Fully digital intensity modulated LIDAR

AbstractIn several applications, such as collision avoidance, it is necessary to have a system able to rapidly detect the simultaneous presence of different obstacles. In general, these applications do not require high resolution performance, but it is necessary to assure high system reliability also within critical scenarios, as in the case of partially transparent atmosphere or environment in presence of multiple objects (implying multiple echoes having different delay times.) This paper describes the algorithm, the architecture and the implementation of a digital Light Detection and Ranging (LIDAR) system based on a chirped optical carrier. This technique provides some advantages compared to the pulsed approach, primarily the reduction of the peak power of the laser. In the proposed architecture all the algorithms for signal processing are implemented using digital hardware. In this way, some specific advantages are obtained: improved detection performance (larger dynamics, range and resolution), capability of detecting multiple obstacles having different echoes amplitude, reduction of the noise effects, reduction of the costs, size and weight of the resulting equipment. The improvement provided by this fully digital solution is potentially useful in different applications such as: collision avoidance systems, 3D mapping of environments and, in general, remote sensing systems which need wide distance and dynamics

Colorimetric and Fluorescent Sensing of Copper Ions in Water through o-Phenylenediamine-Derived Carbon Dots

Funding Information: This work was supported by Regione Lazio through Progetto di Ricerca POR FESR LAZIO 2014–2020 Id: A0375-2020-36403 according to G09493 del 14 July 2021. M.A. has been supported by MIUR—Ministero dell’Istruzione Ministero dell’Università e della Ricerca (Ministry of Education, University and Research) under the national project FSE/FESR–PON Ricerca e Innovazione 2014–2020 (N° AIM1887574, CUP: E18H19000350007). This research was also supported by Fundação para a Ciência e Tecnologia, FCT/MCTES, through the Associate Laboratory for Green Chemistry—LAQV (grants UIDB/50006/2020 and UIDP/50006/2020). Publisher Copyright: © 2023 by the authors.Fluorescent nitrogen and sulfur co-doped carbon dots (NSCDs) were synthesized using a simple one-step hydrothermal method starting from o-phenylenediamine (OPD) and ammonium sulfide. The prepared NSCDs presented a selective dual optical response to Cu(II) in water through the arising of an absorption band at 660 nm and simultaneous fluorescence enhancement at 564 nm. The first effect was attributed to formation of cuprammonium complexes through coordination with amino functional groups of NSCDs. Alternatively, fluorescence enhancement can be explained by the oxidation of residual OPD bound to NSCDs. Both absorbance and fluorescence showed a linear increase with an increase of Cu(II) concentration in the range 1–100 µM, with the lowest detection limit of 100 nM and 1 µM, respectively. NSCDs were successfully incorporated in a hydrogel agarose matrix for easier handling and application to sensing. The formation of cuprammonium complexes was strongly hampered in an agarose matrix while oxidation of OPD was still effective. As a result, color variations could be perceived both under white light and UV light for concentrations as low as 10 µM. Since these color changes were similarly perceived in tap and lake water samples, the present method could be a promising candidate for simple, cost-effective visual monitoring of copper onsite.publishersversionpublishe

In Situ Growth of Mg-Fe Layered Double Hydroxides (LDH) Film on Titanium Dental Implant Substrates for pH Regulation in Oral Environments

Layered double hydroxides (LDHs) consist of two-dimensional, positively charged lamellar structures with the ability to host various anions in the interlayer spaces, which grants them unique properties and tunable characteristics. LDHs, a class of versatile inorganic compounds, have recently emerged as promising candidates for enhancing osseointegration. A suitable alkaline microenvironment is thought to be beneficial for stimulating osteoblasts’ differentiation (responsible for bone matrix formation) while suppressing osteoclast generation (responsible for bone matrix disintegration). LDHs are prone to adjusting their alkalinity and thus offering us the chance to study how pH affects cellular behavior. LDHs can indeed modulate the local pH, inflammatory responses, and oxidative stress levels, factors that profoundly influence the behavior of osteogenic cells and their interactions with the implant surface. Herein, we deposited Mg–Fe LDH films on titanium substrates for dental implants. The modified Ti substrates was more alkaline in comparison to the bare ones, with a pH higher than 8 after hydrolysis in an aqueous environment

Top-down N-doped carbon quantum dots for multiple purposes: heavy metal detection and intracellular fluorescence

In the present study, we successfully synthesized N-doped carbon quantum dots (N-CQDs) using a top-down approach, i.e., hydroxyl radical opening of fullerene with hydrogen peroxide, in basic ambient using ammonia for two different reaction times. The ensuing characterization via dynamic light scattering, SEM, and IR spectroscopy revealed a size control that was dependent on the reaction time, as well as a more pronounced -NH2 functionalization. The N-CQDs were probed for metal ion detection in aqueous solutions and during bioimaging and displayed a Cr3+ and Cu2+ selectivity shift at a higher degree of -NH2 functionalization, as well as HEK-293 cell nuclei marking

Layered Double Hydroxides (LDHs)

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Effects of progressive halogene substitution on the photoluminescence properties of an erbium-porphyrin complex

We have investigated the photoluminescence properties of porphyrin-based erbium and gadolinium complexes at different levels of halogen substitution. Both the intensity and the decay time of the erbium near-infrared emission correlate with the degree of the halogenation. Conversely, no clear correlation is found with the triplet-state energy levels nor with the intensity of the residual visible emission. Such findings confirm that the key role in the low efficiency of the near-infrared emission is played by the nonradiative quenching of the erbium emitting level due to the vibrational modes of the surrounding C-H bond

Double entry method for the verification of data a chromatography data system receives

The importance of software validation increases since the need for high usability and suitability of software applications grows. In order to reduce costs and manage risk factors, more and more recommendations and rules have been established. In the field of pharmacy the vendors of so-called chromatography data systems (CDSs) had to implement the guidelines of the Code of Federal Regulations Title 21 (CFR 21) during the last few years in order to fulfill the increasing requirements. The CFR 21 part 11 deals with electronic records and signatures. This part is binding for each company in the regulated environment that wishes to create, edit and sign electronic information instead of printing them on paper. Subsection CFR 21 part 11.10(h) explains how to perform an input check for manual user entries as well as for data that will be collected from an external device. In this article we present an approach performing the double entry method on data provided by the hardware instrument in order to investigate possible influences on the raw data by the handling CDS. A software tool has been written which allows us to communicate with a high-performance liquid chromatography (HPLC) detector and acquire data from it. The communication is completely independent of a CDS which is started separately and connected to the same system. Using this configuration we made a parallel data acquisition of two instances at the same time possible. Two CDSs have been tested and for at least one of them it has been shown that a comparison of the acquired data can be done as with the double entry method for the data verification. For the second CDS we checked whether it would be applicable after a few modifications. The given approach could be either used for a live data verification of produced raw data or as a single test during a software operational qualification to verify the data acquisition functionality of the software

Detection of Heavy Metals in Water Using Graphene Oxide Quantum Dots: An Experimental and Theoretical Study

In this work, we investigate by ab initio calculations and optical experiments the sensitivity of graphene quantum dots in their use as devices to measure the presence, and concentration, of heavy metals in water. We demonstrate that the quenching or enhancement in the optical response (absorption, emission) depends on the metallic ion considered. In particular, two cases of opposite behaviour are considered in detail: Cd2+, where we observe an increase in the emission optical response for increasing concentration, and Pb2+ whose emission spectra, vice versa, are quenched along the concentration rise. The experimental trends reported comply nicely with the different hydration patterns suggested by the models that are also capable of reproducing the minor quenching/enhancing effects observed in other ions. We envisage that quantum dots of graphene may be routinely used as cheap detectors to measure the degree of poisoning ions in water

Simultaneous measurements of heat capacity, thermal conductivity, and thermal diffusivity of liquid crystals in phase transitions

Photoacoustic measurement, in the gas-microphone configuration, is shown to be a useful technique for investigating, simultaneously, the anomalies found in the specific heat, thermal conductivity, and diffusivity of liquid crystals in the vicinity of phase transitions

Design, Synthesis and Optoelectronic Properties of Aminoacid Derivatives of Poly(arylene ethynylene) Platforms: Hybrid Bio-Synthetic Systems for Sensoring Applications

By means of the modular construction of a large series of poly(arylene ethynylene)s (PAEs) employing Pd-promoted synthetic routes, molecular models of type A-C equivalent to C-B-C equivalent to C-A and B-C equivalent to C-A-C equivalent to C-B, and polymers of type [-C equivalent to C-A-] n and [-C equivalent to C-A-C equivalent to C-B-](n) carrying a variety of aminoacidic side arms, have been prepared and fully characterized towards their application as sensing materials. The introduction of different aminoacidic groups as side substituents on the conjugated backbone may allow the tuning of the recognition ability of the receptor site towards given analytes. The luminescent sensing properties of these materials towards metal ions were investigated. The flexibility of the synthetic route allows tuning of binding activity, molecular recognition and opto- and electro- properties of the materials, as well as the responses upon exposure to metal ions. All compounds showed high selectivity towards Hg(II) ions, and a signal amplification in Hg(II) detection was observed for the polymeric compound in comparison with small molecule analogues. Further functionalization of aminoacid substituted PAEs with ferrocene moieties allows the electrochemical sensing by change in the oxidation potential of Fe(II)/Fe(III) redox couple, and its dependence with the interaction of aminoacidic side arms with given analytes