ライフサイエンスコーパス: pyrolysis

1 synthesised from sodium alginate via furnace pyrolysis.

2 rete Sb-SnO2 islands, were prepared by spray pyrolysis.

3 ime by ultrasonic atomization-assisted spray pyrolysis.

4 completely overcome after 10 min of reactive pyrolysis.

5 l and thus to be accessible via flash vacuum pyrolysis.

6 housand,) with that of the CH3Cl released on pyrolysis.

7 e development of catalysts in catalytic fast pyrolysis.

8 a novel synthetic route based on flame spray pyrolysis.

9 tions, and energy balances from biomass slow pyrolysis.

10 anted in it by PANI/mesoporous silica during pyrolysis.

11 rrier to inhibit the Fe agglomeration during pyrolysis.

12 DMS-decorated carbon networks via a one-step pyrolysis.

13 nusual combination of mechano-plasticity and pyrolysis.

14 ic network was investigated using analytical pyrolysis.

15 n method that appeals to this application is pyrolysis.

16 ramolecular precursor followed by controlled pyrolysis.

17 l contact with the N and C precursors during pyrolysis.

18 llowed by adsorption of furfuryl alcohol and pyrolysis.

19 Dimethyl ether pyrolysis (2% CH3OCH3/Ar) was observed behind the reflec

20 Post-pyrolysis air oxidation (PPAO) at 400 degrees C of anoxi

21 ns were determined applying 800 degrees C of pyrolysis and 1800 degrees C of atomization temperatures

22 ough postsynthetic modification, followed by pyrolysis and acid leaching.

23 The method was optimized by building up pyrolysis and atomization curves in sample medium and by

24 simulate thermochemical conversion via fast pyrolysis and catalytic upgrading of bio-oil to renewabl

25 ly, N-CDs were prepared from L-asparagine by pyrolysis and characterized by different spectroscopic a

26 ied rice straw (Ms) were prepared by ashing, pyrolysis and citric acid modification, respectively, an

27 ion) and haloketone formation (increased for pyrolysis and decreased for oxidation).

28 nt and speciation in biochars generated from pyrolysis and gasification of oak and corn stover were d

29 or haloacetonitrile formation (unchanged for pyrolysis and increased for oxidation) and haloketone fo

30 ture, was found to be a breakdown product of pyrolysis and not part of the nanostructure.

31 ng a thermal separation probe to perform the pyrolysis and sample introduction.

32 re fabricated via two-photon lithography and pyrolysis and shown to reach the Hashin-Shtrikman and Su

33 d chitosan-ruthenium-silica mesophase before pyrolysis and silica removal.

34 ciation in chars derived from thermal (i.e., pyrolysis) and hydrothermal treatments of municipal sewa

35 unburned and burned detritus under hypoxic (pyrolysis) and oxic conditions (thermal oxidation) at 25

36 ssions, food production and industries, coal pyrolysis, and various biological activities).

37 tensity (CI) to more accurately characterize pyrolysis, and we document variation in charcoal chemica

38 ng devices can be equivalent to a laboratory pyrolysis apparatus, the potential for unexpected chemis

39 and structure-controllable ultrasonic spray pyrolysis approach using energetic carbon precursors.

40 Metal-nitrogen-carbon materials prepared via pyrolysis are promising single-atom catalysts but often

41 features down to 200 mum are obtained after pyrolysis at 1000 degrees C in a nitrogen atmosphere.

42 and short-chain polyphosphates formed after pyrolysis at 250-600 degrees C.

43 ; uncertainties represent 1 SD), mainly coal pyrolysis at low temperature ( approximately 650 degrees

44 As such, this study has assessed the pyrolysis behaviour of PV cells and has indicated the en

45 te and separate high-value alkylphenols from pyrolysis bio-oil, produced directly from lignocellulosi

46 By applying this procedure to pyrolysis bio-oil, the primary products (phenol/4-alkylp

47 but much shorter heating durations than slow-pyrolysis biochars, resulting in differing physicochemic

48 rbon sequestration potentials than most slow-pyrolysis biochars.

49 Additionally, typical literature known pyrolysis biomass marker were confirmed by their element

50 chanisms (Maillard reaction, caramelisation, pyrolysis) by which they were formed.

51 (the carbon-rich solid formed during biomass pyrolysis) can provide carbon-negative bioenergy if the

52 Here, a ramped pyrolysis carbon isotope technique is employed to invest

53 n comparing the different use options of the pyrolysis char, the most favorable result is obtained fo

54 Pyrolysis combustion flow calorimetry reveals that these

55 g biomass conversion technologies (microwave pyrolysis, combustion, wet lipid extraction, and hydroth

56 rder of magnitude higher for low temperature pyrolysis compared to high temperature combustion.

57 with classical methods for polymer analysis, pyrolysis-comprehensive two-dimensional gas chromatograp

58 from different feedstock and over a range of pyrolysis conditions are redox-active and reversibly acc

59 Biochars produced under pyrolysis conditions at 500-600 degrees C contain sulfat

60 x properties of chars formed under different pyrolysis conditions has been performed.

61 ns, implying considerable latitude to choose pyrolysis conditions to optimize for desired biochar pro

62 tion temperature is often used as a gauge of pyrolysis conditions, pyrolysis duration also changes ch

63 and wood) under wildfire charring- and slow-pyrolysis conditions.

64 arrier accessible under typical flash vacuum pyrolysis conditions.

65 ood on glowing embers, that is, slow burning pyrolysis conditions.

66 ple, under matrix photolysis or flash vacuum pyrolysis conditions.

67 marily when the enzyme is activated prior to pyrolysis, consistent with increased lignin degradation

68 However bio-oil from fast pyrolysis contains a large amount of oxygen, distributed

69 ded quantitatively either under flash vacuum pyrolysis, conventional heating, or microwave irradiatio

70 High-temperature pyrolysis conversion of organic analytes to H(2) in hydr

71 Overall, these results suggest that soil pyrolysis could be a viable thermal treatment to quickly

72 raction followed by double-shot microfurnace pyrolysis coupled to gas chromatography mass spectrometr

73 IS) for lignin quantification via analytical pyrolysis coupled to gas chromatography with mass-spectr

74 A combination of flash pyrolysis coupled with gas chromatography mass spectrome

75 fingerprint of the colloids was obtained by pyrolysis coupled with gas chromatography-mass spectrome

76 th carbon isotope values generated by online pyrolysis (delta(13)C(pyr)) to characterize and quantify

77 sotope signature of AEOs generated by online pyrolysis (delta(13)Cpyr), natural abundance radiocarbon

78 I and GHG emissions (gCO2e/MJ-fuel) for fast pyrolysis derived fuels range from 1.52 to 2.56 and 22.5

79 formance and GHG reduction potential of fast pyrolysis-derived fuels are highly sensitive to the choi

80 ten used as a gauge of pyrolysis conditions, pyrolysis duration also changes charcoal physicochemical

81 etene curcumin is formed as a consequence of pyrolysis during common household cooking, showing stron

82 ger sized mode dominating under slow burning pyrolysis (Dva approximately 600 nm).

83 forded 3-styrylindazole 58, which on further pyrolysis eliminated N2 to generate 3- and 2-phenylinden

84 Via flash vacuum pyrolysis, even metaparacyclophanes as small and straine

85 e second measures gas yields from laboratory pyrolysis experiments on core samples.

86 Although the different steps (extraction and pyrolysis) fractionate between (12)C and (13)C, the isot

87 atoms per nm(2) ) are prepared via a facile pyrolysis-free route involving a one-step ball milling o

88 s of 44 using the falling solid flash vacuum pyrolysis (FS-FVP) method afforded cyclopenta[def]phenan

89 drazone using the falling solid flash vacuum pyrolysis (FS-FVP) method.

90 were generated by falling solid flash vacuum pyrolysis (FS-FVP).

91 cm(-1) by a combination of mild flash vacuum pyrolysis (FVP) at 200-600 degrees C with low temperatur

92 Flash vacuum pyrolysis (FVP) of 1-(5-(13)C-5-tetrazolyl)isoquinoline

93 Flash vacuum pyrolysis (FVP) of azides is an extremely valuable metho

94 Both photolysis and flash vacuum pyrolysis (FVP) of tetrazoles (1/5) are known to generat

95 1,5-a]quinoline by conventional flash vacuum pyrolysis (FVP) were observed by IR spectroscopy.

96 luable soil amendment as well as bio-oil and pyrolysis gas (py-gas) that can be used for energy.

97 techniques used in SOPs identification, like pyrolysis gas chromatography mass spectrometry (Py-GC/MS

98 Often pyrolysis gas chromatography mass spectrometry has been

99 tion, and quantitative analysis method using pyrolysis gas chromatography mass spectrometry to improv

100 Pyrolysis gas chromatography/mass spectrometry (Py-GC-MS

101 A novel analytical approach based on pyrolysis-gas chromatography coupled with mass spectrome

102 In this study Curie-Point pyrolysis-gas chromatography-mass spectrometry combined

103 Samples were analyzed using pyrolysis-gas chromatography-mass spectrometry with in s

104 The find was analyzed using pyrolysis-gas chromatography-mass spectrometry, X-ray mi

105 y chemical characterisation using whole-rock pyrolysis-gas chromatography-mass spectrometry.

106 was analysed using elemental analysis (EA), pyrolysis-gas chromatography/flame ionisation detection

107 aphy/flame ionisation detection (Py-GC/FID), pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS

108 rm infrared microspectroscopy (mu-FTIR), and pyrolysis-gas chromatography/mass spectrometry (pyr-GC/M

109 at affected lignin chemistry on the basis of pyrolysis-gas chromatography/mass spectrometry analysis.

110 the WEOM chemical composition, measured with pyrolysis-gas chromatography/mass spectrometry, this bei

111 zation was performed by CLSM, AFM, ATR-FTIR, pyrolysis GC-MS, and ICP-MS techniques.

112 Pyrolysis-GC-MS analysis showed more reduction in the le

113 nd Raman spectroscopy) and complimented with pyrolysis-GC-MS, while the colour changes were evaluated

114 state-of-the-art methods, such as TGA-MS and pyrolysis-GC.

115 By using a novel quantitative pyrolysis-GC/MS analysis for rubber polymer, we detected

116 Pyrolysis-GC/MS and 2D-NMR analysis of P. radiata TE cul

117 ds were identified in TEs by thioacidolysis, pyrolysis-GC/MS and/or 2D-NMR in CCR-RNAi lines, providi

118 into transportation fuels via catalytic fast pyrolysis has attracted much attention.

119 ss, metal, semiconductor and polymer layers; pyrolysis has potential not to promote chemical oxidatio

120 ow the use of sequential high-pressure water pyrolysis (HPWP) to replicate petroleum generation and e

121 iate that was generated by high-vacuum flash pyrolysis (HVFP) of the corresponding p-tosylhydrazone s

122 ning chemical components into SO2 by thermal pyrolysis in a high temperature furnace at atmospheric p

123 e)4 with ammonia followed by low-temperature pyrolysis in ammonia.

124 biose were synthesized and subjected to fast pyrolysis in an atmospheric pressure chemical ionization

125 and post exposure bake settings followed by pyrolysis in an inert environment.

126 Wastewater biosolids pyrolysis is a promising technology that could help faci

127 Carbon pyrolysis is a widespread method for synthesizing carbon

128 n of bio-oil recovered from corn stover fast pyrolysis is blended and co-fired with bituminous coal t

129 chanisms possibly involved in cellulose fast pyrolysis is challenging.

130 omposed of uranium oxide using aerosol spray pyrolysis is characterized with respect to the various p

131 Pyrolysis is indispensable for synthesizing highly activ

132 t carbohydrate product of cellulosic biomass pyrolysis is the anhydrosugar levoglucosan (1,6-anhydro-

133 otein synthesis (MPS) via gas chromatography-pyrolysis-isotope ratio mass spectrometry.

134 mporally quantify MPS via gas chromatography:pyrolysis:isotope ratio mass spectrometer.

135 Further pyrolysis leads to complex ceramic structures that are o

136 rocarbons (PAHs) was not observed, with post-pyrolysis levels well below applicable standards.

137 ectrometry (FT-ICR-MS) for the analysis of a pyrolysis liquid from brown coal.

138 Pyrolysis liquids from coal are complex mixtures of orga

139 regarding high-molecular-weight compounds in pyrolysis liquids, although their characterization is im

140 tional liquid chromatography-based analyses, pyrolysis mass spectrometry achieved at least 250-fold h

141 dification, thermal drying, incineration and pyrolysis may decrease NH3 (9-11%) and GHG (11-18%) emis

142 gn a gradient electrospinning and controlled pyrolysis method to synthesize various controllable 1D n

143 article were synthesized using a flame spray pyrolysis method.

144 our composition gradient electrospinning and pyrolysis methodology may lead to further developments i

145 ant inbred maize (Zea mays) population using pyrolysis molecular-beam mass spectrometry to establish

146 Flash vacuum pyrolysis of 1,3-bis-iodomethyl-benzene (m-C8H8I2) produ

147 loss are the predominant reactions for fast pyrolysis of 1,6-anhydrocellodextrins; and 5) HAGBC can

148 Similar pyrolysis of 2-phenyl-5-styryltetrazole 43 afforded 3-st

149 Flash vacuum pyrolysis of 44 using the falling solid flash vacuum pyr

150 (N-C-CoO(x) ) was created through the direct pyrolysis of a metal-organic complex with a NaCl templat

151 ere, we create these microstructures via the pyrolysis of a microporous polymer (PIM-1) under low con

152 g a scalable, one-step process involving the pyrolysis of a polyaniline aerogel synthesized in the pr

153 The solution-based pyrolysis of a series of heterobimetallic Schiff base co

154 orks codoped with nitrogen and phosphorus by pyrolysis of a supermolecular aggregate of self-assemble

155 hysical barriers during the condensation and pyrolysis of a titania precursor, preventing the titania

156 "PMCS") are successfully synthesized by the pyrolysis of an imidazolate framework using a mesoporous

157 Many studies related to catalytic fast pyrolysis of biomass have been published.

158 n the experimental studies on catalytic fast pyrolysis of biomass is also summarized with the emphasi

159 Fast pyrolysis of biomass is recognized as an efficient and f

160 g of short range ordered carbon derived from pyrolysis of biomass waste.

161 manipulation of the primary products of fast pyrolysis of carbohydrates.

162 first observation of graphitic cones in the pyrolysis of carbon.

163 drolysis was conclusively ruled out for fast pyrolysis of cellobiose, cellotriose, and 1,6-anhydrocel

164 The method was then used to examine fast pyrolysis of cellobiose.

165 and small molecules was predominant for the pyrolysis of cellulose.

166 provide insights into the mechanisms of fast pyrolysis of cellulose.

167 Through flash vacuum pyrolysis of CF3 S(O)NCO at ca. 1200 K, sulfinyl isocyan

168 methyl sulfide (DMS), was generated by flash pyrolysis of CH3SO2OOSO2CH3 and subsequently isolated in

169 developed by using simple microwave assisted pyrolysis of citric acid and sodium thiosulphate.

170 s are synthesized through controlled thermal pyrolysis of citric acid and urea.

171 ere synthesized using the one-step microwave pyrolysis of citric acid in the presence of diethylenetr

172 d graphene layers on alumina are obtained by pyrolysis of Co(OAc)2/phenanthroline.

173 cobalt-based catalysts have been prepared by pyrolysis of cobalt complexes with nitrogen ligands on d

174 Pyrolysis of contaminated soils at 420 degrees C convert

175 degrees C) microwave-assisted (MW-assisted) pyrolysis of DIR allows for simultaneously efficient fas

176 ared by a facile and scalable method through pyrolysis of electrospun polyimide.

177 tensity of ions from the aerosol produced by pyrolysis of ethyl cellulose are observed in the mass sp

178 esized by facile approach involving a direct pyrolysis of ferrous gluconate and a following removal o

179 e in high yields (up to 66%) by flash vacuum pyrolysis of FSO(2)N(3).

180 The pyrolysis of H4S was simulated with kinetic Monte Carlo

181 n a simple, scalable and two-step method via pyrolysis of iron acetate and phenanthroline and subsequ

182 rrent understanding of the chemistry in fast pyrolysis of lignocellulose and focuses on the developme

183 the characterization of aqueous phases from pyrolysis of lignocellulosic biomasses.

184 de (RDA/ICE) reaction under the flash-vacuum pyrolysis of maleic anhydride adducts is developed.

185 hether chloromethane (CH3Cl) detected during pyrolysis of Martian soils by the Viking and Curiosity M

186 duce stable molten metal alloy catalysts for pyrolysis of methane into hydrogen and carbon.

187 Pyrolysis of MOF-nanoparticle composites forms highly po

188 Finally, the controlled pyrolysis of MUV-3 results in a N-doped graphitic nanoco

189 of 3D graphitic carbon networks through the pyrolysis of nanosized ZIF-67 crystals.

190 Pyrolysis of nitrogen-ligated cobalt(II) acetate support

191 errestrial environment CH3Cl released during pyrolysis of organic matter derives from the methoxyl po

192 ay derive from the incomplete combustion and pyrolysis of organic matter.

193 former of dihydroxycarbene (1cc) by means of pyrolysis of oxalic acid, isolation of the lower-energy

194 own to 1.2 mum were fabricated by controlled pyrolysis of patterned photoresist.

195 oducing liquid transportation fuels via fast pyrolysis of perennial grasses: switchgrass and miscanth

196 orous graphitic carbon for iodine loading by pyrolysis of polyaniline coated cellulose wiper.

197 ed by high-temperature (up to 900 degrees C) pyrolysis of polyimide precursor hollow-fiber membranes.

198 synthesis of layered SiCN-MoS2 structure via pyrolysis of polysilazane functionalized MoS2 flakes.

199 Exothermic pyrolysis of refuse, which is hypothesized to be initiat

200 elatively slow rate of heating and prolonged pyrolysis of resinites using this new methodology, combi

201 d oxidized nitrogen-bearing compounds during pyrolysis of scooped aeolian sediments and drilled sedim

202 The pyrolysis of SiO(2)@MOF composite affords single-atom Fe

203 Upon flash vacuum pyrolysis of sulfinyl azide CF3S(O)N3 at 350 degrees C,

204 as sample (10% v/v H2S) that was produced by pyrolysis of sulfur-rich kerogen.

205 ) during low temperature (150-400 degrees C) pyrolysis of the carbonaceous chondrite Murchison with c

206 y influenced by the vitrification during the pyrolysis of the galvanic sludge.

207 es of copper, nickel and cobalt, followed by pyrolysis of the mixtures in an argon flow at 700 degree

208 Pyrolysis of the MOF-shell composites produces hollow ca

209 imethylsilylcyclobutylidene was generated by pyrolysis of the sodium salt of the tosylhydrazone deriv

210 Pyrolysis of these hybrid materials under nitrogen at 70

211 O, and other trace gases were evolved during pyrolysis of two mudstone samples acquired by the Curios

212 Additionally, the pyrolysis of vitamin E acetate also produces carcinogen

213 cycle assessment, the climate impact of the pyrolysis of woodchips in Stockholm is compared with two

214 The pyrolysis of woodchips produces heat and power for the c

215 har is the product of incomplete combustion (pyrolysis) of organic material.

216 be applied to various heterogenic combustion/pyrolysis or reaction model systems, such as fossil- or

217 Under flash vacuum pyrolysis or under microwave irradiation, 1-methyl- and

218 Here, we investigate its pyrolysis pathways by selecting n-heptane-4-sulfonic aci

219 isation of power is achieved, building a new pyrolysis plant becomes a better climate option than con

220 A fast-pyrolysis probe/tandem mass spectrometer combination was

221 ate and high temperature and a non-catalytic pyrolysis process are presented.

222 y nanojunction is synthesized using a simple pyrolysis process followed by a hydrothermal treatment.

223 out through a facile, one-step, solid-state pyrolysis process in an inert atmosphere.

224 s a green, environmentally friendly and mild pyrolysis process that improves the dimensional stabilit

225 A mechano-plastic pyrolysis process that overcomes this limitation is repo

226 A novel pyrolysis process using wastewater biosolids-derived bio

227 s using a two-step, diffusion-assisted spray pyrolysis process.

228 rm discotic liquid crystal phases during the pyrolysis process.

229 Dip coating and pyrolysis processes are used to create multi-layer asymm

230 ke of crack cocaine contains cocaine and its pyrolysis product, anhydroecgonine methyl ester (AEME).

231 lly increased the complete silylation of the pyrolysis products and the chromatographic resolution, r

232 For this purpose polymer characteristic pyrolysis products and their indicative fragment ions we

233 n increased fragmentation of ethyl cellulose pyrolysis products during ionization.

234 n was utilized to determine the initial fast-pyrolysis products for four different selectively (13)C-

235 tive response factors (RRFs) for the various pyrolysis products obtained were determined and applied.

236 ensitivity for the caffeine standard and the pyrolysis products of ethyl cellulose is maintained or i

237 To determine the true primary pyrolysis products, a very fast heating pyroprobe was co

238 eaction and facilitate the derivatization of pyrolysis products, by enabling the materials to react w

239 e of the noncannabinoid plant components and pyrolysis products, followed by a discussion of 3 synthe

240 r accounting for 3.9-44.5% of the quantified pyrolysis products.

241 etection of molecular ions of combustion and pyrolysis products.

242 ther accounting for 62-96% of all quantified pyrolysis products.

243 solids played an important role in upgrading pyrolysis products.

244 ty of the ionization methods to ionize known pyrolysis products: glycolaldehyde, hydroxyacetone, furf

245 Ramped pyrolysis profiles indicate that the organic material wa

246 apidly through a very hot oven (flash vacuum pyrolysis) promotes high-temperature thermal reactions i

247 4 mmol H2 g(-1) plastic was obtained for the pyrolysis-reforming of HDPE waste in the presence of the

248 show that hydrogen can be produced from the pyrolysis-reforming process, but also carbon nanotubes a

249 from waste plastics is reported here using a pyrolysis-reforming technology comprising a two-stage re

250 truction zones in the various combustion and pyrolysis regions of a cigarette during puffing.

251 cursors transform to ORR-active sites during pyrolysis remains unclear.

252 amine into an as-drawn CNT fiber followed by pyrolysis results in a direct insulation-to-conduction t

253 Ramped pyrolysis (RP) targets distinct components of soil and s

254 pping of a biochar produced from corn stover pyrolysis shows individual sulfur-containing mineral par

255 to avoid losses of Cl, Br, and I during the pyrolysis step, with concomitant use of Pd as a permanen

256 r and/or tarry deposits generated during the pyrolysis step.

257 Fast moving bed pyrolysis strategy ensures the mixed metal precursors ra

258 Herein, we present a fast moving bed pyrolysis strategy to immobilize HEA-NPs on granular sup

259 In this paper, a slow pyrolysis system for generating heat and biochar from li

260 on a glass substrate with the chemical spray pyrolysis technique.

261 By regulating the thermal-pyrolysis temperature and ratio of reactants, the maximu

262 genic carbon to a lesser extent with greater pyrolysis temperature due to lower charging and discharg

263 gth, 606.440nm in a graphite tube applying a pyrolysis temperature of 1000 degrees C and a molecule f

264 alladium+citric acid modifier and applying a pyrolysis temperature of 1000 degrees C and a volatilisa

265 After a pyrolysis temperature of 1100 degrees C, the pristine an

266 conditions were found to be 213.561nm with a pyrolysis temperature of 1300 degrees C, a volatilizatio

267 Under experimental conditions of pyrolysis temperature of 640 degrees C and atomization t

268 ernary-doped carbon (HQDC-X, X refers to the pyrolysis temperature) can be fabricated by directly pyr

269 ng three easily measured biochar parameters- pyrolysis temperature, H/C molar ratio, and %biochar yie

270 igher ionic strength and lower pH, and (iii) pyrolysis temperature-dependent: 500 < 700 << 300 degree

271 phate being less extractable with increasing pyrolysis temperature.

272 The use of pyrolysis-temperature-based or averaged emission profile

273 om corn stalk biochar produced at increasing pyrolysis temperatures (350-650 degrees C) and from the

274 n electrocatalysts (Ni-PACN) with a range of pyrolysis temperatures and Ni loadings and correlated th

275 ts degradation of the cellulosic fraction at pyrolysis temperatures of 250 degrees C, whereas at high

276 barriers of 74-82 kcal/mol, consistent with pyrolysis temperatures of 900 to 1100 degrees C.

277 ible applications include verifying declared pyrolysis temperatures of biochars and evaluating ecosys

278 way, and porosity of biochar are observed at pyrolysis temperatures ranging from 250 to 550 degrees C

279 In the presence of the clay, at lower pyrolysis temperatures, the biochar develops a higher po

280 Unlike most titania nanomaterials, during pyrolysis the NPs undergo no transition from the anatase

281 count of the use low-temperature MW-assisted pyrolysis to effect this change.

282 ination to form silica replicas or reductive pyrolysis to form electrically conductive carbon replica

283 nts (tetraphenylporphyrin, TPP), followed by pyrolysis to N-doped porous carbon supported SACs (M(1)/

284 1,2-azaborine, is generated by flash vacuum pyrolysis, trapped under cryogenic conditions, and studi

285 The loss or retention of isotope labels upon pyrolysis unambiguously revealed three major competing m

286 relevant for the mechanistic understanding, pyrolysis under flow conditions or in solution or the so

287 tain the cylindrical shape of bacteria after pyrolysis under high temperatures, while heteroatoms inc

288 confirmed in biochar produced by pilot plant pyrolysis units.

289 Low temperature pyrolysis upon fuel addition resulted in "tar-ball" type

290 l assembly technique called ultrasonic spray pyrolysis (USP).

291 The divergence between pyrolysis vapors and biochar in the distribution of WSOC

292 An empirical model of biomass slow pyrolysis was developed and applied to several pathways

293 that the carbonaceous material produced via pyrolysis was dispersed in the form of a layer coating t

294 adical chemistry with tar aerosols from wood pyrolysis was investigated in a flow reactor.

295 two-photon lithography and high-temperature pyrolysis, we have created micro-sized pyrolytic carbon

296 Compared to anhydrous pyrolysis where oil expulsion is limited, gas yields are

297 esizing Fe(1)(II)-N(4) sites via "noncontact pyrolysis" wherein the Fe precursor is not in physical c

298 that hydrocarbons are contributed by biomass pyrolysis, while abiotic sulfate (SO(4) (2-)) reduction

299 of different P species in the pyrochars from pyrolysis, with both total P and polyphosphate being les

300 Pyrolysis yielded an abundance of fragment ions (e.g., 1