Chloride Compounds Research Articles

Use of Guanidine-Containing Organomineral Complexes for Protection of Soft Polyvinyl Chloride Compounds from Photo- and Biodegradation

Use of Guanidine-Containing Organomineral Complexes for Protection of Soft Polyvinyl Chloride Compounds from Photo- and Biodegradation

Adaptations to cationic biocide exposure differentially influence virulence factors and pathogenicity in Pseudomonas aeruginosa

ABSTRACT Cationic biocides (CBs), which include quaternary ammonium compounds (QACs), are employed to mitigate the spread of infectious bacteria, but resistance to such surface disinfectants is rising. CB exposure can have profound phenotypic implications that extend beyond allowing microorganisms to persist on surfaces. Pseudomonas aeruginosa is a deadly bacterial pathogen that is intrinsically tolerant to a wide variety of antimicrobials and is commonly spread in healthcare settings. In this study, we pursued resistance selection assays to the QAC benzalkonium chloride and quaternary phosphonium compound P6P–10,10 to assess the phenotypic effects of CB exposure in P. aeruginosa PAO1 and four genetically diverse, drug-resistant clinical isolates. In particular, we sought to examine how CB exposure affects defensive strategies and the virulence-associated “offensive” strategies in P. aeruginosa. We demonstrated that development of resistance to BAC is associated with increased production of virulence-associated pigments and alginate as well as pellicle formation. In an in vivo infection model, CB-resistant PAO1 exhibited a decreased level of virulence compared to wild type, potentially due to an observed fitness cost in these strains. Taken together, these results illustrate the significant consequence CB resistance exerts on the virulence-associated phenotypes of P. aeruginosa.

New Prospective Insecticidal Agents Based on N-(arylcarbamothioyl)arylmide Derivatives Against Spodoptera frugiperda: Design, Synthesis, Toxicological, Biological, Biomedical Studies and Antibacterial Activity.

In this work, a novel series of N-(arylcarbamothioyl)arylmide) 2-11 were synthesized by treating One-Pot three-multicomponent of Aroyl chloride, ammonium isothiocyanate and amine compounds under refluxing conditions. Using spectroscopic methods, the chemical structure of the novelty developed compounds were investigated. After five days, the proposed derivatives' insecticidal bioassay was assessed using the median lethal concentration (LC50) against the second & fourth larvae of Spodoptera frugiperda as toxicity agents. The findings showed that, to varying degrees, every tested substance exerted insecticidal effects on S. frugiperda larvae in both of their instars. Compound 9 was the most poisonous of them all, having an LC50 against larvae in their second and fourth instars of 60.45 and 123.21 mg/L, respectively. Additionally, a few biological and biochemical characteristics of the substances that were generated in a lab setting were also looked at. Furthermore, this work discusses how to discover novel compounds that may one day be employed as insecticidal agents. Finally, all the designed components were monitored for their antibacterial effectiveness toward both Gram-positive & Gram-negative bacteria.

Unveiling the intricacies of steel corrosion induced by chloride: Insights from reactive molecular dynamics simulation

Corrosion of reinforcing steels induced by chloride has long been a focal point of research, yet the atomic behavior and mechanism is not fully understood. In present study, we developed a reactive force field (ReaxFF) incorporating the Fe/Cl system based on Density Functional Theory calculations to elucidate atomic-scale behavior and mechanism underlying chloride-induced corrosion of reinforcing steel. Results from ReaxFF simulations employing this force field indicate that the initiation of steel corrosion is catalytically induced by chloride present in the outer layer, and the electron transfer between atoms is identified as a critical factor in corrosion. Specifically, Fe atoms become positively charged, detaching from the matrix surface and dissolving into the solution to form iron chloride compounds with surface Cl, while oxygen atoms turn negatively charged, progressively infiltrating the matrix and combining with Fe to create intricate iron oxide compounds. Furthermore, the entire dynamic process of corrosion oxidation on the surface of the ferritic matrix and the formation of product species has been fully captured. This ongoing corrosion process leads to significant matrix loss from metal surface and a reduction in structural integrity.

Numerical and experimental investigation of 2-thiazoline-2-thiol and nitrotetrazolium blue chloride compound as levelers for through-hole copper electroplating

Leveler is essential in the electroplating process of the through-hole (TH), the adsorption characteristics of which are strongly influenced by the aspect ratios of the THs. However, only a single kind of leveler usually appears in the most frequently performed THs’ filling electrolyte, which is highly possible to limit the electrolyte's capability to fill THs and improve the copper film properties. In this paper, two levelers, 2-Thiazoline-2-Thiol (T1) and Nitrotetrazolium Blue chloride (NBT), with significant molecular weight differences, were combined to fill THs with multiple ARs. The interactions among the leveler compounds and other additives become the primary factor controlling the THs electroplating process, which was systematically investigated through a combination of flow field numerical simulation and electrochemical measurements. T1 presents a weaker inhibition effect and is more sensitive to convection than NBT, which also exhibits a convection-enhanced inhibition effect with other additives. The convection of the electrolyte in the THs center continuously decreases with the ARs, guiding to the increasing electroplating rate at the THs center, high throwing power (TP) of 141%, and flawless filling of the THs with ARs of 4.75:1∼1.9:1 in 2.5 h. The copper film on the surface maintains extremely high flatness and low thickness.

Are Mouthwashes Really Effective against Candida spp.?

Oral candidiasis is an opportunistic infection caused by fungi of the genus Candida. Nystatin, fluconazole, and miconazole are the most widely used antifungal drugs in dentistry, but in recent years, they have been shown to be less effective due to the increase in the resistance to antifungal drugs. The growing challenge of antifungal resistance emphasizes the importance of exploring not only alternative strategies in the fight against Candida spp. infections but also supportive treatment for pharmacological treatment for oral candidiasis. This review aims to evaluate and compare the in vitro reports on antifungal efficacy against Candida spp. exhibited by mouthwashes distributed on the European market. The research question was elaborated through the PEO framework recommended by PRISMA 2020. A bibliographic search strategy was developed for the scientific online databases Pubmed and ScienceDirect. According to the eligibility criteria, 21 papers were included in this study over a 27-year period. Mouthwashes containing chlorhexidine digluconate, cetylpyridinium chloride, hexetidine, and fluorine compounds among others, and natural antimicrobials, such as menthol, thymol, eucalyptol, and Glycyrrhiza glabra extracts, have demonstrated antifungal effectiveness. Nonetheless, the methodological variance introduces ambiguity concerning the comparative efficacy of distinct molecules or mouthwash formulations and complicates the evaluation and the comparison of results between studies. Some mouthwashes commercially available in Europe have the potential to be used in anti-Candida therapy and prevention since they have shown antifungal effect.

Assessment of marine and urban-industrial environmental impact on stone acting as the base of a quaternary bronze sculpture

This work investigates the influence of a marine and urban-industrial environment on the deterioration of a funerary memorial in Getxo (Basque Country, Spain). The sculpture and artificial stone materials as well as their degradation products were characterised via a multi-analytical approach. An in situ characterisation of the bronze statue and its artificial limestone base was carried out with portable Energy Dispersive X-Ray Fluorescence (ED-XRF) and Raman spectrometers. In addition, several samples of white crusts as well as metal runoff crusts and biological patina were collected and some of them were prepared as cross-sections. High Resolution Micro-X-ray fluorescence and micro-Raman spectroscopy were used as non-destructive methods to detect original and degradation compounds. The test of soluble salts was also carried out on the samples and ion chromatography was employed in the laboratory. Exclusively calcite salt-efflorescences were found at the monument side with ED-XRF and Raman spectroscopy. While their morphology was compact at unsheltered sites, they showed a lamellar structure at sheltered locations, whose increased volume strongly influences the destruction of the memorial. The spectroscopic characterization of metal runoff showed that its excessive occurrence on the memorial surface was due to the dissolution of the copper-alloy caused by chemical reactivity with the surrounding acidic atmosphere. The formation of brochantite Cu4(SO4)(OH)6, posnjakite Cu4(SO4)(OH)6·(H2O), langite Cu4(SO4)(OH)6·2(H2O), or malachite Cu2(CO3)(OH)2 was favored exclusively in metal runoff crusts at unsheltered locations. However, much thinner crusts collected at sheltered sites showed a different composition, with copper species such as moolooite (Cu(C2O4)·nH2O) and atacamite Cu2Cl(OH)3. The soluble salt extraction showed a variable concentration of soluble ions depending on the area where the samples come from. The sample from north west sheltered location showed the highest content of sulfate, nitrate and chloride compounds. In addition, the concentration of fluoride and nitrate reflects the impact of contamination of surrounding industries.

Thermodynamic Analysis of Chloride Corrosion in Steel for Energy System Applications in Fe-O-Cl-Na Environments

The assumptions of contemporary energy policies are increasing the share of renewable energy sources. Biomass combustion is developing as an alternative to fossil fuels. However, it faces challenges such as limited corrosion resistance of steel boiler components due to chloride compounds in flue gases and fly ash. This paper provides a comprehensive thermodynamic analysis of chloride-induced corrosion in steel in the Fe-O-Cl-Na environment, focusing on the influence of steam concentration in the gas phase. The study was performed by using the general thermodynamic rules, the thermodynamic properties of the pure components involved in the reaction, and the properties of the solutions formed in the liquid and gas phases. The study also examined the impact of alkali metal chlorides, particularly NaCl, on the formation of NaFeO2 in the passive oxide scale layer Fe3O4/Fe2O3. Furthermore, it investigated the condensation of NaCl vapour formation of low-melting eutectic mixtures in deposits and the resulting consequences on the corrosion process. The role of HCl in the chlorination and oxidation process of steel in melted ash deposits was also discussed. The presented thermodynamic analysis was compared with assumptions of an “active oxidation” model. This study can be a valuable resource for experimental research planning and a guide for preventing corrosion in industrial settings.

Structure of Manganese Chloride and Threonine Crystals Formed by Slow Vaporization Method

Crystals of complex compounds are used in technology, optics, medicine, pharmacy, surface treatment, etc. The study of the crystal structure of complex compounds is important because they are widely used in industry and exhibit mechanical, thermal and a number of other valuable properties. Study of the crystal structure of complex compound of manganese chloride with the amino acid threonine, as well as the study of its physicochemical and biological properties. For the synthesis of complex compound, the method of slow evaporation was used. The composition of the formed crystals of the compound was analyzed by X-ray diffraction and spectroscopic structural analyses. the structure of the complex compound MnСl2×C4H9NO3manganese chloride and the amino acid threonine was studied. As a result of the study, it was established that the crystal structure of the compound MnСl2×C4H9NO3belongs to the orthorhombic system with space symmetry P212121.

Green synthesis of novel coumarin derivatives via grinding approach and their antimicrobial evaluation

ABSTRACT Herein, a rapid, clean, less expensive and environmentally friendly route to a novel series of coumarins bearing thiazoles or 1,3,4-thiadiazoles was developed via grinding method under solvent conditions. Thus, 6-bromo-3-(2-bromoacetyl)-2-chromen-2-one was treated with cyanothioacetamide to produce thiazole-2-acetonitrile derivative 2, which was then transformed to iminocoumarins by reacting with hydroxyaldehydes. Hydrolysis of iminocoumarins by conc. HCl furnished coumarins. Furthermore, treatment of compound 2 with phenylisothiocyanate produced thioanilide which interacts with hydrazonoyl chloride and/or α-halocarbonyl compounds afforded 1,3,4-thiadiazole and thiophene derivatives, consequently. All the newly prepared coumarins were screened against six pathogenic microorganisms. The results indicated that compounds 7 and 12 were the most effective against Bacillus pumilis, while compound 4b was highly active against Streptococcus faecalis. Also, compound 5b was highly active against Enterobacter cloacae. Compounds 2 and 7 were higher active compared with reference drug ketoconazole against fungi Saccharomyces cerevisiae.

Acoustic shock wave induced chemical reactions–A case study of NaCl single crystal

Herein, we report the catalytic-free acoustic shock wave-induced synthesis of the non-stoichiometry compound of sodium chloride (Na3Cl2-P4/m) from the stoichiometry NaCl (B1). The shocked NaCl crystal structure is formed as a mixed phase together with the NaCl (B1) and (Na3Cl2-P4/m) thereby the formation of non-stoichiometry compound of Na3Cl2 is confirmed by the diffraction, vibrational, spectroscopic and microscopic techniques. X-ray photoelectron spectroscopic study reveals the positive energy shift of Na 1 s peak which confirms the formation of higher coordination number Na3Cl2 (six to eight) such that it can be considered as Na rich structure. The typical cubic morphology has changed into butterfly wing structure under shocked conditions which is found to be novel, to date. Due to the formation of Na-rich crystal structure, the electrical properties of the shocked crystal are greatly altered. The maximum values of the real part of the impedance of the control and shocked crystals are 1.9 × 107 ohm and 1.0 × 107 ohm, respectively at the lower frequency regions. The present study offers a new platform to synthesize the stable non-stoichiometry NaCl structures under ambient conditions by low pressure acoustic shock waves which could bring about new understanding and implications on NaCl crystals and their applications.

Magnetic coupling interaction-related photoluminescence behaviors in all-inorganic manganese chloride perovskites

Manganese halides, as dilute magnetic semiconductor materials, have magnetic coupling interactions that play an essential role in their photoluminescence (PL); however, such interactions remain controversial. AMnCl3 (AMC, A = K, Rb, and Cs) and their hydrates AMnCl3·2H2O (AMCH, A = K, Rb, and Cs) are both in the ABX3 configuration but exhibit a wide variety of structures with different connectivity types and dimensions. Their magnetic coupling interaction has been demonstrated. However, few studies have systematically investigated the PL in conjunction with the magnetic coupling interaction over these chloride compounds. In this paper, the effect of the magnetic coupling interaction on AMC and AMCH PL is mainly revealed by temperature-dependent PL spectra and lifetimes. The MnX6 (X6 = Cl4(H2O)2 or Cl6) cluster connection types affect the Mn2+–Mn2+ distances. The magnetic coupling interaction between MnX6 octahedrons affects the radiative transitions of manganese chlorides, which is influenced by the Mn2+–Mn2+ distance, local symmetry, and water ligand. The Mn2+–Mn2+ distance and the magnetic coupling interaction also affect their lifetimes. Variations in magnetic coupling interactions can shift emission wavelength, especially dual-emissions and near-infrared (NIR) emission at lower temperatures while A+ = K+. This work helps researchers understand the optical process of Mn2+ ions in different manganese compounds and provides new insights into the design of tailored Mn2+ ion phosphors.

Interaction of Valine with Biometal Chlorides in an Aqueous Environment at 25°C

Research in medical biology and pharmacology can expand understanding of the interactions of biometals with amino acids, which are key components of biological systems. This may lead to the development of new complexes that can be used in medicine, for example, to develop new drugs with antimicrobial activity or to maintain metabolic balance in the body. Research purpose:obtaining complex compounds of biometals, cobalt chloride, nickel chloride and manganese chloride with the amino acid valine, as well as the study of their physicochemical and biological properties. For the analysis, the Kjeldahl method was used to determine the nitrogen content. The composition of the formed crystals was analyzed by IR spectroscopy. The structure and shape of cobalt, nickel and manganese crystals were determined using a microscope. The identity of the obtained compounds was confirmed by IR spectroscopy and microscopic analyses. We can conclude that valine in the complex is coordinated to metal ions through the oxygen atoms of the carboxyl and nitrogen groups of the amine groups.

Interaction of Threonine with Biometal Chlorides in an Aqueous Environment at 25°C

The method for the synthesis of complexes with transition group biometal salts with the amino acid threonine includes improvement of reaction conditions, selection of reagents and analytical methods to confirm the formation of complexes. Research purpose: obtaining complex compounds of biometals, cobalt chloride, nickel chloride and manganese chloride with the amino acid threonine, as well as the study of their physicochemical and biological properties. In the synthesis of complex compounds, the preparative method was used. Compositions of the formed crystals were analyzed by IR spectroscopy. The structure and shape of cobalt, nickel and manganese crystals were determined using a microscope. The identity of the obtained compounds was confirmed by IR spectroscopy and microscopic analyses. We can conclude that threonine in the complex is coordinated to metal ions through the oxygen atoms of the carboxyl and nitrogen groups of the amine groups.

Current Strategies in Controlling Aspergillus flavus and Aflatoxins in Grains during Storage: A Review

Aspergillus flavus is a ubiquitous pathogen that can infect many foods and grains, and it produces large amounts of aflatoxins during their storage. Aflatoxins are considered highly toxic and carcinogenic to humans, and they cause great damage to crop production, food security, and human health. Thus, controlling A. flavus and aflatoxins in grains presents a great challenge to humans worldwide. Over the past decade, many strategies have been demonstrated to be useful in controlling A. flavus and aflatoxins during food storage. These methods involve physical agents, chemical agents, biological agents, etc. Some of these methods are currently used in actual production. In this review, we summarize the reported methods for controlling A. flavus and aflatoxins during food storage in the past ten years and elucidate their advantages and disadvantages. The methods discussed include irradiation technology; low oxygen atmospheres; chemical fungicides (benzalkonium chloride, iodine, ammonium bicarbonate, and phenolic and azole compounds); biological agents from plants, animals, and micro-organisms; and aflatoxin elimination methods. We expect that this review will promote the applications of current strategies and be useful for the development of novel technologies to prevent or eliminate A. flavus and aflatoxins in food and feed during storage.

DNA adductomics aided rapid screening of genotoxic impurities using nucleosides and 3D bioprinted human liver organoids

Current genotoxicity assessment methods are mainly employed to verify the genotoxic safety of drugs, but do not allow for rapid screening of specific genotoxic impurities (GTIs). In this study, a new approach for the recognition of GTIs has been proposed. It is to expose the complex samples to an in vitro nucleoside incubation model, and then draw complete DNA adduct profiles to infer the structures of potential genotoxic impurities (PGIs). Subsequently, the genotoxicity is confirmed in human by 3D bioprinted human liver organoids. To verify the feasibility of the approach, lansoprazole chloride compound (Lanchlor), a PGI during the synthesis of lansoprazole, was selected as the model drug. After confirming genotoxicity by Comet assay, it was exposed to different models to map and compare the DNA adduct profiles by LC-MS/MS. The results showed Lanchlor could generate diverse DNA adducts, revealing firstly its genotoxicity at molecular mechanism of action. Furthermore, the largest variety and content of DNA adducts were observed in the nucleoside incubation model, while the human liver organoids exhibited similar results with rats. The results showed that the combination of DNA adductomics and 3D bioprinted organoids were useful for the rapid screening of GTIs.

Chemical characterization of refuse derived fuel (RDF) using Py-GC/MS

The conversion of municipal solid waste (MSW) to refuse-derived fuel (RDF) and its utilization as an alternative fuel in the cement industry has been an emerging trend. However, RDF is highly heterogeneous, with its complex composition changing with season and source. This work is focused on the chemical characterization of six RDF samples listed as A, B, C, D, E, and F from different locations across the country using pyrolysis gas chromatography-mass spectrometry (Py-GC/MS), thermogravimetric instrument and CHONS elemental analyzer. Qualitative and semi-quantitative results were obtained using EGA, single-shot and double-shot analysis methods. EGA has been used to derive qualitative results in correlation with TGA. FTIR analysis was carried out to understand the initial functional characterization. XRF analysis along with ICP-MS triple quad revealed the inorganic makeup of the samples. Single-shot results indicated that apart from non-hydrocarbon gases (CO2 and O2), the long-chain alkenes were most abundant, followed by alkanes, aromatic compounds, and ketones. Double-shot analysis indicated the presence of chloride and sulphur-based compounds in RDF samples as limiting components. Polystyrene contribution to LHV of RDF has been highlighted. The study can be further used to conduct compositional studies of RDF and its pyrolytic behavior in the gasifier. It will further strengthen the future gasifier models where pyrolysis is one of the critical steps. This technique will be very helpful in obtaining a better characterization of volatile and non-volatile (bio-oil and ash) fractions of the pyrolytic products.

Alternative during‐growth chlorination of sputtered CdTe films and their implementation as activating layers in CdS/CdTe solar cells

AbstractCadmium telluride is an efficient light absorbing material successfully used in solar cell technology. The efficiency of such photovoltaic devices is strongly dependent on post‐deposition thermal treatments in the presence of chlorine. The benefits of this process on the absorbing layer include removal of intragrain defects, grain growth enhancement, and grain boundaries passivation. The absorber chlorination is a crucial step for which CdCl2 is the most common choice. Its use, however, has been overshadowed by the toxicity of Cd‐ and Cl‐containing vapors and residues. In this work, chlorine was incorporated in CdTe films during growth using sputtering targets with different chloride compounds: CdCl2, TeCl4, BaCl2, CaCl2, or LiCl. After characterizing these films, CdTe:CdCl2 and CdTe:TeCl4 were selected as feasible absorbers for testing their performance in photovoltaic devices. Efficiencies near 7% were obtained in as‐grown unoptimized cells in which the absorber consisted of two layers: pristine CdTe and CdTe:CdCl2 or CdTe:TeCl4. The chlorinated layers acted as Cl sources for the adjacent CdTe and CdS, which produced a homogeneous distribution of chlorine throughout the cell. In the during‐growth activating‐layer (DG‐AL) method used here, the chlorine diffusion during growth had a doping effect, passivated grain boundaries and defects, improved the back contact characteristics by reducing the CdTe work function, and lowered the pinhole formation probability by producing a compact chlorinated CdTe layer.

ASPHYDROXEL: ASPHALT CARBON DIOXIDE CAPTURE BY SYNTHESIS OF POTASSIUM HYDROXIDE FOR UTILIZATION OF PALM OIL BUNCH ASH WASTE

Environmental pollution is the most common problem faced by Indonesia, for example, industrial waste. The country of Indonesia once occupied the first position in Southeast Asia, as a country with the worst air quality. In addition, Indonesia is the largest producer of crude palm oil (CPO) and palm oil plantations in the world. The industry produces the most solid waste in the form of empty palm oil bunches and requires a large area to store it. In order to reduce the storage area needed, empty palm oil bunches are burned to ashes or palm oil fuel ash (POFA). Therefore, we have the idea of absorbing CO2 gas and utilizing POFA as a mixture of concrete and asphalt, by converting it into a potassium chloride compound. Then, the electrolysis process is carried out to produce potassium hydroxide compounds. The potassium hydroxide compound will later be mixed with asphalt to produce Asphydroxel asphalt, which absorbs carbon dioxide. In implementing Asphydroxel, several parties are involved, such as oil palm smallholders, palm oil mills, asphalt company research teams, asphalt companies, and the government. It is predicte that this idea will prevent the buildup of bunch ash waste and air pollution which cause climate change

Characterisation and agronomic evaluation of acidified food waste anaerobic digestate products

Raw liquid anaerobic digestate was synthesised into nutrient-dense solid digestates via acidification and evaporation. Acidification retained ammonium in the digestate whilst also donating the anion to free ammonium to form an ammonium salt. Digestate was treated with the addition of sulphuric, nitric, and phosphoric acid resulting in the formation of ammonium sulphate, ammonium nitrate and ammonium phosphate, respectively then evaporated into a solid fertiliser product. FTIR, XRD and SEM-EDS collectively confirm that the addition of acids completely converted the free ammonium in the raw digestate into their respective ammonium salt counterparts. Compounds of potassium chloride, silicon dioxide, calcium carbonate, magnesium ammonium phosphate, sodium nitrate, and sodium chloride were identified in all solid digestate samples. Plant growth and grain yield was higher in urea ammonium nitrate, raw liquid digestate and acidified digestate products compared to control and unacidified solid digestate. Urea ammonium nitrate and ammonium nitrate solid digestate had the highest dry shoot, likely due to the high available nitrogen found in both fertilisers. Overall, acidification and evaporation of liquid digestate can efficiently transform it into a valuable solid fertiliser with a high nutrient density. This process not only has the potential to mitigate handling and storage constraints of low nutrient density digestate in anaerobic digestion facilities but also offers a sustainable alternative to conventional fertilisers.