A Novel Environmental Quality Criterion for Acidification in Swedish Lakes – An Application of Studies on the Relationship Between Biota and Water Chemistry

The recovery from acidification has led to the demand for more precise criteria for classification of acidification. The Swedish Environmental Protection Agency has revised Sweden’s Ecological Quality Criteria for acidification to improve the correlation between the chemical acidification criteria and biological effects. This paper summarises the most relevant findings from several of the studies commissioned for this revision. The studies included data on water chemistry in 74 reference lakes in southern Sweden with data on fish in 61 of the lakes, as well as data on littoral fauna in 48 lakes. We found that the acidity variable most strongly correlated to the biota was the median pH from the current year. Our results probably do not reflect the mechanisms behind the negative effects of acidity on the biota, but are fully relevant for evaluation of monitoring data. The biogeochemical models used for predicting acidification reference conditions generate a pre-industrial buffering capacity. In order to get an ecologically more relevant criteria for acidification based on pH, we transferred the estimated change in buffering capacity into a corresponding change in pH. A change of 0.4 units was defined as the threshold for acidification. With this criterion a considerably lower number of Swedish lakes were classified as acidified when compared with the present Ecological Quality Criteria.     

Trends in the Water Chemistry of High Altitude Lakes in Europe

Here we present the chemical trends of seven high altitude lakes, analysed within the AL:PE and MOLAR Projects of the EU (1999) and selected on the basis of the availability of complete and reliable data for the period 1984–1999. The lakes are representative of the Scandinavian Alps, the Cairngorm Mountains in Scotland, the Alps and the Pyrenees. Significant trends were identified for some indicators of acidification, for instance pH and alkalinity, but not all lakes reacted similarly to decreasing depositions of sulphate and base cations. Differences in lake response are discussed in relation to recent variations of atmospheric deposition chemistry and associated changes in climatic conditions. Beside individual variations of the studied lakes, depending, among other things, on altitude and morphology, catchment characteristics and climate trends play a major role for the reaction of high altitude lakes on changes in atmospheric depositions.     

Development of Stream Water Chemistry during Spring Melt in a Northern Hardwood Forest

The role of snowmelt and subsurface hydrology in determiningthe chemistry of a small headwater stream in the TurkeyLakes Watershed (TLW) was evaluated for the spring meltperiods 1992 to 1996. Spring runoff is the dominanthydrological event at the TLW each year. Processesoccurring within the snowpack during snowmelt wereprincipally responsible for the above-ground changes inchemical fluxes relative to bulk deposition (the effect ofwinter throughfall was minimal). Large changes in chemicalfluxes occurred below ground. Organic matter decomposition,weathering, nitrification, and element cycling are some ofthe more important below-ground processes that operateduring the snow accumulation and ablation season and controlthe composition of the water ultimately appearing in thestream. Maximum stream discharge was accompanied byelevated concentrations of H⁺, NO₃ ^-, K⁺,NH₄ ⁺, DOC, Al and Mn, but reduced levels ofCa²⁺, Mg²⁺, SO₄ ^2- and SiO₂. Theconcentration-discharge relationships were consistent withwater movement through and above the forest floor duringpeak discharge, a flowpath facilitated by rapid infiltrationof meltwater and the existence of a relatively impermeablelayer in the mineral soil creating a perched water table. Averaged over the five periods of snow accumulation andablation, it was estimated that pre-melt stream flow, andwater routed through the forest floor and through the uppermineral soil contributed 9, 28 and 63%, respectively, ofthe discharge measured at the outlet of the catchment. Theforest floor contribution would be greater at peak dischargeand at higher elevations. An end-member mixing modelestimated concentrations of SO₄ ^2-, NO₃ ^-,Cl^-, Ca²⁺, Mg²⁺, Na⁺ and Al that werecomparable to average values measured in the stream. Othervariables (NH₄ ⁺, H⁺, K⁺ and DOC) wereover-estimated implying retention mechanisms operatingoutside the model assumptions.     

Long Term Effects of Acid Irrigation at the Höglwald on Seepage Water Chemistry and Nutrient Cycling

In order to test the hypothesis of aluminium toxicity induced by acid deposition, an experimental acid irrigation was carried out in a mature Norway spruce stand in Southern Germany (Höglwald). The experiment comprised three plots: no irrigation, irrigation (170 mm a^?1), and acid irrigation with diluted sulphuric acid (pH of 2.6–2.8). During the seven years of acid irrigation (1984–1990) water containing 0.43 mol_c m^?2 a^?1 of protons and sulphate was added with a mean pH of 3.2 (throughfall?+?acid irrigation water) compared to 4.9 (throughfall) on both control plots. Most of the additional proton input was consumed in the organic layer and the upper mineral soil. Acid irrigation resulted in a long lasting elevation of sulphate concentrations in the seepage water. Together with sulphate both aluminium and appreciable amounts of base cations were leached from the main rooting zone. The ratio between base cations (Ca?+?Mg?+?K) and aluminium was 0.79 during acid irrigation and 0.92 on the control. Neither tree growth and nutrition nor the pool of exchangeable cations were affected significantly. We conclude that at this site protection mechanisms against aluminium toxicity exist and that additional base cation runoff can still be compensated without further reduction of the supply of exchangeable base cations in the upper mineral soil.     

Impact of Lime and Ash Applications on Soil Solution Chemistry of an Acidified Podzolic Soil

Soil solution samples were taken from two sites (Horröd and Hasslöv) in the south part of Sweden to evaluate how soil solution chemistry responded to different treatmentswith dolomite and wood ash. At Horröd, samples were taken four years after application of wood ash, 4.28 ton ha^-1 and dolomite, 3.25 ton ha^-1. At Hasslöv dolomite, 3.45 ton ha^-1 and 8.75 ton ha^-1 was applied and samples were taken 15 yr later. It was found that treatment with dolomite at one site (Hasslöv) resulted in higher pH values (<2 pH units) and higher nitrification. It was also found at this site that the total Al and the inorganic Al concentrations decreased with dolomite treatment. The Ca, Mg, DOC, Fe, SO₄ ^2- and Cl^- concentrations, mainly in the topsoil, were found to be higher at both sites, following dolomite treatment; Ca and Mg concentrations were 2–8 times higher (<820 M) than in controls (<70 M). Wood ash was found to have less impact. The PO₄ concentration in the O2 horizon at Hasslöv decreased due to dolomite-treatment. ANOVA (Analyse of Variance) and PLS (Partial Least Square) were used to evaluate the data from the two sites.     

Wood Plastic Composite Panels: Influence of the Species,Formulation Variables and Blending Process on the Density and Withdrawal Strength of Fasteners

In this work, the influence of four variable parameters including fiber types (poplar and rice straw), fiber contents (45, 60, and 75 wt%), fiber sizes (20–40 and 40–60 mesh), and blending methods (hot-pressing and extrusion) on the physico-mechanical properties of wood plastic composite panels were studied. Generally, the results showed that each of the above-mentioned parameters had significant effect on the nail and screw withdrawal strength (pull-out load) and density, whereas their interactions did not have highly impressive effects on the properties. All tested properties vary significantly with fiber origin. Composites filled with larger fiber size, produced panels with higher withdrawal strength and density. The effect of blending method on density was maximal. Withdrawal strength values of each sample decreased with increase in fiber loading. The lowest withdrawal strength values of nail and screw were obtained from the samples filled with rice straw. It was found that strength properties of the composites can be improved moderately by adding 45 wt% fiber, 20–40 mesh particle and poplar flour. According to the results, the blending method is a significant variable in the determination of withdrawal strength. Therefore, the blending method can be recommended based on the end product applications.     

Mechanical Properties, Water Vapor Permeability and Water Affinity of Feather Keratin Films Plasticized with Sorbitol

In poultry industry chicken feathers are normally hydrolyzed and used to prepare animal feed. In this work the use of this material to prepare films was investigated. Keratins were extracted from chicken feathers with 2-mercaptoethanol in concentrated urea solution using sodium dodecyl sulfate (SDS). The effect of varying the amount of sorbitol on properties of chicken feather keratin (CFK) was investigated. As the concentration of plasticizer increased, the moisture content (MC) of these films increase, the monolayer MC increased from 0.060 (without plasticizer) to 0.482 g water/g dry matter (0.30 g sorbitol/g keratin). The water vapor permeability (WVP) varied between 0.096 g/m s Pa and 8.098 g/m s Pa for films without sorbitol and with 0.30 g sorbitol/g keratin, respectively. Film strength decreased from 5.13 MPa to 0.45 MPa and the elongation at break achieved the maximum value of 52.75% for samples with 0.02 g sorbitol/g keratin. The dry matter density didn’t change significantly, varying between 0.86–0.89 g/cm³ for all samples. Films with potential applications in food packaging can be obtained from CFKs. However, further researches are necessary to decrease film solubility and increase mechanical resistance.     

Polylactic Acid Composites Utilising Sequential Surface Treatments of Lignocellulose: Chemistry,Morphology and Properties

Polylactic acid (PLA)—maple fibre composites have been synthesised using a series of sequentially modified cellulose fibres (namely alkylation followed by either acetylation or silanation). Confirmations of the sequential modifications were made using Fourier Transform Infrared Spectroscopy and Inductively Coupled Plasma—Atomic Emission Spectroscopy and the new surface morphologies analysed using Scanning Electron Microscopy. The key advantage of the use of sequential treatments (with initial alkali treatment) was the allowance for direct grafting of suitable chemical groups onto the cellulose in the fibre due to the removal of lignin, hemicellulose and other surface impurities. However, a balance was found to exist between alkali exposure time, concentration and resulting fibre integrity. The conditions used resulted in a loss in fibre weight, fibre moisture content and tensile strength. Sequential treatments with acetylation or silane resulted in a 15–21% strength recovery from that of the alkali treated composite. Factors that influenced this recovery in strength were the improved fibre-polymer interface, namely the hydrophilic balancing of the fibres and this further affected the thermal-hydrolysis of the PLA during composite fabrication.     

Monitoring Studies of Precipitation and Cap Cloud Chemistry at Holme Moss in the Southern Pennines

Weekly collections of samples of precipitation and hill cloudwater have been made at Holme Moss (530 m.a.s.l.) in the southernPennines covering a six-year period (1994–1999). In addition continuous meteorological measurements have been conducted at thesite for a five year period (1995–1999). The concentrations of major ions in the samples have been determined by ion chromatography. Analysis of ion concentrations as a function ofwind direction reveals that the ions with anthropogenic sources (SO₄ ^–, NO₃ ^–, NH₄ ⁺, H⁺) exhibit higher concentrations during easterly wind directions whilst the ions with predominantly marine origins (Na⁺, Cl^–, Ca⁺⁺, Mg⁺⁺, K⁺) have concentrations thatare not significantly dependant on wind direction. Precipitation and cloud deposition are strongly correlated to south-westerly wind directions with a secondary peak occurring for north-easterly directions. Fifty nine per cent of ion deposition by rain was found to occur during wind from the SSW to W sector.The average concentrations of ions in cloud water were found tobe much higher than those in rain (by factors of between 2.5 and4.2). It is thought that the high precipitation and annual deposition of ions by precipitation at Holme Moss is due in partto the enrichment of ion concentrations in precipitation by thescavenging of more concentrated cap cloud droplets (the `seeder-feeder effect'). Comparison with data from a nearby lower level site shows encouraging agreement with the scheme currently used in the U.K. deposition mapping procedure to incorporate the influence of orography on deposition by precipitation.     

齐鲁石化公司局域电网谐波源的治理

根据齐鲁石化公司局域电网谐波源的测试结果，并结合公司新区电网的特点，确定了谐波源治理方案，并在工程中实施。测试结果表明，治理效果达到了设计要求，电网的电压畸变率被控制在国家标准允许的范围之内。     

Implications of Heterogeneous Chemistry of Nitric Acid for Nitrogen Deposition to Marine Ecosystems: Observations and Modeling

Size resolved particle composition and nitric acid (HNO₃)measurements from the ASEPS'98 experiment conducted in the BalticSea are used to provide observational evidence of substantialgas-particle transfer of oxidized nitrogen (N) compounds in themarine boundary layer. We then focus on the importance ofHNO₃ reactions on sea salt particles in determining spatio-temporal patterns of N dry deposition to marine ecosystems.Modelling results obtained assuming no kinetic or chemical limiton HNO₃ uptake and horizontally homogeneous conditions withnear-neutral stability, indicate that for wind speeds 3.5 – 10 ms^-1 transfer of HNO₃ to the particle phase to formparticle nitrate (NO₃ ^-) may decrease the N depositionvelocity by 50%. We extend this research using the CHEM-COASTmodel to demonstrate that, in a sulphur poor environment undermoderate wind speeds with HNO₃ concentrations representativeof those found in the marine boundary layer, inclusion ofheterogeneous reactions on sea spray significantly reducesmodelled NO₃ ^- deposition in the near coastal zone.     

超临界水氧化技术发展现状及展望

介绍了超临界水氧化法的研究现状与进展，阐述了其原理、特点、工艺流程及反应器，并对其应用领域做了重点描述，指出了其应用中存在的主要问题及今后的研究方向。     

Modelling Easily Biodegradability of Materials in Liquid Medium-Relationship Between Structure and Biodegradability

In the present project, twenty materials (e.g., polyhydroxybutyrate-hydroxyvalerate, polycaprolactone, cellulose acetate, polyacticacid, polyethylene), representing varied biodegradability levels were studied. An aerobic respirometric test, based on the CEN Draft, was setup. The biodegradability of each plastic film was evaluated by measuring the percentage of carbon converted into CO₂ during 35 days. The values of the CO₂ production were plotted versus days as a cumulative function. In order to reduce its number of points, the cumulative curve was modeled using a sigmoïd function (Hill sigmoïd). This model was compared to one found in the literature. A _i ² test showed that the biodegradation curve was more accurately fitted with the model than the previous one. Three kinetic parameters were determined by this Hill model: one represents the maximal percentage of carbon converted into CO₂, the second the half-life time in days of the degrading part of the material and the third one the curve radius.In addition, the following analyses were carried out on each sample: elemental analysis, thickness, hydrophobicity and surface free energy measurements. In order to compress the information and to keep only relevant pieces, these parameters were submitted to a Principal Component Analysis. PCA found linear combinations of variables that describe major trends in the data. The two principal components which separate groups of materials were closely related to a chemical and a physical axis respectively. Materials showing a high biodegradability were related to high oxygen (and nitrogen) contents and low hydrophobicity: Material thickness did not influence the likeliness to biodegradability described by the maximum biodegradation rate. Finally, this study established the correlation between the biodegradation and the structure of biopolymers.     

Preparation and Properties of Water and Glycerol-plasticized Sugar Beet Pulp Plastics

Sugar beet pulp (SBP), the residue from sugar extraction, was compounded and turned into in situ thermoplastic composite materials. The compounding was performed using a common twin- screw compounding extruder and water and glycerol were used as co-plasticizers. The melt compounding of SBP utilized the water-soluble characteristics of pectin which is one of main components of SBP. The structure of SBP was destroyed under extrusion and pectin was partially released and plasticized by water and glycerol. Scanning electron microscopy revealed that the cellulose microfibrils were dispersed in the matrix of pectin and other ingredients. Effects of the water and glycerol co-plasticizers on rheological, tensile and dynamic mechanical properties of the SBP plastics were investigated. Effects of relative humidity of the environment on the tensile and dynamical mechanical properties of the neat SBP compounds were also evaluated. The results demonstrated that SBP could be processed as a plastic with water and glycerol as co-plasticizers using traditional processing equipments.     

Chemistry,Mineralogy and Morphology of Spodosols at Two Swedish Sites Used to Assess Methods of Counteracting Acidification

The chemistry, mineralogy and morphology of two soil profiles developed on till material of granitic and gneissic composition in south-western Sweden were studied in relation to podzolization processes. These soils were used for treatments with lime and wood ash. The profiles do not show characteristic Podzol morphology but qualify as Spodosols under Soil Taxonomy criteria and are probably typical for the coniferous forest soils of south-western Sweden. Podzolization features are clear but less well expressed than in classic Podzols. The distribution of major elements shows podzolization features with accumulation of sesquioxides in the B horizons and depletion in the eluvial horizons. Quartz and feldspars dominate the bulk soils reflecting the clear relationship between the composition of the soil and the underlying bedrock. Low amounts of clay contain an interlayered vermiculitic phase as the main phyllosilicate in which the degree of interlayering, known to be pH dependent, varies with depth and is at a maximum in the Bhs horizon. In the B horizons there are small but significant amounts of imogolite-type material which affect the adsorption of sulphate.     

多杂质水网络超结构模型及其同步设计法研究

研究了存在回用、再生回用和再生循环的多杂质水网络,修正了水网络同步设计的超结构模型.该模型可以合理表征有效物质回收、杂质问存在反应以及废物处理等多种技术.采用通用代数建模系统(GAMS)编程,求解了多杂质水网络混合整数非线性规划(MINLP)问题.同步设计的脱硫实例优化方案与文献值相比,年度总费用可降低8%以上.求解石油化工中常见的含碳稀氨水回收例题,优化设计结果可以满足各组分单独回收要求,避免杂质间反应,提高了水的重复利用率.     

A Comparative Study Between Technological Properties of Cashew Tree Gum and Arabic Gum

Arabic gum (AG) is the most common emulsifier used for beverage emulsions. Cashew tree gum (CG) is a biological macromolecule that has been proposed as a substitute for the AG, although their technological properties comparison is still necessary. The aim of this study was to evaluate an isolation method for CG, and then evaluate CG technological properties in comparison to AG. The CG isolation methodology was improved using a small solvent amount. CG zeta-potential ranged from +8.0 mV (pH 2) to ?9.7 mV (pH 5), while the electric charge in solution of AG ranged from ?2.7 mV (pH 2) to ?28.6 mV (pH 6). As compared to AG, the CG showed a 50 % higher swelling, a 36 % lower oil absorption capacity, a slightly lower (4–8 %) solubility and lower consistency. CG is a feasible polyelectrolyte, promotes lower consistency solutions, and exhibits good swelling property.     

改性膨润土对水中蒽的吸附和解吸

分别用长碳链季铵盐阳离子型表面活性剂溴化十六烷基三甲铵（HDTMAB）、短碳链季铵盐阳离子型表面活性剂四甲铵化溴（TMAB）及非离子型表面活性剂聚乙二醇（PEG）对天然膨润土进行改性。比较了不同类型改性膨润土对水中蒽的吸附性能,探讨了吸附机理。实验结果表明,天然膨润土及改性膨润土对水中蒽的吸附能力依次为HDTMAB改性膨润土〉PEG改性膨润土〉TMAB改性膨润土〉天然膨润土;吸附等温线均是直线,说明该吸附行为是分配作用的结果。不同蒽初始质量浓度下,各种改性膨润土对蒽的吸附量由大至小的顺序为HDTMAB改性膨润土〉PEG改性膨润土〉TMAB改性膨润土,而天然膨润土对蒽的吸附量随蒽初始质量浓度的变化很小。改性膨润土加入量为30～80g/L时,各种改性膨润土对水中蒽的去除率均可达到90％以上,且解吸率均在5％以下。     

A Comparison of Loch Chemistry from 1955 and 1999 in the Cairngorms,N.E. Scotland

The Cairngorms in north-east Scotland is remote from pollutant sources although it currently receives ca. 10 kg ha¹ yr¹ S and ca. 11 kg ha¹ yr¹ N deposition from the atmosphere.In 1955, 15 lochs (lakes) at a range of altitudes were sampled and analysed for major ion concentrations. A new survey of these and an additional 23 lochs and their catchment soils was conducted in 1999 to determine the impact of acid deposition, and the changes in loch chemistry since the 1955 survey. The bedrock geology of this region has a strong influence on the loch chemistry. Surface waters were generally more acidic in high altitude areas due to predominantly poorly buffered, thin alpine soils developed on granitic parent material (mean acid neutralising capacity (ANC) for 23 lochs = 30 eq L¹). At lower altitudes where the geology is dominated by Dalradian metamorphic rocks surface waters are comparatively base rich and have higher ANC (mean ANC for 15 lochs = 157 eq L¹). Surface water nitrate concentrations show a negative relationship with soil C:N status, in that higher nitrate only occurs at low soil C:N ratios. A comparison of data for 1955 and 1999 shows that sulphate concentrations are significantly lower (67.8 and 47.5 eq L¹, respectively), and pH has improved (pH 5.6 and 5.9) in response to decreased S deposition since the mid 1970s. However, mean nitrate concentrations were found to increase from 2.48 >eq L¹ in 1955 to 5.65 eq L¹ in 1999. Differences in the sampling and laboratory methods from 1955 and 1999 are acknowledged in the interpretation of data.     

Long-term Changes in Environmental Variables of Traunsee,an Oligotrophic Austrian Lake Impacted by the Salt Industry,and Two Reference Sites Hallstättersee and Attersee

Morphometric, hydrological and basic physico-chemicalcharacteristics of three deep Alpine lakes, Traunsee,Hallstättersee and Attersee as well as their long-termbahaviour are presented. The deep Alpine lakesHallstättersee and Traunsee have been influenced by saltmining and the traditional salt industry for over 100 years. Waste products from these activities, entering the lakes, have mainlyaffected the chemistry of these water bodies, especially bysubstantially increasing the chloride concentrations up to 170 mg L^-1. As a consequence of the increased density, mixing conditions of the lakes were altered. The resulting incomplete mixing led to oxygen depletionin deeper layers. In addition, increased nutrientload from the catchment rised the trophic level in the 70s and 80sof the last century in turn, affecting the oxygen content in thehypolimnion. Finally a situation developed where the risk becamehigh for these lakes to become meromictic induced by humanactivity. In fact, Hallstättersee became facultativelymeromictic. This process was interrupted by increased chlorideinput of more than 30 mg L^-1 due to accidental wash outfrom an upstream salt mine rendering Hallstätterseehomogenous in 1978 to 1980 resulting in complete over-turn. Conditions substantially improved in both lakes after miningpractices were altered and restoration measures againsteutrophication were initiated. Chloride and phosphorusconcentrations declined, while oxygen conditions substantiallyimproved in the following years. Conditions in Traunseesubstantially improved and chloride levels near the sedimentdecreased to less than 140 mg L^-1. The third lakeconsidered here, Attersee, always remained in a near-naturalstate although some signs of increased nutrient levels becamevisible in the late 1970s. Chloride concentrations of around 3 mgL^-1 in this lake can be considered as background levels.Attersee can now serve as a reference site for deep Alpine lakesbecause of its ultra-oligotrophic and pristine nature.