Mercury (II) removal from aqueous solutions by iron nanoparticles synthesized from extract of Eucalyptus grandis.

Artisanal mining is the main source of mercury emissions in South America, which generates a serious environmental impact due to this toxic metal, recent research is directed to minimize the impact, therefore this study focuses on the green synthesis of nanoparticles for the absorption of mercury in water. For the synthesis of iron nanoparticles, an extract of Eucalyptus grandis was used with iron chloride salts using water as solvent. The synthesized nanoparticles showed a specific surface area of 131.90 m2/g, determined by Brunauer-Emmett-Teller isotherm (BET). Nanoparticles were characterized by Fourier transformed infrared spectroscopy (FTIR) and transmission electron microscopy (MET). The behavior of nanoparticles synthesized during Hg (II) retention was evaluated measuring pH, temperature, nanoparticle dosing, presence of other ions and comparing with other adsorbents. All analyses measured by atomic absorption spectroscopy by the cold vapor technique (CVAAS), presenting a retention percentage for Hg (II) between 75.05 and 79.59% with pH between 4 and 7. The adsorption isothermal was adjusted to the Freundlich model and the percentage of retention of Hg by the synthesized nanoparticle was 79.26%. This work shows a method for obtaining an environmentally friendly mercury adsorbent from iron and E. grandis with a mercury retention capacity comparable to commercial adsorbents.

Characterization and determination of the quality of rosins and turpentines extracted from Pinus oocarpa and Pinus patula resin.

Rosins and turpentines present in pine resins have been widely used both industrially (coatings, electronics and paint) and pharmaceuticals (ointments). Among the main components of these matrices is abietic acid. This study focuses on the characterization and evaluation of the quality of rosins and turpentines in addition to the quantification of abietic acid in rosins. Rosin and spirit of turpentine were obtained separately through the distillation method from P patula and P. oocarpa resin, species grown in the Department of Cauca-Colombia. Resin-tapping was made using the traditional method (cup and gutter). Quality indicators were determined according to ASTM standards. Solubility tests and identification of functional groups were performed on the obtained rosin by ultraviolet-visible spectroscopy (UV-Vis), infrared (IR) and nuclear magnetic resonance (1H-NMR). The abietic acid present in the rosins was determined by high performance liquid chromatography (HPLC). According to their high acid value and low percentage of unsaponifiable matter, the extracted rosins are considered of medium-high quality. Quantification of abietic acid by HPLC showed 14.85 ± 0.24% and 16.09 ± 0.11% for P. patula and P. oocarpa rosin respectively.

Green method to determine triazine pesticides in water using Rotating Disk Sorptive Extraction (RDSE).

The following work presents the development of the solid phase extraction technique with rotary disk (RDSE) in which the analysis for seven triazines in surface waters was first implemented. All the variables involved in extraction have been studied and optimized using a solid phase of octadecyl (C18) deposited on surface of the disk. Triazines were analyzed quantitatively by gas chromatography with simple quadruple mass detector, recoveries obtained for seven triazines were between 80% and 120%, accuracy expressed as RSD was between 3.21% and 6.34%, and detection limit of the method was between 0.020-0.056 µgL-1 according to each analyte, which indicates a good reproducibility and precision of the method. Finally, the method was applied to analyze the objective compounds in water samples obtained in the Bolo River (Palmira-Colombia), in which triazines were not detected.

Determinación y comparación cualitativa de cannabinoides presentes en productos naturales comerciales del departamento del Cauca, Colombia / Determination and qualitative comparison of cannabinoids present in commercial natural products of the Cauca Department-Colombia

RESUMEN Actualmente, hay un creciente interés por el estudio de Cannabis sativa y sus componentes ya que se le atribuye propiedades terapéuticas en el tratamiento de enfermedades. En Colombia y específicamente en el departamento del Cauca se comercializan productos de cannabis tanto para fines no medicinales como terapéuticos. En consecuencia, es necesario el análisis de estos productos de manera que se pueda conocer la composición de los mismos y el posible efecto que pueda tener sobre la salud. El análisis de los componentes de estos productos se llevó a cabo empleando la cromatografía líquida de alta resolución (CLAR) y espectrometría de masas (EM), de tal manera que permitieron la identificación de las principales especies cannabinoides; Δ9-tetra hidrocannabinol (THC), cannabidiol (CBD), cannabinol (CBN), cannabigerol (CBG). La separación de los analitos se llevó a cabo mediante la implementación de una columna analítica C18 de fase reversa, elución isocrática 1 mL/ min, presión del sistema 800 PSI, una mezcla de acetonitrilo ACN y buffer fosfato (KHPO4) en relación 65/35 como fase móvil, volumen de inyección de 10 µL, un tiempo de análisis de 15 min, y detección a 220 nm.

SUMMARY Cannabis sativa has now experienced an increasing interest in the study of its components since it is attributed therapeutic properties in the treatment of diseases. In Colombia and specifically in the Cauca Department, Cannabis products are marketed both for non-medicinal and therapeutic purposes. Consequently, it is necessary to analyze these products in such a way that the composition of the products and their possible effect on health can be known. The analysis ofthe components of these products was carried out using high performance liquid chromatog-raphy (HPLC) and mass spectrometry (MS), in such a way that they allowed the identification of the main cannabinoid species; Δ9-tetra hydrocannabinol (THC), cannabidiol (CBD), cannabinol (CBN), cannabigerol (CBG). The separation of the analytes was carried out by means of the implementation of a reverse phase C18 analytical column, isocratic elution 1 mL/min, system pressure 800 PSI, a mixture of acetonitrile ACN and phosphate buffer (KHPO4) in relation 65/35 as mobile phase, injection volume of10 µL, analysis time of15 min, and detection at 220 nm.

Presence of PAHs in water and sediments of the Colombian Cauca River during heavy rain episodes, and implications for risk assessment.

In Colombia little attention has been paid to river pollution with Polycyclic Aromatic Hydrocarbons (PAHs). Low environmental control and legislation in such emerging region could significantly contribute to high PAHs releases. In this study, we report the presence of PAHs in water and sediments of the Cauca River (Colombia). Three sampling campaigns were carried out between May 2010 and June 2011, and the samples were collected at eight relevant sites. The sampling time included measuring before, during, and after a season of heavy rains, which were influenced by the global coupled ocean-atmospheric phenomenon, which affected tropical countries with huge flooding, commonly called "La Niña", and/or "El Niño" Southern Oscillation (ENSO). The highest mean ∑PAH concentrations were 4476.5 ng/l and 1582.7 ng/g in water and sediments, respectively. The PAHs most detected were Benzo[b]fluoranthene, Benzo[k]fluoranthene, and Pyrene in sediments; and Fluorene, Acenaphtylene, and Anthracene in water. After the season of rains statistically significant higher PAH concentrations were detected. The results of the study were compared to other rivers worldwide at both environmental compartments, and did not show concentrations of special concern. In some sites, concentrations detected of PAHs were higher than screening benchmarks for ecological protection. Estimation of human health risks was carried out, and the results suggested some likely carcinogenic effects due to PAHs especially in children exposed during current recreational swimming and adults working in low technology sand extraction.