Search

This study investigates the gasification of cellulose, lignin, corn stover (rich in cellulose) and walnut shells (rich in lignin) using CaO as a catalyst. The objective was to understand the effect of the different biomass components on the gasification products and the performance of the CaO catalyst. Notable results indicate distinctive product distribution: cellulose yields higher liquid (58%) and CO (95.36%) products, while lignin produces increased H2 (47.88%), CH4 (34.34%), and CO2 (29.58%). Gasification of biomass feedstocks, corn stover (cellulose-rich) and walnut shell (lignin-rich), aligns with pure cellulose and lignin trends. Catalyst characterization highlights that cellulose exhibits a greater tendency for coke formation, leading to elevated tar compounds and coke deposition on the catalyst surface. The solid residue from cellulose gasification displays a smaller pore volume (5.70 m2/g) and specific surface area, indicating undesirable catalyst rearrangement. XRD analysis indicates a higher carbonation rate of CaO in lignin-rich gasification, leading to increased CaCO3 formation. Further results show a higher CO2 concentration (3.35 mol/kg) and lower CO production (0.54 mol/kg) in corn stover gasification, contrasting with walnut shell (CO2: 14.24 mol/kg, CO: 1.24 mol/kg). The study underscores the quantitative assessment of biomass composition for optimizing gasification processes, vital for catalyst selection and ensuring efficient CO2 capture in industrial applications. [ABSTRACT FROM AUTHOR]

Accelerated carbonation experiments about the development of carbonation rates of ordinary Portland cement concrete under different artificial climates were carried out. Six water cement ratios and six climate condition combinations of temperature and relative humidity were used. Results indicate that changes of concrete carbonation rate with environmental temperature agree the Arrhenius law well, which suggests concrete carbonation rate has obvious dependence on temperature. The higher the temperature is, the more quickly the concrete carbonates, and at the same time it is also affected by environmental relative humidity. Thereafter, the apparent activation energy E of concrete carbonation reaction was obtained, ranging from 16.8 to 20.6 kJ/mol corresponding 0.35-0.74 water cement ratio, and lower water cement ratio will cause the apparent activation energy increase. Concrete carbonation rates will increase 1.1-1.69 times as temperature increase every 10 °C at the temperature range of 10 to 60 °C. [ABSTRACT FROM AUTHOR]

The single influence of capillary porosity and coupling effects of absolute basicity and capillary porosity on concrete carbonation were investigated. The experimental results showed that carbonation rate of concrete at a given absolute basicity (AB) increased moderately with the increase of the porosity ranging from 6.2% to 9.25%, and increased rapidly with porosity from 9.25% to 12.8%.The coupling effect mainly embodied in disappeared mutation point of capillary porosity, and the distributing regions of carbonation depth were clearly partitioned in the coupling influence of absolute basicity and capillary porosity. A design method on carbonation related durability of concrete based on the coupling effects was proposed. [ABSTRACT FROM AUTHOR]