FUNGITOXICITY OF CHLORINATED HYDROCARBON INSECTICIDES IN RELATION TO WATER SOLUBILITY AND VAPOR PRESSURE

1960 ◽  
Vol 38 (2) ◽  
pp. 163-175 ◽  
Author(s):  
Lloyd T. Richardson ◽  
D. M. Miller
Keyword(s):  
Vapor Pressure ◽  
Water Solubility ◽  
High Water ◽  
Assay Method ◽  
Vapor Pressures ◽  
Response Curves ◽  
Chlorinated Hydrocarbon ◽  
High Degree ◽  
Dosage Response Curve ◽  
Bio Assay

Fungitoxicity, in terms of inhibition of mycelial growth, was demonstrated with eight chlorinated hydrocarbon insecticides by the culture plate bio-assay method. All of the dosage–response curves thus derived were bimodal rather than linear. Evidence is presented to show that the shape of these curves is governed by two physical properties of the compounds: water solubility (which was determined experimentally) and vapor pressure. The concentration of insecticide in solution governs the initial rise of each dosage–response curve which is extended to a peak because of supersaturation and is followed by a decline as normal saturation is regained. The concentration of toxicant vapor in contact with the organism governs the second rise in the curve to a level dependent on the vapor pressure of the compound. Lindane has a high degree of fungitoxicity because of its relatively high water solubility. Heptachlor, chlordane, and aldrin are also highly toxic because of their vapor pressures. DDT, methoxychlor, dieldrin, and endrin are weakly fungitoxic because of both low water solubility and low vapor pressure.

EVALUATION OF PROTEIN IN FOODS: IV. A SIMPLIFIED CHEMICAL SCORE

1959 ◽  
Vol 37 (1) ◽  
pp. 1293-1299 ◽  
Author(s):  
J. M. McLaughlan ◽  
C. G. Rogers ◽  
D. G. Chapman ◽  
J. A. Campbell
Keyword(s):  
Rapid Screening ◽  
Assay Method ◽  
Efficiency Ratio ◽  
Lysine Concentration ◽  
Chemical Score ◽  
Group A ◽  
High Degree ◽  
The Relationship ◽  
Bio Assay

Available evidence has shown that most common foods are deficient in lysine, methionine, or in methionine and cystine. Based on the determination of these amino acids, a simplified chemical score was developed and compared with protein efficiency ratio (P.E.R.) values determined with the same samples. Each of 43 foods was assigned to either of two categories: (a) foods apparently deficient in lysine or (b) in methionine (+ cystine). With 16 foods in the former group there was a high degree of correlation between lysine concentration and P.E.R. With 27 foods in the latter group, a good correlation was found between the methionine (+ cystine) concentration and P.E.R. Since the regression lines for the two groups were different, a factor was added to the methionine (+ cystine) values to simplify the relationship. That foods deficient in lysine or in methionine (+ cystine) fell into two distinct groups appeared to be substantiated by data available in the literature. Because the simplified method is relatively rapid, yields reproducible results, and correlates with animal assays, it is proposed as a rapid screening procedure for the evaluation of protein in foods, but is not intended to replace the rat bio-assay method.

scholarly journals Efficient Homogeneous TEMPO-mediated Oxidation of Cellulose  in Lithium Bromide Hydrates

2021 ◽  
Author(s):  
Xiaotong Fu ◽  
Fulong Zhang ◽  
Cuihua Dong ◽  
Wenyuan Zhu ◽  
Kaifeng Xiong ◽  
...  
Keyword(s):  
Selective Oxidation ◽  
Water Solubility ◽  
Lithium Bromide ◽  
High Water ◽  
Amorphous Structure ◽  
Cellulose Oxidation ◽  
Homogeneous Oxidation ◽  
Fractionation Analysis ◽  
Ft Ir ◽  
High Degree

Abstract An appropriate cellulose-dissolving solvent is critical for the homogeneous oxidation of cellulose using TEMPO (2, 2, 6, 6-tetramethylpiperidine-1-oxyl)-mediated system. Herein, TEMPO/NaClO/NaClO2 system in lithium bromide hydrates (LBHs) was developed for the homogeneous selective-oxidation of cellulose, which was two-stage protocol involving cellulose dissolution and homogeneous oxidation. Specifically, cellulose was firstly dissolved in LiBr⋅3.5H2O and offered the optimal pH (5.6) for the subsequent TEMPO/NaClO/NaClO2 oxidation without precipitation of the cellulose chains. Effect of reaction conditions on cellulose oxidation was investigated. The results showed that high degree of oxidation (DO) and evenly distributed carboxyl could be achieved. The particle size gradually decreased with DO, and oxidized cellulose with high water solubility and amorphous structure could be obtained. Furthermore, FT-IR, 13C NMR and fractionation analysis verified that cellulose was successfully converted and the carboxyl uniformly distributed onto the cellulose chains. This TEMPO-mediated system using LBHs as solvent presented an efficient method on the homogeneous selective oxidation of primary hydroxyl in cellulose.

EVALUATION OF PROTEIN IN FOODS: IV. A SIMPLIFIED CHEMICAL SCORE

1959 ◽  
Vol 37 (11) ◽  
pp. 1293-1299 ◽  
Author(s):  
J. M. McLaughlan ◽  
C. G. Rogers ◽  
D. G. Chapman ◽  
J. A. Campbell
Keyword(s):  
Rapid Screening ◽  
Assay Method ◽  
Efficiency Ratio ◽  
Lysine Concentration ◽  
Chemical Score ◽  
Group A ◽  
High Degree ◽  
The Relationship ◽  
Bio Assay

Available evidence has shown that most common foods are deficient in lysine, methionine, or in methionine and cystine. Based on the determination of these amino acids, a simplified chemical score was developed and compared with protein efficiency ratio (P.E.R.) values determined with the same samples. Each of 43 foods was assigned to either of two categories: (a) foods apparently deficient in lysine or (b) in methionine (+ cystine). With 16 foods in the former group there was a high degree of correlation between lysine concentration and P.E.R. With 27 foods in the latter group, a good correlation was found between the methionine (+ cystine) concentration and P.E.R. Since the regression lines for the two groups were different, a factor was added to the methionine (+ cystine) values to simplify the relationship. That foods deficient in lysine or in methionine (+ cystine) fell into two distinct groups appeared to be substantiated by data available in the literature. Because the simplified method is relatively rapid, yields reproducible results, and correlates with animal assays, it is proposed as a rapid screening procedure for the evaluation of protein in foods, but is not intended to replace the rat bio-assay method.

Volatility of Antioxidants and Antiozonants. 1. Pure Compounds in Absence of Rubber

1964 ◽  
Vol 37 (1) ◽  
pp. 210-220 ◽  
Author(s):  
R. B. Spacht ◽  
W. S. Hollingshead ◽  
H. L. Bullard ◽  
D. C. Wills
Keyword(s):  
Vapor Pressure ◽  
Aromatic Amine ◽  
Quantitative Data ◽  
Surface Effects ◽  
Vapor Pressures ◽  
Pure Compounds ◽  
Different Temperatures ◽  
Amine Compounds

Abstract Comparable volatility data are presented for three phenolic and five aromatic amine compounds. Vapor pressure curves for the materials are given along with the vapor pressure equations derived from these curves. The equations are used to calculate temperatures at which the eight compounds would have equal vapor pressure. Vapor pressures of each material are calculated at specified temperatures. Data are given for several methods of determining actual losses of antioxidants at several different temperatures and at several different airflows. Surface effects are also studied. In general, all methods give the same relative rating of the eight materials, but quantitative data vary considerably with the method used.

A Fluorescence Quenching Analysis of the Binding of Fluoroquinolones to Humic Acid

2017 ◽  
Vol 71 (11) ◽  
pp. 2512-2518 ◽  
Author(s):  
Ryan P. Ferrie ◽  
Gregory E. Hewitt ◽  
Bruce D. Anderson
Keyword(s):  
Humic Acid ◽  
Fluorescence Quenching ◽  
Water Solubility ◽  
Binding Constants ◽  
High Water ◽  
Static Quenching ◽  
Temperature Range ◽  
Equilibrium Binding ◽  
Quenching Analysis ◽  
High Water Solubility

Fluorescence quenching was used to investigate the interaction of six fluoroquinolones with humic acid. Static quenching was observed for the binding of ciprofloxacin, enoxacin, fleroxacin, levofloxacin, norfloxacin, and ofloxacin to humic acid. The equilibrium binding constants were found from Stern–Volmer plots of the data. The quenching experiments were repeated over a temperature range of 25–45 ℃ and van’t Hoff plots were generated. From these linear plots, thermodynamic values were calculated for Δ H, Δ G, and Δ S for each of the fluoroquinolones. The equilibrium binding constants were found to be <1 for all the antibiotics studied. The calculated ΔH values were all negative and ranged from −9.5 to −27.6 kJ/mol. The high water solubility of the antibiotics and low ΔH of binding suggests that the antibiotics will be transported easily through the environment. Finally, whether the fluoroquinolones are in a protonated, deprotonated, or partially protonated state is found to correlate to the strength of binding to humic acid.

Novel tetrazole PtII and PdII complexes with enhanced water solubility: synthesis, structural characterization and evaluation of antiproliferative activity

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Tatiyana V. Serebryanskaya ◽  
Alexander S. Lyakhov ◽  
Ludmila S. Ivashkevich ◽  
Yuri V. Grigoriev ◽  
Andreii S. Kritchenkov ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
High Performance ◽  
Water Solubility ◽  
Thermal Analyses ◽  
High Water ◽  
Acetonitrile Solution ◽  
X Ray ◽  
Molecular And Crystal Structures ◽  
Tetrazole Derivatives ◽  
High Water Solubility

AbstractNovel platinum(II) and palladium(II) chlorido complexes with tetrazole derivatives 1-(2-hydroxyethyl)tetrazole (het) and 1-[tris(hydroxymethyl)methyl]tetrazole (thm), viz. cis-[Pt(het)2Cl2], trans-[Pt(het)2Cl2], trans-[Pt(thm)2Cl2], trans-[Pd(het)2Cl2], and trans-[Pd(thm)2Cl2], were synthesized. The compounds were characterized by elemental and high-resolution electrospray ionization (HRESI) mass spectrometry, high-performance liquid chromatography (HPLC), 1H, 13C and 195Pt nuclear magnetic resonance (NMR) spectroscopy, thermal analyses, and Infrared (IR) spectroscopy. Molecular and crystal structures of trans-[PdL2Cl2] and trans-[PtL2Cl2] (L = het, thm) were established by single-crystal X-ray analysis. The complex cis-[Pt(het)2Cl2] was found to undergo cis–to–trans isomerization upon heating in acetonitrile solution and in the solid state. The synthesized complexes show rather high water solubility lying in the range of 2–10 mg/L.

scholarly journals Optimization and Modeling of an Emulsion Polymerization Reactor

2021 ◽  
Author(s):  
Narges Ghadi
Keyword(s):  
Emulsion Polymerization ◽  
Water Solubility ◽  
Monomer Conversion ◽  
High Water ◽  
Oscillatory Behavior ◽  
Operating Conditions ◽  
Polymer Properties ◽  
Continuous Polymerization ◽  
Simulation Results ◽  
The Impact

A mathematical model was developed to simulate emulsion polymerization in batch, semi-batch and continuous reactors for monomers with high water solubility and significant desorption such as vinyl acetate. The effects of operating conditions such as initiator and emulsifier concentration as well as reactor temperature have been studied. The simulation results revealed the sensitivity of polymer properties and monomer conversion to variation of these operating conditions. Furthermore, the impact of monomer soluble impurities on reduction of monomer conversion has been investigated. In order to control polymer molecular weight, application of chain transfer agents such as t-nonyl mercaptan was suggested. Generally, the simulation results fitted well [with] experimental data from the literature. Several optimizing policies were considered to enhance the reaction operation for better product quality. During continuous polymerization, the reactor demonstrates oscillatory behavior throughout the operation. A new reactor train configuration was consistent with the aim of damping the oscillations and producing high-quality latex.

scholarly journals CCN activity of organic aerosols observed downwind of urban emissions during CARES

2013 ◽  
Vol 13 (4) ◽  
pp. 9355-9399 ◽  
Author(s):  
F. Mei ◽  
A. Setyan ◽  
Q. Zhang ◽  
J. Wang
Keyword(s):  
Chemical Composition ◽  
Water Solubility ◽  
Volume Fraction ◽  
Field Studies ◽  
High Water ◽  
Carbonaceous Aerosols ◽  
Mass Spectral ◽  
Least Squares Fit ◽  
The Relationship ◽  
Aerosol Chemical Composition

Abstract. During the Carbonaceous Aerosols and Radiative Effects Study (CARES), activation fraction of size-resolved aerosol particles and aerosol chemical composition were characterized at the T1 site (~60 km downwind of Sacramento, California) from 10 June to 28 June 2010. The hygroscopicity of CCN-active particles (κCCN) with diameter from 100 to 171 nm, derived from the size-resolved activated fraction, varied from 0.10 to 0.21, with an average of 0.15, which was substantially lower than that proposed for continental sites in earlier studies. The low κCCN value was due to the high organic volume fraction, averaged over 80% at the T1 site. The derived κCCN exhibited little diurnal variation, consistent with the relatively constant organic volume fraction observed. At any time, over 90% of the size selected particles with diameter between 100 and 171 nm were CCN active, suggesting most particles within this size range were aged background particles. Due to the large organic volume fraction, organic hygroscopicity (κorg) strongly impacted particle hygroscopicity and therefore calculated CCN concentration. For vast majority of the cases, an increase of κorg from 0.03 to 0.18, which are within the typical range, doubled the calculated CCN concentration. Organic hygroscopicity was derived from κCCN and aerosol chemical composition, and its variations with the fraction of total organic mass spectral signal at m/z 44 (f44) and O : C were compared to results from previous studies. Overall, the relationships between κorg and f44 are quite consistent for organic aerosol (OA) observed during field studies and those formed in smog chamber. Compared to the relationship between κorg and f44, the relationship between κorg and O : C exhibits more significant differences among different studies, suggesting κorg may be better parameterized using f44. A least squares fit yielded κorg = 2.04 (± 0.07) × f44 − 0.11 (± 0.01) with the Pearson R2 value of 0.71. One possible explanation for the stronger correlation between κorg and f44 is that the m/z 44 signal (mostly contributed by the CO2+ ion) is more closely related to organic acids, which may dominate the overall κorg due to their relatively high water solubility and hygroscopicity.

Sign in / Sign up

Export Citation Format

Share Document