Abstract
The aim of the work was to compare the water retention and moisture sorption of viscose (CV) and cotton (Co) fibers carboxymethylated from aqueous media, in presence of NaOH, with sodium monochloroacetate. It was shown previously that under the same treatment conditions, the degree of carboxymethylation was higher in CV and so was the depth within fiber structures to which the carboxymethylation reactions occurred. It was also shown previously, that in terms of their capacity for sorption of a cationic dye (methylene blue), the Co performed better than CV. In this work, the same fibers were tested for their water retention and moisture sorption propensities. The two were sensitive both to the degree of carboxymethylation and the inherent properties of fibers (accessibility, degree of swelling, hornification). But the moisture sorption levels were less sensitive to the degree of carboxymethylation and more to inherent fiber properties whereas the reverse was observed for water retention. In contrast to the prior observations with dye sorption, CV performed better than Co in both moisture sorption and water retention. The poor performance of CV in dye sorption was attributed to the greater depth of carboxymethylation within the fibers that hindered dye permeation, but the same feature was observed to result in better performance (water retention) or not to hinder performance (moisture sorption). These observations highlight the contrasting effects that may arise, of a given set of treatment parameters (fiber type, alkali level in treatment), on efficacy of the product performance.
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Introduction
The carboxymethylation of cellulose is of interest for use in applications such as products for water or moisture sorption (Miyamoto et al. 2018; Chen et al. 2022), or in the removal of contaminants from wastewater (Yan et al. 2011; Wang et al. 2019, 2023). The carboxymethyl derivative of cellulose is obtained through a Williamson-type etherification of a hydroxyl group, in presence of alkali, through nucleophilic substitution with monochloroacetic acid (Mischnick and Momcilovic 2010). To create robust structures capable of withstanding the mechanical stresses generated in such applications, the carboxymethyl cellulose may be deposited and fixed on a carrier (Ibrahim et al. 2020), fibers may be spun from dopes containing carboxymethyl cellulose for assembly into networks (Wang et al. 2023), or cellulose fibers may first be assembled into networks and then subjected to the derivatization reaction (Rácz et al. 1995). The latter route is of interest for sectors such as textiles and nonwovens, where large-scale chemical treatments of fibrous assemblies are a routine part of operations. However, one limitation in the textiles and nonwovens sectors is the strong preference for water as solvent, as most chemical treatment operations are performed in open-to-air vessels. Thus, although optimal reaction yields in carboxymethylation of cellulose is known to be achieved in alcohol-rich media (Gu et al. 2012; Heinze et al. 2018; Li et al. 2022; Liao et al. 2022; Liu et al. 2023; Thakur et al. 2023), aqueous media-based carboxymethylation is preferred in textile treatments.
The carboxymethylation from aqueous media proceeds in a heterogeneous mode, i.e., the reactions occur from liquid media on solid fibrous substrates. In such conditions, the availability of accessible sites (or accessibility) becomes important in governing the progress in reactions, i.e., how much of the fibrous substrate is derivatized and how the introduced functional groups are distributed through the fiber bulk. The source of cellulose acquires importance, as both native and regenerated cellulosic fibers may be employed in the creation of fibrous networks, and they differ in morphological features (e.g., total porosity and the distribution of pores through their structures) as well as supramolecular structure (e.g., degrees of polymerization and of crystallinity)—and both may act to determine the accessibility in fibers. Also of interest is performance, i.e., will celluloses from different sources, with the same overall degree of carboxymethylation, perform to the same level in a given test, e.g., of dye or water sorption.
In previous communications (Bogner et al. 2024a, b), we reported on the carboxymethylation of viscose (CV) and cotton (Co) fibers—a regenerated and native cellulosic respectively—from aqueous solutions of sodium monochloroacetate and NaOH. The treatment parameters were varied: NaOH level in reaction media (0.5 M and 4.0 M), temperature (30 °C and 50 °C) and the content of sodium monochloroacetate, to obtain CV and Co fibers with a range of carboxymethyl group contents. It was determined that under comparable treatment conditions, the degree of carboxymethylation was greater in CV as compared to Co, and also that the depths in fibers to which carboxymethylation occurred, was higher in CV as compared to Co. When the fibers were tested for performance in terms of their capability for sorption of a cationic dye (methylene blue), the molar ratio of dye sorption to carboxyl groups on fibers was higher in Co as compared to CV. The differences were attributed to greater restrictions on permeation of the dye through the CV as compared to Co fibers. In this communication, we report on measurements of the performance of the derivatized CV and Co fibers in their capacity for interactions with liquid water (measured through water retention) and water vapor (measured through moisture sorption). The results of measuring the degree of crystallinity in fibers and of their degrees of polymerization are also reported.
Materials
The viscose (CV) fibers were donated by Kelheim Fibres GmbH (Germany) and the cotton (Co) was donated by Gebr. Otto Baumwollfeinzwirnerei GmbH + Co. KG (Dietenheim, Germany). The procedures for their cleaning, their carboxymethylation treatments and the resulting degrees of carboxymethylation are all reported previously (Bogner et al. 2024a, b).
In brief, CV and Co fibers were cleaned, and awarded carboxymethylation treatments from aqueous reaction media containing sodium monochloroacetate and NaOH. The alkali content in reaction media was maintained at either 0.5 M or 4.0 M, and the treatment temperature at 30 °C or 50 °C. Fibers that were only cleaned and treated only with 4.0 M NaOH were employed as reference. The carboxymethylation degree was estimated from sample carboxyl contents. The values, as determined with potentiometric titration, are summarized in Table 1.
Methods
Fourier transform infrared (FTIR) spectroscopy
FTIR spectroscopy, with measurements both in Attenuated Total Reflectance (ATR) mode and transmittance mode (KBr pelleting), was previously utilized to assess the uniformity of carboxymethyl group distribution through fiber structures (Bogner et al. 2024a, b). The same spectra are utilized here to assess changes in crystallinity of fibers as a result of treatments.
Gel permeation chromatography (GPC)
The average molecular weight and molar mass distribution in selected samples was determined with gel permeation chromatography (GPC), following a method described previously (Pitkänen and Sixta 2020; Rissanen et al. 2023). The device was a Dionex Ultimate 3000 HPLC Module (Thermo Fisher Scientific Inc., Waltham USA) equipped with a Shodex DRI (RI-101) detector (Showa Denko, Ogimachi, Japan) and a Viscotek/Malvern SEC/MALS 20 multi-angle light scattering (MALS) detector (Malvern Panalytical Ltd., Malvern, UK). The fiber specimens (50 ± 5 mg) were activated through sequential immersion in water, acetone, and dimethylacetamide (DMAc), before being dissolved in 5 ml of a 90 g/l LiCl/DMAc (saturated solution) and diluted to a concentration of 1.0 mg/ml with pure DMAc. The analyses were performed in ambient temperature by injecting 100 µl volumes at a flow rate of 0.75 ml/min through a set of four PLgel MIXED-A columns (Agilent Technologies Inc., Palo Alto, USA).
The DRI and MALS detector constants were established and tested with polystyrene standards dissolved in 90 g/L LiCl/DMAc. The polystyrene standards were obtained from Polymer Standards Service (Mainz, Germany): one with narrow molecular weight distribution (Mw = 96,000 g/mol, D = 1.04, refractive index increment, ∂n/∂c, 0.146 ml/g) and one with broad molecular weight distribution (Mw = 248,000 g/mol, D = 1.73). The standards employed for calibration were cello-oligosaccharides (cellobiose, cellotriose, cellotetraose, cellopentaose) and linear xylo-oligosaccharides (xylobiose, xylotriose, xylotetraose) purchased from Megazyme Ltd. (Wicklow, Ireland). A ∂n/∂c value of 0.136 ml/g measured at 488 nm was used for the cellulose dissolved in 90 g/L LiCl/DMAc.
Protonation/deprotonation
The moisture sorption and water retention measurements described below were performed both on protonated and deprotonated specimens. For that, specimens were immersed for 1 h at ambient temperature in solutions of 0.1 M HCl (protonation) or 0.1 M NaOH (deprotonation), and then rinsed repeatedly with deionized water until the pH of the rinse water was similar to that of fresh deionized water. The wet specimens after the last rinsing step were used directly for measurements of water retention, but the specimens were allowed to dry in ambient atmosphere prior to measurements of moisture sorption.
Intrinsic viscosity determination
According to SCAN-CM 15:88, the standard for Scandinavian pulp, paper, and board testing, the intrinsic viscosities, η (ml/g), of the materials were evaluated. Thereby the viscosity was determined in a cupri-ethylenediamine solution via a capillary-tube viscometer. The Mark-Houwink equation was used to calculate the degree of polymerization (DP).
Moisture sorption/desorption
The moisture sorption and desorption equilibria and kinetics over the humidity range 0–90% at 25 °C, was measured on an automated multi-sample Dynamic Vapor Sorption analyzer (Vsorp, proUmid GmbH & Co. KG, Ulm, Germany). About 100 mg specimens were placed in aluminum dishes and loaded onto the device, where the atmosphere was initially conditioned to 0% relative humidity. The specimen masses were recorded every 10 min until attainment of equilibrium (defined as mass change of less than 0.05% over 300 min), whereupon the relative humidity was raised to the next level. This procedure was repeated as relative humidity levels were raised stepwise from 0% through 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% (sorption phase of measurement) and lowered in the reverse order (desorption phase of measurement). The moisture level in specimens at any given point was quantified in terms of the moisture regain (MR), calculated as shown in Eq. 1:
where, MR = moisture regain (%,), mx = mass of specimen (g) at given point, m0 = equilibrium mass of specimen (g) at 0% relative humidity.
The fitting of kinetic and equilibrium sorption models to experimental data was achieved by non-linear regression with the software SigmaPlot (version 14.0, Systat Software GmbH, Germany).
Water retention
About 0.1 g fiber specimens, after protonation/deprotonation and rinsing, were transferred to filtration tubes of 0.45 µm porosity, centrifuged for 10 min at 4000 × g, weighed, dried in ambient atmosphere and reweighed. The water retention values (WRV) were calculated with Eq. 2.
where, WRV = water retention value (%), mwet = mass of wet fiber after centrifugation (g), mdry = mass of fiber after drying in ambient atmosphere (g).
Results and discussion
FTIR spectroscopy
Typical FTIR spectra of CV and Co fibers, from reference treatments (i.e., only cleaned, and treated with 4.0 M NaOH alone) and carboxymethylation treatments (in 0.5 M NaOH and 4.0 M NaOH), from both ATR and transmission mode of measurements, are shown in Fig. S1, along with assignments for the absorbance peaks discussed below.
Cellulose swells in aqueous solutions of NaOH, with a transition observed at ca. 4.0 M, from intercrystalline to intracrystalline swelling (Klemm et al. 1998a). Both inter- and intracrystalline swelling may lead to porosity and therefore accessibility changes. Intracrystalline swelling leads also to an irreversible transformation in the crystal structure of native celluloses (e.g., Co) from polymorph type I to type II (O’Sullivan 1997). That can be detected in FTIR spectra, as demonstrated previously (Manian et al. 2022), from changes in peak intensity, shape or position at the wavenumber regions of 3484–3488 cm−1, 3410–3450 cm−1, 3300–3340 cm−1, 3270 cm−1, 1429 cm−1, 1163 cm−1, 1111 cm−1 and 893 cm−1. Regenerated celluloses (e.g., CV) originally exhibit polymorph type II in their crystalline domains, which is thermodynamically the most stable among all cellulosic polymorphs, and thus intracrystalline swelling does not change the polymorph type.
The Co fibers subjected only to cleaning or to carboxymethylation treatments in 0.5 M NaOH (at either 30 °C or 50 °C), all exhibited evidence of polymorph type I in their spectra; while those treated in 4.0 M NaOH alone, or carboxymethylated in 4.0 M NaOH (at 30 °C or 50 °C), showed evidence of polymorph type II. This was observed in both ATR mode (representative of the fiber surface) and transmission mode (representative of the fiber bulk). It shows that under the treatment conditions employed in experiments, there was thorough impregnation of NaOH solutions through the fiber structures. All CV fibers exhibited evidence of the polymorph type II in their spectra.
The spectra may also be utilized to evaluate indices of crystallinity in the fibers, from the ratios of absorbance intensities at wavenumber regions of 1376 cm−1/2902 cm−1 (“Total Crystallinity Index, TCI”) (Nelson and O’Connor 1964), 1420 cm−1/893 cm−1 (“Lateral Order Index, LOI”) (O’Connor et al. 1958) and 3366 cm−1/1336 cm−1 (“Hydrogen Bond Intensity, HBI”) (Nada et al. 2000). The TCI and LOI are directly proportional, and the HBI is inversely proportional, to the degree of crystallinity (Oh et al. 2005a, b). The indices from FTIR spectroscopy have been shown to correlate with degrees of crystallinity derived from X-ray Diffraction (XRD) (Nelson and O’Connor 1964). The proportionality of LOI with XRD results for polymorph type I is not the same as with polymorph type II, but the proportionalities of TCI and HBI do not vary with polymorph type.
The FTIR crystallinity indices of the CV and Co fibers, from both the ATR and transmission modes of measurements, are shown in Fig. S2. The TCI and LOI from transmission mode measurements were greater than those from the ATR mode, while the converse was observed for the HBI. That suggests differences in crystallinity between the fiber bulk and their surfaces. Only marginal and inconsistent differences could be discerned in the indices as function of fiber type (Co vs. CV), treatment type (i.e., NaOH content in treatment), or the degree of carboxymethylation. The exception was the consistent differences in LOI between the type I polymorph (i.e., Co not treated with 4.0 M NaOH) and type II polymorph (i.e., Co treated with 4.0 M NaOH and all CV fibers). That may be attributed to the difference between the polymorph types in proportionality of the LOI with degree of crystallinity.
Intrinsic viscosities, DP and molar mass distribution
The degree of polymerization (DP) was calculated from the intrinsic viscosity values determined by dissolving the samples in a cupri-ethylenediamine solution according to a common procedure (SCAN-CM 15:88). The commonly reported procedures for determination of molecular weight and molecular weight distribution of carboxymethyl cellulose with GPC involve dissolution of the polymer in eluent made of water alone or water containing NaOH, CH3COOH/CH3COONa, NaCl, Na2SO4, NaNO3 or NaNO3/NaH2PO4 (Eremeeva and Bykova 1998; Wach et al. 2003; Cleaver 2015a, b; Iwata 2021; Kunjalukkal Padmanabhan et al. 2023). The minimum degree of substitution required for water solubility of carboxymethyl cellulose is about 0.4 (BeMiller 2019), but the degree of substitution measured in this work ranged between 0.01–0.07 (Co) and 0.01–0.09 (CV) (Bogner et al. 2024a, b). Thus, the eluent employed for GPC measurements was that commonly used for cellulose (LiCl/DMAc). The chromatograms are shown in Fig. S3 and the derived parameters are listed in Table 2.
The chromatograms of most carboxymethylated samples (marked with an asterisk in Table 1) showed signs of molecular aggregation in eluent (see Fig. S3), in that larger weight fractions were observed in the higher molecular weight region, as compared to the reference (i.e., only cleaned fibers). One possible reason may be presence of moisture, as that has been shown to induce molecular aggregation between polymer chains in solutions of cellulose in LiCl/DMAc (Potthast et al. 2002; Röder et al. 2002). It is also possible that the chosen eluent system was not suitable for the carboxymethylated samples despite the relatively low degrees of substitution. Thus, more work will be required towards optimization of the measurement methodology in future, in terms of either the sample preparation regime and/or choice of eluent. Nevertheless, the viscometry results showed that the degree of polymerization was greater in Co as compared to CV (which was expected) and that the carboxymethylation treatments reduced the degree of polymerization on average by about 10% in CV and about 15% in Co fibers. It shows no significant oxidative damage during treatments, which is also supported by the fact there were no significant changes in fiber carboxyl content after treatments with alkali alone (see Table 1).
Water retention (WRV)
The WRV of the protonated and deprotonated forms of fibers are plotted against their carboxyl contents in Fig. 1. In both sets (i.e., protonated and deprotonated), the WRV increased in the order of fiber type/NaOH level: Co/0.5 M < Co/4.0 M ≅ CV/0.5 M < CV/4.0 M. In other words, at comparable levels of carboxymethylation, the WRV was higher in CV as compared to Co, and in fibers from 4.0 M NaOH treatments as compared to 0.5 M NaOH treatments. And, the WRV of Co from the 4.0 M NaOH treatments and CV from the 0.5 M NaOH treatments, were similar.
The effect of carboxymethylation degree on WRV was found to be greater in the deprotonated as compared to protonated fibers. In the protonated set, the WRV did not change with increase in carboxyl content among fibers from the 0.5 M NaOH treatments; and among fibers from the 4.0 M NaOH treatments, a gradual rise in WRV was observed, with both CV and Co exhibiting similar gradients. In the deprotonated set, the WRV increased with rise in carboxyl content in all fibers, with the gradients increasing in the following order of fiber type/NaOH level: Co/0.5 M ≅ CV/0.5 M < Co/4.0 M < CV/4.0 M; i.e., the gradient was higher in fibers from the 4.0 M NaOH as compared to 0.5 M NaOH treatments, and in CV as compared to Co.
The WRV of deprotonated forms of fibers was higher than that of the protonated forms, and the proportion varied only with the degree of carboxymethylation. The ratio of WRVs, deprotonated-to-protonated, increased from about 1 (observed in the reference fibers), in near-linear fashion, to about 2 in fibers with the highest degree of carboxymethylation in the experimental set, with no differences being apparent as function of either the fiber type or the NaOH level.
Moisture sorption isotherms
The moisture sorption isotherms measured on all fibers, both protonated and deprotonated forms, exhibited the characteristics of a Type II isotherm in the IUPAC classification (Thommes et al. 2015), which is typical for moisture sorption on cellulose. Selected examples from the deprotonated set are shown in Fig. 2. A hysteresis was observed, i.e., at equivalent humidity levels, the moisture regain equilibria from the desorption phase were greater than that from the sorption phase. The aggregate hysteresis was calculated with Eq. 3, and the values are shown in Fig. S4.
where, ΣH = aggregate hysteresis, ΣMR%Desorp = sum of moisture regain equilibria in the range 10–80% of relative humidity from the desorption phase of measurement, ΣMR%Sorp = sum of moisture regain equilibria in the range 10–80% of relative humidity from the sorption phase of measurement.
Generally, no significant differences were observed in aggregate hysteresis levels between the protonated and deprotonated forms of fibers or as function of fiber type, the NaOH level and degree of carboxymethylation.
Moisture regain equilibria (sorption phase)
The equilibria at each of the relative humidity levels (10–90%), as function of the degree of carboxymethylation and NaOH level during treatment, on both the protonated and deprotonated forms of fibers, are shown in Fig. 3 and 4 respectively.
At each humidity level, at comparable levels of carboxymethylation, moisture regain equilibria generally increased in the order of fiber type/NaOH level: Co/0.5 M < Co/4 M < CV/0.5 M ≅ CV/4 M. In other words, the highest moisture regain was observed in CV, with no significant differences between fibers from 4.0 M NaOH or 0.5 M NaOH treatments. The moisture regain in Co was lower, and fibers treated in 4.0 M NaOH exhibited greater moisture regain than fibers treated in 0.5 M NaOH. This was observed for both the protonated and deprotonated forms of fibers.
The sensitivity of moisture regain equilibria to degree of carboxymethylation was greater in Co as compared to CV. The protonated forms of CV exhibited almost no change in moisture sorption with rise in carboxymethylation degree, but in their deprotonated form, there was a gradual rise in moisture regain with increase in carboxymethylation degree. The change in moisture regain of Co with rise in carboxymethylation degree was higher. The gradients were higher in the deprotonated as compared to protonated forms, and in fibers from the 4.0 M NaOH as compared to 0.5 M NaOH treatments.
The moisture regain equilibria of deprotonated forms was greater than the corresponding protonated forms, and the proportions varied with the degree of carboxymethylation and relative humidity. The ratios, deprotonated-to-protonated, were always in the region of 1 for the reference fibers at all humidity levels. For fibers with the highest degree of carboxymethylation, the ratios were in the region of 1.07 at 10% relative humidity, between 1.08–1.10 in the relative humidity interval 20–60%, and increased from about 1.11–1.20 as the relative humidity increased from 70 to 90%. At each humidity level, the ratios changed in near-linear fashion with degree of carboxymethylation. No significant influence appeared of either fiber type or NaOH level.
Guggenheim-Anderson-de Boer (GAB) model
The Type II isotherms observed in the sorption phase of moisture sorption/desorption measurements were characterized with the GAB model, shown in Eq. 4.
where, υ = equilibrium moisture regain (g/g), υm = moisture sorbed as a monomolecular layer (g/g), C = energy constant, proportional to the difference in free enthalpy of water between its pure liquid state and in the monolayer, k = average measure of the difference in free enthalpy of water between its pure liquid state and in the sorbed layers beyond the first (i.e., monolayer), p/po = relative humidity expressed as partial pressure.
Like the Brunauer–Emmett–Teller (BET) model commonly used for Type II isotherms, the GAB model also describes multilayer sorption. While the BET is based on the assumption that adsorbate-sorbent interactions do not extend beyond the first sorbed layer (i.e., monomolecular layer), the GAB model is based on the principle that adsorbate-sorbent interactions extend beyond the first sorbed layer and diminish progressively to zero over a finite distance (Timmermann 2003; Thommes et al. 2015). The thermodynamic state of sorbate molecules in that distance, differs from that of sorbate as pure liquid, by an average factor ‘k’ (0 < k ≤ 1). The BET and GAB models are related, in that CBET ≡ CGAB∙ k, and when k = 1, the GAB equation reduces to that of the BET. The advantage of GAB is the broader range of humidity available for model fitting (up to p/po = 0.8–0.9) as compared to the BET (up to p/po = 0.3).
The values of the parameter υm are plotted in Fig. 5 for both CV and Co as function of the degree of carboxymethylation. At comparable degrees of carboxymethylation, the υm increased in the order of fiber type / NaOH level: Co/0.5 M < Co/4.0 M ≤ CV/4.0 M < CV 0.5 M. In other words, the υm was generally greater in CV as compared to Co. In Co, the υm was higher for fibers from the 4.0 M NaOH as compared to the 0.5 M NaOH treatments, but the reverse was observed in CV fibers. There was some overlap in υm values between CV and Co from the 4.0 M NaOH treatments.
Changes to the υm with rise in degree of carboxymethylation were higher in Co as compared to CV fibers, and higher in fibers from the 4.0 M NaOH treatments as compared to the 0.5 M NaOH treatments. There were no significant differences of the υm between the protonated and deprotonated forms of the fibers.
Values of the parameters k and C are shown in Fig. S5. Neither parameter changed significantly with the degree of carboxymethylation, either in the protonated and deprotonated forms of the fibers. The values for the deprotonated forms were only marginally greater than for the protonated forms. Whereas the values of C did not change significantly between fiber types or treatment conditions; the values of k were marginally greater for CV as compared to Co and for fibers from treatment in 4.0 M NaOH as compared to 0.5 M NaOH.
Moisture sorption kinetics
The moisture sorption rates of cellulosic materials are frequently derived from the “Parallel Exponential Kinetics” (PEK) model (Kohler et al. 2003), depicted in Eq. 5.
where, Mt = moisture regain (%) at time ‘t’ (min)M∞1, M∞2 = moisture regain equilibria attained through each of the two independent processes, τ1, τ2 = characteristic times (min) to reach 0.6321 M∞ in the individual processes.
In the model, the total moisture sorption is envisaged to be the sum of two first-order processes that occur in parallel but are independent of each other. One of the processes is labeled “slow” and the other “fast”, and each has their individual contribution, which sum up to the total moisture regain at equilibrium. The model is intended as a ‘pragmatic, numerical’ approach to highlight differences between materials, without attempting to characterize any of the underlying sorbate-adsorbent interaction mechanisms. Nevertheless, use of the PEK model is robustly criticized for being inadequate, principally on grounds that the derived parameters are not representative of any physical phenomena or of structural elements in cellulose (Thybring et al. 2019).
For that reason, in this work, the PEK model was employed to derive “t50”, defined as the time (in minutes) required for sorption of half the equilibrium moisture regain. A direct determination from experimental data was not feasible, since each sample was measured only once per 10 min, and that would not allow for a good resolution in the results. Hence, the experimental data were first modeled with Eq. 5 (standard error of fits ranged between 0.007–0.062), and the t50 were derived from the obtained model. To normalize for differences in sorption levels, the t50 divided by the equilibrium moisture regain (i.e., t50/MReq) was employed to highlight differences in the rate of sorption between experimental substrates. Higher values indicate lower rates of sorption. See Fig. S6 and S7 for results from the protonated and deprotonated forms of the fibers respectively.
There were generally no differences of t50/MReq between the deprotonated and protonated sets except in the humidity interval of 0–10%, where the deprotonated fibers exhibited slower sorption rates. In both sets, the t50/MReq increased gradually with rise in degree of carboxymethylation in the humidity interval of 0–60% (see parts a–f in Fig. S6 and S7), but at higher humidity levels, there appeared no influence of degree of carboxymethylation on the sorption rate (see parts g–i in Fig. S6 and S7). No differences could be discerned between fiber types or of the alkali level in treatment, except among protonated fibers in the humidity interval of 30–60%, where the sorption rate of CV fibers was generally slower than that of the Co (see parts d–f in Fig. S6).
Discussion
Cellulose interactions with water increase with rising charge density, and the extents are proportional to the polarity of polymer functional groups as well as the electric field intensities of counter ions. Carboxyl groups are more polar than hydroxyls and thus carboxymethylation promotes greater interactions with water; the electric field intensity of sodium ions is greater than that of hydrogen and thus water interactions with the sodium salt of carboxyl groups (i.e., their deprotonated form) is greater than with their protonated form (Berthold et al. 1994, 1996; Hubbe and Rojas 2008; Zhang et al. 2018). These trends were observed also in the results of this work. Both water retention and water vapor (i.e., moisture) sorption generally increased with the degree of carboxymethylation; and for both parameters, the values for deprotonated forms of fibers were greater than that of the corresponding protonated forms. The ratio of values, deprotonated-to-protonated, from measurements of both water retention and moisture sorption, were found to change only with degree of carboxymethylation with no influence from other variables (i.e., fiber type and NaOH level in treatment). Only in case of moisture sorption, the relative humidity was also observed to influence the ratios. Of interest are the differences observed as function of fiber type and of NaOH level in treatment, at comparable degrees of carboxymethylation. The changes in degree of polymerization on carboxymethylation, of on average ca. 10% and 15% in CV and Co respectively, are too low to have contributed significantly to the observed changes in water retention and moisture sorption.
The water retention, a measure of fiber swelling in water, increased in the order of fiber type /NaOH level Co/0.5 M < Co/4.0 M ≅ CV/0.5 M < CV/4.0 M. The swelling level of carboxymethyl cellulose is inversely proportional to the degree of polymerization of the cellulose. The CV fibers exhibited a lower degree of polymerization than Co, which will contribute to the observed order. Treatments with 4.0 M NaOH is known to increase porosity and thereby also the water retention (Jaturapiree et al. 2008; Öztürk et al. 2009). Evidence of that was observed in this work, from the differences of water retention between fibers that were only cleaned and those that were treated with 4.0 M NaOH alone. A further contribution is the depth to which the carboxymethylation occurs within fibers. It has been shown that the water retention is greater for cellulosics carboxymethylated through the bulk as compared to when the substitution is limited to the surface alone (Torgnysdotter and Wågberg 2003; Hubbe and Rojas 2008). In previous work (Bogner et al. 2024a, b), we reported evidence of greater depths of carboxymethylation in CV as compared to Co and in fibers from treatment in 4.0 M NaOH as compared to 0.5 M NaOH, from FTIR spectroscopy and dye sorption measurements; and that appears reflected in the results of water retention as well.
The change in moisture regain equilibria with rise in degree of carboxymethylation was lower in CV as compared to Co. The baseline of moisture sorption in CV fibers, i.e., in the reference fibers, was significantly greater than that in Co, which may be attributed to the greater levels of accessibility in CV as compared to Co (Bredereck and Hermanutz 2005). Thus, it appears the carboxymethylation resulted in smaller improvements of moisture sorption in the CV relative to the initially high moisture regain. A further difference was that CV fibers from 0.5 M NaOH treatments exhibited greater moisture regain as compared to fibers from 4.0 M NaOH treatments, whereas the reverse was observed for the Co. The difference may be attributed to greater hornification in the viscose after the 4 M NaOH treatments. The fibers after carboxymethylation treatments were washed and dried. Drying causes irreversible losses of pore volume in cellulose (termed ‘hornification’), and the extents increase with the degree of swelling before the drying step (Klemm et al. 1998b; Jaturapiree et al. 2011). Swelling levels are higher in CV as compared to Co (You et al. 2021), and thus hornification levels in CV would also be higher.
The differences described above in moisture regain equilibria were also reflected in in the GAB model parameter of υm, whereas no significant differences were observed in the parameters k and C. For polysaccharides in general, caution is recommended in the attribution of physical significance to GAB model parameters, as the parameter estimates do not match results of other independent measurements of the same phenomena (Timmermann 2003; Thybring et al. 2021). Thus, υm may be regarded as a measure of accessibility in general, but not specifically of moisture sorbed in a monomolecular layer. The C and k are to be understood as indicators of profile shape of the type II isotherm, the former of the knee in the lower range of humidity (at ca. 30% relative humidity) and the latter of upswing in the higher range of humidity (at ca. 70% relative humidity). Thus, the GAB model parameter estimates indicate that the accessibility among the different samples increased in the order of fiber type/NaOH level: Co/0.5 M < Co/4.0 M ≤ CV/4.0 M < CV 0.5 M, and that there were no significant differences in the shapes of the isotherm profiles.
The moisture sorption rates were found to become slower with rise in the degree of carboxymethylation (the t50/MReq increased gradually), but such effects were evident only until relative humidity of 60%. The sorption at higher humidity levels is dominated by capillary condensation, as indicated by the upward swing in sorption equilibria beginning at ca. 70% relative humidity, and here there was no influence of carboxymethylation level on sorption rates. Beyond isolated effects, the fiber type or alkali level in treatment were not observed to influence the moisture sorption rates.
No significant differences of hysteresis in the moisture sorption–desorption cycle were observed between any of the samples. Hysteresis is related to water-induced “plasticization” or softening of the polymer (Hou et al. 2022), and it appears that the carboxymethylation, in the range of values obtained in this work, did not influence that aspect of fiber properties.
Conclusion
A greater impact of fiber carboxymethylation was observed on their interactions with liquid water (i.e., water retention) as compared to water vapor (i.e., moisture sorption), as the differences in water retention between the carboxymethylated and reference fibers were greater than that of moisture sorption. In addition to the degree of carboxymethylation, the underlying structure also influenced the response of fibers to liquid water and to moisture, in terms of accessibility, swellability (which is related to the degree of polymerization) and hornification levels. No effect of the distribution of substituted carboxymethyl groups through fiber structures could be detected on moisture sorption levels, but there was evidence of it in their water retention values. Interestingly, whereas a greater depth of carboxymethylation promoted higher water retention (as observed in this work), it was observed to militate against carboxyl group accessibility to dye molecules (observed in previous work). Thus, a greater depth of carboxymethylation would be detrimental or conducive to performance depending on the metric: dye sorption or water retention, respectively. It highlights the contrasting effects that may arise, of a given set of treatment parameters (fiber type, alkali level in treatment), on efficacy of the product performance.
Comparisons between the fiber types of the level of carboxymethylation at the core regions, and assessments of the impact of pore distribution in fibers on the distribution of substituted carboxymethyl groups are works in progress. Of interest will also be to determine if the carboxymethylation changed fiber mechanical properties and if there was any fibrillation of the fibers. Further questions of interest include: the behavior of fibers in measurements of metal complexation, the effect of using a different alkali in treatments (e.g., KOH), and differences between the fiber types in other modification reactions (e.g., acetylation).
Data availability
All data that support the findings of this study are available from the corresponding author, APM, upon reasonable request.
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Funding
Open access funding provided by University of Innsbruck and Medical University of Innsbruck. The research leading to these results was performed in the frame of the project “Textile Competence Center Vorarlberg 2 (Project No. 882502)” funded under the COMET program – Competence Centers for Excellent Technologies – by the Federal Ministry for Climate Protection, Environment, Energy, Mobility, Innovation and Technology (BMK) and the Federal Ministry for Digitization and Business Location (BMDW), with co-financing from the federal province of Vorarlberg. The COMET program is administered by the Austrian Research Promotion Agency (FFG).
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Paul Bogner: investigation, methodology, visualization, writing—original draft; Inge Schlapp-Hackl: investigation, writing—review & editing, Michael Hummel: investigation, writing—review & editing, Thomas Bechtold: conceptualization, supervision, writing—review & editing; Tung Pham: conceptualization, supervision, writing—review & editing, funding acquisition; Avinash P. Manian: conceptualization, supervision, writing—review & editing.
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Bogner, P., Schlapp-Hackl, I., Hummel, M. et al. Carboxymethylation of viscose and cotton fibers: comparisons of water retention and moisture sorption. Cellulose (2024). https://doi.org/10.1007/s10570-024-06144-9
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DOI: https://doi.org/10.1007/s10570-024-06144-9