Development of healing model and simplified characterization test procedure for asphalt concrete

2020 ◽  
pp. 121515
Author(s):  
Morteza Ashouri ◽  
Yizhuang Wang (David) ◽  
Yeong-Tae Choi ◽  
Youngsoo Kim (Richard)
Keyword(s):  
Asphalt Concrete ◽  
Test Procedure ◽  
Characterization Test ◽  
Healing Model

Analysis of Thermal Fatigue Distress of Asphalt Concrete Pavements

1996 ◽  
Vol 1545 (1) ◽  
pp. 43-49 ◽  
Author(s):  
N. Mike Jackson ◽  
Ted S. Vinson
Keyword(s):  
Thermal Fatigue ◽  
Asphalt Concrete ◽  
Thermal Loading ◽  
Test Procedure ◽  
Fatigue Cracking ◽  
Thermal Cracking ◽  
The United States ◽  
Tensile Creep ◽  
Concrete Pavements ◽  
Test Procedures

Thermal cracking of asphalt concrete pavements is responsible for millions of dollars in annual maintenance and rehabilitation costs in the United States and Canada. Thermal cracking typically is associated with low temperatures in northern climates and at high elevations. Another form of thermal cracking, known as thermal fatigue cracking, has been proposed by several researchers as a potential mode of distress in regions with relatively moderate climates. The objectives were to evaluate the possibility of the occurrence of the thermal fatigue cracking mode of distress and to identify a suitable laboratory test procedure to facilitate a mechanistic analysis of this mode of distress. The most promising test procedures evaluated included the direct tensile creep test and the thermal stress restrained specimen test. The results suggest that thermal fatigue distress in asphalt concrete mixtures is not a viable mode of distress in the absence of environmental aging. From the data presented and results documented by others, it is evident that distress often attributed to thermal fatigue cracking is more likely the result of low-temperature cracking of environmentally aged mixtures or subgrade-related distress. It is concluded that fatigue distress due to thermal loading of semirestrained pavements does not occur.

Benefits from Computerized Adaptive Testing as Seen in Simulation Studies

1999 ◽  
Vol 15 (2) ◽  
pp. 91-98 ◽  
Author(s):  
Lutz F. Hornke
Keyword(s):  
Measurement Error ◽  
Computerized Adaptive Testing ◽  
Test Procedure ◽  
Adaptive Testing ◽  
Parameter Estimates ◽  
Simulation Studies ◽  
Computerized Adaptive Test ◽  
Item Banks ◽  
Item Parameters ◽  
General Reliability

Summary: Item parameters for several hundreds of items were estimated based on empirical data from several thousands of subjects. The logistic one-parameter (1PL) and two-parameter (2PL) model estimates were evaluated. However, model fit showed that only a subset of items complied sufficiently, so that the remaining ones were assembled in well-fitting item banks. In several simulation studies 5000 simulated responses were generated in accordance with a computerized adaptive test procedure along with person parameters. A general reliability of .80 or a standard error of measurement of .44 was used as a stopping rule to end CAT testing. We also recorded how often each item was used by all simulees. Person-parameter estimates based on CAT correlated higher than .90 with true values simulated. For all 1PL fitting item banks most simulees used more than 20 items but less than 30 items to reach the pre-set level of measurement error. However, testing based on item banks that complied to the 2PL revealed that, on average, only 10 items were sufficient to end testing at the same measurement error level. Both clearly demonstrate the precision and economy of computerized adaptive testing. Empirical evaluations from everyday uses will show whether these trends will hold up in practice. If so, CAT will become possible and reasonable with some 150 well-calibrated 2PL items.

Evaluating the Validity of a Bayesian Program for Predicting Stage in Hodgkin’s Disease

1981 ◽  
Vol 20 (03) ◽  
pp. 174-178 ◽  
Author(s):  
A. I. Barnett ◽  
J. Cynthia ◽  
F. Jane ◽  
Nancy Gutensohn ◽  
B. Davies
Keyword(s):  
New England ◽  
Hodgkin's Disease ◽  
Bayesian Model ◽  
Medical Center ◽  
Hodgkin’S Disease ◽  
Test Procedure ◽  
Disease Patient ◽  
Probabilistic Information ◽  
Probabilistic Forecasts ◽  
England Medical

A Bayesian model that provides probabilistic information about the spread of malignancy in a Hodgkin’s disease patient has been developed at the Tufts New England Medical Center. In assessing the model’s reliability, it seemed important to use it to make predictions about patients other than those relevant to its construction. The accuracy of these predictions could then be tested statistically. This paper describes such a test, based on 243 Hodgkin’s disease patients of known pathologic stage. The results obtained were supportive of the model, and the test procedure might interest those wishing to determine whether the imperfections that attend any attempt to make probabilistic forecasts have gravely damaged their accuracy.

Reliability of Laboratory Tests for the Control of Oral Anticoagulation

1974 ◽  
Vol 32 (02/03) ◽  
pp. 483-491
Author(s):  
E. A Loeliger ◽  
M. J Boekhout-Mussert ◽  
L. P van Halem-Visser ◽  
J. D. E Habbema ◽  
H de Jonge
Keyword(s):  
Human Brain ◽  
Laboratory Tests ◽  
Test Procedure ◽  
Rabbit Brain ◽  
Normal Range ◽  
Test Procedures ◽  
Discrimination Power ◽  
Power Of The Test ◽  
Assay Procedure ◽  
Low Sensitivity

SummaryThe present study concerned the reproducibility of the so-called prothrombin time as assessed with a series of more commonly used modifications of the Quick’s onestage assay procedure, i.e. the British comparative reagent, homemade human brain thromboplastin, Simplastin, Simplastin A, and Thrombotest. All five procedures were tested manually on pooled lyophilized normal and patients’ plasmas. In addition, Simplastin A and Thrombotest were investigated semiautomatically on individual freshly prepared patients’ plasmas. From the results obtained, the following conclusions may be drawn :The reproducibility of results obtained with manual reading on lyophilized plasmas is satisfactory for all five test procedures. For Simplastin, the reproducibility of values in the range of insufficient anticoagulation is relatively low due to the low discrimination power of the test procedure in the near-normal range (so-called low sensitivity of rabbit brain thromboplastins). The reproducibility of Thrombotest excels as a consequence of its particularly easily discerned coagulation endpoint.The reproducibility of Thrombotest, when tested on freshly prepared plasmas using Schnitger’s semiautomatic coagulometer (a fibrinometer-liJce apparatus), is no longer superior to that of Simplastin A.The constant of proportionality between the coagulation times formed with Simplastin A and Thrombotest was estimated at 0.64.Reconstituted Thrombotest is stable for 24 hours when stored at 4° C, whereas reconstituted Simplastin A is not.The Simplastin A method and Thrombotest seem to be equally sensitive to “activation” of blood coagulation upon storage.

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