Effect of Cross-Linking Waste Protein with Diepoxides on its Biodegradation under Anaerobic Conditions

Biodegradability testing was performed in an aqueous environment under anaerobic conditions after inoculation with digested sludge from municipal wastewater treatment plant. In cross-linking with 1,2:3,4-diepoxybutane in limits 0.8–9.1% weight, biodegradability degree decreased from 76.8 to 62.2%; when 1,2:7,8 diepoxyoctane in quantities 1.1–13.2% weight was used, biodegradability degree dropped more prominently – from 72.3 to 22.8%. There is obviously a direct connection between growing cross-link degree (assessed by so-called fixation index) and decreasing readiness to biodegradation, apparently owing to build-up of a network forming an obstacle to access of micro-organisms and enzymes.     

Anaerobic Biodegradation of Poly (Lactic Acid) Film in Anaerobic Sludge

The anaerobic biodegradation rates of four different sizes of poly (lactic acid) (PLA) films (thickness 25???m) in anaerobic sludge at 55?°C were examined. The anaerobic biodegradation rates of small pieces of PLA film were slower than for large pieces of PLA film. We also examined whether PLA film could also be used as a reference material in the anaerobic biodegradation test in addition to PLA powder. The anaerobic biodegradation rate of PLA film became slower with lower activity sludge, but the rate of decrease was gradual, and the anaerobic biodegradation rate of PLA film was faster than the PLA powder (125?C250???m). The anaerobic biodegradation rate of the PLA powder (125?C250???m) reflected the plastic anaerobic biodegradation activity of the sludge more accurately than the thin PLA film (thickness 25???m). Consequently, PLA powder (125?C250???m) is more suitable than thin PLA film (thickness?<?25???m) for use as a reference material to assess the plastic anaerobic biodegradation activity of the sludge in an anaerobic biodegradation test at 55?°C.     

Biodegradation Behavior of Composite Films with Poly (Vinyl Alcohol) Matrix

The main objective of this study was to develop biodegradable, composite materials, based on poly (vinyl alcohol), bacterial cellulose and chitosan for possible application in packaging industry. Two composite materials were prepared, one containing poly (vinyl alcohol) (PVA) and bacterial cellulose (BC), named PVA/BC, and the other containing PVA, BC but also chitosan (CTS), named PVA/BC/CTS. The biodegradation behavior was studied in a fed-batch bioreactor, in aerobic and anaerobic conditions, using activated sludge. Biodegradation tests were based on weight loss measurements. Structural changes were confirmed by Fourier transform infrared spectroscopy (FTIR) and the morphological ones by scanning electron microscopy (SEM). After 4?weeks, the biodegradation experiments have shown a relative high degradation of the PVA/BC/CTS film compared with the PVA/BC one. These results were confirmed by spectral analysis and also by SEM images. Besides, the SEM images revealed that biodegradation occurs also inside the composite materials, not only on the surface.     

Anaerobic Biodegradation of Blends Based on Polyvinyl Alcohol

The presented work deals with blends composed of polyvinyl alcohol (PVA) and biopolymers (protein hydrolysate, starch, lignin). PVA does not belong to biologically inert plastics but its degradation rate (particularly under anaerobic conditions) is low. A potential solution to the issue problem lies in preparation of blends with readily degradable substrates. We studied degradation of blow-molded films made of commercial PVA and mentioned biopolymers in an aqueous anaerobic environment employing inoculation with digested activated sludge from the municipal wastewater treatment plant. Films prepared in the first experimental series were to be used for comparing biodegradation of blends modified with native or plasticized starch; in this case effect of plasticization was not proved. The degree of PVA degradation after modification with native or plasticized starch increases in a striking and practically same manner already at a starch level as low as approximately 5 wt.%. Films of the second experimental series were prepared as additionally modified with protein hydrolysate and lignin. Only lignin-modified samples exhibited a somewhat lower degree of biodegradation but regarding the measure of lignin present in blend this circumstance is not essential. Level of biodegradation with all discussed films differed only slightly—within range of experimental error.     

Anaerobic Biodegradation of Polyvinyl Alcohol Modified by Extracellular Polysaccharides

This work focused on anaerobic biodegradation of blends composed of glycerol-plasticized polyvinyl alcohol (PVA) and biopolymer (starch, gellan, xanthan) in an aqueous environment, after inoculation with digested activated sludge from a municipal wastewater treatment plant. Glycerol degradability is comparable to degradability of used modifying agents. Modifying agents added in the 20–40 wt% range proportionally increased biodegradation degree (D_t) calculated from balance of transformed carbon in the system. Biodegradation degree of polysaccharides and glycerol attained 95% and over. For PVA it was only 6.5% (in breakdown times up to 500 h). Content of polysaccharides favorably affects biodegradation degree of polyvinyl alcohol blends, but at the expense of reduced mechanical properties of resultant products.     

Comparison of the food waste degradation rate and microbial community in the matrix between two biodegradation agents in a food waste disposer

To reduce the proportion of food waste in municipal solid waste, a food waste biodegradation experiment with two biodegradation agents was conducted for seven weeks with 500 g of food waste added every day into each disposer. The agent containing four biodegradation bacterial strains showed higher degradation rates and matrix temperatures than that containing two. Furthermore, significant differences in the microbiological community structures of the matrixes were found not only between the two biodegradation systems but also among different stages in the same degradation system based on DGGE profiles. The F2 strain exhibited the highest DGGE optical density (OD) value among biodegradation systems and at all experimental stages, suggesting it was a dominant strain during food waste degradation.     

Fungal Degradation of Poly(Butylene Adipate-Co-Terephthalate) in Soil and in Compost

The present work mainly dedicated to fungal degradation of poly(butylene adipate-co-terephthalate) [PBAT], to enclose the role of fungi in a real process of biodegradation, the degree of degradation, and to understand the kinetics of PBAT biodegradation. Respirometer tests were realized in soil at 30 °C, and in compost at 30 and 58 °C. Results have shown that temperature is one of the essential parameters governing the fungal degradation of PBAT. Moreover, the final rates of PBAT biodegradation in an inoculated compost with fungi and in a real compost were found comparable, which means that the selected fungi were efficient as much as a mixture of bacteria and fungi. The curves of PBAT biodegradation were modeled by Hill sigmoid. Fungal degradation was completed by investigating the physical and the chemical properties of the polymer during the process of degradation using several analytical methods such as matrix assisted laser desorption ionization-time of fly spectroscopy, size exclusion chromatography, and differential scanning calorimetry. These experiments led to a better understanding of the various stages of fungal degradation of PBAT: hydrolysis as well as mineralization. Furthermore, the analysis of metabolizing products was investigated also.     

Assessing the biodegradation potential of polymers in screening- and long-term test systems

This paper presents a test scheme for assessing the biodegradation potential of polymers, starting with aquatic screening systems (aerobic and anaerobic) and continuing to long-term systems. At the end of the scheme the material has to prove its behavior under the relevant disposal conditions. Aerobic screening was performed mainly under aquatic conditions, but also in soil, using BOD-respirometry. Carbon balances were performed to obtain a better evaluation of the biodegradation potential. Under anaerobic conditions, biodegradation in an aquatic medium was followed by measuring CH₄ and CO₂ production. Polymers not fully degraded in the screening systems were tested in aquarium systems for at least 1 year. Biodegradation was followed by monitoring the DOC released in the water, mass loss, and microbial growth on the samples and in the water as well as via FTIR spectroscopy and SEM pictures. Results are presented for the polymers PHB, PHBV, PCL, Mater-Bi AI05H and ZF03U, and Bioceta. By combining the data from the screening with the aquarium system, a good picture of the degradation behavior of the polymers is obtained.Paper presented at the Bio/Environmentally Degradable Polymer Society—Third National Meeting, June 6–8, 1994, Boston, Massachusetts.     

Structure and Morphology of Microbial Degraded Poly(ε-caprolactone)/Graphite Oxide Composite

Biodegradation of poly(ε-caprolactone) composite with graphite oxide (GO) by the action of Bacillus subtilis (BS) was studied in this work. Nanocomposite produced in a form of thin film was exposed to nutrient cultivation medium with BS as well as to abiotic nutrient medium (control run) at 30 °C. The matrix itself was exposed to the same conditions for comparison. Biodegradation was demonstrated by the weight loss and the decrease of molecular weight during 21 days of the experiment as well as by changes in the surface morphology and structure. Both degraded and control materials were characterized by confocal laser scanning microscopy, differential scanning calorimetry, thermogravimetry, and Fourier transform infrared spectroscopy with attenuated total reflectance. The bacterial growth expressed as the measure of the optical density/turbidity in McFarland units and pH of medium were measured in situ during the experiment. Lipolytic activity of BS was determined by spectrophotometric assay. Degradation process was accompanied by the increase of matrix crystallinity degree. GO served as nucleating agent and facilitated absorption of cultivation media into the composite which led to the increase of the crystallinity degree also for control nanocomposite specimens. It was not evaluated to be promoter of biodegradation. The surface cracks formation was initiated by BS action. Large surface cracks were formed on BS-degraded composite surfaces while surface erosion was more significant on BS-degraded matrix.     

Use of bio‐traps with multiple substrates and electron acceptors to optimize remediation

Bio‐Traps® were used to investigate biodegradation of benzene, methyl tertiary butyl ether (MTBE), and tertiary butyl alcohol (TBA) under different conditions at a fractured rock site to aid the selection of a bioremediation approach. The Bio‐Traps were amended with the ¹³C‐labeled constituent of interest and sampled sequentially at 15‐, 30‐, 60‐, and 90‐day intervals. The conditions tested were biodegradation during operation of an air sparge system, amendment with nitrate during the air sparge operation, anaerobic biodegradation with the system turned off, and anaerobic biodegradation with nitrate amendment. There was increased biomass with nitrate amendment whether the air sparge system was on or off for all the constituents of interest. The diversity of the microbial community, determined by phospholipid fatty acid analysis, decreased with nitrate amendment as more specialized degraders were selected. The most negative indicators of potential biodegradation performance were observed with the anaerobic control. There was less biomass overall, less incorporation of ¹³C into biomass, and decreased membrane permeability. As testing with additional amendments continues at the site, it is not yet certain which treatment might be selected for bioremediation, but the Bio‐Trap tests thus far have identified that the in situ, natural attenuation condition is least favorable for biodegradation. © 2009 Wiley Periodicals, Inc.     

Active and Intelligent Films Made from Starchy Sources/Blackberry Pulp

Functional, active and intelligent films were prepared from biopolymeric matrices (plantain starch and pre-gelatinized plantain flour) with and without the addition of a natural filler (blackberry pulp) using the casting methodology. A thorough examination of the physicochemical, antioxidant and antimicrobial properties of the both the matrices used and the developed films was then carried out. The films developed from matrices incorporating the blackberry pulp were more amorphous, thicker, less sensitive to moisture, and with higher melting temperatures than the films made without this natural filler. The degree of substitution, average molecular weight and attenuated total reflectance Fourier transform infrared spectroscopy of the films made with blackberry pulp suggest that the starch chains were cross-linked. This is probably because the citric acid contained in the pulp functions as a cross-linking agent. Films with added blackberry pulp responded to changes in pH, i.e. were pH-sensitive, and also showed antimicrobial activity especially against Escherichia coli. In general, the addition of blackberry pulp improved the physicochemical and mechanical properties of the films developed due to cross-linking, as well as increasing their antioxidant activity.     

The Effect of Natural Tree Gum and Environmental Condition on the Degradation of a Typical Automotive Clear Coat

In this work the effects of natural gum and its simulated compound (Arabic gum) on an acrylic based clear coat applied on different basecoats were studied. The experiments were conducted at various aging processes to simulate the real outdoor conditions by the aid of different analytical techniques including optical microscopy, scanning electron microscopy, ATR-FTIR spectroscopy, DMTA and micro hardness measurements, by which the chemical and mechanical responses of the system were investigated. Results showed that, Arabic and natural gums, due to their sticky nature in the slurry state, can strongly attach to the clear coat surface and perform a significant stress during the drying process. It was shown that, this stress was responsible for the surface cracks produced by gums, indicating a physical degradation mechanism. However, it was revealed that, biological materials could also affect the clear coat chemically. In addition, different surface cracks produced by gums on the clear coat applied on silver and black basecoats were observed and attributed to their surface chemistry and mechanical properties differences. It was shown that different amounts of aluminum flakes existed in the basecoat layers of silver and black system can effectively influence the curing degree of the clear coats applied on the se systems. This leads to different cross-linking density, toughness and surface chemistries. Therefore, different interactions of clear coats and gums, as well as stress distribution and relaxation behaviors of these two systems were found effective in such degradations. Comparison of the mechanical properties and visual effects of gums on clear coats indicated a more severe degradation under the post aging, due to the greater effect of UV light.     

厌氧折流板污泥对偶氮染料酸性大红GR的生物降解性能研究

研究了厌氧折流板反应器（ABR）活性厌氧污泥对偶氮染料酸性大红GR的吸附与生物降解性能，并与失活污泥进行了对比。试验结果表明，35℃时厌氧活性污泥2h、12h、6d的脱色率分别为78.2%、86.0%、98.9%。无论在反应初始阶段还是稳定阶段，ABR活性厌氧污泥对染料的去除效果都明显优于失活污泥。而且在初始COD为1152mg/L的，由于非有效吸附位置染料脱落等原因，反应期间，失活污泥混合液中染料浓度还会升高。情况下，活性厌氧污泥混合液出水COD为86.0mg/L，去除率约为92.5%。这说明ABR厌氧污泥微生物在短时间内便可以得到驯化，一旦厌氧微生物适应生长环境，生物降解便开始对染料发挥作用。     

Microbial characteristics associated with six different organic wastes undergoing anaerobic decomposition in batch vial conditions.

In this study, the biodegradation characteristics of six plant-based wastes were compared in anaerobic batch vial systems. The highest gas accumulation and methane (CH4) concentrations (approximately 70%) were observed in samples containing copy paper, newspaper and box paper materials, whereas the lowest were observed in samples containing wood and leaves. In samples containing steamed rice and fruit, the methanogenic activity was inhibited, which resulted in acid accumulation. The high biodegradation activity of newspaper samples was also associated with high adenosine triphosphate levels and dehydrogenase activity. No significant differences were, however, observed in the dehydrogenase activity of the samples. High bioluminescence was observed in samples with high biodegradation activities, indicative of low toxicity.     

Compartment model of aerobic and anaerobic biodegradation in a municipal solid waste landfill

The mathematical formulations in a one-dimensional compartment model of the biodegradation of organic landfill components are described. The model is designed to switch between anaerobic and aerobic conditions, depending on the local oxygen concentration. The model also includes the effect of environmental factors, such as moisture content, pH, and temperature, on reaction rates. The model includes not only biodegradation processes for carbon compounds (acetate, CO2, CH4), but also for nitrogen compounds involved in nitrification and denitrification due to their significance in landfills. Two example runs to simulate anaerobic and aerobic waste were conducted for a single landfill unit cell by changing the organic content and diffusion coefficient.     

Design and Characterization of PVA–Methacrylic Acid Based Smart Polymeric System for Controlled Release of Metoprolol

In the present work covalently crosslinked smart polymeric system of hydrogel based on poly vinyl alcohol (PVA) and methacrylic acid (MA) was designed by free radical polymerization with different compositions using glyoxal (40 % water solution) as crosslinker. It was observed that swelling of hydrogel had a pronounced enhancing effect on increasing the concentration of MA due to availability of more ionized carboxylic groups of MA but produced an opposite effect on increasing the concentration of glyoxal owing to less porous structure. As far as PVA is concerned, swelling did not show significant effect on increasing the concentration of PVA. Hydrophilic polymer PVA rich in hydroxyl group pertained to be highly interactive with water. It was examined that the release of metoprolol tartrate decreased with increased concentration of glyoxal, but increased with increase in concentration of MA. PVA/MA hydrogel was characterized by Fourier transform infrared spectroscopy and X-ray diffraction to study the structure and crystallinity of hydrogel respectively. Morphology was studied through scanning electron microscopy. Furthermore differential scanning calorimetry and thermogravimetric analysis were also performed to characterize thermal stability. It may be concluded that the mechanism of drug release was mainly non-Fickian diffusion.     

大豆油乙氧基化合物的生物降解

采用振荡培养实验和活性污泥模拟实验对大豆油乙氧基化合物（SOE）进行了生物降解研究。实验结果表明，振荡培养实验中SOE的初级生物降解度随平均环氧乙烷加成数的增多而略有下降，且SOE-4，SOE-10，SOE-20的初级生物降解度在第6天时分别为97．3％，91．1％，89．4％；活性污泥模拟实验中SOE的初级生物降解度随平均环氧乙烷加成数的增多而增加，且SOE-4，SOE-10，SOE-20的初级生物降解度在第8天时分别为29．0％，81．2％，100．0％。用激光粒度仪测量SOE水合物在不同静置时间时的粒径分布及分散度结果表明，随静置时间的延长，平均环氧乙烷加成数少的SOE水合物粒径逐渐增大，且分散性或水溶性变差，易产生团聚导致初级生物降解度降低。对水溶性或分散性较差的表面活性剂，建议以振荡培养实验研究其生物降解性较为恰当。     

Intrinsic and Stimulated In Situ Biodegradation of Hexachlorocyclohexane (HCH)

The feasibility of the biodegradation of HCH and its intermediates has been investigated. A recent characterisation of two sites in The Netherlands has shown intrinsic biodegradation of HCH. At one site, breakdown products (monochlorobenzene, benzene and chlorophenol) were found in the core of the HCH-plume, whereas the HCH-concentration decreased over time and space. Characterisation of a second, industrial site indicated less intrinsic biodegradation and the need to stimulate biodegradation. In the laboratory, enhanced HCH degradation was tested with soil and groundwater material from both sites, and the required conversion to the intermediates benzene and monochlorobenzene was demonstrated. Furthermore, the biodegradation of these intermediates could be initiated by adding low amounts of oxygen (<5%). Adding nitrate enhanced this degradation. We hypothesise that this occurs through anaerobic nitrate reducing conversion of oxidised intermediates.At the non-industrial other site, intrinsic degradation took place, as shown in the laboratory experiments. Interpretation of the field data with computer codes Modflow and RT3D was performed. As a result of the modelling study, it has been proposed to monitor natural attenuation for several years before designing the final approach.At the industrial site, the results of the batch experiments are applied. Anaerobic HCH degradation to monochlorobenzene and benzene is stimulated via the addition of an electron donor.Infiltration facilities have been installed at the site to create an anaerobic infiltration zone in which HCH will be degraded, and these facilities are combined with the redevelopment of the site.     

Enhanced Mineralization of PLA Meltblown Materials Due to Plasticization

Polylactic acid (PLA) is one of the important biodegradable polymers. It is widely used in many industrial applications such as films and fibers. Its biodegradability is based on data derived mostly from composting processes. For a broad application of the PLA material in personal care products, an understanding of anaerobic biodegradability is essential because soiled personal care products are usually disposed of in sanitary landfills, where biodegradability mechanisms are predominately in anaerobic conditions. Extensive laboratory results are acquired to elucidate the effects of the temperature on the PLA anaerobic sludge biodegradation. When the temperature is higher than PLA glass transition temperature (T_g), anaerobic degradation is accelerated. A plausible mechanism to explain this observation is that amorphous part of the polymer is easily accessible by microorganisms. When the degrading temperature is below PLA glass transition temperature, sample mineralization under anaerobic conditions is apparently slowed. The mechanisms elucidated by T_g modification can be utilized to control the rate of PLA biodegradation for sustainable waste management.     

废旧硬质聚氨酯泡沫塑料的木质素改性及再生

采用含有二乙二醇(DEG)和乙醇胺(ETA)的双组分解交联剂降解废旧硬质聚氨酯泡沫塑料(PU硬泡),并利用降解得到的低聚物多元醇与木质素复合制备出性能增强的再生PU硬泡。通过对制备的再生PU硬泡的红外光谱、密度、吸水率、抗压强度、热稳定性、导热系数、热重曲线等进行分析测试,考察m(DEG)∶m(ETA)对再生PU硬泡性能的影响。实验结果表明:m(DEG)∶m(ETA)=1∶3时废旧PU硬泡的降解效果最好;木质素加入量为2.0%(w)时再生PU硬泡的密度低、抗压强度高、保温性能良好,达到国家标准《建筑绝热用硬质聚氨酯泡沫塑料》(GB/T 21558—2008)的品质要求。