碎砖骨料再生混凝土配合比研究

用正交法试验分析了碎砖骨料混凝土的配合比，提出水灰比和碎砖骨料掺量分别是影响混凝土强度和流动性的主要因素。倡导用碎砖做混凝土骨料，保护生态环境。     

铝氧化物-水界面化学及其在水处理中的应用

天然水体中,铝氧化物矿物表面上的吸附等各种反应在很大程度上影响着金属阳离子、无机阴离子和一些天然有机物的迁移转化和归趋.在水处理等工业领域中,铝氧化物由于其水合表面的吸附能力而被用做离子交换剂和催化剂载体.因此,对铝氧化物表面化学过程的研究具有重要意义.铝氧化物-水界面上的反应十分复杂,对各种无机、有机污染物的吸附结合能力取决于氧化物固相表面性质、溶液条件和吸附质的性质.从对铝氧化物表面荷电特性和吸附活性的认识出发,就各种铝氧化物的结构特征和表面反应活性及其在水处理技术中的应用进行了简要综述.     

海水环境下玻璃纤维增强复合材料力学性能演化规律研究

目的 研究海水环境下海流能发电机组叶片用玻璃纤维复合材料力学性能的变化规律.方法 在实验室内通过海水浸泡试验、拉伸试验、弯曲试验以及剪切试验,测定叶片用玻璃纤维树脂基复合材料的吸水特性,以及在人工海水介质中各项力学性能参数的演变规律.结果 随着浸泡时间的增加,玻璃纤维树脂基复合材料吸水率先逐步增大、后趋于稳定,总吸水率约0.075％.抗拉强度呈先降低、后提高、又降低的趋势,抗拉强度最高可超过1100 MPa,最小值约为940 MPa.弹性模量和弯曲强度呈逐渐降低的趋势,弹性模量降幅约9.5％,弯曲强度降幅约为30％.弯曲模量变化起伏不定,变化幅度在15％以内.材料剪切强度呈先增大、后降低的趋势,最小值为189 MPa,较初始值高10 MPa.剪切模量呈先降低、后提高的现象,在浸泡28 d时,剪切模量最小,为16.4 GPa.结论 玻璃纤维增强树脂基复合材料经过长期海水浸泡后,拉伸及抗剪切性能略有降低,但降幅不大,抗弯性能下降明显,需要在叶片结构设计和强度计算时,充分考虑抗弯性能衰减的负面影响.     

冀西北黄土丘陵沟壑区梯田地埂植物篱的固埂作用与效益分析

经对张家口地区梯田地埂植物篱的研究表明 ,其固埂作用非常显著 ,且能够改善土壤的理化性状及水分状况 ,有效地拦蓄地表径流及泥沙 ,提高作物产量 ,具有明显的经济效益 ,在当地具有很广泛的推广应用价值     

菌株HX5对多种染料的吸附作用

研究了HX5生长菌体对分属活性、酸性、碱性、直接和分散5大类的26种染料的吸附性能．结果表明，HX5生长菌体可在5h内完全吸附直接染料和分散染料，碱性染料在生长菌体上完全吸附脱色的时间为12h，其次是活性染料，最不易吸附的为酸性染料．染料在生长菌体上的吸附由染料分子的结构和性质所决定，直接染料分子呈线性平面结构、疏水性较强，易于吸附，完全吸附脱色的时间为5h；分散性染料水溶性较差，在静电力的诱导之下即可在较短时间内完全吸附脱色；碱性染料分子带正电，与带负电荷的菌丝球表面异性电荷相吸从而发生吸附脱色；活性染料分子中的氨基质子化后与菌丝球表面相互吸引，氨基质子化的程度越高，吸附效果也就越好；酸性染料分子中氨基质子化程度受到结构本身的限制，以及不存在带正电荷的基团，因而吸附效果最差．     

Adsorption and correlation with their thermodynamic properties of triazine herbicides on soils

IntroductionAdsorptionofherbicidesonsoilfromwaterisanimportantfactoraffectingtheirfate,biologicalactivity,andpersistenceinsoil watersystem .Itisoftenaffectedbyseveralpropertiesofsoil.Betterunderstandingofadsorptionanditsaffectingfactorswillmakeitpossibletoadjusttheherbicidedosageaccordingtosoilproperties,thusreducingtheenvironmentalpollutionofherbicidesintheenvironment.Fig .1　StructuresofthreetriazineherbicidesAmongthepost emergentherbicides,triazineherbicidesaremostcommonlyusedworldwideonco…     

Starch, Poly(lactic acid), and Poly(vinyl alcohol) Blends

Research on biodegradable materials has been stimulated due to concern regarding the persistence of plastic wastes. Blending starch with poly(lactic acid) (PLA) is one of the most promising efforts because starch is an abundant and cheap biopolymer and PLA is biodegradable with good mechanical properties. Poly(vinyl alcohol) (PVOH) contains unhydrolytic residual groups of poly(vinyl acetate) and also has good compatibility with starch. It was added to a starch and PLA blend (50:50, w/w) to enhance compatibility and improve mechanical properties. PVOH (M_W 6,000) at 10%, 20%, 30%, 40%, 50% (by weight) based on the total weight of starch and PLA, and 30% PVOH at various molecular weights (M_W 6,000, 25,000, 78,000, and 125,000 dalton) were added to starch/PLA blends. PVOH interacted with starch. At proportions greater than 30%, PVOH form a continuous phase with starch. Tensile strength of the starch/PLA blends increased as PVOH concentration increased up to 40% and decreased as PVOH molecular weight increased. The increasing molecular weight of PVOH slightly affected water absorption, but increasing PVOH concentration to 40% or 50% increased water absorption. Effects of moisture content on the starch/PLA/PVOH blend also were explored. The blend containing gelatinized starch had higher tensile strength. However, gelatinized starch also resulted in increased water absorption.     

双室火灾烟气特性的实验研究

本文在１／２缩尺建筑模型中，取双室－走廊结构，以标准木垛为火源，对建筑火灾的初始阶段进行了实验模拟。着重研究了火灾初期的烟气特性及其变化，包括烟气温度及烟气中ＣＯ＿２气体和炭颗粒浓度。本文目的在于在探索和发展中等尺寸火灾实验模拟手段和方法的同时，定性地确定火源功率对烟气特性的影响，并积累一定的实验数据，为建筑火灾的分析和模化提供实验基础和依据。     

Mechanical Properties with the Functional Group of Additives for Starch/PVA Blend Film

This paper deals with the mechanical properties and degree of swelling (DS) of starch/PVA blend film with the functional groups i.e., hydroxyl and carboxyl group, of additives. Starch/PVA blend films were prepared by using the mixing process. Glycerol (GL) with 3 hydroxyl group, sorbitol (SO) with 6 hydroxyl group, succinic acid (SA) with 2 carboxyl group, malic acid (MA) with 1 hydroxyl and 2 carboxyl group, tartaric acid (TA) with 2 hydroxyl and 2 carboxyl group and citric acid (CA) with 1 hydroxyl and 3 carboxyl group were used as additives. The results of measured tensile strength (TS) and elongation (%E) verified that both hydroxyl and carboxyl group as a functional groups increased the flexibility and strength of the film. Values of DS for GL-added and SA-added films were low. However, DS values of the films added MA, TA or CA with both hydroxyl and carboxyl group were comparatively high. When the film was dried at low temperature, the properties of the films were evidently improved. The reason is probably because the hydrogen bonding was activated at low temperature.     

Mechanical and Barrier Properties of Biodegradable Films Made from Chitosan and Poly (Lactic Acid) Blends

Biodegradable film blends of chitosan with poly(lactic acid) (PLA) were prepared by solution mixing and film casting. The main goal of these blends is to improve the water vapor barrier of chitosan by blending it with a hydrophobic biodegradable polymer from renewable resources. Mechanical properties of obtained films were assessed by tensile test. Thermal properties, water barrier properties, and water sensitivity were studied by differential scanning calorimeter analysis, water vapor permeability measurements, and surface-angle contact tests, respectively. The incorporation of PLA to chitosan improved the water barrier properties and decreased the water sensitivity of chitosan film. However, the tensile strength and elastic modulus of chitosan decreased with the addition of PLA. Mechanical and thermal properties revealed that chitosan and PLA blends are incompatible, consistent with the results of Fourier transform infrared (FTIR) analysis that showed the absence of specific interaction between chitosan and PLA.