J. Environ. Eng. Manage., 20(1), 9-17 (2010) 9 CO2 EMISSION FROM MUNICIPAL SOLID WASTE INCINERATOR: IPCC FORMULA ESTIMATION AND FLUE GAS MEASUREMENT Tsao-Chou Chen and Cheng-Fang Lin* Graduate Institute of Environmental Engineering National Taiwan University Taipei 106, Taiwan Key Words: Municipal solid waste, incineration, greenhouse gases, statistical analysis, carbon dioxide ABSTRACT Although most of the air pollutants can be removed with air pollution control facilities, the greenhouse gas (carbon dioxide) is unavoidably released into the atmosphere from the flue gas during waste incineration. The amounts of CO2 emitted from municipal solid waste incinerators are usually estimated following the guidelines set down by the Intergovernmental Panel on Climate Change (IPCC). However, there is lack of studies investigating the difference between IPCC estimation and actually measured values from the waste incinerators. In this study, the substantial CO2 emissions from Taipei City's three incinerators were compared with the estimated figures with IPCC Guidelines. In both cases, the seasonal emission data exhibit non-normal distribution. Statistical analysis depicts a significant difference of 71% in the 95% confidence interval between the emission estimated from the IPCC Guidelines and the flue gas measurements. The correlation between the waste components and the emissions was evaluated as well. The results of the correlation analysis for the components of waste material and CO2 emissions show that there is a significant correlation between plastics and the IPCC estimated emission and there is a significant correlation with garden trimmings for the measured CO2 emissions. INTRODUCTION Incineration is currently the preferred treatment operation for municipal solid wastes (MSW). Theoretically and virtually, all the volatile carbon content in MSW will be converted into CO2 emissions. During incineration of MSW, most of the greenhouse gases (GHGs) in the emissions consist of CO2 and N2O, of which CO2 being higher and more important than N2O [1-3]. CO2 emissions, in particular, have played the most significant role on global warming [4]. In densely populated urban areas, the scarcity of land and a desire to promote waste disposal makes incineration, the primary alternative of waste disposal. This makes the CO2 emissions generated during the incineration process and their effect on climate change an important issue for municipal authorities to tackle with MSW management. By applying the life-cycle inventory method and incorporating a compensatory system for waste, a unit function for emissions may be set up to assess the amount of GHGs released by different types of waste disposal schemes. Studies have shown *Corresponding author Email: [email protected] that when the different types of waste disposal methods are ranked based on their contribution to GHG, waste recycling will contribute to the smallest amount of GHG emissions, while incineration is second lowest to waste recycling [1,5-7]. The CO2 released from biomass materials (e.g. paper, food and wood waste) during incineration is excluded from the GHG assessment [1-3] and this will help to lower GHG emissions. The recovery of residual metals from incineration and the conversion of thermal energy from the burning process into electricity also offset GHG emissions. This may be due to displaced electric utility generation and decreased energy consumption for the production processes using recycled inputs [1]. The Intergovernmental Panel on Climate Change (IPCC), however, includes the fossil and biogenic CO2 emissions produced for waste incineration with energy recovery when assessing GHG emissions. Fossil CO2 emissions are included into the national emissions under the energy sector, while biogenic CO2 emissions should be included in the energy sector and report as an information item [3] for avoiding double counting J. Environ. Eng. Manage., 20(1), 9-17 (2010) 10 activity data with energy sector. While there has a separate set of guidelines for the CO2 emissions produced when waste disposal is used to generate energy, there is still some difference in emission offset between the method adopted for calculating CO2 emissions and the method used by the U.S. Environmental Protection Agency when looking at the conversion of thermal energy from waste incineration into electricity and the recovery of residual metal in the waste management sector. The default emission factors from the IPCC formula was widely used by the most communities for assessing CO2 emissions during waste incineration. Hence, it is highly possible to perceive a significant discrepancy between the assessed emissions and the actual emissions. The Kyoto Protocol requires the signatory states to commit to a reduction in GHG emissions and to set up a GHG emissions trading scheme. This makes the question of a discrepancy between the CO2 emissions released by the MSW incinerator during the burning process and the IPCC assessed value an important one. Relevant data from cities with a comprehensive waste management system are therefore needed in order to conduct an in-depth study and analysis of IPCC estimates and actual CO2 emissions. Almost every country has set environmental regulations that limit the emission of pollutants in the flue gas from incinerators when burning the waste. Environmental authorities also set methods and procedures to measure concentrations of concerned pollutants. There is, however, little regulation of CO2 emissions that could provide actual amount of CO2 generated in a MSW incinerator. The objective of this study is to investigate the difference between the IPCC default values for calculating the CO2 emissions in a MSW incinerator and the actual measured values from the flue gas during actual operations. MATERIALS AND METHODS factors from 2006 IPCC Guidelines for National Greenhouse Gas Inventories [3] were used in estimating the CO2 emissions over three successive years (2005-2007) for the studied area and were compared with the actual CO2 measurements in the flue gas released from Taipei City incinerators during regular operation over the same period. Pre-processing, postprocessing and the environmental effects of GHGs that might be indirectly emitted in the waste management system will not be considered. Electricity was not treated as a substitute for emission volume in order to comply with the IPCC Guidelines method for calculating CO2 emissions. 2. Estimation of IPCC CO2 Emissions from Flue Gas The IPCC formula for calculating CO2 emissions from waste incinerator uses the fossil carbon content burnt in the waste as the input parameter. The product of the oxidation factor and amount of fossil carbon oxidized give the CO2 emission. The related data involve the waste components, total mass, dry matter content, total carbon content, fossil carbon fraction and oxidation factor. The collection, transportation and incineration/disposal of waste in Taipei City are all carried out by government authorities. The defined categories of waste were household waste, garden (yard) and park waste, and commercial/institutional waste. This agrees well with the general definition for MSW used in the IPCC Guidelines [3]. According to CO2 emission estimation method suggested by the IPCC Guidelines, this study used Tier 2a method [3] to estimate the amount of CO2 emissions produced by incineration after wastes were transported to the incinerator and were sampled to reveal the waste physical composition. To facilitate the comparison of the CO2 emissions from each unit of waste incinerated, the estimation method was modified as follows: CO2 Emissions = MSW 1. Data Acquisition The Taipei City is the studied region in this research. The total city area is 271.8 km2 and the population is 2.6 million with an average population density of 9,700 people km-2. Three incinerators have been built in Neihu, Muzha and Beitou since 1991. The three incinerators have a capacity of handling 3,900 t d-1 of municipal refuse. All three city incinerators were equipped with air pollution control devices (APCDs). Neihu and Beitou incinerators have semidry scrubbers, activated carbon and bag house, while the Muzha incinerator has an electrostatic precipitator, wet scrubber and catalytic oxidation unit. The main function of the APCD is to reduce and remove particulates, acid gases [8,9], dioxins [10] and heavy metals emitted into the atmosphere from the flue gas. The MSW CO2 emissions formula and emission ∑ (WF j j dm j CF j FCF j OF j ) 44 3 10 12 (1) where CO2 emissions in kg t-1 waste; MSW = mass of municipal solid waste as wet weight incinerated, t waste; WFj = fraction of waste type/material of component j in the MSW (as wet weight incinerated); dmj = dry mass content in the component j of the MSW incinerated, (fraction); CFj = fraction of carbon in the dry matter (i.e., carbon content) of component j; FCFj = fraction of fossil carbon in the total carbon of component j; OFj = oxidation factor, (default value for MSW = 100%); 44/12 = conversion factor from C to CO2; 103 = conversion factor from t to kg; j = component of the Taipei City’s MSW incinerated; and ∑ WF j j = 1. Chen and Lin: CO2 Emission from MSW Incinerator 3. Sampling and Calculation of CO2 Emissions from Flue Gas Taiwan environmental regulations require MSW incinerators to file reports as stationery sources on a quarterly basis each year. The reports have to present measurements for particulate, acid gases, heavy metals and dioxins [11]. As carbon dioxide emission is not the required monitored parameter, CO2 emission data were not directly obtainable. Therefore, CO2 emission was calculated by taking CO2 fractional composition from quarterly flue gas measurements using the dry gas calibration values over 3 successive years (2005-2007). The following formula was employed to calculate CO2 generation for a total of 36 samples. CO2 (mg m-3) = [CO 2 (%)]( 10 4 )[44 (g mol -1 )] 22.4 (L mol-1 ) (2) CO2 (kg h-1) = [CO2 (mg m-3)][dry gas (Nm3 min-1)] [60 (min h-1)][10-6 (kg mg-1)] (3) The hourly CO2 emissions thus obtained is then divided by the hourly waste-combustion rate. These result in the measured CO2 emissions in the flue gas per each metric ton of wet waste incinerated. 4. Data Processing and Analysis Data collected for CO2 emissions of the three Taipei City incinerators were on a quarterly basis from 2005 through 2007 from the flue gas emissions. The monitored values and estimation methods were then used to generate 36 emission samples to facilitate statistical analysis [12]. The emission unit used was 11 the CO2 emissions per ton of wet MSW (CO2 kg t-1 waste). Using the results of combustible fractions in received waste [13-15], the combustible materials burned at each incinerator and the actual flue gas measurements from three incinerators, the quarterly CO2 emissions data were sorted and statistically analyzed. All the statistical tests were carried out using SPSS 11.0 (SPSS Inc., Chicago, USA). RESULTS AND DISCUSSION 1. Analysis of Measured CO2 Emissions The descriptive statistics of flue gas measurements and the fraction of combustible material in waste over the past 3 years are shown in Table 1. Flue gas measurements gave mean of 964 kg t-1 waste for CO2 emissions from 36 samples with a standard deviation of 187 kg t-1, indicating significant variation between the individual measurements. The amount of CO2 emitted during incineration is affected by the differences in the burned waste components. Among the waste categories, the greatest variations in individual sample values was food waste with a standard deviation of 11.9 and the mean variance over 3 years was 23%. This shows that biogenic and fossil carbon fraction in the waste are the major uncertainty factors, due to a variety of MSW [16]. In the IPCC Guidelines, Taiwan is assigned to the South-Eastern Asia where the default value for the food waste component is 43.5%. The actual food waste measurements from Taipei City were therefore obviously lower than the IPCC default at 47%. Comparative analysis shows that the percentage of food waste in Taipei City MSW is also lower than the IPCC's global default value of 39.5% (the lower and upper bounds of global food Table 1. Statistics of the measured CO2 emission and Taipei City MSW components 95% Confidence Interval for Mean Lower Upper Std. Deviation Minimum Maximum 1,027 187 635 1,630 38.0 3.0 44.4 5.3 9.5 3.4 22.6 0.0 56.7 12.0 4.8 23.4 19.7 1.4 0.5 3.2 19.4 17.4 0.4 8.6E-02 6.3 27.4 22.1 2.4 0.9 4.6 11.9 6.9 2.9 1.1 1.1 10.1 6.8 0.0 0.0 23.3 46.4 48.7 12.0 6.5 1.2 0.6 2.5 0.7 0.8 0.4 1.8 0.3 1.5 0.8 3.3 1.2 1.0 0.6 2.2 1.3 0.0 0.0 0.0 0.0 4.0 2.3 7.5 6.3 N Mean Measured CO2 emission (kg t-1 waste) 36 964 901 Combustible fraction Papers (wt%) Textiles (wt%) 36 36 41.2 4.1 36 36 36 36 36 36 36 36 36 Garden trimmings (wt%) Food waste (wt%) Plastics (wt%) Leather and rubber (wt%) Others (wt%) Incombustible fraction Iron (wt%) Other metal (wt%) Glass (wt%) Others (wt%) J. Environ. Eng. Manage., 20(1), 9-17 (2010) 12 Expected normal 2 agrees with the results of the significance test and probably does not follow normal distribution (Fig. 1a). The emission data would therefore tend to follow a lognormal distribution [3,18]. (a) 1 2. Analysis of Estimated CO2 Emissions 0 -1 -2 400 600 800 1000 1200 1400 1600 1800 Measured value (CO2 kg t-1 waste) Expected normal 2 (b) 1 0 -1 -2 0 200 400 600 800 1000 1200 1400 Estimated value (CO2 kg t-1 waste) Fig. 1. Q-plot of (a) measured and (b) estimated CO2 emissions in flue gas from incinerated MSW. waste fractions were 34 and 45% respectively with a confidence interval of 95%) [3]. The average amount of CO2 emissions (964 kg t1 ), is less than 1,179 kg t-1 emitted in France [17]. Thus, it is reasonable to state that the default values assigned by the IPCC on a regional basis for developed, developing and other countries around the world are not justified. To explore the distribution of measured CO2 emissions, the Shapiro-Wilk normal test was used, as there were less than 50 samples available. The statistics value is found to be 0.932 with the significance probability (p) of 0.044. The null hypothesis was rejected as the p value is less than 0.05. The skewness was 1.086 (positively skewed) with the Kurtosis coefficient of 3.307 (leptokurtic), indicating that CO2 emissions follow a non-normal distribution. The measured data from the 3-year period were sorted in ascending order and tested using the normal probability plot. These results show that the cumulative probability of the observations diverged from the straight line of cumulative probability distribution defined by the normal distribution theory. These results show that the distribution of measured CO2 emissions in flue gas Using the IPCC Guidelines, the estimated CO2 emissions from 36 samples have a mean and standard deviation of 567 and 187 kg t-1 waste, respectively. The mean CO2 emission was lower than the measured value of 397 CO2 kg t-1 waste, or 41% of the mean measured emission. The individual variation between the estimated values was also greater than the measured emissions. The statistics of the measured, estimated and calibrated flue gas CO2 emission is shown in Table 2. To investigate the distribution of the estimated CO2 emissions based on MSW components, the same hypothesis of normal distribution test was used here. The Shapiro-Wilk normal test gave the statistic of 0.849. The null hypothesis is rejected as the significant probability p = 0.010 (< 0.05). The skewness thus calculated was 2.071 (positively skewed) with a Kurtosis coefficient of 7.720 (leptokurtic), indicating that the estimated CO2 emission from the IPCC Guidelines does not follow a normal distribution. The estimated emissions were also clustered more closely to the mode and around the lower bound compared to the measured emissions with some extreme data points near the upper bound. The data have trouble breaking the lower boundary of the emissions and tend to extend towards the high end as well. This kind of skewed result is referred to in statistics as the "floor effect". Here it is probably the result of the limits imposed by the waste categories' default emission factors. When tested against the normal probability plot (Fig. 1b), the results show that most of the plots have a cumulative probability variance diverged from the normal distribution theory's cumulative probability distribution line. The divergence is also more obvious than the distribution chart for the measured emissions (Fig. 1a), showing that the distribution of the CO2 emissions in the incinerators' flue gas estimated from the components of the incinerated MSW agrees with the results of the significance test that it does not follow normal distribution model. 3. Analysis of CO2 Emissions from Incinerated MSW For the estimated and measured CO2 emissions from the incinerators, first, the total amount of MSW and the components of the waste incinerated quarterly over 3 years were added up then multiplied against the estimated and measured CO2 emissions for each ton of MSW incinerated in each quarter and in each year. Then, they were added up on a quarterly basis in order Chen and Lin: CO2 Emission from MSW Incinerator 13 Table 2. Statistics of the measured, estimated and calibrated flue gas CO2 emission 95% Confidence Interval for Mean Lower Upper N Mean Std. Deviation Minimum Maximum Measured CO2 emission (kg t-1 waste) 36 964 901 1,027 187 635 1,629 Estimated CO2 emission (kg t-1 waste) 36 567 503 630 187 238 1,343 Calibrated CO2 emission (kg t-1 waste) 36 970 861 1,077 320 408 2,296 Table 3. Descriptive statistics for waste incinerated and CO2 emissions each quarter in Taipei City, 2005-2007 Waste incinerated (t) Measured CO2 emission (t) Estimated CO2 emission (t) N Total Amount 12 12 12 1,843,600 1,775,000 1,014,200 to calculate the estimated and measured CO2 emissions from the incineration of Taipei City MSW. The formula is as follows: ∑ (IM −3 pij W pij 10 ) (4) ij EEij = ∑ (IE pij W pij 10 −3 ) (5) ij where MEij = measured CO2 emission in flue gas after MSW incineration (CO2 ton per quarter, i: year, from 2005-2007; j = quarter (1-4)); IMpij = measured CO2 emission in flue gas per ton of MSW from each incinerator each quarter in each year) (CO2 kg t-1 waste; p: incinerator, Neihu, Muzha and Peitou); Wpij = amount of MSW incinerated from each incinerator each quarter in each year (ton per quarter); 10-3 = conversion factor from kg to t; EEij = estimated CO2 emission in flue gas from incineration of MSW (CO2 ton per quarter); IEpij = estimated CO2 emission in flue gas per ton of MSW from each incinerator each quarter in each year (CO2 kg t-1 waste). The results from this study on the amount of incinerated waste and their CO2 emission are summarized as descriptive statistics in Table 3. The calculations and statistical analysis give 12 sample points for the amount of waste incinerated each quarter as well as the measured and estimated CO 2 emissions (Table 3). There was a total of 1,843,600 t of MSW incinerated in Taipei City. Using the quarterly flue gas measurements and incineration volume, the total CO2 emissions over the three years was 1,775,000 t. The IPCC Guidelines uses a separate method that calculates the total emissions based on the components, default emission factors and incineration volume. IPCC formula gave a total for CO2 emissions of 1,014,200 t over the three-year period. A comparison of the two results shows that, while conditions such as the MSW incineration volume and component Std. Deviation 12,700 15,100 16,000 Measured emission Estimated emission 180000 160000 Emission of CO2 in Ton MEij = Quarterly amount Maximum Mean 177,000 153,600 171,700 147,900 119,600 84,500 Minimum 140,200 124,400 62,000 140000 120000 100000 80000 60000 40000 20000 0 1st 2nd 3rd 4th 1st 2nd 3rd 4th 1st 2nd 3rd 4th 2005 2006 2007 Quarters Fig. 2. Comparison of quarterly measured and estimated CO2 emissions from incinerated MSW. for each quarter over the 3 years are identical, both CO2 emissions are different. Figure 2 shows quite clearly that the measured CO2 emissions in flue gas were significantly higher than the values calculated using the IPCC Guidelines. The difference in CO2 emissions over the three years was as high as 760,800 t. The mean measured CO2 emissions from the three incinerators each quarter over three years compared to the mean CO2 emissions estimated using the IPCC Guidelines was significantly lower by 397 kg t-1 of MSW incinerated. If the average amount of waste incinerated in each quarter over the three years was used as a reference, the emissions using the IPCC Guidelines is, on average, 63,400 t less CO2 emissions for each quarter, and 253,600 t less CO2 emissions each year. According to the IPCC Guidelines, this difference in estimated CO2 emissions could, through the emission exchange system, convert to 447,600 t of MSW for incineration. This implies that there was a 14 J. Environ. Eng. Manage., 20(1), 9-17 (2010) discrepancy in the amounts of MSW incineration/disposal. The major difference may be due to the biogenic CO2 emissions in the incinerated waste not being deducted from the measured CO2 emissions in the flue gas. The IPCC, therefore, recommends the use of field sites measurements for emissions in order to reduce the uncertainty and discrepancy of CO2 emission [3,16]. 4. Analysis of CO2 Emissions and Component of MSW After statistically testing the distribution of measured and estimated CO2 emissions, it is ascertained that the emissions were non-normal in their distribution and there are some obvious discrepancies in practice. This study intended to determine if the estimated fossil carbon component in MSW significantly affected the measured CO2 emissions in the flue gas during incineration and if the amount of emissions exhibited any correlation with the components of MSW. The non-parametric statistical test was used to test divergence and correlation. This avoids the prerequisite assumption of normality and homogeneity of variance used in parametric statistics. First, the variance between the measured and estimated CO2 emissions in flue gas was tested. Wilcoxon signed-ranks test was used in order to take the magnitude of the variance and its positive and negative signs into account. Results of the test are shown in Table 4. Table 4 shows that the estimated CO2 emissions using the components of incinerated waste according to IPCC Guidelines are lower than the actual measured CO2 emissions in flue gas in 34 samples (negative ranks row) and higher than the actual measured CO2 emissions in 2 samples (positive ranks row). The test converts the magnitude of the variance in estimated and measured emissions into absolute ranks. Taking the 34 CO2 emissions with values lower than the measured values' mean rank of 19.0 and the 2 CO2 emissions with values higher than measured values' mean rank of 10.5, the variance between the means of these two ranks were then tested if they were statistically significant. The test results are shown in Table 4. The variance test of the two mean ranks gives a Z value of -4.902, and double-sided testing gives a p value of 0.000 (< 0.05), showing that the IPCC estimated emissions when compared to actual measured emissions results in a visibly different and lower value for CO2 emissions in flue gas. From the analysis, it is justified to state that in practice MSW incineration counted more CO2 emissions. It is therefore necessary to understand how the estimate produced using the IPCC Guidelines can be corrected in order to match a better amount of CO2 released into the atmosphere from the flue gas after MSW incineration. This will help preserve the fairness of the GHG emissions trading scheme. First, the means for the measured CO2 emissions and the IPCC Guidelines’ estimated emissions were established. The difference between the upper and lower bounds for both values (95% confidence interval) were divided by the difference between the upper and lower bounds for the IPCC estimates (95% confidence interval). The resultant upper and lower bounds accounted for around 63 and 79% of the original estimates, respectively. Using the difference between the two, one can find the mean of 71% as a calibration factor. To determine if there was a difference between the calibrated CO2 emission and the measured CO2 emission in flue gas after the correction factor is substituted into the IPCC estimate, the 36 estimated CO2 emission samples were each multiplied by a coefficient of 1.71 to correct the emission. The Wilcoxon signed-ranks test was then used to analyze the variance between the measured CO2 emission and calibrated CO2 emission. Table 4. Wilcoxon signed-ranks test on CO2 emission in flue gas N Negative ranks Positive ranks Ties Total Negative ranks Calibrated CO2 emission — Measured Positive ranks CO2 emission Ties Total a Estimated CO2 emission < Measured CO2 emission b Estimated CO2 emission > Measured CO2 emission c Estimated CO2 emission = Measured CO2 emission d Calibrated CO2 emission < Measured CO2 emission e Calibrated CO2 emission > Measured CO2 emission f Calibrated CO2 emission = Measured CO2 emission g Based on positive ranks. Estimated CO2 emission — Measured CO2 emission 34a 2b 0c 36 21d 15e 0f 36 Mean rank 19.0 10.5 17.3 20.1 Sum of ranks 645 21 Z test Asymp. Sign (2-tailed) -4.902g 0.000 -0.487g 0.626 364 302 Chen and Lin: CO2 Emission from MSW Incinerator The result showed that the two mean ranks returned a variance test result Z of -0.487. In double-sided test, the p value was 0.626 (> 0.05). This did not reach the 0.05 required for significance. The null hypothesis that the estimated and the calibrated emission had equivalent mean ranks can therefore be accepted. This test indicated that the measured CO2 emission and the IPCC Guidelines' estimated emission multiplied by the calibration factor of 1.71 had no significant variance as shown in Table 4. When comparing the mean measured CO2 emission of 964 kg t-1 waste and the mean calibrated CO2 emission of 970 kg t-1 waste, the variance between the two is 6 CO2 kg t-1 waste, or 0.6% of the mean measured CO2 emission. This shows that there is no statistical difference between the calibrated CO2 emission data and the measured CO2 emission in flue gas. To facilitate the comparison of the descriptive statistics for calibrated emission with the measured emissions, the data were listed in the calibrated CO2 emissions shown in Table 2. The IPCC CO2 emission was estimated based on the components of the MSW. There are uncertainty factors involved when collecting and analyzing samples of waste components [16]. For better understanding of the causes of the variance, the degree of association between CO2 emission and waste component was analyzed. Using the Spearman rank order correlation coefficient, the correlation between the two was calculated as shown in Table 5. The correlation coefficients in Table 5 form a correlation matrix. The correlation coefficient rs was calculated by taking the pair-wise difference in two variables for each sample value to analyze their correlation. The result is between -1 and 1, and the closer the value is to ±1, the higher the level of correlation. From Table 5, it may be seen that the significant correlation exists between the measured CO2 emission in the incinerated MSW and its components in the following categories: garden trimmings and food waste. The two correlation coefficients are 0.401 positive correlation and -0.493 negative correlation, with the 15 variance of 16 and 24%, respectively, suggesting a medium level of correlation. With CO2 emission calculated using the IPCC Guidelines, significant correlation existed for food waste, others and plastics. The correlation coefficients were -0.524, -0.540 and 0.985, with variances of 27, 29 and 97% respectively. Food waste and others both have a medium degree of negative correlation, while plastics have high degree of positive correlation. According to the IPCC Guidelines, plastics default dry matter content, total carbon content and fossil carbon fraction values are 100, 75 and 100%, respectively. The estimated CO2 emission above and the correlation test with MSW content indicate that the magnitude of estimated CO2 emissions using the IPCC Guidelines is affected by the default values for dry matter content and carbon content. This is the reason why plastics with a default dry matter content and carbon fossil fraction of 100%, have a high degree of correlation with the emissions. The explained variation between the two is 97% as well, so the higher plastic content in the waste components translates to more statistical significance when calculating the estimated CO2 emissions. For the measured CO2 emissions in flue gas, however, if biogenic CO2 was not excluded then the plastics correlation coefficient is just 0.137, its explained variation just 1.9% and is not statistically significant. At the same time, a significant positive correlation existed between the measured CO2 emission and the MSW component for garden trimmings. This, however, was assigned a fossil carbon fraction of 0% in the IPCC Guidelines. And while the explained variation between two are just 16%, it still exhibits a medium degree of significant correlation statistically. If the fraction of garden trimmings in MSW components increases then their statistical significance on the measured CO2 emission in flue gas would increase as well. The only category to show statistical significance for both measured and estimated CO2 emissions in the correlation with MSW components is the food waste. The rest of the components have a negative correlation. The variation was 24 and 27% respectively. According to IPCC Guide- Table 5. Correlation coefficient between MSW component and CO2 emissions Measured CO2 emission (rs) Sig. (2-tailed) R2 Papers Textiles Garden trimmings Food waste Plastics Leather and rubber Others 0.244 0.152 0.059 0.178 0.300 0.032 0.401* 0.015 0.160 -0.493** 0.002 0.243 0.137 0.427 0.019 -0.161 0.347 0.026 -0.250 0.141 0.063 -0.524** 0.001 0.274 0.985** 0.000 0.970 -0.124 0.471 0.015 -0.540** 0.001 0.292 Estimated CO2 0.043 emission (rs) 0.084 0.805 0.626 Sig. (2-tailed) 0.002 0.007 R2 *Correlation is significant at the 0.05 level (2-tailed). **Correlation is significant at the 0.01 level (2-tailed) -0.078 0.652 0.006 16 J. Environ. Eng. Manage., 20(1), 9-17 (2010) lines, food waste was assigned a default value of 38% for total carbon content in percent of dry weight. This is the lowest default value out of all of the MSW components, showing that food waste has a lower total carbon content compared to other MSW components. Therefore, food waste, compared to other waste materials of equivalent mass, produces significantly less CO2 emissions after incineration. Hence, this phenomenon is presented in the correlation test for both measured and estimated CO2 emissions. When estimating CO2 emissions, the IPCC Guidelines eliminates the CO2 emissions from food waste, garden trimmings and paper as they are biogenic in origin. While for measured CO2 emissions in flue gas, incinerating food waste contributes significantly less CO2 emissions when compared to other waste categories. Garden trimmings provide significantly higher contribution of CO2 emissions while paper exhibits less significance difference. These might be the main causes for the difference between the IPCC estimation and the actual measured values in Taipei City. trimmings and plastics therefore merits further study because they achieved statistically significant correlation with the measured and estimated CO2 emissions. This would reduce the greater tendency for this type of waste to release CO2 emissions directly into the atmosphere during incineration. To avoid excessive divergence between the estimated emissions and the actual measured CO2 emissions in flue gas and help maintain the fairness of future international emission trading schemes, and to better manage and understand the amount of carbon dioxide emitted into the environment, the 95% confidence interval values from the descriptive statistics of waste components' combustible fraction (Table 1) can be used for comparison. If the component fraction used for the estimation falls within the mean confidence interval, then multiply the total CO2 emissions estimated using the IPCC Guidelines by the calibration factor of 1.71. This will provide a better estimate of the actual total CO2 emissions released into the atmosphere from MSW incineration. REFERENCES CONCLUSIONS AND RECOMMENDATIONS When no flue gas emission measurements are available, IPCC Guidelines offers default emission factors to generate a quick and convenient way of estimating the CO2 emissions from waste incineration. The CO2 estimate produced using the IPCC method, however, is prone to differences between the actual emissions. In this study, the measured CO2 emissions in flue gas from MSW incinerators in Taipei City were compared with the estimated emissions using IPCC formula. The results show that both data follow non-normal distribution and the emissions are significantly different in terms of their statistical and practical significance. For a confidence interval of 95%, the IPCC estimates are significantly different from the measured emissions in flue gas by 71%. As for waste categories that affect CO2 emissions of actual incinerating operations, garden trimmings show a positive correlation while the food waste shows a negative correlation. The variations for the two are 16 and 24% respectively. As for the waste categories that exhibit a significant discrepancy based on the IPCC Guidelines’ default emission factor for incinerated waste and their estimated emissions, food waste and the other components show a negative correlation with a variation of 27 and 29%, respectively. Plastics exhibit a high degree of positive correlation with an explained variation of 97%. The fraction of food waste, garden trimmings and plastics in MSW components therefore are key factors affecting the CO2 emissions in the flue gas. The CO2 emissions contributed by these types of waste in the flue gas are probably the main cause of the difference between measured and estimated emissions. The choice of disposal methods for garden 1. U.S. Environmental Protection Agency (USEPA), Solid Waste Management and Greenhouse Gases: A Life-cycle Assessment of Emissions and Sinks. 3rd Ed., USEPA, Washington, DC (2006). 2. 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Discussions of this paper may appear in the discussion section of a future issue. All discussions should be submitted to the Editor-in-Chief within six months of publication. Manuscript Received: May 11, 2009 Revision Received: August 23, 2009 and Accepted: September 9, 2009
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