Correction to: Role of casting and curing conditions on the strength and drying shrinkage of greener concrete

Environmental Science and Pollution Research -     

Role of casting and curing conditions on the strength and drying shrinkage of greener concrete

The shrinkage of cement-based materials is a critical dimensional property that needs proper attention as it can influence the corresponding characteristics especially when the preparation of such cement-based material is done in hot weather. Studies have shown that the casting or curing conditions influence the performance of concrete. However, there is limited understanding of the combined role of casting temperature and curing conditions, especially for concrete made with unconventional binders. In this study, five supplementary cementitious materials (SCMs) were utilized as the substitute of the ordinary Portland cement (OPC) at different ratios to produce greener concrete and improve its characteristics and sustainability. The influence of four casting temperatures (i.e., 25 °C, 32 °C, 38 °C, and 45 °C) and two curing regimes (i.e., covering of samples using wet burlap and applying curing compound on the surface of samples) on the corresponding compressive strength and drying shrinkage at various ages was studied. The outcomes of this research revealed that the composition of the binders has a substantial impact on the characteristics of concrete. In addition, the casting temperature and curing regimes also have a huge role on the compressive strength of concrete produced with binary binders. For example, the compressive strength at 3 days of concrete made at 25 °C made with binary binders was reduced up to 31% compared to that made with only OPC as the binder when cured using wet burlap. Nonetheless, less than 38 ℃ was suitable to minimize the durability issues in the studied blended cement mixes.

     

Biochemical assessment of lead,phenol, and benzene-contaminated water on the heart and blood of Albino rats

A study was performed to evaluate the effect of contaminated water on the tissues of Rattus novergicus (albino rats). Test rats were given water contaminated with lead (0.015 µg L^?1 tap water), phenol (0.05 mL L^?1 tap water), and benzene (0.05 mL L^?1 tap water), while control rats were given tap water over a period of 65 days after which the activity of selected enzymes of the heart and serum was assayed, and hematological parameters and serum lipid profiles were also determined. Generally, a significant (p < 0.05) drop in the activity of the enzymes was observed in the heart of test rats relative to the control rats. However, the serum activities increased significantly in the test group compared to the control group (p < 0.05). The concentrations of serum cholesterol, low-density lipoprotein (LDL), and triglycerides of the test rats were found to be significantly higher than those of the control rats (p < 0.05). Concentrations of hemoglobin, red blood cell count, and packed cell volume of test rats were observed to be significantly lower than those of the control rats (p < 0.05). The experimental results indicated that consumption of water contaminated with lead, phenol, and benzene may damage the heart, increase the risk of atherosclerosis as reflected by the serum lipid profile, and anemia as suggested by abnormal hematological properties.     

High boron removal by functionalized magnesium ferrite nanopowders

Hydroxyl-enriched materials are promising boron adsorbents. However, the use of these materials is hampered by issues of separation, recovery, and selectivity, notably due to the presence of interfering ions. Therefore, we synthesized here a cheap magnetic nanopowder, which was further functionalized with polyvinyl alcohol and glycidol to produce boron-selective adsorbents. We studied their selectivity and removal efficiency using batch and fixed-bed systems. Sorption was studied at both concentrated and trace amounts of boron. Results show that nanopowders have 5.3–6.5 nm pore sizes and 145–203 m²/g surface areas, using Brunauer–Emmett–Teller analysis. Polyvinyl alcohol-functionalized particles removed 93 % of boron at 5 mg/L at pH 7 in 30 min, whereas only 68 % of boron was removed by glycidol-functionalized particles. However, at higher boron concentration, of 50 mg/L, glycidol-functionalized particles showed higher adsorption affinity of 68.9 mg/g. We conclude that internal hydroxyl groups of polyvinyl alcohol-functionalized particles are less accessible at higher boron concentration. This is the first report on magnesium ferrites for boron recovery. The spent adsorbents were separated easily from the aqueous media by an external magnet and repeatedly used. Overall, our findings demonstrated that the hydroxyl-enriched magnetic nanopowders are a better alternative to the existing boron adsorbents regarding magnetic separation, reusability, and selectivity.     

Trace elements in particulate matter of ambient air at petroleum filling stations

Size segregated suspended particulate matter (PM_2.5 and PM_10-2.5) in air at four major petroleum-filling stations in Ile-Ife, Nigeria, were monitored using double staged “Gent” stacked samplers to assess variations in mass loads and elemental concentrations of 25 elements. Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, Zr, Cs, Ta, W, and Pb were determined in both fractions by external ion beam proton-induced X-ray emission technique. Enrichment factors and pollution indices were calculated and results revealed that most elements were anthropogenic in both fractions with concentrations exceeding the World Health Organization guideline standards.     

Sub-cooled and flashing liquid jets and droplet dispersion I. Overview and model implementation/validation

Many accidents involve two-phase releases of hazardous chemicals into the atmosphere. This paper describes the results of a third phase of a Joint Industry Project (JIP) on liquid jets and two-phase droplet dispersion. The aim of the project is to increase the understanding of the behaviour of sub-cooled non-flashing and superheated flashing liquid jets, and to improve the prediction of initial droplet size, droplet dispersion and rainout.Phase III of the JIP first included scaled experiments for materials with a range of volatilities (water, cyclohexane, butane, propane and gasoline). These experiments were carried out by Cardiff University including measurements of flow rate and initial droplet size across the full relevant range of superheats. See the companion paper II for further details of these experiments and the derivation of new refined correlations for droplet size distribution and Sauter Mean Diameter. Furthermore large-scale butane experiments were carried out by INERIS (France) to ensure that for more realistic scenarios the derived droplet size correlations are accurate.Model validation and model improvements were carried out by DNV Software, including validation of release rate and initial droplet size against the above scaled and large-scale experiments. New correlations for droplet size distribution and Sauter Mean Diameter (SMD) were implemented into the Phast discharge model. These were compared against a range of other droplet size and rainout correlations published in the literature, in conjunction with validation against an extensive set of experiments. It was shown that the new droplet size correlation agrees better against experimental data than the existing Phast correlation. To further improve the rainout prediction, the Phast dispersion model (UDM) was also extended to allow simultaneous modelling of a range of droplet sizes and distributed rainout (rather than rainout at one point).     

Uptake of Ni2+ and rhodamine B by nano-hydroxyapatite/alginate composite beads: batch and continuous-flow systems

Alginate encapsulated nano-hydroxyapatite beads were synthesized and characterized by Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller surface analysis, and X-ray diffraction. Their adsorptive potential for Ni²⁺ and rhodamine B was explored in batch mode and by fixed-bed column passage. In the batch system, maximum uptake capacity for Ni²⁺ was 360 mg g^?1 and 480 mg g^?1 for rhodamine B. In the presence of humic acid, sorption was enhanced. For the continuous-flow system, adsorption was effective at low flow rate. For both pollutants, mass transport resistance increased during adsorption. The overall rates of rhodamine B and Ni²⁺ uptake were found to be controlled by external mass transfer.     

Fixed-bed column sorption of borate onto pomegranate seed powder-PVA beads: a response surface methodology approach

Pomegranate seed powder (PS) was functionalized with polyvinyl alcohol (PVA) and utilized for boron removal from the aqueous system. Results of Brunauer--Emmett--Teller (BET) surface area analysis and Boehm titration indicated notable decrease in total surface area and increase in acidic surface functional groups of PS after PVA modification. Enhanced sorption is indicative of complex formation between diol groups of the pomegranate seed powder--polyvinyl alcohol (PS–PVA) and borate ions. Under column test, the saturated sorption capacity of boron was noted to be dependent on flow rate and bed height. The developed central composite design (CCD) was adequate to elucidate the sorption mechanism. Mathematical modeling of the column data was conducted, and a modified-dose-response model was the most suitable to describe the breakthrough curve and observed to be consistent with CCD analysis. This is further supported by extensive error analyses conducted between the model predicted and experimental data.     

Metal partitioning in sediment pore water from the Ondo coastal region,Nigeria

Distribution and equilibrium partitioning of metals (Cd, Cu, Cr, Fe, Ni, Pb, Mn, and Zn) between pore water and surface sediments at the Ilaje coast of Ondo State, Nigeria, were studied. The Ilaje River can be one of the interesting research locations because of its economic nature and history of oil pollution. Seasonal variations were observed to investigate possible variations in the availability of metals for organisms throughout the year. The concentrations in both sediments and pore water during the dry and wet seasons were as follows: Cu?>?Fe???Mn?>?Pb?>?Ni?>?Cr?>?Cd?>?Zn. The pore water–sediment partition coefficient (K _p) showed that Zn and Cd were highly mobile while Fe and Cu have restricted mobility. Dissolved organic carbon (DOC) in pore water had a strong influence on mobility and bioavailability of all the metals (p?K _oc), increased levels of Fe and Cu were linked to lithological origin. Concentrations of Pb and Ni were associated with petroleum-related sources. The significance of the field-based techniques for ecotoxicological purposes is discussed.     

Acute toxicity of acaricide in lizards (Agama agama) Inhabiting dog kennel in Ibadan, Nigeria: An environmental hazard in urban vector control

Acute toxicity of an acaricide (Nuvan^® 1000 EC) in lizards (Agama agama) was observed within 2 minutes spraying of the acaricide in an enclosed dog kennel; heavily infested by ticks in urban area of Ibadan city, South western Nigeria. The acaricide was used at the 0.5% concentration recommended by the manufacturer (Novartis). A lizard which emerged from the kennel during the acaricide spraying exhibited acute signs of toxicity which consisted of shivering, gasping and death. The clinical signs of the acute toxicity manifested in the affected lizard resembled central nervous system (CNS) breakdown or neurotoxicity. Also, two lizards (one female and one male) were found dead in the kennel in the second and third days after the single acaricide spraying operation. The acute acaricide toxicity in lizards observed in this study portrayed the danger of environmental hazard to non-target commensal organisms and it is the first reported case in the area.