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ESR of E' centres in unstrained geological quartz grains.

E1' centres are detectable by ESR spectroscopy in unstrained quartz extracted from weathered rock of Cretaceous age. These centres completely disappear when the samples are irradiated with an artificial gamma-dose of about 200 Gy. The concentration of E1' centres thermally (re)generated at 310 degrees C can be reduced drastically under the influence of gamma-quanta, too. The gamma-radiation induces thermally unstable components in the quartz matrices that start to decay at around 100 degrees C.

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Highly dense protein layers confirmed by atomic force microscopy and quartz crystal microbalance.

Protein adsorption on a gold surface is investigated by comparing the results of quartz crystal microbalance method and atomic force microscopy. The adsorption of streptavidin on functional gold surfaces is directly monitored by a quartz crystal microbalance, and confirmed by atomic force microscopy. For this investigation, a modified gold substrate is fabricated to obtain a topographic image of streptavidin molecules. Both methods show a correlation in terms of the highly dense protein single-layer formation, and the modified gold electrode shows a slightly denser protein layer formation because of the difference in substrate geometry as compared with that of a mica surface.

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Measurement of the dynamics of exocytosis and vesicle retrieval at cell populations using a quartz crystal microbalance.

The quartz crystal microbalance-dissipation technique (QCM-D) is used in two different measurement strategies to monitor the mass change and rigidity of populations of excitable cells during exocytosis and subsequent retrieval of dense-core vesicles. Two cell lines, NG 108-15 and PC 12, were grown to confluence on piezoelectric quartz crystals and were examined separately to demonstrate differences in release and retrieval with cells of different morphology, size, and number of dense-core vesicles. Stimulating the cells to exocytosis with media containing an elevated potassium concentration resulted in an increase in the frequency response corresponding to loss of mass from the cells owing to release of vesicles. In Ca2+-free media, the response was completely abolished. The amplitude and peak area in the frequency response corresponding to mass change with stimulated release was larger for PC 12 cells than for NG 108-15 cells, whereas the initial rate constants for the frequency responses were similar. The data suggest (1) that a greater number and larger size of vesicles in PC 12 cells results in a greater amount of release from these cells vs NG 108-15 cells, (2) the recycling of vesicles utilizes similar fusion/retrieval mechanisms in both cell types, (3) that the control of excess retrieval might be related to the number and size of released vesicles, and (4) that measured retrieval has a rapid onset, masking exocytosis and implying a rapid retrieval mechanism in the early stages of release. These results demonstrate that measurements of complex dynamic processes relating to dense-core vesicle release and retrieval can be simultaneously accomplished using the QCM-D technique.

Animals↗

Determination of boron by using a quartz crystal resonator coated with N-methyl-D-glucamine-modified poly(epichlorohydrin).

A nongravimetric quartz crystal resonator for determination of boron was proposed. The key step is the preparation of a polymer that forms a complex with boron (from borate ion). The polymeric film is deposited on one face of an electrode-separated quartz crystal. The backbone of the polymer is poly(epichlorohydrin), which is modified to anchor N-methyl-D-glucamine. After reticulation and reduction, the film presents high stability and sensitivity to boron at pH 8.5. A carrier solution containing 50 mM EDTA ensures high conductivity and the elimination of several interfering metal ions. Boron is strongly retained by the film, and a positive shift of the oscillating frequency is proportional to its concentration. Boron is eluted with 1 mL of a 1 M mannitol solution. For a 0.160-mL sample loop and concentration up to 600 microM, the calibration sensitivity was 1.67 Hz/microM and the LOD was 2 microM. This limit could be lowered to 0.3 microM by using a 1.00-mL sample loop. In both cases, it was possible to detect 3 ng of boron. It was estimated that the nongravimetric sensor is at least 10 times more sensitive that a hypothetical gravimetric sensor.

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Effect of polyelectrolyte multilayers on the response of a quartz crystal microbalance.

The effect of a polyelectrolyte (PE) multilayers made by a layer-by-layer technique on the response of a quartz crystal microbalance (QCM) is studied by using novel mathematical methods based on the Möbius transformations and their matrix representations in the complex plane. In the first method, the basic properties of the Möbius transformation are used for obtaining the PE bilayer matrix from the QCM impedance measurements taken at four different numbers of layers. In the second method, nonlinear fitting with concomitant error estimation is used for obtaining the elements of the bilayer matrix. The methods are applied to a multilayer composed of 150 bilayers of poly(sodium 4-styrenesulfonate) and poly(diallyldimethylammonium) chloride on a quartz crystal resonator. The structure of the system is discussed, and the bulk acoustic impedance and areal mass density of the bilayer are calculated from the layer matrix.

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Organic vapor sensing with ionic liquids entrapped in alumina nanopores on quartz crystal resonators.

We report on a concept for vapor sensing with the quartz crystal microbalance where the vapor phase is absorbed into small droplets of an ionic liquid. The liquid is contained in the pores of a nanoporous alumina layer, created on the front electrode of the quartz crystal by anodization. Ionic liquids are attractive for vapor sensing because--being liquids--they equilibrate very fast, while at the same time having negligible vapor pressure. Containing the ionic liquids inside cylindrical cavities of a solid matrix removes all problems related to the liquid's softness as well as the possibility of dewetting and flow. The absence of viscoelastic effects is evidenced by the fact that the bandwidth of the resonance remains unchanged during the uptake of solvent vapor. The Henry constants for a number of solvents have been measured.

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The quartz crystal microbalance as a continuous monitoring tool for the study of endothelial cell surface attachment and growth.

The quartz crystal microbalance (QCM) was used to monitor endothelial cell (EC) adhesion on the gold surface of an oscillating quartz crystal contained in a QCM device. A number of parameters were investigated. First, we observed differential QCM O-ring toxicities for ECs. Second, appropriate conditions for cell culture and QCM cell environment were identified that can eliminate large-scale frequency oscillations in the measurements. These artifacts are not due to added cells but originate in the time-dependent evaporation of water. Having eliminated these artifacts, we then demonstrated that the measured steady-state crystal frequency shift, Delta f, and motional resistance shift, DeltaR, were determined by the number of firmly attached ECs requiring trypsinization from the crystal surface. Last, following steady-state attachment of ECs, the EC growth stimulation by fibroblast growth factor was monitored in a continuous fashion by measuring f and R values over a 72 h. period. We observed the Delta f values to increase in a way that reflected the increase in EC number bound to the QCM surface. Following addition of ECs to the QCM, the time-dependent increase in DeltaR can be interpreted in terms of increase by the ECs of the energy dissipation properties of the solution at the solution-gold surface interface. This effect is due to their rapid surface attachment and the elaboration of their cytoskeletal properties. These results indicate that the QCM technique can be used for the study of EC attachment and growth and suggest its potential for the real time study of per unit surface area cell mass distribution dynamics and viscoelastic properties and the cells' responses to stresses or perturbations brought about using biologically active molecules.

Animals↗

Collapse and swelling of thermally sensitive poly(N-isopropylacrylamide) brushes monitored with a quartz crystal microbalance.

Thermally sensitive poly(N-isopropylacrylamide) (PNIPAM) brushes grafted on SiO2-coated quartz crystal surface were prepared with a surface-immobilized initiator. Using quartz crystal microbalance (QCM), we investigated the collapse and swelling of the brushes in water in real time. Both frequency and dissipation of PNIPAM brushes were found to gradually change throughout a temperature range 20-38 degrees C, indicating that PNIPAM brushes undergo a continuous collapse transition in contrast with PNIPAM chains free in dilute solution exhibiting a sharp coil-to-globule transition. This result is in accordance with the previous theoretical prediction. The nonuniformity and stretching of PNIPAM brushes as well as the cooperativity between collapse and dehydration transitions are thought to be responsible for the continuity. On the other hand, a hysteresis was also observed in the cooling process. This is not only due to the intrachain and interchain interactions formed in the collapsed state but also to the nonuniform structure and stretching of the high-density brushes.

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Measurements of interfacial viscoelasticity with a quartz crystal microbalance: influence of acoustic scattering from a small crystal-sample contact.

We discuss the influence of a limited contact size on measurements of high-frequency interfacial viscoelasticity performed with a combination of a quartz crystal microbalance (QCM) and the Johnson-Kendall-Roberts (JKR) apparatus. In this instrument, a sphere-plate contact is established between an elastomeric lens and a quartz resonator. The analysis is carried out in the frame of the sheet-contact model, which states that both the shift of resonance frequency and the bandwidth are proportional to the contact area as long as the contact area is much smaller than the crystal itself. In particular, the ratio of the shift in bandwidth and the shift in frequency (termed the D-f ratio) is predicted to be constant and independent of geometry. However, the experiment does show a slight increase in the D-f ratio with the contact radius when the contact radius is comparable to the wavelength of sound inside the crystal. This effect can be explained by acoustic scattering.

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A prospective randomized controlled study of phototherapy using blue and blue-green light-emitting devices, and conventional halogen-quartz phototherapy.

OBJECTIVE: To determine the efficacy of blue versus blue-green phototherapy using new light sources with narrow luminous spectra. The devices made of high-intensity gallium nitride light-emitting diodes (LEDs) were also compared to conventional halogen-quartz bulbs phototherapy. DESIGN: Prospective open randomized study. PARTICIPANTS: A total of 114 jaundiced, but otherwise healthy term infants who met the entry criteria for phototherapy set by the American Academy of Pediatrics' Practice Parameter. MAIN OUTCOME MEASURES: The duration of phototherapy and the rate of decrease in total serum bilirubin (TSB). RESULTS: The mean TSB concentrations at initiation and termination of treatment, as well as the duration of phototherapy and the rate of decrease in TSB, were not statistically different in newborns receiving blue LED, blue-green LED or conventional phototherapy. The average rate of decrease in TSB (slope), after adjustment by a linear regression analysis for confounding factors, was -3.61 micromol/hour (95% confidence limits -5.47, -1.75) in the 25 newborns receiving blue LED phototherapy compared with -2.57 micromol/hour (-4.32, -0.82) in the 22 newborns treated with blue-green LED phototherapy and -3.42 micromol/hour (-5.02, -1.81) in the 57 newborns who received conventional phototherapy. CONCLUSIONS: When using low light irradiance, there was no statistically significant difference in the effectiveness of phototherapy using blue-green LEDs, blue LEDs or conventional halogen-quartz bulbs.

Bilirubin↗

Real-time monitoring of formaldehyde-induced DNA-lysozyme cross-linking with piezoelectric quartz crystal impedance analysis.

A novel method for monitoring, in real time, the formaldehyde (FA)-induced DNA-protein cross-linking process with the piezoelectric quartz crystal impedance (PQCI) technique is proposed. The method was used to monitor FA-induced DNA-lysozyme cross-link formation. Lysozyme was directly immobilized on the silver electrode surface of a piezoelectric quartz crystal by adsorption. The lysozyme-coated piezoelectric sensor was in contact with FA and DNA solutions. The time courses of the resonant frequency and equivalent circuit parameters of the sensor during the cross-linking were simultaneously obtained and are discussed in detail. On the basis of the feature of the multi-dimensional information provided by the PQCI technique, it was concluded that the observed frequency decrease could be mainly ascribed to the mass increase resulting from the cross-linking. According to the frequency decrease with time, the kinetics of the cross-linking process were quantitatively studied. A piezoelectric response model for the cross-linking was theoretically derived. Fitting the experimental data to the model, the kinetic parameters, such as the binding and dissociation rate constants (k(1) and k(-1)) and the cross-linking equilibrium constant (Ka), were determined. At 37 degrees C, the k(1), k(-1) and Ka values obtained were 7.0 (+/-0.1) x 10(-5) (microg ml(-1))(-1) s(-1), 6.6 (+/-0.1) x 10(-3) s(-1) and 1.06 (+/-0.02) x 10(-2) (microg ml(-1))(-1), respectively.

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Molecular dynamics simulations of hydration, dissolution and nucleation processes at the alpha-quartz (0001) surface in liquid water.

Molecular dynamics simulations have been employed to investigate the hydration and dissolution of alpha-quartz (0001) surfaces in a liquid water environment. Our study indicates that the structure of the water layers near the surfaces is affected by the nature of the substrate surface and by temperature. Ordered mono-layers of interfacial water molecules form in the region of the substrate where the surface is highly charged and built up of Si-O-Si bridges. As the temperature is increased this ordered mono-layer structure is gradually lost. When the surface is terminated by silanol groups, the water retains liquid-like properties even at low temperature and the molecules are distributed in a random manner, without the formation of distinct ordered mono-layers of water molecules near the surface. Taking into account the entropy of the system, the calculated energies of stepwise dissolution of a silicon species from the surface suggest that on thermodynamic grounds the complete dissolution of silicon atoms from the quartz surfaces in a liquid water environment is an endothermic process, but that the formation of a -Si(OH)3 species at the surface would be possible. In addition, if the Si(OH)(4) species were to be dissolved, it would remain near the surface, and re-deposition at the defect-free surface is thermodynamically preferred, although there is an activation enthalpy to the first step in the process of nucleation of Si(OH)4 at the perfect surface.

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Defect analysis in natural quartz from Brazilian sites for ionising radiation dosimetry.

The impurity-related point defects and the dosimetry properties of quartz irradiated with gamma- and X-rays doses were investigated for natural crystals taken from different geologies. The specimens were initially irradiated with gamma particles from (137)Cs to determine the sensitivity and repeatability of thermoluminescence (TL) emission at approximately 503 K. The dose response was investigated in the range 1-20 mGy. The energy dependence was considered in the range 16-65 keV with X rays and with gamma rays from 137Cs and 60Co. It was found that quartz material from two geologies exhibit a linear relationship between TL intensities and absorbed doses with high angular coefficients. Its sensitivities are higher than that found for LiF TLD-100 dosemeters irradiated in the same conditions. The results were discussed in relation to pre-existing impurity contents and the formation of Al-hole centres.

Brazil↗

Counting function for a sphere of anisotropic quartz.

We calculate the leading Weyl term of the counting function for a monocrystalline quartz sphere. In contrast to other studies of counting functions, the anisotropy of quartz is a crucial element in our investigation. Hence we do not obtain a simple analytical form, but we carry out a numerical evaluation. To this end we employ the Radon transform representation of the Green's function. We compare our result to a previously measured unique data set of several tens of thousands of resonances.

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Oxygen self-diffusion in alpha-quartz.

We have studied the formation energy of the simplest oxygen defects in alpha-quartz, the oxygen vacancy and interstitial, by an ab initio approach based on density functional theory in the local density approximation. We have determined the formation energies and entropies and the migration paths and energies. From our results we can conclude that oxygen diffuses in quartz by an interstitial mechanism: the interstitial has a dumbbell structure; one of the constitutive atoms jumps towards a neighboring oxygen site. The activation energy amounts to 4.7 eV in the intrinsic regime and 2.8 eV in the extrinsic regime.

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Application of the statistical dynamical theory to gamma-ray diffraction experiments on low-dislocation quartz single crystals.

Highly monochromatic (Deltalambda/lambda = 10(-6)) short-wavelength (lambda = 0.03 Å) gamma radiation has been used in the study of the diffraction processes in real single crystals. Dislocation-free silicon crystals and quartz crystals with small concentrations of chaotically distributed dislocations were investigated. The experimental results were processed with use of statistical dynamical theories of diffraction, both fundamental and advanced. It is shown that the advanced version is more reliable in both cases. However, the values of the average lattice phase E, describing the long-range distortions of the lattice, can differ markedly from the value of 1 for quartz crystals, and parameter L = -ln(E) has a square dependence on the extinction length.

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Crystal structure of moganite-type phosphorus oxynitride: relationship to other twinned-quartz-based structures.

The structure of moganite-type phosphorus oxynitride quenched from high-pressure high-temperature conditions has been refined using neutron powder diffraction data. This moganite-type structure, space group I2/a, Z = 12, is slightly less distorted with respect to the Imab aristotype than is moganite (a monoclinic form of silica). A close topological relationship has been identified between the moganite-type and orthorhombic BeH(2) structures indicating that SiO(2), PON and BeH(2) all adopt structures belonging to the twinned-quartz-based group. This group represents another possible structure type for systems composed of corner-sharing AX(4) tetrahedra. Structures of this group are obvious candidates for intermediate phases between the cristobalite and quartz types.

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Nearly perfect large-area quartz: 4 meV resolution for 10 keV photons over 10 cm(2).

The perfection of two commercial top-grade quartz crystal wafers has been investigated using Bragg reflection at theta(B)=89.77 degrees of a 2.0 meV bandwidth beam of 9.979 keV X-rays by the (7\bar4\bar34) lattice planes. Topographic images show small defect concentrations (<or=5 cm(-2)). Energy scan widths are below 3 meV over 8 mm x 8 mm areas and 4 meV over the whole wafer ( approximately 11 cm(2)). This suggests that quartz can be a useful optical material.

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