Related Experiment Video
Updated: Aug 13, 2025

Author Spotlight: Optimizing Hollow-Fiber Membranes for Continuous Liquid-Liquid Extraction of Medium-Chain Fatty Acids
Published on: August 9, 2024
Isolation of Carboxylic Acids and NaOH from Kraft Black Liquor with a Membrane-Based Process Sequence
Silvia Maitz1, Lukas Wernsperger1, Marlene Kienberger1
1Institute of Chemical Engineering and Environmental Technology, Graz University of Technology, Inffeldgasse 25c, 8010 Graz, Austria.
Abstract:
In kraft pulping, large quantities of biomass degradation products dissolved in the black liquor are incinerated for power generation and chemical recovery. The black liquor is, however, a promising feedstock for carboxylic acids and lignin. Efficient fractionation of black liquor can be used to isolate these compounds and recycle the pulping chemicals. The present work discusses the fractionation of industrial black liquor by a sequence of nanofiltration and bipolar membrane electrodialysis units. Nanofiltration led to retention of the majority of lignin in the retentate and to a significant concentration increase in low-molecular-weight carboxylic acids, such as formic, acetic, glycolic and lactic acids, in the permeate. Subsequent treatment with bipolar membrane electrodialysis showed the potential for simultaneous recovery of acids in the acid compartment and the pulping chemical NaOH in the base compartment. The residual lignin was completely retained by the used membranes. Diffusion of acids to the base compartment and the low current density, however, limited the yield of acids and the current efficiency. In experiments with a black liquor model solution under optimized conditions, NaOH and acid recoveries of 68-72% were achieved.
More Related Videos
16:33Methods for Facilitating Microbial Growth on Pulp Mill Waste Streams and Characterization of the Biodegradation Potential of Cultured Microbes
Published on: December 12, 2013
07:25Green and Low-cost Production of Thermally Stable and Carboxylated Cellulose Nanocrystals and Nanofibrils Using Highly Recyclable Dicarboxylic Acids
Published on: January 9, 2017
Related Concept Videos
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
Preparation of Carboxylic Acids: Overview
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...
Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
Reducing carboxylic acid derivatives like acyl chlorides (RCOCl), esters (RCO2R′), and nitriles (RCN) using milder aluminum hydride agents like lithium tri-tert-butoxyaluminum hydride [LiAlH(O-t-Bu)3] and diisobutylaluminum hydride [DIBAL-H]...