Potassium Release Kinetics and Water Retention of Controlled-Release Fertilizers Based on Chitosan Hydrogels

Controlled release fertilizer (CRF) hydrogels were prepared from poly(vinyl alcohol), poly(vinyl alcohol)/chitosan and chitosan using glutaraldehyde as a crosslinker. Intermolecular interactions of the CRF hydrogels were elucidated using FTIR. Water absorbency characteristics of the CRF hydrogels were also studied. It was found that the CRF hydrogels exhibited the equilibrium swelling ratio (SR) in the range 70–300%. The water retention of soil containing the CRF hydrogels was also examined. It was found that the CRF hydrogels increased the water retention of the soil. After 30 days, soil containing the PVA-, PVA/CS- and CS-hydrogels showed the water retention capacities of 25%, 10% and 4%, respectively. While the soil without the CRF hydrogel had already given off most of the water. The release behavior of potassium from the CRF hydrogels, both in deionized water and in soil, was investigated. In soil, the potassium release mechanism from the PVA- and PVA/CS-hydrogels were non-Fickian diffusion. On the other hand, the CS hydrogel showed, n value that was close to 1.0 corresponding to case II transport. In deionized water, all the CRF hydrogels showed small values of release exponent (n < 0.5) indicating a quasi-Fickian diffusion mechanism.     

Release Characteristics of Nutrients from Polymer-coated Compound Controlled Release Fertilizers

Reliable information regarding release characteristics of nutrients from a polymer-coated controlled release fertilizer (CRF) is essential for beneficial agronomic and environmental results. Significant knowledge regarding nitrogen release from polymer-coated urea was gained while the information regarding the release of the different nutrients contained in polymer-coated compound N–P–K CRF remains limited. An experiment in which major factors affecting the differential release of nutrients from two coated compound CRF was performed in free water, water saturated sand and sand at field capacity. In general, nitrate release was the fastest, followed by ammonium and potassium whereas phosphate was significantly slower, with a rate of linear release in free water 45–70% slower than that of nitrate. Little differences were obtained for the lag periods of nitrate, ammonium and potassium release (2–10 days) under the experimental conditions, whereas for P they were one order of magnitude larger. The main factor slowing the release was assumed to be the lower solubility of ions with P being the least soluble. Release into free water was, expectedly, somewhat faster than that into saturated sand and significantly faster as compared to sand at field capacity and particularly so for P. Raising the temperature from 20 °C to 40 °C increased the rate of linear release of the different nutrients. The energy of activation, EA_rel, estimated for the linear release, of the different nutrients, was narrow ranging between 37 to 46 (KJ mol⁻¹) whereas the mean values obtained for the two CRF, differing by 50% in coating thickness, was non-significant. However, EA_rel was significantly different in different media. The complex effect of temperature on the lag period and nutrient interactions during release deserve further investigation.     

Amylose Modified Starches as Superabsorbent Systems for Release of Potassium Fertilizers

Journal of Polymers and the Environment - High-amylose maize starch (AS) was modified by graft copolymerization with sodium acid maleate and disodium maleate, using the KMnO4-NaHSO3 redox system,...     

煤及煤矸石中砷的释放

研究了煤及煤矸石中砷的释放特征。采用XRD技术对煤样中的主要矿物成分进行了分析。表征结果显示,煤样中的主要矿物组成为碳酸盐矿物、硅酸盐矿物,以及一定量的SiO2、TiO2、硫化物矿物和硫酸盐矿物。实验结果表明：煤中砷的赋存形态主要以残渣态和硫化物结合态为主;在煤燃烧过程中,当燃烧温度为1 000 ℃时,1号矿井的煤样燃烧后灰渣中的砷含量为1.385 μg/g,砷的释放率为40.10%,2号矿井的煤样燃烧后灰渣中的砷含量为1.531 μg/g,砷的释放率为56.04%;在煤矸石的淋溶过程中,在淋溶液体积为100 mL的条件下,当淋溶液pH为5时淋出液中的ρ（砷）为19.27 μg/L,当淋溶液pH为7时淋出液中的ρ（砷）为7.78 μg/L。     

Evaluation of Risk from Using Poultry Litter to Remediate and Reuse Contaminated Estuarine Sediments

The availability of heavy metals in contaminated sediment evaluated for beneficial reuse, before and after chemical amendment, was evaluated using poultry manure as the amendment. The dredged sediment was only slightly contaminated with heavy metals. Availability tests on the amended sediment showed an increase in heavy metals, most likely because of poultry feed amendments passed to the manure. There would be difficulty finding one chemical amendment to reduce the availability of a number of heavy metals because the metals exhibit different chemical properties. © 2001 John Wiley & Sons, Inc.     

Polychloroprene Degradation by Photo-Fenton. Conductivity Measures as New Approach for Detecting/Evaluation of Degradation Products

In the present work the photo-degradation of polychloroprene (PCP) in toluene solution catalyzed by FeCl₃·6H₂O and polychromatic light was investigated based on FTIR and ¹³C NMR spectroscopies, on conductivity measurements and DSC technique. The band in the 1700–1790 cm⁻¹ range in the FTIR spectrum characterized the presence of carbonyl products due to the degradation of the PCP on the solution exposed to polychromatic light. The formation of carbonyl on degraded PCP was confirmed by the presence of signal on ¹³C NMR at δ 203.5. Products of PCP degradation, such as acid chlorides, generated in the toluene solution migrate to the aqueous phase (in contact with toluene phase) and the conductivity of aqueous phase increased as the time is elapsed. The area related to the PCP melting-peak on the DSC (film casted after the PCP-FeCl₃·6H₂O toluene solution has been exposed to polychromatic light) significantly decreased in comparison to that in the DSC of the raw PCP cast film.     

Release of nitrogen and trace metal species from field stacked biosolids

Concerns over elevated nitrate (NO3-) levels found in groundwater near former biosolid stockpiling locations resulted in the Maine Department of Environmental Protection (MDEP) imposing stricter regulations governing the stockpiling of biosolids in October 2002. The goals of this study were to measure the amount and speciation of nitrogen (N) and trace metals leaving stockpiled biosolids and travelling through the soil column. The biosolids were placed on plastic-lined cells to collect all leachate. Ammonium (NH4+), ranging from 2000 to 4900 mg L(-1), was the dominant N species (90% of total N) in the leachate from the Class B lime-stabilized biosolids in the lined cell experiment. Nitrate (NO3-) and nitrite (NO2-) concentrations were negligible, remaining below 0.25 and 0.1 mg L(-1), respectively. Dissolved organic carbon (DOC) concentrations as high as 8900 mg L(-1) and chemical oxygen demand (COD) as high as 37 000 mg L(-1) were measured in the leachate leaving the lined cell. Fifteen zero-tension pan lysimeters (ZTP-lysimeter) were installed in a 90 m2 plot at depth intervals of 30, 60, and 100 cm. Leachate passing through the soil column underlying the biosolids stockpile was collected in the ZTP-lysimeters. The average ZTP-lysimeter NH4+ concentrations ranged from 1400 mg L(-1) at 60 cm depth to 145 mg L(-1) at 90 cm depth. The average ZTP-lysimeter DOC concentrations ranged from 2000 mg L(-1) at 60 cm to 525 mg L(-1) at 90 cm. Trace metal determinations of the leachate collected from the lined cell and ZTP-lysimeters showed arsenic loading rates exceeded the state limits of 0.5 kg ha(-1) year(-1) by an order of magnitude. Arsenic concentrations were in excess of several thousand milligrams per litre in the lined-cell leachate and several hundred milligrams per litre in the ZTP-lysimeters as deep as 90 cm under the biosolid stockpile. Phosphorus, iron and manganese in excess of several thousand milligrams per litre were observed in both the lined-cell leachate and ZTP-lysimeters. Significant concentrations of other trace metals were found at depth in the zero-tension ZTP-lysimeter plot. Trace metals were largely mobilized by the DOC from the biosolids and due to the presence of anaerobic environment, especially in the underlying soil.     

废水处理三维电极体系中填料的选择评价方法

以瞬时电流效率和电耗为衡量标准,对填充活性炭、涂膜活性炭和石英砂3种填料的废水处理三维电极体系进行了研究。实验结果表明：活性炭的瞬时电流效率最高、电耗最低;3种填料对苯酚的选择性氧化系数依次为0.63,0.57,0.46,表明3种填料对苯酚的降解能力依次降低;在初始苯酚质量浓度为600mg/L、Na₂SO₄质量分数为3%、电流为1A、进水流量为0.60L/h的条件下,以活性炭作为填料,苯酚废水的COD去除率可达80.52%。     

模糊综合评价在焦化废水处理技术中的应用

采集某焦化厂废水处理系统的数据,选取当前常用的3种焦化废水处理技术和该焦化厂现用废水处理技术建立了较为完整的模糊综合评价数学模型,选择技术综合评价的评价因素集,利用判断矩阵分析法确定各评价因素的权重,建立了各定量因素指标的隶属函数,确定了各定性因素指标的模糊评语集,最后以模糊矩阵的合成运算完成模糊综合评价.4种焦化废水处理技术的综合性能优劣次序为:该焦化厂现用废水处理技术>普通活性污泥法>湿式催化氧化法>多相光催化氧化法.     

Development of Cellulose from Sugarcane Bagasse and Polyacrylamide-Based Hydrogel Composites by Gamma Irradiation Technique: A Study of Controlled-Release Behavior of Urea

Journal of Polymers and the Environment - Cellulose was successfully purified from sugarcane bagasse by gamma irradiation technique. The crystallinity of cellulose was reduced by gamma irradiation....     

Fabrication of Biodegradable Superabsorbent Using RSM Design for Controlled Release of KNO<Subscript>3</Subscript>

Present study envisaged the sequential experimental design approach for the development of biodegradable Gelatin-Tapoica/polyacrylamide superabsorbent. Percentage water uptake efficacy of candidate sample was optimized using Response Surface Methodology (RSM) design under microwave irradiation. Different process variables such as potassium persulphate and ammonium persulphate (KPS:APS) ratio, pH, reaction time concentration of acrylamide and N,N-methylene-bis-acrylamide (MBA) were investigated as a function of percentage swelling using sequential experimental design. Maximum liquid efficacy of 1550% was obtained at KPS:APS?=?1.0:0.5; acrylamide?=?7.67?×?10^?1 mol L^?1; MBA?=?1.76?×?10^?2 mol L^?1; pH 10 and time?=?110 s. The 3D crosslinked network formed was characterized using Fourier Transformation Infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscopic (SEM) techniques and thermal stability was ensured by Thermal gravimetric Analysis/Differential Thermal Analysis/Differential Thermal Gravimetric (TGA/DTA/DTG) studies. Superabsorbent synthesized could increase the moisture content in different type of soils and was found to enhance the water-holding capability of the soil upto 60 days in clayey, 40 days in sandy and 51 days in mixture of two soils under controlled conditions. Further, candidate polymer was investigated for the in-vitro controlled release of the KNO₃ with diffusion exponent ‘n’ was found to be 0.4326 indicating Fickian type diffusion. Also, initial diffusion coefficient (D_I?=?3.49?×?10^?5 m² h^?1) was found to be greater than the lateral diffusion coefficient (D_L?=?3.76?×?10^?6 m² h^?1) indicated rapid release of KNO₃ during initial hours with slow release afterwards. The ecofriendly nature of the synthesized polymer was also tested by conducting biodegradation studies and it was found to degrade upto 94% and 88.1% within 70 days with degradation rate of 1.34 and 1.26% per day using composting method and vermicomposting method respectively. So, the synthesized candidate polymer was found to be boon for agriculture-horticulture sector with wide applicability.     

Bioremediation of Dinitrotoluene in Aged Clay and Sandy Soils Using Pseudomonas Organisms,Spizizen Nutrient Medium and Prairie Silt Loam

This article describes the utility of Spizizen medium in effecting the release of 2,4 dinitrotoluene (DNT) from plasticized propellant in aged clay soil and of added Pseudomonas organisms in enhancing the rate of degradation of DNT in clay and sandy soils. DNT is an environmental problem because of its toxicity to mammals. It is proposed that the citrate in Spizizen medium chelates metals that form the aggregates of humin in aged clay soils, thereby releasing propellant components. Lack of awareness of DNT mobilization by citrate or other polyanions may lead to a potential underestimation of the 2,4 DNT present in aged contaminated soil and a potential increased release of DNT following exposure to solvents containing citrate or other polyanions. DNT in contaminated sandy soils was rapidly degraded when Pseudomonas and Spizizen medium were added (85% degraded in 20 days). Pseudomonas isolated/Torn soils at the Badger Plant have particular utility for the in situ degradation of 2,4 DNT in clay and sandy soils because they metabolize Spizizen medium, thrive in diverse climates, and have been selected for their ability to grow in soils contaminated with DNT. Mixture of either the contaminated clay soil or the contaminated sandy soil with uncontaminated prairie silt loam (20:80 ratio) facilitated management of the treatment process. This observation is important because of the widespread distribution, and hence low cost, of this soil type in the central United States.     

Development of Urea Uptake and Release Studies Using N,N-Dimethylacrylamide/Maleic Acid/Citric Acid Based Macrogel

Journal of Polymers and the Environment - Recently, the use of polymers in agricultural and horticultural applications has been seen as a solution to reduce water consumption and excess fertilizer...     

Release of Metals from Buildings,Constructions and Products during Atmospheric Exposure in Stockholm

This article presents results from investigations of run-off frommaterials used on buildings and other constructions obtained byshort term exposures of smaller model surfaces and one year exposures of larger materials surfaces on buildings and other constructions. Elevated concentrations of metals in run-off wereobserved for a wide range of different materials used on buildings and other constructions. Sources of metal emission tothe environment includes copper (Cu) surfaces, galvanized steel,impregnated wood, lead (Pb) surfaces, asphalt surfaces, paintedmaterial stainless steel and concrete. Metal emission rates fromsurfaces of copper and galvanized steel were measured from surfaces on buildings during 12 months exposure. The magnitude of metal emission form other surfaces was also estimated and theapplicability of these data for calculations of metal flows inan urban environment is discussed.     

Evaluation of commercial landscaping mulch for possible contamination from CCA

Wood treated with chromated copper arsenate (CCA) is found in construction and demolition (C&D) debris, and a common use for wood recycled from C&D debris is the production of mulch. Given the high metals concentrations in CCA-treated wood, a small fraction of CCA-treated wood can increase the metal concentrations in the mulch above regulatory thresholds. The objective of this study was to determine the extent of contamination of CCA-treated wood in consumer landscaping mulch and to determine whether visual methods or rapid X-ray fluorescence (XRF) technology can be used to identify suspect mulch. Samples were collected throughout the State of Florida (USA) and evaluated both visually and chemically. Visual analysis focused on documenting wood-chip size distribution, whether the samples were artificially colored, and whether they contained plywood chips which is an indication that the sample was, in part, made from recycled C&D wood. Chemical analysis included measurements of total recoverable metals, leachable metals as per the standardized synthetic precipitation leaching procedure (SPLP), and XRF analysis. Visual identification methods, such as colorant addition or presence of plywood, were found effective to preliminarily screen suspect mulch. XRF analysis was found to be effective for identifying mulch containing higher than 75 mg/kg arsenic. For mulch samples that were not colored and did not contain evidence of C&D wood, none exceeded leachable metal concentrations of 50 microg/L and only 3% exceeded 10 mg/kg for recoverable metals. The majority of the colored mulch made from recycled C&D wood contained from 1% to 5% CCA-treated wood (15% maximum fraction) resulting in leachable metals in excess of 50 microg/L and total recoverable metals in excess of 10 mg/kg. The maximum arsenic concentration measured in the mulch samples evaluated was 230 mg/kg, which was above the Florida residential direct exposure regulatory guideline of 2.1 mg/kg.     

Starch-Chitosan Hydrogels for the Controlled-Release of Herbicide in Agricultural Applications: A Study on the Effect of the Concentration of Raw Materials and Crosslinkers

Journal of Polymers and the Environment - Present work aims to synthesize the herbicide-loaded bio-based hydrogels and study the release mechanism. The different ratios of starch and chitosan were...     

Characterization and Release Kinetics of Allylthiosufinate and its Transforments from Poly(d,l-Lactide) Microspheres

In this work was described poly(d,l-lactide) microwave synthesis using tin(II) 2-ethylhexanoate initiated ring-opening polymerization. Polymerization was performed at 100 °C with monomer to initiator molar ratio ([M]/[I]) of 5,000 in 30 min. The achieved number average molar mass of obtained polymers (determined by gel permeation chromatography) was 102,320 g/mol, with the polydispersion index, Q, 2.80. Structural characterization was performed by FT-IR spectroscopy followed characteristic bands. For applicative purposes the obtained polymer was purified during the procedure of microsphere preparation. Biodegradable microspheres prepared from poly(d,l-lactide) have been widely studied in recent years and have become well established controlled drug delivery systems. In this work microspheres were loaded with allyl thiosulfinate (allicin) and its transforments products (ajoene and vinyldithiine), as pharmacological active substances. The morphology of the microspheres was analyzed using a scanning electron microscope. Allicin was synthesized by acid oxidation of allyl disufide and purification of obtained products by liquid–liquid extraction with diethyl ether. Obtained allicin, purity 73%, was transformed using microwave in acetone solution, at solvent boiling temperature, for 5 min. For the quality and quantity analysis of allicin and its transformation process was used LC/MS chromatography. (E)- and (Z)-ajoene were detected at retention time 3.1 and 3.3 min, respectively, whence 3-vynil-4H-1,2-dithiine and 2-vynil-4H-1,3-dithiine were detected at 4.3 and 4.8 min, respectively. Retention time of allicin was 2.93 min, according to liquid chromatography results. HPLC method was used for assessment of pharmaceutical substances (alicine and alicine transforments) releasing from microspheres at room temperature in solutions with different pH (pH = 3 and pH = 8) for 24 h.     

Supercritical Fluids-Assisted Processing Using CO2 Foaming to Enhance the Dispersion of Nanofillers in Poly(butylene succinate)-Based Nanocomposites and the Conductivity

Journal of Polymers and the Environment - With the rapid development of electronic information technology, traditional metal conductive materials can no longer satisfy the needs of a wider...     

硫铁矿烧渣制备聚合硫酸铁工艺评述

对国内用硫铁矿烧渣制备磷合硫酸铁各方法的优缺点进行了分析和比较。