燃烧氧化-非分散红外吸收测定水中总有机碳方法的改进

总有机碳测定的方法分为差减法和直接法。现对测定方法进行改进,将差减法和直接法测定结果结合,先将样品进行酸化初步吹扫,再使用差减法测定总有机碳。试验结果显示,无论在标准曲线、精密度试验、加标回收试验还是标准样品测定方面,改进法均优于直接法测定结果,且能较好地缩短测量时间。     

大气颗粒物中元素碳的直接测定

对原来用元素分析仪测定大气颗粒物样品中有机碳、元素碳的方法[1 ] 进行改进 ,将差减法间接测定元素碳改为一步直接测定元素碳。有机碳、元素碳的测量标准偏差的平均值分别为 0 35 %、0 34% ,提高了元素碳的测量精度 ,同时避免了误差传递 ,解决了差减法测定元素碳时出现负值的情况。     

利用TOC-5000A总有机碳分析仪测定环境水样中包含全部颗粒态有机碳的研究

本文结合TOC总有机碳分析仪和SSM固体样品燃烧装置各自的特点，探索了测定环境水样中包含全部颗粒态有机碳的测定方法．此方法能够全面反映环境水样中总有机碳的含量     

深圳市饮用水源中CODMn与TOC的相关性研究

通过对深圳市饮用水源中CODMn和TOC测定结果的相关性分析,结果表明,水库内监测点位及监测区域CODMn与TOC相关性良好,水库外监测点位及监测区域CODMn与TOC相关性不显著,而整个监测区域的CODMn与总有机碳相关性令人满意。因此,提出了TOC值可直接作为饮用水源在线监测有机污染物的综合评价指标,同时也实现了湿式氧化法测定TOC在地表水监测中的应用。     

化学需氧量和总有机碳在水质在线监测中的比较

化学需氧量（COD）和总有机碳（TOC）是定量表示水体受有机物污染的2个重要代表性指标。传统的COD在线监测方法在监测有机污染物方面存在一定的挑战,系统比较了COD和TOC在线监测方法在特殊水质中的应用。结果显示：TOC对难氧化有机物的氧化效率高达98%,高氯离子和无机还原性离子对TOC测量误差影响分别约为10%和7%。TOC可更直接、更准确地反映出水体受有机物污染的情况,最后对TOC指标在水质在线监测中的推广应用提出建议。     

总有机碳的测定及其在染料废水监测中的应用

总有机碳能够完全反映水中有机污染程度,已被许多国家所采用,我国也将它列入“污水综合排放标准”中。文章采用德国耶那仪器有限公司的Multi N/C TOC分析仪,用燃烧氧化-非分散红外吸收法分别测定直接染料、活性染料、分散染料、还原染料废水的TOC,并测定相关废水的COD值。实践证明在同类特定染料废水中,TOC与COD之间具有较好的相关性,因此可用TOC监测染料废水污染程度,该方法快速、简便、准确度高。     

高温红外吸收法测定水煤浆中可燃硫方法研究

研究采用高温红外吸收法直接测定水煤浆中可燃硫方法,确定了用浆状水煤浆试样或粉末固体试样的样品制备和红外测硫仪的炉温设定范围(900℃～950℃),通过与间接差减法测定结果对比分析,表明此法可行.     

中国部分城市自来水的总有机碳测定

自来水是城镇居民的主要生活用水来源,用总有机碳(TOC)方法可快速监测其有机污染情况,保障人民生活质量。测定了国内13个城市的自来水TOC值,一定程度上反映了当前国内自来水的有机污染现状。     

京杭大运河(苏北段)底泥中汞的总量与形态的分布研究

对京杭大运河(徐州段)底泥中的18个样品进行研究,分别用冷原子荧光仪和总有机碳测定仪测定,对底泥中的汞的总量和形态进行测定.结果表明,汞在底泥中的含量主要以残渣态存在,可交换态很少,占总合量的0.04%～1.839%,总有机碳的含量与汞的总量分布没有相关性.     

大气总悬浮颗粒中有机碳的测定

本文提出一种新的高灵敏度测定总悬浮颗粒中有机碳的方法一元素分析法。该方法是在氧化炉最佳温度为６００℃时，一步测定出样品中有机碳的含量，并成功地对齐齐哈尔市大气总悬浮颗粒中的有机碳进行了连续的监测。结果表明，总悬浮颗粒中有机碳的含量有较明显的变化规律。     

Variation of total organic carbon content along the stream Harsit, Eastern Black Sea Basin, Turkey

The TOC in surface waters and wastewater is an important analytical parameter describing the total content of all organic substances containing carbon. In practice, the TOC originated from natural and anthropogenic sources, and even if it is not directly responsible for dangers on human health, its determination is important for any kind of water that is used by public. The aim of this study was to determine variation of total organic carbon (TOC) and total carbon (TC) content in the stream Harsit, which courses in Eastern Black Sea Region, Turkey. Sampling was fortnightly conducted in each of the four seasons between March 2009 and February 2010. A total of 230 water samples were collected from ten sampling stations along the main branch of the stream Harsit with 143 km of length. Obtained TOC values were evaluated and used to classify the water quality of stream Harsit, according to the Turkish Water Pollution Control Regulation (TWPCR). The annual average TOC content values for the stations were found between 2.33 and 6.97 mg/L. It was seen that the TOC content have increased along the streamcourse of Harsit until the fourth station, where reaches its maximum value. The TOC content, then, has decreased and the minimum value was observed in the eighth station. The results showed that, except in winter season, maximum TOC content observed in many of the water samples were above Class I water standard indicated in TWPCR, which classifies the water resources according to the different area of uses. It was also found that TOC has a small contribution to TC and the highest TOC content in stream waters were measured in Gumushane station where direct discharge of city wastewaters and solid waste dumping to the stream were observed.     

Assessment of relative accuracy in the determination of organic matter concentrations in aquatic systems

Accurate determinations of total (TOC), dissolved (DOC) and particulate (POC) organic carbon concentrations are critical for understanding the geochemical, environmental, and ecological roles of aquatic organic matter. Of particular significance for the drinking water industry, TOC measurements are the basis for compliance with US EPA regulations. The results of an interlaboratory comparison designed to identify problems associated with the determination of organic matter concentrations in drinking water supplies are presented. The study involved 31 laboratories and a variety of commercially available analytical instruments. All participating laboratories performed well on samples of potassium hydrogen phthalate (KHP), a compound commonly used as a standard in carbon analysis. However, problems associated with the oxidation of difficult to oxidize compounds, such as dodecylbenzene sulfonic acid and caffeine, were noted. Humic substances posed fewer problems for analysts. Particulate organic matter (POM) in the form of polystyrene beads, freeze-dried bacteria and pulverized leaf material were the most difficult for all analysts, with a wide range of performances reported. The POM results indicate that the methods surveyed in this study are inappropriate for the accurate determination of POC and TOC concentration. Finally, several analysts had difficulty in efficiently separating inorganic carbon from KHP solutions, thereby biasing DOC results.     

万峰湖总有机碳空间分布特征

于2012年9月对万峰湖(水库)的总有机碳(TOC)空间分布特征进行研究,结果显示:TOC含量范围为0.41~3.94 mg/L。TOC在纵向分布上的差异不显著,在垂向分布上,总体呈现出上层中层下层的趋势。TOC在垂向上的分布差异主要源于万峰湖属于深水水库,不同深度水层因光照和温度差异所导致生物量的多寡是致使万峰湖出现上层TOC浓度明显高于中层和下层的主要因素。     

Total organic carbon analyzers as tools for measuring carbonaceous matter in natural waters

For some utilities, new US drinking water regulations may require the removal of disinfection byproduct (DBP) precursor material as a means of minimizing DBP formation. The Environmental Protection Agency's Stage 1 DBP Rule relies on total organic carbon (TOC) concentrations as a measure of the effectiveness of treatment techniques for removing organic material that could act as DBP precursors. Accordingly, precise and accurate methods are needed for the determination of TOC and dissolved organic carbon (DOC) concentrations in raw and finished potable water supplies. This review describes the current analytical technologies and summarizes the key factors affecting measurement quality. It provides a look into the fundamental principles and workings of TOC analyzers. Current peroxydisulfuric acid wet ashing methods and combustion methods are discussed. Issues affecting quality control, such as non-zero blanks and preservation, are covered. Some of the difficulties in analyzing water for TOC and DOC that were identified up to 20 years ago still remain problematic today. Limitations in technology, reagent purity, operator skill and knowledge of natural organic matter (NOM) can preclude the level of precision and accuracy desirable for compliance monitoring.     

Assessment of groundwater quality near the landfill site using the modified water quality index

The purpose of this paper is to assess the groundwater quality near a landfill site using the modified water quality index. A total of 128 groundwater samples were analyzed for pH, electrical conductivity (EC), total organic carbon (TOC), polycyclic aromatic hydrocarbon (PAH), Cd, Pb, Zn, Cu, Cr, and Hg. The analytical results have showed a decreasing trend in concentration for TOC, Cd, Pb, Hg, and Cu and an increasing one for pH, EC, and PAH. The modified water quality index, which was called landfill water pollution index (LWPI), was calculated to quantify the overall water quality near the landfill site. The analysis reveals that groundwater in piezometers close to the landfill is under a strong landfill impact. The LWPI in piezometers ranged from 0.52 to 98.25 with a mean value of 7.99. The LWPI in groundwater from the nearest house wells varied from 0.59 to 0.92. A LWPI value below 1 proves that analyzed water is not affected by the landfill. Results have shown that LWPI is an efficient method for assessing and communicating the information on the groundwater quality near the landfill.     

Multi N/C2100S总有机碳分析仪校准方法的建立

以德国Analytikjena公司Multi N/C 2100S分析仪为例,研究建立了合理可行的总有机碳分析仪校准方法.在总有机碳分析仪检定规程JJG 821-2005的基础上,增加零点漂移、直线性、标准曲线线性和检出限4项特性指标,改变了准确性特性的判定方法.根据仪器的使用频率和稳定性,建议校准周期不超过2年.     

Comparing removal of trace organic compounds and assimilable organic carbon (AOC) at advanced and traditional water treatment plants

Stability of drinking water can be indicated by the assimilable organic carbon (AOC). This AOC value represents the regrowth capacity of microorganisms and has large impacts on the quality of drinking water in a distribution system. With respect to the effectiveness of traditional and advanced processing methods in removing trace organic compounds (including TOC, DOC, UV₂₅₄, and AOC) from water, experimental results indicate that the removal rate of AOC at the Cheng Ching Lake water treatment plant (which utilizes advanced water treatment processes, and is hereinafter referred to as CCLWTP) is 54%, while the removal rate of AOC at the Gong Yuan water treatment plant (which uses traditional water treatment processes, and is hereinafter referred to as GYWTP) is 36%. In advanced water treatment units, new coagulation–sedimentation processes, rapid filters, and biological activated carbon filters can effectively remove AOC, total organic carbon (TOC), and dissolved organic carbon (DOC). In traditional water treatment units, coagulation–sedimentation processes are most effective in removing AOC. Simulation results and calculations made using the AutoNet method indicate that TOC, TDS, NH₃-N, and NO₃-N should be regularly monitored in the CCLWTP, and that TOC, temperature, and NH₃-N should be regularly monitored in the GYWTP.     

Total organic carbon analysis as a precursor to disinfection byproducts in potable water: oxidation technique considerations

In recent years, an increasing number of regulations and methodologies have begun to utilize total organic carbon (TOC) analysis for monitoring microbial contamination and/or disinfectant byproduct (DBP) precursors. This paper highlights some analytical differences and similarities between the two widely used TOC oxidation techniques: UV persulfate and high temperature combustion (HTC). Previous papers have come to different and sometimes contradictory conclusions on this subject. However, these studies either compared instruments with significantly different flow paths or TOC systems from different eras. Unlike previous studies, this paper compares two modern TOC analyzers with nearly identical flow paths for sample recovery, detection limits, and analysis of real world samples. On average, both persulfate and HTC oxidation yielded good recoveries for 10 hard to oxidize compounds and potable water samples from 5 different locations across the USA. In general, persulfate yielded more precise results because of its lower background response relative to sample response while HTC gave slightly higher results (roughly 2% to 3%) for surface water samples.