin II motor of muscle contraction that uses ATP to produce motion essential to function of the organism.

Nanomachine designs inspired by intracellular protein constructs and properties

An elastic extracellular protein provided the starting point that led to the design of energy converting elastic contractile model proteins. On the other hand the elastic intracellular protein titin composed of a linear array of repeating small globular units functions within the muscle cell as a series of shock absorbing elements that irreversibly absorb energy of deformation. When a single globular element is combined with subtending elastic contractile model protein the potential exists for the detection of single molecular events. As seen by single chain force extension studies using the atomic force micro scope (AFM) a single chain of titin globular elements gives a sawtooth profile. Each sawtooth represents a single unfolding globular protein element irreversibly absorbing a unique packet of deformation energy. On the other hand the elastic contractile model proteins give a simple monotonic curve in the AFM single chain force extension curve. By the design of a single globular sensing element subtended by elastic contractile sequences a single chain force extension curve is obtained with a single sawtooth. As a single interaction with the globular element can change the characteristic sawtooth for that globular element it becomes a sensing element for detection of that interaction.

De Novo Design of Diverse Elastic Contractile Protein Machines

The potential for more effective design of new protein based nanomachines arises from the previous de novo design of elastic contractile model proteins capable of performing the set of energy conversions familiar in living organisms. The set of energy conversions involves the intensive variables of mechanical force pressure chemical potential temperature electrochemical potential and electromagnetic radiation covering the frequency range from the ultraviolet to the acoustic. The interconversions of energy involving the 6 intensive variables result in 15 possible pair wise energy conversions. When chemo chemical transduction (the conversion of one chemical energy into another) electro electrical transduction (the use of the reduction of one redox group to change the reduction potential of another redox group) and energy conversions between different frequencies of the electromagnetic radiation spectra are included the number of 15 expands to 18 classes of pair wise energy conversions.

The initial elastic contractile model protein

The starting protein based polymer was found as a repeating pentapeptide sequence in the mammalian elastic protein elastin. The repeating pentapeptide sequence is glycine valine glycine valine proline or Gly Val Gly Val Pro or simply GVGVP which in bovine elastin is found to repeat as many as 11 times in a single unbroken sequence. High molecular weight protein based polymers of this repeating sequence (GVGVP)n were found to be soluble in water at temperatures below 25°C and phase separate on raising the temperature above 25°C to form a more ordered viscoelastic and filamentous state. When cross linked for example by  irradiation the resulting elastic sheets swell on lowering the temperature and contract on raising the temperature above 25ºC and do so when loaded with a weight. Thus the cross linked polymer is capable of thermo mechanical transduction.

Changing hydrophobicity to change temperature range for contraction

Changing the polymer composition by addition of a CH2 group per pentamer achieved by replacing a Val residue by an isoleucine (Ile I) residue makes the polymer more hydrophobic and the contraction begins at 10ºC. When deleting two CH2 groups by replacing a Val residue by an alanine (Ala A) residue the contraction begins on raising the temperature above 45°C. Accordingly the temperature at which contraction occurs becomes lower as a polymer becomes more hydrophobic and higher as a polymer becomes less hydrophobic.

Introduction of functional groups with different states of hydrophobicity

Now it becomes possible to change the temperature of the phase separation by substitution of an aliphatic amino acid residue by an amino acid residue with a functional side chain. For example the charged carboxylate of glutamic acid (Glu E) or of aspartic acid (Asp D) or the charged amino function of lysine (Lys K) are less hydrophobic and more polar than the uncharged (more hydrophobic) state of the side chain. Accordingly changing the pH to form the uncharged side chain lowers the temperature of the transition. When at an intermediate temperature therefore neutralizing the charged side chain lowers the temperature of the transition and drives contraction. Thus the suitably substituted cross linked polymer becomes capable of efficient chemo mechanical transduction. Similarly a redox function can be bound to the protein based polymer. Since the oxidized state can be more polar and the reduced state can be more hydrophobicdesigned polymers capable of electro mechanical transduction result.

Phenomenological control of diverse energy conversions

Thus de novo designs of diverse energy conversions utilizing elastic contractile model proteins are achieved pheno menologically by exercising design control of the temperature at which hydrophobic association occurs. These protein based motors were not simply derivative of then known biological machines. Subsequent extensive analysis of these phenomenological designs gave rise to new understandings of the factors that control hydrophobic association/dissociation and the nature of entropic elasticity. These new understandings referred to as the hydrophobic and elastic consilient mechanisms become the engineering principles for the design of diverse protein based nanomachines.

Relevance to biology s protein based machines

Coherence of phenomena between designed elastic contractile model protein machines and biology s protein machines. When considering coherence of phenomena between the behaviours of elastic contractile model proteins designed for energy conversion and the natural energy converting proteins of the cell the hydrophobically associated state is identified with the contracted (rigor) state of a muscle protein or the taut tense T state of a globular protein such as hemoglobin. Formation of this contracted or T state occurs with loss of hydration. As concerns muscle contraction clinically there are recognized acid rigor (association of protein caused by acids) calcium rigor (contraction caused by excess calcium ion) heat rigor (heating that drives hydrophobic association) and rigor mortis (contraction on loss of ATP e.g. dephosphorylation). These muscle phenomena have demonstrable correlation with the elastic contractile model proteins designed for energy conversion.

Another well characterized protein is hemoglobin with its T (taut) state and R (relaxed) state. Increased temperature favours the T state binding polar oxygen favours the R state that forms with the uptake of water and ionpairing decreases charge to favour the T state. Thus there exists a clear coherence of phenomena.

Remarkable positive cooperativity of designed elastic contractile model proteins when compared to biology s renowned protein machines. These elastic contractile model proteins of translational symmetry are designed as chemo mechanical transductional model proteins that exhibit positive cooperativities with Hill coefficients as large as 8. This is a greater positive cooperativity than seen by Monod and others when concerned with symmetries of associating globular proteins. This was not expected from the prevailing view of cooperativity. As stated by Monod  One may set aside the simple problem of fibrous proteins. Being used as scaffolding shrouds or halyards they fulfill these requirements by adopting relatively simple types of translational symmetries.

In the popular hemoglobin example the Hill coefficient found for the oxygen binding curve is 3.2 which indicates a degree of positive cooperativity much less than that obtained with the most efficient design of elastic contractile model proteins. Thus protein structure with translational symmetry is designed to exhibit positive cooperativity that is central to efficient function (e.g. energy conversion) of nanomachines and exceeds the positive cooperativity considered so remarkable in protein machines of biology.

Direct demonstrations of relevance of the hydrophobic and elastic consilient mechanisms to biology s protein machines. Even though these demonstrations of energy conversion by de novo designed elastic contractile model proteins proceeded visually and convincingly with the above noted coherence of phenomena suggestions that biology s protein based machines functioned similarly were not well received by specialists in their particular protein machine. These new understandings nonetheless have now been demonstrated to be significant in three key classes of biological energy conversion the formation of the proton gradient in the mitochondrion the use of the proton gradient to produce ATP by ATP synthase and the use of ATP to produce motion essential to life. Thus the important new engineering principles did not arise from examination of the more complex site localized and evolutionarily optimized energy converting machines of biology. Instead the new engineering principles arose from the design preparation characterization and data analysis of relatively simple model proteins. In doing so the model proteins could be designed to perform the energy conversions of biology by simple changes made in an elastic repeating sequence derived from the mammalian elastic fiber a fiber not recognized as an energy converting machine of biology.

Hydrophobic and Elastic Consilient Mechanisms Definitions

Definition of consilience. Consilience reflects the presence of a pervasive basic law of nature that underlies otherwise seemingly disparate phenomena. In this case the phenomena involve a diverse set of energy conversions with an underlying common mechanism a common groundwork of explanation in the words of E.O. Wilson. Accordingly the common groundwork of explanation for diverse energy conversions as discovered using designed elastic contractile model proteins is called a consilient mechanism.

The hydrophobic and elastic consilient mechanisms. Two inter linked consilient mechanisms have been identified in studies on the de novo designed elastic contractile model protein machines and also observed in the energy conversion of biology s protein machines. These are the hydrophobic and elastic consilient mechanisms. They derive their consilience from a general applicability in the former case to all amphiphilic polymers in water and in the latter case to all polymers of whatever composition containing chain segments with a backbone mobility that can become damped on deformation whether by extension compression or repulsion.

 

Metastabilities in Nanocrystalline Silicon

Porous silicon (PS) is a form of nanocrystalline. Silicon and has attracted quite a lot of attention because of the possibility of it s wide range of applications in optoelectronic devices gas sensors vapour sensors and chemical sensors. PS consists of nanometer size crystallites of silicon and shows photoluminescence (PL) in the visible in room temperature. The as prepared PS surfaces are naturally terminated with a covalently bonded monolayer of hydrogen but this monolayer does not give protection against chemical absorption and exposure to light. Further it has been found that after short light exposures the dark current (DC) is higher than the annealed state dark current. This higher dark current called persistent photocurrent (PPC) persists for several hours even at room temperature. It has been reported that the LS decreases PL and increases electron spin resonance (ESR). Some of these changes are partly reversible with annealing. Some authors have found that PL does not change when the light soaking is done with the sample in vacuum or in nitrogen atmosphere. On the other hand Matsumoto have reported that for long exposures the dangling bond density (ESR) increases and PL decreases for their sample. Therefore there is a need to study these phenomena more closely.

In this paper it has been reported for the first time that the dangling bond density in the nanocrystalline silicon decreases after light exposures of short durations. This is accompanied by an increase in DC photocurrent (PC) and PL. Rapid cooling from high temperatures to room temperature also gives an increase in DC PC and PL and a decrease in ESR signal. Such an increase in DC after fast cooling has been observed by various authors in doped hydrogenated amorphous silicon (a Si H) also. However no decrease in ESR has been reported for a Si H. Further for long exposures the changes observed are in the opposite direction to the short exposures and are similar to the well known Staebler Wronski effect in a Si H. Authors suggest that the metastable changes caused by the thermal quenching and light exposures might be related to the structural changes in PS.

Experimental Procedure

PS layers were prepared by the standard method of electrochemical anodization of boron doped (100) crystalline silicon wafers having resistivity between 0.6 to 1.0   cm. The electrolyte was HF (49%) mixed with equal volume of ethanol. A current density  20 mA/cm2 was used and a two hours anodization yielded about 70 µm thick PS. Free standing PS were also made by passing 1A current for a few minutes after 2 h of anodization to lift off the PS from the silicon wafer. These gave flakes of size = 2 × 5 mm. After anodization PS was rinsed thoroughly in ethanol to remove HF and dried in air. Freestanding PS samples were mounted on Corning 7059 glass substrate by putting silver paint at the two ends of the sample which also served as electrodes for current measurements. Electrical measurements done on the free standing PS gave results similar to the PS samples attached to the silicon substrate. For the PL and ESR measurements PS removed from the Si wafer in the form of flakes was sealed in 10 1 torr helium atmosphere in a quartz tube. The samples were annealed at 150°C for 1 h in vacuum   10-6 torr for removing the effect of previous light exposures if any and slowly cooled (rate   0.5 K/min) to room temperature (state A). ESR was measured using a X band (Varian E 3) spectrometer at microwave power of 5 mW. For PL the sample was excited by a 15 mW He Ne laser (632 nm) and the emitted light was analyzed using a grating spectrometer and a CCD detector. A bias of 40 V was applied for the DC and PC measurements. The samples showed a symmetric sub ohmic I V behaviour upto this voltaged. For thermal quenching experiments the samples were heated in vacuum (10-6torr) at 150°C for one hour. Then the heater was switched off and chilled water was circulated without breaking the vacuum through the copper block upon which the sample had been mounted using silver paint. Using this set up we could obtain cooling rates upto 400 K/min.

Light soaking was done in vacuum using heat filtered white light from a 250W tungsten halogen lamp kept at a distance of about 15 Cm. X ray diffraction and atomic force microscopy (AFM) show that our PS consists of crystallites of sizes 2 5 nm and bigger. Our Raman measurements show the presence of a Si H (broad peak ~480cm 1) along with a nanocrystalline peak (~512 cm 1) whose position and width depend upon the size distribution of crystallites and the stress present in the porous silicon.

Results

Figure 1 shows the ESR signal of our PS in the annealed state (state A). This ESR signal is asymmetric and is similar to that reported by others. This can be fitted to three signals one isotropic signal with g 2.0055 ± 0.0006 (width ~ 6.4G ± 0.5G) corresponding to the dangling bonds in a Si and two anisotropic signals having g   2.0081 ± 0.0006 (width ~ 1.5G±0.5G) and g1 2.0028 ± 0.0006 (width ~ 1.8G±0.5G). The last two have been attributed to the dangling bonds in PS by some authors.

Fig. 2 shows the variation in current upon light exposures of durations varying between 30s and 4500s. After switching off the light the dark current reaches a value (B1 B8) which is higher than the annealed state (state A) dark current. For short exposures (upto 2700s) the excess DC increases with the duration of exposure (B1 B6 Fig. 2) but start decreasing for long exposures (> 3600 s B7 B8 Fig. 2). For very long exposures (> 6h not shown) the final state DC value is lower than the state A. This is similar to the Staebler Wronski effect in a Si H. The excess dark current persists for several hours even at room temperature.

Fig. 3 shows the effect of exposing the sample to infrared light ( 3600 s) exposures with a maximum at about 2700s exposure time. For the 900s exposure PL increases by about a factor of 2 and ESR decreases by   70% compared to the initial state A. Also it is seen that for very long exposures ESR increases with a decrease in DC PC and PL. Interestingly ESR shows a minimum at about the same exposure duration (2700s) at which DC PC and PL show a maximum.

Let us now look at the thermal quenching results. Fast cooling from I50ºC to room temperature (400 K/min) brings PS to another metastable state (C) which has higher DC PC and PL than the annealed state A. This is also accompanied by a decrease in the ESR signal. The state A can be recovered by annealing at 150°C (1h) and slow cooling but not by IR exposure. Table 1 shows the values of DC PC PL and ESR signal before (state A) and after rapid thermal quenching (state C).

It might be mentioned that the position and shape of the PL and ESR signals do not change significantly after various treatments. It is noted that the increase in DC PC and PL is always accompanied by a decrease in ESR and vice versa. Hence there is an anti correlation between DC PC PPC and PL on one hand and ESR on the other.

Discussion

The decrease in the ESR signal accompanies an increase in PC and PL for short exposures (

 

 

ABOUT NPCS

 

NIIR PROJECT CONSULTANCY SERVICES (NPCS) is a reliable name in the industrial world for offering integrated technical consultancy services. NPCS is manned by engineers, planners, specialists, financial experts, economic analysts and design specialists with extensive experience in the related industries.

Our various services are: Detailed Project Report,  Business Plan for Manufacturing Plant, Start-up Ideas, Business Ideas for Entrepreneurs, Start up Business Opportunities, entrepreneurship projects, Successful Business Plan, Industry Trends, Market Research, Manufacturing Process, Machinery, Raw Materials, project report, Cost and Revenue, Pre-feasibility study for Profitable Manufacturing Business, Project Identification, Project Feasibility and Market Study, Identification of Profitable Industrial Project Opportunities, Business Opportunities, Investment Opportunities for Most Profitable Business in India, Manufacturing Business Ideas, Preparation of Project Profile, Pre-Investment and Pre-Feasibility Study, Market Research Study, Preparation of Techno-Economic Feasibility Report, Identification and Section of Plant, Process, Equipment, General Guidance, Startup Help, Technical and Commercial Counseling for setting up new industrial project and Most Profitable Small Scale Business.

NPCS also publishes varies process technology, technical, reference, self employment and startup books, directory, business and industry database, bankable detailed project report, market research report on various industries, small scale industry and profit making business. Besides being used by manufacturers, industrialists and entrepreneurs, our publications are also used by professionals including project engineers, information services bureau, consultants and project consultancy firms as one of the input in their research.

Our Detailed Project report aims at providing all the critical data required by any entrepreneur vying to venture into Project. While expanding a current business or while venturing into new business, entrepreneurs are often faced with the dilemma of zeroing in on a suitable product/line.

 


And before diversifying/venturing into any product, wish to study the following aspects of the identified product:


• Good Present/Future Demand
• Export-Import Market Potential
• Raw Material & Manpower Availability
• Project Costs and Payback Period


We at NPCS, through our reliable expertise in the project consultancy and market research field, Provides exhaustive information about the project, which satisfies all the above mentioned requirements and has high growth potential in the markets. And through our report we aim to help you make sound and informed business decision.

 

The report contains all the data which will help an entrepreneur find answers to questions like:

• Why I should invest in this project?
• What will drive the growth of the product?
• What are the costs involved?
• What will be the market potential?


The report first focuses on enhancing the basic knowledge of the entrepreneur about the main product, by elucidating details like product definition, its uses and applications, industry segmentation as well as an overall overview of the industry sector in India. The report then helps an entrepreneur identify the target customer group of its product. It further helps in making sound investment decision by listing and then elaborating on factors that will contribute to the growth of product consumption in India and also talks about the foreign trade of the product along with the list of top importing and top exporting countries. Report includes graphical representation and forecasts of key data discussed in the above mentioned segment. It further explicates the growth potential of the product.

The report includes other market data like key players in the Industry segment along with their contact information and recent developments. It includes crucial information like raw material requirements, list of machinery and manufacturing process for the plant. Core project financials like plant capacity, costs involved in setting up of project, working capital requirements, projected revenue and profit are further listed in the report.


Reasons for buying the report:

• This report helps you to identify a profitable project for investing or diversifying into by throwing light to crucial areas like industry size, demand of the product and reasons for investing in the product.

• This report provides vital information on the product like its definition, characteristics and segmentation.

• This report helps you market and place the product correctly by identifying the target customer group of the product.

• This report helps you understand the viability of the project by disclosing details like raw materials required, manufacturing process, project costs and snapshot of other project financials.

• The report provides forecasts of key parameters which helps to anticipate the industry performance and make sound business decision.

 

Our Approach:


• Our research reports broadly cover Indian markets, present analysis, outlook and forecast.

• The market forecasts are developed on the basis of secondary research and are cross-validated through interactions with the industry players. 

• We use reliable sources of information and databases.  And information from such sources is processed by us and included in the report.

 

Our Market Survey cum Detailed Techno Economic Feasibility Report Contains following information:

 

 

Ø  Introduction

·         Project Introduction

·         Project Objective and Strategy

·         Concise History of the Product

·         Properties

·         BIS (Bureau of Indian Standards) Provision & Specification

·         Uses & Applications

 

Ø  Market Study and Assessment

·         Current Indian Market Scenario

·         Present Market Demand and Supply

·         Estimated Future Market Demand and Forecast

·         Statistics of Import & Export

·         Names & Addresses of Existing Units (Present Players)

·         Market Opportunity

 

Ø  Raw Material

·         List of Raw Materials

·         Properties of Raw Materials

·         Prescribed Quality of Raw Materials

·         List of Suppliers and Manufacturers

 

Ø  Personnel (Manpower) Requirements

·         Requirement of Staff & Labor (Skilled and Unskilled) Managerial, Technical, Office Staff and Marketing Personnel

 

Ø  Plant and Machinery

·         List of Plant & Machinery

·         Miscellaneous Items

·         Appliances & Equipments

·         Laboratory Equipments & Accessories

·         Electrification

·         Electric Load & Water

·         Maintenance Cost

·         Sources of Plant & Machinery (Suppliers and Manufacturers)

 

Ø  Manufacturing Process and Formulations

·         Detailed Process of Manufacture with Formulation

·         Packaging Required

·         Process Flow Sheet Diagram

 

Ø  Infrastructure and Utilities

·         Project Location

·         Requirement of Land Area

·         Rates of the Land

·         Built Up Area

·         Construction Schedule

·         Plant Layout and Requirement of Utilities

 

Project at a Glance

Along with financial details as under:

 

  •     Assumptions for Profitability workings

  •    Plant Economics

  •    Production Schedule

  •    Land & Building

            Factory Land & Building

            Site Development Expenses

  •    Plant & Machinery

             Indigenous Machineries

            Other Machineries (Miscellaneous, Laboratory etc.)

  •    Other Fixed Assets

            Furniture & Fixtures

            Pre-operative and Preliminary Expenses

            Technical Knowhow

            Provision of Contingencies

  •   Working Capital Requirement Per Month

             Raw Material

            Packing Material

            Lab & ETP Chemical Cost

           Consumable Store

  •   Overheads Required Per Month And Per Annum

         Utilities & Overheads (Power, Water and Fuel Expenses etc.)

             Royalty and Other Charges

            Selling and Distribution Expenses

  •    Salary and Wages

  •    Turnover Per Annum

  •   Share Capital

            Equity Capital

            Preference Share Capital

 

  •    Annexure 1:: Cost of Project and Means of Finance

  •    Annexure 2::  Profitability and Net Cash Accruals

                Revenue/Income/Realisation

                Expenses/Cost of Products/Services/Items

                Gross Profit

                Financial Charges     

                Total Cost of Sales

                Net Profit After Taxes

                Net Cash Accruals

  •   Annexure 3 :: Assessment of Working Capital requirements

                Current Assets

                Gross Working. Capital

                Current Liabilities

                Net Working Capital

                Working Note for Calculation of Work-in-process

  •    Annexure 4 :: Sources and Disposition of Funds

  •    Annexure 5 :: Projected Balance Sheets

                ROI (Average of Fixed Assets)

                RONW (Average of Share Capital)

                ROI (Average of Total Assets)

  •    Annexure 6 :: Profitability ratios

                D.S.C.R

                Earnings Per Share (EPS)

               

             Debt Equity Ratio

        Annexure 7   :: Break-Even Analysis

                Variable Cost & Expenses

                Semi-Var./Semi-Fixed Exp.

                Profit Volume Ratio (PVR)

                Fixed Expenses / Cost 

                B.E.P

  •   Annexure 8 to 11:: Sensitivity Analysis-Price/Volume

            Resultant N.P.B.T

            Resultant D.S.C.R

   Resultant PV Ratio

   Resultant DER

  Resultant ROI

          Resultant BEP

  •    Annexure 12 :: Shareholding Pattern and Stake Status

        Equity Capital

        Preference Share Capital

  •   Annexure 13 :: Quantitative Details-Output/Sales/Stocks

        Determined Capacity P.A of Products/Services

        Achievable Efficiency/Yield % of Products/Services/Items 

        Net Usable Load/Capacity of Products/Services/Items   

       Expected Sales/ Revenue/ Income of Products/ Services/ Items   

  •    Annexure 14 :: Product wise domestic Sales Realisation

  •    Annexure 15 :: Total Raw Material Cost

  •    Annexure 16 :: Raw Material Cost per unit

  •    Annexure 17 :: Total Lab & ETP Chemical Cost

  •    Annexure 18  :: Consumables, Store etc.,

  •    Annexure 19  :: Packing Material Cost

  •    Annexure 20  :: Packing Material Cost Per Unit

  •    Annexure 21 :: Employees Expenses

  •    Annexure 22 :: Fuel Expenses

  •    Annexure 23 :: Power/Electricity Expenses

  •    Annexure 24 :: Royalty & Other Charges

  •    Annexure 25 :: Repairs & Maintenance Exp.

  •    Annexure 26 :: Other Mfg. Expenses

  •    Annexure 27 :: Administration Expenses

  •    Annexure 28 :: Selling Expenses

  •    Annexure 29 :: Depreciation Charges – as per Books (Total)

  •   Annexure 30   :: Depreciation Charges – as per Books (P & M)

  •   Annexure 31   :: Depreciation Charges - As per IT Act WDV (Total)

  •   Annexure 32   :: Depreciation Charges - As per IT Act WDV (P & M)

  •   Annexure 33   :: Interest and Repayment - Term Loans

  •   Annexure 34   :: Tax on Profits

  •   Annexure 35   ::Projected Pay-Back Period And IRR