Cellulose Sulfate Research Articles

Micro scale chromatography of human plasma proteins for nano LC-ESI-MS/MS

Organic precipitation of proteins with acetonitrile demonstrated complete protein recovery and improved chromatography of human plasma proteins. The separation of 25 μL of human plasma into 22 fractions on a QA SAX resin facilitated more effective protein discovery despite the limited sample size. Micro chromatography of plasma proteins over quaternary amine (QA) strong anion exchange (SAX) resins performed best, followed by diethylaminoethyl (DEAE), heparin (HEP), carboxymethyl cellulose (CMC), and propyl sulfate (PS) resins. Two independent statistical methods, Monte Carlo comparison with random MS/MS spectra and the rigorous X!TANDEM goodness of fit algorithm protein p-values corrected to false discovery rate q-values (q ≤ 0.01) agreed on at least 12,000 plasma proteins, each represented by at least three fully tryptic corrected peptide observations. There was qualitative agreement on 9393 protein/gene symbols between the linear quadrupole versus orbital ion trap but also quantitative agreement with a highly significant linear regression relationship between log observation frequency (F value 4,173, p-value 2.2e-16). The use of a QA resin showed nearly perfect replication of all the proteins that were also found using DEAE-, HEP-, CMC-, and PS-based chromatographic methods combined and together estimated the size of the size of the plasma proteome as ≥12,000 gene symbols.

Using Rheology and Image Processing to Study the Effects of Cellulose Nanocrystal Sedimentation.

The effect of sedimentation on lyotropic liquid crystalline dispersions is both an interesting subject in colloidal science and is of practical importance for understanding changes that can occur during dispersion storage. This research explored how the seemingly subtle changes in average length resulting from a single sedimentation step affected the rheological properties and self-assembly of aqueous dispersions of sulfated cellulose nanocrystals. Sedimentation of a primarily isotropic aqueous cellulose nanocrystal dispersion for 1 month at ambient conditions resulted in an isotropic top phase and a biphasic bottom phase, which were separated for further study. Both atomic force microscopy measurements and intrinsic viscosities determined via Fedor's equation showed preferential fractionation of longer cellulose nanocrystals (CNCs) to the bottom phase. The effects of this fractionation on dispersion rheology and phase behavior were studied by preparing a range of concentrations from each phase. As expected, the concentration for the isotropic-biphasic phase transition was significantly lower for the bottom phase than for the top phase or parent dispersion. Rheological changes were generally subtle, but significant differences were seen in the storage modulus at concentrations approaching rheological gelation. Most notably, quantitative image processing showed that even this simple, single-step fractionation process had a significant impact on the relative proportion of tactoids and chiral helices with planar and homeotropic anchoring in self-assembled cellulose nanocrystal films. These results highlight the impact that changes in polydispersity due to sedimentation can have on the self-assembly of nanomaterial mesogens.

Seaweed-derived etherified carboxymethyl cellulose for sustainable tissue engineering

Biodegradability, biocompatibility, abundant supply from renewable sources, and affordability are the outstanding properties of cellulose that have prompted substantial studies into its potential in biomedical applications. Beyond terrestrial sources of cellulose, seaweeds have attracted much attention as a potential source of cellulose because they are widely available. Cellulose and its byproducts may be extracted from various macroalgae species, including red, green, and brown algae. The extracted cellulose's qualities vary depending on the algae species, age, and extraction process utilized. Cellulose's characteristics are enhanced through chemical modifications, specifically etherification and esterification, which substitute functional groups for hydroxyl groups, yielding a range of products, including cellulose acetate (CA), cellulose nitrate, cellulose sulfate, methylcellulose, and carboxymethyl cellulose (CMC). The ability to modify CMC characteristics for particular applications is explored through techniques including grafting processes mixing, and cross-linking with other polymers. Moreover, tissue engineering is given significant consideration in the growing use of CMC and its altered forms in biological applications. These alterations allow for the production of scaffolds that promote tissue regeneration and cell proliferation, enabling CMC-based scaffolds for various tissue engineering uses. This review provides a comprehensive overview of CMC's properties, modifications, and potential in tissue engineering.

Reversible Li plating regulation on graphite anode through a barium sulfate nanofibers-based dielectric separator for fast charging and high-safety lithium-ion battery

Poor Li plating reversibility and high thermal runaway risks are key challenges for fast charging lithium-ion batteries with graphite anodes. Herein, a dielectric and fire-resistant separator based on hybrid nanofibers of barium sulfate (BS) and bacterial cellulose (BC) is developed to synchronously enhance the battery’s fast charging and thermal-safety performances. The regulation mechanism of the dielectric BS/BC separator in enhancing the Li+ ion transport and Li plating reversibility is revealed. (1) The Max-Wagner polarization electric field of the dielectric BS/BC separator can accelerate the desolvation of solvated Li+ ions, enhancing their transport kinetics. (2) Moreover, due to the charge balancing effect, the dielectric BS/BC separator homogenizes the electric field/Li+ ion flux at the graphite anode-separator interface, facilitating uniform Li plating and suppressing Li dendrite growth. Consequently, the fast-charge graphite anode with the BS/BC separator shows higher Coulombic efficiency (99.0% vs. 96.9%) and longer cycling lifespan (100 cycles vs. 59 cycles) than that with the polypropylene (PP) separator in the constant-lithiation cycling test at 2 mA cm−2. The high-loading LiFePO4 (15.5 mg cm−2)//graphite (7.5 mg cm−2) full cell with the BS/BC separator exhibits excellent fast charging performance, retaining 70% of its capacity after 500 cycles at a high rate of 2 C, which is significantly better than that of the cell with the PP separator (retaining only 27% of its capacity after 500 cycles). More importantly, the thermally stable BS/BC separator effectively elevates the critical temperature and reduces the heat release rate during thermal runaway, thereby significantly enhancing the battery’s safety.

Sulfuric acid solvolysis of cellulose in a butanol-1/benzene mixture for isolating cellulose nanocrystals

The absence of a universal method for isolating cellulose nanocrystals (CNCs) has prompted researchers to explore alternative approaches to traditional sulfuric acid hydrolysis. In this study, the authors continue their previous research by investigating CNC synthesis through cellulose solvolysis in an alcoholic environment. The CNCs were successfully obtained utilizing controlled sulfuric acid solvolysis of sulfate cellulose in a butanol-1/benzene mixture. The highest CNC yield (over 60 %) was achieved at strictly controlled acid-to-benzene ratios in a butanol-1/benzene/sulfuric acid reaction mixture, with a significant reduction in the optimal acid concentration. The study also analyzes the physicochemical properties of the isolated CNCs. No surface alkylation of the synthesized CNCs was observed during the cellulose solvolysis in the butanol-1/benzene mixture. Besides, the properties of these CNCs closely resembled those obtained through traditional sulfuric acid hydrolysis. The paper also discusses the potential mechanism of cellulose solvolysis in the process of CNC production.

Layer-by-Layer Assembling and Capsule Formation of Polysaccharide-Based Polyelectrolytes Studied by Whispering Gallery Mode Experiments and Confocal Laser Scanning Microscopy

The layer-by-layer (LbL) assembling of oppositely charged polyelectrolytes was studied using semi-synthetic polysaccharide derivatives, namely the polycations 6-aminoethylamino-6-deoxy cellulose (ADC) and cellulose (2-(ethylamino)ethylcarbamate (CAEC), as well as the polyanion cellulose sulfate (CS). The synthetic polymers poly(allylamine) (PAH) and poly(styrene sulfonate) (PSS) were employed as well for comparison. The stepwise adsorption process was monitored by whispering gallery mode (WGM) experiments and zeta-potential measurements. Distinct differences between synthetic- and polysaccharide-based assemblies were observed in terms of the quantitative adsorption of mass and adsorption kinetics. The LbL-approach was used to prepare µm-sized capsules with the aid of porous and non-porous silica particle templates. The polysaccharide-based capsule showed a switchable permeability that was not observed for the synthetic polymer materials. At ambient pH values of 7, low-molecular dyes could penetrate the capsule wall while no permeation occurred at elevated pH values of 8. Finally, the preparation of protein-loaded LbL-capsules was studied using the combination of CAEC and CS. It was shown that high amounts of protein (streptavidin and ovomucoid) can be encapsulated and that no leaking or disintegration of the cargo macromolecules occurred during the preparation step. Based on this work, potential use in biomedical areas can be concluded, such as the encapsulation of bioactive compounds (e.g., pharmaceutical compounds, antibodies) for drug delivery or sensing purposes.

The highly differentiated gut of Pachnoda marginata hosts sequential microbiomes: microbial ecology and potential applications

Insect gut microbiomes play a crucial role in the insect development and are shaped, among other factors, by the specialized insect diet habits as well as the morphological structure of the gut. Rose chafers (Pachnoda spp.; Coleoptera: Scarabaeidae) have a highly differentiated gut characterized by a pronounced hindgut dilation which resembles a miniaturized rumen. Specifically, the species Pachnoda marginata has not been previously studied in detail in terms of microbial ecology. Here, we show a fine scale study of the highly compartmentalized gut of P. marginata by using amplicon and metagenomic sequencing to shed light on the bacterial, archaeal and fungal communities thriving in each section of the gut. We found a microbial gradient along the gut from aerobic (foregut) to strictly anaerobic communities (hindgut). In addition, we have characterized interesting biological activities and metabolic pathways of gut microbial communities related to cellulose degradation, methane production and sulfate reduction. Taken together, our results reveal the highly diverse microbial community and the potential of P. marginata gut as a source of industrially relevant microbial diversity.

Flexible high electrochemical active hydrogel for wearable sensors and supercapacitor electrolytes

With the rapid advancement of flexible, portable devices, hydrogel electrolytes have gained considerable attention as potential replacements for conventional liquid electrolytes. A hydrogel electrolyte was synthesised by cross-linking acrylic acid (AA), acrylamide (AM), carboxymethyl cellulose (CMC), and zinc sulphate (ZnSO4). The formation of hydrogen bonds and chelate interactions between the P(AA-co-AM) polymer, CMC, and ZnSO4 created a robust network, enhancing the mechanical properties of the hydrogel electrolytes. Notably, the hydrogel electrolyte containing 0.6 % CMC demonstrated superior mechanical strength (compression strength of 1.22 MPa, tensile stress of 230 kPa, tensile strain of 424 %, adhesion strength of 1.98 MPa on wood). Additionally, the CMC/P(AA-co-AM) hydrogels exhibited commendable electrical performance (38 mS/cm) and a high gauge factor (2.9), enabling the precise detection of physiological activity signals through resistance measurements. The unique network structure of the hydrogel electrolyte also ensured a stable bonding interface between the electrode and the electrolyte. After 2000 charge–discharge cycles, the supercapacitor maintained good capacitance characteristics, with a capacitance retention rate of 71.21 % and a stable Coulombic efficiency of 98.85 %, demonstrating excellent cyclic stability. This study introduces a novel methodology for fabricating multifunctional all-solid-state supercapacitors and suggests that the hydrogel can significantly advance the development of wearable energy storage devices.

Anticoagulation activity of sulfated carboxymethyl cellulose/Azadirachta indica leaf powder-based bio-composite.

Polymeric bio-composites synthesized via a green approach using natural herbs have fascinating anticoagulant activity due to their eco-friendly and non-toxic behavior towards various physical and chemical actions. Herein, we introduce a simple and eco-friendly approach for the fabrication of a new hybrid type of bio-composite based on sulfated carboxymethyl cellulose (S-CMC) and Azadirachta indica leaf powder (S-CMC/NLP). First, a non-toxic sulfating agent called N(SO3Na)3 was used to modify carboxymethyl cellulose into S-CMC. With an ion exchange capacity of 0.25 meq. g-1, the level of sulfation (%) of S-CMC (modified polysaccharide) was measured to be 12.01%. Three types of S-CMC/NLP bio-composites were developed by varying the concentration of NLP. FE-SEM, EDX, and XRD were used to characterize the structural features of S-CMC/NLP bio-composites. FTIR spectroscopy indicated that the S-CMC/NLP bio-composite possesses COO-, -OH and SO3- groups, suggesting the structural similarity to heparin. In addition, the anticoagulant effect of the S-CMC/NLP bio-composite was investigated using PT and APTT assays. The APTT investigation confirmed that following the intrinsic pathway of the coagulation system, 2-NLP/S-CMC bio-composite dose-dependently (0.045-0.28 mg mL-1) prolonged the time of blood coagulation compared to control (pure plasma). The S-CMC/NLP bio-composite showed its potential as a new, safe, and effective candidate for anticoagulant activity.

The influence of nanocellulose from different plant raw materials on the quality indicators of electrical insulation paper

An urgent scientific and practical task for electrical engineering enterprises is to improve the specific characteristics of component transformers and capacitors that use electrical insulating paper. Electrical insulating paper is characterized by a wide list of special quality indicators, the necessary values ​​of which are achieved due to the use of cellulose with special properties and various chemical auxiliary substances. There are known attempts to use nanocellulose (NC) from wood to reduce the consumption of harmful synthetic chemical auxiliaries, but there are practically no research results on the impact of consumption of NC from non-wood plant materials. Therefore, in the work, a comparative study of the effect of NC from hemp fibers and coniferous wood on the target indicators of the quality of electrical insulating paper was carried out. For this, cellulose, suitable for extracting NC from hemp fibers, was obtained by an environmentally safe organosolv method. NC is obtained as a result of acid hydrolysis of organosolv hemp and sulfate unbleached coniferous cellulose, which is traditionally used in the production of electrical insulating paper. Laboratory samples of electrical insulating paper were made with a weight of 65±3 g/m2 from sulfated unbleached coniferous cellulose with the addition from 1% to 5% NC by weight of paper. The research results confirmed the hypothesis that the addition of NC paper pulp from various plant raw materials leads to an increase in the mechanical and electrical strength of the paper. It has been established that the effect of NC from hemp fibers on the quality indicators of electrical insulation paper is not inferior to the effect on them of NC from coniferous wood, and in some cases even a better result is observed. It was established that the introduction of NC into the composition of paper practically does not reduce its degree of polymerization, which is of great importance for maintaining high reliability and a long duration of work of paper insulation. The obtained results have scientific and practical significance for other types of insulating papers: capacitor, cable, telephone, impregnation, transformer, etc.

Comparison of double-filtration plasmapheresis (DFPP) versus heparin-mediated extracorporeal LDL-precipitation (HELP)-apheresis in early-onset preeclampsia

ObjectivesPreeclampsia (PE) is a major cause of maternal and fetal mortality, and preterm birth. Previous studies indicate that lipid-apheresis may prolong pregnancy, namely heparin-mediated extracorporeal LDL-precipitation (HELP)- and dextran sulfate cellulose (DSC)-apheresis. We now report on double membrane plasmapheresis (DFPP) in early-onset preeclampsia (eoPE). Study designOpen pilot study assessing the prolongation of pregnancy in PE by lipoprotein-apheresis (DRKS00004527). Two women with eoPE were treated by DFPP and compared to a historical cohort of 6 patients with eoPE treated by HELP-apheresis (NCT01967355). Main outcome measuresClinical outcome of mothers and babies and prolongation of pregnancies (time of admission to birth). ResultsPatient 1 (33y; 22 + 5/7GW) received 4 DFPP. Delivery day 19; birthweight 270 g; weight at discharge 2134 g on day 132. Patient 2 (35y; 21 + 4/7GW) received 2 DFPP. Delivery day 19; birthweight 465 g; weight at discharge 2540 g on day 104. DFPP was well tolerated by both patients. ConclusionsDFPP proved to be save and pregnancies remained stable as long as 19 days. Although babies were born very preterm both babies could finally be dismissed from hospital. No relevant clinical differences between DFPP and HELP-apheresis could be observed. Therefore, DFPP may extend the range of available apheresis techniques to prolong pregnancies in early-onset preeclampsia. However, further studies are necessary to gain more information. Register(DRKS00004527)

Sulfated cellulose nanofibrils-based hydrogel moist-electric generator for energy harvesting

The excellent hydrophilicity of hydrogel makes it an ideal material for moisture-enable electricity. However, the lack of efficient protonation or ion diffusion leads to poor moisture-electric performance. Herein, a nanocellulose-base hydrogel moisture-electric generator (N-HMEG) is developed by composed of sulfated cellulose nanofibers (SCNF) and polyvinyl alcohol (PVA) with glycerol-water binary solvent. The SCNF and glycerol promote the ion diffusion and hygroscopicity of hydrogel, respectively. A N-HMEG can generate an open-circuit voltage of 0.9 V and short-circuit current density of 92 μA cm−2 at 80% relative humidity. The remarkable performances of N-HMEG can be attributed to the synergistic effect of asymmetric ionic diffusion and redox reaction on the electrode. Furthermore, the large-scale integration of N-HMEGs can be easily accomplished to deliver a voltage of up to 102 V with 130 units in series. The integrated N-HMEGs are demonstrated to provide power for commercial electronics. This work provides an effective method for designing of moisture-electric generators, which will facilitate the development of green power sources in the future.

Methylation-GC-MS/FID-Based Glycosidic Linkage Analysis of Unfractionated Polysaccharides in Red Seaweeds.

Glycosidic linkage analysis was conducted on the unfractionated polysaccharides in alcohol-insoluble residues (AIRs) prepared from six red seaweeds (Gracilariopsis sp., Prionitis sp., Mastocarpus papillatus, Callophyllis sp., Mazzaella splendens, and Palmaria palmata) using GC-MS/FID analysis of partially methylated alditol acetates (PMAAs). The cell walls of P. palmata primarily contained mixed-linkage xylans and small amounts of sulfated galactans and cellulose. In contrast, the unfractionated polysaccharides of the other five species were rich in galactans displaying diverse 3,6-anhydro-galactose and galactose linkages with varied sulfation patterns. Different levels of cellulose were also observed. This glycosidic linkage method offers advantages for cellulose analysis over traditional monosaccharide analysis that is known for underrepresenting glucose in crystalline cellulose. Relative linkage compositions calculated from GC-MS and GC-FID measurements showed that anhydro sugar linkages generated more responses in the latter detection method. This improved linkage workflow presents a useful tool for studying polysaccharide structural variations across red seaweed species. Furthermore, for the first time, relative linkage compositions from GC-MS and GC-FID measurements, along with normalized FID and total ion current (TIC) chromatograms without peak assignments, were analyzed using principal component analysis (PCA) as a proof-of-concept demonstration of the technique's potential to differentiate various red seaweed species.

Properties of APTES-Modified CNC Films.

Sulfated cellulose nanocrystals' (CNCs') facile aqueous dispersibility enables producing films, fibers, and other materials using only water as a solvent but prevents using sulfated CNCs in applications that require water immersion. We report that modifying CNCs with 3-aminopropyl-triethoxysilane (APTES) via a simple, single-pot reaction scheme dramatically improves the hydrolytic stability of CNC films. The effects of APTES modification on CNCs' properties were studied using attenuated total reflectance Fourier transform infrared spectroscopy, atomic force and optical microscopy, thermogravimetric analysis, dynamic light scattering, and ultimate analysis. Substituting a mere 12.6% of the CNCs' available hydroxyl groups with APTES dramatically increased the hydrolytic stability of shear cast films while only having minor impacts on their mechanical properties. In addition, quartz crystal microbalance with dissipation monitoring (QCMD) and multiparametric surface plasmon resonance (MP-SPR) studies showed that the CNC-APTES films also had a greater irreversible binding with carbofuran, a pesticide and emerging contaminant. These results highlight that APTES modification is a promising method for increasing the utility of sulfated CNCs in sensors, adsorbents, and other applications requiring water immersion.

The influence of reed nanocellulose on the quality indicators of paper-basis for wallpapers

Improving the production technology of products with improved quality indicators and with less impact on the environment remains an urgent scientific and practical problem of paper industry enterprises. This refers to the technology for the production of paper-bases for wallpaper using environmentally safe chemical additives, in particular nanocellulose (NC), which was obtained by acid hydrolysis from reed cellulose. The production of cellulose was carried out in two stages - extraction from reed stalks with a solution of alkali and an organosolvent method of cooking in a solution of peracetic acid. The obtained organosolvent cellulose contained the remains of lignin and mineral substances, which allows it to be used for the preparation of NC. As a result of the hydrolysis of organosolvent cellulose, a time-stable NC suspension was extracted, the properties of which were investigated by scanning electron microscopy (morphological changes in the structure of reed cellulose-containing materials), atomic force microscopy (determination of topographic characteristics of NC), analysis of electronic absorption spectra (transparency of NC films). It was established that reed NC films had nanoparticles with a cross-sectional size of 5-25 nm, density up to 1.52 g/cm3, transparency up to 81.6 %, tensile strength up to 65 MPa. For the production of castings of paper-bases for wallpaper samples, sulfated pine bleached cellulose and polyester synthetic fiber were used, to the fibrous mass of which were added the following chemical additives: alkyl ketene dimer, reed NC, binder, and optical brightener. It has been shown that the use of nanocellulose at a rate of 0.35 % to 1.0 % of the paper mass leads to a significant improvement in the physical and mechanical quality indicators of the paper base for wallpaper. It was established that the replacement of 50 % of the synthetic chemical auxiliary substance alkyl ketene dimer with nanocellulose or additional application of nanocellulose at a rate of 0.5 g/m2 on the surface of the casting with 0.7 % alkyl ketene dimer allows to obtain paper that meets the requirements of the standard. The obtained results indicate the prospects of using reed nanocellulose for the production of other mass types of paper and cardboard.

Sulfated cellulose pulp with high water retention and a swollen fiber structure for the preparation of completely dispersed cellulose nanofibers

Sulfated cellulose pulp with high water retention and a swollen fiber structure for the preparation of completely dispersed cellulose nanofibers

Cellulose Sulfate Nanofibers for Enhanced Ammonium Removal.

In this study, a sulfonation approach using chlorosulfonic acid (CSA) to prepare cellulose sulfate nanofibers (CSNFs) from raw jute fibers is demonstrated. Both elemental sulfur content and zeta potential in the CSNFs are found to increase with increasing CSA content used. However, the corresponding crystallinity in the CSNFs decreases with the increasing amount of CSA used due to degradation of cellulose chains under harsh acidic conditions. The ammonium adsorption results from the CSNFs with varying degrees of sulfonation were analyzed using the Langmuir isotherm model, and the analysis showed a very high maximum ammonium adsorption capacity (41.1 mg/g) under neutral pH, comparable to the best value from a synthetic hydrogel in the literature. The high ammonium adsorption capacity of the CSNFs was found to be maintained in a broad acidic range (pH = 2.5 to 6.5).

PREPARATION AND CHARACTERIZATION OF MICROSPHERES UTILIZING RATE-CONTROLLING MEMBRANES FOR THE MANAGEMENT OF DIABETES MELLITUS

The present research work aimed at the formulation of film-coated microspheres incorporating glibenclamide drug and their evaluation for the management of diabetes mellitus (DM). Microspheres were prepared by solvent evaporation methodology by the usage of ethyl cellulose as polymer, ethanol and dichloromethane as solvents and Tween 80® as a non-ionic surfactant. The film-coated membrane was prepared by pan coating method, incorporating ethyl cellulose, isopropyl alcohol, diethyl phthalate and sodium lauryl sulfate. This film membrane was coated on microspheres with the help of a spray gun. The efficiency of entrapment of the film coated microspheres of F5* batch, among different formulations, is highest and comes out to be in the range of 76.65±0.58. The percentage yield was observed to be 73.32±0.14. Morphological studies conducted by scanning electron microscope show spherical microspheres of uniform size. In vitro drug release study conducted of the coated microspheres of glibenclamide shows the highest amount of release of 97.44% in the F5*batch. The best-fit model was determined by the highest R2 value. Further, the developed formulation helps in reduction in dose dumping, with better patient compliance, and also masks the bitter taste of the drug.

Insights into critical rheological and interfacial properties of hydrophobically-modified cellulose sulphate derivatives using molecular modeling

Hydrophobically modified cellulose-based polymers are becoming increasingly popular in product development in several industries, including oilfield chemicals. However, there are few studies on understanding the properties of surface-active cellulose sulphates at the molecular level. In this study, two novel hydrophobically modified cellulosic materials, DPEA-Cell-OSO3− I and DPEA-Cell-OSO3− II, were investigated using the MARTINI forcefield. The chain dynamics and fluid-particle interactions in a saline environment, in the presence of oil molecules, at ambient and increased temperatures, were evaluated. Concentration profiles revealed that the new materials adsorbed well at the oil interface, as supported by low interfacial tension measurements in the range of 10−1 to 10−3 mN/m. This can be related to the strong interactions with the oil molecules as dictated by hydrophobic attractive forces. The rheological analysis illustrated that DPEA-Cell-OSO3− II is a thermo-thickening polymer as the viscosity rose from 2.95 cP at 298 K to 7.38 cP at 333 K. Also, the chain dynamics pattern showed the relevancy to a rheopectic material. DPEA-Cell-OSO3− I, on the other hand, is shear thinning with temperature, and a thixotropic material. Overall, the systemic molecular modeling revealed their lucrative potential applications in oilfield operations, especially for improved oil recovery.

Effects of different salt ions on the structure and rheological behavior of sulfated cellulose nanocrystal hydrogel

Cellulose nanocrystal (CNC) hydrogels are increasingly used in various applications. Here, CNC hydrogels were formed by adding four salt ions (NaCl, KCl, MgCl2, and CaCl2) to sulfated CNC suspensions. NaCl and KCl are monovalent salt ions and MgCl2 and CaCl2 are divalent salt ions; each pair has similar cation charges but different cation radii. This study compared the effects of four salt ions on the structure and rheological behavior of CNC hydrogels. At the same ion concentration, compared with NaCl and KCl, the addition of MgCl2 and CaCl2 significantly reduced the distance between the CNC particles, forming pronounced aggregates and denser network structures. Furthermore, the G′ and G″ of the CNC hydrogels with salt ions followed the order NaCl < KCl < MgCl2 < CaCl2 in the small-amplitude oscillatory shear (SAOS) test, and more viscoelastic hydrogels exhibited relatively lower deformability in the creep-recovery test. Under large-amplitude oscillatory shear (LAOS) conditions, the CNC hydrogels with salt ions exhibited LAOS type III behavior, and the change in yield stress followed the same order as the SAOS results. Among them, CNC hydrogel with CaCl2 exhibited stronger nonlinear response and enhanced strain-stiffening behavior (higher I3/I1 and e3/e1) to resist deformation before 20% strain, as well as an enhanced softening effect (higher |v3/v1|) as the structure was destroyed and rearranged at strains ranging from 20% to 100%. Such CNC hydrogels with different salt ions, which can regulate structural and rheological properties, provide basis for designing hydrogels and meet potential requirements in food and biomedicine fields.