Removal of single and dual ring thiophene’s from dodecane using cavitation based processes

Utilising cavitation for enhancing oxidative desulphurization has been investigated for nearly-two decades with recent investigations shifting focus from low-capacity acoustic cavitation (AC) to scalable hydrodynamic cavitation (HC). This work focuses on developing a viable means for removing thiophene’s from fuels. In the first phase of this work, use of vortex based HC devices for removal of single and dual ring thiophenes from dodecane was investigated. HC was shown to be able to remove single ring thiophene from dodecane without using any external catalyst or additives. However, in absence of catalyst or additives, it was not possible to remove dual ring thiophenes such as dibenzothiophene using HC. Therefore, in the second phase of this work, various strategies based on use of catalyst or additives to augment cavitation based process were investigated. AC based experiments were opted for shortlisting suitable catalysts and additives for intensifying cavitation based processes. The influence of using oxidant (H₂O₂) and carboxylic acid catalysts on efficacy of removal of dual ring thiophenes is presented. Several conditions were tested, and the optimal volumetric ratios of 0.95 v/v % H₂O₂ and 6.25 v/v % HCOOH was identified and utilised throughout the remainder of the study. Regeneration of extractant which accumulates oxidised sulphur species from dodecane was also investigated using AC. The additives and process conditions reported in this work are useful for enhancing desulphurization performance.     

温度对AZO薄膜红外辐射性能的影响

随着全球资源的减少和环境的恶化，节能减排已成为人们关注的焦点，具有保温隔热功能的低辐射玻璃成为研究的热点。提高玻璃保温隔热性能最有效的方法就是在其表面涂覆低辐射率层。原材料丰富、导电性能好、可见光透过率高等优势使得Al掺杂ZnO (AZO)薄膜成为最具潜力的低辐射率层。系统研究了温度对AZO薄膜红外辐射性能的影响，分析了变化机理。首先研究了在一定的温度下持续一段时间后，AZO薄膜的红外比辐射率的变化情况。然后研究了在变温环境中红外比辐射率的变化情况。采用直流磁控溅射法在室温下玻璃基片上沉积500 nm厚的AZO薄膜，将薄膜放到马弗炉中进行热处理，在100～400 ℃空气气氛下保温1 h，随炉冷却。采用X射线衍射仪对AZO薄膜进行物相分析，采用扫描电子显微镜观察薄膜表面形貌变化。利用四探针测试法测量AZO薄膜的电阻率，采用红外比辐射率测试仪测试薄膜红外比辐射率, 可见分光光度计测量可见光谱。测试的结果表明，薄膜热处理前后均为六角纤锌矿结构，(002)择优取向。300 ℃及以下热处理1 h后，(002)衍射峰增强，半高宽变窄，晶粒尺寸长大。随着热处理温度的升高，薄膜的电阻率先减小后增大，200 ℃热处理后的薄膜具有最小的电阻率(0.9×10-3 Ω·cm)。热处理温度升高，晶粒长大使得薄膜电阻率降低。热处理温度过高，薄膜会从空气中吸收氧，电阻率下降。薄膜的红外比辐射率变化趋势和电阻率的一致，在200 ℃热处理后获得最小值(0.48)。自由电子对红外光子有较强的反射作用，当电阻率低，自由电子浓度高的时候，更多的红外光子被反射，红外辐射作用弱，红外比辐射率小。薄膜的可见光透过率随着热处理温度的升高先减小后增大，200 ℃热处理后的薄膜的可见光透过率最小，但仍高达82%。这种变化是由于自由电子浓度变化引起的，自由电子对可见光有很强的反射作用。选取未热处理和200 ℃热处理后的样品进行变温红外比辐射率的测量，将样品放在可加热的样品台上，位置固定，在室温到350 ℃的升温和降温过程中每隔25 ℃测量一次红外比辐射率，结果表明，在室温到350 ℃的温度范围内，AZO薄膜的红外比辐射率在升温过程中随着温度的上升而增大，在降温过程中减小，经过整个升、降温过程后，薄膜的红外比辐射率增大。     

Synthesis and Characteristics of Organic Red‐Emissive Materials Based on Phenanthro[9,10‐d]imidazole

Red emission is one of the three primary colors that are essential for the realization of full‐color displays and solid‐state lightings. A high solid‐state efficiency is a crucial factor for the applications in organic light‐emitting diodes (OLEDs). In this work, two new donor‐acceptor‐donor type phenanthro[9,10‐d]imidazole (PIM)‐based derivatives, (2Z,2′Z)‐2,2′‐(1,4‐phenylene)bis(3‐(4‐(1‐phenyl‐1H‐phenanthro[9,10‐d]imidazol‐2‐yl)phenyl)acrylonitrile) ( PIDSB ) and 2,3‐bis(4′‐(1‐phenyl‐1H‐phenanthro[9,10‐d]imidazol‐2‐yl)‐[1,1′‐biphenyl]‐4‐yl)fumaronitrile ( PIDPh ), are designed and synthesized. Both of them possess high thermal stabilities. PIDPh shows typical characteristics of aggregation‐induced emission enhancement, while PIDSB displays an aggregation‐caused quenching effect. They both exhibit significant red‐shifted emissions compared with PIM owing to intramolecular charge transfer. In the film state, the emission peaks of PIDSB and PIDPh are located at 538 nm and 605 nm with high photoluminescent quantum yields of 63.82 % and 41.26 %, respectively. The non‐doped OLED using PIDPh as the active layer shows the maximum external quantum efficiency of 2.06 % with a very low efficiency roll‐off, and exhibits the electroluminescent peak at 640 nm with a Commission Internationale de l′Éclairage coordinate of (0.617,0.396), meeting well the criteria of red OLEDs.     

A ratio-metric fluorescent sensor design platform with red emission of Europium(III) as built-in fluorescence correction

A Eu^III-containing single molecule BCR-Eu as design platform for ratio-metric fluorescent sensor which includes a blue-emitting coumarin dye, a green-emitting BODIPY fluorophore and a Eu^III moiety as the origin of red light has been designed and synthesized. The compound BCR shows only green emission with large stoke shift when excited in 400 nm due to good fluorescence resonance energy transfer from coumarin to BODIPY. After embedding Eu^III complexes in the molecule, BCR-Eu exhibits dual emission which is equal in magnitude and independent of each other, when excited at the range of 305–365 nm. An emission from Lanthanide complexes as the stable built-in standard fluorescence peak offers a promising opportunity to enhance the precision of bioimaging and also an ideal design platform for future ratio-metric fluorescent sensor.     

New lower bounds on 2-spontaneous emission error designs

The combinatorial object named $t$-spontaneous emission error design ($t$-SEED) was proposed by Beth et al. in 2003 in order to correct errors caused by quantum jumps. The newly rising category of $t$-SEEDs has been studied extensively in recent years. Especially, the maximal possible dimensions for 2-SEEDs with block size 3 were determined completely; lower bounds on 2-SEEDs were established by applying affine groups. In this paper we utilize the action of twisted affine groups on finite fields and obtain new lower bounds on the dimensions of 2-$(q^2,k;m)$ SEEDs, some of which outperform the known ones.     

Uptake,Translocation, and Bioaccumulation of Elements in Forest Nettle (Laportea alatipes)

Elements found in the edible parts of plants are considered to be the main source of nutrients for humans and animals. However, there is insufficient information on the relationship between heavy metal pollution in the growing soil of most edible plants. In this study, the distribution of elements in the edible forest nettle (Laportea alatipes) was evaluated as a function of geographical location. Forest land soils had higher concentrations of minor elements (Cu, Cr, Ni, and Zn) compared to soils from rural and suburban areas. Translocation factors for Cd and Pb showed effective translocation from the roots to the leaves; however, these heavy metals in leaves were still above South African maximum permissible levels for vegetables. Atmospheric depositions may play a significant role in higher Cd and Pb concentrations in the leaves. Bioaccumulation factors showed the plant to accumulate Cu, Mn, and Zn to meet physiological requirement levels. Geoaccumulation indices and enrichment factors showed no soil contamination or minimal enrichment by trace metals. Principal component analysis showed Co, Cr, Cu, Fe, Ni, Pb, and Zn in soil to originate from a common source which may be soil silicates and other minerals.     

基于相关子空间的双峰发射线光谱特征提取与分析

低分辨率天体光谱中呈现的双峰发射线轮廓可能反映着比较珍稀的物理现象，如双活动星系核（AGNs）、双超大质量黑洞（SMBH）、喷流云与窄线区的相互作用，也可能是光谱处理过程产生的低质量特征线。双峰发射线轮廓一般由2个或2个以上的波峰构成，对该特征进行提取并分析，可作为双AGN、星系对、双黑洞等稀有天体更有效的搜寻依据，从而有助于更深入地研究星系乃至宇宙的形成与演化。提出一种新的基于相关子空间的双峰发射线特征提取与分析方法，主要工作分为以下三部分：首先利用稀疏差异因子δ度量双峰发射线光谱中属性差异程度，利用KNN方法约束参与稀疏差异因子计算的光谱范围，在此基础上，针对LAMOST低分辨率光谱给出基于相关子空间的特征提取方法；其次，为了验证稀疏差异因子σ以及KNN的输入参数k对双峰发射线光谱的适应性，选择LAMOST双峰发射线光谱样本及普通星系光谱数据，红移范围z<0.3（确保Hα，Hβ，[OⅢ]λλ4 959, 5 007，[NⅡ]λλ6 548, 6 584，[SⅡ]λλ6 717, 6 731等发射线落在LAMOST波长覆盖范围），获得训练集光谱总数332+332（正负样本）条，并借助人眼检查分析该方法中的两个参数：k和δ阈值α对结果的影响，实验表明，当k=18，α=0.6时，相关属性分布较密集且稀疏点较少，结果比较理想；最后，对332条双峰发射线光谱特征子空间所在的波长区间、双峰红/蓝移间隔、双峰线强比等进行了理论分析、测量及人眼认证的基础上，给出了基于相关子空间的双峰发射线特征表述。此外，从双峰特征子空间上不同的发射线激发机制（[OⅢ]/[NⅡ]/[SⅡ]等禁线、Hα、Hβ等氢线）及相关特征子空间上线强关系等角度，对样本中双峰轮廓进行了分析。     

Tuning Emission Wavelength of Polymorphous Crystal via Controllable Alkyl Chain Stacking and Its Vapor- and Thermo-Responsive Fluorescence

Tuning fluorescence colour of solid-state materials has become a topic of increasing interest for both fundamental mechanism study and practical applications such as sensors, optical recording and security printing. In this work, a fluorescent colour tuneable molecule BA-C16 is rationally designed and facilely synthesized by attaching flexible long alkyl chains to 2-hydroxybenzophenone azine ( BA ), which shows both aggregation-induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. Compared to BA , the simple introduction of long alkyl chains in BA-C16 leads to an emission wavelength redshift from 542 to 558 nm. This strategy of extending emission wavelength is rarely reported, and is ascribed to the enlarged through-space π-conjugation between interplanar molecules in the aggregate of BA-C16 . Three crystals of BA-C16 are obtained with green, yellowish green and yellow emission. According to characterization by X-ray crystallography, X-ray powder diffraction and differential scanning calorimetry, alkyl chains play an important role in inducing different stacking modes of the three crystals, which further leads to polymorph-dependent fluorescence colour. BA-C16 exhibits tuneable solid-state fluorescence upon vapor fumigation, or annealing based on a transition between a “near-monomer” crystalline state and a “dimer” crystalline state. BA-C16 is further applied for rewritable fluorescence printing tuned by vapor- and thermal-treatment.