2019
DOI: 10.1016/j.renene.2019.04.063
|View full text |Cite
|
Sign up to set email alerts
|

Synchronously electricity generation and degradation of biogas slurry using microbial fuel cell

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
8
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
7
2
1

Relationship

0
10

Authors

Journals

citations
Cited by 30 publications
(12 citation statements)
references
References 38 publications
0
8
0
Order By: Relevance
“…Wang et al [ 126 ] designed a dual-chamber microbial fuel cell with corn stalk biogas slurry as the anode ( Figure 3 ). The anode compartment and cathode compartment of the biofuel cell are separated by a proton exchange membrane and the proton exchange membrane is pre-treated with an H 2 O 2 solution (30%, 80 °C), deionized water and H 2 SO 4 solution (0.5 mol/L) for 1 h and then washed three times with deionized water.…”
Section: Key Technologymentioning
confidence: 99%
“…Wang et al [ 126 ] designed a dual-chamber microbial fuel cell with corn stalk biogas slurry as the anode ( Figure 3 ). The anode compartment and cathode compartment of the biofuel cell are separated by a proton exchange membrane and the proton exchange membrane is pre-treated with an H 2 O 2 solution (30%, 80 °C), deionized water and H 2 SO 4 solution (0.5 mol/L) for 1 h and then washed three times with deionized water.…”
Section: Key Technologymentioning
confidence: 99%
“…(GACTGGAGTTCCTTGGVACCCGAGAATTCCAGACTACHVGGGTATCTAATCC) [19,20], followed by a second round of ampli cation with the same primer pairs. After ampli cation, gel electrophoresis was performed to detect the ampli ed products.…”
Section: Microbial Analysismentioning
confidence: 99%
“…Then, according to the manufacturer's (Shenggong Biotechnology Co., Ltd., Shanghai, China) instructions, DNA was extracted from samples using the Soil DNA kit. The rst round of polymerase chain reaction (PCR) ampli cation was performed using the primers targeting the V3/V4 region of the bacterial 16S rRNA genes: 341F (CCCTACACGACGCTCTTCCGATCTG (barcode) CCTACGGGNGGCWGCAG) and 805R (GACTGGAGTTCCTTGGVACCCGAGAATTCCAGACTACHVGGGTATCTAATCC) [22,23], followed by a second round of ampli cation with the same primer pairs. After ampli cation, gel electrophoresis was performed to detect the ampli ed products.…”
Section: Microbial Analysismentioning
confidence: 99%