CO2 laser irradiation of raw and bleached cotton fabrics,with focus on water and dye absorbency

In this research, the effect of carbon dioxide laser irradiation on various properties of raw and bleached cotton fabrics, including fabric weight, bending rigidity, wetting, and air permeability, as well as dyeing, was examined and compared. The experiments were carried out at three different laser powers ranging from 4.5 to 6 W to determine the effect of laser treatment on fabric properties. In particular, the influence of laser irradiation on the dyeing properties of treated fabrics with CI Reactive Blue 198 was studied. The colour change of laser‐treated fabrics was determined by calculation of the K/S values as a function of fabric reflectance. The morphological changes in laser‐treated fabrics were observed by scanning electron microscopy. The effects of laser treatment on the properties of raw and bleached cotton fabrics were varied. For instance, the wettability of raw cotton samples was reduced after laser irradiation, whereas the wettability of bleached cotton fabrics was greater. Possible reasons for the various dyeing behaviours observed with irradiation at different laser powers are discussed.     

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;     

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     

Tearing mode interlaminar fracture toughness of composite materials

The Simplified Split Cantilever Beam (SSCB) is proposed in this work and compared with the Split Cantilever Beam (SCB) to obtain the tearing mode interlaminar fracture toughness. The materials considered are single‐fiber system composites and interply hybrid composites. For interply hybrid composites, three different types of stacking sequence for SSCB specimens, which are [0/0//0],[0/0//0]. and [0/0//0], are tested to compare their suitability. Finite element analysis combined with a modified crack closure integral has been applied to separate the different components of the strain‐energy release rate. In addition, the method of compliance calibration was used to calculate Gc values. The effects of crack growth, initial crack length, specimen width, and number of glass fiber plies were also studied. The results show that SSCB testing has a more dominant Mode III component and more stable Gc values than SCB testing. For SSCB testing, the crack growth and the specimen width for the range considered have no clear effects on the interlaminar fracture toughness, but the initial crack length should be carefully selected to obtain corrected values. The tearing mode interlaminar fracture toughness of interply hybrid composites is higher than that of carbon/epoxy composites, and the three different types of stacking sequence considered are all suitable to approximate the Mode III interlaminar fracture toughness for interply hybrid composites.     

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     

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     

Morphological studies of the modified materials: Low-density polyethylene/poly(acrylic acid)/europium(III) and low-density polyethylene/poly(acrylic acid)/uranyl ion

The morphology of low-density polyethylene (LDPE) modified by in situ sorption and thermal polymerization of acrylic acid (AA) in the matrix was examined. The microstructure of the LDPE/poly(acrylic acid) (PAA) materials after Eu³⁺ and UO ion exchange was investigated. The phase behavior of these materials was analyzed using X-ray diffraction, scanning electron microscopy (SEM), and thermal measurements (DSC). The X-ray dif-fraction studies showed that PAA is located at amorphous region of the matrix. The LDPE/PAA surface, as investigate by SEM, was apparently homogeneous before and after Eu³⁺ and UO ion exchange, respectively. Two T_g values were found for the LDPE/PAA material before and after Eu³⁺ ion exchange. Also, three and four T_g values were found for LDPE/PAA after UO ion exchange depending on the amount of UO in the modified matrix. This indicates microphase domains in the LPDE/PAA-, LPDE/PAA/Eu³⁺-, and LPDE/PAA/UO -modified materials, although a lack of visible phase separation in the micrographs was observed. © 1996 John Wiley & Sons, Inc.     

The effect of side chains on the partial specific volumes of poly(o-alkylphenyl methacrylate)s and polydiitaconates

Partial specific volumes ν of a series of poly(o-alkyl phenyl methacrylate)s and polydiitaconates were determined by density measurements, in toluene and tetrahydrofuran solutions, respectively. The effect of the size and nature of the side groups on partial specific volume is analyzed. Good agreement is found between the experimental ν values and those obtained theoretically from the group contribution method.     

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     

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.     

Influence of anionic form on thermal degradation of TMAHP–cellulose

Trimethylammoniumhydroxypropyl (TMAHP)–cellulose in 10 anionic forms (F^?, Cl^?, Br^?, I^?, HSO, NO, OH^?, HCO, H₂PO, CH₃COO^?) was prepared, and the influence of each anion on thermal degradation in inert atmosphere was studied. With the help of dynamic and isothermal thermogravimetry (TG) it was found that H₂PO ions had the greatest retarding effect on TMAHP–cellulose degradation. From the values of rate constants it can be seen that all ionic forms of TMAHP–cellulose have the starting rate of thermal degradation greater than unmodified cellulose. The calculated values of activation energy of thermal degradation for different ionic forms are decreasing in following sequence: H₂PO > F^? > NO > I^? > Br^? > HCO > Cl^? > HSO > OH^? > unmodified cellulose > CH₃COO^?. From the results of pyrolyse measurements in combination with gas chromatography and mass spectrometry (Py–GC–MS) it follows that the products of the elimination of quarternary ammonium salts are trimethylamine, 3-hydroxy-2-propanone, and, in the case of OH^? form, water. In all other ionic forms the third product is the corresponding acid.     

Conductive Composites of Polyurethane Resins and Ionic Liquids

Composites of PUR and IL were prepared and specific conductivities and Shore A hardness were determined. IL were based on 1‐alkyl‐3‐methylimidazolium salts with counterions BF, PF, triflate, or ethylsulfate. Presence of IL increased the conductivity by five orders of magnitude. Variation of alkyl chain length and nature of counterions only had little effect on the conductivity. Presence of IL had a plasticizing effect, which was most pronounced for the IL with dodecyl groups and PF as counterion. In broadband dielectric measurements, the complex conductivity showed a characteristic dispersion that is caused by the interplay between (hopping) transport of charge carriers and electrode polarization.

     

Effect of pH,ionic strength,and temperature on uranyl ion adsorption by poly(N‐vinyl 2‐pyrrolidone‐g‐tartaric acid) hydrogels

Poly‐electrolyte N‐vinyl 2‐pyrrolidone‐g‐tartaric acid (PVP‐g‐TA) hydrogels with varying compositions were prepared in the form of rods from ternary mixtures of N‐vinyl 2‐pyrrolidone/tartaric acid/water. The effect of external stimuli, such as the solution pH, ionic strength, and temperature, on uranyl adsorption by these hydrogels was investigated. Uranyl adsorption capacities of the hydrogels were determined to be 53.2–72.2 (mg UO/g dry gel) at pH 1.8, and 35.3–60.7 (mg UO/g dry gel) at pH 3.8, depending on the amount of TA in the hydrogel. The adsorption studies have shown that the temperature and the ionic strength of the swelling solution also influence uranyl ion adsorption by PVP‐g‐TA hydrogels. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2219–2226, 2000     

Regression‐based model for elastic constants of 2D braided/woven open mesh angle‐ply composites

The elastic constants of closed mesh braided/woven fabrics are generally obtained from finite element analysis, fabric geometry model, and modified classical laminate plate theory. These models are complex and often impractical for industrial design purposes and do not address the cases of open mesh braided/woven fabrics. This paper proposes an alternative to existing models and software packages. Simple regression‐based empirical equations were developed to obtain E_x, E_y, G_xy, and ν_xy of braided/woven fabrics at any angle‐ply angle using the braid/weave unit cell volume fraction (V_f0), the fiber volume fraction (V_f), and the elastic constants of an equivalent angle‐ply laminate (E, E, G, ν). Design equation predictions were verified by comparing them to a previously validated modified classical laminate plate theory (CLPT) model using various fiber/resin combinations. Excellent agreement was found for each set of results. POLYM. COMPOS., 26:152–164, 2005. © 2005 Society of Plastics Engineers     

Mechanical properties of polyethylene/ethylene vinyl acetate filled with calcium carbonate

The tensile behavior of polyethylene/ethylene vinyl acetate (PE/EVA) polymer blends filled with calcium carbonate (CaCO₃) was studied using tensile and viscoelastic tests. The relations between tensile properties (modulus, strength, etc) of oriented and unoriented PE/EVA-CaCO₃, and void volume of polymer/CaCO₃ interface, PE/EVA blend ratio, and CaCO₃ content were investigated. The results indicated that the tensile strength and elongation of PE/EVA-CaCO₃ decreased with CaCO₃ content and PE blend ratio for unoriented PE/EVA-CaCO₃ systems. In the case of oriented samples, the relative modulus (E/E, where E and E are the modulus of oriented composites and the modulus of oriented matrix, respectively) of PE/EVA-CaCO₃ is larger than that of PE/CaCO₃ by increasing the EVA content relative to PE and CaCO₃. The value of E/E can be simply expressed as the function of void volume and CaCO₃ modulus to polymer matrix modulus.     

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^*.     

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.     

Electrochemical synthesis and properties of poly(3‐methylthiophene): Novel synthesis of poly(3‐methylthiophene) with pentachlorostannate and hexachloroantimonate

Poly(3‐methylthiophene) (P3‐MeT) doped with different anions were prepared electrochemically in the presence of tetraalkylammonium salts. The new poly(3‐methylthiophene) SnCl and SbCl (P3‐MeT SnCl₅ and P3‐MeT SbCl₆) were prepared electrochemically using tetra‐n‐butylammonium pentachlorostannate and tetra‐n‐butylammonium hexachloroantimonate as the supporting electrolytes. The effect of current density, salt concentration, reaction temperature, and the nature of solvents on the polymer yield and polymer conductivities have been investigated. Cyclic voltammetry of poly(3‐methylthiophene) has been examined at platinum electrode in 1,2‐dichloroethane medium containing n‐Bu₄NSnCl₅, Bu₄NSbCl₆, and Bu₄NClO₄ as the supporting electrolytes in the range of −1.0 to 1.7 V versus SCE in the presence and absence of 3‐methylthiophene. Electrical conductivity, magnetic susceptibility measurements, and structural determination by elemental analysis and infrared studies were also made. Scanning electron microscopy revealed a globular, branched, fibrous and a spongy, fibrous morphology of poly(3‐methylthiophene) SnCl, ClO, and SbCl, respectively. The thermal analysis of the polymers was also investigated. Possible causes for the observed lower conductivity of these polymers have also been discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 91–102, 1999