Large area continuous multilayer graphene membrane for water desalination

This manuscript reports the preparation of a large area (84 cm) desalination membrane based on multilayers (11 nm thickness) of B,N-codoped defective graphene. The process consists of coating a porous ceramic α-AlO support (100 nm pore size) with a continuous nanometric (50 nm) chitosan film containing adsorbed (NH)BO. Subsequent pyrolysis in the presence of hydrogen converts chitosan into multilayer defective B,N-codoped graphene. The partial removal of B and N dopant atoms by H during the pyrolysis causes the generation of subnanometric pores due to atom vacancy, as determined by control experiments in the absence of this gas. A NaCl and KCl removal efficiency from brackish water higher than 95% for a permeate flux of 24.3 L m h at 10 bars were achieved.This work was financially supported by: i) Project NOR-WATER funded by INTERREG VA Spain-Portugal cooperation programme, Cross-Border North Portugal/Galiza Spain Cooperation Program (POCTEP) and ii) Base Funding - UIDB/50020/2020 of the Associate Laboratory LSRE-LCM - funded by national funds through FCT/MCTES (PIDDAC). P.H. Presumido acknowledges FCT for his scholarship (SFRH/BD/138756/2018). V.J.P. Vilar acknowledges the FCT Individual Call to Scientific Employment Stimulus 2017 (CEECIND/01317/2017). Financial support by the Spanish Ministry of Science and Innovation (Severo Ochoa SEV2016 and RTI2018-890237-CO2-R1) and Generalitat Valenciana (Prometeo 2017-83) is also gratefully acknowledged

Turning carbon dioxide and ethane into ethanol by solar-driven heterogeneous photocatalysis over ruo2-and nio-co-doped srtio3

The current work focused on the sunlight-driven thermo-photocatalytic reduction of carbon dioxide (CO), the primary greenhouse gas, by ethane (C H), the second most abundant element in shale gas, aiming at the generation of ethanol (EtOH), a renewable fuel. To promote this process, a hybrid catalyst was prepared and properly characterized, comprising of strontium titanate (SrTiO) co-doped with ruthenium oxide (RuO) and nickel oxide (NiO). The photocatalytic activity towards EtOH production was assessed in batch-mode and at gas-phase, under the influence of different conditions: (i) dopant loading; (ii) temperature; (iii) optical radiation wavelength; (vi) consecutive uses; and (v) electron scavenger addition. From the results here obtained, it was found that: (i) the functionalization of the SrTiO with RuO and NiO allows the visible light harvest and narrows the band gap energy (ca. 14–20%); (ii) the selectivity towards EtOH depends on the presence of Ni and irradiation; (iii) the catalyst photoresponse is mainly due to the visible photons; (iv) the photocatalyst loses > 50% efficiency right after the 2nd use; (v) the reaction mechanism is based on the photogenerated electron-hole pair charge separation; and (vi) a maximum yield of 64 µmol EtOH g was obtained after 45-min (85 µmol EtOH g h) of simulated solar irradiation (1000 W m) at 200 C, using 0.4 g L of SrTiO:RuO:NiO (0.8 wt.% Ru) with [CO ]:[C H ] and [Ru]:[Ni] molar ratios of 1:3 and 1:1, respectively. Notwithstanding, despite its exploratory nature, this study offers an alternative route to solar fuels’ synthesis from the underutilized C H and CO.This work was financially supported by the Base Funding—UIDB/50020/2020 of the Associate Laboratory LSRE-LCM—funded by national funds through FCT/MCTES (PIDDAC). Larissa O. Paulista also wants to acknowledge for her doctoral fellowship (reference SFRH/BD/137639/2018), supported by FCT. Tânia F. C. V. Silva and Vítor J. P. Vilar acknowledge the FCT Individual Call to Scientific Employment Stimulus 2017 (CEECIND/01386/2017 and CEECIND/01317/2017, respectively). Josep Albero and Hermenegildo García are also grateful to the Spanish Ministry of Science and Innovation (RTI2018-098237-CO2-R1 and Severo Ochoa), Generalitat Valencia (Prometeo 2017/083) and European Union’s Horizon 2020 research and innovation programme under grant agreement No 862453, project FlowPhotochem, by financial contribution