Nitrogen content carbon

Because the basic-oxygen process uses a refining agent containing practically no nitrogen, the product has a low nitrogen content. Oxygen residues depend on the carbon content. 

Halogen, sulphur, nitrogen content Ash content Analysis of ash Organic content by BOD, COD, PV or total carbon methods completed... 

To obtain the free base, 34 g (0.256 mol) of N-ethyl-3-piperidinol and 20 g (0.22 mol) of diphenylacetyl chloride were mixed in 80 cc of isopropanol and the solution was refluxed for 2 hours. The isopropanol was evaporated in vacuo at 30 mm pressure, the residue was dissolved in 150 cc of water and the aqueous solution was extracted several times with ether. The aqueous solution was then neutralized with potassium carbonate and extracted with ether. The ethereal solution was dried over anhydrous potassium carbonate and the ether removed by distillation. The product was then distilled at its boiling point 180° to 181°C at 0.13 mm of mercury whereby 14 g of a clear yellow, viscous liquid was obtained. The nitrogen content for CjiHjjNOj was calculated as 4.33% and the nitrogen content found was 4.21%. 

Solid fuels, unlike gases and liquids, are entirely characterized by their composition. For example, coal can be characterized by its carbon, hydrogen, oxygen, sulfur, and nitrogen content. The water and mineral content of coal are also important means of differentiating coals from various sources. 

In the last decade there has been increased interest in the ferritic steels stimulated originally by the availability of new steel-making processes which gave hope that the brittleness problem could be solved by suitable control of carbon and nitrogen contents. This hope has only been partially realised, but as a result a number of new grades have been marketed which do represent useful additions to the range. These have became known collectively as Super Ferrities . Some examples are in Table 3.12. A substantial amount of relevant information was presented at the conference indicated in Reference 5. 

Here, the 21% of oxygen originally present in air has reacted on a 1 1 volume basis with carbon to produce one volume of carbon dioxide. The nitrogen content of the air does not take part in the reaction process. 

Stable isotope analyses of the organic fraction of bone and of food samples was carried out on a Micromass Prism Mass Spectrometer in the Stable Isotope Laboratory, Department of Physics, University of Calgary, under the direction of H.R. Krouse. Collagen samples were combusted in a Carlo Erba gas analyser which provides information on the carbon and nitrogen content of the samples andintroduces Nior CO gases into the mass spectrometer for analysis of nitrogen or carbon stable isotopes, respectively. 

C to 800°C), the decrease of nitrogen content is frequently accompanied with the degradation of the film. In this process, nitrogen atoms bonded to sp hybridized carbon are preferentially removed and those bonded to sp hybridized carbon are relatively stable, resulting in the graphi-tization of the film [64-67]. 

U. Schenk, R. Manderschied, J. Hugen, and H.-J. Weigel, Effects of CO, enrichment and intraspecific competition on biomass partitioning, nitrogen content and microbial biomass carbon in soil of perennial ryegrass and white clover, J. Exp. Bot. 46 987 (1995). 

The parent siliceous materials of the SBA-15 and MLV types were synthesised after typical procedures [2], The carbon replicas were prepared via polymerisation, catalysed by ferric chloride, of pyrrole introduced into the mesopores of matrices [3]. The products were characterised by the nitrogen adsorption, TEM, and thermal analysis (DTG, DTA). The nitrogen content in carbons was determined using elemental analysis, XPS, and EDX, while the Si and Fe contents, with XPS. The replicas of SBA-15 and MLV-0.75 are denoted as CMK-3Nx and OCM-.Nx, respectively, were x refers to the number of g of FeCl3 per 1 g of silica used for preparations. 

The titrimetric determination of soil constituents is most commonly applied to a limited number of soil analyses, namely, organic carbon, nitrogen compounds, carbonates, and chlorides. Determination of acid content by titration is generally not done because the titration curves are not amenable to typical titration analysis. Because of the color of soil and the fact that it is a suspension when stirred, it is often necessary to remove the constituent of interest before titration. In other cases, it is possible to do a direct titration using an appropriate indicator. However, even in these cases, detection of the end point is difficult. 

---