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PubMed1989

Pulpal and micro-organism responses to two experimental dental bonding systems.

Several new bonding systems have been reported that promote strong adhesion. This in vivo study involves treatment with two experimental bonding systems of Class V cavity preparations in the teeth of three Macaca fascicularis primates and reports the pulpal responses and degree of micro-organism invasion associated with each treatment. In each monkey, the teeth in the upper left quadrant were treated with the experimental solution, containing 2.5% aluminum nitrate + 1.5% oxalic acid + 4.9% NPG, followed by application of PMDM and Silux XL composite. The lower right quadrant was treated with the experimental solution, containing 5.7% NPG + 2.4% nitric acid, followed by PMDM and Silux XL composite. The upper right and lower left quadrants were treated with clinical materials to establish positive and negative controls. After four, 25, and 59 days, the teeth were removed and underwent routine histological and bacteriological evaluation. Slight pathological conditions were noted for superficial and deep responses, but all values approached 0.0 by the 59th day. Micro-organisms were seen under only 12% of the restorations. Both experimental systems appear to be safe for human clinical trials.

Animals↗

PubMed2004

Controlled dissolution for elemental analysis of sample layers by inductively coupled plasma-mass spectrometry: a feasibility study.

Aqueous acid mixtures at room temperature are used to partially dissolve steel samples. The dissolved elements are washed off the surface, diluted, and then determined by inductively coupled plasma-mass spectrometry (ICP-MS) using a magnetic sector mass analyzer. The amount of material removed is measured from the amount of Fe dissolved and increases linearly with HNO(3) concentration in the etch acid. Analyte concentrations in the solid are determined from the signal ratio of analyte ion/Fe(+). The shape of a plot of mass of element removed vs. nitric acid concentration yields information about the efficiency of the removal process and the likely chemical form of the element in the sample. For elements like Mn, Al, and W in steel, these plots have the same linear shape as that for the major element (Fe), and the measured concentrations agree well with the certified values. For problem elements like Nb and Ta, the plots have two linear regions with different slopes, and measured concentrations are lower than the certified values. Laser ablation ICP-MS and scanning electron microscopy (SEM) measurements show these elements to be associated together in the solid in refractory grains that are not dissolved to the same extent as the Fe matrix. For steel, the amount of Fe dissolved corresponds to an average depth of at least 4 microm, or 20 000 atomic layers.

Journal Article↗

PubMed1983

[Determination of the nutritional value of lignocellulose materials].

The determination of the nutritive value of various secondary wood products was conducted by the method of the in-vitro digestibility of dry matter (Mellenberger et al., 1970) and by detergent analyses of fibre (Goering and Van Soest, 1970). Rumen contents for trials in vitro were obtained from adult wethers having a permanent rumen fistula and fed good meadow hay ad lib. The animals also had free access to water and mineral lick for sheep. Out of the 11 lignocellulose materials tested, digestibility in vitro higher than 60% (equivalent to the digestibility of high-quality meadow hay) was only found in three samples. These are: a) beech sawdust II treated with 0.1M sulphuric acid at the hydromodulus of 1:8, temperature 100 to 130 degrees C for two hours, and pressure of 0.25 MPa and then with 0.47M nitric acid at the hydromodulus of 1:13, temperature 100 degrees C for two hours and pressure of 0.25 MPa; b) beech sawdust III treated as beech sawdust II and then neutralized with ammonia to pH 8; c) aspen sawdust treated hydrobarothermically at a temperature of 280 degrees C and pressure of 7 MPa in saturated vapour medium (Canon system). The high digestibility of these samples was due to a low lignin content so that the polysaccharides (cellulose and hemicelluloses) of these secondary wood sources could be sufficiently utilized by rumen microflora.

Animals↗

PubMed1997

Intracolonic release of nitric oxide during trinitrobenzene sulfonic acid rat colitis.

Nitric oxide is thought to play an important role in modulating the inflammatory process. Recently an increase in the inducible form of nitric oxide synthase (iNOS) has been found in the rat trinitrobenzene sulfonic acid model of experimental colitis, and inhibition of nitric oxide synthase activity resulted in an amelioration of tissue injury. The aim of our study was to evaluate in vivo intracolonic release of nitric oxide in this model of colitis. Experimental colitis was induced in male Sprague-Dawley rats by a single intracolonic administration of trinitrobenzene sulfonic acid. Nitrite levels were determined in rectal dialysates by HPLC. The tissue myeloperoxidase and iNOS and the luminal leukotriene B4 were also measured. Nitrite levels were significantly increased in rectal dialysates during colitis and correlated significantly with tissue myeloperoxidase and iNOS activity. The correlation between nitrite dialysate levels and wall iNOS activity confirms that nitrite in dialysates is produced by inflammatory cells and not by colonic bacterial flora. Determination of nitrite levels in rectal dialysates seems a valuable method to monitor colonic inflammation in rat trinitrobenzene sulfonic acid colitis.

Animals↗

PubMed1999

Effect of passivation on the dissolution behavior of Ti6A14V and vacuum-brazed Ti6A14V in Hank's ethylene diamine tetra-acetic acid solution Part I Ion release.

This work aims to investigate the effects of three factors, namely: (1) two differently prepared materials (as-polished Ti6A14V and 2 h brazed Ti6A14V); (2) three different surface passivation treatments (34% nitric acid passivation, 400 degrees C heated in air, and aged in 100 degrees C de-ionized water); and (3) periods of immersion time (up to 32 days), on trace element release in Hank's ethylene diamine tetra-acetic acid (EDTA) solution. After passivation and autoclaving treatment, the specimens were immersed in 8.0 mM EDTA in Hank's solution and maintained at 37 degrees C for periods of time up to 32 days. The 400 degrees C -treated specimens exhibit a substantial reduction in constituent release, which may be attributed to the higher thickness and rutile structure of the surface oxides. For acid-passivated and water-aged treatments, a highly significant decrease in the trace levels of Ti, A1, and V is detected from the brazed Ti6A14V compared to those obtained from the Ti6A14V specimens. It is hypothesized that an anatase-rutile transformation of surface TiO_2 is likely to occur, accelerated by the elements of copper and nickel in the brazed specimens. In addition, a significant time-related decrease in constituent release rate is observed for all kinds of specimens throughout the 0-8 day experimental period. The implication of the results is discussed.

Journal Article↗

PubMed2005

Removal of copper from industrial sludge by traditional and microwave acid extraction.

This work elucidates the removal of copper from industrial sludge by traditional and microwave acid extraction. The effects of acid concentration, extraction time, sludge particle size and solid/liquid (S/L) ratio on copper removal efficiency were evaluated. Leaching with more concentrated acid yielded greater copper content from the industrial sludge. The experimental findings reveal that the most economical traditional extraction conditions were the use of 1N sulfuric or nitric acid for 60 min at an S/L ratio of 1/20; however, at an S/L ratio of 1/6, the extraction time needed to achieve the same copper removal efficiency was increased to 36 h. Increasing the microwave power and reducing the S/L ratio increased the copper extraction efficiency and the effect in the larger S/L ratio system was more significant. A comparison of the results of microwave-assisted (microwave only) and microwave-enhanced (microwave with addition of active carbon) acid extraction demonstrated that under both conditions, S/L ratio=1/6 and 1/20; adding active carbon shortened the extraction time required to achieve 80% copper extraction efficiency from 20 to 10 min. These experimental results indicate that the most important factors that most strongly affected microwave acid extraction were the addition of a microwave absorber, the microwave power input and the S/L ratio. The sludge particle size did not significantly affect the copper extraction. The results reveal that sulfuric acid was an effective extractant and that the copper fraction in the extracted sludge shifted from being mostly bound to the Fe-Mn oxides and organic matter, to being mostly bound to organic matter and remaining as a residue during acid extraction.

Acids↗

PubMed1984

A rapid and safe method of estimating nanomole quantities of P, K+, Na+, Ca2+, and Mg2+ in plant material by perchloric acid digestion.

A method for the determination of nanomole amounts of P and major cations in samples of dried plant tissue is described. Samples weighing 2-7 mg were digested by refluxing tissue in a mixture of perchloric and nitric acids, under conditions which minimized the hazards associated with perchloric acid digestion. In most tissues analyzed, reproducibility between triplicate samples was less than +/- 5%. However, where the amount of P in the tissue was very low (samples contained about 50 nmol P each), the variation between triplicates was greater.

Calcium↗

PubMed2000

Assessment of decalcifying protocols for detection of specific RNA by non-radioactive in situ hybridization in calcified tissues.

For the best performance of in situ analysis of specific RNA expression in calcified tissues, it is necessary to choose an appropriate protocol to decalcify the tissues. We evaluated the usefulness of various acid-based decalcifying reagents with reference to 28 S rRNA staining by in situ hybridization using a thymine-thymine dimerized oligonucleotide probe. The reagents evaluated were 10% nitric acid, 10% HCl, 5% formic acid, 5% trichloroacetic acid, Morse's solution, Plank-Rychlo's solution, and K-CX solution, all of which are commonly used to decalcify tissues, and their effects on retention of morphology and RNA were compared with EDTA-based solutions. When normal mouse mandible was used as a model tissue, well-preserved morphology of ameloblasts was obtained from sections decalcified with Morse's solution, 10% HCl, Plank-Rychlo's solution, and K-CX solution, and best retention of 28 S rRNA was obtained with 5% formic acid and Morse's solution. We recommend Morse's solution to decalcify tissues to be processed for the rapid analysis of specific RNA expression. Indeed, we detected specific mRNAs strongly in sections treated with Morse's solution, and quantitative analysis showed that the ratio of signal intensities of 28 S rRNA and the specific mRNAs correlated with each other depending on decalcifying solutions.

Animals↗

PubMed2006

Modeling of electrodialytic and dialytic removal of Cr, Cu and As from CCA-treated wood chips.

A one-dimensional model is developed for simulating the electrodialytic and dialytic treatment of a saturated bed of wood chips containing chromium, copper and arsenic. The movement of Cr, Cu and As is mathematically modeled taking into account the diffusion transport resulting from the concentration gradients of their compounds and the electromigration of their ionic, simple and complex species during the operation. The model also includes the electromigration of the non-contaminant principal ionic species in the system, H(+) and OH(-), proceeding from the electrolysis at the electrodes, Na(+) and NO(3)(-) used as electrolyte solutions in the electrode compartments, and oxalate ions and protons incorporated with the oxalic acid solution during wood chips incubation. The model simulation also takes into account that OH(-) generated on the cathode, during electrodialytic remediation, is periodically neutralized by addition of nitric acid in the cathode compartment. The anion and cation-exchange membranes are simply represented as ionic filters that preclude the transport of co-ions (the cations and anions respectively) with the exception of H(+), which is retarded but considered to pass through the anion-exchange membrane.

Arsenates↗

PubMed2002

Microwave-assisted Acid decomposition of animal- and plant-derived samples for element analysis.

A single microwave-assisted acid-decomposition procedure is proposed for sample preparation of plant- and bovine-derived materials prior to multielement determination by inductively coupled plasma-optical emission spectrometry (ICP-OES). The procedure involved sample grinding in a cryogenic mill to reduce particle sizes and increase the surface area for acid attack, followed by decomposition under high pressure and temperature. A single heating program was employed and efficiently destroyed most of the organic matrix by using small volumes of nitric acid and hydrogen peroxide. Accuracy of the elemental analysis was indicated by the good agreement between certified and found values of elements in plant and animal samples at 95% confidence level. The sample preparation procedure was fast and reproducible, and proved to be efficient for elemental analysis in agricultural and food-related samples by a sensitive multielement technique such as ICP-OES.

Animals↗

PubMed2004

Morphological investigation of chemically treated poly(ethylene terephthalate)-based activated carbons.

Complementary techniques, including low-temperature nitrogen adsorption and small-angle X-ray scattering (SAXS), are applied to detect the effects of surface functionalization on the morphology of activated carbon derived from poly(ethylene terephthalate) (PET). Scanning electron microscopy (SEM) is also employed as an auxiliary method to visualize the surface below the micron scale. The SEM images reveal a micron-sized ridgelike texture. Room temperature acid treatment makes the ridges become more pronounced, while treatment with boiling acid uncovers fiberlike structures of roughly 1 microm diameter. All samples display an apparent surface fractal dimension of Ds = 2.4 in the wave vector range 0.001-0.02 A(-1). Nitric acid at room temperature increases the surface oxygen content only by 3 at. %, while all the adsorption properties and structural parameters reported in this paper are virtually unaffected. Significant differences in the morphology at submicron scales appear only after boiling acid treatment. The resulting carbon remains highly microporous, but the loss of Brunauer-Emmett-Teller (BET) surface area from about 1150 to 304 m2/g is approximately 75%. In addition to the principal peak at around 8 A, fresh peaks appear in the polydisperse Horvath-Kawazoe (HK) pore size distribution owing to the burnoff of intervening walls. The average width of the slitlike pores calculated from the Dubinin-Radushkevich (DR) plot increases from 8.4 to 11 A. The minimum slit width where the applied probe molecules, that is, nitrogen and hexane, can enter increases from about 5 to about 5.4 A. The separation distance of the basic structural units is practically unchanged. When, however, this carbon is in contact with hexane, this distance expands from about 19 to 27 A. The swelling is consistent with the deformable nature of this sample also illustrated by the low-pressure hysteresis and the reduced helium density. Particular attention was paid to the surface areas derived from low-temperature nitrogen adsorption and X-ray measurements. Owing to the wide spatial range of the structures in these samples, estimates of the specific surface area of activated carbons can be substantially in error unless both upper and lower q ranges of the SAXS spectra are taken into account. Surface areas derived from the adsorption data either by the BET or the DR approaches were always below the values obtained by standard SAXS. As an example, the carbon sample functionalized at room temperature gave surface area values of 1114, 1293, and 1970 m2/g, respectively. The possibility that this difference is caused by inaccessible pores was excluded by contrast variation measurements with hexane.

Journal Article↗

PubMed2004

Adsorption of valeric acid from aqueous solution onto activated carbons: role of surface basic sites.

Adsorption of valeric acid was studied on two activated carbons of different origins, wood and bituminous coal. The effect of oxidation on the adsorption uptake was investigated. Both initial samples were oxidized with nitric acid, which caused the introduction of a significant number of oxygen-containing groups onto the carbon surface. Boehm titration, potentiometric titration, thermal analysis, and sorption of nitrogen were used for detailed surface characterization. Valeric acid adsorption from aqueous solution was measured at 333 K. The calculated isotherms showed a good fitting to the Freundlich equation. The capacity coefficients revealed a direct correlation with the number of basic groups present on the surface. The amount of valeric acid adsorbed at its low concentration is dependent on the number of basic groups, whereas at high concentration the amount adsorbed depends on the volume of micropores smaller than 10 A, where the adsorption potential is the strongest.

Journal Article↗

PubMed1989

Health effects of acid aerosols formed by atmospheric mixtures.

Under ambient conditions, sulfur and nitrogen oxides can react with photochemical products and airborne particles to form acidic vapors and aerosols. Inhalation toxicological studies were conducted, exposing laboratory animals, at rest and during exercise, to multicomponent atmospheric mixtures under conditions favorable to the formation of acidic reaction products. Effects of acid and ozone mixtures on early and late clearance of insoluble radioactive particles in the lungs of rats appeared to be dominated by the oxidant component (i.e., the mixture did cause effects that were significantly different from those of ozone alone). Histopathological evaluations showed that sulfuric acid particles alone did not cause inflammatory responses in centriacinar units of rat lung parenchyma (expressed in terms of percent lesion area) but did cause significant damage (cell killing followed by a wave of cell replication) in nasal respiratory epithelium, as measured by uptake of tritiated thymidine in the DNA of replicating cells. Mixtures of ozone and nitrogen dioxide, which form nitric acid, caused significant inflammatory responses in lung parenchyma (in excess of effects seen in rats exposed to ozone alone), but did not damage nasal epithelium. Mixtures containing acidic sulfate particles, ozone, and nitrogen dioxide damaged both lung parenchyma and nasal epithelia. In rats exposed at rest, the response of the lung appeared to be dominated by the oxidant gas-phase components, while responses in the nose were dominated by the acidic particles. In rats exposed at exercise, however, mixtures of ozone and sulfuric acid particles significantly (2.5-fold) elevated the degree of lung lesion formation over that seen in rats exposed to ozone alone under an identical exercise protocol.

Acid Rain↗

PubMed2001

Selective leaching of elements associated with Mn-Fe oxides in forest soil, and comparison of two sequential extraction methods.

For selective dissolution of Mn oxides as components of soil (easily reducible oxides) 0.05 mol L(-1) and 0.1 mol L(-1) NH2OH.HCl acidified to pH 2 and for dissolution of Fe oxides (crystalline form of the oxides) 0.25 mol L(-1) NH2OH.HCl in 25% acetic acid, 0.2 mol L(-1) oxalate buffer and 0.1 mol L(-1) ascorbic acid in oxalate buffer were tested. Dissolved elements were determined by ICP-MS and ICP-OES. The studies indicate that the use of 0.05 mol L(-1) NH2OH.HCl in nitric acid solution (pH 2) and 0.1 mol L(-1) ascorbic acid in 0.2 mol L(-1) oxalate buffer led to selective leaching of trace metals bound by Mn and Fe oxide phases in soil. Comparison of different extraction schemes indicates that the trace elements investigated are mainly bound to minerals consisting of crystalline Fe oxides and insoluble minerals (under the extraction conditions used). The studies also indicate that Mn oxides and organic matter retain a major mobile fraction of the elements investigated in the soil.

Chemistry Techniques, Analytical↗

PubMed2006

Performance of sulphonic cation exchangers in the recovery of ammonium from basic and slight acidic solutions.

Two sulphonated polystyrene-divinylbenzene cation exchangers (gel type Purolite SGC 100 x 10 MBH and macroporous Purolite C160 MBH) have been investigated for NH(4)(+) ions uptake from the ammonium-rich simulated solutions, corresponding to the caustic condensate of the nitrogen fertilizers production. One component (NH(3) or NH(4)NO(3)) solutions and the mixtures with varying molar ratio of these compounds have been used at the total concentration 0.214 mol/L. Batch and column experiments have been conducted to establish the influence of the matrix structure on the performance of the cation exchangers investigated during the sorption and the desorption. Batch sorption isotherms and breakthrough curves have shown the similar behaviour of the cation exchangers in the removal of NH(4)(+) and NH(3). On decreasing the influent pH from 11.4 to 5.74 a decrease in breakthrough capacity (BC) from 2.57 to 1.93 mol/L was observed. The distribution coefficients (K(d)), calculated from the batch sorption isotherms, are higher for the basic feed solution than for slightly acidic one. Both the degree of the cation exchanger regeneration (N/N(0)) and the efficiency of the NH(4)(+) ions recovery (N(R)), obtained using 0.7 bed volume (BV) of eluent (20% nitric acid) are lower for Purolite C 160 MBH than those for Purolite SGC 100 x 10 MBH. Using 5 BV of eluent the efficiency of the ammonium recovery amounted to 100% for both cation exchangers investigated. With respect to the efficiency of NH(4)(+) ions sorption and regeneration cation exchangers investigated are applicable for the recovery of ammonium ions from caustic condensate in the nitrogen fertilizers production.

Adsorption↗

PubMed1997

Inhibitory effects of a fullerene derivative, dimalonic acid C60, on nitric oxide-induced relaxation of rabbit aorta.

Dimalonic acid C60 (10(-5) M), a new fullerene derivative, produced an augmentation of phenylephrine-induced tone and reduced both the acetylcholine-induced maximum relaxation and the amplitude of substance P (10(-8) M)-induced relaxation in endothelium-containing thoracic aorta of rabbit; the acetylcholine- and substance P-induced relaxation was restored in the presence of superoxide dismutase (250 U/ml). Dimalonic acid C60 (10(-5) M) did not influence the phenylephrine-induced contractile response in the absence of endothelium, but the acetylcholine-induced relaxation was eliminated by removal of the endothelium. Superoxide anion generation, using hypoxanthine (1 mM)/xanthine oxidase (16 mU/ml), reduced the acetylcholine-induced relaxation and produced an augmentation of phenylephrine-induced tone in endothelium-containing strips; these effects were negated by the addition of superoxide dismutase (250 U/ml). A nitric oxide-generating agent, S-nitroso-N-acetylpenicillamine, caused relaxation of aorta without endothelium in a concentration-dependent manner, and the concentration-response curve was shifted to the right in the presence of dimalonic acid C60. This inhibitory effect of dimalonic acid C60 was also masked in the presence of superoxide dismutase. Sodium nitroprusside-induced relaxation was not affected by either dimalonic acid C60 or superoxide dismutase. These observations suggest that dimalonic acid C60 inhibits endothelium (nitric oxide)-dependent agonist-induced relaxation through the production of superoxide.

Acetylcholine↗

PubMed2004

Temporal variation in daily concentrations of ozone and acid-related substances at Saturna Island, British Columbia.

A multiple linear regression model was used to investigate seasonal and long-term trends in concentrations of ozone (O3) and acid-related substances at the Saturna Island monitoring station in southwestern British Columbia from 1991 to 2000. Statistically significant primary (dominant) cycles with a period of 1 yr were found for O3, sulfur dioxide (SO2), nitric acid (HNO3), and aerosol concentrations of sulfate (SO4(2-)), calcium (Ca2+) and chloride (Cl-). Of these, peak median concentrations occurred during the spring for O3 and Ca2+, during the warmer, drier months (April-September) for SO4(2-) and HNO3, and during the cooler, wetter months (October-March) for SO2 and Cl-. Statistically significant secondary cycles of 6 months duration were seen for concentrations of O3, SO4(2-), HNO3, Ca2+, and Cl-. Daily maximum O3 concentrations exhibited a statistically significant increase over the period of record of 0.33 +/- 0.26 ppb/yr. Statistically significant declines were found for concentrations of SO2, SO4(2-), HNO3, Ca2+, and potassium, ranging from 20 to 36% from levels at the start of the sampling period. Declines in ambient concentrations of SO2, SO4(2-), and HNO3 reflect local declines in anthropogenic emissions of the primary precursors SO2 and NOx over the past decade. Trends in Ca2+ and potassium ion concentrations are in line with a broader North American declining trend in acid-neutralizing cations.

Acid Rain↗

PubMed1994

One- and two-electron oxidations of methionine by peroxynitrite.

Peroxynitrite is stable, but its acid, HOONO, either rearranges to form nitrate or oxidizes nearby biomolecules. We report here the reactions of HOONO with methionine and the methionine analog 2-keto-4-thiomethylbutanoic acid (KTBA). These oxidations proceed by two competing mechanisms. The first yields the sulfoxide; the second-order rate constants, k2, for this process for methionine and KTBA are 181 +/- 8 and 277 +/- 11 M-1.s-1, respectively, at pH 7.4 and 25 degrees C. In the second mechanism, methionine or KTBA undergoes a one-electron oxidation that ultimately gives ethylene. We propose that the one-electron oxidant is an activated form of peroxynitrous acid, HOONO*, that is formed in a steady state mechanism. The ratios of the second-order rate constants for the ethylene-producing reaction (k*2) and the first-order rate constant to produce nitric acid (kN) for methionine and KTBA, k*2/kN, are 1250 +/- 290 and 6230 +/- 1390 M-1, respectively. Both ceric and peroxydisulfate ions also oxidize KTBA to ethylene, confirming a one-electron transfer mechanism. The yields of neither MetSO nor ethylene are affected by several hydroxyl radical scavengers, suggesting that a unimolecular homolysis of HOONO to HO. and .NO2 is not involved in these reactions. HOONO* gives hydroxyl radical-like products from various substrates but displays more selectivity than does the hydroxyl radical; thus, HOONO* is incompletely trapped by typical HO. scavengers. However, a mechanism involving dissociation of HOONO* to caged radicals cannot be ruled out at this time.

Chelating Agents↗