Acid Hydrolysis Research Articles

Characterization of cellulose nanocrystals from Zhombwe (Neorautanenia brachypus (harms) CA Sm.) bagasse.

Increased awareness of environmental pollution has changed focus to the use of biodegradable materials because they lack persistence in the environment. This article focused on the production of cellulose nanocrystals from Zhombwe, Neorautanenia brachypus (Harms) CA Sm. bagasse using steam explosion, alkaline treatment, bleaching, purification, and acid hydrolysis. The chemical composition after the treatments was determined using TAPPI standards. Further characterization was done using x-ray Diffraction (XRD), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The nanoscale dimensions and morphology of the extracted nanocrystals was determined through field emission scanning electron microscopy (FE-SEM). FTIR spectroscopy and DSC confirmed the removal of noncellulosic compounds. XRD revealed that N. brachypus bagasse contained cellulose type I, which partly endured morphological change to polymorph II after purification and hydrolysis. FE-SEM revealed elliptical to rod-shaped structures after acid hydrolysis, which had a mean length and width of 1103 nm and 597 nm respectively. TAPPI tests revealed that successive chemical treatments increased crystallinity by 29.7%, enriched cellulose content by 74.2%, reduced lignin content by 21.7%, and reduced hemicellulose to less than 1%. The semicrystalline nature of the material produced in our work is a promising candidate for swelling hydrogel applications in areas such as wound dressing, heavy metal removal, controlled drug delivery, agriculture, and sanitary products. Future studies may focus on surface modification of nanocrystals to improve their thermal stability and therefore expand their range for potential industrial applications.

Effect of Glycerol and Sisal Nanofiber Content on the Tensile Properties of Corn Starch/Sisal Nanofiber Films

Currently, petroleum-derived plastics are widely used despite the disadvantage of their long degradation time. Natural polymers, however, can be used as alternatives to overcome this obstacle, particularly cornstarch. The tensile properties of cornstarch films can be improved by adding plant-derived nanofibers. Sisal (Agave sisalana), a very common low-cost species in Brazil, can be used to obtain plant nanofibers. The goal of this study was to obtain sisal nanofibers using low concentrations of sulfuric acid to produce thermoplastic starch nanocomposite films. The films were produced by a casting technique using commercial corn starch, glycerol, and sisal nanofibers, accomplished by acid hydrolysis. The effects of glycerol and sisal nanofiber content on the tensile mechanical properties of the nanocomposites were investigated. Transmission electron microscopy findings demonstrated that the lowest concentration of sulfuric acid produced fibers with nanometric dimensions related to the concentrations used. X-ray diffraction revealed that the untreated fibers and fibers subjected to acid hydrolysis exhibited a crystallinity index of 61.06 and 84.44%, respectively. When the glycerol and nanofiber contents were 28 and 1%, respectively, the tensile stress and elongation were 8.02 MPa and 3.4%. In general, nanocomposites reinforced with sisal nanofibers showed lower tensile stress and higher elongation than matrices without nanofibers did. These results were attributed to the inefficient dispersion of the nanofibers in the polymer matrix. Our findings demonstrate the potential of corn starch nanocomposite films in the packaging industry.

A Highly Stable, Multifunctional Janus Dressing for Treating Infected Wounds.

The limited and unstable absorption of excess exudate is a major challenge during the healing of infected wounds. In this study, a highly stable, multifunctional Janus dressing with unidirectional exudate transfer capacity is fabricated based on a single poly(lactide caprolactone) (PLCL). The success of this method relies on an acid hydrolysis reaction that transforms PLCL fibers from hydrophobic to hydrophilic in situ. The resulting interfacial affinity between the hydrophilic/phobic PLCL fibers endows the Janus structure with excellent unidirectional liquid transfer and high structural stability against repeated stretching, bending, and twisting. Various other functions, including wound status detection, antibacterial, antioxidant, and anti-inflammatory properties, are also integrated into the dressing by incorporating phenol red and epigallocatechin gallate. An in vivo methicillin-resistant Staphylococcus aureus-infected wound model confirms that the Janus dressing, with the capability to remove exudate from the infected site, not only facilitates epithelialization and collagen deposition, but also ensures low inflammation and high angiogenesis, thus reaching an ideal closure rate up to 98.4% on day 14. The simple structure, multiple functions, and easy fabrication of the dressing may offer a promising strategy for treating chronic wounds, rooted in the challenges of bacterial infection, excessive exudate, and persistent inflammation.

Photolysis of tolfenamic acid in aqueous and organic solvents: a kinetic study.

Tolfenamic acid (TA) is a non-steroidal anti-inflammatory drug that was studied for its photodegradation in aqueous (pH 2.0-12.0) and organic solvents (acetonitrile, methanol, ethanol, 1-propanol, 1-butanol). TA follows first-order kinetics for its photodegradation, and the apparent first-order rate constants (k obs) are in the range of 0.65 (pH 12.0) to 6.94 × 10-2 (pH 3.0) min-1 in aqueous solution and 3.28 (1-butanol) to 7.69 × 10-4 (acetonitrile) min-1 in organic solvents. The rate-pH profile for TA photodegradation is an inverted V (∧) or V-top shape, indicating that the cationic form is more susceptible to acid hydrolysis than the anionic form of TA, which is less susceptible to alkaline hydrolysis. The fluorescence behavior of TA also exhibits a V-top-shaped curve, indicating maximum fluorescence intensity at pH 3.0. TA is highly stable at a pH range of 5.0-7.0, making it suitable for formulation development. In organic solvents, the photodegradation rate of TA increases with the solvent's dielectric constant and solvent acceptor number, indicating solute-solvent interactions. The values of k obs decreased with increased viscosity of the solvents due to diffusion-controlled processes. The correlation between k obs versus ionization potential and solvent density has also been established. A total of 17 photoproducts have been identified through LC-MS, of which nine have been reported for the first time. It has been confirmed through electron spin resonance (ESR) spectrometry that the excited singlet state of TA is converted into an excited triplet state through intersystem crossing, which results in an increased rate of photodegradation in acetonitrile.

Development and validation of stability-indicating method of etrasimod by HPLC/DAD/MS/MS technique with greenness profiling

Etrasimod, a novel selective sphingosine-1-phosphate receptor modulator, was recently approved by the U.S. Food and Drug Administration and the European Medicinal Agency for the treatment of moderately to severely active ulcerative colitis in adults. In this research, the forced degradation study as an integral part of drug product and packaging development, which generates data on degradation mechanisms, is published. The development and validation of the stability-indicating method using a superior high-performance liquid chromatography technique coupled with a diode array detector and tandem mass spectrometer was performed to support the forced degradation study and monitor the formation of degradation products. Etrasimod demonstrated good stability under elevated temperature and basic stress conditions, while acidic hydrolysis, oxidative, and photolytic degradation produced eight degradation products. The knowledge of degradation products will be useful in the long-term stability study for establishing the acceptance criteria of etrasimod as a drug substance and dosage form during quality control and stability assessment. The eco-friendliness of the developed forced degradation procedure was evaluated using various greenness appraisal tools. The green metric tools showed that the forced degradation procedure obeys eco-friendly conditions.

Quaternization of Methyl Picolinate with Some Phenacyl Bromides. Synthesis of DL-Baikiain Alkaloid

By fusing methyl picolinate with phenacyl bromides, the corresponding phenacyl salts were obtained, cyclization of which in acetic anhydride led to previously undescribed 3-aryl-1H-pyrido[2,1-c][1,4]oxazinium bromides. Reduction of the quaternary salts of methyl picolinate followed by acid hydrolysis leads to the alkaloid DL-baikiain.

Nanocellulose-Based Resistive Sensors for Air Humidity Measurements

Introduction. The measurement of relative air humidity plays a crucial role in various aspects of human life, such as climate control systems, medical breath and skin hydration monitoring. Typically, humidity sensors use inorganic materials and petroleum-derived polymers. However, there is a growing trend towards the transition to biodegradable materials, which eliminates the need for waste disposal.Problem Statement. Currently, nanocellulose (NC) has been being explored as a promising material for humidity sensors. However, the influence of the chemical composition and nanoparticle size of NC on the sensor characteristics remains understudied.Purpose. This study aims to investigate the influence of the chemical composition and structure of NC on the parameters of humidity sensors.Materials and Methods. NC has been synthesized from reed stalks and wheat straw bz the oxidation and acid hydrolysis methods. NC-film sensors having a mass within 0.3—3 mg have been fabricated. The static parameters (response, sensitivity, reversibility, and repeatability) and the dynamic parameters (short and long-term stability, response and recovery time) of the sensors have been analyzed.Results. The manufacturing method influences the NC chemical composition, while the origin material affects its structure. The sensors produced by the oxidation method have demonstrated improved sensitivity (2.69 · 106), response (0.2 (%RH)–1), recovery time (60 s) and long-term stability (1.44%) as compared with those made by the hydrolysis method. Additionally, the application of wheat straw NC as origin material has resulted in improved reversibility (5%), repeatability (5% deviation), short-term stability (30% deviation), and response time (1 s) as compared with the reed stalks NC.Conclusions. It has been established that the origin material of nanocellulose influences the reversibility, repeatability, response time, and short-term stability of the sensors. The manufacturing method has effect on the sensitivity, response, recovery time, and long-term stability of the sensors.

Structural elucidation a complex galactosyl andglucosyl-rich pectin from the pericarp of immature fruits of Juglans mandshurica Maxim.

A glucosyl-rich pectin, JMMP-3 (Mw, 2.572 × 104g/mol, O-methyl % = 3.62%), was isolated and purified from the pericarp of the immature fruit of Juglans mandshurica Maxim. (QingLongYi). The structure of JMMP-3 was studied systematically by infrared spectroscopy, monosaccharide compositions, methylation analysis, partial acid hydrolysis, and 1/2D-NMR. The backbone of JMMP-3 possessed a smooth region (→ 4GalA1 →) and a hairy region (→ 4GalA1 → 2Rha1 →) with a molar ratio of 2: 5. The substitution of four characteristic side chains (R1-R4) occurs at C-4 of → 2,4)-α-Rhap-(1→, where R1 is composed of → 5)-α-Araf-(1→, R2 is composed of → 4)-β-Galp-(1 → and β-Galp-(1→, R3 is composed of α-Glcp-(1→, →4)-α-Glcp-(1 → and → 4,6)-α-Glcp-(1→, and R4 is composed of → 5)-α-Araf-(1→, β-Galp-(1→, → 4)-β-Galp-(1→, → 3,4)-β-Galp-(1→, → 4,6)-β-Galp-(1 → and → 2,4)-β-Galp-(1 → . In addition, the antitumor activity of JMMP-3 on HepG2 cells was preliminarily investigated.

Optimizing cultural conditions and pretreatment for high-value single-cell protein from vegetable waste

The study aimed to produce single-cell protein (SCP) from vegetable waste through solid-state fermentation (SSF) using tomato, capsicum, eggplant, and cucumber waste. Three yeast strains, namely Candida tropicalis, Candida krusei, and Saccharomyces cerevisiae were selected to optimize cultural conditions without pretreatment of the substrate to obtain a higher yield of SCP. The study identified the best-performing yeast strains and optimized the acid and thermal hydrolysis pretreatment of vegetable waste using central composite design by response surface methodology. The substrate was pretreated with varying concentrations of sulfuric acid (2 %, 4 %, and 6 % w/v) at temperatures of 120°C, 140°C, and 160°C. The study demonstrated that SCP production could be enhanced with the acid and thermal hydrolysis of nutrient-supplemented vegetable waste by using optimized cultural conditions. Without pretreatment of vegetable waste, the yeast combination of Saccharomyces cerevisiae and Candida tropicalis achieved a maximum protein content of 10.8 mg/g of dry biomass (an increment of 63.6 % compared to control). With the same yeast strains, pretreatment of vegetable waste (with 4 % sulfuric acid at 140°C) and supplemented with a nutrient source increased SCP production to 21.9 and 31.7 mg/g (an increment of 231.8 % and 375.8 % compared to control), respectively. The study's findings suggest that SCP production from vegetable waste can be optimized through SSF and acid-thermal hydrolysis pretreatment, which could be a promising approach for efficient waste management.

Biorefinery of red seaweed Palmaria palmata for production of bio-based chemicals and biofuels

The seaweed Palmaria palmata was used as feedstock for production of chemical/fuel precursors (acetone, butanol, ethanol) and biogas. Palmaria palmata consists of xylan as major cell wall polysaccharide, as well as galactan and glucan. First, the biomass was subjected to acid hydrolysis at laboratory scale to solubilise fermentable sugars using acetic or hydrochloric acid as catalysts. Differences were observed in composition and amenability to hydrolysis of seaweeds from different harvests. Highest saccharification yields were obtained using HCl (pH 1.7, 120 °C, up to 80 % of xylose). Hydrolysates were fermented to acetone-butanol-ethanol by Clostridium beijerinckii reaching yields of 0.28 g products/g consumed sugars. The process by-products (solids after acetic acid hydrolysis and spent fermentation broth) were used as feedstocks for anaerobic digestion showing biogas yields between 310 and 650 L/kg dry organic material when mixed in different ratios with sugar beet pulp. Subsequently, the hydrolysis and fermentation processes were upscaled up to a 100-L pilot volume where nanofiltration was implemented to increase sugar concentration and remove salts. While high monomeric sugar yields were replicated during upscaling, fermentation inhibition was observed in the upscaled process. This paper shows Palmaria palmata to be a suitable feedstock for the co-production of bio-butanol and biogas and highlights process development needs to desalt and detoxify seaweed hydrolysates prior to fermentation.

The promotion and inhibition of proteolysis in silages during ensiling of citrus waste

Although waste generated from the production of citrus fruit juice is a suitable raw material for ensiling, excessive proteolysis greatly reduces the quality of silages and economic benefits. The driving force and factors influencing proteolysis during ensiling remain poorly understood. In this study, the degree of silage proteolysis was systematically evaluated through the analysis of silage composition, proteolysis promotion and inhibition under various ensiling factors were quantified, and the causes of proteolysis were explored through changes of microbiome. A reduction in soluble protein (SP) and in-solution protein (ISP) contents coupled with an increase in NH3-N were found after ensiling. A decrease in free amino acid content was evident in upper and middle sections, whereas there was an increase in the bottom section. The strongest proteolysis of silages was observed in the middle section. The main factor accelerating hydrolysis of protein into amino acid (the first stage of proteolysis) was acid protease activity (APA). The hydrolysis of amino acid into NH3-N (the second stage of proteolysis) was principally inhibited by lactic acids, acetic acids, pH, and soluble carbon, and accelerated by APA, moisture and total carbon. Acid protease was probably constituted mainly microbial protease, able to tolerate a pH range of 3.44–3.77. Bacterial coupled colony (B-CC), Trichocomaoute, and Trichocomaceae-1 presumably promoted the production and activity of acid protease. As inferred, the first stage of proteolysis was promoted by B-CC and fungal coupled colony (F-CC), and inhibited by Trichocomaoute. While the second stage of proteolysis was likely promoted by P. kudriavzevii and F-CC, and inhibited by B-CC and Trichocomaoute. Thus, the use of homofermentative lactic acid bacteria in raw materials is recommended to reduce the degree of proteolysis, particularly in the middle section of the silo.

Weak acid hydrolysis strategy to oxygen vacancy enriched BiOBrnI1-n nanosheet for photodegrading various contaminants

BiOBrnI1-n solid solution enriched with oxygen vacancies (OVs) was obtained using simple hydrolysis method and exhibited excellent ability to remove various contaminants, inclusive of bisphenol A (BPA), rhodamine B (RhB), methyl orange (MO), tetracycline hydrochloride (TCH) and sulfamethazine (SMT). The photocatalytic degradation efficiency of optimal BiOBrnI1-n catalyst for BPA is 128 and 13.8 times higher than that of BiOBr and BiOI, respectively. The excellent degradation activity benefits from the suitable energy band potential, interior electric field and superior charge separation efficiency. The test of catalytic cycles confirms the high reusability of BiOBrnI1-n. Photoinduced h+, ·O2−, and e− serve as reactive species in the degradation process. This work provides an effective photocatalyst for the photodegradation of various contaminants.

Monocomponent Biosorption of Copper Ions (II) onto Nanocrystalline Cellulose from Coconut Husk Fibers

Introduction: Nanocrystalline cellulose (NCC) is one of the most suitable cellulose derivatives for the treatment of wastewater. Various agricultural wastes have been used for the extraction of NCC. Coconut wastes have been widely studied as potential adsorbents for the removal of pollutants, including dyes and heavy metals. Methods: In this work, nanocrystalline cellulose (NCC) was successfully isolated from coconut husk fibers through alkaline pretreatment accompanied by sulfuric acid hydrolysis. Then, the ability of NCC to adsorb Cu2+ from aqueous solution in batch studies was investigated. Results: Results indicated that the optimal hydrolysis parameters were achieved at 50° C for 45 min with 64% sulfuric acid to extract NCC as rod-like particles with diameters between 4-10 nm. The potential of NCC as a biosorbent to remove copper ions (Cu2+) from aqueous solution was investigated in terms of batch mode and maximum adsorption capacity (qm) of 79.491 mg/g of Cu2+. The adsorption efficiency of Cu2+ions increased with an increase in the adsorbent dosage, decreased with an increase in the initial concentration of contaminant, and increased with the contact time. Under optimal conditions, adsorption kinetic followed a pseudo-second-order kinetic model and the adsorption isotherm fitted most closely with the Langmuir model. Conclusion: According to a literature review, NCC from coconut husk fibers has not been used for the adsorption of heavy metals, mainly copper ions. This study shows that NCC from coconut husk fibers can be used as a low-cost and environmentally friendly adsorbent for the removal of Cu2+ from aqueous solutions.

Chitin Nanocomposites for Fused Filament Fabrication: Flexible Materials with Enhanced Interlayer Adhesion.

In this work, we present a series of nanocomposites for Fused filament fabrication (FFF) based on polycaprolactone (PCL) and chitin nanocrystals (ChNCs). The ChNCs were synthesized by acid hydrolysis using HCl or lactic acid (LA). The approach using LA, an organic acid, makes the ChNCs synthesis more sustainable and modifies their surface with lactate groups, increasing their compatibility with the PCL matrix. The ChNCs characterization by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy revealed that both ChNCs presented similar morphologies and crystallinity, while differential scanning calorimetry and thermogravimetric analysis proved that they can bear temperatures up to 210 °C without degrading, which allows their processing in the manufacturing of PCL composites by twin-screw extrusion. Therefore, PCL composites in the form of filaments containing 0.5-1.0 wt % ChNCs were produced and used as feedstock in FFF, and standard tensile and flexural specimens were printed at different temperatures, up to 170 °C, to assess the influence of the ChNCs in the mechanical properties of the material. The tensile testing results showed that the presence of ChNCs enhances the strength and ductility of the PCL matrix, increasing the elongation at break around 20-50%. Moreover, the vertically printed flexural specimens showed a very different bending behavior, such that the pure PCL specimens presented a brittle fracture at 7% strain, while the ChNCs composites were able to bend over themselves. Hence, this work proves that the presence of ChNCs aims to improve the interlayer adhesion of the objects manufactured by FFF due to their good adhesive properties, which is currently a concern for the scientific community and the industrial sector.

Synthesis, Characterization and Application of New Polymers Imprinted with Zinc (II) Ions

In this work, molecularly imprinted polymers with zinc imprints and their comparison polymers without imprints were synthesized. A comparative characterization of the physical parameters of the synthesized zinc-imprinted (ZnIP) and non-imprinted (NIP) polymers was carried out using the methods of elemental analysis, conductometry, scanning electron microscopy, and IR-Fourier spectroscopy. The ability of the resulting polymers to molecularly recognize zinc was evaluated. Based on experimental data on static adsorption, the adsorption capacity of ZnIP and NIP was determined using an atomic emission spectrometer. It was found that ZnIP is characterized by better physical parameters and a higher ability for molecular recognition of zinc compared to NIP. ZnIP with zinc imprints were found to have better sorption capacity for zinc than their reference polymers. The sorption of zinc by molecular imprinted ZnIP is mainly due to the complex formation and pores of the initial carbon product. The synthesized ZnIP have increased porosity. The presence of pores with a diameter <50 nm in ZnIP is associated with voids formed after acid hydrolysis, which is clearly visible in images recorded by scanning electron microscopy. Thus, the possibility of using ZnIP as a selective sorbent has been established.

The composition and flavor change mechanism of membrane-filtered sugarcane syrup during the acid hydrolysis process based on 1H NMR and GC–IMS

Nuclear magnetic resonance (NMR) spectroscopy and gas chromatography-ion mobility spectrometry (GC-IMS) were employed to comprehensively characterize both non-volatile and volatile components present in membrane-filtrated sugarcane syrup (MS). A total of 19 non-volatile compounds and 65 volatile compounds were successfully identified within the MS sample. Among the volatile compounds, 12 were determined to be key aroma contributors based on their Relative Odor Activity Values (ROAV). Our investigation elucidated that hydrolysis and Maillard reactions serve as the primary pathways during acid hydrolysis, with reaction kinetics strengthened by increasing heating temperature and citric acid concentration, thereby enhancing the caramel and roasted aromas of MS. These findings not only contribute to a deeper understanding of the composition of sugarcane syrup but also offer valuable insights into flavor characterization and quality control within the sugarcane industry. Furthermore, this research lays a foundation for future studies aimed at optimizing processing techniques to enhance syrup flavor and overall product quality.

Synthesis of cellulose nano fiber from palmyrah fruit fiber and its applicability as a reinforcement agent on starch based biodegradable film

The global trend in packaging is shifting towards environmentally friendly, natural materials that decompose easily. Among the bio-based packaging materials, starch is a renewable, biodegradable, bio-compatible, and easily accessible source. However, starch-based biodegradable films depict weak mechanical properties compared with synthetic polymers. This problem can be solved by incorporating reinforcement fillers into the starch matrix. Palmyrah fruit (Borassus flabellifer L.) waste can be a good source to obtain fillers due to its high cellulose content. The aim of the study was to investigate the reinforcement of starch-based biodegradable films with the incorporation of pure cellulose nanofiber (CNF) obtained from palmyrah fruit fiber (PFF). Chemical treatments such as alkaline treatment (4% NaOH), bleaching [1% Ca(OCl)2], and acid hydrolysis (10 moldm-3 H2SO4) were done successively to obtain pure CNF from PFF. CNF was characterized using FTIR and particle size distribution (PSD) was analyzed by granulometry. The yield of CNF from PFF was 37.890±0.008 %. The results of FTIR depicted CNF was synthesized successfully. Five different biodegradable films were prepared by varying the amount of palmyrah tuber starch (4.5-2.5 w/w %) and CNF (0.0-2.0 w/w %) while the amount of glycerin (1.5 w/w %) and gelatin (1 w/w %) were kept constant. PSD results revealed that nano-sized CNF (10-100 nm) was synthesized successfully. The optimized film was selected based on the tensile strength and low water vapor transmission rate. Optimized film formulation, with palmyra tuber starch (3 w/w %) and CNF (1.5 w/w %) showed desirable physical, mechanical and optical properties, including the thickness, moisture content, water vapor transmission rate, water uptake, transparency at 600 nm, water activity, water solubility and tensile strength of 0.192±0.004 mm, 11.07±0.04 %, 3.870±0.005 g/m2.day, 22.34±0.05 %, 3.97±0.01 %, 0.440±0.001, 51.68±0.140 % and 9.55 MPa respectively. All films showed excellent soil biodegradability within two weeks. In conclusion, palmyra fruit CNF can be effectively used to reinforce starch-based biodegradable packaging films.

Isolation and Characterization of Spherical Cellulose Nanocrystals Extracted from the Higher Cellulose Yield of the Jenfokie Plant: Morphological, Structural, and Thermal Properties.

Scholars are looking for solutions to substitute hazardous substances in manufacturing nanocellulose from bio-sources to preserve the world's growing environmental consciousness. During the past decade, there has been a notable increase in the use of cellulose nanocrystals (CNCs) in modern science and nanotechnology advancements because of their abundance, biocompatibility, biodegradability, renewability, and superior mechanical properties. Spherical cellulose nanocrystals (J-CNCs) were successfully synthesized from Jenfokie micro-cellulose (J-MC) via sulfuric acid hydrolysis in this study. The yield (up to 58.6%) and specific surface area (up to 99.64 m2/g) of J-CNCs were measured. A field emission gun-scanning electron microscope (FEG-SEM) was used to assess the morphology of the J-MC and J-CNC samples. The spherical shape nanoparticles with a mean nano-size of 34 nm for J-CNCs were characterized using a transmission electron microscope (TEM). X-ray diffraction (XRD) was used to determine the crystallinity index and crystallinity size of J-CNCs, up to 98.4% and 6.13 nm, respectively. The chemical composition was determined using a Fourier transform infrared (FT-IR) spectroscope. Thermal characterization of thermogravimetry analysis (TGA), derivative thermogravimetry (DTG), and differential thermal analysis (DTA) was conducted to identify the thermal stability and cellulose pyrolysis behavior of both J-MC and J-CNC samples. The thermal analysis of J-CNC indicated lower thermal stability than J-MC. It was noted that J-CNC showed higher levels of crystallinity and larger crystallite sizes than J-MC, indicating a successful digestion and an improvement of the main crystalline structure of cellulose. The X-ray diffraction spectra and TEM images were utilized to establish that the nanocrystals' size was suitable. The novelty of this work is the synthesis of spherical nanocellulose with better properties, chosen with a rich source of cellulose from an affordable new plant (studied for the first time) by stepwise water-retted extraction, continuing from our previous study.

Metal Ion-Induced Acid Hydrolysis Strategy for the One-Step Synthesis of Tough and Highly Transparent Hydrolyzed Polyacrylamide Hydrogels.

Polyacrylamide (PAM) hydrogel is hard to enhance through coordination bonds because amide groups rarely coordinate with metal ions strongly in an aqueous solution. It is known that the aqueous solution of ZrOCl2.8H2O can be strongly acidic depending on its concentration. Consequently, through a facile one-step metal ion-induced acid hydrolysis strategy (MIAHS), tough and highly transparent hydrolyzed PAM physical hydrogels are prepared by using ZrOCl2.8H2O in this work. The formation of the partially hydrolyzed PAM physical hydrogels elucidates that the side reaction of imidization during common acid hydrolysis of PAM can be perfectly overcome because the structure of the Zr(IV) ion and its interaction with amide groups promote selective acidic hydrolysis from amide to carboxyl groups. Compared to most coordination cross-linked hydrogels, which need at least two-step fabrication, the hydrolyzed PAM hydrogel via MIAHS can be obtained by one-step synthesis due to the weak interaction between amide groups and Zr(IV). The obtained PAM hydrogel cross-linked by hydrogen bonds and coordination bond between Zr(IV) and carboxyl is a multibond network (MBN) and can achieve hierarchical energy dissipation, which exhibits excellent mechanical properties (tensile strength of 3.15 MPa, elongation at break of 890%, and toughness of 17.0 MJ m-3), high transparence (transmittance of 95%), and outstanding conductivity (5.6 S m-1) at water content of 80 wt %. The high gauge factor (from 2.24 to 12.8 as the strain increases from 0 to 400%) endows the hydrolyzed PAM hydrogels with promising application as strain sensors. Furthermore, in addition to ZrOCl2.8H2O, the fact that various hydrolyzable compounds of Ti(IV), Zr(IV) Hf(IV), and Sn(IV) can also fabricate tough hydrolyzed PAM hydrogels verifies the universality of MIAHS. Therefore, the simple, efficient, and universal MIAHS will shed new light on preparing functional PAM-based hydrogels.

Characterization and isolation method of Gigantochloa scortechinii (Buluh Semantan) cellulose nanocrystals

This study explored the impact of sodium hydroxide and benzoylation treatment on the production of cellulose nanocrystals from Semantan bamboo (Gigantochloa scortechinii). Bamboo cellulose nanocrystals (BCNs) were obtained via acid hydrolysis, with the effectiveness of an isolation method and chemical treatments demonstrated in removing non-cellulosic constituents. X-ray diffraction analysis revealed a crystalline cellulose II structure for benzoylated BCN (B) and a crystalline cellulose I structure for NaOH-treated BCN (S), with BCN (S) exhibiting a higher crystallinity index (80.55 %) compared to BCN (B) (67.87 %). The yield of BCN (B) (23.68 ± 1.10 %) was higher than BCN (S) (20.65 ± 2.21 %). Transmission electron microscopy images showed a mean diameter of 7.95 ± 2.79 nm for BCN (S) and 9.22 ± 3.38 nm for BCN (B). Thermogravimetric analysis indicated lower thermal stability for BCN (B) compared to BCN (S), with charcoal residues at 600 °C of 31.06 % and 22 %, respectively. Zeta potential values were −41.60 ± 1.97 mV for BCN (S) and −21.80 ± 2.54 mV for BCN (B). Gigantochloa scortechinii holds significant potential for sustainable and eco-friendly applications in the construction, furniture, and renewable energy industries. These findings highlight the versatility and potential of BCNs derived from Gigantochloa scortechinii for various applications.