Tailoring planar slip to achieve pure metal-like ductility in body-centred-cubic multi-principal element alloys.

Uniform tensile ductility (UTD) is crucial for the forming/machining capabilities of structural materials. Normally, planar-slip induced narrow deformation bands localize the plastic strains and hence hamper UTD, particularly in body-centred-cubic (bcc) multi-principal element high-entropy alloys (HEAs), which generally exhibit early necking (UTD < 5%). Here we demonstrate a strategy to tailor the planar-slip bands in a Ti-Zr-V-Nb-Al bcc HEA, achieving a 25% UTD together with nearly 50% elongation-to-failure (approaching a ductile elemental metal), while offering gigapascal yield strength. The HEA composition is designed not only to enhance the B2-like local chemical order (LCO), seeding sites to disperse planar slip, but also to generate excess lattice distortion upon deformation-induced LCO destruction, which promotes elastic strains and dislocation debris to cause dynamic hardening. This encourages second-generation planar-slip bands to branch out from first-generation bands, effectively spreading the plastic flow to permeate the sample volume. Moreover, the profuse bands frequently intersect to sustain adequate work-hardening rate (WHR) to large strains. Our strategy showcases the tuning of plastic flow dynamics that turns an otherwise-undesirable deformation mode to our advantage, enabling an unusual synergy of yield strength and UTD for bcc HEAs.

High-Efficiency Oxygen Reduction Reaction Revived from Walnut Shell.

The development of inexpensive and efficient electrocatalysts for oxygen reduction reactions (ORR) remains a challenge with respect to renewable energy technologies. In this research, a porous, nitrogen-doped ORR catalyst is prepared using the hydrothermal method and pyrolysis with walnut shell as a biomass precursor and urea as a nitrogen source. Unlike past research, in this study, urea is not directly doped; instead, a new type of doping is carried out after annealing at 550 °C. In addition, the sample's morphology and structure are analyzed and characterized by scanning electron microscopy (SEM) and X-ray powder diffraction (XRD). A CHI 760E electrochemical workstation is used to test NSCL-900's performance in terms of oxygen reduction electrocatalysis (ORR). It has been found that the catalytic performance of NSCL-900 is significantly improved compared with that of NS-900 without urea doping. In a 0.1 mol/L KOH electrolyte, the half-wave potential can reach 0.86 V (vs. RHE) and the initial potential is 1.00 V (vs. RHE). The catalytic process is close to four-electron transfer and there are large quantities of pyridine nitrogen and pyrrole nitrogen.

Highly Efficient Oxygen Reduction N-Doped Carbon Nanosheets Were Prepared by Hydrothermal Carbonization.

A metal-free carbon catalyst is a kind of oxygen reduction catalyst with great prospects. It is an important material with potential to replace the traditional Pt catalyst. In this paper, a kind of irregular and ultra-thin carbon nanosheet (K180M-300-900) with high catalytic activity was synthesized by hydrothermal calcination using okra as a biomass and NH4Cl as an N source. The prepared nitrogen-doped metal-free catalyst with high pyridine-N and graphitic-N provides an extremely large number of active sites and has certain lattice defects. Ultra-thin carbon nanosheets promote sufficient contact between the catalyst and electrolyte, promote the diffusion of oxygen, and result in a faster transfer rate of electrons. The initial potential and half-slope potential of K180M-300-900 are 0.99 V and 0.82 V, respectively, which are comparable to those of 20% Pt/C. In addition, the stability and methanol tolerance of this catalyst (K180M-300-900) are better than 20% Pt/C, so it has great development potential and application value. This result provides a new method to prepare metal-free carbon materials that will take the place of traditional Pt catalysts.

Nanosheets with High-Performance Electrochemical Oxygen Reduction Reaction Revived from Green Walnut Peel.

The synthesis of metal-free carbon-based electrocatalysts for oxygen reduction reactions (ORR) to replace conventional Pt-based catalysts has become a hot spot in current research. This work proposes an activation-assisted carbonization strategy, to manufacture N-doped ultra-thin carbon nanosheets (GWS180M800) with high catalytic activity, namely, melamine is used as an accelerator/nitrogen source, and walnut green peels biological waste as a carbon source. The melamine acts as a nitrogen donor in the hydrothermal process, effectively enhancing the nitrogen doping rate. The content of pyridine nitrogen groups accounts for up to 48.5% of the total nitrogen content. Electrochemical tests show that the GWS180M800 has excellent ORR electrocatalytic activity and stability, and makes a quasi-four-electron ORR pathway clear in the alkaline electrolyte. The initial potential and half slope potential are as high as 1.01 and 0.82 V vs. RHE, respectively. The GWS180M800 catalyst has a better ability to avoid methanol cross poisoning than Pt/C has. Compared with 20 wt% Pt/C, GWS180M800 has improved methanol tolerance and stability. It is a metal-free biochar ORR catalyst with great development potential and application prospects. This result provides a new space for the preparation of valuable porous nano-carbon materials based on carbonaceous solid waste and provides new ideas for catalyzing a wide range of electrochemical reactions in the future.

Awn Stem-Derived High-Activity Free-Metal Porous Carbon for Oxidation Reduction.

Designing oxygen reduction reaction (ORR) catalysts with excellent performance has far-reaching significance. In this work, a high-activity biomass free-metal carbon catalyst with N and S co-doped was successfully prepared by using the KOH activated awn stem powder as the precursor with organic matter pore-forming doping technology, which is named TAAS. The content of pyridine nitrogen groups accounts for up to 36% of the total nitrogen content, and a rich pore structure is formed on the surface and inside, which are considered as the potential active centers of ORR. The results show that the specific surface area of TAAS reaches 191.04 m2/g, which effectively increases the active sites of the catalyst, and the initial potential and half slope potential are as high as 0.90 and 0.76 V vs. RHE, respectively. This study provides a low-cost, environmentally friendly and feasible strategy for the conversion of low-value agricultural and forestry wastes into high value-added products to promote sustainable development of energy and the environment.

An Ultra-Low Modulus of Ductile TiZrHfTa Biomedical High-Entropy Alloys through Deformation Induced Martensitic Transformation/Twinning/Amorphization.

Biomedical alloys are paramount materials in biomedical applications, particularly in crafting biological artificial replacements. In traditional biomedical alloys, a significant challenge is simultaneously achieving an ultra-low Young's modulus, excellent biocompatibility, and acceptable ductility. A multi-component body-centered cubic (BCC) biomedical high-entropy alloy (Bio-HEA), which is composed of non-toxic elements, is noteworthy for its outstanding biocompatibility and compositional tuning capabilities. Nevertheless, the aforementioned challenges still remain. Here, a method to achieve a single phase with the lowest Young's modulus among the constituent phases by precisely tuning the stability of the BCC phase in the Bio-HEA, is proposed. The subtle tuning of the BCC phase stability also enables the induction of stress-induced martensite transformation with extremely low trigger stress. The transformation-induced plasticity and work hardening capacity are achieved via the stress-induced martensite transformation. Additionally, the hierarchical stress-induced martensite twin structure and crystalline-to-amorphous phase transformation provide robust toughening mechanisms in the Bio-HEA. The cytotoxicity test confirms that this Bio-HEA exhibits excellent biocompatibility without cytotoxicity. In conclusion, this study provides new insights into the development of biomedical alloys with a combination of ultra-low Young's modulus, excellent biocompatibility, and decent ductility.

Iron-modified carriers accelerate biofilm formation and resist anammox bacteria loss in biofilm reactors for partial denitrification-anammox.

The slow formation of anammox biofilms presents a bottleneck for resolving anammox bacterial loss and achieving stable performance in biofilm-based partial denitrification-anammox (PD-A) processes. This study utilized iron-modified (K1/Fe3O4 NPs) carriers, which were prepared and used for the first time in PD-A processes. Parallel moving bed biofilm reactors (MBBRs) indicated that iron-modified carriers facilitated the formation of biofilms at a faster rate than K1 carriers, consequently improving the nitrogen removal performance of the process by over 40 %. 16S rDNA analysis showed that anammox bacteria were approximately four times more abundant in the iron-modified carrier biofilm than in the K1 carrier biofilm. XPS and zeta potential analysis suggested that the improved microbial affinity of the iron-modified carrier surface caused this. As a result, the iron-modified carriers facilitated the formation of anammox biofilms and enhanced PD-A performance.

Comparing the long-term responses of soil microbial structures and diversities to polyethylene microplastics in different aggregate fractions.

Microplastics (MPs) alter soil aggregation stability. However, studies have yet to determine whether these alterations further affect microbial community structures and diversities within different soil aggregates and whether they influence the responses of soil microbial structures and diversities to MPs in different aggregate fractions. In this study, long-term soil incubation experiments and soil fractionation were combined to investigate the effects of polyethylene microplastics (PE-MPs) on soil aggregate properties and microbial communities in soil aggregates with different particle sizes. Results showed that the existence of PE-MPs significantly reduced the physicochemical properties of soil aggregates, inhibited the activities of soil enzymes, and changed the richness and diversity of bacterial and fungal communities. Such variations exerted notable differences in soil aggregate levels. The response sensitivity of bacteria in the silt and clay fraction was higher than that in the macroaggregate fraction, but the response sensitivity of fungi in the macroaggregate fraction was higher than that in the silt and clay fraction. Relationships and path analysis between soil aggregate properties and microbial communities after PE-MPs addition were proposed. PE-MPs affected microbial community structures by directly and indirectly influencing soil microenvironmental conditions. The relative abundances of Acidobacteria, Gemmatimonadetes, Bacteroides, Basidiomycota, Chtridiomyota, and Glomeromycota were significantly correlated with physicochemical properties and soil enzyme activities. Enzyme activities were direct factors influencing soil microbial community structures, and physicochemical properties (i.e., dissolved organic carbon, soil available phosphorus) could indirectly affect these structures by acting on soil enzyme activities. Our findings helped improve our understanding of the responses of soil microbial structures and diversities to MPs through the perspective of different soil aggregates.

Inhibitory effect of microplastics on soil extracellular enzymatic activities by changing soil properties and direct adsorption: An investigation at the aggregate-fraction level.

Microplastics (MPs), as a new type of environmental pollutant, pose a serious threat to soil ecosystems. The activities of soil extracellular enzymes produced by microorganisms are the potential sensitive indicators of soil quality. However, little is known about the response mechanism of enzyme activities toward MPs on a long-term scale. Moreover, information on differences in enzyme activities across different soil aggregates is lacking. In this study, 150 days of incubation experiments and soil aggregate fractionation were combined to investigate the influence of MPs on extracellular enzyme activities in soil. 28% concentration of polyethylene with size 100 µm was adopted in the treatments added with MPs. The results show that MPs inhibited enzyme activities through changing soil nutritional substrates and physicochemical properties or through adsorption. Moreover, MPs competed with soil microorganisms for physicochemical niches to reduce microbial activity and eventually, extracellular enzyme activity. Enzyme activities in different aggregate-size fractions responded differently to the MPs exposure. The catalase in the coarse particulate fraction and phenol oxidase and ß-glucosidase in the micro-aggregate fraction exerted the greatest response. With comparison, urease, manganese peroxidase, and laccase activities showed the greatest responses in the non-aggregated silt and clay fraction. These observations are believed to stem from differences in the key factors determining the enzyme activities in different aggregate-size fractions. The inhibitory pathway of microplastics on activities of extracellular enzymes in soil varies significantly across different aggregate fractions.

Decrease in bioavailability of soil heavy metals caused by the presence of microplastics varies across aggregate levels.

Microplastics can alter the physicochemical and biogeochemical processes in soil, but whether these alterations have further the effects on the transformation of soil heavy metal speciation, and if so, whether these effects vary across soil aggregate levels remain unknown. Herein, long-term soil culture experiments and soil fractionation are combined to investigate the effects of microplastics on chemical speciation of Cu, Cr, and Ni with different particle-size soil aggregates. Results show that microplastics in soil decrease the exchangeable, carbonate-bound, and Fe-Mn oxide-bound fractions of metals but increase their organic-bound fractions via direct adsorption and indirect effects on the soil microenvironment conditions. The findings suggest that microplastics can promote the transformation of heavy metal speciation from bioavailable to organic bound. Such promotion exerts notable differences across soil aggregate levels. The transformation of soil heavy metal speciation is greater in larger aggregates than in smaller aggregates in the early incubation period with microplastics but shows the opposite trend in the later incubation period. Therefore, this process is more sensitive to long-term microplastic pollution in smaller aggregates than in larger aggregates, most likely owing to the lag in the influence of microplastics on metal speciation transformation in the smaller aggregates.

Sorghum-Waste-Derived High-Surface Area KOH-Activated Porous Carbon for Highly Efficient Methylene Blue and Pb(II) Removal.

With the development of the environment and human society, the removal of metal ions and dyes in wastewater treatment remains an urgent problem to solve. In this work, two biomass carbon adsorbents were synthesized by a KOH activation and carbonization route using sorghum stem and root as carbon precursors. In comparison with the samples without KOH activation, the pore structure of the KOH-activated carbon has been dramatically improved. The findings show that the specific surface areas of the adsorbents by sorghum stem (S1) and sorghum root (R1) were 948.6 and 168.1 m2 g-1, respectively. Meanwhile, the abundant OH- and COO- groups on the surface of these adsorbents endow them with negative polarity, thereby exhibiting excellent adsorption performance for removing methylene blue (MB) and Pb(II) from wastewater. The adsorption amount and removal rate of S1 were 98.1 mg g-1 and 98.08%, respectively, for MB, whereas those of R1 were 197.6 mg g-1 and 98.82% for the Pb(II) ion, respectively. Our findings offer an invaluable insight into designing and synthesizing a highly efficient sustainable adsorbent to remove MB and Pb(II) based on biomass agricultural waste.

Study on In-Situ Synthesis Process of Ti-Al Intermetallic Compound-Reinforced Al Matrix Composites.

In this study, ball-milled powder of Ti and Al was used to fabricate Ti-Al intermetallic compound-reinforced Al matrix composites by an in-situ reaction in cold-pressing sintering and hot-pressing sintering processes. The detailed microstructure of the Ti-Al intermetallic compound-reinforced Al composite was characterized by optical microscopy (OM), X-ray diffraction (XRD), energy dispersive spectrometry (EDS), and electron backscattered diffraction (EBSD). The results indicate that a typical core-shell-like structure forms in the reinforced particles. The shell is composed of a series of Ti-Al intermetallic compounds and has good bonding strength and compatibility with the Al matrix and Ti core. With cold-pressing sintering, the shell around the Ti core is closed, and the shell thickness increases as the milling time and holding time increase. With hot-pressing sintering, some radiating cracks emerge in the shell structure and provide paths for further diffusion of Ti and Al atoms. The Kirkendall effect, which is caused by the difference between the diffusion coefficients of Ti and Al, results in the formation of cavities and a reduction in density degree. When the quantity of the intermetallic compounds increases, the hardness of the composites increases and the plasticity decreases. Therefore, factors that affect the quantity of the reinforcements, such as the milling time and holding time, should be determined carefully to improve the comprehensive properties of the composites.

Postoperative complications in patients with cochlear implants and impacts of nursing intervention.

CONCLUSION: This study shows that cochlear implantation is relatively safe surgery with few major complications and within acceptable limits. However, close follow-up observation and effective medical and nursing intervention could alleviate further complications and thus become key elements for promoting recovery of patients undergoing such surgery. OBJECTIVES: Cochlear implantation has become an effective method for curing patients disabled by profound hearing loss in China. However, full exploration of the associated complications remains to be completed. The objective of this study was thus to analyse the postoperative complications in patients with cochlear implants (CIs) in order to design improved measures for clinical and nursing interventions. METHODS: A retrospective study of 262 patients receiving CIs at the Department of Otorhinolaryngology/Head and Neck Surgery, Chinese People's Liberation Army General Hospital, Beijing, China from March 1997 to December 2006 was conducted. RESULTS: Among 262 patients, 4 cases (1.5%) had 1 or more major complications requiring substantial medical or nursing interventions, including 1 case of cerebrospinal fluid (CSF) otorrhoea accompanied by meningitis, 2 cases of facial nerve paresis and 1 case of perforation of tympanic membrane. Forty cases (15.3%) had some form of minor complication that settled spontaneously or easily with conventional treatments and nursing, of which dizziness and vomiting was the most frequent (4.2%), followed by CSF gusher without otorrhoea and/or induced meningitis (2.7%), tinnitus (1.9%) and facial nerve partially exposed without paralysis (1.5%). Eleven cases (4.2%) had some symptoms associated with installation of the cochlear device. Except for one patient who had no response after implantation because his auditory nerves were underdeveloped, all the patients who received appropriate treatment and nursing intervention had a favourable prognosis.