LEADER 05115nam 2200613 450 001 9910465419203321 005 20200903223051.0 010 $a3-03813-319-1 035 $a(CKB)3710000000221824 035 $a(EBL)1869238 035 $a(SSID)ssj0001343420 035 $a(PQKBManifestationID)11951774 035 $a(PQKBTitleCode)TC0001343420 035 $a(PQKBWorkID)11309590 035 $a(PQKB)10032483 035 $a(MiAaPQ)EBC1869238 035 $a(Au-PeEL)EBL1869238 035 $a(CaPaEBR)ebr10906063 035 $a(OCoLC)891395346 035 $a(EXLCZ)993710000000221824 100 $a20091020h20092009 uy| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aSintering of systems with interacting components /$fA.P. Savitskii 210 1$aStafa-Zuerich ;$aUnited Kingdom :$cTrans Tech,$d[2009] 210 4$dİ2009 215 $a1 online resource (292 p.) 225 1 $aMaterials science foundations,$x1422-3597 ;$vvolumes 57-58 300 $aBased on the earlier work : Liquid phase sintering of the systems with interacting components. 311 $a0-87849-150-3 320 $aIncludes bibliographical references. 327 $aSintering of Systems with Interacting Components; Arnold Savitskii ; Brief Annotation; Preface to the English Edition; Preface to the Russian Edition; Introduction; Table of Contents; Table of Contents; CHAPTER 1. SINTERING OF SINGLE PHASES; 1.1. Mechanisms of Sintering; 1.2. Factors Affecting Sintering; CHAPTER 2. PRINCIPAL AND RELATED PROBLEMS; 2.1. Driving Forces for Sintering; Definition of the Term "Sintering"; 2.2. Diffusion Interaction between Solid and Liquid Metals; 2.3. Plastic Flow in the Diffusion Zone; 2.4. Growth of Powder Compacts during Liquid-Phase Sintering 327 $a2.5. Dilatometry of Powder Compacts during Liquid-Phase Sintering2.6. Formation of Liquid Phase in Systems with Intermetallic Compounds; CHAPTER 3. VOLUME CHANGES OF TWO-COMPONENT COMPACTS DURING SINTERING; 3.1 Model of Two-Component Powder Compact Being Sintered in the Solid State; 3.2. Volume Changes of Ti-Ni Powder Compacts during Sintering; 3.3. Model of Powder Compact Being Sintered in the Presence of a Liquid Phase; 3.4. Amount of Growth of Powder Compacts during Liquid-Phase Sintering; 3.5. Degree of Densification of Compacts during Liquid-Phase Sintering 327 $a3.6. Overall Magnitude of Compact Volume Changes during Liquid-Phase SinteringCHAPTER 4. SINTERING OF SYSTEMS WITH CONSIDERABLE SOLUBILITY IN THE SOLID PHASE; 4.1. Effect of Titanium Particle Size on Compact Growth in the Ti-Al System; 4.2. Dilatometric and Structural Studies of Growth Process in the Ti-Al System; 4.3. Volume Growth as a Method for Obtaining Highly Porous Ti-Al Alloys; 4.4. Volume Changes Exhibited by Al-Zn Compacts; 4.5. Liquid-Phase Sintering of Powder Compacts in the Al-Mg System; CHAPTER 5. SYSTEMS WITH CONSIDERABLE SOLUBILITY OF THE COMPONENTS IN THE SOLID AND LIQUID 327 $a5.1. Volume Changes of Compacts in the Cu-Sn System5.2. Dilatometric and Structural Studies of Liquid-Phase Sintering in the Cu-Sn System; 5.3. Volume Changes in Cu-Al Compacts; 5.4. Aluminium Bronze, Parts made from which Change Little in Size during Sintering; CHAPTER 6. Al-Cu SYSTEM WITH HIGH SOLUBILITY IN THE LIQUID PHASE; 6.1. Volume Changes of Al-Cu Compacts during Sintering; 6.2. Effect of Porosity upon Volume Changes; 6.3. Effect of Aluminium Particle Size; 6.4. Alloy and Structure Formation; 6.5. Sintering in the Presence of a Large Amount of Liquid Phase; 6.6. Exothermal Sintering 327 $a6.7. Optimisation of Liquid-Phase Sintering Regimes6.8. Possibility of Decreasing Compact Growth during Sintering; CHAPTER 7. SINTERING OF ALUMINIUM WITH TRANSITION METALS; 7.1. Liquid-Phase Sintering of the Al-Cr System; 7.2. Liquid-Phase Sintering of the Al-Ti System; 7.3. Liquid-Phase Sintering of the Al-Ni System; 7.4. Liquid-Phase Sintering of the Al-Fe System; CONCLUSION; References 330 $aThe aim of this publication is to acquaint those readers who are interested in the fundamentals of powder materials sintering, with the latest scientific achievements which are important to its successful practice. The book contains new information, not previously known in the West, as well as offering a totally fresh view of this vital issue. The work discloses to western eyes a new scientific trend in the science of sintering systems with interacting components; a trend of which many experts are unaware. The new approach will considerably enrich and advance investigations into the theory and 410 0$aMaterials science foundations ;$vv. 57-58. 606 $aSintering 608 $aElectronic books. 615 0$aSintering. 676 $a671.373 700 $aSavit?skii?$b A. P. 701 $aSavit?skii?$b A. P$0941559 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910465419203321 996 $aSintering of systems with interacting components$92124127 997 $aUNINA LEADER 05251nam 2200637Ia 450 001 9910137967603321 005 20230802002407.0 010 $a3-527-64195-5 010 $a1-283-86988-8 010 $a3-527-64196-3 010 $a3-527-64194-7 035 $a(CKB)3280000000000390 035 $a(EBL)843679 035 $a(OCoLC)797919442 035 $a(SSID)ssj0000622301 035 $a(PQKBManifestationID)11388576 035 $a(PQKBTitleCode)TC0000622301 035 $a(PQKBWorkID)10642080 035 $a(PQKB)11183637 035 $a(MiAaPQ)EBC843679 035 $a(Au-PeEL)EBL843679 035 $a(CaPaEBR)ebr10577669 035 $a(CaONFJC)MIL418238 035 $a(EXLCZ)993280000000000390 100 $a20110819d2012 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 00$aOrganoselenium chemistry$b[electronic resource] $esynthesis and reactions /$fedited by Thomas Wirth 210 $aWeinheim $cWiley-VCH$dc2012 215 $a1 online resource (464 p.) 300 $aDescription based upon print version of record. 311 $a3-527-32944-7 320 $aIncludes bibliographical references and index. 327 $aOrganoselenium Chemistry: Synthesis and Reactions; Contents; Preface; List of Contributors; 1: Electrophilic Selenium; 1.1 General Introduction; 1.1.1 Synthesis of Electrophilic Selenium Reagents; 1.1.2 Reactivity and Properties; 1.2 Addition Reactions to Double Bonds; 1.2.1 Addition Reaction Involving Oxygen-Centered Nucleophiles; 1.2.2 Addition Reaction Involving Nitrogen-Centered Nucleophiles; 1.2.3 Addition Reactions Involving Carbon-Centered Nucleophiles; 1.2.4 Addition Reaction Involving Chiral Nucleophiles or Chiral Substrates; 1.3 Selenocyclizations; 1.3.1 Oxygen Nucleophiles 327 $a1.3.2 Nitrogen Nucleophiles1.3.3 Competition between Oxygen and Nitrogen Nucleophiles; 1.3.4 Carbon Nucleophiles; 1.3.5 Double Cyclization Reactions; References; 2: Nucleophilic Selenium; 2.1 Introduction; 2.1.1 Development of Nucleophilic Selenium Reagents; 2.1.2 Examples of Recent Applications; 2.2 Properties of Selenols and Selenolates; 2.2.1 Electronegativity of Selenium; 2.2.2 Tautomerism of Selenols; 2.2.3 Nucleophilicity of Selenolates; 2.3 Inorganic Nucleophilic Selenium Reagents; 2.3.1 Conventional Reagents; 2.3.2 New Reagents; 2.4 Organic Nucleophilic Selenium Reagents 327 $a2.4.1 Preparation 2.4.2 Structure; 2.4.3 Ammonium Selenolates (NH4+); 2.4.4 Selenolates of Group 1 Elements (Li, Na, K, and Cs); 2.4.5 Selenolates of Group 2 Elements (Mg, Ca, and Ba); 2.4.6 Selenolates of Group 3 Elements (Sm, Ce, Pr, Nb, and U); 2.4.7 Selenolates of Group 4 Elements (Ti, Zr, and Hf); 2.4.8 Selenolates of Group 5 Elements (V, Nb, and Ta); 2.4.9 Selenolates of Group 6 Elements (Mo and W); 2.4.10 Selenolates of Group 7 Elements (Mn and Re); 2.4.11 Selenolates of Group 8 Elements (Fe, Ru, and Os); 2.4.12 Selenolates of Group 9 Elements (Co, Rh, and Ir) 327 $a2.4.13 Selenolates of Group 10 Elements (Ni, Pd, and Pt)2.4.14 Selenolates of Group 11 Elements (Cu, Ag, and Au); 2.4.15 Selenolates of Group 12 Elements (Zn, Cd, and Hg); 2.4.16 Selenolates of Group 13 Elements (B, Al, Ga, and In); 2.4.17 Selenolates of Group 14 Elements (Si, Ge, Sn, and Pb); 2.4.18 Selenolates of Group 15 Elements (P, As, Sb, and Bi); References; 3: Selenium Compounds in Radical Reactions; 3.1 Homolytic Substitution at Selenium to Generate Radical Precursors; 3.1.1 Bimolecular SH2 Reactions: Synthetic Considerations; 3.1.1.1 Radical Reagents 327 $a3.1.2 Alkyl Radicals from Selenide Precursors 3.1.3 Acyl Radicals from Acyl Selenide Precursors; 3.1.4 Imidoyl Radicals from Imidoyl Selenides; 3.1.5 Other Radicals from Selenide Precursors; 3.2 Selenide Building Blocks; 3.3 Solid-Phase Synthesis; 3.4 Selenide Precursors in Radical Domino Reactions; 3.5 Homolytic Substitution at Selenium for the Synthesis of Se-Containing Products; 3.5.1 Intermolecular SH2 onto Se; 3.5.2 Intramolecular SH2: Cyclization onto Se; 3.6 Seleno Group Transfer onto Alkenes and Alkynes; 3.6.1 Seleno-Selenation; 3.6.2 Seleno-Sulfonation; 3.6.3 Seleno-Alkylation 327 $a3.7 PhSeH in Radical Reactions 330 $aSelenium-based methods in synthetic chemistry have developed rapidly over the past years and are now offering highly useful tools for organic synthesis. Filling the gap for a comprehensive handbook and ready reference, this book covers all modern developments within the field, including biochemical aspects. The chemistry chapters are organized according to the different reactivities of various selenium compounds and reagents, with each chapter dealing with a special reaction type. Also includes a table with 77Se NMR shifts to aid in practical problems.From the Contents 606 $aOrganoselenium compounds 606 $aSelenium compounds 615 0$aOrganoselenium compounds. 615 0$aSelenium compounds. 676 $a547.05724 701 $aWirth$b Thomas$f1964-$0893873 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910137967603321 996 $aOrganoselenium chemistry$91996683 997 $aUNINA LEADER 05128nam 22006491 450 001 9910789641103321 005 20080410150822.0 010 $a0-567-66122-9 010 $a1-283-27115-X 010 $a9786613271150 010 $a0-567-58124-1 024 7 $a10.5040/9780567661227 035 $a(CKB)2670000000113785 035 $a(EBL)766071 035 $a(OCoLC)748242280 035 $a(SSID)ssj0000555284 035 $a(PQKBManifestationID)12242707 035 $a(PQKBTitleCode)TC0000555284 035 $a(PQKBWorkID)10518605 035 $a(PQKB)10321704 035 $a(Au-PeEL)EBL766071 035 $a(CaPaEBR)ebr10495220 035 $a(CaONFJC)MIL327115 035 $a(OCoLC)870415132 035 $a(UtOrBLW)bpp09257986 035 $a(MiAaPQ)EBC766071 035 $a(EXLCZ)992670000000113785 100 $a20150227d2007 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aPaul's argumentation in Galatians $ea pragma-dialectical analysis /$fMika Hietanen 210 1$aLondon ;$aNew York :$cT & T Clark,$d2007. 215 $a1 online resource (241 p.) 225 1 $aLibrary of New Testament studies ;$v344.$aEuropean studies on Christian origins 225 1 $aT & T Clark library of biblical studies 300 $aDescription based upon print version of record. 311 $a0-567-03127-6 320 $aIncludes bibliographical references (pages 199-211) and indexes. 327 $aPreface -- List of Figures -- List of Tables -- Part 1. Introduction: 1.1 General Presentation of the Task ; 1.2 Overview of Paul's Argumentation ; 1.3 Problems in the Argumentation in Galatians 3.1-5.12 1.4 Specific Presentation of the Task -- Part 2. The method: 2.1 Background ; 2.2 General Characteristics of the Method ; 2.3 Metatheoretical Premisses ; 2.4 Speech Act Theory ; 2.5 A Model for Critical Discussion ; 2.6 Reconstructing Argumentative Discourse -- Part 3. Analysis: 3.1 The Analytical Procedure ; 3.2 Higher-Order Conditions ; 3.3 The Stages of the Argumentation ; 3.4 Gal. 3.1-5, the Galatians' Reception of the Spirit ; 3.5 Gal. 3.6-14, Abraham's Faith ; 3.6 Gal. 3.15-18, Testamental Practice and Inheritance ; 3.7 Gal. 3.19-25, the Purpose and Function of the Law ; 3.8 Gal. 3.26-29, Equality 'in Christ' ; 3.9 Gal. 4.1-7, the Freedom of God's Children ; 3.10 Gal. 4.8-11, Paul's Concern for the Galatians ; 3.11 Gal. 4.12-20, Paul's Relationship with the Galatians ; 3.12 Gal. 4.21-31, an Allegory of Hagar and Sarah ; 3.13 Gal. 5.1-12, Freedom versus Circumcision -- Part 4- Overview and conclusion. 4.1 An Analytic Overview ; 4.2 Violation of Rules and Quality of Argumentation ; 4.3 Conclusion: Paul's Argumentation in Galatians. 330 $a"Galatians is a polemical letter which contains a substantial amount of argumentative passages. Paul evidently wanted to persuade by using the best arguments possible to convince his addressees. Using a state-of-the-art method from the discipline of argumentation analysis, Paul's argumentation can be analysed with a precision that standard exegetical methods cannot provide. The pragma-dialectical method developed in Amsterdam facilitates an analysis which is both descriptive and normative. On the one hand, Paul's argumentation can be described, such as the relationship between premisses and conclusions, the structure of the arguments, and features relating to rhetorical strategy. On the other hand, the method makes it possible to evaluate Paul's argumentation against a set of rules for sound reasoning. Fallacies and problematic arguments can be described accurately. The spiritual nature of Paul's matters do not relieve him of rationality, and Paul himself does not argue as if it did. Paul's argumentation is found problematic in several respects. There is a tension in the text: Paul works a great deal to argue his claims while at the same time giving the impression that he merely wants to declare his standpoints and does not want to carry out an argumentation at all. Many of the conclusions are presented as self-evident, even when they are not. Paul's style is far from an ideal model of the resolution of a dispute. Paul relies heavily on an argumentative strategy with maximal use of rhetorical devices. The analysis shows that a contemporary method of argumentation analysis provides tools necessary to adequately describe and understand both individual arguments and the overarching strategy of the argumentation in a Pauline text."--Bloomsbury Publishing. 410 0$aLibrary of New Testament studies ;$v344. 410 0$aLibrary of New Testament studies.$pEuropean studies on Christian origins. 410 0$aT & T Clark library of biblical studies. 606 $aRhetoric, Ancient$xHistory 606 $2Biblical studies & exegesis 615 0$aRhetoric, Ancient$xHistory. 676 $a227.406 700 $aHietanen$b Mika$01503525 801 0$bUtOrBLW 801 1$bUtOrBLW 906 $aBOOK 912 $a9910789641103321 996 $aPaul's argumentation in Galatians$93731995 997 $aUNINA