An attempt to compare the performance of bioscrubbers and biotrickling filters for degradation of ethyl acetate in gas streams

2005 ◽  
Vol 80 (11) ◽  
pp. 1252-1260 ◽  
Author(s):  
Michalis Koutinas ◽  
Ludmila G Peeva ◽  
Andrew G Livingston
2012 ◽  
Vol 87 (6) ◽  
pp. 785-790 ◽  
Author(s):  
Tiantian Song ◽  
Chunping Yang ◽  
Guangming Zeng ◽  
Guanlong Yu ◽  
Chao Xu

2017 ◽  
Vol 61 ◽  
pp. 215-221 ◽  
Author(s):  
F. Spennati ◽  
A. Mannucci ◽  
G. Mori ◽  
C. Giordano ◽  
G. Munz

2017 ◽  
Vol 61 ◽  
pp. 215-221
Author(s):  
F. Spennati ◽  
A. Mannucci ◽  
G. Mori ◽  
C. Giordano ◽  
G. Munz

2014 ◽  
Vol 26 (12) ◽  
pp. 2500-2507 ◽  
Author(s):  
Lu Wang ◽  
Chunping Yang ◽  
Yan Cheng ◽  
Jian Huang ◽  
Haining Yang ◽  
...  

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
M Diab-Assaf ◽  
RI Taleb ◽  
W Shebaby ◽  
A Mansour ◽  
CJ Moussa ◽  
...  

Planta Medica ◽  
2006 ◽  
Vol 72 (11) ◽  
Author(s):  
RM Marçal ◽  
DM Ptak ◽  
RR Krempser ◽  
MR Krempser ◽  
SV Floresta ◽  
...  

ENTOMON ◽  
2019 ◽  
Vol 44 (2) ◽  
pp. 117-126
Author(s):  
Rhitayu Chakraborti ◽  
Probir Kumar Bandyopadhyay

Study to assess the larvicidal property of Lantana camara leaves against Aedes triseriatus larvae found that the ethyl acetate extract had profound larvicidal action with the crude extract having a LC50 value of 409.831ppm. GC-MS analysis of the ethyl acetate extract confirmed the presence of twenty-one compounds out of which beta-caryophyllene covered the highest percentage of the chromatogram area. Further tests with beta-caryophyllene against the mosquito larvae proved it to be the active ingredient of L. Camara with a LC50 value of 104.243ppm.


1963 ◽  
Vol 43 (3) ◽  
pp. 345-360 ◽  
Author(s):  
Stanley Kushinsky ◽  
Jane (Wu) Tang

ABSTRACT A convenient and mild procedure is described in this paper whereby free and conjugated oestrogens may be extracted from urine. The extracts containing approximately 90 per cent of the oestrogens are devoid of most of the extraneous material and may be reduced in volume to less than 1/15 of that of the urine. The procedure consists of the following steps: (1) a 10 per cent (v/v) solution of a high molecular weight secondary amine (Amberlite LA-2, Rohm and Haas) in ethyl acetate is washed with formic acid and water, (2) the oestrogens in urine (acidified to pH 2 or 3 with H2SO4) are extracted with the LA-2 solution, (3) the oestrogen fraction is back-extracted from the organic solution with dilute aqueous ammonia.


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