Photography and the Elphinstone Institution of Bombay

Abstract

Ralizing the potentials of photography, the Court of Directors of the East India company recommended to the Government of Bombay as early as 1845 ‘the encouragement of the study of this useful art of photography in any of the seientific or educational institutions under the control or inf1uence of your government’. They also offered to furnish students with the requisite apparatus, if they found it necessary to procure them from England¹. The proposal was repeated in their dispatch dated 29th December 1854, when they again expressed their desire to establish training in photography. Thereupon, W. Hart, Secretary to the Government of Bombay, requested the Board of Education of Bombay Presidency to submit a scheme for carrying out this project². Mr Stowell, Secretary to the Board of Education, called for the opinions of the Principal of the Elphinstone Institution, and of its Professor of Chemistry³. A small but interesting episode of early photography in India had its beginning in this way.     

Machine learning in continuous casting of steel: a state-of-the-art survey

Journal of Intelligent Manufacturing - Continuous casting is the most important route for the production of steel today. Due to the physical, mechanical, and chemical components involved in the...     

On the integration of SIC and MIMO DoF for interference cancellation in wireless networks

Recent advances in MIMO degree-of-freedom (DoF) models allowed MIMO research to penetrate the networking community. Independent from MIMO, successive interference cancellation (SIC) is a powerful physical layer technique used in multi-user detection. Based on the understanding of the strengths and weaknesses of MIMO DoF and SIC, we propose to have DoF-based interference cancellation (IC) and SIC help each other so that (i) precious DoF resources can be conserved through the use of SIC and (ii) the stringent SINR threshold criteria can be met through the use of DoF-based IC. In this paper, we develop the necessary mathematical models to realize the two ideas in a multi-hop wireless network. Together with scheduling and routing constraints, we develop a cross-layer optimization framework with joint DoF IC and SIC. By applying the framework on a throughput maximization problem, we find that SIC and DoF IC can indeed work in harmony and achieve the two ideas that we propose.     

Engineering of Saccharomyces cerevisiae for the production of (+)-ambrein

The triterpenoid (+)-ambrein is the major component of ambergris, a coprolite of the sperm whale that can only be rarely found on shores. Upon oxidative degradation of (+)-ambrein, several fragrance molecules are formed, amongst them (−)-ambrox, one of the highest valued compounds in the perfume industry. In order to generate a Saccharomyces cerevisiae whole-cell biocatalyst for the production of (+)-ambrein, intracellular supply of the squalene was enhanced by overexpression of two central enzymes in the mevalonate and sterol biosynthesis pathway, namely the N-terminally truncated 3-hydroxy-3-methylglutaryl-CoA reductase 1 (tHMG) and the squalene synthase (ERG9). In addition, another key enzyme in sterol biosynthesis, squalene epoxidase (ERG1) was inhibited by an experimentally defined amount of the inhibitor terbinafine in order to reduce flux of squalene towards ergosterol biosynthesis while retaining sufficient activity to maintain cell viability and growth. Heterologous expression of a promiscuous variant of Bacillus megaterium tetraprenyl-β-curcumene cyclase (BmeTC-D373C), which has been shown to be able to catalyse the conversion of squalene to 3-deoxyachillol and then further to (+)-ambrein resulted in production of these triterpenoids in S. cerevisiae for the first time. Triterpenoid yields are comparable with the best microbial production chassis described in literature so far, the methylotrophic yeast Pichia pastoris. Consequently, we discuss similarities and differences of these two yeast species when applied for whole-cell (+)-ambrein production.     

Liquid marbles,formation and locomotion using external fields and forces

Liquid marbles may be traditionally formed by rolling a droplet on a bed of non-wetting particles resulting in encapsulation and stabilisation. Particles used in this process may range from nanometre to millimetre if handled with sufficient care. This method, however, runs the risk of droplet coalescence and is limited to non-wetting particles. Currently there exist some alternative methods of formulation including using electrostatics to either deliver a particle bed to the droplet or pull the droplet to the particles. The former has shown some promise in potential batch processes but is hindered by interparticle forces. Additional production methods include a form of blender, but this has shown to be unable to produce marbles of a narrow size distribution. Once formed, liquid marbles have demonstrated value as potential blood typing devices, as micro-reaction vessels due to the inherent barrier between the internal phase and the substrate whilst maintaining gas permeability, and as contaminant sensors. Liquid marbles also demonstrate a remarkable level of elasticity under compressive force and reduced evaporation rates when compared to bare water droplets, a function of the size and composition of the stabilising particles. In addition to this, liquid marbles have been proposed as actuators. Locomotion may easily be induced in these structures, using electrostatics, sound, magnetism or light depending on the particle/liquid combinations used in formation, and the environment of deployment. This review seeks to present and summarise recent advances in the field of liquid marble manufacture and methods for actuation. We also aim to highlight potential future avenues of further study within this arena.     

In Situ Analysis of the Thermal Evolution of Electrodeposited Fe-C Coatings

Metallurgical and Materials Transactions A - Fe-C coatings with a high amount of carbon were electrodeposited from an iron-sulfate electrolyte. Citric acid as an additive in the electrolyte not...