Low Purity Research Articles

CO2 capture utilizing Li4SiO4 from spent lithium-ion batteries and iron tailings offers eco-friendly benefits

Carbon capture and storage stand as a pivotal technology in the battle against global climate change. The development of economically viable CO2 capture materials, coupled with the recycling of solid wastes, poses a significant challenge in the pursuit of carbon neutrality. Herein, we propose a process to synthesize a promising high-temperature sorbent, Li4SiO4, using spent lithium-ion batteries and iron tailings. Li4SiO4 synthesized under optimal process conditions demonstrates exceptional CO2 capacity and cycle stability (0.25 g/g, 100 cycles), with a preparation cost merely amounting to 1/7 of traditional methods, rendering it industrially feasible. Moreover, elucidating the intricate relationship between impurity elements in the feedstock and the CO2 capture capacity of the adsorbent holds considerable significance in guiding material synthesis strategies. A systematic evaluation of solid waste purity and impurity elements on CO2 capture capacity, through a combination of experiments and theoretical calculations, reveals that lower purity solid waste containing favorable impurities (96.78 % Li2CO3 and 90.35 % SiO2) enhances the CO2 capture efficiency of the synthesized Li4SiO4. This innovative work establishes a direct link between trace impurities and macroscopic properties, providing a viable decarbonization pathway and fostering high-value secondary utilization of solid waste under short and economical processes.

NEural Engine for Discovering Luminous Events (NEEDLE): identifying rare transient candidates in real time from host galaxy images

ABSTRACT Known for their efficiency in analysing large data sets, machine learning-based classifiers have been widely used in wide-field sky survey pipelines. The upcoming Vera C. Rubin Observatory Legacy Survey of Space and Time (LSST) will generate millions of real-time alerts every night, enabling the discovery of large samples of rare events. Identifying such objects soon after explosion will be essential to study their evolution. Using ∼5400 transients from the Zwicky Transient Facility (ZTF) Bright Transient Survey as training and test data, we develop NEEDLE (NEural Engine for Discovering Luminous Events), a novel hybrid (convolutional neural network + dense neural network) classifier to select for two rare classes with strong environmental preferences: superluminous supernovae (SLSNe) preferring dwarf galaxies, and tidal disruption events (TDEs) occurring in the centres of nucleated galaxies. The input data includes (i) cutouts of the detection and reference images, (ii) photometric information contained directly in the alert packets, and (iii) host galaxy magnitudes from Pan-STARRS (Panoramic Survey Telescope and Rapid Response System). Despite having only a few tens of examples of the rare classes, our average (best) completeness on an unseen test set reaches 73 per cent (86 per cent) for SLSNe and 80 per cent (87 per cent) for TDEs. While very encouraging for completeness, this may still result in relatively low purity for the rare transients, given the large class imbalance in real surveys. However, the goal of NEEDLE is to find good candidates for spectroscopic classification, rather than to select pure photometric samples. Our system will be deployed as an annotator on the UK alert broker, Lasair, to provide predictions of real-time alerts from ZTF and LSST to the community.

A Whole-Process Visible Strategy for the Preparation of Rhizomucor miehei Lipase with Escherichia coli Secretion Expression System and the Immobilization.

Rhizomucor miehei (RM) lipase is a regioselective lipase widely used in food, pharmaceutical and biofuel industries. However, the high cost and low purity of the commercial RM lipase limit its industrial applications. Therefore, it is necessary to develop cost-effective strategies for large-scale preparation of this lipase. The present study explored the high-level expression of RM lipase using superfolder green fluorescent protein (sfGFP)-mediated Escherichia coli secretion system. The sfGFP(-15) mutant was fused to the C-terminus of RM lipase to mediate its secretion expression. The yield of the fusion protein reached approximately 5.1g/L with high-density fermentation in 5-L fermentors. Unlike conventional secretion expression methods, only a small portion of the target protein was secreted into the cell culture while majority of the fusion protein was still remained in the cytoplasm. However, in contrast to intracellular expression, the target protein in the cytoplasm could be transported efficiently to the supernatant through a simple washing step with equal volume of phosphate saline (PBS), without causing cell disruption. Hence, the approach facilitated the downstream purification step of the recombinant RM lipase. Moreover, contamination or decline of the engineered strain and degradation or deactivation of the target enzyme can be detected efficiently because they exhibited bright green fluorescence. Next, the target protein was immobilized with anion-exchange and macropore resins. Diethylaminoethyl sepharose(DEAE), a weak-basic anion-exchange resin, exhibited the highest bind capacity but inhibited the activity of RM lipase dramatically. On the contrary, RM lipase fixed with macropore resin D101 demonstrated the highest specific activity. Although immobilization with D101 didn't improve the activity of the enzyme, the thermostability of the immobilized enzyme elevated significantly. The immobilized RM lipase retained approximately 90% of its activity after 3-h incubation at 80°C. Therefore, D101 was chosen as the supporting material of the target protein. The present study established a highly efficient strategy for large-scale preparation of RM lipase. This innovative technique not only provides high-purity RM lipase at a low cost but also has great potential as a platform for the preparation of lipases in the future.

Wastewater treatment, hydrogen and energy recovery using electrochemical advanced oxidation

Electrochemical advanced oxidation processes (EAOPs) offer several advantages over conventional Advanced Oxidation Processes (AOPs) such as UV/H2O2 and H2O2/O3. This includes the absence of chemical additives and ease of control. However, high energy consumption hampers the industrial application of EAOPs. Currently, the hydrogen generated at the cathode is vented and wasted, because of its low gas purity and difficulty in collecting it. But it also underscores an opportunity where the reactor design can be improved to facilitate the collection of high-purity hydrogen for energy savings. In our study, The EAOPs reactor was designed with a proton exchange membrane (PEM) for hydrogen generation. The hydrogen at the cathode chamber is then supplied to a fuel cell to generate electricity. The energy efficiency of the EAOPs-fuel cell system is evaluated through the wastewater treatment performance and energy saving that fuel cells achieve. To optimize the EAOPs-fuel cell system, various operational conditions, including different anode types, salt concentrations, and target organic compounds, were examined to optimize the system. Our experimental results indicate that the EAOPs-fuel cell system exhibits energy-efficient performance across various operational conditions. Notably, the highest energy efficiency and recovery ratio were achieved when operating at 3 V with boron-doped diamond (BDD) as the anode. Furthermore, we investigated the impact of mass transfer on the system's energy efficiency, considering both the initial organic concentration and flow velocity. This study provided valuable insights into combining the effect of EAOPs and hydrogen fuel cells, contributing to the understanding and optimizing the oxidation performance. It also contributes to developing sustainable and cost-effective advanced oxidation technologies with wide-ranging water treatment applications.

Dual targeting negative enrichment strategy for highly sensitive and purity detection of CTCs.

Circulating tumor cells (CTCs) have significant clinical value in early tumor detection, dynamic monitoring and immunotherapy. CTC detection stands out as a leading non-invasive approach for tumor diagnostics and therapeutics. However, the high heterogeneity of CTCs and the occurrence of epithelial-mesenchymal transition (EMT) during metastasis pose challenges to methods relying on EpCAM-positive enrichment. To address these limitations, a method based on negative enrichment of CTCs using specific leukocyte targets has been developed. In this study, aiming to overcome the low purity associated with immunomagnetic beads targeting solely the leukocyte common antigen CD45, we introduced CD66b-modified immunomagnetic beads. CD66b, a specific target for neutrophils with abundant residues, was chosen as a complementary approach. The process involved initial collection of nucleated cells from whole blood samples using density gradient centrifugation. Subsequently, magnetically labeled leukocytes were removed by magnetic field, enabling the capture of CTCs with higher sensitivity and purity while retaining their activity. Finally, we selected 20 clinical blood samples from patients with various cancers to validate the effectiveness of this strategy, providing a new generalized tool for the clinical detection of CTCs.

A simple method for the preparation of cordierite ceramics with high strength and low thermal expansion coefficient

AbstractCordierite ceramics have great application prospects due to their very low coefficient of thermal expansion. However, the low purity of ceramics leads to their unsatisfactory fracture strength, which has always been a research focus. Herein, by applying external pressure to the green body of mixed raw materials and optimizing the synthesis temperature, high‐purity cordierite powder was prepared, and then it was used as the starting material for the fabrication of high‐strength cordierite ceramics. The optimal sample exhibited a flexural strength of 146 MPa, which is about 1.4 times that of the cordierite ceramics reported in the literature. This is attributed to applied external pressure increasing the contact area of raw materials, leading to a more thorough reaction, and the content of the α‐cordierite phase is 98.4 wt% in the sample synthesized at 1275°C. Concurrently, the samples possessed a thermal expansion coefficient of only 1.9 × 10−6°C−1 (room temperature to 800°C). In addition, the increase in columnar crystal volume fraction is also one of the reasons for the high strength and low thermal expansion coefficient of cordierite ceramics.

Comparing skin swabs, buccal swabs, and toe clips for amphibian genetic sampling, a case study with a small anuran (Acris blanchardi).

Multiple methods for collecting genetic samples from amphibians exist, each with their own implications for study design, animal welfare, and costs. Toe clipping is one common method, but there is ongoing debate regarding its potential detriment. Less invasive methods should be implemented, if efficacious, as amphibians are a particularly vulnerable vertebrate group. Skin and buccal swabbing are less invasive methods for genetic sampling, but the potential for contamination and a lower yield of DNA may exist. To compare these methods, we gathered skin swabs, buccal swabs, and toe clips from the same individuals of a relatively small anuran species, Blanchard's Cricket Frog (Acris blanchardi). We then compared DNA yield, DNA purity, amplification success rate, and genotypic data quality among sample types. We found toe clips and buccal swabs generated similar DNA yield and purity, with skin swabs yielding significantly less DNA of significantly lower purity than the other sample types. Amplification success rate was significantly higher using toe clips compared to the other sample types, though buccal swab samples amplified more readily than skin swabs. Genotypic data from toe clips and buccal swabs did not differ significantly in quality, but skin swab data quality was significantly lowest among sample types. Thus, skin swabbing could produce erroneous data in some situations, but buccal swabbing is likely an effective substitute to toe clipping, even for small species. Our results can help future researchers select which genetic sampling method might best suit their research needs.

Preparation of (S)-epichlorohydrin using a novel halohydrin dehalogenase by selective conformation adjustment.

Chiral epichlorohydrin (ECH) is an attractive intermediate for chiral pharmaceuticals and chemicals preparation. The asymmetric synthesis of chiral ECH using 1,3-dicholoro-2-propanol (1,3-DCP) catalyzed by a haloalcohol dehalogenase (HHDH) was considered as a feasible approach. However, the reverse ring opening reaction caused low optical purity of chiral ECH, thus severely restricts the industrial application of HHDHs. In the present study, a novel selective conformation adjustment strategy was developed with an engineered HheCPS to regulate the kinetic parameters of the forward and reverse reactions, based on site saturation mutation and molecular simulation analysis. The HheCPS mutant E85P was constructed with a markable change in the conformation of (S)-ECH in the substrate pocket and a slight impact on the interaction between 1,3-DCP and the enzyme, which resulted in the kinetic deceleration of the reverse reactions. Compared with HheCPS, the catalytic efficiency (kcat(S)-ECH/Km(S)-ECH) of the reversed reaction dropped to 0.23-fold (from 0.13 to 0.03mM-1s-1), while the catalytic efficiency (kcat(1,3-DCP)/Km(1,3-DCP)) of the forward reaction only reduced from 0.83 to 0.71mM-1s-1. With 40mM 1,3-DCP as substrate, HheCPS E85P catalyzed the synthesis of (S)-ECH with the yield up to 55.35% and the e.e. increased from 92.54 to >99%. Our work provided an effective approach for understanding the stereoselective catalytic mechanism as well as the green manufacturing of chiral epoxides.

Development of an electroanalytical methodology for the identification and quantification of cocaine in samples seized using a carbon paste electrode modified with multi-walled carbon nanotubes

Among the drugs of abuse, cocaine (COC) is the second most commonly used worldwide due to its stimulating and psychoactive effects. Currently, this drug is classified, according to the World Drug Report (WDR), as an illicit substance and is frequently seized by law enforcement agencies. Additionally, it can cause social problems due to its abusive use. This study describes the development of an electroanalytical methodology using square wave voltammetry (SWV) associated with a single electrode of carbon paste modified with 10 % MWCNTs (multi-walled carbon nanotubes) to quantify COC in seized samples containing up to 20% cocaine (low purity index) in the state of Espírito Santo (Brazil). SWV parameters, including Es = 10 mV, a = 30 mV, and f = 15 Hz, were optimized utilizing a Britton-Robinson buffer solution of 0.1 mol/L (pH 10) as a supporting electrolyte through the implementation of experimental design (CCD). COC showed an oxidation peak at approximately 1.0 V, with low limits of quantification and detection (1.90 × 10−6 mol L−1 and 5.75 × 10−7 mol L−1, respectively), in the linear range from 2.36 × 10−6 mol L−1 to 1.38 × 10−5 mol L−1, with the proposed methodology. Thus, this research develops a fast and low-cost technique in favor of the police, allowing the R2 = 99%. The results obtained in the intraday calibration curves present a relatively low standard deviation (RSD < 8%), indicating a good repetition of the value production of an electrode for less than USD 1.42 per analysis.

Membrane pre-concentration as an efficient strategy to enhance the enrichment of rare earth by MgO precipitation

Taking advantage of the environmentally-friendly properties of a magnesium salt leaching agent, magnesium oxide (MgO) was used as a precipitant to enrich rare earth (RE) from leaching liquor in the magnesium salt system. This approach not only tackles the issue of ammonia–nitrogen pollution but also enables efficient magnesium recycling. However, due to the high concentration of magnesium ions and the low concentration of RE ions in the leaching solution, the precipitation kinetics of RE concentrates are sluggish, leading to low RE purity in the resulting precipitated product. In this work, we proposed a novel strategy that combines complexation-ultrafiltration (UF) pre-concentration with subsequent MgO precipitation to enhance the hydrolysis of MgO, promoting the precipitation of RE. We further improved the RE enrichment efficiency by optimizing membrane type, complexing agent selection, concentration levels, precipitation temperature, and MgO dosage. Under the conditions of concentrating the leaching solution using optimal UF membrane and employing glyphosate as the complexing agent, the RE ions concentration increased from 101 to 3940 mg/L, and we successfully separated magnesium ions with a separation factor of 36.4. A comparison between direct MgO precipitation and the pre-concentration approach revealed an 80 % reduction in precipitation time and an 80 % decrease in MgO usage with pre-concentration. Furthermore, this combined process led to an 8 % increase in RE recovery and a 2.8-fold enhancement in RE purity, and similar results were obtained when using actual mine leaching solutions. Additionally, the glyphosate present in the UF permeate and the precipitated mother liquor can be efficiently reclaimed through resin adsorption. This proposed process holds significant potential for engineering applications aimed at enriching RE.

Recent Advances in Microfluidic-Based Extracellular Vesicle Analysis.

Extracellular vesicles (EVs) serve as vital messengers, facilitating communication between cells, and exhibit tremendous potential in the diagnosis and treatment of diseases. However, conventional EV isolation methods are labor-intensive, and they harvest EVs with low purity and compromised recovery. In addition, the drawbacks, such as the limited sensitivity and specificity of traditional EV analysis methods, hinder the application of EVs in clinical use. Therefore, it is urgent to develop effective and standardized methods for isolating and detecting EVs. Microfluidics technology is a powerful and rapidly developing technology that has been introduced as a potential solution for the above bottlenecks. It holds the advantages of high integration, short analysis time, and low consumption of samples and reagents. In this review, we summarize the traditional techniques alongside microfluidic-based methodologies for the isolation and detection of EVs. We emphasize the distinct advantages of microfluidic technology in enhancing the capture efficiency and precise targeting of extracellular vesicles (EVs). We also explore its analytical role in targeted detection. Furthermore, this review highlights the transformative impact of microfluidic technology on EV analysis, with the potential to achieve automated and high-throughput EV detection in clinical samples.

Abstract GS03-06: Genomic and transcriptomic profiling of primary tumors from patients with HR+, HER2-, node-positive, high-risk early breast cancer in the monarchE trial

Abstract Background Two years of adjuvant abemaciclib combined with endocrine therapy (ET) resulted in significant and clinically meaningful improvement in invasive disease-free survival (IDFS) and distant relapse-free survival (DRFS) in patients (pts) with HR+, HER2-, node-positive, high-risk early breast cancer in the monarchE trial (NCT03155997). Abemaciclib benefit was sustained beyond the completion of treatment (tx) with deepening magnitude of absolute benefit in IDFS and DRFS at 5 years. Here, we evaluate comprehensive molecular profiling of archived primary tumor tissue and association with clinical outcomes. Methods For biomarker analysis, a proportionally stratified random sampling case-cohort design was utilized to include all patients who experienced an IDFS event at a pre-specified interim analysis with a median follow up of 54 months. A cohort of 895 pts (189 with IDFS event) in the abemaciclib + ET arm was matched 1:1 with 903 pts (270 with IDFS event) in the ET arm. Baseline primary tumor samples underwent exome-capture RNA sequencing (RNAseq; n=1324, 23% intent-to-treat (ITT) population) and paired tumor-normal (germline blood samples) whole-exome sequencing (WES; n=1234, 22% ITT population). Expression-based intrinsic subtypes (i.e., luminal A (LumA), luminal B (LumB), HER2-enriched (HER2E), basal- and normal-like) were characterized using the Absolute Intrinsic Molecular Subtyping model. The 21-gene expression signature score (Oncotype DX test) was inferred from RNAseq; samples were categorized into lower (0-25) and high (26-100) risk groups. To investigate associations of biomarkers with abemaciclib benefit, WES genomic events including oncogenic and hotspot mutations by OncoKB, and copy number events, of incidence &amp;gt;9% were pre-selected. Results The biomarker subset of monarchE was reflective of the ITT population. A total of 1190 tumors (abemaciclib+ET n= 605; ET alone n=585) yielded adequate RNAseq results. Intrinsic subtype distribution was consistent across tx arms (Table A). Low tumor purity limited assessment of the normal-like subtype. The 4-year IDFS benefit of abemaciclib was consistent across all subtypes. LumA cancers had the lowest risk of recurrence while HER2E and basal-like subtypes had the highest. Inferred 21-gene expression signature score showed similar benefits from abemaciclib in both lower and high-risk groups (Table B). A total of 1173 tumors yielded adequate WES results (abemaciclib+ET n=580; ET alone n=593). Consistent abemaciclib benefit was observed across the most frequently altered genes (Table C). In exploratory analysis, lower benefit from abemaciclib was seen in the subset of focal-high level MYC amplified tumors (n=176, HR 1.30, 95% CI, 0.77, 2.20) compared to MYC non-amplified tumors (n=997, HR 0.62, 95% CI, 0.47, 0.80, nominal interaction p=0.014). The treatment benefit of abemaciclib was observed across all subpopulations of altered genes based on gene expression data. Conclusions Adjuvant abemaciclib+ET maintained IDFS benefit compared to ET alone across all molecular subtypes as measured by RNAseq. Benefit was consistent across most altered genes assessed by WES, except for the subset of tumors with MYC amplification. Additional research is necessary to confirm these findings. Table. Citation Format: Nicholas Turner, Jorge Reis-Filho, Matthew Goetz, Christine Desmedt, Sarat Chandarlapaty, Hironobu Sasano, Carlos Arteaga, Sherene Loi, Stephanie Graff, Deli Liu, Vanessa Rodrik-Outmezguine, Anthony Sireci, Cynthia Sandoval Rubenstein, Helen Won, Lacey M. Litchfield, Maria Munoz, Stephen Johnston. Genomic and transcriptomic profiling of primary tumors from patients with HR+, HER2-, node-positive, high-risk early breast cancer in the monarchE trial [abstract]. In: Proceedings of the 2023 San Antonio Breast Cancer Symposium; 2023 Dec 5-9; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2024;84(9 Suppl):Abstract nr GS03-06.

Unlocking functional lipid ingredients from algae by food-grade biosolvents and ultrasound-assisted extraction for nutritional applications

Algae are a sustainable source of healthy and functional lipids. The production of extracts suitable for food and nutraceutical industries requires food-grade solvents, which may have low lipid extraction yield and/or purity. This work aimed to assess the efficiency of biosolvents ethanol (E) and ethyl acetate (EA) in obtaining food-grade lipid ingredients from an algae blend, Fucus vesiculosus, Ulva sp., and Chlorella vulgaris, in comparison with the Folch method. Ultrasound (UAE) was assayed to enhance the biosolvent extraction. The results showed that the different extraction approaches can significantly influence the extraction yield, lipid purity, and lipid composition, including fatty acid (FA) content. EA and EA + UAE produced high lipid purity (>74%) extracts with high polyunsaturated FA (≤77.5%) and n-3 FA (≤74.4%) contents, despite the lower extraction yield. E + UAE may be used to obtain lipid-rich ingredients from algae blend (57%) and C. vulgaris (91%). All extracts showed anti-inflammatory and antioxidant properties. This study provides relevant information for the production of food-grade lipid ingredients from algae.

Exploring Functionality Gain for (Recombinant) β-Lactoglobulin Through Production and Processing Interventions

AbstractInterventions in the upstream production and further processing of recombinant food proteins affect its properties when used for food application. Often the efficiency of particular interventions is evaluated based on molecular purity and yield rather than final functional properties. Yet, the formulation of foods, including the amount of protein required, can be affected when the functional properties have changed. In this explorative study, we exemplify how far we can extend the functionality range of the major whey protein β-lactoglobulin (BLG), in terms of foaming and (heat-set) gelling, through various interventions. Slight changes in the amino acid sequence of BLG affected its functional properties significantly. Foams were up to ten times more stable, when selecting different natural isoforms of BLG (isoform A instead of B) or when inducing targeted cysteine mutations. The isoform B yielded stronger thermally induced gels (+ 40%) compared to isoform A. During downstream processing of recombinantly secreted BLG, limited purification of up to ~ 67 wt% enabled reasonable foaming properties and superior gelation, while a lower purity of ~ 22 wt% resulted in poor performance in both cases. Post-processing allowed conversion of native whey protein into soluble amyloid-like aggregates. These aggregates resulted in better foam stability (i.e., approximately four times longer than non-aggregated protein), but did not improve gelation. The presented study demonstrates that one should consider not only protein yield and purity, but also functional properties when developing recombinant proteins for food application. In turn, these functional properties are a result of the complete upstream and downstream chain.

Design and operation results of KSTAR ECH system

The electron cyclotron heating (ECH) system at the Korea Superconducting Tokamak Advanced Research (KSTAR) is a crucial heating devices, which is employed in various research endeavors, including plasma startup, wall cleaning, neoclassical tearing mode control, long pulse operation, and hybrid scenarios development from the first plasma operation. For facilitating advanced scenarios development and magnetohydrodynamics research in KSTAR, it was deemed necessary to install a total of 6 MW ECH systems, consisting of four 105/140 GHz and two 170 GHz systems. To address this, a new ECH room was developed and the existing ECH system was totally rearranged. This study describes the design of the novel KSTAR ECH system and its operation results, and discusses the problems that occur during the ECH system operation. Each ECH system to deliver 1 MW for 300 s was designed to enable stable, safe, and efficient operation in the new ECH room and four 105/140 GHz dual frequency ECH were injected to KSTAR successfully. The polarization angle was experimentally confirmed by using an electron cyclotron wall conditioning, and the beam angle change by ECH antenna was verified by a newly developed IR measurement. However, mixed patterns with higher-order modes were observed in the output beam from matching optics unit of some gyrotrons, which affect the operation efficiency and the output power. In future works, we will analyze the causes for low mode purity and improve the operation efficiency.

Electrochemical oxidation of concentrated benzyl alcohol to high-purity benzaldehyde via superwetting organic-solid-water interfaces.

Organic electrosynthesis in aqueous media is presently hampered by the poor solubility of many organic reactants and thus low purity of liquid products in electrolytes. Using the electrooxidation of benzyl alcohol (BA) as a model reaction, we present a "sandwich-type" organic-solid-water (OSW) system, consisting of BA organic phase, KOH aqueous electrolyte, and porous anodes with Janus-like superwettability. The system allows independent diffusion of BA molecules from the organic phase to electrocatalytic active sites, enabling efficient electrooxidation of high-concentration BA to benzaldehyde (97% Faradaic efficiency at ~180 mA cm-2) with substantially reduced ohmic loss compared to conventional solid-liquid systems. The confined organic-water boundary within the electrode channels suppresses the interdiffusion of molecules and ions into the counterphase, thus preventing the hydration and overoxidation of benzaldehyde during long-term electrocatalysis. As a result, the direct production of high-purity benzaldehyde (91.7%) is achieved in a flow cell, showcasing the effectiveness of electrocatalysis over OSW interfaces for the one-step synthesis of high-purity organic compounds.

Facile synthesis of highly stable and efficient MAPbI3 perovskite quantum dots: Spectroscopic characterization and defect analysis

The hybrid methylammonium-based perovskite quantum dots (PQDs) have attracted tremendous attraction for display devices due to their low cost, high luminescence, and color purity. The large-scale production of PQDs is constrained due to the use of toxic and hazardous solvents such as dimethylformamide (DMF) in the synthesis process. Here, a novel approach to prepare PQDs using an environment-friendly solvent, gamma-valerolactone (GVL), is proposed. The synthesized PQDs were found to be uniform with less defect states as compared to the conventionally used DMF solvents, confirmed by different characterizing techniques. The stability of GVL-based PQDs was also found to be improved and proved the efficiency of the present method. Photoluminescence quantum yield (PLQY) of 98 % and single tetragonal CH3NH3PbI3 phase of GVL-derived sample retained over 15 days while the decomposition and degradation were observed in the DMF-derived sample within a short duration. A protocol for the preparation of CH3NH3PbI3 PQDs with less intrinsic defects and uniform optoelectronic properties is presented and paves the way for further modifications and applications.

Isolation of Extracellular Outer Membrane Vesicles (OMVs) from Escherichia coli Using EVscore47 Beads.

Outer membrane vesicles (OMVs) are attractive for biomedical applications based on their intrinsic properties in relation to bacteria and vesicles. However, their widespread use is hampered by low yields and purities. In this study, EVscore47 multifunctional chromatography microspheres were synthesized and used to efficiently isolate functional OMVs from Escherichia coli. Through this technology, OMV loss can be kept to a minimum, and OMVs can be harvested using EVscore47 at 11-fold higher yields and ~13-fold higher purity than those achieved by means of ultracentrifugation. Based on the results presented here, we propose a novel EVscore47-based isolation of OMVs that is fast and scalable.

Selective Recovery of Battery-Grade Li2CO3 from Spent NCM Cathode Materials Using a One-Step Method of CO2 Carbonation Recovery Without Acids or Bases.

The recovery of spent lithium-ion batteries by traditional acid leaching is limited by serious pollution, complicated technology, and the low purity of Li2CO3. To address the problems of the traditional acid leaching process and increasing demand for decarbonization, a technique for the selective carbonation leaching of Li and the recovery of battery-grade Li2CO3 by a simple concentration precipitation process without acids or bases was developed. The coupling of CO2 and reducing agents could effectively promote the precipitation of MCO3 (M=Ni/Co/Mn) and the selective leaching of Li by decreasing the reducing capability needed for transition metals and decreasing the pH of the solution. The optimal selective leaching process of Li was obtained under 1 MPa CO2 with 20 g/L Na2S2O3 at an L/S ratio of 30 mL/g for 1.5 h. FT-IR, XRD, ICP-MS and other methods were used to reveal the multiphase interfacial reaction mechanism of the carbonation reduction of layered cathode materials, which indicated that the reducing agent Na2S2O3 could promote lattice distortion of the cathode materials and effective separation of Li. In summary, a green and economical method for the selective recovery of battery-grade Li2CO3 using a one-step method of CO2 carbonation recovery in a near-neutral environment was proposed.

High purity and recovery of native filamentous hemagglutinin (FHA) from Bordetella pertussis using affinity chromatography

Filamentous hemagglutinin (FHA) is a critical adhesion molecule produced by Bordetella pertussis (BP), the causative agent of highly contagious respiratory infection known as whooping cough. FHA plays a pivotal role in the pathogenesis of whooping cough and is a key component of acellular pertussis vaccines (aPV). However, conventional purification methods for FHA often involve labor-intensive processes and result in low purity and recovery rates. Therefore, this study explores the use of monoclonal and polyclonal antibodies as specific tools to achieve highly pure and efficient FHA purification. To generate FHA-specific antibodies, polyclonal antibodies were produced by immunizing sheep and monoclonal antibodies (MAbs) were generated by immunizing mice with recombinant and native FHA. The MAbs were selected based on affinity, isotypes, and specificity, which were assessed through ELISA and Western blot assays. Two immunoaffinity columns, one monoclonal and one polyclonal, were prepared for FHA antigen purification. The purity and recovery rates of these purifications were determined using ELISA, SDS-PAGE, and immunoblotting. Furthermore, the MAbs were employed to develop an ELISA assay for FHA antigen concentration determination. The study's findings revealed that immunoaffinity column-based purification of FHA resulted in a highly pure antigen with recovery rates of approximately 57% ± 6.5% and 59% ± 7.9% for monoclonal and polyclonal columns, respectively. Additionally, the developed ELISA exhibited appropriate reactivity for determining FHA antigen concentration. This research demonstrates that affinity chromatography is a viable and advantageous method for purifying FHA, offering superior purity and recovery rates compared to traditional techniques. This approach provides a practical alternative for FHA purification in the context of aPV development.