Studying soil organic matter using 13C CP-MAS NMR: the effect of soil chemical pre-treatments on spectra quality and representativity

¹³C CP-MAS NMR spectroscopy is a technique that has proved to be useful in studying soil organic matter (SOM). Nevertheless, NMR spectra exhibit a weak signal and have very low resolution due to: the low natural abundance of ¹³C (1.1 % of C) in SOM, the generally low SOM content of soils, and the presence of paramagnetic impurities. This paper studies the effects of soil chemical pre-treatments on ¹³CP-MAS NMR spectra quality and spectra representativity i.e. soil C mass balance.

After chemical pre-treatment to increase total organic carbon (TOC) content and C/Fe ratio, eight soils characterized by different levels of organic carbon content and C/Fe ratios were studied using ¹³CP-MAS NMR. Moreover, where chemical treatments were not applicable due to high carbon losses, the number of ¹³CP-MAS NMR scans was increased in order to obtain satisfactory spectra.

Results show that chemical pre-treatment of soils with C/Fe > 1 caused high C losses. Bulk soils were therefore studied by increasing the number of ¹³CP-MAS NMR scans. Acceptable spectra were obtained from 8K scans (1K = 1024 transient). On the other hand, even when a large number of scan (32K) are used, soil with C/Fe < 1 cannot be studied. As these soils are characterized by low C losses after HCl treatments (range of 2.9–25.4%), a pre-treatment of at least 1.39 mol l⁻¹ HCl removes excess Fe and at the same time increases C/Fe ratio resulting in 32K scans providing good spectra.     

城市生活垃圾可生物降解有机质成分的测定

卫生填埋是我国现阶段最主要的城市生活垃圾处理方式,定量分析城市生活垃圾可生物降解有机质成分对于研究填埋垃圾的厌氧降解过程具有重要意义.通过一系列常规化学试验,利用抽提差重法、比色法及灼烧差重法,依次测定了垃圾中含水率,挥发分与灰分,脂肪类,易水解物与半纤维素,腐植酸,难水解物、不水解物与纤维素,木质素与固体残渣等成分,为入场垃圾可生化性评价及降解过程中固相成分变化的动态监测提供了一种简便快速的测定方法.     

固相微萃取-气相色谱法测定水中痕量有机氯农药

建立了固相微萃取-气相色谱联用快速测定水中14种痕量有机氯农药的方法,对比研究了浸入式直接固相微萃取与顶空固相微萃取两种方式对不同有机氯农药的富集效率,优化了试验条件.方法线性关系良好,检出限为0.1 ng/L～10 ng/L,定量下限为0.2 ng/L～40 ng/L,RSD＜8%,实际水样的加标回收率为67.0%～133%.     

Effect of clay minerals on extractability of heavy metals and sewage sludge mineralization in soil

An incubation experiment lasting 111 d was carried out to study the effect of the addition of three clay minerals (Na-bentonite, Ca-bentonite, and zeolite) to soil derived from sewage sludge on water-extractable and exchangeable forms of four heavy metals (Zn, Cd, Cu, and Ni), as well as on soil organic matter mineralization, microbial biomass C and the release of inorganic N. The addition of clay minerals led to a significant decrease in water-extractable and exchangeable forms of heavy metals. The extent of decrease ranged from 14 to 75% for the water-extractable heavy metals and from 12 to 42% for the exchangeable form over the incubation time, as compared with untreated soil. The reduction in extractability of heavy metals was greater due to the addition of Na-bentonite and Ca-bentonite than that due to the addition of zeolite. Addition of clay minerals did not affect any of the following microbiological parameters in the soil: microbial biomass C, organic C (C_org) mineralization, and metabolic quotient (qCO₂), and release of inorganic N during the first 3 weeks of incubation. However, as the incubation period increased, these parameters were significantly increased by the addition of clay minerals, especially by the addition of Na-bentonite and Ca-bentonite. This result is explained by a strong reduction in extractability of heavy metals after the addition of Na-bentonite and Ca-bentonite.     

PARTICULATE ORGANIC MATTER IN THE NORTHERN AND CENTRAL ADRIATIC

The particulate organic matter distribution and its elemental composition in the northern and central Adriatic Sea during different seasonal periods are shown, highlighting the principal processes and factors influencing their distribution and characteristics.

In the low salinity waters the concentrations of particulate carbon, nitrogen and phosphorus were higher and more variable than in the dense waters, mainly due to dilution effects which induce an abundant phytoplankton growth.

Generally in summer the particulate organic matter distribution followed the trophic gradient while in winter resuspension events often became more important. Differences between summer and winter were more evident in the diluted waters and were mainly due to the seasonal heat exchanges and to the fresh water inputs.

Marked differences in C/P ratios were observed in the POM: high ratios in the northern diluted waters and low in the more saline waters and in the central Adriatic.     

PAB在有机废水处理中的应用

综述了光合细菌独特的生理特性和其处理高浓度有机废水的原理,介绍了近年来国内外利用光合细菌处理有机废水的研究成果,并对光合细菌用于废水生物处理的前景及存在的问题进行了评述。     

Carbon materials-catalyzed hydroliquefaction of flame-retardant plastics in organic solvents

Flame-retardant plastics, such as desktop and laptop personal computer bodies, could be completely liquefied by carbon materials-catalyzed hydroliquefaction in tetralin without using H₂ as a hydrogen source. Active carbons with larger surface areas (1450–3450 m²/g) acted as superior catalysts in transferring tetralin hydrogens to plastics. On the other hand, carbon blacks and fullerene-rich soot were less active catalysts. Graphite and mesocarbon microbeads did not show any catalytic effects. Benzene, toluene, and ethylbenzene were obtained as recyclable hydrocarbons; their total amounts varied from 4 wt% to 12 wt% depending on the types of plastics and the carbon materials used. Organic bromides such as polybromodioxins were not contained in the gases and oils of the product. Received: July 19, 2000 / Accepted: September 17, 2000     

微污染水源水的控制技术

饮用水水源的污染日益严重,对人类的健康和传统净水工艺都构成了较大的威胁,更加剧了水资源的危机,文中阐述了近年来我国处理微污染水源水的主要技术,强化混凝处理技术,臭氧活性炭联用深度处理技术,生物活性炭深度处理技术,光催化氧化法技术,膜法深度处理技术,吸附预处理技术,生物预处理技术等,并给出了各种处理方法的优缺点。     

新型转式垃圾焚烧炉焚烧技术研究

研究了新型转式焚烧炉稳定燃烧工艺和有机垃圾在新型转式焚烧炉中焚烧过程HCl和NOx释放和控制特性。结果表明,新型转式焚烧炉采用二次燃烧技术,能有效控制和降低二次污染物的生成。     

Remediation of soil and groundwater contaminated with organic chemicals using stabilized nanoparticles: Lessons from the past two decades

▪ Overviewed evolution and environmental applications of stabilized nanoparticles. ▪ Reviewed theories on particle stabilization for enhanced reactivity/deliverability. ▪ Examined various in situ remediation technologies based on stabilized nanoparticles. ▪ Summarized knowledge on transport of stabilized nanoparticles in porous media. ▪ Identified key knowledge gaps and future research needs on stabilized nanoparticles. Due to improved soil deliverability and high reactivity, stabilized nanoparticles have been studied for nearly two decades for in situ remediation of soil and groundwater contaminated with organic pollutants. While large amounts of bench- and field-scale experimental data have demonstrated the potential of the innovative technology, extensive research results have also unveiled various merits and constraints associated different soil characteristics, types of nanoparticles and particle stabilization techniques. Overall, this work aims to critically overview the fundamental principles on particle stabilization, and the evolution and some recent developments of stabilized nanoparticles for degradation of organic contaminants in soil and groundwater. The specific objectives are to: 1) overview fundamental mechanisms in nanoparticle stabilization; 2) summarize key applications of stabilized nanoparticles for in situ remediation of soil and groundwater contaminated by legacy and emerging organic chemicals; 3) update the latest knowledge on the transport and fate of stabilized nanoparticles; 4) examine the merits and constraints of stabilized nanoparticles in environmental remediation applications; and 5) identify the knowledge gaps and future research needs pertaining to stabilized nanoparticles for remediation of contaminated soil and groundwater. Per instructions of this invited special issue, this review is focused on contributions from our group (one of the pioneers in the subject field), which, however, is supplemented by important relevant works by others. The knowledge gained is expected to further advance the science and technology in the environmental applications of stabilized nanoparticles.