Cooking with active oxygen and solid alkali (CAOSA) is an efficient pretreatment method for biomass. For better grading of the lignin yellow liquor, the different lignin fractions and the recovered solid alkali were obtained using a simultaneous acid-alkali graded separation method. The results indicated that the recovery rate of solid alkali was 67.25 %, and the grading of lignin components was characterized by smaller dispersion coefficients, and more stable properties and structure. Lignin fractions with low dispersion coefficients possess more key structures, including the Phenol hydroxyl group (ArOH), Methoxy (OMe), and β-aryl ether (β-O-4), and have better thermal properties. The low molecular weight L4 has the highest ArOH content (2.1 mmol/g), which provides better antioxidant properties. The CAOSA process destroyed the S-unit and prevented lignin from condensation. Furthermore, the CAOSA process protected carbohydrates, which could effectively prevent them from dehydrating and re-polymerizing into pseudo-lignin. This allowed the pulp to remain natural, which was beneficial for subsequent transformation and utilization. Overall, the efficient separation of biomass components and lignin grading method proposed by combining the CAOSA process with the acid-alkali grading separation method has a strong application prospect and provides a theoretical basis for the high-value utilization of biomass and lignin.
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http://dx.doi.org/10.1016/j.ijbiomac.2024.134521 | DOI Listing |
Anal Chim Acta
February 2025
School of Electric Power Engineering, South China University of Technology, Guangzhou, Guangdong, 510641, China; Guangdong Province Key Laboratory of Efficient and Clean Energy Utilization, Guangzhou, Guangdong, 510641, China. Electronic address:
Background: Rapid and accurate detection of the biomass potassium (K) content in biomass is crucial for mitigating ash deposition and fouling issues in biomass fuel combustion processes. Laser-induced breakdown spectroscopy (LIBS) offers a promising approach for rapid analysis of biomass elemental. However, the accuracy of LIBS detection is susceptible to chemical matrix effects.
View Article and Find Full Text PDFSci Rep
January 2025
School of Civil Engineering and Communication, North China University of Water Resources and Electric Power, Zhengzhou, 450045, People's Republic of China.
As one of the bulk solid wastes in the Yellow River basin in China, fluorite tailings urgently need to be utilized as resources. In this paper, NaOH and NaCO were used for alkali thermal activation of ground fluorite tailings under different temperature conditions, and the reactivity was analyzed by XRD, SEM and compressive strength after hydration, so as to evaluate the feasibility of fluorite tailings as geopolymer precursor. The results show that the fluorite tailings can exhibit certain reactivity under alkaline heat excitation, and significant amorphous glass phase can be detected.
View Article and Find Full Text PDFMolecules
December 2024
School of Resources and Safety Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
As a large-volume industrial solid waste generated during the production of wet-process phosphoric acid, the primary disposal method for phosphogypsum (PG) currently involves centralized stockpiling, which requires substantial land use. Additionally, PG contains impurities, such as phosphorus, fluorine, and alkali metals, that may pose potential pollution risks to the surrounding environment. However, the mechanisms governing the co-release of phosphorus and fluorine impurities alongside valuable metal cations during leaching remain unclear, posing challenges to efficient disposal and utilization.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Beijing Key Laboratory of Lignocellulosic Chemistry, and Engineering Research Center of Forestry Biomass Materials and Energy, Ministry of Education, Beijing Forestry University, Beijing 100083, China. Electronic address:
J Am Chem Soc
January 2025
Department of Materials Science, Fudan University, Shanghai 200433, China.
Borohydrides, known for ultrahigh hydrogen density, are promising hydrogen storage materials but typically require high operating temperatures due to their strong thermodynamic stability. Here we introduce a novel light-induced destabilization mechanism for hydrogen storage reaction of borohydrides under ambient conditions photogenerated vacancies in LiH. These vacancies thermodynamically destabilize B-H bonds through the spontaneous "strong adsorption" of BH groups, which trigger an asymmetric redistribution of electrons, enabling hydrogen release at near room temperature, approximately 300 °C lower than the corresponding thermal process.
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