Factors Affecting Degradation of MSMA in Soil

Weed Science ◽  
1986 ◽  
Vol 34 (5) ◽  
pp. 781-787 ◽  
Author(s):  
Khalid H. Akkari ◽  
Robert E. Frans ◽  
Terry L. Lavy

The effects of herbicide concentration, soil water content, and temperature on the fate and degradation of the monosodium salt of methylarsonic acid (MSMA) were evaluated in four soils. Available arsenicals were extracted, purified, and separated using reversed-phase high-performance liquid chromatography (HPLC). Residual MSMA was determined with a graphite furnace atomic absorption spectrophotometer at 193.7 nm. Initial loss of MSMA was rapid, and degradation followed first-order kinetics. The rate of change of the rate constant was temperature dependent only at soil water contents less than field capacity. MSMA dissipation was significantly faster in finer textured soils with continuous flooding and under controlled laboratory conditions (<180 days) than under field (ca. 350 days) conditions. Also, in finer textured soils, degradation of MSMA resulted in significant increases in arsenate and cacodylic acid (dimethyl arsinic acid) over native levels under flooded conditions. However, MSMA treatments contributed only a small fraction to total soil arsenic which dissipated to original concentrations by 120 days. The results indicate that under present recommended use patterns it is highly unlikely that MSMA will accumulate in the environment or carry over from one growing season to the next.

1989 ◽  
Vol 35 (1) ◽  
pp. 43-47 ◽  
Author(s):  
H Tsuchiya ◽  
T Hayashi ◽  
M Tatsumi ◽  
Y Hoshino ◽  
S Ohtani ◽  
...  

Abstract We describe a method used for determining serotonin and tryptamine in urine after oral loading with their precursor amino acid. Several factors affecting prepurification and chromatographic separation of both indoleamines were optimized, including sample extraction and mobile-phase composition. Under optimal conditions, serotonin and tryptamine are extracted from urine samples together with an internal standard, and then they are separated by reversed-phase chromatography followed by native fluorescence detection. The analytical procedure is simple enough to apply to routine analysis and performable at low cost. Sensitivity and selectivity of the method are satisfactory enough to determine urinary serotonin and tryptamine. By pursuing urinary excretion of serotonin and tryptamine after oral loading with L-tryptophan (30 mg per kilogram body weight), our method proves that urinary excretion of both indoleamines increases immediately after loading and reaches a maximum in about 45 min.


Author(s):  
Raju Chandra ◽  
Manisha Pant ◽  
Harchan Singh ◽  
Deepak Kumar ◽  
Ashwani Sanghi

A reliable and reproducible reversed-phase high performance liquid chromatography (RP-HPLC) was developed for the quantitative determination of Remipril drug content from marketed bulk tablets. The active ingredient of Remipril separation achieved with C18 column using the methanol water mobile phase in the ratio of 40:60 (v/v). The active ingredient of the drug content quantify with UV detector at 215 nm. The retention time of Remipril is 5.63 min. A good linearity relation (R2=0.999) was obtained between drug concentration and average peak areas. The limit of detection and limit of quantification of the instrument were calculated 0.03 and 0.09 µg/mL, respectively. The accuracy of the method validation was determined 102.72% by recoveries method.


2017 ◽  
pp. 96-103 ◽  
Author(s):  
Gillian Eggleston ◽  
Isabel Lima ◽  
Emmanuel Sarir ◽  
Jack Thompson ◽  
John Zatlokovicz ◽  
...  

In recent years, there has been increased world-wide concern over residual (carry-over) activity of mostly high temperature (HT) and very high temperature (VHT) stable amylases in white, refined sugars from refineries to various food and end-user industries. HT and VHT stable amylases were developed for much larger markets than the sugar industry with harsher processing conditions. There is an urgent need in the sugar industry to be able to remove or inactivate residual, active amylases either in factory or refinery streams or both. A survey of refineries that used amylase and had activated carbon systems for decolorizing, revealed they did not have any customer complaints for residual amylase. The use of high performance activated carbons to remove residual amylase activity was investigated using a Phadebas® method created for the sugar industry to measure residual amylase in syrups. Ability to remove residual amylase protein was dependent on the surface area of the powdered activated carbons as well as mixing (retention) time. The activated carbon also had the additional benefit of removing color and insoluble starch.


Sign in / Sign up

Export Citation Format

Share Document