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از ساعت 7 صبح تا 10 شب
ویرایش: 3
نویسندگان: Gordon Gilmore. David Joss
سری:
ISBN (شابک) : 1119896088, 9781119896081
ناشر: Wiley
سال نشر: 2024
تعداد صفحات: 542
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 14 مگابایت
در صورت تبدیل فایل کتاب Practical Gamma-ray Spectrometry به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
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Cover Title Page Copyright Contents Preface to the Third Edition Preface to the Second Edition Preface to the First Edition Internet Resources Within the Book About the Website Chapter 1 Radioactive Decay and the Origin of Gamma and X‐Radiation 1.1 Introduction 1.2 Beta Decay 1.2.1 β− or Negatron Decay 1.2.2 β+ or Positron Decay 1.2.3 Electron Capture (EC) 1.2.4 Multiple Stable Isotopes 1.3 Alpha Decay 1.4 Spontaneous Fission (SF) 1.5 Exotic Decay Modes 1.6 Gamma Emission 1.6.1 The Electromagnetic Spectrum 1.6.2 Some Properties of Nuclear Transitions 1.6.3 Lifetimes of Nuclear Energy Levels 1.6.4 Width of Nuclear Energy Levels 1.6.5 Internal Conversion 1.6.6 Abundance, Yield and Emission Probability 1.6.7 Ambiguity in Assignment of Nuclide Identity 1.7 Other Sources of Photons 1.7.1 Annihilation Radiation 1.7.2 Bremsstrahlung 1.7.3 Prompt Gamma‐Rays 1.7.4 X‐rays 1.7.4.1 X‐ray Nomenclature 1.7.4.2 X‐ray Energies 1.7.4.3 X‐rays and Identification 1.7.4.4 The Energy Widths of X‐rays 1.8 The Mathematics of Decay and Growth of Radioactivity 1.8.1 The Decay Equation 1.8.2 Growth of Activity in Reactors 1.8.3 Growth of Activity from Decay of a Parent 1.8.3.1 Transient Equilibrium – t1/2 Parent > t1/2 Daughter 1.8.3.2 Secular Equilibrium – t1/2 Parent ≫ t1/2 Daughter 1.8.3.3 No Equilibrium – t1/2 Parent < t1/2 Daughter 1.8.3.4 Multiple Parent–Daughter Relationships 1.9 The Chart of the Nuclides 1.9.1 A Source of Nuclear Data 1.9.2 A Source of Generic Information 1.9.2.1 Thermal Neutron Capture (n, γ) 1.9.2.2 Fast Neutron Reactions, (n, p), etc. 1.9.2.3 Fission Reactions (n, f) Practical Points Further Reading Chapter 2 Interactions of Gamma Radiation with Matter 2.1 Introduction 2.2 Mechanisms of Interaction 2.2.1 Photoelectric Absorption 2.2.2 Compton Scattering 2.2.3 Pair Production 2.3 Total Attenuation Coefficients 2.4 Interactions Within the Detector 2.4.1 The Very Large Detector 2.4.2 The Very Small Detector 2.4.3 The ‘Real’ Detector 2.4.4 Summary 2.5 Interactions Within the Shielding 2.5.1 Photoelectric Interactions 2.5.2 Compton Scattering 2.5.3 Pair Production 2.6 Bremsstrahlung 2.7 Attenuation of Gamma Radiation 2.8 The Design of Detector Shielding Practical Points Further Reading Chapter 3 Semiconductor Detectors for Gamma‐Ray Spectrometry 3.1 Introduction 3.2 Semiconductors and Gamma‐Ray Detection 3.2.1 The Band Structure of Solids 3.2.2 Mobility of Holes 3.2.3 Creation of Charge Carriers by Gamma Radiation 3.2.4 Suitable Semiconductors for Gamma‐Ray Detectors 3.2.5 Newer Semiconductor Materials 3.3 The Nature of Semiconductors 3.4 The Manufacture of Germanium Detectors 3.4.1 Introduction 3.4.2 The Manufacturing Process 3.4.3 Lithium‐Drifted Detectors 3.4.4 Detector Configurations 3.4.5 Absorption in Detector Caps and Dead Layers 3.4.6 Detectors for Low‐Energy Measurements 3.4.7 Well Detectors 3.5 Detector Capacitance 3.5.1 Microphonic Noise 3.6 Charge Collection in Detectors 3.6.1 Charge Collection Time 3.6.2 Shape of the Detector Pulse 3.6.3 Timing Signals from Germanium Detectors 3.6.4 Electric Field Variations Across the Detector 3.6.5 Removing Weak Field Regions from Detectors 3.6.6 Trapping of Charge Carriers 3.6.7 Radiation Damage 3.7 Packaging of Detectors 3.7.1 Construction of the Detector Mounting 3.7.2 Loss of Coolant 3.7.3 Demountable Detectors 3.7.4 Electrical Cooling of Detectors 3.8 Position‐Sensitive Detectors 3.8.1 Segmentation 3.8.2 Gamma‐Ray Tracking Practical Points Further Reading Chapter 4 Electronics for Gamma‐Ray Spectrometry 4.1 The General Electronic System 4.1.1 Introduction 4.1.2 Electronic Noise and Its Implications for Spectrum Resolution 4.1.3 Pulse Shapes in Gamma Spectrometry Systems 4.1.4 Impedance – Inputs and Outputs 4.1.5 The Impedance of Cabling 4.1.6 Impedance Matching 4.2 Detector Bias Supplies 4.3 Preamplifiers 4.3.1 Resistive Feedback Preamplifiers 4.3.2 Reset Preamplifiers 4.3.3 The Noise Contribution of Preamplifiers 4.3.4 The Rise Time of Preamplifiers 4.3.5 Intelligent Preamplifiers and High‐Voltage Supplies 4.4 Amplifiers and Pulse Processors 4.4.1 The Functions of the Amplifier 4.4.2 Pulse Shaping 4.4.3 The Optimum Pulse Shape 4.4.4 The Optimum Pulse Shaping Time Constant 4.4.5 The Gated Integrator Amplifier 4.4.6 Pole‐zero Cancellation 4.4.7 Baseline Shift 4.4.8 Pile‐up Rejection 4.4.9 Amplifier Gain and Overview 4.5 Resolution Enhancement 4.5.1 New Semiconductor Materials 4.6 Multichannel Analysers and Their Analogue‐to‐Digital Converters 4.6.1 Introduction 4.6.2 Pulse Range Selection 4.6.3 The ADC Input Gate 4.6.4 The ADC 4.6.4.1 The Wilkinson ADC 4.6.4.2 The Successive Approximation ADC 4.6.5 MCA Conversion Time and Dead Time 4.6.6 Choosing an ADC 4.6.7 Linearity in MCAs 4.6.8 Optimum Spectrum Size 4.6.9 MCA Terms and Definitions 4.6.10 A Short History of MCA Systems 4.6.11 Simple MCA Analysis Functions 4.7 Live Time Correction and Loss‐Free Counting 4.7.1 Live Time Clock Correction 4.7.2 The Gedcke–Hale Method 4.7.3 Use of a Pulser 4.7.4 Loss‐Free Counting (LFC) 4.7.5 MCA Throughput 4.8 Spectrum Stabilization 4.8.1 Analogue Stabilization 4.8.2 Digital Stabilization 4.9 Coincidence and Anticoincidence Gating 4.10 Multiplexing and Multiscaling 4.11 Digital Pulse Processing Systems Practical Points Further Reading Chapter 5 Statistics of Counting 5.1 Introduction 5.1.1 Statistical Statements 5.2 Counting Distributions 5.2.1 The Binomial Distribution 5.2.2 The Poisson and Gaussian Distributions 5.3 Sampling Statistics 5.3.1 Confidence Limits 5.3.2 Combining the Results from Different Measurements 5.3.3 Propagation of Uncertainty 5.4 Peak Area Measurement 5.4.1 Simple Peak Integration 5.4.2 Peaked‐Background Correction 5.5 Counting Decision Limits 5.5.1 Critical Limit (LC): ‘Is the Net Count Significant?’ 5.5.2 Upper Limit (LU): ‘Given That This Count Is Not Statistically Significant, What Is the Maximum Statistically Reasonable Count?’ 5.5.3 Confidence Limits 5.5.4 Detection Limit (LD): ‘What Is the Minimum Number of Counts that I Can Be Confident of Detecting?’ 5.5.5 Determination Limit (LQ): ‘How Many Counts Would I Have to Have to Achieve a Particular Statistical Uncertainty?’ 5.5.6 Other Calculation Options 5.5.7 Minimum Detectable Activity (MDA): ‘What Is the Least Amount of Activity I Can Be Confident of Measuring?’ 5.5.8 Uncertainty of the LU and MDA 5.5.9 An Example by Way of Summary 5.6 Special Counting Situations 5.6.1 Non‐Poisson Counting 5.6.2 Low Numbers of Counts 5.6.3 Non‐Poisson Statistics Due to Pile‐up Rejection and Loss‐Free Counting 5.7 Optimizing Counting Conditions 5.7.1 Optimum Background Width 5.7.2 Optimum Peak Width 5.7.3 Optimum Spectrum Size 5.7.4 Optimum Counting Time 5.8 Uncertainty Budgets 5.8.1 Introduction 5.8.2 Accuracy and Precision 5.8.3 Types of Uncertainty 5.8.4 Types of Distribution 5.8.5 Uncertainty on Sample Preparation 5.8.6 Counting Uncertainties 5.8.7 Calibration Uncertainties 5.8.7.1 Nuclear Data Uncertainty 5.8.7.2 Uncertainty on Efficiency Calibration Standards 5.8.8 An Example of an Uncertainty Budget Practical Points Further Reading Chapter 6 Resolution: Origins and Control 6.1 Introduction 6.2 Charge Production – ωP 6.2.1 Germanium Versus Silicon 6.2.2 Germanium Versus Sodium Iodide 6.2.3 Temperature Dependence of Resolution 6.3 Charge Collection – ωC 6.3.1 Mathematical Form of ωC 6.4 Electronic Noise – ωE 6.4.1 Parallel Noise 6.4.2 Series Noise 6.4.3 Flicker Noise 6.4.4 Total Electronic Noise and Shaping Time 6.5 Resolving the Peak Width Calibration Practical Points Further Reading Chapter 7 Spectrometer Calibration 7.1 Introduction 7.2 Reference Data for Calibration 7.3 Sources for Calibration 7.4 Energy Calibration 7.4.1 Errors in Peak Energy Determination 7.5 Peak Width Calibration 7.5.1 Factors Affecting Peak Width 7.5.2 Algorithms for Peak Width Estimation 7.5.3 Estimation of the Peak Height 7.5.4 Anomalous Peak Widths 7.6 Efficiency Calibration 7.6.1 Which Efficiency? 7.6.2 Full‐energy Peak Efficiency 7.6.3 Is an Efficiency Calibration Curve Necessary? 7.6.4 The Effect of Source‐to‐Detector Distance 7.6.5 Calibration Errors Due to Difference in Sample Geometry 7.6.6 An Empirical Correction for Sample Height 7.6.7 Effect of Source Density on Efficiency 7.6.7.1 Corrections Based on Estimated Mass Attenuation Coefficients 7.6.7.2 Empirical Correction for Self‐absorption 7.6.8 Efficiency Loss Due to Random Summing (Pile‐up) 7.6.9 True Coincidence Summing 7.6.10 Corrections for Radioactive Decay 7.6.11 Electronic Timing Problems 7.7 Absolute Total Efficiency 7.8 Mathematical Efficiency Calibration 7.8.1 Empirical Mathematics 7.8.2 Gamma Spectrometry Goes to Monte Carlo 7.8.3 Do Monte Carlo‐Based Programs Work? 7.8.4 Efficiency Calibration Software 7.8.5 Using Monte Carlo to Assist Other Methods 7.8.5.1 Efficiency Transfer 7.8.5.2 The Representative Point (RP) Method 7.8.6 The Virtual Gamma Spectrometry Laboratory Practical Points Further Reading Chapter 8 True Coincidence Summing 8.1 Introduction 8.2 The Origin of Summing 8.3 Summing and Solid Angle 8.4 Spectral Evidence of Summing 8.5 Validity of Close Geometry Calibrations 8.5.1 The Effect of TCS on Efficiency Calibration 8.6 Summary 8.7 Summing in Environmental Measurements 8.8 Achieving Valid Close Geometry Efficiency Calibrations 8.9 TCS, Geometry and Composition 8.10 Achieving ‘Summing‐Free’ Measurements 8.10.1 Using the ‘Interpolative Fit’ to Correct for TCS 8.10.2 Comparative Activity Measurements 8.10.3 Using Correction Factors Derived from Efficiency Calibration Curves 8.10.4 Correction of Results Using ‘Bodged’ Nuclear Data‘Bodge’ is British slang for a clumsy, messy, inelegant or inadequate solution to a problem. 8.11 Mathematical Summing Corrections 8.12 Software for Correction of TCS 8.12.1 GESPECOR 8.12.2 Calibrations Using Summing Nuclides 8.12.3 TCS Correction in Spectrum Analysis Programs 8.13 Using Coincidences for Measurement Practical Points Further Reading Chapter 9 Computer Analysis of Gamma‐Ray Spectra 9.1 Introduction 9.1.1 Can You Trust the ‘black box’? 9.2 Methods of Locating Peaks in the Spectrum 9.2.1 Using Regions of Interest 9.2.2 Locating Peaks Using Channel Differences 9.2.3 Derivative Peak Searches 9.2.4 Peak Searches Using Correlation Methods 9.2.5 Checking the Acceptability of Peaks 9.3 Library‐Directed Peak Searches 9.4 Energy Calibration 9.5 Estimation of the Peak Centroid 9.6 Peak Width Calibration 9.7 Determination of the Peak Limits 9.7.1 Using the Width Calibration 9.7.2 Individual Peak Width Estimation 9.7.3 Limits Determined by a Moving Average Minimum 9.8 Measurements of Peak Area 9.9 Full‐Energy‐Peak Efficiency Calibration 9.10 Multiplet Peak Resolution by Deconvolution 9.11 Peak Stripping as a Means of Avoiding Deconvolution 9.12 Spectrum Smoothing 9.13 The Analysis of the Sample Spectrum 9.13.1 Peak Location and Measurement 9.13.2 Corrections to the Peak Area for Peaked‐Background 9.13.3 Upper Limits and Minimum Detectable Activity 9.13.4 Activity Estimations Using Efficiency Curves 9.13.5 Comparative Activity Estimations 9.13.6 Corrections Made by the Spectrum Analysis Program 9.13.6.1 Random Summing Correction 9.13.6.2 Other Corrections 9.14 Nuclide Identification 9.14.1 Simple Use of Lookup Tables 9.14.2 Taking into Account Other Peaks 9.15 The Final Report 9.16 Setting up Nuclide and Gamma‐Ray Libraries 9.17 Buying Spectrum Analysis Software 9.18 Reading the Manual 9.19 The Spectrum Analysis Programs Referred to in the Text Practical Points Further Reading Chapter 10 Scintillation Spectrometry 10.1 Introduction 10.2 The Scintillation Process 10.3 Scintillation Activators 10.4 Lifetime of Excited States 10.5 Temperature Variation of the Scintillator Response 10.6 Scintillator Detector Materials 10.6.1 Sodium Iodide – NaI(Tl) 10.6.2 Bismuth Germanate – BGO 10.6.3 Caesium Iodide – CsI(Tl) and CsI(Na) 10.6.4 Undoped Caesium Iodide – CsI 10.6.5 Barium Fluoride – BaF2 10.6.6 Caesium Fluoride – CsF 10.6.7 Rare‐Earth Halides – LaCl3(Ce), LaBr3(Ce) and CeBr3 10.6.8 Other Scintillators 10.7 Photomultiplier Tubes 10.8 The Photocathode 10.9 The Dynode Electron Multiplier Chain 10.10 Photodiode Scintillation Detectors 10.11 Silicon Photomultipliers 10.12 Construction of the Complete Detector 10.12.1 Detector Shapes 10.12.2 Optical Coupling of the Scintillator to the Photomultiplier 10.13 The Resolution of Scintillation Systems 10.13.1 Statistical Uncertainties in the Detection Process 10.13.2 Factors Associated with the Scintillator Crystal 10.13.3 The Variation of Resolution with Gamma‐Ray Energy 10.14 Electronics for Scintillation Systems 10.14.1 High‐Voltage Supply 10.14.2 Preamplifiers 10.14.3 Amplifiers 10.14.4 Multi‐channel Analysers and Spectrum Analysis 10.15 Comparison of Sodium Iodide and Germanium Detectors Practical Points Further Reading Chapter 11 Low Count‐Rate Systems 11.1 Introduction 11.2 Counting with High Efficiency 11.2.1 MDA: Efficiency and Resolution 11.2.2 MDA: Efficiency, Background and Counting Period 11.2.2.1 Variation of BS, the Compton Continuum Due to the Sample, with Detector Size 11.2.2.2 Variation of BE, the Environmental Background, with Detector Size 11.2.2.3 The Effect of Resolution on Relative MDA and Count Period 11.2.2.4 Is Bigger MUCH Better? 11.3 The Effect of Detector Shape 11.3.1 Low‐Energy Measurements 11.3.2 Well Detectors 11.3.3 Sample Quantity and Geometry 11.4 Low Background Systems 11.4.1 The Background Spectrum 11.4.2 Low Background Detectors 11.4.3 Detector Shielding 11.4.4 The Graded Shield 11.4.5 Airborne Activity 11.4.6 The Effect of Cosmic Radiation 11.4.6.1 Direct Interaction of Secondary Cosmic Radiation 11.4.6.2 Cosmic Neutron‐Induced Activity 11.4.7 Underground Measurements 11.5 Active Background Reduction 11.5.1 Compton Suppression Systems 11.5.1.1 Design Considerations – Spectrometry (HPGe) Detector 11.5.1.2 Design Considerations – Guard Detector 11.5.1.3 Disadvantages of Compton Suppression 11.5.2 Veto Guard Detectors 11.6 Limiting Electronic Noise 11.7 Ultra‐low‐Level Systems Practical Points Further Reading Chapter 12 High Count‐Rate Systems 12.1 Introduction 12.2 Detector Throughput 12.3 Preamplifiers for High Count Rate 12.3.1 Energy Rate Saturation 12.3.2 Energy Resolution 12.3.3 Dead Time 12.4 Amplifiers 12.4.1 Time Constants and Pile‐up 12.4.2 The Gated Integrator 12.4.3 Pole‐Zero Correction 12.4.4 Amplifier Stability – Peak Shift 12.4.5 Amplifier Stability – Resolution 12.4.6 Overload Recovery 12.5 Digital Pulse Processing 12.6 The ADC and MCA 12.7 Dead Times and Throughput 12.7.1 Extendable and Non‐extendable Dead Time 12.7.2 Gated Integrators 12.7.3 DSP Systems 12.7.4 Theory Versus Practice 12.7.4.1 Semi‐Gaussian Analogue Versus Digital Processor 12.7.4.2 Gated Integrator Analogue Versus Digital Processor 12.7.5 Modern DSPEC and LYNX Digital Systems 12.8 System Checks Practical Points Further Reading Chapter 13 Ensuring Quality in Gamma‐Ray Spectrometry 13.1 Introduction 13.2 Nuclear Data 13.3 Radionuclide Standards 13.4 Maintaining Confidence in the Equipment 13.4.1 Setting Up and Maintenance Procedures 13.4.2 Control Charts 13.4.3 Setting Up a Control Chart 13.5 Gaining Confidence in the Spectrum Analysis 13.5.1 Test Spectra with Known Peaks 13.5.1.1 The IAEA G1 Test Spectra 13.5.1.2 The Sanderson Test Spectra 13.5.1.3 Programs for Mathematically Creating Test Spectra 13.5.2 Test Spectra Created by Counting 13.5.2.1 The 1995 IAEA Test Spectra 13.5.2.2 The 1997 NPL Test Spectra 13.5.2.3 The 2002 IAEA Test Spectra 13.5.2.4 The CTBTO Spectrum 13.5.2.5 Finding Test Spectra 13.5.3 Measuring Test Samples – Intercomparison Exercises 13.5.3.1 NPL Environmental Radioactivity Proficiency Test Exercises 13.5.3.2 The IAEA Proficiency Exercises 13.5.4 Assessing Spectrum Analysis Performance 13.5.5 Assessment of Intercomparison Exercises 13.6 Maintaining Records 13.7 Accreditation Practical Points Further Reading Chapter 14 Gamma Spectrometry of Naturally Occurring Radioactive Materials (NORM) 14.1 Introduction 14.2 The NORM Decay‐Series 14.2.1 The Uranium Series – 238U 14.2.2 The Actinium Series – 235U 14.2.3 The Thorium Series – 232Th 14.2.4 Radon Loss 14.2.5 Natural Disturbance of the Decay‐Series 14.3 Gamma Spectrometry of the NORM Nuclides 14.3.1 Measurement of 7Be 14.3.2 Measurement of 40K 14.3.3 Gamma Spectrometry of the Uranium/Thorium Series Nuclides 14.3.4 Allowance for Natural Background 14.3.5 Resolution of the 186 keV Peak 14.3.6 Other Spectral Interferences and Summing 14.4 Nuclear Data of the NORM Nuclides 14.5 Measurement of Chemically Modified NORM 14.5.1 Measurement of Separated Uranium 14.5.2 Measurement of Separated Thorium 14.5.3 ‘Non‐natural’ Thorium 14.5.4 Measurement of Gypsum – A Cautionary Tale Practical Points Further Reading Chapter 15 Applications 15.1 Monitoring Radon in Water 15.1.1 The Principle of the Method 15.1.2 Detector Background 15.1.3 Taking Water Samples 15.1.4 Background Measurement 15.1.5 Standardization 15.1.6 Spectrum Acquisition 15.1.7 Analysis of the Spectra 15.2 Whole Body Counting 15.2.1 The Background Problem 15.2.2 Whole Body Counting Is Different 15.2.3 Is There a Standard Body? 15.3 Gamma Spectrometry and the CTBT 15.3.1 Background 15.3.2 The Global Verification Regime 15.3.3 Nuclides Released in a Nuclear Explosion 15.3.4 Measuring the Radionuclides 15.3.4.1 Radioactive Particulate Monitoring 15.3.4.2 Noble Gas Monitoring 15.3.5 Current Status 15.4 Gamma Spectrometry of Nuclear Industry Wastes 15.4.1 Measurement of Isotopically Modified Uranium 15.4.2 Measurement of Transuranic Nuclides 15.4.3 Waste Drum Scanning 15.5 Safeguards 15.5.1 Enrichment Meters 15.5.2 Plutonium Spectra 15.5.3 Fresh and Aged Samples 15.5.4 Absorption of Gamma‐Rays 15.5.5 Hand‐held Monitors 15.6 PINS – Portable Isotopic Neutron Spectrometry 15.7 Gamma‐Ray Imaging 15.8 Investigating the Structure of the Atomic Nucleus Using Gamma‐Ray Spectroscopy Further Reading Chapter 16 Choosing and Setting Up a Detector, and Checking Its Specifications 16.1 Introduction 16.2 Setting Up a Germanium Detector System 16.2.1 Installation – The Detector Environment 16.2.1.1 The Counting Room 16.2.1.2 The Electrical Supply 16.2.1.3 Placement of the Detector 16.2.2 Liquid Nitrogen Supply 16.2.3 Shielding 16.2.4 Cabling 16.2.5 Installing the Detector 16.2.6 Preparation for Powering‐up 16.2.7 Powering‐up and Initial Checks 16.2.7.1 Resistive Feedback Preamplifier Systems 16.2.7.2 Transistor Reset (TRP) Preamplifier Systems 16.2.8 Switching Off the System 16.3 Optimizing the Electronic System 16.3.1 General Considerations 16.3.2 DC Level Adjustment and Baseline Noise 16.3.3 Setting the Conversion Gain and Energy Range 16.3.4 Pole‐zero (PZ) Cancellation 16.3.4.1 Oscilloscope and Source 16.3.4.2 Oscilloscope and Square Wave 16.3.4.3 Automatic Correction 16.3.5 Incorporating a Pulse Generator 16.3.5.1 With a Resistive Feedback Preamplifier 16.3.5.2 With a Transistor Reset Preamplifier 16.3.6 Baseline Restoration (BLR) 16.3.7 Optimum Time Constant 16.4 Checking the Manufacturer\'s Specification 16.4.1 The Manufacturer\'s Specification Sheet 16.4.2 Detector Resolution and Peak Shape 16.4.3 Detector Efficiency Coaxial Detectors 16.4.3.1 Well Detectors 16.4.4 Peak‐to‐Compton (P/C) Ratio 16.4.5 Window Thickness Index 16.4.6 Physical Parameters Practical Points Further Reading Chapter 17 Troubleshooting 17.1 Fault‐finding 17.1.1 Equipment Required 17.1.2 Fault‐finding Guide 17.2 Preamplifier Test Point and Leakage Current 17.2.1 Resistive Feedback (RF) Preamplifiers 17.2.2 Transistor Reset and Pulsed Optical Reset Preamplifiers 17.3 Thermal Cycling of the Detector 17.3.1 The Origin of the Problem 17.3.2 The Thermal Cycling Procedure 17.3.3 Frosted Detector Enclosure 17.4 Ground Loops, Pick‐up and Microphonics 17.4.1 Ground Loops 17.4.2 Electromagnetic Pick‐up 17.4.2.1 Common Mode Rejection 17.4.2.2 Mains Supply Problems 17.4.3 Microphonics 17.4.3.1 Mechanisms and Checks 17.4.3.2 Solutions Practical Points Appendix A Sources of Information A.1 Introduction A.2 Nuclear Data A.2.1 Sources of Nuclear Data A.2.2 Online Sources of Gamma‐Ray Emission Data A.2.2.1 DDEP A.2.2.2 Lara A.2.2.3 ENSDF A.2.2.4 NuDat 3.0 A.2.2.5 IAEA A.2.3 Nuclear Databases Offline and in Print A.3 Internet Sources of Other Nuclear Data A.4 Chemical Information A.5 Further Research A.6 Practical Gamma‐Ray Spectrometry Website Appendix B Gamma‐ and X‐Ray Standards for Detector Calibration Appendix C X‐Rays Routinely Found in Gamma Spectra Appendix D Gamma‐Ray Energies in the Detector Background and the Environment Appendix E Chemical Names, Symbols and Relative Atomic Masses of the Elements Glossary Index EULA