Suspended particle size distribution and the performance of deep bed filters

1992 ◽  
Vol 26 (12) ◽  
pp. 1571-1575 ◽  
Author(s):  
R.I. Mackie ◽  
Renbi Bai
Author(s):  
S.G. PEARSON ◽  
B.C. VAN PROOIJEN ◽  
F.P. DE WIT ◽  
H. MEIJER-HOLZHAUER ◽  
A.P. DE LOOFF ◽  
...  

2009 ◽  
Vol 135 (5) ◽  
pp. 306-316 ◽  
Author(s):  
Rajat Kanti Chakraborti ◽  
Joseph F. Atkinson ◽  
Jagjit Kaur

1996 ◽  
Vol 34 (9) ◽  
pp. 133-140 ◽  
Author(s):  
J. S. Chang ◽  
L. J. Tsai ◽  
S. Vigneswaran

Suspended particle size is one of the main factors which affect the performance of the microfiltration. Experimental results with bi and trimodal suspensions of latex particles clearly showed that the permeate flux and the quality were significantly affected by the particle size and its distribution, especially when the particle size was smaller than the pore size of the membrane.


1982 ◽  
Vol 60 (8) ◽  
pp. 1101-1107
Author(s):  
C. V. Mathai ◽  
A. W. Harrison

As part of an ongoing general research program on the effects of atmospheric aerosols on visibility and its dependence on aerosol size distributions in Calgary, this paper presents the results of a comparative study of particle size distribution and visibility in residential (NW) and industrial (SE) sections of the city using a mobile laboratory. The study was conducted in the period October–December, 1979. An active scattering aerosol spectrometer measured the size distributions and the corresponding visibilities were deduced from scattering coefficients measured with an integrating nephelometer.The results of this transit study show significantly higher suspended particle concentrations and reduced visibilities in the SE than in the NW. The mean values of the visibilities are 44 and 97 km for the SE and the NW respectively. The exponent of R (particle radius) in the power law aerosol size distribution has a mean value of −3.36 ± 0.24 in the SE compared with the corresponding value of −3.89 ± 0.39 for the NW. These results arc in good agreement with the observations of Alberta Environment; however, they are in contradiction with a recent report published by the City of Calgary.


2014 ◽  
Author(s):  
Cameron R. Turner ◽  
Matthew A. Barnes ◽  
Charles C.Y. Xu ◽  
Stuart E. Jones ◽  
Christopher L. Jerde ◽  
...  

1. Detecting aquatic macroorganisms with environmental DNA (eDNA) is a new survey method with broad applicability. However, the origin, state, and fate of aqueous macrobial eDNA - which collectively determine how well eDNA can serve as a proxy for directly observing organisms and how eDNA should be captured, purified, and assayed - are poorly understood. 2. The size of aquatic particles provides clues about their origin, state, and fate. We used sequential filtration size fractionation to measure, for the first time, the particle size distribution (PSD) of macrobial eDNA, specifically Common Carp (hereafter referred to as Carp) eDNA. We compared it to the PSDs of total eDNA (from all organisms) and suspended particle matter (SPM). We quantified Carp mitochondrial eDNA using a custom qPCR assay, total eDNA with fluorometry, and SPM with gravimetric analysis. 3. In a lake and a pond, we found Carp eDNA in particles from >180 to <0.2 µm, but it was most abundant from 1-10 µm. Total eDNA was most abundant below 0.2 µm and SPM was most abundant above 100 µm. SPM was ≤0.1% total eDNA, and total eDNA was ≤0.0004% Carp eDNA. 0.2 µm filtration maximized Carp eDNA capture (85%±6%) while minimizing total (i.e., non-target) eDNA capture (48%±3%), but filter clogging limited this pore size to a volume <250 mL. To mitigate this limitation we estimated a continuous PSD model for Carp eDNA and derived an equation for calculating isoclines of pore size and water volume that yield equivalent amounts of Carp eDNA. 4. Our results suggest that aqueous macrobial eDNA predominantly exists inside mitochondria or cells, and that settling plays an important role in its fate. For optimal eDNA capture, we recommend 0.2 µm filtration or a combination of larger pore size and water volume that exceeds the 0.2 µm isocline. In situ filtration of large volumes could maximize detection probability when surveying large habitats for rare organisms. Our method for eDNA particle size analysis enables future research to compare the PSDs of eDNA from other organisms and environments, and to easily apply them for ecological monitoring.


Sign in / Sign up

Export Citation Format

Share Document