Research article Topical Sections

Evolution of activation energy during hot deformation of Al–15% B4C composites containing Sc and Zr

  • During hot deformation, the activation energy, Q, is an essential parameter that indicates the difficulty level in the hot working processing. The evolution of the activation energies of three Al–15% B4C composites (the base material, S40 with 0.4% Sc and SZ40 with 0.4% Sc and 0.2% Zr) was investigated using high-temperature flow stress data based on a revised Sellar’s constitutive equation. The microstructure evolution during hot deformation was characterized using a transmission electron microscope. The calculated activation energy maps reveal that the activation energy during hot deformation was related to the microstructure change in addition to deformation conditions. For the base composite, the variation of the activation energy was small because the microstructure barely changed during deformation. For the Sc and Zr containing composites (S40 and SZ40), dynamic precipitation occurred at high deformation temperature and the activation energy map can be divided in two regions. The activation energy decreases with an increase of deformation temperature to the minimum level in the region I where the composites were in the solid solution condition. It follows by an increase with increasing temperature in the region II where dynamic precipitation occurred. Based on the combination of the activation energy map with the flow instability zone, the optimum hot workability of a composite in term of excellent processability was proposed at the domain where the less energy of hot deformation was required.

    Citation: Jian Qin, Zhan Zhang, X.-Grant Chen. Evolution of activation energy during hot deformation of Al–15% B4C composites containing Sc and Zr[J]. AIMS Materials Science, 2019, 6(4): 484-497. doi: 10.3934/matersci.2019.4.484

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  • During hot deformation, the activation energy, Q, is an essential parameter that indicates the difficulty level in the hot working processing. The evolution of the activation energies of three Al–15% B4C composites (the base material, S40 with 0.4% Sc and SZ40 with 0.4% Sc and 0.2% Zr) was investigated using high-temperature flow stress data based on a revised Sellar’s constitutive equation. The microstructure evolution during hot deformation was characterized using a transmission electron microscope. The calculated activation energy maps reveal that the activation energy during hot deformation was related to the microstructure change in addition to deformation conditions. For the base composite, the variation of the activation energy was small because the microstructure barely changed during deformation. For the Sc and Zr containing composites (S40 and SZ40), dynamic precipitation occurred at high deformation temperature and the activation energy map can be divided in two regions. The activation energy decreases with an increase of deformation temperature to the minimum level in the region I where the composites were in the solid solution condition. It follows by an increase with increasing temperature in the region II where dynamic precipitation occurred. Based on the combination of the activation energy map with the flow instability zone, the optimum hot workability of a composite in term of excellent processability was proposed at the domain where the less energy of hot deformation was required.


    The tuberculosis (TB) is caused by the bacterium Mycobacterium tuberculosis. The bacteria usually attack the lungs, but TB bacteria can attack any part of the body such as the kidney, spine, and brain [1]. TB is contagious, which means the bacteria easily spread from an infected person to someone else. One can get TB by breathing in air droplets from a cough or sneeze of an infected person. Once infected, the individual is at the highest risk of developing TB disease within the first two years, and there is still no vaccine able to prevent pulmonary TB, the most common form of the disease [2,3,4]. Pulmonary TB is typical and infectious, which is responsible for 1.5 million deaths each year. Not all infected with TB bacteria becomes sick. As a result, two TB-related conditions exist: latent TB infection (LTBI) and TB disease [1].

    In mainland of China, although the governments do their best to control TB, China has the second highest number of TB cases in the world. According to the global TB report in 2018, the number of TB in China was 823,342, the death number of TB was 3149 [1]. Particularly, pulmonary TB in Jiangsu province, China, showed a slow oscillatory trend. In 2015, reported cases were 36,039 and deaths 91; 2016, cases 36,647, deaths 93; 2017, cases 28,402, deaths 97; 2018, cases 33,566, deaths 80; and 2019, cases 32,880, deaths 90 [5]. Therefore, TB is still a major infectious disease that needs to be controlled whether in China or in Jiangsu province, China.

    In order to estimate the relationship between variables described disease dynamics, a classical statistical approach is the use of time series analysis of the incident cases. For example, Ekpenyong et al. [6] established an ARMA(1,0,1)×(1,1,2)12 model to analyze and predict the monthly TB cases in University of Calabar Teaching Hospital based on data from 1990–2015. Moosazadeh et al. [7] used monthly TB incidence data recorded in the Iranian National Tuberculosis Control Program for time series analysis and selected SARIMA(0,1,1)×(0,1,1)12 as the most adequate model for prediction. Li et al. [8] used hybrid ARIMA-EGARCH model to analyze the visceral leishmaniasis data in Kashgar, China and the visceral leishmaniasis cases were simulated by ARIMA(2,1,2)(1,1,1)12-EGARCH(1,1) model, and found that the root-mean-square error was 7.23% in the validation phase, which offered a scientific basis to control visceral leishmaniasis spread in Kashgar prefecture of Xinjiang, China.

    On the other hand, in China, there is experiencing challenge of public health caused by air pollution [9]. And numerous epidemiological studies showed that air pollution associate with risk of various disease [10,11,12,13,14,15]. Recently, Peng et al. [16] found that long-term exposure to PM2.5 increases the risk of death among TB patients, and claimed that the control of ambient air pollution may help decreasing the mortality of TB. Liu et al. [17] showed that the short-term exposure of PM10 and PM2.5 could significantly increase the risk of death of residents, and the increase of PM10 and PM2.5 in short-term was significantly correlated with the total mortality, cardiovascular death and respiratory death. Tang et al. [9] and He et al. [18,19] focused on how air pollution affects the dynamics of epidemic models, and found that only taking sustained, long-term and high-intensity emission reduction measures can effectively reduce the air quality index and the number of respiratory cases.

    Based on the discussions above, in this study, we apply time-series approach to analyze the impact of air quantity on the spreading of TB in Jiangsu province, China during the years 2015 to 2019, and predict the trend of TB epidemic in 2020.

    The required information was collected as two parts: Information regarding TB cases: The number of TB cases was collected from the Jiangsu Disease Control Center from January 2015 to December 2019 (60 months) [5] (see Figure 1). Information regarding air pollution including air quality index (AQI), particulate matter <2.5μm in diameter (PM2.5) and particulate matter <10μm in diameter (PM10), was gathered from the National Meteorological Information Center [20] (See Figure 2 for details).

    Figure 1.  Time series of the monthly reported TB cases from January 2015 to December 2019.
    Figure 2.  Time series of the monthly AQI, PM2.5 and PM10 in Jiangsu, China from January 2015 to December 2019.

    The ARIMA model is one of the most important and basic models. According to whether the model contains seasonal components, it can be divided into continuous ARIMA(p,d,q) model, seasonal ARIMA(P,D,Q)S model and product seasonal ARIMA(p,d,q)×(P,D,Q)S model. p,d,q and P,D,Q are the order values of continuous and seasonal autoregressive (AR), difference (I), and moving average (MA), respectively. s represents a seasonal period. Briefly, the ARIMA univariate analysis models consist of 3 sub-processes: model identification, parameter estimation and model diagnosis. By repeating these three steps, the optimal prediction model is screened out [21].

    The following steps are used to fit the model:

    ● Firstly, the stationarity of the original sequence is tested by using the disease sequence diagram and Augmented Dickey-Fuller (ADF) test. If the sequence is non-stationary, in order to eliminate the trend and seasonality of the sequence, the first-order ordinary difference (d=1) and the first-order seasonal difference (D=1) are applied to make it stable. We further analyze the stationary series.

    ● Secondly, we examine the autocorrelation function (ACF) and partial autocorrelation function (PACF) graphs to identify the parameters in the model, p and q, respectively. Then, the maximum likelihood estimation (MLE) method is used to estimate the parameters in the model. In order to evaluate the suitability of the established ARIMA model, the parameters and residual of the model are tested respectively, and Ljung-Box (Q) test is applied to check whether the residual of the model is white noise.

    ● Finally, if several models satisfy the condition that the parameters are significant and the residual sequence of the model is white noise, then the optimal univariate model can be selected by using Akaike information criterion (AIC), Schwarz Bayesian information criterion (SBC) and mean absolute percentage error (MAPE) and root mean square error (RMSE) indicators of the model.

    In order to establish the optimal multivariate model, we consider the air quality variables as regression variables into the model to test whether they can improve the prediction performance of ARIMA model. The cross-correlation function (CCF) analysis is performed on the number of TB cases and climate data to find the best predictor and its optimal lag period to be included in the final model. In order to eliminate the trending and seasonal characteristics of each meteorological variable sequence, we differentially process each meteorological variable to achieve stability. Next, we perform a pre-whitening process to establish an optimal ARIMA model for each individual meteorological variable, which is used as a filter to filter the input and the output sequence. And the cross-correlation coefficient of the filtered output and the input sequence is calculated by the CCF, so the pre-whitening process is completed. By means of the Cross-Correlation diagram to judge the hysteresis relationship between the input and the output sequence, the climatic variables (P<0.05) which are significantly correlated with the number of TB cases are included in the multivariate ARIMA model.

    Simply speaking, the ARIMA model with input variables is called a dynamic regression model, abbreviated as ARIMAX. The optimal selection criteria for the ARIMAX model are still AIC and MAPE. The MAPE is calculated for training and validation data to assess the predictive validity of the models. Smaller the values of this metric indication, the better the predictive performance. The MAPE equals to:

    MAPE=100%nnt=1|XtˆXtXt|,

    where Xt is the actual value and ˆXt the forecast value. The difference between Xt and ˆXt is divided by the actual value Xt again. The absolute value in this calculation is summed for every forecasted point in time and divided by the number of fitted points n. Multiplying by 100% makes it a percentage error.

    All data are analyzed by using packages tseries,fUnitRoots,zoo,forecast and TSA of the software R (version 3.6.3). The ARIMA and ARIMAX models are constructed by using the processed data.

    From January 2015 to December 2019, there were 167,534 TB cases in Jiangsu, China. The annual TB cases were 36,039, 36,647, 28,402, 33,566, 32,880, respectively [5]. Figure 3 shows that the number of TB cases has seasonal fluctuations with an annual cycle. During the period of March, the seasonal index (or called season exponent, which is reflects a stable relationship between the average number of newly TB cases and the average number of total newly TB) is the largest.

    Figure 3.  Season index of TB cases from January 2015 to December 2019.

    Therefore, the multiplicative seasonal ARIMA model is used. The ADF test of the original sequence shows P=0.523>5%, indicating that the sequence of TB cases is not a stationary sequence. To eliminate the trend and seasonality, the original sequence is pre-processed using first-order ordinary difference (d=1) and first-order seasonal difference (D=1), then we can obtain a stationary sequence (ADF Test, P=0.01) (see Figure 4).

    Figure 4.  Time series of stationary sequence obtained from first-order ordinary difference (d=1) and first-order seasonal difference (D=1).

    Next, autocorrelation function (ACF) and partial autocorrelation function (PACF) analyses are performed. ACF shows q=0, 1 or 2, and PACF shows p=0 or 1. Considering the seasonal autocorrelation, since the data are collected monthly, S is equal to 12 (See Figure 5).

    Figure 5.  ACF and PACF figures after differencing.

    According to the criterion of minimum information, the model ARIMA(1,1,0)×(0,1,1)12 has the minimum value of AIC=670.203, AICc=670.761, SBC = 675.753 in two candidate models which are the optimal model (see Table 1).

    Table 1.  Goodness of fits for plausible ARIMA models.
    Model AIC AICc SBC
    ARIMA(1,1,0)×(0,1,1)12 670.203 670.761 675.753
    ARIMA(1,1,0)×(1,1,0)12 673.439 673.997 678.989

     | Show Table
    DownLoad: CSV

    The parameter estimation results of the model and white noise test results are shown in Table 2 and Table 3. All parameters in the ARIMA(1,1,0)×(0,1,1)12 model are statistically significant.

    Table 2.  Parameters estimation for ARIMA(1,1,0)×(0,1,1)12.
    Parameter Coefficient Standard error T-value P-value
    AR(1) -0.556 0.121 -4.584 <0.001
    SMA(1) -0.638 0.283 -2.255 0.014

     | Show Table
    DownLoad: CSV
    Table 3.  White noise test results of residual sequences.
    Model Lag χ2 DF P-value
    ARIMA(1,1,0)×(0,1,1)12 6 5.176 5 0.395
    12 11.634 11 0.392
    18 18.150 17 0.379

     | Show Table
    DownLoad: CSV

    Finally, ARIMA(1,1,0)×(0,1,1)12 model is employed for fitting TB cases from January 2015 to December 2019. The fitting and forecasting results are shown in Figure 6. And in the case of predicting in 2020, MAPE=6.243%<10%. Almost the statistic data are located in the confidence interval of 95%. Hence we can use ARIMA(1,1,0)×(0,1,1)12 model to predict new TB cases in Jiangsu in short term.

    Figure 6.  The prediction results of ARIMA(1,1,0)×(0,1,1)12 model.

    In order to find the best multivariate model, we consider air pollution variables (AQI, PM2.5 and PM10) as regression variables into the model, namely, ARIMAX model. By calculating the cross-correlation (CCF) between TB cases and air quality series, the best predictor and its lag order are found and finally incorporated into the model. Table 4 lists the optimal models for each meteorological sequence in pre-whitening. The P-values of the residual sequences are significantly greater than 0.05. Parameters are significantly passed. Significant air quality variables independently associated with TB cases by cross-correlations are shown in Figure 7.

    Table 4.  Comparisons of ARIMA models.
    Air quality Optimization model AIC AICs SBC
    AQI ARIMA(0,1,1)×(0,1,1)12 368.496 369.054 374.047
    PM2.5 ARIMA(0,1,1)×(1,1,0)12 330.791 331.349 336.342
    PM10 ARIMA(0,1,1)×(1,1,0)12 379.408 379.966 384.958

     | Show Table
    DownLoad: CSV
    Figure 7.  Cross-correlations between the pre-whitened TB cases and air quality factors from 2015 to 2019.

    From Figure 7, we can know that the monthly average AQI at a lag of 5 months, PM2.5 at a lag of 0 month and PM10 at a lag of 0 month or 13 months are significantly related to the number of TB cases, which can be included in the multivariate ARIMAX model. And hence, there are four ARIMAX models, but only two of which pass the parameter test, i.e., ARIMA(1,1,0)×(0,1,1)12+PM2.5 and ARIMA(1,1,0)×(0,1,1)12+PM10 (see Table 5). And ARIMA(1,1,0)×(0,1,1)12+PM2.5 with 0-month lag has the smallest AIC = 664.066 and MAPE = 5.891%, which is the best model. And the numerical prediction results of ARIMA(1,1,0)×(0,1,1)12+PM2.5 model are shown in Figure 8.

    Table 5.  Parameters estimation for ARIMA(1,1,0)×(0,1,1)12 with different air qualities.
    Air quanlity Lag Coefficient Standard error T-value P-value AIC MAPE
    PM2.5 0 12.223 4.760 2.568 0.006 664.066 5.891%
    PM10 0 6.193 3.120 1.985 0.026 666.414 5.957%

     | Show Table
    DownLoad: CSV
    Figure 8.  The prediction results of ARIMA(1,1,0)×(0,1,1)12+PM2.5 model.

    TB is a chronic infectious disease that seriously endangers people's health. In the present paper, based on the reported TB cases, we establish ARIMA and ARIMAX models to study the trend of TB epidemic in Jiangsu, China by using the method of time series analysis.

    Although the research of time series data has developed rapidly in recent years, most of it focuses on one-dimensional time series, and there are few studies on multi-dimensional time series. Our ARIMAX model of multiple time series of air quantity and the reported TB cases is a useful attempt.

    It is worthy to note that, in [16], the authors found that long-term exposure to PM2.5 increases the risk of death from TB and other diseases among TB patients. And in the present paper, we investigate the impact of AQI, PM2.5 and PM10 on the spreading of TB in Jiangsu, China, and find that long-term exposure to PM2.5 is closed related to the spreading of TB. More precisely, when the monthly PM2.5 with 0-month lag is introduced into the ARIMA model, the results reveal that ARIMA(1,1,0)×(0,1,1)12+PM2.5 with 0-month lag model can improve the predictive performance of the ARIMA model. These results can be seen as supplements of the results in [16], and may provide a scientific basis for the prevention and control of TB.

    The authors would like to thank the anonymous referees for very helpful suggestions and comments which led to improvement of our original manuscript. This research was supported by the National Natural Science Foundation of China (Grant No. 61672013, 11601179, 61772017 and 11961071), Research project of philosophy and Social Sciences in Jiangsu Province, China (2019SJA1671), Huaian Key Laboratory for Infectious Diseases Control and Prevention, China (HAP201704), and Innovation and Entrepreneurship Training Program for College Students in Jiangsu Province (201710323027Y and 201810323013Z), National Innovation Training Program for College Students, China (201810323007).

    The authors declare that they have no competing interests.



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