Using landfill leachate to indicate the chemical and biochemical activities in elevated temperature landfills.

Landfill leachate properties contain important information and can be a unique indicator for the chemical and biochemical activities in landfills. In the recent decade, more landfills are experiencing elevated temperature, causing an imbalance in the decomposition of solid waste and affecting the properties of the landfill leachate. This study analyzes the properties of leachate from two landfills that were experiencing elevated temperature (ETLFs), samples were collected from both elevated temperature impacted and non-impacted areas in each landfill. The accumulation of volatile fatty acids (VFA) in leachates from elevated temperature impacted areas of both landfill sites revealed that methanogenesis was inhibited by the elevated temperature, which was further confirmed by the more acidic pH, higher H/C elemental ratio, and lower degree of aromaticity of the elevated temperature impacted leachates. Also, carbohydrates depletion indicated possible enhancement of hydrolysis and acidogenesis by elevated temperature, which was supported by compositional comparison of isolated acidic species by negative-ion electrospray ionization (ESI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICRMS) at 21 T derived from both elevated temperature impacted and non-impacted areas in the same landfill site. Furthermore, leachate organics fractionation showed that leachates not impacted by elevated temperature contain less hydrophilic fraction and more humic fraction than elevated temperature-impacted leachates for both ETLFs.

Molecular characterization of root exudates using Fourier transform ion cyclotron resonance mass spectrometry.

The release of root exudates (REs) provides an important source of soil organic carbon. This work revealed the molecular composition of REs of different plant species including alfalfa (Medicago sativa L.), bean (Phaseolus vulgaris L.), barley (Hordeum vulgare L.), maize (Zea mays), wheat (Triticum aestivum L.), ryegrass (Lolium perenne L.) and pumpkin (Cucurbita maxima) using electrospray ionization coupled with Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS). The combination of positive ion mode (+ESI) and negative ion mode (-ESI) increased the number of the molecules detected by ESI FT-ICR MS, and a total of 8758 molecules were identified across all the samples. In detail, lipids and proteins and unsaturated hydrocarbons were more easily detected in +ESI mode, while aromatic compounds with high O/C were readily ionized in -ESI mode, and only 38% of the total assigned formulas were shared by -ESI and +ESI modes. Multivariate statistical analysis of the formulas indicated that the close related plants species secreted REs with similar molecular components. Moreover, the unsaturation degree and nitrogen content were the two key parameters able to distinguish the similarities and differences of molecular components of REs between plant species. The results provided a feasible analysis method for characterization of the molecular components of REs and for the first time characterized the molecular components of REs of a variety of plant species using ESI FT-ICR MS.

Molecular level characterization of the biolability of rainwater dissolved organic matter.

The atmospheric wet deposition has been recognized as a significant allochthonous source of dissolved organic carbon (DOC) to the ocean. However, few studies have examined the biolability of rainwater dissolved organic matter (DOM) at the molecular level. Rainwater samples were collected and incubated with ambient microbes. DOC, UV-vis spectroscopy, formic acid (FA), acetic acid (AA), and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICRMS) were applied. Approximately 50 ± 16 % of rainwater DOC and ~90 % of FA and AA were bioconsumed within 28 days. The contribution of FA and AA to the total BDOC was ~30 %, which was the largest known biolabile fraction in rainwater DOC. In contrast, only approximately 15 % of formulae identified by FT-ICRMS were consumed, which were characterized by higher saturation, higher heteroatom content and lower modified aromaticity. Among the major high molecular weight secondary organic carbon (HWW-SOC)-like compounds, organosulfate contained the largest fraction of consumed formulae, while biogenic volatile organic-derived CHO compounds had the lowest. Our study for the first time provided both quantitative and qualitative understanding of the bioavailability of rainwater DOM, which is essential for understanding their effects on the biogeochemical cycles and the environmental health in the receiving waters.

Improved understanding of dissolved organic matter transformation in concentrated leachate induced by hydroxyl radicals and reactive chlorine species.

Concentrated leachate (CL) is commonly featured with high salt and dissolved organic matters (DOM). In this study, molecular transformation of DOM was revealed to identify the reactive mechanisms with (non-) radical reactive species in ozonation, electrolysis and E+-ozonation processes. Chlorine ions were efficiently activated into non-radical reactive chlorine species (RCS) with 245.7 mg/L, which was more dominant in electrolysis. Compared to ozonation, C•OH was increased from 2.6 × 10-4 mg/L into 5.8 × 10-4 mg/L and the generation of Cl•/ClO• could be concluded according to the decline of non-radical RCS in E+-ozonation process. For chromophoric and fluorescent DOM, aromatic compounds and polymerization degree dramatically decreased in E+-ozonation. Lipid-like and CRAM/lignin-like compounds were substantially degraded, as •OH and ClO•/Cl• shows an affinity towards oxygen-containing organic compounds via single electron transfer by attracting OH bonds. Especially, carbon/hydrogen/oxygen (CHO-containing) compounds were readily to be degraded with the removal efficiency of 92.5 %, 97.0 % and 98.4 % in electrolysis, ozonation and E+-ozonation, respectively. Moreover, nitrogen atoms have a negative effect on DOM degradation, and thus, carbon/hydrogen/nitrogen and carbon/hydrogen/nitrogen/sulfur (CHN- and CHNS-containing) compounds were considered as refractory compounds. This paper is expected to shed light on the synergetic effect in E+-ozonation and transformation of refractory DOM in CL treatment.