Nanofiltration for the removal of algal metabolites and the effects of fouling

2010 ◽  
Vol 61 (5) ◽  
pp. 1189-1199 ◽  
Author(s):  
M. B. Dixon ◽  
C. Falconet ◽  
L. Ho ◽  
C. W. K. Chow ◽  
B. K. O'Neill ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Drinking Water ◽  
Membrane Fouling ◽  
Size Exclusion ◽  
Low Molecular Weight ◽  
Test Unit ◽  
Organic Micropollutants ◽  
Bench Scale ◽  
Over Time

Nanofiltration (NF) has been shown to be an effective way of removing organic micropollutants from drinking water due to its size exclusion properties. A rapid bench scale membrane test unit was utilised to trial six NF membranes to remove the algal metabolites, microcystin, cylindrospermopsin, 2-methylisoborneol (MIB) and geosmin (GSM). Membrane fouling due to the algal metabolites was observed for both charged and neutral metabolites. MIB and GSM were removed effectively by low molecular weight cut-off (MWCO) membranes but less effectively by a higher MWCO membrane. Removal of MIB and GSM by the higher MWCO membrane was improved as the membrane fouled. Microcystin was initially removed to above 90% by tight NF membranes but fouling of several membranes caused decreased percent removals over time. Tight NF membranes afforded removals of 90–100% for cylindrospermopsin, while removal by the higher MWCO membrane was lower but improved with time due to fouling.

scholarly journals Pilot Study on the Combination of Different Pre-Treatments with Nanofiltration for Efficiently Restraining Membrane Fouling While Providing High-Quality Drinking Water

Membranes ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 380
Author(s):  
Yan Chen ◽  
Huiping Li ◽  
Weihai Pang ◽  
Baiqin Zhou ◽  
Tian Li ◽  
...  
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Membrane Fouling ◽  
Membrane Surface ◽  
Post Treatment ◽  
Size Exclusion ◽  
Transmembrane Pressure ◽  
Feed Water ◽  
High Quality ◽  
Treated Water

Nanofiltration (NF) is a promising post-treatment technology for providing high-quality drinking water. However, membrane fouling remains a challenge to long-term NF in providing high-quality drinking water. Herein, we found that coupling pre-treatments (sand filtration (SF) and ozone–biological activated carbon (O3-BAC)) and NF is a potent tactic against membrane fouling while achieving high-quality drinking water. The pilot results showed that using SF+O3-BAC pre-treated water as the feed water resulted in a lower but a slowly rising transmembrane pressure (TMP) in NF post-treatment, whereas an opposite observation was found when using SF pre-treated water as the feed water. High-performance size-exclusion chromatography (HPSEC) and three-dimensional excitation–emission matrix (3D-EEM) fluorescence spectroscopy determined that the O3-BAC process changed the characteristic of dissolved organic matter (DOM), probably by removing the DOM of lower apparent molecular weight (LMW) and decreasing the biodegradability of water. Moreover, amino acids and tyrosine-like substances which were significantly related to medium and small molecule organics were found as the key foulants to membrane fouling. In addition, the accumulation of powdered activated carbon in O3-BAC pre-treated water on the membrane surface could be the key reason protecting the NF membrane from fouling.

Characterisation of Persistent Anti-Xa Activity Following Administration of the Low Molecular Weight Heparin Enoxaparin Sodium (Clexane)

1994 ◽  
Vol 72 (02) ◽  
pp. 275-280 ◽  
Author(s):  
David Brieger ◽  
Joan Dawes
Keyword(s):  
Molecular Weight ◽  
Enoxaparin Sodium ◽  
Antithrombin Iii ◽  
Anticoagulant Activity ◽  
Active Material ◽  
Biologically Active ◽  
Size Exclusion ◽  
Low Molecular Weight ◽  
Exclusion Chromatography ◽  
Liver And Kidney

SummaryIt is widely reported that persistent anti-Xa activity follows administration of low molecular weight heparins. To identify the effectors of this activity we have injected 125I-labelled Enoxaparin sodium into rabbits and subsequently analysed the circulating radiolabelled material and anti-Xa activity by affinity and size exclusion chromatography. Antithrombin III-binding material derived from the injected drug was responsible for all the anti-Xa amidolytic activity. At early times after injection additional anticoagulant activity which was largely attributable to tissue factor pathway inhibitor was measured by the Heptest clotting assay after removal of glycosaminoglycans from plasma samples. Small radiolabelled fragments, including penta/hexasaccharide with affinity for antithrombin III, were detectable in the circulation 1 week later, and sulphated oligosaccharides persisted for 3-4 weeks. Significant quantities of radiolabel remained in the liver and kidney several weeks post-injection; these organs may sequester some of the injected drug and give rise to circulating biologically active material by degradation and secretion of catabolic products into the plasma.

Comparison of exopolysaccharides from mucoid and nonmucoid strains of Clavibacter michiganensis subspecies sepedonicus

1993 ◽  
Vol 39 (3) ◽  
pp. 291-296 ◽  
Author(s):  
Paul J. Henningson ◽  
Neil C. Gudmestad
Keyword(s):  
Molecular Weight ◽  
High Performance ◽  
Size Exclusion ◽  
Enzyme Linked Immunosorbent Assay ◽  
Low Molecular Weight ◽  
Neutral Sugar ◽  
Clavibacter Michiganensis ◽  
Serological Reaction ◽  
Molecular Weights ◽  
Exclusion Chromatography

The exopolysaccharides produced by six strains of Clavibacter michiganensis ssp. sepedonicus were isolated and purified by liquid chromatography. Neutral sugar composition and molecular weights were determined for each polysaccharide fraction, using gas chromatography and high-performance size-exclusion chromatography. The serological reaction of each fraction was tested using enzyme-linked immunosorbent assay. Exopolysaccharide from nonmucoid strains contained only low molecular weight polysaccharides (1.5 × 103 to 1.1 × 104). Exopolysaccharide from mucoid and intermediate strains could be separated into low (4.0 × 103 to 1.1 × 104) molecular weight and high (5.0 × 105 to 1.6 × 106) molecular weight fractions. High molecular weight polysaccharides were composed almost exclusively of galactose, glucose, and fucose. The ratios of these sugars were highly variable among strains. Low molecular weight polysaccharides were primarily composed of galactose with significant and varying amounts of glucose, rhamnose, mannose, and ribose. All polysaccharide fractions except one, produced by a nonmucoid strain, reacted in the immunoassay test.Key words: exopolysaccharide, polysaccharide, Clavibacter, michiganensis, sepedonicus.

Assimilable organic carbon and biodegradable organic carbon removal by nanofiltration: full and bench-scale evaluation

2001 ◽  
Vol 1 (4) ◽  
pp. 35-42 ◽  
Author(s):  
I.C. Escobar ◽  
A.A. Randall ◽  
S.K. Hong
Keyword(s):  
Molecular Weight ◽  
Ionic Strength ◽  
Organic Carbon ◽  
Effective Means ◽  
High Hardness ◽  
Full Scale ◽  
Significant Fraction ◽  
Size Exclusion ◽  
Small Molecular Weight ◽  
Bench Scale

The main objective of this research was to evaluate the effectiveness of nanofiltration (NF) at full and bench scale for controlling AOC and BDOC, which are the main indicators of biological stability of the finished potable water. One of the major observations from full-scale operation was that nanofiltration was a very effective means to reduce BDOC, but conversely, did not reject a significant fraction of AOC. The high BDOC rejection by nanofiltration (NF) membranes at full scale can be explained by size exclusion, since a significant fraction of BDOC consists of compounds, such as humic and fulvic acids, which are larger than the pores of NF membranes (molecular-weight cutoff ≈200 daltons). The insignificant AOC rejection observed in full-scale systems was probably due to the low pH, high hardness, and high ionic strength (TDS) of the raw water. Bench scale tests using simulated waters clearly demonstrated that AOC removal by NF membranes decreases markedly with decreasing pH, and increasing hardness and ionic strength, implying that electrostatic repulsion plays a significant role in AOC removal mechanisms. These solution environments repress the electrostatic interaction between charged organic compounds and membranes, allowing passage of small molecular weight compounds and thus reducing AOC rejection.

scholarly journals Biologically active ion exchange (BIEX) for NOM removal and membrane fouling prevention

2017 ◽  
Vol 17 (4) ◽  
pp. 1178-1184 ◽  
Author(s):  
M. Schulz ◽  
J. Winter ◽  
H. Wray ◽  
B. Barbeau ◽  
P. Bérubé
Keyword(s):  
Molecular Weight ◽  
Biological Activity ◽  
Ion Exchange ◽  
Membrane Fouling ◽  
Building Blocks ◽  
Biologically Active ◽  
Low Molecular Weight ◽  
Effective Removal ◽  
Pre Treatment ◽  
The Impact

The natural organic matter (NOM) removal efficiency and regeneration behavior of ion-exchange filters with promoted biological activity (BIEX) was compared to operation where biological activity was suppressed (i.e. abiotic conditions). The impact of BIEX pre-treatment on fouling in subsequent ultrafiltration was also investigated. Biological operation enhanced NOM removal by approximately 50% due to an additional degradation of smaller humic substances, building blocks and low molecular weight acids. Promotion of biological activity significantly increased the time to breakthrough of the filters and, therefore, is expected to lower the regeneration frequency as well as the amount of regenerate of which to dispose. Pre-treatment using BIEX filters resulted in a significant decrease in total and irreversible fouling during subsequent ultrafiltration. The decrease was attributed to the effective removal of medium and low molecular weight NOM fractions. The results indicate that BIEX filtration is a robust, affordable and easy-to-operate pre-treatment approach to minimize fouling in ultrafiltration systems and enhance the quality of the produced permeate.

Structural features of low-molecular-weight heparins affecting their affinity to antithrombin

2009 ◽  
Vol 102 (11) ◽  
pp. 865-873 ◽  
Author(s):  
Antonella Bisio ◽  
Davide Vecchietti ◽  
Laura Citterio ◽  
Marco Guerrini ◽  
Rahul Raman ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Nmr Spectra ◽  
Biological Activities ◽  
Anticoagulant Activity ◽  
2D Nmr ◽  
Structural Features ◽  
Size Exclusion ◽  
Low Molecular Weight ◽  
Low Molecular Weight Heparins ◽  
2D Nmr Spectra

SummaryAs part of a more extensive investigation on structural features of different low-molecular-weight heparins (LMWHs) that can affect their biological activities, Enoxaparin,Tinzaparin and Dalteparin were characterised with regards to the distribution of different chain length oligosaccharides as determined by size-exclusion (SE) chromatography, as well as their structure as defined by 2D-NMR spectra (HSQC). The three LMWHs were also fractionated into high affinity (HA) and no affinity (NA) pools with regards to their ability to bind antithrombin (AT).The HA fractions were further subfractionated and characterised. For the parent LMWHs and selected fractions,molecular weight parameters were measured using a SE chromatographic system with a triple detector (TDA) to obtain absolute molecular weights. The SE chromatograms clearly indicate that Enoxaparin is consistently richer in shorter oligosaccharides than Tinzaparin and Dalteparin. Besides providing the content of terminal groups and individual glucosamine and uronic acid residues with different sulfate substituents, the HSQC-NMR spectra permitted us to evaluate and correlate the content of the pentasaccharide, AT-binding sequence A-G-A*-I-A (AT-bs) through quantification of signals of the disaccharide sequence G-A*.Whereas the percent content of HA species is approximately the same for the three LMWHs, substantial differences were observed for the chain distribution of AT-bs as a function of length, with the AT-bs being preferentially contained in the longest chains of each LMWH. The above information will be useful in establishing structure-activity relationships currently under way. This study is therefore critical for establishing correlations between structural features of LMWHs and their AT-mediated anticoagulant activity.

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