Sustainable Production of Chitin Nanowhiskers from Crustacean Biomass Using Cost-Effective Ionic Liquids: Strategies to Avoid Byproduct Formation

: Nanochitin, especially in the form of chitin nanowhiskers (ChNWs), represents a significant advance in biopolymer technology due to its high specific surface area, superior tensile strength, and excellent thermal stability. Derived from crustacean waste, which contains 15–40% of chitin, these materials provide a sustainable option that diverts waste from landfills and contributes to environmental conservation. Traditional methods of isolating nanochitin are energy-intensive and generate substantial waste. This study introduces a more sustainable method using inexpensive ionic liquids (ILs) such as [Hmim][HSO 4 ] and [HN 222 ][HSO 4 ], which bypass the costly and destructive steps of traditional procedures. This study also identified the byproduct in IL-mediated chitin hydrolysis reaction as calcium sulfate dihydrate and presented a solution to circumvent the byproduct formation. The effectiveness of the [HN 222 ][HSO 4 ] IL in producing ChNWs from both purified chitin and crustacean biomass was assessed, showing a high yield and maintaining the purity and structural integrity of chitin, thereby demonstrating a significant reduction in the environmental footprint of ChNW production.


Introduction
Nanochitin, i.e., chitin in its nanostructure form, is considered to be one of the important biopolymeric nanomaterials due to its high specific surface area, high tensile strength, and thermal stability, as well as renewability and abundance [1].Chitin is an abundant biopolymer [2] made of repeating 2-(acetylamino)-2-deoxy-D-glucose β-linked units [3], and is found in the shells of arthropods (crabs, lobster, and shrimps), the cell walls of fungi, insect cuticles (e.g., fly larvae), some mushrooms, and yeasts [4].
Sustain.Chem.2024, 5 131 Crustacean waste biomass is, by far, the most abundant source of chitin and contains 15-40% of this polymer [29,30].Crustacean waste is considered an environmental hazard [31] since it is either dumped back into the ocean or disposed of in landfills.Using chitinous waste to manufacture chitinous products keeps waste out of landfills, benefits the environment, conserves resources, and provides additional revenue to agricultural and aquacultural businesses.However, the recovery of "bulk" chitin is challenging due to the chitinous matrix structure, which contains strong covalent and hydrogen bonds between layers of proteins (20-40%) and chitin.In addition, crustacean waste is also rich in minerals (20-50%).
To obtain nanochitin from biomass, conventional methods include two steps.The first step aims to recover chitin as pure as possible from the shell matrix.However, this initial step is destructive, wasteful, and energy-demanding since it involves deproteinization to remove proteins present in a shell matrix (using bases, e.g., NaOH) and, in the case of crustacean biomass, demineralization to remove minerals (using acids, e.g., HCl).Bleaching/discoloration is often required [32,33].The process is conducted at relatively high temperatures (60-100 • C), and for a long time [34,35], utilizing ~1.2 kWh of electricity and generating > 500 L acidic and basic aqueous waste per 1 kg of "bulk" chitin.
A dual catalyst-solvent treatment of biomass with 1-butyl-3-methylimidazolium hydrogen sulfate ([C 4 mim][HSO 4 ]) recently showed the potential of this IL to bypass the first step of "bulk" chitin isolation in producing nanowhiskers [50,51].In this process, biomass was pretreated with the IL and hydrolyzed in an IL-water (3:1) mixture.After quenching the reaction, the thick white gel-looking suspension was ultrasonicated, centrifuged, washed, and lyophilized.The overall mass yield of nanofillers was 79%, much higher than that reported for HCl hydrolysis (45-55%).No deacetylation took place during the treatment, and the degree of acetylation (%DA) was the same as that of commercial chitin.
Despite all its advantages and potential applications in biomass processing, [C 4 mim][HSO 4 ] is costly, mainly due to its manufacturing method.The method involves the formation of 1-butyl-3-methylimidazolium bromide ([C 4 mim]Br) by adding butyl bromide to methylimidazole, followed by an anion exchange process with sodium hydrogen sulfate [52][53][54][55].Factors that add to the high cost include the limited sizes of ion-exchange columns and high resource (i.e., resin and solvent) consumption.In addition, this is a traditional batch process and not a continuous manufacturing.
Since IL cost, biomass load, and IL recovery are three parameters likely to exert a significant influence on the final cost of chitin nanowhiskers [56], the manufacturing scale synthesis of the ILs must not only utilize inexpensive reagents but also be simple, straightforward, and easily scalable.The first study that evaluated the costs of hydrogen sulfate-based ILs on a bulk scale was conducted by Chen et al. [57].The study considered factors such as raw material cost, other operating costs (salary/wages), utility costs (e.g., electricity and cooling water), and wastewater treatment [58,59]  , within a price range for typical organic solvents (USD 1.44-1.56kg −1 ) [57].In this work, we assess the effectiveness of these cost-effective ILs (Figure 1) for isolating chitin nanowhiskers from both purified chitin and crustacean biomass and evaluate the properties of the resultant materials.
Sustain.Chem.2024, 5, FOR PEER REVIEW 3 effectiveness of these cost-effective ILs (Figure 1) for isolating chitin nanowhiskers from both purified chitin and crustacean biomass and evaluate the properties of the resultant materials.

Determination of Chitin Content in Biomass
The Black and Schwartz method was used to determine the amount of chitin in biomass [62].Ground and sieved crustacean biomass (1 g) was weighed into a 50 mL round bottom flask equipped with a Teflon-coated magnetic stir bar and a condenser.Then, 24 mL of 1 M HCl was added and the mixture was heated under reflux with stirring at 750 rpm for 1 h.After 1 h, the flask was removed from heat and cooled to room temperature.The reaction mixture was transferred to a centrifuge tube and centrifuged at 3750 rpm for 10 min in a Beckman Coulter Allegra X-15R Refrigerated Centrifuge (Beckman, Brea, CA, USA).Then, the supernatant was carefully separated from the solids, 25 mL of fresh DI water was added, and the resultant suspension was centrifuged again.Centrifugation, aqueous phase decantation, and fresh DI water addition steps were consecutively repeated until the washings were no longer acidic.The remaining solid was transferred to its initial (water-rinsed) round bottom flask now with 24 mL of 1.25 M aqueous NaOH, and the mixture was heated under reflux with stirring at 750 rpm for 1 h.After 1 h, the reaction was once again removed from heat, cooled down and its content transferred to new centrifuge tubes, and centrifuged for 10 min at 3800 rpm.The supernatant was decanted and discarded, and the remaining solid was washed with the addition of fresh DI water, followed by centrifugation, again at 3750 rpm, for 10 min.The solid was repeatedly washed and centrifuged with fresh DI water (8 more times) until the supernatant was neutral.When the supernatant was neutral, it was decanted and discarded, and the remaining solid was transferred onto a Petri dish and dried overnight in an 80 °C Cole-

Determination of Chitin Content in Biomass
The Black and Schwartz method was used to determine the amount of chitin in biomass [62].Ground and sieved crustacean biomass (1 g) was weighed into a 50 mL round bottom flask equipped with a Teflon-coated magnetic stir bar and a condenser.Then, 24 mL of 1 M HCl was added and the mixture was heated under reflux with stirring at 750 rpm for 1 h.After 1 h, the flask was removed from heat and cooled to room temperature.The reaction mixture was transferred to a centrifuge tube and centrifuged at 3750 rpm for 10 min in a Beckman Coulter Allegra X-15R Refrigerated Centrifuge (Beckman, Brea, CA, USA).Then, the supernatant was carefully separated from the solids, 25 mL of fresh DI water was added, and the resultant suspension was centrifuged again.Centrifugation, aqueous phase decantation, and fresh DI water addition steps were consecutively repeated until the washings were no longer acidic.The remaining solid was transferred to its initial (waterrinsed) round bottom flask now with 24 mL of 1.25 M aqueous NaOH, and the mixture was heated under reflux with stirring at 750 rpm for 1 h.After 1 h, the reaction was once again removed from heat, cooled down and its content transferred to new centrifuge tubes, and centrifuged for 10 min at 3800 rpm.The supernatant was decanted and discarded, and the remaining solid was washed with the addition of fresh DI water, followed by centrifugation, again at 3750 rpm, for 10 min.The solid was repeatedly washed and centrifuged with fresh DI water (8 more times) until the supernatant was neutral.When the supernatant was neutral, it was decanted and discarded, and the remaining solid was transferred onto a Petri dish and dried overnight in an 80 • C Cole-Parmer StableTemp gravimetric convection oven (Charleston, SC, USA), and weighed to obtain the percent of chitin from biomass.The determination of chitin content was carried out in triplicate.

1.
Pretreatment with ILs-For chitin pretreatment, a suspension of chitin in IL (1:10 w/w) was prepared by thoroughly mixing chitin in the IL (for example, 0.76 g chitin was added and mixed in 7.64 g [HSO 4 ] − -based IL), resulting in a well-blended paste.
The prepared paste was then properly sealed, encased with a parafilm, and kept in the oven (45-65 • C) for 24 h.For biomass pretreatment, a 3 wt% crushed crustacean biomass was prepared by thoroughly mixing the biomass in the IL (for example, 1.5 g crushed crustacean biomass was added and mixed in 48.5 g of the [HSO 4 ] − -based IL), resulting in a paste.The properly blended paste was subsequently sealed, covered with a parafilm, and kept in the oven (45-65 • C) for 24 h.

2.
Isolation of Chitin Nanowhiskers-After letting the mixture in the containers settle for 24 h, 30% DI water with respect to IL (i.e., 16.7 g of water per 48.5 g of the IL) was added to each flask.Each flask was equipped with a stirring bar and a condenser, and then heated to 110 • C in an oil bath, for 6-48 h.In the case of biomass, this resulted in a significant production of foam.After heating, 50 mL DI water was added to each flask.Following that, the mixtures were moved to 15 mL centrifuge tubes, and centrifuged (Eppendorf 5430 R, Enfield, CT; rotor CE 11017, 7830 rpm).The liquid was decanted, fresh water was added, the precipitate was stirred with a spatula, and the suspension was centrifuged again.This process was repeated 10 more times until a neutral pH was obtained.After washing, the suspensions were ultrasonicated (VibraCell Ultrasonicator, model CV 33, Newtown, CT, USA) for 10 min with 30 s cycles for the uniform distribution of particles.The suspension was then split into 2 parts.One part was diluted and analyzed using Transmission Electron Microscopy (TEM, Hitachi H-9500, Tokyo, Japan).The second part was frozen at −20 • C, and then subjected to a lyophilization (Labconco FreeZone Plus Cascade Benchtop Freeze Dryer System, Kansas City, MO, USA) process for approximately 72 h, resulting in the production of nanocrystals with precise dimensions.

Characterization 2.4.1. Estimation of Crystallinity
The crystallinity of the nanocrystals generated directly from crustacean biomass was measured using a powder X-ray diffractometer (HD 2711N, Rigaku, Tokyo, Japan) with Ni-filtered Cu Kα radiation and λ = 1.542Å, at 44 mA and 40 kV.Diffractograms were collected under a scanning rate of 1 • min −1 over the 2θ region ranges from 5 to 50 • .Origin software (OriginLab Corporation, Northampton, MA, USA) was used for removing the background, and then for the smoothening and baseline correction of the recorded data.The Peak Analyzer tool was employed to automatically identify and analyze a wide range of multiple peaks, and the crystallinity of the product was finally computed using the equation: ∑ area o f crystalline peaks ∑ area o f crystalline peaks and amorphous scattering × 100 (1)

Crystallite Size Determination
The crystallite size was calculated using the Scherrer equation [63], previously employed for chitin [64]: where β represents the crystallite size perpendicular to the lattice plane represented by ( 020) and (110) peaks, k is the Scherrer constant for a given crystal shape (k = 0.91), λ represents the wavelength of the incident X-rays (1.54 Å), L represents the width of the peak at half of its maximum in radians (FWHM), and θ is the position of the peak (half of the plotted 2θ value).

Transmission Electron Microscopy
The morphology, including the distribution of nanocrystals (diluted 30-fold before analysis), size, and shape, was evaluated using a Transmission Electron Microscope (Hitachi H-9500, Tokyo, Japan).

Field Emission Scanning Electron Microscopy
A field emission scanning electron microscope (FE-SEM, S/N 4300, Hitachi, Chiyoda, Tokyo, Japan) was used for the visualization of gypsum crystals.For this, the samples were mounted on the sample stage with adhered carbon tape (Ted Pella Inc., Redding, CA, USA) and visualized at 500-5000 magnification, with an accelerating voltage of 15,000 V. Quartz PCI Imaging software (Version 8, Quartz Imaging Corp., Vancouver, BC, Canada) (https://www.quartzimaging.com/pci-microscope-imaging-software.html,accessed on 1 April 2024) was used to analyze the recorded images.

Thermal Gravimetric Analysis
The thermal stability of the generated nanocrystals was examined using a thermogravimetric analyzer (TGA, Pyris1, PerkinElmer Inc., Shelton, CT, USA).The samples were kept under controlled conditions at a temperature of 21 ± 1 • C with a relative humidity (RH) of 65 ± 2% before analysis.An inert atmosphere was maintained by flowing nitrogen at a rate of 20 mL min −1 .The thermal analysis was carried out at a heating rate of 10 • C min −1 , spanning the temperature range of 40 to 600 • C. The data generated were analyzed with the assistance of Pyris software (PerkinElmer Inc., Shelton, CT, USA).

Attenuated Total Reflectance (ATR) Fourier-Transform Infrared Spectroscopy (FTIR)
The structural characterization of the isolated nanocrystals was confirmed using an ATR FTIR Spectrum-400 instrument (PerkinElmer, Waltham, MA, USA).The samples were kept under controlled conditions at a temperature of 21 ± 1 • C with an RH of 65 ± 2% and then placed on a chemically inert Zn-Se-diamond crystal stage for analysis.A total of 64 scans were conducted, covering the spectral range from 650 to 4000 cm −1 , and the spectral resolution was set at 4 cm −1 .The results were recorded and interpreted with the aid of OPUS Bruker software (Bruker, Billerica, MA, USA).

Degree of Acetylation
FTIR spectroscopy was employed to assess the degree of acetylation (%DA) of the chitin nanocrystals, following the same procedure detailed by Beil et al. [65].First, the calibration curve was constructed as follows.The ATR FTIR spectra (64 scans) were recorded for chitin and chitosan with known %DA (15, 24, 30, and 86%).The spectra were converted to Transmittance, then smoothed employing a 9-point Savitzky-Golay algorithm, and the first derivatives of the spectra were calculated.The first derivative ATR FTIR values at 1383 cm −1 (MB1), 1327 cm −1 (MB2), and 1163 cm −1 (RB) were determined and the ratios (MB1 + MB2)/RB were found.The data were then plotted as %DA vs. (MB1 + MB2)/RB.This calibration curve (Figures S2 and S3, ESI) was used to determine the %DA for prepared samples.] was prepared by mixing triethylamine with sulfuric acid through a simple Brønsted acid-base proton transfer reaction [60,61].

Results and Discussion
As an initial step, the ILs were tested for the preparation of ChNWs from pure chitin, to determine their ability to hydrolyze the glycosidic linkages (Figure S1 , respectively), the pretreatment temperature was kept higher than their melting points.After pretreatment, DI water was added and the solutions were heated to 110 • C for 48 h under reflux.The precipitate was centrifuged, washed with water, and ultrasonicated.The suspension was then split into two parts.One part was diluted and used for Transmission Electron Microscopy (TEM) imaging while the second one was dehydrated using freeze-drying and used for further characterization.Based on the IL used to prepare the ChNWs from chitin, the products were denoted as ChNWs/Ch/[C 4  ], respectively.Such moderate yield was reported in the literature in other acidic systems, where the acidic hydrolysis of chitin leads to the formation of not only ChNWs but also chitin oligomers [71,72].Decreasing the time to 24 h during subsequent studies produced the nanomaterial in the same yields.
The dimensional parameters of the ChNWs processed using each IL were obtained from TEM.A 10-times dilution of the original suspensions, obtained after ultrasonication, with a concentration of ~0.1 mg mL −1 was the most suitable for TEM imaging.As shown in the TEM images (Figure 2), the morphology of the nanowhiskers was highly regular.The ChNWs from [Hmim][HSO 4 ] and [HN 222 ][HSO 4 ] presented elongated crystalline rod-like nanoparticles, characterized by pointed ends, with diameters ranging between 20 and 22 nm, and lengths ranging between 230 and 246 nm (Table 1).Given the obtained results, we estimated the average aspect ratio (L/d) to be ~12 to 12.5.These findings correlate with those previously reported when using [C 4 mim][HSO 4 ] for hydrolysis, with diameters of 21.7 ± 5.5 nm and lengths of 216 ± 78 nm.Overall, the ChNWs obtained showed a similar length and diameter, i.e., avg.230 ± 12 nm and 21.3 ± 0.9 nm, respectively.For comparison, the aspect ratio of ChNWs obtained through hydrolysis with HCl can range from 15 to 120, depending on the chitin source used [73].The size of ChNWs is directly dependent on the biomass it was isolated from.For example, the hydrolysis of α-chitin from shrimp shells using 3 N HCl results in nanowhiskers with an average length and width of 216 ± 91 nm and 16.4 ± 5.8 nm [74].When chitin is sourced from Riftia tubes, the resulting ChNWs have a length range from 500 nm to a few µm [75].The size of the nanowhiskers from Oyster and Button mushrooms ranging from 50 to 200 nm in length and ~11 nm in diameter [76].Attenuated Total Reflectance (ATR) Fourier-Transform Infrared Spectroscopy (FTIR) was then used to detect chemical modifications to the chitin due to the IL treatment.The spectral peaks were compared with those identified in standard chitin reference upon the normalization of the FTIR spectra (Figure 3; expanded spectra of different FTIR regions are shown in Figures S4-S6, ESI).Independent of the IL used for hydrolysis, the obtained ChNW/Ch/ILs showed almost identical spectrum profiles (Figure 3).The spectra of ChNW/Ch/ILs were not only similar to each other but also to the spectrum of pure chitin Attenuated Total Reflectance (ATR) Fourier-Transform Infrared Spectroscopy (FTIR) was then used to detect chemical modifications to the chitin due to the IL treatment.The spectral peaks were compared with those identified in standard chitin reference upon the normalization of the FTIR spectra (Figure 3; expanded spectra of different FTIR regions are shown in Figures S4-S6, ESI).Independent of the IL used for hydrolysis, the obtained ChNW/Ch/ILs showed almost identical spectrum profiles (Figure 3).The spectra of ChNW/Ch/ILs were not only similar to each other but also to the spectrum of pure chitin that was used as the starting material and to those reported in the literature (summarized in Table S1, ESI).Thus, the peak attributed to O(3)H• • • O(5) from the ring in the α-chitin was located at the same position in all ChNW/Ch/ILs and chitin standard, at 3438 cm −1 .The peaks were also of the same intensity, indicating no hydrolysis-induced changes in -O-H stretching.The same observation (i.e., peaks of close intensity situated at the same wavenumber for both ChNW/Ch/ILs products and pure chitin standard) is valid for the N-H stretching and bending, at 3103 cm −1 and 1556 cm −1 , respectively.Similarly, no differences were found in the location or intensity of Amide III peaks (namely, C-N and N-H) at 1311 cm −1 and N-H peak at 3261 cm −1 .Both the intensity and the wavenumber of the vibration modes of carbonyl (Amide I), namely, the C=O• • • H-N vibration at 1654 cm −1 and the -CH 2 OH• • • O=C band at 1620 cm −1 , were also retained, indicating no changes in amide-type of hydrogen bonding.Concerning C-O, the stretching of glycosidic linkage (the asymmetric bridge oxygen stretching) is indicated by a peak at 1154 cm −1 , and pyranose ring stretching was found at 895 cm −1 .
N-H) at 1311 cm −1 and N-H peak at 3261 cm −1 .Both the intensity and the wavenumber of the vibration modes of carbonyl (Amide I), namely, the C=O … H-N vibration at 1654 cm −1 and the -CH2OH … O=C band at 1620 cm −1 , were also retained, indicating no changes in amide-type of hydrogen bonding.Concerning C-O, the stretching of glycosidic linkage (the asymmetric bridge oxygen stretching) is indicated by a peak at 1154 cm −1 , and pyranose ring stretching was found at 895 cm −1 .As for CH bonds, a symmetric stretching vibration of the CH3 group from -NHC(O)CH3 amide bond, a asymmetric stretching vibration of the CH2 group from CH2OH, and stretching vibrations of CH in the pyranose ring appeared at 2964, 2930, and 2886 cm −1 , respectively.The CH3 deformation appeared at 1378 cm −1 in both standard and nanowhiskers, whereas -CH2 ending in CH2OH showed up at 1425 cm −1 .The bands at 970 cm −1 and 873 cm −1 correspond to vibrations of CH3 wagging and the C-H vibrations of CH3 in the ring structure.Overall, the obtained ChNW/Ch/ILs produced in this study did not indicate any significant change in chemical functional groups compared to the native chitin.This finding differs from what was shown before for acid hydrolysis [77], which reported that the use of an acidic environment leads to partial chitin deacetylation.
Powder X-ray diffraction (pXRD) was used to elucidate the degree of crystallinity of all products (Figure 4).For that, the diffractograms obtained for ChNW/Ch/ILs samples were compared with the diffractogram of pure chitin.In all diffractograms, the peaks were found at 9.24°, 12.69°, 19.23°, 20.58°, 23.18°, and 26.27°, corresponding to (0 2 0), (0 2 1), (1 1 0), (1 2 0), (1 3 0), and (0 1 3) reflections, respectively [78,79].The crystallinity index (CrI) was determined using the peak height method based on a comparison of the intensity of a crystalline reflection 19.23° (I110) and the height of amorphous scattering (16°, Iam) [80,81].However, the reliability of this method is based on the precision of background subtraction and the presence of both anhydrous and hydrated polymorphs [82].Therefore, we As for CH bonds, a symmetric stretching vibration of the CH 3 group from -NHC(O)CH 3 amide bond, a asymmetric stretching vibration of the CH 2 group from CH 2 OH, and stretching vibrations of CH in the pyranose ring appeared at 2964, 2930, and 2886 cm −1 , respectively.The CH 3 deformation appeared at 1378 cm −1 in both standard and nanowhiskers, whereas -CH 2 ending in CH 2 OH showed up at 1425 cm −1 .The bands at 970 cm −1 and 873 cm −1 correspond to vibrations of CH 3 wagging and the C-H vibrations of CH 3 in the ring structure.Overall, the obtained ChNW/Ch/ILs produced in this study did not indicate any significant change in chemical functional groups compared to the native chitin.This finding differs from what was shown before for acid hydrolysis [77], which reported that the use of an acidic environment leads to partial chitin deacetylation.
Powder X-ray diffraction (pXRD) was used to elucidate the degree of crystallinity of all products (Figure 4).For that, the diffractograms obtained for ChNW/Ch/ILs samples were compared with the diffractogram of pure chitin.In all diffractograms, the peaks were found at 9.24  , corresponding to (0 2 0), (0 2 1), (1 1 0), (1 2 0), (1 3 0), and (0 1 3) reflections, respectively [78,79].The crystallinity index (CrI) was determined using the peak height method based on a comparison of the intensity of a crystalline reflection 19.23 • (I 110 ) and the height of amorphous scattering (16 • , I am ) [80,81].However, the reliability of this method is based on the precision of background subtraction and the presence of both anhydrous and hydrated polymorphs [82].Therefore, we have also employed the peak deconvolution method that typically provides higher accuracy [83,84].This method is based on calculating the ratio between the area of crystalline peaks and the total area of a pXRD pattern.Figures S8-S13 and Tables S2-S7 (ESI) provide the calculated peak fitting of the diffraction profiles, the calculated peak locations, areas under the peak, and full width at half maximum (FWHM) values.
While starting chitin was found to be 84% crystalline, the crystallinity values of ChNWs from [HN 222 ][HSO 4 ] was similar (84.5%), slightly lower for [Hmim][HSO 4 ] (79.8%), and significantly higher for the [C 4 mim][HSO 4 ] IL (92.6%,Table 2).The crystallite size values (Tables 2, S8 and S9, ESI) were calculated using Scherrer's equation [63].Specifically, the crystallite size (a measure of the coherent volume for chitin in the diffraction peak) of each type of nanowhiskers was determined for two of the most prominent crystalline peaks of chitin, at the (0 2 0) and (1 1 0) planes, and was found to be between 6.9 and 8.6 nm (at the (0 2 0) plane) and between 5.2 and 7.5 nm (at the (1 1 0) plane), consistent with those observed previously.Thus, nanowhiskers obtained using HCl-hydrolysis from crab chitin demonstrated a crystallinity index of 86%, whereas the crystallite dimensions at the (0 2 0) and (1 1 0) planes for CtNWs were 9.2 nm and 6.5 nm, respectively [85].Likewise, the acid hydrolysis of α-chitin from shrimp shells produced nanowhiskers with a crystallinity index of 93.6% and crystallite dimensions of 6.3 nm at the (1 1 0) plane [86].However, since the peaks were not fitted most appropriately for detailed structural reporting (chi-squared in the range of 10 −4 ), it would be advisable that researchers use the crystallite size data with appropriate caution.
Sustain.Chem.2024, 5, FOR PEER REVIEW 9 have also employed the peak deconvolution method that typically provides higher accuracy [83,84].This method is based on calculating the ratio between the area of crystalline peaks and the total area of a pXRD pattern.Figures S8-S13 and Tables S2-S7 (ESI) provide the calculated peak fitting of the diffraction profiles, the calculated peak locations, areas under the peak, and full width at half maximum (FWHM) values.2).The crystallite size values (Table 2 and Tables S8 and S9, ESI) were calculated using Scherrer's equation [63].Specifically, the crystallite size (a measure of the coherent volume for chitin in the diffraction peak) of each type of nanowhiskers was determined for two of the most prominent crystalline peaks of chitin, at the (0 2 0) and (1 1 0) planes, and was found to be between 6.9 and 8.6 nm (at the (0 2 0) plane) and between 5.2 and 7.5 nm (at the (1 1 0) plane), consistent with those observed previously.Thus, nanowhiskers obtained using HCl-hydrolysis from crab chitin demonstrated a crystallinity index of 86%, whereas the crystallite dimensions at the (0 2 0) and (1 1 0) planes for CtNWs were 9.2 nm and 6.5 nm, respectively [85].Likewise, the acid hydrolysis of α-chitin from shrimp shells produced nanowhiskers with a crystallinity index of 93.6% and crystallite dimensions of 6.3 nm at the (1 1 0) plane [86].However, since the peaks were not fitted most appropriately for detailed structural reporting (chi-squared in the range of 10 -4 ), it would be advisable that researchers use the crystallite size data with appropriate caution.Table 2. Crystallinity index (CrI, %) determined via peak height and peak deconvolution methods and crystallite size (nm) at the (0 2 0) and (1 1 0) planes.The degree of acetylation (%DA) was also determined for pure chitin and all ChNWs/ Ch/ILs, using the first derivative of FTIR spectra (Figure S13, Table S10, ESI), as reported by Beil et al. [65].The technique compares the heights of the C-H deformation band (1383 cm −1 , MB1), the amide III band (1327 cm −1 , MB2), and the bridge oxygen stretching band (1163 cm −1 , RB) in the first derivative ATR FTIR spectra with those obtained for several external standards (chitins and chitosans with a known value of %DA).A calibration curve (also called a standard curve) was generated by plotting the value [(MB1 + MB2)/RB] against %DA for a series of reference standards.Back calculations using this calibration curve (Figure S2, ESI) revealed the %DA in the range of 97-100% in all cases.

Preparation and Characterization of Chitin Nanowhiskers from Crustaceous Biomass
As demonstrated in the previous section, all three ILs, i.e., [C 4 mim][HSO 4 ], [Hmim][HSO 4 ], and [HN 222 ][HSO 4 ], were able to hydrolyze chitin and produced ChNWs with similar dimensions.These same ILs were then used to simultaneously pulp and hydrolyze crustacean biomass (shrimp shells, SS) using a two-step procedure, sim-ilar to the one described for commercial chitin.Briefly, SS was first pretreated with [C 4 mim][HSO 4 ] [50,51], [Hmim][HSO 4 ], or [HN 222 ][HSO 4 ] for 48 h, followed by the addition of DI water and 110 • C heating under reflux for 48 h.In comparing the reactions between the ILs with the two starting materials (chitin or SS), it is worth noting that the reaction with SS proceeded much more vigorously than the same reaction with chitin, and created foam in all cases, likely due to the release of carbon dioxide from calcium carbonate (CaCO 3 , present in the SS) under acidic conditions.After dilution with water, centrifugation, washing, and lyophilization, the product yield was 75-80% based on chitin available in the SS (Table 3), with yields significantly higher than those obtained from pure chitin.].It is also worth noting that the same byproduct was formed regardless of the "inexpensive" IL's identity, excluding any compound that could be derived from the ILs themselves.Also important is that the byproduct formed only in the case of IL reactions with biomass but was not seen when pure chitin polymer was hydrolyzed using these ILs, despite identical reaction conditions.This suggests that the formation of the byproduct had something to do with minerals present in biomass.Upon examining the FTIR spectra (Figure 6) of the obtained ChNWs, it became evident that while the location and intensity of the peaks of ChNWs/SS/[C4mim][HSO4] closely resembled those of commercially available chitin [50,51], there were significant differences in the spectra of ChNWs/SS produced using "inexpensive" ILs, i. [HSO4] exhibited peaks typical for chitin; however, the intensities of many peaks were found to be somewhat greater than those typically associated with the biopolymer.This was particularly true for weak vibrations at 3483 and 3437 cm −1 , normally associated with water molecules, weak peaks in the region 820-650 cm −1 , and medium/strong vibrations at 1155 and 1116 cm −1 , characteristic of sulfate ion [87,]- [89].The FTIR spectrum of ChNWs/SS/[HN222][HSO4] also showed peaks of enhanced intensities similar to the ones described for ChNWs/SS/[Hmim][HSO4].In this sample, additional peaks at 3152, 1555, 1401, 1170, and 974 cm −1 were identified, which did not match either chitin or sulfate (indicated in Figure 6a-d in blue color).The peaks did not belong to ionic liquids (Figure S7).We suggest that the reader consult the SI file, where the expansion of the FTIR regions is provided.Byproduct formation was reproducible in both cases.It is also worth noting that the same byproduct was formed regardless of the "inexpensive" IL's identity, excluding any compound that could be derived from the ILs themselves.Also important is that the byproduct formed only in the case of IL reactions with biomass but was not seen when pure chitin polymer was hydrolyzed using these ILs, despite identical reaction conditions.This suggests that the formation of the byproduct had something to do with minerals present in biomass.
Since one of the goals of this work was to generate high-purity chitin, identifying the new material was of great importance.An analysis of the literature identified the peaks at 11.56, 20.68, 23.33, and 29.07° 2θ as calcium sulfate dihydrate (also known as gypsum, Ca(SO4)•2H2O) [90].TEM images did not show the presence of gypsum, likely because of the mineral being dissolved in water during the preparation of the sample for TEM analysis.On the other hand, lyophilized samples were expected to contain both chitin nanocrystals and gypsum after water removal.When the ChNWs/SS/[HN222][HSO4] lyophilized sample was dispersed in a small amount of water and placed onto a carbon tape, Sustain.Chem.2024, 5, FOR PEER REVIEW 13 followed by slow water evaporation, Scanning Electron Microscopy (SEM) imaging revealed the presence of gypsum crystals (Figure 8).The reaction of acidic ILs with SS resulted in foam formation, which was attributed to CO2 release from CaCO3 in acidic conditions.This same reaction generates CaSO4, which was previously reported to be ~5-10 times less soluble in the presence of 10% of alkylimidazolium hydrogen sulfate ILs than in pure water (0.055 mol/kg) [92], which would induce the coprecipitation of CaSO4 together with ChNWs.However, a comparatively lesser decrease in the solubility of CaSO4•2H2O was observed for [C4mim][HSO4] when compared with [C2mim][HSO4], indicating an influence of the alkyl chain at the N2 atom of the imidazolium cation on the mineral's aqueous solubility [92].With respect to the discussed reactions, no gypsum was detected when [C4mim][HSO4] was used to recover ChNWs from biomass, while a significant amount of gypsum was detected when [Hmim][HSO4] was used.Considering that the difference between the ILs is only the butyl substituent on the N2 atom of imidazolium, we hypothesize that it is a protonated nitrogen atom of the cation of the IL that participates in the byproduct formation.The protonated ammonium or imidazolium could be stabilizing CO3 2-from the CaCO3 mineral of SS in solution through electrostatic interactions.It could also undergo deprotonation and The reaction of acidic ILs with SS resulted in foam formation, which was attributed to CO 2 release from CaCO 3 in acidic conditions.This same reaction generates CaSO 4 , which was previously reported to be ~5-10 times less soluble in the presence of 10% of alkylimidazolium hydrogen sulfate ILs than in pure water (0.055 mol/kg) [92], which would induce the coprecipitation of CaSO 4 together with ChNWs.However, a comparatively lesser decrease in the solubility of CaSO 4 •2H 2 O was observed for [C 4 mim][HSO 4 ] when compared with [C 2 mim][HSO 4 ], indicating an influence of the alkyl chain at the N2 atom of the imidazolium cation on the mineral's aqueous solubility [92].With respect to the discussed reactions, no gypsum was detected when [C 4 mim][HSO 4 ] was used to recover ChNWs from biomass, while a significant amount of gypsum was detected when [Hmim][HSO 4 ] was used.Considering that the difference between the ILs is only the butyl substituent on the N2 atom of imidazolium, we hypothesize that it is a protonated nitrogen atom of the cation of the IL that participates in the byproduct formation.The protonated ammonium or imidazolium could be stabilizing CO 3 2− from the CaCO 3 mineral of SS in solution through electrostatic interactions.It could also undergo deprotonation and react with CO 2 liberated by the reaction of [HSO 4 ] − with CaCO 3 with the formation of carbamates.
Regardless, the next step was adjusting the reaction conditions to minimize the formation of gypsum.Hence, the pretreatment step was eliminated.However, when SS was treated with [Hmim][HSO 4 ] without pretreatment, there still was a significant amount of gypsum present.Decreasing the reaction time first to 24 h, then to 12 h, and then to 6 h did not result in the removal of gypsum.Contrarily, the treatment of SS with [HN 222 ][HSO 4 ] provided a pure chitin product upon excluding the pretreatment step and reducing the reaction time to 24 h.Eliminating the pretreatment step aimed to remove the need for 24 h heating at 90 • C, leading to a favorable result.
The yield of the product decreased from 79 to 72%, whereas ChNWs' dimensions remained approximately the same (Table 4), not surprising considering that TEM imaging was only suitable for chitin visualization.The crystallinity, determined using the peak fitting method, was found to be 79.4%, a value very similar to that of ChNWs/SS/[C 4 mim][HSO 4 ] (80.6%, Tables S8 and S9, ESI).The crystallite size was determined to be 7.1 nm at the (0 2 0) plane and 6.1 nm at the (1 1 0) plane (Table S9, ESI), also very close to that obtained for ChNWs/SS/[C 4 mim][HSO 4 ] (8.4 and 5.6 nm at the (0 2 0) and (1 1 0) planes).The %DA calculated was found to be ~100%.Thermal analysis data have shown that T 50%dec was 341.7 • C, compared with 347 • C reported for pure chitin [93].This innovative approach to producing ChNWs from crustacean biomass will contribute to advancing the circular economy concept.Crustacean biomass (e.g., shrimp shells) which would normally be sent to a waste treatment process (landfill) can be valorized through this process.Furthermore, the environmental impact of nanochitin production is considerably diminished through this method.By reducing hazardous chemical use and waste generation, the process aligns with global sustainability goals, notably cutting CO 2 emissions by approximately 75%.
To make sure that the process is environmentally viable, future research will perform an environmental life cycle assessment (LCA) The International Standardization Organization (ISO) defines the framework and guidelines for LCA.The framework includes goal and scope definition, inventory analysis, impact assessment, and result interpretation [94,95].The system boundary shall encompass all the activities associated with the collection and transportation of the crustacean shells to the biorefinery, processing, and conversion into nanostructured chitin.
Finally, techno-economic considerations are an integral part of defining the sustainability of a product.Process simulation models can help to estimate the material and energy balances of the process pathways producing nanostructured chitin using the process data from the experimental tasks.The economic analysis encompasses the estimation of the capital investment, operational expenses, and production costs.

Conclusions
This research introduces a sustainable and cost-effective method for producing nanochitin using inexpensive ionic liquids (ILs) such as [HN 222 ][HSO 4 ], presenting a significant advancement over traditional chitin extraction processes.As mentioned in the introduction of this work, the applications to chitin nanowhiskers are broad, including packaging replacements, medical devices, and flexible electronics, to name but a few.Importantly for all the aforementioned applications, the IL reduces the overall production costs by simplifying the process, eliminating the need for initial purification steps, and reducing the consumption of chemicals and energy.
The scalability of this process promises broader implementation across sectors utilizing biopolymers.Future research should focus on further cost reductions for IL production and on evaluating the lifecycle impacts of these materials to enhance their commercial and environmental viability.This approach not only demonstrates a technological innovation in the production of chitin nanowhiskers but also exemplifies the application of green chemistry principles in materials science, setting a template for sustainable material production.The chitin nanowhiskers produced maintain high crystallinity and dimensional stability, making them suitable for various industrial applications including biomedicine, packaging, and electronics.

Figure 5 .
Figure 5. TEM micrograph of a dilute suspension of chitin nanowhiskers derived from purified chitin using (a) [C 4 mim][HSO 4 ], (b) [Hmim][HSO 4 ], and (c) [HN 222 ][HSO 4 ].HV 300 kV.Magnification: 30,000×; scale bar 200 nm.Since one of the goals of this work was to generate high-purity chitin, identifying the new material was of great importance.An analysis of the literature identified the peaks at 11.56, 20.68, 23.33, and 29.07 • 2θ as calcium sulfate dihydrate (also known as gypsum, Ca(SO 4 )•2H 2 O) [90].TEM images did not show the presence of gypsum, likely because of the mineral being dissolved in water during the preparation of the sample for TEM analysis.On the other hand, lyophilized samples were expected to contain both chitin nanocrystals and gypsum after water removal.When the ChNWs/SS/[HN 222 ][HSO 4 ]lyophilized sample was dispersed in a small amount of water and placed onto a carbon tape, followed by slow water evaporation, Scanning Electron Microscopy (SEM) imaging revealed the presence of gypsum crystals (Figure8).

Figure 6 .
Figure 6.FTIR spectra of pure chitin (aqua) and chitin nanowhiskers (ChNWs) obtained from SS: ChNWs/SS/[C4mim][HSO4] (blue), ChNWs/SS/[Hmim][HSO4] (brown and grey, two trials), and ChNWs/SS/[HN222][HSO4] (orange and green, two trials).Powder X-ray diffractograms (Figure7) of ChNWs/SS/[Hmim][HSO4] and ChNWs/SS/[HN222][HSO4] confirmed the presence of chitin (at 9.24°, 12.69°, 19.23°, 20.58°, 23.18°, and 26.27°, respectively[78,79]), but also peaks that did not belong to the biopolymer, at 11.56, 20.68, 23.33, and 29.07° 2θ.The amount of chitin was significantly greater in ChNWs/SS/[HN222][HSO4], whereas ChNWs/SS/[Hmim][HSO4] showed a significant amount of byproduct.Interestingly, no byproduct formation was detected in ChNWs/SS/[C4mim][HSO4].It is also worth noting that the same byproduct was formed regardless of the "inexpensive" IL's identity, excluding any compound that could be derived from the ILs themselves.Also important is that the byproduct formed only in the case of IL reactions with biomass but was not seen when pure chitin polymer was hydrolyzed using these ILs, despite identical reaction conditions.This suggests that the formation of the byproduct had something to do with minerals present in biomass.Since one of the goals of this work was to generate high-purity chitin, identifying the new material was of great importance.An analysis of the literature identified the peaks at 11.56, 20.68, 23.33, and 29.07° 2θ as calcium sulfate dihydrate (also known as gypsum, Ca(SO4)•2H2O)[90].TEM images did not show the presence of gypsum, likely because of the mineral being dissolved in water during the preparation of the sample for TEM analysis.On the other hand, lyophilized samples were expected to contain both chitin nanocrystals and gypsum after water removal.When the ChNWs/SS/[HN222][HSO4] lyophilized sample was dispersed in a small amount of water and placed onto a carbon tape,

Figure 8 .
Figure 8. Gypsum crystals as obtained from biomass using [Hmim][HSO4] and [HN222][HSO4] (left, right) looking identical to those provided in ref.[91].No coating was used for imaging.Note that no ChNWs could be seen at this low magnification.

Figure 8 .
Figure 8. Gypsum crystals as obtained from biomass using [Hmim][HSO 4 ] and [HN 222 ][HSO 4 ] (left, right) looking identical to those provided in ref.[91].No coating was used for imaging.Note that no ChNWs could be seen at this low magnification.
Overall, the [HN 222 ][HSO 4 ] IL performed very similarly to the [C 4 mim][HSO 4 ] IL for biomass treatment and required milder reaction conditions, i.e., no pretreatment and 12 h reflux.

Table 1 .
Dimensional parameters of the ChNWs isolated from chitin using different ILs.

Table 1 .
Dimensional parameters of the ChNWs isolated from chitin using different ILs.

Table 3 .
Dimensional parameters of the ChNWs isolated from shrimp shells (SS) using different ILs.