Comparative Analysis of Hydrate Nucleation for Methane and Carbon Dioxide

Research in the field of hydrate formation requires more focus upon its modelling to enable the researchers to predict and assess the hydrate formation and its characteristics. The main focus of the study was to analyze the deviations induced in various parameters related to hydrate nucleation caused by the choice of different measuring correlations or methods of their sub-components. To serve this purpose under a range of operational conditions, parameters of hydrate nucleation such as rates of nucleation and crystal growth, critical radius of the nucleus, and theoretical induction time for carbon dioxide and methane were considered in this study. From these measurements, we have quantitatively compared the ease of hydrate formation in CO2 and CH4 systems in terms of nucleation while analyzing how various correlations for intermediate parameters were affecting the final output. Values of these parameters were produced under the considered bracket of operational conditions and distributed among six cases using both general and guest-gas specific correlations for gas dissolution and fugacity and their combinations. The isotherms and isobars produced from some of the cases differed from each other considerably. The rate of nucleation in one case showed an exponential deviation with a value over 1 × 1028 at 5 MPa, while the rest showed values as multiples of 106. These deviations explain how sensitive hydrate formation is to processing variables and their respective correlations, highlighting the importance of understanding the applicability of semi-empirical correlations. An attempt was made to define the induction time from a theoretical perspective and derive a relevant equation from the existing models. This equation was validated and analyzed within these six cases from the experimental observations

Determination of protein transporter function using Raman spectroscopy

Transporter proteins are essential across the tree of life as they provide a cell with a means of exchanging vital metabolites with the external milieu. Characterizing the function of transporters is challenging and traditionally uses methods involving radiolabelled substrates, which requires prolonged exposure times and specialist equipment. Here, we provide an alternative method to the classical uptake assay using Raman spectroscopy to detect the uptake of alkyne-labelled substrates and determine transporter function. As a proof of principle, we demonstrate the method using a candidate nucleotide transporter (ThNTT4) expressed in Escherichia coli, which is shown to transport alkyne-labelled ATP molecules (N6pATP), which was readily detected using Raman spectroscopy. We show that ATP transport can be detected in a time-dependent manner using alkyne labels and demonstrate the substrate specificity of the transporter for purine but not pyrimidine substrates. This work establishes that Raman spectroscopy is an excellent alternative to using radioactive substrates in analysing, not only pathogen transporters, but potentially any transporter in which its substrate can be alkyne tagged