Removal of dyes from water using Citrullus lanatus seed powder in continuous and discontinuous systems.

The objective of this study is to develop a low-cost biosorbent using residual seeds of the Citrullus lanatus fruit for the removal of cationic dyes. Physicochemical parameters such as pH, adsorbent mass, contact time, and temperature were evaluated for their effects on dye removal. The biosorbent is composed of lignin and cellulose, exhibiting a highly heterogeneous surface with randomly distributed cavities and bulges. The adsorption of both dyes was most effective at natural pH with a dosage of 0.8 g L-1. Equilibrium was reached within 120 min, regardless of concentration, indicating rapid kinetics. The Elovich model and pseudo-second-order kinetics were observed for crystal violet and basic fuchsin dye, respectively. The Langmuir model fitted well with the equilibrium data of both dyes. However, the increased temperature had a negative impact on dye adsorption. The biosorbent also demonstrated satisfactory performance (R = 43%) against a synthetic mixture of dyes and inorganic salts, with a small mass transfer zone. The adsorption capacities for crystal violet and basic fuchsin dye were 48.13 mg g-1 and 44.26 mg g-1, respectively. Thermodynamic studies confirmed an exothermic nature of adsorption. Overall, this low-cost biosorbent showed potential for the removal of dyes from aqueous solutions.

In this work, a novel biosorbent was developed using residual Citrullus lanatus fruit seeds that can efficiently remove cationic dyes from aqueous solutions. The biosorbent's composition includes lignin and cellulose, and its surface structure is highly heterogeneous, consisting of randomly distributed cavities and bulges. The biosorbent demonstrated a rapid and efficient adsorption capacity for both crystal violet and basic fuchsin, regardless of dye concentration. Moreover, the biosorbent was successfully employed in the treatment of a synthetic mixture containing several dyes and inorganic salts. Finally, the application of the biosorbent in continuous adsorption showed a low zone of mass transfer and high breakthrough time, indicating it to be an excellent material for fixed-bed operation. Overall, this study provides a low-cost and efficient alternative for the removal of dyes from aqueous solutions, with promising practical applications.

Preparation of alumina-supported Fe-Al-La composite for fluoride removal from an aqueous matrix.

Using groundwater for human consumption is an alternative for places with no nearby surface water resources. Fluoride is commonly found in groundwater, and the consumption of this water for a prolonged time in concentrations that exceed established limits by WHO and Brazilian legislation on water potability (1.5 mg L-1) can cause harmful problems to human health. For this reason, fluoride removal is an important step before water consumption. In this work, activated alumina was impregnated with Fe-Al-La composite and employed for the first time as an adsorbent for fluoride removal from an aqueous environment. XRD, SEM/EDS, FT-IR, and point of zero charge were used to characterize the prepared adsorbent. The adsorptive performance of adsorbent material was investigated by employing a 23-central composite design (CCD), and the obtained experimental conditions were pH = 6.5 and adsorbent dosage = 3.0 g L-1. A maximum adsorption capacity of 8.17 mg g-1 at 298 K and pH = 6.5 was achieved by Langmuir isotherm to describe the adsorption. The kinetic model that better described experimental data was Avrami, with the kav parameter increasing with the initial concentration from 0.076 to 0.231 (min-1)nav. The nature of adsorption was found to be homogeneous, and it occurs in a monolayer. The fluoride removal performance for the prepared adsorbent was higher than granular activated alumina, showing that supporting Fe-Al-La at the alumina surface increased its fluoride adsorption capacity from 16 to 42% at the same experimental conditions. Finally, the influence of co-existing ions Cl-, SO42-, and NO3- was evaluated in fluoride adsorption, and the material presented great selectivity to fluoride. Thus, Fe-Al-La/AA adsorbent is a promising material for fluoride removal from water.

Adsorption kinetics and equilibrium of Ni2+, Cu2+, Co2+, and Ag+ on geopolymers derived from ashes: application to treat effluents from the E-Coat printing process.

Geopolymers were obtained from ashes through an alternative geopolymerization process and applied to remove Ni2+, Cu2+, Co2+, and Ag+ from synthetic aqueous media and real effluents. The study in synthetic solutions revealed that pseudo-second-order and general order models were the best to fit the kinetic curves. To represent the equilibrium curves, Langmuir and Freundlich were the most adequate. The geopolymer derived from bottom ash (GHA) was superior to adsorb Cu+2, Co+2, and Ag+1 than the geopolymer derived from fly ash (GFA). GHA reached adsorption capacities of 279.5, 288.2, and 462.8 mg g-1 for Co+2, Cu+2, and Ag+1, respectively. Otherwise, GFA was the best for Ni+2 removal, with an efficiency of 95% in low concentrations. In treating real effluents of the E-coat printing process, both GHA and GFA were efficient, with the removal of higher than 85% for all the metals. In brief, it can be stated that GFA and GHA prepared are promising materials to remove metals from aqueous media (synthetic and real), presenting fast adsorption kinetics, high adsorption capacity, and high metal removal percentage.

Effective removal of non-steroidal anti-inflammatory drug from wastewater by adsorption process using acid-treated Fagopyrum esculentum husk.

In this work, buckwheat husks (Fagopyrum esculentum) were modified by acid treatment and posteriorly employed to remove the ketoprofen in batch adsorption. The characterization results indicated that a more irregular surface with new empty spaces was generated after acid treatment. The adsorptive process was favored at acidic pH = 3. The dosage of 0.85 g L-1 was fixed for the kinetic and isothermal tests, obtaining good removal and capacity indications. The kinetic studies were better represented by pseudo-second-order, obtaining an experimental capacity of 74.3 mg g-1 for 200 mg L-1 of ketoprofen. An increase in temperature negatively affected the adsorption isotherm curves, resulting in a maximum capacity of 194.1 mg g-1. Thermodynamic results confirmed the exothermic nature of the process with physical forces acting. The adsorbent presented high efficiency in treating a synthetic effluent containing different drugs and salts, 71.2%. Therefore, adsorbent development from buckwheat husks treated with a strong acid is an excellent alternative, given the good removal results and the low cost for its preparation.

Effective adsorptive removal of textile pollutant using coal bottom ash with high surface area obtained by alkaline fusion route.

In this work, coal bottom ash was modified by alkaline fusion route in order to improve its pore properties and make it a potential adsorbent to remove crystal violet dye from aqueous medium. The solids were characterized and posteriorly subjected to kinetic, isotherm, and thermodynamic studies, as well as regenerated and reused for five adsorption tests. The alkaline fusion step resulted in the amorphization of material and generation of high surface area (102 m 2 g -1) and pore volume (0.180 cm 3 g-1), resulting in superior performance compared to the raw material. Kinetic and equilibrium studies showed that the adsorption process was better adjusted by the pseudo-second order and Langmuir models, respectively. The maximum adsorption capacity at equilibrium was 177. 37 mg g-1, with the adsorptive step occurring spontaneously and endothermically. The adsorbent maintained notable levels of dye removal after five consecutive cycles of thermal regeneration and reuse. Besides, the adsorbent was able to remove 64% of the colour of simulated industrial wastewater. Therefore, the alkaline fusion step proved to be a route capable of transforming the coal bottom ash into an adsorbent with improved textural and adsorptive properties.

Synthesis of geopolymers from fly and bottom ashes of a thermoelectrical power plant for metallic ions adsorption.

A series of geopolymers were synthesized from fly and bottom ashes of a thermoelectrical power plant located in the Brazilian southern, aiming to add value for these wastes. The geopolymers were prepared in conventional and ultrasound-assisted ways and used to uptake Ag+, Co2+, Cu2+, and Ni2+ from aqueous solutions. All materials were characterized by infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and N2 adsorption isotherms (BET and BJH methods). The results revealed that the geopolymers obtained from the conventional method presented slightly higher values of surface area and total pore volume. However, in some cases, the adsorption potential was better for the ultrasound synthesized materials. The geopolymers prepared from both methods presented good adsorption performance concerning Ag+ and Cu2+, Co2+ and Ni2+. The removal percentages were higher than 90%. In addition, the adsorption capacities were within the literature range. These findings show that the ultrasound technique is not essential to improve the geopolymers production process compared to the conventional process, which generated material with better performance for heavy metals adsorption. Besides, it was possible to aggregate value for fly and bottom ashes, generating promising adsorbent materials.

Optimization of ketoprofen adsorption from aqueous solutions and simulated effluents using H2SO4 activated Campomanesia guazumifolia bark.

This study used the bark of the forest species Campomanesia guazumifolia modified with H2SO4 to absorb the anti-inflammatory ketoprofen from aqueous solutions. FTIR spectra confirmed that the main bands remained after the chemical treatment, with the appearance of two new bands related to the elongation of the carbonyl group present in hemicellulose. Micrographs confirmed that the surface started to contain a new textural shape after acid activation, having new pores and cavities. The drug adsorption's optimum conditions were obtained by response surface methodology (RSM). The adsorption was favored at acidic pH (2). The dosage of 1 g L-1 was considered ideal, obtaining good indications of removal and capacity. The Elovich model very well represented the kinetic curves. The isotherm studies indicated that the increase in temperature negatively affected the adsorption of ketoprofen. A maximum adsorption capacity of 158.3 mg g-1 was obtained at the lower temperature of 298 K. Langmuir was the best-fit isotherm. Thermodynamic parameters confirmed the exothermic nature of the system (ΔH0 = -8.78 kJ mol-1). In treating a simulated effluent containing different drugs and salts, the removal values were 35, 50, and 80% at 15, 30, and 180 min, respectively. Therefore, the development of adsorbent from the bark of Campomanesia guazumifolia treated with H2SO4 represents a remarkable alternative for use in effluent treatment containing ketoprofen.

Woody residues of the grape production chain as an alternative precursor of high porous activated carbon with remarkable performance for naproxen uptake from water.

Activated carbon prepared from grape branches was used as a remarkable adsorbent to uptake naproxen and treat a synthetic mixture from aqueous solutions. The material presented a highly porous texture, a surface area of 938 m2 g-1, and certain functional groups, which were key factors to uptake naproxen from effluents. The maximum adsorption capacity predicted by the Langmuir model for naproxen was 176 mg g-1. The thermodynamic study revealed that the adsorption process was endothermic and spontaneous. The linear driving force (LDF) model presented a good statistical adjustment to the experimental decay data. A suitable interaction pathway of naproxen adsorption onto activated carbon was proposed. The adsorbent material was highly efficient to treat a synthetic mixture containing several drugs and salts, reaching 95.63% removal. Last, it was found that the adsorbent can be regenerated up to 7 times using an HCl solution. Overall, the results proved that the activated carbon derived from grape branches could be an effective and sustainable adsorbent to treat wastewaters containing drugs.

One step acid modification of the residual bark from Campomanesia guazumifolia using H2SO4 and application in the removal of 2,4-dichlorophenoxyacetic from aqueous solution.

The residual bark of the tree species Campomanesia guazumifolia was successfully modified with H2SO4 and applied to remove the toxic herbicide 2.4-dichlorophenoxyacetic (2.4-D) from aqueous solutions. The characterization techniques made it possible to observe that the material maintained its amorphous structure; however, a new FTIR band emerged, indicating the interaction of the lignocellulosic matrix with sulfuric acid. Micrographs showed that the material maintained its irregular shape; however, new spaces and cavities appeared after the acidic modification. Regardless of the herbicide concentration, the system tended to equilibrium after 120 min. Using the best statistical coefficients, the Elovich model was the one that best fitted the kinetic data. The temperature increase in the system negatively influenced the adsorption of 2.4-D, reaching a maximum capacity of 312.81 mg g-1 at 298 K. The equilibrium curves showed a better fit to the Tóth model. Thermodynamic parameters confirmed the exothermic nature of the system (ΔH0 = -59.86 kJ mol-1). As a residue obtained from urban pruning, the bark of Campomanesia guazumifolia treated with sulfuric acid is a promising and highly efficient alternative for removing the widely used and toxic 2.4-D herbicide from aqueous solutions.

Effective treatment of hospital wastewater with high-concentration diclofenac and ibuprofen using a promising technology based on degradation reaction catalyzed by Fe0 under microwave irradiation.

Real hospital wastewater was effectively treated by a promising technology based on degradation reaction catalyzed by Fe0 under microwave irradiation in this work. Fe0 powders were synthesized and characterized by different techniques, resulting in a single-phase sample with spherical particles. Optimum experimental conditions were determined by a central composite rotatable design combined with a response surface methodology, resulting in 96.8% of chemical oxygen demand reduction and 100% organic carbon removal, after applying MW power of 780 W and Fe0 dosage of 0.36 g L-1 for 60 min. Amongst the several organic compounds identified in the wastewater sample, diclofenac and ibuprofen were present in higher concentrations; therefore, they were set as target pollutants. Both compounds were completely degraded in 35 min of reaction time. Their plausible degradation pathways were investigated and proposed. Overall, the method developed in this work effectively removed high concentrations of pharmaceuticals in hospital wastewater.

Chitin-psyllium based aerogel for the efficient removal of crystal violet from aqueous solutions.

A new alternative aerogel was prepared from low-cost chitin and psyllium biopolymers to adsorb crystal violet (CV) dye from liquid media and possibly treat effluents containing other dyes. The aerogel was characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM), which demonstrated that aerogel has a typical structure of amorphous materials and presented a randomly interconnected porous structure that resembles an open pore network. 2.5 g L-1 of aerogel was able to remove 86.00% of CV from solutions, and the natural pH of the CV solution was considered the more adequate for adsorption. The pseudo-second-order (PSO) model satisfactorily described the adsorption kinetics, and the Freundlich model was suitable to represent the adsorption equilibrium. The maximum experimental capacity achieved was 227.11 mg g-1, which indicates that aerogel is very efficient and competitive with several adsorbents. Tests using a simulated effluent showed that aerogel has excellent potential to treat real colored effluents.

Adsorption and mass transfer studies of methylene blue onto comminuted seedpods from Luehea divaricata and Inga laurina.

In this work, comminuted seedpods of the forest species Luehea divaricata (LDPR) and Inga laurina (ILPR) were used as alternative and environmental-friendly adsorbents for the methylene blue (MB) removal from aqueous solutions. Batch adsorption experiments were carried out at the native pH of the solution (pH = 8.7), with curves of removal and adsorption capacity crossed at 0.75 g L-1, having 125 mg g-1 for LDPR and 115 mg g-1 for ILPR. The kinetic models of pseudo-first-order (PFO) and HSDM-Crank were the most adequate to represent MB dye concentration decay data for both biosorbents. The equilibrium curves were better adjusted by the Langmuir model for both adsorbents, with maximum adsorption capacity increased from 279 to 325 mg g-1 for LDPR, and 199 to 233 mg g-1 for ILPR, as a function of an increase in temperature from 298 to 328 K. The thermodynamic parameters showed that both systems are spontaneous with a dominance of physisorption. Mass transfer analysis indicates that the external mass transfer is the limiting step, with Bi < 0.5. Surface diffusion increased with the adsorption capacity, presenting linear and exponential behavior for the ILPR and PLPR adsorbents, respectively. Both materials proved to be efficient in treating a simulated effluent with similar industrial wastewater characteristics, reaching superior values at 70% of color removal.

Transforming pods of the species Capparis flexuosa into effective biosorbent to remove blue methylene and bright blue in discontinuous and continuous systems.

This study investigates, for the first time, the applicability of seed pods from Capparis flexuosa as an alternative biosorbent to remove methylene blue and bright blue from aqueous medium using continuous and batch systems. The biosorbent was characterized by different techniques, whose particles presented rough surface and large pores and functional groups existing on its surface. In the batch system, an adsorptive capacity of 96.40 mg g-1 and 80% of methylene blue removal was reached with 0.9 g L-1 of adsorbent at pH 10, whereas 109.7 mg g-1 and 83% of bright blue removal was observed using 0.8 g L-1 of adsorbent at pH 2.0. The Elovich model adjusted the experimental data satisfactorily for both dyes. Tóth model for the MB best described the equilibrium data, and the Langmuir model for the bright blue both favored by the increase of temperature and dyes' concentration. The maximum capacities obtained were 280.78 mg g-1 and 342.85 mg g-1 for methylene blue and bright blue, respectively. The thermodynamic parameters indicated spontaneous processes, with endothermic behavior for both dyes. The fixed adsorption experiments using Capparis flexuosa seed pods showed adsorptive capacities of 158.65 and 205.81 mg g-1 for the methylene blue and bright blue, respectively. The overall results indicated that the pods of the Capparis flexuosa could be an ecological, effective, and economical alternative in the removal of dyes for both continuous and batch systems.

Adsorption of ibuprofen, ketoprofen, and paracetamol onto activated carbon prepared from effluent treatment plant sludge of the beverage industry.

The presence of emerging contaminants such as pharmaceuticals in aquatic means presents as a serious threat, since their real consequences for the environment and human health are not well known. Therefore, this work consisted of preparing and characterize sludge-derived activated carbons (beverage sludge activated carbon - BSAC and acid-treated beverage sludge activated carbon - ABSAC) to investigate their use in the pharmaceuticals adsorption in aqueous media. The morphology study has demonstrated that ABSAC, unlike BSAC, exhibited an abundant porous structure, with smaller particles and bigger roughness. Adsorption results indicated that the ABSAC was more effective that BSAC, since it presented superior surface area (642 m2 g-1) and total pore volume (0.485 cm3 g-1) values. Pseudo-second-order kinetic model was more suitable to predict experimental data. Sips model best described the equilibrium data, with maximum adsorption capacities of 145, 105, and 57 mg g-1 for paracetamol, ibuprofen, and ketoprofen, respectively. Besides, the sludge-derived adsorbent was highly efficient in the treatment of a simulated drug effluent, removing 85.16% of the pharmaceutical compounds. Therefore, the material prepared in this work possesses intrinsic characteristics that make it a remarkable adsorbent to be applied in the treatment of pharmaceutical contaminants contained in industrial wastewater.

Stable Resin Bonding to Y-TZP Ceramic with Air Abrasion by Alumina Particles Containing 7% Silica.

PURPOSE: To evaluate the influence of new air-abrasion powders with different silica concentrations (silica-coated aluminum oxide) and aging on the bond strength between composite cement and Y-TZP ceramic. MATERIALS AND METHODS: Ceramic slices (7 x 6.3 x 2 mm3) were randomly allocated into 8 groups (n = 20) considering different surface treatments (SiC: silica-coated aluminum oxide particles; AlOx: aluminum oxide particles; 7% Si and 20% Si: experimental powders consisting of 7% and 20% silica-coated of AlOx respectively) and aging (baseline: 24 h at 37°C in water; aged: 90 days at 37°C in water + 12,000 thermal cycles). A blinded researcher performed the air-abrasion procedure for 10 s (identical parameters for all groups). Composite resin cylinders (Ø = 3 mm) were cemented onto the silanized ceramic surfaces, light cured, and subjected to shear bond-strength testing (wire loop Ø = 0.5 mm). The topography of the powders and air-abraded surfaces was analyzed using SEM and atomic force microscopy (AFM). The elemental composition of the powders and air-abraded surfaces was analyzed with energy dispersive spectroscopy (EDS), and surface wetting of the air-abraded surfaces was also determined by contact-angle measurements. RESULTS: Under baseline conditions, all groups presented similar bond strengths, but only SiC and 7% Si yielded unaltered bond strength after aging. SiC and 7% Si presented lower contact angles. All groups presented similar surface topographies. The silica content was also similar among groups, except for AlOx. CONCLUSION: 7% Si and SiC presented similar bond strength and better bonding performance after aging than AlOx and 20% Si. A higher silica concentration was not able to promote stable adhesion of composite cement after aging.

Synthesis of a novel CoFe2O4/chitosan magnetic composite for fast adsorption of indigotine blue dye.

A novel CoFe2O4/chitosan magnetic composite, where CoFe2O4 is known as cobalt ferrite, was synthetized, characterized and applied to adsorb indigotine blue dye (IBD). According to the central composite design (CCD), adsorption of IBD onto CoFe2O4/chitosan composite was favored when initial pH and adsorbent dosage were 3.0 and 0.75 g L-1, respectively. Adsorption was a fast process, well represented by pseudo-first order model, being the equilibrium reached at 15 min. Concerning the equilibrium behavior, the adsorption was satisfactorily modeled by the Langmuir model, reaching maximum adsorption capacity of 380.88 mg g-1 at 328 K. The thermodynamic parameters indicated a spontaneous, favorable and endothermic adsorption process. CoFe2O4/chitosan magnetic composite is an efficient adsorbent to remove dyes from aqueous media, presenting advantages like fast kinetic, high adsorption capacity and interesting magnetic properties that allows the easy separation after the adsorption operation.

Alternative synthesis for ZnFe2O4/chitosan magnetic particles to remove diclofenac from water by adsorption.

An easy preparation of magnetic particles with a chitosan external layer and zinc ferrite as core material was proposed. ZnFe2O4/chitosan particles were produced without any calcination step, characterized in detail, and, for the first time, applied for diclofenac (DCF) uptake from aqueous solution. The magnetic properties were checked, and revealed that the adsorbent particles have ability to be separated from the solution by an external magnetic field. Adsorption of DCF onto ZnFe2O4/chitosan particles was a fast process, well represented by pseudo-second order kinetic model, favored at initial pH of 4, with 0.2 g L-1 of adsorbent dosage and, reached the equilibrium within 20 min. The S-shaped equilibrium isotherms were well predicted by BET liquid-phase multilayer model. The adsorption was an exothermic, spontaneous and favorable process. The feasibility to produce chitosan magnetic particles, coupled with fast adsorption kinetics, high capacity (188 mg g-1), reusability (4 times) and the possibility to employ ZnFe2O4/chitosan particles for DCF adsorption, even in more concentrated solutions, were positive outcomes of this study.

Development of CO2 activated biochar from solid wastes of a beer industry and its application for methylene blue adsorption.

An alternative activated biochar was developed from barley malt bagasse (BMB) through pyrolysis followed by CO2 activation. The materials BMB, biochar and activated biochar (CO2-biochar) were characterized and tested as adsorbents for the removal of methylene blue (MB) from aqueous solutions. Adsorption kinetics, equilibrium and thermodynamics were studied. It was found that BMB and biochar presented surface area values lower than 1 m2 g-1, while CO2-biochar was a typical mesoporous material with surface area around 80 m2 g-1. As consequence, the adsorption potential for methylene blue was in the following order CO2-biochar ≫ biochar > BMB. Adsorption kinetics of MB on CO2-biochar followed the pseudo-second order model. Langmuir presented the best fit with the equilibrium adsorption isotherms. The maximum adsorption capacity was 161 mg g-1. MB adsorption on CO2-biochar was spontaneous, favorable and exothermic. Pyrolysis followed by CO2 activation was a suitable route to produce an alternative mesoporous adsorbent from barley malt bagasse.

Production of cellulolytic enzymes and application of crude enzymatic extract for saccharification of lignocellulosic biomass.

In this study, the optimal conditions for production of cellulolytic enzymes by Trichoderma reesei NRRL-6156 using the solid-state fermentation were assessed in conical flasks and validated in a packed-bed bioreactor. Afterwards, the crude enzymatic extract obtained in the optimized condition was used for hydrolysis of sugarcane bagasse in water and ultrasound baths. The enzyme activities determined in this work were filter paper, exocellulase, endocellulase, and xylanase. The optimized condition for production was moisture content 68.6 wt% and soybean bran concentration 0.9 wt%. The crude enzymatic extract was applied for hydrolysis of sugarcane bagasse, being obtained 224.0 and 229 g kg(-1) at temperature of 43.4 °C and concentration of enzymatic extract of 18.6 % in water and ultrasound baths, respectively. The yields obtained are comparable to commercial enzymes.

Carbon nanotubes as supports for inulinase immobilization.

The commercial inulinase obtained from Aspergillus niger was non-covalently immobilized on multiwalled carbon nanotubes (MWNT-COOH). The immobilization conditions for the carbon nanotubes were defined by the central composite rotational design (CCRD). The effects of enzyme concentration (0.8%-1.7% v/v) and adsorbent:adsorbate ratio (1:460-1:175) on the enzyme immobilization were studied. The adsorbent:adsorbate ratio variable has positive effect and the enzyme concentration has a negative effect on the inulinase immobilization (U/g) response at the 90% significance level. These results show that the lower the enzyme concentration and the higher the adsorbent:adsorbate ratio, better is the immobilization. According to the results, it is possible to observe that the carbon nanotubes present an effective inulinase adsorption. Fast adsorption in about six minutes and a loading capacity of 51,047 U/g support using a 1.3% (v/v) inulinase concentration and a 1:460 adsorbent:adsorbate ratio was observed. The effects of temperature on the immobilized enzyme activity were evaluated, showing better activity at 50 °C. The immobilized enzyme maintained 100% of its activity during five weeks at room temperature. The immobilization strategy with MWNT-COOH was defined by the experimental design, showing that inulinase immobilization is a promising biotechnological application of carbon nanotubes.