温压工艺中聚合物添加剂的加入方式

采用温压技术制备铁基粉末冶金材料,研究了干混和湿混两种聚合物添加剂加入方式及压制温度对生坯和烧结体性能的影响,并对其作用机理进行了探讨.试验结果表明,干混混合粉生坯及烧结体的性能略高于湿混混合粉生坯及烧结体的性能,但前者的最佳压制温度范围略高.     

秦山核电站邻近水域海水光的穿透性能变化研究

本文运用水体可见光的传输机理，讨论了光的传输特性与水中悬浮泥沙，色素和黄色物质的定量关系。同时简述了在秦山核电站邻近海域１９９５年１０月￣１９９６年７月间４个航次的有关水光学特征现场测量过程和实验室分析方法。最后，通过水体中太阳光透透深度和真空层，研究了该邻近海域的光穿透性能的季节性变化。研究表明，核电站运行以来，秦山核电站邻近海域水的光穿透性能变化很小。     

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。     

通信电缆、光缆及材料环境试验研究

简述了通信电缆、光缆及材料环境试验研究概况,进行了线缆 土壤腐蚀数据积累及规律性研究,取得了大量数据和研究成果,将 成果应用到国民经济建设中,为线缆的护层结构设计、材料选择、生 产维护和制定标准规范提供了科学依据。     

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     

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.