Investigation on vermilion,gingiva, and tooth color of young Uygur and Han populations in Xinjiang,China

This study examines oral tissue color in Uygur and Han Chinese populations. The color of oral tissues is of great significance in dental field. It remains uncertain whether there is any difference in the color of oral tissues between different nationalities or ethnicities. Little is known about the color of oral tissues in different Chinese populations. The study included 263 Uygur and Han students aged 18–22 years. The color of anterior teeth, vermilion, and attached gingiva in the subjects was measured by spectrophotometry and expressed through the CIELCh system. The t test and ANOVA was used to analyze color difference between groups. Distribution ranges for L (lightness), C (chroma) and h (hue angle) of anterior teeth, vermilion, and attached gingiva in these two ethnicities were obtained. Significant differences in color of oral tissues between Uygur and Han Ethnicities were found out. The Uygur and Han populations have similar spatial distribution ranges for the color of oral tissues, with slight differences that displayed strong regularities, suggesting that the color of oral tissues was associated with race. In addition, there was a trend of decreasing lightness (especially for maxillary anterior teeth), increasing chroma and redder hue from the center of teeth toward the sides in both ethnicities. There were differences in the color of teeth and attached gingiva between sexes in the Uygur and Han populations. The color of the upper vermilion differed significantly from that of the lower vermilion. © 2010 Wiley Periodicals, Inc. Col Res Appl, 2010     

Color variability for a wine sample poured into a standard glass wine sampler

Spectroradiometric color measurements were performed at 26 regularly spaced points of a standard wine sampler into which 100 cc of wine were poured. Our goal is to describe the color changes occurring in this system, but not to propose a new method for wine‐color measurement. Three samples of three different wines (red, rosé and white) were studied. From experimental measurements, lines of constant lightness (L), chroma (C_,10) and hue‐angle (h_ab,10) were plotted for each wine poured into the wine sampler, as well as lines of constant CIELAB color differences (ΔE_,10), with respect to a reference point placed at the axis of the wine sampler and at the zone with the greatest diameter. Considering different points of the wine sampler, the color attribute undergoing the greatest change was lightness (ΔL about 16.0, 15.0 and 11.0 for the red, rosé and white wines, respectively), followed by chroma (ΔC_,10 about 2.8, 3.8 and 2.6 for the red, rosé and white wines, respectively) and hue(ΔH_,10 lower than 1.0 for all the wines). Lightness variations were related mainly to the thickness differences between various zones of the wine sampler. Large color differences were found among the different points of the wine poured into the wine sampler (about 20.0, 21.0 and 14.0 CIELAB units, for the red, rosé and white wines, respectively). Panels should be aware of these large color variations when wine is visually assessed using standard wine samplers. It should be concluded that a single color specification for a wine poured into a wine sampler gives incomplete information, but hue, which is the main color attribute considered by observers, is nearly constant in the wine sampler. © 2003 Wiley Periodicals, Inc. Col Res Appl, 28, 473–479, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.10200     

Riemannian formulation and comparison of color difference formulas

Study of various color difference formulas by the Riemannian approach is useful. By this approach, it is possible to evaluate the performance of various color difference formulas having different color spaces for measuring visual color difference. In this article, the authors present mathematical formulations of CIELAB (ΔE), CIELUV (ΔE), OSA‐UCS (ΔE_E) and infinitesimal approximation of CIEDE2000 (ΔE₀₀) as Riemannian metric tensors in a color space. It is shown how such metrics are transformed in other color spaces by means of Jacobian matrices. The coefficients of such metrics give equi‐distance ellipsoids in three dimensions and ellipses in two dimensions. A method is also proposed for comparing the similarity between a pair of ellipses. The technique works by calculating the ratio of the area of intersection and the area of union of a pair of ellipses. The performance of these four color difference formulas is evaluated by comparing computed ellipses with experimentally observed ellipses in the xy chromaticity diagram. The result shows that there is no significant difference between the Riemannized ΔE₀₀ and the ΔE_E at small color difference, but they are both notably better than ΔE and ΔE. © 2011 Wiley Periodicals, Inc. Col Res Appl, 2011;     

Estimation of hue discrimination thresholds using a computer interactive method

An experimental approach is described for measuring colour discrimination thresholds of human observers. Special software was developed for the accurate display of colour pairs on a high resolution CRT, using serial feedback from a spectroradiometer. Discrimination thresholds between a test and a target colour are determined by repeatedly showing an observer a circle composed of four separate quadrants, one of which has a different colour from the other three. Three quadrants are of the test colour and one of the target colour, or vice versa. Observers are asked to select the quadrant that differs from the others. An experiment is described where hue‐dependent effects affecting hue discrimination are investigated. Eighteen hue threshold values around the hue circle, at constant L = 51 and C = 25, were measured for three observers. Hue thresholds were found to vary around the hue circle, exhibiting an abrupt change in the blue to purple region (240° ≤ h_ab,10 = 300°) This change is not fully accounted for by any CIELAB‐based colour difference formula, including the most recent CIEDE2000 formula. © 2005 Wiley Periodicals, Inc. Col Res Appl, 30, 410–415, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.20153     

Extending CIELAB: Vividness, , depth, , and clarity,

CIE L*, a*, b* is a rectangular coordinate system used extensively for numerical color communication and quality assurance. Often the a*, b* coordinates are rotated to cylindrical polar coordinates of (radial distance) and h_ab (angle measured counterclockwise from the a* axis), reasonably relating to chroma and hue. When each coordinate is considered independently, it is observed that colors in our daily experiences do not change in a similar independent fashion. Changes in concentration for mixtures of colorants result in changes in both chroma and lightness. Directly illuminated three‐dimensional colored objects change in both chroma and lightness between direct illumination and either shadow or highlight. Two new coordinates are defined for CIELAB: vividness, , and depth, . Each represents a Euclidean distance from a color defined by L* and to of 0 and either L* = 0 for vividness or L* = 100 for depth. Image‐based visualizations were made to demonstrate how changes in these variables led to color changes more representative of our daily experiences. For cases where a color and background had the same lightness, it was observed that colors became less distinct with a reduction in chroma. A third dimension was defined, clarity, , a Euclidean distance from a color defined by L*, a*, and b* to its background color, similarly defined. © 2013 Wiley Periodicals, Inc. Col Res Appl, 39, 322–330, 2014     

Study on the thermal stability of heterogeneous nucleation effect of polypropylene nucleated by different nucleating agents

The thermal stability of the heterogeneous nucleation effect of polypropylene (PP) nucleated with an organic phosphate (A) and two kinds of sorbitol derivatives (B and D) was investigated by DSC multiscanning. For pure PP, the peak temperature of crystallization (T) was little changed with an increasing number of DSC scans, indicating that nucleation of PP is thermally stable. For the PP nucleated with an organic phosphate (PPA), the temperatures at the onset of crystallization (T) and at the completion of crystallization (T); the peak temperature of crystallization (T) and melting (T); and the heat of crystallization (ΔH_c) and fusion (ΔH_m) of PP are higher than those of pure PP and were little influenced with an increasing number of DSC scans. For PP nucleated with the sorbitol derivatives (PPB and PPD), the T, T, T, and T decreased with an increasing the number of scans. These results indicated that the thermal stability of heterogeneous nucleation effect of the nucleating agent A is higher than that of nucleating agents B and D. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1643–1650, 2002     

Forced oscillations in continuous flow stirred tank reactors with nonlinear step growth polymerization

The self-step growth polymerization of RA_f monomers in homogeneous, continuous flow stirred tank reactors (HCSTRs) is simulated under conditions of periodic feed concentration (with frequency ω and amplitude α). By having periodic operation, the polydispersity index of the polymer is found to increase by about 35% over the values at steady state. Periodic operation of HCSTRs is found to lead to gelation only for certain values of the frequency and the dimensionless residence time τ^*. Gelling envelopes have been obtained to give conditions under which HCSTRs should be operated. These envelopes can be described in terms of two critical dimensionless residence times, τ and τ such that nongelling operation is always ensured when τ^* < τ. For τ^* > τ, periodic operation always leads to gelation, and HCSTRs cannot be used. For τ < τ^* < τ, the gelling behavior is found to depend on the functionality f, amplitude α, and the dimensionless residence time τ^*.     

Evaluating the 1931 CIE color‐matching functions

The use of colorimetry within industry has grown extensively in the last few decades. Central to many of today's instruments is the CIE system, established in 1931. Many have questioned the validity of the assumptions made by Wright¹ and Guild,² some suggesting that the 1931 color‐matching functions are not the best representation of the human visual system's cone responses. A computational analysis was performed using metameric data to evaluate the CIE 1931 color‐matching functions as compared to with other responsivity functions. The underlying assumption was that an optimal set of responsivity functions would yield minimal color‐difference error between pairs of visually matched metamers. The difference of average color differences found in the six chosen sets of responsivity functions was small. The CIE 1931 2° color‐matching functions on average yielded the largest color difference, 4.56 ΔE. The best performance came from the CIE 1964 10° color‐matching functions, which yielded an average color difference of 4.02 ΔE. An optimization was then performed to derive a new set of color‐matching functions that were visually matched using metameric pairs of spectral data. If all pairs were to be optimized to globally minimize the average color difference, it is expected that this would produce an optimal set of responsivity functions. The optimum solution was to use a weighted combination of each set of responsivity functions. The optimized set, called the Shaw and Fairchild responsivity functions, was able to reduce the average color difference to 3.92 ΔE. In the final part of this study a computer‐based simulation of the color differences between the sets of responsivity functions was built. This simulation allowed a user to load a spectral radiance or a spectral reflectance data file and display the tristimulus match predicted by each of the seven sets of responsivity functions. © 2002 Wiley Periodicals, Inc. Col Res Appl, 27, 316–329, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.10077     

Several features of vinyl chloride–diallyl phthalate suspension copolymerization

Vinyl chloride–diallyl phthalate (VC–DAP) suspension copolymerization was carried out in a 5‐L autoclave and 200‐mL stainless steel vessel at 45°C. The apparent reactivity ratios of VC–DAP suspension copolymerization system were calculated as r_VC = 0.77 and r_DAP = 0.37. It shows that VC–DAP copolymer contains no gel when the feed concentration of DAP (f) is lower than a critical concentration (f_cr, inside the range of 0.466–0.493 mmol/mol VC at 80–85% conversion), the polymerization degree (DP) of copolymer increases with the increase of f and conversion. VC–DAP copolymer is composed of gel and sol fractions when f is larger than f_cr. The DP of sol fraction decreases as f increases, but the gel content and the crosslinking density of gel increase. The gel content also increases as conversion increases. The results also show that the index of polydispersity of molecular weight of sol changes with f, a maximum value appears when f is close to f_cr. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 156–162, 2000     

Some aspects of the visual scaling of large colour differences—II

In an earlier article the authors related visually‐ scaled large colour differences to ΔE* values calculated using four colour‐difference formulae. All four metrics yielded linear regressions from plots of visual colour difference against ΔE*, and ΔE gave the best linear fit, but the correlations were rather low. In an effort to clarify matters, the previous investigation is expanded to include data not hitherto examined. The link between visual colour difference and ΔE* colour metrics is further explored in terms of a power law relationship over a wide range of lightness, hue, and chroma variations within CIELAB colour space. It is shown that power‐law fits are superior to linear regressions in all cases, although correlations over large regions of the colour space are not very high. Partitioning of the experimental results to give reduced data sets in smaller regions is shown to improve correlations markedly, using power‐law fits. Conclusions are drawn concerning the uniformity of CIELAB space in the context of both linear and power‐law behavior. © 2000 John Wiley & Sons, Inc. Col Res Appl, 25, 116–122, 2000     

Numerical and experimental investigation of three-dimensional flow in extrusion dies

The univariant element, Q₁ P₀, and the multivariant elements, QP₀ and R P₀, are compared for the numerical simulation of the flow in extrusion dies. The pressure distribution obtained by using the Q₁ P₀ element was found to be afflicted with the checkerboard pressure mode. On the other hand, the multivariant elements, Q P₀ and R P₀, gave accurate and physically reasonable velocity and pressure distributions. The computed values of the pressure drop across extrusion dies matched well with the pressure drop determined experimentally.     

Intrinsic birefringence of nylon 6

Different values are reported in the literature for the intrinsic birefringence of the crystalline (Δn) and the amorphous (Δn) phases in nylon 6. Mostly, these values have either been determined by extrapolation (and then it is assumed that Δn = Δn) or calculated theoretically. In this study, intrinsic birefringence values Δn and Δn for nylon 6 were determined using the Samuels two-phase model which correlates sonic modulus with structural parameters. Three series of fiber samples were used: (1) isotropic samples of different degrees of crystallinity for estimation of E and E moduli at two temperatures. The following modulus values were obtained: 1.62 × 10⁹ and 6.66 × 10⁹ N/m² for 28.5°C, and 1.81 × 10⁹ and 6.71 × 10⁹ N/m² for ?20°C; (2) anisotropic, amorphous fiber samples for estimation of Δn = 0.076 and E = 1.63 × 10⁹ N/m² at 28.5°C; (3) semicrystalline samples of various draw ratios for estimations of Δn = 0.089 and Δn = 0.078. All measurements were carried out with carefully dried samples to avoid erroneous results caused by moisture.     

Competitive adsorption of uranyl ions in the presence of Pb(II) and Cd(II) ions by poly(glycidyl methacrylate) microbeads carrying amidoxime groups and polarographic determination

The adsorption capacity of UO in the presence of Pb(II) and Cd(II) ions was investigated with amidoximated poly(glycidyl methacrylate) (PGMA) microbeads with an average size of 135 μm packed in a glass column (0.5‐cm i.d. and 20‐cm length, flow rate = 3 mL/min) under competitive conditions. A differential pulse polarography technique was used for the determination of trace quantities of uptaken elements by the measurement of the reduction peak currents at ?200/?950, ?400, and ?600 mV (vs a saturated calomel electrode) for UO, Pb(II), and Cd(II) ions, respectively. When only UO was found in the eluate, its adsorption was 85.3% from a 50 μM initial solution. However, when there was UO with binary systems of Pb(II) or Cd(II), it was 78.2 and 76.3%, respectively. On the other hand, in a ternary mixture of UO with Pb(II) and Cd(II), the adsorption was found to be 75.2% with the same initial concentration. According to the results, the competitive adsorption studies showed that these amidoximated PGMA microbeads had good adsorption selectivity for UO with the coexistence of Pb(II) and Cd(II) ions. The ionic strength of the solution also influenced the UO adsorption capacity of the amidoximated PGMA microbeads. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 4168–4172, 2007     

Über die Katalyse der Cooxidation von cis-Oct-4-en und n-Butyraldehyd

The Catalysis of the Co-Oxidation of cis-Oct-4-ene and n-Butyric Aldehyde The co-oxidation of cis-oct-4-ene and n-butyric aldehyde in the absence of catalysts, or in the presence of molybdenum and Co(acac)₃, resp., was studied in dependence on the aldehyde/olefin ratio, on the temperature and other reaction conditions. Under the same conditions, the noncatalyzed co-oxidation converted 50%, the MoO₂(acac)₂-catalyzed one 68%, and the Co(acac)₃-catalyzed one 40% of the reacted olefin into the epoxide. The cis/trans-epoxide ratio in the molybdenum-catalyzed co-oxidation was nearly 2 independent of the aldehyde/olefin ratio. In the non-catalyzed co-oxidation the cis/trans-epoxide ratio depends linearly on the aldehyde/olefin ratio (cis/trans E. = 0,58 + 0,90 n/n). From these dependences we can conclude that the homolytic mechanism of epoxide formation decreases and the polar mechanism (Priležaev-reaction) increases with increasing aldehyde/olefin ratio. Optimization of the epoxide yields according to a Box-Hunter experimental plan gave the following reaction conditions to yield 95% epoxide based on reacted olefin: 70°C, Δn_S/n = 0,49, n/n = 3,5 · 10⁻³, n/n = 0,53. The co-oxidation in the presence of other molybdenum catalysts of the chloro-nitrosyl-complex type and of the carbonyl-complex type as well as the co-oxidation with other aldehydes were studied, too.     

Color managing the third edition of Billmeyer and Saltzman's Principles of Color Technology

Commercial ICC‐compliant color‐management software was used to produce color‐managed CMYK‐encoded images for the third edition of Principles of Color Technology. Custom profiles were created for a Scitex Eversmart Pro flatbed scanner and a Kodak Approval proofing device. This enabled objects such as color‐order systems and colorimetric‐encoded, computer‐generated graphical images to be reproduced with reasonable colorimetric accuracy. The GretagMacbeth ColorChecker Color Rendition Chart was used as an independent verification target. Its printed reproduction had an average error of 4.2 ΔE (6.4 ΔE^*_ab). Colorimetric‐rendering device profiles enabled the visualization of the book's color gamut and of a calibrated visible spectrum. © 2002 Wiley Periodicals, Inc. Col Res Appl, 27, 360–373, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.10083     

The viscoelastic properties of rubber–resin blends. III. The effect of resin concentration

The viscoelastic properties of a rubber–resin blend, which influences performance of the blend as a pressure-sensitive adhesive, depend upon the structure of the resin as well as its molecular weight. The effect of the concentration of a compatible resin in the blend was examined using a mechanical spectrometer. Four types of resins were used. These are the rosin esters, polyterpenes, pure monomer resins such as polystyrene and poly(vinyl cyclohexane), and petroleum stream resins. Each was examined in blends with both natural rubber and styrene–butadiene rubber over a range of concentrations. It is shown that the temperature of the tan δ peak for compatible systems can be predicted by the Fox equation, T = W₁T + W₂T, where W₁ and W₂ are the weight fractions of the resin and rubber, respectively, and the T_g's are the tan δ peak temperatures in K. The plateau modulus G for a blend can be identified as the G′ value in the rubbery plateau at the point where tan δ is at a minimum. The relationship between G and G, the plateau modulus for the undiluted elastomer, is shown to be proportional to the volume fraction of the elastomer raised to the 2.3–2.4 power for natural rubber with six different compatible resins. The exponent for styrene–butadiene rubber is 2.5–2.6 with four different resins. Using these relationships, both the tan δ peak temperature and plateau modulus can be predicted for a rubber–resin system from data on the unmodified elastomer and on one typical rubber–resin blend.     

Elastic characteristics of branched-network polymers

The computed dependencies of elastic characteristics of branched-network polymers were obtained on the basis of the Takayanagi series model. The moduli ratio (λ) for branched-network and branched polymers increases as a result of an increase of the moduli ratio of network and branched phases (E/E) and the network phase fraction (V_net). The λ-increase as a function of V_net is larger than in the case of the E/E dependence. On the basis of computed dependencies, the experimental results for the radiation crosslinked SBS block copolymer were considered. The experimental results agree with the computed de-pendencies for the hetergeneous branched-network polymers with E/E ≈︁ 20. The influence of entanglements on the elastic characteristics of branched-network polymers is discussed. © 1996 John Wiley & Sons, Inc.     

Melting behavior of poly(trimethylene terephthalate)

In this study, the melting behavior of isothermally crystallized polytri‐ methylene terephthalate (PTT) was investigated. Multiple melting behaviors in DSC heating trace were found because two populations of lamellar stacks were formed during primary crystallization and the recrystallization at heating process, respectively. This fact could be also confirmed from the result of optical microscopy observation. The Hoffman–Weeks equation was applied to obtain equilibrium melting temperature (T). The T value of PTT is about 525 K, which is 10 K higher than that reported. Combining the enthalpy of fusion from the DSC result and the degree of crystallinity from WAXD result, the value of the equilibrium‐melting enthalpy ΔH was deduced to be approximately 28.8 kJ mol^?1. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2426–2433, 2002     

Solution and diffusion properties of cyclohexane,cyclohexanol, and cyclohexanone in poly(ethylene glycol) by inverse gas chromatography

The solution and diffusion properties of cyclohexane, cyclohexanol, and cyclohexanone in poly(ethylene glycol) (PEG) and crosslinked PEG have been studied in the temperature range of 368.15 to 403.15 K using inverse gas chromatography (IGC) technique. The infinite dilute activity coefficient (Ω) and diffusion coefficient (D) have been determined for the above solvent/polymer systems. Accordingly, several thermodynamic functions, the diffusion pre‐exponential factor, and activation energy have been attained. The results showed a decrease in Ω and an increase in D with rising temperature. The order of the relative magnitude of Ω and D of the solvents were explained by comparing their interactions with the polymer and their collision diameters, respectively. Moreover, Ω and D in crosslinked PEG were smaller than those in PEG at various temperatures. The analysis of Ω, the infinite dilute selectivity and capacity showed the possibility of using crosslinked PEG as an appropriate membrane material for the separation of cyclohexane, cyclohexanol, and cyclohexanone mixture. A thermodynamic study also implied that the solvent sorptions in the polymers were all enthalpically driven in the experimental range. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.