scholarly journals Non-Destructive Detection of Pentachlorophenol Residues in Historical Wooden Objects

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1052
Author(s):  
Ida Kraševec ◽  
Nataša Nemeček ◽  
Maja Lozar Štamcar ◽  
Irena Kralj Cigić ◽  
Helena Prosen
Keyword(s):  
Indoor Air ◽  
Room Temperature ◽  
Quantitative Methods ◽  
Solid Phase ◽  
Contact Mode ◽  
Solvent Extraction Method ◽  
Museum Objects ◽  
Wooden Furniture ◽  
Non Destructive ◽  
Heritage Collections

Wood is a natural polymeric material that is an important constituent of many heritage collections. Because of its susceptibility to biodegradation, it is often chemically treated with substances that can be harmful to human health. One of the most widely used wood preservatives was pentachlorophenol (PCP), which is still present in museum objects today, although its use has been restricted for about forty years. The development of non-destructive methods for its determination, suitable for the analysis of valuable objects, is therefore of great importance. In this work, two non-destructive solid-phase microextraction (SPME) methods were developed and optimized, using either headspace or contact mode. They were compared with a destructive solvent extraction method and found to be suitable for quantification in the range of 7.5 to 75 mg PCP/kg wood at room temperature. The developed semi-quantitative methods were applied in the wooden furniture depot of National Museum of Slovenia. PCP was detected inside two furniture objects using headspace mode. The pesticide lindane was also detected in one object. The indoor air of the depot with furniture was also sampled with HS SPME, and traces of PCP were found. According to the results, SPME methods are suitable for the detection of PCP residues in museum objects and in the environment.

scholarly journals Plasticiser loss in heritage collections: its prevalence, cause, effect, and methods for analysis

2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Rose King ◽  
Josep Grau-Bové ◽  
Katherine Curran
Keyword(s):  
Indoor Air ◽  
Science Research ◽  
Conservation Practices ◽  
Preventive Conservation ◽  
Migration Rates ◽  
Poly Vinyl Chloride ◽  
Surrounding Environment ◽  
Heritage Science ◽  
Non Destructive ◽  
Heritage Collections

AbstractPlasticiser loss is a topic frequently mentioned in discussions on the degradation of plastic artefacts in museum collections, particularly for plasticised poly (vinyl chloride) and cellulose acetate. Plasticisers may migrate to the plastic’s surface and remain as a deposit, or volatilise into the surrounding environment, both presenting an aesthetic issue and impacting the future stability of the plastic. This paper draws on the work of conservation science, materials degradation, and indoor air quality/emissions studies, to review our current understanding of plasticiser loss. The influence of the material’s intrinsic properties, and environmental factors on migration rates are discussed and related to preventive conservation practices. The methods by which plasticiser migration is studied, including characterisation, are also reviewed, with a particular focus on minimally invasive and non-destructive methods suitable for heritage science research.

scholarly journals 68Ga, 44Sc and 177Lu-labeled AAZTA5-PSMA-617: synthesis, radiolabeling, stability and cell binding compared to DOTA-PSMA-617 analogues

2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Jean-Philippe Sinnes ◽  
Ulrike Bauder-Wüst ◽  
Martin Schäfer ◽  
Euy Sung Moon ◽  
Klaus Kopka ◽  
...  
Keyword(s):  
Human Serum ◽  
Room Temperature ◽  
Solid Phase ◽  
Negative Influence ◽  
Binding Motif ◽  
Lncap Cells ◽  
Cell Binding ◽  
Binding Characteristics

Abstract Background The AAZTA chelator and in particular its bifunctional derivative AAZTA5 was recently investigated to demonstrate unique capabilities to complex diagnostic and therapeutic trivalent radiometals under mild conditions. This study presents a comparison of 68Ga, 44Sc and 177Lu-labeled AAZTA5-PSMA-617 with DOTA-PSMA-617 analogues. We evaluated the radiolabeling characteristics, in vitro stability of the radiolabeled compounds and evaluated their binding affinity and internalization behavior on LNCaP tumor cells in direct comparison to the radiolabeled DOTA-conjugated PSMA-617 analogs. Results AAZTA5 was synthesized in a five-step synthesis and coupled to the PSMA-617 backbone on solid phase. Radiochemical evaluation of AAZTA5-PSMA-617 with 68Ga, 44Sc and 177Lu achieved quantitative radiolabeling of > 99% after less than 5 min at room temperature. Stabilities against human serum, PBS buffer and EDTA and DTPA solutions were analyzed. While there was a small degradation of the 68Ga complex over 2 h in human serum, PBS and EDTA/DTPA, the 44Sc and 177Lu complexes were stable at 2 h and remained stable over 8 h and 1 day. For all three compounds, i.e. [natGa]Ga-AAZTA5-PSMA-617, [natSc]Sc-AAZTA5-PSMA-617 and [natLu]Lu-AAZTA5-PSMA-617, in vitro studies on PSMA-positive LNCaP cells were performed in direct comparison to radiolabeled DOTA-PSMA-617 yielding the corresponding inhibition constants (Ki). Ki values were in the range of 8–31 nM values which correspond with those of [natGa]Ga-DOTA-PSMA-617, [natSc]Sc-DOTA-PSMA-617 and [natLu]Lu-DOTA-PSMA-617, i.e. 5–7 nM, respectively. Internalization studies demonstrated cellular membrane to internalization ratios for the radiolabeled 68Ga, 44Sc and 177Lu-AAZTA5-PSMA-617 tracers (13–20%IA/106 cells) in the same range as the ones of the three radiolabeled DOTA-PSMA-617 tracers (17–20%IA/106 cells) in the same assay. Conclusions The AAZTA5-PSMA-617 structure proved fast and quantitative radiolabeling with all three radiometal complexes at room temperature, excellent stability with 44Sc, very high stability with 177Lu and medium stability with 68Ga in human serum, PBS and EDTA/DTPA solutions. All three AAZTA5-PSMA-617 tracers showed binding affinities and internalization ratios in LNCaP cells comparable with that of radiolabeled DOTA-PSMA-617 analogues. Therefore, the exchange of the chelator DOTA with AAZTA5 within the PSMA-617 binding motif has no negative influence on in vitro LNCaP cell binding characteristics. In combination with the faster and milder radiolabeling features, AAZTA5-PSMA-617 thus demonstrates promising potential for in vivo application for theranostics of prostate cancer.

scholarly journals Ag Nanoparticles Sensitized In2O3 Nanograin for the Ultrasensitive HCHO Detection at Room Temperature

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Shiqiang Zhou ◽  
Mingpeng Chen ◽  
Qingjie Lu ◽  
Yumin Zhang ◽  
Jin Zhang ◽  
...  
Keyword(s):  
Indoor Air ◽  
Ag Nanoparticles ◽  
Room Temperature ◽  
Unsolved Problem ◽  
Air Pollutant ◽  
Ag Nps ◽  
Performance Targets ◽  
Fabrication Cost ◽  
Low Concentrations ◽  
Stringent Performance

AbstractFormaldehyde (HCHO) is the main source of indoor air pollutant. HCHO sensors are therefore of paramount importance for timely detection in daily life. However, existing sensors do not meet the stringent performance targets, while deactivation due to sensing detection at room temperature, for example, at extremely low concentration of formaldehyde (especially lower than 0.08 ppm), is a widely unsolved problem. Herein, we present the Ag nanoparticles (Ag NPs) sensitized dispersed In2O3 nanograin via a low-fabrication-cost hydrothermal strategy, where the Ag NPs reduces the apparent activation energy for HCHO transporting into and out of the In2O3 nanoparticles, while low concentrations detection at low working temperature is realized. The pristine In2O3 exhibits a sluggish response (Ra/Rg = 4.14 to 10 ppm) with incomplete recovery to HCHO gas. After Ag functionalization, the 5%Ag-In2O3 sensor shows a dramatically enhanced response (135) with a short response time (102 s) and recovery time (157 s) to 1 ppm HCHO gas at 30 °C, which benefits from the Ag NPs that electronically and chemically sensitize the crystal In2O3 nanograin, greatly enhancing the selectivity and sensitivity.

Room temperature rectification in tapered-channel thermal diodes through nanoscale confinement-induced liquid–solid phase change

2021 ◽  
Vol 129 (7) ◽  
pp. 075103
Author(s):  
Matt Jacobs ◽  
Xinran Zhou ◽  
Edgar Olivera ◽  
Ryan Sheil ◽  
Shu Huang ◽  
...  
Keyword(s):  
Phase Change ◽  
Room Temperature ◽  
Solid Phase ◽  
Tapered Channel

scholarly journals The effect of short-term storage temperature on the key headspace volatile compounds observed in Canadian faba bean flour

2021 ◽  
pp. 108201322199884
Author(s):  
Rami Akkad ◽  
Ereddad Kharraz ◽  
Jay Han ◽  
James D House ◽  
Jonathan M Curtis
Keyword(s):  
Fatty Acids ◽  
Volatile Compounds ◽  
Room Temperature ◽  
Unsaturated Fatty Acids ◽  
Solid Phase ◽  
Short Term ◽  
Bean Flour ◽  
Odour Activity Value ◽  
Short Term Storage ◽  
Term Storage

The odour emitted from the high-tannin fab bean flour ( Vicia faba var. minor), was characterized by headspace solid-phase microextraction/gas chromatography-mass spectrometry (HS-SPME/GC–MS). The relative odour activity value (ROAV) was used to monitor the changes in key volatile compounds in the flour during short-term storage at different temperature conditions. The key flavour compounds of freshly milled flour included hexanal, octanal, nonanal, decanal, 3-methylbutanal, phenyl acetaldehyde, (E)-2-nonenal, 1-hexanol, phenyl ethyl alcohol, 1-octen-3-ol, β-linalool, acetic acid, octanoic acid, and 3-methylbutyric acid; these are oxidative degradation products of unsaturated fatty acids and amino acids. Despite the low lipid content of faba beans, the abundances of aldehydes arising during room temperature storage greatly contributed to the flavour of the flour due to their very low odour thresholds. Two of the key volatiles responsible for beany flavour in flour (hexanal, nonanal) increased greatly after 2 weeks of storage at room temperature or under refrigerated conditions. These volatile oxidation products may arise as a result of enzymatic activity on unsaturated fatty acids, and was seen to be arrested by freezing the flour.

The formation of iron(III) oxide hydroxides from iron(II) oxalate

1976 ◽  
Vol 29 (10) ◽  
pp. 2149 ◽  
Author(s):  
RJ Atkinson
Keyword(s):  
Sodium Hydroxide ◽  
Intermediate Product ◽  
Room Temperature ◽  
Oxidation Process ◽  
Solid Phase ◽  
Bubble Flow ◽  
Air Bubble ◽  
Dissolved Iron ◽  
Complete Reaction ◽  
Iron Concentrations

FeC2O4,2H2O(s) suspensions in sodium hydroxide solutions were oxidized by a fast air-bubble flow at room temperature until complete reaction had occurred. With amounts of NaOH in the range OH/Fe initial mole ratio ≤1.0, the reaction is FeC2O4, 2H2(s)+ OH-(aq)+ �O2(g) → ⅔γFeOOH(s)+1/3Fe(C2O4)33-(aq)+13/6H2O With OH/Fe mole ratio ≥ 2.0 the reaction is FeC2O4, 2H2(s)+ 2OH-(aq)+ �O2(g) → αFeOOH(s)+(C2O4)33-(aq)+ 5/2 H2O Mixtures of goethite (α-FeOOH) and lepidocrocite (γ-FeOOH) form at intermediate OH/Fe mole ratio. The oxidation process occurs in a solid-phase intermediate product. Comparisons with similar oxidations of iron(11)sulphate solutions showed that γ-FeOOH formation was favoured and α-FeOOH formation inhibited in the iron(11) oxalate oxidation. These differences are related to pH and dissolved iron concentrations.

THE SYSTEM: BISMUTH–CADMIUM–MERCURY

1965 ◽  
Vol 43 (7) ◽  
pp. 1924-1928 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark
Keyword(s):  
Binary System ◽  
Ternary Alloy ◽  
Room Temperature ◽  
Solid Phase ◽  
Liquidus Surface ◽  
Molar Volumes ◽  
X Ray

The liquidus surface of this ternary alloy has been determined, together with the nature of the solid phase separating from various melts. The densities and molar volumes of the binary system: Cd—Hg have been determined and it is shown that there is marked contraction when the α and β phases form from the components. X-ray powder photographs of various Cd—Hg alloys at room temperature have been made and the limits of homogeneity determined.

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