Modification of PET Ion-Track Membranes by Silica Nanoparticles for Direct Contact Membrane Distillation of Salt Solutions.

The paper describes desalination by membrane distillation (MD) using ion-track membranes. Poly(ethylene terephthalate) (PET) ion-track membranes were hydrophobized by the immobilization of hydrophobic vinyl-silica nanoparticles (Si NPs). Si NPs were synthesized by the sol-gel method, and the addition of the surfactant led to the formation of NPs with average size of 40 nm. The thermal initiator fixed to the surface of membranes allowed attachment of triethoxyvinyl silane Si NPs at the membrane surface. To further increase hydrophobicity, ethoxy groups were fluorinated. The morphology and chemical structure of prepared membranes were characterized by SEM, FTIR, XPS spectroscopy, and a gas permeability test. Hydrophobic properties were evaluated by contact angle (CA) and liquid entry pressure (LEP) measurements. Membranes with CA 125-143° were tested in direct contact membrane distillation (DCMD) of 30 g/L saline solution. Membranes showed water fluxes from 2.2 to 15.4 kg/(m2·h) with salt rejection values of 93-99%.

Functionalization of PET Track-Etched Membranes by UV-Induced Graft (co)Polymerization for Detection of Heavy Metal Ions in Water.

Nowadays, water quality monitoring is an essential task since environmental contamination and human exposure to heavy metals increased. Sensors that are able to detect ever lower concentrations of heavy metal ions with greater accuracy and speed are needed to effectively monitor water quality and prevent poisoning. This article shows studies of the modification of flexible track-etched membranes as the basis for the sensor with various polymers and their influence on the accuracy of detection of copper, cadmium, and lead ions in water. We report the UV-induced graft (co)polymerization of acrylic acid (AA) and 4-vinylpyridine (4-VPy) on poly(ethylene terephthalate) track-etched membrane (PET TeMs) and use them after platinum layer sputtering in square wave anodic stripping voltammetry (SW-ASV) for detection of Cu2+, Cd2+, and Pb2+. Optimal conditions leading to functionalization of the surface and retention of the pore structure were found. Modified membranes were characterized by SEM, FTIR, X-ray photoelectron spectroscopy (XPS) and colorimetric analysis. The dependence of the modification method on the sensitivity of the sensor was shown. Membrane modified with polyacrylic acid (PET TeMs-g-PAA), poly(4-vinylpyridine) (PET TeMs-g-P4VPy), and their copolymer (PET TeMs-g-P4VPy/PAA) with average grafting yield of 3% have been found to be sensitive to µg/L concentration of copper, lead, and cadmium ions. Limits of detection (LOD) for sensors based on PET TeMs-g-PAA are 2.22, 1.05, and 2.53 µg/L for Cu2+, Pb2+, and Cd2+, respectively. LODs for sensors based on PET TeMs-g-P4VPy are 5.23 µg/L (Cu2+), 1.78 µg/L (Pb2+), and 3.64 µg/L (Cd2+) µg/L. PET TeMs-g-P4VPy/PAA electrodes are found to be sensitive with LODs of 0.74 µg/L(Cu2+), 1.13 µg/L (Pb2+), and 2.07 µg/L(Cd2+). Thus, it was shown that the modification of membranes by copolymers with carboxylic and amino groups leads to more accurate detection of heavy metal ions, associated with the formation of more stable complexes.

Fe3O4 Nanoparticles for Complex Targeted Delivery and Boron Neutron Capture Therapy.

Magnetic Fe3O4 nanoparticles (NPs) and their surface modification with therapeutic substances are of great interest, especially drug delivery for cancer therapy, including boron-neutron capture therapy (BNCT). In this paper, we present the results of boron-rich compound (carborane borate) attachment to previously aminated by (3-aminopropyl)-trimethoxysilane (APTMS) iron oxide NPs. Fourier transform infrared spectroscopy with Attenuated total reflectance accessory (ATR-FTIR) and energy-dispersive X-ray analysis confirmed the change of the element content of NPs after modification and formation of new bonds between Fe3O4 NPs and the attached molecules. Transmission (TEM) and scanning electron microscopy (SEM) showed Fe3O4 NPs' average size of 18.9 nm. Phase parameters were studied by powder X-ray diffraction (XRD), and the magnetic behavior of Fe3O4 NPs was elucidated by Mössbauer spectroscopy. The colloidal and chemical stability of NPs was studied using simulated body fluid (phosphate buffer-PBS). Modified NPs have shown excellent stability in PBS (pH = 7.4), characterized by XRD, Mössbauer spectroscopy, and dynamic light scattering (DLS). Biocompatibility was evaluated in-vitro using cultured mouse embryonic fibroblasts (MEFs). The results show us an increasing of IC50 from 0.110 mg/mL for Fe3O4 NPs to 0.405 mg/mL for Fe3O4-Carborane NPs. The obtained data confirm the biocompatibility and stability of synthesized NPs and the potential to use them in BNCT.