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1.
Membranes (Basel) ; 12(5)2022 May 08.
Article in English | MEDLINE | ID: mdl-35629828

ABSTRACT

Hybrid ceramic membranes (i.e., membranes with a layer-by-layer (LbL) coating) are an emerging technology to remove diverse kinds of micropollutants from water. Hybrid ceramic membranes were tested under laboratory conditions as single-channel (filter area = 0.00754 m2) and multi-channel (0.35 m2) variants for the removal of pharmaceuticals (sulfamethoxazole, diclofenac, clofibric acid, and ibuprofen) and typical wastewater pollutants (i.e., COD, TOC, PO4-P, and TN) from drinking water and treated wastewater. The tests were conducted with two low transmembrane pressures (TMP) of 2 and 4 bar and constant temperatures and flow velocities, which showed rejections above 80% for all the tested pharmaceuticals as well for organic pollutants and phosphorous in the treated wastewater. Tests regarding sufficient cleaning regimes also showed that the LbL coating is stable and resistant to pHs between 2 and 10 with the use of typical cleaning agents (citric acid and NaOH) but not to higher pHs, a commercially available enzymatic solution, or backwashing. The hybrid membranes can contribute to the advanced treatment of water and wastewater with low operational costs, and their application at a larger scale is viable. However, the cleaning of the membranes must be further investigated to assure the stability and durability of the LbL coating.

2.
Membranes (Basel) ; 11(4)2021 Apr 10.
Article in English | MEDLINE | ID: mdl-33920279

ABSTRACT

Layer-by-Layer (LbL) technology was used to coat alumina ceramic membranes with nanosized polyelectrolyte films. The polyelectrolyte chains form a network with nanopores on the ceramic surface and promote the rejection of small molecules such as pharmaceuticals, salts and industrial contaminants, which can otherwise not be eliminated using standard ultrafiltration methods. The properties and performance of newly developed hybrid membranes are in the focus of this investigation. The homogeneity of the applied coating layer was investigated by confocal fluorescence microscopy and scanning transmission electron microscopy (STEM). Properties such as permeability, bubble point, pore size distribution and Zeta potential were determined for both pristine and LbL coated membranes using various laboratory tests. Subsequently, a thorough comparison was drawn. The charging behavior at solid-liquid interface was characterized using streaming potential techniques. The retention potential was monitored by subjecting widely used pharmaceuticals such as diclofenac, ibuprofen and sulfamethoxazol. The results prove a successful elimination of pharmaceutical contaminants, up to 84% from drinking water, by applying a combination of polyelectrolyte multilayers and ceramic membranes.

3.
Part Fibre Toxicol ; 8: 9, 2011 Feb 23.
Article in English | MEDLINE | ID: mdl-21345205

ABSTRACT

BACKGROUND: Engineered nanomaterials display unique properties that may have impact on human health, and thus require a reliable evaluation of their potential toxicity. Here, we performed a standardized in vitro screening of 23 engineered nanomaterials. We thoroughly characterized the physicochemical properties of the nanomaterials and adapted three classical in vitro toxicity assays to eliminate nanomaterial interference. Nanomaterial toxicity was assessed in ten representative cell lines. RESULTS: Six nanomaterials induced oxidative cell stress while only a single nanomaterial reduced cellular metabolic activity and none of the particles affected cell viability. Results from heterogeneous and chemically identical particles suggested that surface chemistry, surface coating and chemical composition are likely determinants of nanomaterial toxicity. Individual cell lines differed significantly in their response, dependent on the particle type and the toxicity endpoint measured. CONCLUSION: In vitro toxicity of the analyzed engineered nanomaterials cannot be attributed to a defined physicochemical property. Therefore, the accurate identification of nanomaterial cytotoxicity requires a matrix based on a set of sensitive cell lines and in vitro assays measuring different cytotoxicity endpoints.


Subject(s)
Cell Line/drug effects , Nanostructures/chemistry , Nanostructures/toxicity , Toxicity Tests/methods , Animals , Cell Death/drug effects , Cell Line/metabolism , Humans , Oxidative Stress , Particle Size , Reactive Oxygen Species/metabolism , Soot/chemistry , Soot/pharmacology , Toxicity Tests/standards
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