Natural ink production and printability studies for smart food packaging

Versatile smart packages provide information on the freshness of the content and help protect the content from microorganisms. In this sense, in this study both natural antimicrobial properties and pH sensitive natural dyes were obtained from red beet. Inks were prepared and printed using this dye and their suitability for smart packaging was investigated. For this purpose, red beet was cut into small sizes and mixed separately in ethanol and water (1:2) at 200 rpm. The betaine dye was taken up in solvent. These solvents were removed with evaporator and precipitated with centrifugation and dried in a vacuum oven. The chemical structure of the obtained dye was illuminated by Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy (ATR-FTIR). The color character was determined by UV spectroscopy. Pink colored natural ink was produced by using ink varnish with carboxymethyl cellulose polymer and solid dye. Screen printing was made with this ink and the color, gloss, and lightfastness characters of prints were examined. Antimicrobial effects of the obtained prints were measured against Staphylococcus aureus and Escherichia coli. Mordanting studies were performed with (KAl[SO₄]₂.12H₂O) and change in color character was measured. The prints produced using the red beet extract have a yellow-orange color in the basic state; in acid cases it was determined to have a pink-purple color. In addition, it has been found that the ink prints obtained from red beet have antimicrobial properties against bacteria. Results prove that produced samples have good antimicrobial, pH indicator, and printability properties. This colorant can be used in smart food packaging.     

Voltammetric characterization of selective potassium ion transfer across micro-water/1,2-dichloroethane interface facilitated by a novel calix[4]arene derivative

In this study, transfer reactions of alkali and alkaline-earth metal ions across a micro-water/1,2-dichloroethane (1,2-DCE) interface facilitated by a novel calix[4]arene derivative, 5,11,17,23-tetra-tert-butyl-25,27-bis(2′amino-methylpyridine)-26,28-dihydroxy calix[4]arene (APHC4), were investigated by cyclic and differential pulse voltammetry techniques. Well-defined voltammetric behavior was obtained only for K⁺ ion among the used metal ions. The electrochemical data were used to determine the stoichiometry and the appropriate association constant of the occurring complex between K⁺ ion and APHC4. The obtained steady-state voltammograms indicated that the facilitated transfer process occurs with a TIC/TID mechanism according to 1:1 stoichiometry. The logarithm of the association constant () of K(APHC4)⁺ complex in the DCE phase was calculated to be 6.32. Also, the availability of the facilitated transfer for the design of an amperometric screening sensor for K⁺ ion was evaluated in the range of 50–500 μmol dm⁻³.     

Changes in Total Polar Compounds,Peroxide Value,Total Phenols and Antioxidant Activity of Various Oils Used in Deep Fat Frying

In this study, the effect of deep fat frying on oil degradation, total phenols (TP) and total antioxidant activity (TAA) of hazelnut, corn, soybean and olive oils were investigated. Oil degradation and oxidation were monitored by measuring the total polar compounds (TPC) and the peroxide value (PV). The amount of TPC in corn, soybean and olive oils increased significantly with the time increment (p < 0.05). The PV of the oils did not exceed the maximum acceptable limit of 10 mequiv O₂/kg after 125 min frying except for hazelnut oil (10.64 mequiv O₂/kg). Deep-fat frying did not cause any significant change in the TP of corn oil, soybean oil and olive oil (p < 0.05). A significant decrease in the antioxidant activity was observed after 50 min frying using hazelnut oil and corn oil (p < 0.05). However, the antioxidant activity of soybean oil and olive oil significantly decreased after 75 and 25 min frying, respectively.     

Investigation of ethanol conversion for hydrogen fuel cells using computer simulations

Ethanol conversion to hydrogen has been investigated by a series of thermodynamic analyses and computer simulations within the context of a cost‐effective fuel processor/fuel cell system where heat exchange is of great importance. Two different methods, multi‐reaction equilibria and Gibbs free energy minimisation, are used for the thermodynamic analyses. The computer simulations consider the catalytic conversion of ethanol to hydrogen on a bimetallic Pt–Ni catalyst by indirect partial oxidation (IPOX) which consists of total oxidation (TOX), steam reforming (SR) and water–gas shift (WGS) reactions. The results indicate that there is an optimal water:fuel ratio for maximum hydrogen production at each operating condition for hydrogen yields calculated as a percentage of the theoretical value. Mass‐based hydrogen yields are also presented considering fuel economy especially for vehicular applications. Finally, the benefits of using a secondary WGS reactor and the comparison of the results of the two thermodynamic methods are highlighted. Copyright © 2005 Society of Chemical Industry     

Biodegradation kinetics of the soluble slowly biodegradable substrate in polyamide carpet finishing wastewater

BACKGROUND: Carpet manufacturing and finishing with purely synthetic fibers has received relatively little attention, compared to other textile processing types. This study evaluates the biodegradation kinetics of organic compounds generated from polyamide‐based carpet manufacturing. RESULTS: Experiments were conducted on pre‐washing and dyeing/softening wastewater effluents. Model evaluation of oxygen uptake rate profiles with dual hydrolysis kinetics revealed that the soluble slowly hydrolysable chemical oxygen demand (COD) was the major fraction, constituting nearly 97% of the biodegradable COD and 78% of total COD content. Degradation of the slowly hydrolysable COD fraction was characterized with a rate coefficient of 0.72 day^?1, a significant rate limiting step for substrate utilization. Model simulation of system performance indicated that an unusually long hydraulic retention time was required for an activated sludge system to reduce the effluent COD concentration. CONCLUSION: Compared to domestic wastewater, two additional hydrolysable COD fractions with different degradation kinetics were characterized. The dyeing and softening step had the highest slowly biodegradable organic matter content, with the lowest degradation rate. Simulation results showed that soluble slowly hydrolysable COD degradation did not cause any problem in terms of effluent quality. With the system operated under reduced solids retention time, the effluent COD quality was significantly influenced by the slow hydrolysis rate of soluble hydrolysable matter. Copyright © 2007 Society of Chemical Industry     

Joint quantity flexibility for multiple products in a decentralized supply chain

In this study, we analyze a decentralized supply chain with a single retailer and a single manufacturer where the retailer sells multiple products in a single period. The products differ in terms of a limited number of features only. The retailer places initial orders based on preliminary demand forecasts at the beginning of the period and has an opportunity to modify its initial order after receiving perfect demand information. However, the final orders of the retailer are constrained by its initial orders. The manufacturer has two options for procurement. The first procurement option is regular delivery at the beginning of the period, after the initial orders of the retailer. The next one is expedited delivery, after the updated orders are received. In this setting, our objective is to characterize the optimal policies for the retailer and the manufacturer, and assess the benefits of flexibility.     

Integrated photochemical and biological treatment of a commercial textile surfactant: Process optimization,process kinetics and COD fractionation

The biodegradability of surfactants is a frequent and complex issue arising both at domestic as well as industrial treatment facilities. In the present experimental study, the integrated photochemical (H₂O₂/UV-C) and biochemical (activated sludge) treatment of a commercial grade nonionic/anionic textile surfactant formulation was investigated. Photochemical baseline experiments have shown that once the initial pH and H₂O₂ dose were optimized, practically complete COD removal (COD_o = 500 ± 30 mg L⁻¹) could be achieved. Once the COD was elevated to values being typical for the textile fabric preparation stage, treatment efficiency was seriously retarded provided that the photochemical treatment conditions remained constant. Moreover, a definite relationship existed between H₂O₂ consumption and COD removal for H₂O₂/UV-C advanced oxidation of the textile surfactant. In the second part of the study, COD abatement was modeled for the biodegradation of untreated and photochemically pretreated textile surfactant formulation according to their COD fractions. Results have indicated that the readily biodegradable and rapidly hydrolysable COD fractions of the textile surfactant solution could be appreciably increased upon exposure to an optimum H₂O₂ concentration (60 mM; i.e. 2.1 g H₂O₂ (g COD_o)⁻¹) and extended UV-C irradiation times (i.e. 90 and 120 min).     

Investigations of nickel(II) removal from aqueous solutions using tea factory waste

This paper presents the data for the effect of adsorbent dose, initial metal concentration, solution pH, agitating rate and temperature on the adsorption of nickel(II) on waste tea. Batch adsorption studies have been carried out. The equilibrium nature of nickel(II) adsorption at different temperature (25-60 degrees C) has been described by the Freundlich and Langmuir isotherm. The adsorption capacity (Q(0)) calculated from Langmuir isotherm was 15.26 mg Ni(II) g(-1) at initial pH of 4.0 at 25 degrees C. The results of the thermodynamic investigations indicate that the adsorption reactions are spontaneous (DeltaG degrees <0), slightly endothermic (DeltaH degrees > 0) and irreversible (DeltaS degrees > 0).