Oil/Suspended Particulate Material Interactions and Sedimentation

The interactions of physically dispersed oil droplets with suspended particulate material (SPM) can be important for the transport of bulk quantities of spilled crude oil and polycyclic aromatic hydrocarbons (PAH) to subtidal sediments. The literature regarding oil/SPM interactions is reviewed, and results from whole-oil droplet/SPM interaction kinetics and pure-component (Prudhoe Bay crude oil distillate cut) equilibrium partitioning experiments are presented. The effects of oil type, SPM characteristics, and salinity on the interaction rates are examined, and the importance of whole-oil droplet/SPM interactions on particle agglomeration and settling behavior are discussed. Whole-oil droplet/SPM interactions are retarded as oil droplet dispersion into the water column is inhibited by oil viscosity increases due to evaporation weathering and water-in-oil emulsification. Compared to whole oil droplet/SPM interactions, dissolved-component/SPM adsorption is not as significant for transport of individual components to sediments. The information presented in this paper can be used to augment computer-based models designed to predict oil-spill trajectories, oil-weathering behavior, and spilled oil impacts to the marine environment.     

Metal Contamination of the Natural Environment in Norway from Long Range Atmospheric Transport

Long range atmospheric transport is the most important sourceof contamination to the natural environment in Norway with manyheavy metals. Investigations based on aerosol studies, bulkdeposition measurements and moss analysis show that airborne transport from other parts of Europe is the major mode for supplyof vanadium, zinc, arsenic, selenium, molybdenum, cadmium, tin,antimony, tellurium, thallium, lead, and bismuth, whereas metalssuch as chromium, nickel, and copper are mainly derived from point sources within Norway and in northwestern Russia close tothe Norwegian border. Elements associated with long range transport show substantial enrichment in the humus horizon of natural soils in southern Norway, sometimes to levels suspected to cause effects on soil microbial processes. E.g. lead concentration values of 150–200 ppm are observed in the mostcontaminated areas in the south as compared to about 5 ppm inthe far north. Elements such as lead and cadmium also show enrichment in some terrestrial food chains. These elements alsoshow considerably elevated levels over background concentrationsin the water and sediment of small lakes in the southern part ofthe country. Retrospective studies based on ombrogenous peatcores indicate that long range transport has been a significantsource of heavy metal contamination in southern Norway for thelast couple of centuries. The deposition of most heavy metals inNorway has been considerably reduced over the last 20 yr, withthe exception of contributions in the north from Russian smelters.     

Enhancing Performance of Sphingobacterium spiritivorum in Bioremediation Phenanthrene Contaminated Sand

Many biodegradation studies have focused on survival of isolated bacteria to increase the bacteria population and subsequently enhance the efficiency of polycyclic aromatic hydrocarbon (PAH) biodegradation. However, there is limited research on enhancing the performance of isolated bacteria through reinoculation. Thus, this study was designed to evaluate the effects of reinoculation on the performance of Sphingobacterium spiritivorum in degradation of phenanthrene contaminated sand. Experiments were performed in three different reactors. Inoculation was performed once (day 0) in reactor 1. In reactor 2, inoculation was performed twice (day 0 and day 5). The bacteria was isolated from reactor 2 and inoculated into reactor 3. The study results show reactor 3 having the highest degradation rate (13.61 mg/kg/day) and percentage removal (95.36 percent). In contrast, without reinoculation in reactor 1, 68.93 percent of phenanthrene was removed. Thus, the performance of S. spiritivorum in phenanthrene degradation can be enhanced through reinoculation. © 2014 Wiley Periodicals, Inc.     

Material Properties and Influence of Molecular Weight and Testing Rate on Adhesion Properties of Epoxidized Natural Rubber-Based Adhesives

The effect of molecular weight and testing rate on peel and shear strength of epoxidized natural rubber (ENR-50)-based adhesive was investigated using petro resin as the tackifier. Toluene and polyethylene terephthalate were used as the solvent and substrate respectively. Peel and shear strength were determined by a Llyod Adhesion Tester operating at different rates of testing. Result shows that peel strength and shear strength increases up to an optimum molecular weight of 4.2 × 10⁴ g/mol of ENR-50. This observation is attributed to the combined effects of wettability and mechanical strength of rubber for peel strength. For shear strength, it is ascribed to the optimum cohesive and adhesive strength. Both peel strength and shear strength increases with increasing rate of testing, an observation which is associated to the viscoeslastic response of the adhesive. Thermal study, SEM and FTIR study confirms the miscibility of tackifier with ENR-50.     

Biodegradation of Injection Molded Starch-Poly (3-hydroxybutyrate-co-3-hydroxyvalerate) Blends in a Natural Compost Environment

Injection molded specimens were prepared by blending poly (hydroxybutyrate-co-valerate) (PHBV) with cornstarch. Blended formulations incorporated 30% or 50% starch in the presence or absence of poly-(ethylene oxide) (PEO), which enhances the adherence of starch granules to PHBV. These formulations were evaluated for their biodegradability in natural compost by measuring changes in physical and chemical properties over a period of 125 days. The degradation of plastic material, as evidenced by weight loss and deterioration in tensile properties, correlated with the amount of starch present in the blends (neat PHBV < 30% starch < 50% starch). Incorporation of PEO into starch-PHBV blends had little or no effect on the rate of weight loss. Starch in blends degraded faster than PHBV and it accelerated PHBV degradation. Also, PHBV did not retard starch degradation. After 125 days of exposure to compost, neat PHBV lost 7% of its weight (0.056% weight loss/day), while the PHBV component of a 50% starch blend lost 41% of its weight (0.328% weight loss/day). PHB and PHV moieties within the copolymer degraded at similar rates, regardless of the presence of starch, as determined by ¹H-NMR spectroscopy. GPC analyses revealed that, while the number average molecular weight (Mn) of PHBV in all exposed samples decreased, there was no significant difference in this decrease between neat PHBV as opposed to PHBV blended with starch. SEM showed homogeneously distributed starch granules embedded in a PHBV matrix, typical of a filler material. Starch granules were rapidly depleted during exposure to compost, increasing the surface area of the PHBV matrix.     

Elaboration of a Bio-Colored Material Based on Natural Dye and Polybutylene Succinate: Comparative Study with Colored Polylactic Acid

Journal of Polymers and the Environment - In the context of sustainable development and natural products valorization, new ecological materials enter a logic aimed at removing the causes of...     

A New Test Method for Determining Biodegradation of Plastic Material Under Controlled Aerobic Conditions in a Soil-Simulation Solid Environment

A new test method is described for assessing biodegradation of plastic material under simulated soil conditions. An inert substrate can be activated with soil extract and nutrient and used in place of soil in biodegradation tests. The biodegradation level is evaluated by determining the carbon dioxide (CO₂) production released by the test reactors. Effects of substrate nature, solution pH, nutrient composition, soil extract concentration, and activation duration on CO₂ production were investigated, and the experimental conditions were optimized. Results obtained with cellulose showed a biodegradation rate of 80% within 28 days. Moreover, with this kind of substrate, reaction products and residues can be easily extracted and analysed.     

Interactions between biological and abiotic pathways in the reduction of chlorinated solvents

While biologically mediated reductive dechlorination continues to be a significant focus of chlorinated solvent remediation, there has been an increased interest in abiotic reductive processes for the remediation of chlorinated solvents. In situ chemical reduction (ISCR) uses zero‐valent iron (ZVI)–based technologies, such as nanoscale iron and bimetallic ZVI, as well as naturally occurring reduced minerals incorporating dual‐valent iron (DVI), such as magnetite, green rust, and iron sulfides that are capable of dechlorinating solvents. A more recent area of development in ISCR has been in combining biological and abiotic processes. There are several ways in which biological and abiotic processes can be combined. First, the interaction between the two may be “causative.” For example, the Air Force Center for Engineering and the Environment's biogeochemical reductive dechlorination (BiRD) technology combines a mulch barrier with hematite and gypsum to create an iron‐sulfide‐based reducing zone. Biodegradation under sulfate‐reducing conditions produces sulfide that combines with the hematite to form iron sulfides. As such, the BiRD technology is “causative”; the biological processes create reducing minerals. The biological generation of other reducing minerals such as magnetite, siderite, and green rust is feasible and is, with magnetite, observed in nature at some petroleum sites. A second type of interaction between abiotic and biotic processes is “synergistic.” For example, biological processes can enhance the activity of reduced metals/minerals. This is the basis of the EHC® ISCR technologies, which combine ZVI with a (slowly) degradable carbon substrate. This combination rapidly creates buffered, strongly reducing conditions, which result in more complete solvent degradation (i.e., direct mineralization). The extent and level of reducing activity commonly observed are much greater when both the carbon substrate and the ZVI are present. When the carbon substrate is expended, the reducing activity due to ZVI alone is much less. The understanding of biogeochemical processes and their impact on abiotic processes is still developing. As that understanding develops, new and improved methods will be created to enhance volatile organic compound destruction. © 2009 Wiley Periodicals, Inc.     

萃取浓缩-薄涂柱气相色谱法测定煤焦油废水中的联苯和菲

用苯萃取浓缩煤焦油废水中的联苯和菲,然后用薄涂柱气相色谱法进行测定。试验表明：该法具有色谱柱温低、快速、准确等特点。     

Natural and anthropogenic arsenic in soil in the Boston Basin

Naturally occurring and anthropogenic arsenic concentrations in soils, in conjunction with the current knowledge of its potential risk to human health, demonstrate a critical environmental and public health issue. These widespread arsenic concentrations potentially affect large human populations. There are locations worldwide where naturally occurring arsenic is considered to be and documented as a potential human health risk through the use of established risk assessment calculation approaches or as demonstrated by clearly measurable health or agricultural effects. This natural arsenic, exposed due to human activity and coupled with anthropogenic contributions, may be the number‐one soil contact environmental health issue in the world. Considering the relatively high natural arsenic concentrations in some New England locations, and with the advantage of access to a large soil arsenic database, this issue has been addressed as described herein for the Boston Basin and related areas. The article provides a summary of some large natural and anthropogenic arsenic data sets with comparison between them and a derivation of the natural and anthropogenic components in the Boston Basin. © 2010 Wiley Periodicals, Inc.     

A Review of the Fate and Effects of Silicones in the Environment

Silicones are well-known useful materials varying in structure, reactivity, and chemical and physical properties, but they all contain a covalent bond between the silicon atom and an organic group. Most common of these polymers are those based on polydimethylsiloxane (PDMS) having a siloxane (Si–O–Si) repeat unit and two methyl groups on each silicon atom. All these polymers are manmade, and the organosilicon linkage is not found in nature. It was therefore erroneously assumed that these polymers do not degrade naturally in the environment. It is the purpose of this review to refute this myth and to describe the degradation processes of PDMS in the environment and any potential ecological impact on the terrestrial, aquatic, and atmospheric compartments. Although it was found that minor degradation takes place by hydrolysis of PDMS to dimethylsilandiol followed by oxidation of the methyl group to aldehyde and ultimately to CO₂ by Arthobacter and Fusarium oxysporium schlechtendahl, the major degradation processes are abiotic. High molecular weight PDMS are initially depolymerized by soil hydrolysis of the siloxane bonds to yield organosilanol terminated oligomers. These organosilanols and low molecular weight linear PDMS and cyclics are evaporated into the atmosphere and are oxidized there by hydroxyl radicals to benign silica, water, and CO₂.     

Role of Hydrophilic and Hydrophobic Interactions in Structure Development of Zein Films

Zein has been studied for its potential as a biobased polymeric material. Due to the fact that films made exclusively from zein are brittle, composites of zein and oleic acid were prepared in our lab and formed into flexible films. Film properties were believed related to their structure. X-ray scattering measurements on zein films suggested the formation of layers along the plane of the film. Oleic acid seemed to play an important role in layer formation. However, X-ray measurements could not yield information on the nature of the interface between oleic acid and zein. Surface plasmon resonance (SPR) was used to further investigate interaction between zein and oleic acid. Dynamic adsorption of zein from alcoholic solutions onto hydrophilic and hydrophobic surfaces generated by self-assembled monolayers of 11-mercaptoundecanoic acid or 1-octanethiol was monitored by SPR. It was observed that zein had a greater affinity for hydrophilic than for hydrophobic surfaces under the prevalent experimental conditions. A mechanism for structure development of zein-oleate films was proposed based on these results and previous X-ray measurements. It is suggested that the structure development involves hydrophilic adsorption of fatty acids onto the zein surface followed by hydrophobic associations leading to a layered film structure organization.     

Material reuse and recycling in construction works in Japan

Journal of Material Cycles and Waste Management - The status of material reuse and recycling in Japan is reviewed with an emphasis on the efforts by the national government. First, the national...     

Effects of Liming on the Aquatic Fauna in a Norwegian Watershed: Why Do Crustaceans and Fish Respond Differently?

We studied the effects of liming on fish and crustaceans in a watershed which is in a region known to have one of the highest diversity of aquatic biota in Norway. This watershed, Enningdal, is shared between Norway (1/3) and Sweden (2/3) and includes 61 lakes  >  1.0 ha in Norway. Liming started on a large scale in the 1980s. Currently, a total of 26 of lakes (43%) are limed, covering 93% of the total lake area. The mean value ± S.D. of pH and the concentration of inorganic labile Al in these lakes is 6.62 ± 0.35 and 3 ± 4 μg l⁻¹, respectively. Historical data of fish communities have been obtained from surveys, while test-fishing and sampling of crustaceans were conducted in 24 lakes in recent years (2002–2004). The present study shows that crustaceans to a greater extent than fish has responded to improved water quality after more than 20 years of liming. Of a total of 120 fish populations, 42 (35%) have gone extinct. Only five of the lost fish populations (12%) have been re-established, all due to human re-introductions. Physical barriers are considered to be the main factor preventing fish from invading limed lakes. In contrast, crustaceans have been re-established in most limed lakes. This may be mainly due to their good spreading capacity. However, they might also have survived in refuges within the watershed, or as resting-eggs in the sediment.     

循环经济发展中的物质代谢分析

介绍了循环经济发展过程中物质代谢系统边界的确定、代谢主体的认定、物质流的组成,分析了单位产值物质需求量、人均物质消耗强度和物质生产力等物质代谢效率的评价指标,探讨了物质代谢调控对象和手段,提出了当前循环经济理论研究应该从物质代谢入手,从产品的整个生命周期来研究经济系统与生态环境之间的物质流动规律,以形成闭合的物料循环系统。     

Chemical Treatments of Natural Fiber for Use in Natural Fiber-Reinforced Composites: A Review

Studies on the use of natural fibers as replacement to man-made fiber in fiber-reinforced composites have increased and opened up further industrial possibilities. Natural fibers have the advantages of low density, low cost, and biodegradability. However, the main disadvantages of natural fibers in composites are the poor compatibility between fiber and matrix and the relative high moisture sorption. Therefore, chemical treatments are considered in modifying the fiber surface properties. In this paper, the different chemical modifications on natural fibers for use in natural fiber-reinforced composites are reviewed. Chemical treatments including alkali, silane, acetylation, benzoylation, acrylation, maleated coupling agents, isocyanates, permanganate and others are discussed. The chemical treatment of fiber aimed at improving the adhesion between the fiber surface and the polymer matrix may not only modify the fiber surface but also increase fiber strength. Water absorption of composites is reduced and their mechanical properties are improved.     

Material cycles in Asia: especially the recycling loop between Japan and China

In this article, we clarify the current status of Japanese exports and Chinese imports of secondary resources. A total of around 10 million metric tons (t) of secondary resources are exported annually from Japan to China, Hong Kong, and Korea. Hong Kong plays the role of a transshipment point, especially regarding the trade in plastic waste, and China imports much from the USA and Japan, often through Hong Kong. The secondary resources exported from Japan include both byproducts from manufacturing processes and end-of-life products or materials. The great demand in China, and the difference in prices between countries, drive this transboundary shipment, although Japan has enacted various recycling laws that were implicitly intended to promote domestic recycling. In China, the imported secondary resources are recycled, usually by means of primitive and low-cost hand labor. The greatest concern is whether there are still improper (illegal or polluting) recycling activities in China. International material cycles should prevent environmental pollution and ensure efficient resource utilization. To that end, the following measures are needed: cooperative control of the trade of secondary resources between countries, the alignment of domestic laws with the regulations in other countries based on the actual trade activities, and the realization of sound practices for global resources management.     

Removal of Oil from the Sea Surface through Particulate Interactions: Review and Prospectus

The fate of oil spilled in coastal zones depends in large part on the interactions with environmental factors existing within a short time of the spill event. In addition to weathering which produces changes in the chemistry of the hydrocarbon stock, physical interactions between oil and suspended particulate matter (SPM), both organic and inorganic, play a role in determining the dispersal and sedimentation rates of the spill. This in turn affects the degradation rate of the oil. This paper provides a comprehensive literature review of the role of oil–particle interactions in removal of petroleum hydrocarbons from the sea surface and provides estimates of the degree to which SPM may augment the deposition of oil. Both field and laboratory observations have shown widely varying rates of oil removal due to particulate interactions. The discussion covers the interaction between oil weathering, injection, sinking, adsorption, microbial processes, flocculation and ingestion by zooplankton, which all contribute to packaging oil and SPM into settling aggregates.