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Single layer graphene oxide (SLGO) was studied as a novel coating material to drastically improve the antifouling performance of polyether sulfone (PES) hollow fiber (HF) membranes in membrane bioreactor (MBR) application. By selectively modifying the membrane surface, only a small amount of SLGO coating (6.2 mg m −2 ) was needed to achieve acceptable membrane performance. The UV treatment of the SLGO coating further assisted in improving the antifouling properties of the as-prepared PES HF membranes. By comparing the transmembrane pressure of pristine PES HF and PES_GO 6.20_ UV X (X = 0–1.5 h) membranes in a MBR for wastewater treatment at a fixed water flux, the PES_GO 6.20_ UV 1.0 membrane coated with 1 h UV-treated SLGO was demonstrated to substantially relieve the bio-fouling problem. To understand the influence of SLGO modification on membrane performance, FESEM, ATR-FTIR, and AFM analyses were conducted to characterize the as-prepared membranes, and the SLGO deposition mechanism was also proposed in this study. 

We demonstrated for the first time that inkjet printing can be a low-cost, easy, fast, and scalable method for depositing ultrathin (7.5–60 nm) uniform graphene oxide (GO) nanofiltration membranes on polymeric supports for highly effective water purification. A large area (15 × 15 cm 2 ) GO nanofiltration membrane was printed successfully on a modified polyacrylonitrile (M-PAN) support. Water permeance and rejection of small organic molecules (<1 nm, charged and uncharged) of printed GO membranes can be adjusted by controlling the GO “ink” concentration and/or printing time. Compared with commercial polymeric nanofiltration membranes, printed GO membranes, after optimization, showed approximately one order of magnitude higher water permeance and much higher rejection (>95%) of small organic molecules. Printed GO membranes also showed excellent performance in removing pharmaceutical contaminants, with ∼95% rejection and <10% water permeance decline over extended-period permeation testing. We believe that inkjet printing could be an effective method for preparing ultrathin GO membranes for effective water nanofiltration purification. 

The majority of harmful atmospheric CO and NO_xemissions are from vehicle exhausts. Although there has been success addressing NO_xemissions at temperatures above 250 °C with selective catalytic reduction technology, emissions during vehicle cold start (when the temperature is below 150 °C), are a major challenge. Herein, we show we can completely eliminate both CO and NO_xemissions simultaneously under realistic exhaust flow, using a highly loaded (2 wt %) atomically dispersed palladium in the extra‐framework positions of the small‐pore chabazite material as a CO and passive NO_xadsorber. Until now, atomically dispersed highly loaded (>0.3 wt %) transition‐metal/SSZ‐13 materials have not been known. We devised a general, simple, and scalable route to prepare such materials for Pt^IIand Pd^II. Through spectroscopy and materials testing we show that both CO and NO_xcan be simultaneously completely abated with 100 % efficiency by the formation of mixed carbonyl‐nitrosyl palladium complex in chabazite micropore.

 

The majority of harmful atmospheric CO and NO_xemissions are from vehicle exhausts. Although there has been success addressing NO_xemissions at temperatures above 250 °C with selective catalytic reduction technology, emissions during vehicle cold start (when the temperature is below 150 °C), are a major challenge. Herein, we show we can completely eliminate both CO and NO_xemissions simultaneously under realistic exhaust flow, using a highly loaded (2 wt %) atomically dispersed palladium in the extra‐framework positions of the small‐pore chabazite material as a CO and passive NO_xadsorber. Until now, atomically dispersed highly loaded (>0.3 wt %) transition‐metal/SSZ‐13 materials have not been known. We devised a general, simple, and scalable route to prepare such materials for Pt^IIand Pd^II. Through spectroscopy and materials testing we show that both CO and NO_xcan be simultaneously completely abated with 100 % efficiency by the formation of mixed carbonyl‐nitrosyl palladium complex in chabazite micropore.