Ni₃S₂ nanocrystals wrapped by thin carbon layer and anchored on the sheets of reduced graphene oxide (Ni₃S₂@C/RGO) have been synthesized by a spray-coagulation assisted hydrothermal method and combined with a calcination process. Cellulose, dissolved in Thiourea/NaOH aqueous solution is chosen as carbon sources and mixed with graphene oxide via a spray-coagulation method using graphene suspension as coagulation bath. The resulted cellulose/graphene suspension is utilized as solvent for dissolving of Ni(NO₃)₂ and then used as raw materials for hydrothermal preparation of the Ni₃S₂@C/RGO composites. The structure of the composites has been investigated and their electrochemical properties are evaluated as anode material for lithium-ion batteries. The Ni₃S₂@C/RGO sample exhibits increasing reversible capacities upon cycles and shows a superior rate performance as well. Such kinds of promising performance have been ascribed to the wrapping effect of carbon layer which confines the dislocation of the polycrystals formed upon cycles and the enhanced conductivity as the integration of RGO conductive substrate. Discharge capacities up to 850 and 630 mAh·g⁻¹ at current densities of 200 and 5000 mA·g⁻¹, respectively, are obtained. The evolution of electrochemical performance of the composites with structure variation of the encapsulated Ni₃S₂ nanocrystals has been revealed by ex-situ TEM and XRD measurements.

This thesis reports the preparation of chitosan/polyacrylamide/graphene oxide nanocomposites (CAGs) and a study of its adsorption properties of methylene blue (MB) solution. Initially, we synthesized CAGs by blending and freeze-drying methods. Then, we conducted a series experiments by removing MB from aqueous solution to test its adsorption properties and adsorption mechanism. We used UV-Vis spectrophotometry to determine the concentration of residual methylene blue accurately and efficiently, which has a specific absorption peak at 662 nm in the UV-Vis spectrum, in aqueous solution. When the graphene oxide content in the composite was 20 wt%, the adsorption capacity reached maximum values. The chemical properties and surface structure of the nanomaterials were analyzed using FT-IR, TGA, SEM, and BET. Also, we carried out experiments to measure the adsorption properties of the CAGs by varying several factors, such as initial concentration, adsorption time, and pH, etc. The outcomes revealed that the adsorption equilibrium was developed after 2800 min at 20 °C (room temperature) with an adsorbent dosage of 0.01 g mL⁻¹. The ion adsorption equilibrium data were well-fitted by the Langmuir isotherm with a maximum monolayer capacity of 510.2 mg/g. Kinetic researches disclosed that the adsorption procedure was defined by a pseudo-second-order model. Thermodynamic researches revealed that the enthalpy change (ΔH⁰) as well as Gibbs free energy change (ΔG⁰) of the adsorption procedure was negative, indicating that the adsorption procedure was spontaneous and exothermic. After three cycles, the removal efficiency was still 90.18%. Therefore, in conclusion, we believe that the CAGs is a good adsorption material for organic dyes due to its good adsorption and recyclable properties.

In this study, a solar single/double-effect switching LiBr-H₂O absorption refrigeration system was investigated to make full use of solar energy and give full play to the advantages of solar refrigeration systems. A corresponding thermodynamic dynamic mathematical model was developed. The operation characteristics of the system operating continuously for one week were analyzed. In order to highlight the advantages of the solar single/double-effect switching absorption refrigeration system, it was compared with other forms of solar refrigeration systems and compression refrigeration systems. The practical application potential of the single/double-effect switching LiBr-H₂O absorption refrigeration system was evaluated from the perspective of economy and environmental effect. The results showed that the system could achieve the switching operation between single-effect mode and double-effect mode under weather conditions of high solar radiation intensity, and the daily cooling efficiency on such days was relatively high. After an auxiliary heater was added, the primary energy savings of the solar single/double-effect switching LiBr-H₂O absorption refrigeration system were 25–52%, depending on the area of the collector and the volume of the storage tank. The solar fraction of the system was about 71.99% for continuous operation during the whole refrigeration season. However, the initial investment cost of the system equipment accounted for 89.66% of the total cost. Compared with the traditional compression refrigeration system, the initial investment cost of the solar single/double-effect switching LiBr-H₂O absorption refrigeration system was higher, but it had a better environmental protection effect.

Iron-based oxygen carriers (OCs) have received much attention due to their low costs, high mechanical strengths and high-temperature stabilities in the chemical looping gasification (CLG) of biomass, but their chemical reactivity is very ordinary. Converter steel slags (CSSs) are steelmaking wastes and rich in Fe₂O₃, CaO and MgO, which have good oxidative ability and good stability as well as catalytic effects on biomass gasification. Therefore, the composite OCs prepared by mechanically mixing CSSs with iron-based OCs are expected to be used to increase the hydrogen production in the CLG of biomass. In this study, the catalytic performance of CSS/Fe₂O₃ composite OCs prepared by mechanically mixing CSSs with iron-based OCs on the gasification of brewers’ spent grains (BSGs) were investigated in a tubular furnace experimental apparatus. The results showed that when the weight ratio of the CSSs in composite OCs was 0.5, the relative volume fraction of hydrogen reached the maximum value of 49.1%, the product gas yield was 0.85 Nm³/kg and the gasification efficiency was 64.05%. It could be found by X-ray diffraction patterns and scanning electron microscope characterizations that the addition of CSSs helped to form MgFe₂O₄, which are efficient catalysts for H₂ production. Owing to the large and widely distributed surface pores of CSSs, mixing them with iron-based OCs was beneficial for catalytic steam reforming to produce hydrogen.

Unlike the hot-melting processing of thermoplastic plastics, the processing of starch-based material relies on the addition of solvents, resulting in their low productivity, hindering large-scale industrialized production. A strategy to realize the high production efficiency of starch-based material, an environmentally friendly modification process without waste liquid generation, was designed to prepare a hot-melting starch (HMS) that can be repeatedly hot melted. Ball milling, enzymatic digestion, and deep eutectic solvent (DES) plasticization modification were combined to prepare the HMS. Ball milling destroyed the starch’s particles and the crystallinity, exposing the hydroxyl group, which allowed amylase to achieve enzymatic hydrolysis more easily. After enzymatic hydrolysis, the molecular chains of modified starch were shortened and the entanglement of molecular chains was reduced, which promoted the slip of molecular chains. The plasticization of DES, which promoted by the broken starch particles and the destroyed crystal structure, formed stronger hydrogen bonds and facilitated hot melting. Furthermore, due to the excellent hot-melting properties, HMS can be combined with sisal fiber and polycaprolactone (PCL) under solvent-free conditions. The tensile strength of HMS/sisal fiber/PCL was increased by 109%; meanwhile, the water contact angle was stabilized at 104°, when the blending ratio of hot-melting starch was 67.5% compared with HMS.