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14 декабря, 2021
Biogas technology is viewed as one of the renewable technologies in Africa that can help eases its energy and environmental problems. To date, some digesters have been installed in several sub-Saharan countries, utilising a variety of waste such as from slaughterhouses, municipal wastes, industrial waste, animal dung and human excreta. Small-scale biogas plants are located all over the continent but very few of them are operational. In most African countries, for example, Burundi, Ivory Coast, and Tanzania, biogas is produced through anaerobic digestion of human and animal excreta using the Chinese fixed-dome digester and the Indian floating-cover biogas digester, which are not reliable and have poor performance in most cases (Omer and Fadalla, 2003). These plants were built for schools, health clinics and mission hospitals and small-scale farmers, in most cases by nongovernmental organisations. In Africa the interest in biogas technology has been further stimulated by the promotional efforts of various international organisations and foreign aid agencies through their publications, meetings and visits. Most of the plants have only operated for a short period due to poor technical quality. Table 3 gives a list of the African countries with biogas production units as at 2007. There is thus a need to introduce more efficient reactors to improve both the biogas yields and the reputation of the technology. The development of large-scale anaerobic digestion technology in Africa is still embryonic, but with a lot of potentials.
No of small/ |
No of |
Level of technology development |
||||
Country |
Geographical characteristic |
Region |
medium digester (< 100m3) |
Large scale digester (>100m3) |
||
Landlocked |
Coastal |
|||||
Botswana |
* |
Southern Africa |
Several |
Few |
Low |
|
Burkina Faso |
* |
West Africa |
Few |
— |
Low |
|
Burundi |
* |
Central Africa |
Several |
Several |
High |
|
Cameroon |
* |
Central Africa |
Few |
— |
Low |
|
Congo- Brazzaville |
* |
Central Africa |
Several |
Few |
Low |
|
Cote d’Ivoire |
* |
West Africa |
Several |
Few |
Low |
|
Egypt |
* |
North Africa |
Several |
Few |
High |
|
Eritrea |
* |
East Africa |
Few |
— |
Low |
|
Ethiopia |
* |
East Africa |
Few |
— |
Low |
|
Ghana |
* |
West Africa |
Several |
Few |
High |
|
Guinea |
* |
West Africa |
Few |
— |
Low |
|
Kenya |
* |
East Africa |
Several |
Several |
High |
|
Lesotho |
* |
Southern Africa |
Few |
— |
Medium |
|
Malawi |
* |
Southern Africa |
Few |
— |
Low |
|
Mali |
* |
West Africa |
Several |
Few |
High |
|
Morocco |
* |
North Africa |
Several |
— |
Medium |
|
Namibia |
* |
Southern Africa |
Few |
— |
Low |
|
Nigeria |
* |
West Africa |
Few |
Few |
Low |
|
Rwanda |
* |
Central Africa |
Several |
Few |
High |
|
Sierra Leone |
* |
West Africa |
Few |
— |
Low |
|
South Africa |
* |
Sothern Africa |
Several |
Several |
High |
|
Sudan |
* |
East Africa |
Few |
— |
Low |
|
Swaziland |
* |
Southern Africa |
Several |
— |
Medium |
|
Tanzania |
* |
East Africa |
Several |
Several |
High |
|
Tunisia |
* |
North Africa |
Few |
— |
Low |
|
Uganda |
* |
East Africa |
Few |
— |
Low |
|
Zimbabwe |
* |
Southern Africa |
Several |
Few |
Medium |
Sources: Karekezi, (2002), Allafrica. com, (2000), Akinbami et al, (2001), Spore, (2004), Amigun and von Blottnitz, (2007). Table 2. Countries with documented biogas producing units in Africa as at 2007 |
Some of the first biogas digesters were set up in Africa in the 1950s in South Africa and Kenya. In other countries such as in Tanzania, biogas digesters were first introduced in 1975 and in others even more recently (South Sudan in 2001). To date, biogas digesters have been installed in several sub-Saharan countries including Burundi, Botswana, Burkina Faso, Cote d’Ivoire, Ethiopia, Ghana, Guinea, Lesotho, Namibia, Nigeria, Rwanda, Zimbabwe, South Africa and Uganda (Winrock International, 2007). Biogas digesters have utilized a variety of inputs such as waste from slaughterhouses, waste in urban landfill sites, industrial waste (such as bagasse from sugar factories), water hyacinth plants, animal dung and human excreta. Biogas digesters have been installed in various places including commercial farms (such as in chicken and dairy farms in Burundi), a public latrine block (in Kibera, Kenya), prisons in Rwanda, and health clinics and mission hospitals (in Tanzania) (Winrock International, 2007). However, by far the most widely attempted model is the household biogas digester — largely using domestic animal excreta (Table 2). This is due to the fact that this technology is closely linked to poverty alleviation and rural development. The biogas produced from these household-level systems has been used mostly for cooking, with some use for lighting.
Global experience shows that biogas technology is a simple and readily usable technology that does not require overtly sophisticated capacity to construct and manage. It has also been recognized as a simple, adaptable and locally acceptable technology for Africa (Gunnerson and Stuckey, 1986; Taleghani and Kia, 2005). There are some cases of successful biogas intervention in Africa, which demonstrate the effectiveness of the technology and its relevance for the region. The lessons learned from biogas experiences in Africa suggest that having a realistic and modest initial introductory phase for Biogas intervention; taking into account the convenience factors in terms of plant operation and functionality; identifying the optimum plant size and subsidy level; and; having provision for design adaptation are key factors for successful biogas implementation in Africa (Biogas for better life, 2007). Biogas technology has multiple beneficial effects.
Anaerobic digestion (AD) is an attractive treatment for this waste of difficult disposal. AD processes transform the organic matter contained in a certain waste in biogas as main product. This process is carried out for different kind of microorganisms which work in a coordinate and interdependent chain until biogas obtaining.
Anaerobic treatment of moderate and high strength wastes with high biodegradable content presents a number of advantages in comparison to the classical aerobic processes: a) quite a high degree of purification with high-organic load feeds can be achieved; b) low nutrient requirements are necessary; c) small quantities of excess sludge are usually produced and finally, d) a combustible biogas is generated. The production of biogas enables the process to generate or recover energy instead of just energy-saving; this can reduce operational costs as compared with other processes such as physical, physico-chemical or biological aerobic treatments (Borja et al., 2006).
Previous works carried out at pilot-scale have shown that most of agro-industrial residues, such as sugar beet pulp, potato pulp, potato thick stillage and brewer’s grains, can be treated anaerobically with an efficient solids stabilisation and energy recovery, if the applied process-type (one or two stages) is selected according to the C:N ratio of the residues. These works demonstrated that at hydraulic retention times (HRT) of between 10 and 20 days, normally, the 50-60% of the organic matter was degraded. The ultimate anaerobic biodegradability was higher and lied between 76% (brewer’s grain) and 88% (potato pulp), which demonstrated that more than 60% of the available energy potential could be used in the industrial processes. The gas production varied between 300 and 500 m3 biogas per ton of dry matter with a methane content of 60-70%. The undigested solids, which were separated from the effluent of the reactors could be completely stabilised after a short aerobic post-treatment to be used as a soil conditioner (Borja et al., 2006).
A number of kinetic models have been proposed for the process of anaerobic digestion. Early models were based on a single-culture system and used the Monod equation or variations. More recently, several dynamic simulation models have been developed based on a continuous multi-culture system; these correspond to the major bioconversion steps in anaerobic digestion but again make the assumption that culture growth obeys Monod type kinetics. Doubt has been expressed by several investigators on the validity of applying the Monod equation to waste treatment as the specific growth rate is expressed only as a function of the concentration of the limiting substrate in the reactor. The Monod equation contains no term relating to input substrate concentration; this implies that the effluent substrate concentration is independent of the input concentration. Experimental results do not always agree with this implication; for example the anaerobic digestion of dairy manure, beef cattle manure at mesophilic and thermophilic temperatures, rice straw or poultry litter (Borja et al., 2003).
Deviation from the Monod relationship in many digestion systems may be due to their complexity. This complexity has necessitated the use of generalized measures of feed and effluent strength, namely total Chemical Oxygen Demand (COD) and volatile solids (VS), which may not truly reflect the nature of the growth-limiting substrate. Utilizable carbon in the digester is derived from the hydrolysis of polymeric compounds, constituting the waste, by exo-enzymes in the extracellular medium or on the surface / vicinity of the microorganisms: only these hydrolysed, assimilable compounds can be considered as the growth-limiting substrate in terms of the Monod relationship. Extra-cellular hydrolysis is often considered the rate-limiting step in anaerobic digestion of organic wastes (Borja et al.,
2003) and for a model to be truly valid this must be taken into account.
Multi-culture system kinetics may be desirable in view of the heterogeneous nature of the microbial population performing the various bioconversion steps involved. However, the kinetic models based on this premise necessarily involve a number of kinetic equations and coefficients making them highly complex, as shown by the reported models (Borja et al., 2003). Complexity does not necessarily equate to accuracy and there is still a strong case in favour of a simpler kinetic treatment based on a single culture system. Methanogenesis is particularly suited to this approach as there is a strong holistic characteristic in the process. Various cultures and bioconversion steps in digestion are interdependent and the whole process has certain self-regulatory characteristics within the process limits.
Kincannon and Stover (1982) proposed a widely used mathematical model to determine the kinetic constants for immobilized systems and high-rate reactors. In this model the substrate utilization rate is expressed as a function of the organic loading rate by monomolecular kinetics for biofilm reactors such as rotating biological contactors and biological filters (Kapdan and Erten, 2007). A special feature of the modified Stover-Kincannon model is the utilization of the concept of organic loading rate as the major parameter to describe the kinetics of an anaerobic filter in terms of organic matter removal and methane production (Buyukkamaci and Filibeli, 2002; Kapdan and Erten, 2007).
The modified Stover-Kincannon model allows to calculate the maximum substrate utilization rate by the microorganisms (Rmax) and the saturation constant (Kb) in anaerobic digestion processes (Yu et al., 1998). Therefore, this model allows determining the effluent substrate concentration for a known volume of reactor and an initial concentration of the substrate. The modified Stover-Kincannon model has been used for different substrates and reactor configurations: anaerobic hybrid reactors treating petrochemical waste (Jafarzadeh et al., 2009), anaerobic treatment of synthetic saline wastewater by Halanaerobium lacusrosei (Kapdan and Erten, 2007), anaerobic digestion of soybean wastewaters (Yu et al., 1998) and molasses (Buyukkamaci and Filibeli, 2002) in a filter and in a hybrid reactor, respectively.
The aim of the present study was focused on the AD of two-phase OMSW at two different influent substrate concentrations and on the determination of kinetics constants of the system using the above-mentioned modified Stover-Kincannon model.
Peter Hass
IPSOS Industrial Consulting GmbH, Berlin,
Germany
The increasing number of biogas plants which is favored now as a part of the energy concept of the German Government and the European Union has major impact on traditional gas distribution and transmission systems. In addition, synthetic methane gas or hydrogen injections must be considered in the near future which will originate from wind power generation (conversion of excess capacities). The main aspect of this change is the resulting calorific value which may be subject to changes in a short time which must therefore be measured, calculated and permanently surveyed.
This chapter describes the basics of gas mixing and the various situations which may be encountered and must be handled in the transportation or distribution process. There are some limitations which must be considered for industrial consumers and power plants. Measurements and simulations are required to survey and control the process of gas distribution and finally generate figures for accounting and billing. Some typical examples are presented to give an insight into real situations and projects.
The problems and limitations of the gas distribution process in heterogeneous networks and biogas injections are discussed with respect to the IT-structure and organizational environment. The final benefit that can be achieved is an individual calorific value for each consumer in the grid enabling a fair billing despite the variations of many gas injections from many sources.
As mentioned previously, the temperature and substrate compostion have a high effect on biogas production. Their effects are confirmed by the study published by several researchers. As an example the results, obtained by Derbal et al. (Derbal & al., 2011) can be cited.
The obtained values of different parameters of the (co)-digestion experiments under mesophilic and thermophilic conditions are presented (see figure 2, 3, 4, 5, 6). It should be noted that the volume of the mesophilic co-digester which is 2000 m3 is 20 times larger than pilot scale digesters 500 l. Therefore, the absolute biogas volume produced is different from the other cases and no comparison can be made. However, a comparison for different parameters is presented as follows:
0,5
0,45
0,4
0,35
0,3
CO
■E 0,25 0,2 0,15 0,1 0,05 0
Fig. 2. Comparison of gas production (GP)
The use of gas production rate GPR as a comparison parameter led us to include the data from the industrial scale digester. The results shown on Figure 3 confirm that the combined effect of temperature and solid waste addition is positive and considerable. Moreover, thermophilic co-digestion presents the best GPR results wich are confirmed by values of
□ A. D. T=35°C
□ A. D. T=35°C
□ A. Co-D. T=35°C
□ A. Co-D. T=55°C
Fig. 3. Comparison of gas production rate (GPR)
SGP of Figure 4. SGP is in relation with the biodegradability of the substrate and with anaerobic process reaction. SGP increased from 0.14 to 0.33 for digestion of wastewater sludge alone when temperature increased from mesophilic conditions (35°C) to thermophilic ones (55°C), whereas for a wastewater sludge mixed with solid waste this parameter increased from
0. 31 to 0.51. Adding solid waste under mesophilic comditions results in an increase of SGP from 0.14 to 0.31, whereas under thermophilic conditions SGP increased from 0.33 to 0.51. The combined effect of increasing temperature from mesophilic conditions to thermophilic ones and adding solid waste to wastewater sludge increased SGP from 0.14 to 0.51. Figure 5 presents the comparison of COD removal in the different studied cases. It increased from 24% for wastewater sludge alone under mesophilic conditions to 49.35% for wastewater sludge mixed with solid waste under thermophilic conditions. Moreover, for TVS thermophilic, co-digestion presents the best removal rate, 52.93%, as shown in Table 5. As a treatment system, anaerobic co-digestion under thermophilic conditions presents the best removal rates as well as specific gas production. It should be noted that changing working conditions from mesophilic to thermophilic ones increases anaerobic kinetic rates and as such the treatment capacity of a known volume will be increased as well. Adding solid waste contributes to the increase of biodegradable organic matter in the substrate (Figure 6).
As a conclusion of this sludy, the obtained results show that thermophilic co-digestion gives the best results. Although the temperature has an effect on the biogas production, it remains however quite relative compared to the effect of solid waste. These results confirm that the combined effect of the temperature and solid waste improves considerably the biogas production rate (GPR). The moving from mesophilic to thermophilic conditions, for waste sludge alone makes GPR pass from 0.18 to 0.39 m3/m3*d and for the waste sludge mixed with solid waste from 0.29 to 0.96 m3/m3*d.
The analysis of produced biogas showed that the percentage of biomethane is very high 60.37 and 64.44 for the digestion of sludge waste in mesophilic and thermophic phases, respectively and 65.8 and 60.61 for the co-digestion of solids waste with sludge waste in mesophilic and thermophilic cases, respectively.
Hydrogen generation in microbiological processes can be realized both by eucariota (green algae), procariota (cyanobacteria) in direct or indirect splitting of water under illumination, as well as in the fermentation and photofermentation reactions in presence of organic substances and numerous strains of bacteria. Due to very low yields of hydrogen obtained in presence of algae and cyanobacteria this paper will concentrate only on fermentative processes.
Dark fermentation process towards hydrogen is performed in presence of organothrophic bacteria. Large variety of microorganisms is involved in these reactions, therefore this paper will focus only on the description of three groups of microorganisms.
The first group belongs to anaerobic, gram-negative, mesophilic bacteria of Clostridium and Bacillus type. C. acetobutylicum (Chin, 2003), C. butyricum (Masset, 2010, Cai, 2010) C. pasterianum, C. bifermentants (Wang, 2003), C. beijerinckii (Skonieczny, 2009), C. tyrobutyricum (Jo, 2008), C. saccharoperbutylacetonicum ( Alalayaha, 2008), B. lichemiformis (Kalia, 1994), B. coagulans (Kotay, 2007) are the most popular representatives of this group. This strains of bacteria can form spores capable to survive in extreme conditions such as low and high temperature, different pH, irradiation, extreme dry conditions or presence of deadly chemical compounds (eg. NaCl). Bacteria cells under these conditions goes to anabiosis: complete reduction of metabolic processes. The separation of already divided DNA occurs at this stage with simultaneous surrounding by two cytoplasmic membranes. The endospore formed under unfavourable conditions can return to normal activity under appropriate conditions. In this process the external protection of outer coating is destroyed. Appropriate temperature, pH and presence of feed compounds facilitate formation of vegetative cells and their growth (Setlow, 2007). In some cases presence and increase of concentration of specific compounds is the biochemical signal to stop the endospore phase. Presence of alanine, serine, cysteine together with lactic acid accelerate germination C. botulinum bacteria (Plowman, 2002).
The second group of fermentative bacteria active in hydrogen generation belongs to anaerobic gram-negative bacteria. The best activity in biohydrogen generation via dark fermentation was found for the following strains: Enterobacter asburiae (Jong-Hwan, 2007), Enterobacter cloacae (Mandal, 2006), Enterobacter aerogenes (Jo, 2008), Escherichia coli (Turcot, 2008), Klebsiella oxytoca (Wu, 2010) or Citrobacter Y19 (Oha, 2003). These strains of bacteria can tolerate oxygen in environment. Here, in aerobic condition the oxygen respiration can occurs. The change of metabolic pathway provides method for survival under variable conditions of environment. These bacteria show better biological activity in comparison with those active only in completely anaerobic conditions. However, in aerobic conditions no hydrogen formation is observed. This effect is caused by inhibition of hydrogenase, enzyme catalyzing hydrogen generation.
Thermophilic bacteria operating at 60-85 oC belongs to the third group of bacteria generating hydrogen in fermentative processes (Zhang, 2003). The following strains of thermophilic bacteria of Thermoanaerobacterium thermosaccharolyticum (Thonga, 2008) and hyperthermophilic of Thermatoga neapolitana (Mars, 2010, Eriksen, 2008), Thermococcus kodakaraensis (Kanai, 2005), or Clostridium thermocellum (Lewin, 2006) can generate hydrogen in presence of organic substrates at relatively high temperatures. It was established that thermophilic bacteria are the most effective from all those already described.
Application of C. saccharolyticus and Thermatoga elfii thermophilic bacteria results in 80 % yield of the theoretical one (theoretically 4 moles of glucose can be transformed into acetic acid with 100% yield) while applying saccharose or glucose (Vardar-Schara,2008), respectively. High yield in hydrogen generation is explained by Guo et al. (Guo, 2010) who assumes that high temperature can accelerate hydrolysis of substrates engaged in this process. At the same time Valdes-Vazquez et al. (Valdes-Vazquez, 2005) demonstrates that such results are not surprising, because optimal activity of hydrogenase is 50-70 °C. Unfortunately, the high yield of hydrogen generation with thermophilic bacteria is not equivalent to total amount of generated gas (Hallenbeck, 2009). In this situation the construction of bigger reactors is required what in consequence increase total costs. Moreover, reaction performed at higher temperatures require additional thermal energy supplied to the bioreactor.
Photofermentation in hydrogen generation is the process which requires appropriate strain of bacteria, organic substances (mainly VFA) and light with appropriate intensity. The following strains of bacteria indicate activity in photoproduction of hydrogen: Rhodobacter sphaeroides (Koku, 2002), Rhodobacter capsulatus (Obeid, 2009), Rhodovulum sulfidophilum (Maeda, 2003), or Rhodopseudomonas palustris (Chen, 2008). The research of new strains active in photogeneration of hydrogen is performed in numerous laboratories all over the world. These efforts were recently awarded by discovery of activity in Rheudopseudomanas faecalis (Ren, 2009).
Rhodobacter sphaeroides belong to the group of bacteria the best recognized in hydrogen generation. These gram-negative bacteria belongs to the purple non-sulfur (PNS) Proteobacteria subgroup (Porter, 2008). The morphology is different because the shape of these bacteria as well as their dimensions strongly depends on the medium (see Fig. 3). In medium containing sugars the dimensions are limited to 2.0-2.5 x 2.5-3.0 pm, whereas under other conditions they can vary from 0.7 to 4.0 pm (Garrity, 2005).
Fig. 3. Rhodobacter sphaeroides ATCC 17039 (Garrity, 2005). |
Rhodobacter spheroides indicate strong chemotaxis with certain sugars, aminoacids and several organic acids (Packer, 2000). They are also capable to accept molecular nitrogen. Their metabolism is very elastic because they can germinate both in aerobic conditions (with or without light) as well as in anaerobic environment, in presence of light.
Under aerobic conditions this strain is used in purification of animal wastes (Huang, 2001) and biotransformation of toxins present in plant extracts (Yang, 2008). In the absence of oxygen Rhodobacter spheroids can be used in synthesis of carotenoides (Chen, 2006) and the most of all in hydrogen generation (Kars, 2010).
The measured results of the total accumulated temperature of each treatment were shown in table 4-8.
Soil depth cm |
Intervaltreatments |
A |
B |
C |
D |
E |
F |
1 |
435.6 |
438.4 |
427.5 |
463.2 |
526.9 |
396.1 |
|
0 |
2 |
408.7 |
403.9 |
415.8 |
430 |
479.6 |
401.8 |
3 |
418.1 |
410.2 |
369.6 |
431.3 |
511.8 |
369.1 |
|
Mean |
420.8 |
417.5 |
404.3 |
441.5 |
506.1 |
389 |
|
1 |
395 |
380.5 |
395.6 |
410 |
435.7 |
380.8 |
|
5 |
2 |
393.1 |
397.2 |
386.8 |
392.4 |
425.4 |
377.6 |
3 |
380.7 |
397.4 |
391.8 |
405.7 |
446.5 |
370.5 |
|
Mean |
389.6 |
391.7 |
391.4 |
402.7 |
440.1 |
374.7 |
|
1 |
356.5 |
356 |
343.2 |
366.4 |
381.3 |
350.4 |
|
10 |
2 |
365.8 |
367.1 |
358.5 |
378.2 |
407.2 |
335.7 |
3 |
362.8 |
354.8 |
359.4 |
367.2 |
413 |
344.4 |
|
Mean |
361.7 |
359.3 |
353.7 |
370.6 |
400.5 |
343.5 |
|
1 |
339.2 |
332.4 |
330.5 |
346.7 |
370.4 |
337.1 |
|
15 |
2 |
348.1 |
346 |
346.6 |
359.8 |
385.5 |
342.3 |
3 |
342.9 |
341.3 |
335.4 |
348.6 |
398.8 |
323.8 |
|
Mean |
343.4 |
339.9 |
337.5 |
351.7 |
384.9 |
334.4 |
Table 4-8. The total accumulated temperature of each treatment |
Analysis of variance of the total accumulated temperature of each treatment was shown in table 4-9.
Soil depth cm |
Source |
SS |
DF |
MS |
F |
P-value |
F0.05 |
Interval |
3016.57 |
2 |
1508.29 |
6.3092 |
0.0169 |
4.1028 |
|
0 |
Treatment |
25517.2 |
5 |
5103.44 |
21.3477 |
4.84E-05 |
3.3258 |
Error |
2390.63 |
10 |
239.06 |
||||
Total |
30924.4 |
17 |
|||||
Interval |
58.83 |
2 |
29.42 |
0.3999 |
0.6806 |
4.1028 |
|
5 |
Treatment |
6241.93 |
5 |
1248.39 |
16.9726 |
0.000133 |
3.3258 |
Error |
735.53 |
10 |
73.55 |
||||
Total |
7036.3 |
17 |
|||||
Interval |
324.96 |
2 |
162.48 |
2.1843 |
0.1633 |
4.1028 |
|
10 |
Treatment |
5774.55 |
5 |
1154.91 |
15.526 |
0.000195 |
3.3258 |
Error |
743.86 |
10 |
74.39 |
||||
Total |
6843.37 |
17 |
|||||
Interval |
432.25 |
2 |
216.13 |
4.113 |
0.0497 |
4.1028 |
|
15 |
Treatment |
5264.62 |
5 |
1052.92 |
20.037 |
6.42E-05 |
3.3258 |
Error |
525.47 |
10 |
52.55 |
||||
Total |
6222.34 |
17 |
Table 4-9. Analysis of variance of the total accumulated temperature of each treatment |
Multiple comparisons of the total accumulated temperature of different soil depths among treatments were shown in table 4-10.
Table 4-10 showed that there were significant differences between plastic film and three kinds of biogas fibre residue film, black film and control while the soil depth was 0cm and 10cm. There were significant differences between the black film and control; there were significant differences between A, B treatment of biogas residue fibre film and control; there were no significant differences between C treatment of biogas residue fibre mulch and control; there were significant differences between black film and C treatment of biogas residue fibre film. While the soil depth was 5 cm, there were significant differences between plastic film and three kinds of biogas fibre residue film, black film and control; there were significant differences between A, B treatment of biogas fibre residue film, black film and control. While soil depth was 15 cm, there were significant differences between plastic film and three kinds of biogas fibre residue film, black film and control; there were significant differences between the black film and C treatment of biogas residue fibre film and control.
While the soil depth was 0 cm, 5 cm, 10 cm, the total accumulated temperature of A, B treatment of biogas residue film obviously increased than control, and C did not significantly increase; while the soil depth was 0cm, the total accumulated temperature of A treatment increased 31.8 °С, B increased 28.5 °С, and C increased 15.3°C than control; while the soil depth was 5cm, the total accumulated temperature of A treatment increased 17°C, B increased 17.3C, and C increased 15.2°C than control; while the soil depth was 10cm, the total accumulated temperature of A treatment increased 18.2 °С, B increased 15.8 °С, and C increased 10.2 °С than control. While the soil depth was 15 cm, the total accumulated temperature of three kinds of biogas fibre residue film nearly closed to control, and was less than the black film and plastic film. There was no significant difference between the three kinds of biogas residue fibre film.
0 |
A B C D E F |
420.8 417.5 404.3 441.5 506.1 389 |
31.8* 28.5* 15.3 52.5** 117.1** |
85.3** 88.6** 101.8** 64.6** |
20.7 24 37.2* |
16.5 13.2 |
3.3 |
28.13 |
40.01 |
A |
391.4 |
17* |
48.7** |
11.3 |
1.8 |
0.3 |
15.6 |
22.19 |
|
B |
391.7 |
17.3* |
48.4** |
11 |
2.1 |
||||
C |
389.6 |
15.2 |
50.5** |
13.1 |
|||||
D |
402.7 |
28.3* |
37.4** |
||||||
E |
440.1 |
65.7** |
|||||||
F |
374.4 |
||||||||
A |
361.7 |
18.2* |
38.8** |
8.9 |
8 |
2.4 |
15.68 |
22.32 |
|
B |
359.3 |
15.8* |
41.2** |
11.3 |
5.6 |
||||
C |
353.7 |
10.2 |
46.8** |
16.9* |
|||||
10 |
D |
370.6 |
27.1** |
271** |
|||||
E |
400.5 |
57** |
|||||||
F |
343.5 |
||||||||
A |
343.4 |
9 |
41.5** |
8.3 |
5.9 |
3.5 |
13.19 |
18.76 |
|
B |
339.9 |
5.5 |
45** |
11.8 |
2.4 |
||||
C |
337.5 |
3.1 |
47.4** |
14.2* |
|||||
D |
351.7 |
17.3* |
33.2** |
||||||
E |
384.9 |
50.5** |
|||||||
F |
334.4 |
Уі — У F |
E |
Уі — yj Уі — Ус |
LSD0.05 LSD0.01 |
ІУ, — Ув |
Notes: The significance of symbols was as same as table 4-4. |
Table 4-10. Multiple comparisons of the total accumulated temperature of different soil depths among treatments |
Chitosan is available commercially in three forms: solution, flake and powder. The prices of chitosan in the forms of solution, flake and powder range between 50 to 70 baht/L, 700 to 900 baht/kg and 750 to 2,300 baht/kg, respectively. Chitosan in the form of freely moving polymeric chains has previously been found to enhance sludge granulation and shorten the start-up period of UASB systems (El-Mamouni et al., 1998; Lertsittichai et al., 2007; Liu et al.,
2002; Thaveesri et al., 1995).
The effectiveness in enhancing granulation of different forms of chitosan, i. e. solution, bead and powder, has also been studied by Nuntakumjorn et al. (2008). They prepared chitosan solution by dissolving chitosan in acetic acid solution (1% w/v). In preparing chitosan powders, they used a spray dryer to spray-dry chitosan solution (1% w/v). In preparing the chitosan beads, they dropped the chitosan solution (4% w/v) into a solution of KOH and ethanol. The chitosan beads were found to have spherical shape, white color and looked like glutinous pellets. The appearance of the chitosan beads is shown in Fig. 6.
(a) (b) Fig. 6. (a) Chitosan beads in the KOH/Ethanol solution (b) SEM micrograph with 3500x of chitosan powders (from Nuntakumjorn et al., 2008) |
Nuntakumjorn et al. (2008) used two identical reactors, with a working volume of 5.3 L, running in parallel. A sludge suspension with an initial VSS concentration of 12 g VSS/L was inoculated into the reactors. The acclimation of the sludge was carried out until the COD removal was approximately 80%. The reactors were run with a HRT of 1.5 day corresponding to an OLR of 1.45 g COD/L-d. Chitosan in the different forms was introduced into the reactors on the second operating day of the start-up period at dose rates of 2 mg chitosan/g suspended solids.
A summary of the results of Nuntakumjorn et al. (2008) is as follows. When comparing between the UASB with no chitosan addition and the UASB with chitosan addition in the solution form, the UASB with chitosan addition was found to have a 9 to 59% lower effluent COD, 5 to 7% higher COD removal, up to 25% higher biogas production rate, 21 to 39% lower biomass washout, 37% larger particle size and 4 day longer sludge retention time.
When comparing between the UASB with chitosan addition in the solution form and with addition in the bead form, the UASB with chitosan solution was found to have 5 to 17% lower effluent COD, 16 to 45% higher COD removal, 7 to 20% lower biomass washout and 3 to 17% higher biogas production than the UASB with chitosan beads. The reduced effectiveness of chitosan in the bead form might be caused by a lower amount of chitosan in the bead form and by insufficient contact between the chitosan beads and biomass.
When comparing between the UASB with no chitosan addition and the UASB with chitosan addition in the powder form, no differences were found in terms of COD removal, biogas production and biomass washout. The average COD removal of the UASB with chitosan addition was approximately 80% and that without chitosan was approximately 81%. The biogas production rate was 9.85 L/d and 10.23 L/d for the UASB with and without chitosan addition, respectively. Both UASB reactors had biomass washout in the range of 0.6 to 1.5 g VSS/L. Although chitosan powders have net positive charge, the electrostatic interaction between the negatively charged bacteria was not significantly reduced. Nuntakumjorn et al. (2008) concluded that chitosan powders does not enhance the granulation process and UASB performance.
The conditioning with air and / or liquid gas to adjust the technical combustion characteristics may influence both the methane number and the condensation of higher hydrocarbons in the combustion gas mixture.
The methane number — equivalent to the octane number of petrol — is a statement of the antiknock properties of fuel combustion in a engine, where the term anti-knock refers to the tendency to uncontrolled and undesirable self-ignition. Methane has by definition a methane number of 100, hydrogen a methane number of 0. A methane number of 80 for example means that the gas mixture associated with this methane number has the same antiknock properties as a mixture of 80% vol. methane and 20 vol. -% hydrogen. Some inert mixture components such as CO2 increase the methane number, higher hydrocarbons, reduce it. The calculated methane numbers (Gascalc, E. on Ruhrgas) of L gases are generally greater than those of H gases (nitrogen not factored out). As a lower limit for the smooth operation of modern engines, a methane number of MZ > 70 is considered necessary (DIN 51624, 2008).
For multi-component mixtures such as natural gases, the condensation and boiling curves do not lie together, but span a conditional area, where different gas-liquid compositions are possible. Between the critical pressure and the cricondenbar point with increasing temperature, and between the critical temperature and the criconden therm point with falling pressure, condensate (retrograde condensation) can form when the throttle curve touches the dew line, intersects or the final state lies in the two-phase region (Honer zu Siederdissen & Wundram, 1986).
An admixture of propane / butane to natural gas and processed biogas generally manifests itself in a shift of the dew curve to higher temperatures. According to (Oellrich et al., 1996), in the case of Russian H gas, condensation is only to be expected at temperatures of -35 ° C, while it will occur with Dutch L gas already at -5 ° C. If liquid gas/air is admixed within the limits described in DVGW worksheet G 260, the criconden therm point moves toward +15 ° C or +45 ° C, but at higher pressures. For mixtures of natural gas and processed conditioned biogas, this is to be expected to a lesser degree, since the concentrations of propane / butane are correspondingly smaller.
It should be noted that the calculation of the condensation curves of natural gases requires an analysis that takes into account the higher hydrocarbons, since even small amounts in the ppm range result in a significant shift. Furthermore, the process of condensation is not in itself critical, but the quantity of condensate is the decisive criterion. For large flow rates, a seemingly low volume of condensate can therefore lead to problems (Oellrich et al., 1996).
The following Table 10 and Figure 13 show cases of condensation in conditioning by the addition of LPG, in order to meet the North Sea I specification. The lowest and the highest admixtures were selected for the diagrams. It should be noted that at the highest level of admixing, the restrictions imposed by G 486 were not observed.
Initial concentration of CH4 in the biogas in Vol.-% |
LPG addition to biogas in Vol.-% |
Calorific value in kWh/m3 |
Wobbe Index in kWh/m3 |
rel. Density |
Methane number |
94,000 |
9,400 |
11,960 |
14,339 |
0,696 |
71 |
94,000 |
12,600 |
12,432 |
14,642 |
0,721 |
67 |
96,000 |
8,100 |
11,965 |
14,654 |
0,667 |
72 |
96,000 |
11,300 |
12,442 |
14,946 |
0,693 |
67 |
98,000 |
6,800 |
11,970 |
14,998 |
0,637 |
73 |
98,000 |
9,900 |
12,438 |
15,268 |
0,664 |
67 |
99,500 |
5,800 |
11,971 |
15,276 |
0,614 |
74 |
99,500 |
8,900 |
12,443 |
15,534 |
0,642 |
67 |
Table 10. Cases of condensation for mixtures of the North See I H gas specification |
Kondensationslinien (SRK-Gleichung)
Fig. 13. Condensation curves for mixtures of the North See I H gas specification
In summary, it can be said that the criconden therm points of the H gases in Germany lie below temperatures of -20 ° C. An exception to this are the higher caloric mixtures of the North Sea quality — here, 0 ° C is also possible. However, the mixtures were ignored in the calculation of the limits in G 486 and DIN 51 624, so that it applies mainly to the higher LPG quantities added. Generally, this means that process procedures, in which pressure and temperature lie in the two-phase region, should be avoided.
This section shows a summary of all the mixing rates of LPG and / or air to attain the base gas properties under consideration.
The use of biogas has a potential improve the quality of life in the rural areas through reduced drudgery in women and children, reduced indoor smoke, improved sanitation and better lighting (Amigun and Blottnitz, 2011). Wood fuel gathering is a hard and time consuming duty for women. For instance, it is estimated that women can spend 2-6 hours in collecting wood fuel (DFID, 2002) depending on the country and region. For instance, one study in Limpopo, South Africa found that the rural women spend 5-6 hours (Masekoameng et al., 2005), while another study in a different region of South Africa report that the women spend over two hours. This takes away time that could be better utilized in other productive activities such as income generation or education particularly for girls who have to be absent from school to undertake such task. Biogas plants thus can help in reducing the workload of women and girls in collecting firewood.
health problems caused by the smoke inherent to traditional ways of cooking and heating, particularly open fires include: sneezing, nausea, headache, dizziness, eye irritation and respiratory illnesses (Onguntoke et al., 2010). Biogas improves health of the rural people by providing a cleaner cooking fuel thus avoiding these health problems. Women and children have the greatest risk of these health problems and children under 5 years are at high risk of contracting acute respiratory illnesses such as, pneumonia. Often, the rural population are also faced with lack of sanitation, resulting in water borne diseases affecting mainly women and children. Operating a biogas plant implies that manure is directly fed to the plant keeping the kitchen smoke free and farmyard cleaner.
Anaerobic microorganisms, especially methanogens are highly susceptible to changes in environmental conditions. Many researchers evaluate the performance of an anaerobic system based on its methane production rate because methanogenesis is regarded as a rate — limiting step in anaerobic treatment of wastewater. Methanogens are highly vulnerable and extremely low growth rate in an anaerobic treatment system require careful maintenance and monitoring of the environmental conditions. A temperature change in the substrates or substrates concentration can lead to shutdown of gas production (Novaes, 1986).
The microbial metabolism processes are dependent on many parameters, so that for an optimum fermenting process, numerous parameters must be taken into consideration and be controlled. Some of these environmental conditions are shown in the Table 1 (Deublein and Steinhauser, 2008). A brief discussion of the factors more reported in literature is shown follows.
Operation Parameters |
Inhibitors |
Hydrogen partial pressure |
Oxygen (O2) |
Concentration of the microorganisms |
Sulfur compounds |
Type of substrate |
Organic acids (fatty acids and amino acids) |
Specific surface of material |
Nitrate (NO3-) |
Disintegration |
Ammonium (NH4+) and ammonia (NH3) |
Cultivation, mixing and volume load |
Heavy Metals |
Light and Mixing |
Tannins |
Temperature |
Disinfectants, herbicides and insecticides |
Alkalinity and pH |
Degree of decomposition of organic matter |
Organic Loading Rate (OLR) |
Foaming |
Nutrients (C/N/P-ratio) Trace elements |
Scum |
Precipitants (calcium carbonate, MAP, apatite) Biogas removal |
Table 1. Environmental conditions and inhibitors in the degradation methanogenic (Deublein and Steinhauser, 2008). |