Factors affecting the enzymic susceptibility of alkali and acid pretreated sugar-cane bagasse

Acid and alkali pretreatments were studied to identify those factors which are critical in determining the susceptibility of a lignocellulosic substrate (bagasse) to enzymic hydrolysis. The different effects of each treatment on the structure of the bagasse affected the subsequent susceptibility to enzymic attack in different ways. The acid treatments appeared to act by disrupting the lignin structure, probably by hydrolysing the carbohydrate chains attached to the lignin, as well as the lignin itself. The attack on the carbohydrate content removed outlying material in the cell wall (i.e. hemicellulose and amorphous cellulose) to expose a ‘core’ of more resistant regions. The alkali treatments appeared to produce a more open structure by penetrating the inner layers and selectively removing hemicellulose molecules as well as breaking some lignin—carbohydrate bonds. The different treatments resulted in structural changes which were found to affect the hydrolysis mechanism.     

Comparison of ionic liquid,acid and alkali pretreatments for sugarcane bagasse enzymatic saccharification

BACKGROUND: Much attention has been given to applying ionic liquids (ILs) as an alternative pretreatment method for lignocellulosic biomass. This study aims to select the most suitable type of IL for pretreating sugarcane bagasse (SCB). The potential of ILs for pretreatment was evaluated and compared with conventional pretreatment media, acids and alkalis. The performance of the pretreatment media was evaluated based on the amount of reducing sugar produced from enzymatic saccharification, the energy requirement, and changes in the chemical structure and crystallinity index of the pretreated bagasse. RESULTS: 1‐ethyl‐3‐methylimidazolium acetate [EMIM]oAc was selected as the most suitable IL for SCB pretreatment. The optimum yields of reducing sugar obtained from [EMIM]oAc‐, alkali‐, and acid‐pretreated SCB were 69.5%, 92.8% and 41.3%, respectively. Although a lower yield of reducing sugar was obtained, [EMIM]oAc pretreatment required the least energy to pretreat 1 kg of SCB. Moreover, the percentage of SCB loss during [EMIM]oAc pretreatment was the lowest. [EMIM]oAc‐pretreated SCB also had the lowest crystallinity index (CI) with the most amorphous structure. CONCLUSION: [EMIM]oAc appears to be another option for pretreating SCB, and other issues such as the recyclability of [EMIM]oAc is worth investigating. Copyright © 2011 Society of Chemical Industry     

Preparation of sulfuric acid ([3-(3-silicapropyl)sulfanyl]propyl)ester: A new and recyclable catalyst for the formylation and acetylation of alcohols under heterogeneous conditions

We describe a simple and efficient procedure for the preparation of sulfuric acid ([3-(3-silicapropyl)sulfanyl]propyl)ester (3) by the reaction of 3-(thio(propy-3-yl)silica)-propanol (2) and chlorosulfonic acid in chloroform. 3-(Thio(propy-3-yl)silica)-propanol was prepared by the reaction of 3-mercaptopropylsilica (MPS) with 3-chloropropanol in refluxing toluene. This solid sulfuric acid ([3-(3-silicapropyl)sulfanyl]propyl)ester is employed as a new catalyst for the formylation of alcohols with ethyl formate under mild and heterogeneous conditions at room temperature with good to excellent yields. Also, 3 can catalyze the acetylation of various alcohols by the reaction of alcohols with ethyl acetate under reflux conditions or with acetic anhydride at room temperature.     

In situ X-ray analysis under controlled potential conditions: An innovative setup and its application to the investigation of ultrathin films electrodeposited on Ag(1 1 1)

An innovative setup to combine electrochemical and in situ surface X-ray diffraction (SXRD) measurements is described. This electrochemical cell has a different design from the other ones commonly used for X-ray diffraction studies. It allows the sample surface to stay always completely immersed into the solution under controlled potential conditions even during the SXRD measurements. The X-ray beam crosses the liquid (about 1 cm) and the cell walls. Because of the high X-ray energy, the beam attenuation is negligible and by an appropriate positioning of the detector arm slits it is possible to minimize the diffuse scattering induced by the liquid and cell walls in order to still detect the minima of the crystal truncation rods (CTRs). The liquid solution in the cell is managed by a special device, which allows the controlled exchange of the electrolyte solutions necessary in the electrochemical atomic layer epitaxy (ECALE) growth. The whole setup can be remotely controlled from outside the experimental hutch by a dedicated computer. As an example we report measurements on S layers deposited at underpotential on the Ag(1 1 1) surface, and on CdS films of increasing thickness.