Search results for "METHANE"
showing 10 items of 1763 documents
SPECTROSCOPY AND NON-EQUILIBRIUM DISTRIBUTION OF VIBRATIONALLY EXCITED METHANE IN A SUPERSONIC JET
1998
Abstract High-resolution spectra of supersonic jets of vibrationally excited methane have been recorded by diode laser in the 8 μm region. A formalism for the description of energy distribution is proposed. It allows to estimate populations of vibrational polyads. Under these non-equilibrium conditions, translational temperature is also measured from line profiles. For relaxation, it is shown that vibrational relaxation between polyads is negligible whereas strong redistribution of population arises inside each polyad. Spectroscopically, observed lines involving the first four excited polyads allows cross-checked tests for energy level analysis.
N-Alkyl Ammonium Resorcinarene Salts as High-Affinity Tetravalent Chloride Receptors.
2016
N-Alkyl ammonium resorcinarene salts (NARYs, Y=triflate, picrate, nitrate, trifluoroacetates and NARBr) as tetravalent receptors, are shown to have a strong affinity for chlorides. The high affinity for chlorides was confirmed from a multitude of exchange experiments in solution (NMR and UV/Vis), gas phase (mass spectrometry), and solid-state (X-ray crystallography). A new tetra-iodide resorcinarene salt (NARI) was isolated and fully characterized from exchange experiments in the solid-state. Competition experiments with a known monovalent bis-urea receptor (5) with strong affinity for chloride, reveals these receptors to have a much higher affinity for the first two chlorides, a similar af…
Methane and leachate pollutant emission potential from various fractions of municipal solid waste (MSW): effects of source separation and aerobic tre…
2002
The effects of source-separation of putrescibles as well as aerobic pre-treatment and landfill aeration on the pollutant emission potential of methane and leachate pollutants were studied in the fresh (PFMSW) and composted (CPFMSW) source-separated putrescible fraction of municipal solid waste, and in the grey waste, and in lysimeter landfilled grey waste and ten-year-old unsorted MSW from our landfill lysimeter study. After 0, 23 and 51 days, an aerobic lysimeter experiment, an elution test and biochemical methane potential (BMP) test was done on samples. PFMSW had high methane (CH4) potential (410 m3CH4 t-1TS) as well as a high amount of ammonium-nitrogen (3.6 kg NH4-N) was eluted, where…
Die vielfältigen additionsprodukte von phenylen-, naphthylen-, biphenylylen- und methylendiphenylendimethacrylaten mit radikalen aus 2,2'-azoisobutyr…
1976
Die Reaktionen von Phenylen-, Naphthylen-, Biphenylylen- und Methylendiphenylendimethacrylaten (1–4) wurden teils mit 2,2'-Azoisobutyronitril (AIBN) in Substanz oder anionisch in Losung mit Butyllithium oder Natriumdihydronaphthylid (Naphthalinnatrium), teils mit grosem Uberschus an AIBN stark verdunnt in siedendem Benzol durchgefuhrt. Neben unloslichen (vernetzten) Polymeren wurden losliche erhalten, darunter Cyclopolymere vom Typ 9, wie die Ergebnisse der Hydrolyse und anschliesende Umsetzung mit Diazomethan zu Poly(methacrylsaure-methylester)n zeigten. Die Verdunnungsreaktion ergab die Produkte 5 der unterdruckten Polymerisation, der innermolekularen Addition mit Kopf/Schwanz- und Schwan…
Synthesis and characterization of optically active 2,4-disubstituted-2-oxazolines and their polymerization
1994
Four different optically active 2,4-disubstituted-2-oxazolines were synthesized and characterized. Cationic polymerization of these oxazolines were studied. Three of the oxazolines could be polymerized using methyl trifluoromethanesulfonate as initiator. S-(–)-2-Phenyl-4-isopropyl-2-oxazoline could not be polymerized under the conditions used.
Poly(THF-co-cyano ethylene oxide): Cyano Ethylene Oxide (CEO) Copolymerization with THF Leading to Multifunctional and Water-Soluble PolyTHF Polyelec…
2016
Cyano-functional polyether copolymers based on THF were prepared via cationic ring-opening copolymerization of THF with cyano ethylene oxide (CEO). The CEO content of poly(tetrahydrofuran) (polyTHF) based copolymers varied from 3.3 to 29.3%, and molecular weights ranged from 5100 to 31900 g·mol–1 with Mw/Mn in the range of 1.31 to 1.74 (SEC in THF, PS standards). The polymerization was conducted with methyl trifluoromethanesulfonate (MeOTf) as an initiator. Kinetic studies concerning incorporation of both monomers were performed via NMR spectroscopy. The cyano groups at the poly(THF-co-CEO) copolymers enable direct access to amino (polyTHF–NH2) and carboxyl groups (polyTHF–COOH) in facile o…
Simultaneous application of vacuum and sweep gas in a polypropylene membrane contactor for the recovery of dissolved methane from water
2021
Abstract Vacuum and nitrogen as sweep gas were used simultaneously (combination mode) to generate the driving force in a microporous polypropylene membrane contactor for the recovery of dissolved methane from water. Experiments were carried out under different liquid flow-rates (5.0–28.0 L h−1), N2 flow-rates (0.5–1.5 L h−1) and vacuum pressures (0–480 mbar). The maximum removal efficiency of methane was >90% at moderate values of gas-to-liquid ratios (G/L) and vacuum of 0.2 and ≤ 200 mbar, respectively. Removal efficiencies obtained in combination mode were usually higher than when using vacuum or sweep gas, separately. To achieve a methane content >35% in the recovered gas, G/L values low…
Recovery of dissolved methane through a flat sheet module with PDMS, PP, and PVDF membranes
2022
Abstract A degassing contactor using a flat sheet membrane module (FM) was operated in sweep gas mode to study the performance of several commercial polymer membranes, both dense (polydimethylsiloxane, PDMS) and microporous (polypropylene, PP, and polyvinylidenefluoride, PVDF), for the recovery of dissolved methane from water. Non-steady state experiments were conducted at different liquid (QL, 3.5–40.5 L h-1) and gas flow rates (QN2, 0.05–15.00 L h-1). In the case of PDMS, PP, and when PVDF was operated at moderate high QL (≥ 21 L h-1), similar methane removal efficiencies (RE) were obtained. In the case of PVDF operated at relatively low QL (3.5 L h-1), a lower RE was observed. A model fo…
Multiconfigurational second-order perturbation study of the decomposition of the radical anion of nitromethane
2004
The doublet potential energy surfaces involved in the decomposition of the nitromethane radical anion (CH(3)NO(2) (-)) have been studied by using the multistate extension of the multiconfigurational second-order perturbation method (MS-CASPT2) in conjunction with large atomic natural orbital-type basis sets. A very low energy barrier is found for the decomposition reaction: CH(3)NO(2) (-)--[CH(3)NO(2)](-)--CH(3)+NO(2) (-). No evidence has been obtained on the existence of an isomerization channel leading to the initial formation of the methylnitrite anion (CH(3)ONO(-)) which, in a subsequent reaction, would yield nitric oxide (NO). In contrast, it is suggested that NO is formed through the …
Hydrogen and methane yields of untreated, water-extracted and acid (HCl) treated maize in one- and two-stage batch assays
2011
Abstract In the present study, two-stage H 2 and CH 4 production was compared with one-stage CH 4 production from maize subjected to water extraction and acid (HCl) treatment. In addition, the effect of duration (2 and 14 days) of the first-stage H 2 process on the H 2 yields and subsequent CH 4 yields from the second-stage was also investigated. Results showed that the average H 2 yields from untreated maize were 5.6 and 9.9 ml/g volatile solids added (VS added ) after 2 and 14 days, respectively. On the other hand, H 2 yields from water-extracted and HCl-treated maize were 18.0 and 20.5 ml/gVS added (14 d), respectively. On comparison to one-stage CH 4 assays, the average increase in CH 4…