Related Experiment Video
Updated: Jun 8, 2026

Pretreatment of Lignocellulosic Biomass with Low-cost Ionic Liquids
Published on: August 10, 2016
Hydrolysis of cellulose by using catalytic amounts of FeCl₂ in ionic liquids
Furong Tao1, Huanling Song, Lingjun Chou
1Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, PR China.
Abstract:
Microcrystalline cellulose (MCC) is hydrolyzed to an appreciable extent (70 %) by using 1-(4-sulfonic acid) butyl-3-methylimidazolium hydrogen sulfate (IL-1) as effective catalyst. Valuable chemicals, such as 5-hydroxymethyl furfural (HMF) and furfural, are obtained in relatively high yields (15 % and 7 %, respectively). Interestingly, the introduction of FeCl₂ as catalyst into IL-1 further enhances the catalytic activity, as proved by the higher conversion of MCC (84 %) and higher yields of HMF and furfural (34 % and 19 %, respectively) under the same experimental conditions, although small amounts of levulinic acid (LA) and total reducing sugars (TRS) were also found. The hydrolysis of MCC scarcely proceeded, or showed a lower efficiency, in the absence of catalyst (4 %) or with Al₂O₃ (7 %), inorganic acids (≤65 %), or several other ionic liquids (≤24 %) as catalyst. Dimers of furan compounds were detected as the main byproducts, as analyzed by HPLC-MS; from the mass spectrometry analysis, the components of the gas-phase products were determined to be methane, ethane, CO, CO₂, and H₂. A mechanism to explain the high activity of FeCl₂ in the IL-1 system is proposed. Recycling of the IL-1 catalyst showed an almost constant activity during five successive trials. The simple and effective catalyst system may prove valuable in facilitating the energy-efficient and cost-effective conversion of biomass into biofuels and platform chemicals.
Related Concept Videos
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...
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
Cellulose and Pectic Polysaccharides
As a cell matures, its cell wall specializes according to its type. For example, the parenchyma cells of...
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Hydrolysis
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...

