Block copolymer based novel magnetic mixed matrix membranes-magnetic modulation of water permeation by irreversible structural changes

This contribution focuses on understanding the effect of magnetic field intensity on the performance of novel hydrophilic and hydrophobic mixed matrix membranes (MMMs). The hydrophilic MMMs were made up of polymeric nanoparticles (PNPs) that were synthesized through polymerization-induced self-assembly (PISA) and iron oxide nanoparticles prepared in presence of poly (methacrylic acid)-b-poly quaternized (2-dimethylamino)ethyl methacrylate. The hydrophobic MMMs were prepared by the addition of iron oxide nanoparticles with different surface properties to a linear poly (methacrylic acid)-b-poly (methylmethacrylate) diblock copolymer dissolved in tetrahydrofuran (THF). Three different types of hydrophilic membranes were prepared with polymeric nanoparticles of different morphologies (spherical, vermicular and vesicular). In case of the hydrophobic membranes, six different membranes containing different iron oxide core coated with different stabilizers such as poly (methacrylic acid), quaternized poly(2-dimethylamino)ethyl methacrylate and meso-2, 3-dimercaptosuccinic acid were prepared. An external magnetic field with intensity values up to 1.15 T was used for the permeation studies and the results were compared with those obtained in the absence of magnetic field. The collected data indicate an increase in the water flux of up to 16% and 29% under the magnetic field for hydrophobic and hydrophilic membranes, respectively. The STEM analyses suggest that the magnetic nanoparticles move within the membrane structure during the application of the magnetic field. This displacement/rearrangement causes constant changes in the membrane structure (structure of the active layer) and consequently on the membrane permeability. These results suggest that the application of the magnetic field could be used as a pretreatment step to obtain high flux membranes

Antifouling Activity of Halogenated Compounds Derived from the Red Alga Sphaerococcus coronopifolius: Potential for the Development of Environmentally Friendly Solutions

Nowadays, biofouling is responsible for enormous economic losses in the maritime sector, and its treatment with conventional antifouling paints is causing significant problems to the environment. Biomimetism and green chemistry approaches are very promising research strategies for the discovery of new antifouling compounds. This study focused on the red alga Sphaerococcus coronopifolius, which is known as a producer of bioactive secondary metabolites. Fifteen compounds, including bromosphaerol (1), were tested against key marine biofoulers (five marine bacteria and three microalgae) and two enzymes associated with the adhesion process in macroalgae and invertebrates. Each metabolite presented antifouling activity against at least one organism/enzyme. This investigation also revealed that two compounds, sphaerococcinol A (4) and 14R-hydroxy-13,14-dihydro-sphaerococcinol A (5), were the most potent compounds without toxicity towards oyster larvae used as non-target organisms. These compounds are of high potential as they are active towards key biofoulers and could be produced by a cultivable alga, a fact that is important from the green chemistry point of view

Bicompartmentalized polymer particles by tandem ROMP and ATRP in miniemulsion

This Study describes an original approach to prepare biphasic particles by simultaneous ring-opening metathesis polymerization (ROMP) of norbornene and atom-transfer radical polymerization (ATRP) of methyl methacrylate under miniemulsion conditions. A single water-soluble ruthenium macrocatalyst was used to initiate ROMP and mediate ATRP. All situations led to high conversions, and well-distributed particles containing two incompatible homopolymers grown under controlled conditions could indeed be prepared

Impact of RGD Nanopatterns Grafted onto Titanium on Osteoblastic Cell Adhesion

This work reports on the synthesis of titanium bone implants functionalized with nanoparticles (NPs) containing Arg-Gly-Asp-Cys peptide (RGDC) and shows the adhesion behavior of cells seeded on these materials. RGDC peptides were first: conjugated to a norbornenyl-poly(ethylene oxide) macromonomer (Nb-PEO). Then, functional NPs with a size of similar to 300 nm and constituted of polynorbornene core surrounded by poly(ethylene oxide) shell were prepared by ring-opening metathesis polymerization in dispersed medium. The grafting density of these NPs on the titanium surface is up to 2 NPs.mu m(-2) (80 pmol of RGDC per cm(-2) of NP surface). Cell adhesion was evaluated using preosteoblast cells (MC3T3-E1). Results of cells cultured for 24 h showed that materials grafted with NPs functionalized with RGDC peptides enhance specific cell adhesion and can create filopodia-like among NP sites by stressing the cells

Nano-porous structures via

International audienceControl of film structures made from a polystyrene-polystyrene sodium sulfonate-polystyrene (PS-PNaSS-PS) copolymer micellar solution is investigated in a THF/water mixture. Four different copolymers (varying molecular weights) are synthesised via RAFT (Reversible Addition Fragmentation chain Transfer) polymerisation. Depending on parameters such as copolymer molecular weight, solvent composition and copolymer concentration, the PS-PNaSS-PS triblock self-assembles into different morphologies in solution and dry state. The effect of each parameter is investigated using characterization techniques such as AFM, TEM, Cryo-TEM, SEM and SAXS. The morphologies obtained for PS-PNaSS-PS are found to be extremely sensitive when the water content of the micellar solution is low. Among the structures observed, a highly ordered nano-porous film is obtained using a PS10k-PNaSS6k-PS10k triblock copolymer solution containing 3.0 wt% of water. This micellar solution is used to prepare a porous membrane for filtration applications. Pure water filtration data suggest a pore size in the range of ultrafiltration, making these membranes attractive for applications in the food industry, for bacteria, virus and protein removal