Wetting and Imbibition Characteristics of Pseudomonas fluorescens Biofilms Grown on Stainless Steel.

This study aims to provide insights into biofilm resistance associated with their structural properties acquired during formation and development. On this account, the wetting and imbibition behavior of dehydrated Pseudomonas fluorescens biofilms grown on stainless steel electropolished substrates is thoroughly examined at different biofilm ages. A polar liquid (water) and a non-polar liquid (diiodomethane) are employed as wetting agents in the form of sessile droplets. A mathematical model is applied to appraise the wetting and imbibition performance of biofilms incorporating the evaporation of sessile droplets. The present results show that the examined biofilms are hydrophilic. The progressive growth of biofilms leads to a gradual increase of substrate surface coverage─up to full coverage─accompanied by a gradual decrease of biofilm surface roughness. It is noteworthy that just after 24 h of biofilm growth, the surface roughness increases about 6.7 times the roughness of the clean stainless steel surface. It is further found that the imbibition of liquid in the biofilm matrix is restricted only to the biofilm region under the sessile droplet. The lack of further capillary imbibition into the biofilm structure, beyond the droplet deposition region, implies that the biofilm matrix is not in the form of an extended network of interconnected micro/nanopores. All in all, the present results indicate a resilient biofilm structure to biocide penetration despite its hydrophilic nature.

Adsorption of DBT and 4,6-DMDBTon nanoporous activated carbons: the role of surface chemistry and the solvent.

Adsorption of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) from solutions in hexane and hexadecane respectively as well as in acetonitrile for both thiophenic compounds was investigated with sorbents of three activated carbons and their oxidized counterparts. The raw sorbents were of different surface acidity. Oxygen surface groups created after oxidation increased the adsorption of thiophenic compounds via polar interactions.

Metal Organic Frameworks as Desulfurization Adsorbents of DBT and 4,6-DMDBT from Fuels.

Ultradeep desulfurization of fuels is a method of enormous demand due to the generation of harmful compounds during the burning of sulfur-containing fuels, which are a major source of environmental pollution. Among the various desulfurization methods in application, adsorptive desulfurization (ADS) has low energy demand and is feasible to be employed at ambient conditions without the addition of chemicals. The most crucial factor for ADS application is the selection of the adsorbent, and, currently, a new family of porous materials, metal organic frameworks (MOFs), has proved to be very effective towards this direction. In the current review, applications of MOFs and their functionalized composites for ADS are presented and discussed, as well as the main desulfurization mechanisms reported for the removal of thiophenic compounds by various frameworks. Prospective methods regarding the further improvement of MOF's desulfurization capability are also suggested.

Graphene Oxide Based Magnetic Nanocomposites with Polymers as Effective Bisphenol-A Nanoadsorbents.

Magnetic graphene oxide was impregnated with polymers for the preparation of nanocomposite adsorbents to be examined for the adsorptive removal of a typical endocrine disruptor, bisphenol-A (BPA) from aqueous solutions. The polymers used were polystyrene, chitosan and polyaniline. The nanocomposites prepared were characterized for their structure, morphology and surface chemistry. The nanocomposites presented an increase adsorptive activity for BPA at ambient conditions, compared to pure magnetic oxide, attributed to the synergistic effect of the polymers and the magnetic graphene oxide. The increased adsorption of BPA exhibited by the nanocomposites with chitosan and polyaniline could be attributed to the contribution of amine groups.