Roald N. Leif

The aqueous solubility of trichloroethene (TCE) and tetrachloroethene (PCE) as a function of temperature

Abstract Using a flexible Au bag autoclave and a precision high-pressure liquid chromatography pump to control pressure, the liquid–liquid aqueous solubilities of TCE and PCE were measured as a function of temperature from 294 to 434 K (at constant pressure). The results were used to calculate the partial molal thermodynamic quantities of the organic liquid aqueous dissolution reactions: Δ Ḡ soln , Δ H soln , Δ S soln and Δ C p soln . Calculated values for these quantities at 298 K for TCE are: Δ Ḡ soln =11.282 (±0.003) kJ/mol, Δ H soln =−3.35 (±0.07) kJ/mol, Δ S soln =−49.07 (±0.24) J/mol K, and Δ C p soln =385.2 (±3.4) J/mol K. Calculated values for these quantities at 298 K for PCE are: Δ Ḡ soln =15.80 (±0.04) kJ/mol, Δ H soln =−1.79 (±0.58) kJ/mol, Δ S soln =−59.00 (±1.96) J/mol K and Δ C p soln =354.6 (±8.6) J/mol K. These thermodynamic quantities may be used to calculate the solubility of TCE and PCE at any temperature of interest. In the absence of direct measurements over this temperature range, the Henrys Law constants for TCE and PCE have been estimated using the measured aqueous solubilities and calculated vapor pressures.

Aqueous oxidation of trichloroethene (TCE): a kinetic analysis

Abstract An empirical kinetic rate law appropriate for many ground waters (neutral pH, aerobic) has been determined for the aqueous oxidation of trichloroethene (TCE), one of the most volumetrically important chlorinated hydrocarbon pollutants. Mass balances were monitored by measuring both the rate of disappearance of TCE and the rate of appearance of CO 2 and Cl − . Dilute buffer solutions were used to fix pH and stoichiometrically sufficient amounts of dissolved O 2 were used to make the reactions pseudo zero-order in O 2 . Using a standard chemical kinetic approach, two orders-of-magnitude in initial TCE concentration were spanned and the resulting double-log plot (log concentration vs. log initial rate) was used to determine the rate constant ( k =5.77±1.06×10 −7 s −1 ) and “true” (i.e., with respect to concentration, not time) reaction order ( n c =0.85±0.03) for the rate law. By determining rate constants over the temperature interval 343–373 K, the Arrhenius activation energy (E a ) for the reaction was determined to be 108.0±4.5 kJ/mol. The rate law and derived kinetic parameters may be used in reactive transport simulators in order to account for aqueous oxidation of TCE as a function of temperature.

An Efficient, Optimized Synthesis of Fentanyl and Related Analogs

The alternate and optimized syntheses of the parent opioid fentanyl and its analogs are described. The routes presented exhibit high-yielding transformations leading to these powerful analgesics after optimization studies were carried out for each synthetic step. The general three-step strategy produced a panel of four fentanyls in excellent yields (73–78%) along with their more commonly encountered hydrochloride and citric acid salts. The following strategy offers the opportunity for the gram-scale, efficient production of this interesting class of opioid alkaloids.

Derivatization of pinacolyl alcohol with phenyldimethylchlorosilane for enhanced detection by gas chromatography–mass spectrometry

AbstractA derivatization procedure for the qualitative gas chromatography–mass spectrometry (GC-MS) analysis of pinacolyl alcohol (PA) that employs phenyldimethylchlorosilane (PhDMClS) and the promoter N-methylimidazole is described. While PA, underivatized, can be detected using conventional gas chromatographic methods, its polarity and low boiling point make its detection in complex matrices challenging. The silylation procedure described herein generates a PA-derivative exhibiting an increased on-column retention time, thus shifting its GC-MS signal away from commonly encountered, volatile, interfering analytes. Derivatized PA could be distinguished from other PhDMClS-derivatized isomeric alcohols by its unique retention time and mass spectrum. The derivatization was demonstrated to perform well in the GC-MS analysis and identification of PA in samples from Proficiency Tests administered by the Organisation for the Prohibition of Chemical Weapons (OPCW). FigureNMI-Accelerated Silylation of Pinacolyl Alcohol for GC-MS Analysis

Rapid and mild silylation of β‐amino alcohols at room temperature mediated by N‐methylimidazole for enhanced detectability by gas chromatography/electron ionization mass spectrometry

RATIONALE In this work, we expand the use of in situ activation of chloro(dimethyl)phenylsilane using N-methylimidazole (NMI) for the effective derivatization of β-aminoethyl alcohols. Due to its enhanced nucleophilic character, NMI is expected to act as an efficient activator in these reactions. METHODS The derivatization of a panel of β-aminoethyl alcohols was accomplished by reacting the analyte with chloro(dimethyl)phenylsilane in the presence of either NMI or pyridine. After the addition of chloro(dimethyl)phenylsilane, the vials were gently tumbled for 1 h at ambient temperature. The phenyldimethylsilyl derivatives were identified using gas chromatography/electron ionization mass spectrometry (GC/EI-MS). RESULTS A total of ten β-aminoethyl alcohols were successfully derivatized via in situ activation of chloro(dimethyl)-phenylsilane with NMI. Derivatization with NMI was significantly more efficient than with pyridine by a factor of 3-6 for the studied alcohols. The derivatizations in the presence of NMI were found to occur in just 1 h and were conveniently executed at ambient temperature. CONCLUSIONS The use of the nitrogenous base NMI in order to activate chloro(dimethyl)phenylsilane for the efficient silylation of a panel of β-aminoethyl alcohols has been demonstrated. The present work shows that NMI is an efficient base for the smooth derivatization of these types of alcohols. Furthermore, the installation of the bulky PDMS group onto these alcohols adds to the certainty that this is a viable approach for the installation of the more commonly employed, trimethylsilyl group. Published in 2014. This article is a U.S. Government work and is in the public domain in the USA.

Deterministic control over high-Z doping of polydicyclopentadiene-based aerogel coatings.

We report on simple and efficient routes to dope polydicyclopentadiene (PDCPD)-based aerogels and their coatings with high-Z tracer elements. Initially, direct halogenation of PDCPD wet gels and aerogels with elemental iodine or bromine was studied. Although several pathways were identified that allowed doping of PDCPD aerogels by direct addition of bromine or iodine to the unsaturated polymer backbone, they all provided limited control over the amount and uniformity of doping, especially at very low dopant concentrations. Deterministic control over the doping level in polymeric aerogels and aerogel coatings was then achieved by developing a copolymerization approach with iodine and tin containing comonomers. Our results highlight the versatility of the ring-opening metathesis polymerization (ROMP)-based copolymerization approach in terms of functionalization and doping of low density polymeric aerogels and their coatings.

Analysis of chemical warfare agents by gas chromatography-mass spectrometry: methods for their direct detection and derivatization approaches for the analysis of their degradation products

Abstract Chemical warfare agents (CWAs) are unarguably one of the most feared toxic substances produced by mankind. Their inception in conventional warfare can be traced as far back as the Middle Ages but their full breakthrough as central players in bellic conflicts was not realized until World War I. Since then, more modern CWAs along with efficient methods for their manufacture have emerged and violently shaped the way modern warfare and diplomatic relations are conducted. Owing to their mass destruction ability, counter methods to mitigate their impact appeared almost immediately on par with their development. These efforts have focused on their efficient destruction, development of medical countermeasures and their detection by modern analytical chemistry methods. The following review seeks to provide the reader with a broad introduction on their direct detection by gas chromatography-mass spectrometry (GC-MS) and the various sample derivatization methods available for the analysis of their degradation products. The review concentrates on three of the main CWA classes and includes the nerve agents, the blistering agents and lastly, the incapacitating agents. Each section begins with a brief introduction of the CWA along with discussions of reports dealing with their detection in the intact form by GC-MS. Furthermore, as products arising from their degradation carry as much importance as the agents themselves in the field of forensic analysis, the available derivatization methods of these species are presented for each CWA highlighting some examples from our lab in the Forensic Science Center at the Lawrence Livermore National Laboratory.

Assessing the reliability of the NIST library during routine GC-MS analyses: Structure and spectral data corroboration for 5,5-diphenyl-1,3-dioxolan-4-one during a recent OPCW proficiency test.

Revision of the NIST library spectrum for the compound 5,5-diphenyl-1,3-dioxolan-4-one is presented. After the synthesis and characterization (by NMR and MS) of 5,5-diphenyl-1,3-dioxolan-4-one, it was found that its mass spectral data did not match the one found in the NIST database. Herein, we present a revised version of the spectrum corresponding to the material and a comparative analysis to the previously published data.

Rhodotorula taiwanensis MD1149 produces hypoacetylated PEFA compounds with increased surface activity compared to Rhodotorula babjevae MD1169

Biosurfactants have several desirable characteristics in the industrial sector: detergency, antimicrobial effects, skin hydration, and emulsibility. Several yeast glycolipids are currently being utilized in these capacities: sophorolipids, ustilagic acid, and mannosylerythritol lipids (MELs). An emerging class of glycolipids, termed polyol esters of fatty acids (PEFA), have recently been reported for Rhodotorula babjevae, a basidiomycetous yeast species that secretes hyperacetylated congeners of PEFA (typically with 3–6 acetylation modifications). While screening Rhodotorula species for surfactant production, we identified a new environmental isolate identified as Rhodotorula taiwanensis MD1149 that dropped the surface tension of the liquid medium, indicating that it produced a potent biosurfactant. Acid depolymerization of the purified biosurfactants, followed by gas chromatography-mass spectrometry (GC-MS) analysis revealed that the biosurfactants were composed of PEFA compounds composed mainly of mannitol and arabitol esters of 3-hydroxy fatty acid, 3-methoxy fatty acid, and fatty acids with a single double bond; chain lengths were mainly C16 and C18. Liquid chromatography-mass spectrometry (LC-MS) confirmed the predicted accurate mass of these compounds. Interestingly, PEFA compounds produced by Rhodotorula taiwanensis MD1149 were more surface active due to their hypoacetylation profile (0–4 acetylation modifications) compared to Rhodotorula babjevae MD1169. These disparate surface active properties, based on acetylation, change the hydrophilic-lipophilic balance (HLB) of these compounds, and their potential utility within industrial applications.

Efficient derivatization of methylphosphonic and aminoethylsulfonic acids related to nerve agents simultaneously in soils using trimethyloxonium tetrafluoroborate for their enhanced, qualitative detection and identification by EI-GC–MS and GC–FPD

Trimethyloxonium tetrafluoroborate (TMO·BF4) has been used in the simultaneous derivatization of phosphonic and 2-aminoethylsulfonic acids related to nerve agents in different soils for their enhanced detection and identification by electron ionization gas chromatography-mass spectrometry (EI-GC-MS). The panel of acids consisted of five Schedule 2 phosphonic acids (methyl methylphosphonic acid, ethyl methylphosphonic acid, isopropyl methylphosphonic acid, pinacolyl methylphosphonic acid and cyclohexyl methylphosphonic acid) along with two sulfonic acids, N,N-diethyl-2-aminoethylsulfonic acid and N,N-diisopropyl-2-aminoethylsulfonic acid. The acids were converted to their corresponding methyl esters at ambient temperature when present at a 10μgg-1 concentration in three separate soils: Virginia type A soil, Ottawa sand and Nebraska EPA soil. The concentration of the acids reflects values typically encountered during proficiency tests (PTs) administered annually by the Organisation for the Prohibition of Chemical Weapons (OPCW). Derivatization times to yield detectable signals for the methyl ester products for all the acids was found to vary among all three soil samples, however, it was found that generally the most optimal time across all the matrices involved was 3h after the addition of TMO·BF4. Concomitantly, the analysis of the samples was complemented using GC coupled to flame photometric detection (GC-FPD). The inclusion of GC-FPD in the analysis yielded stronger signals for all seven methylated analytes making their detection after merely 3h possible relative to the ones initially obtained with EI-GC-MS. Regarding the three soils employed in our study, a greater methylating efficiency was found in the Virginia type A soil and Ottawa sand yielding results that were significantly larger in magnitude to those found during the same time points for the Nebraska EPA soil sample. Prolonged reaction times (up to 72h) were explored to find the time for the highest yield of methyl ester production were found instead to be deleterious to the process showcasing the importance of the fast yielding nature of the process specifically in situations where time-sensitive analysis is crucial (e.g. OPCW-PT).