挥发性脂肪酸对厌氧干式发酵产甲烷的影响

为了提高中温干式厌氧间歇发酵效率,研究了发酵过程中间产物———挥发性脂肪酸对产甲烷的影响。实验分2批进行,第1批在牛粪发酵过程中分别添加乙酸、丙酸和丁酸,第2批发酵添加易产生挥发酸的厨余垃圾混合发酵。结果显示,添加单一挥发酸的发酵过程中,添加丙酸的产甲烷速度较慢,因为丙酸降解生成乙酸的速度较慢,减慢了甲烷的形成;混合发酵过程厨余垃圾产甲烷速度比牛粪快,发酵过程产生2个产气高峰;牛粪和厨余垃圾固体物质含量比在11∶1到5∶1范围内较好,比牛粪单独发酵产气多,产酸高但不酸败,产生的挥发酸主要是乙酸和丙酸,其中比例为7∶1混合发酵的产甲烷速率最大,为4.89 mL/(g VS·d)。实验表明,牛粪厌氧干式发酵过程添加一定量的厨余垃圾可加快挥发酸的产生并提高挥发酸产量,从而提高甲烷的产量,但是总挥发酸长时间超过10 000 mg/L,pH降到不适于产甲烷菌生长的范围时,将抑制甲烷的生成,挥发酸积累导致厌氧发酵酸败。     

浓度波扩散模型在玉米秸秆厌氧干发酵中的应用及验证

将Vavilin的浓度波扩散模型引入到玉米秸秆厌氧干发酵中,使用MATLAB7.0软件运用最小二乘法,计算初始含水量为70%的中温玉米秸秆干发酵过程中Ds、DB和ρm等相关模型系数,并通过不同初始含水量(75%、80%和85%)实验来进行验证,结果表明,所得模型系数在含水量70%~80%时预测效果较好,能较为准确地反映发酵过程中的传质过程。     

餐厨垃圾单相厌氧酸化系统恢复参数

针对现今餐厨垃圾单相厌氧酸化系统缺乏有效的恢复性监控指标,提出可有效表征酸化系统恢复的监控指标。在中温条件下,连续对餐厨垃圾单相厌氧消化系统进行负荷冲击及恢复,分别对p H、沼气产率及成分、挥发性脂肪酸组成成分、总碱度(TA)和碳酸氢盐碱度(BA)及其组合指标进行监测分析。结果表明,传统单因子参数不能有效地指示系统恢复,选取VFA/BA和丙酸/乙酸的比值作为餐厨垃圾单相厌氧酸化系统恢复指示性参数。在酸化系统恢复过程中,当丙酸/乙酸≤1.4、VFA/BA≤0.4时,表明系统中各种挥发酸浓度值已恢复正常,且具有足够的缓冲能力,可提高反应器负荷,保证反应器恢复启动运行。     

Long-term thermophilic mono-digestion of rendering wastes and co-digestion with potato pulp

In this study, mono-digestion of rendering wastes and co-digestion of rendering wastes with potato pulp were studied for the first time in continuous stirred tank reactor (CSTR) experiments at 55 °C. Rendering wastes have high protein and lipid contents and are considered good substrates for methane production. However, accumulation of digestion intermediate products viz., volatile fatty acids (VFAs), long chain fatty acids (LCFAs) and ammonia nitrogen (NH₄-N and/or free NH₃) can cause process imbalance during the digestion. Mono-digestion of rendering wastes at an organic loading rate (OLR) of 1.5 kg volatile solids (VS)/m³ d and hydraulic retention time (HRT) of 50 d was unstable and resulted in methane yields of 450 dm³/kg VS_fed. On the other hand, co-digestion of rendering wastes with potato pulp (60% wet weight, WW) at the same OLR and HRT improved the process stability and increased methane yields (500–680 dm³/kg VS_fed). Thus, it can be concluded that co-digestion of rendering wastes with potato pulp could improve the process stability and methane yields from these difficult to treat industrial waste materials.     

Application of an early warning indicator and CaO to maximize the time–space-yield of an completely mixed waste digester using rape seed oil as co-substrate

In order to increase the organic loading rate (OLR) and hereby the performance of biogas plants an early warning indicator (EWI-VFA/Ca) was applied in a laboratory-scale biogas digester to control process stability and to steer additive dosing. As soon as the EWI-VFA/Ca indicated the change from stable to instable process conditions, calcium oxide was charged as a countermeasure to raise the pH and to bind long-chain fatty acids (LCFAs) by formation of aggregates. An interval of eight days between two increases of the OLR, which corresponded to 38% of the hydraulic residence time (HRT), was sufficient for process adaptation. An OLR increase by a factor of three within six weeks was successfully used for biogas production. The OLR was increased to 9.5 kg volatile solids (VS) m^?3 d^?1 with up to 87% of fat. The high loading rates affected neither the microbial community negatively nor the biogas production process. Despite the increase of the organic load to high rates, methane production yielded almost its optimum, amounting to 0.9 m³ (kg VS)^?1. Beneath several uncharacterized members of the phylum Firmicutes mostly belonging to the family Clostridiaceae, a Syntrophomonas-like organism was identified that is known to live in a syntrophic relationship to methanogenic archaea. Within the methanogenic group, microorganisms affiliated to Methanosarcina, Methanoculleus and Methanobacterium dominated the community.     

Recovery of volatile fatty acids via membrane contactor using flat membranes: Experimental and theoretical analysis

Volatile fatty acid (VFA) separation from synthetic VFA solutions and leachate was investigated via the use of a membrane contactor. NaOH was used as a stripping solution to provide constant concentration gradient of VFAs in both sides of a membrane. Mass flux (12.23 g/m² h) and selectivity (1.599) observed for acetic acid were significantly higher than those reported in the literature and were observed at feed pH of 3.0, flow rate of 31.5 ± 0.9 mL/min, and stripping solution concentration of 1.0 N. This study revealed that the flow rate, stripping solution strength, and feed pH affect the mass transfer of VFAs through the PTFE membrane. Acetic and propionic acid separation performances observed in the present study provided a cost effective and environmental alternative due to elimination of the use of extractants.     

再生水中消毒副产物——卤乙酸的测定方法研究

参照美国国家环保局(USEPA)推荐的饮用水卤乙酸类消毒副产物测定方法(Method 552.3),通过优化该方法的预处理条件和改变检测方法,提出了酸化萃取-衍生化-中和萃取-GC-MS测定再生水中卤乙酸含量的分析方法,并分析了北方某市再生水中4种卤乙酸类消毒副产物含量。结果表明,该方法适用于我国再生水水质,能够有效地消除再生水中共存污染物的干扰;其相对标准偏差(n=7)小于10%,方法的精密度较好;检出限与USEPA方法基本一致;样品加标回收率满足USEPA 6251B标准方法中(100±30)%要求;再生水中的卤乙酸比自来水高出几十倍,对环境和人类存在一定的潜在危害。     

The effects of pH, bromide and nitrite on halonitromethane and trihalomethane formation from amino acids and amino sugars

In this study, the effects of pH, bromide and nitrite on the formation of halonitromethanes (HNMs) and trihalomethanes (THMs) from eight amino acids (glycine, alanine, serine, cysteine, aspartic acid, glutamic acid, lysine and histidine) and four amino sugars (glucosamine, galactosamine, N-acetylglucosamine and N-acetylneuraminic acid) were examined for chlorination and ozonation followed by chlorination. During ozonation-chlorination, two amino acids, glycine and lysine, exhibited distinctly higher HNM formation than the other compounds. The formation of HNMs was higher at pH 8 than 6. Glycine and lysine also produced higher levels of THMs than the other compounds at pH 8. The presence of nitrite resulted in an increase in HNM formation. The presence of bromide increased the HNM formation, especially brominated HNM species. Bromine incorporation factors of trihalogenated HNMs were higher than those of THMs. For chlorination alone, HNM levels were about the detection limit (4 nM or 0.7 μg L⁻¹) at pH 6 and 8, and in the presence of bromide or nitrite. Amino acids and amino sugars tested, except glycine and lysine, showed relatively low levels of THM (∼15 μg L⁻¹) formation.     

Determination of C(5)-C(12) perfluoroalkyl carboxylic acids in river water samples in the Czech Republic by GC-MS after SPE preconcentration

A method employing solid phase extraction followed by gas chromatography-mass spectrometry with negative chemical ionization has been developed for determination of ultratrace concentrations of perfluoroalkyl carboxylic acids in river water. The effects of the experimental parameters, such as the pH, additions of NaCl and an ion-pairing agent (tetraethylammonium bromide) and the kind of the elution agent, on the efficiency of the test acid extraction have been studied. The analyte extraction recoveries and the limits of detection and determination have been found. The method developed has been tested on determinations of perfluoroalkyl carboxylic acids in the waters of the two largest Czech rivers, Vltava and Labe (Elbe). The best extraction results have been attained without any alteration of the sample pH, with an addition of tetrabutylammonium bromide (a concentration of 50 μg mL⁻¹ in the sample) and using methanol as the elution agent. Under these conditions, the recoveries of the test acids in the spiked real samples are within ranges from 60% to 104% and 53% to 111% for analyte concentration levels of 1.40 ng mL⁻¹ and 0.14 ng mL⁻¹, respectively, depending on the lengths of the perfluorinated chains of the acids. In general, the recovery decreases with increasing length of this chain. The method developed exhibits very low limits of detection and determination and the results are fully comparable with those obtained when using more expensive HPLC-MS/MS instrumentation. Typical values amount to tenths to tens of pg mL⁻¹ and units to one hundred pg mL⁻¹ for the limits of detection and determination, respectively; the measuring sensitivity increases with increasing length of the analyte chain. The analyzes of real samples from the Vltava and Elbe rivers have demonstrated that the results obtained are similar to the values published for contamination of the Elbe and other rivers in western and central Europe. The concentrations determined are of the order of units to tens of pg mL⁻¹ and the C₈-C₁₀ acids occur most often.