Analysis of acids and degradation products related to iron and sulfur in the Swedish warship Vasa

Holzforschung ◽  
2008 ◽  
Vol 62 (6) ◽  
Author(s):  
Gunnar Almkvist ◽  
Ingmar Persson

Abstract Aqueous wood extracts from the historic Swedish warship Vasa have been analyzed by 1H-NMR spectroscopy, ion chromatography, and matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry as part of studies on the chemical degradation related to increased levels of iron and sulfur. The results show that low molecular organic acids have accumulated in the Vasa wood after the 1961 salvage. The increased acidity was found in a context of chemical degradation of the wood polymers and the conservation agent polyethylene glycol (PEG) in iron-rich parts of the timber. Formic, glycolic and oxalic acid are all possible end-products of oxidative degradation of wood polymers, whereas hydrolysis of acetyl groups in xylan may have contributed to increased concentrations of acetic acid. MALDI-TOF spectra of PEG displaced towards low-molecular PEG oligomers, as reported earlier, were accompanied by increased levels of formic acid, indicating oxidative degradation of PEG. PEG with a carboxylic acid end group (PEGC) was observed to a minor degree in the wood. However, analysis of stored conservation treatment solutions showed high concentrations of PEGC yielding significant contributions to the acidity during the 1960s conservation period. PEGC was probably formed as a result of microbial processes during the early conservation regime. Calculations using concentrations and well-established acidity constants show that oxalic and formic acid are the primary contributors to a low pH in the wood. The increased acidity in the interior of the wood was found in the absence of sulfur compounds but in a context of iron. The majority of the sub-samples with significant levels of sulfate in the surface region with a prospective sulfur oxidation, however, showed neither a decreased pH nor significant depolymerization. This indicates that oxidation pathways of organically bound sulfur do not necessarily produce strong acids, and thereby free protons, as the final product. These observations imply opposing effects of iron and reduced sulfur species, with iron acting as a initiator in oxidative reactions of Fenton type, whereas the reduced organic sulfur compounds may act as anti-oxidants.

2020 ◽  
Vol 20 (4) ◽  
pp. 1264-1270
Author(s):  
Xiang Tu ◽  
Shaohua Chen ◽  
Siyu Wang ◽  
Haiqing Liao ◽  
Xuejiao Deng

Abstract This study investigated the pollution status of volatile organic sulfur compounds (VOSCs) and the factors influencing their spatial distribution in the Xi River in Shenyang, China. A method for simultaneous determination of 14 VOSCs that cause odor in water samples was developed by using purge and trap coupled with gas chromatography and a flame photometric detector. The results indicated that each target compound could be identified from 15 sampling sites, and the total concentration of 14 VOSCs ranged from 2.575 to 52.981 μg L−1. Dimethyl sulfide (DMS) was the most important contaminant with an average concentration of 4.029 μg L−1, a detection rate of 93.33% and a variation coefficient of 0.72. The VOSCs were primarily distributed in suburban and rural sections, and the suburban section was the worst in regard to pollution by VOSCs. Dimethyl trisulfide was primarily distributed in urban and suburban sections of the Xi River due to industrial emissions. Ethanethiol, DMS, and ethyl methyl sulfide, which are typical by-products of microbial anaerobic decomposition from domestic wastewater, were found in abundance in the suburban section. Diethyl sulfide, diethyl disulfide, methyl propyl disulfide, and 1-propyl disulfide representing agricultural nonpoint source pollution were mostly distributed in the rural section.


Tetrahedron ◽  
2004 ◽  
Vol 60 (17) ◽  
pp. 3873-3881 ◽  
Author(s):  
Naoki Saito ◽  
Chieko Tanaka ◽  
Yu-ichi Koizumi ◽  
Khanit Suwanborirux ◽  
Surattana Amnuoypol ◽  
...  

2007 ◽  
Vol 25 (9) ◽  
pp. 1082-1088 ◽  
Author(s):  
Carol Aghajanian ◽  
Howard A. Burris ◽  
Suzanne Jones ◽  
David R. Spriggs ◽  
Marvin B. Cohen ◽  
...  

Purpose To establish the maximum-tolerated dose (MTD), dose-limiting toxicity (DLT), safety, pharmacokinetics, and pharmacodynamics of ixabepilone when administered as a 1-hour infusion every 3 weeks to patients with advanced solid tumors or relapsed/refractory non-Hodgkin's lymphoma. Dosing schedules of 40 mg/m2 and 50 mg/m2 over 3 hours were also evaluated. Patients and Methods Sixty-one patients were enrolled using an initial accelerated dose-escalation phase followed by a standard dose-escalation phase, with doses of ixabepilone ranging from 7.4 to 65 mg/m2. The pharmacokinetics of ixabepilone and two of its chemical degradation products were evaluated. Plasma pharmacodynamics were evaluated for both 1- and 3-hour infusions using an assay that measures the amount of endogenous tubulin in peripheral-blood mononuclear cells that exists in the polymerized versus the unpolymerized state. Response evaluation was performed every 6 weeks. Results The most common DLTs were neutropenia, stomatitis/pharyngitis, myalgia, and arthralgia. The MTD of ixabepilone as a 1-hour infusion every 3 weeks was established as 50 mg/m2. The maximum plasma concentration and area under the plasma concentration time curve appeared to increase less than proportionally to dose. Durable objective responses were seen in eight patients, including two complete responses. Five of the responders had experienced treatment failure with a taxane. Conclusion The recommended dose of ixabepilone for the initiation of phase II studies on the basis of these results is 50 mg/m2 over 1 hour every 3 weeks. The promising efficacy and tolerability results demonstrated by ixabepilone in this study warrant its continued development.


2016 ◽  
Vol 79 (13-14) ◽  
pp. 919-926 ◽  
Author(s):  
Ana Protić ◽  
Marina Radišić ◽  
Jelena Golubović ◽  
Biljana Otašević ◽  
Mira Zečević ◽  
...  

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