Control optimisatlion of CO(2) cycles for medium temperature retail food refrigeration systems

This is the post-print version of the final paper published in International Journal of Refrigeration. The published article is available from the link below. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. Copyright @ 2009 Elsevier B.V.This paper describes a detailed procedure into the investigation of optimised control strategies for CO2 cycles in medium temperature retail food refrigeration systems. To achieve this objective, an integrated model was developed composing of a detailed condenser/gas cooler model, a simplified compressor model, an isenthalpic expansion process and constant evaporating temperature and superheating. The CO2 system can operate subcritically or transcritically depending on the ambient temperature. For a transcritical operation, a prediction can be made for optimised refrigerant discharge pressures from thermodynamic cycle calculations. When the system operates in the subcritical cycle, a floating discharge pressure control strategy is employed and the effect of different transitional ambient temperatures separating subcritical and transcritical cycles on system performance is investigated. The control strategy assumes variable compressor speed and adjustable air flow for the gas cooler/condenser to be modulated to achieve the constant cooling load requirement at different ambient conditions.DEFR

Evaluation of Supermarket Energy Use and Emissions with Various Technology Options

In this paper, an operational supermarket in the UK has been selected to be modelled by the previously developed supermarket energy simulation software ‘SuperSIM’. Detailed information of the supermarket and model development procedures are explained. The model was previously validated through comparisons with site measurements of space air temperature and humidity and energy consumptions. It is therefore used to simulate, quantify and evaluate supermarket energy performance at various technology options in terms of heat recovery from refrigerant discharge, high efficiency condensers and evaporators and store locations etc

Modelling and performance evaluation of a low-temperature ammonia-water absorption refrigeration system

This paper presents the simulation of a low-temperature gas-fired ammonia-water absorption chiller for refrigeration applications. The model was developed as part of a research effort to investigate microturbine-based tri-generation systems for application in the food retail industry. The absorption chiller model was developed in the TRNSYS environment by integrating the main component models in the system and will form part of an overall TRNSYS-based supermarket model. The chiller model was validated against experimental results obtained on a 12 kW absorption chiller in the laboratory. The model was subsequently used to investigate the influence of important design and operating parameters on the performance of the chiller. © The Author 2009. Published by Oxford University Press. All rights reserved

Performance analysis of finned-tube CO2 gas cooler with advanced 1D-3D CFD modelling development and simulation

Research data for this article: Data not available / Data will be made available on request.Supplementary material is available online at: https://www.sciencedirect.com/science/article/pii/S1359431120307122?via%3Dihub#s0070 .Due to natural refrigerant applied, CO2 transcritical refrigeration and heat pump systems have been widely applied and attracted more attentions. As a main component, CO2 gas cooler plays an important role in the system performance and thus requires further development for design and control optimizations with advanced technology. Correspondingly, a new coupled 1D and 3D Computational Fluid Dynamics (CFD) model on a finned-tube CO2 gas cooler has been proposed and developed. The CFD model has been validated by comparing with literatures for parameters including airside heat transfer coefficient, refrigerant side temperature profile as well as heating capacity. The model has been applied to predict the heat exchanger performance at different operating conditions of both air and refrigerant sides and maldistributions of air flow inlet. It is found from the simulation results that the refrigerant temperature decreases abruptly in the first coil row and the refrigerant temperature profile along the heat exchanger tubes is affected by thermal conduction between two adjacent tube rows through fins. In addition, the higher air flow inlet velocity can reduce greatly the coil approach temperature and thus improve the system efficiency. Similar effect can also be found from refrigerant pressure. Furthermore, the non-uniform air flow patterns can affect considerably the coil performance in terms of the refrigerant temperature profile, coil approach temperature, coil heating capacity and system energy efficiency. The developed CFD model can be an efficient tool for the performance evaluation and optimisation of the CO2 gas cooler and its associated system.The authors would like to acknowledge the support received from Research Councils UK (ESPRC, EP/R000298/1) for this research project

Proteomic analysis at the sites of clinical infection with invasive Streptococcus pyogenes

Invasive Streptococcus pyogenes infections are rare, with often-unexplained severity. Prompt diagnosis is desirable, as deaths can occur rapidly following onset and there is an increased, but preventable, risk to contacts. Here, proteomic analyses of clinical samples from invasive human S. pyogenes infections were undertaken to determine if novel diagnostic targets could be detected, and to augment our understanding of disease pathogenesis. Fluid samples from 17 patients with confirmed invasive S. pyogenes infection (empyema, septic arthritis, necrotising fasciitis) were analysed by proteomics for streptococcal and human proteins; 16/17 samples had detectable S. pyogenes DNA. Nineteen unique S. pyogenes proteins were identified in just 6/17 samples, and 15 of these were found in a single pleural fluid sample including streptococcal inhibitor of complement, trigger factor, and phosphoglycerate kinase. In contrast, 469 human proteins were detected in patient fluids, 177 (38%) of which could be identified as neutrophil proteins, including alpha enolase and lactotransferrin which, together, were found in all 17 samples. Our data suggest that streptococcal proteins are difficult to detect in infected fluid samples. A vast array of human proteins associated with leukocyte activity are, however, present in samples that deserve further evaluation as potential biomarkers of infection

The novel use of phase change materials in an open type refrigerated display cabinet: A theoretical investigation

In this paper, 2D CFD models have been developed for a prototype refrigerated open type multi-deck display cabinet with and without integrated phase change material (PCM). The models can predict the effect of adding a PCM container on cabinet efficiencies, air temperature distributions, product temperatures and air flow patterns inside the cabinet at a range of operating conditions including space air temperatures and evaporator air velocities. To validate the cabinet models, the prototype cabinet was mounted in an air conditioned chamber and extensive experiments were conducted at constant space air temperature and relative humidity. The cabinet models have therefore been validated through comparison with experiment results for air temperatures at different locations of the airflow path and of food products. Simulation results show that significant energy can be saved through the installation of a PCM container. Further benefits include greater stabilization of product temperatures during defrost periods for the modified display cabinet. Consequently, the validated models can be used to explore and analyse the cabinet performance and control strategies at various operating and design conditions.Work presented in this paper was carried out with financial support from the Department of Environment, Food and Rural Affairs (Defra: AFM280). The authors would like to acknowledge the support of Defra and the input from the collaborating partners

Personalised randomised controlled trial designs—a new paradigm to define optimal treatments for carbapenem-resistant infections

Antimicrobial resistance is impacting treatment decisions for, and patient outcomes from, bacterial infections worldwide, with particular threats from infections with carbapenem-resistant Enterobacteriaceae, Acinetobacter baumanii, or Pseudomonas aeruginosa. Numerous areas of clinical uncertainty surround the treatment of these highly resistant infections, yet substantial obstacles exist to the design and conduct of treatment trials for carbapenem-resistant bacterial infections. These include the lack of a widely acceptable optimised standard of care and control regimens, varying antimicrobial susceptibilities and clinical contraindications making specific intervention regimens infeasible, and diagnostic and recruitment challenges. The current single comparator trials are not designed to answer the urgent public health question, identified as a high priority by WHO, of what are the best regimens out of the available options that will significantly reduce morbidity, costs, and mortality. This scenario has an analogy in network meta-analysis, which compares multiple treatments in an evidence synthesis to rank the best of a set of available treatments. To address these obstacles, we propose extending the network meta-analysis approach to individual randomisation of patients. We refer to this approach as a Personalised RAndomised Controlled Trial (PRACTical) design that compares multiple treatments in an evidence synthesis, to identify, overall, which is the best treatment out of a set of available treatments to recommend, or how these different treatments rank against each other. In this Personal View, we summarise the design principles of personalised randomised controlled trial designs. Specifically, of a network of different potential regimens for life-threatening carbapenem-resistant infections, each patient would be randomly assigned only to regimens considered clinically reasonable for that patient at that time, incorporating antimicrobial susceptibility, toxicity profile, pharmacometric properties, availability, and physician assessment. Analysis can use both direct and indirect comparisons across the network, analogous to network meta-analysis. This new trial design will maximise the relevance of the findings to each individual patient, and enable the top-ranked regimens from any personalised randomisation list to be identified, in terms of both efficacy and safety

Characterization and genomic analyses of two newly isolated Morganella phages define distant members among Tevenvirinae and Autographivirinae subfamilies

Morganella morganii is a common but frequent neglected environmental opportunistic pathogen which can cause deadly nosocomial infections. The increased number of multidrug-resistant M. morganii isolates motivates the search for alternative and effective antibacterials. We have isolated two novel obligatorily lytic M. morganii bacteriophages (vB_MmoM_MP1, vB_MmoP_MP2) and characterized them with respect to specificity, morphology, genome organization and phylogenetic relationships. MP1s dsDNA genome consists of 163,095bp and encodes 271 proteins, exhibiting low DNA (10kb chromosomal inversion that encompass the baseplate assembly and head outer capsid synthesis genes when compared to other T-even bacteriophages. MP2 has a dsDNA molecule with 39,394bp and encodes 55 proteins, presenting significant genomic (70%) and proteomic identity (86%) but only to Morganella bacteriophage MmP1. MP1 and MP2 are then novel members of Tevenvirinae and Autographivirinae, respectively, but differ significantly from other tailed bacteriophages of these subfamilies to warrant proposing new genera. Both bacteriophages together could propagate in 23 of 27M. morganii clinical isolates of different origin and antibiotic resistance profiles, making them suitable for further studies on a development of bacteriophage cocktail for potential therapeutic applications.This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, COMPETE 2020 (POCI-01-0145-FEDER-006684) and the Project PTDC/BBB-BSS/6471/2014 (POCI-01-0145-FEDER-016678). RL contributed to the genome sequencing analysis, supported by the KU Leuven GOA Grant ‘Phage Biosystems’. JP acknowledges the project R-3986 of the Herculesstichting.info:eu-repo/semantics/publishedVersio

Phosphoinositide-3 kinase inhibition modulates responses to rhinovirus by mechanisms that are predominantly independent of autophagy

Human rhinoviruses (HRV) are a major cause of exacerbations of airways disease. Aspects of cell signalling responses to HRV infection remain unclear, particularly with regard to signalling via PI3K, and the PI3K-dependent pathway, autophagy. We investigated the roles of PI3K and autophagy in the responses of epithelial cells to major and minor group HRV infection. The PI3K inhibitor 3-MA, commonly used to inhibit autophagy, markedly reduced HRV-induced cytokine induction. Further investigation of potential targets of 3-MA and comparison of results using this inhibitor to a panel of general and class I-selective PI3K inhibitors showed that several PI3Ks cooperatively regulate responses to HRV. Targeting by siRNA of the autophagy proteins Beclin-1, Atg7, LC3, alone or in combination, or targeting of the autophagy-specific class III PI3K had at most only modest effects on HRV-induced cell signalling as judged by induction of proinflammatory cytokine production. Our data indicate that PI3K and mTOR are involved in induction of proinflammatory cytokines after HRV infection, and that autophagy has little role in the cytokine response to HRV or control of HRV replication

Anthropogenic perturbation of the carbon fluxes from land to ocean

A substantial amount of the atmospheric carbon taken up on land through photosynthesis and chemical weathering is transported laterally along the aquatic continuum from upland terrestrial ecosystems to the ocean. So far, global carbon budget estimates have implicitly assumed that the transformation and lateral transport of carbon along this aquatic continuum has remained unchanged since pre-industrial times. A synthesis of published work reveals the magnitude of present-day lateral carbon fluxes from land to ocean, and the extent to which human activities have altered these fluxes. We show that anthropogenic perturbation may have increased the flux of carbon to inland waters by as much as 1.0 Pg C yr-1 since pre-industrial times, mainly owing to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (~0.4 Pg C yr-1) or sequestered in sediments (~0.5 Pg C yr-1) along the continuum of freshwater bodies, estuaries and coastal waters, leaving only a perturbation carbon input of ~0.1 Pg C yr-1 to the open ocean. According to our analysis, terrestrial ecosystems store ~0.9 Pg C yr-1 at present, which is in agreement with results from forest inventories but significantly differs from the figure of 1.5 Pg C yr-1 previously estimated when ignoring changes in lateral carbon fluxes. We suggest that carbon fluxes along the land–ocean aquatic continuum need to be included in global carbon dioxide budgets.Peer reviewe