Kitchen waste valorization through a mild-temperature pretreatment to enhance biogas production and fermentability: Kinetics study in mesophilic and thermophilic regimen

Biowaste valorization through anaerobic digestion is an attractive option to achieve both climate protection goals and renewable energy production. In this paper, a complete set of batch trials was carried out on kitchen waste to investigate the effects of mild thermal pretreatment, temperature regimen and substrate/inoculum ratio. Thermal pretreatment was effective in the solubilisation of macromolecular fractions, particularly carbohydrates. The ability of the theoretical methodologies in estimating hydrogen and methane yields of complex substrates was evaluated by comparing the experimental results with the theoretical values. Despite the single batch configuration, a significant initial hydrogen production was observed, prior to methane yield. Main pretreatment effect was the gain in hydrogen production; the extent was highly variable according to the other parameters values. High hydrogen yields, up to 113 mL H2/g VSfed, were related to the prompt transformation of soluble sugars. Thermophilic regimen resulted, as expected, in faster digestions (up to 78 mL CH₄/gVS/day) and sorted out pH inhibition. The relatively low methane yields (342–398 mL CH₄/g VS_fed) were the result of the consistent lignocellulosic content and low lipid content. Thermal pretreatment proved to be a promising option for the enhancement of hydrogen production in food waste dark fermentation.     

Hydrogen storage and distribution systems

Hydrogen storage and transportation or distribution is closely linked together. Hydrogen can be distributed continuously in pipelines or batch wise by ships, trucks, railway or airplanes. All batch transportation requires a storage system but also pipelines can be used as pressure storage system. Hydrogen exhibits the highest heating value per weight of all chemical fuels. Furthermore, hydrogen is regenerative and environment friendly. There are two reasons why hydrogen is not the major fuel of toady’s energy consumption: First of all, hydrogen is just an energy carrier. And, although it is the most abundant element in the universe, it has to be produced, since on earth it only occurs in the form of water. This implies that we have to pay for this energy, which results in a difficult economic task, because since the industrialization we are used to consuming energy for free. The second difficulty with hydrogen as an energy carrier is the low critical temperature of 33 K, i.e. hydrogen is a gas at room temperature. For mobile and in many cases also for stationary applications the volumetric and gravimetric density of hydrogen in a storage system is crucial. Hydrogen can be stored by six different methods and phenomena: high pressure gas cylinders (up to 800 bar), liquid hydrogen in cryogenic tanks (at 21 K), adsorbed hydrogen on materials with a large specific surface area (at T < 100 K), absorbed on interstitial sites in a host metal (at ambient pressure and temperature), chemically bond in covalent and ionic compounds (at ambient pressure), oxidation of reactive metals e.g. Li, Na, Mg, Al, Zn with water. These metals easily react with water to the corresponding hydroxide and liberate the hydrogen from the water. Finally, the metal hydroxides can be thermally reduced to the metals in a solar furnace.     

炼油厂恶臭污染物的防治

论述了炼厂恶臭气体的防治方法，主要从密闭的生产装置、酸性水储罐及污水处理系统几个方面进行了分析并提出了目前为解决恶臭污染采取的方法。     

紫外—双氧水和亚铁离子体系对硝基苯光降解的研究

研究了以５００Ｗ直管高压汞灯为光源，在双氧水和亚铁离子的体系中，对硝基苯进行光降解的可能性。结果表明，在实验条件下，本系统对硝基苯有明显的降解效果。浓度为５０ｍｇ／Ｌ的硝基苯经过６０ｍｉｎ的光照，其降解率可达９１．７％。此外，还探讨 铁离子浓度、双氧水浓度、硝基苯浓度、ｐＨ值等因素对光降解的影响。     

Production of hydrogen by steam gasification of dehydrochlorinated poly(vinyl chloride) or activated carbon in the presence of various alkali compounds

Steam gasification of dehydrochlorinated poly(vinyl chloride) (PVC) or activated carbon was carried out in the presence of various alkali compounds at 3.0 MPa and 560°C–660°C in a batch reactor or in a semi-batch reactor with a flow of nitrogen and steam. Hydrogen and sodium carbonate were the main products, and methane and carbon dioxide were the minor products. Yields of hydrogen were high in the presence of sodium hydroxide and potassium hydroxide. The acceleration effect of the alkali compounds on the gasification reaction was as follows: KOH > NaOH > Ca(OH)₂ > Na₂CO₃. The rate of gasification increased with increasing partial steam pressure and NaOH/C molar ratio. However, the rate became saturated at a molar ratio of NaOH/C greater than 2.0.     

刺激性气体HCl在不同尺度火灾实验中的释放行为

火灾是一种灾害性燃烧现象 ,给人员和财产安全带来极大损失。氯化氢 (HCl)是火灾烟气中阻碍人员逃生的最重要的刺激性气体之一。以典型的小尺度和大尺度实验为例 ,分析了加热程度和通风供氧对常用有机材料起火后释放HCl的影响 ,发现不论小尺度还是大尺度 ,HCl的形成只与燃烧过程有关 ,与氧化过程无关 ,HCl的生成率不随通风情况不同而改变。实验中影响HCl释放的主要因素是热 (辐射加热热流密度或温度 )。当超过CCl键发生断裂的温度后 ,继续升温HCl释放速率不发生改变 ,出现稳定释放阶段。在反映HCl释放过程不同尺度间存在共性 ,因此 ,利用小尺度的结果进行释放规律内在机理的探索是合理的方法     

Comparative evaluation of sizing of metal hydride (MH) hydrogen storage tank filled with different alloys

This study presents a comparative analysis of sizing of metal hydride tank filled with different alloys. Alloys include solid solutions and intermetallic compounds of the generic families AB₅, AB₂, AB, A₂B. The effects of the different alloys on the sizing of metal hydride hydrogen storage tanks are complicated and depend on many factors. In this paper, a thermoeconomic optimization analysis with a simple algebraic formula was presented for the estimation of optimum metal hydride tank surface area for heat transfer enhancement. The optimum area of the metal hydride tank filled with commercially available different alloys (LaN₅, Ti_0,98Zr_0,02V_0,43Fe_0,09Cr_0,05Mn_1,5, TiFe, Mg₂NiH₄) was evaluated and compared by the developed method. The optimum net savings and the value of payback were determined for four alloys. It is found that mathematical model can be employed for the determination of optimum metal hydride tank design and increasing net savings according to alloy types. The optimum areas of the tanks filled with four alloys (LaN₅, Ti_0,98Zr_0,02V_0,43Fe_0,09Cr_0,05Mn_1,5, TiFe, Mg₂NiH₄) were calculated as 0.136, 0.130, 0.133, and 0.173 m², respectively. The optimum net savings for tanks filled with four alloys (LaN₅, Ti_0,98Zr_0,02V_0,43Fe_0,09Cr_0,05Mn_1,5, TiFe, Mg₂NiH₄) are about 461.0, 409.3, 419.6, and 979.6 $ and the values of payback are about 1.98, 2.1, 2.17, and 1.37 years, respectively. Excessive area of the metal hydride tank would not be as economical as the optimum tank area. Thermal management of metal hydride tank must be designed for optimum points calculated at which maximum savings occur.     

The effect of alkyl chain length on the degradation of alkylimidazolium- and pyridinium-type ionic liquids in a Fenton-like system

Background, aim, and scope  Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them, the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride. Materials and methods  The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide. All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with the aid of ¹H NMR. Results  Degradation of ionic liquids in this system was quite effective. Increasing the H₂O₂ concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance to degradation was weaker, the shorter the alkyl chain. Discussion  The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Conclusions  The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium chloride when the resistance of imidazolium ionic liquids decreases with increasing H₂O₂ concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Recommendations and perspectives  Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the future structural design as well as tailor the technological process of these chemicals     

UV/H_2O_2/草酸高铁铵体系中孔雀石绿的光降解研究

研究了UV/H2O2/草酸高铁铵体系下孔雀绿(Malachite green,MG)光降解过程中的影响因素,包括MG的初始浓度、初始pH值、投加H2O2浓度和草酸高铁铵浓度等。结果表明:MG初始浓度越低光降解越快,碱性条件有利于MG的降解,其最佳降解pH为11.0;随H2O2浓度的增加,MG降解率先增加后减少,在100mmol/L时,降解率最高;MG降解率随草酸高铁铵浓度增加而增加,于10.0mmol/L时MG降解率最高;UV/H2O2/草酸高铁铵体系的降解效果较强,交叉实验结果表明H2O2:草酸高铁铵浓度比在1～20:1时降解率均高于。因此该体系具有快速、简单、经济并高效率等特点,可应用于染料废水的降解和脱色工艺中。     

高温(70℃)玉米秸秆水解液产氢行为及群落结构

考察了高温条件下(70℃)牛粪堆肥、土壤、厌氧污泥、腐烂秸秆种接种物利用玉米秸秆水解液的产氢行为。结果表明:牛粪堆肥接种时达到最大的产气量(1355.7mL/L)和氢气产量(608.4mL/L),随后依次为腐烂秸秆、厌氧污泥和土壤。修改的Gompertz方程可以较好描述产氢量随时间变化趋势(R2>0.99)。牛粪堆肥接种时达到最大的产氢潜力(676.0mL/L),而土壤接种时的迟滞时间最小(9.8h)。DGGE图谱显示:不同接种物对应不同的微生物群落结构。Bacillus thermozeamaize,Enterobacter sp.JDM-19和Thermoanaerobacterium polysaccharolyticum strain,KMTHCJT和可能分别是牛粪堆肥,厌氧污泥和腐烂秸秆接种条件下的关键产氢微生物。