生物导热基本方程的三维非定常代数显式解析解

对目前比较通用的生物导热基本方程Pennes方程,给出了其三维非定常情况下的代数显式解析解。据知,以前很少有发表过这类严格的几何多维解析解。它除了有不可代替的理论价值外,还可以作为标准解来校验日益发达的数值解以及作为基础来研究计算传热学的数值计算方法。另外,文章的特殊求解方法也有发展价值之处。     

舌模型建构与三维温度场数值模拟初探

舌体的三维温度场的建立可直观反映全舌空间温度的分布情况,能够深层次分析全舌的传热特性。本文选择猪舌为实验研究对象,建构舌体真实血管分布的物理模型为计算机可识别的数字模型,在此基础上用有限元方法对舌体三维温度场的数值模拟做了初步探索。讨论了血管形状分布,血液灌注率,代谢热与生物体三维温度场变化规律的相关性。     

基于模拟方法生成血管树的人舌三维温度场数值模拟

采用分步模拟方法生成血管树并以此作为物理模型,进行舌体三维温度场的实验研究与数值计算。计算分为舌体组织和血液温度场数值模拟两部分,相应数学模型也包括舌体组织控制方程、血液控制方程及两者之间的耦合方程。在考虑了血液与组织间的耦合换热,舌津液蒸发的影响基础上,采用数值模拟得到的舌面对流换热系数,使计算结果与红外热像验证极为近似。以模拟方法生成的血管树替代生物体的血管铸型,在某种意义上说将生物体三维传热计算方法的研究推向了一个新的层面。     

聚焦超声源对生物媒质加热的理论研究

用差分法求解生物热传导方程,研究了凹球面聚焦超声换能器用于热疗时在人体组织内产生的稳态温度场.引入热焦距及等温线,分析了换能器参数、生物组织特性参数对有效治疗区的影响,并对声场和温度场特征进行了比较关键词：聚焦超声热疗生物组织温度场     

激光诱导间质热疗中生物组织的温度场研究

激光诱导间质热疗疗效评估的前提是必须获得准确的激光在不同功率、不同照射时间的生物组织温度场分布.利用多物理场直接耦合分析软件COMSOLMultiphysics构建了在组织光学参量不变情况下的三维有限元传热模型.该模型基于Pennes生物传热方程和轴对称高斯形状的激光光束热源方程,参量针对离体猪肝组织,考虑到了生物组织热物性密度、比热和热导率随温度变化的情况.仿真获得激光功率为0.77W、0.95W、1.23W,照射时间为10~90s,径向距离0~2mm范围和轴向距离0~4mm范围的温度场数据集.利用拟合算法,获得了自变量为激光功率、照射时间、径向距离和轴向距离的生物组织温度场分布模型.将功率为0.88W和1.05W时的结果与Pennes方程结果相比较,两者误差在5%以内.     

基于有限元的舌体三维温度场数值模拟

依据生物体自然形态所进行的三维温度场建构与计算是近年来国内外生物传热研究中的焦点之一.采用血管铸型的方法获取猪舌的血管树,通过数码成像及逆向建模将其转换为计算机可识别的数字模型.以Pennes方程为基准方程,对自然形态和实际传热状态下的舌体三维温度场进行了重构计算,并获得成功.通过此方法可获取其它生物体器官三维空间的温度分布,对本研究而言,舌体三维温度场计算的成功为探索生物传热与中医舌诊的机理研究搭建了技术平台.     

Luminescence and Energy Transfer in Frozen Solutions of Uranyl Sulfate in Selective Excitation

Luminescence spectra of vitrified solutions of uranyl sulfate in a concentrated sulfuric acid are investigated in the range 4.2–80 K in selective laser excitation. It is shown that the luminescence spectra are a superposition of two components — the component that is related to the resonance excitation of uranyl complexes and the component that is caused by the luminescence of uranyl complexes sensitized by the transfer of electron-excitation energy from the resonance-excited centers. The nonselective character is established for the spectral migration of electron-excitation energy with participation of the bending vibrations of the uranyl complex that ensure direct vibrational transitions between neighboring electronic energy levels. The temperature evolution of the luminescence spectra can be described within the framework of the model of configuration coordinates with allowance for only the linear terms of vibronic interaction.     

温度对稀土离子掺杂ZBLAN玻璃上转换发光的影响

研究了Er3+,Pr3+和Yb3+共掺杂ZBLAN玻璃在960nm激光泵浦下的上转换发光的温度特性.温度变化范围为室温到300℃.结果表明Pr3+离子的发光强度随温度的增加,先增加;达到极大后,随温度的增加下降.Er3+发光强度随温度增加单调下降.     

荧光粉CaWO4：Eu3+中WO42-与Eu3+间的能量转递

通过高温固相法分别制备了CaWO₄和CaWO₄:1%Eu³⁺ 样品. 测量了样品不同温度(10–300 K)的荧光光谱、荧光衰减曲线和 时间分辨荧光光谱. 样品的荧光光谱表明: 在240 nm紫外光激发下, 两个样品在430 nm处都展现出来源于WO₄^2-的蓝色发射; 样品CaWO₄:Eu³⁺的Eu³⁺(⁵D₀→⁷F_{1, 2, 3,4})的特征发射则归属于WO₄^2-到Eu³⁺ 间的能量传递.由样品室温(300K)荧光衰减曲线发现: 纯CaWO₄的荧光寿命为8.85μs,Eu³⁺掺杂之后WO₄^2-的荧光寿命缩短至6.27μs,这从另一方面证明了WO₄^2-与Eu³⁺间能量传递的存在. 由荧光寿命得到T=300K时, CaWO₄: 1%Eu³⁺中WO₄^2-与Eu³⁺间的能量传递效率(η_ET)为29.2%, 能量传递速率(ω_ET)为4.65×10⁴ s^-1.通过时间分辨荧光光谱, 获得了从WO₄^2-到Eu³⁺之间的能量传递的时间演变过程,当温度由10 K增加到300 K时, 能量传递出现的时间单调变小. 测试了不同温度(10–300 K)对CaWO₄:Eu³⁺的荧光寿命的影响, 发现在10–50K时,Eu³⁺的荧光寿命增加, 但温度超过50K时发生猝灭, 荧光寿命开始下降; WO₄^2-的荧光寿命则是随着温度的升高逐渐缩短.关键词：能量传递红色荧光粉温度依赖4：Eu³⁺')\" href=\"#\">CaWO₄：Eu³⁺     

荧光粉CaWO4：Eu3+中WO2-4与Eu3+间的能量转递*

通过高温固相法分别制备了CaWO4和CaWO4：1%Eu3+样品.测量了样品不同温度(10-300 K)的荧光光谱、荧光衰减曲线和时间分辨荧光光谱.样品的荧光光谱表明：在240 nm紫外光激发下,两个样品在430 nm处都展现出来源于WO2?4的蓝色发射;样品CaWO4：Eu3+的Eu3+(5D0→7F1,2,3,4)的特征发射则归属于WO2?4到Eu3+间的能量传递.由样品室温(300 K)荧光衰减曲线发现：纯CaWO4的荧光寿命为8.85μs, Eu3+掺杂之后WO2?4的荧光寿命缩短至6.27μs,这从另一方面证明了WO2?4与Eu3+间能量传递的存在.由荧光寿命得到T =300 K时, CaWO4：1%Eu3+中WO2?4与Eu3+间的能量传递效率(ηET)为29.2%,能量传递速率(ωET)为4.65×104 s?1.通过时间分辨荧光光谱,获得了从WO2?4到Eu3+之间的能量传递的时间演变过程,当温度由10 K增加到300 K时,能量传递出现的时间单调变小.测试了不同温度(10-300 K)对CaWO4：Eu3+的荧光寿命的影响,发现在10-50 K时, Eu3+的荧光寿命增加,但温度超过50 K时发生猝灭,荧光寿命开始下降;WO2?4的荧光寿命则是随着温度的升高逐渐缩短.     

Intermolecular Processes in Excited Electronic States in the Gas Phase (Review)

A brief review of works on the temperature dependences of the rate constants k_q of the intermolecular processes proceeding in the excited electronic states in the gas phase is given. The dependences k_q(T) for such biomolecular processes as intermolecular vibrational energy transfer in the triplet state vibrational quasi-continuum, triplet-triplet electron excitation energy transfer, and intermolecular photoinduced electron transfer have been compared. The experimental data have shown that in the gas phase for all analyzed intermolecular processes both an increase and a decrease in k_q with increasing temperature (T) is observed, which is not associated with the specific intermolecular interactions leading to the formation of long-lived components. The change in the type of temperature dependence is due to the change in the mechanisms of the radiationless transitions with increasing density of vibrational levels in the final electronic state. The applicability of the known models based on the theory of radiationless transitions for predicting the temperature dependences k_q(T) is discussed. __________ Translated from Zhurnal Prikladnoi Spektros-kopii, Vol. 72, No. 4, pp. 429–439, July–August, 2005.     

激光诱导间质热疗中生物组织的温度场研究

激光诱导间质热疗疗效评估的前提是必须获得准确的激光在不同功率、不同照射时间的生物组织温度场分布.利用多物理场直接耦合分析软件COMSOL Multiphysics构建了在组织光学参量不变情况下的三维有限元传热模型.该模型基于Pennes生物传热方程和轴对称高斯形状的激光光束热源方程,参量针对离体猪肝组织,考虑到了生物组织热物性密度、比热和热导率随温度变化的情况.仿真获得激光功率为0.77 W、0.95 W、1.23 W,照射时间为10~90 s,径向距离0~2 mm范围和轴向距离0~4 mm范围的温度场数据集.利用拟合算法,获得了自变量为激光功率、照射时间、径向距离和轴向距离的生物组织温度场分布模型.将功率为0.88 W和1.05 W时的结果与Pennes方程结果相比较,两者误差在5%以内.     

铌锰锆钛酸铅铁电陶瓷电滞回线的温度和频率响应

研究了Pb［(Zr052Ti048)095(Mn1/3Nb2/3)005］O3 (PMnN_PZT) 铁电陶瓷电滞回线的温度和频率响应,结果显示在高频和室温条件下测试铁电特性时,电滞回线呈现“束腰”形状,而不是通常所看到的方形回线 . 在低频和高温条件下测试时才能观察到正常的方形回线,同时,诸如矫顽场、极化强度、 内偏场这些重要的铁电参数也会随频率和温度发生显著的变化. 剩余极化强度随频率和温度 的大幅增长表明“束腰” 电滞回线有可能是由于缺陷偶极子引起的. 电滞回线形状与温度 和频率存在较强的相关性说明缺陷偶极子存在一特征弛豫时间,缺陷偶极子反转响应速度由 此弛豫时间决定.关键词：电滞回线氧空位频率响应温度响应     

肿瘤热疗计划中三维温度分布的不确定性研究

本文采用Monte—Carlo方法对肿瘤热疗计划中组织的三维温度场进行了模拟,并研究了肿瘤区域、血液灌注率、 加热功率等参数的不确定性对组织温度造成的影响。本文结果对优化热疗参数及制定临床治疗方案具有重要的参考价值。     

激光热疗中生物组织的光热描述及研究进展

激光热疗中,激光与生物组织相互作用研究应包含两个方面：一是光子在生物组织中的迁移规律,基于传输理论的Ｍｏｎｔｅ－Ｃａｒｌｏ方法能较为真实地模拟光在生物组织内的分布,并进一步获得热源的分布;另一方面是热在生物组织中的传导,经典的Ｐｅｎｎｅｓ方程和基于微结构的Ｗｅｉｎｂａｕｍ与Ｊｉｊｉ模型从不同层面描述生物组织中的传热问题,两者的统一是至关重要的,文中对此进行了阐述,文中还报道了用光学方法对组织热凝固     

Temperature Dependence of the Efficiency of Collisional Transfer of Vibrational Energy in Mixtures of Vibrationally Excited Triplet Molecules with Foreign Gases

By the pressure dependences of the decay rates of delayed fluorescence activated by vibrational excitation of triplet molecules of benzophenone and anthraquinone, the efficiencies of collisional transfer of vibrational energy (V–V-transfer) in the vibrational quasi-continuum of the triplet state have been estimated. It is shown that the efficiencies of the process in mixtures with foreign gases increase with increasing dipole moment and polarizability of colliding molecules. In the temperature range 433–513 K, we obtained an inverse temperature dependence of the V–V-transfer efficiency, which is satisfactorily described by empirical relations taking into account long-range attractive forces. The results obtained point to the determining role of long-range attractive forces in quasi-resonance V–V-transfer of vibrational energy by molecules excited in vibrational quasi-continuum.     

Calculation of entropy of mixing of liquid metal alloys in a hard sphere system

A semi-empirical model, based on the hard sphere system, is used to determine the entropy of mixing of simple as well as compound-forming alloys. For the compound-forming liquid solutions, the method leads to fairly accurate results, showing thereby that the usual theory of hard spheres mixtures can be applied to compound forming alloys also. It has been shown that the compound formation is very sensitive to the temperature of the mixture. Numerical applications are attempted for NaHg and NaGa.     

Temperature Dependence of the Triplet–Triplet Energy Transfer Efficiencies in Carbonyl Vapors

The temperature dependences of the rate constants k _TT and the efficiencies _DA of triplet–triplet transfer of the energy of electronic excitation in a gas phase for a number of donor–acceptor pairs (benzophenone–diacetyl, anthraquinone–diacetyl, carbazole–diacetyl, and naphthalene–diacetyl) were studied. It is shown that for gas phase systems the k _TT and _DA constants can both increase and decrease with increase in the temperature over the range 360–510 K. To explain the temperature changes of the k _TT values, the experimental rate constants were compared with those calculated by a classical model (Marcus' equation). In the temperature range under study, the influence of the average vibrational energy <E _vib> of the donor and acceptor molecules was taken into account to estimate the free energy change G, which varied from 0.4 to –1.2 eV. It is established that the increase in k _TT with temperature for certain gas-phase systems and decrease for others represent the typical, for a gas-phase system, transition from a normal region (increase in k _TT) to an inverted one (decrease in k _TT) with monotonic variation of G, including the temperature increase of <E _vib> of the molecules.