Cellulose Ethers Research Articles

Influence of cellulose ethers chemistry and substitution degree on the setting and early-stage hydration of calcium sulphoaluminate cement

The setting and hydration process of calcium sulphoaluminate (CSA) cement within 24 h in the presence of five grades of cellulose ethers (CE) that have different chemistry or substitution degrees were studied by the Vicat test, ultrasonic test and isothermal calorimetry. X-ray diffraction (XRD) was further utilized to characterize the mineral phases of hydrates. Test results reveal that hydroxyethyl cellulose (HEC) prolongs the setting time less than hydroxyethyl methyl cellulose (HEMC) or hydroxypropyl methyl cellulose (HPMC). Higher CE dosage causes very limited change to the setting time of the mortar with HEMC/HPMC but narrows their gap with HEC. CE advance the second exothermal peak of CSA cement hydration where HEC works the most while highly-substituted HEMC/HPMC do the least. The trend is more pronounced at high dosage. The total hydration heat and the crystalized phases of hydrates are impacted slightly. CE work similarly in mortar on hydration to that in cement paste, but their effect is greatly weakened. A model is proposed to illustrate the hydration process. CE film is suggested to work as a medium for easier water migration that helps with the acceleration of the cement hydration reaction.

A detailed study on the rheological behavior of a novel cellulose-based hydrophobically-modified polymer

Hydrophobically-modified cellulose derivatives have been considered for improved oil recovery applications. However, the subsurface reservoir environment defined by combinations of brine salinity, temperature, and porous media-induced shear can pose an adverse challenge to the mobility control prospects of these materials. Previous studies have focused mostly on amphiphilic cellulose ethers. This study is based on a cellulose ester, herein, a novel polymeric surfactant derived from sodium cellulose sulfate is investigated. Rheological studies were carried out on the novel material under variable external reservoir conditions. From the results, the amphiphilic polymer was able to initiate associative behavior at a low concentration of 0.15 g/L. The biopolymeric surfactant exhibited tolerance to temperature and shear over the tested range of 35 °C to 75 °C, and 100 RPM to 250 RPM respectively by retaining its original rheological profile. The viscosity improved over a brine salinity range of 10,000ppm to 60,000ppm as it increased from 45.75 cp to 49.1 cp. From these findings, it can be inferred that the novel cellulose derivative is a good mobility control agent, and should be considered for oilfield applications that target cheap, cost-effective, and environmental-friendly operations.

Experimental study on dynamic and static structure establishment and recovery rate of fresh cement paste by composite thickening agents

The rheological and thixotropic properties, as well as the establishment of dynamic and static structures effectively reflect the workability of the cement paste. In order to investigate the effects of organic and inorganic composite thickening agents on fresh cement paste, the rheological curves, structural recovery rate, storage modulus G′ and loss modulus G″ of cement pastes mixed with limestone powder (LP), re-dispersible polymer powder (RPP) and hydroxypropyl methyl cellulose ether (HPMC) were tested by Anton Paar MCR 102 rotary rheometer. The results showed that LP and RPP reduced the yield stress and enhanced workability, and LP also improved the establishment of static structures. The incorporation of HPMC facilitated the recovery rate of static structure, and obviously improved the deformation resistance of the cement paste by reducing the difference between the G′ and the G″. However, a single thickening agent was hard to balance the rheological parameters of the pastes. While the combination of LP, RPP and HPMC could improve the rate of structure establishment and recovery, and increase the deformation resistance as well as the stability of the paste. The dense filling effect of LP, the film-forming and bridging effect of RPP, and the winding and water retention effects of HPMC together made up the synergistic effect to further improve the stability of the pastes.

Physicochemical Properties of Cellulose Ethers

Cellulose ethers are naturally derived ingredients that are commonly used in personal care products as rheology modifiers, film formers, stabilizers, and sensorial agents. In this work, we investigated the physicochemical properties of various grades of hydroxyethylcellulose (HEC), hydroxypropylcellulose (HPC), hydroxypropylmethylcellulose (HPMC), methylcellulose (MC), and sodium carboxymethylcellulose (CMC). In addition, we also studied the influence of hydrophobic modification on the structure of HEC by carrying out experiments with cetyl hydroxyethylcellulose (HMHEC). Rheological, friction coefficient, dynamic vapor sorption (DVS), surface tension analysis, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) data were generated for the cellulose ethers in order to obtain information about their viscosity, lubricity, moisture absorption, solubility in the bulk solution phase, physical properties, and thermal degradation profile, respectively.

Influence of aluminum sulfate on mobility and adhesion of hydroxyethyl methyl cellulose in cement-based materials for tunnel linings

Cellulose ether allows for high adhesion of fresh cement-based materials for hard rock tunnel linings. Alternatively, accelerator is used when a fast stiffening rate is required to support the surrounding rock. However, the influence of the addition of accelerator on the performance of cellulose ether has not been explored previously. In this study, four types of hydroxyethyl methyl cellulose with different viscosity levels and pure aluminum sulfate were used. The viscosifying property of the hydroxyethyl methyl cellulose in an aqueous solution with varying concentrations and temperatures was first examined. Furthermore, the hydrodynamic diameter and the concentration of hydroxyethyl methyl cellulose in the extracted interstitial fluid of the fresh mixtures was measured by performing the dynamic light scattering (DLS) test and the total organic carbon (TOC) test. In addition, the adhesion of the materials was tested both in the fresh and hardened state. Results indicate that the addition of aluminum sulfate contracts the pores in the fresh material and hinders the mobility of the hydroxyethyl methyl cellulose, especially for the ones with a high viscosity level. It is also shown that both hydroxyethyl methyl cellulose and aluminum sulfate enhance the adhesion of the fresh material, which can be attributed to improved shear resistance.

"ON THE IMPORTANCE OF VARIATION OF ALKALISATION CONDITIONS ON CELLULOSE ETHER SYNTHESIS"

With a multivariate approach, we investigate and correlate the effect of mercerization conditions on the properties of a cellulose ether. We have chosen to work with carboxymethylcellulose (CMC) for analytical reasons. As expected, the DS was found to increase when the NaOH/AGU (anhydroglucose unit) stoichiometric ratio (r) was increased (range 1.0–1.3) and [NaOH] was decreased (range 50-30%). However, such changes also favoured the formation of unwanted side products. Decreased (r) and increased [NaOH] resulted in increased heterogeneity, and thus the quantities of insoluble particles and unreacted chemicals also increased. As another result, the prediction between mercerisation and synthesis weakens. Consequently, a DS of 0.18–0.7 was obtained; the measured solubility was much lower than expected. A non-statistical distribution of substituents was further found. Interestingly, the relative importance of substitution at increases with an increased [NaOH].

Impact of instrumental settings in electrospray ionization ion trap mass spectrometry on the analysis of O-methoxyethyl-O-methyl cellulose: a comprehensive quantitative evaluation

The hydroxyethyl substitution along and among the polymer chains of respective cellulose ethers (HEC and HEMC) can be analyzed by ESI-IT-MS after permethylation of the free OH-groups, partial hydrolysis, and mABA labeling. This method requires the correct quantification of the molar ratios of the constituents belonging to a particular degree of polymerization (DP) with respect to their numbers of MeOEt and Me groups without any discrimination along the MS analysis pathway. The influence of the chemistry on the ionization and the impact of the voltages controlling the ion transport (Cap Exit, Octopoles) and the ion storage efficiency (Trap Drive, TD) on a relative quantification were studied using binary equimolar mixtures of cellobiose with increasing number of methoxyethyl and decreasing number of methyl groups (Δ m/z 88, 2× MeOEt). No suppression effects were observed in concentration-dependent measurements. Choice of Cap Exit is especially crucial for low m/z with less MeOEt residues. An equation describing the relationship between Oct 2 DC, m/z, and TDmax (TD at maximum intensity) was established from the experimental data and applied to calculate TDmax for higher DPs (larger COS). Optimized conditions allowed to determine the correct molar ratio of binary mixtures. Measurements of overlapping m/z segments and subsequent interrelation of the data gave complete substitution profiles for MeOEt/Me celluloses in accordance with reference data. The study generally makes aware of potential erroneous quantification in ESI-IT-MS analysis using internal standards of similar chemistry or in relative quantification of analytes, even for those with related structures.Graphical abstract

CoFe2O4@Methylcellulose/AC as a New, Green, and Eco-friendly Nano-magnetic adsorbent for removal of Reactive Red 198 from aqueous solution

• Methylcellulose (MC) was played an essential role to improve the nanomagnetic adsorbent structure for the Reactive Red 198 (RR198) adsorption. • CoFe 2 O 4 @MC/AC was synthesized as a novel nanomagnetic adsorbent with a facile, simple, and green microwave-assisted coprecipitation method. • The physical and chemical structure of CoFe 2 O 4 @MC/AC were approved with FTIR, FESEM, EDS, Mapping, Line Scan, XRD, VSM, and BET techniques. • The isotherm, kinetic and thermodynamic of RR198 adsorption were investigated. • CoFe 2 O 4 @MC/AC exhibited good chemical stability and reusability. Methylcellulose (MC) is the most common commercial cellulose ether and the most attractive biopolymer due to its cheap cost of biodegradability, biocompatibility, hydrophilicity, and lack of toxicity. In this study, CoFe 2 O 4 @MC/activated carbon (AC) was synthesized as a unique magnetic nano-adsorbent in the presence of MC biopolymer for Reactive Red 198 (RR198) dye removal. The nano-magnetic adsorbent was characterized by FESEM (Field emission scanning electron microscopy), EDS (Energy-dispersive X-ray spectroscopy), Mapping, Linescan, BET (Brunauer–Emmett–Teller), FTIR (Fourier Transform Infrared Spectroscopy), XRD (X-Ray Diffraction), and VSM (Vibrating-Sample magnetometer). For simple separation by external magnetic fields, the Ms value was 57.91 emu/g. According to XRD analysis, the nano-adsorbent maintains its crystal structure, with an average crystal size of 11 nm. The maximum removal efficiencies of RR198 for synthetic and real wastewater samples under optimal conditions (an initial concentration of 10 mg/L, pH 3, contact time of 10 min, nanocomposite dose of 1.5 g/L, and a temperature of 25 °C) were 92.2% and 78%, respectively. The adsorption experiments were fitted well with the Freundlich isotherm (R 2 = 0.989) and pseudo -second-order kinetic (R 2 = 0.995). The values of entropy changes (ΔS = 35.087 kJ/mol.k), enthalpy changes (ΔH = -9.862 kJ/mol), and negative Gibbs free energy changes (ΔG) showed that the adsorption process was exothermic. Finally, the reusability findings showed that after six recovery cycles, the efficiency decreased slightly (90.1%). In the end, it can be concluded that the prepared CoFe 2 O 4 @Methylcellulose/AC can be used as an efficient adsorbent for the removal of RR198 from an aqueous solution.

Rheological Properties and Early-Age Microstructure of Cement Pastes with Limestone Powder, Redispersible Polymer Powder and Cellulose Ether.

In order to study the synergistic effects of organic and inorganic thickening agents on the rheological properties of cement paste, the rheological parameters, thixotropy cement-paste containing limestone powder (LP), re-dispersible polymer powder (RPP), and hydroxypropyl methylcellulose ether (HPMC) were investigated using the Anton Paar MCR 102 rheometer at different resting times. The early-age hydration process, hydration products, and microstructure were also analyzed with scanning electron microscopy (SEM) and thermogravimetry analyses (TGA). The results showed that the addition of LP, RPP, and HPMC affected the rheological properties of cement paste, but the thickening mechanism between organic and inorganic thickening agents was different. The small amount of LP increased the plastic viscosity but decreased the yield stress of cement paste due to its dense filling effect. Adding 1% of RPP improved the thixotropic property of cement paste by 50%; prolonging the standing time could improve the thixotropic performance by as much as two times. Only 0.035% HPMC added to the cement paste increased the plastic viscosity by 20%, while the yield stress increased nearly twice. The more HPMC added, the more significant effect it showed. Cement paste compounds with LP, RPP, and HPMC balanced the yield stress and plastic viscosity and improved the thixotropy. The C-L6-R1.0-H0.035 paste presented as a pseudoplastic, its rheological indexes were close to one, and it was hardly affected by the resting time. The composite superposition effect of organic and inorganic thickening agents reduced the impact of resting time for all pastes. As the organic thickening component inhibited the hydration more than the LP promoted the hydration of the cement paste, indicating that the C-L6-R1.0-H0.035 paste remained in the particle fusion stage after curing for three days, as shown by the SEM images.

Are cellulose ethers safe for the conservation of artwork? New insights in their VOC activity by means of Oddy testing

Cellulose ethers, like methyl cellulose (MC) or hydroxypropyl cellulose (HPC), are widely used in conservation. They also occur as additives and rheology modifiers in various products like dispersions or gels. Do such products release harmful volatile organic compounds (VOC) during their accelerated aging? A mass testing series utilizing the Oddy test of 60 commercial cellulose ethers ranks the products in safe for permanent use (P, no corrosion), only for temporary use (T, slight corrosion), and unsuitable at all (F, heavy corrosion). Results show that 55% of the products passed the test whereas 33% are for temporary use as slight corrosion occurred on at least one metal coupon and only 11% failed the Oddy test. Raman measurements of the corrosion products identified oxides like massicot, litharge, cuprite, and tenorite among carbonates (hydrocerussite, plumbonacrite), and acetates like basic lead acetate, lead acetate trihydrate as well as lead formate as main phases. For example, commercial, industrial Klucel® G (HPC) scored a T rating through slight corrosion on the lead coupon. Basic lead acetate among other phases indicates the presence of acetic acid. Additional measurements of the sample with thermal desorption GC–MS utilizing the BEMMA scheme confirm the high acetic acid outgassing and reveal the presence of a small amount of formaldehyde.

High-purity cellulose production from birch wood by γ-valerolactone/water fractionation and IONCELL-P process

This study presents an environmentally friendly process to produce high-purity cellulose (dissolving pulp) from birch wood by combining γ-valerolactone (GVL)/water fractionation and ionic liquid treatment of pulp, IONCELL-P (IP). A paper grade pulp was produced from optimal GVL cook with a similar composition to birch kraft pulp and was bleached with ECF sequence before the hemicelluloses were removed using the IONCELL-P process. The purity of the GVL-IP pulp significantly exceeded that of commercial prehydrolysis kraft (PHK) and prehydrolysis soda-anthraquinone (PH-Soda-AQ) pulps. IONCELL-P extraction removed more than 90% of the hemicelluloses, resulting in a dissolving pulp with a purity of 96% and a high molecular mass fraction, 2.3 times higher than that of a conventional PHK pulp. GVL-IP pulps are suitable not only for regenerated cellulose fibers or films, but also for high-purity, high-viscosity cellulose acetate and ethers, which cannot be produced in an environmentally friendly way by conventional processes.

Spatial Distribution of Functional Groups in Cellulose Ethers by DNP-Enhanced Solid-State NMR Spectroscopy

Spatial Distribution of Functional Groups in Cellulose Ethers by DNP-Enhanced Solid-State NMR Spectroscopy

Anti-prion activity of cellulose ether is impaired in mice lacking pre T-cell antigen receptor α, T-cell receptor δ, or lytic granule function

The anti-prion activity of cellulose ether (CE) has been reported in rodents, but the mechanism of action is not well understood. As defects in early T-cell development have been reported in Tga20 mice which show only a slight effect of CE administration, we investigated the involvement of immune functions in the CE action. We confirmed an insertion of the prion protein transgene into the pre T-cell antigen receptor α gene of Tga20 mice, and its impaired expression in the thymus and other tissues. The influence of immune suppression on the CE effect was then examined in high CE-responder mice treated with immunosuppressive agents or neonatal thymectomy. As neonatal thymectomy significantly reduced the CE effect, we compared the influence of various T-cell defects in mice with similar genetic backgrounds. The CE effect was increased or unchanged in mice with defects in the αβ T-cell lineage, whereas it was abolished in T-cell receptor δ deficient mice. Further, when other immune defects were examined, the CE effect was reduced in mice with lysosomal trafficking dysfunction, but was unchanged in mice deficient in B-cell differentiation or toll-like receptor 4 signaling. These findings collectively suggest that the mechanism of CE action may involve γδ T cells and lytic granule function, as well as immune factors like natural killer T cells which are lacking in pre T-cell antigen receptor α deficient mice and neonatally thymectomized mice.

The Influence of Cellulose Ethers on the Physico-Chemical Properties, Structure and Lipid Digestibility of Animal Fat Emulsions Stabilized by Soy Protein.

This study explores the influence of carboxymethylcelullose (CMC) and methylcelullose (MC), added by simultaneous (sim) and sequential (seq) emulsification methods, on the structure, rheological parameters and in vitro lipid digestibility of pork lard O/W emulsions stabilized by soy protein concentrate (SPC). Five emulsions (SPC, SPC/CMC-sim, SPC/CMC-seq SPC/MC-sim, SPC/MC-seq) were prepared in vitro. The presence of CMC and MC, and the stage of incorporation affected the emulsion microstructure. In the SPC emulsion, lipid droplets were entrapped by a protein layer that was thicker when MC was added, providing greater resistance against environmental stresses during gastrointestinal digestion. At 37 °C, CMC incorporation produced a structural reinforcement of the SPC emulsion, whereas MC addition did not affect the network rigidity, although a delaying effect on the crossover temperature was observed, which was more evident in SPC/MC–seq. The presence and stage of CMC and MC incorporation affected the rate and extent of lipolysis, with SPC/MC-seq presenting an inferior concentration of free fatty acids. The lower extent of lipolysis observed in SPC/MC-seq may be positive in the manufacture of animal fat products in which reduced fatty acid absorption is intended.

Electrostatic spraying synthesis of energetic RDX@NGEC nanocomposites

It displays a favorable spherical morphology of the energetic RDX@NGEC nanocomposites and the 3D distribution of Raman mapping images, as well as the gas products detected by IR, and the mechanism of the desensitization. • Electrospray technology is utilized to assemble a novel energetic RDX@NGEC nanocomposites successfully. • The obtained RDX@NGEC composites exhibit favorable thermal decomposition and significant reduced sensitivity. • The mechanism of coating process, thermal decomposition and desensitization was proposed and discussed. • This construction strategy of novel energetic binder NGEC-based composites provides an application potential in propellants. Recently, an emerging category of thermal plastic energetic binder: nitrate glycerol ether cellulose (NGEC) exhibits promising application in propellants with extraordinary mechanical performance, and can be considered for using in military system instead (or partial) of traditional nitrocellulose (NC). In this paper, the electrostatic spraying technology is performed to synthesis a novel kind of nanocomposites energetic materials (nEMs) (hexahydro-1,3,5-trinitro-1,3,5-triazine) RDX@NGEC by adjusting the mass ratio of NGEC:RDX (0:5 ∼ 2.5:2.5). The results demonstrate that the NGEC patches with content of 30% were coated relatively uniformly on the surface of RDX crystal, and an ideal spherical structure, with dramatically reduced particle size (100 ∼ 800 nm) was obtained. Most importantly, the thermal decomposition properties are investigated systematically by traditional DSC (differential scanning calorimeter) analysis, DSC-TG-IR (DSC-thermogravimetric analysis-fourier-transform infrared spectroscopy) combining technology, where the kinetic parameters of thermal decomposition reaction are also calculated by two traditional methods: the Kissinger and Ozawa methods. It reveals that the process of the decomposition is mainly controlled by RDX when content of NGEC is low (10%∼20%), and the decomposition peak of NGEC is gradually appearing with the increasing content of NGEC (30%∼50%). Furthermore, the impact and friction sensitivities are tested and have been reduced about 1 ∼ 3 times. The mechanism of the sensitivity reduction, coating process and decomposition are also discussed detailly. Hence, this preparation and properties strategy of novel energetic RDX@NGEC nanocomposites may provide foundational theory research and exhibits application potential in propellants and explosives.

Spatial distribution of functional groups in cellulose ethers by DNP Enhanced Solid-State NMR Spectroscopy

Spatial distribution of functional groups in cellulose ethers by DNP Enhanced Solid-State NMR Spectroscopy

Application-Driven Material Design of Printable Strain Hardening Cementitious Composites (SHCC)

The creation of concrete shells from customized prefabricated modules is a novel approach that facilitates the construction of free-form surfaces considerably. In the framework of the Adaptive Concrete Diamond Construction (ACDC) project at TU Dresden, a material for 3D printing of the outer contours of such modules has been developed based on the principles of Strain Hardening Cementitious Composite (SHCC). In addition to its high ductility, the required material must also be suitable for 3D printing while enabling the achievement of high geometric accuracy in the manufacture of the modules. To gain the required performance, cellulose ether and starch ether were used specifically to extend the open time, for a longer period of maintaining initial workability, as well as for enhancing shape stability and surface quality. An extensive experimental program was carried out to evaluate the outcomes of the material modifications, including flow table tests, water retention tests, and several specific tests to determine the adhesiveness of the fresh SHCC. For hardened SHCC, surface roughness was assessed using a laser 3D scanner in addition to testing its mechanical properties.

Modulation of viscosity, microstructure and lipolysis of W/O emulsions by cellulose ethers during in vitro digestion in the dynamic and semi-dynamic gastrointestinal models

In this study, W/O emulsions incorporated with various proportions of two hydrocolloids, namely, methylcellulose (MC) and hydroxypropyl methylcellulose (HPMC), were prepared. The shear viscosity, microstructure, and lipolysis of the W/O emulsions before and during in vitro digestion in the dynamic (DIVHS) and semi-dynamic gastrointestinal models were evaluated and compared. The shear viscosity of both emulsions increased with the addition of MC and HPMC content up to a certain limit (0.5–2%), whereas it significantly decreased at a higher addition level (4%) due to the increased flocculation and coalescence in higher cellulose ethers. The HPMC emulsions (2 wt % in aqueous phases) showed higher viscosity and larger droplet size than the equivalent MC emulsions before and during simulated digestion, accompanied by the lower extent of lipolysis. These results are in line with the formation of a more compact and stronger gel structure in HPMC emulsions, which could retard lipase adsorption at the W–O interface. For both emulsions at the same concentration (40 wt%), a higher extent of free fatty acid (FFA) release was found during digestion in the dynamic system (HPMC ꞊ 62%, MC ꞊ 72%) compared to that in the semi-dynamic model (HPMC ꞊ 58%, MC ꞊ 70%). This behavior was supported by the smaller droplet size of emulsions digesta collected from the dynamic system having a larger surface area. Overall, the present study suggested that the dynamic DIVHS system was more effective in enzymatic hydrolysis of the W/O emulsions investigated than the semi-dynamic model under the current experimental conditions. This work had provided valuable insights into the modulation of the structural and digestive properties of W/O emulsions by the addition of MC and HPMC, which could be meaningful for the development of healthier emulsion-based food products (e.g., margarine and spreads) with reduced lipid digestibility.

Simultaneous Physico-Mechanical and In Vivo Assessment towards Factual Skin Performance Profile of Topical Polymeric Film-Forming Systems.

Topical film-forming systems (FFS) change drastically after solvent displacement, therefore indicating their skin metamorphosis/transformation as a property of special regulatory and research interest. This paper deals with the lack of suitable characterization techniques, suggesting a set of methods able to provide a comprehensive notion of FFS skin performance. After screening the physico-chemical, mechanical and sensory properties of FFS and resulting films, an elaborate three-phase in vivo study was performed, covering skin irritation, friction and substantivity. Upon removal of 24-hour occlusion, no significant change in erythema index was observed, while the film-former type (cellulose ether, acrylate and/or vinyl polymer) affected transepidermal water loss (TEWL); hydrophobic methacrylate copolymer-based samples decreased TEWL by 40–50%, suggesting a semi-occlusive effect. Although both the tribological parameters related to the friction coefficient and the friction curve’s plateau provided valuable data, their analysis indicated the importance of the moment the plateau is reached as the onset of the secondary formulation, while the tertiary state is still best described by the completion of the film’s drying time. The final part of the in vivo study proved the high in-use substantivity of all samples but confirmed the optimal 4:1 ratio of hydrophobic cationic and hydrophilic polymers, as indicated during early physico-mechanical screening.

Cellulose-Based Nanofibers Processing Techniques and Methods Based on Bottom-Up Approach-A Review.

In the past decades, cellulose (one of the most important natural polymers), in the form of nanofibers, has received special attention. The nanofibrous morphology may provide exceptional properties to materials due to the high aspect ratio and dimensions in the nanometer range of the nanofibers. The first feature may lead to important consequences in mechanical behavior if there exists a particular orientation of fibers. On the other hand, nano-sizes provide a high surface-to-volume ratio, which can have important consequences on many properties, such as the wettability. There are two basic approaches for cellulose nanofibers preparation. The top-down approach implies the isolation/extraction of cellulose nanofibrils (CNFs) and nanocrystals (CNCs) from a variety of natural resources, whereby dimensions of isolates are limited by the source of cellulose and extraction procedures. The bottom-up approach can be considered in this context as the production of nanofibers using various spinning techniques, resulting in nonwoven mats or filaments. During the spinning, depending on the method and processing conditions, good control of the resulting nanofibers dimensions and, consequently, the properties of the produced materials, is possible. Pulp, cotton, and already isolated CNFs/CNCs may be used as precursors for spinning, alongside cellulose derivatives, namely esters and ethers. This review focuses on various spinning techniques to produce submicrometric fibers comprised of cellulose and cellulose derivatives. The spinning of cellulose requires the preparation of spinning solutions; therefore, an overview of various solvents is presented showing their influence on spinnability and resulting properties of nanofibers. In addition, it is shown how bottom-up spinning techniques can be used for recycling cellulose waste into new materials with added value. The application of produced cellulose fibers in various fields is also highlighted, ranging from drug delivery systems, high-strength nonwovens and filaments, filtration membranes, to biomedical scaffolds.