Denitrification performance and microbial community of bioreactor packed with PHBV/PLA/rice hulls composite.

In this study, a novel biodegradable PHBV/PLA/rice hulls (PPRH) composite was applied and tested as biofilm attachment carrier and carbon source in two bioreactors for biological denitrification process. The denitrification performance, effect of operational conditions and microbial community structure of PPRH biofilm were evaluated. The batch experiment results showed that PPRH-packed bioreactor could completely remove 50 mg L-1 of NO3--N at natural pH (ca. 7.5) and room temperature. The continuous flow experiments indicated that high NO3--N removal efficiency (77%-99%) was achieved with low nitrite (<0.48 mg L-1) and ammonia (<0.81 mg L-1) accumulation, when influent NO3--N concentration was 30 mg L-1 and hydraulic retention time was 2-6 h. Furthermore, the microbial community analysis indicated that bacteria belonging to genus Diaphorobacter in phylum Proteobacteria were the most dominant and major denitrifiers in denitrification. In summary, PPRH composite was a promising carbon source for biological nitrate removal from water and wastewater.

The structural and functional properties of polysaccharide foulants in membrane fouling.

Polysaccharide foulant is known to play a crucial role in membrane fouling, however the detailed influential mechanisms and the pertinence to specific structure of polysaccharides, as well as intermolecular interactions among them with and without divalent cation are still indistinct. In this study, seven polysaccharides including agarose, sodium alginate, carrageenan, pectin, starch, sodium carboxymethylcellulose (CMC) and xanthan gum, with different chain and molecular structures, were used as model foulants to investigate the role of structural and functional features of polysaccharides in membrane fouling. Two Hermia's models (classical and mass-transfer models) as well as the resistance-in-series model were used to analyze the fouling mechanism. Results show that the spatial configuration of foulant molecule is significant in membrane fouling which actually controls the resistance of gel layer formed on membrane. Polysaccharides with different properties show distinct fouling mechanisms which are in accordance with the four models described by Hermia respectively. Cations may change the interaction of polysaccharide foulant which further leads to the structural change of the gel layer. It turns out that mass-transfer model is more suitable for interpreting of crossflow filtration data. So far, little has been known about the effects of molecule structure of polysaccharides on membrane fouling. In this paper, we provide a basic database for polysaccharide fouling which will work as a theoretical basis for finding more effective measures to prevent and control membrane fouling.

The role of transparent exopolymer particles (TEP) in membrane fouling: A critical review.

Transparent exopolymer particles (TEP) as gel-like particulate acidic polysaccharide have been commonly found in marine, surface water and wastewater. Currently, increasing interest has been devoted to TEP-associated membrane fouling in different membrane systems for water and wastewater treatment, thus this review attempts to provide a holistic view and critical analysis with regard to the definition, formation, detection and properties of TEP, which could ultimately determine its fouling potential. It appears that there is not a common consensus on the actual role of TEP in membrane fouling development due to the subjective definition and highly debatable detection method of TEP. It was clearly demonstrated in this review that the formation of TEP was largely related to cations in water and wastewater which indeed determined the cross-linking degree of precursor materials (e.g. polysaccharides) via intermolecular interactions, and subsequently the quantity of TEP formed. The binding between cations ions (e.g. monovalent, divalent and trivalent cations) and polysaccharide not only depends on the functional groups of polysaccharide, but also its spatial configuration. These in turn suggest that the formation, property and ultimate fouling potential of TEP would be closely related to the type and concentration of cations, while well explaining the controversial reports on TEP-associated fouling in the literature. In addition, the fouling mechanisms of TEP are also elucidated with details in this review, including (i) the formation of TEP-associated gel layer on membrane surface; (ii) carrying microorganisms to membrane surface via protobiofilm and (iii) trapping of deformable TEP in membrane pores. Consequently, it is apparent that TEP is an ignored determinant of membrane fouling, which has not yet been seriously addressed in the design and operation of membrane systems for water and wastewater treatment.

Comparative toxicity of pristine graphene oxide and its carboxyl, imidazole or polyethylene glycol functionalized products to Daphnia magna: A two generation study.

To investigate the chronic toxicity of graphene oxide (GO) and its functionalized products (GO-carboxyl, GO-imidazole and GO-polyethylene glycol), a two-generation study was conducted using the aquatic model species Daphnia magna. Each generation of daphnids were exposed for 21 days to 1.0 mg L-1 graphene material, with body length, neonate number, time of first brood and the intrinsic rate of natural increase (r) assessed as endpoints. Chronic exposure to GO, GO-carboxyl, and GO-imidazole had no adverse effect on body length or offspring number in the daphnid F0 generation, however, this exposure paradigm led to significant growth or reproduction inhibition in the following generation. Meanwhile, GO was found to show the strongest inhibitory effect, sequentially followed by GO-carboxyl and GO-imidazole. With exposure to GO-polyethylene glycol, no significant effects on growth or reproduction were observed for both F0 and F1 generation daphnids. These results reveal that carboxyl, imidazole and polyethylene glycol functional attachments alleviate the bio-toxicity of GO, especially polyethylene glycol. The increased C/O atomic ratio present in GO-carboxyl, GO-imidazole and GO-polyethylene glycol due to functionalization may mainly explain the reduced toxicity.

Intermolecular interactions of polysaccharides in membrane fouling during microfiltration.

Membrane technology has been widely employed for seawater desalination, water and wastewater reclamation, while membrane fouling still remains as a major challenge. The polysaccharides in extracellular polymeric substances (EPS) have been recognized as an important foulant that causes serious membrane fouling, while the detailed structure of polysaccharides and the intermolecular interactions between them have not been adequately disclosed. In this study, two different polysaccharides and their mixtures were used to study the intermolecular cross-linking of polysaccharides as well as its effects on membrane fouling. Results demonstrated that the fouling propensities of distinct polysaccharides were completely different, which was attributed to the different intermolecular interactions lying in polysaccharides. The cross-linking among molecules of polysaccharide, regardless of the homogeneity, was found to form complex networks and determine the effective dimension of polysaccharides. Depending on the effective dimension of foulants, pore blocking and cake layer occurred subsequently during filtration processes. In light of this, it potentially gives new insights into the fouling behaviours by combining the structure-function knowledge of polysaccharides with their fouling propensity. In addition, transparent exopolymeric particles (TEP) measurement was found to provide an intuitionistic evaluation of the complex networks formed from polysaccharides, so that may act as a good indicator of fouling during membrane filtration.

Interactions of natural organic matter on the surface of PVP-capped silver nanoparticle under different aqueous environment.

It is now widely accepted that coating on the nano-surface would critically dictate the uptake and cytotoxicity of engineering nanomaterials. However, the influence of natural organic matter (NOM) on the surface is quite limited to humic substances, while the diversity of NOM is neglected. In the present study, we tried to investigate the change of surface in the coexistence of bovine serum albumin (BSA) and humic acid (HA). The isothermal titration calorimetric measurements show that HA can combine with BSA in both freshwater or seawater, however, the patterns are different. In freshwater, HA lowered the adsorption of BSA on PVP-capped AgNPs through complexation with BSA, which prevented the contact of sulfur in BSA with PVP-AgNPs. Then in seawater, BSA retained its sulfur availability to bind with PVP-AgNPs. Furthermore, the toxicity of PVP-AgNPs incubated in the BSA/HA solution was evaluated by measuring the level of reactive oxygen species generated by Escherichia coli. The results indicated that, in seawater, the adsorbed BSA promoted the toxicity of PVP-AgNPs in the presence of Ca2+ and Mg2+, but the presence of HA limited this effect.