Acceptor-rich bulk heterojunction polymer solar cells with balanced charge mobilities

In this work, we reported efficient polymer solar cells with balanced hole/electron mobilities tuned by the acceptor content in bulk heterojunction blend films. The photovoltaic cells were fabricated with two new wide band-gap D-A polymers PBDDIDT and PBDDIDTT as the donor material. The molecular conformations of new polymers are carefully evaluated by theoretical calculations. The results of photovoltaic studies show that two devices reach their optimal conditions with rich PC₇₁BM content up to 80% in blend films, which is uncommon with most of reported PSCs. The as-cast devices based on PBDDIDT and PBDDIDTT reveal good photovoltaic performance with PCE of 7.04% and 6.40%, respectively. The influence of PC₇₁BM content on photovoltaic properties is further detailed studied by photoluminescence emission spectra, charge mobilities and heterojunction morphology. The results exhibit that more efficient charge transport between donor and acceptor occurs in rich PC₇₁BM blend films. Meanwhile, the hole and electron mobilities are simultaneously enhanced and afford a good balance in rich PC₇₁BM blend films (D/A, 1:4) which is critical for the improvement of current density and fill factors.     

Moisture transfer and stress development during high-temperature drying of Chinese fir

Abstract

The knowledge of moisture content (MC) and drying stress are crucial parameters to control the drying process and maintain the quality of dried wood. Herein, we investigated the pattern of moisture transfer and stress development in Chinese fir during the high-temperature drying process. The MC in each layer of lumber was separated into bound water and free water via nuclear magnetic resonance (NMR), and the drying and residual stress were measured using prong test method. There was different MC in each layer along the thickness, resulting in an MC gradient that initially increased and then decreased, which is consistent with the trend of drying stress. The T₂₁ peak indicating bound water shifted to the left especially when MC was below the fiber saturation point, signifying that the discharge of moisture became difficult with prolonged drying time. The ratio of bound water to free water was different in each layer, indicating that the moisture transfer was different along the thickness. Furthermore, the residual stress was greater than the corresponding drying stress though the disparity reduced gradually, which suggests that the MC gradient was the largest affecting factor for drying stress at high MC stages but decreased to some extent as the drying process continued.     

杨木NaOH浸渍渗透特性研究

通过自制设备对杨木NaOH浸渍渗透过程进行了实验研究。结果表明,杨木NaOH浸渍过程纵向边材渗透性能明显优于心材,而横向渗透差异较小;横向渗透为逐层渗透过程,单位渗透体积量与渗透时间呈线性关系;纵向渗透过程可分为快速渗透阶段(第一阶段)和慢速渗透阶段(第二阶段)两个阶段。在本实验条件下适当提高浸渍温度和NaOH浓度均能不同程度地改善浸渍渗透效果,而木块厚度和含水率对渗透过程均有不同程度的负面影响。     

稻草常压酸水解工艺的研究

研究了稻草常压酸水解工艺,通过单因素实验确定了酸水解适宜的工艺条件,并以还原糖提取率为评价指标,评价了稻草的常压酸水解效果。结果表明,稻草适宜的酸水解工艺条件为:酸水解温度100℃、酸水解时间3 h、质量分数为3%的硫酸、固液比1∶4,在此工艺条件下稻草酸水解得率为73%,还原糖提取率约为17%,多戊糖去除率约为65%;酸水解后的稻草中多戊糖含量为12.2%,用酸水解后稻草生产的人纤浆基本能够达到人纤浆质量标准的要求。     

制浆过程木材浸渍研究进展

从多个角度对木材浸渍研究进展进行了分析论述,全面阐述了基于渗透理论及扩散理论的木材浸渍理论模型,介绍了木材浸渍研究的3种常用连续测量方法,详细论述了木材浸渍的影响因素及改善措施。     

不同复配乳化剂合成乳液对汽车工业滤纸强度性能的影响

以苯乙烯和丙烯酸酯为主要单体,设计多种复配乳化剂方案,通过单体预乳化、半连续乳液聚合法合成苯丙乳液,用作汽车发动机空气滤清器滤纸浸渍树脂.研究了多种复配乳化剂合成苯丙乳液浸渍对汽车工业滤纸抗张强度、耐破度及挺度的影响,筛选出对滤纸强度性能作用效果良好的复配乳化剂.结果表明,合成乳液浸渍对提高汽车工业滤纸抗张强度、挺度及耐破度作用显著,OP-10/FR-1、OR-2/DSB、FOR-3/RE-610复配乳化剂乳液浸渍的汽车工业滤纸抗张强度高于3.15kN/m、挺度大于3.45 mN·m、耐破度在250 kPa以上.     

Comparative study on pyrolysis and catalytic pyrolysis upgrading of biomass model compounds: Thermochemical behaviors,kinetics, and aromatic hydrocarbon formation

In order to understand the pyrolysis mechanism, reaction kinetic and product properties of biomass and select suitable agricultural and forestry residues for the generation desired products, the pyrolysis and catalytic pyrolysis characteristics of three main components (hemicellulose, cellulose, and lignin) of biomass were investigated using a thermogravimetric analyzer (TGA) with a fixed-bed reactor. Fourier transform infrared spectroscopy (FTIR) and elemental analysis were used for further characterization. The results showed that: the thermal stability of hemicellulose was the worst, while that of cellulose was higher with a narrow range of pyrolysis temperatures. Lignin decomposed over a wider range of temperatures and generated a higher char yield. After catalytic pyrolysis over HZSM-5 catalyst, the conversion ratio increased. The ratio for the three components was in the following order: lignincellulose < biomass < xylan. The Starink method was introduced to analyze the thermal reaction kinetics, activation energy (Ea), and the pre-exponential factor (A). The addition of HZSM-5 improved the reactivity and decreased the activation energy in the following order: xylan (30.54%) > biomass(15.41%) > lignin (14.75%) > cellulose (6.73%). The pyrolysis of cellulose gave the highest yield of bio-oil rich in levoglucosan and other anhydrosugars with minimal coke formation. Xylan gave a high gas yield and moderate yield of bio-oil rich in furfural, while lignin gave the highest solid residue and produced the lowest yield of bio-oil that was rich in phenolic compounds. After catalytic pyrolysis, xylan gave the highest yield of monocyclic aromatic hydrocarbons, 76.40%, and showed selectivity for benzene and toluene. Cellulose showed higher selectivity for xylene and naphthalene; however, lignin showed enhanced for selectivity of C10 + polycyclic aromatic hydrocarbons. Thus, catalytic pyrolysis method can effectively improve the properties of bio-oil and bio-char.     

A novel and multifunctional flame retardant nucleating agent towards superior fire safety and crystallization properties for biodegradable poly (lactic acid)

In engineering application area, it has always been a challenge to simultaneously improve flame-retardant performance and crystallization rate of polylactic acid (PLA) biomaterials, thus restricting their extensive application. In this work, a multifunctional additive (4,4′-(phenylphosphoryl)bis(piperazine-4,1-diyl))bis(diphenylphosphine oxide) (PDPO) was successfully synthesized and used to fabricate flame retardant PLA biocomposites. The crystallization behavior, fire safety, mechanical properties and flame retardant mechanisms of PLA biocomposites were studied in detail. The results indicated that PDPO notably improved the crystallization rate and crystallinity of PLA biocomposites. When 4 wt% PDPO was incorporated, PLA/PDPO biocomposites successfully passed UL-94V-0 grade and their LOI values were improved from 19.0% of pure PLA to 29.4%. The introduction of PDPO promoted the premature degradation and carbonization of PLA substrate, and inhibited the transesterification of the PLA during thermal pyrolysis process. Besides, PDPO decomposed and produced the Ph and PO, which efficiently exerted the free radical trapping effect in vapor phase. Therefore, the spread of fire for PLA/PDPO was declined and even self-extinguished. Meanwhile, the low addition of PDPO presented little effect on the mechanical properties of PLA composites. This flame retardant PLA biocomposites showed broad application prospects in emerging fields such as electronic devices, automobiles, and 3D printing materials.     

木材学国家精品课程深化教学的思考

结合"木材学"国家精品课程建设中的一些实际情况,从加强师资队伍和实践教学的建设、推进教学方法以及考核体系的改革和创新四个方面对如何更好地深化教学进行了论述,为培养优秀人才奠定了基础。