LEADER 05194nam 22006134a 450 001 9910143962903321 005 20210104162156.0 010 $a1-280-85416-2 010 $a9786610854165 010 $a3-527-60766-8 010 $a1-61583-208-4 010 $a3-527-60708-0 024 3 $z9783527312320 035 $a(CKB)1000000000375908 035 $a(EBL)481785 035 $a(OCoLC)70113405 035 $a(SSID)ssj0000118310 035 $a(PQKBManifestationID)11133249 035 $a(PQKBTitleCode)TC0000118310 035 $a(PQKBWorkID)10053081 035 $a(PQKB)11166711 035 $a(MiAaPQ)EBC481785 035 $a(EXLCZ)991000000000375908 100 $a20060525d2005 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCarrier-bound immobilized enzymes$b[electronic resource] $eprinciples, applications and design /$fLinqiu Cao 210 $aWeinheim $cWiley-VCH$dc2005 215 $a1 online resource (581 p.) 300 $aDescription based upon print version of record. 311 $a3-527-31232-3 320 $aIncludes bibliographical references and index. 327 $aCarrier-bound Immobilized Enzymes; Foreword; Contents; 1 Introduction: Immobilized Enzymes: Past, Present and Prospects; 1.1 Introduction; 1.2 The Past; 1.2.1 The Early Days (1916-1940s); 1.2.2 The Underdeveloped Phase (1950s); 1.2.3 The Developing Phase (1960s); 1.2.4 The Developed Phase (1970s); 1.2.5 The Post-developed Phase (1980s); 1.2.6 Rational Design of Immobilized Enzymes (1990s-date); 1.3 Immobilized Enzymes: Implications from the Past; 1.3.1 Methods of Immobilization; 1.3.2 Diversity versus Versatility; 1.3.3 Complimentary versus Alternative 327 $a1.3.4 Modification versus Immobilization1.3.4.1 Enhanced Stability; 1.3.4.2 Enhanced Activity; 1.3.4.3 Improved Selectivity; 1.4 Prospective and Future Development; 1.4.1 The Room for Further Development; 1.4.2 An Integration Approach; 1.5 References; 2 Adsorption-based Immobilization; 2.1 Introduction; 2.2 Classification of Adsorption; 2.3 Principles Involved in Absorptive Enzyme Immobilization; 2.3.1 Monolayer Principle; 2.3.2 Stabilization Principle; 2.3.3 Enzyme Distribution; 2.4 Requirement of the Carriers; 2.4.1 Physical Requirements; 2.4.1.1 Pore-size and Available Surface 327 $a2.4.1.2 Internal Structure2.4.1.3 Density of Binding Functionality; 2.4.1.4 Particle Size; 2.4.2 Chemical Nature of the Carriers; 2.4.2.1 Nature of Binding Functionality; 2.4.2.2 The Role of the Spacer; 2.4.2.3 The Nature of the Backbone; 2.5 Factors Which Dictate Enzyme Catalytic Performance; 2.5.1 Activity; 2.5.1.1 Diffusion-controlled Activity; 2.5.1.2 Conformation-controlled Activity; 2.5.1.3 Substrate-controlled Activity; 2.5.1.4 Loading-controlled Activity; 2.5.1.5 Medium-dependent Activity; 2.5.1.6 Microenvironment-dependent Activity; 2.5.1.7 Carrier Nature-dependent Activity 327 $a2.5.1.8 Enzyme Nature-dependent Activity2.5.1.9 Additive-dependent Activity; 2.5.1.10 Hydrophilicity-dependent Activity; 2.5.1.11 Orientation-determined Activity; 2.5.1.12 Binding Nature-controlled Enzyme Activity; 2.5.1.13 Binding Density-controlled Enzyme Activity; 2.5.1.14 Reactor-dependent Activity; 2.5.1.15 Pore-size-dependent Activity; 2.5.1.16 Water-activity-dependent Activity; 2.5.2 Stability; 2.5.2.1 Conformation-controlled Stability; 2.5.2.2 Confinement-controlled Stability; 2.5.2.3 Enzyme Loading-dependent Stability; 2.5.2.4 Diffusion-controlled Stability 327 $a2.5.2.5 Cross-linking-dependent Stability2.5.2.6 Carrier Nature-controlled Stability; 2.5.2.7 Aquaphilicity-controlled Stability; 2.5.2.8 Medium-controlled Stability; 2.5.2.9 Temperature-dependent Stability; 2.5.2.10 Microenvironment-controlled Stability; 2.5.2.11 Binding Nature-controlled Enzyme Stability; 2.5.2.12 Binding Density-controlled Enzyme Stability; 2.5.2.13 Additive-dependent Stability; 2.5.2.14 Enzyme Orientation-dependent Stability; 2.5.2.15 Enzyme-dependent Stability; 2.5.3 Selectivity; 2.5.3.1 Conformation-controlled Selectivity; 2.5.3.2 Diffusion-controlled Selectivity 327 $a2.5.3.3 Binding Functionality-controlled Selectivity 330 $aThe first systematic overview of this key technique since the early 1990s, this authoritative reference is the only handbook available to include all recent developments. The author draws on his wide-ranging experience in both academia and industry to systematically cover all types of enzyme immobilization methods, such as adsorption-based and covalent immobilization, as well as enzyme entrapment and encapsulation. Throughout, a careful review of materials and techniques for the generation of functional immobilized enzymes benefits both developers and users of carrier-bound enzymes.A must 606 $aImmobilized enzymes 608 $aElectronic books. 615 0$aImmobilized enzymes. 676 $a572.7 700 $aCao$b Linqiu$0863246 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910143962903321 996 $aCarrier-bound immobilized enzymes$91926966 997 $aUNINA LEADER 05286nam 2200673Ia 450 001 9910830648403321 005 20170815110139.0 010 $a1-282-30160-8 010 $a9786612301605 010 $a0-470-18682-8 010 $a0-470-18832-4 035 $a(CKB)1000000000376540 035 $a(EBL)469085 035 $a(OCoLC)609847800 035 $a(SSID)ssj0000353967 035 $a(PQKBManifestationID)11249009 035 $a(PQKBTitleCode)TC0000353967 035 $a(PQKBWorkID)10302259 035 $a(PQKB)11076582 035 $a(MiAaPQ)EBC469085 035 $a(PPN)241414458 035 $a(EXLCZ)991000000000376540 100 $a20731212d1966 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aMulti-sulfur and sulfur and oxygen five- and six-membered heterocycles$hPart one$b[electronic resource] /$fDavid S. Breslow, Herman Skolnik 205 $a99th ed. 210 $aNew York $cInterscience$d1966 215 $a1 online resource (635 p.) 225 1 $aChemistry of heterocyclic compounds ;$v21/1 300 $aDescription based upon print version of record. 311 $a0-470-38195-7 320 $aIncludes bibliographies. 327 $aMULTI-SULFUR AND SULFUR AND OXYGEN FIVE- AND SIXMEMBERED HETEROCYCLES; CONTENTS OF PART ONE; 1. C2O2S Ring Systems; I. C2O2S 1, 3, 2-Dioxathiolane and 1, 3, 2-Dioxathiole; A. Sulfite Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Physical Properties; 3. Reactions; 4. Uses; B. Sulfate Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Reactions; C. Sulfate Esters of Enediols; D. 1, 3, 2-Dioxathiolan-4-one 2-Oxides; II. C4-C2O2S 2, 4-Dioxa-3-thiabicyclo[3. 2. 0]heptane; III. C2O2S-C2O2S 1, 3, 2-Dioxathiolo[1, 3, 2]dioxathiole Glyoxal Sulfate 327 $aIV. C2O2S-C4O Furo[3, 4-d]-l, 3, 2-dioxathioleV. C2O2S-C4S Thieno[3, 4-d]-1, 3, 2-dioxathiole; VI. C2O2S-C5 3aH-Cyclopenta-1, 3, 2-dioxathiole; VII. C2O2S-C5O 4H-Pyrano[3, 4-d]-1, 3, 2-dioxathiole; VIII. C2O2S-C6 1, 3, 2-Benzodioxathiole; A. Sulfite Esters; B. Sulfate Esters; IX. C2O2S-C7 4H-Cyclohepta-1, 3, 2-dioxathiole; X. C2O2S-C4O-C4O 1, 7, 11, 13-Tetraoxa-12-thiadispiro-[4. 0. 4. 3]trideca-3, 9-diene-2, 8-dione; XI. C2O2S-C4N-C5N 6H-Cyclohepta-1, 3, 2-dioxathiol-4, 8-imine; XII. C2O2S-C5-C6 8H-Indeno[1, 2-d}-1, 3, 2-dioxathiole 327 $aXIII. C2O2S-C4O2-C50 4H, 6H-1, 3, 2-Dioxathiolo[4, 5]-pyrano[3, 2-d]-m-dioxinXIV. C2O2S-C6C6; A. Naphtho[1, 2-d}-1, 3, 2-dioxathiole; B. Naphtho[2, 3-d]-1, 3, 2-dioxathiole; XV. C2O2S-C6-C6-C6; A. Anthra[1, 2-d]-1, 3, 2-dioxathiole; 1. Sulfite Esters; 2. Sulfate Esters; B. Anthra[2, 3-d]-1, 3, 2-dioxathiole; C. Phenanthro[9, 10-d]-1, 3, 2-dioxathiole; XVI. C2O2S-C4N-C4N-C9O2 [1, 3, 2]Dioxathiolo-[4', 5' : 8, 9][1, 6]dioxacycloundeca[2, 3, 4-gh]-pyrrolizine; XVII. C2O2S-C4N-C4N-C10O2 Spiro[1, 6]dioxacyclododeca-[2, 3, 4-gh]-pyrrolizine-9(8H), 4'-[ 1, 3, 2]-dioxathiolane 327 $aXVIII. C2O2S-C5-C6-C6-C6A. Cyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]-dioxathiole; B. Cyclopenta[1, 2]phenanthro[1, 10a-d][1, 3, 2]-dioxathiole; XIX. C2O2S-C6-C6-C6-C6; A. Chryseno[5, 6-d]-1, 3, 2-dioxathiole; B. 4, 9-o-Benzenonaphtho[2, 3-d]-1, 3, 2-dioxathiole; XX. C2O2S-C4O-C4O-C5-C6-C6 3H, 9H-11b, 13a-Epoxycyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]dioxathiole; 2. C2OS2 Ring Systems; I. 1, 2, 5-Oxadithia Compounds; A. C2OS2 1, 2, 5-Oxadithiolane; B. C2OS2-C4SThieno[3, 4-c][1, 2, 5]oxadithiole; C. C2OS2-C6 2, 1, 3-Benzoxadithiole; D. C2OS2-C6-C6 Naphth[1, 2-c][1, 2, 5]oxadithiole 327 $aII. 1, 3, 4-Oxadithia CompoundsC2OS2 1, 3, 4-Oxadithiolane; 3. C2S3 Ring Systems; I. 1, 2, 3-Trithia Compounds; A. C2S3 1,2,3-Trithiole; B. C2S3-C6 Benzotrithiole; C. C2S3-C4N2-C6 Trithiolo[4, 5-b]quinoxaline; II. 1, 2, 4-Trithia Compounds; A. C2S3 1, 2, 4-Trithiolane; B. Spiro Derivatives of 1, 2, 4-Trithiolane; 4. C3OS Ring Systems; I. 1, 2-Oxathia Compounds; A. C3OS 5H-1, 2-Oxathiole, 3H-1, 2-Oxathiole, and 1, 2-Oxathiolane; 1. 3H-1, 2-Oxathiole; 2. 5H-1, 2-Oxathiole; 3. 1, 2-Oxathiolane; a. 1, 2-Oxathiolane 2, 2-Dioxide; (1) Preparation; (a) From 3-Chloroalkanesulfonic Acids 327 $a(b) From 3-Hydroxyalkanesulphonic Acids 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$v21/1. 606 $aOrganosulfur compounds 606 $aHeterocyclic compounds 615 0$aOrganosulfur compounds. 615 0$aHeterocyclic compounds. 676 $a547.594 676 $a547/.59/05 700 $aBreslow$b David Samuel$f1916-$0893559 701 $aSkolnik$b Herman$0893560 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830648403321 996 $aMulti-sulfur and sulfur and oxygen five- and six-membered heterocycles$91996096 997 $aUNINA LEADER 04016oam 2200721zu 450 001 9911007276703321 005 20210803002710.0 010 $a9781938549557 010 $a1938549554 010 $a9781680159691 010 $a1680159690 035 $a(CKB)2670000000560707 035 $a(SSID)ssj0001406808 035 $a(PQKBManifestationID)12483819 035 $a(PQKBTitleCode)TC0001406808 035 $a(PQKBWorkID)11421945 035 $a(PQKB)11417492 035 $a(FR-PaCSA)88949264 035 $a(FRCYB88949264)88949264 035 $a(MiAaPQ)EBC31870550 035 $a(Au-PeEL)EBL31870550 035 $a(BIP)62930758 035 $a(BIP)42926677 035 $a(EXLCZ)992670000000560707 100 $a20160829d2014 uy 101 0 $aeng 135 $aurun| ||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCOMSOL for engineers 205 $a1st ed. 210 31$a[Place of publication not identified]$cMercury Learning and Information$d2014 215 $a1 online resource (266 p.) 225 1 $aMultiphysics Modeling Series 300 $aBibliographic Level Mode of Issuance: Monograph 311 08$a9781938549533 311 08$a1938549538 330 $aCOMSOL Multiphysics software is one of the most valuable software modeling tools for engineers and scientists. This book is designed for engineers from the fields of mechanical, electrical, and civil disciplines, and introduces multiphysics modeling techniques and examples accompanied by practical applications using COMSOL 4.x. The book includes a companion CD-ROM with files of over 25 models, images, and code. The main objective is to introduce readers to use COMSOL as an engineering tool for modeling by solving examples that could become a guide for modeling similar or more complicated problems. The objective is to provide a collection of examples and modeling guidelines through which readers can build their own models. Readers are assumed to be familiar with the principles of numerical modeling and the finite element method (FEM). The book takes a flexible-level approach for presenting the materials along with using practical examples. The mathematical fundamentals, engineering principles, and design criteria are presented as integral parts of examples. At the end of each chapter are references that contain more in-depth physics, technical information, and data; these are referred to throughout the book and used in the examples. COMSOL for Engineers could be used to complement another text that provides background training in engineering computations and methods. Examples provided in this book should be considered as "lessons" for which background physics could be explained in more detail. FEATURES Includes a companion CD-ROM with files of over 25 models, images, code Uses progressive approach in terms of examples and models eBook Customers: Companion files are available for downloading with order number/proof of purchase by writing to the publisher at info@merclearning.com. 410 0$aMultiphysics Modeling Series 606 $aEngineering$xData processing 606 $aEngineering$xMathematical models 606 $aEngineering$xComputer simulation 606 $aPhysics$xData processing 606 $aPhysics$xMathematical models 606 $aPhysics$xComputer simulation 606 $aEngineering & Applied Sciences$2HILCC 606 $aApplied Mathematics$2HILCC 615 0$aEngineering$xData processing. 615 0$aEngineering$xMathematical models. 615 0$aEngineering$xComputer simulation. 615 0$aPhysics$xData processing. 615 0$aPhysics$xMathematical models. 615 0$aPhysics$xComputer simulation. 615 7$aEngineering & Applied Sciences 615 7$aApplied Mathematics 676 $a620.00285/53 700 $aTabatabaian$b Mehrzad$0948349 801 0$bPQKB 906 $aBOOK 912 $a9911007276703321 996 $aCOMSOL for engineers$93959570 997 $aUNINA