Mechanism of additional carrier with seasonal temperature changes enhanced ecological floating beds for non-point source pollution water treatment.

The continuous performance and denitrification characteristics of carriers were investigated in two modified enhanced ecological floating beds (EFBs), one with only ceramsite and the other with ceramsite and extra additional stereo-elastic packing. Over a period of more than 414 days, the extra carrier was found to improve nitrogen removal while enhancing the system's resistance to seasonal temperature variations. The denitrification of all carriers in EFBs was inhibited in practice by seasonal temperature change, especially temperature rose from below 20 °C to above 20 °C and the inhibition rate of nitrous nitrogen (NO2--N) reduction was consistently above 91%, which was higher than that of nitrate nitrogen (NO3--N). However, the denitrification process including the rate and the resistance to temperature changes of ceramsite in the same EFBs with stereo-elastic packing at different temperatures, was consistently improved. The removal rate of NO3--N and NO2--N increased by up to 23.5% and 19.5%, respectively. The potential denitrification rates of all carriers increased with time which was also evidenced by in PICRUSt results, which showed that the abundances of predicted functional genes encoding NO3--N and NO2--N reductase increased over time. The dominant denitrifier also differed over time due to seasonal temperature changes.

Silica mitigated calcium mineral scaling in brackish water reverse osmosis.

Although the autopsies of reverse osmosis (RO) membranes from full-scale, brackish water desalination plants identify the co-presence of silica and Ca-based minerals in scaling layers, minimal research exists on their formation process and mechanisms. Therefore, combined scaling by silica and either gypsum (non-alkaline) or amorphous calcium phosphate (ACP, alkaline) was investigated in this study for their distinctive impacts on membrane performance. The obtained results demonstrate that the coexistence of silica and Ca-based mineral salts in feedwaters significantly reduced water flux decline as compared to single type of Ca-based mineral salts. This antagonistic effect was primarily attributed to the silica-mediated alleviation of Ca-based mineral scaling. In the presence of silica, silica skins were immediately established around Ca-based mineral precipitates once they emerged. Sheathing by the siliceous skins hindered the aggregation and thus the morphological evolution of Ca-based mineral species. Unlike sulfate precipitates, ACP precipitates can induce the formation of dense and thick silica skins via an additional condensation reaction. Such a phenomenon rationalized the notion concerning a stronger mitigating effect of silica on ACP scaling than gypsum scaling. Meanwhile, coating by silica skins altered the surface chemistries of Ca-based mineral precipitates, which should be fully considered in regulating membrane surface properties for combined scaling control. Our findings advance the mechanistic understanding on combined mineral scaling of RO membranes, and may guide the appropriate design of membrane surface properties for scaling-resistant membrane tailored to brackish water desalination.

Silica scaling of reverse osmosis membranes preconditioned by natural organic matter.

Reverse osmosis (RO) membranes were preconditioned in this study with humic acid, sodium alginate, or bovine serum albumin, and subsequently examined for silica scaling using the water matrix representative of concentrated brackish groundwater. The results suggested that water matrix combined with organic foulants affected silica scaling. High ambient pH favored the moderate silica ionization and thus the silica homogeneous polymerization to potentially form low molecular weight silica oligomers. The resulting scaling layer was dense and highly impermeable. Under the high Ca proportion at a given hardness, membrane scaling was enhanced through the Ca-induced silica scaling and the formation of intermolecular bridges between adjacent silica species. In contrast, high Mg hardness may facilitate the sustainable growth of silica oligomers to form the ringed high molecular weight oligomers by reducing the required energy for chain deformation. The deposition of these oligomers caused a loose scaling layer with reduced hydraulic resistance to water permeation. During the scaling tests under similar water matrix, the membranes slightly fouled by organics suffered severe flux decline due to an available space provided by the pre-existing organic fouling layer for subsequent silica scaling.

Dependence of initial silica scaling on the surface physicochemical properties of reverse osmosis membranes during bench-scale brackish water desalination.

Silica scaling of reverse osmosis membranes in brackish water desalination is less understood than hardness scaling due to the complex silica behaviors at the membrane/water interface. In this study, -COOH, -SO3H, -NH2 and -OH functional groups were introduced onto polyamide membranes to create distinct surface physicochemical properties. The resulting membranes were further studied under similar scaling conditions to yield temporal flux loss data that were empirically interpreted by a logistic growth model. The scaled membranes were also characterized by complementary analytical techniques. It was found that permeate flux loss was strongly correlated to the initial silica layer formed by direct interaction between reactive silanol (Si-OH) and reciprocal groups on the membrane surface, rather than the entire scaling layer. Importantly, membrane surface properties dictated the initial silica layer formation through three possible mechanisms, i.e., electrostatic repulsion, competitive adsorption, and interfacial energy change. Of these, electrostatic repulsion was identified as the primary one. Therefore, by modifying the membrane surface properties, the three aforementioned mechanisms may be enhanced to favor the formation of a loose, disordered initial silica scaling layer. Accordingly, membrane flux loss may be mitigated. This finding provided important insights into the design heuristics of scaling-resistant reverse osmosis membrane for brackish water desalination.

An ectopic study of apatite-coated silk fibroin scaffolds seeded with AdBMP-2-modified canine bMSCs.

The present study was undertaken to evaluate ectopic new bone formation effects of apatite-coated silk fibroin scaffolds (mSS) seeded with adenovirus-mediated bone morphogenic protein-2 gene (AdBMP-2) transduced canine bone marrow stromal cells (bMSCs) in nude mice. In this study, bMSCs derived from canine were cultured and transduced with AdBMP-2 adenovirus-mediated enhanced green fluorescent protein gene (AdEGFP) in vitro. Osteogenic differentiation of bMSCs was determined by alkaline phosphatase (ALP) activity analysis, and the transcript levels for BMP-2, osteopontin (OPN), osteocalcin (OCN) and bone sialoprotein (BSP) genes via real-time quantitative PCR (RT-qPCR) analysis. The ectopic bone formation effects of mSS seeded with AdBMP-2-modified bMSCs were evaluated through histological and histomorphological analysis 4, 8 and 12 weeks post-operation in nude mice. ALP activity was statistically increased in the AdBMP-2 group, when compared with control groups. The mRNA expression of BMP-2, OPN, OCN and BSP was also statistically up-regulated 6 and 9 days after AdBMP-2 transduction. Significantly higher bone volume was achieved in AdBMP-2-transduced bMSCs/mSS constructs than that of AdEGFP-transduced bMSCs/mSS or bMSCs/mSS groups at 4, 8 and 12 weeks (P < 0.01). These results demonstrated that mSS seeded with AdBMP-2-transduced canine bMSCs can promote ectopic new bone formation and maturation in nude mice, suggesting the potential of this silk-scaffold-based tissue-engineered bone for further bone regeneration studies in canine models.

Ectopic study of calcium phosphate cement seeded with pBMP-2 modified canine bMSCs mediated by a non-viral PEI derivative.

We have evaluated the ectopic new bone formation effects of CPC (calcium phosphate cement) seeded with pBMP-2 (plasmids containing bone morphogenetic protein-2 gene) transfected canine bMSCs (bone marrow stromal cells) mediated by a non-viral PEI (polyethylenimine) derivative (GenEscort™ II) in nude mice. Canine bMSCs were transfected with pBMP-2 or pEGFP (plasmids containing enhanced green fluorescent protein gene) mediated by GenEscort™ II in vitro, and the osteoblastic differentiation was explored by ALP (alkaline phosphatase) staining, ARS (alizarin red S) staining and RT-qPCR (real-time quantitative PCR) analysis. Ectopic bone formation effects of CPC/pBMP-2 transfected bMSCs were evaluated and compared with CPC/pEGFP transfected bMSCs or CPC/untransfected bMSCs through histological, histomorphological and immunohistochemical analysis 8 and 12 weeks post-operation in nude mice. Transfection efficiency was up ∼35% as demonstrated by EGFP (enhanced green fluorescent protein) expression. ALP and ARS staining were stronger with pBMP-2 gene transfection, and mRNA expression of BMP-2 (bone morphogenetic protein-2), Col 1 (collagen 1) and OCN (osteocalcin) in pBMP-2 group was significantly up-regulated at 6 and 9 days. Significantly higher NBV (new bone volume) was achieved in pBMP-2 group than in the control groups at 8 and 12 weeks (P<0.05). In addition, immunohistochemical analysis indicated higher OCN expression in pBMP-2 group (P<0.01). We conclude that CPC seeded with pBMP-2 transfected bMSCs mediated by GenEscort™ II could enhance ectopic new bone formation in nude mice, suggesting that GenEscort™ II mediated pBMP-2 gene transfer is an effective non-viral method and CPC is a suitable scaffold for gene enhanced bone tissue engineering.

BMP-2 gene modified canine bMSCs promote ectopic bone formation mediated by a nonviral PEI derivative.

The study was to explore the effects of BMP-2 gene modified canine bone marrow stromal cells (bMSCs) mediated by a nonviral PEI derivative (GenEscort™ II) in promoting bone formation in vitro and in vivo. Canine bMSCs were cultured and transfected with plasmids containing bone morphogenetic protein-2 gene (pBMP-2) or enhanced green fluorescent protein gene (pEGFP). Gene transfection conditions were initially optimized by varying GenEscort™ II/plasmid ratios. Osteogenic differentiation of gene modified bMSCs was investigated via alkaline phosphatase (ALP) activity analysis and real-time quantitative PCR (RT-qPCR) analysis in vitro. The bone formation ability of pBMP-2 transfected bMSCs combined with apatite-coated silk scaffolds (mSS) was explored and compared with pEGFP transfected bMSCs/mSS or untreated bMSCs/mSS at 8, 12 weeks after operation. Results showed that gene transfection efficiency reached up to 36.67 ± 4.12% as demonstrated by EGFP expression. ALP staining and activity assay were stronger with pBMP-2 gene transfection, and the mRNA expression of BMP-2, bone sialoprotein (BSP), Runt-related transcription factor 2 (Runx-2), and osteopontin (OPN) up-regulated in bMSCs 3, 6, 9 days in pBMP-2 group. Besides, the tissue-engineered bone complex with pBMP-2 modified bMSCs achieved significantly increased de novo bone formation compared with control groups (p < 0.01). We conclude that pBMP-2 transfection mediated by GenEscort™ II could enhance the osteogenic differentiation of canine bMSCs and promote the ectopic new bone formation in nude mice. GenEscort™ II mediated pBMP-2 gene transfer appears to be a safe and effective nonviral method for gene enhanced bone tissue engineering.