UV-Visible Spectrophotometry of Water and Wastewater ( 2 )

Publication series :2

Author: Thomas   Olivier;Burgess   Christopher  

Publisher: Elsevier Science‎

Publication year: 2017

E-ISBN: 9780444639004

P-ISBN(Paperback): 9780444638977

Subject: O657.3 spectrochemical analysis (method of spectrology)

Keyword: 仪器分析法(物理及物理化学分析法),物理学,废水的处理与利用

Language: ENG

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Description

UV-Visible Spectrophotometry of Water and Wastewater, Second Edition, represents an update to the first book dedicated to the use of UV spectrophotometry for water and wastewater quality monitoring. Using practical examples, the book illustrates how this technique can be a source of new methods of characterization and measurement.

Easy and fast to run, this simple and robust analytical technique must be considered as one of the best ways to obtain a quantitative estimation of specific or aggregate parameters (e.g., Nitrate, TOC) and simultaneously qualitative information on the global composition of water and its variation.

This second edition presents the current methods and applications for water quality monitoring based on UV spectra, including the most recent works and developments. After the introduction of the basics for UV spectrophotometry understanding, the applications of UV measurement are presented, both from the family of chemicals and water quality parameters and from the type of water.

Writing from years of experience in the development and applications of UV systems and from scientific and technical works, the authors provide several useful examples showing the great interest of UV spectrophotometry for water quality monitoring. At the end of the book, the UV spectra library of the first edition is updated with dozens of new chemicals of interest.

  • Adds dozens of new chemicals of interest to the first library of UV-sp

Chapter

1.3.4 Procedures and Best Practices for Assuring Spectrophotometer Performance

1.3.4.1 Wavelength Accuracy and Reproducibility

1.3.4.2 Absorbance, Accuracy and Reproducibility

1.3.4.3 Stray-Light

1.3.4.4 Resolution

1.3.4.5 Optimal Spectrophotometric Range

1.4 Sample Presentation

1.4.1 Cuvettes

1.4.2 Cleaning Procedures

1.5 Factors Influencing Spectral Characteristics

1.5.1 Sample Handing and Storage

1.5.2 Turbidity

1.5.3 Solvent Quality and Polarity

1.5.4 pH

1.5.5 Ionic Strength

1.5.6 Temperature

1.5.7 Data Treatment

1.5.7.1 Averaging and Smoothing

1.5.7.2 Derivatives

1.5.7.3 Spectral Correction

1.6 Data Integrity and Security

References

Further Reading

2 From Spectra to Qualitative and Quantitative Results

2.1 Introduction

2.2 Basic Handling of UV Spectra

2.2.1 One Spectrum Transformation

2.2.1.1 Coloured Scale

2.2.1.2 Derivative Spectra

2.2.1.3 Shape Factor

2.2.1.4 Smoothing

2.2.2 Two-Spectra Comparison

2.2.2.1 Differential Spectrum

2.2.2.2 Direct Comparison

2.2.2.3 Normalisation

2.2.3 Evolution Study from a Spectra Set

2.2.3.1 Isosbestic Points

2.2.3.2 Hidden Isosbestic Points

2.2.3.3 Application: Variability Estimation

2.3 Concentration Calculation

2.3.1 Ideal Case: Pure Solution with No Interference

2.3.1.1 Simple Absorptiometry for One Analyte

2.3.1.2 Two Analytes

2.3.1.3 Multicomponent Method by Multilinear Regression (MLR)

2.3.2 Real Samples: Compensation of Interferences

2.3.2.1 Two Wavelengths Approach

2.3.2.2 Spectra Slopes

2.3.2.3 Derivative Methods

2.3.2.4 Polynomial Compensation of Interferences

2.3.2.5 Chemometric Analysis: PCA, PCR and PLS

2.3.2.6 Ultra-violet spectral deconvolution (UVSD)/Semideterministic Method

2.3.3 Real Samples: Pretreatment Steps for Improving UV Response

2.4 Examples of Application

Acknowledgements

References

3 Organic Constituents

3.1 Introduction

3.2 Coloured Organic Compounds

3.2.1 Dyes

3.2.1.1 Azoic Dyes

3.2.1.2 Anthraquinonic Dyes

3.2.1.3 Other Dyes

3.2.2 Coloured Reagents

3.2.2.1 pH Indicators

3.2.2.2 Redox Indicator

3.2.2.3 Complexometry Indicators

3.3 UV-Absorbing Organic Compounds

3.3.1 Aldehydes and Ketones

3.3.2 Aldehydes

3.3.2.1 Ketones

3.3.3 Amines

3.3.4 Aniline

3.3.4.1 Chloroanilines

3.3.4.2 Toluidine and Anisidine

3.3.4.3 Other Aromatic Amines

3.3.4.4 Applications

3.3.5 Benzene and Related Compounds

3.3.5.1 BTEX

3.3.5.2 Chlorobenzene

3.3.6 Pesticides

3.3.6.1 Herbicides

3.3.6.2 Insecticides

3.3.7 Pharmaceuticals

3.3.8 Phenols

3.3.8.1 Alkylphenols

3.3.8.2 Chlorophenols

3.3.8.3 Nitrophenols

3.3.8.4 Polyphenols

3.3.8.5 Phenol Index

3.3.9 Phthalates

3.3.10 Polycyclic Aromatic Hydrocarbons

3.3.10.1 Solvent Effect

3.3.10.2 Influence of the Number of Aromatic Rings

3.3.10.3 Isomeric PAH UV Spectra

3.3.10.4 Introduction of a Five-Membered Cycle in the PAH Structure

3.3.10.5 PAH (Index)

3.3.11 Sulphur Organic Compounds

3.3.12 Surfactants

3.4 Solid-Phase Extraction and UV-Visible Spectrophotometry

3.5 Nonabsorbing Organic Compounds

3.5.1 Carbonyl Compounds: Use of Absorbing Derivatives

3.5.2 Aliphatic Amines and Amino Acids: Photo-Oxidation

3.5.3 Carbohydrates: Photodegradation

Ackowledgments

References

Further Reading

4 Aggregate Organic Constituents

4.1 Introduction

4.2 Dissolved Organic Matter

4.3 Reference Methods Assistance

4.3.1 TOC, DOC Explanation

4.3.2 BOD Measurement

4.3.3 COD Final Determination

4.4 UV Estimation of TOC, DOC, COD, and BOD5

4.4.1 UV-Spectra Exploitation From a Limited Number of Wavelengths

4.4.2 UV-Spectra Exploitation From a Multiwavelengths Approach

4.4.3 Validation

4.5 UV Recovery of Organic Pollution Parameters

References

5 Mineral Constituents

5.1 Introduction

5.2 Inorganic Nonmetallic Constituents

5.2.1 N Compounds

5.2.2 General Procedure

5.2.3 Nitrate

5.2.4 Nitrite

5.2.5 TKN

5.2.6 Ammonium

5.2.7 P Compounds

5.2.8 General Procedure

5.2.9 Orthophosphates

5.2.10 Total Phosphorus

5.2.11 S Compounds

5.2.12 Cl Compounds

5.2.13 Chloride

5.2.14 Hypochlorite

5.2.15 Organochlorine Compounds

5.3 Metallic Constituents

5.3.1 Chromium (Direct Measurement)

5.3.1.1 Hexavalent Chromium

5.3.1.2 Trivalent Chromium

5.3.2 Metallic Constituents Determination by Complexometry

References

6 Physical and Aggregate Properties

6.1 Introduction

6.2 Colour

6.2.1 Determination of Colour

6.2.2 Relation Between Colour and Visible Absorbance

6.3 Physical Diffuse Absorption

6.3.1 Some Elements on Diffusion of Light by Particles

6.3.2 Methods for the Study of Heterogeneous Fractions

6.3.3 UV-Visible Responses of Mineral Suspensions

6.3.4 UV Responses of Microorganisms

6.3.5 UV Responses of Wastewater

6.4 TSS Estimation

6.4.1 Turbidimetry

6.4.2 UV Estimation of TSS

References

7 Natural Water

7.1 Introduction

7.2 Significance of UV Spectra of Natural Water

7.3 Quality of Natural Water

7.3.1 Water Quality Variation Along a River

7.3.2 Rain Influence on River Water Quality

7.3.3 Wetland Water Quality

7.3.4 Lakes Water Quality

7.3.5 Groundwater Quality

7.4 Recent Advances in Freshwater Quality UV Monitoring

7.4.1 About Isosbestic Point(s)

7.4.2 Relation Between Parameters (DOC/NO3)

7.4.3 Second Derivative Renewal

7.4.4 High-Frequency Monitoring

7.5 Point Source and Accidental Discharge

7.5.1 Discharge in River

7.5.2 Discharge in Sea

7.5.3 Accidental Discharge

Acknowledgments

References

8 Drinking Water

8.1 Introduction

8.2 From Resources to Tap Water

8.2.1 Baseline Conditions

8.2.2 Rainfalls Conditions

8.3 Production of Tap Water in a Large Treatment Plant

8.3.1 Routine Monitoring

8.4 Early Warning Systems

8.5 Disinfection by-Products

8.6 Bottled Drinking Waters

8.6.1 Spring Water

8.6.2 Mineral Water

8.6.3 Other Bottled Waters

References

9 Urban Wastewater

9.1 Introduction

9.2 Sewers

9.2.1 Fresh Domestic Effluent

9.2.2 Variation of Quality According to Time

9.2.3 Evolution Along the Sewer

9.2.4 Effect of Rain

9.3 Synthesis and Other Applications

9.4 Treatment Processes

9.4.1 Primary Settling Assistance

9.4.2 Physico-Chemical Treatment Assistance

9.4.3 Jar Test

9.4.4 Problem of Sample Aging

9.4.5 Biological Processes

9.4.6 Complementary Technique: Membrane Filtration and Activated Carbon

9.5 Applications

9.5.1 Fixed Biomass Treatment Plant

9.5.2 Extensive Process

9.5.3 Ozone Treatment for Treated Effluent

9.6 Classification of Wastewater

9.6.1 Typology of Urban Wastewater from UV Spectra Shape

9.6.2 Automatic Classification of Water and Wastewater

Acknowledgments

References

10 Industrial Wastewater

10.1 Introduction

10.2 Wastewater Characteristics

10.2.1 Generalities

10.2.2 Influence of Industry Nature

10.2.3 Variability of Industrial Wastewater Quality

10.2.4 Quantitative Estimation

10.3 Treatment Processes

10.3.1 Physico-chemical Processes

10.3.2 Biological Processes

10.3.3 Hyphenated Processes

10.4 Waste Management

10.4.1 Sampling Assistance

10.4.2 Treatability Tests Assistance

10.4.3 Spills Detection

10.4.4 Shock Loading Management

10.4.5 External Waste Management

10.5 Environmental Impact

10.5.1 Discharge

10.5.2 Groundwater Survey

Acknowledgments

References

11 Leachates and Organic Extracts From Solids

11.1 Introduction

11.2 Landfill Leachates

11.2.1 Leachate Characterisation

11.2.1.1 Direct Examination of UV Spectra

11.2.1.2 pH Effect

11.2.2 Leachate Treatment

11.2.2.1 Coagulation–Flocculation With FeCl3

11.2.2.2 Photo-Oxidation

11.3 Polluted Soils

11.3.1 Polluted Soils Characterisation

11.3.1.1 Polycyclic Aromatic Hydrocarbons

11.3.1.2 Petroleum Hydrocarbons

11.3.2 Treatment of Polluted Soils

11.3.2.1 Polycyclic Aromatic Hydrocarbons

11.3.2.2 Petroleum Hydrocarbons

11.4 Solid Wastes Treatment by Composting

11.4.1 Characterisation of Solid Wastes

11.4.2 Composting of Solid Wastes

11.5 Soils, Sediments, and Wetlands

11.5.1 Soils

11.5.2 Sediments

11.5.3 Wetlands

References

Further Reading

12 UV Spectra Library

12.1 Introduction

12.2 Spectra Acquisition

12.3 Spectra of Compounds

12.3.1 Acids and Salts

12.3.1.1 Acetic Acid

12.3.1.2 Butyric Acid

12.3.1.3 EDTA

12.3.1.4 Formic Acid

12.3.1.5 Oxalic Acid

12.3.1.6 Propionic Acid

12.3.1.7 Sodium Salicylate

12.3.1.8 Potassium Sodium Tartrate

12.3.2 Aldehydes and Ketones

12.3.2.1 Acetaldehyde

12.3.2.2 Acetone

12.3.2.3 Benzaldehyde

12.3.2.4 2-Butanone

12.3.2.5 Butyraldéhyde

12.3.2.6 Diisobutylketone

12.3.2.7 Formaldehyde

12.3.2.8 Isobutyl Methyl Ketone

12.3.3 Amines and Related Compounds

12.3.3.1 Aniline

12.3.3.2 p-Anisidine

12.3.3.3 2-Chloroaniline

12.3.3.4 4-Chloroaniline

12.3.3.5 2-Chloro-4-Methylaniline

12.3.3.6 3,4-Dichloroaniline

12.3.3.7 Diethylamine

12.3.3.8 Diethanolamine

12.3.3.9 Glutamic Acid

12.3.3.10 Glycine

12.3.3.11 4-Nitroaniline

12.3.3.12 m-Toluidine

12.3.3.13 p-Toluidine

12.3.3.14 Tyrosine

12.3.3.15 4,4’-Diaminodiphenylmethane

12.3.4 Benzene and Related Compounds

12.3.4.1 Benzene

12.3.4.2 Chlorobenzene

12.3.4.3 Ethylbenzene

12.3.4.4 Toluene

12.3.4.5 m-Xylene

12.3.4.6 o-Xylene

12.3.4.7 p-Xylene

12.3.5 Pesticides

12.3.5.1 2-4-Dichlorophenoxy Acetic Acid (2-4 D)

12.3.5.2 Alachlor

12.3.5.3 Atrazine

12.3.5.4 Carbaryl

12.3.5.5 Chlorpyrifos

12.3.5.6 Chlortoluron

12.3.5.7 Diazinon

12.3.5.8 Dichlorprop

12.3.5.9 Dimethoate

12.3.5.10 Dinoterb

12.3.5.11 Diquat

12.3.5.12 Diuron

12.3.5.13 Hexazinone

12.3.5.14 Isoproturon

12.3.5.15 Linuron

12.3.5.16 Malathion

12.3.5.17 Metazachlor

12.3.5.18 Metolachlor

12.3.5.19 Paraquat

12.3.5.20 Parathion

12.3.5.21 Simazine

12.3.5.22 Terbuthylazine

12.3.5.23 Terbutryn

12.3.6 Pharmaceuticals

12.3.6.1 1,7 Ethinylestradiol

12.3.6.2 Acetaminohen

12.3.6.3 Atenolol

12.3.6.4 Caffeine

12.3.6.5 Carbamazepine

12.3.6.6 Ciprofloxacine

12.3.6.7 Clofibric Acid

12.3.6.8 Diatrozoate

12.3.6.9 Diclofenac

12.3.6.10 Erythromycine

12.3.6.11 Ibuprofen

12.3.6.12 Methylparaben

12.3.6.13 Sulfamethoxazole

12.3.6.14 Trimethoprim

12.3.6.15 Warfarin

12.3.7 Phenol and Related Compounds

12.3.7.1 Phenol

12.3.7.2 4-Chloro-3-Methylphenol

12.3.7.3 2-Chlorophenol

12.3.7.4 3-Chlorophenol

12.3.7.5 4-Chlorophenol

12.3.7.6 m-Cresol

12.3.7.7 o-Cresol

12.3.7.8 p-Cresol

12.3.7.9 4,5-Dichlorocatechol

12.3.7.10 2,3-Dichlorophenol

12.3.7.11 2,4-Dichlorophenol

12.3.7.12 2,5-Dimethylphenol

12.3.7.13 4,6-Dinitro-2-Methylphenol

12.3.7.14 2-Nitrophenol

12.3.7.15 3-Nitrophenol

12.3.7.16 4-Nitrophenol

12.3.7.17 Pentachlorophenol

12.3.7.18 Pyrocatechol

12.3.7.19 2-Tert-Butyl-4-Methylphenol

12.3.7.20 2,4,6-Trichlorophenol

12.3.7.21 2,4,6-Trimethylphenol

12.3.7.22 Bisphenol A

12.3.8 Phthalates

12.3.8.1 Butyl Benzyl Phthalate

12.3.8.2 Di-Butyl Phthalate

12.3.8.3 Di-Ethyl Phthalate

12.3.8.4 Potassium Hydrogen Phthalate

12.3.8.5 DEHP

12.3.9 Polycyclic Aromatic Hydrocarbons

12.3.9.1 Acenaphthene

12.3.9.2 Acenaphthylene

12.3.9.3 Anthracene

12.3.9.4 Benzo(a)anthracene

12.3.9.5 Benzo(a)pyrene

12.3.9.6 Benzo(b)fluoranthene

12.3.9.7 Benzo(g,h,i)perylene

12.3.9.8 Benzo(k)fluoranthene

12.3.9.9 Chrysene

12.3.9.10 Dibenz(a,h)anthracene

12.3.9.11 Fluoranthene

12.3.9.12 Fluorene

12.3.9.13 Indeno(1,2,3-cd)pyrene

12.3.9.14 Naphthalene

12.3.9.15 Phenanthrene

12.3.9.16 Pyrene

12.3.10 Surfactants

12.3.10.1 Alkyl Diphenyloxide Disulfonate, Disodium Salt

12.3.10.2 Dodecyl Benzene Sulfonate

12.3.10.3 Nonyl Phenol Ethoxylate

12.3.10.4 Octyl Phenol Ethoxylate

12.3.10.5 Sodium-N-Methyl-N-Oleoyl-Taurate

12.3.11 Solvents

12.3.11.1 Acetone

12.3.11.2 Acetonitrile

12.3.11.3 Ethanol

12.3.11.4 Hexane

12.3.12 Inorganic Compounds

12.3.12.1 Ammonium Chloride

12.3.12.2 Hydrogen Peroxide

12.3.12.3 Iodine

12.3.12.4 Potassium Cyanide

12.3.12.5 Potassium Dichromate

12.3.12.6 Potassium Iodate

12.3.12.7 Potassium Iodide

12.3.12.8 Potassium Metaperiodate

12.3.12.9 Potassium Permanganate

12.3.12.10 Sodium Chlorate

12.3.12.11 Sodium Chromate

12.3.12.12 Sodium Cyanide

12.3.12.13 Sodium Hypochlorite

12.3.12.14 Sodium Nitrate (Low Concentration)

12.3.12.15 Sodium Nitrate (High Concentration)

12.3.12.16 Sodium Nitrite (Low Concentration)

12.3.12.17 Sodium Nitrite (High Concentration)

12.3.12.18 Sodium Tetraborate Decahydrate

Acknowledgments

References

Index

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