American Journal of Analytical Chemistry 

About: American Journal of Analytical Chemistry is an academic journal published by Scientific Research Publishing. The journal publishes majorly in the area(s): Adsorption & Detection limit. It has an ISSN identifier of 2156-8251. It is also open access. Over the lifetime, 964 publications have been published receiving 10036 citations. The journal is also known as: AJAC.

Characterization of Cellulosic Fibers by FTIR Spectroscopy for Their Further Implementation to Building Materials

Abstract: Nowadays, the material recycling is a growing trend in development of building materials and therefore using of secondary raw materials for production new building materials is in accordance with sustainable development in civil engineering. Therefore, it is increasingly becoming crucial to accelerate the transition from application of non-renewable sources of raw materials to renewable raw materials. One fast renewable resource is natural plant fibers. The use of the cellulosic fibers as environmentally friendly material in building products contributes to the environmental protection and saves non-renewable resources of raw materials. Wood fibers and recycled cellulose fibers of waste paper appear as suited reinforcing elements for cement-based materials. In this paper, there is used application of Fourier transform infrared spectroscopy (FTIR) on cellulose fibers coming from different sources. FTIR spectra of cellulose fiber samples are investigated and compared with reference sample of cellulose.

Optimized Assay for Hydrogen Peroxide Determination in Plant Tissue Using Potassium Iodide

Abstract: Here, we present an optimization of colorimetric determination of hydrogen peroxide content in plants using potassium iodide. Our method is based on a one step buffer (extraction and reaction) for the determination of H2O2 in different plant tissues and overcomes interference of soluble antioxidant and color background. A particular attention is paid to buffer pH shown to be tissue dependent. With this inexpensive microplate method, it is possible to analyze 12 experimental samples in about 45 min all in triplicates, with blanks, controls and standard curve.

Biosensors for Pesticide Detection: New Trends

Abstract: Due to the large amounts of pesticides commonly used and their impact on health, prompt and accurate pesticide analysis is important. This review gives an overview of recent advances and new trends in biosensors for pesticide detection. Optical, electrochemical and piezoelectric biosensors have been reported based on the detection method. In this review biosensors have been classified according to the immobilized biorecognition element: enzymes, cells, antibodies and, more rarely, DNA. The use of tailor-designed biomolecules, such as aptamers and molecularly imprinted polymers, is reviewed. Artificial Neural Networks, that allow the analysis of pesticide mixtures are also presented. Recent advances in the field of nanomaterials merit special mention. The incorporation of nanomaterials provides highly sensitive sensing devices allowing the efficient detection of pesticides.

Development and Validation of Two Methods to Quantify Volatile Acids (C2-C6) by GC/FID: Headspace (Automatic and Manual) and Liquid-Liquid Extraction (LLE)

Abstract: The concentration of the volatile fatty acids (VFA) is an important indicator of the status of an-aerobic processes, but most of the existing methods require sample pretreatment and are labor-intensive. It was developed and validated a rapid Gas Chromatographic (GC) method to quantify seven VFA (acetic, propionic, isobutyric, butyric, isovaleric, valeric and caproic), acetone, methanol, ethanol and n-butanol by headspace (automatic and manual) and liquid-liquid extraction (LLE) with diethyl ether (only VFA). The determination was made in a Shimadzu Gas Chromatograph equipped with a Flame Ionization Detector (GC/FID), a headspace auto-sampler and an HP-INNOWAX column. Isobutanol and crotonic acid were utilized as internal standards (IS). The validation parameters evaluated were: precision (coefficient of variation—C.V.% for the retention times, from 0.02 to 0.87), linearity (R2 = 0.9291 - 0.9997), limits of detection (from 3.97 to 36.45 mg·L﹣1) and instrumental precision (from 0.01 to 0.53), which provide evidence that the methods are adequate to determine these analytes in samples from anaerobic reactors and from the environment.

Normalized Rare Earth Elements in Water, Sediments, and Wine: Identifying Sources and Environmental Redox Conditions

Abstract: The concentrations of the rare earth elements (REE) in surface waters and sediments, when normalized on an element-by-element basis to one of several rock standards and plotted versus atomic number, yield curves that reveal their partitioning between different sediment fractions and the sources of those fractions, for example, between terrestrial-derived lithogenous debris and seawater-derived biogenous detritus and hydrogenous metal oxides. The REE of ancient sediments support their partitioning into these same fractions and further contribute to the identification of the redox geochemistry of the sea water in which the sediments accumulated. The normalized curves of the REE that have been examined in several South American wine varietals can be interpreted to reflect the lithology of the bedrock on which the vines may have been grown, suggesting limited fractionation during soil development.