Empirical prediction of smoke production in the ISO Room Corner Fire Test by use of ISO Cone Calorimeter Fire Test data

The combustion conditions in the ISO Room Corner Fire Test make it possible to predict full scale smoke production by use of prediction models and bench scale fire test data procured by the ISO Cone Calorimeter Fire Test. The full scale smoke production is governed by the type of material burning only if the rate of heat release is less than 400–600 kW. For higher rates of heat release, the smoke production is more governed by the combustion conditions. The influence of the combustion conditions on the full scale smoke production reduces the possibilities of smoke prediction to materials causing flashover within 10 min in the ISO Room Corner Fire Test. The smoke to heat ratio S_Q (m²MJ) was used to compare smoke production between the scales. In general, the comparison revealed that the smoke yield was significantly less in full scale than in bench scale, especially for the plastics. Plastics do yield more smoke than wood based materials in both scales, but the differences in full scale are not as extreme as indicated by the bench scale smoke data. No simple correlations between the scales seem to exist. Multiple regression studies on empirical smoke prediction models show that bench scale fire parameters can be used to predict full scale fire performance. A quite accurate empirical smoke prediction model is presented for the group of materials which caused flashover within 10 min. The model predicts the full scale rate of smoke production at a rate of heat release of 400 kW. The presented results might be used to assess the fire safety hazard of visible smoke, but benchmarks of smoke hazard do not seem to exist. Thus further studies and agreement on safety levels and principles are needed for general visibility analysis concerning fire safety engineering purposes. Copyright © 1999 John Wiley & Sons, Ltd.     

Isolation,characterization and enzymatic modification of water soluble xylans from Eucalyptus grandis wood and sugarcane bagasse

BACKGROUND: There is growing interest in utilizing xylans as biodegradable polymers to replace synthetic additives, coatings and encapsulation matrices. However, techniques are required to reduce the water solubility of the xylan for such applications. The study objective was to isolate and characterize water soluble xylans from Eucalyptus grandis wood and sugarcane (Saccharum officinarum L) bagasse for subsequent precipitation in water by enzymatic modification. RESULTS: The water soluble xylans were extracted from E. grandis and bagasse using two mild alkali‐low‐temperature extraction methods in which the xylan was recovered either by ultra‐purification (Hoije) or ethanol precipitation (Lopez). Yields of 66 and 35% were obtained for the xylan extracted from bagasse and E. grandis, respectively, using the Hoije method and 28 and 12%, respectively, using the Lopez method. The xylans were hydrolysed by selective removal of arabinose and 4‐O‐methylglucuronic acid (4‐O‐MeGlcA) side chains by treatment with α‐L ‐arabinofuranosidase and α‐D ‐glucuronidase, respectively. The α‐L ‐arabinofuranosidase removed about 14% of the available arabinose in the xylans extracted from bagasse using the Hoije method, which led to precipitation in water. However, the α‐D ‐glucuronidase removed only 2% 4‐O‐MeGlcA of the available 4‐O‐MeGlcA from the xylans extracted from bagasse and E. grandis using both the Hoije and Lopez methods, and failed to show visible precipitation of the xylan in water. CONCLUSION: The xylans extracted from bagasse suited the substrate specificities of the α‐L ‐arabinofuranosidase for side chain removal and precipitation in water. However, the dosage of α‐D ‐glucuronidase for precipitating the xylan would need to be increased. Copyright © 2012 Society of Chemical Industry     

Quantitative analysis of oil removal from cotton fabrics through thein situ formation of microemulsions by solid-state nuclear magnetic resonance

Solubilization and subsequent removal of soybean oil from cotton fabrics through thein situ formation of microemulsions were evaluated by solid-state nuclear magnetic resonance (NMR) spectrometry. Regions of water-in-oil and oil-in-water microemulsions were identified for systems that contained polyoxyethylene (60) sorbitol hexaoleate, soybean oil, and an aqueous phase composed of water/ethanol or isopropanol (80:20 wt%) at 25°C. The amount of oil removed from the cotton fabrics was determined by solid-state NMR after constructing a calibration curve relating the intensity of camphor/oil NMR signals (I_c/I_o) to their molar ratio (M_c/M_o). A precision Crockmeter (Mul-Tech Industries, New York, NY) was used to reproducibly remove soybean oil stain from cotton fabric, which was subsequently analyzed by NMR. Typically, more than 90% of the oil stain was removed after 200 revolutions of the Crockmeter finger with 2 wt% surfactant at 25°C. Increasing the amount of surfactant to 6 wt% improved soybean oil removal from the fabric to 99 wt%.     

Efficiency of Ozonation and AOP for Methyl-tert-Butylether (MTBE) Removal in Waterworks

Methyl-tert-butylether (MTBE) is attracting more and more attention since it was discovered in groundwater and other raw water sources for waterworks and proved to difficult to remove during conventional treatment steps in drinking water production. Therefore advanced treatment processes have to be evaluated in addition to established treatment technologies. Laboratory based experiments were carried out studying ozonation with varying ozone concentrations at different pH values. For the elimination of MTBE the degradation through hydroxyl radicals was identified as the main degradation pathway. No decline of MTBE concentration occurred in experiments with molecular ozone, but AOP (Advanced Oxidation Processes) experiments where hydrogen peroxide (H₂O₂) was added showed a more efficient elimination. However, no complete mineralization was achieved — tert-butyl alcohol (tBA) and tert-butyl formate (tBF) were identified as metabolites. In natural waters (i.e., groundwater, bank filtrated water, and drinking water) the efficiency of MTBE removal was strongly dependent on the content of natural organic matter and alkalinity because of their scavenging characteristics. However, bromate formation was observed as well and could cause problems for drinking water production. Comparison with data gained from waterworks showed that conventional ozonation techniques as applied in waterworks are not able to remove MTBE efficiently.     

Extraction of Condensed Tannins from Cervid Feed and feces and Quantification using a Radial Diffusion Assay

A radial diffusion assay was employed to quantify condensed tannins (CT) in feed and feces of mule deer (Odocoileus hemionus) and white-tailed deer (O. virginianus). This biological assay measures the precipitation of bovine serum albumin (BSA), with the area of the precipitation ring being proportional to the amount of extracted CT applied to the well. CT extracted from the bark of white spruce (Picea glauca) was used as the standard. CT were extracted with 70% (v/v) aqueous acetone and precipitated with 50% (v/v) aqueous methanol or 70% (v/v) aqueous acetone. Functional range of CT weights for suitable ring measurement was 0.5–4.0 mg, and equilibrium was achieved within an incubation period of 24 hr. Methanol (50%) was a more effective precipitation solvent than acetone (70%) having 13 ± 4% greater specific activity (P < 0.05) and superior capabilities for predicting CT content. Precipitation rings were evaluated on images magnified on a photocopier. Ring diameters measured on a 200% enlarged photocopy provided the most precise estimate of ring area (R² = 0.98). This convenient method reduced analysis times and enhanced accuracy and precision of tannin quantification. Analytical consequences and future research requirements are considered.     

Pharmacological Perspectives on the Detoxification of Plant Secondary Metabolites: Implications for Ingestive Behavior of Herbivores

Plant secondary metabolites (PSMs) are a major constraint to the ingestion of food by folivorous and browsing herbivores. Understanding the way in which mammalian detoxification pathways are adapted to deal with PSMs is crucial to understanding how PSMs influence ingestive behavior of herbivores and hence their fitness and the impact that they have on vegetation. Pharmacological concepts can provide insights into the relationship between the absorption and metabolic fate of PSMs and ingestive behavior. Lipophilic PSMs will be absorbed into the bloodstream and must be removed fast enough to prevent their accumulation to toxic levels. Elimination depends on their metabolism, usually by cytochrome P450 enzymes, to more polar metabolites that can be excreted by the kidney. The concentration of PSM in blood (C) is a better measure of exposure to a toxin compared to the amount ingested because there can be great variability in the rate and degree of absorption from the gut. C rises and falls depending on the relative rates of absorption and elimination. These rates depend in part on metabolic and transport processes that are saturable and liable to inhibition and induction by PSMs, indicating that complex interactions are likely. Herbivores can use diet choice and the rate and amount of PSM consumption to prevent C from reaching a critical level that produces significant adverse effects.     

Method to produce 9(S)-hydroperoxides of linoleic and linolenic acids by maize lipoxygenase

Seed from maize (corn) Zea mays provides a ready source of 9-lipoxygenase that oxidizes linoleic acid and linolenic acid into 9(S)-hydroperoxy-10(F), 12(Z)-octadecadienoic acid and 9(S)-hydroperoxy-10(E), 12(Z), 15(Z)-octadecatrienoic acid, respectively. Corn seed has a very active hydro-peroxide-decomposing enzyme, allene oxide synthase (AOS), which must be removed prior to oxidizing the fatty acid. A simple pH 4.5 treatment followed by centrifugation removes most of the AOS activity. Subsequent purification by ammonium sulfate fractional precipitation results in negligible improvement in 9-hydroperoxide formation. This facile alternative method of preparing 9-hydroperoxides has advantages over other commonly used plant lipoxygenases.     

Stannous chloride—an effective reducing agent for the removal of selenium(IV) from acidic solution

BACKGROUND: Selenium removal from aqueous solutions can be a significant industrial problem, particularly in the metallurgical industry. In order to evaluate new reducing agents for this application, the reduction of selenious acid (H₂SeO₃) species with stannous ions (Sn²⁺) from weakly acidic sulfate solutions containing 300 mg L^?1 of selenium at 23 °C was studied. RESULTS: At initial pH values < 1.3 and molar ratio ≥ 2, less than 0.5 µg L^?1 of selenium(IV) remained in solution after reduction. The reductive precipitation reaction started as soon as the stannous ions were added to the selenium‐bearing solution and was completed in less than 5 min. The reaction products, characterized using X‐ray diffraction, electron microscopy, particle and surface area measurements, X‐ray photoelectron spectroscopy and chemical analysis, were composed of approximately equal amounts of tin selenide and tin dioxide. In addition to tin selenide a minor amount of selenium(IV) was found to be removed via adsorption on the tin dioxide formed in situ. Tests with a complex industrial solution also resulted in full and stable selenium precipitation. CONCLUSION: Stannous ions were found to be very effective in removing selenious ions from synthetic and industrial solutions, producing very stable precipitates. Copyright © 2012 Society of Chemical Industry     

Effect of bamboo oil on antioxidative activity and nitrite scavenging activity

The purposes of this study were to investigate the effects of the bamboo oil on antioxidative activity and nitrite scavenging activity in vitro and in vivo. When the bamboo oil concentration was increased from 10 to 90 μL/mL, the DPPH scavenging rate increased from 15.6 to 98.2%. However, at bamboo oil concentrations above 110 μL/mL, it was not increased. The superoxide anion radical scavenging rate increased from 54.8 to 89.1% when the bamboo oil concentration increased from 110 to 150 μL/mL. When the bamboo oil was incubated for 20 h, the linoleic acid scavenging rate was approximately 91.2%, similar to that of ascorbic acid. The glutathione production using bamboo oil in vivo was 59.0 μM/g of liver, which was about 6.5-fold higher than that of the control. In the case of the activities of glutathione peroxidase and catalase, they were 16.8 U/mg of protein and 295 KU/mg of protein, respectively, approximately 5.6-fold higher and 3.0-fold higher than that of the control. The nitrite scavenging activity was increased from 60.1 to 93.9% at pH of 1.2 when the saturation time was increased from 2 months to 8 months. However, at more than 10 months of saturation, this level was not increased. These results suggest that the bamboo oil of Phyllostachys nigra var. henonis can be used in bioactive and functional materials.     

The effect of lauric acid shock loads on the biological and physical performance of granular sludge in UASB reactors digesting acetate

The specific activity of acetotrophic methanogens and the physical behaviour of granular sludge in laboratory-scale upflow anaerobic sludge bed (UASB) reactors subjected to shock loads of lauric acid in the absence and presence of calcium were studied. In the absence of calcium, lauric acid completely inhibited acetotrophic methanogens above a threshold level of 100 mg C_12:0dm^?3, whereas no inhibition occurred below this threshold concentration. Addition of an equivalent amount of calcium to wastewater containing lauric acid prevented inhibition of acetotrophic methanogens at least up to 1500 mg C_12:0dm^?3. Addition of less than an equivalent amount of calcium apparently removed more than a stoichiometric amount of lauric acid: 50 % inhibition occurred at approximately 700 mg ‘free’ or excess C_12:0dm^?3. The results indicate that complete sludge wash-out from conventional UASB reactors is likely to occur within 2-8 h if the system is overloaded with an influent containing more than 100 mg C_12:0dm^?3. Calcium did not prevent wash-out.     

3, 4‐Dihydroxymandelic acid amides of alkylamines as antioxidants for lipids

The antioxidative and radical scavenging activity of the 3, 4‐dihydroxymandelic acid (DHMA) amides of hexylamine, 2‐ethylhexylamine, octylamine, and cyclohexylamine was determined by several physicochemical test systems. The amides were synthesized by protecting group‐free coupling of in situ prepared N‐hydroxysuccinimidylester of DHMA and the amines. The radical scavenging activity was determined using the DPPH (2, 2‐diphenyl‐1‐picrylhydrazyl) method and by quenching superoxide anions generated using a horse radish peroxidase/H₂O₂ system. In the DPPH assay, all amides show higher radical scavenging activity (EC₅₀ 0.09‐0.12 mol/mol_DPPH) compared to the standard antioxidants ascorbic acid (EC₅₀ 0.27 mol/mol_DPPH) and tocopherol (EC₅₀ 0.25 mol/mol_DPPH). The amides are also more potent superoxide radical scavengers (IC₅₀ < 600 nm) than standard ascorbic acid (IC₅₀ 700 nm). Activity against lipid peroxidation was determined by accelerated autoxidation of highly unsaturated oils and squalene using the Rancimat. Again, the antioxidative potentials of the DHMA amides against lipid oxidation as determined by the Rancimat, are at least equal or higher compared to the standard lipid antioxidants tocopherol, BHT, BHA, and ascorbylpalmitate (concentration in soybean oil 0.05%, all other oils 0.025%, squalene 0.005%). In squalene, an equi‐amount mixture of DHMA octylamide and α‐tocopherol shows a synergistic effect. Last but not least, the amides are able to protect an emulsion of linoleic acid/β‐carotene against oxidation initiated by N, N‐azodiisobutyramidine dihydrochloride (IC₅₀ 0.19‐0.77 mmol/l, ascorbic acid > 0.9, tocopherol 0.08). The DHMA octylamide in combination with ascorbic acid shows a synergistic antioxidative effect in the emulsion model. In conclusion, the new alkylamides of DHMA are easy to synthesize, potent radical scavengers and protect lipids, in particular the highly unsaturated, both in bulk and in emulsions against autoxidation.     

Prediction of Zeolite-Cemented Sand Tensile Strength by GMDH type Neural Network

Soil tensile strength (q_t) plays an important role in controlling cracks and tensile failures particularly in the design of foundations that usually fail under tensile stresses at the bottom of the treated layer. Soil-cement mixtures are used in many engineering applications including building of stabilized pavement bases and canal lining. Splitting tensile test (STT) is one of the common applied methods for indirect determination of q_t. Given that the determination of q_t of artificially cemented soils from STT—especially for samples with long curing time—is relatively costly and time-consuming, there is a need to develop some empirical models that can estimate determinable properties simply. In the current study, it has been analyzed that whether the Group Method of Data Handling (GMDH)-type Neural Network (NN) is suitable to predict the q_t of sands stabilized with zeolite and cement. For this purpose, a program of STT considering three distinct porosity ratios, four cement contents and six different percent of cement replacement by zeolite in 42, 56 and 90 days of curing time is performed in present study. Active particle (AP) has been introduced as a new parameter for modeling the GMDH-type NN. The performances of the proposed models reveal that GMDH is a reliable and accurate approach to predict the q_t of sands stabilized by zeolite-cement mixture. Proposing an equation in current study, it can be interpreted that AP is one of the key parameters to predict the q_t of zeolite-cemented sands. The sensitivity analysis on the proposed GMDH model with the best performance has shown that the proposed q_t is considerably influenced by cement content variations.     

Feasibility of Palm Oil as the Feedstock for Biodiesel Production via Heterogeneous Transesterification

The production of biodiesel has become popular recently as a result of increasing demand for a clean, safe and renewable energy. Biodiesel is made from natural renewable sources such as vegetable oils and animal fats. The conventional method of producing biodiesel is by reacting vegetable oil with alcohol in the presence of a homogenous catalyst (NaOH). However, this conventional method has some limitations such as the formation of soap, usage of significant quantities of wash water and complicated separation processes. Heterogeneous processes using solid catalysts have significant advantages over homogenous methods. Currently, more than 90 % of world biodiesel is produced using rapeseed oil. The production of biodiesel from rapeseed oil is considered uneconomical, considering the fact that palm oil is currently the world's cheapest vegetable oil. Therefore, the focus of this study is to show the feasibility of producing biodiesel from palm oil using montmorillonite KSF as a heterogeneous catalyst. The heterogeneous transesterification process was studied using design of experiment (DOE), specifically response surface methodology (RSM) based on a four‐variable central composite design (CCD) with α = 2. The transesterification process variables were reaction temperature, x₁ (50–190 °C), reaction period, x₂ (60–300 min), methanol/oil ratio, x₃ (4–12 mol mol^–1) and the amount of catalyst, x₄ (1–5 wt %). It was found that the conversion of palm oil to biodiesel can reach up to 78.7 % using the following reaction conditions: reaction temperature of 155 °C, reaction period of 120 min, ratio of methanol/oil at 10:1 mol mol^–1 and amount of catalyst at 4 wt %. From this study, it was shown that montmorillonite KSF catalyst can be used as a solid catalyst for biodiesel production from palm oil.     

Alkaline Pre-treatment of Hardwood Chips Prior to Delignification

Abstract

Hardwood (Betula pendula) chips were extracted having alkaline aqueous solutions with varying chemical charges (1, 2, 3, 4, 6, and 8% of NaOH on wood), treatment times (30, 60, 90, and 120 minutes), and temperatures (130°C and 150°C). The total amount of material removed was in the range 2.1–16.5% of the original dry feedstock. This fraction was characterized in terms of carbohydrates and their degradation products (mainly aliphatic carboxylic acids together with some furanoic compounds), lignin, and extractives. Low alkali charges (1–4% of NaOH) were not sufficient to neutralize all the acids formed (mainly acetic acid from the acetyl groups of xylan). In contrast, an increase in alkali charge (6% and 8% of NaOH) more intensively facilitated the alkali-catalyzed degradation reactions of polysaccharides to various hydroxy acids, which were then typically present as one of the main constituents in the dissolved organic matter, along with other aliphatic carboxylic acids (acetic and formic acids), lignin, extractives, and carbohydrates.     

Effects of relative humidity,temperature, and population density on production of cuticular hydrocarbons in housefly Musca domestica L

The production of cuticular hydrocarbons by both males and females of Musca domestica L. under very wet conditions (90% relative humidity) compared to the production at 50 and 20% relative humidity is delayed up to at least 3 days after emergence from the pupae. Eight days after emergence, however, males contain the same amounts of hydrocarbons at 90, 50, and 20% relative humidity, whereas females at 90% still possess less of these substances than at 50 and 20%. It is suggested that this is due to the fact that males, being more active than females, need more cuticular hydrocarbons to prevent water loss. No indication is found that relative humidity has a different effect on the production of the sex pheromone, muscalure [(Z)-9-tricosene] by females than on the production of the other hydrocarbons. Male and female flies produce more hydrocarbons at 35°C than at 20°C. On females, the relative amounts of nonacosane and methyl- and dimethylnonacosanes are significantly higher at 35°C than at 20°C. Female flies produce some (Z)-9-tricosene after eight generations at low population density in contrast to females at high population density, which did not produce muscalure. We suggest that because of the relatively large contribution to the total population, the properties of a small number of females are likely to be expressed sooner in the next generations of small populations than in those of large populations.     

Pilot‐scale treatment of waste‐water from carbon production by a combined physical–chemical process

BACKGROUND: Due to its strong colour, high concentrations of fluorides and chemical oxygen demand (COD_Cr) and large amount of suspended solids (SS), the waste‐water from carbon production (WCP) seriously affects the stability of the circulating system of Guizhou Branch, Aluminium Corporation of China. In this paper, the performance of a pilot‐scale (24 m³ d^?1) combined treatment plant, consisting of chemical precipitation, coagulation, and Fenton oxidation, for the treatment of WCP was investigated. RESULTS: Lime precipitation and hydrated ferrous sulphate (HFS) coagulation, with polyacrylamide (PAM) as a coagulation aid, proved to be effective in the removal of colour (>70%), suspended solids (SS) (>90%) and fluoride (>80%) from the WCP. Subsequent Fenton oxidation combined with coagulation as a final treatment efficiently removed SS, F^?, COD_Cr, dissolved organic carbon (DOC) and colour. The average total removal efficiencies of these parameters in the pilot‐scale combined technology were as follows: SS = 98.8%, F^? = 95.7%, COD_Cr = 94.8%, DOC = 91.8% and colour = 98.3%, giving an average effluent quality: colour 24 (multiple), COD_Cr 168 mg L^?1, DOC 80 mg L^?1, F^? 38 mg L^?1 and SS 44 mg L^?1, consistent with the reusable water limits for the process. CONCLUSIONS: The current experimental results and the economic evaluation suggest that the combined process could be advantageous and feasible for the treatment of WCP. Copyright © 2009 Society of Chemical Industry     

Modeling and optimization of the process parameters in vacuum drying of culinary banana (Musa ABB) slices by application of artificial neural network and genetic algorithm

The influence of drying temperature, sample slice thickness, and pretreatment on quality attributes like rehydration ratio, scavenging activity, color (in terms of nonenzymatic browning), and texture (in terms of hardness) of culinary banana (Musa ABB) has been evaluated in the present study. A comparative approach was made between artificial neural network (ANN) and response surface methodology (RSM) to predict various parameters for vacuum drying of culinary banana. The effect of process variables on responses during dehydration were investigated using general factorial experimental design. This design was used to train feed-forward back-propagation ANN. The predictive capabilities of these two methodologies for optimization of process parameters were compared in terms of relative deviation (R_d). Results revealed that a properly trained ANN model is found to be more accurate in prediction as compared to RSM. The optimum condition selected from ANN/GA responses on the basis of highest fitness value revealed that culinary banana slices of 6 mm thickness pretreated with 1% citric acid and dried at 76°C resulted in a maximum rehydration ratio of 6.20, scavenging activity of 48.63% with minimum nonenzymatic browning of 25%, and hardness of 43.63 N. Results further revealed that, in the case of rehydration ratio, temperature and pretreatment showed a positive effect while thickness had a negative effect. On the contrary, for scavenging activity, temperature showed the highest negative effect followed by slice thickness and positive effect with pretreatment. For nonenzymatic browning, thickness showed the highest negative effect but temperature and pretreatment showed a positive effect. Similarly, for hardness, all three parameters showed a negative effect.     

Characterization and properties of LDPE film with gallic‐acid‐based oxygen scavenging system useful as a functional packaging material

We prepared and characterized active, oxygen‐scavenging, low density polyethylene (LDPE) films from a non‐metallic‐based oxygen scavenging system (OSS) containing 1, 3, 5, 10, and 20% of gallic acid (GA) and potassium chloride (PC). We compared the surface morphology and mechanical, permeability, and optical properties of the oxygen‐scavenging LDPE film with those of pure LDPE film. The surface morphology, gas barrier, and thermal properties indicate that the OSS was well incorporated into the LDPE film structure. The surface roughness of the film increased with the amount of oxygen scavenging material. The oxygen and water vapor permeability of the developed film also increased with the amount of oxygen scavenging material, though its elongation decreased. The oxygen scavenging capability of the prepared film was analyzed at different temperatures. The initial oxygen content (%) in the vial headspace, 20.90%, decreased to 16.6% at 4 °C, 14.6% at 23 °C, and 12.7% at 50 °C after 7 days of storage with the film containing 20% OSS. The film impregnated with 20% organic oxygen scavenging material showed an effective oxygen scavenging capacity of 0.709 mL/cm² at 23 °C. Relative humidity triggered the oxygen scavenging reaction. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44138.     

Adsorption behavior of aqueous europium on kaolinite under various disposal conditions

This work investigated the adsorption behavior of europium on kaolinite under various disposal conditions. Batch-wise adsorption and precipitation experiments and equilibrium model calculations were performed over a pH range of 4–10 and CO₂ concentration range of 0%, 0.03%, and 10%. Experimental precipitation behaviors are in agreement with the results of equilibrium model calculations using the geochemical code MINTEQA2. Aqueous species of Eu³⁺ exists mainly at pH 5 or below and solid phases of Eu(OH)₃(s), Eu(OH)CO₃(s), and Eu₂(CO₃)₃·3H₂O(s) are formed at higher pH ranges. Adsorption behavior of Eu on kaolinite in the low pH range can be explained by interlayer ion-exchange reaction. The significant increase in adsorbed amount at pH 5–6 is due to the surface complexation at the edge site of kaolinite. In the high pH range, precipitation of Eu contributes mainly to the adsorption quantity. The rapid decrease in adsorbed amount above pH 7 under 10% CO₂ condition occurs by the formation of anionic europium species of Eu(CO₃) ₂ ^- .The adsorption of Eu on kaolinite could be well interpreted by the Freundlich adsorption isotherm. The data except for the highest equilibrium concentration ranges were also explained by Langmuir isotherm and the maximum adsorbed quantity of Eu on kaolinite,b, is 1.2 mg/g.     

The Preozonation of Phenolic Aqueous Solution and Its Effect on the Improvement of Coagulation Treatment

Phenolic solutions are difficult to treat with coagulation processes because phenol is well soluble in water. However, with suitable preozonation, the ozonized organic components can be removed more effectively by coagulation processes. In order to avoid excessive preozonation, a good control on the degree of preozonation is crucial for practical applications. The degree of preozonation of phenolic solution was evaluated by measuring the phenol decomposition rate, ADMI value and ozone outlet concentration during the ozonation. Three characteristic times were observed, namely (1) ADMI value reaches the peak value during preozonation, (2) the ozone outlet concentration starts increasing, and (3) the ADMI value reaches the discharge standard (500 value, EPA Taiwan). These characteristic times provide the useful means as real-time control parameters on the extent of preozonation. The results of HPLC and GPC show that phenol is almost completely decomposed after 43?min of preozonation. The major components after preozonation are oxalic acid and coupling compounds. The preozonized solution, containing phenol decomposition products, was then subjected to coagulation treatments. The coagulation behavior of preozonized solution is dependent on the extent of preozonation. Three types of coagulant were investigated, namely alum, ferric chloride (FeCl₃) and poly aluminum chloride (PAC). Both PAC and FeCl₃ are effective coagulants for COD removal. As an example, phenol solution (initial phenol concentration=300?mg/L, C _{O 3},i=20?mg/L) was preozonized for 50 minutes, followed by FeCl₃ coagulation treatment. After preozonation and coagulation processes, the total COD and ADMI removal rates are as high as 70% and 80%, respectively. Most of the coupling compounds and oxalic acid are removed by the coagulant.