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Rapid Procedure (rapid + procedure)
Selected AbstractsAnaerobic co-digestion of potato processing wastewater with pig slurry and abattoir wastewaterJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2008Maria Monou Abstract BACKGROUND: Small-scale experimental investigations were carried out on the anaerobic digestion of potato processing wastewater and its co-digestion with pig slurry and/or abattoir wastewater. A simple and rapid procedure was used to determine the suitability of these wastes for digestion. RESULTS: During the initial 5-day acclimation phase, the seed (digested brewery waste) was replaced by the test waste before allowing the tests to incubate without further addition, where methanogenesis was measured. Although potato processing wastewater has low pH, with high fat content treatment via anaerobic digestion was still feasible in spite of low methane production. Co-digestion with pig slurry and abattoir wastewater was therefore investigated to enhance the process. Pig slurry improved the process, which, when co-digested with potato processing wastewater in equal ratio achieved 72% volatile solids removal, 35 mL average daily biogas production and 32% maximum methane content in 22 days (following the acclimation period). Co-digestion with abattoir wastewater did not improve the digestion process due to poor buffering and low pH value. CONCLUSION: Anaerobic co-digestion may be a feasible treatment option for industrial bio-wastes and livestock wastes produced in Cyprus and indeed in similar other countries of comparable market size and activities. Copyright © 2008 Society of Chemical Industry [source] Characterization of differential ebulliometers for measuring activity coefficientsAICHE JOURNAL, Issue 1 2000J. David Raal Differential ebulliometry is a powerful and rapid procedure for obtaining infinitely dilute activity coefficients with potentially very good accuracy. Tedious degassing procedures are not necessary, as in a static method, and from only a few measurements full system phase behavior can be evaluated. The principal problem, precise evaluation of the equilibrium liquid composition from the known composition of a prepared solution charged to the apparatus, is well known but has so far defied adequate resolution. A system of exact self-consistent equations was developed for the characterization of an ebulliometer through a dimensionless ebulliometer constant. Evaluation of this constant from typical data and its subsequent use are illustrated for a system of known phase equilibrium behavior. Remarkably, the equations permit evaluation of the effective "static" holdups in various parts of the equipment without any volume measurements. Since one equation is redundant to the main purpose, it can be used for a consistency check of measured and calculated data. The equations also furnish a guide for the operation of ebulliometers. [source] Isomer differentiation by combining gas chromatography, selective self-ion/molecule reactions and tandem mass spectrometry in an ion trap mass spectrometerRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 10 2003Hui-Fen Wu This study presents a novel, simple and rapid procedure for isomer differentiation by combining gas chromatography (GC), a selective self-ion/molecule reaction (SSIMR) and tandem mass spectrometry (MS/MS) in an ion trap mass spectrometer (ITMS). SSIMR product ions were produced from four isomers. For aniline, SSIMR induces the formation of the molecular ion, [M+H]+, [M+CH]+, adduct ions of fragments ([M+F]+, where F represents fragment ions) and [2MH]+. 2 and 3-Picoline produce [M+H]+, [2MH]+ and [M+F]+, while 5-hexynenitrile produces [M+H]+, [M+F]+ and [2M+H]+ ions. The proposed method provides a relatively easy, rapid and efficient means of isomer differentiation via a SSIMR in the ITMS. Typically, isomer differentiation can be achieved within several minutes. The superiority of the SSIMR technique for isomer differentiation over electronic ionization (EI) is also demonstrated. Copyright © 2003 John Wiley & Sons, Ltd. [source] Detection of Phytophthora nicotianae in Soil with Real-time Quantitative PCRJOURNAL OF PHYTOPATHOLOGY, Issue 1 2010Junli Huang Abstract Phytophthora nicotianae is one of the most important soil-borne plant pathogens. A rapid, specific and sensitive real-time polymerase chain reaction (PCR) detection method for P. nicotianae was established, which used primers targeting the internal transcribed spacer (ITS) regions of rDNA genes of Phytophthora spp. Based on the nucleotide sequences of ITS2 of 15 different species of Phytophthora, the primers and probe were designed specifically to amplify DNA from P. nicotianae. With a series of 10-fold DNA dilutions extracted from P. nicotianae pure cultures, the detection limit was 10 pg/,l in conventional PCR, whereas in SYBR Green I PCR the detection limit was 0.12 fg/,l and in TaqMan PCR 1.2 fg/,l, and real-time PCR was 104,105 times more sensitive than conventional PCR. The simple and rapid procedures maximized the yield and quality of recovered DNA from soil and allowed the processing of many samples in a short time. The direct DNA extractions from soil were utilized to yield DNA suitable for PCR. By combining this protocol with the real-time PCR procedure it has been possible to specifically detect P. nicotianae in soil, and the degree of sensitivity was 1.0 pg/,l. The system was applied to survey soil samples from tobacco field sites in China for the presence of P. nicotianae and the analyses of naturally infested soil showed the reliability of the real-time PCR method. [source] | ||||||||||