溴代烷烃与活性氮的反应发光研究

在流动余辉装置上, 利用N₂空心阴极放电制备活性氮, 研究了活性氮与溴代烷烃(CHBr₃、CH₂Br₂、C₂H₅Br、C₄H₉Br) 反应的化学发光.上述所有反应中, 在550～750 nm波段均观察到了较强的NBr (b¹Σ+→X³Σ^-)跃迁发射谱. 同时在活性氮与CHBr₃和CH₂Br₂的反应中, 在流动管下游还观察到了CN (A²π, B²π→X²Σ⁺)的发射谱. 验证性的实验表明, 激发态NBr (b¹Σ⁺)是由二步过程形成: N(⁴S)与溴代烷烃反应生成NBr (X³Σ^-), 再通过N₂ (A ³Σ_u⁺)分子能量转移到激发态NBr (b¹Σ⁺); 而激发态的CN是通过N(⁴S) + CBr→CN(A, B) + Br过程形成的.     

不同温度下VUV光激发的Pr3+离子的发光性质

The luminescent properties of Pr³⁺-doped LaB₃O₆, SrAl₁₂O₁₉, SrB₄O₇ and NaYF₄ in the vaccum ultraviol-et (VUV) range at different temperatures were investigated under the excitation of high-energetic synchrotron radiation. For Pr³⁺ ions in LaB₃O₆, SrAl₁₂O₁₉ and SrB₄O₇, only the parity-forbidden ¹S₀→4f² transitions were observ-ed in the emission spectra at relatively low temperature; but the parity-allowed 4f5d→4f² transitions appeared simultaneously when the temperature was high enough. And the intensity of broad 4f5d→4f² emission increased relative to the intensity of ¹S₀→4f² emissions with increasing temperature. Then the thermal equilibrium model of energy levels was employed to the lowest 4f5d state and ¹S₀ state of Pr³⁺ in the three hosts. The calculated curves were in good agreement with the experimental values, indicating the occurrence of the thermal excitation from ¹S₀ state to 4f5d states at high temperatures when the lowest 4f5d state lies higher than ¹S₀ state and the photon energy is high enough.     

新半金属Fe2LaO4磁电性能的第一性原理计算

利用基于密度泛函理论的第一性原理赝势法设计并优化了含稀土元素的新半金属Fe₂LaO₄。详细计算了其电荷分布,分子磁矩等磁电性能，并结合配位场理论分析了其电子结构。结果表明，Fe₂LaO₄是一种含稀土元素的铁磁性的新ⅡB型半金属；它的稳定相晶格常数约为0.623 nm，分子磁矩约为1.0μ_B；Fe₂LaO₄属软铁磁性半金属；La较多的外层电子增强了Fe₂LaO₄内部的库仑斥力,导致了配合物ML₄和ML₆均受强场作用,从而使Fe₂LaO₄具有软铁磁性；考虑自旋分布后ML₄和ML₆的电子结构分别为a_1g¹↑a_1g¹↓t_1u³↑t_1u³↓e_g²↑e_g²↓t_2g³↑t_2g³↓和a_1g¹↑a_1g¹↓t_1u³↑t_1u³↓t_2g³↑t_2g³↓e_g²↑e_g²↓e_g^*1↑,这些电子属于分子轨道。     

白光LED用Sr0.955Al2Si2-xTixO8：Eu2+荧光粉的晶体结构和光谱特性

由高温固相反应制得Sr_0.955Al₂Si_2-xTi_xO₈：Eu²⁺（x=0~1.0）系列试样,研究了Ti⁴⁺置换Si⁴⁺对其晶体结构和光谱特性的影响。Ti⁴⁺以类质同相替代Si⁴⁺进入晶体晶格中,形成了连续固溶体,其晶胞参数a,b,c,β和晶胞体积V随Ti⁴⁺置换量呈线性递增。Ti⁴⁺置换Si⁴⁺对晶胞参数c的影响显著,b其次,a最小。荧光激发谱为宽带,位于230~400nm,由267nm、305nm、350nm和375nm 4个峰拟合成,表观峰值位于351nm;随着Ti⁴⁺置换量的增加,半高宽（FWHM）从105nm减小到93nm。发射光谱位于380~600nm,表观峰值位于407nm,可由406nm和441nm两峰拟合而成并且随Ti⁴⁺置换量增加线性红移,Ti⁴⁺进入晶格对长波长发射中心影响较少;Ti⁴⁺置换量为1.0时,表观发射峰位从407nm红移至417nm;利用试样荧光光谱和VanUitert经验公式,得出SrAl₂Si₂O₈：Eu²⁺中Sr²⁺的配位数为9。随着Ti⁴⁺置换量Si⁴⁺进入基质晶格,造成Eu-O距离变小,使得Eu²⁺所处的晶体场强度增强,发光中心Eu²⁺的5d能级分裂增大,造成Eu²⁺最低发射能级重心下移,两拟合谱峰峰位均呈线性红移。     

VB2n-(n=8~12)团簇几何结构、电子及热力学特性的理论研究

基于卡里普索结构预测程序和密度泛函理论的第一性原理计算,搜索确定了VB_2n^-（n=8~12）团簇的基态和亚稳态结构。结果发现,V原子的掺杂完全改变了原硼团簇的结构并提高了原体系的稳定性。掺杂体系基态结构分别呈现高对称性的鼓状（VB₁₆^-：C_2v）、管状（VB₁₈^-：C_2v和VB₂₀^-：C_s）及笼状（VB₂₂^-：C₂和VB₂₄^-：D_3h）结构。基于基态结构,研究了体系的电荷转移和极化率,拟合出了光电子能谱、红外和拉曼谱图,分析了流变键和芳香特性。最后,研究了体系的热力学特性,讨论了温度对热力学参数的影响。     

Ni-Co双金属催化剂上沼气重整制氢机理

用传统湿式浸渍法制备了La₂O₃掺杂的商业γ-Al₂O₃负载的沼气重整催化剂Ni-Co/La₂O₃-γ-Al₂O₃, 并用程序升温加氢(TPH)、程序升温氧化(TPO)、程序升温表面反应(TPSR)、程序升温脱附(TPD)及脉冲实验对催化剂进行了表征. 结果表明, 沼气重整过程中Ni-Co/La₂O₃-γ-Al₂O₃催化剂上的表面碳物种主要来源于CH₄的裂解, CO₂的贡献很小. CH₄裂解能够产生三种活性不同的碳物种, 即C_α、C_β与C_γ. 随着反应的进行, C_α物种减小而C_β与C_γ物种增加, 且C_γ物种能够转变为惰性的石墨碳. 重整反应过程中CH₄与CO₂的活化能相互促进. 催化剂表面的O物种与C反应生成CO或与CH_x反应生成CH_xO再分解为CO与吸附态的H物种, 可能是Ni-Co/La₂O₃-γ-Al₂O₃催化剂上沼气重整的速率控制步骤.     

(Zn1-xMnx)C2O4·2H2O在空气中的热分解动力学研究

用热分析（TG-DTG/DTA）、X射线衍射（XRD）技术和透射电镜（TEM）研究了固态物质Zn_1-xMn_xC₂O₄•2H₂O在空气中热分解的过程。热分析结果表明，Zn_1-xMn_xC₂O₄•2H₂O在空气中分两步分解，其失重率与理论计算失重率相吻合。 XRD和TEM结果表明，Zn_1-xMn_xC₂O₄•2H₂O分解的最终产物为Zn_1-xMn_xO,其颗粒大小约为10-13 nm。在非等温条件下对Zn_1-xMn_xC₂O₄•2H₂O的热分解动力学进行了分析。用Friedman法和Flynn-Wall-Ozawa(FWO)法求取了分解过程的活化能E，并用多元线性回归给出了可能的机理函数。Zn_1-xMn_xC₂O₄•2H₂O两步热分解的活化能分别为155.7513 kJ/mol 和215.9397 kJ/mol。     

Bi2WO6量子点(QDs)修饰Bi2MoO6-xF2x异质结的构筑及其催化活性增强机理

采用简单沉积-沉淀法合成了Bi₂WO₆@Bi₂MoO_6-xF_2x（BWO/BMO6-xF2x）异质结,借助XRD、XPS、TEM、SEM、EDS、UV-Vis-DRS、PC和EIS等测试技术对其组成、形貌、光吸收特性和光电化学性能等进行系统表征,并以模型污染物罗丹明B（RhB）的光催化降解作为探针反应来评价Bi₂WO₆@Bi₂MoO_6-xF_2x异质结的光催化活性增强机制。形貌分析表明,所得Bi₂MoO₆微球由大量厚度为20~50 nm的纳米片组成;FE-SEM和HR-TEM分析表明,尺寸约为10 nm的Bi₂WO₆量子点均匀沉积在Bi₂MoO_6-xF_2x微球表面,形成新颖的Bi₂WO₆@Bi₂MoO_6-xF_2x异质结;与纯Bi₂MoO₆或者Bi₂WO₆相比,1∶1Bi₂WO₆@Bi₂MoO_6-xF_2x异质结表现出更好的光催化活性和光电流性质,其对RhB光催化降解的表观速率常数分别为纯BMO和BWO的6.4和11.6倍。PC和EIS图谱分析表明,Bi₂WO₆量子点表面沉积显著提高Bi₂MoO_6-xF_2x光生电子/空穴的分离效率和迁移速率;活性物种捕获实验证明了·O₂^-和h⁺是主要的活性物种。根据实验结果,探讨了F^-掺杂和Bi₂WO₆量子点之间的协同效应对Bi₂MoO₆的光催化活性的影响机制。     

Tm3+/Er3+/Ho3+共掺SiO2-Bi2O3-AlF3-BaF2玻璃发光性能

采用高温熔融法制备了Tm³⁺/Er³⁺/Ho³⁺共掺的铋硅酸盐50SiO₂-40Bi₂O₃-5AlF₃-5BaF₂玻璃。研究了在808 nm激光器（Laser Diode）激发下Tm³⁺/Er³⁺/Ho³⁺共掺的铋硅酸盐在2 060 nm处的发光性能,同时测试及分析了该铋硅酸盐玻璃的差热特性、吸收光谱及荧光光谱。根据吸收光谱以及Judd-Oflet理论,计算了Ho³⁺的Judd-Oflet强度参数Ω_t（t=2,4,6）以及Tm³⁺/Er³⁺/Ho³⁺相应的吸收截面。铋硅酸盐玻璃中,Tm₂O₃、Er₂O₃和Ho2O3掺杂浓度分别为0.75%、1.0%和0.5%时,2 060 nm处Ho³⁺∶⁵I₇→⁵I₈发射峰强度达到最大。对Tm³⁺/Er³⁺/Ho³⁺ 3种离子的光谱性质和离子间可能存在的能量传递也做了分析。Ho³⁺在1 953 nm处的最大吸收截面σ_abs为9.08×10^-21 cm²,在2 060 nm处的最大发射截面σem为11.68×10^-21 cm²,辐射寿命τ_mea为2.75 ms,具有良好的增益效应σ_emτ（3.212×10^-20 cm^-2·ms）。     

Eu3+离子在Ca2PbO4一维结构基质中的发光研究

A Eu³⁺-doped Ca₂PbO₄ with one-dimensional structure was prepared with a solid-state reaction method and its characteristics were investigated. The XRD results show that the substitution of Ca²⁺ by Eu³⁺ has no influence on the structure of Ca₂PbO₄. Under the excitation of ultraviolet light， the Ca₂PbO₄:Eu³⁺ phosphor exhibits strong red emission at about 618 nm which is assigned to the ⁵D₀- ⁷F₂ electric-dipole transition. The compounds Sr₂CeO₄ and Ca₂SnO₄ have the same crystal symmetry as that of Ca₂PbO₄ and it is found that the emission intensity of Ca₂PbO₄∶Eu³⁺ is higher than that of Sr₂CeO₄∶Eu³⁺ and lower than that of Ca₂SnO₄∶Eu³⁺. The excitation spectrum of Ca₂PbO₄∶Eu³⁺ appears to be a broad band with two peaks at about 289 nm and 340 nm. The former peak is attributed to the Eu³⁺-O₂- charge transfer transition， while the latter one may be related to the absorption of Ca₂PbO₄ host or its crystal defects.     

超声波活化处理对微晶纤维素结构和氧化反应性能的影响

采用无污染的超声波技术预处理微晶纤维素, 研究了微晶纤维素在活化前后的超分子结构、形态结构和可及度的变化, 超声波活化对微晶纤维素选择性氧化性能的影响.     

Effects of Ultra-sonification Assisting Polyethylene Glycol Pre-treatment on the Crystallinity and Accessibility of Cellulose Fiber

In order to prepare the advanced cellulosic super-absorbent polymer with high grafting level, we tried the novel ultrasound wave assisting polyethylene glycol (PEG) pre-treatment method to decrease the crystallinity and increase the accessibility of cellulose fiber. The effects of ultrasonification assisting PEG method on the crystallinity and swelling capacity of cellulose fiber were investigated. To optimize the experimental condition, the Taguchi method was employed in the treatment process. The influence factors such as ultrasonic wave power, ultrasonic wave time and PEG molecular weight relative to the crystallinity of cellulose fiber were studied systematically. The degree of crystallinity of cellulose fiber was measured by wide-angle X-ray diffraction (WAXD). The morphology of cellulose fiber was observed by environment scanning electron microscopy (ESEM). The effects of pre-treatment variables on the water absorbency and water retention values of cellulose fiber were also investigated. The research results revealed that, under the optimal experimental condition (ultrasonic powder, 500 W; ultrasonic time, 150 s; PEG molecular weight, 600 g/mol), the crystallinity of cellulose fiber decreased from 72.16 to 42.95%. Accordingly, the absorbency of cellulose fiber increased from 1.436 to 2.063 g/g, and the water retention value increased from 47.21 to 113.4%. However, the morphology of cellulose fiber did not change thoroughly compared with the original cellulose fiber. It can be hypothesized that the original inter- and intra-macromolecular hydrogen bonds in cellulose network were weakened, resulting from the high level dispersion of PEG within cellulose network without breaking the surface morphology of fiber.     

IR Spectroscopic Study of Prepurified Flax

Flax fiber treated by conventional and ultrasonic procedures was studied. IR spectroscopic procedures were developed to estimate the degree of fiber decontamination from lignin and noncellulose fractions and to study supramolecular transformations of cellulose.     

Concentration effects on the isolation and dynamic rheological behavior of cellulose nanofibers via ultrasonic processing

Chemical pretreatment combined with high-intensity ultrasonication was performed to disintegrate cellulose nanofibers from poplar wood powders. The cellulose content in each suspension was treated as the control variable because the suspension concentration significantly influences the properties of the resultant cellulose nanofibers via ultrasonic processing. The as-obtained cellulose nanofibers were characterized by fiber diameter distribution, crystal structure, and rheological analysis. An increase of not more than 1.2 % of the cellulose content resulted in finer nanofibers. Both storage modulus and loss modulus of cellulose nanofiber suspensions rapidly increased with increasing concentration because of the gradual formation of a stronger network structure. In addition, the dynamic mechanical behavior of suspensions with fiber contents lower than 0.8 % was affected by the frequency and temperature alteration in contrast with the suspension with higher fiber contents. The sol–gel transformation and the visco-elastic transition depend on the hydroxyl bonding and the cross-linking extent of cellulose nanofibers in various concentration environments.     

Sonocrystallization of polycarbonate melts

In this paper, we showed the simplified continuous process to crystallize the polycarbonate (PC) melts using sonocrystallization which is based on ultrasonic cavitation and ‘hot spot’ theory. High power ultrasonic wave was introduced to crystallize the PC prepolymers which is generally used for solid‐state polymerization (SSP) to obtain the ultra‐high molecular weight PCs. The structure and properties of PC treated with ultrasonic wave such as torque changes and crystallinities were studied. The experimental results showed that ultrasonic wave could improve the crystallinities of PCs and sonication time was proportional to their crystallinity. This is attributed to the decrease of the specific volume and the resulting shrinkage is compensated by a flux of a polymer melt toward the crystallization front. Torque data were collected directly from the Haake internal mixer and crystallinities were evaluated from differential scanning calorimeter (DSC). This process is an environmentally benign process so that no additional solvents or treatments are needed and will be very useful in the conventional solid‐state process which is used industrially. Copyright © 2007 John Wiley & Sons, Ltd.     

A novel approach for the homogenization of cellulose to use micro‐amounts for stable isotope analyses

Climate reconstructions using stable isotopes from tree‐rings are steadily increasing. The investigations concentrate mostly on cellulose due to its high stability. In recent years the available amount of cellulose has steadily decreased, mainly because micro‐structures of plant material have had to be analyzed. Today, the amounts of cellulose being studied are frequently in the milligram and often in the microgram range. Consequently, homogeneity problems with regard to the stable isotopes of carbon and oxygen from cellulose have occurred and these have called for new methods in the preparation of cellulose for reliable isotope analyses. Three different methods were tested for preparing isotopically homogenous cellulose, namely mechanical grinding, freezing by liquid nitrogen with subsequent milling and ultrasonic breaking of cellulose fibres. The best precision of isotope data was achieved by freeze‐milling and ultrasonic breaking. However, equipment for freeze‐milling is expensive and the procedure is labour‐intensive. Mechanical grinding resulted in a rather high loss of material and it is also labour‐intensive. The use of ultrasound for breaking cellulose fibres proved to be the best method in terms of rapidity of sample throughput, avoidance of sample loss, precision of isotope results, ease of handling, and cost. Copyright © 2009 John Wiley & Sons, Ltd.     

超声波强化提取地骨皮中有机酸的研究

用超声波强化提取地骨皮中有机酸,采用单因素和正交试验方法研究了提取温度、提取时间、料液比、超声波功率对地骨皮中有机酸提取量的影响规律。结果表明超声波提取法的最佳工艺条件为提取温度65℃、提取时间35 min、料液比1∶16、超声波功率135 W,在此条件下地骨皮中总有机酸提取率为2.73%。     

木质纤维素纳米纤丝制备及形态特征分析

以阔叶树材杨木木粉为原料,始终保持纤维处在水润涨的状态下,利用亚氯酸钠在酸性条件下脱除木质素,氢氧化钾脱除半纤维素,然后借助高强度超声波的空化作用,依次制备了综纤维素、纯化纤维素及木质纤维素纳米纤丝(WCNF).通过傅里叶变换红外吸收光谱(FTIR)、X射线衍射(XRD)、扫描电镜(SEM)对WCNF制备过程中的化学组分、晶型结构、结晶度及形态特征变化进行了表征,并进一步利用图像分析系统对WCNF的直径分布进行了测量统计.结果表明,WCNF的主要成分为纤维素,其晶型结构仍为纤维素Ⅰ型,结晶度为65.68%,较之原料木粉提高了12.33%.所得纤丝的直径集中分布在5～32nm之间,长度大于10μm,长径比高于300,纤丝间相互交织成网状缠结结构.WCNF的高结晶度、高长径比、纳米尺度、网状缠结结构,显示其为一种十分理想的增强增韧材料.     

羧甲基纤维素系列高分子表面活性剂超声合成的研究

研究了在超声波作用下羧甲基纤维素的降解反应及ＣＭＣ与具有不同亲水亲油比值的活性大单体「烷基醇（酚）聚氧乙烯醚丙烯酸酯及第三单体」的超声共聚反应。经萃取提纯的共聚产物用ＩＲ，＾１３Ｃ ＮＭＲ和ＵＶ等方法进行表证，证实通过超声反应制得了二元和三元共聚物。     

Effect of surface chemistry and topography of sulphite fibres on the transcrystallinity of polypropylene

In the present study the effect of chemically and mechanically treated cellulose materials on the degree of polypropylene transcrystallisation was investigated. The cellulose materials which were sulphite fibres, microcrystalline cellulose (MCC) and knife milled sulphite fibre, were either chemically treated by esterification or mechanically treated by beating. The esterified cellulose materials did not induce a transcrystalline layer, however, all unesterified cellulose materials clearly induced a transcrystalline layer. The fibres which were mechanically treated by beating gave a higher degree of transcrystallisation than the untreated ones. Our results show the importance of the surface chemistry of the added fibres on the growth of transcrystallisation in polypropylene composite materials.