Halloysite aluminosilicate nanotubes with a 15 nm lumen, 50 nm external diameter, and length of 800 +/- 300 nm have been developed as an entrapment system for loading, storage, and controlled release of anticorrosion agents and biocides. Fundamental research to enable the control of release rates from hours to months is being undertaken. By variation of internal fluidic properties, the formation of nanoshells over the nanotubes and by creation of smart caps at the tube ends it is possible to develop further means of controlling the rate of release. Anticorrosive halloysite coatings are in development and a self-healing approach has been developed for repair mechanisms through response activation to external impacts. In this Perspective, applications of halloysite as nanometer-scale containers are discussed, including the use of halloysite tubes as drug releasing agents, as biomimetic reaction vessels, and as additives in biocide and protective coatings. Halloysite nanotubes are available in thousands of tons, and remain sophisticated and novel natural nanomaterials which can be used for the loading of agents for metal and plastic anticorrosion and biocide protection.

The corrosion of metals is one of the main destructive processes that leads to huge economic losses. Polymer coating systems are normally applied on a metal surface to provide a dense barrier against the corrosive species in order to protect metal structures from corrosive attack. When the barrier is damaged and the corrosive agents penetrate to the metal surface the coating system can not stop the corrosion process. The most effective solution so far for designing anticorrosion coatings for active protection of metals is to employ chromate-containing conversion coatings.[1] However, hexavalent chromium species are responsible for several diseases, including DNA damage and cancer, [2] which is the main reason for banning Cr 6+ -containing anticorrosion coatings in Europe from 2007. The deposition of thin inorganic or hybrid films on metallic surfaces has been suggested as a pretreatment to provide an additional barrier against the corrosion species and mainly to improve adhesion between the metal and polymer coating system.[3] The films are usually deposited by the plasma polymerization technique or the sol-gel route. Sol-gel-derived thin films that contain either inorganic (phosphates, vanadates, borates, and cerium and molybdenum compounds) or organic (phenylphosphonic acid, mercaptobenzothiazole, mercaptobenzoimidazole, triazole) inhibitors are investigated as substitutes for chromates. [3a-e] Among them, the highest activity is shown for sol-gel coatings with a cerium dopant of a critical concentration in the 0.2-0.6 wt % range. However, the negative effect of the free inhibitor occluded in the sol-gel matrix on the stability of the protective film is observed for all types of inhibitors (for instance, a higher concentration of Ce leads to the formation of microholes in the sol-gel film [3f] ). This shortcoming calls for the development of nanometer-scale reservoirs to isolate an inhibitor inside and prevent its direct interaction with the sol-gel matrix. Nanoreservoirs should be homogeneously distributed in the film matrix and should possess controlled and corrosion-stimulated inhibitor release to cure corrosion defects.Mixed-oxide nanoparticles (e.g. ZrO 2 /CeO 2 ), [4] b-cyclodextrin-inhibitor complexes, [3c] hollow polypropylene fibers, [5] and conducting polyaniline [6] have been explored as prospective reservoirs for corrosion inhibitors to be incorporated in the protective film. The common mechanism of the nanoreservoir activity is based on the slow release of inhibitor triggered by corrosion processes. Ion exchangers have also been investigated as 'smart' reservoirs for corrosion inhibitors. Chemically synthesized hydrocalmite behaves as an anion exchanger: adsorbing corrosive chloride ions and releasing corrosion-inhibiting nitrite anions. [7] Despite considerable efforts devoted to the development of new, complex anticorrosion systems, practically no single solution is able to fulfill the requirements of sufficient corrosion protection while avoiding chromates in the coating, especially in the ...

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A search for sub-GeV dark matter production mediated by a new vector boson A , called dark photon, is performed by the NA64 experiment in missing energy events from 100 GeV electron interactions in an active beam dump at the CERN SPS. From the analysis of the data collected in the years 2016, 2017, and 2018 with 2.84 × 10 11 electrons on target no evidence of such a process has been found. The most stringent constraints on the A mixing strength with photons and the parameter space for the scalar and fermionic dark matter in the mass range 1 GeV are derived. Thus, demonstrating the power of the active beam dump approach for the dark matter search.

The temperature-dependent behavior of hollow polyelectrolyte multilayer capsules consisting of poly(diallyldimethylammonium chloride) (PDADMAC) and poly(styrene sulfonate) (PSS) with a different number of layers was investigated in aqueous media using confocal laser scanning microscopy, scanning and transmission electron microscopy, atomic force microscopy, and elemental analysis. Capsules with an even number of layers exhibited a pronounced shrinking at elevated temperature resulting in a transition to a dense sphere, whereas capsules with an odd number of layers swelled during heating to 5-fold of their initial size followed by their rupture. This effect increases for odd layer numbers and decreases for even layer numbers with increasing layer number. According to elemental analysis, an excess of PDADMAC monomers exists within the multilayers of capsules with an odd number of layers leading to a repulsion between the positive charges, whereas shells with an even number of layers have a balanced ratio between the oppositely charged polyions, so that the temperature-dependent behavior is controlled by the different interactions between polyelectrolytes and the bulk water. At a certain temperature, the polyelectrolyte material softens thus facilitating any rearrangement. Besides incubation temperature, the duration of heating has an influence on the restructuring of the multilayers.

Halloysite clay nanotubes were investigated as a tubular container for the corrosion inhibitor benzotriazole. Halloysite is a naturally occurring cylindrical clay mineral with an internal diameter in the nanometer range and a length up to several micrometers, yielding a high-aspect-ratio hollow tube structure. Halloysite may be used as an additive in paints to produce a functional composite coating material. A maximum benzotriazole loading of 5% by weight was achieved for clay tubes of 50 nm external diameters and lumen of 15 nm. Variable release rates of the corrosion inhibitor were possible in a range between 5 and 100 h, as was demonstrated by formation of stoppers at tube openings. The anticorrosive performance of the sol-gel coating and paint loaded with 2-5% of halloysite-entrapped benzotriazole was tested on copper and on 2024-aluminum alloy by direct exposure of the metal plates to corrosive media. Kinetics of the corrosion spot formation at the coating defects was analyzed by the scanning vibrating electrode technique, and an essential damping of corrosion development was demonstrated for halloysite-loaded samples.

In this review, the recent achievements in the synthesis of inorganic nanomaterials inside the spatially confined volume of individual micro‐ and submicroreactors (emulsions, micelles, organized thin films, polyelectrolyte capsules, etc.) are presented. The advantages and shortcomings of each type of microreactor are discussed. Particular attention is paid to polyelectrolyte capsules as confined microreactors with controlled shell permeability and the possibility of shell engineering on the nanolevel, thus tailoring different functionalities. Nanomaterials synthesized inside a confined multifunctional microreactor have several advantages: i) absence of particle aggregates, ii) amorphous or metastable crystal phases, and iii) unique composite inorganic/inorganic and inorganic/organic structures.

The development of active corrosion protection systems for metallic substrates is an issue of prime importance for many industrial applications. The present work shows a new contribution to the development of a new protective system with self-healing ability composed of hybrid sol−gel films doped with nanocontainers that release entrapped corrosion inhibitor in response to pH changes caused by corrosion process. A silica−zirconia based hybrid film was used in this work as an anticorrosion coating deposited on 2024 aluminum alloy. Silica nanoparticles covered layer-by-layer with polyelectrolyte layers and layers of inhibitor (benzotriazole) were randomly introduced into the hybrid films. The hybrid film with the nanocontainers reveals enhanced long-term corrosion protection in comparison with the undoped hybrid film. The scanning vibrating electrode technique also shows an effective self-healing ability of the defects. This effect is obtained due to regulated release of the corrosion inhibitor triggered by the corrosion processes started in the cavities. The approach described herein can be used in many applications where active corrosion protection of materials is required.