In the recent years structural health monitoring (SHM) has gathered spectacular attention in civil engineering applications. Application of such composites enable to improve the safety and performance of structures. Recent advances in nanotechnology have led to development of new family of sensors – self-sensing materials. These materials enable to create the so-called “smart concrete” exhibiting self-sensing ability. Application of selfsensing materials in cement-based materials enables to detect their own state of strain or stress reflected as a change in their electrical properties. The variation of strain or stress is associated with the variation in material’s electrical characteristics, such as resistance or impedance. Therefore, it is possible to efficiently detect and localize crack formation and propagation in selected concrete element. This review is devoted to present contemporary developments in application of nanomaterials in self-sensing cement-based composites and future directions in the field of smart structures.

With the increase in use and application of carbon nanomaterials and the frequent presence of fluoroquinolones and tetracyclines antibiotics in the aquatic environment, their interactions have attracted extensive attention. In this study, adsorption of two antibiotics: oxytetracycline (OTC) and ciprofloxacin (CIP) by four carbon-based nanomaterials (graphene oxide, reduced graphene oxide, multiwalled carbon-nanotubes, oxidized multiwalled carbon-nanotubes) affected by pH was investigated. The experiment was performed in two steps: (i) adsorption of OTC and CIP at different pH values, (ii) adsorption isotherm studies of both antibiotics on four carbon-based nanomaterials. Both steps were conducted using the batch equilibration technique. The results showed that the adsorption of both antibiotics on studied adsorbents was highly pH-dependent. The highest adsorption was obtained at pH 7.0, implying the importance of the zwitterionic antibiotics forms to adsorption. Antibiotics adsorption isotherms at three given pH values followed the order of pH 7.0 > 1.0 > 11.0, which confirmed zwitterionic species of OTC and CIP as having the greatest ability to adsorb on carbonaceous nanomaterials. Electrostatic interaction, π-π EDA interaction, hydrophobic interaction for both antibiotics, and additionally hydrogen bond for CIP were possible mechanisms responsible for OTC and CIP adsorption onto studied nanomaterials. These results should be important to understand and assess the fate and interaction of carbon-based nanomaterials in the aquatic environment. This study can also be important for the use of carbon nanomaterials to remove antibiotics from the environment.

A revolutionary invention from Nanoseen, a nanotechnology startup headquartered in Poland, is likely to soon help solve the widespread problem of access to clean, fresh water

The aim of this paper is to present characteristics, toxicity and environmental behavior of nanoparticles (NPs) (silver, copper, gold, zinc oxide, titanium dioxide, iron oxide) that most frequently occur in consumer products. In addition, NPs are addressed as the new aquatic environmental pollutant of the 21st century. NPs are adsorbed onto particles in the aquatic systems (clay minerals, fulvic and humic acids), or they can adsorb environmental pollutants (heavy metal ions, organic compounds). Nanosilver (nAg) is released from consumer products into the aquatic environment. It can threaten aquatic organisms with high toxicity. Interestingly, copper nanoparticles (Cu-NPs) demonstrate higher toxicity to bacteria and aquatic microorganisms than those of nanosilver nAg. Their small size and reactivity can cause penetration into the tissues and interfere with the metabolic systems of living organisms and bacterial biogeochemical cycles. The behavior of NPs is not fully recognized. Nevertheless, it is known that NPs can agglomerate, bind with ions (chlorides, sulphates, phosphates) or organic compounds. They can also be bound or immobilized by slurry. The NPs behavior depends on process conditions, i.e. pH, ionic strength, temperature and presence of other chemical compounds. It is unknown how NPs behave in the aquatic environment. Therefore, the research on this problem should be carried out under different process conditions. As for the toxicity, it is important to understand where the differences in the research results come from. As NPs have an impact on not only aquatic organisms but also human health and life, it is necessary to recognize their toxic doses and know standards/regulations that determine the permissible concentrations of NPs in the environment.

Hybrid filter material was obtained via modification of polypropylene (PP) nonwoven with nanosize zinc oxide particles of a high aspect ratio. Modification was conducted as a three-step process, a variant of hydrothermal method used for synthesis of nano-ZnO, adopted for coating three dimensional polymeric nonwoven filters. The process consisted of plasma treatment of nonwoven to increase its wettability, deposition of ZnO nanoparticles and low temperature hydrothermal growth of ZnO rods. The modified nonwovens were investigated by a high resolution scanning electron microscopy (HR-SEM). It has been found that the obtained hybrid filters offer a higher filtration efficiency, in particular for so called most penetrating particle sizes.

The aim of the presented research was to test different carbon supports, such as graphene oxide (GO), graphene oxide modified with ammonia (N-GO), and reduced graphene oxide (rGO) for catalysts used in a low-temperature fuel cell, specifically a proton exchange membrane fuel cell (PEMFC). Modification of the carbon supports should lead to different catalytic activity in the fuel cell. Reduction of GO leads to partial removal of oxygen groups from GO, forming rGO. Modification of GO with ammonia results in an enrichment of GO structure with nitrogen. A thorough analysis of the used supports was carried out, using various analytical techniques, such as FTIR spectroscopy and thermogravimetric (TGA) analysis. Palladium and platinum catalysts deposited on these supports were produced and used for the oxygen reduction reaction (ORR). Catalytic activity tests of the prepared catalysts were carried out in a home-made direct formic acid fuel cell (DFAFC). The tests showed that the enrichment of the GO structure with nitrogen caused an increase in the catalytic activity, especially for the palladium catalyst. However, reduction of GO resulted in catalysts with higher activity and the highest catalytic activity was demonstrated by Pt/rGO, because platinum is the most catalytically active metal for ORR. The obtained results may be significant for low-temperature fuel cell technology, because they show that a simple modification of a carbon support may lead to a significant increase of the catalyst activity. This could be useful especially in lowering the cost of fuel cells, which is an important factor, because thousands of fuel cells running on hydrogen are already in use in commercial vehicles, forklifts, and backup power units worldwide. Another method used for lowering the price of current fuel cells can involve developing new clean and cheap production methods of the fuel, i.e. hydrogen. One of them employs catalytic processes, where carbon materials can be also used as a support and it is necessary to know how they can influence catalytic activity.