Solution behavior of a surfactant aldehyde–the oxidation product of an alcohol ethoxylate

It has previously been shown that alcohol ethoxylates readily undergo autoxidation and that one of the major oxidation products is the surfactant aldehyde, i.e. an ethoxylate carrying a –CH₂CHO group at the terminal end of the polyoxyethylene chain. In this work the cloud point, phase behavior and aggregation characteristics of the surfactant aldehyde produced by oxidation of C₁₂H₂₅(OCH₂CH₂)₅OH (C₁₂E₅) are determined and compared with the values obtained with the parent surfactant. It was found that the physico–chemical behavior of the two species was very similar, which indicates that a considerable portion of the aldehyde group is in hydrated state, i.e. the surfactant aldehyde consists of a mixture of aldehyde in carbonyl form and the corresponding geminal diol. The cloud point of the surfactant aldehyde decreased rapidly with time, even when it was stored at low temperature. Also the parent surfactant and its homologue C₁₂E₆ exhibited a decrease in cloud point during storage. For instance, a 1% aqueous solution of C₁₂E₆ showed a cloud point decrease from 62 to 32°C after 4 months storage at 40°C. Such a change in solution behavior can have important practical implications.     

Modification of polysulfone membranes 5. Effect of n-butylamine and allylamine plasma

This paper describes some properties of microwave plasma polymers of n-butylamine and allylamine deposited on the surface of polysulfone substrate. Contact angle evaluation, ATR-FTIR spectroscopy, X-ray photoelectron spectroscopy analysis and estimation of pore size distribution of ultrafiltration polysulfone membranes were used. It was found that addition of Ar to the amine vapor significantly stabilized the plasma and converted it to the ablation mode. The surface became more hydrophilic and the surface groups were enriched in oxygen. Both amines gave deposits of various compositions: the n-butylamine polymer was not as enriched in amines as the polymer formed from allylamine. However, the amounts of nitrogen in both deposits indicated allylamine to be the precursor for the preparation of membranes with weakly basic functionalities. When porous membranes are modified, the ultrafilters obtained may be named `fouling protected' as they do not foul so intensively with proteins as their unmodified analogues. To a lesser extent, similar behavior was shown by membranes modified by deposition of plasma-polymerized n-butylamine.     

Socio-Economic Impact of the Covid-19 Pandemic in the U.S.

This paper proposes a dynamic cascade model to investigate the systemic risk posed by sector-level industries within the U.S. inter-industry network. We then use this model to study the effect of the disruptions presented by Covid-19 on the U.S. economy. We construct a weighted digraph G = (V,E,W) using the industry-by-industry total requirements table for 2018, provided by the Bureau of Economic Analysis (BEA). We impose an initial shock that disrupts the production capacity of one or more industries, and we calculate the propagation of production shortages with a modified Cobb–Douglas production function. For the Covid-19 case, we model the initial shock based on the loss of labor between March and April 2020 as reported by the Bureau of Labor Statistics (BLS). The industries within the network are assigned a resilience that determines the ability of an industry to absorb input losses, such that if the rate of input loss exceeds the resilience, the industry fails, and its outputs go to zero. We observed a critical resilience, such that, below this critical value, the network experienced a catastrophic cascade resulting in total network collapse. Lastly, we model the economic recovery from June 2020 through March 2021 using BLS data.     

Enhancement of the Efficacy of Photodynamic Inactivation of Candida albicans with the Use of Biogenic Gold Nanoparticles

This study reports on successful photodynamic inactivation of planktonic and biofilm cells of Candida albicans using Rose Bengal (RB) in combination with biogenic gold nanoparticles synthesized by the cell‐free filtrate of Penicillium funiculosum BL1 strain. Monodispersed colloidal gold nanoparticles coated with proteins were characterized by a number of techniques including SEM–EDS, TEM, UV–Vis absorption and fluorescence spectroscopy, as well as Fourier transform infrared spectroscopy to be 24 ± 3 nm spheres. A Xe lamp (output power of 20mW, delivering intensity of 53 mW cm^?2) was used as a light source to study the effects of RB alone, the gold nanoparticles alone and the RB‐gold nanoparticle mixture on the viability of C. albicans cells. The most effective reduction in the number of planktonic cells was found after 30 min of Xe lamp light irradiation (95.4 J cm^?2) and was 4.89 log₁₀ that is 99.99% kill for the mixture of RB with gold nanoparticles compared with 2.19 log₁₀ or 99.37% for RB alone. The biofilm cells were more resistant to photodynamic inactivation, and the highest effective reduction in the number of cells was found after 30 min of irradiation in the presence of the RB–gold nanoparticles mixture and was 1.53 log₁₀, that is 97.04% kill compared with 0.6 log₁₀ or 74.73% for RB. The probable mechanism of enhancement of RB‐mediated photodynamic fungicidal efficacy against C. albicans in the presence of biogenic gold nanoparticles is discussed leading to the conclusion that this process may have a multifaceted character.     

Sensitivity of the NTB phase formation to the molecular structure of imino-linked dimers

ABSTRACT

Here we report on the synthesis and mesomorphic properties of a series of imino-linked dimeric molecules. In order to improve our understanding of the structure–N_TB phase correlations, we have studied the impact of geometric and electronic factors arising from varying mesogenic units, different spacer lengths and from the ratio (n/m) between the lengths of terminal chains (n) and spacer (m). From the perspective of the molecular geometry, the results show that the stability of the N_TB phase results from increasing effective molecular bending and with the broadening of the mesogenic unit, in particular near the spacer, and that the n/m ratio plays a substantial role in conjunction with the specific mesogenic unit. A computational study of the electronic properties shows that a broadening of the mesogenic core in the vicinity of the spacer is associated with an increased anisotropy of the electrostatic potential distribution. Within a given series of materials our study suggests that the incidence of the N_TB phase and its thermal stability are governed by the synergy of specific geometrical factors and the anisotropy of the electrostatic potential distribution of the mesogenic core.     

Photochemical Reduction of Carbon Dioxide Catalyzed by a Ruthenium‐Substituted Polyoxometalate

A polyoxometalate of the Keggin structure substituted with Ru^III, ⁶Q₅[Ru^III(H₂O)SiW₁₁O₃₉] in which ⁶Q=(C₆H₁₃)₄N⁺, catalyzed the photoreduction of CO₂ to CO with tertiary amines, preferentially Et₃N, as reducing agents. A study of the coordination of CO₂ to ⁶Q₅[Ru^III(H₂O)SiW₁₁O₃₉] showed that 1) upon addition of CO₂ the UV/Vis spectrum changed, 2) a rhombic signal was obtained in the EPR spectrum (g_x=2.146, g_y=2.100, and g_z=1.935), and 3) the ¹³C NMR spectrum had a broadened peak of bound CO₂ at 105.78 ppm (Δ_1/2=122 Hz). It was concluded that CO₂ coordinates to the Ru^III active site in both the presence and absence of Et₃N to yield ⁶Q₅[Ru^III(CO₂)SiW₁₁O₃₉]. Electrochemical measurements showed the reduction of Ru^III to Ru^II in ⁶Q₅[Ru^III(CO₂)SiW₁₁O₃₉] at ?0.31 V versus SCE, but no such reduction was observed for ⁶Q₅[Ru^III(H₂O)SiW₁₁O₃₉]. DFT‐calculated geometries optimized at the M06/PC1//PBE/AUG‐PC1//PBE/PC1‐DF level of theory showed that CO₂ is preferably coordinated in a side‐on manner to Ru^III in the polyoxometalate through formation of a Ru? O bond, further stabilized by the interaction of the electrophilic carbon atom of CO₂ to an oxygen atom of the polyoxometalate. The end‐on CO₂ bonding to Ru^III is energetically less favorable but CO₂ is considerably bent, thus favoring nucleophilic attack at the carbon atom and thereby stabilizing the carbon sp² hybridization state. Formation of a O₂C–NMe₃ zwitterion, in turn, causes bending of CO₂ and enhances the carbon sp² hybridization. The synergetic effect of these two interactions stabilizes both Ru–O and C–N interactions and probably determines the promotional effect of an amine on the activation of CO₂ by [Ru^III(H₂O)SiW₁₁O₃₉]^5?. Electronic structure analysis showed that the polyoxometalate takes part in the activation of both CO₂ and Et₃N. A mechanistic pathway for photoreduction of CO₂ is suggested based on the experimental and computed results.     

Differential pulse voltammetry in analysis of disinfectants — 2-mercaptobenzothiazole, 4-chloro-3-methylphenol, triclosan, chloramine-T

The aim of this work was to study the possibility of simultaneous voltammetric determination of some disinfectants used as components in cosmetic products. The examined compounds were: triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol), chloramine-T (N-chloro-p-toluenesulfonamide sodium salt), 4-chloro-3-methylphenol and 2-mercaptobenzothiazole. Measurements were performed using glassy carbon electrode immersed in Britton-Robinson buffers which acted as supporting electrolytes. The dependence of oxidation and reduction potentials on pH was examined using cyclic voltammetry. Britton-Robinson buffer of pH 9.9 was chosen for further studies to ensure the best separation of compounds. The resultant oxidation potentials indicate the possibility to simultaneously determine some of the disinfectants.. Oxidation reactions of mixtures containing two compounds (4-chloro-3-methylphenol and chloramine-T, 2-mercaptobenzothiazole and 4-chloro-3-methylphenol, 2-mercaptobenzothiazole and triclosan) were recorded as differential pulse voltammograms.     

Analysis of anthocyanin pigments in Lonicera (Caerulea) extracts using chromatographic fractionation followed by microcolumn liquid chromatography-mass spectrometry

Anthocyanins from the fruit Lonicera caerulea L. var. kamtschatica (blueberry honeysuckle, Caprifoliaceae) were studied via (semi)preparative chromatographic fractionation followed by MS and μLC/MS analysis. The extraction procedure was optimized with respect to analytical purposes as well as its potential use for the preparation of nutraceuticals. The highest yield of anthocyanins was obtained using acidified methanol as the extraction medium. A comparable total anthocyanin content was obtained using a mixture of methanol and acetone. However, when Lonicera anthocyanins were in contact with acetone, a condensation reaction occurred to a large extent and related 5-methylpyranoanthocyanins were found. The effect of other extraction media, including ethanol as a "green" solvent, is also discussed. The potential of two fractionation procedures for extract purification differing in their chromatographic selectivity and scale was studied (i.e. using a Sephadex LH-20 gel column and a reversed phase). Fractions obtained by both procedures were used for a detailed analysis. MS and μLC/MS(2) methods were used for monitoring anthocyanin and 5-methylpyranoderivatives content as well as identifying less common and more complex dyes (dimer of cyanidin-3-hexoside, cyanidin-ethyl-catechin-hexosides, etc.). These more complex dyes are most likely formed during fruit treatment.     

Development of a proficiency testing scheme for a limited number of participants in the field of natural water analysis

A proficiency testing (PT) scheme was developed for a limited number of analytical laboratories participating in the analysis of natural water in Israel. Three fit-for-intended-use reference materials (RMs) were prepared for a pilot PT from natural water: RM-blank and two in-house reference materials (IHRMs) with seven analytes fortified to achieve different levels of analyte concentrations. The measurands for the PT participants were the traceable spike values certified in the IHRMs, i.e., added mass concentrations of the analytes. The RM-blank and IHRMs were found to be homogeneous and stable over 11 days, the time necessary for the experimental part of the PT. The RMs were distributed to the PT participants as unknown test items similar to routine samples. The test results were evaluated using their deviations from the IHRM-certified values. Eight Israeli laboratories took part in the interlaboratory comparison. Individual laboratory performance and metrological compatibility of the PT results of the participants, as a local group of laboratories, were evaluated for every analyte.     

Modifying of etching anisotropy of silicon substrates by surface active agents

The influence of alcohol additives on etch rate anisotropy of Si(hkl) planes has been studied. The etching processes were carried out in 3 and 5 M KOH aqueous solutions saturated and non-saturated with alcohols. Isopropanol, 1-propanol and tert-butanol were examined. It has been showed that the etching process cannot be controlled only by the surface tension of the solution. Saturation of the etching solution with alcohols modifies etch rate anisotropy, lowering the ratio of the etch rate of (110) and vicinal planes to the etch rate of (100) plane. The morphology of Si(hkl) planes etched in 3 M KOH solution saturated with tert-butyl alcohol has been studied in detail. Smooth (331) and (221) planes have been achieved in this solution. The (100) plane turned out to be densely covered by hillocks, opposite to the (100) plane etched in weak-alkaline solution saturated with isopropanol. To explain this phenomenon, the mechanism of hillocks formation on Si(100) surface has been proposed.