Preface

Based on the author's forty years of teaching experience, this unique textbook covers both basic and advanced concepts of optimization theory and methods for process systems engineers. Topics covered include continuous, discrete and logic optimization (linear, nonlinear, mixed-integer and generalized disjunctive programming), optimization under uncertainty (stochastic programming and flexibility analysis), and decomposition techniques (Lagrangean and Benders decomposition). Assuming only a basic background in calculus and linear algebra, it enables easy understanding of mathematical reasoning, and numerous examples throughout illustrate key concepts and algorithms. End-of-chapter exercises involving theoretical derivations and small numerical problems, as well as in modeling systems like GAMS, enhance understanding and help put knowledge into practice. Accompanied by two appendices containing web links to modeling systems and models related to applications in PSE, this is an essential text for single-semester, graduate courses in process systems engineering in departments of chemical engineering.

Based on the author's forty years of teaching experience, this unique textbook covers both basic and advanced concepts of optimization theory and methods for process systems engineers. Topics covered include continuous, discrete and logic optimization (linear, nonlinear, mixed-integer and generalized disjunctive programming), optimization under uncertainty (stochastic programming and flexibility analysis), and decomposition techniques (Lagrangean and Benders decomposition). Assuming only a basic background in calculus and linear algebra, it enables easy understanding of mathematical reasoning, and numerous examples throughout illustrate key concepts and algorithms. End-of-chapter exercises involving theoretical derivations and small numerical problems, as well as in modeling systems like GAMS, enhance understanding and help put knowledge into practice. Accompanied by two appendices containing web links to modeling systems and models related to applications in PSE, this is an essential text for single-semester, graduate courses in process systems engineering in departments of chemical engineering.

AIChE JournalVolume 33, Issue 2 p. 319-321 R & D Note Chemical comminution of coal A. H. Mamaghani, A. H. Mamaghani Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this authorJ. K. Beddow, J. K. Beddow Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this authorA. F. Vetter, A. F. Vetter Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this author A. H. Mamaghani, A. H. Mamaghani Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this authorJ. K. Beddow, J. K. Beddow Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this authorA. F. Vetter, A. F. Vetter Center for Particulate Materials Processing Sciences, Department of Chemical and Materials Engineering, University of Iowa Iowa City, IA 52242Search for more papers by this author First published: February 1987 https://doi.org/10.1002/aic.690330221Citations: 2AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume33, Issue2February 1987Pages 319-321 RelatedInformation

Biotechnology and BioengineeringVolume 21, Issue 12 p. 2359-2363 Communications to the EditorFree Access Nonporous magnetic supports for proteases, cell-lytic enzymes, and ribonuclease: Limits of reactant size P. J. Halling, P. J. Halling Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this authorJ. A. Asenjo, J. A. Asenjo Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this authorP. Dunnill, P. Dunnill Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this author P. J. Halling, P. J. Halling Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this authorJ. A. Asenjo, J. A. Asenjo Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this authorP. Dunnill, P. Dunnill Department of Chemical and Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, EnglandSearch for more papers by this author First published: December 1979 https://doi.org/10.1002/bit.260211217Citations: 14AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume21, Issue12December 1979Pages 2359-2363 ReferencesRelatedInformation

Event Abstract Back to Event Sulfated Glycopolymers for glycosaminoglycan mimics and nanomedicine Yoshiko Miura1, Tomohiro Fukuda2 and Yu Hoshino1 1 Kyushu University, Department of Chemical Engineering, Japan 2 National Institute of Technology, Toyama college, Department of Applied Chemistry and Chemical Engineering, Japan Glycosaminoglycans (GAGs) are polysaccharides found in living systems that play key roles in biological activities and also function as polyelectrolyte. The preparation of GAGs is important in view of biomaterials development, and total syntheses have been energetically studied by many researchers. However, it is difficult to attain the total syntheses of GAGs due to the complex chemical structure and large molecular sizes. We investigated the preparation GAGs mimic polymer and application of nanomedicine via glycopolymer methods. We tried to reconstruct the function of GAGs by glycopolymers of regioselective sulfated saccharides. Glycopolymers provides the strong binding based on the multivalency. In addition, glycopolymer libraries are easily prepared by the radical polymerization. We prepared the phenyl acrylamides with sulfonated N-acetyl glucosamines (GlcNAc) of 6-sulfo-. 3-sulfo-, 4-sulfo and 3,4, 6-sulfo-GlcNAc. The monomers of sulfonated GlcNAc were synthesized by glycosylation, regioselective sulfonation of GlcNAc and condensation with acrylate. The monomers were polymerized with other vinyl monomers to prepare the glycopolymer and glyconanoparticles (Figure 1). We investigated the affinities of the GAGs mimic glycopolymers with pathogen proteins. The glycopolymers with 6-sulfo-GlcNAc exhibited the inhibitory effect on Alzheimer’s amyloid beta peptides. The inhibitory effects depended on the sugar ratio and the molecular weights of the polymers. The GAGs mimic array was prepared to analyze the interaction with amyloid beta peptides. The enzyme (b-secretase) for Alzheimer disease was also inhibited by the GAGs mimic polymers. The nanoparticle with GAGs mimic monomer was also prepared to capture the specific proteins. These results showed the usefulness of the glycopolymers comparing to the real GAGs. The glycopolymers are applicable to the many kinds of materials including synthetic polymer, particle, nanoparticles and thin layer formations, which are useful for bionanomaterial and nanomedicine fabrications. Keywords: Biomimetic, polymer, Polymeric material, Bioactive molecule Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016. Presentation Type: New Frontier Oral Topic: Protein interactions with biomaterials Citation: Miura Y, Fukuda T and Hoshino Y (2016). Sulfated Glycopolymers for glycosaminoglycan mimics and nanomedicine. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.00918 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Mar 2016; Published Online: 30 Mar 2016. Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Yoshiko Miura Tomohiro Fukuda Yu Hoshino Google Yoshiko Miura Tomohiro Fukuda Yu Hoshino Google Scholar Yoshiko Miura Tomohiro Fukuda Yu Hoshino PubMed Yoshiko Miura Tomohiro Fukuda Yu Hoshino Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Event Abstract Back to Event A mechanically robust injectable hydrogel scaffold for adipose-derived stem cell delivery for the treatment of peripheral arterial disease Stuart Young1, Lauren E. Flynn2 and Brian G. Amsden1 1 Queen's University, Department of Chemical Engineering, Canada 2 University of Western Ontario, Department of Chemical and Biochemical Engineering, Canada Introduction: Peripheral arterial disease can lead to critical limb ischemia with high risks of amputation and mortality. A promising treatment involves delivering adipose-derived stem cells (ASCs) to stimulate revascularization and functional recovery. However, when delivered via intramuscular injection in saline, substantial ASC loss occurs. To improve ASC retention and survival, a modular delivery gel was developed composed of: i) methacrylated glycol chitosan (MGC) functionalized with GGGGRGDS, and ii) a diacrylate triblock copolymer of poly(ethylene glycol) (PEG) and poly(trimethylene carbonate) (PTMC) to improve mechanical robustness. A thermal initiator system of ammonium persulfate (APS) and N,N,N′,N′-tetramethylethylenediamine (TEMED) was optimized for in situ gelation following injectable delivery. Methods: MGC was prepared as previously reported[1]. The N terminus of GGGGRGDS peptide was acrylated and conjugated to MGC via Michael addition. Acrylated PEG-PTMC of varying block lengths was prepared by ring-opening polymerization of TMC initiated by PEG (4, 10, or 20 kg·mol-1) (TMC:PEG MW = 1:10 – 1:2)) using HCl as a monomer activator, followed by reaction with acryloyl chloride. Polymer structure and functionalization were confirmed by 1H NMR and GPC. To form gels, APS and TEMED (2.5 to 10 mM) were added to solutions of MGC and PEG-PTMC. Initiation sensitivity and crosslinking time were assessed by rheometry at 20 °C and 37°C. Gels were equilibrated in PBS, after which the swelling ratio and mechanical properties were measured. Isolated bovine ASCs[2], expanded to passage 2, were suspended in the pre-polymer solutions. APS/TEMED was added, and the suspension injected via 25G needle into molds and crosslinked by heating (37°C). ASC viability (LIVE/DEAD staining) and metabolic activity (MTT assay) were monitored over 7 days. Results: The MGC had a 5% degree of methacrylation and 5% degree of peptide functionalization, while the PEG-PTMC had > 99% acrylation. Pre-polymer solutions showed no gelation over 10 min at 20 °C (Fig. 1a). Upon heating, gelation time was directly related to initiator concentration (Fig. 1b). The swelling, equilibrium compressive modulus, and maximum strain of PEG-PTMC hydrogels was dependent on the overall molecular weight and PEG/PTMC ratio (Fig. 2). By blending MGC with PEG-PTMC, gel stiffness was significantly reduced to the range of native tissue (~10-15 kPa), while improving elastic resiliency under dynamic loading. Further, the metabolic activity of encapsulated ASCs was maintained over 7 d of culture. Discussion: Blending of MGC with PEG-PTMC facilitated adjustment of gel mechanical properties while improving resiliency under dynamic loading. The APS/TEMED crosslinking approach provided an injectable delivery method with high stimuli sensitivity. Sustained ASC metabolic activity in culture suggests the gel could promote ASC survival and retention, thereby promoting their regenerative effects in ischemic regions.

ADVERTISEMENT RETURN TO ISSUEEditorialNEXTTwenty-Five Years of Green Chemistry and Green Engineering: The End of the BeginningPaul T. Anastas and David T. AllenView Author Information Center for Green Chemistry and Green Engineering, School of Forestry and Environmental Studies, Department of Chemical and Environmental Engineering, Yale University, United States Center for Energy and Environmental Resources, Department of Chemical Engineering, The University of Texas at Austin, United StatesCite this: ACS Sustainable Chem. Eng. 2016, 4, 11, 5820Publication Date (Web):November 7, 2016Publication History Received13 October 2016Published online7 November 2016Published inissue 7 November 2016https://doi.org/10.1021/acssuschemeng.6b02484Copyright © 2016 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views2235Altmetric-Citations25LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (150 KB) Get e-AlertsSUBJECTS:Chemical engineering and industrial chemistry,Green chemistry,Molecular design Get e-Alerts

Journal of Applied Polymer ScienceVolume 37, Issue 10 p. 3057-3060 NoteFree Access Cellulose-induced crosslinking of polyethylene P. Cousin, P. Cousin Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorP. Bataille, P. Bataille Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorH. P. Schreiber, H. P. Schreiber Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorS. Sapieha, Corresponding Author S. Sapieha Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaPulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, Canada===Search for more papers by this author P. Cousin, P. Cousin Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorP. Bataille, P. Bataille Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorH. P. Schreiber, H. P. Schreiber Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaSearch for more papers by this authorS. Sapieha, Corresponding Author S. Sapieha Pulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, CanadaPulp and Paper Research Institute of Canada and Chemical Engineering Department, Ecole Polytechnique de Montréal, P.O. Box 6079, Station “A”, Montréal, Québec, H3C 3A7, Canada===Search for more papers by this author First published: 20 May 1989 https://doi.org/10.1002/app.1989.070371020Citations: 21AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL References 1 A. J. Michell, Appita, 39, 223 (1986). 2 C. Klason, J. Kubat, and H. E. Stromvall, Int. J. Polym. Mater., 10, 159 (1984). 3 E. P. Plueddemann, Silane Coupling Agents, Plenum, New York, 1982. 4 R. T. Woodhams, C. Thomas, and D. K. Rodgers, Polym. Eng. Sci., 24, 1166 (1984). 5 E. M. Kampouris and A. G. Andreopoulos, J. Appl. Polym. Sci., 34, 1209 (1987). 6 Ger. Pat. 2,440,668 (1975). 7 B. N. Misra, J. K. Jassal, and C. S. Pande, Ind. J. Chem., 16A, 1033 (1978). 8 W. N. Martin, Can. Pat. 893153 (1972). 9 P. Allard, Y. H. Zang, and S. Sapieha, to appear. 10 S. Sapieha, J. F. Pupo, and H. P. Schreiber, J. Appl. Polym. Sci., 37, 233 (1989). Citing Literature Volume37, Issue1020 May 1989Pages 3057-3060 ReferencesRelatedInformation

The Effect of Pressure on Electronic Structure H. G. Drickamer, H. G. Drickamer Department of Chemistry and Chemical Engineering, University of Illinois, Urbana, IllinoisSearch for more papers by this authorJ. C. Zahner, J. C. Zahner Department of Chemistry and Chemical Engineering, University of Illinois, Urbana, IllinoisSearch for more papers by this author H. G. Drickamer, H. G. Drickamer Department of Chemistry and Chemical Engineering, University of Illinois, Urbana, IllinoisSearch for more papers by this authorJ. C. Zahner, J. C. Zahner Department of Chemistry and Chemical Engineering, University of Illinois, Urbana, IllinoisSearch for more papers by this author Book Editor(s):I. Prigogine, I. Prigogine University of Brussels, Brussels, BelgiumSearch for more papers by this author First published: 01 January 1962 https://doi.org/10.1002/9780470143506.ch4Citations: 10Book Series:Advances in Chemical Physics AboutPDFPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Citing Literature Advances in Chemical Physics, Volume 4 RelatedInformation

Journal of Polymer Science Part C: Polymer LettersVolume 24, Issue 6 p. 273-281 Article Dynamics of polystyrene sulfonate ionomers in solution. A neutron spin-echo study B. Nyström, Corresponding Author B. Nyström Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwayDepartment of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwaySearch for more papers by this authorJ. Roots, J. Roots Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwaySearch for more papers by this authorJ. S. Higgins, J. S. Higgins Department of Chemical Engineering and Chemical Technology, Imperial College, London SW 7 2 BY, EnglandSearch for more papers by this authorB. Gabrys, B. Gabrys Department of Chemical Engineering and Chemical Technology, Imperial College, London SW 7 2 BY, EnglandSearch for more papers by this authorD. G. Peiffer, D. G. Peiffer Corporate Research Science Laboratories, Exxon Research and Engineering Company, Clinton Township-Route 22 East, Annandale, New Jersey 08801Search for more papers by this authorF. Mezei, F. Mezei Institut Laue-Langevin, 156X, 38042 Grenoble Cédex, FranceSearch for more papers by this authorB. Sarkissian, B. Sarkissian Institut Laue-Langevin, 156X, 38042 Grenoble Cédex, FranceSearch for more papers by this author B. Nyström, Corresponding Author B. Nyström Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwayDepartment of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwaySearch for more papers by this authorJ. Roots, J. Roots Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, 0315 Oslo 3, NorwaySearch for more papers by this authorJ. S. Higgins, J. S. Higgins Department of Chemical Engineering and Chemical Technology, Imperial College, London SW 7 2 BY, EnglandSearch for more papers by this authorB. Gabrys, B. Gabrys Department of Chemical Engineering and Chemical Technology, Imperial College, London SW 7 2 BY, EnglandSearch for more papers by this authorD. G. Peiffer, D. G. Peiffer Corporate Research Science Laboratories, Exxon Research and Engineering Company, Clinton Township-Route 22 East, Annandale, New Jersey 08801Search for more papers by this authorF. Mezei, F. Mezei Institut Laue-Langevin, 156X, 38042 Grenoble Cédex, FranceSearch for more papers by this authorB. Sarkissian, B. Sarkissian Institut Laue-Langevin, 156X, 38042 Grenoble Cédex, FranceSearch for more papers by this author First published: June 1986 https://doi.org/10.1002/pol.1986.140240607Citations: 11AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume24, Issue6June 1986Pages 273-281 RelatedInformation

Peter Zandstra speaks to Emily Culme-Seymour, Assistant Commissioning Editor Peter Zandstra graduated with a Bachelor of Engineering degree from McGill University (QC, Canada) in the Department of Chemical Engineering, and obtained his PhD degree from the University of British Columbia (BC, USA) in the Department of Chemical Engineering and Biotechnology, under the supervision of Jamie Piret and Connie Eaves. He continued his research training as a Post Doctoral Fellow in the field of Bioengineering at the Massachusetts Institute of Technology (MA, USA; with Doug Lauffenburger) before being appointed to the University of Toronto (ON, USA) in 1999. He holds an academic appointment as a Professor at the University of Toronto's Institute of Biomaterials and Biomedical Engineering, and he is cross-appointed with the Departments of Chemical Engineering and Applied Chemistry, and the Donnelly Centre for Cellular and Biomolecular Research. Zandstra is a Canada Research Chair in Stem Cell Bioengineering and is a recipient of a number of awards and fellowships including the Premiers Research Excellence Award (2002), the Edgar William Richard Steacie Memorial Fellowship (2006), the John Simon Guggenheim Memorial Foundation Fellowship (2007) and the McLean Award (2009). Zandstra is a fellow of the American Institute for Medical and Biological Engineering and the American Association for the Advancement of Science. Zandstra currently serves as associate editor for several journals. In addition to his academic appointment, he serves as the Chief Scientific Officer for the Centre for Commercialization of Regenerative Medicine in Toronto (ON, Canada).

Journal Article Comparison of Principal Component Analysis and Multivariate Curve Resolution-Alternating Least Squares Analysis of XPS Spectral Maps Get access F B Lavoie, F B Lavoie Department of Chemical and Biotechnological Engineering, Université de Sherbrooke. Sherbrooke, (QC) J1K 2R1 Canada Search for other works by this author on: Oxford Academic Google Scholar N Braidy, N Braidy Department of Chemical and Biotechnological Engineering, Université de Sherbrooke. Sherbrooke, (QC) J1K 2R1 Canada Search for other works by this author on: Oxford Academic Google Scholar S Biais, S Biais Centre de caractérisation des matériaux. Université de Sherbrooke. Sherbrooke, (QC) J 1K 2R1 Canada Search for other works by this author on: Oxford Academic Google Scholar R Gosselin R Gosselin Department of Chemical and Biotechnological Engineering, Université de Sherbrooke. Sherbrooke, (QC) J1K 2R1 Canada Search for other works by this author on: Oxford Academic Google Scholar Microscopy and Microanalysis, Volume 20, Issue S3, 1 August 2014, Pages 658–659, https://doi.org/10.1017/S1431927614005017 Published: 27 August 2014

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Environmental Microbiology ReportsVolume 13, Issue 1 p. 3-7 Crystal Ball Are we really studying persister cells? Sooyeon Song, Sooyeon Song Department of Animal Science, JeonBuk National University, Jeonju-si, Jeollabuk-do, 54896 Republic of KoreaSearch for more papers by this authorThomas K. Wood, Corresponding Author Thomas K. Wood [email protected] Department of Chemical Engineering, Pennsylvania State University, University Park, PA, 16802-4400 USAFor correspondence. E-mail [email protected]; Tel. (+)1 814-863-4811; Fax (1) 814-865-7846.Search for more papers by this author Sooyeon Song, Sooyeon Song Department of Animal Science, JeonBuk National University, Jeonju-si, Jeollabuk-do, 54896 Republic of KoreaSearch for more papers by this authorThomas K. Wood, Corresponding Author Thomas K. Wood [email protected] Department of Chemical Engineering, Pennsylvania State University, University Park, PA, 16802-4400 USAFor correspondence. E-mail [email protected]; Tel. (+)1 814-863-4811; Fax (1) 814-865-7846.Search for more papers by this author First published: 03 May 2020 https://doi.org/10.1111/1758-2229.12849Citations: 15Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume13, Issue1February 2021Pages 3-7 RelatedInformation

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