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  • 1
    Keywords: Forschungsbericht ; Schwimmbad ; Wasseraufbereitung ; Filtration
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (55 Seiten, 6,04 MB) , Illustrationen, Diagramme
    Language: German
    Note: Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
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  • 2
    Keywords: Forschungsbericht ; Brackwasser
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (46 Seiten, 1,73 MB) , Illustrationen, Diagramme
    Language: German
    Note: Förderkennzeichen BMBF 02WM1355D. - Verbund-Nummer 01156460 , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
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  • 3
    Keywords: Forschungsbericht ; Schwimmbad ; Wasseraufbereitung ; Filtration
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (62 Seiten, 2,57 MB) , Illustrationen, Diagramme
    Language: German
    Note: Laufzeit 18 Monate mit kostenneutraler Verlängerung auf 24 Monate, Projektbeginn: 01.10.2012, Projektende Phase I: 31.12.2014 , Bewilligungsempfänger: W.E.T. Wasser, Energie, Technologie GmbH , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Bericht deutsch. - Anhang englisch. - Zusammenfassungen in deutscher und englischer Sprache
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  • 4
    Keywords: Forschungsbericht ; Wasserversorgung
    Type of Medium: Online Resource
    Pages: Online-Ressource (209 S., 19 MB) , Ill., graph. Darst., Kt.
    Language: German , English
    Note: Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Förderkennzeichen BMBF 02WM1083. - Verbund-Nr. 01078904. - Engl. Berichtsblatt u.d.T.: SMART - Sustainable management of available water resources with innovative technologies - Projektphase 2 : part 5: Brackish water treatment using membrane filtration , Systemvoraussetzungen: Acrobat reader. , Mit dt. u. engl. Zsfassung
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  • 5
    Keywords: Forschungsbericht ; Trinkwasseraufbereitung
    Type of Medium: Online Resource
    Pages: Online-Ressource (24 S., 2,14 MB) , Ill., graph. Darst.
    Language: German
    Note: Förderkennzeichen BMBF 02WT0707. - Verbund-Nr. 01051732. - [Engl. T.: Development of novel processes for simultaneous elimination of organic pollutants and nitrate from drinking water by means of biodegradable solid substrates] , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden. - Auch als gedr. Ausg. vorhanden , Systemvoraussetzungen: Acrobat reader.
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  • 6
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Environmental chemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (582 pages)
    Edition: 1st ed.
    ISBN: 9783527614448
    DDC: 572
    Language: English
    Note: Intro -- Refractory Organic Substances in the Environment -- Contents -- Preface -- List of Authors -- List of Abbreviations -- 1 Setting the Scene -- 1.1 The Relevance of Reference Materials - Isolation and General Characterization -- 1.1.1 Introduction -- 1.1.2 Concept of Standard and Reference Material -- 1.1.3 Reference Materials in the ROSIG Priority Program -- 1.1.4 Experimental Details -- 1.1.4.1 Origin of the Samples -- 1.1.4.2 Isolation -- 1.1.4.3 Analytical Methods -- 1.1.5 Discussion -- 1.1.5.1 Mass Balance of the Isolates -- 1.1.5.2 Spectroscopic Characterization in the UV and Visible Range -- 1.1.5.3 Elemental Analysis -- 1.1.5.4 Proton and Complexation Capacities -- 1.1.5.5 Size-exclusion Chromatography -- 1.1.6 Conclusions -- References -- Additional References for ROS Literature -- 1.2 Element Determination and its Quality Control in Fractions of Refractory Organic Substances and the Corresponding Original Water Samples -- 1.2.1 Introduction -- 1.2.2 Description of Analytical Methods -- 1.2.2.1 Sample Treatment -- 1.2.2.2 Flame and Graphite Atomic Absorption Spectrometry (FAAS, GF-AAS) -- 1.2.2.3 Inductively Coupled Plasma Mass Spectrometry (ICP-MS) -- 1.2.2.4 Inductively Coupled Plasma Isotope Dilution Mass Spectrometry (ICP-IDMS) -- 1.2.2.5 Instrumental Neutron Activation Analysis (INAA) -- 1.2.2.6 Total Reflection X-Ray Fluorescence Spectrometry (TXRF) -- 1.2.3 Results of the Interlaboratory Study -- 1.2.3.1 Element Concentrations in ROS Fractions and their Original Samples -- 1.2.3.2 Relative Enrichment Factors of Elements in Separated FA and HA Fractions -- 1.2.3.3 Quality Control of Analytical Data -- References -- 2 Structural Investigations -- 2.1 Heavy Metal and Halogen Interactions with Fractions of Refractory Organic Substances Separated by Size-exclusion Chromatography -- 2.1.1 Introduction. , 2.1.2 SEC/ICP-MS System and the Isotope Dilution Technique -- 2.1.3 Determination of Heavy Metal-ROS Complexes in Fractions Separated by SEC -- 2.1.4 Correlation of Metal-ROS Complexes with other Analytical Data -- 2.1.5 Kinetically Stable Cr(III) and Co(III) Complexes of ROS -- 2.1.6 Determination of Halogen-ROS Compounds in Fractions separated by SEC -- 2.1.7 Conclusions -- References -- 2.2 Characterization of Refractory Organic Substances and their Metal Species by Combined Analytical Procedures -- 2.2.1 Introduction -- 2.2.2 Size Distribution and Stability of ROS-Metal Species Assessed by Ultrafiltration, EDTA Exchange, and Atomic Spectrometry -- 2.2.3 On-site Characterization of Aquatic Refractory Organic Substances and their Metal Species by Mobile Fractionation and Exchange Techniques -- 2.2.4 Conclusions -- References -- 2.3 Application of Nuclear Magnetic Resonance Spectroscopy to Structural Investigations of Refractory Organic Substances - Principles and Definitions -- 2.3.1 Potential of Nuclear Magnetic Resonance (NMR) Spectroscopy for ROS Structure Elucidation -- 2.3.2 Quantification of Solution-state and Solid-state NMR Spectra of ROS -- 2.3.3 Assignment of ROS NMR Signals -- References -- 2.4 Structural Characterization of Refractory Organic Substances by Solid-state High-resolution (13)C and (15)N Nuclear Magnetic Resonance -- 2.4.1 Introduction -- 2.4.2 Pulse Sequences Used -- 2.4.2.1 Cross Polarization Magic Angle Spinning (CPMAS) -- 2.4.2.2 Magic Angle Spinning (MAS) or Bloch-decay Spectra -- 2.4.2.3 Dipolar Dephasing Techniques (DD Techniques) -- 2.4.3 Lake Hohloh Samples -- 2.4.3.1 (13)C Solid-state Spectra -- 2.4.3.2 Proton Solution Spectra -- 2.4.3.3 (15)N CPMAS Spectra -- 2.4.4 Comparison of Samples from Different Locations -- 2.4.4.1 (13)C Solid-state Spectra -- 2.4.4.2 (15)N CPMAS Spectra -- 2.4.5 Conclusions. , 2.4.5.1 Methods -- 2.4.5.2 Structural Results -- References -- 2.5 Quantification of Substructures of Refractory Organic Substances by Means of Nuclear Magnetic Resonance -- 2.5.1 Introduction -- 2.5.2 Experimental Details -- 2.5.2.1 Nuclear Magnetic Resonance -- 2.5.2.2 Multistage Ultrafiltration -- 2.5.3 Results from Solution-state NMR investigations -- 2.5.3.1 General Considerations -- 2.5.3.2 Aliphatic Structural Moieties -- 2.3.3.3 Aromatic Structural Moieties -- 2.5.4 Combination of Multistage Ultrafiltration and Two-dimensional HMQC NMR -- 2.5.5 Conclusions -- References -- 2.6 Nuclear Magnetic Resonance Spectroscopy Investigations of Silylated Refractory Organic Substances -- 2.6.1 Introduction -- 2.6.1.1 Functional Group Analysis in Refractory Organic Substances -- 2.6.1.2 Silylation of Refractory Organic Substances -- 2.6.2 Materials and Methods -- 2.6.3 Two-dimensional NMR Spectroscopy of Silylated Natural Organic Matter -- 2.6.3.1 Comparative Analysis of 2D NMR Spectra -- Visualization of Conformity and Variation by Calculation of Minimum and Difference Spectra -- 2.6.4 NMR Functional Group Analysis of FA and HA Fractions Isolated from Samples of Different Origin -- 2.6.4.1 Comparison of BS1 FA, HO10 FA, FG1 FA, HO13 FA and SUW FA -- 2.6.4.2 Comparison of BS1 HA, HO13 HA, and SUW HA -- 2.6.4.3 Comparison of Results from NMR Functional Group Analysis with Data Obtained from Complementary Methods -- 2.6.5 Conclusions -- References -- 2.7 Isotopic Evidence for the Origin and Formation of Refractory Organic Substances -- 2.7.1 Variations of Stable Isotope Abundances in the Course of the Synthesis and Diagenesis of Biomass -- 2.7.2 Bulk Isotope Analysis -- 2.7.3 Pyrolysis-Gas Chromatography/Mass Spectrometry-Isotope-ratio Mass Spectrometry (Py-GC/MS-IRMS) -- 2.7.4 Bulk Isotopic Analyses of the Reference Samples. , 2.7.4.1 Differences Between the Isotope Content of the Reference Samples -- 2.7.5 Formation of Refractory Organic Substances in a Peat Profile of the Hohlohsee -- 2.7.5.1 Bulk Isotope Analyses on Hohlohsee Samples -- 2.7.5.2 δ(13)C Values of Pyrolysis Products of Sphagnum Peat and DOM from Bog Water -- References -- 2.8 Analytical Pyrolysis of Humic Substances and Dissolved Organic Matter in Water -- 2.8.1 Introduction -- 2.8.2 Methods -- 2.8.3 Characterization and Differentiation of Structural Properties -- 2.8.4 Pyrolysis-Field Ionization Mass Spectrometry -- 2.8.5 Structural Variations as a Result of Sampling Season and Year -- 2.8.6 Quality Control and Changes During Sample Storage -- 2.8.7 Correlations between (13)C NMR and Py-FIMS -- 2.8.8 Developments of Quantitative GC/MS -- 2.8.8.1 Determination of Hexose Subunits of Cellulose by Py-GC/MS -- 2.8.8.2 Determination of Solvent-extracted Fatty Acids by GC/MS -- 2.8.9 Conclusions -- References -- 2.9 Characterization of Refractory Organic Substances by HPLC/MS -- 2.9.1 Introduction -- 2.9.2 Experimental Details -- 2.9.2.1 Mass Spectrometry -- 2.9.2.2 Size-exclusion Chromatography (SEC) -- 2.9.3 Results and Discussion -- 2.9.3.1 Mass Spectra of Refractory Organic Substances -- 2.9.3.2 Size-exclusion Chromatography of Refractory Organic Substances -- References -- 2.10 UV-Visible Spectroscopy and the Potential of Fluorescent Probes -- 2.10.1 UV-Visible Absorption Spectroscopy -- 2.10.2 Colorimetric Analysis -- 2.10.3 Fluorescence of Refractory Organic Substances -- 2.10.4 Aging of Refractory Organic Substances -- 2.10.5 Complexing of Heavy Metals -- References -- 2.11 Stationary and Time-resolved Fluorescence for Refractory Organic Substances Characterization -- 2.11.1 Introduction -- 2.11.2 Experimental Details -- 2.11.3 Results and Discussion. , 2.11.3.1 Steady-state Fluorescence of Humic Substances -- 2.11.3.2 Time-resolved Fluorescence of Humic Substances -- 2.11.3.3 Fluorescence of Chemically Altered Humic Substances -- 2.11.4 Conclusions -- References -- 2.12 Structural Characterization of Refractory Organic Substances by Pyrolysis-GC/FTIR -- 2.12.1 Introduction -- 2.12.2 Experimental Details -- 2.12.2.1 Sample Preparation -- 2.12.2.2 Curie-point Pyrolysis -- 2.12.2.3 Flash Pyrolysis -- 2.12.2.4 GC/FTIR Spectroscopy -- 2.12.3 Results and Discussion -- References -- 2.13 X-ray Microscopy Studies of Refractory Organic Substances -- 2.13.1 Introduction -- 2.13.2 X-ray Microscopy -- 2.13.3 Results -- 2.13.3.1 Refractory Organic Substances in Soils -- 2.13.3.2 Flocculation of Refractory Organic Substances by Cations -- 2.13.3.3 Spectromicroscopy of Refractory Organic Substances -- 2.13.4 Conclusions -- References -- 2.14 Fractionation of Refractory Organic Substances by Electrophoresis -- 2.14.1 Introduction -- 2.14.2 Experimental Details -- 2.14.3 Results and Discussion -- 2.14.4 pH-dependence -- 2.14.5 Electrophoresis with Organic Modifiers -- 2.14.6 Micellar Electrokinetic Chromatography -- 2.14.7 Electrophoresis in Sieving Media -- 2.14.8 Isoelectric Focusing -- 2.14.9 Characterization of Degradation Products of Refractory Organic Substances -- 2.14.10 Hydrothermolysis -- 2.14.11 Pyrolysis -- 2.14.12 Conclusions -- References -- 2.15 Occurrence of Amino Acids, Carbohydrates, and Low-molecular-weight Organic Acids in Refractory Organic Substances -- 2.15.1 Introduction -- 2.15.2 Experimental Details -- 2.15.2.1 Samples -- 2.15.2.2 Determination of Amino Acids -- 2.15.2.3 Determination of Carbohydrates -- 2.15.2.4 Determination of Low-molecular-weight Organic Acids -- 2.15.3 Results and Discussion -- 2.15.3.1 Acid-hydrolyzable Amino Acids and Carbohydrates. , 2.15.3.2 Enzymatically Hydrolyzable Amino Acids and Carbohydrates.
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 21 (1987), S. 349-357 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 8
    Publication Date: 2020-09-18
    Description: Recorded molecular weights (MWs) for humic substances (HS) range from a few hundred to millions of daltons. For purposes of defining HS as a specific class of chemical compounds, it is of particular importance to ascertain if this broad range of MWs can be attributed to actual variability in molecular properties or is simply an artifact of the analytical techniques used to characterize HS. The main objectives of this study were (1) to establish if a preferential range of MWs exists for HS and (2) to determine any consistent MW properties of HS. To reach the goal, we have undertaken an approach to measure under standardized conditions the MW characteristics of a large set of HS from different natural environments. Seventy-seven humic materials were isolated from freshwater, soil, peat, and coal, such that each possessed a different fractional composition:  humic acid (HA), fulvic acid (FA), and a nonfractionated mixture of HA and FA (HF). Size exclusion chromatography (SEC) was used as the analytical technique to determine molecular weight characteristics. The MW distributions were characterized by number (Mn) and weight (Mw) average MW, and by polydispersity. The complete range of Mw values varied within 4.7−30.4 kDa. The maximum Mw values were observed for peat HF and soil HA, whereas the smallest weights were measured for river water HF. Maximum values of polydispersity (3.5−4.4) were seen for peat HF and soil HA, while much lower values (1.6−3.1) were found for all preparations isolated with XAD-resins. Statistical evaluation showed consistent Mw and Mn variations with the HS source, while polydispersity was mostly a function of the isolation procedure used. A conclusion was made that HS have a preferential range of MW values that could characterize them as a specific class of chemical compounds.
    Type: Article , PeerReviewed
    Format: text
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