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911.
This paper presents an experimental characterization of the strain dependency of the complex modulus of bituminous mixtures for strain amplitude levels lower than about \(110~\upmu\mbox{m}/\mbox{m}\). A series of strain amplitude sweep tests are performed at different temperatures (8, 10, 12 and 14°C) and frequencies (0.3, 1, 3 and 10 Hz), during which complex modulus is monitored. For each combination of temperature and frequency, four maximum strain amplitudes are targeted (50, 75, 100 and \(110~\upmu\mbox{m}/\mbox{m}\)). For each of them, two series of 50 loading cycles are applied, respectively at decreasing and increasing strain amplitudes. Before each decreasing strain sweep and after each increasing strain sweep, 5 cycles are performed at constant maximum targeted strain amplitude.Experimental results show that the behavior of the studied material is strain dependent. The norm of the complex modulus decreases and phase angle increases with strain amplitude. Results are presented in Black and Cole–Cole plots, where characteristic directions of nonlinearity can be identified. Both the effects of nonlinearity in terms of the complex modulus variation and of the direction of nonlinearity in Black space seem to validate the time–temperature superposition principle with the same shift factors as for linear viscoelasticity.The comparison between results obtained during increasing and decreasing strain sweeps suggests the existence of another phenomenon occurring during cyclic loading, which appears to systematically induce a decrease of the norm of the complex modulus and an increase of the phase angle, regardless of the type of the strain sweep (increasing or decreasing).  相似文献   
912.
Advanced material characterization of asphalt concrete is essential for realistic and accurate performance prediction of flexible pavements. However, such characterization requires rigorous testing regimes that involve mechanical testing of a large number of laboratory samples at various conditions and set-ups. Advanced measurement instrumentation in addition to meticulous and accurate data analysis and analytical representation are also of high importance. Such steps as well as the heterogeneous nature of asphalt concrete (AC) constitute major factors of inherent variability. Thus, it is imperative to model and quantify the variability of the needed asphalt material’s properties, mainly the linear viscoelastic response functions such as: relaxation modulus, \(E(t)\), and creep compliance, \(D(t)\). The objective of this paper is to characterize the inherent uncertainty of both \(E(t)\) and \(D(t)\) over the time domain of their master curves. This is achieved through a probabilistic framework using Monte Carlo simulations and First Order approximations, utilizing \(E^{*}\) data for six AC mixes with at least eight replicates per mix. The study shows that the inherent variability, presented by the coefficient of variation (COV), in \(E(t)\) and \(D(t)\) is low at small reduced times, and increases with the increase in reduced time. At small reduced times, the COV in \(E(t)\) and \(D(t)\) are similar in magnitude; however, differences become significant at large reduced times. Additionally, the probability distributions and COVs of \(E(t)\) and \(D(t)\) are mix dependent. Finally, a case study is considered in which the inherent uncertainty in \(D(t)\) is forward propagated to assess the effect of variability on the predicted number of cycles to fatigue failure of an asphalt mix.  相似文献   
913.
运用基于密度泛函理论(DFT)框架下的超软赝势平面波(USPP)方法,计算了立方相CeO2的几何结构、弹性性质、电子结构和光学性质,并采用HSE06杂化泛函矫正了带隙.所得晶格参数及体模量与先前文献报道数据基本吻合.计算出了二阶弹性常数及德拜温度值,并给出了能带结构、态密度、差分电荷密度的分布情况.最后,为了阐明CeO2的光学跃迁机制,计算并分析了其复介电常数、折射率、吸附光谱、反射光谱等光学性质.  相似文献   
914.
基于贝叶斯推理提出了一种可实现误差模式选择的桥梁车辆荷载识别方法。该方法通过静力影响线构建车辆荷载与实测响应的关系表达式,并建立修正曲面以消除动力效应造成的识别误差。引入与结构响应大小和车速相关的五种误差模式。根据假设的先验分布推导车辆轴重参数的后验分布,以获得车辆荷载的最优估计值和置信区间,并计算各误差模式的后验概率。分别采用简支梁数值算例和某连续梁桥动载试验,对该方法在不同车速工况下的识别精度和可靠性进行了验证。结果表明,修正曲面可以有效消除车辆动力冲击的影响,提高了荷载识别精度;荷载识别结果以置信区间形式呈现,可量化荷载识别结果的不确定性;贝叶斯方法能够识别出最佳误差模式,进一步提升了荷载识别的鲁棒性。  相似文献   
915.
为研究古尔班通古特沙漠砂混凝土框架节点的抗震性能,对 9 个缩尺比为 1/2 的框架节点进行了拟静力试验研究,研究了沙漠砂替代率、轴压比和配箍率对节点破坏模式、耗能能力、延性、刚度和恢复力模型的影响。研究结果表明:沙漠砂替代率由 0% 逐渐增加到 80% 时,试件的破坏现象、骨架曲线、耗能、刚度退化主要受沙漠砂混凝土的强度和应力?应变关系影响,延性逐渐降低,且沙漠砂替代率为 80% 的构件其延性较首个试件降低了 11.48%;轴压比由 0.2 逐渐增加到 0.6 时,峰值荷载提高约 3%,延性降低约 5%,等效黏滞阻尼系数增加约 18%,刚度退化程度增加;配箍率由 0.50% 逐渐增加到 2.52% 时,峰值荷载提高近 10%,延性提高约 6%,等效黏滞阻尼系数增加约25%,刚度退化减缓。整体而言,沙漠砂混凝土框架节点的抗震性能与普通混凝土试件相似。建立了沙漠砂混凝土框架节点的三折线恢复力模型,且计算模型与试验结果吻合良好。  相似文献   
916.
The study conducted proved that triombrast (dose dependently) > hexabrics > Ultravist > or = melitrast = omnipac in a concentration interval of 0.03-30.0 mg iodine/ml in vitro and in a dose interval of 0.5-2.0 g iodine/kg in vivo activate the complement system (CS) according to the alternative way in the blood of "sensitive" rats. The degree of CS activation by radiopaque agents (ROA) is significantly determined mathematically by their viscosity and relation of the number of iodine atoms to the number of ions or dissolved particles, and by their hydrophilic (for nonion CS) and osmotic (for ion monomeric CS) properties.  相似文献   
917.
Pulmonary diseases caused by dust occupy a leading place in occupational morbidity structure. Those diseases inspire much attention due to their high prevalence, especially in ecologically hazardous regions where the workers are under "double exposure". Upper respiratory tract diseases serve as a trigger for all respiratory disorders in workers exposed to dust. Early diagnosis of respiratory disorders includes history, clinical data, X-ray examination and assessment of pulmonary ventilation and together with concurrent cardiovascular diagnosis is necessary for well-justified prophylaxis.  相似文献   
918.
Like umblical enteric remnants (eg, umblical sinus and omphalomesenteric fistula), enteric remnants can be seen on the dorsal aspect of the body (dorsal enteric sinus, dorsal enteric fistula IDEF], dorsal enteric diverticulum) in conjunction with complete cleft of the vertebral column. Complete cleft of the vertebral column associated with gastrointestinal tract and central nervous system anomalies is known as "split notochord syndrome" (SNS). The authors present an unreported variant of SNS having dorsal enteric diverticulum adjacent to the DEF. The patient died 17 days after surgical repair.  相似文献   
919.
Despite the fact that target antigens and the genetic basis of several autoimmune diseases are now better understood, the initial events leading to a loss of tolerance towards self-components remain unknown. One of the most attractive explanations for autoimmune phenomena involves various infections as possible natural events capable of initiating the process in genetically predisposed individuals. The most accepted explanation of how infection causes autoimmunity is based on the concept of "molecular mimicry" (similarity between the epitopes of an autoantigen and the epitopes in the environmental antigen). Infectious stimuli may also participate in the development of autoimmunity by inducing an increased expression of stress proteins (hsp), chaperones and transplantation antigens, which leads to abnormal processing and presentation of self antigens. Superantigens are considered to be one of the most effective bacterial components to induce inflammatory reactions and to take part in the development and course of autoimmune mechanisms. It has long been known that defects in the host defense mechanism render the individual susceptible to infections caused by certain microorganisms. Impaired exclusion of microbial antigens can lead to chronic immunological activation which can affect the tolerance to self components. Defects in certain components of the immune system are associated with a higher risk of a development of autoimmune disease. The use of animal models for the studies of human diseases with immunological pathogenesis has provided new insights into the influence of immunoregulatory factors and the lymphocyte subsets involved in the development of disease. One of the most striking conclusion arising from work with genetically engineered immunodeficient mouse models is the existence of a high level of redundancy of the components of the immune system. However, when genes encoding molecules involved in T cell immunoregulatory functions are deleted, spontaneous chronic inflammation of the gut mucosa (similar to human inflammatory bowel disease) develops. Surprisingly, when such immunocompromised animals were placed into germfree environment, intestinal inflammation did not develop. Impairment of the mucosal immune response to the normal bacterial flora has been proposed to play a crucial role in the pathogenesis of chronic intestinal inflammation. The use of immunodeficient models colonized with defined microflora for the analysis of immune reactivity will shed light on the mode of action of different immunologically important molecules responsible for the delicate balance between luminal commensals, nonspecific and specific components of the mucosal immune system.  相似文献   
920.
CONCLUSION: We conclude that despite inevitable variability the clinical picture of JME is characteristic. It is easy to diagnose JME if one thinks of it while the history should be thoroughly analyzed. An EEG recording during sleep confirms the diagnosis. An early diagnosis of JME permits adequate prognosis of the subsequent course of epilepsy, and adequate therapy brings remission in most of the patients. If treatment starts following the large number of severe GTC seizures, the response to therapy is incomplete. The persistency of the illness throughout the life, the need for continuous medication and therapeutic unresponsiveness in cases with late diagnosis, do not justify the increasing misconception that JME is of benign nature. Diagnosis of JME is rare because of insufficient familiarily of physicians with the illness. BACKGROUND: Juvenile myoclonic epilepsy (JME) is an idiopathic generalized epileptic syndrome characterized with the combination of myoclonic, generalized tonic-clonic (GTC) and absence seizures that are readily provoked by sleep deprivation. PATIENTS: Forty-three patients, aged from 14 to 51 years, participated in a 5-year follow-up study. Diagnosis was made according to the criteria (Table 1) for diagnosis of JME set by Panayiotopoulos et al. (1994). Nineteen patients made their first contact with a neurologist at the Institute of Neurology and were diagnosed as JME, while the remaining 24 were referred to from other medical institutions with a diagnosis of therapy resistant to focal epilepsy. All patients underwent a somatic and neurological examination, "mini mental test," EEG in waking and CT scan of the brain. Some patients had EEG performed during sleep and some had MRI of the head. RESULTS: JME began between 9 and 26 (average 17) years. All patients had myoclonic seizures, 98% had GTC and 23% absence seizures. The first myoclonic seizure occurred between 9 and 24 years while the frst GTC seizure occurred between 10 and 32 years. Myoclonic seizures (83% of patients) and GTC seizures (70% of patients) occurred most often immediately after awaking. The most frequent provocative factors were insufficient sleep, alcohol abuse and tiredness. Epilepsy in the family was present in 39%, focal neurological deficiency in 9% and pathological findings on of CT and MRI in 7% of patients. Waking EEG was pathological in 77% of patients; it included generalized spike-wave discharges in 73%, multiple spike-wave complexes in 33% and focal discharges in 12% of patients, respectively. In all 26 patients tested, sleep EEG was pathological most often with multiple spike-wave complexes in 85% and 3-4 Hz spike-wave complexes in 57% of patients. The correct diagnosis of JME following a comprehensive examination was made in 24 (56%) patients after a delay of 1 to 35 years. In 24 patients with delayed diagnosis of JME the replacement of earlier medication with valproic acid (VPA) induced remission in 18 patients (75%) while 1 patient (4%) experienced a reduction in the number of seizures. Five patients (21%) did not respond to VPA medication: 2 due to a weak compliance, another 2 due to inefficient medication and 1 because of the preexistent malabsorption syndrome. In 19 patients (44%) with initial diagnosis of JME, VPA was introduced immediately upon diagnosis. Of them, 15 (79%) had excellent response to VPA, 1 refused therapy and for 3 patients there is no information. In 2 patients VPA was substituted due to side effects (hepatotoxicity and alopetia) with lamotrigine (low doses), which brought about decrease in frequency and mitigation in myoclonic seizures.  相似文献   
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