Reduction Discoloration of Reactive Dyed Cotton Waste and Chemical Recycling via Ionic Liquid

The textile industry generates large volumes of waste throughout its production process.Most of this waste is colored,therefore,discoloration is an important step toward recycling and reusing this waste.This study focused on the chemical reductive discoloration of textile waste composed of cotton dyed with reactive dye.The experimental design demonstrated the significant influence of the concentration of reducing agent and time of reaction on the degree of whiteness of the cotton fibers.The concentration of the alkaline agent was not significant in the process.The optimization of the reaction conditions lead to Berger degree of 50.5±3.5.The discolored cotton was chemically recycled through dissolution in ionic liquid 1-ethyl-3-methylimidazolium chloride and regeneration in film form in water.The microstructure of the regenerated cellulose films was evaluated by Scanning Electron Microscopy(SEM)indicating complete dissolution and uniform regeneration.The discoloration process reduced the polymerization degree and crystallinity index of the cotton fibers but retained the cellulose I structure.The dissolution and cellulose regeneration process results in transparent films with an amorphous structure.The thermal behavior,evaluated by thermogravimetric analysis,indicated that residues and regenerated film presented a main decomposition step.The maximum decomposition rate temperature of the regenerated films was approximately 40℃lower than the cotton fibers,which correlates well with the reduction in polymerization degree and amorphous structure.In general,the study demonstrated that textile cotton waste dyed with reactive dyes can be chemically discolored to form transparent and amorphous films,contributing to the development of sustainable strategies for the textile industry.

Adsorptive Properties of Dyes to Cellulosic Sheet and Discoloration of Dye Solution by UV-ray Irradiation

The adsorptive properties and selectivity of dyes and water molecules to cellulosic sheet, dependence of adsorptive properties of dyes on the concentration of dye solution, and discoloration of the dye solution due to the UV-ray irradiation were determined for 18 kinds of commercial dyes. The results are as follows： 1） the adsorptive properties of dyes to cellulose sheet differed greatly, but did not depend on the dye types such as acidic, basic and so on; 2） adsorptive properties of dyes to cellulosic sheet de- pended on the concentration of dye solution and were classified into 4 types： concentration-independent, increasing or decreasing with dye concentration, and having a maximum. This classification was irrelevant to the dye types; 3） the irradiation of UV-ray did not cause significant discoloration of dye solution itself, which suggested that wood components as well as dye molecules influence the discoloration of wood.

Discoloration of Congo Red by Rod-Plate Dielectric Barrier Discharge Processes at Atmospheric Pressure

A dielectric barrier discharge （DBD） reactor with a rod-plate electrode configuration was used for the oxidative decomposition of Congo red dye in an aqueous solution. Plasma was generated in the gas space above the water interface under atmospheric pressure. Discharge characteristics were analyzed by voltage-current waveforms. Effects of applied voltage, initial conductivity, and initial concentration were also analyzed. Congo red discoloration increased with increased applied voltage and decreased conductivity. The initial conductivity significantly influenced the Congo red discoloration. Under the same conditions, the highest discoloration rate was obtained at 25 mg/L. The presence of ferrous ions in the solutions had a substantial positive effect on Fenton dye degradation and flocculation. At an applied voltage of 20 kV, about 100% of dye was degraded after 4 min of Fe^2＋/DBD treatment. Results showed that adding a certain dosage of hydrogen peroxide to the wastewater could enhance the discoloration rate. Possible pathways of Congo red discoloration by DBD plasma were proposed based on GC/MS, FTIR, and UV-vis spectroscopy analyses.

Correlation of discoloration and biomechanical properties in porcine sclera induced by genipin

·AIM: To study the feasibility of using the discoloration to evaluate the biomechanical properties after treating with genipin.·METHODS: Porcine cadaver eyes were treated for30 min with 1.0%(by w/v) genipin. Untreated samples were used as controls. After treatment, scleral strips of4.0 ×10.0-mm2 were cut. The denaturation temperature(Td) measurement and stress-strain test were performed after taking photograph to analyze the color.·RESULTS: Within 24 h after treating with genipin, the sclera exhibited a bluish color which became deeper with time. And the denaturation temperature also was increased gradually. Compared with untreated groups, at1, 6, 12, 24 and 36 h after treatment, the ultimate stress were increased by 56%, 153%, 173%, 225% and 211%respectively. The Young’s modulus at 10% strain also increased by 170%, 246%, 264%, 389% and 288%respectively. There were strong correlation between the discoloration and the biomechanical properties(ΔE-Ultimate stress:R2=0.892, P =0.00; ΔE-Young’s modulus:R2=0.602, P =0.00).·CONCLUSION: Genipin could be used to strengthen collagen gradually in a relatively short time span. And the biomechanical properties could be reliably evaluated via simple visible discoloration.

Effect of drying methods on the discoloration of three major domestic softwood species in Korea

Japanese pine, Korean pine and larch are three major softwood species in Korea. Their colors are relatively light, thus easily discolored due to drying and UV irradiation. In this study, they were dried with five different drying methods, steam treated and exposed to weathering. Their colors were measured using a spectrophotometer and comparisons made both among species and drying methods. For Japanese and Korean pines, high temperature dried and steam-dried specimens showed distinct color differences compared with the controls. Steam treatment discolored the dried specimens of Japanese and Korean pines but did not discolor those of larch. After weathering for 144 days the specimens of Japanese pine showed slight color differences among drying methods.

Effects of gold plating on the resistance to high temperature discoloration of the cavity for ceramic packages

The effects of thickness and types of gold plating on the resistance to hightemperature discoloration of gold plating on cavity surface of ceramic package were investigated. Itwas found that the thicker gold plating, the less discoloration degree for ceramic packages.Non-cyanide gold plating performed better resistance to high-temperature aging than cyanide goldplating. The relationship between the gold plating thickness and the amount of diffused Ni to thegold plating of ceramic packages with Au/Ni and Au/Ni-Co platings after heating at 420℃ for 15 minwas also studied. When the gold plating thickness reach 2.0 μm and 1.6 μm for Au/Ni and Au/Ni-Coplating systems, respectively, no discoloration was observed on the gold plating surface of cavity,and the corresponding diffused Ni amounts (mass fraction) are 1.0% and 0.4%, while the diffused Coto the gold plating is 0.04%.

In-situ pressure-induced BiVO_(4)/Bi_(0.6)Y_(0.4)VO_(4) S-scheme heterojunction for enhanced photocatalytic overall water splitting activity

Step-scheme(S-scheme)heterojunctions in photocatalysts can provide novel and practical insight on promoting photogenerated carrier separation.The latter is critical in controlling the overall efficiency in one-step photoexcitation systems.In this study,a nanosized BiVO4/Bi0.6Y0.4VO4 solid solution was prepared by a coprecipitation method following with hydrothermal or calcination processes.The S-scheme heterojunction was fabricated by in-situ pressure-induced transformations of bismuth vanadate from the tetragonal zircon phase to the monoclinic scheelite phase,which led to the formation of BiVO4 nanoparticles with a diameter of approximately 5 nm on the surface of BiVO_(4)/Bi_(0.6)Y_(0.4)VO_(4)/Bi_(0.6)Y_(0.4)VO_(4) with S-scheme heterojunctions showed significantly enhanced photocatalytic overall water splitting activity compared with using bare BiVO_(4)/Bi_(0.6)Y_(0.4)VO_(4).Characterization of the carrier dynamics demonstrated that a superior carrier separation through S-type heterojunctions might have caused the enhanced overall water splitting(OWS)activity.Surface photovoltage spectra and the results of selective photodeposition experiments indicated that the photogenerated holes mainly migrated to the BiVO4 nanoparticles in the heterojunction.This confirmed that the charge transfer route corresponds to an S-scheme rather than a type-II heterojunction mechanism under light illumination.This study presents a facile and efficient strategy to construct S-scheme heterojunctions through a pressure-induced phase transition.The results demonstrated that S-scheme junctions composed of different crystalline phases can boost the carrier separation capacity and eventually improve the photocatalytic OWS activity.

Pressure-induced growth of coralloid-like FeF_(2) nanocrystals to enable high-performance conversion cathode

Fluoride ferrous(FeF_(2))is viewed as a promising conversion cathode material for next-generation lithiumion batteries(LIBs)due to its high theoretical specific capacity and low cost.Unfortunately,issues such as poor intrinsic conductivity,iron dissolution,and phase separation hinder the application of FeF_(2)in highenergy cathodes.Here,a pressure-induced morphology control method is designed to prepare coralloidlike FeF_(2)nanocrystals with nitrogen-rich carbon coating(c-FeF_(2)@NC).The coralloid-like interconnected crystal structure of c-FeF_(2)@NC contributes to reducing interfacial resistance and enhancing the topotactic transformation during the conversion reaction,and the nitrogen-rich carbon(NC)coating can enhance interfacial stability and kinetic performance.When used as a conversion cathode for LIBs,c-FeF_(2)@NC exhibits a high initial reversible capacity of 503.57 mA h g^(-1)and excellent cycling stability of497.61 m A h g^(-1)with a low capacity decay of 1.19%over 50 cycles at 0.1 A/g.Even at 1 A/g,a stable capacity of 263.78 mA h g^(-1)can still be retained after 200 cycles.The capability of c-FeF_(2)@NC as a conversion cathode for sodium-ion batteries(SIBs)was also evaluated to expand its field of application.Furthermore,two kinds of full batteries have been assembled by employing c-FeF_(2)@NC as cathodes and quantitative limited-Li(LLi)and pre-lithiated reduced graphene oxide(PGO)as anodes,respectively,to envisage the feasibility of practical applications of conversion materials.

Evaluation of Teeth Discoloration Induced by Endomethasone, AH+, Canason and Apexit Paste

Objective: The aim of this study was to investigate, in vitro, the color changes of the teeth, induced by endodontic sealers. Materials and Methods: Forty-five mature maxillary and mandibular anterior teeth, extracted for periodontal reasons, were collected. After the chemo-mechanical instrumentation of the root canal, teeth were filled with four endodontic sealers (Endomethason, AH+, Canason and Apexit). Depending on canal sealers and the CEJ (Cement Enamel Junction), teeth were divided into 8 experimental groups (n = 5) and one control group/CG (n = 5). Teeth color changes (L*a*b*/CIE Commission Internationaled’ Eclaraige) were determinated by a spectrophotometer Vita Easyshade in 4 stages (Baseline, Week 0, 4 and 12). Results: Between the EOCEJ and CG for the parameter L*, there was a statistical significance (p 0.05). The L*a*b* results were: L* (83.6 ± 4.8 → 83.6 ± 4.9);a* (﹣2.68 ± 1.02 → ﹣1.12 ± 0.72) and b* (20.2 ± 4.5 → 24.4 ± 4.2). Conclusions: All endodontic sealers may cause teeth discoloration.

Pressure-Induced Charge-Order Melting and Reentrant Charge Carrier Localization in the Mixed-Valent Pb3Rh7O15

The mixed-valent Pb3Rh7O15 undergoes a Verwey-type transition at Tv≈180K, below which the development of Rh3＋3＋/Rh4＋4＋ charge order induces an abrupt conductor-to-insulator transition in resistivity. Here we investigate the effect of pressure on the Verwey-type transition of Pb3Rh7O15 by measuring its electrical resistivity under hydrostatic pressures up to 8GPa with a cubic anvil cell apparatus. We find that the application of high pressure can suppress the Verwey-type transition around 3GPa, above which a metallic state is realized at temperatures below ～70K, suggesting the melting of charge order by pressure. Interestingly, the low-temperature metallic region shrinks gradually upon further increasing pressure and disappears completely at P〉7GPa, which indicates that the charge carriers in Pb3Rh7O15 undergo a reentrant localization under higher pressures. We have constructed a temperature-pressure phase diagram for Pb3Rh7O15 and compared to that of Fe3O4, showing an archetype Verwey transition.

Effects of gold plating on the resistance to high temperature discoloration of the cavity for ceramic packages

The effects of thickness and types of gold plating on the resistance to high temperature discoloration of gold plating on cavity surface of ceramic package were investigated. It was found that the thicker gold plating, the less discoloration degree for ceramic packages. Non-cyanide gold plating performed better resistance to high-temperature aging than cyanide gold plating. The relationship between the gold plating thickness and the amount of diffused Ni to the gold plating of ceramic packages with Au/Ni and Au/Ni-Co platings after heating at 420℃for 15 min was also studied. When the gold plating thickness reach 2.0 μm and 1.6 μm for Au/Ni and Au/Ni-Co plating systems, respectively, no discoloration was observed on the gold plating surface of cavity, and the corresponding diffused Ni amounts (mass fraction) are 1.0% and 0.4%, while the diffused Co to the gold plating is 0.04%.

Discoloration on Methylene Blue Solutions by Direct and Catalytic Ozonation

During textile manufacturing, huge amounts of wastewaters characterized by removed impurities and high concentrations of dye are produced. These wastewaters cause several problems when they are discharged to the environment. The use of ozone in wastewater treatment results of interest. In this work we propose to assess the discoloration rate of different synthetic wastewaters as a function of pH, dye concentration (methylene blue (MB)) and reaction time. A comparison of discoloration rate between conventional ozonation and catalytic ozonation salts of copper, zinc, silver and nickel was also performed. For the optimization of the ozonation process of colored solutions, it was used a central composite experimental design with five replicates of the center point resulting to evaluate the influence of the independent variables at different ranges of pH, [MB] and time. In the catalyst-assisted ozonation, [MB], pH and the reaction time were fixed to 100 mg/L, 5.5 and 15 min, respectively. The optimized experimental conditions to provide maximum discoloration were pH=3.3;[MB]=8.6 mg/L and time=74.3 min. Regarding the catalyst-assisted ozonation, it was found that CuSO4 catalyst gave better color reduction if compared with other catalysts assayed.

Pressure-induced phase transition and electronic structure evolution in layered semimetal HfTe_(2)

Motivated by the recent experimental work,the pressure-induced structural transition of well-known two-dimensional(2D)1T-Hf Te_(2)was investigated up to 50 GPa through the advanced CALYPSO structure search technique combined with the first-principles calculations.Our calculations suggested that the 1T-Hf Te_(2)will first transform to C2/m phase at 3.6 GPa with a volume reduction of 7.6%and then to P62m phase at 9.6 GPa with a volume collapse of 4.6%.The occurrences of 3D C2/m and P62m phases mainly originated from the enhanced Te-Te interlayer coupling and the drastic distortions of Hf-Te polyhedrons in P3m1 phase under compression.Concomitantly,the coordination number of Hf atoms increased from six in P3m1 to eight in C2/m and eventually to nine in P62m at elevated pressure.The metallic and semimetallic nature of C2/m and P62m phases were characterized,and the evidence of the reinforced covalent interactions of Te-Hf and Te-Te orbitals in these two novel high-pressure phases were manifested by the atom-projected electronic DOS and Bader charge.

Energy Spectrum of La3Lu2Ga3O12：Cr^3＋ and Its Pressure-Induced R-Line-Shift Reversal

By means of both the theory for pressure-induced Shifts （PS） of energy spectra and the theory for shifts of energy spectra due to electron-phonon interaction （EPI）, the normal-pressure energy spectra of α and β centers of Cr^3＋ ions for LLGG：Cr^3＋ and the PS＇s of R1 lines and U band of these centers have been calculated at 10 K, respectively. The total calculated results are in very good agreement with the experimental data. For LLGG：Cr^3＋, the pressureinduced low-high crystal-field transition and the reversal of R1-line PS take place. The pressure-dependent variation of Rmix^ei （2E - 4T2） [mixing-degree of （t2^2 （^3T1）e^4T2） and （t2^3 E） base-wavefunctions in the wavefunction of R1 state without EPI] plays a key role for the reversal of R1-line PS. The behavior of the pure electronic PS of R1 line is quite different from that of the PS of R1 line due to EPI. It is the combined effect of them that gives rise to the total PS of R1 line. The comparison between R1-line PS＇s of GSGG：Cr^3＋ and LLGG：Cr^3＋ has been made. It is found that a peak of R1-line PS appears at Rmix^ei （^2E - ^4T2） ≈ 0.08.

Dynamic Investigations of Pressure-Induced Abnormal Phase Transitions in PbTiO3

The effects of pressure on phonon modes of ferroeleetrie tetragonal P4mm and paraelectric cubic Pm3m PbTiOa are systematically investigated by using first-principles simulations. The pressure-induced tetragonal-to-cubie and subsequent cubic-to-tetragonal phase transitions are the second-order transitions, which are different from the phase transitions induced by temperature [Phys. Rev. Lett. 25 （1970） 167]. As pressure increases, the lowest A1 and E modes of the tetragonal phase become softer and converge to the F1u mode of the cubic phase. As pressure further increases, the lowest Flu mode first hardens and then softens again, and finally diverges into A1 and E modes. The behaviors of optical phonon modes confirm the ferroelectric-to-paraelectric-to-ferroeleetric phase transitions.

Pressure-Induced Metallization and Electrical Phase Diagram for Polycrystalline CaB_6 under High Pressure and Low Temperature

The electrical properties of polycrystaltine CaB6 are revealed by in-situ resistance measurements under high pressure and low temperature. Due to the existence of grain boundaries, polycrystalline CaB6 behaves with semiconducting transport properties, which is different from the semimetallic CaB6 single crystals. The temperaturedependent resistance measurement results show that before the structural phase transition at 12.3 GPa the high pressure first induces the metallization at 6.5 GPa for CAB6. Moreover, the phase diagram for CaB6 is drawn based on the investigated electric conducting properties and at least three different conducting phases are found even at moderate high pressure and low temperature, indicating that the electric nature of CaB6 is very sensitive to the environment.

Revealing the Pressure-Induced Softening/Weakening Mechanism in Representative Covalent Materials

Diamond, cubic boron nitride(c-BN), silicon(Si), and germanium(Ge), as examples of typical strong covalent materials, have been extensively investigated in recent decades, owing to their fundamental importance in material science and industry. However, an in-depth analysis of the character of these materials' mechanical behaviors under harsh service environments, such as high pressure, has yet to be conducted. Based on several mechanical criteria, the effect of pressure on the mechanical properties of these materials is comprehensively investigated.It is demonstrated that, with respect to their intrinsic brittleness/ductile nature, all these materials exhibit ubiquitous pressure-enhanced ductility. By analyzing the strength variation under uniform deformation, together with the corresponding electronic structures, we reveal for the first time that the pressure-induced mechanical softening/weakening exhibits distinct characteristics between diamond and c-BN, owing to the differences in their abnormal charge-depletion evolution under applied strain, whereas a monotonous weakening phenomenon is observed in Si and Ge. Further investigation into dislocation-mediated plastic resistance indicates that the pressure-induced shuffle-set plane softening in diamond(c-BN), and weakening in Si(Ge), can be attributed to the reduction of antibonding states below the Fermi level, and an enhanced metallization, corresponding to the weakening of the bonds around the slipped plane with increasing pressure, respectively. These findings not only reveal the physical mechanism of pressure-induced softening/weakening in covalent materials, but also highlights the necessity of exploring strain-tunable electronic structures to emphasize the mechanical response in such covalent materials.

The Thermal and Mechanical Properties of Ultra-High Molecular Weight Polyethylene/Montmorillonite (UHMWPE/MMT) Nanocomposites Hybrid Gel Using Pressure-Induced Flow (PIF) Processing

Hybrid organic-inorganic polymer nanocomposites incorporating organically modified montmorillonite (MMT) and ultra-high molecular weight polyethylene (UHMWPE) were examined. UHMWPE/MMT hybrid nanocomposites were prepared using gel and pressure-induced flow(PIF) processing methods at a gel weight concentration of 8% UHMWPE with various organoclay contents (0, 0.4, 0.8, 1.2, and 1.6 parts per hundred parts). The interlayer properties of the nanocomposites were studied by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The thermal and mechanical interfacial properties of the nanocomposites were investigated through thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and the use of a universal test machine (UTM). TEM indicates that the nanocomposites are formed upon dispersion of MMT in the polymer matrix. From the DSC, TGA, and DMA results, we find that the thermal stability of the UHMWPE nanocomposites increases as the MMT content increases. The nanocomposites show higher tensile strengths than pure UHMWPE gel sheet. These findings indicate that the interfacial and mechanical properties are improved by the addition of MMT and PIF processing.

Pressure-induced phase transition of B-type Y_2O_3

The synthesized monoclinic（B-type） phase of Y2O3 has been investigated by in situ angle-dispersive x-ray diffraction in a diamond anvil cell up to 44 GPa at room temperature. A phase transition occurs from monoclinic（B-type） to hexagonal（A-type） phase at 23.5 GPa and these two phases coexist even at the highest pressure. Parameters of isothermal equation of state are V0= 69.0（1）A3, K0= 159（3） GPa, K0= 4（fixed） for the B-type phase and V0= 67.8（2） A3, K0= 156（3） GPa,K＇0= 4fixed for the A-type phase. The structural anisotropy increases with increasing pressure for both phases.

Discoloration Range and Shroud Image Depth Values Cannot Be Satisfied by the Same Proton Energy

The radiative hypothesis has been revisited showing other characteristics, produced by the protons used as dyes in total disagree with the ones of the Body Image that appears on the Shroud of Turin. Our investigations highlight that for the protons to reach 3.7 cm in air, the distance that measures the range of discoloration effects, must be emitted with an energy of about 1.5 MeV using Wilson and Brobeck’s empirical formula and 1.35 MeV using Bethe’s. This last formula provides a result closer to reality. Bethe shows that the penetration depth is greater than that calculated empirically. Such a value of proton energy (1.35 MeV) makes it possible to satisfy the discoloration effects range for the Shroud but it is incompatible with a depth of penetration in linen that is only 200 nm. Moreover, using the same subatomic particles, we obtained on the colored linen a distribution of energy represented by regression but not linear. Thus, also the possible I(z) correlation, between color intensity and body-sheet distance, which should be due to the oxidizing action of protons, does not agree with that extracted from the Shroud of Turin.