民用蜂窝煤燃烧排放颗粒物的化学组成和稳定碳同位素特征

本文选用了镜质组反射率在0.77%-1.88%之间5 种不同成熟度的煤, 将其制成民用蜂窝煤球, 研究民用蜂窝煤燃烧排放颗粒物（PM）的化学组成, 包括元素（C、N、O、S）、有机碳（OC）、元素碳（EC）和水溶性无机离子（WSII）, 稳定碳同位素组成特征和质量吸收效率值（MAE）, 并讨论了它们与煤成熟度之间的关系.结果表明, 5 种原煤C、N、O、S 元素组成差别不大, 但是燃烧后排放的PM 化学组成差别比较大.无烟煤燃烧排放的PM 粒径分布呈双峰结构, 峰值分别在0.09 μm 和0.25 μm; 而烟煤PM 的峰值为0.58 μm.无烟煤排放PM 的颗粒数远小于烟煤.PM、OC 和EC 的排放受煤成熟度的影响非常大, 无烟煤排放的量最小, 分别为2.21 g/kg、0.22 g/kg 和0.004 g/kg; 成熟度最低的烟煤排放量最大, 分别为70.3 g/kg 、46.1 g/kg 和2.42 g/kg.PM、OC 和EC 的排放因子与煤的成熟度成幂指数关系.EC 的MAE 在0.17-21.9 m^2/g 之间, 与煤成熟度呈指数相关关系.燃煤WSII 的平均排放因子为801 mg/kg, WSII 当中含量最高的是NH4^＋ 和24SO4^2- , 平均分别占WSII总量的23.5%和44.4%.燃煤排放PM 的δ^13C 变化范围为–24.5‰-–22.8‰, 平均值为–23.6‰.以上研究有助于人们从原煤性质的角度去考察民用燃煤对人类健康和气候变化的影响, 并为大气污染源解析提供一些科学依据.     

Effects of Coal Rank and High Organic Sulfur on the Structure and Optical Properties of Coal-based Graphene Quantum Dots

Coal‐based graphene quantum dots (GQDs) were successfully produced via a one‐step chemical synthesis from six different coal ranks, from which two superhigh organic sulfur (SHOS) coals were selected as natural S‐doped carbon sources for the preparation of S‐doped GQDs. The effects of coal properties on coal‐based GQDs were analyzed by means of high‐resolution transmission electron microscopy (HRTEM), X‐ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X‐ray photoelectron spectroscopy (XPS), ultraviolet‐visible (UV‐Vis) absorption spectroscopy, and fluorescence emission spectra. It was shown that all coal samples can be used to prepare GQDs, which emit blue‐green and blue fluorescence under ultraviolet light. Anthracite‐based GQDs have a hexagonal crystal structure without defects, the largest size, and densely arranged carbon rings in their lamellae; the high‐rank bituminous coal‐based GQDs are relatively reduced in size, with their hexagonal crystal structure being only faintly visible; the low‐rank bituminous coal‐based GQDs are the smallest, with sparse lattice fringes and visible internal defects. As the metamorphism of raw coals increases, the yield decreases and the fluorescence quantum yield (QY) initially increases and then decreases. Additionally, the surface of GQDs that were prepared using high‐rank SHOS coal (high‐rank bituminous coal) preserves rich sulfur content even after strong oxidation, which effectively adjusts the bandgap and improves the fluorescence QY. Thus, high‐rank bituminous coal with SHOS content can be used as a natural S‐doped carbon source to prepare S‐doped GQDs, extending the clean utilization of low‐grade coal.     

Development of a CO2 emission factor in Korea from sub-bituminous coal by the classification method

While the Intergovernmental Panel on Climate Change classifies coal as anthracite, bituminous coal, and sub-bituminous coal, Korea only distinguishes coal as anthracite and bituminous coal while sub-bituminous coal is considered bituminous coal. As a result, Korea conducted research in the CO₂ emission factors of anthracite and bituminous coal, but largely ignored sub-bituminous coal. Therefore, the purpose of this research is to develop the CO₂ emission factor of sub-bituminous coal by classifying sub-bituminous coal from resources of bituminous coal activities collected in Korea between 2007 and 2011. The 2007–2011 average carbon content of sub-bituminous coal was analyzed to be 69.63 ± 3.11 %, the average hydrogen content 4.97 ± 0.37 %, the inherent moisture 12.60 ± 4.33 %, the total moisture 21.91 ± 5.45 %, and the dry-based gross calorific value was analyzed to be 5,914 ± 391 kcal/kg; using these analyzed values, the as-received net calorific value was found to be 20.75 ± 7.59 TJ/Gg and the CO₂ emission factor was found to be 96,241 ± 4,064 kg/TJ. In addition, the 62.7 million ton amount for the 2009 greenhouse gas emission from sub-bituminous coal as estimated with the analyzed value of this study is an amount that is equivalent to 11.1 % of the 2009 total greenhouse gas emission amount of 564.7 million tons, and this amount is larger than the 9.3 % for the industrial processes sector, 3.3 % for the agricultural sector and 2.5 % for the waste sector. Therefore, it is important to reflect the realities of Korea when estimating the greenhouse gas emission from such sub-bituminous coals.     

液氮溶浸对不同煤阶含水煤样渗流特性的影响

中国包含多种煤阶煤层,由于煤质、地质条件等差异,不同煤层中的水分赋存情况也具有较大差异性。煤阶、饱水度作为影响液氮低温致裂效果的两个重要因素,有必要对其进行深入研究。为此,分别选择褐煤、烟煤与无烟煤3种煤阶煤样,并制备得出饱水度分别为0%、33%与99%的煤样进行液氮溶浸处理,使用摄像机定点拍摄、观察煤样表面宏观裂隙处理前后的演化规律,并对煤样进行氮气渗流试验。试验结果表明：液氮溶浸后褐煤因产生的一条与多条贯穿裂隙发生整体结构上的断裂,烟煤表面有新裂隙产生,原生宏观裂隙有一定的扩展与延伸,无烟煤表面宏观裂隙无明显发育;煤样饱水度越高,液氮的致裂增透效果越显著;液氮溶浸对3种煤阶煤样的致裂增透效果关系为：褐煤>烟煤>无烟煤,在完全干燥状态下,由于热应力不足以破坏颗粒间链接,烟煤与无烟煤的增透效果近似相等;对于褐煤,液氮溶浸处理对完全干燥状态下的煤体即产生有效致裂,渗透率平均增幅高达559.35%,对于烟煤,在饱水度为33%和99%的状态下,液氮溶浸对煤体具有明显致裂效果,渗透率平均增幅分别为330.60%和448.77%,对于无烟煤,在饱水度为99%的状态下液氮溶浸处理才能对煤体产生有效致裂,渗透率平均增幅为185.53%。     

论煤地质学与碳中和

煤基碳排放构成了中国碳排放总量中最重要的部分,做好煤基碳减排和煤炭高效洁净低碳化利用是实现“碳中和”国家目标的重要途径,碳中和背景下的煤地质学发展值得关注。系统评述与碳中和相关的煤地质学研究领域,分析煤地质学在碳中和研究与工程实践中的作用和应用前景,探讨碳中和背景下煤地质学的重要发展方向。取得以下认识:推进清洁煤地质研究、服务煤的高效洁净化燃烧,勘探开发煤系天然气低碳燃料、优化一次能源结构和化石能源结构,开展煤化工资源勘查与开发地质保障研究、推动煤炭的低碳能源转化和新型煤化工产业发展,深化瓦斯地质研究、提高煤矿瓦斯（井下）抽采率、控制煤矿瓦斯的大气排放和泄漏,研究煤层甲烷天然逸散和煤层自燃排放、控制煤层露头的天然排放,发展煤层CO₂地质封存与煤层气强化开发（CO₂-ECBM）技术、推动碳捕获、利用与封存（CCUS）技术发展及其在火力电厂烟气碳减排中的商业化应用,研究煤炭勘查企业的碳足迹、实现企业净零排放,是与煤地质学紧密相关的碳减排技术路径;其中煤层甲烷与煤系气高效勘探开发、深部煤层CO₂-ECBM、煤层露头气体逸散与自燃发火控制、洁净煤地质与煤炭精细勘查是碳中和背景下煤地质学优先发展的重要领域。      

Changes in hydrocarbon maturity indices with coal rank and type,Buller Coalfield,New Zealand

The Buller Coalfield (South Island, New Zealand) is an inverted late Paleogene Basin that contains middle Eocene bituminous coals which exhibit considerable variation in both coal rank (across-basin), and coal type (in-seam). Twenty-two fractionated bitumen extracts of Brunner Coal Measures coal samples from 12 drillholes were analyzed by GC and GC–MS to characterize the effect of coal rank and type on conventional hydrocarbon maturity indices at the beginning and end of the oil window (0.56–1.26% Ro_max).The Carbon Preference Index, pristane/phytane and isoprenoid/n-alkane ratios evolve throughout the high volatile bituminous B rank stage, while other biomarker ratios [18α(H)-22,29,30-trisnorneohopane/17α(H)-22,29,30-trisnorhopane (Ts/Tm), 18α(H),21β(H)-30-norneohopane (C₂₉ Ts)/17α(H),21β(H)-30-norhopane and C₃₀ diahopane/hopane] do not show appreciable change in value until medium volatile bituminous rank. Various aromatic based ratios appear to be more effective in delineating rank throughout the entire oil window; in particular the Methylphenanthrene Index and vitrinite reflectance are positively correlated over the entire bituminous rank range. However, subtle changes in depositional conditions (variable coal type) complicate these rank estimates. Within a given coal seam, variation in CPI, isoprenoid/n-alkane and hopane/sterane ratios appear to be related to the hydrogen content of the coal, while the homohopane index and the oleanane/hopane ratio covary with sulfur content. As with depressed vitrinite reflectance values, MPI is similarly lowered in the perhydrous samples. The mechanisms that control these hydrocarbon parameters during deposition and diagenesis are complex and convoluted, however, changes in bacterial activity and community (with marine incursion) appear to play an important role. Due to these anomalies, none of the hydrocarbon maturity indices calculated can be singularly used to constrain coal rank.     

Methane exchange between coal-bearing basins and the atmosphere: the Ruhr Basin and the Lower Rhine Embayment, Germany

A precise knowledge of methane exchange processes is required to fully understand the recent rise of atmospheric methane concentration. Three of these processes take place at the lithosphere/atmosphere boundary: bacterial consumption of methane and emission of bacterial or thermogenic methane. This study was initiated to quantify these processes on a regional scale in the Ruhr Basin and the Lower Rhine Embayment. Since these areas are subject to bituminous coal and lignite mining, natural and anthropogenically-induced methane exchange processes could be studied. The methane emission and consumption rates and their carbon isotope signal were measured at the lithosphere/atmosphere boundary using flux chambers. On most of the soils studied, methane consumption by bacteria was identified. Thermogenic methane was released only at some of the natural faults examined. In active and abandoned bituminous coal mining areas methane emissions were restricted to small areas, where high emission rates were measured. The carbon isotope composition of methane at natural faults and in mining subsidence troughs was typical of thermogenic methane (−45 to −32 ‰ δ¹³C). Methane exchange balancing revealed that natural methane emissions from these two basins represent no source of atmospheric importance. However, methane release by upcast mining shafts dominates the methane exchange processes and is by about two orders of magnitude greater than methane consumption by bacterial oxidation in the soils.     

Petrographic variation in the Springfield (No. 9) coal in Western Kentucky

The Springfield (Western Kentucky No. 9) coal of the Carbondale Formation (Middle Pennsylvanian) in the Western Kentucky Coal Field of the Illinois Basin was sampled in eleven mines from one to three channels of three equal benches. The rank of the coal is high-volatile C bituminous in the Moorman Syncline and in the Henderson Basin and high-volatile B bituminous in the Webster Syncline. The percentage of total vitrinite macerals and of total vitrinite plus liptinite was found to decrease significantly from the bottom bench through to the top bench. In a comparison of the sources of variation within the set of maceral data it was found that the only significant variation in the vitrinite and vitrinite plus liptinite percentages was between the benches. Both the rank of the coal and the maceral percentages are varying in a predictable manner.     

宁夏煤变质规律初探

宁夏煤炭资源丰富,煤类多,在区域和垂向上呈现出明显的规律性。晚古生代煤层以中、高变质的烟煤、无烟煤为主,中生代煤层以低变质的烟煤为主,从各含煤区分布看,贺兰山、香山含煤区多为高变质的烟煤和无烟煤,灵盐、固原含煤区以低变质烟煤为主,青铜峡-固原深断裂西部的煤变质程度明显高于东部。分析认为深成变质作用对各时代煤变质具有普遍意义,在此基础上,岩浆热力变质作用和动力变质作用也是导致局部地区煤变质增高的因素,如贺兰山含煤区的汝箕沟矿区,受隐伏岩浆热力影响,以岭大井田为中心,呈现北东向展布的半环带状煤级分带;香山含煤区各时代煤类分布方向与区域构造线方向一致,推测可能在深成变质作用下叠加了岩浆热力变质和动力变质作用。     

Nuclear magnetic resonance studies of ancient buried wood—II. Observations on the origin of coal from lignite to bituminous coal

Coalified logs ranging in age from Late Pennsylvania to Miocene and in rank from lignite B to bituminous coal were analyzed by ¹³C nuclear magnetic resonance (NMR) utilizing the cross-polarization, magic-angle spinning technique, as well as by infrared spectroscopy. The results of this study indicate that at least three major stages of coalification can be observed as wood gradually undergoes transformation to bituminous coal. The first stage involves hydrolysis and loss of cellulose from wood with retention and differential concentration of the resistant lignin. The second stage involves conversion of the lignin residues directly to coalified wood of lignitic rank, during which the oxygen content of intermediate diagenetic products remains constant as the hydrogen content and the carbon content increases. These changes are thought to involve loss of methoxyl groups, water, and C₃ side chains from the lignin. In the third major stage of coalification, the coalified wood increases in rank to subbituminous and bituminous coal; during this stage the oxygen content decreases, hydrogen remains constant, and the carbon content increases. These changes are thought to result from loss of soluble humic acids that are rich in oxygen and that are mobilized during compaction and dewatering. Relatively resistant resinous substances are differentially concentrated in the coal during this stage. The hypothesis that humic acids are formed as mobile by-products of the coalification of lignin and function only as vehicles for removal of oxygen represents a dramatic departure from commonly accepted views that they are relatively low-molecular-weight intermediates formed during the degradation of lignin that then condense to form high-molecular-weight coal structures.     

煤田火区碳排放量计算模型和关键参数研究

完善碳排放清单,是进行减排工作的基础,为了查明煤田火区对大气碳排放的贡献量,以煤氧复合作用学说为理论基础,从不同的研究思路出发,提出了烧失煤量法和排放通量法两种火区碳排放量计算模型。在明确模型中关键参数“释放因子”“排放系数α”“排放通量”“排放系数β”的具体含义的基础上,重点对各参数所对应的获取途径进行了研究论述：(1)释放因子通过在室内进行煤自燃模拟实验得出;(2)排放系数α通过煤岩吸附实验结合火区实地勘测得出;(3)排放通量通过对火区现场煤自燃气体排放及环境因素的实时监测得出;(4)排放系数β通过对遥感图像裂隙信息的提取得到。上述两种计算模型在我国乌达实验区进行了实际应用,并对其可实现性进行了检验。     

Interactions between organic matter and minerals in two bituminous coals of different rank

The association between specific mineral and organic constituents in two Asturian bituminous coals of different rank was studied. For this, raw coals were fractionated by density and the variation of a number of parameters was followed in parallel. Results of coal chemical analyses, including analyses for 22 elements, were used to establish the elemental association with coal organic matter. Petrographic analyses determined the distribution of macerals among densimetric fractions, vitrinite reflectance being at a minimum in the intermediate density fractions. Mineral species were identified by X-ray diffraction, FT-IR spectroscopy and Mössbauer spectroscopy. Comparison of trends for different parameters determined using this set of techniques allowed classification of the various minerals according to their association with organic matter. Carbonates seem to be specifically associated with the organic matter of the low-volatile bituminous coal whereas sulfides concentrate in the organic matter of the high-volatile bituminous coal. Vitrinite is the maceral exhibiting the most probable association with inorganic matter. The possibility of a merely physical association of fine-grained detrital minerals with organic matter cannot be excluded; nevertheless, one must bear in mind that even this type of interaction is important due to its effect on various coal preparation and utilization processes.     

邯郸-峰峰矿区不同变质程度煤中有机氮的赋存形态

氮是煤中的常见元素之一,煤中氮的赋存形态多样且随煤阶发生变化。以邯郸-峰峰矿区为例,利用X射线光电子能谱（XPS）实验,研究不同变质程度煤（R_ran=1.08%~3.67%）中有机氮的赋存形态,探讨煤中各形态有机氮相对含量随煤阶的变化规律。结果表明:按N 1s XPS谱图分峰峰值的结合能可将煤中氮的形态归为N-6、N-5、N-Q和N-X四种;研究区煤中N-5的相对含量最高,且随着煤阶的增高而降低;N-Q的相对含量随着煤阶的增高而增高;煤中N-6的相对含量随煤阶呈“增-减-稳”的变化规律;N-X的相对含量为9.1%~35.1%,其与煤阶关系不明显;在煤阶R_ran=1.08%~1.47%的范围内,煤的N 1s XPS谱图中缺失N-Q分峰,表明褐煤中相对含量最高的质子化吡啶氮在此阶段已几乎全部去质子化而转化为吡啶氮。不同变质阶段氮的赋存形态变化特征对燃煤发电及煤化工领域煤化学参数选取提供参考。      

Initial volatilization temperatures and average volatilization rates of coal — Their relationship to coal rank and other characteristics

Two thermal parameters, initial volatilization temperature (IVT) and average volatilization rate (AVR), have been determined by thermogravimetric analysis in argon for 38 coal samples ranging in rank from lignite to low-volatile bituminous. Both IVT and AVR are correlated with percent volatile matter and vitrinite reflectance.The IVT values increase gradually from about 250 to 445°C with increasing rank; however, a change in slope is observed in the region of high-volatile bituminous coals (from about 340°C to about 380°C) when IVT's are plotted against percent volatile matter or percent fixed carbon. The changes in slope near 340°C and near 380°C occur at “coalification jumps” recognized on the basis of changes in the optical and chemical character of the macerals. In general, AVR values decrease gradually with increasing rank for the lignite and sub-bituminous coals and for the medium- and low-volatile bituminous coals; however, a sharp increase in AVR occurs in high-volatile bituminous coals. The change in slope of the IVT curves and sharp increase in the AVR values for high-volatile bituminous coals reflect the development of new, higher vapor pressure organic compounds produced during this stage of the coalification process.A plot of AVR vs IVT reveals three regions which correspond to: (1) lignite and sub-bituminous coals; (2) high-volatile bituminous coals; and (3) medium- to low-volatile bituminous coals.     

超低排放燃煤电厂一次颗粒物和黑碳实时排放特征

燃煤电厂是大气一次污染物的重要排放源,其超低排放改造改变了大气颗粒物排放特征。为满足当前高时间分辨率排放清单构建的需要,燃煤电厂颗粒物实时排放质量浓度及关键组分比值亟需更新。本研究基于稀释通道采样系统,对某超低排放改造后的燃煤电厂开展实测,获得该燃煤电厂可吸入颗粒物(PM10)、细颗粒物(PM2.5)、超细颗粒物(PM1.0)和黑碳(BC)的实时排放质量浓度,更新各污染物排放因子,分析PM1.0/PM2.5、PM2.5/PM10和BC/PM2.5质量浓度比值(文中以上比值均为质量浓度比值)日变化。结果表明,上述污染物排放平均质量浓度分别为(5.0±6.0)mg/m^3、(5.0±5.9)mg/m^3、(4.9±5.9)mg/m^3和(36.6±28.3)μg/m^3;对应的排放因子分别为0.03 kg/t、0.03 kg/t、0.03 kg/t和0.2 mg/kg。该燃煤电厂颗粒物排放质量浓度表现出明显的日间变化,高值时段(20:30至次日10:30)PM2.5平均质量浓度是低值时段(10:30~20:30)的12.2倍,推测可能与不同时段的污染控制措施效率变动有关。作为不完全燃烧的产物,黑碳排放高值时段(06:00~12:00和14:30~19:00)的质量浓度是低值时段(00:00~05:00)相应值的1.5~2.4倍,推测与煤的添加和锅炉燃烧效率有关。颗粒物及组分质量浓度的日变化在构建高时间分辨率排放清单时需予以考虑。本研究实测所得PM2.5/PM10和BC/PM2.5比值分别为1.00±0.01和0.03±0.04,均远高于清单编制技术手册中推荐的燃煤电厂相应比值0.3和0.002,采用现有清单编制技术手册的相应比值可能低估了燃煤电厂细颗粒物和黑碳排放,需引起重视。     

Assessment of greenhouse gas emissions from coal and natural gas thermal power plants using life cycle approach

The importance of mitigation of climate change due to greenhouse gas (GHG) emissions from various developmental and infrastructure projects has generated interest at global level to reduce environmental impacts. Life cycle assessment may be used as a tool to assess GHG emissions and subsequent environmental impacts resulting from electricity generation from thermal power plants. This study uses life cycle approach for assessing GHG emissions and their impacts due to natural gas combined cycle (NGCC) and imported coal thermal power plants using the IPCC 2001 and Eco-Indicator 99(H) methods in India for the first time. The total GHG emission from the NGCC thermal power plant was 584 g CO₂ eq/kWh electricity generation, whereas in case of imported coal, it was 1,127 g CO₂ eq/kWh electricity generation. This shows that imported coal has nearly ~2 times more impacts when compared to natural gas in terms of global warming potential and human health as disability-adjusted life years from climate change due to GHG emissions such as carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O).     

Environmental geochemistry and health of fluorine in Chinese coals

Fluorine is one of the potential hazardous trace elements in coal. Fluorine may be released into atmosphere mostly during coal combustion process. When the coal is burning indoors without any controlling methods (chimney), the fluorine will pollute the room and is absorbed by food fired (dried) over stoves. Now many people have suffered from fluorosis due to coal burning indoors in Southwest China. In this paper, the concentration, distribution, mode of occurrences and impact factors of fluorine in Chinese coals are analyzed. The environmental impacts and typical features of fluorosis are studied. It is concluded that the value of fluorine in Chinese coals ranges from 20 to 300 mg/kg, and with average value of 122 mg/kg from 5,603 coal samples. It is higher than the average value of the world coals (80 mg/kg). In provincial coalfields of the SW China, the content of F is highest and many people have been affected due to coal combustion indoors.     

深部煤层封存CO_2的地质主控因素探讨

目前世界上多数国家都以CO2捕获和封存作为CO2减排的有效措施之一。向深部不可采煤层中封存CO2能一举两得,既可实现CO2减排的目的,又能置换出煤层甲烷气体。从实验室研究角度出发,分析了煤级、温度、压力、水分及氮气对煤吸附CH4、CO2的影响,并结合煤层气开发选区评价方法,探讨了影响煤层封存CO2的地质主控因素,认为煤种、煤厚、煤层埋深、渗透率是主要控制因素,而地质构造、水文地质、甲烷气含量等为次一级控制因素。综合分析认为,我国煤层封存CO2的潜力很大,而华北地区是深部煤层封存CO2的首选地区。     

Hydrocarbon genesis of Jurassic coal measures in the Turpan Basin, China

A typical case of coal-derived oils in China, i.e. the crude oils from the Middle-Lower Jurassic coal measure strata in the Turpan Basin, is presented. By means of oil-source correlation, it is confirmed that low maturity crude oil in the Shengjinkou oil field is derived from the coal-bearing Qiketai Formation of Middle Jurassic age, a brackish lacustrine sediment. Mature crude oils in the Qiketai oil field, and in well Taican 1, are sourced from the Badaowan Formation of Lower Jurassic age, which contains coal seams as thick as 100 m. Results show that commercial accumulations of liquid crude oils can be generated from coals and coal measure strata containing high volatile coal of bituminous rank. Despite unfavourable types of source material, the total hydrocarbon-generating potential can be great due to the unusual abundance of organic matter.     

早白垩世泥炭地净初级生产力及其控制因素--来自二连盆地吉尔嘎郎图凹陷6号煤的证据

现代泥炭地中蕴藏着巨量的碳,泥炭地生产力的高低会影响全球碳循环及全球气候变化。前人对全新世以来泥炭地生产力做了大量研究,但对前第四纪的“深时”阶段的泥炭地生产力则极少涉及,其主要原因是缺少精确的定年方法。以二连盆地吉尔嘎郎图凹陷早白垩世6号煤为例,利用地球物理测井信号进行频谱分析并获得煤层中米兰科维奇旋回周期参数（123 ka（偏心率）:38.1 ka（斜率）:22.1 ka（岁差））,将米兰科维奇旋回作为“深时”地层时间的“度量”工具,计算出6号煤层碳的聚集速率为35.1~38.9 g C/（m2·a）,进一步推算出其所代表的泥炭地的碳聚集速率为46.2~51.2 g C/（m2·a）,净初级生产力（NPP）为231~256 g C/（m2·a）。将该计算结果与全新世同一纬度带泥炭地生产力水平比较,并结合前人研究成果综合分析影响因素,得出早白垩世泥炭地生产力水平主要受温度和大气中二氧化碳含量控制,而这两种因素又与气候相关联,则泥炭地生产力的研究可能对进一步了解古气候提供帮助。