Sulphate and Nitrate in Precipitation and Soil Water in Pine Forests in Latvia

The SO₄–S and NO₃–N concentrations and pH in bulk precipitation, throughfall, stemflow and soil water for the 1994–2004 period were studied in pine forests in Latvia (Rucava and Taurene Integrated Monitoring stations). The SO₄–S and NO₃–N concentrations decreased over the study period, simultaneously with a decrease of acidity in precipitation. The changes were more evident in the western part of Latvia, probably due to declining long-range air pollution from West Europe. The trend of decreasing sulphate concentrations and increasing pH in precipitation were not followed by respective changes in soil water. In the upper soil horizon sulphate ion concentrations and acidity increased in soil water. Over the observation period, nitrate concentrations also showed an increasing trend in soil water at Rucava and Taurene, but these changes were not statistically significant.     

硫酸锰渣污染土壤中重金属的形态分布及生物活性

测定了硫酸锰渣污染土壤中Cu,Zn,Cd,Pb,Mn的总量和各形态含量.结果表明重金属总量远超过环境背景值和土壤环境二级标准.重金属各形态分布特征:Cu,有机态>残渣态>铁锰氧化态>碳酸盐态>可交换态;Zn,残渣态>铁锰氧化态>有机态>碳酸盐态>可交换态;Cd,铁锰氧化态>可交换态>碳酸盐态>残渣态>有机态;Pb,铁锰氧化态>残渣态>有机态>碳酸盐态>可交换态;Mn,铁锰氧化态>残渣态>可交换态>有机态>碳酸盐态.重金属的生物可利用性系数和迁移系数均为Cd>Mn>Pb>Cu>Zn.     

Temperature Effects on Soil Mineralization of Polylactic Acid Plastic in Laboratory Respirometers

A respirometric system was used to analyze the biodegradation of high molecular weight (120,000 to 200,000 g mol^–1) polylactic acid (PLA) plastic films in soil under laboratory conditions. The respirometric system consisted of air-conditioning pretraps, a soil reactor, and a carbon dioxide (CO₂) posttrap. A 200-g homogeneous soil mixture of all-purpose potting soil : manure soil : sand [1 : 1 : 1 (w/w)] and 1.5 g of PLA plastic films in 1 × 1-cm² squares was added to each bottle. The respirometers were placed in a 28, 40, or 55°C water bath for 182 days. Treatments (three replicates) included native corn starch (positive control), polyethylene (Glad Cling Wrap; negative control), and three PLA films: Ca-I (Cargill Dow Polymers LLC, monolayer), GII (Cargill Dow Polymers LLC, Generation II), and Ch-I (Chronopol; monolayer). The degree of polymer mineralization was indicated by the cumulative CO₂ liberated from each respirometer. The initial average mineralization rate and total percentage mineralized of the PLA plastic films at 28, 40, and 55°C was 24.3, 41.5, and 76.9 mg/day with a 27, 45, and 70% carbon loss, respectively. No decrease in soil pH was observed after 182 days of mineralization. Hence, increase in soil temperature drastically enhanced the biodegradation of PLA plastic films in soil under laboratory conditions (P < 0.0001).     

Mechanical and Barrier Properties of Biodegradable Films Made from Chitosan and Poly (Lactic Acid) Blends

Biodegradable film blends of chitosan with poly(lactic acid) (PLA) were prepared by solution mixing and film casting. The main goal of these blends is to improve the water vapor barrier of chitosan by blending it with a hydrophobic biodegradable polymer from renewable resources. Mechanical properties of obtained films were assessed by tensile test. Thermal properties, water barrier properties, and water sensitivity were studied by differential scanning calorimeter analysis, water vapor permeability measurements, and surface-angle contact tests, respectively. The incorporation of PLA to chitosan improved the water barrier properties and decreased the water sensitivity of chitosan film. However, the tensile strength and elastic modulus of chitosan decreased with the addition of PLA. Mechanical and thermal properties revealed that chitosan and PLA blends are incompatible, consistent with the results of Fourier transform infrared (FTIR) analysis that showed the absence of specific interaction between chitosan and PLA.     

Nitrogen Budget of a Spruce Forest Ecosystem After Six-year Addition of Ammonium Sulphate in Southwest Sweden

A nitrogen (N) budget was constructed for a period of 6 years (1988–1993) in a Norway spruce stand with current deposition of 19 kg N and 22 kg S ha⁻¹ year⁻¹. The stand was fertilized annually by addition of 100 kg N and 114 kg S ha⁻¹ (NS). Above and below ground biomass, litterfall, fine- root litter production, soil solution and net mineralization were measured to estimate pools, fluxes and accumulation of nitrogen. The average needle litterfall in control (C) and NS plots in 1993 was 2.2 and 2.5 ton ha⁻¹ year⁻¹, respectively. The fine root litter production prior to treatment (1987) was 4.4 ton ha⁻¹ year⁻¹ and after treatment (1993) it was 4.5 and 3.9 ton ha⁻¹ year⁻¹ in C and NS plots, respectively. Net N mineralization in the soil profile down to 50 cm was estimated to be 86 and 115 kg ha⁻¹ year⁻¹ in C and NS plots, respectively in 1992. During the treatment period the uptake of N in the needle biomass in C and NS plots was 29 and 77 kg ha⁻¹ year⁻¹, respectively. No N was accumulated in needles of C plot where the NS plots accumulated 34 kg ha⁻¹ year⁻¹. Of the annually added inorganic N to NS plots 47% was accumulated in the above and below ground biomass and 37% in the soil. N fluxes via fine-root litter production in the C plots were much higher (54 kg ha⁻¹ year⁻¹) than that via litterfall (29 kg ha⁻¹ year⁻¹). The corresponding values in the NS plots were 65 and 43 kg ha⁻¹ year⁻¹, respectively. Most of the net N mineralization occurred in the FH layer and upper mineral soil. It is concluded that fine root litter and litterfall play an important role in the cycling of N. Despite a high N uptake the losses of N in litterfall and fine root litter resulted in an incorporation of N in soil organic matter.     

Synthesis and Characterization of Lactic Acid Oligomers: Evaluation of Performance as Poly(Lactic Acid) Plasticizers

The use of fully bio-based and biodegradable materials for massive applications, such as food packaging, is an emerging tendency in polymer research. But the formulations proposed in this way should preserve or even increase the functional properties of conventional polymers, such as transparency, homogeneity, mechanical properties and low migration of their components to foodstuff. This is not always trivial, in particular when brittle biopolymers, such as poly(lactic acid) (PLA), are considered. In this work the formulation of innovative materials based on PLA modified with highly compatible plasticizers, i.e. oligomers of lactic acid (OLAs) is proposed. Three different synthesis conditions for OLAs were tested and the resulting additives were further blended with commercial PLA obtaining transparent and ductile materials, able for films manufacturing. These materials were tested in their structural, thermal and tensile properties and the best formulation among the three materials was selected. OLA with molar mass (M_n) around 1,000 Da is proposed as an innovative and fully compatible and biodegradable plasticizer for PLA, able to replace conventional plasticizers (phthalates, adipates or citrates) currently used for films manufacturing in food packaging applications.     

Facile Preparation of Chitosan Films for High Performance Removal of Reactive Blue 19 Dye from Aqueous Solution

This study aimed at finding effective strategies for high-performance removal of reactive blue 19 (RB19) dye from aqueous solution. Chitosan (CS) films had been prepared by using solvent casting with mild drying for this purpose. The CS films were characterized by X-ray diffraction, field-emission scanning electron microscopy, and Fourier transform infrared (FTIR) spectroscopy. The performance of RB19 removal using CS were evaluated by varying contact time, solution pH, initial dye concentration, and adsorbent dosage. Adsorption isotherms, kinetics, and desorption were investigated by batch experiments. Results showed that CS films exhibited the optimal adsorption performance for RB19 removal and high maximum adsorption capacities of RB19, which were 799 and 822.4 mg g^?1 at 20 and 40 °C, respectively. Adsorption kinetic data were well described by the pseudo-second-order kinetic model. FTIR analyses further indicated that interactions between RB19 and the CS film occurred during adsorption. The CS films also exhibited satisfactory desorption of RB19 at about 80 % after 30 min of desorption at pH 11. Our study demonstrated that the CS films can be easily prepared and applied for effective removal of RB19 in treatment of wastewater.     

Effects of Long-Term Application of Ammonium Sulphate on Nitrogen Fluxes in a Beech Ecosystem at Solling, Germany

To study the effects of elevated inputs of acidity and nitrogen (N), 1000 mmol m^-2 a^-1 of ammonium sulphate (NH₄NO₃) equivalent to an input of potential acidity of 2000 mmol m^-2 a^-1 was applied annually for 11 yr between 1983 and 1993 in a beech forest at Solling, Germany. Most of the applied NH₄ ⁺ was nitrified in the litter layer and in the upper mineral soil. N in soil leachate quickly responded to the elevated input, but most of the applied N was stored in the soil or left the ecosystem via pathways other than soil output. Leaching of N from the soil increased until the last year of N addition. After the last N application, N fluxes decreased rapidly to low values. The buffering of acidity produced by the nitrification of the applied NH₄ ⁺ was caused mainly by three different processes: (i) sulphur (S) retention, (ii) release of aluminium, (iii) release of base cations. Retention of S took place mostly in the subsoil. 72% of the S input was recovered in output after 14 years of the experiment. Due to the increased fluxes of mobile anions with soil solution, outputs of cations increased drastically.     

衣康酸/苯乙烯磺酸共聚物的合成及其阻垢性能研究

以衣康酸(IA)和苯乙烯磺酸(SSA)为原料,合成IA／SSA共聚物阻垢剂,确定的最佳合成条件：反应温度为103℃,反应时间为2h,引发剂用量为7％(占单体总质量),IA：SSA质量比为2．8：1。在此工艺条件下合成的IA／SSA共聚物阻垢剂,其阻碳酸钙垢的阻垢率可达99％。     

Post-Glacial Lead Dynamics in a Forest Soil

The use of alkyl-Pb additives in gasoline during the 20th century resulted in widespread Pb pollution. The objective of this study was to determine the relative importance of atmospherically deposited Pb and Pb released through weathering to soil Pb pools at the Hubbard Brook Experimental Forest, New Hampshire. We employed a selective extraction method to estimate the amount of Pb that was: water-soluble + exchangeable (EX); inorganically bound (IB); organically bound (ORG); bound to amorphous oxides (AMOX); and bound in crystalline minerals (RES). After normalizing crystalline-Pb concentrations to the immobile element Ti, we estimated that 14.1 kg ha^-1 of Pb has been weathered from Hubbard Brook soils in the 12,000–14,000 yr since deglaciation – a long-term average release of 1.0–1.2 g ha^-1 a^-1. Analysis of Ti-normalized total Pb concentrations indicated a net post-glacial decrease of 7.2 kg ha^-1 in the total Pb pool – consisting of a net accumulation of 4.9 kg ha^-1 in the O horizon, and a net loss of 12.1 kg ha^-1 from mineral soil. Atmospheric deposition of Pb between 1926 and 1989 (estimated as 8.7 kg ha^-1) was a major source of Pb in the post-glacial period. Together, long-term weathering release and 20th century atmospheric deposition could account for all of the Pb in the EX, IB, ORG, and AMOX fractions. Lead from gasoline appears to constitute a major fraction of the total Pb burden in Hubbard Brook soils. Periodic analysis of soil Pb fractions may be useful in monitoring the fate of Pb in forest soils.     

Degradation of Polylactic Acid (PLA) Plastic in Costa Rican Soil and Iowa State University Compost Rows

In this study the degradation of polylactic acid (PLA) plastic films in Costa Rican soil and in a leaf composting environment was investigated. Three types of PLA films were used: Ch-I, (PLA monolayer plastic films from Chronopol, Golden, CO), GII (PLA trilayer plastic films from Cargill Dow Polymers LLC, Minnetonka, MN), and Ca-I (PLA monolayer plastic films from Cargill Dow Polymers LLC). The average soil temperature and moisture content in Costa Rica were 27°C and 80%, respectively. The average degradation rate of PLA plastic films in the soil of the banana field was 7675 M _w/week. Two compost rows were set up at the Iowa State University (ISU) (Ames) compost site. Temperature and relative humidity of the compost rows were kept at 55 ± 5°C and 50 ± 10% RH, respectively. The degradation rates of GII and Ca-I in the compost rows were 113,290 and 71,283 M _w/week, respectively. Therefore, it was estimated that in Costa Rican soil and in compost rows, PLA would be visibly degraded in 6 months and in 3 weeks, respectively.     

Aging of Toughened Polylactic Acid Nanocomposites: Water Absorption,Hygrothermal Degradation and Soil Burial Analysis

The environmental aging behaviour of montmorillonite (MMT) filled polylactic acid (PLA) nanocomposites (PLA/MMT) and linear low density polyethylene (LLDPE)-toughened PLA (PLA/LLDPE ratio = 90/10) nanocomposites (PLA/LLDPE/MMT) were investigated in this study. The nanocomposites were subjected to water absorption, hygrothermal degradation and soil burial analysis. Both PLA/MMT and PLA/LLDPE/MMT nanocomposites were immersed in distilled water at three different temperatures (room temperature, 60, and 90 °C) and the weight difference before and after immersion was calculated. The kinetics of water absorption for both nanocomposites followed the Fick’s second law of diffusion, where a linear relationship exists between the initial moisture absorption at any time t and t ^1/2 (the square root of time), followed by a horizontal plateau (saturation). The equilibrium moisture content (M _m ) and diffusion coefficient (D) of PLA nanocomposites increased with the addition of MMT (2 phr) and LLDPE. However, the D values of both nanocomposites decreased by increasing MMT (4 phr). The M _m for PLA/MMT and PLA/LLDPE/MMT nanocomposites increased by increasing immersion temperature (60 °C) and prolonged immersion resulted in hygrothermal degradation of both nanocomposites. The hygrothermal degradation studies showed that PLA degrades much faster at 90 °C as compared to 60 °C in both the nanocomposites. The addition of MMT and LLDPE improved the hygrothermal stability of PLA in both nanocomposites. Soil burial test revealed deterioration of impact strength in all samples while the rate of biodegradation was retarded in the presence of MMT and LLDPE.     

Performance of Cow Dung Reinforced Biodegradable Poly(Lactic Acid) Biocomposites for Structural Applications

In this work, performance of cow dung (CD) reinforced poly(lactic acid) (PLA) biocomposites was investigated for the potential use in load bearing application. CD of average 4 mm size was blended with PLA at different CD ratios (0–50 wt%) and their effects on the biocomposite properties were studied. The results showed an improvement in the flexural properties, while the tensile and impact strength dropped by 20 and 28% with the addition of 50% CD. The decline in the tensile and impact strength was due to micro-cracking and voids formation at higher CD content. Also, the incorporation of CD slightly decreased the thermal stability of the biocomposite. However, dynamic mechanical properties of the biocomposites generally improved. SEM analysis of tensile and impact fractured surfaces indicated that the CD had a reasonable adhesion with matrix. Moreover, the SEM micrographs of soil burial studies showed an accelerated degradation of higher CD wt% biocomposites.     

C9-AA水溶性石油树脂的制备及其阻垢性能

以乙烯生产过程中的副产物C9馏分和丙烯酸为原料,采用自由基溶液聚合,合成具有阻垢性能的C9-AA水溶性石油树脂。考察了引发剂AIBN和溶剂的加入量、C9-AA加入量、Ca^2＋浓度、循环冷却水pH和养护时间对C9-AA水溶性石油树脂阻垢性能的影响,并对其阻垢效果进行了评价。在Ca^2＋质量浓度小于或等于600mg／L、循环冷却水pH小于或等于9．3、C9-AA水溶性石油树脂加入量大于或等于15mg／L的条件下,C9—AA水溶性石油树脂对循环冷却水的阻垢率达到90％以上,其有效作用时间为60h。     

Physical Determinants of Methane Oxidation Capacity in a Temperate Soil

Methane oxidation capacity of soil from an experimentalsite in Northwest England was strongly dependent on temperatureand percentage water holding capacity. The soil had a distincttemperature optimum of 25 °C, with capacity for net methaneoxidation being completely lost below 5 and greater than37 °C. Optimum percentage water holding capacity for methaneoxidation was in the range 30–60%, with significant reductions inmethane oxidation rates in soils outside this range. Organic andmineral layers within the soil showed differences in potentialmethane oxidation rate, with methane oxidation being most rapid inthe buried organic layer and least rapid in the surface organiclayer. The importance of soil structure and gas diffusionlimitation is underlined, as is the strong temperature dependenceof methane oxidation when such diffusion limitation is removed.     

Nitrous Oxide Concentrations in the Soil of a Mown Grassland: Comparison of Model Results with Soil Profile Measurements

Nitrous oxide (N₂O) concentrations in the soilprofile of a fertilized grassland on the Swiss plateauwere measured at irregular intervals during one year.Air samples were taken from air-permeable tubesinstalled at depths between 2 and 100 cm belowthe surface. Highest concentrations in thetopsoil were observed following precipitationafter fertilization. In the subsoil,concentrations were highest when the soil watercontent fell below about 92% after a wet periodand mineral nitrogen was available from priorfertilization. N₂O concentrations in thetopsoil were simulated with the process-basedgrassland ecosystem model PaSim 2.5 (PastureSimulation Model) and compared with measured soilN₂O concentrations. The model simulated wellthe concentration peaks after fertilizeradditions and the concentrations in winter. Butthe simulated baseline concentrations during thegrowing season were overestimated. Possiblecauses for this discrepancy are discussed andsuggestions are made to improve the model.     

从醇/酮装置酸性废水中回收甲酸

采用共沸—分馏组合法从环己醇和环己酮生产装置产生的酸性废水中回收甲酸,确定了适宜挟带剂的种类及加入量。采用共沸—分馏组合法可获得甲酸质量分数达80%以上的甲酸水溶液,甲酸回收率达70%以上。回收甲酸后,酸性废水的COD由1.0×105~1.6×105m g/L降至500m g/L以下,COD去除率达到99%以上。