Cellulose Crystals Research Articles

Chitosan coatings reinforced with cellulose crystals and oregano essential oil as antimicrobial protection against the microbiological contamination of stone sculptures

The proliferation of microorganisms in outdoor stone sculptures and cultural objects can damage the structure and aesthetics of the materials through biodeterioration mechanisms. Biocides and synthetic products are often used to prevent this phenomenon, despite their negative impact on the environment and human health. Less toxic alternatives with reduced environmental impact can be an option for the preventive conservation of stone sculptures to reduce the environmental impact. In this work, chitosan formulations reinforced with two types of cellulose crystals (microcrystalline cellulose (MCC) or cellulose nanocrystals (CNCs)) and with or without citric acid and sodium tripolyphosphate were prepared. The films obtained with these formulations showed low solubility, and those only containing MCC or CNCs had the lowest wettability. The formulation containing 2% (w/v) MCC was selected for further analysis and supplemented with oregano essential oil (OEO) at 1% (v/v) and 2% (v/v), exhibiting low solubility, swelling and wettability when polymerised in film form. Inoculation of the films with Staphylococcus aureus, Bacillus cereus, Pseudomonas aeruginosa and Rhodotorula spp. resulted in total or partial inhibition of their growth, as well as a 60–100% reduction in Penicillium chrysogenum growth, depending on the concentration of OEO. The formulation with 2% (v/v) OEO was applied to samples of granite, marble and limestone, forming a protective, yet irregular coating on their surfaces. The wettability of the stones’ surfaces was reduced without becoming completely water-repellent and the coating did not cause visible colour changes.

Research and Application of Chemical Sand Control without Blockage in WellBore

Abstract The main sand control methods for oil production wells in a certain Oilfield include mechanical filling sand control, artificial well bore reconstruction with coated sand, and phenolic resin sand control. Mechanical filling for sand control requires the well bore to be intact, with residual pipe columns in the well that cannot meet the testing fluid profile, and subsequent processing often requires major repairs; The construction pressure of artificial well bore is high, and the production of chemical resin sand control is significantly reduced. In order to ensure the consolidation strength, both sand control processes are under displacement operations, and the well bore above the top boundary of the perforated layer is fixed with a plug that needs to be drilled. Research on a new type of chemical sand control technology for well bore without blockage. By using biomass cellulose crystals with smaller particle size and resin in the sand fixing agent combination, the sand particles in the formation are well coated, and condensation reaction occurs to achieve the goal of sand control. The casing will not solidify to create well bore blockage, avoiding later drilling and plugging operations. The construction pressure is low, the damage to the casing is small, and it has a certain degree of selectivity. After sand control, the water content can be reduced by more than 10%. It is suitable for sand control operations in casing damage wells, casing change wells, high inclination wells, and horizontal wells, and can be used for packer construction. As of December 2023, there have been 8 on-site applications with a success rate of 100%, Average water content reduced by 13%, and a cumulative recovery of 2936 tons of oil production. This has safely and efficiently solved the sand control problem in complex well conditions.

Investigation of the microscopic damage mechanisms in cotton fibers induced by mechanical friction

For the problem of friction damage in cotton fiber processing, a multi-scale combination of investigation methods is proposed. The surface of damaged cotton fiber is detected by relevant test means with damage features such as dislocations, defects and cracks. The internal pyranose ring and glycosidic bond fail, the crystallinity decreases, and the number of hydrogen bonds decreases. Anisotropy exists in the frictional properties of the microscopic surface of the cotton fiber. The results of molecular dynamics simulation showed that the cellulose main chain failed mainly at the glycosidic bond, and the side chain failed mainly at the hydroxymethyl functional group. Its interchain hydrogen bond O3H…O5 was the least damaged. The cellulose crystal (200) surfaces had poor abrasion resistance, and the frictional properties of each crystal surface were anisotropic. The results of the study provide a theoretical basis for improving friction and wear problems in cotton fiber processing.

Tunicate cellulose nanocrystals strengthened injectable stretchable hydrogel as multi-responsive enhanced antibacterial wound dressing for promoting diabetic wound healing

The intricate microenvironment of diabetic wounds characterized by hyperglycemia, intense oxidative stress, persistent bacterial infection and complex pH fluctuations hinders the healing process. Herein, an injectable multifunctional hydrogel (QPTx) was developed, which exhibited excellent mechanical performance and triple responsiveness to pH, temperature, and glucose due to dynamic covalent cross-linking involving dynamic Schiff base bonds and phenylboronate esters with phenylboronic-modified quaternized chitosan (QCS-PBA), polydopamine coated tunicate cellulose crystals (PDAn@TCNCs) and polyvinyl alcohol (PVA). Furthermore, the hydrogels can incorporate insulin (INS) drugs to adapt to the complex and variable wound environment in diabetic patients for on-demand drug release that promote diabetic wound healing. Based on various excellent properties of the colloidal materials, the hydrogels were evaluated for self-healing, rheological and mechanical properties, in vitro insulin response to pH/temperature/glucose release, antibacterial, antioxidant, tissue adhesion, coagulation, hemostasis in vivo and in vitro, and biocompatibility and biodegradability. By introducing PDAn@TCNCs particles, the hydrogel has photothermal antibacterial activity, enhanced adhesion and oxidation resistance. We further demonstrated that these hydrogel dressings significantly improved the healing process compared to commercial dressings (Tegaderm™) in full-layer skin defect models. All indicated that the glucose-responsive QPTx hydrogel platform has great potential for treating diabetic wounds.

Development of Biodegradable Bioplastics with Sericin and Gelatin from Silk Cocoons and Fish Waste.

The bioplastics sector promotes environmentally friendly means of cutting down on the usage of fossil fuels, plastic waste, and environmental pollution. Plastic contamination has detrimental effects on both ecological systems and the global food supply. The approach we present here to resolve this issue involves the integration of sericin and gelatin, obtained from cocoon and fish waste, respectively, with nano-reinforced cellulose crystals, to develop a biodegradable and compostable plastic material. The use of cocoon and fish wastes for the extraction of sericin and gelatin presents an environmentally beneficial approach since it contributes to waste reduction. The sericin level found in silk cocoon waste was determined to be 28.08%, and the gelatin amount in fish waste was measured to be 58.25%. The inclusion of sericin and gelatin in bioplastics was accompanied by the incorporation of glycerol, vinegar, starch, sodium hydroxide, and other coloring agents. Fourier transform infrared (FTIR) examination of bioplastics revealed the presence of functional groups that corresponded to the sericin and gelatin components. The tensile strength of the bioplastic material was measured to be 27.64 MPa/psi, while its thickness varied between 0.072 and 0.316 mm. The results of burial experiments indicated that the bioplastic material had a degradation rate of 85% after 14 days. The invention exhibits potential as a viable alternative for packaging, containment, and disposable plastic materials. The use of this sustainable approach is recommended for the extraction of sericin and gelatin from silk cocoons and fish waste, with the intention of using them as raw materials for bioplastic production.

Evaluating how citrus fiber affects the cell structure and functions of starch-based foam

This work used a proper content of citrus fiber (10 wt% ∼ 30 wt%, dry starch base) to improve the cell structures and functions of starch foam. The insoluble fiber promoted cell nucleation in the starch melt, whereas the soluble pectin improved the starch matrix's strength by forming ester bonding with starches as confirmed by FTIR results. This effectively modified the starch foaming process and endowed the obtained foams with an increased cell density (from 83.37 to 123.44 cell/cm3×104) and a reduced foam density (from 0.457 to 0.142 g/cm3). The foam containing 20 wt% citrus fiber exhibited the highest expansion ratio of 5.20. Due to the improved structures and the tortuous path effect of cellulose crystals, the prepared foams significantly presented a strengthened compression performance and improved moisture resistance. Meanwhile, the fiber-loaded foams displayed a high free radical-scavenging activity (60.30 % ∼ 85.75 %), showing good antioxidant activity. It is therefore believed that this study could provide a facile and green way for producing starch-based foams with desirable functions.

Cellulose nanocomposite tough hydrogels: synergistic self‐healing, adhesive and strain‐sensitive properties

AbstractRecent advancements are notable in electrically conductive hydrogels emulating human skin functions. However, a significant challenge remains: crafting a single conductive gel that integrates self‐healing, robust mechanical strength, and excellent electrical traits. Our innovation lies in a strong, lightweight, curable gel achieved through multiple coordination bonds between cellulose crystals and acid‐treated multi‐walled carbon nanotubes (MWCNTs) in a polymer network. Embedded MWCNTs act as dynamic bridges within a porous structure, giving exceptional mechanical performance. Reversible coordination interactions confer remarkable recovery and reliable mechanical and electrical self‐healing. Additionally, these ionic gels function as adaptable stress sensors, detecting significant movements like finger and joint motions. This work introduces MWCNT‐incorporated nanomaterials with good stretchability, high ion conductivity, remarkable self‐healing nature, and good stress sensitivity. Such proteins hold promise for electronic sensors, wearable devices, and healthcare monitoring, unveiling a path to diverse applications. Our study addresses challenges and unlocks possibilities for materials that can adapt, withstand, and sense in innovative ways. © 2024 Society of Chemical Industry.

Camellia Oleifera shells derived nano cellulose crystals conjugated with gallic acid as a sustainable Pickering emulsion stabilizer

Lately, emulsions with low-fat and natural stabilizers are predominant. This study extracted the nano cellulose crystals (NCs) from Camellia Oleifera shells, and their gallic acid (GA) conjugates were synthesized by free-radical grafting. Pickering emulsions were prepared using NCs 1 %, 1.5 %, 2.5 %, and gallic acid conjugates NC-GA1, NC-GA2, and NC-GA3 as stabilizers. The obtained nano cellulose crystals exhibited 18–25 nm, −40.01 ± 2.45 size, and zeta potential, respectively. The contact angle of 83.4° was exhibited by NC-GA3 conjugates. The rheological, interfacial, and microstructural properties and stability of the Pickering emulsion were explored. NC-GA3 displayed the highest absorption content of 79.12 %. Interfacial tension was drastically reduced with increasing GA concentration in NC-GA conjugates. Rheological properties suggested that the low-fat NC-GA emulsions showed a viscoelastic behavior, increased viscosity, gel-like structure, and increased antioxidant properties. Moreover, NC-GA3 displayed reduced droplet size and improved emulsion temperature and storage stability (28 days) against phase separation. POV and TBARS values were reduced with the NC-GA3 (P < 0.05). This work confirmed that grafting phenolic compounds on NCs could enhance bioactive properties, which can be used in developing low-fat functional foods. NC-GA conjugates can potentially fulfill the increasing demand for sustainable, healthy, and low-fat foods.

Tunable Construction of Chiral Nematic Cellulose Nanocrystals/ZnO Films for Ultra-Sensitive, Recyclable Sensing of Humidity and Ethanol.

The investigation of functional materials derived from sustainable and eco-friendly bioresources has generated significant attention. Herein, nanocomposite films based on chiral nematic cellulose crystals (CNCs) were developed by incorporating xylose and biocompatible ZnO nanoparticles (NPs) via evaporation-induced self-assembly (EISA). The nanocomposite films exhibited iridescent color changes that corresponded to the birefringence phenomenon under polarized light, which was attributed to the formation of cholesteric structures. ZnO nanoparticles were proved to successfully adjust the helical pitches of the chiral arrangements of the CNCs, resulting in tunable optical light with shifted wavelength bands. Furthermore, the nanocomposite films showed fast humidity and ethanol stimuli response properties, exhibiting the potential of stimuli sensors of the CNC-based sustainable materials.

Interfacial interactions between spider silk protein and cellulose studied by molecular dynamics simulation.

Due to their excellent biocompatibility and degradability, cellulose/spider silk protein composites hold a significant value in biomedical applications such as tissue engineering, drug delivery, and medical dressings. The interfacial interactions between cellulose and spider silk protein affect the properties of the composite. Therefore, it is important to understand the interfacial interactions between spider silk protein and cellulose to guide the design and optimization of composites. The study of the adsorption of protein on specific surfaces of cellulose crystal can be very complex using experimental methods. Molecular dynamics simulations allow the exploration of various physical and chemical changes at the atomic level of the material and enable an atomic description of the interactions between cellulose crystal planes and spider silk protein. In this study, molecular dynamics simulations were employed to investigate the interfacial interactions between spider silk protein (NTD) and cellulose surfaces. Findings of RMSD, RMSF, and secondary structure showed that the structure of NTD proteins remained unchanged during the adsorption process. Cellulose contact numbers and hydrogen bonding trends on different crystalline surfaces suggest that van der Waals forces and hydrogen bonding interactions drive the binding of proteins to cellulose. These findings reveal the interaction between cellulose and protein at the molecular level and provide theoretical guidance for the design and synthesis of cellulose/spider silk protein composites. MD simulations were all performed using the GROMACS-5.1 software package and run with CHARMM36 carbohydrate force field. Molecular dynamics simulations were performed for 500 ns for the simulated system.

The mechanism of solid acid-catalyzed bamboo sawdust liquefaction under polyol systems.

Solid acid catalysts are widely used in the field of biomass catalytic conversion owing to their advantages of low environmental pollution, easy separation and reusability. Nevertheless, there are relatively few studies on the mechanism of solid acid liquefaction for biomass. In this study, the effect of acid strength and acid amount of various solid acids on the liquefaction efficiency has been investigated using waste bamboo sawdust generated from the pulp and paper industry as the raw material. In addition, the physicochemical changes of cellulose, hemicellulose and lignin during the reaction process of bamboo sawdust have been studied, and the liquefaction mechanism of bamboo sawdust under the action of various solid acids has been concluded. As a result, the liquefaction efficiency of bamboo sawdust under the polyol system of PEG400/propanetriol is mainly related to the acid strength of the solid acid, and the greater the acid strength of the solid acid, the better the catalytic effect on the bamboo sawdust, in which the residual amount of bamboo sawdust liquefaction catalyzed by the SPA catalyst is only 17.72%. Noteworthy, the most difficult component to liquefy is the crystallization of natural cellulose I into cellulose II during the reaction process, which is the primary obstacle to the complete liquefaction of bamboo sawdust by solid acid. Overall, these findings are valuable for the high value utilization of waste bamboo sawdust in the pulp and paper industry, as well as the application of solid acid catalytic technology for biomass.

Magnetic Multienzyme@Metal-Organic Material for Sustainable Biodegradation of Insoluble Biomass.

Biodegradation of insoluble biomass such as cellulose via carbohydrase enzymes is an effective approach to break down plant cell walls and extract valuable materials therein. Yet, the high cost and poor reusability of enzymes are practical concerns. We recently proved that immobilizing multiple digestive enzymes on metal-organic materials (MOMs) allows enzymes to be reused via gravimetric separation, improving the cost efficiency of cereal biomass degradation [ACS Appl. Mater. Interfaces 2021, 13, 36, 43085-43093]. However, this strategy cannot be adapted for enzymes whose substrates or products are insoluble (e.g., cellulose crystals). Recently, we described an alternative approach based on magnetic metal-organic frameworks (MOFs) using model enzymes/substrates [ACS Appl. Mater. Interfaces 2020, 12, 37, 41794-41801]. Here, we aim to prove the effectiveness of combining these two strategies in cellulose degradation. We immobilized multiple carbohydrase enzymes that cooperate in cellulose degradation via cocrystallization with Ca2+, a carboxylate ligand (BDC) in the absence and presence of magnetic nanoparticles (MNPs). We then compared the separation efficiency and enzyme reusability of the resultant multienzyme@Ca-BDC and multienzyme@MNP-Ca-BDC composites via gravimetric and magnetic separation, respectively, and found that, although both composites were effective in cellulose degradation in the first round, the multienzyme@MNP-Ca-BDC composites displayed significantly enhanced reusability. This work provides the first experimental demonstration of using magnetic solid supports to immobilize multiple carbohydrase enzymes simultaneously and degrade cellulose and promotes green/sustainable chemistry in three ways: (1) reusing the enzymes saves energy/sources to prepare them, (2) the synthetic conditions are "green" without generating unwanted wastes, and (3) using our composites to degrade cellulose is the first step of extracting valuable materials from sustainable biomasses such as plants whose growth does not rely on nonregeneratable resources.

Birefringence Behaviors of Cellulose Nanocrystals under Varied Concentrations, Ultrasonication Treatments, and Different Solvents

Self-assembly of cellulose nanocrystal (NCC) in suspension has unique characteristics under polarize observation which is called as birefringence behaviors. However, the study about these phenomena is lacking especially when the NCC is prepared in dried powder form. Here, we reported the behaviors of commercial NCC obtained from CelluForce NCC, NCV100-NASD90 dispersed in different concentrations (0.1% to 8% weight/weight); ultrasonic times (0 to 45 minutes); solvents (Benzene, N,N-Dimethylacetamide (DMA), Ethanol, Dimethylformamide, Acetone, Acetic acid 1%, and Water) for their birefringence manners. In addition, nanocellulose obtained from TEMPO mediated oxidation and organic acid hydrolysis were also reported. Dried powder NCC showed shear thickening behavior at high concentration and well-dispersed at acetic acid and water solvent indicated the redispersable NCC. While, cellulose NCC, NCV100-NASD90 considerably low dispersion in non-polar solvents. Birefringence appears only when the suspension was in anisotropic state due to stirring. As sonication times increased, the birefringence clearly visible which suggested the defibrillation of aggregated cellulose crystal. The results of this study authenticated that redispersable NCC could be obtained from dried powder cellulose and provided birefringence behavior by managing concentration levels, sonication times and perfect solvents to dilute.

Thermal pretreatment of willow branches impacts yield and pore development of activated carbon in subsequent activation with ZnCl2via modifying cellulose structure

Development of pore structures of activated carbon (AC) from activation of biomass with ZnCl2 relies on content and structure of cellulose/hemicellulose in feedstock. Thermal pretreatment of biomass could induce dehydration and/or aromatization to change structure of cellulose/hemicellulose. This might interfere with evolution of structures of AC, which was investigated herein via thermal pretreatment of willow branch (WB) from 200 to 360 °C and the subsequent activation with ZnCl2 at 550 °C. The results showed that thermal pretreatment at 360 °C (WB-360) could lead to substantial pyrolysis to form biochar with yield of 31.9%, accompanying with nearly complete destruction of cellulose crystals and remarkably enhanced aromatic degree. However, cellulose residual in WB-360 could still be activated to form AC-360 with specific surface area of 1837.9 m2·g−1, which was lower than that in AC from activation of untreated WB (AC-blank, 2077.8 m2·g−1). Nonetheless, the AC-200 from activation of WB-200 had more developed pores (2113.9 m2·g−1) and superior capability for adsorption of phenol, due to increased permeability of ZnCl2 to the largely intact cellulose structure in WB-200. The thermal pretreatment did increase diameters of micropores of AC but reduced overall yield of AC (26.8% for AC-blank versus 18.0% for AC-360), resulting from accelerated cracking but reduced intensity of condensation. In-situ IR characterization of the activation showed that ZnCl2 mainly catalyzed dehydration, dehydrogenation, condensation and aromatization but not cracking, suppressing formation of derivatives of cellulose and lignin in bio-oil. The thermal pretreatment formed phenolic —OH and C=O with higher chemical innerness, which changed reaction network in activation, shifting morphology of fibrous structures in AC-blank to "melting surface" in AC-200 or AC-280.

Dynamic Structural Change of Plant Epidermal Cell Walls under Strain.

The molecular foundations of epidermal cell wall mechanics are critical for understanding structure-function relationships of primary cell walls in plants and facilitating the design of bioinspired materials. To uncover the molecular mechanisms regulating the high extensibility and strength of the cell wall, the onion epidermal wall is stretched uniaxially to various strains and cell wall structures from mesoscale to atomic scale are characterized. Upon longitudinal stretching to high strain, epidermal walls contract in the transverse direction, resulting in a reduced area. Atomic force microscopy shows that cellulose microfibrils exhibit orientation-dependent rearrangements at high strains: longitudinal microfibrils are straightened out and become highly ordered, while transverse microfibrils curve and kink. Small-angle X-ray scattering detects a 7.4nm spacing aligned along the stretch direction at high strain, which is attributed to distances between individual cellulose microfibrils. Furthermore, wide-angle X-ray scattering reveals a widening of (004) lattice spacing and contraction of (200) lattice spacing in longitudinally aligned cellulose microfibrils at high strain, which implies longitudinal stretching of the cellulose crystal. These findings provide molecular insights into the ability of the wall to bear additional load after yielding: the aggregation of longitudinal microfibrils impedes sliding and enables further stretching of the cellulose to bear increased loads.

Small-angle neutron scattering from cellulose solutions in phosphoric acid at different water content

Cellulose from biomass is an abundant and renewable alternative source for chemicals and fuels, yet its utilization by chemical or biological process requires pre-treatment in order to release the macromolecules from their tightly packed crystal structure. Phosphoric acid (PA) has been known for many years to be an efficient solvent for crystalline cellulose. It is also established that a certain quantity of water content in PA is required for efficient pretreatment. This study uses small-angle neutron scattering (SANS) measurements to evaluate cellulose dissolution in deuterated phosphoric acid (dPA), at different wt% dPA between 78 and 97 % (different D2O content). The SANS method is useful for this purpose due to the availability of deuterated dPA, its contrast in scattering length density towards cellulose, and its low incoherent scattering cross-section. The results indicate that most of the cellulose in 2 wt% solution is dissolved in PA as individual chains, at acid content of 81–94 wt% PA. Structural differences of the dissolved cellulose in PA of the various water compositions in this range are insignificant. At 78 % dPA the cellulose crystal still seem to be disrupted, yet the structure can be modeled as mass-surface fractals of small fibrils with irregular surface, possibly due to dissolved chain segments, which are aggregated as mass fractals of rods. At 97 % dPA evidence for a small content of undissolved fibrils is noted.

Optimization of culture conditions to express AA9 Polysaccharide monooxygenases AN3860 in Escherichia coli

Lignocellulose biomass is a copious source for second generation biomaterial production. The participant of Polysaccharide monooxygenases enzyme (PMO) in the reactions which convert lignocellulose biomass into monosaccharides enhances the activity and improve the efficiency of hydrolysis of hydrolase enzymes on lignocellulose substrate. Enzyme AN3860, obtained from Aspergillus nidulans strain belonging to AA9 PMO, is expected to catalyze flexibly at C1 and C4 carbon positions of β-glycosidic linkage. As an enzyme with high potential of improving cellulose crystals hydrolysis capacity, AN3860 was successfully cloned into the expression system of E. coli BL21 (DE3) strain. In this study, the culture process of recombinant strain with AN3680 gene is optimized to increase the target proteins yield, thus ensure the outcome of purification process, and save production cost. The results demonstrate that the E. coli recombinant strains grow sufficiently in TB (Terrific Broth) culture media and the highest yield of AN3680 protein achieved when the concentration of Isopropyl β-D-1-thiogalactopyranoside (IPTG) is 0.05 mM and the temperature of the reaction is 30 0C at 150 rpm. After 6 hours of induction, the biomass reaches 500 mg/L and the yield of AN3860 account for (7-10) % total protein generated. The recombinant AN3860 protein is later harvested on larger scale and purified by Ni-NTA column chromatography method for analysis of bioactivities on lignocellulose substrates in the future. ® 2022 Journal of Science and Technology - NTTU

Green and efficient utilization of cellulose by in situ regenerating rod‐like cellulose crystals in dry blending rubber compounds

AbstractThe crystalline cellulose has captured much attention as reinforcement material in rubber composites, but no successful cases have been found till now. Here, a facile approach of cellulose utilization was proposed by in‐situ regenerating cellulose in dry rubber matrix. Cellulose was dissolved in ionic liquid (IL), and then directly mixed with dry rubber, silica, and other ingredients. Taking advantages of the strong interaction between IL and silica, the dissolution equilibrium of cellulose/IL was destroyed and resulted in the regeneration of cellulose crystals in rubber matrix. The regenerated cellulose appeared at dry blending stage, and showed an ideal rod‐like shape (10–100 nm in diameter and 200–500 nm in length). While it grew in size at curing stage, and finally reached 100–200 nm in diameter and 1–2 μm in length. The regenerated cellulose exhibited pronounced reinforcement efficiency. This methodology has no any waste liquid discharged, and has a promising use in the preparation of cellulose/rubber composites.Highlights Nanosized rod‐like cellulose was regenerated in dry rubber, instead of latex. Regeneration of cellulose was due to interaction between ionic liquid and silica. The in situ regenerated cellulose dispersed well in cured rubber compounds. The regenerated cellulose exhibited a good reinforcement efficiency in rubber. The whole machining process had no any waste liquid discharged.

Acid-modified pea protein isolate and okara cellulose crystal: A co-emulsifier to improve physico-chemical stability of fat-reduced eggless mayonnaise

Mayonnaise, a high fat emulsified food, always contains egg yolk as a source of emulsifier. Lowering fat content and restricting use of egg yolk are promising ways to enhance nutritive profile and attraction to vegan trend. This work aimed to prepare fat-reduced eggless mayonnaise with good physicochemical stability using pea protein isolate (PPI) in combination with cellulose crystals as a co-emulsifier. Emulsifying property of Okara cellulose crystals (OC) and modified OC using gallic acid (OCG) was investigated. The cellulosic materials possessed effective emulsifying property, particularly at increased concentration. The present work suggested that acid-aided hydrolysis could improve emulsifying property of PPI. Then, the acid-modified PPI (aPPI) together with OC or OCG were employed at different ratios as a co-emulsifier for fat-reduced eggless mayonnaise preparation. The co-emulsifier could improve dispersibility and rheological property of the mayonnaise effectively. In addition, the cellulosic materials improved oxidative stability of the mayonnaises, particularly for OCG. This behavior might be expected since a steric hindrance effect of the interfacial films of co-emulsifier, in addition to antioxidant capacity of OCG. Thus, the innovative addition of the dual modes of emulsifying and antioxidant actions could be used to improve physicochemical stability and reduce fat content of eggless mayonnaise.

Matrix polysaccharides affect preferred orientation of cellulose crystals in primary cell walls

Matrix polysaccharides affect preferred orientation of cellulose crystals in primary cell walls