Enantiomer fractions instead of enantiomer ratios

The use of enantiomer ratios (ERs) to indicate the relative amounts of a pair of enantiomers in a sample has some disadvantages. Enantiomer fractions (EFs) are proposed as an alternative expression to eliminate the difficulties.     

Alkaline hydrolysis of humic substances--spectroscopic and chromatographic investigations.

To find out more on the structure of humic substances (HS), isolated dissolved organic carbon (DOC) samples from a brown water lake and a wastewater effluent were fractionated and subjected to alkaline hydrolysis. UV/Vis and fluorescence spectroscopy, as well as size-exclusion chromatography with on-line detection of UV absorption, fluorescence and DOC concentration were used to investigate the structural changes caused by the hydrolysis reaction. Following hydrolysis, the fluorescence intensity increased considerably despite a decrease in the UV absorption. The UV absorption and the DOC data from the SEC experiments revealed a strong shift to smaller molecular sizes after hydrolysis. The spectra of the hydrolysed samples, as well as the size-exclusion chromatograms, were compared to spectra of hydroxybenzoic acids and hydroxycinnamic acids. From this comparison, it can be concluded that the hydrolysis products have a structure similar to these organic acids.     

Performance of some growth variables

European beech (Fagus sylvatica L.), Norway spruce (Picea abies L. Karst.) and Silver fir (Abies alba Mill.) were exposed to low concentrations of ozone (O(3)) and sulfur dioxide (SO(2)), alone and combined, and simulated acid rain (pH 4.0) in sheltered open-top chambers in Hohenheim (Southwest Germany) for almost five years. The concentrations of O(3) and SO(2) used were related to annual ambient average found in southern West Germany. Two control chambers were ventilated with charcoal filtered air and rainfall was simulated at pH 4.0 and 5.0. Because of large dense plant growth in the chambers it was only possible to measure uncompleted growth of shoots in the upper canopy. Therefore, growth analysis was restricted to this area. The treatment with acidic precipitation decreased the annual shoot growth of beech and reduced leaf surface area of those trees. Exposure to SO(2), O(3) alone and in combination resulted in further reduction of shoot length and leaf surface area. Fumigation with SO(2) and O(3) + SO(2) caused insignificant decreases of shoot length, total dry weight and needle surface area of spruce. The lateral leader shoot growth of spruce exposed to O(3) was significantly reduced only in the last year of the experiment. Growth rates of the spruce exposed to charcoal filtered air and non-acidic precipitation were reduced more than those of beech and fir. Growth variables determined for fir reflected different rates of incremental change. Exposure to O(3) resulted in the largest dry matter production of all fir groups but those exposed to charcoal filtered air and non-acidic precipitation responded with the best lateral leader shoot growth, lowest specific leaf area (SLA) and leaf area ratio (LAR) respectively indicating best metabolic efficiency. At the conclusion of this study a classification of sensitivity was developed for the tree species.     

Impact of Fenton and ozone on oxidation of wastewater containing nitroaromatic compounds

Fenton and ozone treatment was investigated at laboratory scale for the degradation of aqueous solutions of nitrobenzene (NB).Effects of reactants concentration (O3,H2O2,and Fe(II)),temperature,and pH on NB degradation were monitored.Reaction kinetic of these processes was also assessed.A rapid reaction took place for Fenton process at higher initial concentration of H2O2,higher temperatures,and more acidic conditions(pH 3).Similarly, ozonation reaction exhibited rapid rates for higher ozone dose,higher temperatures,and more basic conditions(pH 11).Complete NB degradation in 65 min Was achieved using Fenton process.The conditions of complete elimination of 100 mg/L of initial NB concentration,were 250 mg/L of H2O2 concentration,pH 3,and 10 mg/L of Fe(Ⅱ) concentration.Under these conditions,55% organic carbon elimination Was achieved.Total organic carbon mineralization Was attained in 240 min reaction time by Fenton process with 900 mg/L of H2O2 concentration,and 30 mg/L of Fe(II) concentration.Fenton reaction showed a pseudo-first order kinetic;the reaction rate constant Was ranged from 0.0226 to 0.0658 min-1.Complete NB degradation wag also achieyed for an ozone dose of the order of 2.5 g/L.The ozonation Was studied at different ozone doses.different initial pH(7-11)and at difierent temperatures(15-35℃).NB ozonation kinetic Was represented by a bi-molecular kinetic model which was reduced to pseudo-first order kinetic.The pseudo-first order reaction rate constant was determined to increase at 20℃ from 0.004 to 0.020 min-1 as the used ozone increased from 0.4 to 1.9g/L.