Structure and Reactivity of Dissolved Organic Matter as Determined by Ultra-high Resulution [i.e. Resolution] Electrospray Ionization Mass Spectrometry PDF Download
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Author: Sunghwan Kim
Publisher:
ISBN:
Category : Biogeochemistry
Languages : en
Pages :
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Abstract: There is currently little molecular level information available for dissolved organic matter (DOM). In this study, electrospray ionization mass spectrometry (ESI-MS) with ultra-high resolution has been used to study DOM at a molecular level. High resolution mass spectra of DOM routinely contains several thousand peaks with a multitude of peaks in each nominal mass region. To study the spectra at the molecular level, the individual peaks need to be examined, a process that is arduous and time consuming. In this study, use of the van Krevelen diagram is demonstrated as an innovative graphical interpretation tool for ultra-high resolution mass spectrometric data of DOM. Plotting of ESI-FT ICR-MS data from DOM indicates that lignin or tannin type molecules compose the main portion of readily ionizable DOM molecules. In addition, many peaks corresponding to hydrogen deficient molecules are observed. These hydrogen deficient molecules found in DOM samples can be related to black carbon derived material. The process of consumption and utilization of DOM by microorganisms is investigated by employing plug-flow thin film bioreactors and ultra-high resolution mass spectrometry of DOM from inflow and outflow water samples. It is shown that the DOM molecules are subject to modifications to lower molecular weight molecules by micro-organisms. Applying van Krevelen analyses for mass spectral data reveals that relative importance of the peaks with low H/C ratios (especially the peaks in the region that has been assigned to black carbon molecules) are generally increased from inflow to outflow water samples. This is consistent in two sets of bioreactor samples collected from two different locations. The current study clearly demonstrates that the method employed in a significant breakthrough in the ability to recognize such a biologically refractory form of DOM.
![Structure and Reactivity of Dissolved Organic Matter as Determined by Ultra-high Resulution [i.e. Resolution] Electrospray Ionization Mass Spectrometry PDF](https://books.google.com/books/content/images/frontcover/YZvojwEACAAJ?fife=w80-h100)
Author: Sunghwan Kim
Publisher:
ISBN:
Category : Biogeochemistry
Languages : en
Pages :
Get Book Here
Book Description
Abstract: There is currently little molecular level information available for dissolved organic matter (DOM). In this study, electrospray ionization mass spectrometry (ESI-MS) with ultra-high resolution has been used to study DOM at a molecular level. High resolution mass spectra of DOM routinely contains several thousand peaks with a multitude of peaks in each nominal mass region. To study the spectra at the molecular level, the individual peaks need to be examined, a process that is arduous and time consuming. In this study, use of the van Krevelen diagram is demonstrated as an innovative graphical interpretation tool for ultra-high resolution mass spectrometric data of DOM. Plotting of ESI-FT ICR-MS data from DOM indicates that lignin or tannin type molecules compose the main portion of readily ionizable DOM molecules. In addition, many peaks corresponding to hydrogen deficient molecules are observed. These hydrogen deficient molecules found in DOM samples can be related to black carbon derived material. The process of consumption and utilization of DOM by microorganisms is investigated by employing plug-flow thin film bioreactors and ultra-high resolution mass spectrometry of DOM from inflow and outflow water samples. It is shown that the DOM molecules are subject to modifications to lower molecular weight molecules by micro-organisms. Applying van Krevelen analyses for mass spectral data reveals that relative importance of the peaks with low H/C ratios (especially the peaks in the region that has been assigned to black carbon molecules) are generally increased from inflow to outflow water samples. This is consistent in two sets of bioreactor samples collected from two different locations. The current study clearly demonstrates that the method employed in a significant breakthrough in the ability to recognize such a biologically refractory form of DOM.
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Zeitungsausschnitte.
Author: Carla Jean Steinbring
Publisher:
ISBN:
Category :
Languages : en
Pages : 71
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Author: Christopher L. Osburn
Publisher: Frontiers Media SA
ISBN: 2889450813
Category :
Languages : en
Pages : 244
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Book Description
A substantial increase in the number of studies using the optical properties (absorbance and fluorescence) of dissolved organic matter (DOM) as a proxy for its chemical properties in estuaries and the coastal and open ocean has occurred during the last decade. We are making progress on finding the actual chemical compounds or phenomena responsible for DOM’s optical properties. Ultrahigh resolution mass spectrometry, in particular, has made important progress in making the key connections between optics and chemistry. But serious questions remain and the last major special issue on DOM optics and chemistry occurred nearly 10 years ago. Controversies remain from the non-specific optical properties of DOM that are not linked to discrete sources, and sometimes provide conflicting information. The use of optics, which is relatively easier to employ in synoptic and high resolution sampling to determine chemistry, is a critical connection to make and can lead to major advances in our understanding of organic matter cycling in all aquatic ecosystems. The contentions and controversies raised by our poor understanding of the linkages between optics and chemistry of DOM are bottlenecks that need to be addressed and overcome.
Author: Meilin Wu
Publisher: Frontiers Media SA
ISBN: 2832515762
Category : Science
Languages : en
Pages : 392
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Author: Vanessa-Nina Roth
Publisher:
ISBN:
Category :
Languages : en
Pages : 164
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Author: Reid Milstead
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
Dissolved organic matter (DOM) is a complex heterogeneous mixture of organic compounds that is found in all water systems. DOM is derived from both terrestrial and microbial sources. The composition of DOM can vary greatly depending on a number of variables, including time of year, surrounding groundcover type, and water column depth. The characterization of DOM composition is increasingly performed using high-resolution mass spectrometry, although different instrumentation and techniques may yield different results. Importantly, DOM plays a key role in a number of chemical processes in both natural and engineered systems, such as the generation of carbon dioxide (CO2) from surface waters, the degradation of aquatic contaminants, and the formation of disinfection byproducts (DBPs) during drinking water treatment. The composition of DOM determines its reactivity in all of these processes. Using both bulk and high-resolution analytical techniques, the photooxidation of DOM can be explored. DOM compounds that are more oxidized and aromatic tend to be associated with the consumption of oxygen and the production of CO2. Bulk scale measurements show that DOM becomes less aromatic and lower in molecular weight as a result of partial photooxidation. High-resolution mass spectrometry also provides evidence of oxygen addition and the loss of CO2 from DOM during irradiation experiments. However, the chemical formulas that are most photolabile vary depending on the initial composition of DOM. Using light exposure experiments the kinetics of degradation of four contaminants were quantified for a large set of diverse waters. Using this information, we evaluated the relationships between indirect photolysis rate constants and the formation of photochemically produced reactive intermediates (PPRI) using linear regression analysis. Additionally, quencher experiments were performed to identify the PPRI associated with the degradation of each contaminant in all waters. Triplet state DOM (3DOM) and singlet oxygen (1O2) were identified as critical for atorvastatin, carbamazepine, and sulfadiazine, while hydroxyl radical (•OH) is important for benzotriazole. Our results suggest that quenching experiments should be used with caution due to the non-targeted nature of quenching compounds and the interconnection of PPRI. All of these factors result in probe compounds possibly overstating the importance of PPRI in the indirect photolysis of common contaminants. The characterization of DOM in drinking waters reveals a high degree of variability in DOM composition and reactivity with chlorine, particularly in groundwater samples. Despite the variability in DOM composition, novel DBPs with up to three halogen substituents are compositionally similar among all waters. These novel DBPs are positively correlated with trihalomethane and, to a lesser extent, the formation of haloacetonitriles. This suggests that some low molecular weight DBPs and novel DBPs detected via high-resolution mass spectrometry share similar aromatic precursors, providing evidence that low molecular weight DBPs are useful proxies for the formation of unknown, unidentified high molecular weight DBPs. Compared to Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS), Orbitrap MS yields significantly fewer formula matches and appears to have a bias towards sulfur-containing formulas and against nitrogen-containing formulas. Additionally, the choice of calibration method is particularly important for the less powerful Orbitrap MS. The matched formulas yielded from Orbitrap MS tend to be more oxidized and less highly saturated than those yielded by FT-ICR MS. Despite these differences, the formulas produced by both instruments tend to yield similar relative differences between samples, suggesting that Orbitrap MS is an acceptable replacement for FT-ICR MS in some cases.
Author: Albert Lebedev
Publisher: ILM Publications
ISBN: 1906799121
Category : Science
Languages : en
Pages : 544
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"In full colour throughout, this book describes the power of mass spectrometry in resolving environmental issues, demonstrating how real-world complex problems can be solved in a simple and elegant way."--Worldcat.
Author: Reid Milstead
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
Dissolved organic matter (DOM) is a complex heterogeneous mixture of organic compounds that is found in all water systems. DOM is derived from both terrestrial and microbial sources. The composition of DOM can vary greatly depending on a number of variables, including time of year, surrounding groundcover type, and water column depth. The characterization of DOM composition is increasingly performed using high-resolution mass spectrometry, although different instrumentation and techniques may yield different results. Importantly, DOM plays a key role in a number of chemical processes in both natural and engineered systems, such as the generation of carbon dioxide (CO2) from surface waters, the degradation of aquatic contaminants, and the formation of disinfection byproducts (DBPs) during drinking water treatment. The composition of DOM determines its reactivity in all of these processes. Using both bulk and high-resolution analytical techniques, the photooxidation of DOM can be explored. DOM compounds that are more oxidized and aromatic tend to be associated with the consumption of oxygen and the production of CO2. Bulk scale measurements show that DOM becomes less aromatic and lower in molecular weight as a result of partial photooxidation. High-resolution mass spectrometry also provides evidence of oxygen addition and the loss of CO2 from DOM during irradiation experiments. However, the chemical formulas that are most photolabile vary depending on the initial composition of DOM. Using light exposure experiments the kinetics of degradation of four contaminants were quantified for a large set of diverse waters. Using this information, we evaluated the relationships between indirect photolysis rate constants and the formation of photochemically produced reactive intermediates (PPRI) using linear regression analysis. Additionally, quencher experiments were performed to identify the PPRI associated with the degradation of each contaminant in all waters. Triplet state DOM (3DOM) and singlet oxygen (1O2) were identified as critical for atorvastatin, carbamazepine, and sulfadiazine, while hydroxyl radical (•OH) is important for benzotriazole. Our results suggest that quenching experiments should be used with caution due to the non-targeted nature of quenching compounds and the interconnection of PPRI. All of these factors result in probe compounds possibly overstating the importance of PPRI in the indirect photolysis of common contaminants. The characterization of DOM in drinking waters reveals a high degree of variability in DOM composition and reactivity with chlorine, particularly in groundwater samples. Despite the variability in DOM composition, novel DBPs with up to three halogen substituents are compositionally similar among all waters. These novel DBPs are positively correlated with trihalomethane and, to a lesser extent, the formation of haloacetonitriles. This suggests that some low molecular weight DBPs and novel DBPs detected via high-resolution mass spectrometry share similar aromatic precursors, providing evidence that low molecular weight DBPs are useful proxies for the formation of unknown, unidentified high molecular weight DBPs. Compared to Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS), Orbitrap MS yields significantly fewer formula matches and appears to have a bias towards sulfur-containing formulas and against nitrogen-containing formulas. Additionally, the choice of calibration method is particularly important for the less powerful Orbitrap MS. The matched formulas yielded from Orbitrap MS tend to be more oxidized and less highly saturated than those yielded by FT-ICR MS. Despite these differences, the formulas produced by both instruments tend to yield similar relative differences between samples, suggesting that Orbitrap MS is an acceptable replacement for FT-ICR MS in some cases.
Author: Nicholas D. Ward
Publisher: Frontiers Media SA
ISBN: 2889661547
Category : Science
Languages : en
Pages : 203
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Book Description
The goal of this research topic was to motivate innovative research that blurs traditional disciplinary and geographical boundaries. As the scientific community continues to gain momentum and knowledge about how the natural world functions, it is increasingly important that we recognize the interconnected nature of earth systems and embrace the complexities of ecosystem transitions. We are pleased to present this body of work, which embodies the spirit of research spanning across the terrestrial-aquatic continuum, from mountains to the sea. Publisher’s note: In this 2nd edition, the following article has been updated: Sawakuchi HO, Neu V, Ward ND, Barros MdLC, Valerio AM, Gagne-Maynard W, Cunha AC, Less DFS, Diniz JEM, Brito DC, Krusche AV and Richey JE (2017) Carbon Dioxide Emissions along the Lower Amazon River. Front. Mar. Sci. 4:76. doi: 10.3389/fmars.2017.00076
