PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Pyrolysis”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,315 records · Page 73Linked to original sources

The feasibility of inert colloidal processing of silicon nanoparticles.

Silicon nanoparticles have important applications, including nonvolatile floating-gate memory devices. To prevent device performance variations, particle size and oxide thicknesses need to be controlled with a high degree of precision. Additionally, producing well-ordered, two-dimensional arrays of nanoparticles may require the exploitation of self-assembly techniques and colloidal forces, which in turn requires that silicon nanoparticles first come into contact with liquids. Until recently, aerosol silicon nanoparticle collection into liquid was assumed to be an inert process. Once formed, the silicon nanoparticle colloid was assumed to be inert. In fact, silicon nanoparticles produced in the aerosol phase by dilute silane pyrolysis and size classified with a differential mobility analyzer undergo a size reduction upon collection in ethylene glycol, water, and ethanol. Unclassified polydisperse silicon aerosol nanoparticles with an average diameter of 11 nm become monodisperse when collected in a colloid and have a final particle diameter of 2-5 nm. Further evidence suggests that silicon nanoparticles collected in ethanol react with the ethanol to produce tetraalkylorthosilicate-like species. Collections of aerosol silicon nanoparticles in degassed water do not show measurable differences between the aerosol and colloidal size distributions. This reduced reactivity to the solvent indicates that the presence of dissolved oxygen in the solvent may be responsible for the reactivity between the silicon nanoparticles and the solvent.

Journal Article↗

Thermal stability of organic monolayers chemically grafted to minerals.

The thermal degradation of monolayers of alkylsilicon hydrides (RSiH(3)), alkylphosphonic acids (RP(O)(OH)(2)), and alkyldimethylchlorosilanes (R(CH(3))(2)SiCl) supported on silica, alumina, titania, zirconia, and calcium hydroxyapatite particles was investigated using thermal gravimetric analysis (TGA). The common feature in the TGA was a dramatic weight loss between approximately 200 and approximately 600 degrees C (N(2) atmosphere), which was not present for bare minerals, and, thus, was assigned to the degradation of the surface grafted organic species. The onset of weight loss and the temperature of maximal weight loss rate (T(MAX)) showed no dependence on the mineral and were determined by the nature of the chemical group directly attached to the surface. The T(MAX) values were approximately 400-450 degrees C (monolayers of RSiH(3) and RP(O)(OH)(2)) and approximately 250 degrees C (monolayers of RSi(CH(3))(2)Cl). The activation energies (E(A)) of the degradation processes were determined using TGA at multiple heating rates. Surprisingly, the substrate material did not show a significant effect on E(A). For example, all the monolayers of octadecyl groups (R=C(18)H(37)) supported on silica, alumina, titania, and zirconia showed closed E(A) values approximately 265+/-15 kJ/mol. The weight loss, IR, MS, and chemical analysis data suggested that monolayer degradation occurred through pyrolysis of the hydrocarbon moieties (R groups) via cleavage of the CC and SiC (monolayers of silanes) or CC and PC bonds (monolayers of phosphonic acids). The inorganic portion of the molecule remained attached to the surface of the mineral (presumably as silicates or phosphates).

Journal Article↗

Examination of cadmium sorption characteristics for a boreal soil near Fairbanks, Alaska.

The objective of this research was to better understand cadmium (Cd) mobility in an organic-rich, boreal soil. Cadmium was selected for the study because of its tendency to be more mobile in soils than other heavy metals, such as lead or mercury. The release of metals from soil is a concern for northern regions where soils are gradually warming, resulting in an increased rate of natural organic matter (NOM) decomposition and soil erosion. Soil samples were collected from three principle soil horizons at a research site in the Caribou-Poker Creeks Research Watershed (CPCRW), near Fairbanks, Alaska. A dilute Cd solution was added to the soil and the soil solution was allowed to mix for 72 h. The soil solution was then passed through a 75 microm sieve and a 0.3 microm filter. Particulate samples retained on the sieve and filter were analyzed by atomic absorption (AA) to determine how much Cd was bound to the different size particles. The NOM in each particle size fraction was analyzed by pyrolysis-gas chromatography/mass spectrometry (py-GC/MS) to determine the nature of the NOM present. Our results showed that the concentration of Cd was almost equal for the different particle sizes in each horizon. That is, the amount of Cd associated with particles larger than 75 microm was nearly the same, on a per mass basis, as the amount of Cd associated with particles ranging in size between 0.3 and 75 microm. Since the mass ratio of Cd to solids normally increases as particle size decreases, this result suggested unusual sorption behavior. Based on the Cd distribution among the particles and the percentage of NOM in each particle size range, it is believed that NOM is a primary factor influencing the sorption behavior of Cd in the boreal soil tested.

Absorption↗

Adsorption of Paraquat dichloride from aqueous solution by activated carbon derived from used tires.

The removal of pesticide from wastewater under different batch experimental conditions, using a car tire derived activated carbon was investigated. The pesticide utilized in the study was Paraquat dichloride (1,1-dimethyl-4,4-bipyridyl dichloride), which is a well known herbicide. The adsorbent was produced from the pyrolysis and activation of used tires (TAC). The performances of this adsorbent and a commercial activated carbon F300 (CAC) have been compared. It was determined that the adsorption of Paraquat was weakly pH dependent. The effects of particle size, carbon dosage, temperature and the initial concentration of the Paraquat were studied. Further experiments investigating the regeneration capabilities of the tire-supplied carbon were performed. The regenerated carbons that were washed with basic pH solution were found to have the best sorption capacity recovery. It was found that the rate of sorption of Paraquat onto the carbon is very fast with almost 90% of the maximum possible adsorption taking place in the first 5 min. Nevertheless, the batch sorption kinetics was fitted for a first-order reversible reaction, a pseudo-first-order reaction and a pseudo-second-order reaction. The pseudo-second-order chemical reaction model appears to provide the best correlation. The applicability of the Langmuir isotherm for the present system has been evaluated at different temperatures. The isotherms show that the sorption capacity of CAC decreases with temperature and the dominant mechanism of CAC adsorption is physical sorption.

Adsorption↗

Use of a transient model to simulate fluidized bed incineration of sewage sludge.

This paper presents a mathematical model dedicated to fluidized bed incineration of sludge. The main assumptions as well as the principal equations of the model are presented. Basically, this model relies on instantaneous pyrolysis of sludge and on a five zones description of the hydrodynamics into the incinerator. Its originality is essentially due to the introduction of a two-dimensional buffer zone between the bubble and the emulsion phase. The chemistry of the gaseous system is described by chemical equilibrium. Results of a start up procedure have been presented in order to illustrate the ability of the model to describe transient behavior. To validate the model from an energetic point of view, different types of sludge (primary, activated and digested) have been computed and compared to industrial data and to results obtained from a simple calculation. The lower dryness limit corresponds to self incineration of the sludge. The higher one corresponds to maximal thermal level that should not be exceeded within the furnace.

Computer Simulation↗

Recycling of auto shredder residue.

Currently, about 75% of end-of-life vehicle's (ELV) total weight is recycled in EU countries. The remaining 25%, which is called auto shredder residues (ASR) or auto fluff, is disposed of as landfill because of its complexity. It is a major challenge to reduce this percentage of obsolete cars. The European draft directive states that by the year 2006, only 15% of the vehicle's weight can be disposed of at landfill sites and by 2015, this will be reduced to 5%. The draft directive states that a further 10% can be incinerated. The quantities of shredder fluff are likely to increase in the coming years. This is because of the growing number of cars being scrapped, coupled with the increase in the amount of plastics used in cars. In Sweden, some current projects are focusing on recycling of ASR material. In this paper some different alternatives for using this material are reported. The hypothetical injection of ASR into a blast furnace concentrating on ASR's effect to some blast furnace (BF) parameters has been completed using a blast furnace mass balance model. As a result, in principle, ASR can be used as reducing agent in the BF process if certain conditions are met. The particle size of ASR material must be controlled to ensure optimal gasification of the material in the raceway. Regarding the chemical composition of ASR, the non-ferrous content can affect the pig iron quality, which is difficult to rectify at a later point. The most attractive recycling alternative is to use the products obtained from pyrolysis of ASR in appropriate metallurgical processes.

Argon↗

Synthesis, characterization and thermolysis studies on triazole and tetrazole based high nitrogen content high energy materials.

This paper reports the synthesis, characterisation and thermolysis studies of hydrazinium azotetrazolate (HAZ) and 1,1'-dinitro-3,3'-azo-1,2,4-triazole (N-DNAT). TGA and DSC results suggested that HAZ decomposes in the range of 150-180 degrees C and N-DNAT in the range of 160-170 degrees C, respectively. The pattern of decomposition of HAZ dihydrate and N-DNAT has been predicted with the help of pyrolysis GC/MS technique and a probable decomposition mechanism has been proposed. The theoretically predicted performance data suggests the potential nature of HAZ and N-DNAT for their use in propellant/explosive as well as in gas generator formulations.

Hot Temperature↗

Effect of temperature on the release of hexadecane from soil by thermal treatment.

A natural organic soil (2.5% of total organic carbon) was artificially contaminated with hexadecane, and thermally treated under an inert medium up to different final temperatures (150-800 degrees C) for 30 min to simulate ex situ thermal process conditions. The experiments were conducted using a complete organic soil, instead of the clays or isolated soil fractions that are commonly used. Neat and contaminated samples were separately heated to understand the impact of the soil itself and the contaminant in the release of volatiles. The soil quality as well as the quality and amount of volatile compounds generated during the process were monitored. More than 80-88% of the initial hexadecane content in the soil matrix was recovered in liquids traps after the thermal treatment, therefore the contaminant could be recovered for further recycling. The high amount of hexadecane collected without suffering chemical transformations indicated that the main mechanism for the hexadecane removal was evaporation. The analysis of the light gases released from contaminated samples indicated negligible or null hexadecane pyrolysis reaction rates, confirming that the evaporation/desorption of the contaminant are the processes that governed the removal of the contaminant from the soil. For the soil tested, of a relatively low surface area, good removal efficiencies (higher than 99.9%) were detected at about 300 degrees C, being higher temperatures not necessary to significantly improve the contamination removal.

Alkanes↗

Activated carbon from vetiver roots: gas and liquid adsorption studies.

Large quantities of lignocellulosic residues result from the industrial production of essential oil from vetiver grass (Vetiveria zizanioides) roots. These residues could be used for the production of activated carbon. The yield of char obtained after vetiver roots pyrolysis follows an equation recently developed [A. Ouensanga, L. Largitte, M.A. Arsene, The dependence of char yield on the amounts of components in precursors for pyrolysed tropical fruit stones and seeds, Micropor. Mesopor. Mater. 59 (2003) 85-91]. The N(2) adsorption isotherm follows either the Freundlich law K(F)P(alpha) which is the small alpha equation limit of a Weibull shaped isotherm or the classical BET isotherm. The surface area of the activated carbons are determined using the BET method. The K(F) value is proportional to the BET surface area. The alpha value increases slightly when the burn-off increases and also when there is a clear increase in the micropore distribution width.

Adsorption↗

Organic matter transformation in the environment investigated by quantitative electron paramagnetic resonance (EPR) spectroscopy: studies on lignins.

The lignins separated from angiosperm and gymnosperm trees, peat and xylitic brown coal were investigated by quantitative EPR. Observed free radicals in lignins are sensitive to alkaline environment. Gaseous ammonia interacting with solid lignins in resonance cavity shifts quinone-hydroquinone equilibria towards formation of semiquinone anions. Complexation of copper(II) by lignins causes drastic decrease of the semiquinones in the matrices. Formation of lignin-Pb(II) complexes yielded radicals characterised by unusually low g-value (1.9999-2.0003). Monomeric structural units of the investigated lignins were recognised by pyrolysis with in situ methylation by tetramethylammonium hydroxide. Although for the natural lignins the mixture of normal semiquinone signals at g about 2.0034 and signals at g 1.9999 were observed, some monomeric components of lignins (e.g., caffeic acid, pyrogallol) gave pure lines at g = 1.9999. The bacterial oxidative biodegradation of lignin monomeric components and their Pb(II) complexes resulted in increase of the radical signals.

Bacillus subtilis↗

Theoretical prediction of gas-phase infrared spectra of imidazo[1,2-a]pyrazinediones and imidazo[1,2-a]imidazo[1,2-d]pyrazinediones derived from glycine.

Imidazo[1,2-a]pyrazine-3,6-diones and imidazo[1,2-a]imidazo[1,2-d]pyrazine-3,8-diones can be produced by pyrolysis of simple amino acids. While such bicyclic and tricyclic amidines were detected and characterized by IR spectroscopy for some alpha-substituted amino acids, the parent systems composed of glycine fragments are unknown up to now. IR spectra for five amidines derived from glycine were calculated by using different semi-empirical (PM3, AM1, MNDO and MINDO/3), HF, and hybrid DFT (B3LYP, B3P86 and B3PW91) methods in conjunction with 6-31G(d) basis set (for HF and DFT). Vibration frequencies in the experimental IR spectra were predicted based upon the B3LYP data, by correcting the calculated wavenumbers by a scaling factor of 0.959. The behavior of most characteristic bands (nu(CX), nu(NH), etc.) and their shifts with respect to such bands in the spectra of alanine and alpha-aminoisobutyric acid derivatives studied before, are discussed. Performance of the semi-empirical methods was tested, bearing in mind possible future needs for IR spectra predictions for larger molecular systems of similar chemical nature; the use of MINDO/3 and MNDO is recommended. A basis set effect on the B3LYP fundamental vibration frequencies for hexahydroimidazo[1,2-a]pyrazine-3,6-dione was studied by varying Pople basis sets from minimal STO-3G to 6-311++G(d, p). No significant improvements were found beyond the 6-31G(d) basis set, which thus can be recommended to predict IR spectra for the amidines and similar molecules.

Amidines↗

Optical absorption of sodium copper chlorophyllin thin films in UV-vis-NIR region.

The optical absorption studies of sodium copper chlorophyllin thin films (SCC), prepared by spray pyrolysis, in the UV-vis-NIR region was reported for the first time. Several new discrete transitions are observed in the UV-vis region of the spectra in addition to a strong continuum component in the IR region. The spectra of the infrared absorption allow characterization of vibration modes for the powder and thin films of SCC. The absorption spectrum recorded in the UV-vis region showed different absorption bands, namely the Soret (B) in the region 340-450 nm and Q-band in the region 600-700 nm and other band labeled N in the 240-320 region. Some important spectral parameters namely optical absorption coefficient (alpha), molar extinction coefficient (epsilon(molar)), oscillator strength (f), electric dipole strength (q(2)) and absorption half bandwidth (Deltalambda) of the principle optical transitions were evaluated. The analysis of the absorption coefficient in the absorption region revealed direct transitions and the energy gap was estimated as 1.63 eV. Discussion of the obtained results and their comparison with the previous published data are also given.

Absorption↗

Comment on gas phase infrared spectrum and ab initio calculations of phosphorus(III) thiocyanide, SPCN.

We show that two of the three bands assigned to SPCN are assignable to cyanogen and that the bands assigned to SPCl are done so in error, with the 712 cm(-1) band in the spectrum of Allaf and Odeh assignable to HCN. There is no evidence for either ClPS or SPCN in the spectra shown. Finally low resolution IR spectroscopy by itself, whilst useful in assisting in the identification of pyrolysis products does not provide unambiguous identification and requires support by rigorous computation, band modelling and correct use of the literature. None of these are evidenced in the present paper of Allaf and Odeh nor indeed in the work that was the subject of our previous criticism and re-analysis.

Gases↗

Polynuclear transition metal complexes with thiocarbohydrazide and dithiocarbamates.

Sn(tch)2{MCl2}2 was prepared from the precursor Sn(tch)2 and MCl2. It was subsequently allowed to react with diethyldithiocarbamate which yielded the trinuclear complexes of the type Sn(tch)2{M2(dtc)4}, where tch=thiocarbohydrazide, M=Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and dtc=diethyldithiocarbamate. They were characterized on the basis of microanalytical, thermal (TGA/DSC), spectral (IR, UV-vis, EPR, (1)H NMR) studies, conductivity measurement and magnetic moment data. On the basis of spectral data a tetrahedral geometry has been proposed for the halide complexes, Sn(tch)2{MCl2}2 except for Cu(II) which exhibits a square planar coordination although the transition metal ion in Sn(tch)2{M2(dtc)4} achieves an octahedral geometry where the dithiocarbamato moiety acts as a symmetrical bidentate ligand. The bidentate nature has been established by the appearance of a sharp single nu(C-S) around 1000 cm(-1). A downfield shift observed in NH(a) and NH(b) protons on moving from Sn(tch)2 to Sn(tch)2{MCl2}2 is due to the drift of electrons toward metal atoms. A two-step pyrolysis has been observed in the Sn(tch)2{MCl2}2 complexes while their dithiocarbamato derivatives exhibit a three-stage degradation pattern. Finally, the in vitro antibacterial activity of Sn(tch)2{M2(dtc)4} and the mononuclear Sn(tch)2 has been carried out on bacterial strains Escherichia coli and Salmonella typhi. The compounds were found to be active against the test organisms. The activity of the complexes is enhanced with increasing concentration. The maximum activity in both the strains was achieved by cobalt(II) dithiocarbamate complex. Minimum activity was found for Sn(tch)2 which generally increases with the introduction of transition metal ion in the complex.

Anti-Bacterial Agents↗

Phase association of polycyclic aromatic hydrocarbons in the Minjiang River Estuary, China.

Persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) are of great concern due to their persistence, bioaccumulation and toxic effects. In this work the levels of 16 priority PAHs were determined in water, pore water, sediment, soil and vegetable samples from Minjiang River Estuary, China. Total PAH concentrations varied from 9.9 to 474 microg/l in water, 82.1 to 239 microg/l in pore water, 112 to 877 ng/g dry wt. in surficial sediments, 128 to 465 ng/g dry wt. in soil and 8600 to 111,000 ng/g dry wt. in Chinese vegetables. Overall, the mean concentrations of PAHs were present in higher levels in pore water than that in surface water, due possibly to higher concentrations of dissolved organic carbon or colloids with which the hydrophobic pollutants were strongly associated. Such a concentration gradient implies a potential flux of pollutants from sediment pore water to overlying water. Contamination was dominated by high molecular mass PAH compounds in all samples, indicating combustion-derived sources (for example, pyrolysis at high temperature). The levels of PAHs in water and vegetable were relatively high in comparison to other studies, although PAHs in sediment and soil were comparable to those found in many other similar environments. The ratios of selected PAHs indicated again that PAHs in Minjiang River Estuary were mainly derived from incomplete combustion of fossil fuel.

China↗

Characteristic of polycyclic aromatic hydrocarbon concentrations and source identification for fine and coarse particulates at Taichung Harbor near Taiwan Strait during 2004-2005.

Fine (PM(2.5)) and coarse (PM(2.5-10)) particulate concentrations of ambient air polycyclic aromatic hydrocarbons (PAHs) were measured simultaneously from February 2004 to January 2005 at the Taichung Harbor (TH) sampling site near Taiwan of central Taiwan. Particle-bound polycyclic aromatic hydrocarbons (PAHs) were collected on quartz filters; the collected sample was Soxhlet extracted with a dichloromethane (DCM)/n-hexane mixture (50/50, v/v) for 24 h, and then the extracts were analyzed by gas chromatography-mass spectrometry (GC-MS). The results indicated that vehicle emissions, coal combustion, incomplete combustion and pyrolysis of fuel and oil burning were the main source of PAHs near Taiwan Strait of central Taiwan. Diagnostic ratios and principal component analysis (PCA) were also used to characterize and identify PAHs emission sources in this study.

Air Pollutants↗

Mercury in urban soils: a comparison of local spatial variability in six European cities.

The objective of this study was to quantify and assess for the first time the variability of total mercury in urban soils at a European level, using a systematic sampling strategy and a common methodology. We report results from a comparison between soil samples from Aveiro (Portugal), Glasgow (Scotland), Ljubljana (Slovenia), Sevilla (Spain), Torino (Italy) and Uppsala (Sweden). At least 25 sampling points (in about 4-5 ha) from a park in each city were sampled at two depths (0-10 and 10-20 cm). Total mercury was determined by pyrolysis atomic absorption spectrometry with gold amalgamation. The quality of results was monitored using certified reference materials (BCR 142R and BCR 141R). Measured total mercury contents varied from 0.015 to 6.3 mg kg(-1). The lowest median values were found in Aveiro, for both surface (0-10 cm) and sub-surface (10-20 cm) samples (0.055 and 0.054 mg kg(-1), respectively). The highest median mercury contents in soil samples were found in samples from Glasgow (1.2 and 1.3 mg kg(-1), for surface and sub-surface samples, respectively). High variability of mercury concentrations was observed, both within each park and between cities. This variability reflecting contributions from natural background, previous anthropogenic activities and differences in the ages of cities and land use, local environmental conditions as well as the influence of their location within the urban area. Short-range variability of mercury concentrations was found to be up to an order of magnitude over the distance of only a few 10 m.

Cities↗