1,223 research outputs found

    Waveforms of the repeated impact SHPB test of granite samples.

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    Waveforms of the repeated impact SHPB test of granite samples.</p

    SHPB device.

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    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 -

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    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

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    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 ā€œone-stepā€ technique, a solution is used for the deposition of a precursor layer which is dripped and subsequently annealed. In the ā€œtwo-stepā€ sequential technique, a PbI<sub>2</sub> precursor layer is converted into perovskite. We show that, on ZnO, the annealing treatment of the ā€œone-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 ā€œone-stepā€ technique gives better results for the sensitization of smooth oxide underlayers whereas the ā€œtwo-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 ā€œone-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 ā€œone-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

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    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

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    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. Freqā€‰ā‰„ā€‰9 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

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    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

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    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

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    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 RNAā€“DNA 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 DNAā€“DNA duplex structure present at the concatemer junction when the DNA is not transcribed and the RNAā€“DNA 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 DNAā€“DNA duplex at the concatemer junction site are significantly more stable than the corresponding base pairs in the RNAā€“DNA hybrid that forms when the site is transcribed. Because of their energetic preference for the DNAā€“DNA duplex, these 5 bp favor the collapse of the transcription bubble. Four of the 5 bp with enhanced stability in the DNAā€“DNA 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 RNAā€“DNA 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 DNAā€“DNA double-helical structure

    Facile Construction of Yttrium Pentasulfides from Yttrium Alkyl Precursors: Synthesis, Mechanism, and Reactivity

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    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>āˆ’</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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