A magnetic amino enriched hydrothermal carbon production with molasses as carbon source

Author(s):  
Nahui Zhang ◽  
Xuelei Jiang ◽  
Dezhang Ren ◽  
Yunjie Liu ◽  
Yonglian Li ◽  
...  
1996 ◽  
Vol 34 (1-2) ◽  
pp. 417-423 ◽  
Author(s):  
G. J. Hatziconstantinou ◽  
P. Yannakopoulos ◽  
A. Andreadakis

Primary sludge hydrolysis can enrich primary effluent with the soluble organics which in turn can be a valuable carbon source to subsequent nutrient removal processes. By controlling hydraulic retention time and temperature it is possible to confine the anaerobic digestion of the primary sludge to the acidogenic and acetogenic phase (hydrolysis/fermentation process), and take advantage of the soluble organics produced. This paper presents the results of a research involving bench and pilot scale experiments related to primary sludge hydrolysis. The pilot scale sedimentation tank (4.10 m in diameter, 3.20 m in depth) operated over an expended period of 21 months as a conventional clarifier and following this as a fermentor unit employing sludge recirculation. Parallel to the pilot scale experiments, several batch and continuous flow bench scale experiments were conducted in order to determine the factors controlling the production of soluble organics and the effect of the latter on the denitrification process. The conclusions drawn were that a) a soluble COD production of the order of 5-6% in terms of sludge TCOD can be expected in a batch fermentor operating with HRT≅2days at T≤ 20°C, b) in a continuous flow fermentor, combinations of T>20°C and SRT>2 should be applied in order to achieve a production of the order of 10%, c) significant soluble carbon production can be achieved in primary sedimentation tanks (over 30% in terms of influent SCOD) when relatively increased SRTs (4 to 5 days) in combination with sludge recirculation are employed, under T>22°C, and d) increased denitrification performance of the order of 9 mgNOx/g MLSS.hr, can be achieved with hydrolysate as a carbon source.


Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


2018 ◽  
Author(s):  
Zhanyu Li ◽  
Mengru Zhang ◽  
Yu Zhang ◽  
Shuang Liu ◽  
Jinbo Zhao ◽  
...  

Deployment of organoboron in lieu of the strongly basic <br>organometallic reagents as carbon source in Cu-catalyzed <br>cyclopropene carbometallation opens unprecedented three-<br>component reactivity for stereoselective synthesis of poly-substituted cyclopropanes. A proof-of-principle demonstration of this novel carbometallation strategy is presented herein for a highly convergent access to poly-substituted aminocyclopropane framework via <br>carboamination. Preliminary results on asymmetric desymmetrization with commercial bisphosphine ligands attained high levels of enantioselection, offering a straightforward access to enantioenriched aminocyclopropanes bearing all-three chiral centers, including an all-carbon quaternary center. This strategy may underpin a host of novel synthetic protocols for poly-substituted cyclopropanes. <br>


Author(s):  
Kavitha K ◽  
Asha S ◽  
Hima Bindu T.V.L ◽  
Vidyavathi M

The safety and efficacy of a drug is based on its metabolism or metabolite formed. The metabolism of drugs can be studied by different in vitro models, among which microbial model became popular. In the present study, eight microbes were screened for their ability to metabolize phenobarbital in a manner comparable to humans with a model to develop alternative systems to study human drug metabolism. Among the different microbes screened, a filamentous fungi Rhizopus stolonifer metabolized phenobarbital to its metabolite which is used for further pharmacological and toxicological studies. The transformation of phenobarbital was identified by high- performance liquid chromatography (HPLC). Interestingly, Rhizopus stolonifer sample showed an extra metabolite peak at 3.11min. compared to its controls. The influence of different carbon sources in media used for growth of fungus, on metabolite production was studied, to find its effect in production of metabolite as the carbon source may influence the growth of the cell.


Crop Science ◽  
1980 ◽  
Vol 20 (2) ◽  
pp. 208-213 ◽  
Author(s):  
T. A. Kerby ◽  
D. R. Buxton ◽  
K. Matsuda
Keyword(s):  

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