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1 n important precursor of this compound under pyrolytic and aqueous heating conditions.
2 ition to diamond starting at 50 GPa for both pyrolytic and polycrystalline graphite, we also record t
3 ree of hydrogen and oxygen compared to other pyrolytic approaches and yields either nitrogen-doped or
4 anosecond timescales by shock compression of pyrolytic as well as polycrystalline graphite to pressur
5 ngly, CCR suppression substantially promoted pyrolytic breakdown of cell wall polysaccharides, a phen
6 r 10-20 cycles in H2SO4 on all materials but pyrolytic carbon (PyC).
7 l that simulates dynamic adsorption of H2 on pyrolytic carbon can reproduce many aspects of the exper
8 easily, and cheaply fabricated by depositing pyrolytic carbon into a quartz theta nanopipet.
9                             It consists of a pyrolytic carbon nanoelectrode obtained by chemical vapo
10                      The pores formed in the pyrolytic carbon nanoribbons range in size from sub-nano
11 crystals with multilayered graphitic carbon, pyrolytic carbon or inert metals have been obtained, but
12 mally black silicon substrate with amorphous pyrolytic carbon.
13  in defining the structure and properties of pyrolytic carbons.
14                                        Under pyrolytic conditions the acidity/basicity of Maillard re
15 the degradation of glucose was studied under pyrolytic conditions using excess sodium glycinate the r
16 mation of HMF and chlorinated products under pyrolytic conditions using glucose or sucrose and amino
17 ning 2,3-butanedione were investigated under pyrolytic conditions using glycine, sodium glycinate and
18         A kinetic analysis was performed for pyrolytic conditions, and benzene, toluene, and xylene w
19 ations of organic materials under controlled pyrolytic conditions, with the advantage of increasing t
20  half to surface adsorption processes in the pyrolytic conversion of analytes to H2.
21 d nona-BDE profiles suggested photolysis and pyrolytic debromination of BDE-209 in the air samples.
22  carbon filling of one of the barrels by the pyrolytic decomposition of butane, followed by electrode
23 l as an additional peak corresponding to the pyrolytic dehydration product, 1-hexadecene.
24 e harnessing a ring-contracting flash vacuum pyrolytic extrusion of sulfur dioxide from the respectiv
25                                              Pyrolytic fragmentation of about one-third of the analyt
26                 The delta(13)C values of the pyrolytic fragments (CO, CH4, C2H4) are shown to be high
27                                     Ideally, pyrolytic fragments will originate from unique sites wit
28 ic graphene oxide (PGO) and hydrogen-reduced pyrolytic graphene oxide (HPGO).
29 method is used to treat graphite oxide (GO), pyrolytic graphene oxide (PGO) and hydrogen-reduced pyro
30 cken liver sulfite oxidase (SO) bound at the pyrolytic graphite "edge" or modified gold electrodes sh
31 on of HLM directly onto polished basal plane pyrolytic graphite (BPG), edge plane pyrolytic graphite
32 plane pyrolytic graphite (EPPG), basal plane pyrolytic graphite (BPPG), and the basal surface of high
33  capsulatus was immobilized on an edge-plane pyrolytic graphite (EPG) electrode to construct a hypoxa
34 l plane pyrolytic graphite (BPG), edge plane pyrolytic graphite (EPG), glassy carbon (GC), or high-pu
35 lline boron-doped diamond (pBDD), edge plane pyrolytic graphite (EPPG), basal plane pyrolytic graphit
36 butanol/hexane solution onto highly oriented pyrolytic graphite (HOPG) and carbon-coated Si(100) spon
37 te polymer film formation on highly oriented pyrolytic graphite (HOPG) and chemically modified HOPG.
38 ectroactivity of basal plane highly oriented pyrolytic graphite (HOPG) and two types of aluminum allo
39 lfonate (AQDS) is studied on highly oriented pyrolytic graphite (HOPG) as a model sp(2) surface.
40 rphyrin (CoOEP) supported on highly oriented pyrolytic graphite (HOPG) at the phenyloctane/CoOEP/HOPG
41 at airborne contamination of highly oriented pyrolytic graphite (HOPG) causes the nonideal asymmetry
42  These molecules assemble on highly oriented pyrolytic graphite (HOPG) from aqueous solutions to form
43                              Highly oriented pyrolytic graphite (HOPG) is an important electrode mate
44 structure of 1-octadecanol on highly ordered pyrolytic graphite (HOPG) is observed.
45 methylammonium (FcTMA(+)) at highly oriented pyrolytic graphite (HOPG) is used as a model system to d
46 ials, aluminum and highly oriented (ordered) pyrolytic graphite (HOPG) never before used for this pur
47 e sample of interest and of a highly ordered pyrolytic graphite (HOPG) reference sample, was reviewed
48 HBC-solvent dispersion and a highly oriented pyrolytic graphite (HOPG) substrate.
49 Ru(3)(CO)(12) precursor on a highly oriented pyrolytic graphite (HOPG) surface modified with one-atom
50  on five different grades of highly oriented pyrolytic graphite (HOPG) that vary in step-edge height
51 G), and the basal surface of highly oriented pyrolytic graphite (HOPG), encompassing five distinct gr
52 and GO are similar to that of highly ordered pyrolytic graphite (HOPG), which has no band-gap.
53 t" on mica and "flat" on the highly oriented pyrolytic graphite (HOPG).
54 elmy plate measurements using highly ordered pyrolytic graphite (HOPG).
55 lti-walled carbon nano tube (MWCNT) modified pyrolytic graphite (MPG) electrode is prepared and appli
56 o a dense gold nanoparticle (AuNP) film on a pyrolytic graphite (PG) electrode.
57                       Films were prepared on pyrolytic graphite (PG) electrodes by casting mixtures o
58 abolism of styrene using DNA/enzyme films on pyrolytic graphite (PG) electrodes monitored via Ru(bpy)
59 [PVP-Ru(bpy)2(2+), bpy = 2,2'-bipyridine] on pyrolytic graphite (PG) electrodes were evaluated for th
60 taining DNA and N-acetyltransferase (NAT) on pyrolytic graphite (PG) electrodes.
61  force microscopy (AFM) at a highly oriented pyrolytic graphite and voltammetry at a glassy carbon el
62 ricated by forming the wells on a conductive pyrolytic graphite chip (1 in. x 1 in.) with a single co
63 orests were grown in printed microwells on a pyrolytic graphite detection chip and decorated with cap
64 nticipated Fe(II/III) couple only, PFV using pyrolytic graphite edge (PGE) electrodes demonstrates th
65 me bacterial enzyme were immobilized on both pyrolytic graphite edge and alkanethiol-modified Au elec
66                  Hydrogenase was adsorbed to pyrolytic graphite edge and carbon felt electrodes.
67 nolayers of the bacterial diheme enzyme at a pyrolytic graphite edge electrode give catalytic, reduct
68 tammetry (PFV) with the enzyme adsorbed at a pyrolytic graphite edge electrode.
69 idation of 5-hydroxytryptophan (5-HTPP) at a pyrolytic graphite electrode at pH 7.5, two quasi-revers
70 n electrochemically oxidized highly oriented pyrolytic graphite electrode or a graphene oxide suspens
71 reduction currents produced at an edge-plane pyrolytic graphite electrode was diagnosed analytically
72 ous incubation of tobacco peroxidase and the pyrolytic graphite electrode with the cross-coupling rea
73 -pyrenebutyric acid frameworks on edge plane pyrolytic graphite electrodes (PGE/MWNT/Py) to which an
74  showed reversible FeIII/FeII voltammetry on pyrolytic graphite electrodes and catalytic current for
75 plet deposits of DDPD in HDOP at basal plane pyrolytic graphite electrodes are studied by voltammetri
76 ive films were grown layer by layer on rough pyrolytic graphite electrodes featuring 4-nm underlayers
77 llopolymers were assembled layer by layer on pyrolytic graphite electrodes to make sensors that selec
78 can be covalently attached to functionalized pyrolytic graphite electrodes using peptidic coupling.
79       In vivo damaged DNA was immobilized on pyrolytic graphite electrodes using the layer-by-layer (
80 ons and double-stranded (ds)-DNA on oxidized pyrolytic graphite electrodes was evaluated for detectio
81      Cross-linked myoglobin-polyion films on pyrolytic graphite electrodes were used in strongly acid
82 ube and graphite powder-modified basal plane pyrolytic graphite electrodes.
83 lt to fabricate graphene and highly oriented pyrolytic graphite electrodes.
84         At the octanoic acid/highly oriented pyrolytic graphite interface, the molecules self-assembl
85 ed anthracene derivatives on highly oriented pyrolytic graphite is investigated using scanning tunnel
86 olayer films of MoS2 grown on highly ordered pyrolytic graphite substrate.
87 rface coverage of ca. 70% on highly oriented pyrolytic graphite substrates.
88 orce microscopy (AFM) on the highly oriented pyrolytic graphite surface and differential pulse (DP) v
89 ing palladium mesowires on a highly oriented pyrolytic graphite surface and then transferring these m
90 rtically stacked bilayers on highly oriented pyrolytic graphite surface were determined to be ordered
91 0.00microl were directly introduced into the pyrolytic graphite tube without use of a chemical modifi
92 The slurries were directly introduced in the pyrolytic graphite tubes.
93 ymer or complex assembled in microwells on a pyrolytic graphite wafer are housed in dual microfluidic
94 s indium tin oxide, aluminum, highly ordered pyrolytic graphite, and glassy carbon, was achieved usin
95  carbon allotropes, including the edge-plane pyrolytic graphite, graphite powder, and glassy carbon,
96 ammetry in comparison with naked basal plane pyrolytic graphite, similar catalytic behavior is also s
97 SiO(x)/Si(100), and nonpolar, highly ordered pyrolytic graphite, surfaces.
98 ure adhesion of graphene atop highly ordered pyrolytic graphite, utilizing atomic-scale 'blisters' cr
99 other flat substrates such as highly ordered pyrolytic graphite.
100 dsorbed at the basal plane of highly ordered pyrolytic graphite.
101 sulfonic acid) (p-AHNSA) modified edge plane pyrolytic graphite.
102 anomechanical exfoliation of highly oriented pyrolytic graphite.
103 solution across a surface of highly oriented pyrolytic graphite.
104                                              Pyrolytic loss of N2 from 46b generates C15H10 intermedi
105 for gamma-irradiated bacterial samples using pyrolytic methylation and compared for electron ionizati
106 fire may be enriching soils in (15)N through pyrolytic N isotope fractionation.
107 owed that PAH input to lake sediments was of pyrolytic origin, likely dominated by coal and later in
108 -14 cm in the 1950s indicated that Re was of pyrolytic origin.
109 lucose and cellulose in terms of predominant pyrolytic pathways.
110 in landscape fires (indicated by the rise in pyrolytic polycyclic aromatic hydrocarbons) and a declin
111                                          The pyrolytic products not only retain the microcubic morpho
112 oils rather than that commonly attributed to pyrolytic products.
113 plies generally to all compounds analyzed by pyrolytic PSIA.
114 mation of anhydrosugars was the preferential pyrolytic reaction for glucose, while the formation of c
115 t formation of lonsdaleite above 170 GPa for pyrolytic samples only.
116              We also observed changes in the pyrolytic signals of polyethylene with decreasing debris
117 n two groups: contaminated by atmospheric or pyrolytic sources.
118 nnels even though these were observed in the pyrolytic studies of phenylacetylene.
119                                We report the pyrolytic synthesis of homogeneously alloyed CdS(x)Se(1-
120                              The single step pyrolytic synthesis was simple to perform while yielded
121                                              Pyrolytic treatment reduced total petroleum hydrocarbons
122            The maximum extractable yield of 'pyrolytic' unsubstituted PAHs for grass (22 mug g(-1) at
123                                     GC/MS of pyrolytic volatiles yielded only guaiacyl derivatives, i

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