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1 osed matrix cleanup minimizes fouling of the pyrolytic AAS platform, enables reliable reuse of SPE ca
2 n important precursor of this compound under pyrolytic and aqueous heating conditions.
3 ition to diamond starting at 50 GPa for both pyrolytic and polycrystalline graphite, we also record t
4 sed sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic source
5 ree of hydrogen and oxygen compared to other pyrolytic approaches and yields either nitrogen-doped or
6 anosecond timescales by shock compression of pyrolytic as well as polycrystalline graphite to pressur
7 ngly, CCR suppression substantially promoted pyrolytic breakdown of cell wall polysaccharides, a phen
8 r 10-20 cycles in H2SO4 on all materials but pyrolytic carbon (PyC).
9 l that simulates dynamic adsorption of H2 on pyrolytic carbon can reproduce many aspects of the exper
10              In this study, readily prepared pyrolytic carbon electrodes are explored in several powe
11 easily, and cheaply fabricated by depositing pyrolytic carbon into a quartz theta nanopipet.
12 of 1 nm curled graphene fragments within the pyrolytic carbon microstructure, the interactions among
13                             It consists of a pyrolytic carbon nanoelectrode obtained by chemical vapo
14                      The pores formed in the pyrolytic carbon nanoribbons range in size from sub-nano
15 crystals with multilayered graphitic carbon, pyrolytic carbon or inert metals have been obtained, but
16                                              Pyrolytic carbon provides an alternative to classic amor
17 s architectures of three-dimensional printed pyrolytic carbon shell reinforcements and electrodeposit
18 ature pyrolysis, we have created micro-sized pyrolytic carbon with a tensile strength of 1.60 +/- 0.5
19 with the electrolyte and another filled with pyrolytic carbon.
20 mally black silicon substrate with amorphous pyrolytic carbon.
21  in defining the structure and properties of pyrolytic carbons.
22                                     Coupling pyrolytic chemical transformation to mass transport and
23 ix regia seed pod was carried out in an N(2) pyrolytic condition with the primary objective of undert
24                                        Under pyrolytic conditions the acidity/basicity of Maillard re
25 the degradation of glucose was studied under pyrolytic conditions using excess sodium glycinate the r
26 mation of HMF and chlorinated products under pyrolytic conditions using glucose or sucrose and amino
27 ning 2,3-butanedione were investigated under pyrolytic conditions using glycine, sodium glycinate and
28         A kinetic analysis was performed for pyrolytic conditions, and benzene, toluene, and xylene w
29 ations of organic materials under controlled pyrolytic conditions, with the advantage of increasing t
30 iii) CD-MOF-derived materials prepared under pyrolytic conditions.
31  half to surface adsorption processes in the pyrolytic conversion of analytes to H2.
32 of pore size and porosity was observed after pyrolytic conversion of PIM-1 to CMS membranes, attribut
33 d nona-BDE profiles suggested photolysis and pyrolytic debromination of BDE-209 in the air samples.
34  carbon filling of one of the barrels by the pyrolytic decomposition of butane, followed by electrode
35  ab initio molecular simulations, we explore pyrolytic decomposition pathways of the most used precur
36 l as an additional peak corresponding to the pyrolytic dehydration product, 1-hexadecene.
37  a gap of less than 5 nm, fabricated via the pyrolytic deposition of carbon followed by the electroch
38 e harnessing a ring-contracting flash vacuum pyrolytic extrusion of sulfur dioxide from the respectiv
39                                              Pyrolytic fragmentation of about one-third of the analyt
40                 The delta(13)C values of the pyrolytic fragments (CO, CH4, C2H4) are shown to be high
41                                     Ideally, pyrolytic fragments will originate from unique sites wit
42 ic graphene oxide (PGO) and hydrogen-reduced pyrolytic graphene oxide (HPGO).
43 method is used to treat graphite oxide (GO), pyrolytic graphene oxide (PGO) and hydrogen-reduced pyro
44 cken liver sulfite oxidase (SO) bound at the pyrolytic graphite "edge" or modified gold electrodes sh
45 sembly at the 1-phenyloctane/highly oriented pyrolytic graphite (1-PO/HOPG) interface.
46 on of HLM directly onto polished basal plane pyrolytic graphite (BPG), edge plane pyrolytic graphite
47 plane pyrolytic graphite (EPPG), basal plane pyrolytic graphite (BPPG), and the basal surface of high
48  capsulatus was immobilized on an edge-plane pyrolytic graphite (EPG) electrode to construct a hypoxa
49 l plane pyrolytic graphite (BPG), edge plane pyrolytic graphite (EPG), glassy carbon (GC), or high-pu
50 lline boron-doped diamond (pBDD), edge plane pyrolytic graphite (EPPG), basal plane pyrolytic graphit
51 butanol/hexane solution onto highly oriented pyrolytic graphite (HOPG) and carbon-coated Si(100) spon
52 te polymer film formation on highly oriented pyrolytic graphite (HOPG) and chemically modified HOPG.
53 ectroactivity of basal plane highly oriented pyrolytic graphite (HOPG) and two types of aluminum allo
54 lfonate (AQDS) is studied on highly oriented pyrolytic graphite (HOPG) as a model sp(2) surface.
55 rphyrin (CoOEP) supported on highly oriented pyrolytic graphite (HOPG) at the phenyloctane/CoOEP/HOPG
56 at airborne contamination of highly oriented pyrolytic graphite (HOPG) causes the nonideal asymmetry
57  These molecules assemble on highly oriented pyrolytic graphite (HOPG) from aqueous solutions to form
58                              Highly oriented pyrolytic graphite (HOPG) is an important electrode mate
59 structure of 1-octadecanol on highly ordered pyrolytic graphite (HOPG) is observed.
60 methylammonium (FcTMA(+)) at highly oriented pyrolytic graphite (HOPG) is used as a model system to d
61 ials, aluminum and highly oriented (ordered) pyrolytic graphite (HOPG) never before used for this pur
62 e sample of interest and of a highly ordered pyrolytic graphite (HOPG) reference sample, was reviewed
63 hyrin oligomer adsorbed on a highly oriented pyrolytic graphite (HOPG) substrate.
64 HBC-solvent dispersion and a highly oriented pyrolytic graphite (HOPG) substrate.
65 Ru(3)(CO)(12) precursor on a highly oriented pyrolytic graphite (HOPG) surface modified with one-atom
66  on five different grades of highly oriented pyrolytic graphite (HOPG) that vary in step-edge height
67 adgroups can be assembled on highly oriented pyrolytic graphite (HOPG) to generate nanometer-resoluti
68 G), and the basal surface of highly oriented pyrolytic graphite (HOPG), encompassing five distinct gr
69 as also been imaged at "aged" highly ordered pyrolytic graphite (HOPG), where apparently enhanced ele
70 and GO are similar to that of highly ordered pyrolytic graphite (HOPG), which has no band-gap.
71 tane and covalently modified highly-oriented pyrolytic graphite (HOPG).
72 t" on mica and "flat" on the highly oriented pyrolytic graphite (HOPG).
73 elmy plate measurements using highly ordered pyrolytic graphite (HOPG).
74 lti-walled carbon nano tube (MWCNT) modified pyrolytic graphite (MPG) electrode is prepared and appli
75 o a dense gold nanoparticle (AuNP) film on a pyrolytic graphite (PG) electrode.
76                       Films were prepared on pyrolytic graphite (PG) electrodes by casting mixtures o
77 abolism of styrene using DNA/enzyme films on pyrolytic graphite (PG) electrodes monitored via Ru(bpy)
78 [PVP-Ru(bpy)2(2+), bpy = 2,2'-bipyridine] on pyrolytic graphite (PG) electrodes were evaluated for th
79 taining DNA and N-acetyltransferase (NAT) on pyrolytic graphite (PG) electrodes.
80  force microscopy (AFM) at a highly oriented pyrolytic graphite and voltammetry at a glassy carbon el
81 cene derivatives adsorbed at highly oriented pyrolytic graphite as simple models.
82 ricated by forming the wells on a conductive pyrolytic graphite chip (1 in. x 1 in.) with a single co
83 orests were grown in printed microwells on a pyrolytic graphite detection chip and decorated with cap
84 nticipated Fe(II/III) couple only, PFV using pyrolytic graphite edge (PGE) electrodes demonstrates th
85 me bacterial enzyme were immobilized on both pyrolytic graphite edge and alkanethiol-modified Au elec
86                  Hydrogenase was adsorbed to pyrolytic graphite edge and carbon felt electrodes.
87 nolayers of the bacterial diheme enzyme at a pyrolytic graphite edge electrode give catalytic, reduct
88 tammetry (PFV) with the enzyme adsorbed at a pyrolytic graphite edge electrode.
89 nsitive voltammetric method using edge plane pyrolytic graphite electrode (EPPGE) as a novel sensor i
90 idation of 5-hydroxytryptophan (5-HTPP) at a pyrolytic graphite electrode at pH 7.5, two quasi-revers
91 n electrochemically oxidized highly oriented pyrolytic graphite electrode or a graphene oxide suspens
92 reduction currents produced at an edge-plane pyrolytic graphite electrode was diagnosed analytically
93 ous incubation of tobacco peroxidase and the pyrolytic graphite electrode with the cross-coupling rea
94 catalyze O(2) reduction when adsorbed onto a pyrolytic graphite electrode.
95 -pyrenebutyric acid frameworks on edge plane pyrolytic graphite electrodes (PGE/MWNT/Py) to which an
96  showed reversible FeIII/FeII voltammetry on pyrolytic graphite electrodes and catalytic current for
97 plet deposits of DDPD in HDOP at basal plane pyrolytic graphite electrodes are studied by voltammetri
98 ive films were grown layer by layer on rough pyrolytic graphite electrodes featuring 4-nm underlayers
99 llopolymers were assembled layer by layer on pyrolytic graphite electrodes to make sensors that selec
100 can be covalently attached to functionalized pyrolytic graphite electrodes using peptidic coupling.
101       In vivo damaged DNA was immobilized on pyrolytic graphite electrodes using the layer-by-layer (
102 ons and double-stranded (ds)-DNA on oxidized pyrolytic graphite electrodes was evaluated for detectio
103      Cross-linked myoglobin-polyion films on pyrolytic graphite electrodes were used in strongly acid
104 ube and graphite powder-modified basal plane pyrolytic graphite electrodes.
105 lt to fabricate graphene and highly oriented pyrolytic graphite electrodes.
106 hanically exfoliated mica and highly ordered pyrolytic graphite flakes used as reference substrates.
107         At the octanoic acid/highly oriented pyrolytic graphite interface, the molecules self-assembl
108 ed anthracene derivatives on highly oriented pyrolytic graphite is investigated using scanning tunnel
109 e electrowetting response of highly oriented pyrolytic graphite over a wide range of electrolyte conc
110                               The edge plane pyrolytic graphite sensing platform is recommended as a
111 active crystalline layer (denoted as RZx) on pyrolytic graphite sheets (PGS), which was then utilized
112 olayer films of MoS2 grown on highly ordered pyrolytic graphite substrate.
113 rface coverage of ca. 70% on highly oriented pyrolytic graphite substrates.
114 orce microscopy (AFM) on the highly oriented pyrolytic graphite surface and differential pulse (DP) v
115 ing palladium mesowires on a highly oriented pyrolytic graphite surface and then transferring these m
116 rtically stacked bilayers on highly oriented pyrolytic graphite surface were determined to be ordered
117 0.00microl were directly introduced into the pyrolytic graphite tube without use of a chemical modifi
118 The slurries were directly introduced in the pyrolytic graphite tubes.
119 ymer or complex assembled in microwells on a pyrolytic graphite wafer are housed in dual microfluidic
120 s indium tin oxide, aluminum, highly ordered pyrolytic graphite, and glassy carbon, was achieved usin
121  carbon allotropes, including the edge-plane pyrolytic graphite, graphite powder, and glassy carbon,
122 ammetry in comparison with naked basal plane pyrolytic graphite, similar catalytic behavior is also s
123 SiO(x)/Si(100), and nonpolar, highly ordered pyrolytic graphite, surfaces.
124 ure adhesion of graphene atop highly ordered pyrolytic graphite, utilizing atomic-scale 'blisters' cr
125 other flat substrates such as highly ordered pyrolytic graphite.
126 dsorbed at the basal plane of highly ordered pyrolytic graphite.
127 s, mediating the affinity to highly oriented pyrolytic graphite.
128 anomechanical exfoliation of highly oriented pyrolytic graphite.
129 sulfonic acid) (p-AHNSA) modified edge plane pyrolytic graphite.
130 solution across a surface of highly oriented pyrolytic graphite.
131 ork is self-assembled on the highly-oriented-pyrolytic-graphite substrate.
132                                              Pyrolytic loss of N2 from 46b generates C15H10 intermedi
133  methylated homologues can serve as specific pyrolytic markers for chitin.
134            The method can be applied to most pyrolytic materials where quantitative oxygen conversion
135 for gamma-irradiated bacterial samples using pyrolytic methylation and compared for electron ionizati
136 fire may be enriching soils in (15)N through pyrolytic N isotope fractionation.
137 owed that PAH input to lake sediments was of pyrolytic origin, likely dominated by coal and later in
138 -14 cm in the 1950s indicated that Re was of pyrolytic origin.
139 lucose and cellulose in terms of predominant pyrolytic pathways.
140 in landscape fires (indicated by the rise in pyrolytic polycyclic aromatic hydrocarbons) and a declin
141                                          The pyrolytic products not only retain the microcubic morpho
142 oils rather than that commonly attributed to pyrolytic products.
143 plies generally to all compounds analyzed by pyrolytic PSIA.
144 mation of anhydrosugars was the preferential pyrolytic reaction for glucose, while the formation of c
145  that transition metals in clay can catalyze pyrolytic reactions at relatively low temperatures to de
146 transformations, contaminant desorption, and pyrolytic reactions occurring when contaminated soils ar
147 ) .) with phenyl (C(6) H(5) .) radicals in a pyrolytic reactor coupled with single photon ionization
148 otron-based mass spectrometry coupled with a pyrolytic reactor.
149 ate heterojunction, growing from the surface pyrolytic reconstruction of Ti-BPDC, works in a direct Z
150 etal catalysts can significantly enhance the pyrolytic remediation of soils contaminated with polycyc
151 t formation of lonsdaleite above 170 GPa for pyrolytic samples only.
152              We also observed changes in the pyrolytic signals of polyethylene with decreasing debris
153 n two groups: contaminated by atmospheric or pyrolytic sources.
154 nnels even though these were observed in the pyrolytic studies of phenylacetylene.
155 he 3dTM-SSCs generation through a controlled pyrolytic synthesis are discussed, with focus on elucida
156                                We report the pyrolytic synthesis of homogeneously alloyed CdS(x)Se(1-
157                              The single step pyrolytic synthesis was simple to perform while yielded
158 tep sequential extraction protocol (SEP) and pyrolytic thermodesorption.
159 were toxic; thus, high removal efficiency by pyrolytic treatment does not guarantee detoxification.
160 ne removal efficiency was observed after the pyrolytic treatment of Fe-enriched bentonite (1.8% wt io
161  model was tested with pilot-scale data from pyrolytic treatment of soils contaminated with crude oil
162  mathematical methods to inform the reliable pyrolytic treatment of specific soil/contaminant systems
163                                          The pyrolytic treatment of those precursors combined with st
164                                              Pyrolytic treatment reduced total petroleum hydrocarbons
165 (e.g., clays) can significantly decrease the pyrolytic treatment temperature and energy requirements
166            The maximum extractable yield of 'pyrolytic' unsubstituted PAHs for grass (22 mug g(-1) at
167                                     GC/MS of pyrolytic volatiles yielded only guaiacyl derivatives, i

 
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