Sagar Roy

A Bilayered Structure Comprised of Functionalized Carbon Nanotubes for Desalination by Membrane Distillation

The development of a novel carbon nanotube (CNT) immobilized membrane comprised of a double-layer structure is presented for water desalination by membrane distillation. The bilayered structure is comprised of CNTs functionalized with a hydrophobic octadecyl amine group on the feed side and carboxylated CNTs on the permeate side. The latter is more hydrophilic. The hydrophobic CNTs provide higher water vapor permeation, while the hydrophilic CNTs facilitate the condensation of water vapor. Together, these led to superior performance, and flux in a direct contact membrane distillation mode was found to be as high as 121 kg/m(2)h at 80 °C. The bilayered membrane represented an enhancement of 70% over the unmodified membrane and 37% over a membrane which had a monolayered structure where only the feed side was CNT-modified.

Carbon nanotube-immobilized super-absorbent membrane for harvesting water from the atmosphere

This paper describes the development of a carbon nanotube (CNT)-immobilized membrane for harvesting pure water from air. The CNTs were incorporated into a layer of super-absorbing poly(acrylamide-co-acrylic acid) which was cast over a porous hydrophilized polypropylene support. The super-absorbing polymer tended to bind to the water molecules to form water clusters. The incorporation of CNTs led to the interruption of specific water–polymer as well as water–water interactions to generate more free water which permeated more easily through the membrane. The CNTs were functionalized with carboxylic groups to improve the dispersibility into the polymer matrix. The water vapor extraction efficiency reached over 50%, and the presence of CNTs led to an enhancement in water vapor removal by as much as 45% and in the mass transfer coefficient by 44%.

Effect of carbon nanotube (CNT) functionalization in epoxy-CNT composites

Abstract The effect of carbon nanotube (CNT) functionalization in altering the properties of epoxy-CNT composites is presented. The presence of functional groups effectively influenced the colloidal behavior of CNTs in the precursor epoxy resin and the hardener triethylenetetramine (TETA), which affected the synthesis process and eventually the interfacial interactions between the polymer matrix and the CNTs. The physical, thermal, and electrical properties of the composites exhibited strong dependence on the nature of functionalization. At a 0.5-wt% CNT loading, the enhancement in tensile strength was found to be 7.2%, 11.2%, 11.4%, and 14.2% for raw CNTs, carboxylated CNTs, octadecyl amide-functionalized CNTs, and hydroxylated CNTs, respectively. Glass transition temperatures (Tg) also varied with the functionalization, and composites prepared using hydroxylated CNTs showed the maximum enhancement of 34%.

Immobilization of Graphene Oxide on the Permeate Side of a Membrane Distillation Membrane to Enhance Flux

In this paper, a facile fabrication of enhanced direct contact membrane distillation membrane via immobilization of the hydrophilic graphene oxide (GO) on the permeate side (GOIM-P) of a commercial polypropylene supported polytetrafluoroethylene (PTFE) membrane is presented. The permeate side hydrophilicity of the membrane was modified by immobilizing the GO to facilitate fast condensation and the withdrawal of the permeate water vapors. The water vapor flux was found to be as high as 64.5 kg/m2·h at 80 °C, which is 15% higher than the unmodified membrane at a feed salt concentration of 10,000 ppm. The mass transfer coefficient was observed 6.2 × 10−7 kg/m2·s·Pa at 60 °C and 200 mL/min flow rate in the GOIM-P.