Preparation of Surgical Thread from a Bioplastic Based on Nopal Mucilage.

Currently, natural materials represent a sustainable option for the manufacture of biopolymers with numerous industrial applications and characteristics comparable with synthetic materials. Nopal mucilage (NM) is an excellent natural resource for the synthesis of bioplastics (BPs). In the present research, the fabrication of biopolymers by using NM is addressed. Changes in the plasticizer (sorbitol and cellulose) concentration, in addition to the implementation of two sources of starch (corn starch (CS) and potato starch (PS)) to obtain the surgical thread, were analyzed. The NM extracted was close to 14% with ethanol. During the characterization of the extract, properties such as moisture, humidity, viscosity, and functional groups, among others, were determined. In the CS and PS analysis, different structures of the polymeric chains were observed. BP degradation with different solvents was performed. Additionally, the addition of sorbitol and cellulose for the BP mixtures presenting the highest resistance to solvent degradation and less solubility to water was conducted. The obtained thread had a uniform diameter, good elasticity, and low capillarity compared to other prototypes reported in the literature.

Removal of Anionic and Cationic Dyes Present in Solution Using Biomass of Eichhornia crassipes as Bioadsorbent.

The discharge of large amounts of effluents contaminated with gentian violet (GV) and phenol red (PR) threatens aquatic flora and fauna as well as human health, which is why these effluents must be treated before being discarded. This study seeks the removal of dyes, using water lily (Eichhornia crassipes) as an adsorbent with different pretreatments. PR and GV were analyzed by a UV-visible spectrophotometer. Equilibrium experimental data showed that Freundlich is the best model to fit PR and SIPS for GV, showing that the adsorption process for both dyes was heterogeneous, favorable, chemical (for GV), and physical (for PR). The thermodynamic analysis for the adsorption process of both dyes depends directly on the increase in temperature and is carried out spontaneously. The Pseudo first Order (PFO) kinetic model for GV and PR is the best fit for the dyes having an adsorption capacity of 91 and 198 mg/g, respectively. The characterization of the materials demonstrated significant changes in the bands of lignin, cellulose, and hemicellulose, which indicates that the functional groups could participate in the capture of the dyes together with the electrostatic forces of the medium, from which it be concluded that the adsorption process is carried out by several mechanisms.

3,5-Dinitrosalicylic Acid Adsorption Using Granulated and Powdered Activated Carbons.

Some nitroaromatic compounds are found in wastewater from industries such as the weapons industry or the wine industry. One of these compounds is 3,5-dinitrosalicylic acid (DNS), widely used in various tests and frequently found as an emerging pollutant in wastewater and to which the required attention has not been given, even though it may cause serious diseases due to its high toxicity. This study investigated the adsorption of DNS using granulated activated carbon (GAC) and powdered activated carbon (PAC) at different temperatures. The results show that in equilibrium, the adsorption takes place in more than one layer and is favorable for the removal of DNS in both GAC and PAC; The maximum adsorption capacity was obtained at 45 °C, with values of 6.97 mg/g and 11.57 mg/g, respectively. The process is spontaneous and exothermic. In addition, there was a greater disorder in the solid-liquid interface during the desorption process. The predominant kinetics using GAC (7.14 mg/g) as an adsorbent is Elovich, indicating that there are heterogeneous active sites, and when PAC (10.72 mg/g) is used, Pseudo-second order kinetics predominate, requiring two active sites for DNS removal. External mass transfer limitations are only significant in GAC, and ATR-FTIR studies in PAC demonstrated the participation of functional groups present on the adsorbent surface for DNS adsorption.