The waste water from food processing contains dissolved salts and organic matter. The amount of each depends upon the product being processed and the procedure being used. The suitability for irrigation of food processing waste water from 20 plants processing nine food products was assessed from the standpoint of electrical conductivity (EC), chloride and sodium concentrations, sodium-adsorption-ratio (SAR), and chemical oxygen demand (COD). Waste water from plants processing green beans (Phaseolus vulgaris L.), squash (Cucurbita pepo var. melopepo Alef.), tomatoes (Lycopersicon esculentum Mill.), corn (Zea mays L.), steam peeled potatoes (Solanum tuberosum L.) and sweet potatoes (Ipomoea batatas Lam.), and poultry is suitable for irrigation under most conditions. Waste water from some pea (Pisum sativum L.) and lima beans (Phaseolus lunatus L.) processing plants may be suitable for irrigation, but is of questionable suitability from others. Waste water from lye-peel potato processing is not suitable for irrigation.

Japan's Specifications and Standards for Food Additives, 7th Edition (JSFA-VII) does not set limits for total contents of water-soluble chlorides and water-soluble sulfates (water-soluble inorganic salts) in food color aluminum lakes (FC-Als). However, the regulatory limit is 2% in JECFA and CFR. We used column switching suppressor-type ion chromatography (CSS-IC) for determination of anions. The total contents of water-soluble inorganic salts in FC-Als (112 qualified samples) were determined using the modified CSS-IC from fiscal year 1998 to fiscal year 2003. Total contents of water-soluble inorganic salts in four samples exceeded 2%. From an international point of view, it is desirable that the total content of water-soluble inorganic salts in FC-A1 should again be regulated in Japan.

In this study, Sea Water Bread (SWB), made with food grade sea water was compared with control bread made with Tap Water (TWB). Sea water’s influence on chemical-nutritional properties of bread was investigated. Contents of salt, macro/micro-elements, basic nutrients, polyphenols, antioxidant activity, olfactory characteristics, and volatile components were analyzed. Chlorides’ analysis showed SWB had a lower salt content than TWB and it was confirmed by ICP-OES investigation. An electronic nose confirmed differences between the groups of aromatic molecules of the bread typologies, as well as the profiles of the volatile molecules by GC-MS.

This study aimed to determine the quality of drinking water supplied in different types of food stalls in Jashore Municipality, Bangladesh. A total of 35 water samples were collected from different tea stalls, street side fast food stalls, normal restaurants and well-furnished restaurants. The water quality was evaluated by determining the distinct physical, chemical and biological parameters. The results revealed that the water used in the food stalls and restaurants for drinking purpose was in desired quality in terms of turbidity, electrical conductivity, pH, total dissolved solids, nitrate (NO₃⁻), sulfate (SO₄²⁻), phosphate (PO₄³⁻), chloride (Cl⁻), sodium (Na) and potassium (K) concentrations. The values were within the permissible limit proposed by the Bangladesh Bureau of Statistics and the World Health Organization. Concentrations of calcium (Ca) and magnesium (Mg) found in several samples were higher than the World Health Organization standard. Iron (Fe) concentrations were higher than the permissible limit of the World Health Organization. Only 46% exceeded the permissible limit of Bangladesh Bureau Statistics. The threatening result was that the samples were contaminated by fecal coliform, indicating that the people of Jashore Municipality may have a greater chance of being affected by pathogenic bacteria. The drinking water provided in the street side fast food stalls was biologically contaminated. The findings demonstrate that the drinking water used in food stalls and restaurants of Jashore Municipality did not meet up the potable drinking water quality standards and therefore was detrimental to public health.

Food safety issues and increases in food borne illnesses have promulgated the development of new sanitation methods to eliminate pathogenic organisms on foods and surfaces in food service areas. Electrolyzed oxidizing water (EO water) shows promise as an environmentally friendly broad spectrum microbial decontamination agent. EO water is generated by the passage of a dilute salt solution (approximately 1% NaCl) through an electrochemical cell. This electrolytic process converts chloride ions and water molecules into chlorine oxidants (Cl2, HOCl/ClO-). At a near-neutral pH (pH 6.3-6.5), the predominant chemical species is the highly biocidal hypochlorous acid species (HOCl) with the oxidation reduction potential (ORP) of the solution ranging from 800 to 900 mV. The biocidal activity of near-neutral EO water was evaluated at 25 °C using pure cultures of Escherichia coli, Salmonella typhimurium, Staphylococcus aureus, Listeria monocytogenes, and Enterococcus faecalis. Treatment of these organisms, in pure culture, with EO water at concentrations of 20, 50, 100, and 120 ppm total residual chlorine (TRC) and 10 min of contact time resulted in 100% inactivation of all five organisms (reduction of 6.1-6.7 log10 CFU/mL). Spray treatment of surfaces in food service areas with EO water containing 278-310 ppm TRC (pH 6.38) resulted in a 79-100% reduction of microbial growth. Dip (10 min) treatment of spinach at 100 and 120 ppm TRC resulted in a 4.0-5.0 log10 CFU/mL reduction of bacterial counts for all organisms tested. Dipping (10 min) of lettuce at 100 and 120 ppm TRC reduced bacterial counts of E. coli by 0.24-0.25 log10 CFU/mL and reduced all other organisms by 2.43-3.81 log10 CFU/mL.

The effect of esterification on hydrolyzed rice starch was analyzed, for this aim rice starch was hydrolyzed and subsequently esterified with lauroyl chloride at three modification levels. Starch derivatives were characterized regarding their degree of substitution (DS), water solubility index, z-potential, gelatinization, and digestibility properties. DS of derivatives of rice starch laurate ranged from 0.042 to 1.86. It was determined that after esterification the water solubility index increased from 3.44 to 53.61%, the z-potential decreased from −3.18 to −11.27, and the content of slowly digestible starch (SDS) decreased from 26.22 to 5.13%. Different emulsions with starch concentrations ranging from 6 to 30 wt% were evaluated. The most stable emulsions were those having 20 and 30 wt% of rice starch laurate.

Groups of 0+ Atlantic salmon (Salmo salar) smolts were transferred to duplicate seawater tanks, and subjected to five different ration levels, 0% (starved), 25%, 50%, 75% or 100% (full fed). Waste feed was collected after each meal. After six weeks all groups were re-fed in excess. During the trial period body weight and length increased significantly in the 50, 75 and 100% groups, while no significant changes in body weight were observed in the 0% and 25% groups. A significant decrease in SGR was observed in the 0 and 25% groups during the first month in sea water. After re-feeding, SGR increased in all groups. All groups, except the previously starved group, showed peak SGR between weeks 6-8 and 8-12. Food restriction at 0% and 25% of full ration for a period of six weeks resulted in significant osmotic disturbances. After six weeks in sea water, plasma Cl⁻ levels were higher in the 0% group than in the other groups. Branchial Na⁺,K⁺-ATPase activity increased in all groups following exposure to seawater. Re-feeding caused a transient increase in branchial Na⁺,K⁺-ATPase activity after two weeks in the previously starved group, with a concurrent reduction in plasma Cl⁻ levels. Previous exposure to different ration levels significantly influenced growth rate and mean body size. Compensatory growth and partial size compensation was seen in the 0, 25 and 50% feed deprivation groups, whereas full size compensation was found in the 75% group.

In this work, an ecologically friendly, cheap, and highly efficient hydrophobic deep eutectic solvent based liquid phase microextraction procedure was developed and coupled with flame atomic absorption spectrometry for determination of cadmium. Hydrophobic deep eutectic solvent (HDES) was prepared by mixture of trihexyltetradecylphosphonium chloride and pivalic acid and used as extraction solvent. The formation of cadmium complex was achieved by sodium diethyldithiocarbamate trihydrate. Response Surface Methodology by Box–Behnken Design and three different models was used for optimizing experimental conditions and statistical analysis. Analytical parameters such as limit of detection, limit of quantification, relative standard deviation and enhancement factor were calculated as 1.6 µg L⁻¹, 5.0 µg L⁻¹, 3.3% and 43, respectively. Finally, the developed liquid phase microextraction method was applied to some food and water samples.

Bisphenol A (BPA) contamination in foods and beverages usually occurs as a result of migration from the packages that contain it. In this context, a simple, easy-to-use, and efficient method was developed for the spectrophotometric determination of BPA in food, milk, and water samples in contact with plastic products after preconcentration by ultrasonic-thermostatic-assisted cloud point extraction (UTA-CPE). The method is based on the charge transfer-sensitive complexation of BPA with 3-methylamino-7-dimethylaminophenothiazin-5-ium chloride (AzB) in the presence of cetyltrimethylammonium bromide (CTAB) at pH 8.5 and then extraction of the formed complex into the micellar phase of polyethylene glycol dodecyl ether (Brij 35). The effects of the analytical variables affecting complex formation and extraction efficiency were systematically studied and optimized. Under optimized conditions, a good linear relationship was obtained in the range of 1.2–160 μg L⁻¹ with a detection limit of 0.35 μg L⁻¹. After preconcentration of a sample of 20 mL, a sensitivity enhancement factor was found to be 180. The accuracy and reliability of the method were evaluated by recovery studies from the spiked quality control samples and intraday and interday precision studies. From the studies conducted, the extraction efficiency (E%) was in the range of 94–103% with a relative standard deviation lower than 5.2% (as RSD%, n = 5). The method was successfully applied to the preconcentration and determination of BPA from the selected sample matrices. Graphical Abstract Migration of bisphenol A into the foodstuffs