Purity Of Cellulose Research Articles

Bacterial Cellulose Purification with Non-Conventional, Biodegradable Surfactants

Bacterial cellulose (BC) is a versatile biopolymer with significant potential across biomedical, food, and industrial applications. To remove bacterial contaminants, such as protein and DNA, BC pellicles undergo purification, which traditionally relies on harsh alkali treatments, such as sodium hydroxide or strong surfactants, which present environmental concerns. In response, this study evaluates the efficacy of various non-conventional surfactants—both non-biodegradable and biodegradable—as alternatives for BC purification. Among the surfactants tested, sodium cocoyl isethionate (SCI), a mild anionic and biodegradable surfactant, emerged as particularly effective, achieving an 80.7% reduction in protein content and a 65.19% reduction in double-stranded DNA (dsDNA) content relative to untreated samples. However, these advantages were not without additional challenges, such as the appearance of residual surfactants. Given SCI’s promising performance and biodegradability, it was further examined in two-step treatment protocols; additionally, sodium dodecyl sulfate (SDS) was also examined as a more traditional anionic surfactant as well as NaOH. For the two-step treatment protocol, BC pellicles were treated with one reagent for 3 h, followed by a second reagent for an additional 3 h. Notably, by using NaOH as the final step in the two-step treatment protocol, residual surfactant was not detected in the FTIR analysis. Overall, this work demonstrates that SCI, in addition to subsequent NaOH treatment, can be used as a surfactant-based approach for BC purification, representing a potential environmentally friendly alternative to traditional surfactant-based approaches for BC purification.

Low-cost bacterial cellulose production from agricultural waste for antibacterial applications

Various carbon sources can be utilized for the biosynthesis of bacterial cellulose (BC), with agricultural wastes being explored as sustainable options. In this study, glucose was extracted from bamboo dust via mild acid hydrolysis to prepare a modified medium combining extracted glucose with Hestrin-Schramm (HS) medium for BC biosynthesis using Acetobacter xylinus NCIM 2526. Chitosan, a biopolymer, was incorporated into the BC synthesis medium at concentrations of 0.2%, 0.6%, and 1% (w/v) after 2 days of shaking incubation, producing chitosan-incorporated BC membranes through in situ synthesis. Fourier transform infrared (FTIR) spectroscopy confirmed cellulose in the BC produced from the modified medium and chitosan in BC membranes with 0.2% and 0.6% (w/v) chitosan. Changes in physical and crystalline morphology were further characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The purity of cellulose was validated through chemical solubility tests, while energy-dispersive X-ray (EDX) analysis confirmed the presence of chitosan in the BC membranes. The average yields were 5.8 ± 0.21 g/l for pure BC, 5.2 ± 0.21 g/l for BC with 0.2% (w/v) chitosan, and 4.6 ± 0.21 g/l for BC with 0.6% (w/v) chitosan after 7 days. The medium with 1% (w/v) chitosan did not produce BC membranes. BC synthesized with 0.2% chitosan exhibited similar physical and chemical properties to pure BC and demonstrated good antimicrobial properties, suggesting its potential use in bandages and wound dressings.

Fractionation of Winemaking Grape Stalks by Subcritical Water Extraction to Obtain Added-Value Products.

Grape stalks (GSs) from winemaking were submitted to a green process to valorise its lignocellulosic biomass that applied subcritical water extraction (SWE) at 170 °C and 180 °C to obtain active extracts and cellulose-enriched fractions. The sum of the total phenolic content of the soluble extract and the solid residue fractions from the SWE exceeded that of the GS, which suggests the generation of compounds with antioxidant properties through SWE. All SWE fractions showed high antioxidant power. The increased temperature promoted the extraction of polyphenolic compounds, enhancing the antioxidant power of both extracts and solid residues. These solid residue fractions were bleached with alkaline hydrogen peroxide solutions (4 and 8% v/v) to purify cellulose. After two bleaching cycles, no notable delignification progress was observed, as the bleaching yield or whiteness index did not significantly change in the further cycles. The first bleaching cycle led to a significant reduction in the lignin content at both SWE temperatures. The cellulose purity was higher in the samples obtained at 170 °C and bleached with 4% alkaline hydrogen peroxide. SWE at 180 °C led to greater cellulose oxidation during the bleaching step regardless of the hydrogen peroxide concentration.

Integrated formic acid and deep eutectic solvent mediated sustainable synthesis of cellulose nanocrystals from Sterculia foetida shells

The present study reports the green synthesis of cellulose nanocrystals from the shells of Sterculia foetida (SFS) cellulose. Three different methods, alkali, acid and organic acid, were screened for the maximum cellulose extraction. A maximum cellulose yield, 30.6 ± 0.84 w/w, was obtained using 90% formic acid at 110 °C in 120 min. The extracted cellulose was characterized and identified by instrumental analyses. SEM analysis showed skeletal rod-like microfibril structures and similar intra-fibrillar widths. CP/MAS 13C NMR and FTIR spectrum revealed the purity of cellulose and the absence of other components like hemicellulose and lignin. XRD study revealed a cellulose crystallinity index of 88.07%. BET analysis showed a good surface area (3.3213 m2/g) and a micro-pore area of 1.871 m2/g. The cellulose nanocrystals were synthesized from the extracted cellulose using deep eutectic solvents (DES), choline chloride and lactic acid (1:2 ratio). The cellulose nanocrystals (CNC) synthesized from DES-based exhibited zeta potential and particle size of −16.7 mV and 576.3 d.nm. DES-synthesized cellulose nanocrystals were spherical-like shapes, as observed from TEM images. The present results exposed that formic acid is an effective and green catalyst for the extraction of cellulose and DES for the sustainable synthesis of CNC.

Applying Subcritical Water Extraction to Obtain Bioactive Compounds and Cellulose Fibers from Brewer Spent Grains

Of the three types of waste generated in beer processing, brewer’s spent grain (BSG) is the most abundant and has a high potential for valorization. In this work, defatted BSG (DB) was subjected to an extraction process with subcritical water at different temperatures to obtain extracts rich in phenols and the cellulosic fractions, which were also purified by using hydrogen peroxide (H2O2). The results showed that the dry extracts obtained at 170 °C were richer in phenolics (24 mg Gallic Acid Equivalent (GAE) g−1 DB), but with lower antioxidant capacity (71 mg DB·mg−1 2,2-diphenyl-1-pikryl-hydrazyl). This extract also showed the highest antibacterial potential against L. innocua (80 mg·mL−1) and E. coli (140 mg·mL−1) than those obtained at lower temperatures. The purification of cellulose from the treated residues, using hydrogen peroxide, revealed that DB is a limited source of cellulose material since the bleached fractions showed low yields (20–25%) and low cellulose purity (42–71%), even after four bleaching cycles (1 h) at pH 12 and 8% H2O2. Despite this, the subcritical water extraction method highlights the potential of a simple process as a technological option to convert underutilized side streams like beer bagasse into added-value, potential ingredients for innovative food and pharmaceutical applications.

Hydrothermal extraction of microcrystalline cellulose from post-consumer indigo denim fabrics and evaluation of its UV blocking property

Abstract Waste cotton clothes, including post-consumer denim fabrics, are abundant biopolymer sources due to their high cellulose content. These waste materials commonly end up in landfills, posing health and environmental concerns and losing valuable cellulosic materials. To address these, this study aims to extract and characterize microcrystalline cellulose (MCC) from post-consumer indigo denim fabrics using a one-step hydrothermal method and evaluate its UV-blocking properties. FTIR and TGA analysis of raw and bleached denim confirmed the presence and purity of cotton cellulose and the indigo dye. Extracted MCC yielded 70-84%, with a degree of polymerization (DP) of 281-299. XRD analysis of the MCC showed a cellulose Type I structure. FTIR suggests the removal of amorphous phases of cellulose, leaving the crystalline structure. SEM meanwhile revealed rod-shaped and rough-surfaced MCC particles with diameters of 10-20 μm and lengths of 45-60 μm. Both FTIR and SEM indicated the retention of indigo dye on MCC surface. Increased acid hydrolysis time led to smaller particle sizes and higher degree of crystallinity (CrI). Indigo PVA-MCC films showed good transparency and effective UV blocking. These results indicate the successful conversion of denim to MCC via the hydrothermal method and the stability of indigo dye in the cellulose matrix.

A soft processing technology for the extraction of cellulose from plant residues and agri-food wastes

In this study, cellulose was extracted from giant cane (GC), Posidonia oceanica seagrass (PO), coffee silverskin (CS), and brewer's spent grain (BSG) as alternatives to conventional sources of cellulose. The extraction protocol involved three steps: i) hemicellulose and lignin removal through alkaline hydrolysis in a 5% (w/v) NaOH solution (solid-to-liquid ratio = 1:100 g/mL, T = 25 °C, t = 2 h, ω = 300 rpm), ii) removal of organic compounds and ashes through a 95% (v/v) ethanol solution (solid-to-liquid ratio = 1:25 g/mL, T = 25 °C, t = 0.5 h, ω = 500 rpm), and iii) double bleaching in a 1% (w/v) acidic (pH = 4) NaClO2 solution (solid-to-liquid ratio = 1:50 g/mL, T = 90 °C, t = 1.5 h, ω = 500 rpm). Yield, purity, crystallinity degree, and morphology of cellulose extracted through a soft-chemical cascade process were assessed by gravimetric, infrared (FT-IR), nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM) analyses. Averaged cellulose extraction yields of 36.4, 38.6, 23.1, and 22.2% for GC, PO, CS, and BSG were obtained, respectively. All cellulose samples had high purity, though lower than the ultra-pure bacterial cellulose, which was due to the slight contamination from unremoved hemicellulose and lignin residues. Cellulose samples exhibited similar chemical features and the typical fibril-like morphology of microcrystalline cellulose (6–13 μm in width). The versatility of the proposed extraction procedure supports the sustainable conversion of low-cost organic biomasses to valuable products with manifold industrial applications (e.g., food packaging).

Supercritical carbon dioxide–activated copper/bacterial cellulose aerogels for the capture of hydrophobic organic liquids

In this study, bacterial cellulose was derived from coconut water via fermentative production of nata de coco, a common food in Southeast Asia. Bacterial cellulose offers distinct advantages over plant cellulose resources, including three-dimensional structure, high porosity, high cellulose purity, and the absence of required polluting treatments, making it an ideal candidate for the facile preparation of various functional aerogel materials. Surface modification of nata de coco-derived cellulose fibers was obtained by incorporating Cu species (approximately 15 wt%) through an aqueous reaction of Cu(CH3COO)2 with N2H4 at room temperature. The Cu-coated bacterial cellulose aerogels were fabricated via supercritical carbon dioxide drying to maintain the natural three-dimensional matrix and subsequently characterized by various techniques confirming high porosity and crystallinity and successful Cu coating onto the cellulose fiber surface. The Cu-containing aerogel showed a significantly improved adsorption uptake for n-hexane (12.6 g g−1) in comparison with pure bacterial cellulose–based aerogel (3.2 g g−1). Furthermore, notable adsorption performances of 13.6–19.9 g g−1 were found for cyclohexane, ethyl acetate, and soybean oil, indicating the high efficiency of the supercritical carbon dioxide–activated bacterial cellulose aerogel containing Cu species in the adsorption of water-insoluble liquids. Notably, applying supercritical carbon dioxide drying afforded the stable aerogel structure for reusing over several cycles with almost unchanged trapping capacity.

Optimization of Cellulose Recovery Using Deep Eutectic Solvent Fractionation: A Response Surface Method Approach

Lignocellulosic biomass is a crucial renewable energy source for producing biofuels and valuable compounds, making it an attractive alternative to fossil resources. In this study, an environmentally friendly method was developed for cellulose fractionation from sugarcane bagasse using deep eutectic solvents (DESs), focusing on achieving high cellulose purity and specific physicochemical properties. The effects of different parameters were investigated by comparing four DESs: choline chloride–lactic acid (ChCl-LA), choline chloride–glycerol (ChCl-G), choline chloride–urea (ChCl-U), and choline chloride–polyalcohol (ChCl-P), under various reaction temperatures and times. The fractionation process was conducted under standard conditions at a temperature of 100 °C for 120 min with a 1:1 molar ratio. The results indicated that all DESs produced comparable cellulose recovery, ranging from 91.83% to 97.07%. A relatively high cellulose recovery was observed in the presence of ChCl-LA, at 95.47%. In addition, ChCl-LA demonstrated the highest efficiency in removing hemicellulose and lignin, at 95.36% and 93.38%, respectively, and high recovery yields of 70.45% for hemicellulose, and 70.66% for the lignin fraction. The fractionation conditions were further optimized using response surface methodology (RSM), achieving a ChCl-LA ratio of 1:2 v/v at 120 °C for 120 min. This resulted in impressive yields: 97.86% cellulose recovery, 96.50% hemicellulose removal, 74.40% hemicellulose recovery, 77.3% lignin recovery, and 71.5% lignin yield from sugarcane bagasse. These results closely match the predicted values, emphasizing the effectiveness of the process and its potential for economic application in lignocellulosic biorefinery operations.

A tree-ring cellulose extraction device adapted to radiocarbon analysis

AbstractTree-ring cellulose is a commonly used material for radiocarbon analysis. Extracting cellulose is labor-consuming and several devices that enable batchwise extraction have been developed. However, these devices bear the risk of sample contamination. The present study describes a new device which improves upon two aspects of currently available devices. First, to prevent cross-sample-contamination, we redesigned the drainage module to enable independent removal of chemical waste from each individual sample funnel. Second, we added covers to the sample funnels to reduce the risk of external contamination. Cellulose purity (i.e., holocellulose) was confirmed by Fourier Transform Infrared (FTIR) Spectroscopy. Furthermore, accuracy of the radiocarbon analysis was confirmed by results of 14C-blank samples and samples of known age. In conclusion, while maintaining labor-saving, our modified device significantly reduces the risk of sample contamination during extraction of tree-ring cellulose.

Preparation and characterization of Baijiu Jiuzao cellulose nanofibers-kafirin composite bio-film with excellent physical properties

Jiuzao is the main solid by-products of Baijiu industry, which contain a high amount of underutilized cellulose and proteins. In recent years, cellulose nanofibers mixed with proteins to prepare biodegradable bio-based film materials have received widespread attention. In this study, we propose a novel method to simultaneously extract kafirin and cellulose from strong-flavor type of Jiuzao, and modify cellulose to prepare cellulose nanofibers by the TEMPO (2,2,6,6-tetramethylpiperidine-1-oxide) oxidation-pressure homogenization technique, and finally mix kafirin with cellulose nanofibers to prepare a new biodegradable bio-based composite film. Based on the analysis of one-way and response surface experiments, the highest purity of cellulose was 82.04 %. During cellulose oxidation, when NaClO was added at 25 mmol/g, cellulose nanofibers have a particle size of 80–120 nm, a crystallinity of 65.8°. Finally, kafirin and cellulose nanofibers were mixed to prepare films. The results showed that when cellulose nanofibers were added at 1 %, the film surface was smooth, the light transmittance was 60.8 %, and the tensile strength was 9.17 MPa at maximum, which was 104 % higher than pure protein film. The contact angle was 34.3°. This paper provides new ideas and theoretical basis for preparing biodegradable bio-based composite film materials, and improves the added value of Jiuzao.

Effect of Drying Methods on the Thermal and Mechanical Behavior of Bacterial Cellulose Aerogel.

Bacterial cellulose (BC) presents significant promise as a biomaterial, boasting unique qualities such as exceptional cellulose purity, robust mechanical strength, heightened crystalline structure, and biodegradability. Several studies have highlighted specific effects, such as the impact of dehydration/rehydration on BC tensile strength, the influence of polymer treatment methods on mechanical properties, the correlation between microorganism type, drying method, and Young's modulus value, and the relationship between culture medium composition, pH, and crystallinity. Drying methods are crucial to the structure, performance, and application of BC films. Research findings indicate that the method used for drying can influence the mechanical properties of BC films, including parameters such as tensile strength, Young's modulus, and water absorption capacity, as well as the micromorphology, crystallinity, and thermal characteristics of the material. Their versatility makes them potential biomaterials applicable in various fields, including thermal and acoustic insulation, owing to their distinct thermal and mechanical attributes. This review delves into the thermal and mechanical behavior of bacterial cellulose aerogels, which are profoundly impacted by their drying mechanism.

Obtaining Cellulose Fibers from Almond Shell by Combining Subcritical Water Extraction and Bleaching with Hydrogen Peroxide.

Almond shell (AS) represents about 33% of the almond fruit, being a cellulose-rich by-product. The use of greener methods for separating cellulose would contribute to better exploitation of this biomass. Subcritical water extraction (SWE) at 160 and 180 °C has been used as a previous treatment to purify cellulose of AS, followed by a bleaching step with hydrogen peroxide (8%) at pH 12. For comparison purposes, bleaching with sodium chlorite of the extraction residues was also studied. The highest extraction temperature promoted the removal of hemicellulose and the subsequent delignification during the bleaching step. After bleaching with hydrogen peroxide, the AS particles had a cellulose content of 71 and 78%, with crystallinity index of 50 and 62%, respectively, for those treated at 160 and 180 °C. The use of sodium chlorite as bleaching agent improved the cellulose purification and crystallinity index. Nevertheless, cellulose obtained by both bleaching treatments could be useful for different applications. Therefore, SWE represents a promising green technique to improve the bleaching sensitivity of lignocellulosic residues, such as AS, allowing for a great reduction in chemicals in the cellulose purification processes.

Closer Approach towards the Preparation of Cellulose and Microcrystalline Cellulose from Corn Husks

AbstractIn this work, cellulose was effectively produced from corn husks by a simple and eco‐friendly method. Major influencing variables for cellulose extraction were examined, and the highest yield of lignin and hemicellulose cleavage was achieved after corn husks were treated in 12.5 wt % NaOH solution at solid/liquid ratio (S/L) of 1:10 g mL−1, 70 °C for 90 min. Subsequent bleaching conducted in 10 wt % H2O2 solution at 80 °C for 90 min produced cellulose with a lightness value (L*) of ∼87, chromaticity indexes a* = −1.85, b* = 2.94 with high purity, 90.86 %, and crystallinity, 64.94 %. Fourier transform infrared, scanning electron microscopy, and x‐ray diffraction analysis showed a clear transition in morphology, structure modification, and crystallinity consistent with the alteration of the chemical composition from raw material to delignified residue and the bleached one. To synthesize microcrystalline cellulose (MCC), the hydrolysis was investigated in H2SO4 solutions of different concentrations and durations via monitoring particle size distribution by laser diffraction spectroscopy. At the most efficient conditions (30 wt % H2SO4, 18 h, 45 °C, 1:10 S/L ratio), the obtained MCC reached an average particle size of 42.68 µm, crystallinity degree of 61.6 %, and cellulose purity of 92.5 %. Meanwhile, similar parameters with 4 N HCl solution produced MCC with the same purity but higher crystallinity (65.6 %), higher mean size, 67.62 µm, and higher aspect ratio. SEM images showed that 4 N HCl caused less detrimental and erosive action, and less fragmentation on cellulose microfibrils compared to 30 wt % H2SO4. The study's outcome supports the feasibility of corn husks to produce cellulose and MCC for further applications.

Ionic liquid pretreatment of lignocellulose for complete hemicellulose removal to produce high-purity cellulose mixed esters

Strategic valorization of agricultural waste can serve as waste management and promote sustainable biorefineries. Sugarcane bagasse is a readily available lignocellulosic biomass and can be converted into valuable cellulose-based thermoplastics. However, the cellulose purity significantly influences the material properties of the resulting thermoplastics, potentially limiting their applications. Therefore, conventional production necessitates harsh pretreatment of lignocellulose to isolate high-purity cellulose, followed by chemical modification. Here, we demonstrate a facile and green pretreatment method for complete removal of hemicellulose by incubating bagasse in a mixed system of an ionic liquid, 1-ethyl-3-methylimidazolium acetate (EmimOAc), and dimethyl sulfoxide (DMSO) at 140 °C, followed by precipitation in water, achieving >99 % hemicellulose removal. The pretreated bagasse, containing 71 % cellulose and 28 % lignin, underwent homogeneous transesterification with vinyl decanoate and isopropenyl acetate, using EmimOAc as both the solvent and catalyst, assisted by a co-solvent of DMSO. The polysaccharide derivative in the resulting acylated bagasse was separated from the lignin derivative by precipitation in methanol. The obtained polysaccharide derivative with high cellulose purity displayed a high weight-average molar mass of 1.5×106 g mol−1 and a polydispersity of 4. It also exhibited superior thermal stability (thermal degradation temperature, Td−5 %: 359 °C; glass transition temperature, Tg: 144 °C) compared to pulp-derived cellulose acetate decanoate (Td−5 %: 349 °C; Tg: 129 °C).

Nanofibrillated cellulose derived from rice bran, wheat bran, okara as novel dietary fibers: Structural, physicochemical, and functional properties

The structural, physicochemical, and functional properties of nanofibrillated cellulose (NFC) derived from rice bran (RB), wheat bran (WB), and okara were investigated and explored its potential as novel dietary fibers (DF). Cellulose microfibers (CMF) with cellulose purity of 87.4 % (RB), 92.1 % (WB), and 95.1 % (okara) were prepared by alkali and bleaching treatment, respectively. Subsequently, cellulose microfibers were prepared into NFCs with nanoscale diameters by dynamic high-pressure microjet treatment. Fourier transform infrared (FTIR) spectroscopy demonstrated a significant decrease in the intensity of characteristic absorption peaks of lignin and hemicellulose after chemical treatment. X-ray diffraction results indicated the order of relative crystallinity is: NFC (56.9 %) > CMF (50.8 %) > DF (26.1 %). Moreover, NFC exhibits higher water/oil holding capacity, swelling capability, nitrite/cholesterol/sodium cholate adsorption capacity than CMF and DF. Besides, NFC exhibited superior ability to inhibit starch and lipid digestion compared to DF. Consequently, NFC holds great promise as a novel dietary additive in the food industry. [Display omitted]

Influences of fractional separation on the structure and reactivity of wheat straw cellulose for producing 5-hydroxymethylfurfural

High-efficient production of 5-hydroxymethylfurfural (HMF), a “sleeping giant” in sustainable chemistry, from cellulose depends significantly on the effective separation of cellulose from lignocellulosic biomass. Herein, we report the fractional separation of wheat straw cellulose (WSC) from wheat straw under solvothermal conditions using a mixed solvent of γ-valerolactone (GVL) and H2O as the separating solvent, wherein the impacts of fractional separation parameters (solvent composition, temperature, and time) on removals of lignin and hemicellulose as well as purity and recovery of cellulose were studied by a Box-Behnken Design of response surface method. The optimization of the solvothermal parameters enabled an optimal fractional separation condition (VGVL: ∼ 60.0 vol%, T: 205 oC, t: ∼1.7 h) that led to a higher purity (89.4%) and recovery (86.7%) of cellulose in WSC. A further correlation of the removals of lignin and hemicellulose as well as purity and recovery of cellulose with the yield of HMF excluded an independent influence of the above factors. Instead, a comprehensive contribution of high fractional separation efficiency (defined as the product of cellulose purity and recovery) and low crystallinity of WSC was found to improve the HMF yield. However, the heat- and freeze-dryings of WSC after the solvothermal separation were found to lower the HMF yield because it re-improved the crystallinity of WSC. A high HMF yield of 58.6 mol% was achieved after reacting wet-WSC in a mixed solvent of 1,4-dioxane and H2O at 180 oC for 20 min, which was 1.5 fold higher than that from microcrystalline cellulose. This work highlights the importance of enhancing the fractional separation efficiency of cellulose from lignocellulosic biomass whereas avoiding drying process for future HMF biorefinery.

Juncus rigidus high biomass and cellulose productivity under wastewater salinity stress - A paradigm shift to the valorization of RO reject water

The use of water purifiers is intensively catching up and disposing of reverse osmosis reject water is of great concern. Reject water management using conventional methods is costly and harmful to the environment. To address this issue, the present study aims to utilize reverse osmosis reject wastewater using an eco-friendly approach. Juncus rigidus was treated with reject wastewater containing different salinity levels. Wastewater-treated plant dry biomass increased with increasing reject water salinity, and 625.3 g dry biomass recovered in treatment-B (~18,520 ppm). However, ~23,220 ppm wastewater salinity was lethal to the plants. The cellulose was extracted by alkali hydrolysis. The cellulose content in the wastewater-treated biomass was significantly higher in Treatment-B compared to both the control and Treatment-A (~12,744 ppm). The water salinity enhanced the cellulose (26.49 %) production in J. rigidus. Cellulose purity was confirmed using spectroscopic and thermogravimetric means. XRD shows highest crystallinity Index (77.29) with a d-spacing of 4.7 Å and 5.7 nm crystallite size in treatment-B. FTIR results reveal well-defined relevant peaks for OH, CH, CO, CH2, C-O-C, CO groups in treatment-B cellulose. Salinity impacts carboxyl groups in treatment B cellulose with a sharper and intense peak at 1644 cm−1 responsible for water absorption. Treatment-B exhibits higher thermal stability due to increased crystallinity. DSC shows endothermic depolymerization of cellulose with distinct peaks for different treatments. Morphological traits got better with increasing salinity with no adverse effect on cellulose. Salinity moderately affected the water absorption capacity of cellulose. All cellulose samples were devoid of gram-negative bacteria known by microbial test. This pioneering work underscores the plant's remarkable capacity not only to accomplish the circular economy by the valorization of wastewater obtained from various water purifiers for Juncus cultivation for cellulose production for diverse applications but also to generate income from wastewater.

Karakterisasi Biofilm Selulosa Bakteri dengan Modifikasi Gliserol secara Ex Situ

Bacterial cellulose (BC) is biomaterial from bacterial fermentation that contain high purity of cellulose, but 90% of BC pellicles retained water from the fermentation process. In this study, BC was modified with glycerol immersion in different concentrations (0%; 2,5%; 5%; 7,5%; 10%). For wide application, water content on BC must be removed by drying. Various oven drying condition are temperature 80 °C and 120 °C and time 60 minutes. The physical and mechanical properties of the dried BC biofilm were determined including tensile strength and elasticity. BC biofilm bound was identified by FTIR and EDX. The results showed that glycerol concentration was able to increase biofilm elasticity from 3.46% to 27.743%. However, glycerol immersion above 7.5% caused a decrease in the tensile strength of BC biofilm. The drying variation of 120 °C produces the highest tensile strength of 7.161 MPa when soaked in 7.5% glycerol. The drying variation of 80 °C produced a biofilm with the best elasticity of 27.473%. The results of FTIR and EDX analysis confirmed that there were differences in the contents of the modified BC.

Combining subcritical water extraction and bleaching with hydrogen peroxide to obtain cellulose fibres from rice straw

Cellulose fibres from rice straw (RS) were obtained by applying a combined and green process consisting of subcritical water extraction (SWE) (at 160 and 180 °C), followed by bleaching with hydrogen peroxide (H2O2). The bleaching variables were optimised for both extraction residues (R160 and R180), obtaining optimum conditions for 4 % H2O2 at pH 12 for 1 h of reaction. Under these conditions, four successive bleaching cycles were applied to promote cellulose purification in both R160 and R180 lignocellulosic samples, which were characterised as to their yield, whiteness index (WI), chemical composition, microstructural characteristics, degree of crystallinity, and thermal stability. The samples pre-extracted with SWE at 180 °C were more susceptible to bleaching than those pre-treated at 160 °C, being richer in cellulose (86.2 vs. 72.4 %), with higher WI (80.1 vs. 78) and yield (46.2 vs. 36.7 %) after the four bleaching cycles. Likewise, the R180 bleached fractions had higher crystallinity (67 vs. 63%) and were more thermostable than the R160 bleached fibres. Therefore, the SWE at 180 °C, followed by four bleaching cycles with H2O2 (4 %, at pH 12, for 1 h), can be considered a green and more sustainable alternative for obtaining cellulose fibres from RS with high cellulose purity.