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Intensification of Biobased Processes

Intensification of Biobased Processes

Andrzej Górak | Andrzej Stankiewicz

(2018)

Additional Information

Abstract

In recent years bioprocessing has increased in popularity and importance, however, bioprocessing still poses various important techno-economic and environmental challenges, such as product yields, excessive energy consumption for separations in highly watery systems, batch operation or the downstream processing bottlenecks in the production of biopharmaceutical products. Many of those challenges can be addressed by application of different process intensification technologies discussed in the present book.

The first book dedicated entirely to this area, Intensification of Biobased Processes provides a comprehensive overview of modern process intensification technologies used in bioprocessing. The book focusses on four different categories of biobased products: bio-fuels and platform chemicals; cosmeceuticals; food products; and polymers and advanced materials. It will cover various intensification aspects of the processes concerned, including (bio)reactor intensification; intensification of separation, recovery and formulation operations; and process integration. This is an invaluable source of information for researchers and industrialists working in chemical engineering, biotechnology and process engineering.


Prof. Andrzej Górak is a Professor at Lodz University of Technology, Poland and an Emeritus Professor of TU Dortmund University. He is an Editor of Chemical Engineering and Processing: Process Intensification and a Board Member of the European Process Intensification Centre (EUROPIC).

His scientific interests are reactive and bioreactive separation processes, process intensification, computer aided process engineering. His research is also focused on experimental investigations of reactive and hybrid separation processes such as reactive distillation and membrane separations.

Andrzej Stankiewicz is Full Professor at Delft University of Technology (Chair of Intensified Reaction and Separation Systems) and Director of TU Delft Process Technology Institute. He is author of numerous publications on chemical reaction engineering, industrial catalysis and process intensification, including the world’s first book on Process Intensification: Re-Engineering the Chemical Processing Plant.

Prof. Stankiewicz is an Editor of Chemical Engineering and Processing: Process Intensification and a Series Editor of the Green Chemistry Books Series. He was the founder and first Chairman of the Working Party on Process Intensification at the European Federation of Chemical Engineering, and currently chairs the Board of the European Process Intensification Centre (EUROPIC).

His current research interests are control of molecular interactions and intensification of chemical processes using electric and electromagnetic fields. And he has been awarded the prestigious Advanced Investigator Grant by the European Research Council (with co-workers) and a grant by the Bill and Melinda Gates Foundation.

Table of Contents

Section Title Page Action Price
Cover Cover
Intensification of Biobased Processes i
Preface vii
Dedication xi
Contents xiii
Chapter 1 - Intensified Fermentation Processes and Equipment 1
1.1 Introduction 1
1.2 Fermentation 3
1.2.1 Fermentation Processes 3
1.2.2 Fermentation Equipment 4
1.3 Fermentation Fundamentals and Rate-limiting Factors 6
1.3.1 Stoichiometry/Kinetics 6
1.3.2 Operation Modes: Use of the Invested Utilities to the Max 7
1.3.3 Transport Limitations 9
1.3.4 Scale Dependency of Flow Regimes and Transport 9
1.3.5 Biomass Retention 9
1.4 Hydrodynamics 10
1.4.1 Hydrodynamics in Non-stirred Fermenters 10
1.4.1.1 Power Input 10
1.4.1.2 Fluid Flow Regimes 11
1.4.1.3 Liquid Flow and Velocity 12
1.4.2 Hydrodynamics in Stirred Fermenters 13
1.4.2.1 Power Input 13
1.4.2.2 Flow Regimes 14
1.4.3 Mass Transfer 15
1.4.4 Heat Transfer 18
1.4.5 Liquid Mixing 20
1.5 Fermentation Intensification 22
1.6 Examples 24
1.6.1 Bioethanol Production with Saccharomyces cerevisiae: Smart Integration (FI Principle 4) 24
1.6.2 Biopharmaceuticals Production with Mammalian Cells: Jump via Cell Retention (FI Principles 2 and 4) 25
1.6.3 Bakers’ Yeast Production: Debottlenecking Oxygen Transfer (FI Principle 3) 26
1.6.4 Synergistic Production of Complex and Non-natural Compounds via Fermentation (FI Principles 1 and 4) 28
1.7 Fermentation Intensification Limits 28
1.7.1 Bakers’ Yeast Case 31
1.7.2 BDO Case 34
1.8 Conclusions and Outlook 35
Abbreviations 38
Acknowledgements 38
References 38
Chapter 2 - Rotating Bioreactors: Concept, Designs and Applications 42
2.1 Introduction 42
2.2 Background 43
2.2.1 Bioreactor Design Requirements for Microbial Transformations 43
2.2.2 Rotating Reactor: Design Concept, Characteristics and Processing Benefits 45
2.3 Rotating Reactors for Microbial Fermentation and Biotransformation Applications 46
2.3.1 Rotating Fluidised Bed 46
2.3.2 Rotating Bed Bioreactors 49
2.3.3 Rotating Biofilm Contactors 54
2.3.4 Rotating Membrane Bioreactors 57
2.4 Summary and Outlook 58
References 59
Chapter 3 - Intensified Downstream Processing in Biofuels Production 62
3.1 Introduction 62
3.2 Types of Biofuels 63
3.3 Biodiesel 65
3.3.1 Dividing-wall Column (DWC) Technology 66
3.3.2 Reactive Distillation 67
3.3.3 Reactive Dividing-wall Column 69
3.3.4 Other PI Techniques 70
3.4 Bioethanol 71
3.4.1 Extractive Dividing-wall Column 72
3.4.2 Heat Pump Assisted Extractive Distillation 72
3.5 Biobutanol 76
3.6 Dimethyl Ether 77
3.6.1 DWC Ternary Separation 79
3.6.2 Reactive DWC 80
3.6.3 Reactive Distillation 81
3.6.4 Catalytic Cyclic Distillation 82
3.7 Concluding Remarks 83
References 84
Chapter 4 - Improving Fermentation by Product Removal 86
4.1 Introduction 86
4.2 The Roles of ISPR 88
4.2.1 Improving the Product Formation Rate and Yield of Product on Substrate 88
4.2.2 Avoiding Product Degradation 91
4.2.3 Improving Downstream Processing 91
4.3 Process Design Aspects 92
4.3.1 Configurations 92
4.3.2 Batch Versus Continuous Operating Mode 93
4.3.3 The Importance of Cell Reuse in ISPR 95
4.3.4 Recycles 96
4.3.5 Modelling and Simulation 96
4.3.6 Calculating Generic Conditions at Which ISPR is Appropriate 98
4.4 ISPR for Phase Separating Compounds 98
4.4.1 General Considerations 98
4.4.2 Example: Development of ISPR for 2-butanol Production 101
4.4.3 Example: Development of ISPR for Sesquiterpene Production 102
4.5 Concluding Remarks 104
Appendix. Comparison of Performance of Base Case and ISPR Case 105
References 106
Chapter 5 - Liquid–Liquid Extraction in Processing of Bioproducts 109
5.1 Introduction to Liquid–Liquid Extraction 109
5.2 Process Intensification in Liquid–Liquid Extraction 110
5.2.1 Intensification Using New Materials in Extraction Systems 111
5.2.1.1 Water-based and Renewable Solvents 112
5.2.1.2 Ionic Liquids (ILs) and Deep Eutectic Solvents (DES) 113
5.2.1.3 Surfactants, Microemulsions and Micelles 114
5.2.2 Intensification by Novel Equipment and External Force 114
5.2.2.1 Intensification in Equipment for Liquid–Liquid Extraction 114
5.2.2.2 External Force Assisted Extraction 115
5.2.3 Intensification by Integrated and Hybrid Extraction Methods 117
5.2.3.1 Integrated Solvent Extraction Strategies 117
5.2.3.2 Intensification by Hybrid Separation Methods 117
5.3 Application of Liquid–Liquid Extraction to Bioproducts 118
5.3.1 Recovery of Fermentation-derived Products 119
5.3.1.1 Recovery of Antibiotics 119
5.3.1.2 Recovery of Carboxylic Acids and Organic Acids 120
5.3.1.3 Other Fermentation-derived Products 120
5.3.1.4 Extraction of Biopolymers and Cellular Components 121
5.3.2 Biofuels, Platform Chemicals and Biomass Hydrolysate Products 122
5.3.2.1 Biofuels 122
5.3.2.2 Platform Chemicals 123
5.3.2.3 Biomass Hydrolysate Components and Impurities 123
5.3.3 Microalgal Bio-based Products 123
5.4 Conclusions and Outlook 124
References 125
Chapter 6 - Organic Solvent Nanofiltration for an Intensified Processing of Renewable Raw Materials 132
6.1 Introduction 132
6.1.1 Oils and Fats 133
6.1.2 Current Processes and Challenges 133
6.2 Organic Solvent Nanofiltration 134
6.2.1 Fundamentals, Benefits and Constraints 134
6.2.2 Membrane Modules, Cascades and Membrane-assisted Processes 135
6.3 Applications 137
6.3.1 Solvent Recovery 138
6.3.2 Deacidification 139
6.4 Conclusion 141
References 142
Chapter 7 - Green Fuels and Fuel Additives Production in Simulated Moving Bed Reactors 145
7.1 Simulated Moving Bed Reactor Technology – What is it 145
7.2 Design and Modelling of Simulated Moving Bed Reactor Processes 148
7.3 Simulated Moving Bed Reactor in the Context of Bio-based Industries: Production of Fuels and Fuel Additives 152
7.3.1 Production of Acetals from Bioethanol 154
7.3.2 Valorization of Bioglycerol 158
7.4 Conclusions 161
Nomenclature 162
Greek Letters 162
Superscripts and Subscripts 162
Abbreviations 163
Acknowledgements 163
References 163
Chapter 8 - Intensification of Enzymatic Hydrolysis of Cellulose Using High Frequency Ultrasound 166
8.1 Introduction 166
8.2 Theoretical Background 169
8.2.1 Fundamental Aspects of Ultrasound and Cavitation 169
8.2.2 Overview of Cavitation-assisted Enzymatic Hydrolysis 171
8.2.3 Overview of the Effects of Ultrasound on Enzymes 173
8.3 Experimental Section 174
8.3.1 Materials 174
8.3.2 Procedures and Sample Preparations 175
8.3.3 Brunauer–Emmett–Teller (BET) and X-ray Diffraction (XRD) Surface Analysis 176
8.4 Results and Discussion 177
8.4.1 Enzymatic Hydrolysis of Cellulose in the Presence and Absence of Ultrasound 177
8.4.2 Effects of the Frequency of Ultrasound on Enzymatic Hydrolysis 179
8.4.3 BET and XRD Studies 180
8.5 Energy, Cost, and Scale-up Considerations 182
8.6 Conclusions 184
Acknowledgements 184
References 185
Chapter 9 - Process Intensification for Hydroprocessing of Vegetable Oil 188
9.1 Introduction 188
9.2 Experimental 191
9.2.1 Catalyst Coatings for Microchannel Reactors 191
9.2.2 Microchannel Plate Pretreatment and Catalyst Coating 192
9.2.3 Experimental Setup 192
9.2.4 Catalyst Activity Test and Jatropha Properties 194
9.3 Results and Discussion 195
9.3.1 Physicochemical Properties of the Catalyst 195
9.3.2 195
9.3.3 C9–C14 Hydrocarbons Yield 196
9.3.4 C15–C18 Hydrocarbons Yield 197
9.3.5 >C18 Oligomerized Products Yield 198
9.3.6 Influence of Pressure on Product Yield in the Microchannel Reactor 198
9.3.7 Kinetics and Thermodynamics of Vegetable Oil Hydroprocessing 200
9.3.8 Computational Dynamics Studies 200
9.3.8.1 Molar Flow Rate Variation of Reactant and Products in COMSOL 200
9.3.8.2 Concentration, Temperature and Velocity Profile for Triglyceride Hydroprocessing in the Microchannel Reactor 202
9.3.8.3 Concentration Profile of Products 204
9.4 Conclusion 205
Acknowledgements 207
References 207
Chapter 10 - Enzymatic Reactive Absorption and Distillation 210
10.1 Introduction 210
10.1.1 Reactive Absorption (RA) and Distillation (RD) 211
10.1.2 Enzymatic Reactive Absorption (ERA) and Distillation (ERD) 212
10.2 Technical Realization 215
10.2.1 Equipment for ERA and ERD Processes 215
10.2.1.1 Columns 215
10.2.1.2 Rotating Packed Beds 216
10.2.1.3 Membrane Contactors 218
10.2.1.4 Criteria for Equipment Selection 219
10.2.2 Application of Enzymes 219
10.2.2.1 Homogeneous Application and Recovery 220
10.2.2.2 Heterogeneous Enzyme Application 222
10.3 Modeling and Design 225
10.3.1 Modeling of Continuous ERA and ERD 226
10.3.2 Reaction Kinetics for Enzyme Reactions 228
10.4 Application Examples 229
10.4.1 Application of ERA for CO2 Capture 230
10.4.1.1 Challenges in Conventional CO2-capture Processes 230
10.4.1.2 Carbonic Anhydrase in CO2-capture Processes 231
10.4.1.3 Performance of Enzyme-enhanced Absorption Processes 232
10.4.2 Application of ERD 234
10.4.2.1 Transesterification to Butyl Butyrate 235
10.4.2.2 Resolution of Secondary Alcohols 236
10.4.2.3 The Potential of ERD 237
10.5 Conclusions 238
Acknowledgements 240
References 240
Chapter 11 - Process Intensification of Immobilized Enzyme Reactors 249
11.1 Introduction 249
11.2 Enzymes as Catalysts 250
11.3 Enzymatic Reactors: Conventional Versus Process Intensified Reactors 251
11.3.1 Conventional Reactors and Enzyme Catalysis 251
11.3.2 Process Intensified Enzymatic Reactors (PI-ER) 252
11.3.2.1 Enzymatic Membrane Reactor (EMR) 252
11.3.2.2 Enzymatic Microreactors 255
11.3.2.3 Immobilized Monolithic Enzyme Reactors (IMERs) 258
11.3.2.4 Rotating Packed Bed Reactors (RPBs) 260
11.3.2.5 Spinning Mesh Disc Reactor (SMDR) 261
11.4 Conclusion 263
References 263
Chapter 12 - Process Intensification of Enzymatic Biotransformation Processes 268
12.1 Introduction 268
12.1.1 Enzymatic Biotransformation 268
12.1.2 Process Intensification 271
12.2 Process Intensification and Biotransformation 272
12.3 Case Study 1 – Extractive Biotransformation of Naphthalene 277
12.4 Case Study 2 – Intensification of Enzymatic Hydrolyis of Triglyceride Ester 279
12.5 Conclusions 284
References 285
Chapter 13 - Microalgae: From Bio-based Curiosity Towards a Bulk Feedstock 289
13.1 Microalgae and Their Potential for Bulk-commodities and Biofuels 289
13.2 Cultivation of Microalgae: Current State and Emerging Trends 290
13.2.1 Current Phototrophic Cultivation 290
13.2.2 Novel Reactor Designs 293
13.2.2.1 Panel Photobioreactors 293
13.2.2.2 Tubular Photobioreactors with Wavy Two-phase Flow 293
13.2.2.3 Thin-layer Systems – Sloped Shallow Ponds 293
13.2.2.4 Biofilm Systems 294
13.3 From Single to Multiple Products 294
13.3.1 Necessity for Low Cost- and Mild Technologies 294
13.3.2 Harvesting Microalgae 295
13.3.3 Cell Disruption 296
13.3.4 Extraction 297
13.4 Concluding Remarks 298
13.4.1 State-of-development of Microalgae for Bulk Products 298
13.4.2 Further Steps Towards Feasible Bulk-commodity Production 299
References 299
Chapter 14 - Process Intensification in Glutamic Acid Production 303
14.1 Introduction 303
14.2 Current Production Process and the Challenges in Sustainability 304
14.3 Process Intensification Approaches Towards Sustainability 306
14.4 Process Intensification in Glutamic Acid Production Through a Membrane-integrated Reactor System 307
14.5 The Fermentation Media for the Bioprocess 311
14.6 Fermentation 311
14.7 Analytical Determination for Process Monitoring 312
14.8 Membrane Fouling and Cleaning 312
14.9 Analysis of Process Intensification Through a Membrane-integrated Hybrid Reactor System 313
14.9.1 Production Parameters 313
14.9.2 Plant Configuration 315
14.9.3 Space Intensification 317
14.9.4 Flexibility in Capacity and Application 319
14.9.5 Energy Intensity 319
14.9.6 Labour Intensity 320
14.9.7 Eco-friendliness 321
14.9.8 Economic Gain 321
14.10 Conclusion 325
References 325
Chapter 15 - Intensified Production of Recombinant Proteins 327
15.1 Introduction 327
15.1.1 Recombinant Monoclonal Antibodies as Pharmaceuticals 327
15.1.2 Development and Production of a Recombinant Monoclonal Antibody 328
15.1.3 State-of-the-art Monoclonal Antibody Production 328
15.1.3.1 Upstream: Cultivation of Cells 328
15.1.3.2 Downstream: Monoclonal Antibody Capture and Polishing 329
15.2 Continuous Cultivation of Mammalian Cell Cultures 331
15.2.1 Perfusion Culture Systems 331
15.2.2 Steady State Operation of Continuous Bioreactors 332
15.3 Continuous Countercurrent Chromatography in Monoclonal Antibody Capture 333
15.3.1 Principles of Countercurrent Chromatography 333
15.3.2 Periodic Countercurrent Chromatography 335
15.3.3 Performance Comparison of Capture Processes 335
15.4 Continuous mAb Polishing 337
15.4.1 Multi-column Countercurrent Solvent Gradient Purification 337
15.4.2 Integrated Protein PEGylation 340
15.5 Conclusions 341
References 342
Chapter 16 - Intensification of Aqueous Two-phase Extraction for Protein Purification 344
16.1 Introduction 344
16.2 Thermodynamic Background 345
16.2.1 ATPS Phase Equilibria 345
16.2.2 Protein Partitioning 346
16.2.2.1 Measurement of the Second Osmotic Virial Coefficient 348
16.2.2.2 Measurement of Osmotic Cross Virial Coefficient 349
16.2.3 Results–Estimating Partition Coefficients in ATPE 350
16.3 Purification of Enzymes in a Mixer–Settler Apparatus 352
16.3.1 Single Stage Experiments 353
16.3.2 Multistage Experiments 355
16.4 Centrifugal Partition Chromatography 356
16.4.1 Experimental 358
16.4.2 Results 358
16.4.2.1 Hydrodynamic Behavior 358
16.4.2.2 Activity Balance for Laccase Separation Using the Combination of a CPC and ATPE 359
16.5 Conclusion 361
References 361
Chapter 17 - Intensification of Functional Foods Production 365
17.1 Functional Foods 365
17.2 Food Processes Intensification 367
17.3 Process Intensification of Functional Foods Based on Nanodispersion Production 368
17.3.1 Formation of Nanodispersions 369
17.3.2 Classification of the Techniques for Production of Nanodispersions Based on Nature of Solvent Used 370
17.3.2.1 Emulsification-evaporation Technique 370
17.3.2.2 Emulsification–Diffusion Technique 371
17.3.2.3 Solvent-displacement Technique 371
17.3.3 Process Intensification 372
17.4 Preparation of Functional Nano-sized Lycopene from Tomato Processing Wastes 373
17.4.1 Materials and Methods 373
17.4.2 Results and Discussions 374
17.4.3 Conclusions 377
17.5 Concluding Remarks 377
Acknowledgements 378
References 378
Chapter 18 - Microwave-enhanced Extraction of Natural and Food Products: from Academia to Innovative and Large-scale Applications 381
18.1 Introduction 381
18.2 Microwave Heat Transfer 382
18.3 Microwave-assisted Extraction 383
18.3.1 Microwave Combined with Solvent Extraction 384
18.3.1.1 Microwave-assisted Solvent Extraction (MASE) 384
18.3.1.2 Vacuum Microwave-assisted Extraction (VMASE) 384
18.3.1.3 Microwave Integrated Soxhlet Extraction (MIS) 384
18.3.2 Microwave Extraction with Water Distillation 385
18.3.2.1 Compressed Air Microwave Distillation (CAMD) 385
18.3.2.2 Microwave Hydrodistillation (MWHD) 385
18.3.2.3 Vacuum Microwave Hydrodistillation (VMHD) 385
18.3.2.4 Microwave Accelerated Steam Distillation (MASD) 385
18.3.3 Microwave Combined with Solvent-free Distillation 386
18.3.3.1 Solvent-free Microwave-assisted Extraction (SFME) 386
18.3.3.2 Vacuum Solvent-free Microwave-assisted Extraction (VSFME) 386
18.3.4 Microwave-assisted Hydrodiffusion 386
18.3.4.1 Microwave Hydrodiffusion and Gravity (MHG) 386
18.3.4.2 Vacuum Microwave Hydrodiffusion and Gravity (VMHG) 387
18.3.5 Microwave Steam Diffusion (MSDF) 388
18.3.6 Industrial Application of Microwave-assisted Extraction 389
18.4 Applications 389
18.4.1 Antioxidants 389
18.4.2 Flavors and Fragrances 390
18.4.3 Natural Colors 391
18.4.4 Fats and Oils 392
18.5 Applications of Microwave Extraction in Industry 394
Acknowledgements 394
References 394
Chapter 19 - Intensified Food Processing Through Membrane Operations 397
19.1 Introduction 397
19.2 Fundamentals of Membrane Operations 398
19.2.1 Pressure-driven Membrane Operations 398
19.2.2 Membrane Contactors 402
19.2.3 Pervaporation 405
19.2.4 Electrodialysis 406
19.3 Integrated Membrane Operations in Food Processing 407
19.3.1 Fruit Juice Processing 407
19.3.2 Must and Wine Processing 416
19.3.3 Milk and Whey Processing 420
19.4 Conclusions 424
References 425
Chapter 20 - Intensified Brewing Systems 430
20.1 Introduction 430
20.2 Short Overview on Brewing 431
20.2.1 Malting 431
20.2.2 Mashing 432
20.2.2.1 Traditional Equipment 433
20.2.3 Wort Boiling 434
20.2.3.1 Traditional Technology 435
20.2.4 Fermentation and Maturation 436
20.3 Bottlenecks to Process Intensification 437
20.4 Intensification of Brewing Processes 439
20.4.1 High Gravity Brewing 439
20.4.2 Intensifying Enzymatic Activity in Mashing 440
20.4.3 Intensification in Wort Treatment 445
20.4.3.1 Pre-treatment of Hops 445
20.4.3.2 Rectification Systems for Minimum Evaporation 445
20.4.3.3 Specific Technologies for Volatile Removal 446
20.4.4 Fermentation and Maturation 447
20.4.4.1 Continuous Fermentation and Maturation 448
20.4.4.2 Yeast Modification 448
20.4.4.3 Additives to Maturation 449
20.4.5 Pasteurization 449
20.4.6 Deaeration of Water 449
20.4.7 Dealcoholization 450
20.4.8 From Batch to Continuous 451
20.4.9 Synergy in Process Steps 452
20.5 New Energy Concepts Based on Intensified Brewing Systems 452
20.5.1 Low Temperature Heat Supply and Heat Integration 452
20.5.2 Hydrodynamic Cavitation in Brewing 457
References 457
Chapter 21 - Novel Processing Concepts for Making Fibrous Food Products 462
21.1 Introduction 462
21.2 Current Processes for Making Meat Analogs 464
21.2.1 Mixing Proteins with Hydrocolloids 464
21.2.2 Extrusion 465
21.2.3 Mycoprotein 466
21.3 Novel Processing Concepts 466
21.3.1 Spinning 466
21.3.2 Cultured Meat 468
21.3.3 Structuring with Simple Shear Flow 468
21.4 Comparing Structuring Methods 470
21.5 Ingredients for Meat Analogs 471
21.5.1 Plant Proteins 472
21.5.2 Solidification Properties 472
21.5.3 Minor Components for Taste and Color 473
21.5.4 Fat or Oil 474
21.6 Future Outlook 474
References 475
Chapter 22 - The Usefulness of Direct Digital Manufacturing for Biomedical Applications 478
22.1 Introduction 478
22.2 General Overview 480
22.3 DDM for Biomedical Applications 481
22.3.1 DDM for Pharmaceutics 481
22.3.2 DDM for Surgical Planning and Training 482
22.3.3 DDM for Tissue Engineering 483
22.4 Conclusion 485
Acknowledgements 485
References 485
Chapter 23 - Alternative Energy Forms in Manufacturing, Processing and Applications of Biopolymers and Biomaterials 488
23.1 Introduction 488
23.2 Electric Fields 491
23.3 Magnetic Fields 492
23.4 Microwave Fields 494
23.5 Plasma 497
23.6 Acoustic Fields 497
23.7 Energy of Light 500
23.8 Concluding Remarks – From Lab-scale Research to Commercial-scale Manufacturing 501
References 502
Subject Index 507