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ویرایش:
نویسندگان: Paul R. Loconto
سری:
ISBN (شابک) : 1032195622, 9781032195629
ناشر: CRC Press
سال نشر: 2022
تعداد صفحات: 167
[169]
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 15 Mb
در صورت تبدیل فایل کتاب Laboratory Experiments in Trace Environmental Quantitative Analysis به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب آزمایشات آزمایشگاهی در ردیابی تجزیه و تحلیل کمی محیطی نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
این کتاب با بهروزرسانی کامل و بهموقع، اصول، تکنیکها و کاربردهایی را در این زیرشاخه شیمی تحلیلی برای تعیین کمیت آثار مواد شیمیایی آلی و معدنی بالقوه سمی موجود در هوا، خاک، ماهی و آب و همچنین سرم ارائه میکند. پلاسما، ادرار و سایر مایعات بدن.
A thorough and timely update, this book presents principles, techniques, and applications in this sub-discipline of analytical chemistry for quantifying traces of potentially toxic organic and inorganic chemical substances found in air, soil, fish, and water, as well as serum, plasma, urine, and other body fluids.
Cover Half Title Title Page Copyright Page Dedication Table of Contents Preface About the Author Photos Chapter 1 Introduction 1.1 What Might a Typical Laboratory Schedule Look Like? 1.2 How Is the Instructional Laboratory Configured? 1.3 How to Weigh the Right Way Chapter 2 An Introduction to pH Measurement: Estimating the Degree of Purity of Snow, Measuring Soil pH: Introduction to Ion Chromatography 2.1 Background and Summary of Method 2.2 Experiment 2.2.1 Glassware Needed per Student 2.2.2 Chemical Reagents/pH Meter Needed per Student Workstation 2.2.3 Ion Chromatograph 2.2.4 Procedure 2.3 Suggested Reading Chapter 3 Introduction to the Visible Spectrophotometer 3.1 Background and Summary of Method 3.2 Experiment 3.2.1 Glassware Needed per Student or Group 3.2.2 Chemical Reagents Needed per Student or Group 3.2.3 Miscellaneous Item Needed per Student or Group 3.2.4 Spectrophotometer 3.2.5 Product Line History of the Spec 20 3.2.6 Troubleshooting the Spec 20 3.2.7 Procedure 3.3 For the Report 3.4 Suggested Reading Chapter 4 Visible Spectrophotometric Determination of Trace Levels of Iron in Groundwater 4.1 Background and Summary of Method 4.2 Experiment 4.2.1 Volumetric Glassware Needed per Student 4.2.2 Gravity Filtration Setup 4.2.3 Chemical Reagents Needed per Student or Group 4.2.4 Spectrophotometer 4.2.5 Procedure 4.2.6 Determination of Total Fe by FLAA or ICP-AES 4.3 For the Notebook 4.4 Suggested Reading Chapter 5 Spectrophotometric Determination of Phosphorus in Eutrophicated Surface Water 5.1 Background and Summary of Method 5.2 Experiment 5.2.1 Preparation of Chemical Reagents 5.2.1.1 5 M Sulfuric Acid 5.2.1.2 Molybdate Reagent 5.2.1.3 1% Ascorbic Acid 5.2.1.4 Preparation of Stock Phosphorus 5.2.2 Procedure 5.3 For the Notebook 5.4 Suggested Reading Chapter 6 Determination of Anionic Surfactants by Mini-Liquid–Liquid Extraction (MINI-LLE) in an Industrial Wastewater Effluent Using Ion Pairing with Methylene Blue 6.1 Background and Summary of Method 6.2 Experiment 6.2.1 Preparation of Chemical Reagents 6.2.1.1 Methylene Blue (MB) 6.2.1.2 3 M Sulfuric Acid 6.2.1.3 To Prepare a 0.5 M Sulfuric Acid Solution 6.2.1.4 To Prepare a 0.1 M Sodium Hydroxide Solution 6.2.1.5 To Prepare the Wash Solution 6.2.1.6 To Prepare the MB Reagent 6.2.2 Preparation of the 100 ppm Surfactant Stock Solution and General Comments on Standards 6.2.3 Operation and Calibration of the Orion SA 720A pH Meter 6.2.4 Procedure to conduct a miniaturized liquid-liquid extraction (LLE) 6.3 For the Report (a Written Laboratory Report Due on This Experiment) 6.4 Suggested Reading Chapter 7 Comparison of Ultraviolet and Infrared Absorption Spectra of Chemically Similar Organic Compounds 7.1 Background and Summary of Method 7.1.1 UV-Vis Absorption Spectroscopy 7.1.2 Mid-Infrared Absorption Spectroscopy 7.2 Experiment 7.2.1 Items/Accessories Needed per Student or Group 7.2.2 Preparation of Chemical Reagents 7.2.3 Procedure to Obtain UV Absorption Spectra for Two Sets of Chemically Similar Organic Compounds: (1) Alkane Sulfonates vs. Alkyl Sulfates and (2) Two Esters with Different Carbon Backbones 7.2.4 Procedure to Obtain FTIR Absorption (Transmission) Spectra for Various Organic Compounds 7.3 For the Report 7.4 Suggested Reading Chapter 8 Determination of Oil and Grease and of Total Petroleum Hydrocarbons in Wastewater via Reversed-Phase Solid-Phase Extraction Techniques (RP-SPE) and Quantitative Fourier-Transform Infrared (FTIR) Spectroscopy 8.1 Background and Summary of Method 8.2 Experiment 8.2.1 Preparation of Chemical Reagents 8.2.2 Reagents Needed per Student or Group of Students 8.2.3 Apparatus Needed per Group 8.2.4 Procedure 8.2.5 Percent Recovery Study 8.2.6 Probe Sonication: Liquid–Solid Extraction 8.2.7 Calibration of the FTIR Spectrophotometer 8.2.8 Isolation, Recovery, and Quantitation of Oil and Grease from Wastewater Samples 8.3 Calculations 8.4 Suggested Reading Chapter 9 Determination of the Degree of Hardness in Various Sources of Groundwater Using Flame Atomic Absorption Spectroscopy 9.1 Background and Summary of Method 9.2 Experiment 9.2.1 Preparation of Chemical Reagents 9.2.2 Chemicals/Reagents Needed per Student or Group 9.2.3 FLAA Operating Analytical Requirement 9.2.4 Preparation of the Calibration Curve 9.2.5 Procedure 9.3 For the Lab Notebook (No Report Necessary) 9.4 Suggested Reading Chapter 10 Determination of Lead in Drinking Water Using Graphite Furnace Atomic Absorption Spectroscopy (GFAA): External Standard vs. Standard Addition Calibration Mode 10.1 Background and Summary of Method 10.2 Experiment 10.2.1 Preparation of Chemical Reagents 10.2.2 Reagents Needed per Student or Group 10.2.3 Procedure 10.2.4 Using the WinLab® Software 10.2.5 Preparation of the Stock Reference Pb Standard and Start of the Autosampler 10.3 For the Notebook 10.4 Suggested Readings Chapter 11 A Comparison of Soil Types via a Quantitative Determination of the Chromium Content Using Visible Spectrophotometry and Flame Atomic Absorption Spectroscopy or Inductively Coupled Plasma–Optical Emission Spectrometry 11.1 Background and Summary of Method 11.2 Experiment 11.2.1 Chemical Reagents Needed per Student or Group 11.2.2 Procedure for Alkaline Digestion 11.2.3 Procedure for Conducting Visible Spectrophotometric Analysis 11.2.4 Procedure for Atomic Absorption Spectrophotometric Analysis or ICP-AES 11.3 For the Report 11.4 Suggested Reading Chapter 12 Data Acquisition and Instrument Control Using the Turbochrom Chromatography Software: An Introduction to High-Performance Liquid Chromatography (HPLC): Evaluating Those Experimental Parameters That Influence Separations 12.1 Background and Summary of Method 12.1.1 HPLC and TEQA 12.1.2 Flow-through Packed Columns 12.1.3 HPLC Also Refers to an Instrument That Is a High-Pressure Liquid Chromatograph 12.2 Experiment 12.2.1 Preparation of Chemical Reagents 12.2.2 Accessories to Be Used with the HPLC per Group 12.2.3 Procedure 12.2.3.1 Initial Observations of a Computer-Controlled High-Performance Liquid Chromatograph 12.2.3.2 Creating a QuickStart Method, Acquiring Data, Optimizing, Calibrating, and Conducting Analysis Using the QuickStart Method 12.2.3.3 Effect of Solvent Strength on k’ 12.2.3.4 Effect of Mobile-Phase Flow Rate on Resolution 12.3 For the Lab Notebook 12.4 Suggested Reading Chapter 13 Identifying the Ubiquitous Phthalate Esters in the Environment Using HPLC, Photodiode Array Detection, and Confirmation by GC-MS 13.1 Background and Summary of Method 13.1.1 Analytical Method Development Using HPLC 13.1.2 GC-MS Using a Quadrupole Mass Spectrometer 13.2 Of What Value Is This Experiment? 13.3 Experiment 13.3.1 Preparation of Chemical Reagents 13.3.2 Accessories to be Used With the HPLC per Student or Group 13.3.3 Procedure 13.4 For the Report 13.5 Suggested Reading Chapter 14 An Introduction to Gas Chromatography: Evaluating Experimental Parameters That Influence Gas Chromatographic Performance 14.1 Background and Summary of Method 14.2 Brief Description of Gas Chromatographs Located in the Hazardous Waste Analysis Lab at Michigan State University 14.3 Principle of Separation in GC 14.4 Experiment 14.4.1 Preparation of Chemical Reagents 14.4.2 Accessories to Be Used with the GC per Group 14.4.2.1 Summary of Turbochrom Methods to Be Used in this Experiment 14.4.3 Procedure 14.4.3.1 Measurement and Adjustment of Carrier Gas Flow Rate and Split Ratio 14.4.3.2 Comparison of the FID vs. the ECD Sensitivity 14.4.3.3 Injection Volume vs. GC Peak Shape 14.4.3.4 Flow Rate vs. Capillary Column Efficiency 14.4.3.5 Column Temperature vs. Capacity Factor 14.5 For the Lab Notebook 14.6 Suggested Readings Chapter 15 Screening for the Presence of BTEX in Wastewater Using Liquid–Liquid Extraction (LLE) and Gas Chromatography: Screening for THMs in Chlorine-Disinfected Drinking Water Using Static Headspace (HS) Gas Chromatography 15.1 Background and Summary of Method 15.2 Of What Value Is This Experiment? 15.3 Experimental 15.3.1 Preparation of Chemical Reagents 15.3.2 Chemicals/Reagents Needed per Group 15.3.3 Items/Accessories Needed per Student or per Group 15.3.4 Preliminary Planning 15.3.5 Procedure for BTEX Instrumental Analysis Using Mini-LLE Techniques 15.3.5.1 Selecting the Most Suitable Extraction Solvent 15.3.5.2 Preparation of the Primary Dilution Standard and Working Calibration Standards 15.3.6 Procedure for THM Instrumental Analysis Using HS Techniques 15.3.7 Procedure to Conduct a Screen for BTEXs via Mini-LLE and Subsequent Injection into a GC-FID 15.3.8 Procedure to Conduct Manual Headspace Sampling and Direct Injection into a GC-ECD 15.4 For the Report 15.5 Suggested Readings Chapter 16 Determination of Priority Pollutant Volatile Organic Compounds (VOCs) in Gasoline-Contaminated Groundwater Using Static Headspace (HS) and Solid-Phase Microextraction Headspace (SPME-HS) and Gas Chromatography 16.1 Background and Summary Method 16.2 Of What Value Is This Experiment? 16.3 Use of t Statistics 16.4 Experimental 16.4.1 Preparation of Chemical Reagents 16.4.2 Chemicals/Reagents Needed per Group 16.4.3 Items/Accessories Needed per Student or per Group 16.4.4 Preliminary Planning 16.4.5 Procedure for BTEX Instrumental Analysis HS Techniques 16.4.6 Technique to Conduct a Manual Headspace Sampling and Direct Injection Using a Gas-Tight Sampling Syringe 16.4.7 Technique to Conduct an SPME Headspace Sampling and Injection/Thermal Desorption Using an SPME Syringe/Fiber Assembly 16.5 For the Report 16.6 Suggested Readings Chapter 17 Determination of the Herbicide Residue Trifluralin in Chemically Treated Lawn Soil by Gas Chromatography Using Reversed-Phase Solid-Phase Extraction (RP-SPE) Sample Prep Techniques 17.1 Background and Summary of Method 17.1.1 Solid-Phase Extraction 17.1.2 Internal Standard Mode of Calibration 17.2 Experiment 17.2.1 Preparation of Chemical Reagents 17.2.2 Chemicals/Reagents/Accessories Needed per Group 17.2.3 Preparation of the Working Calibration Standards 17.2.4 Establishing the Calibration 17.2.5 Isolating Trifluralin from Lawn-Treated Soil Using RP-SPE Techniques 17.3 For the Report 17.4 Suggested Reading Chapter 18 Determination of Priority Pollutant Semivolatile Organochlorine Pesticides: A Comparison of Mini-Liquid–Liquid and Reversed-Phase Solid-Phase Extraction Techniques 18.1 Background and Summary of Method 18.2 Experimental 18.2.1 Preparation of Chemical Reagents 18.2.2 Chemicals/Reagents Needed per Group 18.2.3 Preliminary Planning 18.2.4 Selection of a Suitable Internal Standard 18.2.5 Procedure for Calibration and Quantitation of the GC-ECD 18.2.6 Procedure for Performing Mini-LLE and RP-SPE 18.3 For the Report 18.4 Suggested Reading Chapter 19 Determination of Priority Pollutant Polycyclic Aromatic Hydrocarbons (PAHs) in Contaminated Soil Using RP-HPLC-PDA with Wavelength Programming 19.1 Background and Summary of Method 19.2 Of What Value Is This Experiment? 19.3 Experiment 19.3.1 Preparation of Chemical Reagents 19.3.2 Accessories to Be Used with the HPLC per Group 19.3.3 Procedure 19.3.3.1 Creating the Wavelength Program Method 19.3.3.2 Extraction Procedure for Soil 19.3.3.3 Calculation of the # ppm of Each PAH in Contaminated Soil 19.4 For the Report 19.5 Suggested Reading Chapter 20 How to Set up and Operate an Ion Chromatograph 20.1 Determination of Inorganic Anions Using Ion Chromatography (IC): Anion Exchange IC with Suppressed Conductivity Detection 20.1.1 Background 20.2 How Do I Operate the Ion Chromatograph? 20.3 Is There a Need for Sample Prep? 20.4 How Do I Prepare a Reference Stock Standard for Each Anion? 20.5 How Do I Prepare the Bicarbonate/Carbonate Eluent from Scratch? 20.6 How Do I Prepare a Mixed Anion Stock Standard for IC? 20.7 How Do I Prepare a Four-Level Set of Calibration Standards for IC? 20.8 What Does the Data Look Like? 20.9 Suggested Reading Index