コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 1,10-phenanthroline; pyr(3) = tris-2-pyridyl-methane).
2 es and subsequently activate the C-H bond of methane.
3 rs of groundwater aquifer contamination with methane.
4 photoelectrochemical CO(2) reduction toward methane.
5 mmonia due to its structural similarities to methane.
6 lakes known to contain bacteria that oxidize methane.
7 rial genomes, thus contributing to growth on methane.
8 Q, the diiron(IV) oxidant that hydroxylates methane.
9 their cooperative action converted CO(2) to methane.
10 d for syngas production via dry reforming of methane.
11 ed Ni/MgO catalysts for the dry reforming of methane.
12 out to simulate the benchmark combustion of methane.
13 denitrifiers could have used reduced iron or methane.
14 ic and chemical data in areas with microbial methane.
15 can influence decadal changes in atmospheric methane.
16 te the quantities and sources of groundwater methane.
17 inventories, may be a significant source of methane.
18 s the most efficient catalysts for producing methane.
19 and led to enrichment of (13) C in residual methane.
20 sary to attack the highly inert C-H bonds of methane.
21 or the reaction of Criegee intermediate with methane.
22 fied lakes, where they use oxygen to oxidize methane.
23 a circulation-induced enrichment of gaseous methane a few kilometres above Pluto's plains that favou
24 ve the potential to emit large quantities of methane, a potent greenhouse gas, as the Earth continues
25 to assemble a structural model of the potent methane-activating intermediate as a Pd(III) dimer with
29 (3) surfaces acts as a judicious oxidant for methane activation with mitigated CO(2) formation, even
30 genation, alkane and cycloalkane metathesis, methane activation, metathetic oxidation, CO(2) activati
34 e oxidation (n-DAMO), up to 85% of dissolved methane and more than 99% of nitrogen were removed in pa
37 tron spectroscopy showed that water added to methane and oxygen led to surface methoxy groups and acc
38 er column, but their responses to changes in methane and sulfate supplies remain poorly constrained.
39 one production, increases in the lifetime of methane, and increases in atmospheric aerosol production
41 xposure may affect microbial communities and methane- and sulfur-cycling gene abundances in Arctic ma
43 rogenotrophic pathway-from CO(2) and H(2) to methane-as the terminal step of microbial biomass degrad
46 phylococcus hominis yielded hydrogen, but no methane, authentifying observational data.Three patients
48 tion conditions and the isotopic labeling of methane by deuterium allow for an unambiguous identifica
49 oups of hydrocarbons are reviewed, including methane/C(2) hydrocarbons, normal alkanes, alkane isomer
50 centrations and stable isotope signatures of methane, carbon dioxide and nitrate and monitored microb
51 rrent density of (108 +/- 5) mA cm(-2) and a methane cathodic energy efficiency of 20% using a dilute
52 s (GHGs), but to what extent soil release of methane (CH(4) ) and nitrous oxide (N(2) O) may contribu
53 een shown to account for over half of annual methane (CH(4) ) emissions and can offset summer photosy
57 n and consumption of nitrous oxide (N(2) O), methane (CH(4) ), and carbon dioxide (CO(2) ) are affect
61 most effective C sinks of the biosphere, but methane (CH(4)) emissions can offset their climate cooli
64 idle wells, and ~63,000 active wells, whose methane (CH(4)) emissions remain largely unquantified at
65 e of storing a relatively high amount of dry methane (CH(4)) in the adsorbed phase are largely explor
70 and modelling simulations allow the study of methane (CH(4)) sources and sinks at any geographic loca
79 n the Permian Basin in Texas and New Mexico, methane columns showed maxima over regions with the high
80 y effective and thermally stable to catalyze methane combustion at low temperatures (<500 degrees C)
81 sponsible for the sudden rise of atmospheric methane concentration (XCH(4)) since 2007, but remains d
86 xide-rich ice and/or energetic processing of methane condensed on water ice grains in the cold, outer
87 AOM than sulfate reduction rates at in situ methane conditions were observed, making alternative ele
88 s underlying these results: eCO(2) increased methane-consuming microorganisms more strongly in soils
89 d (605 mL g(-1) VS(fed)) with 22.4% enhanced methane content for 30 mg L(-1) IONPs supplemented bioma
90 ulative enhancements in biomass, biogas, and methane content proffered a net rise of 98.63% in biomet
91 ts (C(2) H(6) /C(2) H(4) ) from conventional methane conversion have not been produced commercially o
94 nly supplies insights into the mechanisms of methane coupling reactions but also illustrates how the
95 ses to demonstrate the presence of a cryptic methane cycle in sulfate-reducing sediments from the con
97 s driven methane production drives a cryptic methane cycling and fuels AOM coupled to the reduction o
98 etary model, we find that pre-photosynthetic methane-cycling microbial ecosystems are much less produ
99 focuses on recent fundamental insights about methane dehydroaromatization (MDA) to benzene over ZSM-5
101 We present ice core isotopic measurements of methane (Delta(14)C, delta(13)C, and deltaD) from the la
104 emissions of greenhouse gases, in particular methane, due to the microbial anaerobic fermentation of
105 d to predict the production of total gas and methane during the fermentation periods, which showed go
107 Pluto is covered by numerous deposits of methane, either diluted in nitrogen or as methane-rich i
111 uction regions, often reporting results as a methane emission intensity (methane emitted as a percent
112 subsets of wells, can increase the lifecycle methane emission intensity by up to a factor of 2-3, bet
113 poral evolution of methane emissions and the methane emission intensity for a variety of well configu
114 letion flowbacks raise the average lifecycle methane emission intensity from 0.79 to 0.81% for flowba
117 ane emissions from a production site and the methane emission intensity would be expected to evolve o
118 atially and statistically analyze 598 direct methane emission measurements from abandoned oil and gas
124 sites will improve inventories and models of methane emissions and clarify pathways toward mitigation
125 oaches to accurately estimate facility-scale methane emissions and perform source attribution at subf
126 s used to estimate the temporal evolution of methane emissions and the methane emission intensity for
129 ts and find that lower-bound reported annual methane emissions averaged 22.1 Gg (-16.9, +19.5) betwee
131 apshots of methane emissions; however, total methane emissions from a production site and the methane
135 mission measurements in China and found high methane emissions from heavy-duty NGVs (90% higher than
138 cities have highlighted the contribution of methane emissions from natural gas distribution networks
139 64 northern California homes to (1) quantify methane emissions from natural gas leaks and incomplete
142 ace-based monitoring for annual reporting of methane emissions from point sources and suggest that fu
143 stry emissions could double by 2030, so that methane emissions from the charcoal industry could outco
144 contributes to uncertainty in inventories of methane emissions from the natural gas supply chain.
146 ate change mitigation, but a renewal of high methane emissions has been reported for these ecosystems
150 aks in U.S. distribution mains, resulting in methane emissions of 0.69 Tg/year (95% cr int: 0.25, 1.2
153 y not be an effective measure for mitigating methane emissions unless best management practices are i
154 und that the old peat contribution to annual methane emissions was large (~30%) compared to intact we
156 seems to be a suitable approach to decrease methane emissions, a relevant cleaner effect that may co
157 ia has the potential to significantly reduce methane emissions, it is unclear if enough farmland exis
159 studies have been instantaneous snapshots of methane emissions; however, total methane emissions from
160 ing results as a methane emission intensity (methane emitted as a percentage of natural gas produced
162 trument (TROPOMI) launched in 2017 that show methane enhancements over production regions in the Unit
164 ated from the formation of coproducts CO and methane, except for hydrogen activation on the Pt NPs.
165 e also find that the pair of CO(2) and C(1) (methane) exhibit a separate pattern of mutual isotopic e
169 y silicon photoelectrodes with an impressive methane Faradaic efficiency of up to 51%, leading to a d
172 on, chamber-measured net ecosystem exchange, methane fluxes) as well as experimental treatments (hete
173 that aqueous dissolution removed >95% of the methane from ~3.5 mm live oil droplets within 14.5 min,
176 signatures that may be useful indicators of methane gas migration, potentially from nearby coal seam
177 reas for the onboard storage of hydrogen and methane gas-alternatives to conventional fossil fuels.
178 ation of *CO to *CHO, a key intermediate for methane generation, compared to the competing step, C-C
179 e simplest Criegee intermediate CH(2)OO with methane has been performed using the density functional
183 cluster ions catalyze the transformation of methane in a gas-phase ion trap experiment via nonoxidat
184 erobic methanotrophic archaea (ANME) consume methane in marine sediments, limiting its release to the
185 less dramatic than previous observations of methane in other basins, it is more prominent than that
186 be an important driver of the conversion of methane in oxygen-limited lake systems and potentially u
187 e the dominant natural source of atmospheric methane in terrestrial and shallow-water areas; in deep-
189 ne resources require efficient conversion of methane into liquid chemicals, whereas an ambient select
191 entifying and quantifying where and how much methane is being released into the ocean remains a major
193 l region of Cthulhu, bright frost containing methane is observed coating crater rims and walls as wel
194 e/methane ratios around 5.3% and (13)C and D methane isotopic compositions around -40 and -240 per mi
195 mages caused by criteria air pollutants, and methane leakage from the natural gas infrastructure.
196 tude than the climate benefits, (3) reducing methane leakage rates from 2.3 to 2.0% increases the net
199 h by $1.1B-$1.4B, (4) although internalizing methane leakage, climate damages, and health damages in
201 ntal implications when gas components (e.g., methane, longer-chained hydrocarbons) dissolve into shal
202 trophs persisted for weeks in the absence of methane, making them a powerful marker for active as wel
203 he last two decades; an increasing number of methane measurements are being made with such systems as
204 sion of CO(2) to fuels and chemicals such as methane, methanol, and C(2+) hydrocarbons or syngas are
207 8 to August 2019, we collected 77 surveys of methane mixing ratios, covering a distance of about 6400
211 analogous to that of the methanotroph enzyme methane monooxygenase that activates methane at ambient
212 atically critical subunit of the particulate methane monooxygenase, the predominant methane oxidation
213 p in both of these processes is catalyzed by methane monooxygenase, which converts methane or ammonia
214 ave the ability to anaerobically oxidize non-methane multi-carbon alkanes such as ethane and n-butane
217 bon atoms for the nonoxidative conversion of methane on Fe(1) (C)SiO(2) and this surface process is i
218 zed by methane monooxygenase, which converts methane or ammonia into methanol or hydroxylamine, respe
219 anol, being electron rich and derivable from methane or CO(2), is a potentially renewable one-carbon
223 mox with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO) microorganisms, at a temperat
224 ox) with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO), up to 85% of dissolved metha
225 ble methane monooxygenase (sMMO) carries out methane oxidation at 4 degrees C and under ambient press
226 ic and anoxic incubations both showed active methane oxidation by a Methylobacter species, with anoxi
227 system for enhanced methanol productivity in methane oxidation by in situ generated hydrogen peroxide
230 NME-1 archaea and SRB, with the capacity for methane oxidation coupled to sulfate reduction, which is
231 performing high-rate (up to 72 muM day(-1) ) methane oxidation in the anoxic hypolimnion of the tempe
234 proof-of-concept, particularly for selective methane oxidation, hydrogen production, water splitting,
240 dustrial Holocene were 22 to 56 teragrams of methane per year (95% confidence interval), which is com
241 er national emissions of 1290 [1246-1342] Gg methane per year or 66% [64-69%] of current GHGI estimat
242 glacial warming were small (<19 teragrams of methane per year, 95% confidence interval) and argue aga
251 results suggest that methyl-compounds driven methane production drives a cryptic methane cycling and
252 0) = 2.1) and vegetated (Q(10) = 2.3) soils, methane production from both fresh and old carbon source
253 Surprisingly, the catalytic activity for methane production increased significantly after every r
254 e oils to ruminant mixed rations will reduce methane production increasing the formation of propionic
255 eration cycle, reaching more than double the methane production rate after eight regeneration cycles.
256 retreatment showed a progressive decrease in methane production rates and poor process stability, lea
257 based waste pretreatments also produced high methane production rates but with some process instabili
262 etween individual sites, with typical ethane/methane ratios around 5.3% and (13)C and D methane isoto
263 inetic isotope effects (KIEs) for the di-pai-methane rearrangement of benzobarrelene fit with statist
266 g, we estimate that 18-27 of the 23-31 Tg of methane released at the seafloor could have reached the
267 responses to potential large-scale seafloor methane releases in ways that provide insight for future
273 289-299] reported laboratory experiments on methane-saturated oil droplets under emulated deep-water
276 at abandoned wells remain the most uncertain methane source in the U.S. and become the most uncertain
278 Under these conditions, the excess amount of methane stored in the pores of Cr-soc-MOF-1 in the form
279 ](4+) (SD/Ag78a; dppm=bis-(diphenylphosphino)methane) that was synthesized through a one-pot reaction
280 nt enabled the direct selective oxidation of methane to dimethyl ether (DME) over Pt/Y(2) O(3) .
281 ts are selective in the direct conversion of methane to HCHO and CO (~94% selectivity with a HCHO/CO
283 ethanol produced in the partial oxidation of methane to methanol over Cu-SSZ-13 in a continuous-flow
287 to allow diffusion of hydrogen, oxygen, and methane to the catalyst active sites, while confining th
288 primarily occur at the depth of the sulfate-methane transition zone or underlying sediment respectiv
289 ones (upon reaction with CO(2) ) and then to methane (upon reaction with hydrogen), simultaneously re
292 o global warming gases of carbon dioxide and methane via dry reforming is environmentally crucial and
294 tion are complex mixtures including ammonia, methane, volatile organic compounds (VOC), and H(2)S.
296 , and warming by other greenhouse gases like methane was not a major factor, the mean surface tempera
297 text]) is an ice-like solid that forms from methane-water mixture under elevated-pressure and low-te
298 the highest activity and selectivity toward methane with an extremely high faradaic efficiency of ~6