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Misr J. Ag. Eng.

, 25(3): 1055- 1066 BIOLOGICAL ENGINEERING


A SIMPLE APPARATUS FOR BIOGAS QUALITY
DETERMINATION

Abdel-Hadi, M. A.

ABSTRACT
A prototype experimental setup was constructed and investigated to
determine the quality of biogas produced during anaerobic fermentation
of cow dung. The technique depends on measuring percentage of carbon
dioxide volume using 40% potassium hydroxide. The biogas and carbon
dioxide percentage were collected from a bench-scale batch anaerobic
digester (vertical type) under room temperature every week for 16 weeks
retention time without mixing to determine the biogas quality throughout
the retention time. The volume of gases was re-calculated for standard
temperature and pressure (STP). The result has been verified by
determining the methane percentage of the same sample of biogas using a
gas chromatography (Chrompack CP 9001) and the carbon dioxide
percentage of the biogas was proportional to its quality.
INTRODUCTION

B
iogas is mainly composed of methane (CH4), carbon dioxide
(CO2) and low amount of other gases (Yadava and Hcssc,
1981). (GTZ, 1999) mentioned that, biogas is a mixture of gases
that is composed chiefly of methane 40-70 vol.%, carbon dioxide 30-60
vol.% and other gases 1-5 vol.% including hydrogen (H2) 0-1 vol.% and
hydrogen sulfide (H2S) 0-3 vol.%. (Tjalfe, 2003) reported the same
percent of methane and carbon dioxide while the other gases 0 - 3 vol.%.
The quality of biogas generated by organic waste materials does not remain
constant but varies with the period of digestion (Khandewal and Mahdi,
1986). The ratio of CH4 to CO2 is normally stable in the reactor and a
change of the ratio can be due to process imbalance. However, the methane
ratio also depends on substrate composition, temperature, pH and pressure
(Liu, 2003). Since the dissolution of CO2 is strongly dependent on pH,
Assist. Professor, Agric. Eng. Dept., Fac. of Agric., Suez Canal Univ.,
41522 Ismailia, Egypt.

Misr J. Ag. Eng., July 2008 1055


fluctuation of pH can also change gas composition.
The important processes in anaerobic digestion are hydrolysis,
fermentation, acetogenesis, and methanogenesis. In the hydrolysis stage,
complex organic materials are broken down into their constituent at parts
such as amino acids, fatty acids, simple sugars and glucose (United Tech.,
2003). In the Acidogenesis process, acidogenic bacteria turn the products of
hydrolysis into simple organic compounds, mostly short chain (volatile)
acids. The transition of the substrate from organic material to organic acids
in the acid forming stages causes the pH of the system to drop. This is
beneficial for the acidogenic and acetagenic bacteria that prefer a slightly
acidic environment, with a pH of 4.5 - 5.5, and are less sensitive to changes
in the incoming feed stream, but is problematic for the bacteria involved in
the next stage of methanogenesis. Methanogens are very sensitive to
changes and prefer a neutral to slightly alkaline environment (Gas
Technology, 2003). If the pH is allowed to fall below 6, methanogenic
bacteria cannot survive. A better indicator is therefore methane production
(Hansson et al., 2002 and Liu, 2003). The change in pH can be both an
indicator and the cause of process imbalance.
The quality of biogas depends mainly on the presence of methane in it. A
good quality of biogas has high percentage of methane. The percentage of
methane in biogas is generally determined by the Orsat apparatus, gas-
chromatograph etc. (Holman, 1995). Savery and Cruzon (1972)
suggested that, the three agents KOH, NaOH and Ca(OH)2 can be used in
chemical scrubbing of biogas. The absorption of CO2 in alkaline solution
is assisted by agitation. The turbulence in the liquid aids to diffusion of
the molecule in the body of liquid and extends the contact time between
the liquid and gas. Another factor governing the rate of absorption is
concentration of the solution. A solution of potassium hydroxide (KOH),
sodium hydroxide (NaOH) and water has enhanced scrubbing capabilities
for CO2 removal because the physical absorption capacity of the water is
increased by the chemical reaction of the KOH and NaOH. Konstandt
(1976) mentioned that the percentage of methane CH4 can be estimated
through recognition of CO2 percentage from this equation:
CH4 = 100% - [CO2% + 0.2% H2S] vol.%

Misr J. Ag. Eng., July 2008 1056


Methane content was measured by absorption of carbon dioxide with10%,
33% and 40% of KOH (APHA et al., 1992; Hamilton and Stephen,
1964; Okeke and Ezekoye, 2006) respectively. The assumption by using
this method was that biogas mainly constituted of methane and carbon
dioxide gas, where the other gases produced during anaerobic process
were neglected. Ergüder et al. (2000) reported that, the gas production in
batch reactors was determined by a water displacement device. The
content of CH4 in biogas was determined as follows: A known volume of
the headspace gas (V1) produced in a serum bottle used in biochemical
methane production (BMP) experiments was syringed out and injected
into another serum bottle which contained 20 g/l KOH solution. This
serum bottle was shaken manually for 3-4 min so that all the CO2 was
absorbed in the concentrated KOH solution. The volume of the remaining
gas (V2), which was 99.9% CH4, in the serum bottle was determined by
means of a syringe. The ratio of V2=V1 provided the content of CH4 in
the headspace gas.
This paper is an attempt to ease the biogas quality determination using a
simple apparatus that use a chemical method such as potassium hydroxide
solution to determine the CO2 percentage. The CO2 percentage in the
biogas is proportional to its quality.
MATERIALS AND METHODS
Biogas Digester
A bench-scale of cylindrical biogas digester (vertical type) as shown in
fig. (1) was constructed at the Agric. Eng. Dep., Fac. of Agric., Suez-
Canal Univ. The digester was fabricated from galvanized steel sheet of
1.5 mm thickness, 45 cm length and 25 cm diameter with total capacity of
22 liters and digestion volume of 16 liters. The digester has inlet and
outlet tube of 50.8 mm (2 in.) diameter for feeding by organic wastes and
rejecting the digested materials. To follow up the digestion processes,
orifice for releasing the produced gas was provided to the digester.
Released gas volume was collected in gasholder and determined by using
the wetted displacement with a previously calibrated scale in liter. The
digestion system was batch anaerobic fermentation under room

Misr J. Ag. Eng., July 2008 1057


temperature (measophilic reaction) for 16 weeks retention time without
mixing to obtain the biogas production.

Gas outlet
Water
Gasholder
Pressure balance Scale (Liter)
chamber
Biogas

Substance inlet Biogas removal

Substance outlet

Fig. (1): Schematic diagram of bench-scale biogas digester (vertical type)

Biogas Quality Determination


The biogas digester and KOH apparatus for determine the biogas quality
were designed and constructed at the Agric. Eng. Dept., Fac. of Agric.,
Suez Canal Univ. The simple apparatus consists of glass U-tube shape
with 12 mm internal diameter for filling by potassium hydroxide solution.
The U-tube hitched with tap to adjust the level of solution with

Misr J. Ag. Eng., July 2008 1058


atmospheric pressure after removal of CO2. The tube was fitted with
injection of samples as a biogas inlet and with gas outlet to release gases
after removal of CO2 as shown in fig. (2).

1
2

8
3
7
6

5
1 - Funnel 2 - Holder 3 - Glass tube 4 –Tap
5 - Flask 6 - Injection of samples 7 - Scale 8 – Gas outlet

Fig. (2): KOH apparatus to determine methane and carbon


dioxide.

The temperature and pH were measured regularly every week using


Jenway temperature and pH meter, model 370pH/mv hand held meter
(Jenway ® 2006) for re-calculated the biogas volume.
Methane percentage was measured using the potassium hydroxide
solution in the laboratory scale investigation. The released gas was
fractioned in a percentage (i.e. methane and CO2 percentage) using the
40% potassium hydroxide. All measurements were carried out under
room temperature and atmospheric pressure. The volume gases were re-
calculated for standard temperature and pressure STP (Hansen et al.,

Misr J. Ag. Eng., July 2008 1059


2004). The percentage of methane in each sample was determined using a
gas chromatography GC (Chrompack CP 9001) at a flow rate of 18
ml/min with helium as the carrier gas. The flame-ionization-detector
(FID) operated at a flow rate of H2 24 ml/ min and makeup N2 of 30ml/
min.
The percentage of CO2 was calculated as follow:
V1  V2
Percentage of CO2  x 100 vol.% (1)
V1
Where
V1 : volume of biogas before removal of CO2, ml
V2 : volume of methane and the other gases after removal of CO2, ml

The volume of biogas, methane and the other gases were re-calculated for
standard temperature and pressure (STP: 0 oC and 1 bar) by using ideal
gas law.
PV = NRT (2)
The atmospheric pressure (P) equal the gas pressure (Pm) during
adjustment the solution level in the apparatus.
Vm .Pm .T
V (3)
VmP.T.Tm
V (4)
Tm
Where
V : gas volume at STP, ml,
Vm : gas volume at room temperature, ml,
T : standard temperature, 0 oC (273 oK) and
Tm : room temperature in oK.
Percentage of CH4 = 100% - [CO2% + 3% (H2S and the other gases)]
vol.,% (5)

Where

Misr J. Ag. Eng., July 2008 1060


3% is the average of H2S and the other gases percentage 1-5 vol.% (GTZ,
1999)
The SPSS statistical package, version 10.0 (SPSS Inc., Michigan, USA),
was used for the statistical analysis. From the data obtained in the
experimental, Bivariate correlations analysis was done to establish the
presence or absence of significant differences in the methane percentage
determination by potassium hydroxide solution 40% and gas
chromatography.
RESULTS AND DISCUSSIONS
The anaerobic process (acetogenesis stage) in digester will normally
leaded to accumulation of volatile fatty acids (VFA) resulting in a
decrease in pH. At the same time, the CO2 gradually increased after the
second week and then reached its to maximum value at the fifth week.
After the fifth week, the pH value slowly gradually increased (fig. 3) this
refers to the digested material has a high buffer capacity. At that time, the
CO2 gradually decreased and methane production gradually increased to
balance the process in the digester.
The results obtained from the experiments can be used to analyze the
quality of biogas as a function of its CO2 percentage. On the other hand,
when CO2 percentage decreased in biogas produced the percentage of
methane will be increased.
Fig. 4 shows the variation of methane percentage and biogas production
at different retention times. It can be seen that the methane percentage of
biogas sample is gradually increases after the second week and then
reaches a maximum value at the middle of the retention time. It can also
be observed that, due to no production of biogas a very negligible
percentage of methane in biogas samples before the second week and
after sixteen weeks from retention time.
Fig. 5 shows the result of methane percentage by GC and KOH solution
method. The methane percentage by GC was less than from KOH method
in the beginning of the retention time anaerobic process due to the other
gases such as H2S and ammonia were high percentage. However, it was
by both methods approximately congruent and the same direction from
fifth week to the end of the retention time.

Misr J. Ag. Eng., July 2008 1061


100 8.00
90 Methan Carbon dioxide pH value 7.80
Methane and Carbon dioxide,

80 7.60
70 7.40
60 7.20

pH value
%

50 7.00
40 6.80
30 6.60
20 6.40
10 6.20
0 6.00
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Hydraulic retention time, week

Fig. (3): Relationship among the methane, carbon dioxide percentage


and the pH value during the retention time.

100 3.5
Methane
90
3.0
Biogas production, l u
80 Biogas production
70 2.5
Methane, %

60 2.0
50
40 1.5
30 1.0
20
0.5
10
0 0.0
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18

Hydraulic retention time, week


Fig. (4): Variation of methane percentage and the biogas
production in different weeks of the retention time.

Misr J. Ag. Eng., July 2008 1062


100
90
80
70
Methane, %

60
50
40
30 Methane, (KOH) method
20
10 Methane, (GC) analysis
0
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Hydraulic retention time, week

Fig. (5): Comparison between methane percentage by KOH


method and GC analysis.

Table (1) shows a comparison between the Std. deviation, the mean and
correlation between the derived KOH solution and GC method.

Table (1): Significance levels of the correlation between


the KOH and GC methods.
Std.
N Mean correlations
Deviation
KOH 14 10.1151 61.7286
0.968**
GC 14 12.1758 61.4786
** Correlation is significant at the 0.01 level

Misr J. Ag. Eng., July 2008 1063


CONCLUSION
- When pH value gradually increased the methane production gradually
increased and at that time the CO2 gradually decreased.
- The CO2 percentage of biogas mixture should be proportional indicator
of its quality.
- The result indicated that, the methane percentage by GC different than
by KOH solution method in the beginning of the retention time
anaerobic process. However, it was nearly in line direction in
middle and end the retention time.
- The statistical analyses result showed that, the correlation was found
significant between the derived KOH solution and GC method at the
0.01 level
- The KOH apparatus is simple and the using easier than other
conventional methods especially in development country and
cheaper than others methods.
REFERENCES
APHA, AWWA, and WEF. (1992). Standard Methods for the
Examination of Water and Wastewater. American Public Health
Association, Washington.
Ergüder, T. H., E. Güven, And G. N. Demirer (2000). Anaerobic
treatment of olive mill waste in batch reactors. Process Biochem. 36:
243–248.
Gas Technology, I. (2003). HIMET-A Two-Stage Anaerobic Digestion
Process for Converting Waste to Energy. Institute of Gas technology,
Chicago IL.
GTZ-GATE (1999). Biogas Digest (Volume I. Biogas Basics) GTZ-
GATE. Eschborn, Germany. http://www2.gtz.de/dokumente/bib/04-
5364.pdf
Hamilton, L. F. and G. S. Stephen (1964). Quantitative chemical
analysis. The machmillan company, New York, pp. 454 – 459.
Hansen, T. L., J. E. Schmidt, I. Angelidaki, E. Marca, J. Jansen, H.
Mosbaek and T. H. Christensen, (2004) Method for determination
of methane potentials of solid organic waste. Waste Management 24:
393–400.

Misr J. Ag. Eng., July 2008 1064


Hansson, M., A. Nordberg, I. Sundh and B. Mathisen (2002). Early
warning of disturbances in a laboratory-scale MSW biogas process.
Water Science and Technology, 5 (10): 255-260.
Holman, J. P. (1995). Experimental methods for engineers, 6th ed. New
Delhi: Tata McGraw-Hill, p. 539-43.
Jenway ® (2006). Operating Manual of the 370 pH/mv meter. Jenway,
Gransmore Green Felsted, Dunmow Essex CM6 3 LB, England.
Khandewal, K. C. and S. S. Mahdi, (1986). Biogas technology:
practical handbook. New Delhi: Tata McGraw-Hill, p. 51-2.
Konstandt, H. G. (1976). Engineering’s operation and economics of
methane gas production. Seminar on Microbial Energy Conversion,
Gottingen, Erich Goetze Verlag, Germany
Liu, J. (2003). Instrumentation, Control and Automation in Anaerobic
Digestion. Ph.D. dissertation, Department of Biotechnology, Lund
University, Sweden.
Okeke, C.E. and V.A. Ezekoye, (2006). Design, construction, and
performance evaluation of plastic biodigester. The Pacific Jo. Sc. Tec.
7(2), Nsukka, Nigeria.
Savery, W. C. and D. C. Cruzon (1972). Methane recovery from
chicken manure. J Water Pollut Control Fed 44: 2349-54.
Tjalfe G. Poulsen (2003). Solid waste management. Chapter 5 Anaerobic
digestion, Aalborg University. Denmark.
United Tech, I. (2003). Anaerobic Digestion, UTI Web Design.
Yadava, L. S. and P. R. Hcssc (1981). The Development and Use of
Biogas Technology in Rural Areas of Asia (A Status Report 1981).
Improving Soil Fertility through Organic Recycling. FAO/UNDP
Regional Project RAS/75/004, Project Field Document No. 10.

Misr J. Ag. Eng., July 2008 1065


‫الملخص العربي‬
‫جھاز بسيط لتقدير جودة الغاز الحيوي‬
‫د‪ .‬محمد على عبد الھادي‬

‫يھدف ھذا البحث إلي تصميم جھاز بسيط لقياس جودة الغاز الحيوي بطريقة كيميائية يعتمد علي‬
‫تقدير نسبة غاز ثاني أوكسيد الكربون في الغاز الحيوي نتيجة امتصاصه بمحلول كيماوي‬
‫ھيدروكسيد البوتاسيم ‪.%٤٠‬‬
‫صمم وصنع الجھاز بالوحدة التجريبية للغاز الحيوي بقسم الھندسة الزراعية ‪ -‬كلية الزراعة ‪-‬‬
‫جامعة قناة السويس‪ .‬والجھاز عبارة عن أنبوب زجاجي علي شكل حرف ‪ U‬بقطر داخلي ‪ ١٢‬مم‬
‫مفتوح من أحد جانبيه إلضافة المحلول الكيماوي ومرتبط باألنبوب صنبور لضبط منسوب‬
‫المحلول في كال الجانبين أثناء القياس لمعادلة الضغط الجوي‪ .‬أجريت تجربة معملية علي روث‬
‫األبقار بالتخمر الالھوائي نظام تغذية مرة واحدة تحت درجة حرارة الغرفة )‪ ٢٢‬م‪ (o‬وبدون تقليب‬
‫لوقت استبقاء ‪ ١٦‬أسبوع في مخمر رأسي مصنع من الحديد المجلفن بسمك ‪ ١.٥‬مم وبقطر‬
‫وارتفاع ‪ ٢٥‬و ‪ ٤٥‬سم علي التوالي وحجم صافي لتخمر المادة ‪ ١٦‬لتر‪.‬‬
‫استخدمت التجربة المعملية في قياس كمية الغاز الحيوي الناتج باللتر باإلزاحة الحجمية يوميا ً مرة‬
‫كل أسبوع‪ .‬كذلك تم تقدير نسبة غاز ثاني أوكسيد الكربون بطريقة ھيدروكسيد البوتاسيم ‪%٤٠‬‬
‫وحساب نسبة الميثان في الغاز الحيوي الناتج مع األخذ في االعتبار درجة الحرارة والضغط‬
‫الجوي أثناء القياس )المعادلة العامة للغازات( تم مقارنة النتائج المتحصل عليھا بھذه الطريقة مع‬
‫التقدير بطريقة الغاز كروماتوجراف )‪gas chromatography (Chrompack CP 9001‬‬
‫كطريقة قياسية لنفس العينات‪.‬‬
‫وقد توصلت النتائج الي‪:‬‬
‫‪ ‬بتقدير نسبة غاز ثاني أوكسيد الكربون في الغاز الحيوي يمكن حساب نسبة غاز الميثان مع‬
‫األخذ في االعتبار نسبة ‪ %٣‬غازات أخري‬
‫‪ ‬وجود عالقة عكسية بين نسبة الميثان وثاني أوكسيد الكربون في الغاز الحيوي‬
‫‪ ‬وجود عالقة طردية بين رقم األس الھيدروجيني داخل المخمر ونسبة الميثان المتحصل عليھا‬
‫وفي نفس الوقت عالقة عكسية مع نسبة ثاني أوكسد الكربون ‪ ،‬وذلك في مدى األس الھيدروجيني‬
‫من ‪ ٦.٤‬إلى ‪٧.٢‬‬
‫‪ ‬يوجد فروق بسيطة بين نسبة غاز الميثان المقدرة بطريقة ھيدروكسيد البوتاسيم ‪%٤٠‬‬
‫والمقدرة بتحليل الغاز كروماتوجراف ‪ gas chromatography‬خاصةً في بداية وقت االستبقاء‪.‬‬
‫‪ ‬وجد ارتباط معنوي مقداره **‪ .968‬عند مستوي ‪ 0.01‬بين التقدير بطريقة ھيدروكسيد‬
‫البوتاسيم ‪ %٤٠‬وتحليل الغاز كروماتوجراف‪.‬‬
‫‪ ‬تصميم وتشغيل الجھاز يعتمد علي المعادلة العامة للغازات )الحرارة والضغط أثناء القياس(‪.‬‬
‫‪ ‬سھولة االستخدام ورخص الثمن بالمقارنة مع الطرق األخرى خاصةً في المناطق النامية‪.‬‬

‫‪Misr J. Ag. Eng., July 2008‬‬ ‫‪1066‬‬

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