1,223 research outputs found
Waveforms of the repeated impact SHPB test of granite samples.
Waveforms of the repeated impact SHPB test of granite samples.</p
SHPB device.
A large number of cracks exist in natural rock masses, which significantly affects the stability of surrounding rocks in engineering under impact loading. Repeated impact tests by Split Hopkinson Pressure Bar are performed on non-penetrating cracked granite specimens with different prefabricated-crack inclination angles (0, 30, 45, 60, and 90Ā°). The damage evolution law of cracked rock under repeated impact loading is investigated. Macroscopic damage variables considering geometric and mechanical parameters of cracks are proposed. Further, a constitutive model for the impact loading test is developed based on the coupling damage. It has been found that, the impact resistance of fractured rock first decreases and then increases with the increased prefabricated-crack inclination angle. The impact resistance for specimens with an inclination angle of 45Ā° is the minimum. Theoretical results from the developed model agree with the experimental data. The model could well describe the progressive damage characteristics of cracked rock masses.</div
S1 Dataset -
A large number of cracks exist in natural rock masses, which significantly affects the stability of surrounding rocks in engineering under impact loading. Repeated impact tests by Split Hopkinson Pressure Bar are performed on non-penetrating cracked granite specimens with different prefabricated-crack inclination angles (0, 30, 45, 60, and 90Ā°). The damage evolution law of cracked rock under repeated impact loading is investigated. Macroscopic damage variables considering geometric and mechanical parameters of cracks are proposed. Further, a constitutive model for the impact loading test is developed based on the coupling damage. It has been found that, the impact resistance of fractured rock first decreases and then increases with the increased prefabricated-crack inclination angle. The impact resistance for specimens with an inclination angle of 45Ā° is the minimum. Theoretical results from the developed model agree with the experimental data. The model could well describe the progressive damage characteristics of cracked rock masses.</div
Effects of Oxide Contact Layer on the Preparation and Properties of CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> for Perovskite Solar Cell Application
In perovskite solar cells, oxide
electron transport layers (ETL)
and their interface with the organometal trihalides are key to achieve
efficient and stable devices. In the present work we investigate ZnO
and TiO<sub>2</sub> ETLs and their influence on the preparation of
CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> film by two different
techniques. In the āone-stepā technique, a solution
is used for the deposition of a precursor layer which is dripped and
subsequently annealed. In the ātwo-stepā sequential
technique, a PbI<sub>2</sub> precursor layer is converted into perovskite.
We show that, on ZnO, the annealing treatment of the āone-stepā
deposited layer is optimum for a duration time of only 2 min. This
duration is much less critical for the TiO<sub>2</sub> underlayer.
Long annealing times produce the degradation of the pigment and formation
of PbI<sub>2</sub>. It is also shown that the āone-stepā
technique gives better results for the sensitization of smooth oxide
underlayers whereas the ātwo-stepā one must be utilized
for rough or structured underlayer sensitization. The best solar cell
performances were achieved by combining a low-overvoltage electrodeposited
ZnO layer, a planar architecture, and a perovskite layer prepared
by a āone-stepā deposition-dripping route. A maximum
overall conversion efficiency of 15% was measured for the ZnO-based
perovskite solar cell. Cell impedance spectra have been measured over
a large applied voltage range. Their analysis, using an ad-hoc equivalent
circuit, shows that charge recombinations are reduced for the āone-stepā
perovskite and that a better interface with the oxide is produced
in that case
Quantitative Detection of OH Radicals for Investigating the Reaction Mechanism of Various Visible-Light TiO<sub>2</sub> Photocatalysts in Aqueous Suspension
The reaction mechanism of visible-light responsive photocatalysts
was explored by analyzing OH radicals (<sup>ā¢</sup>OH) quantitatively
by means of a coumarin fluorescence probe method. The photocatalysts
investigated were various modified TiO<sub>2</sub>, i.e., nitrogen-doped,
Pt-complex-deposited, FeĀ(III)-grafted, and FeĀ(III)-grafted Ru-doped
TiO<sub>2</sub>. The formation rate of <sup>ā¢</sup>OH was measured
to calculate the <sup>ā¢</sup>OH quantum yield from the absorbed
intensity of 470 nm LED light. The highest quantum yield was obtained
for FeĀ(III)-grafted Ru-doped TiO<sub>2</sub>. The <sup>ā¢</sup>OH yield was increased on the addition of H<sub>2</sub>O<sub>2</sub> for the FeĀ(III)-grafted TiO<sub>2</sub>, indicating that H<sub>2</sub>O<sub>2</sub> is supposedly a reaction intermediate for producing <sup>ā¢</sup>OH. The photocatalytic activity for each sample was
obtained by measuring CO<sub>2</sub> generation rate on the acetaldehyde
decomposition in an aqueous suspension system and then it was compared
with the <sup>ā¢</sup>OH formation rate. Although the CO<sub>2</sub> generation rate is positively correlated with the <sup>ā¢</sup>OH formation rate for each photocatalyst, the values of CO<sub>2</sub> generation were extremely larger than those of <sup>ā¢</sup>OH. This finding indicates that the oxidation reaction takes place
dominantly with surface trapped holes which probably exchange with
the <sup>ā¢</sup>OH in solution
Additional file 1: Table S1 of Pan-cancer analysis of frequent DNA co-methylation patterns reveals consistent epigenetic landscape changes in multiple cancers
Frequent co-methylation clusters. Table S2. Cross-check of known tumor suppressor with corresponding cancer co-methylation clusters. The numbers indicate the overlaps between co-methylated clusters and known tumor suppressor in each corresponding cancer type. Freqāā„ā9 genes were obtained from combined co-methylated clusters from all 17 cancer datasets and extracted the genes appeared in over 9 datasets. Figure S1. Protein-protein network query on STRING database for Cluster 1 genes. (DOCX 375Ā kb
sj-docx-1-wmr-10.1177_0734242X231221082 ā Supplemental material for How to influence food waste behaviour of urban residents? The combined effect of network embeddedness and incentive measures
Supplemental material, sj-docx-1-wmr-10.1177_0734242X231221082 for How to influence food waste behaviour of urban residents? The combined effect of network embeddedness and incentive measures by Xiu Cheng, Jie Zhang and Linling Zhang in Waste Management & Research</p
sj-docx-2-wmr-10.1177_0734242X231221082 ā Supplemental material for How to influence food waste behaviour of urban residents? The combined effect of network embeddedness and incentive measures
Supplemental material, sj-docx-2-wmr-10.1177_0734242X231221082 for How to influence food waste behaviour of urban residents? The combined effect of network embeddedness and incentive measures by Xiu Cheng, Jie Zhang and Linling Zhang in Waste Management & Research</p
Site-Resolved Structural Energetics of the T7 Concatemer Junction
The
concatemer junction is a conserved sequence of 8 bp, which
is strategically located at the junction between the head-to-tail
repeats of genomic DNA in T7 and related bacteriophages. The RNA polymerase
pauses at this site to recruit the machinery necessary for cleavage
of the concatemer into single genome DNA. During pausing, the transcription
bubble collapses and the transcription RNAāDNA hybrid is shortened
to only 3 bp. This work addresses the question of the role of the
nucleic acid components of the transcription elongation complex in
this collapse of the transcription bubble. The nucleic acid structures
investigated are the DNAāDNA duplex structure present at the
concatemer junction when the DNA is not transcribed and the RNAāDNA
hybrid formed when the concatemer junction is transcribed. The structural
energetics of each base pair in the two structures is characterized
using imino proton exchange and nuclear magnetic resonance spectroscopy.
The results show that 5 bp in the DNAāDNA duplex at the concatemer
junction site are significantly more stable than the corresponding
base pairs in the RNAāDNA hybrid that forms when the site is
transcribed. Because of their energetic preference for the DNAāDNA
duplex, these 5 bp favor the collapse of the transcription bubble.
Four of the 5 bp with enhanced stability in the DNAāDNA duplex
are located in the downstream half of the concatemer junction site.
This location suggests that only after the entire concatemer junction
is transcribed can the RNAāDNA hybrid accumulate sufficient
structural destabilization to trigger the dissociation of the RNA
and the switch of the DNA template strand from the hybrid structure
to the DNAāDNA double-helical structure
Facile Construction of Yttrium Pentasulfides from Yttrium Alkyl Precursors: Synthesis, Mechanism, and Reactivity
Treatment of the yttrium dialkyl
complex Tp<sup>Me2</sup>YĀ(CH<sub>2</sub>Ph)<sub>2</sub>Ā(THF) (Tp<sup>Me2</sup> = triĀ(3,5 dimethylpyrazolyl)Āborate, THF = tetrahydrofuran) with
S<sub>8</sub> in a 1:1 molar ratio in THF at room temperature afforded
a yttrium pentasulfide Tp<sup>Me2</sup>YĀ(Īŗ<sub>4</sub>-S<sub>5</sub>) (THF) (<b>1</b>) in 93% yield. The yttrium monoalkyl
complex Tp<sup>Me2</sup>CpYCH<sub>2</sub>PhĀ(THF) reacted with
S<sub>8</sub> in a 1:0.5 molar ratio under the same conditions to
give another yttrium pentasulfide [(Tp<sup>Me2</sup>)<sub>2</sub>Y]<sup>+</sup>Ā[Cp<sub>2</sub>YĀ(Īŗ<sub>4</sub>-S<sub>5</sub>)]<sup>ā</sup> (<b>10</b>) in low yield. Further investigations
indicated that the S<sub>5</sub><sup>2ā</sup> anion facilely
turned into the corresponding thioethers or organic disulfides, and
released the redundant S<sub>8</sub>, when it reacted with some electrophilic
reagents. The mechanism for the formation of the S<sub>5</sub><sup>2ā</sup> ligand has been investigated by the controlling of
the reaction stoichiometric ratios and the stepwise reactions
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