Assessing of drinking water quality in Al-karak province in central Jordan; based on water saturation indices.

Jordan is renowned for having limited water resources. The demand for water will increasing rapidly as the country's population grows and the number of refugees increases. In order to maintain the highest water quality for consumers, the Ministry of Water and Irrigation and other governmental agencies are striving to manage Jordan's water resources through continuous monitoring. The main objective was to evaluate the drinking water quality at storage mixing tanks at Al-Karak province, besides, assessing its suitability for safe consumption. The investigation scheme was to monitor Al-Karak's drinking water system for three successive months. The fourteen principal storage tanks for the water distribution system in the area of investigation were sampled. The pH, electrical conductivity (EC), major cations, major anions, total dissolved solids (TDS), total hardness (TH), turbidity, total alkalinity (TA), and heavy metals were measured. The scaling and originality of the dissolved salt elements in the collected water samples and geochemical processes were examined using Piper and Durov diagrams. The indices used in all samples over the period of investigation, are Langelier Saturation Index (LSI), Ryznar Stability Index (RSI), Aggressive Index (AI), Puckorius Scaling Index (PSI), and Water Quality Index (WQI). The results showed that scale development is high in all storage tanks, as the water is calcium carbonate supersaturated, evident from LSI values that ranges 0.5-2. According to the range of RSI values (5.91-6.6), all water tanks are resistant to corrosion. Throughout the period of study (October-December), the estimated WQIs of all samples upon average were found to be less than 50, indicating excellent water quality. Finally, the collected water samples are analyzed and found to be within the acceptable levels of Jordan's drinking water standards.

Pyrolysis of domestic sewage sludge: influence of operational conditions on the product yields using factorial design.

This study aims to investigate a sustainable method for sewage sludge (SS) safe disposal and reuse. The study involved exploring the optimum parameters of thermal treatment of SS by pyrolysis to produce biochar. Based on the analysis of the full factorial design, the effects of pyrolysis conditions: temperature, heating rate, and isothermal time on pyrolysis product yields were evaluated. The average yield of biochar was significantly reduced when the pyrolysis temperature was increased from 300 to 500 °C, while the average yields of bio-oil (BO) and non-condensable gases (NCGs) were increased. The yield of biochar was nearly the same when the heating rate was increased from 5 to 35 °C/min, while the yield of BO was increased and the yield of NCGs was decreased. The average yields of biochar and NCGs were reduced when the isothermal time was increased from 45 to 120 min, while the yield of BO was slightly increased. Factorial design methodology revealed all potential interactions between the variables of the pyrolysis process of SS. To predict pyrolysis product yields, first-order regression models were developed based on the effects' magnitude of the process parameters and their interactions. The models were agreed to the experimental data.

Phenol biodegradation by plant growth promoting bacterium, S. odorifera: kinetic modeling and process optimization.

One of the main organic pollutants that could result from industrial products and chemical transformations is phenol. In the current study, the kinetics of Serratia odorifera, which was isolated from arable soil, was studied by growing it on broth minimal medium spiked with phenol as only carbon source and energy. The newly isolated plant growth-promoting bacterium (PGPB), S. odorifera, was used for the first time for phenol biodegradation. The growth kinetics parameters (phenol-dependent) including maximum specific growth rate (µmax), half-saturation coefficient (Ks), and the Haldane's growth kinetics inhibition coefficient (Ki), were tested via Haldane inhibition model and resulted on the 0.469 (h -1), 26.6 (mgL-1), and 292 (mgL-1), respectively. The sum of squared error (SSR) of 4.89 × 10-3 was fitted to the experimental data by Haldane equation. The results of phenol biodegradation were fitted into the modified Gombertz model. The increase of phenol concentrations led to increases in both the rate of phenol biodegradation and lagging time. The optimal phenol biodegradation and bacterial growth obtained by S. odorifera, were at 28 °C incubation temperature and a pH of 7.0. The pathway of phenol biodegradation by S. odorifera was proposed in the current study to provide a new insight into synchronization of phenol biodegradation and plant growth-promoting bacteria. This may play an important role in remediation of phenol-contaminated soil besides promoting the plant growth, thus lessening the plant stress.

Synchrotron XANES and EXAFS evidences for Cr+6 and V+5 reduction within the oil shale ashes through mixing with natural additives and hydration process.

Solid friable residues (i.e. Ash) from combusted oil shale are a major environmental issue because they are highly enriched with toxic elements following combustion. The synchrotron based techniques X-ray Absorption Fine Structure (XAFS) were used for determining the changes in speciation of Chromium (Cr) and Vanadium (V) in the ash and its mixtures with Red soil and Phosphogypsum as additives, through one-year period of hydration process. The X-ray Absorption Near Edge Structure (XANES) qualitative results indicate that all mixtures exhibits similar patterns showing that Vanadium has remain as pentavalent state, on the contrary Chromium has dramatic decreased from hexavalent to trivalent. This change in Cr speciation became clearer with increasing hydration period. Therefore, the results confirmed the advantage of the hydration process in the Cr(VI) reduction which might be due the domination of carbonate phase within all mixtures, thus hydration caused carbonate dissolution that increase the pH toward more alkaline which caused the Cr(IV) reduction into less-harmful and less mobile Cr(III). This increase in pH was not in favor of changing the V(V) into V(IV) due to its large stability field V(V). The Extend X-ray Absorption Fine Structure (EXAFS) analysis showed that Cr exhibiting a coordination shell of C-atoms as first nearest neighbors backscattering atoms around Cr, and at C-atoms backscattering at medium range order. This confirmed the domination of carbonate media through the best fitting of Cr-C. Which might be attributed to the more alkaline conditions developed during saturation of water (hydration), that accelerates of the reduction of Cr(VI) into Cr(III). This means simply that hydration of the ash can reduce the presence of harmful Cr(VI) in these ash tailings.

Cr(VI)/Cr(III) and As(V)/As(III) ratio assessments in Jordanian spent oil shale produced by aerobic combustion and Anaerobic Pyrolysis.

With the increase in the awareness of the public in the environmental impact of oil shale utilization, it is of interest to reveal the mobility of potentially toxic trace elements in spent oil shale. Therefore, the Cr and As oxidation state in a representative Jordanian oil shale sample from the El-Lajjoun area were investigated upon different lab-scale furnace treatments. The anaerobic pyrolysis was performed in a retort flushed by nitrogen gas at temperatures in between 600 and 800 °C (pyrolytic oil shale, POS). The aerobic combustion was simply performed in porcelain cups heated in a muffle furnace for 4 h at temperatures in between 700 and 1000 °C (burned oil shale, BOS). The high loss-on-ignition in the BOS samples of up to 370 g kg(-1) results from both calcium carbonate and organic carbon degradation. The LOI leads to enrichment in the Cr concentrations from 480 mg kg(-1) in the original oil shale up to 675 mg kg(-1) in the ≥ 850 °C BOS samples. Arsenic concentrations were not much elevated beyond that in the average shale standard (13 mg kg(-1)). Synchrotron-based X-ray absorption near-edge structure (XANES) analysis revealed that within the original oil shale the oxidation states of Cr and As were lower than after its aerobic combustion. Cr(VI) increased from 0% in the untreated or pyrolyzed oil shale up to 60% in the BOS ash combusted at 850 °C, while As(V) increased from 64% in the original oil shale up to 100% in the BOS ash at 700 °C. No Cr was released from original oil shale and POS products by the European compliance leaching test CEN/TC 292 EN 12457-1 (1:2 solid/water ratio, 24 h shaking), whereas leachates from BOS samples showed Cr release in the order of one mmol L(-1). The leachable Cr content is dominated by chromate as revealed by catalytic adsorptive stripping voltammetry (CAdSV) which could cause harmful contamination of surface and groundwater in the semiarid environment of Jordan.

Cypress tree (Cupressus semervirens L.) bark as an indicator for heavy metal pollution in the atmosphere of Amman City, Jordan.

Bio-monitoring of air quality in Amman City was investigated by analyzing 36 cypress tree (Cupressus semervirens L.) bark samples from three sites of different anthropogenic activities at the end of summer season 2001. Cypress barks were found to be a good bio-indicator for air pollution in arid regions. Variation in Pb, Zn, Mn, Cr, Ni, Cd, and Cu contents between sites was observed due to different types of activities. Traffic emissions were found to be the main source of heavy metal pollution in the atmosphere of Amman. Lead content was found to be the highest in highly traffic density areas. The industrial part of the city was characterized by high Zn, Mn, Cr, Ni, and Co contents. No significance variations were found in pH values of the bark between the sites. This was attributed to buffering effect of carbonate in the atmosphere originated from soil of the area.

Qualitative evaluation of the mineralogical and chemical composition of dry deposition in the central and southern highlands of Jordan.

The chemical and mineralogical composition of dry deposition in the western highlands of central and south Jordan at the end of the summer season 2000, reflect the composition of soils in addition to anthropogenic activities at these areas. Calcite predominated in the central region whereas calcite and quartz are the dominant minerals in south Jordan. The concentrations of Hg, Cr, Ni, Cu, Pb and Zn were higher in central Jordan, which might be attributed to higher anthropogenic activities than south. On the other hand, Fe, Mn, Ti, Ba, Sr, Y and Rb were higher in the south of Jordan reflecting the composition of soil at these sites. At Aqaba city, the only port of Jordan, where Cr, Cd, As and S were higher than other areas. This variation might be attributed to the contribution of phosphate dust in the atmosphere through handling processes.