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Chlorine Contribution to Quantitative Structure and Activity Relationship Models of Disinfection By-Products' Quantum Chemical Descriptors and ToxicitiesWang, Fang 27 May 2009 (has links)
Quantitative Structure-Activity Relationship (QSAR) has been applied extensively in predicting toxicity of Disinfection By-Products (DBPs) in drinking water. Among many toxicological properties, acute and chronic toxicities of DBPs have been widely used in health risk assessment of DBPs. These toxicities are correlated with molecular properties, which are usually correlated with molecular descriptors. The primary goals of this thesis are: 1) to investigate the effects of molecular descriptors (e.g., chlorine number) on molecular properties such as energy of the lowest unoccupied molecular orbital (ELUMO) via QSAR modelling and analysis; 2) to validate the models by using internal and external cross-validation techniques; 3) to quantify the model uncertainties through Taylor and Monte Carlo Simulation. One of the very important ways to predict molecular properties such as ELUMO is using QSAR analysis. In this study, number of chlorine (NCl) and number of carbon (NC) as well as energy of the highest occupied molecular orbital (EHOMO) are used as molecular descriptors. There are typically three approaches used in QSAR model development: 1) Linear or Multi-linear Regression (MLR); 2) Partial Least Squares (PLS); and 3) Principle Component Regression (PCR). In QSAR analysis, a very critical step is model validation after QSAR models are established and before applying them to toxicity prediction. The DBPs to be studied include five chemical classes: chlorinated alkanes, alkenes, and aromatics. In addition, validated QSARs are developed to describe the toxicity of selected groups (i.e., chloro-alkane and aromatic compounds with a nitro- or cyano group) of DBP chemicals to three types of organisms (e.g., Fish, T. pyriformis, and P.pyosphoreum) based on experimental toxicity data from the literature. The results show that: 1) QSAR models to predict molecular property built by MLR, PLS or PCR can be used either to select valid data points or to eliminate outliers; 2) The Leave-One-Out Cross-Validation procedure by itself is not enough to give a reliable representation of the predictive ability of the QSAR models, however, Leave-Many-Out/K-fold cross-validation and external validation can be applied together to achieve more reliable results; 3) ELUMO are shown to correlate highly with the NCl for several classes of DBPs; and 4) According to uncertainty analysis using Taylor method, the uncertainty of QSAR models is contributed mostly from NCl for all DBP classes.
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Structural feature based computational approach of toxicity prediction of ionic liquids: Cationic and anionic effects on ionic liquids toxicitySalam, M.A., Abdullah, B., Ramli, A., Mujtaba, Iqbal M. 01 October 2016 (has links)
Yes / The density functional theory (DFT) based a unique model has been developed to predict the toxicity of ionic liquids using structural-feature based quantum chemical reactivity descriptors. Electrophilic indices (ω), the energy of highest occupied (EHOMO) and lowest unoccupied molecular orbital, (ELUMO) and energy gap (∆ E) were selected as the best toxicity descriptors of ILs via Pearson correlation and multiple linear regression analyses. The principle components analysis (PCA) demonstrated the distribution and inter-relation of descriptors of the model. A multiple linear regression (MLR) analysis on selected descriptors derived the model equation for toxicity prediction of ionic liquids. The model predicted toxicity values and mechanism are very consistent with observed toxicity. Cationic and side chains length effect are pronounced to the toxicity of ILs. The model will provide an economic screening method to predict the toxicity of a wide range of ionic liquids and their toxicity mechanism.
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Elumo : - Smart bottenplatta för klivande rullstolarSvensson, Malin, Olsson, Johan January 2022 (has links)
Imagine a power wheelchair that can step over obstacles, step up on sidewalks and drive on lateral slopes whilst the user is still seated upright. Previously these features were impossible, but thanks to Elumo this is no longer the case. Elumo is a six-wheeled base to be used on electric wheelchairs. The base has been developed by Malin Svensson and Johan Olsson during their bachelor’s thesis at the Innovation Engineering Program at Halmstad University. The project took place between autumn 2021 and spring 2022. The development of Elumo started with several user studies conducted by the students, where over 70 wheelchair users responded to a survey concerning the everyday life of a person using wheelchairs. These users were later invited to a user workshop where they could list everyday complaints and possible improvements concerning existing power wheelchairs. One of the most common complaints was getting up on sidewalks and driving on uneven terrain. Both of these problems will be solved with the base Elumo. The technology that makes the stepping-feature and improved suspension possible, is patented by the company EMTW and the students have had a close cooperation with them during the development. Our goal is for “Elumo to become a new product that will focus on the user and will deliver innovative power wheelchairs that provide safety, independence and improve quality of life for people using wheelchairs.”
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