柠条的纤维特性及其双螺杆CMP制浆性能研究

以柠条为原料，分析了其化学组分和纤维形态，并探讨了柠条双螺杆CMP法的制浆工艺以及浆料的纤维形态和成纸的物理性能。研究结果表明：与针、阔叶木相比，柠条原料中纤维素和综纤维素质量分数较低，苯醇抽出物和热水抽出物质量分数较高，柠条纤维长度总体偏短，木质部和皮部的纤维质量平均长度分别为0.621和0.819 mm，还存在部分杂细胞。采用3.5% Na₂SO₃和1.5% NaOH常温预浸12 h、90℃汽蒸1 h后再用双螺杆挤浆机在质量分数35%下进行搓丝，并结合高浓盘磨机磨浆，所得CMP浆得率可达73%。柠条CMP浆基本保持了纤维原有的长度，质量平均长度达0.650 mm，长宽比为32.7，纤维解离较好，但分丝帚化情况不理想，含有部分纤维束和杂细胞。当加拿大游离度为300 mL时，柠条CMP浆成纸的环压强度指数和松厚度较高，分别为8.67（N·m）/g和2.56 cm³/g，抗张指数为19.6（N·m）/g，本色浆白度较高，达50%（ISO）。柠条CMP浆适合配抄瓦楞原纸等包装用纸，漂白后可配抄新闻纸和白板纸。     

Finite element modelling of calendering — some aspects of the effects of temperature gradients and structure inhomogeneities

The compression of a paper web in a calender nip has been simulated using the finite element method. The mechanical properties of the paper were allowed to vary in the thickness and machine directions of the web. This was done in order to model the influence of temperature gradients as well as density variations (due to the presence of fibre floes) on the deformation behaviour in the nip. Paper was assumed to be an elastic-plastic material exhibiting strain hardening. The yielding behaviour was governed by the Drucker-Prager yield condition. Simulations of the deformation behaviour when paper was subjected to a temperature gradient, clearly revealed that the deformation gradually became more concentrated towards the surface layers as the temperature of the surface increased. This is in accordance with experimental results which indicate that temperature-gradient calendering promotes the surface properties, whereas the bulk of the structure is preserved. Modelling the deformation behaviour of a structure containing density variations reveals that the paper may contain an inhomogeneous strain distribution after unloading, i.e. after passage through the nip.     

Catalytic hydrodechlorination of 1-chlorooctadecane, 9,10-dichlorostearic acid, and 12,14-dichlorodehydroabietic acid in supercritical carbon dioxide

Kinetic and thermodynamic analyses of catalytic hydrodechlorinations in supercritical carbon dioxide (SC-CO₂) were performed using 5% Pd supported on γ-Al₂O₃. The selected standard compounds used for the study represented chlorinated wood resins commonly found in pitch deposits; 1-chlorooctadecane (C₁₈-Cl), 9,10-dichlorostearic acid (Stearic-Cl₂), and 12,14-dichlorodehydroabietic acid (DHA-Cl₂). The reaction utilized isopropanol as a hydrogen donor. Pressure, temperature, and the concentrations of isopropanol and palladium were varied to study the effect of each parameter and to optimize the dechlorination yield. The reaction in SC-CO₂ was compared to the one in liquid solvents at atmospheric pressure. By applying a Langmuir–Hinshelwood kinetic model, the rate-determining step of the reaction was deduced to be adsorption of the chlorinated molecules on the palladium surface. The apparent activation energies of the reactions for C₁₈-Cl, Stearic-Cl₂, DHA-Cl₂ were 43±5, 40±7, and 135±7 kJ mol⁻¹, respectively, in SC-CO₂. The relatively high activation energy for DHA-Cl₂ was apparently due to structural differences from the other two compounds. The apparent activation energy of dechlorination of C₁₈-Cl in liquid isopropanol at atmospheric pressure was determined to be 35±3 kJ mol⁻¹, leading to the conclusion that the rate-determining step is the same for this compound in both fluid systems. The enthalpies of desorption of stearic acid and dehydroabietic acid were determined to be 18±2 and 12±2 kJ mol⁻¹, respectively. These values being less than half of the apparent activation energies of dechlorination of their corresponding chlorinated compounds indicates that desorption of the dechlorinated products is not the rate-determining step of the reaction. This was consistent with the conclusion that the rate-determining step is adsorption, on the understanding that the reaction mechanism is same in both fluid systems.     

径向基函数网络在近红外光谱纸浆卡伯值测量的应用

为了提高制浆过程中的在线预测纸浆卡伯值的精度,提出采用径向基函数网络来建立纸浆卡伯值近红外光谱法在线测量模型。结果表明,这种算法由于既考虑到了近红外光谱响应的非线性因素,又可防止BP网络在建模时出现训练速度慢、容易陷入局部最小和“过拟合”的现象,利用这种网络建立的纸浆卡伯值测量模型与一元回归、多元回归、主成分回归等线性方法和BP算法相比,具有更高的预测精度。     

Comparison of Oxygen Transfer Parameters Determined from the Steady State Oxygen Uptake Rate and the Non-Steady-State Changing Power Level Methods

In this study, a laboratory scale Univ. of Cape Town enhanced biological phosphorus removal process was operated under controlled conditions at a solids retention time of 15 days. Results are presented for the process performance and oxygen transfer parameters determined by applying the steady state oxygen uptake rate (OUR) and the changing power level (CPL) techniques, as per ASCE standard guidelines. The testing periods were temporally separated to eliminate interference of the tests. During the application of the CPL method, the sludge volume index gradually increased and higher values of the oxygen transfer rate and alpha were measured, in comparison to the data from the steady state OUR method, under similar process performance. Furthermore, the mass transfer rate decreased as the CPL method of testing continued. In contrast, the oxygen transfer parameters remained uniform during the time when the OUR method was applied. The data indicated that the CPL method resulted in higher and variable oxygen transfer parameters, even though the process performance remained unchanged. Therefore, a more rigorous evaluation of the CPL method is recommended to clarify the validity of the test.     

Quercetagetin loaded in soy protein isolate–κ-carrageenan complex: Fabrication mechanism and protective effect

In the present study, the potential of soy protein isolate (SPI)–κ-carrageenan (κ-CG) complex as a protective carrier for quercetagetin was investigated at different pH values (pH 2.3 and 6.5). The particle size of the ternary aggregates was slightly increased at pH 2.3, yet dramatically decreased at pH 6.5 with increasing quercetagetin concentration. Moreover, the negative ζ-potential of the ternary aggregates was increased significantly (p < 0.05) at pH 6.5. The addition of quercetagetin to the SPI–κ-CG complex could highly quench the intrinsic fluorescence of SPI. Circular dichroism spectra further suggested that the bound quercetagetin could induce the rise of β-sheet and β-turn contents at the cost of α-helix and unordered coil fractions of SPI. In addition, quercetagetin could increase the viscoelasticity of the ternary aggregates at both pH. Furthermore, the SPI–κ-CG complex was found to be superior to single SPI or κ-CG in terms of improving light stability and radical scavenging ability of quercetagetin.     

Conceptual design of kenaf fiber polymer composite automotive parking brake lever using integrated TRIZ–Morphological Chart–Analytic Hierarchy Process method

This paper presents the conceptual design of kenaf fiber polymer composites automotive parking brake lever using the integration of Theory of Inventive Problem Solving (TRIZ), morphological chart and Analytic Hierarchy Process (AHP) methods. The aim is to generate and select the best concept design of the component based on the product design specifications with special attention to incorporate the use of natural fiber polymer composites into the component design. In this paper, the TRIZ contradiction matrix and 40 inventive principles solution tools were applied in the early solution generation stage. The principle solution parameters for the specific design characteristics were later refined in details using the aid of morphological chart to systematically develop conceptual designs for the component. Five (5) innovative design concepts of the component were produced and AHP method was finally utilized to perform the multi-criteria decision making process of selecting the best concept design for the polymer composite automotive parking brake lever component.     

Differences in the chemical structure of the lignins from sugarcane bagasse and straw

Two major residues are produced by the sugarcane industry, the fibrous fraction following juice extraction (bagasse), and the harvest residue (straw). The structures of the lignins from these residues were studied by pyrolysis coupled to gas chromatography-mass spectrometry (Py-GC/MS), nuclear magnetic resonance (NMR), and derivatization followed by reductive cleavage (DFRC). Whereas the lignin from bagasse has a syringyl-rich p-hydroxyphenyl:guaiacyl:syringyl (H:G:S) molar composition of 2:38:60, the lignin from straw is guaiacyl-rich (H:G:S of 4:68:28). The compositional differences were also reflected in the relative abundances of the different interunit linkages. Bagasse lignin was primarily β–O–4′ alkyl-aryl ether substructures (representing 83% of NMR-measurable linkages), followed by minor amounts of β–5′ (phenylcoumarans, 6%) and other condensed substructures. The lignin from straw has lower levels of β-ethers (75%) but higher relative levels of phenylcoumarans (β–5′, 15%) and dibenzodioxocins (5–5/4–O–β, 3%), consistent with a lignin enriched in G-units. Both lignins are extensively acylated at the γ-hydroxyl of the lignin side-chain (42% and 36% acylation in bagasse and straw), predominantly with p-coumarates (preferentially on S-units) but also with acetates (preferentially on G-units) to a minor extent. Tetrahydrofuran structures diagnostically arising from β–β-coupling (dehydrodimerization) of sinapyl p-coumarate or its cross-coupling with sinapyl alcohol were found in both lignins, indicating that sinapyl p-coumarate acts as a monomer participating in lignification. The flavone tricin was also found in the lignins from sugarcane, as also occurs in other grasses.