Mild Alkaline Conditions Research Articles

Ionic nanoporous membranes from self-assembled liquid crystalline brush-like imidazolium triblock copolymers.

There is a need to generate mechanically and thermally robust ionic nanoporous membranes for separation and fuel cell applications. Herein, we report a general approach to the preparation of ionic nanoporous membranes through custom synthesis, self-assembly, and subsequent chemical manipulations of ionic brush block copolymers. We synthesized polynorbornene-based triblock copolymers containing imidazolium cations balanced by counter anions in the central block, side-chain liquid crystalline units, and sidechain polylactide end blocks. This unique platform comprises: (1) imidazolium/bis(trifluoromethanesulfonyl)imide (TFSI) as the middle block, which has an excellent ion-exchange ability, (2) cyanobiphenyl liquid crystalline end block, a sterically hindered hydrophobic segment, which is chemically stable and immune to hydroxide attack, (3) polylactide brush-like units on the other end block that is easily etched under mild alkaline conditions and (4) a polynorbornene backbone, a lightly crosslinked system that offers mechanical robustness. These membranes retain their morphology before and after backbone crosslinking as well as etching of polylactide sidechains. The ion exchange performance and dimensional stability of these membranes were investigated by water uptake capability and swelling ratio. Moreover, the length of the carbon spacer in the imidazolium/TFSI central block moiety endowed the membrane with improved ionic conductivity. The ionic nanoporous materials are unusual due to their singular thermal, mechanical, alkaline stability and ion transport properties. Applications of these materials include electrochemical actuators, solid-state ionic nanochannel biosensors, and ion-conducting membranes.

Barley β-glucan bioactive films: Promising eco-friendly materials for wound healing

Mixtures containing β-glucans were extracted from barley, under both mild and high alkaline conditions, to prepare biodegradable films (MA and HA, respectively), as natural dressings with intrinsic therapeutic properties. An in-depth characterization was performed to evaluate the impact of mild and high alkaline conditions on chemical, physicochemical, and biological features for potential use in wound treatments. Both MA and HA films exhibited a good ability to absorb water and simulate wound fluid, which helps maintain optimal tissue hydration. Moreover, their oxygen permeability (147.6 and 16.4 cm3 × μm/m2 × 24 h × Pa × 107, respectively) appeared adequate for the intended application. Biocompatibility tests showed that the films do not harm human dermal fibroblasts. Impressively, they promote cell attachment and growth, with MA having a stronger effect due to its higher β-glucan content. Furthermore, MA films can modulate macrophage behaviour in an inflamed microenvironment, reducing oxidative stress and pro-inflammatory cytokines, while simultaneously increasing levels of anti-inflammatory cytokines. In a scratch test, HA films allowed for faster fibroblast migration within the first 16 h compared to MA.Overall, this study demonstrates that developing β-glucan based films from barley, through a sustainable and cost-effective process, holds great promise for skin applications. These films exhibit significant potential to promote wound healing and modulate inflammation.

Surface Charge-Modulated Toxicity of Cysteine-Stabilized Silver Nanoparticles.

The toxicity of silver nanoparticles (AgNPs) depends on their physicochemical properties. The ongoing research aims to develop effective methods for modifying AgNPs using molecules that enable control over the processes induced by nanoparticles in both normal and cancerous cells. Application of amino acid-stabilized nanoparticles appears promising, exhibiting tunable electrokinetic properties. Therefore, this study focused on determining the influence of the surface charge of cysteine (CYS)-stabilized AgNPs on their toxicity towards human normal B (COLO-720L) and T (HUT-78) lymphocyte cell lines. CYS-AgNPs were synthesized via the chemical reduction. Transmission electron microcopy (TEM) imaging revealed that they exhibited a quasi-spherical shape with an average size of 18 ± 3 nm. CYS-AgNPs remained stable under mild acidic (pH 4.0) and alkaline (7.4 and 9.0) conditions, with an isoelectric point observed at pH 5.1. Following a 24 h treatment of lymphocytes with CYS-AgNPs, concentration-dependent alterations in cell morphology were observed. Positively charged CYS-AgNPs notably decreased lymphocyte viability. Furthermore, they exhibited grater genotoxicity and more pronounced disruption of biological membranes compared to negatively charged CYZ-AgNPs. Despite both types of AgNPs interacting similarly with fetal bovine serum (FBS) and showing comparable profiles of silver ion release, the biological assays consistently revealed that the positively charged CYS-AgNPs exerted stronger effects at all investigated cellular levels. Although both types of CYS-AgNPs have the same chemical structure in their stabilizing layers, the pH-induced alterations in their surface charge significantly affect their biological activity.

Hexane defatting effects on rapeseed protein extractability and properties at neutral and mild pH 8.5

Rapeseed is a promising plant protein source yet to be fully explored. Traditionally, rapeseed proteins are extracted from hexane-defatted press cake at high alkaline conditions to maximise protein recovery. Instead of the traditional approach, this study explored the effects of extracting proteins from the whole-kernel seed, focusing on assessing the hexane defatting process followed by gentle protein extraction at neutral pH compared with pH 8.5. Extraction at neutral pH resulted in a napin-rich protein extract, while alkaline conditions favoured cruciferin extraction as expected. Hexane defatting destroyed the oil bodies's structure while detaching the cell membrane from the cell wall, causing dehydration, and enabling interactions between the seed constituents. Increasing cycles of hexane treatment greatly reduced the total protein recovery by 9 g/100 g under neutral pH and >60 g/100 g under mild alkaline conditions which affected the protein structure, leading to a more rigid structure with a slightly higher melting temperature.

Mild alkaline conditions affect digester performance and community dynamics during long-term exposure

This paper examines the adaptive responses of microbial communities to gradual shifts in pH toward the mild alkaline range in anaerobic digestion (AD) systems. The results indicate that a pH of 8.0 serves as a critical upper limit for stable AD operation, beyond which microbial efficiency declines, underscoring the importance of microbial resilience against elevated pH stress. Specifically, hydrolysis genera, e.g. Eubacterium and Anaerobacterium, and syntrophic bacteria were crucial for reactor stability. Fibrobacter had also been shown to play a key role in the accumulation of propionate, thus leading to its dominance in the volatile fatty acid profile throughout the experimental phases. Overall, this investigation revealed the potential adaptability of microbial communities in AD systems to mild alkaline pH shifts, emphasizing the hydrolysis bacteria and syntrophic bacteria as key factors for maintaining metabolic function in elevated pH conditions.

De novo synthesis of a novel hapten and development of a monoclonal antibody–based immunoassay for the detection of dichlorvos and trichlorfon

The absence of high-affinity antibodies has hindered the development of satisfactory immunoassays for dichlorvos (DDVP) and trichlorfon (TCP), two highly toxic organophosphorus pesticides. Herein, the de novo synthesis of a novel anti-DDVP hapten was introduced. Subsequently, a specific anti-DDVP monoclonal antibody (Mab) was produced with satisfying affinity to DDVP (IC50: 12.4 ng mL−1). This Mab was highly specific to DDVP, and TCP could readily convert into DDVP under mild alkaline conditions. Leveraging this insight, an indirect competitive ELISA was successfully developed for simultaneous detection of DDVP and TCP. The limit of detection in rice, cabbage and apple for DDVP /TCP was found to be 12.1/14.6 μg kg−1, 7.3/8.8 μg kg−1 and 6.9/8.3 μg kg−1, respectively. This study not only provides an effective strategy for producing a high-quality anti-DDVP Mab but also affords a reliable and cost-effective tool suitable for high-throughput detection of DDVP and TCP in food samples.

Industrial byproducts as adhesive allies: Unraveling the role of proteins and isocyanates in polyurethane wood bonding

Wooden structures are becoming increasingly popular in the construction world. However, these structures often rely on synthetic adhesives, raising concerns about the environmental risks associated with their chemical composition. In response to these concerns, this study aims to explore sustainable alternatives, particularly focusing on polyurethane adhesives that incorporate proteins from industrial byproducts. The investigation involved three protein sources: soybean meal, shrimp shells, and skim milk, modified under mild alkaline conditions to obtain protein concentrates. These concentrates were then incorporated into the adhesives at varying protein contents: 5%, 10%, and 15%. Additionally, two isocyanate systems were examined, one being petrochemical-based and the other a partially bio-based blend. Chemical, thermal, optical, and mechanical characterizations were conducted to evaluate the adhesive performance. This study demonstrates that the adhesives’ thermal properties remain unaffected by both the protein content and the isocyanate system. However, these factors influence the adhesive penetration into the wood substrate. Ultimately, the results suggest that higher protein content offers superior retention of mechanical strength in adhesives compared to the petrochemical reference when subjected to humid conditions. Overall, this research demonstrates the potential of proteins from industrial byproducts as sustainable adhesive allies, providing valuable insights into their interactions with different isocyanates.

Hydrothermal Treatment of Wheat Bran under Mild Acidic or Alkaline Conditions for Enhanced Polyphenol Recovery and Antioxidant Activity.

This study was undertaken to investigate the effects of hydrothermal treatments under mild acid and alkaline conditions on polyphenol release and recovery from wheat bran (WB). After an initial screening of various food-grade substances, strong evidence was raised regarding the potency of citric acid and sodium carbonate to provide WB extracts exceptionally enriched in polyphenols. Thus, these two catalysts were tested under various time and temperature combinations, and the processes were described by linear models based on severity factor. The most effective treatments were those performed with 10% of either citric acid or sodium carbonate, at a constant temperature of 90 °C for 24 h, providing yields in total polyphenols of 23.76 and 23.60 mg g-1 dry mass of ferulic acid equivalents, respectively. Liquid chromatography-mass spectrometry analyses revealed that, while the sodium carbonate treatment afforded extracts enriched in ferulic acid, treatments with citric acid gave extracts enriched in a ferulate pentose ester. The extracts produced from those treatments also exhibited diversified antioxidant characteristics, a fact ascribed to the different polyphenolic composition. To the best of the authors' knowledge, this is the first report demonstrating the effective release of ferulic acid and a ferulate pentose ester from WB, using benign acid and alkali catalysts, such as citric acid and sodium carbonate.

Gallic acid crosslinked peanut protein‐corn starch composite edible films produced at alkaline pH with ultrasound application

AbstractCorn starch and peanut protein blend films were prepared with and without gallic acid addition (0.25%, w/v) at pH 7, 9, and 11 by casting. The ultrasound (160 W, 20 kHz, 10 min) treatment was applied to the film‐forming solutions. This study aimed to develop biopolymer‐based films with gallic acid and to determine the interactions of components at different pHs and with ultrasound. The barrier, optical, mechanical, and thermal properties of films were examined. Moreover, structural characterization of films was conducted by Fourier transform infrared (FTIR), x‐ray diffraction, and trinitro benzenesulfonic acid assay to enlighten the crosslinking interactions of gallic acid with biopolymers at different pHs. At neutral pH, gallic acid behaved as plasticizer. By acting as a crosslinker at pH 9, gallic acid provided the lowest moisture content, darker and more opaque appearance, enhanced barrier performance and thermal stability. The crosslinking degrees of gallic acid‐enriched films were 49.1% (pH 7), 77% (pH 9), and 67.4% (pH 11). Additionally, gallic acid increased antioxidant capacity. The ultrasonication adversely affected the film properties by breaking bonds in the film structure. Peanut protein‐corn starch‐gallic acid films under mild alkaline conditions exhibited outstanding thermal stability, mechanical durability, light, and water barrier characteristics, making them appropriate for sustainable food packaging applications.

Upcycling of protein concentrates from industrial byproducts into polyurethane wood adhesives

Wood structures generally rely on synthetic adhesives for their strength and versatility. However, environmental concerns linked to the chemical composition of these adhesives have stimulated the search for more environmentally friendly adhesives. Researchers have explored replacing petroleum-based constituents with natural raw materials such as lignins, tannins, and proteins. Of these alternatives, proteins, being biological macromolecules, are recognized for their capacity to enhance adhesion to wood substrates. This study considered the development of protein-based adhesives derived from diverse sources, including soybean meal, microbrewery spent grains, shrimp shells, and skim milk powder. These raw materials were subjected to mild alkaline conditions to yield protein concentrates. The resulting adhesives were formulated at various protein content levels: 5%, 10%, 15%, and 20%. The study’s findings showed that the incorporation of proteins into the polyurethane adhesive system not only can preserve but also augment adhesive performance. This enhancement encompasses deeper penetration into wood substrates and an overall improvement in mechanical strength. These results underscore the promise of proteins as a sustainable alternative to petroleum-based polyols in adhesive formulations.

Post‐Synthetic Ensembling Design of Hierarchically Ordered FAU‐type Zeolite Frameworks for Vacuum Gas Oil Hydrocracking

AbstractZeolites hold importance as catalysts and membranes across numerous industrial processes that produce most of the world's fuels and chemicals. In zeolite catalysis, the rate of molecular diffusion inside the micropore channels defines the catalyst's longevity and selectivity, thereby influencing the catalytic efficiency. Decreasing the diffusion pathlengths of zeolites to the nanoscopic level by fabricating well‐organized hierarchically porous architecture can efficiently overcome their intrinsic mass‐transfer limitations without losing hydrothermal stability. We report a rational post‐synthetic design for synthesizing hierarchically ordered FAU‐type zeolites exhibiting 2D‐hexagonal (P6mm) and 3D‐cubic (Ia d) mesopore channels. The synthesis involves methodical incision of the parent zeolite into unit‐cell level zeolitic fragments by in situ generated base and bulky surfactants. The micellar ensembles formed by these surfactant‐zeolite interactions are subsequently reorganized into various ordered mesophases by tuning the micellar curvature with ion‐specific interactions (Hofmeister effect). Unlike conventional crystallization, which offers poor control over mesophase formation due to kinetic constraints, crystalline mesostructures can be developed under dilute, mild alkaline conditions by controlled reassembly. The prepared zeolites with nanometric diffusion pathlengths have demonstrated excellent yields of naphtha and middle‐distillates in vacuum gas oil hydrocracking with decreased coke deposition.

Post-Synthetic Ensembling Design of Hierarchically Ordered FAU-type Zeolite Frameworks for Vacuum Gas Oil Hydrocracking.

Zeolites hold importance as catalysts and membranes across numerous industrial processes that produce most of the world's fuels and chemicals. In zeolite catalysis, the rate of molecular diffusion inside the micropore channels defines the catalyst's longevity and selectivity, thereby influencing the catalytic efficiency. Decreasing the diffusion pathlengths of zeolites to the nanoscopic level by fabricating well-organized hierarchically porous architecture can efficiently overcome their intrinsic mass-transfer limitations without losing hydrothermal stability. We report a rational post-synthetic design for synthesizing hierarchically ordered FAU-type zeolites exhibiting 2D-hexagonal (P6mm) and 3D-cubic (Ia d) mesopore channels. The synthesis involves methodical incision of the parent zeolite into unit-cell level zeolitic fragments by in situ generated base and bulky surfactants. The micellar ensembles formed by these surfactant-zeolite interactions are subsequently reorganized into various ordered mesophases by tuning the micellar curvature with ion-specific interactions (Hofmeister effect). Unlike conventional crystallization, which offers poor control over mesophase formation due to kinetic constraints, crystalline mesostructures can be developed under dilute, mild alkaline conditions by controlled reassembly. The prepared zeolites with nanometric diffusion pathlengths have demonstrated excellent yields of naphtha and middle-distillates in vacuum gas oil hydrocracking with decreased coke deposition.

Activation of periodate by chalcopyrite for efficient degradation of tetracycline hydrochloride

Activation of periodate (PI) has been widely recognized as an efficient and economical technique for the elimination of contaminants. In this study, a novel system with PI triggered by chalcopyrite (CuFeS2) was applied in the decomposition of tetracycline hydrochloride (TC). Effects of CuFeS2 dosage, PI concentration, pH value, inorganic anions, valence state change of Iodine ions (I-) were tested. The experimental findings demonstrated that the CuFeS2/PI system could successfully decompose TC in water under mild alkaline conditions (89.5 %, pH = 8). Compared with the other catalysts and the other CuFeS2/peroxide systems, CuFeS2/PI system exhibited more superior decontamination performance. Involvement of multiple reactive oxygen species such as superoxide radical (·O2–), hydroxyl radical (*OH) and singlet oxygen (1O2) in TC decomposition was confirmed by Electron spin resonance (ESR) tests and quenching experiment, and the interactions between Cu(Ⅱ)/Fe(III) and Cu(I)/Fe(Ⅱ) was confirmed. Based on a calculation using the density functional theory (DFT), the active sites of CuFeS2 for PI activation were revealed. Additionally, the analysis of degradation intermediates was conducted, with the toxicity of the intermediates analyzed. The CuFeS2/PI system was then applied in the treatment of real water samples, and the reusability of CuFeS2 was also investigated. This research presents a novel strategy as well as a theoretical foundation for CuFeS2 triggered PI to remove antibiotic contaminants.

Pitfalls in RNA Modification Quantification Using Nucleoside Mass Spectrometry.

In recent years, there has been a high interest in researching RNA modifications, as they are involved in many cellular processes and in human diseases. A substantial set of enzymes within the cell, called RNA writers, place RNA modifications selectively and site-specifically. Another set of enzymes, called readers, recognize these modifications which guide the fate of the modified RNA. Although RNA is a transient molecule and RNA modification could be removed by RNA degradation, a subclass of enzymes, called RNA erasers, remove RNA modifications selectively and site-specifically to alter the characteristics of the RNA. The detection of RNA modifications can be done by various methods including second and next generation sequencing but also mass spectrometry. An approach capable of both qualitative and quantitative RNA modification analysis is liquid chromatography coupled to mass spectrometry of enzymatic hydrolysates of RNA into nucleosides. However, for successful detection and quantification, various factors must be considered to avoid biased identification and inaccurate quantification. In this Account, we identify three classes of errors that may distort the analysis. These classes comprise (I) errors related to chemical instabilities, (II) errors revolving around enzymatic hydrolysis to nucleosides, and (III) errors arising from issues with chromatographic separation and/or subsequent mass spectrometric analysis.A prominent example for class 1 is Dimroth rearrangement of m1A to m6A, but class 1 also comprises hydrolytic reactions and reactions with buffer components. Here, we also present the conversion of m3C to m3U under mild alkaline conditions and propose a practical solution to overcome these instabilities. Class 2 errors-such as contaminations in hydrolysis reagents or nuclease specificities-have led to erroneous discoveries of nucleosides in the past and possess the potential for misquantification of nucleosides. Impurities in the samples may also lead to class 3 errors: For instance, issues with chromatographic separation may arise from residual organic solvents, and salt adducts may hamper mass spectrometric quantification. This Account aims to highlight various errors connected to mass spectrometry analysis of nucleosides and presents solutions for how to overcome or circumnavigate those issues. Therefore, the authors anticipate that many scientists, but especially those who plan on doing nucleoside mass spectrometry, will benefit from the collection of data presented in this Account as a raised awareness, toward the variety of potential pitfalls, may further enhance the quality of data.

Inhibition of non-specific protein adsorption on PMMA surface: The role of surface modification

Mitigating non-specific adsorption (NSA) occurring on the surface of microfluidic devices plays a critical role in the detection of early protein biomarkers for clinical diagnosis. Surface-modified methods commonly used in the formation of microfluidic channels include BSA coating, PEG grafting, and Plasma cleaning. The surface composition and microstructure of PMMA surfaces were characterized by Fourier transfer infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), water contact angles (CA), and atomic force microscopy (AFM) measurements. The NSA on surfaces of bovine serum albumin (BSA) labeled with fluorescein isothiocyanate (FITC) were investigated by microfluidics and fluorescence microscopy. The results showed that the hydrophobicity of the PMMA surface was enhanced after modification with PEG. We further evaluated their anti-protein adsorption properties under a mild alkaline (PH 7.4) condition, including concentration, reaction time, and sample volume. The BSA coating had the best anti-protein adsorption effect, reaching over 87.6%. The anti-protein adsorption effect of the plasma cleaning method is slightly inferior to that of BSA coating, at 86.1%, but the modification process is simpler and faster. Due to the insufficient stability of PEG, its resistance to protein adsorption decreases as the concentration increases.

Smartphone-Based High-Throughput Fluorimetric Assay for Histidine Quantification in Human Urine Using 96-Well Plates.

A high-throughput fluorimetric assay for histidine was developed, using a 96-well plates platform. The analyte reacts selectively with o-phthalaldehyde under mild alkaline conditions to form a stable derivative. Instrumental-free detection was carried out using a smartphone after illumination under UV light (365 nm). The method was proved to be linear up to 100 μM histidine, with an LLOQ (lower limit of quantification) of 10 μM. The assay was only prone to interference from glutathione and histamine that exist in the urine samples at levels that are orders of magnitude lower compared to histidine. Human urine samples were analyzed following minimum treatment and were found to contain histidine in the range of 280 to 1540 μM. The results were in good agreement with an HPLC corroborative method.

Enhanced Oxidation of Antibiotics by Ferrate Mediated with Natural Organic Matter: Role of Phenolic Moieties.

The increasing presence of antibiotics in water sources threatens public health and ecosystems. Various treatments have been previously applied to degrade antibiotics, yet their efficiency is commonly hindered by the presence of natural organic matter (NOM) in water. On the contrary, we show here that nine types of NOM and NOM model compounds improved the removal of trimethoprim and sulfamethoxazole by ferrate(VI) (FeVIO42-, Fe(VI)) under mild alkaline conditions. This is probably associated with the presence of phenolic moieties in NOMs, as suggested by first-order kinetics using NOM, phenol, and hydroquinone. Electron paramagnetic resonance reveals that NOM radicals are generated within milliseconds in the Fe(VI)-NOM system via single-electron transfer from NOM to Fe(VI) with the formation of Fe(V). The dominance of the Fe(V) reaction with antibiotics resulted in their enhanced removal despite concurrent reactions between Fe(V) and NOM moieties, the radicals, and water. Kinetic modeling considering Fe(V) explains the enhanced kinetics of antibiotics abatement at low phenol concentrations. Experiments with humic and fulvic acids of lake and river waters show similar results, thus supporting the enhanced abatement of antibiotics in real water situations.

Synthesis and Anti-Inflammatory Evaluation of a Library of Chiral Derivatives of Xanthones Conjugated with Proteinogenic Amino Acids.

In recent decades, the relationship between drug chirality and biological activity has been assuming enormous importance in medicinal chemistry. Particularly, chiral derivatives of xanthones (CDXs) have interesting biological activities, including enantioselective anti-inflammatory activity. Herein, the synthesis of a library of CDXs is described, by coupling a carboxyxanthone (1) with both enantiomers of proteinogenic amino esters as chiral building blocks (2-31), following the chiral pool strategy. The coupling reactions were performed at room temperature with good yields (from 44 to 99.9%) and very high enantiomeric purity, with most of them presenting an enantiomeric ratio close to 100%. To afford the respective amino acid derivatives (32-61), the ester group of the CDXs was hydrolyzed in mild alkaline conditions. Consequently, in this work, sixty new derivatives of CDXs were synthetized. The cytocompatibility and anti-inflammatory activity in the presence of M1 macrophages were studied for forty-four of the new synthesized CDXs. A significant decrease in the levels of a proinflammatory cytokine targeted in the treatment of several inflammatory diseases, namely interleukin 6 (IL-6), was achieved in the presence of many CDXs. The amino ester of L-tyrosine (X1AELT) was the most effective in reducing IL-6 production (52.2 ± 13.2%) by LPS-stimulated macrophages. Moreover, it was ≈1.2 times better than the D-enantiomer. Indeed, enantioselectivity was observed for the majority of the tested compounds. Thus, their evaluation as promising anti-inflammatory drugs should be considered.

Secondary Structures of MERS-CoV, SARS-CoV, and SARS-CoV-2 Spike Proteins Revealed by Infrared Vibrational Spectroscopy.

All coronaviruses are characterized by spike glycoproteins whose S1 subunits contain the receptor binding domain (RBD). The RBD anchors the virus to the host cellular membrane to regulate the virus transmissibility and infectious process. Although the protein/receptor interaction mainly depends on the spike's conformation, particularly on its S1 unit, their secondary structures are poorly known. In this paper, the S1 conformation was investigated for MERS-CoV, SARS-CoV, and SARS-CoV-2 at serological pH by measuring their Amide I infrared absorption bands. The SARS-CoV-2 S1 secondary structure revealed a strong difference compared to those of MERS-CoV and SARS-CoV, with a significant presence of extended β-sheets. Furthermore, the conformation of the SARS-CoV-2 S1 showed a significant change by moving from serological pH to mild acidic and alkaline pH conditions. Both results suggest the capability of infrared spectroscopy to follow the secondary structure adaptation of the SARS-CoV-2 S1 to different environments.

Membrane Filtration Applied to the Purification of Sugarcane Bagasse Mild Alkaline Extracts

Sugarcane bagasse (SCB), a by-product of the sugar industry, is composed mainly of cellulose, hemicelluloses, and lignin, and can be used to replace petrochemical polymers in various applications. In this work, SCB was treated under mild alkaline conditions with 1.5% NaOH (m:v) and a solid:liquid ratio of 1:20 (m:v) at 60 °C, during 6 h. A 10 kDa polysulfone hollow fiber membrane was used for the purification of the extract in different filtration modes, namely concentration and diafiltration, and a combination of both modes. Permeate fluxes and rejection rates were evaluated at different transmembrane pressure (TMP) at the shear rate of 10,187 s–1, at 40 °C. In concentration mode, increasing the volume reduction factor up to 6.1 led to a significant increase in the retention rates of acid-soluble lignin (ASL) and xylan, and a decrease in inorganic salt content in the retentate. In diafiltration mode, after 2.9 diavolumes, the acid-insoluble lignin (AIL) and xylan rejection rates drastically increased, as did the rejection rates of ash.