Composite additives regulate physicochemical and microbiological properties in green waste composting: A comparative study of single-period and multi-period addition modes.

Composting additives can significantly enhance green waste (GW) composting. However, their effectiveness is limited due to the short action duration of a single-period addition. Therefore, this study proposes that multi-period additive modes to prolong the action duration, expedite lignocellulose degradation, reduce composting time, and enhance product quality. This study conducted six treatments (T1-T6), introducing a compound additive (BLP) during the mesophilic (MP) and cooling periods (CP). Each treatment consistently maintained 25% total BLP addition of GW dry weight, with variations only in the BLP distribution in different periods. The composition of BLP consists of Wbiochar: Wlactic acid: Wpond sediment in a ratio of 10:1:40. Specifically, T1 added 25% BLP in CP, T2 added 5% in MP and 20% in CP, T3 added 10% in MP and 15% in CP, T4 added 15% in MP and 10% in CP, T5 added 20% in MP and 5% in CP, and T6 added 25% in MP. In this study, composting temperature, pH value, electrical conductivity, total porosity, the contents of lignin, cellulose, hemicellulose, and nutrient, scanning electron microscopy images, germination index, and the successions of different bacteria and fungi at the phylum and genus levels were detailed. Results showed T4 achieved two thermophilic periods and matured in just 25 days. T4 enhanced lignocellulose degradation rates (lignin: 16-53%, cellulose: 14-23%, hemicellulose: 9-48%) and improved nutrient content. The above results, combined with correlation analysis and structural equation model, indicated that T4 may promote the development of dominant bacteria (Proteobacteria, Firmicutes, Actinobacteria, Bacteroidetes) by regulating compost physicochemical properties and facilitate the growth of dominant fungi (Ascomycota and Basidiomycota) by modulating nutrient supply capacity. This ultimately leads to a microbial community structure more conducive to lignocellulose degradation and nutrient preservation. In summary, this study reveals the comprehensive effects of single-period and multi-period addition methods on GW composting, providing a valuable basis for optimizing the use of additives and enhancing the efficiency and quality of GW composting.

Combined addition of biochar, lactic acid, and pond sediment improves green waste composting.

Composting, as an eco-friendly method to recycle green waste (GW), converts the GW into humus-like compounds. However, conventional GW composting is inefficient and generates poor-quality compost. The objective of this research was to investigate the effects of the combined additions of biochar (BC; 0, 5, and 10 %), lactic acid (LA; 0, 0.5, and 1.0 %), and pond sediment (PS; 0, 20, and 30 %) on GW composting. A treatment without additives served as the control (treatment T1). The results showed that treatment R1 (with 5 % BC, 0.5 % LA, and 20 % PS) was better than the treatments with two additives or no additive and required only 32 days to generate a stable and mature product. Compared with T1, R1 improved water-holding capacity, electrical conductivity, available phosphorus, available potassium, nitrate nitrogen, OM decomposition, and germination index by 51 %, 48 %, 170 %, 93 %, 119 %, 157 %, and 119 %, respectively. R1 also increased the activities of cellulase, lignin peroxidase, and laccase. The results showed that the combined addition of BC, LA, and PS increased the gas exchange, water retention, and the microbial secretion of enzymes, thus accelerating the decomposition of GW. This study demonstrated the effects of BC, LA, and PS addition on GW composting and final compost properties, and analyzed the reasons of the effects. The study therefore increases the understanding of the sustainable disposal of an important solid waste.

Synergetic Function of the Single-Atom Ru-N4 Site and Ru Nanoparticles for Hydrogen Production in a Wide pH Range and Seawater Electrolysis.

Hydrogen production by water splitting and seawater electrolysis is a promising alternative to develop clean hydrogen energy. The construction of high-efficiency and durable electrocatalysts for the hydrogen evolution reaction (HER) in a wide pH range and seawater is critical to overcoming the sluggish kinetic process. Herein, we develop an efficient catalytic material composed of a single-atom Ru-N4 site and Ru nanoparticles anchored on nitrogen-doped carbon (Ru1+NPs/N-C) through the coordination-pyrolysis strategy of the melamine formaldehyde resin. The Ru1+NPs/N-C catalyst shows outstanding HER activity with the smallest overpotentials, the lowest Tafel slopes, the highest mass activity and turnover frequency, as well as excellent stability in both acidic and alkaline media. Moreover, Ru1+NPs/N-C shows comparable hydrogen production performance and a higher faradic efficiency to 20% Pt/C in natural seawater and artificial simulated seawater. Theoretical calculations demonstrate that the strong synergistic effects between the Ru-N4 site and Ru nanoparticles modify the electronic structure to accelerate the HER kinetics. Ru nanoparticles can effectively realize dissociation of H2O to generate adsorbed hydrogen and also promote the single-atom Ru-N4 site to combine adsorbed hydrogen to H2 and desorption. This work provides a new perspective for designing high-efficiency hydrogen production electrocatalysts for large-scale seawater electrolysis.

Ferrocene-Labelled Electroactive Aptamer-Based Sensors (Aptasensors) for Glycated Haemoglobin.

Glycated haemoglobin (HbA1c) is a diagnostic biomarker for type 2 diabetes. Traditional analytical methods for haemoglobin (Hb) detection rely on chromatography, which requires significant instrumentation and is labour-intensive; consequently, miniaturized devices that can rapidly sense HbA1c are urgently required. With this research, we report on an aptamer-based sensor (aptasensor) for the rapid and selective electrochemical detection of HbA1c. Aptamers that specifically bind HbA1c and Hb were modified with a sulfhydryl and ferrocene group at the 3' and 5'-end, respectively. The modified aptamers were coated through sulfhydryl-gold self-assembly onto screen printed electrodes, producing aptasensors with built in electroactivity. When haemoglobin was added to the electrodes, the current intensity of the ferrocene in the sensor system was reduced in a concentration-dependent manner as determined by differential pulse voltammetry. In addition, electrochemical impedance spectroscopy confirmed selective binding of the analytes to the aptamer-coated electrode. This research offers new insight into the development of portable electrochemical sensors for the detection of HbA1c.

Facile synthesis of hexagonal α-Co(OH)2 nanosheets and their superior activity in the selective reduction of nitro compounds.

Novel hexagonal α-cobalt hydroxide nanosheets are synthesized through a 2-methylimidazole-induced hydrolysis strategy with cetyltrimethylammonium bromide (CTAB) as a surfactant. The weak alkaline environment provides favorable conditions for the formation of metastable α-Co(OH)2, while the same raw material will produce ß-Co(OH)2 when a strong alkali solution is used. CTAB plays a vital role not only in hexagonal oriented growth, but also in the formation of the hydrotalcite-like structure of α-Co(OH)2 with high crystallinity. The crystallinity of both α- and ß-Co(OH)2 is very poor without CTAB as a surfactant. The Co in this Co(OH)2-x layer presents most of the CoII and a small part of the CoIII, and the interlayer nitrate anion balances the positive charge of the host layer. The redox function produced by the CoII and CoIII of α-Co(OH)2 together with the large layer spacing jointly promotes the electron and mass transfer. The use of hydrazine hydrate for transfer hydrogenation involves the transport of protons and electrons produced by decomposition, and the rapid transport is bound to be conducive to the reduction process. Nitro compounds with varieties of functional groups can be smoothly reduced to the corresponding amines with high selectivity, when α-Co(OH)2 was used as a catalyst under mild conditions.

Support Diminution Design for Layered Manufacturing of Manifold Surface Based on Variable Orientation Tracking.

This article proposes a support diminution design method for layered manufacturing of manifold surface based on variable orientation tracking (VOT). We aim at reducing the external support or upholders to a minimum with maximum possibility theoretically to save material and diminish material stripping effect (MSE), thereby improving the bilateral surface precision either exterior or interior. The cosmic gravity effect criterion is first used to extract surface need support from manifold surface with various materials by considering the balance force involving material characteristics and inclination angle. In the light of this criterion theory, varying the substrate normal orientation (SNO), namely workbench, for each layer in printing coordinate system, may break the balance between gravity and its equilibrium force. Therefore, the optimal SNO can be rigorously calculated using mathematical harmonic analysis among the continuous domain. To serve for the multidegree of freedom (DOF) on account of SNO, a reconfigurable VOT robot with six-axis DOF is developed for 3D printing (3DP). The matched servo controller is successfully implemented to accurate tracking of both orientation and Cartesian coordinates, using forward kinematic chains as well as reverse kinematic tracking. What is more, the end-effector (extruder) is holding perpendicular to the substrate workbench. The physical experiment that takes human external ear auricle, for example, using a layer-based process is implemented via VOT. The MSE due to supporting material can be clearly observed and diminished using an optical microscope. The stripped material from external support via diminution design can be evaluated quantitatively by electronic weighting balance. All of which indicate the findings that external support in 3DP can be virtually reckoned and diminished using VOT rather than the so-called build orientation traversal method. The VOT method upon which we touched can be widely applied to various layered manufacturing of accurate structure, for instance, cantilever, sandwich, and scaffolds in the occasion needing precise curtailment of outer support multimaterial.

A supramolecular pyrenyl glycoside-coated 2D MoS2 composite electrode for selective cell capture.

Here we demonstrate the simple construction and characterization of a pyrenyl glycoside-coated 2D MoS2 material composite capable of selectively capturing proteins and live cells on an electrode, as determined by differential pulse voltammetry.

Probing Mannose-Binding Proteins That Express on Live Cells and Pathogens with a Diffusion-to-Surface Ratiometric Graphene Electrosensor.

This paper describes the development of a "diffusion-to-surface" ratiometric graphene electrosensor for the selective detection of live cells and pathogens that highly express mannose-binding proteins (MBPs). MBPs have been implicated in many pathological processes and are identified on specific types of bacteria. Consequently, MBPs are a promising biomarker for targeted disease diagnosis and therapy. Here, we develop a unique electrosensor that features a ratiometric voltammetric signal for the selective probing of MBPs. Self-assembly of mannosyl anthraquinone (AQ) to a graphene oxide-decorated screen-printed electrode produces the sensor with an inherent surface-controlled voltammetric signal. Subsequently, addition of a redox probe (RP) imparts the system with a diffusion-controlled current, thus enabling a ratiometric sensing rationale for which AQ serves as a reference. While the reference current is hardly compromised by adding analytes, RP exhibits a concentration-dependent current quenching on addition of mannose-selective lectins over other proteins. Importantly, this ratiometric electrosensor has proven to be applicable for the ratiometric probing of alternatively activated macrophages and a Gram-negative bacterium highly expressing MBPs, but shows minimal response to a series of control live cells and bacteria without mannose receptor expression.