Bernard Wiredu

Vanillin based polymers: I. An electrochemical route to polyvanillin

Electrochemical reductive polymerization of divanillin in aqueous sodium hydroxide using a lead cathode gives polyvanillin in 91% yield. The product was characterized by elemental analysis, UV-Vis, FT-IR, 1H, 13C NMR, TGA-DTGA, and GPC.

Brönsted Acidic Ionic Liquid 1-(1-Propylsulfonic)-3-methylimidazolium-Chloride Catalyzed Hydrolysisof D-Cellobiose in Aqueous Medium

Bronsted acidic ionic liquid 1-(1-propylsulfonic)-3-methylimidazolium chloride (PSMIMCl) shows a higher catalytic activity than sulfuric acid in the hydrolysis of D-cellobiose to D-glucose in water at 90–120°C. This catalytic activity enhancement is more significant at higher temperatures, and at 120°C, PSMIMCl produced 64.5% glucose yield, whereas H2SO4 produced only 42.2% after 40 min. reaction, and this is a 52.8% enhancement of catalytic activity due to the alkylimidazolium group attached to the sulfonic acid group. 1H NMR monitoring of the D-cellobiose hydrolysis in PSMIMCl and sulfuric acid mediums failed to reveal intermediates in the hydrolysis reaction, and this is probably due to rapid conversion of the intermediate(s) to a mixture of D-glucose anomers with .

A comparison of dilute aqueous p-toluenesulfonic and sulfuric acid pretreatments and saccharification of corn stover at moderate temperatures and pressures.

Single step pretreatment-saccharification of corn stover was investigated in aqueous p-toluenesulfonic and sulfuric acid media. Dilute aqueous solution of p-toluenesulfonic acid was a better catalyst than aqueous sulfuric acid of the same H(+) ion concentration for single step pretreatment-saccharification of corn stover at moderate temperatures and pressures. For example, 100mg corn stover heated at 150°C for 1h in 0.100 M H(+) aqueous sulfuric acid produced 64 μmol of total reducing sugars (TRS), whereas the sample heated in 0.100 M H(+)p-toluenesulfonic acid produced 165 μmol of TRS under identical conditions. Glucose yield showed a similar trend, as aq. sulfuric acid and p-toluene sulfonic acid media produced 29 and 35 μmol of glucose respectively after 2.5h. Higher catalytic activity of p-toluenesulfonic acid may be due to an interaction with biomass, supported by repulsion of hydrophobic tolyl group by the aqueous phase.

The effect of metal ions as co-catalysts on acidic ionic liquid catalyzed single-step saccharification of corn stover in water

The effects of adding Cr(3+), Mn(2+), Fe(3+), Co(2+) Ni(2+), Cu(2+), Zn(2+) and La(3+) chlorides as co-catalysts to 1-(1-propylsulfonic)-3-methylimidazolium chloride acidic ionic liquid catalyzed saccharification of corn stover in aqueous medium was studied at 140-170 °C, by measuring the total reducing sugar (TRS) and glucose yields. The samples with Mn(2+), Fe(3+), Co(2+) as co-catalysts produced higher TRS yields compared to the sample without the metal ions. The Mn(2+) produced the highest catalytic effect enhancements and produced TRS yields of 68.0%, 72.9%, 90.2% and 87.9% at 140, 150, 160 and 170 °C respectively; whereas the corn stover samples without the Mn(2+) produced TRS yields of 42.9%, 52.3%, 54.4% and 53.5% at the same four temperatures. At higher temperatures of 160 and 170 °C, all metal ions studied produced significant enhancements in glucose yields, except Cr(3+). The addition of La(3+) as a co-catalyst produced the highest glucose yield improvement.

Chemocatalytic hydrolysis of cellulose at 37 °C, 1 atm

The metal salt – Bronsted acidic ionic liquid system composed of ZnCl2·1.74H2O-1-(1-propylsulfonic)-3-methylimidazolium chloride can directly hydrolyze untreated cellulose in 78% total reducing sugar and 19% glucose yield at 37 °C, 1 atm in 4.0 days. The new chemical catalyst is used at a temperature lower than typical cellulase enzyme operating conditions.

Interactions of d-cellobiose with selected chloride salts: A 13 C NMR and FT-IR study

The interactions of cellulose model compound d-cellobiose with chloride salts of Zn(2+), Ca(2+), Li(+), Sn(2+), La(3+), Mg(2+), K(+) and NH4(+) were evaluated by measuring the (13)C NMR chemical shift changes (Δδ) of the disaccharide due to the addition of salts in D2O. The KCl and NH4Cl showed similar Δδ changes due to interactions only with the Cl(-) anion. Whereas other chloride salts showed interactions with both cation and anion. Among these salts the total interactions are in the order: Zn(2+)>Sn(2+)>Li(+)>Ca(2+)~La(3+)>Mg(2+). The FT-IR spectra of D-cellobiose-chloride salt 1:2 mixtures also indicate that KCl and NH4Cl interacts similarly with D-cellobiose in the solid state.

Conversion of levulinic acid and cellulose to γ-valerolactone over Raney-Ni catalyst using formic acid as a hydrogen donor

AbstractThe present study aimed to investigate the conversion of levulinic acid (LA) and cellulose (DP∼450) to γ-valerolactone (GVL) over Raney-Ni catalyst. In this process, hydrogenation was fulfi...