Relative Purity Research Articles

Automating Trace Detection and Chemical Purity Analysis of Carbon Nanotube Mixtures by Non-Negative Matrix Factorization of Spatial Raman Scattering Hyperspectra

Carbon nanotubes come in different species having different properties. So, it is useful to develop automated ways to quantify species purities and trace impurity content. Spatially scanned Raman spectra make hyperspectral data sets that can be used to discriminate between species and determine purities, and their analysis can be automated. A promising analytical machine learning approach is non-negative matrix factorization, which is a multivariate algorithm well adapted to hyperspectral Raman scattering data sets, and, significantly, available in open source. We prepare samples from different concentrations of pure nanotubes and acquire spatially scanned Raman scattering hyperspectra. We compare the known concentrations of the source dispersions to those determined from hyperspectra acquired from deposited materials on substrates. Here, we demonstrate and deal with several metrological issues: We show that the stability of the focusing conditions is critical. We show that if there are strong peaks that are not significant, normalization is helpful. We show that this approach compares favorably to the “best case” situation where the spectra are factored into a priori known library spectra. Scans of around 100 data points provided good bounds on concentrations down to about the parts per thousand level. Using more than one laser wavelength, so that different species are brought into resonance with each laser should enable higher relative purity measurements. However, there is an important consideration if the difference in laser energies is less than or comparable to the phonon energy. Overall, this approach is promising for the determination of chemical purity of carbon nanotubes and could be generalized to other chemical mixtures.

Efficient electroreduction of CO2 to acetate with relative purity of 100% by ultrasmall Cu2O nanoparticle on a conductive metal-organic framework

Efficient electroreduction of CO2 to acetate with relative purity of 100% by ultrasmall Cu2O nanoparticle on a conductive metal-organic framework

Upcycling CO2 into succinic acid via electrochemical and engineered Escherichia coli

Converting CO2 into value-added chemicals still remains a grand challenge. Succinic acid has long been considered as one of the top building block chemicals. This study reported efficiently upcycling CO2 into succinic acid by combining between electrochemical and engineered Escherichia coli. In this process, the Cu-organic framework catalyst was synthesized for electrocatalytic CO2-to-ethanol conversion with high Faradaic efficiency (FE, 84.7 %) and relative purity (RP, 95 wt%). Subsequently, an engineered E. coli with efficiently assimilating CO2-derived ethanol to produce succinic acid was constructed by combining computational design and metabolic engineering, and the succinic acid titer reached 53.8 mM with the yield of 0.41 mol/mol, which is 82 % of the theoretical yield. This study effort to link the two processes of efficient ethanol synthesis by electrocatalytic CO2 and succinic acid production from CO2-derived ethanol, paving a way for the production of succinic acid and other value-added chemicals by converting CO2 into ethanol.

Efficient Capture and Electroreduction of Dilute CO2 into Highly Pure and Concentrated Formic Acid Aqueous Solution.

High-purity CO2 rather than dilute CO2 (15 vol %, CO2/N2/O2 = 15:80:5, v/v/v) similar to the flue gas is currently used as the feedstock for the electroreduction of CO2, and the liquid products are usually mixed up with the cathode electrolyte, resulting in high product separation costs. In this work, we showed that a microporous conductive Bi-based metal-organic framework (Bi-HHTP, HHTP = 2,3,6,7,10,11-hexahydroxytriphenylene) can not only efficiently capture CO2 from the dilute CO2 under high humidity but also catalyze the electroreduction of the adsorbed CO2 into formic acid with a high current density of 80 mA cm-2 and a Faradaic efficiency of 90% at a very low cell voltage of 2.6 V. Importantly, the performance in a dilute CO2 atmosphere was close to that under a high-purity CO2 atmosphere. This is the first catalyst that can maintain exceptional eCO2RR performance in the presence of both O2 and N2. Moreover, by using dilute CO2 as the feedstock, a 1 cm-2 working electrode coating with Bi-HHTP can continuously produce a 200 mM formic acid aqueous solution with a relative purity of 100% for at least 30 h in a membrane electrode assembly (MEA) electrolyzer. The product does not contain electrolytes, and such a highly concentrated and pure formic acid aqueous solution can be directly used as an electrolyte for formic acid fuel cells. Comprehensive studies revealed that such a high performance might be ascribed to the CO2 capture ability of the micropores on Bi-HHTP and the lower Gibbs free energy of formation of the key intermediate *OCHO on the open Bi sites.

Visible emission studies by UV light conversion in (Dy3+/Tb3+) ions pair activated zinc-bismuth-barium borotellurite glasses for achieving intense green and white light

Both white light and green emission properties of (Dy3+/Tb3+) ions pair activated zinc-bismuth-barium borotellurite glasses were studied by ultraviolet light (UV:388 and 366 nm) conversion with a focus on down-conversion process. On the dependences of Tb3+ amounts with co-doping of Dy3+, densities of glasses, excitation, emission, area of the integration in percent, decay times, multipolar interactions, and most responsible photometric parameters are investigated in the current work. These co-activated glasses show a broad color production range (450–700 nm) covering of red (∼622 nm), green (∼545 nm), and blue (∼488 nm) colors under the stimulation of UV light wavelengths. The ratio from Yellow to blue emission was analyzed to study the site symmetry of Dy3+ surrounds. With 388 nm of UV radiation, the area of the integrated intensity under the green (Tb3+:545 nm) peak reaches a maximum of 87 %, while it falls under the yellow (Dy3+:575 nm) peak at about 13 %. The decay times of co-activated glasses were found in decreasing order, followed by fitting with a double-exponential function. The Reisfeld and Dexter's energy transfer mechanism confirmed the reduction in Dy3+ emission and its lifetime values through quadrupole-quadrupole interaction (f = 10). Moreover, photometric properties such as relative color temperatures, color coordinates, and color purity were also discussed and compared to discriminate the potentiality of the present fabricated glasses for use in both white light and green-emitting devices.

Evaluation of novel chromatographic prototypes for supercoiled plasmid DNA polishing.

Since the world first approved gene therapeutics, nucleic acid-based therapies have gained prominence. Several strategies for DNA-based therapy have been approved, and numerous clinical trials for plasmid DNA (pDNA)-based vaccines are currently in development. Due to the rising interest in pDNA for vaccination and gene therapy, plasmid manufacturing must become more effective. One of the most critical steps is downstream processing, involving isolation and purification procedures. To comply with the regulatory guidelines, pDNA must be available as a highly purified, homogeneous preparation of supercoiled pDNA (sc pDNA). This process undertakes several challenges, primarily due to the diversity of molecules derived from the producer organism. In this study, different resins were tested for the adsorption and selective polishing of sc pDNA. To identify optimal pDNA adsorption conditions, batch and column assays were performed with different resins while promoting electrostatic and hydrophobic interactions. The effect of ionic strength, pH, and contact time were evaluated and optimized. Additionally, static and dynamic binding capacities were determined for the selected resins. Analytical chromatography and agarose gel electrophoresis were used to assess the selectivity of the most promising resins toward sc pDNA isoform. Also, genomic DNA, endotoxins, and proteins were quantified to characterize the final sc pDNA quality. At the same time, the recovery and purity yields were evaluated by quantification of sc pDNA after the purification procedure. Overall, the results of the chromatographic assays using agmatine- and arginine-based resins have shown promising potential for sc pDNA polishing. Both resins demonstrated excellent binding capacity for pDNA, with agmatine outperforming arginine-based resin in terms of capacity. However, arginine-based resin exhibited a superior pDNA recovery yield, reaching a notable 52.2% recovery compared to 10.09% from agmatine. Furthermore, both resins exhibited high relative purity levels above 90% for the sc pDNA. The comprehensive characterization of the recovered sc pDNA also revealed a significant reduction in gDNA levels, reinforcing the potential of these prototypes for obtaining high-quality and pure sc pDNA. These findings highlight the promising applications of both resins in scalable pDNA purification processes for gene therapy and biopharmaceutical applications.

Continuously Producing Highly Concentrated and Pure Acetic Acid Aqueous Solution via Direct Electroreduction of CO2.

It is crucial to achieve continuous production of highly concentrated and pure C2 chemicals through the electrochemical CO2 reduction reaction (eCO2RR) for artificial carbon cycling, yet it has remained unattainable until now. Despite one-pot tandem catalysis (dividing the eCO2RR to C2 into two catalytical reactions of CO2 to CO and CO to C2) offering the potential for significantly enhancing reaction efficiency, its mechanism remains unclear and its performance is unsatisfactory. Herein, we selected different CO2-to-CO catalysts and CO-to-acetate catalysts to construct several tandem catalytic systems for the eCO2RR to acetic acid. Among them, a tandem catalytic system comprising a covalent organic framework (PcNi-DMTP) and a metal-organic framework (MAF-2) as CO2-to-CO and CO-to-acetate catalysts, respectively, exhibited a faradaic efficiency of 51.2% with a current density of 410 mA cm-2 and an ultrahigh acetate yield rate of 2.72 mmol m-2 s-1 under neutral conditions. After electrolysis for 200 h, 1 cm-2 working electrode can continuously produce 20 mM acetic acid aqueous solution with a relative purity of 95+%. Comprehensive studies revealed that the performance of tandem catalysts is influenced not only by the CO supply-demand relationship and electron competition between the two catalytic processes in the one-pot tandem system but also by the performance of the CO-to-C2 catalyst under diluted CO conditions.

Optimization of xylanase production by Pichia kudriavzevii and Candida tropicalis isolated from the wood product workshop.

Enzymatic compounds can be found abundantly and provide numerous advantages in microbial organisms. Xylanases are used in various pharmaceutical, food, livestock, poultry, and paper industries. This study aimed to investigate xylanase-producing yeasts, xylose concentration curve and their enzymatic activity under various factors including carbon and nitrogen sources, temperature, and pH. Enzyme activity was evaluated under different conditions before, during, and after purification. The yeast strains were obtained from the wood product workshop and were subsequently cultivated on YPD (yeast extract peptone dextrose) medium. Additionally, the growth curve of the yeast and its molecular identification were conducted. The optimization and design process of xylan isolated from corn wood involved the use of Taguchi software to test different parameters like carbon and nitrogen sources, temperature, and pH, with the goal of determining the most optimal conditions for enzyme production. In addition, the Taguchi method was utilized to conduct a multifactorial optimization of xylanase enzyme activity. The isolated species were partially purified using ammonium sulfate precipitation and dialysis bag techniques. The results indicated that 3 species (8S, 18S, and 16W) after molecular identification based on 18S rRNA gene sequencing were identified as Candida tropicalis SBN-IAUF-1, Candida tropicalis SBN-IAUF-3, and Pichia kudriavzevii SBN-IAUF-2, respectively. The optimal parameters for wheat carbon source and peptone nitrogen source were found at 50°C and pH 9.0 through single-factor optimization. By using the Taguchi approach, the best combination for highest activity was rice-derived carbon source and peptone nitrogen source at 50°C and pH 6.0. The best conditions for xylanase enzyme production in single-factor optimization of wheat bran were 2135.6 U/mL, peptone 4475.25 U/mL, temperature 50°C 1868 U/mL, and pH 9.0 2002.4 U/mL. Among the tested yeast, Candida tropicalis strain SBN-IAUF-1 to the access number MZ816946.1 in NCBI was found to be the best xylanase product. The highest ratio of enzyme production at the end of the delayed phase and the beginning of the logarithmic phase was concluded by comparing the growth ratio of 8S, 16W, and 18S yeasts with the level of enzymatic activity. This is the first report on the production of xylan polymer with a relative purity of 80% in Iran. The extracellular xylanases purified from the yeast species of C. tropicalis were introduced as a desirable biocatalyst due to their high enzymatic activity for the degradation of xylan polymers.

Comparative analysis of reagent kits for DNA extraction from dry blood stains

Neonatal screening is a mandatory newborn screening procedure that detects the presence of genetic diseases. Dry blood stains are used for mass screening of children. This technology is the most affordable and convenient for the transportation and storage of biological material. DNA extraction is one of the important steps in molecular diagnostics, the accuracy of which is particularly important in genetic analysis. Different DNA extraction kits offer different protocols and reagents, which may vary in efficiency and quality of extraction.The aim of our work was to perform a comparative analysis of reagent kits for DNA extraction from dried blood spots.The materials were dried blood drop samples on Guthrie cards obtained from healthy preterm infants on day 3-4 of life as part of a newborn screening program.The study methods included spectrophotometric analysis to determine the concentration and purity of DNA, the simplicity of protocols, the duration of isolation, and the possibility of automating the process were also evaluated. The efficiency of DNA isolation using different reagent kits was additionally monitored by real-time PCR results using a test system to assess the level of TREC and KREC in peripheral blood, since quantitative analysis requires more attention to the material under study.In assessing the purity of the nucleic acid extracted using four kits analyzed, successful deproteinization of DNA samples and relative purity could be observed. The average DNA purity for the “Extra-DNA-Bio” set was 2.2±0.23, for “EXTRA-prep PS” – 1.89±0.23, for “MagnoPrime UNI” with manual and automatic isolation – 2.31±0.21 and 2.85±0.09, respectively. The average DNA concentration for the Extra-DNA-Bio kit was 15.28 μg/mL, for the EXTRA-Prep PS kit it was 16.26 μg/mL, and for the MagnoPrime UNI for manual and automated isolation it was 62.5 μg/mL and 102.28 μg/mL, respectively. According to the applied Kraskell-Wallis criterion and Dunn’s test, significant differences in both TREC and KREC parameters are present between the group of DNA samples extracted using the “MagnoPrime UNI” reagent kit for manual extraction and the groups of samples extracted by other methods (“MagnoPrime UNI” for automatic extraction) or “Extra-DNA-Bio” and “EXTRA-Prep PS” kits.In the course of the present study, four comparable reagent sets demonstrated a high level of convergence of the obtained data, satisfying all the necessary parameters for further molecular genetic analysis, can be used for neonatal screening and in other areas of research requiring DNA extraction from a dried blood spots.

Separation of La/Ce in rare earth polishing powder waste via Two-Stage hydrochloric acid leaching and corresponding leaching mechanism

Rare earth polishing powder waste (REPPW) usually contains lanthanum (La) and cerium (Ce) with content over 50 %, thus its recovery is important for the cyclic utilization of rare earth. In the traditional acid leaching process, La and Ce are simultaneously leached and required further separation. Based on their leaching behavior difference, a two-stage hydrochloric acid leaching process was proposed in this study to recover and primarily separate La and Ce in REPPW. With the optimal operation conditions, La enriched solution with a relative purity of 91.11 % and Ce enriched solution with a relative purity of 92.85 % were obtained and their recovery ratio were 59.47 and 85.15 %, respectively. After precipitation and calcination, products of La2O3 with purity of 83.67 % and CeO2 with purity of 93.38 % were obtained. Besides, individual leaching kinetics of La and Ce in low-acid leaching were studied using various shrinking core models. Based on the analysis of phase components and micromorphology evolution of REPPW during the leaching process, the leaching mechanism of REPPW was determined. Combined the leaching regularity with the fitting results, the leaching process of La was controlled by interfacial transfer and product layer diffusion, and the Ce was by product layer diffusion. The apparent activation energies of the LaOF and CeO2 leaching reactions were 89.97 kJ/mol and 79.03 kJ/mol, respectively.

Enrichment of sialic acid-containing casein glycomacropeptide in protein hydrolysates using phenylboronic acid-functionalized mesoporous silica nanoparticles

Glycomacropeptide (GMP) is a bioactive peptide of high value, rich in glycosylation sites and with physiological and dietary therapeutic value. The enrichment and detection of GMP facilitates the accurate quantification and the identification of adulteration of GMP in food products. In GMP, sialic acid is an abundant glycosyl group and is mainly located at the end of the sugar chain. Here, we propose a novel GMP enrichment strategy based on the affinity of sialic acid for phenylboronic acid groups that shift with environmental pH. As an enrichment material, mesoporous silica nanoparticles were progressively modified with aminopropyl and phenylboronic acid groups. The developed material showed excellent selectivity for sialic acid in the presence of galactose and fucose as interferents. The adsorption behavior of sialic acid-containing GMP fits the Langmuir adsorption model, offering a recovery of 71.72% (in terms of sialic acid content) and a GMP relative purity of 0.957. Results from sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and size exclusion chromatography confirm that the enriched GMP contains almost no other unexpected proteins and peptides, indicating that the developed strategy holds promise for purifying GMP in various dairy systems.

Impact of non-Markovian evolution on characterizations of quantum thermodynamics

Here, we study the impact of non-Markovian evolution on prominent characteristics of quantum thermodynamics such as ergotropy and power. These are benchmarked by the behavior of the quantum speed limit time. We make use of both geometric-based, particularly the quantum Fisher and Wigner–Yanase information metric, and physical properties-based measures, particularly the relative purity measure and relative entropy of coherence measure, to compute the quantum speed limit time. A simple non-Markovian model of a qubit in a bosonic bath exhibiting non-Markovian amplitude damping evolution is considered, which, from the quantum thermodynamic perspective with finite initial ergotropy, can be envisaged as a quantum battery. To this end, we explore the connections between the physical properties-based measures of the quantum speed limit time and the coherent component of ergotropy. The non-Markovian evolution is shown to impact the recharging process of the quantum battery. Furthermore, a connection between the discharging–charging cycle of the quantum battery and the geometric measures of the quantum speed limit time is observed.

Continuous multi-membrane chromatography of large viral particles

Continuous multi-column chromatography (CMCC) has been successfully implemented to address biopharmaceutical biomolecule instability, to improve process efficiency, and to reduce facility footprint and capital cost. This paper explores the implementation of a continuous multi-membrane chromatography (CMMC) process, using four membrane units, for a large viral particle in just few weeks. CMMC improves the efficiency of the chromatography step by enabling higher loads with smaller membranes for multiple cycles of column use and enables steady-state continuous bioprocessing. The separation performance of CMMC was compared to a conventional batch chromatographic capture step used at full manufacturing scale. The product step yield was 80% using CMMC versus 65% in batch mode while increasing slightly the relative purity. Furthermore, the total amount of membrane area required for the CMMC approach was approximately 10% of the area needed for batch operation, while realizing similar processing times. Since CMMC uses smaller membrane sizes, it can take advantage of the high flow rates achievable for membrane chromatography that are not typically possible at larger membrane scales due to skid flow rate limitations. As such, CMMC offers the potential for more efficient and cost-effective purification trains.

Hydrophobic, Ultrastable Cuδ+ for Robust CO2 Electroreduction to C2 Products at Ampere-Current Levels.

Copper (Cu) is the only known material that can efficiently electrocatalyze CO2 to value-added multicarbon products. Owing to the instability of the Cuδ+ state and microscopic structure in reactions, Cu catalysts are still facing big challenges with low selectivity and poor durability, particularly at high current densities. Herein, we report a rational one-step surface coordination approach for the synthesis of Cu dendrites with an ultrastable Cuδ+ state and hydrophobicity (Cu CF), even after exposure to air for over 6 months. As a result, Cu CF exhibited a C2 FE of 90.6% at a partial current density of 453.3 mA cm-2 in a flow cell. A 400 h stable electrolysis at 800 mA and even a ground-breaking stable operation at a large industrial current of 10 A were achieved in the membrane electrode assembly (MEA) form. We further demonstrated a continuous production of C2H5OH solution with 90% relative purity at 600 mA over 50 h in a solid-electrolyte reactor. Spectroscopy and computation results suggested that Cu(II) carboxylate coordination species formed on the surface of Cu CF, which ensured the stability of the Cuδ+ state and hydrophobicity. As a result, rich active sites and a stable three-phase interface on the catalyst surface were achieved, along with the optimized *CO adsorption strength and adsorption configuration. The mixed *CO adsorption configurations on Cu CF made the *CO dimerization process easier, which promoted the conversion of CO2 to C2 products. This work provides a promising paradigm for the design and development of Cu-based catalysts with ultrahigh stability under industrial current densities.

A closer look at the Azzolino collection.

The state of preservation of documents from the historically significant Azzolino collection at the Swedish National Archives has been investigated and analyses carried out of the iron gall inks. The collection shows varied levels of iron gall ink corrosion. An initial visual condition survey was followed by characterisation of the writing ink with XRF spectrometry on a selection of documents. The aim was to investigate whether ink composition could be related to author or geography, and in turn to level of ink corrosion, which could then serve as a basis for decisions on treatment options. Results indicate a relative purity of the inks in this collection in terms of high iron content and low levels of other elements, entailing that elemental analysis is not a good tool to predict potential deterioration of ink in single documents from this historical context. XRF-mapping showed a possibility for discerning authors by ink composition, contributing meaningful information to questions of attribution and historical context for these documents. A tendency for the ink of Queen Christina to contain more copper than inks from the other authors, and the indication that some inks contain calcium, may be of note for further study.

A combined ultrasound + membrane ultrafiltration (USN-UF) process for enhancing saccharides separation from Spirulina (Arthrospira platensis)

In this study the combination of ultrasound (USN) + membrane ultrafiltration (UF) was used to separate Spirulina saccharides (SPS). The results showed that USN significantly (p < 0.05) increased the average high-added-value compounds yield (mainly protein 572.8 mg/g, saccharides 133.6 mg/g and polyphenols 33.6 mg/g, dw) when the setting of 400 W/10 min was applied. Scanning electron microscope (SEM) results showed that USN treatment effectively destroyed Spirulina microstructure. The extraction efficiency differed according to USN total energy consumption, with higher extraction efficiency observed when a cooling system was not used. Different molecular weight cut-offs (MWCOs) membranes were used to separate SPS. Relative high purity SPS (∼70%) were obtained when 4 and 10 kDa membranes were used, while a higher separation efficiency occurred when using 100 and 150 kDa membranes. USN treatment increased the concentration of relatively low molecular weight SPS (4, 10 kDa) in the permeate (p < 0.05) but there was no significant (p > 0.05) effect on the high molecular weight SPS (300, 500 kDa). Membrane fouling was observed during the saccharides UF process, thus indicating that the process could be further improved.

Catalyst-free synthesis of 5-hydroxymethylfurfural from fructose by extractive reaction in supercritical CO2 – subcritical H2O two-phase system

An extractive reaction configuration using supercritical carbon dioxide (scCO2) as the extracting solvent was tested for the production of 5-hydroxymethyl furfural (HMF) from a 5 wt% fructose aqueous feed. In this configuration, extraction of HMF by scCO2 prevents HMF degradation in the aqueous phase. Because of water co-extraction by scCO2, the volume of the reactional mixture was maintained by continuous injection of water. Reaction was operated in a 90 mL high pressure reactor, where an HMF maximum yield of 62.4 % was achieved at 160 °C and 25 MPa, with a CO2 flow rate of 20 g.min−1 for 420 min. This is the first time that HMF is reportedly produced with such a yield by a catalyst-and organic solvent-free process. Besides, the separation efficiency reached 97.3 % and the relative purity of HMF in the extract was 95.8 wt%. Therefore, this configuration avoids post reactional purification which is needed in conventional batch processes or in extractive reaction processes using organic solvents. Based on kinetic and thermodynamic studies, modeling of the extractive reaction process was developed to perform a sensitivity analysis for CO2 flow rate and extraction efficiency, upon the HMF yield. As an example, it was shown that for 800 min reaction duration, a CO2 flow rate of 100 g.min−1 or an extraction efficiency increase by a 10-fold factor could theoretically led to HMF yields of 73.0 % and 73.7 %, respectively.

Anti-Bacterial Activity of Novel Synthesized Chalcone Against S. epidermidis and S. aureus Isolated from Packed Red Cell Blood Product

Bacterial contamination in blood product was still a problem in Indonesia. Various studies to improve the safety of blood product by inhibiting the bacterial growth in blood product was developed. Chalcone, is one of the natural compounds that has ability to inhibit the bacterial growth, so it can be possible to use that compound for anti-bacterial use in the future. This study aim is to evaluate the anti-bacterial activity of novel synthesis chalcone (E)-1-(4-hydroxyphenyl)-3-phenylprop-2-en-1-one against S. epidermidis and S. aureus isolated from packed red cell blood product. A novel chalcone was synthesized by Claisen-Schmidt Methods while anti-bacterial activity test was done by Agar Diffusion Methods. Chalcone that has been synthesized then characterized by Fourier Transform Infra-Red (FTIR) Methods and Gas Chromatography – Mass Spectrometry (GC-MS). Chalcone was synthesized through a condensation reaction between an aldehyde (benzaldehyde) and ketone (acetophenone) with NaOH as alkaline catalyst. The results from sedimentary analysis using FTIR showed an absorption of the C=C group in the typical medium of chalcone compounds, at the wave number of 1516.96 cm-1. The results of GC-MS characterization resulted a GC chromatogram with one peak with time of retention (tR) 19.68 minutes and relative purity 100%. MS mass spectrum shows that the molecular ion (M+) of this compound was detected at 224 which equivalents to the molecular weight of the chalcone compound. Anti-bacterial test showed that the synthetic chalcone compound with 5% concentration had an inhibitory ability of 56.02% on S. epidermidis and 54.10% on S. aureus, while 2.5% chalcone concentration had an inhibitory ability of 29.17% on S. epidermidis and 50.45% on S. aureus, and 1.25% chalcone concentration had inhibitory ability 0% on S. epidermidis and 37.27% on S. aureus.

Direct Production of Ni–Co–Mn Mixtures for Cathode Precursors from Cobalt-Rich Lithium-Ion Battery Leachates by Solvent Extraction

A novel solvent extraction scheme was developed for the processing of Co-rich lithium-ion battery (LIB) leachate to a Ni–Co–Mn (NCM) sulfate mixture that can be directly used in the precursor synthesis of LIB cathodes. Conventional hydrometallurgical recycling of spent LIBs usually aims at separation of Li, Ni, Co, and Mn into pure fractions, which is simplified here. Operating pH and the number of extraction stages for each separation were evaluated from batch equilibrium experiments. Two continuous countercurrent extractions with bis(2-ethylhexyl) hydrogen phosphate (D2EHPA) and one with Cyanex 272 were studied in bench-scale mixer-settler equipment, and a Ni–Co–Mn solution with n(Ni):n(Co) = 14.16 and n(Ni):n(Mn) = 8.06 was obtained. The Ni:Co:Mn molar ratio in the NCM mixture can be adjusted to, for example, 8:1:1 using a Co-rich raffinate from the same process, and no additional transition metal salts are required for tuning the composition. Stripping raffinate containing 102.7 g L−1 Co at 99.8% relative purity was obtained from Cyanex 272 extraction. The main benefit of the process concept is that the solvent extraction separations can be operated with less stringent requirements than when producing pure metal salts.

Plasmonically enhanced two-photon absorption induced photoacoustic microscopy with laser-synthesized TiN nanoparticles

Combining photonic excitation and acoustic detection, photoacoustic imaging (PAI) presents one of the most promising noninvasive biomedical diagnostic modalities, but this technique still lacks efficient nano-sized contrast agents absorbing light in the region of relative tissue transparency (630–900 nm). Here, we explore the use of titanium nitride (TiN) nanoparticles (NPs) fabricated by methods of pulsed laser ablation in liquids as a contrast agent in PAI. When prepared in acetone, the NPs are spherical, have an average size of 25 nm, and exhibit a broad plasmonic absorption peak around 700 nm. We show that solutions of these NPs render possible a strong nonlinear photoacoustic response and the generation of photoacoustic images with 67 μm resolution within the biological transparency window. The observed effect is explained by a plasmonically enhanced two-photon absorption process in TiN NPs. Combined with earlier demonstrated capability of generating photothermal therapeutic effect, relative chemical purity, and excellent biocompatibility, laser-synthesized TiN NPs promise attractive applications in biomedical theranostics involving imaging modalities based on photoacoustics microscopy or tomography.