The impact of inoculum source,inoculum to substrate ratio and sample preservation on methane potential from different substrates

Batch experiments were conducted to evaluate the impact of inoculum sources, inoculum to substrate (IS) ratio and storage conditions on the potential and production rate of methane (CH₄) from different substrates: wheat straw, whole crop maize, cattle manure, grass and cellulose.The results of the test with four inocula and four substrates indicated that inoculum source could have a significant impact on both CH₄ potential (BMP) and the kinetics parameters of different substrates. The two inocula showing the highest BMP and production rates in each period were those coming from a feeding with more than 70% of animal manure under thermophilic conditions. The impact of the IS ratio in the range 0.25–2.5, in terms of g volatile solids (VS) substrate/g VS inoculum, depended on substrate type. Maize silage was more affected to changes in the IS ratio than wheat straw. The optimal IS ratio range for maize was 1.0–1.5, however, a wider IS range can be used in wheat straw (0.5–2.5). The impact of freezing and drying depended on biomass type. Freezing, drying and ensiling of grass increased the CH₄ yield compared to fresh grass. Drying of maize had no impact while freezing reduced the CH₄ potential. Drying and freezing had no impact on straw.     

A Constitutive Equation of Thermoelasticity for Solid Materials

A new constitutive equation of thermoelasticity for crystals is presented based on the interatomic potential and solid mechanics at finite temperature. Using the new constitutive equation, the calculations for crystal copper and graphene are carried out under different loading paths at different temperatures. The calculated results are in good agreement with those of the previous thermoelasticity constitutive equation based on quantum mechanics, which clearly indicates that our new constitutive equation of thermoelasticity is correct. A lot of comparisons also show that the present theory is more concise and efficient than the previous thermal stress theory in the practical application.     

Modified embedded-atom method interatomic potential for the Mg–Zn–Ca ternary system

Mg–Zn–Ca alloys are representative Mg alloys with high formability at room temperature. Their high formability is thought to be related to slip, twinning, and recrystallization of the alloys, but the detailed mechanisms have not yet been clarified. To enable atomistic simulations for investigating those behaviors, an interatomic potential for the Mg–Zn–Ca ternary system was developed. The development was based on the second nearest-neighbor modified embedded-atom method formalism, combining previously developed Mg–Zn and Mg–Ca potentials with the newly developed Zn–Ca binary potential. The Zn–Ca and Mg–Zn–Ca potentials reproduce structural, elastic, and thermodynamic properties of compounds and solution phases of relevant alloy systems in reasonable agreement with experimental data, first-principles and CALPHAD calculations. The applicability of the developed potentials is demonstrated through calculations of the effects of Zn and Ca solutes on the generalized stacking fault energy for various slip systems, segregation energy on twin boundaries, and volumetric misfit strain.     

Clean hydrogen production in a full biological microbial electrolysis cell

The recent interest in microbial electrolysis cell (MEC) technology has led the research platform to develop full biological MECs (bioanode-biocathode, FB-MEC). This study focused on biohydrogen production from a biologically catalyzed MEC. A bioanode and a biocathode were initially enriched in a half biological MFC (bioanode-abiocathode, HB-MFC) and a half biological MEC (abioanode-biocathode, HB-MEC), respectively. The FB-MEC was established by transferring the biocathode of the HB-MEC and the bioanode of the HB-MFC to a two-chamber MEC. The FB-MEC was operated under batch (FB-MEC-B) and recirculation batch (FB-MEC-RB) modes of operation in the anodic chamber. The FB-MEC-B reached a maximum current density of 1.5 A/m² and the FB-MEC-RB reached a maximum current density of 2.5 A/m² at a similar applied voltage while the abiotic control system showed the maximum of 0.2 A/m². Hydrogen production rate decreased in the FB-MEC compared to that of the HB-MEC. However, the cathodic hydrogen recovery increased from 42% obtained in the HB-MEC to 56% in the FB-MEC-B and 65% in the FB-MEC-RB, suggesting the efficient oxidation and reduction rates in the FB-MEC compared to the HB-MEC. The onset potential for hydrogen evolution reaction detected by linear sweep voltammetry analysis were −0.780 and −0.860 V vs Ag/AgCl for the FB-MEC-RB and the FB-MEC-B (−1.26 for the abiotic control MEC), respectively. Moreover, the results suggested that the FB-MEC worked more efficiently when the biocathode and the bioanode were enriched initially in half biological systems before transferring to the FB-MEC compared to that of the simultaneously enriched in one system.     

溶解氧变化对阴极极化下10Ni5CrMo钢氢脆敏感性的影响

摘要：为研究溶解氧质量浓度对10Ni5CrMo钢在阴极极化条件下氢脆敏感性影响规律，对10Ni5CrMo钢进行了阴极极化下的电化学交流阻抗谱测试﹑并采用慢应变速率拉伸实验和断口分析方法研究了海水中溶解氧质量浓度变化和不同阴极极化下10Ni5CrMo钢的氢脆敏感性。结果表明：溶解氧质量浓度变化对10Ni5CrMo钢强度几乎没有影响；同一溶解氧质量浓度下，随极化电位负移，断裂时间、伸长率、断面收缩率明显降低，氢脆系数增加，氢脆敏感性显著提高，极化电位达到-1000mV时，氢脆系数已超过安全区允许的最高值25%，进入危险区；同一极化电位下，随着海水中溶解氧质量浓度减少，材料塑性变差，断裂时间、伸长率和断面收缩率不断降低，氢脆系数增加，氢脆敏感性提高。     

Electrical conductivity of poly(vinyl alcohol)/carbon nanotube multilayer thin films: Influence of sodium polystyrene sulfonate mediated carbon nanotube dispersion

This investigation was aimed to enhance the dispersibility of multi-walled carbon nanotubes (MWCNT) using sodium polystyrene sulfonate (Na-PSS) polyelectrolyte. Subsequently, electrically conducting, multi-layer thin films are prepared utilizing layer by layer assembly method with poly(vinyl alcohol) as a host matrix. The highest extent of MWCNT dispersion was observed in MWCNT:Na-PSS ratio of 1:9 (wt/wt), which was estimated from UV-Vis spectroscopic analysis. Zeta potential measurements of Na-PSS modified MWCNT dispersion showed large negative potentials ranging from −52 to −64 mV in the most stable pH range of 4 to 10, suggesting the colloidal stability is due to the long-range repulsive nature of electrostatic interactions from negatively charged sulfonate groups. Complementary molecular dynamics simulations showed that adsorption of Na-PSS imparts a large negative potential to the carbon nanotube surface, which increases with an increase in Na-PSS concentration. The multi-layer thin film of (1:9) MWCNT:Na-PSS exhibited a DC electrical conductivity of 2.96 × 10² S/m.     

黄沙坪铅锌多金属矿的成矿规律及深部找矿远景

众所周知,矿物质的成分是多种多样的,社会的发展和科学的进步需要运用到多重金属矿物质,在专业人员的勘探与挖掘中,发现了黄沙坪铅锌多金属矿,这个矿区中有丰富的有色金属,这个矿的发掘为研究成矿规律提供了物质基础,同时也为深部找矿提供了可靠的依据。本文主要分析黄沙坪铅锌多金属矿的成矿规律及深部找矿远景。     

Revealing Electrical-Poling-Induced Polarization Potential in Hybrid Perovskite Photodetectors

Despite recent rapid advances in metal halide perovskites for use in optoelectronics, the fundamental understanding of the electrical-poling-induced ion migration, accounting for many unusual attributes and thus performance in perovskite-based devices, remain comparatively elusive. Herein, the electrical-poling-promoted polarization potential is reported for rendering hybrid organic–inorganic perovskite photodetectors with high photocurrent and fast response time, displaying a tenfold enhancement in the photocurrent and a twofold decrease in the response time after an external electric field poling. First, a robust meniscus-assisted solution-printing strategy is employed to facilitate the oriented perovskite crystals over a large area. Subsequently, the electrical poling invokes the ion migration within perovskite crystals, thus inducing a polarization potential, as substantiated by the surface potential change assessed by Kelvin probe force microscopy. Such electrical-poling-induced polarization potential is responsible for the markedly enhanced photocurrent and largely shortened response time. This work presents new insights into the electrical-poling-triggered ion migration and, in turn, polarization potential as well as into the implication of the latter for optoelectronic devices with greater performance. As such, the utilization of ion-migration-produced polarization potential may represent an important endeavor toward a wide range of high-performance perovskite-based photodetectors, solar cells, transistors, scintillators, etc.     

Etching characteristics of thin SiON films using a liquefied perfluorocarbon precursor of C6F12O with a low global warming potential

Perfluorocarbon gas is widely used in the semiconductor industry. However, perfluorocarbon has a negative effect on the global environment owing to its high global warming potential (GWP) value. An alternative solution is essential. Therefore, we evaluated the possibility of replacing conventional perfluorocarbon etching gases such as CHF₃ with C₆F₁₂O, which has a low GWP and is in a liquid state at room temperature. In this study, silicon oxynitride (SiON) films were plasma-etched using inductively coupled CF₄ +C₆F₁₂O+O₂ mixed plasmas. Subsequently, the etching characteristics of the film, such as etching rate, etching profile, selectivity over Si, and photoresist, were investigated. A double Langmuir probe was used and optical emission spectroscopy was performed for plasma diagnostics. In addition, a contact angle goniometer and x-ray photoelectron spectroscope were used to confirm the change in the surface properties of the etched SiON film surface. Consequently, the etching characteristics of the C₆F₁₂O mixed plasma exhibited a lower etching rate, higher SiON/Si selectivity, lower plasma damage, and more vertical etched profiles than the conventional CHF₃ mixed plasma. In addition, the C₆F₁₂O gas can be recovered in the liquid state, thereby decreasing global warming. These results confirmed that the C₆F₁₂O precursor can sufficiently replace the conventional etching gas.