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The traditional method for the identification of paper from different origins relies on microscopy to observe the fiber morphology, which requires professional experience. In this paper, pyrolysis-gas chromatographymass spectrometry was utilized to analyze five types of traditional Chinese handmade papers, e.g., ramie paper, bamboo paper, bark fiber paper (mulberry paper and kozo paper), and Langdu paper. The results demonstrated that this method can be used to differentiate the four types of handmade papers. A high phenolic compound content was detected in bamboo paper; macromolecular triterpenoids, e.g., ß - amyrin, a - amyrin, and stigmastan-3,5-diene were found in mulberry paper and kozo paper; while those compounds were not found in ramie paper. In particular, a large quantity of phytosterol compounds were found for the first time in Langdu paper. This not only can be used to differentiate Langdu paper from others, but also it helps to explain why Langdu paper can resist insect and mildew activities. Results of the study can provide experimental reference for characterization of traditional handmade Chinese papers via pyrolysis-gas chromatography-mass spectrometry. [ABSTRACT FROM AUTHOR]

Reports related to incidences of drug facilitated crimes (DFCs) have notably increased in recently. In such cases, victims report being assaulted or robbed while under the influence of drugs. Lorazepam (LZ) is frequently used in DFCs as it can easily make victims docile owing to its potent numbing effect. Therefore, a straightforward and green analytical method to analyze LZ in spiked food matrices in connection with criminal acts becomes important. The current study reports a simple, green, and high sample throughput analytical method for determining LZ in food and drink matrices commonly encountered in DFCs, based on recently introduced cellulose paper sorptive extraction (CPSE). For the extraction of LZ from food matrices, pristine cellulose paper (CP, commonly used laboratory filter paper) was used as a sorptive medium. Five pieces of CP (1.5″ × 1.5″ each) were dipped into diluted food matrices (cream biscuits and tea) and stirred on a rotary shaker for 30 min at 200 rpm. The CPs were then dried, and the adsorbed LZ was back-extracted into 2 mL of methanol. The extract was then subjected to GC–MS analysis in selected ion monitoring (SIM) mode. Several parameters, including CP size and number, back-extraction solvent type and volume, sample volume, extraction time and stirring speed, pH, ionic strength, elution time and speed, were thoroughly screened and optimized. Under the optimized conditions, the method was found to be linear in the range of 0.2–10 µg·mL−1 (or µg·g−1) with a coefficient of determination (R2) ranging from 0.996–0.998. The limit of detection and limit of quantification for cream biscuits were 0.054 and 0.18 µg·g−1 whereas they were 0.05 and 0.16 µg·mL−1 for tea samples. For all measurements, the relative standard deviations (%RSD) were always below 10%. Two mL of methanol per sample was used during the entire sample preparation process. The greenness of the proposed procedure was evaluated using Analytical Eco-Scale and GAPI greenness assessment tools. Finally, the CPSE–GC–MS method has been applied for the determination of LZ in forensic food samples which were used in DFCs. [ABSTRACT FROM AUTHOR]

The utilization of plant extraction products from Oeneanthe pimpinelloides (Apiaceae family) seeds were investigated in terms of their use as an insecticide control of packaging materials. The aim was to investigate their insecticidal effects against the flour beetle Tribolium castaneum. The Oeneanthe pimpinelloides seeds were extracted with methanol. By using the liquid-liquid extraction method, the hexane extract (II) was separated from the methanol extract (I) and hexane and methanol were evaporated. Then, the chemical composition of each sample was determined via gas chromatography-mass spectrometry. The methanol extract predominantly contained tetrahydrofuran, 1-methoxy-2-propanol, 1-methoxy, 2-butoxyethanol, 1-phenylethanone, cyclohexene carboxylate derivative, (3-phenyl-2-propynylidene) cyclopropane, diphenyldiazene, and dihydroxypropyl ester components, while the hexane fraction contained nonane, 1-octanol, decane, undecane, tridecane, alkyl benzene, benzene sulfonic acid, benzoxazine, and hexadecanoic acid components, as well as some derivatives of them. Each fraction was dissolved in DMSO for impregnation on filter paper. The insecticide effects of the paper samples were determined against Tribolium castneum. According to the results, the mortality started after 3 d for each fraction. After 4 d, the hexane fraction indicated total mortality in comparison with the methanol fraction, which showed partial mortality (3/5). [ABSTRACT FROM AUTHOR]

Once printed, books are always accompanied by the smells of volatile organic compounds (VOCs) which are continuously emitted not only by inks but also by papers themselves throughout their lives. Although the VOCs from papers may bring mild discomfort to readers, they are considered as very important factors that feature the degradation of papers and show potential applications in cultural relic appraisal. In this study, an analytical approach based on solid phase microextraction combined with gas chromatography-mass spectrometry (SPME-GC/MS) was proposed for the evaluation of volatile organic compounds (VOCs) emitted by Chinese traditional handmade papers. The VOCs evaluations and artificial aging processes were both applied to recent-made papers and naturally aged papers from a traditional Chinese calligraphy and painting scroll (collected by the National Museum of China). To be noticed, a large number of aliphatic acids, aldehydes, ketones, furan derivatives, benzene series and terpenoid substances indicated that the VOCs signals not only reveal the degradation of paper but also tentatively reflect the storage environment along hundreds of years ago. The semi-quantitative evaluation of markers indicated that the historical paper is under a serious degradation due to the high capacity it releases. Our results provided a path way to get the degradation information of ancient paintings as well as potential realistic applications such as the conservation of paper-based relics and the environmental protection in libraries and museums. [ABSTRACT FROM AUTHOR]

Pulp-paper mills (PPMs) are known for consistently generating a wide variety of pollutants, that are often unidentified and highly resistant to environmental degradation. The current study aims to investigate the changes in the indigenous bacterial communities profile grown in the sediment co-contaminated with organic and inorganic pollutants discharged from the PPMs. The two sediment samples, designated PPS-1 and PPS-2, were collected from two different sites. Physico-chemical characterization of PPS-1 and PPS-2 revealed the presence of heavy metals (mg kg-1) like Cu (0.009-0.01), Ni (0.005-0.002), Mn (0.078-0.056), Cr (0.015-0.009), Pb (0.008-0.006), Zn (0.225-0.086), Fe (2.124-0.764), Al (3.477-22.277), and Ti (99.792-45.012) along with high content of chlorophenol, and lignin. The comparative analysis of organic pollutants in sediment samples using gas chromatography-mass spectrometry (GC-MS) revealed the presence of major highly refractory compounds, such as stigmasterol, β-sitosterol, hexadecanoic acid, octadecanoic acid; 2,4-di-tert-butylphenol; heptacosane; dimethyl phthalate; hexachlorobenzene; 1-decanol, 2-hexyl; furane 2,5-dimethyl, etc in sediment samples which are reported as a potential toxic compounds. Simultaneously, high-throughput sequencing targeting the V3-V4 hypervariable region of the 16S rRNA genes, resulted in the identification of 1,249 and 1,345 operational taxonomic units (OTUs) derived from a total of 115,665 and 119,386 sequences read, in PPS-1 and PPS-2, respectively. Analysis of rarefaction curves indicated a diversity in OTU abundance between PPS-1 (1,249 OTUs) and PPS-2 (1,345 OTUs). Furthermore, taxonomic assignment of metagenomics sequence data showed that Proteobacteria (55.40%; 56.30%), Bacteoidetes (11.30%; 12.20%), and Planctomycetes (5.40%; 4.70%) were the most abundant phyla; Alphproteobacteria (20.50%; 23.50%), Betaproteobacteria (16.00%; 12.30%), and Gammaproteobacteria were the most recorded classes in PPS-1 and PPS-2, respectively. At the genus level, Thiobacillus (7.60%; 4.50%) was the most abundant genera grown in sediment samples. The results indicate significant differences in both the diversity and relative abundance of taxa in the bacterial communities associated with PPS-2 when compared to PPS-1. This study unveils key insights into contaminant characteristics and shifts in bacterial communities within contaminated environments. It highlights the potential for developing efficient bioremediation techniques to restore ecological balance in pulp-paper mill waste-polluted areas, stressing the importance of identifying a significant percentage of unclassified genera and species to explore novel genes. [ABSTRACT FROM AUTHOR]

In this work, volatile organic compounds (VOCs) in the ambient air of a secondary fiber paper mill were analyzed. For the sake of studying pollution comprehensively, four sites in the paper mill were analyzed and active sampling methods were used. Desorption was carried out with two solvents, carbon disulfide and dichloromethane. The compositions of VOCs were determined by gas chromatography-mass spectrometry (GCMS) method. The main identified substances in the four sites were as follows: (1) waste paper sorting room: alkanes, phenols, and esters; (2) papermaking workshop: benzene series, alkanes, ethers, and phenols; (3) vacuum pump outlet: benzene series and phenols; and (4) office area: benzene series and phenols. Two main toxic substances in VOCs, the benzene series and phenols, were detected in the ambient air of the paper mill. The benzene series existed in three places along the main process of the paper mill and even existed in the office area, which was far away from the production line. Additionally, phenols were detected in all sampling locations in the paper mill. [ABSTRACT FROM AUTHOR]

The present study deals with the bioremediation of potentially hazardous pulp and paper mill effluent by a laccase producing Paenibacillus sp. strain LD-1 (JX499920) isolated from contaminated soil sample by lignin enrichment method. The bacterium effectively reduced pollution parameters (colour 68%, lignin 54%, phenol 86%, BOD 83% and COD 78%) after 144 h of treatment at 34 ± 1 °C and 120 rpm. GC–MS analysis of control and treated samples showed that concentration of most of the low molecular weight phenolic compounds like 2-methoxyphenol, 2,6-dimethoxy phenol, 2-methoxy-4-ethyl-phenol, 3-allyl-6-methoxyphenol, ethanone 1-(-4-hydroxy-3,5-dimethoxyphenyl), benzoic acid, 2-methoxy-4-(1-propenyl) phenol and 4-methoxycinnamic acid present in control untreated effluent were reduced after bacterial treatment. The toxicity assessments were carried out with treated and untreated effluent by studying the growth and germination of seeds of mung bean ( Vigna radiata L.). The mung bean bioassay confirmed the detoxification of effluent after bacterial treatment. [ABSTRACT FROM AUTHOR]

The Jatropha curcas plant (Jatropha) has been proposed as a source of biodiesel fuel, as it yields crude glycerol as an abundant by-product. Its by-products could serve as a starting material in making glycerol for FDA-regulated products. Jatropha is not regarded as a source of edible vegetable oil since it contains phorbol esters (PEs). PEs, even at very low exposure concentrations, demonstrate various toxicities in humans and animals, but may not be detected by routine impurity analyses. Here, we demonstrate the development of a rapid and simplified method for the detection and quantification of Jatropha-derived PE toxins using ambient ionization mass spectrometry. To do this, we successfully coupled a paper spray ambient ionization source with an ion trap portable mass spectrometer. The paper spray source was assembled using chromatography papers, and analyte ions were generated by applying a high voltage to a wetted paper triangle loaded with PE standards. For method development, we used commercially available PE standards on an ion trap portable mass spectrometer. Standard solutions were prepared using ethanol with PE concentrations ranging from 1.0 to 0.0001 mg mL−1. Spike and recovery experiments were performed using USP grade and commercially available glycerol. To discern chemical differences between samples, we applied multivariate data analysis. Based on the results obtained, paper spray coupled with a portable mass spectrometric method can be successfully adopted for the analysis of toxic contaminants present in glycerol-based consumer products with LOD and LOQ of 0.175 μg mL−1 and 0.3 μg mL−1 respectively. This direct, simple design, and low-cost sampling and ionization method enables fast screening with high sensitivity in non-laboratory settings. [ABSTRACT FROM AUTHOR]

In order to search for bio-rational and eco-friendly pest control agents to protect crops from insect infestation, while avoiding the toxic hazards of chemical pesticides, essential oils (EOs) were hydrodistilled from Juniperus procera and Thymus vulgaris and analyzed using gas chromatography–flame ionization detection (GC–FID), and gas chromatography–mass spectrometry (GC–MS). Eugenol (71.3%), β-caryophyllene (11.8%), and α-pinene (6.1%) were isolated as the major components of J. procera EO, whereas thymol (58.1%), p-cymen (10.3%), and carvacrol (8.3%) were the main terpenes in T. vulgaris EO. The EOs and terpenes exhibited considerable bioactivity against the khapra beetle using the contact and fumigation bioassays, where T. vulgaris EO was superior in bioactivity. Among the terpenes tested, carvacrol and eugenol were superior. Regarding contact toxicity using impregnated filter paper and after 24 h of exposure, the LC50 values ranged between 21.4 and 77.0 µL/cm2 against larvae and between 16.1 and 69.6 µL/cm2 against adults. After 48 h, these values decreased remarkably. Upon fumigation and after 48 h of exposure, the LC50 values ranged between 23.0 and 65.3 µL/L against larvae, and from 14.2 to 56.4 µL/L against adults. The botanicals effectively inhibited the acetylcholinesterase activity of the larvae; however, they were safe for the earthworm E. fetida and did not alter the viability of wheat grains. There is a potential for using these botanicals to control T. granarium. However, further investigations are needed to confirm the safety of these phytochemicals before use as grain protectants on a commercial scale. [ABSTRACT FROM AUTHOR]

The age of a relatively old document is one of the pending issues to be resolved in the field of forensic documentary examination. Although nowadays there are a variety of analytical methodologies focused in the analysis of inks for dating documents, the paper analysis has attained little attention. This work aims to develop two complementary approaches for estimating the age of documents based on paper analysis employing the pyrolysis technique coupled to gas chromatography with detection by mass spectrometry (Py-GC/MS): (i) a direct approach using the pyrolytic fingerprints and multivariate regression with artificially aged samples, and (ii) an indirect approach based on the identification of compounds characteristic of the document period. The direct approach has successfully allowed the age estimation of relatively old documents under police custody (up to 30 years of age) and the determination of a relation between the natural and the accelerated aging of paper under the used conditions. This approach is applicable to papers that have the same (or similar) composition and have been stored under comparable storage conditions. Additionally, the indirect approach is presented as an interesting perspective to ratify valuable information of the document age. [ABSTRACT FROM AUTHOR]

Abstract: A set of inks was analyzed using Py/GC/MS technique. They were prepared following some ancient Armenian recipes and then analyzed after being dried in air to obtain solid samples. A simple analytical procedure was adopted which excludes any treatment of the samples and consists in introducing the solid sample directly into the injector of the furnace pyrolyzer. Inks were also written on whatman paper by calamum and analyses of papers containing ink were carried out. A real sample analysis was reported. Comparing the pyrograms it was possible to discriminate fragments derived from ink, from that formed by the decomposition of paper by the influence of ink. In order to understand the origin of the fragments formed during the pyrolysis of inks the standard compounds used to prepare them were carried out, too. [Copyright &y& Elsevier]

Plastics, papers, and textiles are the main dry waste components of municipal solid waste (MSW). Product-oriented pyrolysis of these wastes under proper blend ratio could be important not only for improving the quality of char, oil, or gas from MSW pyrolysis, but also for enhancing the recycle of plastics from MSW. In this study, the pyrolysis characteristics of papers (ivory board, coated duplex board with grey back, kraft paper and offset printing paper), plastics (polypropylene and polyethylene), and textiles (cotton and polyester) were studied using thermogravimetric-Fourier transform infrared (TG-FTIR) analysis, gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) to obtain the optimum blend ratios for the desired products (gas, oil, volatile and char). The synergistic effects amongst different components during pyrolysis were investigated. Results showed that the co-pyrolysis of papers, plastics, and textiles under equal blend ratio promoted the production of aromatics, alkenes, water, alcohol, and phenol in volatile, but inhibited the production of CO 2 , CO, alkanes, and carbonyls. The optimum mass blend ratios were found to be paper: plastic: textile = 25 wt%: 50 wt%: 25 wt% and 12 wt%: 50 wt%: 38 wt%, respectively for obtaining the highest energy share in volatile and gas. While for producing char with higher surface area, higher paper ratio and lower plastics ratio is preferred. When the plastics percentage in mixture was increased from 12.5 wt% to 25 wt%, the oxygenates percentage in pyrolysis oil was reduced from 82 area% to 19 area%, further increase in plastics percentage, or, alterations of papers and textiles percentages did not show significant influence on oil composition, indicating that plastics can be recycled, without lowering the calorific values of pyrolysis oil or MSW for incineration, when their blend ratio in MSW exceeds 25 wt%. • Synergism amongst paper, plastic, textile with different blend ratio investigated. • Optimum blend ratios to obtain desired products (char, gas, oil, volatile) were found. • Non-oxygenates in oil was 80 area% when the plastics percentage was ≥ 25 wt%. • Mixtures with more paper and less plastic can produce chars with high surface area. [ABSTRACT FROM AUTHOR]

Copyright of Studies in Conservation is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Biting lice are widespread ectoparasites of dogs and other animals. Their management is complicated because of growing levels of resistance to commonly applied pediculicides. Thus, the development of novel approaches to their control is of primary clinical interest. Therefore, we examined the chemical composition of garlic, clove, pumpkin, onion and marjoram essential oils through gas chromatography-mass spectrometry (GC-MS) and their individual toxicity against the dog lice Trichodectes canis using a contact filter paper bioassay. GC-MS analysis revealed the presence of 45 compounds in garlic oil, 15 compounds in clove oil, 24 compounds in pumpkin oil, 16 compounds in onion oil and 22 compounds in marjoram oil. 2,3,3-trimethyl Hexane (5.33%), (+-) -(1S, 3R)-4(S)(a)-Methyladamantan (44.35%), 2,6,10,14,18,22-Tetracosahexane, Ethyl-2,6,10,15, 19,23-Hexane (31.67%), (E, E)-2,4-Decadienal (18.64%) and 4-methyl-1-(1-methylethyl)-3-Cyclohexen-1-ol (CAS) (21.01%) were the most abundant compounds in garlic, clove, pumpkin, onion and marjoram oils, respectively. All treated groups except marjoram oil showed high levels of toxicity. Clove, garlic and pumpkin oils demonstrated the best loucidal activity reaching 100% mortality within 15 and 20 minutes. The LC50 values were 10.757, 9.156, 11.325, 27.296 and 15.059 % for garlic, clove, pumpkin, marjoram and onion oils. Based on the LC50 values, the relative efficacies of the tested oils after 35 minutes compared with that of the marjoram oil as a reference material indicated that, clove, garlic, pumpkin and onion oils were 3.0, 2.5, 2.4 and 1.8, respectively more effective than marjoram oil. The LT50 values, post-treatment with 25% were 40.659, 48.335, 39.261, 45.744, and 47.974% respectively. The relative speed of killing lice is almost similar in all tested oils. It could be concluded that clove, garlic and pumpkin oils may offer eco-friendly alternatives of veterinary pediculicides for the control of the dog lice T. canis. [ABSTRACT FROM AUTHOR]

We tested the performance of pyrolysis-comprehensive two-dimensional gas chromatography/mass spectrometry in the course of our cultural heritage studies, and compared its potentialities for the characterization of traditional East Asian handmade papers with those previously obtained by pyrolysis-gas chromatography/mass spectrometry. The evaluation of the two methods was conducted in considering the number of detected peaks, the compounds separation, the sensitivity, and the identification of marker compounds. The results showed that the number of plant markers (triterpenes and phytosterols) detected in a Japanese kozo reference paper was improved in the pyrolysis fingerprint. With a gain in sensitivity in the order of six, the case study of a museum sample confirmed that pyrolysis-comprehensive two-dimensional gas chromatography/mass spectrometry is more efficient for a reliable identification of museum collections samples and/or archaeological samples where tiny quantities of materials are the rule. The present study has been successful in refining a micro-destructive method based on analytical pyrolysis for the characterization of traditional East Asian handmade papers using pyrolysis-comprehensive two-dimensional gas chromatography/mass spectrometry. [ABSTRACT FROM AUTHOR]

At the beginning of the 20th century, the eclectic artist Mariano Fortuny y Madrazo patented two innovative methods for polychrome printing on fabrics and textiles, giving life to Fortuny fabric production in Venice. The first patent was related to colour application, while the second to a special machine that allows continuous printing using cylindrical rollers. Despite the descriptions, the methodology and materials used remain a secret. In collaboration with the Fortuny Museum in Venice, this research aimed at studying and identifying the different steps of Fortuny printing methodologies. Printing matrices, fabrics and raw materials found in the artist's studio were analysed in a multi-analytical campaign through digital microscopy, X-ray fluorescence (XRF), Fourier-transform infrared spectroscopy in attenuated total reflectance (FTIR-ATR), μ-Raman spectroscopy and gas chromatography–mass spectrometry (GC–MS). Three main pigments were identified in paper samples: ivory black, a copper-based pigment, and a carbon black pigment with ultramarine for blues. The pigments were bound with linseed oil and colophony in varying proportions. Polychrome silk fabrics were dyed with a base colour, and then the coloured patterns were superimposed by continuous printing. Prussian blue was identified as one of the textile inks. Results provided a better understanding of printing methodology. [ABSTRACT FROM AUTHOR]

In this study, the dynamics of volatile compound alterations during the storage of ground roasted coffee in various packaging were investigated using solid-phase microextraction-gas chromatography-mass spectrometry. Each type of packaging underwent repeated opening and closing, simulating the gradual consumption behavior of the consumer who consumes ground coffee in smaller doses over time. The experimental results revealed that after 30 days of storage, 35 to 45% of the volatile substances originally present in the coffee were lost regardless of the type of packaging used. Notably, storing coffee in a paper sachet proved to be the least effective method, resulting in a loss of over 80% of all volatile coffee substances during this storage period. [ABSTRACT FROM AUTHOR]

Methylmalonic aciduria is a common inherited metabolic disorder. Methylmalonic acid (MMA), a key indicator of methylmalonic aciduria, increases in the amniotic fluid of affected fetuses. For prenatal diagnosis, the MMA in amniotic fluid can be measured by stable-isotope dilution gas chromatography-mass spectrometry. Here, we quantified the MMA in cell-free amniotic fluid samples that had been dried on filter paper and transported at ambient temperatures, and compared the results with data obtained from the original amniotic fluid. Our results indicated that the filter paper method was reproducible and accurate enough to be applied to clinical analysis. We also used the filter paper method to screen at-risk fetuses and obtained a clear diagnosis in each case. We conclude that our method enables the prenatal diagnosis of methylmalonic aciduria using practical procedures and a simplified method for transporting the samples. [ABSTRACT FROM AUTHOR]

Circaea lutetiana is a medicinal plant in the Onagraceae family. The plant has been used for the treatment of wounds. As its chemical composition possesses valuable components, the infusion has been drunk or washed for treatment of injuries. The paper identified the chemical components of the leaves and stems of the plant Circaea lutetiana. The compositions of Circaea lutetiana leaves and stems were extracted with hexane and analyzed using gas chromatography-mass spectrometry (GC-MS). The method of peak area normalization was used to identify 22 compounds. Among them, The primary compounds (leaves and stems) are esters (30,799%), alkanes (12,69%), fatty acids (carboxylic acids), oxo-fatty acids (7,038%), phytosterols (3,43%), triterpenoids (3,01%). Analysis of each part of the plant (stems, leaves, and fruits) and more detailed information on the specific plants were investigated. [ABSTRACT FROM AUTHOR]

Abstract: Hyphenated techniques like Py-GC/MS (pyrolysis-gas chromatography/mass spectrometry) result often in complex chromatograms containing a high information density. Extracting meaningful information is difficult and time consuming. Especially with automatic sampling, data evaluation becomes a major bottleneck. An effective approach to automate the characterization of chromatograms is presented. The database approach consists basically of three steps: measuring reference substances to generate a database, measuring unknown or difficult samples and using the database for the identification of these samples. The compiled database contains a collection of mass spectra of pyrolysis products with data such as retention index and additional information from which reference substances the pyrolysis products may derive. The developed database approach has been tested on designed mixtures of compounds forming “white pitch”. “White pitch” is a typical type of deposit found in paper production processes deriving from chemicals used in coating processes. [Copyright &y& Elsevier]

The optimization of a clean procedure based on ultrasound-assisted emulsification liquid-liquid microextraction for the sensitive determination of four bisphenols is presented. The miniaturized technique was coupled with gas chromatography-mass spectrometry after derivatization by in situ acetylation. The Taguchi experimental method, an orthogonal array design, was applied to find the optimal combination of seven factors (each factor at three levels) influencing the emulsification, extraction and collection efficiency, namely acetic anhydride volume, sodium phosphate concentration, carbon tetrachloride volume, aqueous sample volume, sodium chloride concentration and ultrasound power and application time. A second factorial design was applied with four factors and five levels for each factor, 25 experiments being performed in this instance. The matrix effect was evaluated, and it was concluded that sample quantification can be done by calibration with aqueous standards. The detection limits ranged from 0.01 to 0.03 ng mL depending on the compound. The environmentally friendly sample pretreatment procedure was applied to study the migration of the bisphenols from different types of samples: thermal printer paper, compact discs, digital versatile discs, small tight-fitting waistcoats, baby's bottles, baby bottle nipples of different materials and children's toys. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

Given the imperative of monitoring organophosphorus pesticides (OPs) residues in the ecosystem, here a novel, facile and sensitive fluorescence sensor is presented for the rapid detection of dimethoate. In this work, surface molecularly imprinted polymer (SMIP) and microfluidic technology had been introduced to enhance the selectivity and portability of the described methodology. Oil-soluble CdSe quantum dots (QDs) synthesized in a green way were used as fluorescent material for the selective detection of dimethoate on the basis of static quenching and photoinduced electron transfer mechanism. Among many kinds of paper materials, glass fiber paper was used as the novel substrate of paper chip due to low pristine fluorescence and better performance when combining CdSe QDs. In the process of molecular imprinting, the interaction between several functional monomers and dimethoate molecule was investigated and simulated theoretically by software to improve the selectivity of the sensor. Consequently, the fabricated novel detection platform could effectively respond to dimethoate in 10 min with the concentration range of 0.45–80 μmol/L and detection limit of 0.13 μmol/L. The recovery in the spiked experiment soybean sample was in an acceptable range (97.6–104.1%) and the accuracy was verified by gas chromatography-mass spectrometry, which signified the feasibility and potential in food sampling. [ABSTRACT FROM AUTHOR]

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Abstract: The thermochemical conversion technique was applied in deinking sludge from the pulp and papermaking industrial to indagate the utilization of sludge biomass to energy, and the pyrolysis characteristics and pyrolytic products of deinking sludge were studied with thermogravimetric analysis (TGA) and pyrolysis coupled with gas chromatograph–mass spectrometer (Py-GC/MS). The static tubular furnace as an applied industrial research was used to study deinking sludge pyrolysis. The solid, gas and liquid of products was characterized by electron probe microanalysis (EPMA), gas chromatograph (GC) and gas chromatograph–mass (GC/MS), respectively. The results revealed that the weight-loss process of deinking sludge was a non-isothermal reaction and composed of four stages, i.e. dewater stage, volatile releasing stage, carbon burnout stage and some calcium carbonate decomposition. Pyrolytic products from deinking sludge in the static tubular furnace were comprised of the gaseous (29.78%), condensed liquid (bio-oil, 24.41%) and solid residues (45.81%). The volatiles from deinking sludge pyrolyzing were almost aromatic hydrocarbons, i.e. styrene, toluene and benzene and few acids and the solid was calcium carbonate (CaCO3) that can be reused as paper filler. Deinking sludge was converted into high-grade fuel and chemicals by means of thermochemical conversion techniques, hence, pyrolysis of paper deinking sludge had a promising development on the comprehensive utilization. [Copyright &y& Elsevier]

This study was designed to examine methanol as a new aging marker of insulating paper. An analytical GC-MS method coupled to headspace injection was developed, followed by a validation. To further validate the possible applicability of methanol for different transformer conditions some laboratory studies were performed such as a stability and an aging test. Oil samples of power transformers of several Belgian nuclear and coal-fired power plants have been analyzed since mid 2009 and are followed-up periodically to correlate the results with the analysis of the furanic compounds which have been used since mid 1980s as oil soluble degradation products of the insulating winding paper. It seemed that while no 2FAL was present some considerable amount of MeOH was detected which revealed some paper degradation. A second real case study was started to further correlate MeOH and 2FAL results. From these laboratory and real case studies it seemed that MeOH is a very promising marker for paper degradation in power transformers. [ABSTRACT FROM AUTHOR]

The presence of the metabolite 11-nor-9-carboxy-delta-9-tetrahydrocannabinol (C-THC) in hair is generally accepted as the definitive proof of delta-9-tetrahydrocannabinol (THC) ingestion. During hair analysis, the removal of any potential C-THC external contamination that could result from marijuana smoke or close personal contact via awash procedure is critical. Here, we performed a series of experiments to demonstrate that C-THC is the reliable indicator of marijuana ingestion when paired with the correct washing procedure to remove potential external contamination. [ABSTRACT FROM AUTHOR]

Background and aim: As a result of population growth, paper and wood products consumption has increased, and restrictions on using forest wood raw materials initiated the utilization poplar trees as fast-growing spices. The aim of this study was to focus on identification and comparison of the phenolic chemical components in poplar woods (populous nigra and populous deltoides). Materials and methods: In this study, three trees from each poplar tree were randomly felled in plantation near Nowshar, Iran. Then three discs were cut from each log. At first, wood was grounded and then wood flour extractive were measured using TAPPI standard procedure. Wood flour was extracted by acetone and extractives residue was added to BSTFA reactor and samples were kept in constant temperature bath at 70oC for an hour. The extractive samples were then analyzed by GC/MS. The compounds were identified using GC diagram which shows abundance and retention time of each compound, and calculation of quartz index and Adams table. Results: The result of GC-MS showed that there exist 68 and 105 compounds in wood of Populus nigra and Populus detoides, respectively. di-Limonene (30.26%), bis (2-ethylhexyl) phthalate (10.07%), Gamma-Sitosterol (1.06%), Hexadecanoic acid (2.0%), gamma-Terpinene (4.02%) and 4-Hydroxy-Benzoic acid (3.62%) were the most important compounds in wood of Populus detoides. There were the Limonene (25.62%), Anymol (5.29%), gamma-Terpinene (3.38%), 1, 2-Benzandicarboxylic acid (2.00%) and bis (2-ethylhexyl) phthalate (0.68%) as the most important compounds in wood of Populus nigra. Conclusion: The gas chromatographs showed that Limonene, Benzene methanol, alpha-Terpineol, beta-Bisabolene, Hexadecanoic acid and bis (2-ethylhexyl) phthalate were the 7 common compounds in the wood of Populus nigra and Populus deltoides. These compounds can play an important role in the durability and consumption of these woods. [ABSTRACT FROM AUTHOR]

Pulps were sampled from three major points of a deinking pulping line and classified as fibers fraction, fines fraction, and aqueous phase, respectively, then extracted with tetrahydrofuran (THF) or methyl tertbutyl ether (MTBE). Sticky contaminants in the extractives were examined by GC-MS analysis. The results showed that the contaminants can be grouped as adhesive substances, wood extractives, ligninderivatives, and other organic acids, of which the adhesive substances were accounted as the major component. Contents of sticky components in each group and their removal were further evaluated according to the related unit operation. Adhesives remaining in fibers and fines fractions were removed by the post-flotation. Wood extractives and degraded residual lignins were also released to some extent from pulp fibers during heat-dispersing, and then removed during the post-flotation. [ABSTRACT FROM AUTHOR]

Food packaging materials may be a potential source of contamination through the migration of components from the material into foodstuffs. Potential migrants can be known substances such as additives (e.g., plasticizers, stabilizers, antioxidants, etc.), monomers, and so on. However, they can also be unknown substances, which could be non-intentionally added substances (NIAS). In the present study, non-targeted analysis using mass spectrometry coupled to gas chromatography (GC-MS) for the identification of migrants in plastic and paper-based candy wrappers was performed. Samples were analyzed after extraction with acetonitrile. Numerous compounds including N-alkanes, phthalates, acetyl tributyl citrate, tributyl aconitate, bis(2-ethylhexyl) adipate, butylated hydroxytoluene, etc. were identified. Many of the compounds detected in plastic samples are not included in the positive list of the authorized substances. One non-intentionally added substance, 7,9-Di-tert-butyl-1-oxaspiro(4,5)deca-6-9-diene-2,8-dione, which has been reported as a degradation product of the antioxidant Irganox 1010, was found in several samples of both plastic and paper packaging. The proposed method was shown to be a useful approach for the identification of potential migrants in packaging samples. The toxicity of the compounds identified was estimated according to Cramer rules. Then, a second targeted analysis was also conducted in order to identify photoinitiators; among the analyzed compounds, only 2-hydroxybenzophenone was found in five samples. [ABSTRACT FROM AUTHOR]

Proton transfer reaction mass spectrometry (PTR-MS) and gas chromatography mass spectrometry GC-MS) allow real-time measurements of various atmospheric volatile organic compounds (VOC). By taking parallel measurements in ambient conditions, two PTR-MSs and two GC-MSs were studied for their ability to measure methanol, acetaldehyde, acetone, benzene and toluene. The measurements were conducted at a rural boreal forest site in southern Finland between 13 April and 14 May 2012. This paper presents correlations and possible biases between the concentrations measured using the four instruments. This paper presents correlations and possible biases between the concentrations measured using the four instruments. A very good correlation was found for benzene and acetone measurements between all instruments (the mean R value was 0.88 for both compounds), while for acetaldehyde and toluene the correlation was weaker (with a mean R value of 0.50 and 0.62, respectively). For some compounds, notably for methane, there were considerable systematic differences in the mixing ratios measured by the different instruments, despite the very good correlation between the instruments (mean R = 0.90). The systematic difference arises as a difference in the linear regression slope between measurements conducted between instruments, rather than as an offset. This mismatch indicates that the systematic uncertainty in the sensitivity of a given instrument can lead to an uncertainty of 50-100% in the methanol emissions measured by commonly used methods. [ABSTRACT FROM AUTHOR]

Surfactants are essential in the pulp recovery process for the removal of ink on paper to be recycled. In order to create a “green” surfactant, seed oil was extracted from Morinda citrifolia L. by Soxhlet extraction for 4–8 h and its composition evaluated by gas chromatography-mass spectrometry (GC-MS). The total ion chromatogram (TIC) of fatty acids of Morinda citrifolia L. (FAMC) indicated that extraction yields the largest amount of unsaturated fatty acids (UFA), specifically C19H34O2 and C21H38O2, at 6 h. All FAMC fractions were evaluated for their suitability as a surfactant for deinking flotation. FAMC isolated after 6 h of extraction yields fatty acids that are the most suitable surfactants, as the fraction consists of mostly unsaturated fatty acids that show good interactions with the structure of common ink molecules. Our results show that the performance of the FAMC taken after 6 h of extraction approaches that of a synthetic surfactant (SS). The appropriate viscous force for deinking flotation was found to be 1.5–2.0 × 10−4 mg/mm s2 when the synthetic surfactant is used compared to 1.0–1.5 × 10−4 mg/mm s2 for FAMC. The higher intermolecular bonding strength in the synthetic surfactant-ink particle system requires higher viscous force. [ABSTRACT FROM AUTHOR]

Microparticles encapsulated with orange essential oil were prepared by improved emulsifying solvent volatilization technology, and modified with chitosan to improve their loading and adhesion properties on paper. Characterization was performed by Zetasizer Nano ZS instrument, transmission electron microscope (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR) spectroscopy, thermogravimetric analyzer (TGA), gas-chromatography-mass spectrometry (GC-MS) and the ultrafast GC Electronic Nose Heracles II, etc. The results showed that for poly (lactic-co-glycolic acid) (PLGA) microparticles and chitosan–PLGA microparticles, respectively, the particle sizes were 233.2 and 277.6 nm, loading capacity was 19.17% and 24.36%, Zeta potential was −8.27 and 5.44 mV, adhesive capacity was 76.32 and 324.84 mg/g, and encapsulation efficiency was 93.23% and 94.06%. GC-MS demonstrated that the embedding process minimally effected the aroma quality of orange essential oil. The ultrafast GC Electronic Nose Heracles II showed that chitosan–PLGA microparticles could effectively slow the release of the orange essential oil. Therefore, this work provides a proposal for a better understanding of biodegradable functional packaging paper. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Chinese Mass Spectrometry Society is the property of Journal of Chinese Mass Spectrometry Society and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The combustion of fuel with high sulfur concentrations produces a large number of sulfur oxides (SOx), which have a range of negative effects on human health and life. The preparation of catalysts with excellent performance in the oxidative desulfurization (ODS) process is highly effective for reducing SOx production. In this paper, cross-linked polyvinylimidazole (VE) was successfully created using a simple ontology aggregation method, after which a catalyst of polyvinylimidazolyl heteropolyacid clusters (VE-HPA) was prepared by adding heteropolyacid clusters. Polyvinylimidazolyl-phosphotungstic acid (VE-HPW) showed an outstanding desulfurization performance, and the desulfurization efficiency reached 99.68% in 60 min at 50 °C with H2O2 as an oxidant. Additionally, the catalyst exhibited recyclability nine consecutive times and remained stable, with a removal rate of 98.60%. The reaction mechanism was eventually proposed with the assistance of the free radical capture experiment and GC-MS analysis. [ABSTRACT FROM AUTHOR]

Photochemical sources of peroxycarboxylic nitric anhydrides (PANs) are utilized in many atmospheric measurement techniques for calibration or to deliver an internal standard. Conventionally, such sources rely on phosphor-coated low-pressure mer- cury (Hg) lamps to generate the UV light necessary to photo-dissociate a dialkyl ketone (usually acetone) in the presence of a calibrated amount of nitric oxide (NO) and oxygen (O2). In this manuscript, a photochemical PAN source in which the Hg lamp has been replaced by arrays of ultraviolet light-emitting diodes (UV-LEDs) is described. The output of the UV-LED source was analyzed by gas chromatography (PAN-GC) and thermal dissociation cavity ring-down spectroscopy (TD-CRDS). Using acetone, diethyl ketone (DIEK), diisopropyl ketone (DIPK), or di-n-propyl ketone (DNPK), respectively, the source produces peroxyacetic (PAN), peroxypropionic (PPN), peroxyisobutanoic (PiBN), or peroxy-n-butanoic nitric anhydride (PnBN) from NO in high yield (>90 %). Box model simulations with a subset of the Master Chemical Mechanism (MCM) were carried out to rationalize products yields and to identify side products. The use of UV-LED arrays offers many advantages over conventional Hg lamp setups, including greater light output over a narrower wavelength range, lower power consumption, and minimal generation of heat. [ABSTRACT FROM AUTHOR]

Recently, Hu et al. have published a very interesting paper concerning the GC-MS analysis of 2-pentanol enantiomers in four types of Baijiu, a strong alcoholic beverage, which is of importance to Chinese social culture [[1]]. The only issue, which in my opinion is disputable, in the paper by Hu et al. is the ions which were chosen for the identification of the title compounds during the GC-MS analysis, identified on page four: " ...and qualitative ions ( I m i / I z i ) of (R)- and (S)-2-pentanol were 75, 73, and 60 and quantitative ions ( I m i / I z i ) were 51." It has to be stressed that the paper by Hu et al. is interesting and that the presented results may find practical application provided that the ions used for the GC-MS analysis of the title compounds are appropriate. References 1 Hu L., Qiu S., Dai Y., Tian L., Wei C. Determination of 2-pentanol enantiomers via chiral GC-MS and its sensory evaluation in Baijiu. [Extracted from the article]

Coffee, one of the most widely consumed beverages in the world, is commercialized as powder and beans in different types of packaging and extracted through several methods. In this regard, the present study focused on evaluating the concentration of two of the most used phthalates in plastic materials (bis(2-ethylhexyl)phthalate (DEHP) and di-butyl phthalate (DBP)) in coffee powder and beverages to assess their migration from different packaging and machines. Furthermore, the levels of exposure to these endocrine disruptors in regular coffee consumers were estimated. Samples of packaged coffee powder/beans (n = 60) from different forms of packaging (multilayer bag, aluminum tin, and paper pod) and coffee beverages (n = 40) that were differently extracted (by professional espresso machine (PEM), Moka pot (MP), and home espresso machine (HEM)) were analyzed by extraction of the lipid fraction, purification, and determination by gas chromatography–mass spectrometry (GC/MS). Risk due to consumption of coffee (1–6 cups) was assessed based on tolerable daily intake (TDI) and incremental lifetime cancer risk (ILCR). No significant differences emerged in DBP and DEHP concentrations among different types of packaging (multilayer, aluminum, and paper), whereas higher levels of DEHP were reported in beverages extracted by PEM (6.65, 2.58–11.32) than by MP (0.78, 0.59–0.91) and HEM (0.83, 0.62–0.98). The presence of higher DEHP levels in coffee beverages than in coffee powder may be due to its leaching through machine components. However, the levels of PAEs did not exceed the specific migration limits (SMLs) set out for food contact materials (FCM), and exposure to PAEs from coffee beverages was low, justifying the small risk due of its consumption. Consequently, coffee can be considered a safe beverage for exposure to some phthalic acid esters (PAEs). [ABSTRACT FROM AUTHOR]

The transfer of dissolved organic matter (DOM) at soil--river interfaces controls the biogeochemistry of micropollutants and the equilibrium between continental and oceanic C reservoirs. Then determining the transfer mechanisms of DOM is of main importance for ecological and geochemical reasons. Is stream DOM the result of the flushing of pre-existing soil DOM reservoirs activated by the modification of water flow paths? The evolution of the chemical composition of stream DOM investigated by thermally assisted hydrolysis and methylation (THM) using tetramethylammonium hydroxide (TMAH) coupled to a gas chromatograph and mass spectrometer (THM-GC-MS) during inter-storm conditions and five storm events with a high-frequency sampling gives new insights on this question. In inter-storm conditions, stream DOM is inherited from the flushing of soil DOM, while during storm events, the modification of the distribution of chemical biomarkers allows the identification of three additional mechanisms. The first one corresponds to the destabilization of microbial biofilms by the increase in water velocity resulting in the fleeting export of a microbial pool. The second mechanism corresponds to the erosion of soils and river banks leading to a partition of organic matter between particles and dissolved phase. The third mechanism is linked to the increase in water velocity in soils that could induce the erosion of macropore walls, leading to an in-soil partitioning between soil microparticles and dissolved phase. The contribution of this in-soil erosive process would be linked to the magnitude of the hydraulic gradient following the rise of water table and could persist after the recession, which could explain why the return to inter-storm composition of DOM does not follow the same temporal scheme as the discharge. Those results are of main importance to understand the transfer of nutrients and micropollutants at the soil--river interfaces during the hot moments that are storm events. [ABSTRACT FROM AUTHOR]

Dual choice bioassays were used to evaluate the antifeedant property of essential oil and methanolic extract of Alpinia galanga (L.) (locally known as lengkuas) against two species of termites, Coptotermes gestroi (Wasmann) and Coptotermes curvignathus (Holmgren) (Isoptera: Rhinotermitidae). A 4-cm-diameter paper disc treated with A. galanga essential oil and another treated with either methanol or hexane as control were placed in a petri dish with 10 termites. Mean consumption of paper discs (miligram) treated with 2,000 ppm of essential oil by C. gestroi was 3.30 ± 0.24 mg and by C. curvignathus was 3.32 ± 0.24 mg. A. galanga essential oil showed significant difference in antifeedant effect, 2,000 ppm of A. galanga essential oil was considered to be the optimum concentration that gave maximum antifeedant effect. The essential oil composition was determined using gas chromatography-mass spectrometry. The major component of the essential oil was 1,8-cineol (61.9%). Antifeedant bioassay using 500 ppm of 1,8-cineol showed significant reduction in paper consumption by both termite species. Thus, the bioactive agent in A. galangal essential oil causing antifeeding activity was identified as 1,8-cineol. Repellent activity shows that 250 ppm of 1,8-cineol caused 50.00 ± 4.47% repellency for C. gestroi, whereas for C. curvignathus 750 ppm of 1,8-cineol was needed to cause similar repellent activity (56.67 ± 3.33%). C. curvignathus is more susceptible compare to C. gestroi in Contact Toxicity study, the lethal dose (LD50) of C. curvignathus was 945 mg/kg, whereas LD50 value for C. gestroi was 1,102 mg/kg. Hence 1,8-cineol may be developed as an alternative control against termite in sustainable agriculture practices. [ABSTRACT FROM AUTHOR]

Carbonyl compounds are ubiquitous in the atmosphere and either emitted primarily from anthropogenic and biogenic sources or they are produced secondarily from the oxidation of volatile organic compounds (VOC). Despite a number of studies about the quantification of carbonyl compounds a comprehensive description of optimised methods is scarce for the quantification of atmospherically relevant carbonyl compounds. Thus a method was systematically characterised and improved to quantify carbonyl compounds. Quantification with the present method can be carried out for each carbonyl compound sampled in the aqueous phase regardless of their source. The method optimisation was conducted for seven atmospherically relevant carbonyl compounds including acrolein, benzaldehyde, glyoxal, methyl glyoxal, methacrolein, methyl vinyl ketone and 2,3-butanedione. O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine hydrochloride (PFBHA) was used as derivatisation reagent and the formed oximes were detected by gas chromatography/mass spectrometry (GC=MS). The main advantage of the im proved method presented in this study is the low detection limit in the range of 0.01 and 0.17 μmolL-1 depending on carbonyl compounds. Furthermore best results were found for extraction with dichloromethane for 30 min followed by derivatisation with PFBHA for 24 h with 0.43mgmL-1 PFBHA at a pH value of 3. The optimised method was evaluated in the present study by the OH radical initiated oxidation of 3-methylbutanone in the aqueous phase. Methyl glyoxal and 2,3-butanedione were found to be oxidation products in the samples with a yield of 2% for methyl glyoxal and 14% for 2,3- butanedione. [ABSTRACT FROM AUTHOR]

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Chinese Mass Spectrometry Society is the property of Journal of Chinese Mass Spectrometry Society and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Utilizing conventional wood preservatives poses potential risks to ecosystems and human health. Therefore, the wood protection industry must develop alternatives that are both efficient and environmentally friendly. In this paper, industrial tobacco waste extracts were used as eco-friendly wood preservatives against wood decay fungi. Three major constituents in the extracts were identified via gas chromatography-mass spectrometry (GC-MS) and included nicotine, neophytadiene, and 2,7,11-cembratriene-4,6-diol. The antifungal activities of waste tobacco extracts and these three major constituents against wood decay fungi were tested. At a concentration of 40 mg/mL, the tobacco waste extract treated with 50% ethanol significantly inhibited the activity of wood decay fungi. This was because the extract contained nicotine as the primary active component and neophytadiene as a synergistic active component. Wood decay resistance tests were conducted on Pinus yunnanensis and Hevea brasiliensis treated with a 50% ethanol extract of tobacco waste at a concentration of 40 mg/mL. The mass losses of Pinus yunnanensis exposed to G. trabeum and T. versicolor were 4.11% and 5.03%, respectively, while the mass losses in Hevea brasiliensis exposed to G. trabeum and T. versicolor were 7.85% and 9.85%, respectively, which were classified as highly resistant. The acute ecotoxicity of the tobacco waste extract was assessed using a kinetic luminescent bacteria test with Aliivibrio fischeri, which revealed significantly lower acute toxicity than a commercial copper-based wood preservative. This study offers insights into high-value utilization of tobacco waste and advancement of natural wood preservatives. [ABSTRACT FROM AUTHOR]

Different grain sources of whiskey have great potential for aroma expression. In this paper, four whiskeys fermented from different raw materials (barley, wheat, highland barley, and sorghum) were compared. Gas chromatography–mass spectrometry (GC-MS) and sensory evaluation were used to determine the composition of the aromatic compounds. A correlation analysis was further conducted between the aromatic compounds and sensory evaluations. Barley whiskey and wheat whiskey had more pronounced fruity, floral, and grain aromas, attributed to esters and terpenes. Barley whiskey had the most compounds (55), followed by highland barley whiskey (54). Highland barley whiskey had the greatest number of unique aroma compounds (seven). It exhibited a unique cocoa aroma related to concentrations of trans-2-nonenal, γ-nonanolactone, 1-nonanol, isoamyl lactate, 2-butanol, and 6-methyl-5-hepten-2-one. Sorghum whiskey had a specific leather and mushroom aroma attributed to 6-methyl-5-hepten-2-one, ethyl lactate, ethyl caprate, phenethyl octanoate, farnesol, α-terpineol, 3-methyl-1-pentanol, and methyleugenol. Alcohols were the main aroma components of grain whiskeys. Isoamyl alcohol (231.59~281.39 mg/L), phenylethyl alcohol (5.755~9.158 mg/L), citronellol (0.224~4.103 mg/L), β-damascenone (0.021~2.431 mg/L), geraniol (0.286~1.416 mg/L), isoamyl acetate (0.157~0.918 mg/L), phenylacetaldehyde (0.162~0.470 mg/L), linalool (0.024~0.148 mg/L), 1-octen-3-ol (0.016~0.145 mg/L), trans-2-nonenal (0.027~0.105 mg/L), and trans-2-octen-1-ol (0.011~0.054 mg/L) were all important aroma compounds in the whiskeys. [ABSTRACT FROM AUTHOR]

Kaffir lime juice, often treated as production waste, can be a good source of terpenes. These compounds undergo various decomposition processes under the influence of external factors, especially during transportation and storage. In this paper, it was possible to monitor changes in the terpene profile of kaffir lime juice under different storage conditions, namely, 4 °C, 20 °C, and 35 °C. The identification of key decomposition products was achieved using gas chromatography–mass spectrometry (GC–MS) and a data mining protocol. It was followed by tracing those products in different storage conditions using a high-throughput proton transfer reaction mass spectrometry (PTR–MS) approach. Based on our findings, degradation pathways were presented, showing that the main products resulting from storage are p-cymene, p-cymenene, terpinene-4-ol, and α-terpineol. It was shown that conversion to p-cymenene occurs after 5 days of storage. Terpinene-4-ol and α-terpineol were found to be the final products of the conversion at all temperatures. Changes in the composition of terpenes are important from the point of view of their bioactive properties. [ABSTRACT FROM AUTHOR]

Overview of the Special Issue Puscas et al. (2022) [[1]] published a research paper entitled "Cytotoxicity Evaluation and Antioxidant Activity of a Novel Drink Based on Roasted Avocado Seed Powder". The purpose of this Special Issue entitled "Spicy and Aromatic Plants" is to expand our knowledge about edible plants, which have been used for thousands of years, by all the peoples of the world, in every household. References 1 Puscas A., Tanislav A.E., Marc R.A., Muresan V., Muresan A.E., Pall E., Cerbu C. Cytotoxicity Evaluation and Antioxidant Activity of a Novel Drink Based on Roasted Avocado Seed Powder. [Extracted from the article]

Fluorine is a naturally occurring element found in soil, water, food materials, and natural minerals such as fluorapatite, sellaite, and cryolite and exists as fluoride compounds with other elements because of high reactivity. The exposure of fluoride to the environment and human beings are industrial factors, food, water, and geogenic factors that impact the health of millions of human beings worldwide. Overexposure to fluoride exceeding the permissible limit (1.5 mg/l as per WHO) causes several diseases in human beings, such as teeth mottling, thyroid inflammation, dental fluorosis, skeletal fluorosis, lesions in the kidney, and other organs. To overcome the deleterious impact of fluoride, its detection at an early stage is very much required. Therefore, feeling the importance of the same, immense efforts have been made to the selective and sensitive determination of fluoride in water by numerous researchers. This review paper summarizes the various conventional methods such as spectroscopic, ion chromatography, ICP-OES, and gas chromatography-mass spectrometry, their advantages, and drawbacks leading to the development of advanced ready-to-use detection strategies such as stamartphones for on-the-spot fluoride detection. This review paper also discusses future directions, which will assist scientists in achieving a new benchmark in developing a reliable, cost-effective, and user-friendly fluoride detector. [ABSTRACT FROM AUTHOR]