Matthew Woolway

Liezl Stander, Matthew Woolway, Terence L. Van Zyl

Chemical plant design and optimisation have proven challenging due to the complexity of these real-world systems. The resulting complexity translates into high computational costs for these systems' mathematical formulations and simulation models. Research has illustrated the benefits of using machine learning surrogate models as substitutes for computationally expensive models during optimisation. This paper extends recent research into optimising chemical plant design and operation. The study further explores Surrogate Assisted Genetic Algorithms (SA-GA) in more complex variants of the original plant design and optimisation problems, such as the inclusion of parallel and feedback components. The novel extension to the original algorithm proposed in this study, Surrogate Assisted NSGA-\Romannum{2} (SA-NSGA), was tested on a popular literature case, the Pressure Swing Adsorption (PSA) system. We further provide extensive experimentation, comparing various meta-heuristic optimisation techniques and numerous machine learning models as surrogates. The results for both sets of systems illustrate the benefits of using Genetic Algorithms as an optimisation framework for complex chemical plant system design and optimisation for both single and multi-objective scenarios. We confirm that Random Forest surrogate assisted Evolutionary Algorithms can be scaled to increasingly complex chemical systems with parallel and feedback components. We further find that combining a Genetic Algorithm framework with Machine Learning Surrogate models as a substitute for long-running simulation models yields significant computational efficiency improvements, 1.7 - 1.84 times speedup for the increased complexity examples and a 2.7 times speedup for the Pressure Swing Adsorption system.

Mohamed Z. Variawa, Terence L. Van Zyl, Matthew Woolway

Real-world optimisation problems typically have objective functions which cannot be expressed analytically. These optimisation problems are evaluated through expensive physical experiments or simulations. Cheap approximations of the objective function can reduce the computational requirements for solving these expensive optimisation problems. These cheap approximations may be machine learning or statistical models and are known as surrogate models. This paper introduces a simulation of a well-known batch processing problem in the literature. Evolutionary algorithms such as Genetic Algorithm (GA), Differential Evolution (DE) are used to find the optimal schedule for the simulation. We then compare the quality of solutions obtained by the surrogate-assisted versions of the algorithms against the baseline algorithms. Surrogate-assistance is achieved through Probablistic Surrogate-Assisted Framework (PSAF). The results highlight the potential for improving baseline evolutionary algorithms through surrogates. For different time horizons, the solutions are evaluated with respect to several quality indicators. It is shown that the PSAF assisted GA (PSAF-GA) and PSAF-assisted DE (PSAF-DE) provided improvement in some time horizons. In others, they either maintained the solutions or showed some deterioration. The results also highlight the need to tune the hyper-parameters used by the surrogate-assisted framework, as the surrogate, in some instances, shows some deterioration over the baseline algorithm.

Terence L. van Zyl, Matthew Woolway, Andrew Paskaramoorthy

Portfolio management is a multi-period multi-objective optimisation problem subject to a wide range of constraints. However, in practice, portfolio management is treated as a single-period problem partly due to the computationally burdensome hyper-parameter search procedure needed to construct a multi-period Pareto frontier. This study presents the \gls{ParDen-Sur} modelling framework to efficiently perform the required hyper-parameter search. \gls{ParDen-Sur} extends previous surrogate frameworks by including a reservoir sampling-based look-ahead mechanism for offspring generation in \glspl{EA} alongside the traditional acceptance sampling scheme. We evaluate this framework against, and in conjunction with, several seminal \gls{MO} \glspl{EA} on two datasets for both the single- and multi-period use cases. Our results show that \gls{ParDen-Sur} can speed up the exploration for optimal hyper-parameters by almost $2\times$ with a statistically significant improvement of the Pareto frontiers, across multiple \glspl{EA}, for both datasets and use cases.

Hayato Kunugi, Mohsen Rahmani, Yosuke Iyama et al.

Deep generative modeling to stochastically design small molecules is an emerging technology for accelerating drug discovery and development. However, one major issue in molecular generative models is their lower frequency of drug-like compounds. To resolve this problem, we developed a novel framework for optimization of deep generative models integrated with a D-Wave quantum annealing computer, where our Neural Hash Function (NHF) presented herein is used both as the regularization and binarization schemes simultaneously, of which the latter is for transformation between continuous and discrete signals of the classical and quantum neural networks, respectively, in the error evaluation (i.e., objective) function. The compounds generated via the quantum-annealing generative models exhibited higher quality in both validity and drug-likeness than those generated via the fully-classical models, and was further indicated to exceed even the training data in terms of drug-likeness features, without any restraints and conditions to deliberately induce such an optimization. These results indicated an advantage of quantum annealing to aim at a stochastic generator integrated with our novel neural network architectures, for the extended performance of feature space sampling and extraction of characteristic features in drug design.