The coulometric determination of sulfur in silicon-iron

A coulometric method for the determination of sulfur in metallurgical products has been developed which meets the needs of production control of low sultur contents. The method is rapid and more precise than the conventional combustion technique.     

Determination of tho2 in thoriated tungsten wire

Dissolution of a thoriated tungsten wire in a mixture of nitric and hydrofluoric acids followed by a sodium hydroxide separation of tungsten and EDTA titration of the thorium is used as an improved method for the determination of thorium in thoriated tungsten wire     

An external secondary ion source for fourier transform mass spectrometry

A differentially pumped external secondary ion source for Fourier transform mass spectrometry is described. Installation does not interfere with other experiments such as laser desorption or photodissociation. Spectra of cesium iodide clusters (with ions up to m/z 8187), polyethylene glycol 1000, and histidine from both glycerol and dithiothreitol-dithioerythritol matrices are reported. The ion with m/z 156 from histidine was recorded with mass resolution of 160,000.     

Using 15N to determine a budget for effluent-derived nitrogen applied to forest

Using stable N isotopes, the fate of effluent-derived N has been determined within a land based municipal effluent irrigation scheme. Over 900 metric tonnes(t) of effluent-derived N have been applied to 192 ha of production conifer forest near Rotorua (NZ) over the past 11 years. The effluent N has a natural isotopic signal, generated by the treatment process, allowing it to be traced into various components of the system. Using this isotopic signal, a realistic approximation of storage capacity of various components of the system has been generated, including a calculation of the contribution of effluent N exiting the catchment via stream flow.Forest storage accounts for 50% of the applied N with a considerable proportion of that immobilized in wood and soil. The wetland, although not intensively sampled, retains 115 t, (13%) of the applied N. Denitrification, including that occurring within the wetland, accounts for 23 t (3%). Nitrogen isotope data confirm that the rise in NO3 concentrations is directly attributable to effluent N. Currently 88% of NO3-N in the stream is effluent-derived. Using current N isotope values for the stream and extrapolating over the discharge period, export of effluent N via the stream is estimated as 263 t (29%) of the applied N. Overall the forest and wetland ecosystem has intercepted or denitrified 65% of applied N, with 29% lost to the stream, and 50 t (5%) unaccounted for.The forest ecosystem is currently over-supplied with N and a number of management implications flows from these findings. In the long term the continued application of effluent N to the current irrigation area is not sustainable.     

Use of double-depleted 13C and 15N culture media for analysis of whole cell bacteria by MALDI time-of-flight and Fourier transform mass spectrometry

In the present paper, results demonstrating the significant advantages of matrix-assisted laser desorption/ionization (MALDI) analysis of whole cell samples of bacteria grown on double isotopically-depleted (13C and 15N) media are presented. It is shown that several advantages accrue for MALDI with a 9.4 T Fourier transform mass spectrometer (FTMS). Of particular note, for analysis of whole cells, sample preparation is simple and chemical interference is reduced. Moreover, ion coalescence problems are minimized, and data-base identification of proteins facilitated. Furthermore, high resolution mass spectra obtained from such whole cells show significant improvement in apparent mass resolving power and mass measurement accuracy, whether time-of-flight or FTMS MALDI is used. As a consequence, it becomes possible to detect subtle details in the chemistry of the organism, such as the presence of both post-translationally modified and unmodified versions of the same proteins. This approach is also adaptable to direct assay of over-expressed proteins from Escherichia coli cultures and should facilitate studies aimed at the detection of medically important cellular biomarker proteins.