We present wetting, hygroscopicity, and interfacial activity of hemicellulose with respect to etherification and contrast it to their potential as interfacial modifiers, which is demonstrated by oil-in-water emulsification containing up to 60 vol% of the oil phase. Tunable amphiphilicity of hardwood and softwood hemicelluloses, xylans, and galactoglucomannans, respectively, was accomplished via controlled etherification. A series of degree of substitution (DS) of hydroxypropylated and 3-butoxy-2-hydroxypropylated ("butylated") grades was synthesized. The hemicellulose ethers were characterized by gel permeation chromatography, spectroscopic techniques, such as NMR, and contact angle measurements. An attenuated total reflectance infrared method was developed for fast identification of the DS. Near infrared analysis was utilized to explore the hygroscopicity of the material and to perform principle component analysis. The modification to butylated grades decreased the hygroscopicity, whereas the hydroxypropylated grades bound moisture. All of the hemicellulose ethers were water-soluble. The interfacial tension of the aqueous hemicellulose solutions was determined by pendant-drop tensiometer, and it was demonstrated to be dependent on the degree of modification.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.biomac.6b00355DOI Listing

Publication Analysis

Top Keywords

interfacial activity
8
hemicellulose ethers
8
etherification wood-based
4
wood-based hemicelluloses
4
interfacial
4
hemicelluloses interfacial
4
activity wetting
4
wetting hygroscopicity
4
hygroscopicity interfacial
4
hemicellulose
4

Similar Publications

Transition-metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS), have emerged as a generation of nonprecious catalysts for the hydrogen evolution reaction (HER), largely due to their theoretical hydrogen adsorption energy close to that of platinum. However, efforts to activate the basal planes of TMDs have primarily centered around strategies such as introducing numerous atomic vacancies, creating vacancy-heteroatom complexes, or applying significant strain, especially for acidic media. These approaches, while potentially effective, present substantial challenges in practical large-scale deployment.

View Article and Find Full Text PDF

Additives-Modified Electrodeposition for Synthesis of Hydrophobic Cu/CuO with Ag Single Atoms to Drive CO Electroreduction.

Adv Mater

January 2025

State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, China.

Copper-based electrocatalysts are recognized as crucial catalysts for CO electroreduction into multi-carbon products. However, achieving copper-based electrocatalysts with adjustable valences via one-step facile synthesis remains a challenge. In this study, Cu/CuO heterostructure is constructed by adjusting the anion species of the Cu ions-containing electrolyte during electrodeposition synthesis.

View Article and Find Full Text PDF

Effects of Maillard Reaction Durations on the Physicochemical and Emulsifying Properties of Chickpea Protein Isolate.

Foods

January 2025

Department of Marine Biopharmacology, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China.

This study investigated the physicochemical and emulsifying properties of chickpea protein isolate (CPI)-citrus pectin (CP) conjugates formed via the Maillard reaction across varying reaction durations. CPI and CP were conjugated under controlled dry-heating conditions, and the resulting conjugates were characterized by measuring their particle size, zeta potential, solubility, thermal stability, surface hydrophobicity, and emulsifying properties. The results showed that as reaction duration increased, the particle size and zeta potential of the CPI-CP conjugates increased significantly, reaching a maximum particle size of 1311.

View Article and Find Full Text PDF

The efficient hydrogenation of 1-butene is an industrially significant reaction for producing fuels and value-added chemicals. However, achieving high catalytic efficiency and stability remains challenging, particularly for cost-effective materials, such as Ni. In this study, we developed a porous Ni-coated Ni foam catalyst by electrostatic spray deposition to address these challenges.

View Article and Find Full Text PDF

Significantly Enhanced Acidic Oxygen Evolution Reaction Performance of RuO Nanoparticles by Introducing Oxygen Vacancy with Polytetrafluoroethylene.

Polymers (Basel)

December 2024

Key Laboratory of Pulp and Paper Science & Technology of Ministry of Education/Shandong Province, State Key Laboratory of Biobased Material and Green Papermaking, Faculty of Light Industry, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.

The supported RuO catalysts are known for their synergistic and interfacial effects, which significantly enhance both catalytic activity and stability. However, polymer-supported RuO catalysts have received limited attention due to challenges associated with poor conductivity. In this study, we successfully synthesized the RuO-polytetrafluoroethylene (PTFE) catalyst via a facile annealing process.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!