Endovascular treatment for massive haemoptysis due to pulmonary pseudoaneurysm: report of 23 cases.

PURPOSE: To evaluate the safety and effectiveness of endovascular treatment for massive haemoptysis caused by pulmonary pseudoaneurysm (PAP). METHODS: The clinical data, imaging data, and endovascular treatment protocol of 23 patients with massive haemoptysis caused by continuous PAP were retrospectively analysed. The success, complications, postoperative recurrence rate, and influence of the treatment on pulmonary artery pressure were also evaluated. RESULTS: Nineteen patients with a bronchial artery-pulmonary artery (BA-PA) and/or nonbronchial systemic artery-pulmonary artery (NBSA-PA) fistula underwent bronchial artery embolization (BAE) and/or nonbronchial systemic artery embolization (NBSAE) + pulmonary artery embolization (PAE). The pulmonary artery (PA) pressures before and after embolization were 52.11 ± 2.12 (35-69 cmH2O) and 33.58 ± 1.63 (22-44 cmH2O), respectively (P = 0.001). Four patients did not have a BA-PA and/or NBSA-PA fistula. Embolization was performed in two patients with a distal PAP of the pulmonalis lobar arteria. Bare stent-assisted microcoils embolization was performed in the other two patients with a PAP of the main pulmonary lobar arteries. The PA pressures of the four patients before and after treatment were 24.50 ± 1.32 (22-28 cmH2O) and 24.75 ± 1.70 (22-29 cmH2O), respectively (P = 0.850). The technique had a 100% success rate with no serious complications and a postoperative recurrence rate of 30%. CONCLUSION: Endovascular treatment is safe and effective for massive haemoptysis caused by PAP. BAE and/or NBSAE can effectively reduce pulmonary hypertension in patients with a BA-PA and/or NBSA-PA fistula.

Controlled Symmetry with Woods-Saxon Stochastic Resonance Enabled Weak Fault Detection.

Weak fault detection with stochastic resonance (SR) is distinct from conventional approaches in that it is a nonlinear optimal signal processing to transfer noise into the signal, resulting in a higher output SNR. Owing to this special characteristic of SR, this study develops a controlled symmetry with Woods-Saxon stochastic resonance (CSwWSSR) model based on the Woods-Saxon stochastic resonance (WSSR), where each parameter of the model may be modified to vary the potential structure. Then, the potential structure of the model is investigated in this paper, along with the mathematical analysis and experimental comparison to clarify the effect of each parameter on it. The CSwWSSR is a tri-stable stochastic resonance, but differs from others in that each of its three potential wells is controlled by different parameters. Moreover, the particle swarm optimization (PSO), which can quickly find the ideal parameter matching, is introduced to attain the optimal parameters of the CSwWSSR model. Fault diagnosis of simulation signals and bearings was carried out to confirm the viability of the proposed CSwWSSR model, and the results revealed that the CSwWSSR model is superior to its constituent models.

Phase-engineered high-entropy metastable FCC Cu2-y Ag y (In x Sn1-x )Se2S nanomaterials with high thermoelectric performance.

Crystal-phase engineering to create metastable polymorphs is an effective and powerful way to modulate the physicochemical properties and functions of semiconductor materials, but it has been rarely explored in thermoelectrics due to concerns over thermal stability. Herein, we develop a combined colloidal synthesis and sintering route to prepare nanostructured solids through ligand retention. Nano-scale control over the unconventional cubic-phase is realized in a high-entropy Cu2-y Ag y (In x Sn1-x )Se2S (x = 0-0.25, y = 0, 0.07, 0.13) system by surface-ligand protection and size-driven phase stabilization. Different from the common monoclinic phase, the unconventional cubic-phase samples can optimize electrical and thermal properties through phase and entropy design. A high power factor (0.44 mW m-1 K-2), an ultralow thermal conductivity (0.25 W m-1 K-1) and a ZT value of 1.52 are achieved at 873 K for the cubic Cu1.87Ag0.13(In0.06Sn0.94)Se2S nanostructured sample. This study highlights a new method for the synthesis of metastable phase high-entropy materials and gives insights into stabilizing the metastable phase through ligand retention in other research communities.

Effect of Rice Husk-Based Silica on the Friction Properties of High Density Polyethylene Composites.

Rice husk ash (RHA)-reinforced composites are now used in many tribological applications. We prepared two kinds of RHAs using different pretreatment and the same pyrolysis process, namely water-treated RHA (WRHA) and acid-treated RHA (ARHA). Comparing the two RHAs, the RHA pretreated with hydrochloric acid (HCl) was found to have a smaller particle size and a more uniform dispersion. Accordingly, the two kinds of RHAs were used as fillers and added to the high-density polyethylene (HDPE) matrix by an extrusion process. The results showed that the friction coefficient (COF) value of the composites with ARHA was reduced to 0.12 when an additional amount of 0.75 wt.% or 1.5 wt.%. WRHA was used as a filler to the amount of 1.5 wt.%, but the COF value was raised to about 0.21. The reason for this phenomenon may be due to its larger particle size and more severe abrasive wear. This work provides a method for making natural biomass fillers that can effectively reduce the COF of HDPE composites with slight decreases in mechanical properties.

Bi-functional hydrogen and coordination bonding surfactant: A novel and promising collector for improving the separation of calcium minerals.

Mono-functional chelating collectors exhibit limited selectivity in the flotation of minerals. In particular, the selective separation of calcium minerals presents a significant challenge because mono-functional chelating collectors, such as fatty acid, indistinguishably adsorb onto mineral surfaces by coordinating with the same metal cation (Ca2+). Thus, there is an urgent need to develop new-mode-functional collectors to separate calcium minerals and a need to understand the underlying chemoselectivity. Given the difference of the hydrogen bonding ability of anions with fluorite, calcite and scheelite surfaces, the introduction of additional hydrogen bonding functional groups into collector molecules is a novel strategy to improve selectivity. In this study, a hydrogen and coordination bonding (bi-functional) collector, 2-cyano-N-ethylcarbamoyl acetamide (CEA) was developed, which could form coordination bonds with the Ca2+ ions (by carbonyl groups) and hydrogen bonds with the anions (by amino groups) on calcium mineral surfaces. The results of flotation tests showed that CEA can selectively separate fluorite and calcite from scheelite at pH 7. The promising selectivity of CEA lies in both the electrical properties and the anions' hydrogen bonding ability with the three calcium minerals. The negatively charged scheelite surfaces are not conducive to coordination bonding with CEA while the positively charged fluorite and calcite surfaces are. Besides, the hydrogen bonding ability of fluorite (F-) and calcite (CO32-) with carbamido in CEA is higher than that of scheelite (WO42-), and this also plays an essential role. This coordination and hydrogen bonding based surfactant design protocol has a great potential in the development of tail-made collectors/depressants for the separation of other oxidized minerals.

Stabilizing sulfur vacancy defects by performing "click" chemistry of ultrafine palladium to trigger a high-efficiency hydrogen evolution of MoS2.

Defect engineering is widely applied in transition metal dichalcogenides to produce high-purity hydrogen. However, the instability of vacancy states on catalysis still remains a considerable challenge. Here, our first-principles calculations showed that, by optimizing the asymmetric S vacancy in the highly asymmetric 1T' crystal of layered bitransition metal dichalcogenides (Co-MoS2) in light of Pd modulation, the relative amount of metastable phase and the quantity of active sites in the structure can be reduced and increased, respectively, leading to a further boosted hydrogen evolution reaction (HER) activity toward layered bi-transition metal dichalcogenides. Thus, we then used a "click" chemistry strategy to make such a catalyst with engineered unsaturated sulfur edges via a strong coupling effect between ultrafine Pd ensembles and Co-MoS2 nanosheets. As expected, the Pd-modulated Co-MoS2 nanosheets exhibited a very low overpotential of 60 mV at 10 mA cm-2 with a small Tafel slope (56 mV dec-1) for the HER in 1.0 M PBS, comparable to those of commercial Pt/C. In addition, their high HER activity was retained in acidic and alkaline conditions. Both the theoretical and experimental results revealed that Pd ensembles can efficiently activate and stabilize the inert basal plane S sites during HER processes as a result of the formation of Pd-S in Co-MoS2. This work not only provides a deeper understanding of the correlation between defect sites and intrinsic HER catalytic properties for transition metal chalcogenide (TMD)-based catalysts, but also offers new insights into better designing earth-abundant HER catalysts displaying high efficiency and durability.