1. 西安科技大学,陕西 西安710054自然资源部煤炭资源勘查与综合利用重点实验室,陕西,西安,710021
2. 自然资源部煤炭资源勘查与综合利用重点实验室,陕西 西安710021西安科技大学煤炭绿色开采地质研究院,陕西,西安,710054
3. 西安科技大学煤炭绿色开采地质研究院,陕西 西安710054陕西省煤层气开发利用有限公司,陕西,西安,710119
4. 陕西省煤层气开发利用有限公司,陕西,西安,710119
[ "马东民(1967 —),男,博士,教授,从事煤与煤层气地质教学研究。通讯地址:陕西省西安市碑林区雁塔中路58号,邮政编码:710054。E-mail: mdm6757@126.com" ]
纸质出版:2020
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马东民, 高正, 陈跃, 等. 不同温度下低、中、高阶煤储层甲烷吸附解吸特征差异[J]. 油气藏评价与开发, 2020,10(4):17-24.
MA Dongmin, GAO Zheng, CHEN Yue, et al. Differences in methane adsorption and desorption characteristics of low, medium and high rank coal reservoirs at different temperatures[J]. Petroleum Reservoir Evaluation and Development, 2020, 10(4): 17-24.
马东民, 高正, 陈跃, 等. 不同温度下低、中、高阶煤储层甲烷吸附解吸特征差异[J]. 油气藏评价与开发, 2020,10(4):17-24. DOI: 10.13809/j.cnki.cn32-1825/te.2020.04.003.
MA Dongmin, GAO Zheng, CHEN Yue, et al. Differences in methane adsorption and desorption characteristics of low, medium and high rank coal reservoirs at different temperatures[J]. Petroleum Reservoir Evaluation and Development, 2020, 10(4): 17-24. DOI: 10.13809/j.cnki.cn32-1825/te.2020.04.003.
为研究不同煤阶CH
4
吸附/解吸特征差异及解吸滞后效应
采集低、中、高煤阶样品
进行显微组分测定、液氮吸附、等温吸附/解吸等实验
系统分析不同煤阶样品物质成分、孔隙结构、吸附/解吸特征差异及解吸滞后效应
结合甲烷吸附热计算结果
从能量角度探讨煤层气解吸滞后机理。结果表明:①煤样的镜质组反射率
R
o
max
分别为0.43 %、1.26 %、3.27 %
低阶煤样品镜质组含量低、惰质组含量高、挥发分高和固定碳高
中、高阶样品则反之;煤变质程度增高
孔隙度、BET比表面积、BJH总孔容、分形维数D
2
呈“V”型变化
D
1
呈倒“V”型变化;②温度相同时
煤阶越高
残余吸附量越大
解吸难度增加。温度升高
残余吸附量呈先上升后下降的趋势
以40 ℃为拐点
温度对气体分子活化程度和煤的孔隙结构均有影响;③压力相同
煤阶越高
甲烷吸附速率越快
低压阶段(
p
4 MPa)
吸附量增加快
高压阶段(
p
4 MPa)
吸附量增加不明显;④DFS4
#
、SGZ11
#
、SH3
#
三个煤样解吸过程中等量吸附热均大于吸附过程中的等量吸附热
表明解吸过程需要持续从体系外吸收热量
而处于吸附态的甲烷由于解吸需要的等量吸附热大于吸附时的等量吸附热需要从外界环境吸取能量
吸附和解吸过程的能量差异会导致解吸滞后;处于游离态的甲烷
由于高压作用下进入微小孔
致使煤基质膨胀变形
孔隙结构改变
导致甲烷解吸受限
造成解吸滞后。
In order to study the difference in adsorption/desorption characteristics and the desorption hysteresis of CH
4
in different coal ranks
low
medium
and high coal rank samples are collected for the experiments of micro-component determination
liquid nitrogen adsorption
and isothermal adsorption/desorption to systematically
analyze the composition
pore structure
differences in adsorption/desorption characteristics and desorption hysteresis effects of different coal rank sample materials. Combined with the calculation results of methane adsorption heat
the mechanism of coalbed methane desorption hysteresis from the energy perspective is discussed. The results show that: ①The reflectance
R
o
max
of the vitrinite group of coal samples are 0.43 %
1.26 %
and 3.27 %
respectively. Low-rank coal samples have low vitrinite group content
high inert matter group content
high volatile content and fixed carbon. Medium-rank and high-rank samples are reversed. The degree of coal metamorphism increases. Porosity
BET specific surface area
BJH total pore volume
and fractal dimension D
2
change in a “V” shape
and D
1
changes in an inverted “V” shape. ②Under isothermal condition
the residual adsorption amount becomes larger as the coal rank rises
and the desorption becomes more difficult. As the temperature rises
the residual adsorption capacity increases first and then decreases. With 40 ℃ as the inflection point
the temperature influences both the degree of activation of gas molecules and the pore structure of coal. ③When the pressure is the same
the higher the coal rank
the faster the methane adsorption rate at the low-pressure stage(
p
4 MPa)
the adsorption capacity increases rapidly at the high-pressure stage(
p
4 MPa)
and the adsorption capacity does not increase significantly. ④For the three coal samples
DFS4
#
SGZ11
#
and SH3
#
in the desorption process
their isosteric heat of adsorption are all greater than that in the adsorption process
indicating that the desorption process needs to continuously absorb heat from outside. Therefore
the methane in the adsorption state needs to absorb energy from the external environment
and the energy difference between the adsorption and desorption processes will cause desorption hysteresis. The methan
e in the free state enters into the micropores due to high pressure
resulting in the expansion and deformation of coal matrix
changes in pore structure
limit of methane desorption
and finally a desorption hysteresis effect.
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