Effect of cation exchange on the distribution and movement of cations in soils with variable charge. I. Effect of lime on potassium and magnesium exchange equilibria

The influence of Ca(OH)₂ on K and Mg exchange equilibria in three New Zealand soils was studied. Calcium hydroxide was mixed with each soil to raise the pH to about 6 or 7. For each Ca(OH)₂ treatment, K and Mg exchange isotherms were determined, from which the equilibrium activity ratios were derived. Exchange coefficients and solution activity ratios were calculated according to the Gapon convention.The addition of Ca(OH)₂ produced varying effects in the Gapon exchange coefficient for both K and Mg. The magnitude and direction of change in the exchange coefficient were related to the cation initially dominating the exchange sites, rate of Ca(OH)₂ addition, soil colloids contributing to the CEC and specific interactions of Ca with these soil colloids.Addition of Ca(OH)₂ reduced the equilibrium activity ratio of all soils. Changes in the bonding strength of K and Mg with increasing CEC were suggested as a possible mechanism for this decrease.     

不同品种磷肥在土壤中的退化研究

对钙镁磷肥（FMP）、过磷酸钙（SSP）和部分酸化磷肥（PAPR）在河南郑州西岗沙土和河南西华县潮土中的退化情况进行了研究。     

Lanthanum-Magnesium and Lanthanum-Manganese Donor-Acceptor-Codoped Semiconducting Barium Titanate

BaTiO₃ powder doped with La donor and codoped with Mn or Mg acceptor was sintered at 1350°C/1 h in air. For Ladoped BaTiO₃, the room-temperature resistivity decreased to a minimum at [La³⁺] ∼ 0.15 mol%. For La-Mn-codoped BaTiO₃, the minimum resistivity occurred at [La³⁺] - 2[Mn²⁺] ∼ 0.15 mol%. When the ceramic was changed to a fine-grained insulator by high donor doping ([La³⁺] >0.15 mol%), its semiconductivity was restored, and the relatively homogeneous, coarse-grained microstructure recurred by codoping with either Mg or Mn acceptor, with the transition at [La³⁺] - 2[Mg²⁺] = 0.15 mol% or [La³⁺] - 2[Mn²⁺] = 0.15 mol%. The analogy of a compensation effect between La-Mn- and La-Mg-codoped BaTiO₃ suggested that Mn acceptor added to BaTiO₃ exists as Mn²⁺ ion in the bulk grain region; its influence on the positive temperature coefficient of resistivity behavior is then discussed.     

氢氧化镁和氧化镁中酸不溶物的研究

产硝后的高镁卤水和硫氢化钡溶液进行反应，生成氢氧化镁，酸不溶物在0．3％（质量分数）左右，但将其煅烧成氧化镁后，酸不溶物高达1．2％-2．5％（质量分数），二者酸不溶物远不成比例关系。通过对样品在分析中穿滤对比、硫酸法测定酸不溶物、碘量法测定硫化物试验，确定在生产过程中，硫氢化钡被氢氧化镁吸附，经过高温煅烧，硫氢化钡被氧化成硫酸钡，成为氧化镁中的酸不溶物，这就是氧化镁和氢氧化镁中酸不溶物不成比例的主要原因。     

钙镁磷肥发展前景综述

我国主要磷资源形成于距今6.5亿至5.5亿年前,1亿年内在扬子古海沉积了105亿t以中、低品位为主的胶磷矿。这类磷矿中的大多数含镁高,是制造钙镁磷肥的最佳原料。利用玻璃结构因子配料法可充分利用磷矿开采过程中废弃的低品位磷矿及顶板剥离层生产钙镁磷肥。并介绍中国的钙镁磷肥与日本、韩国熔成磷肥的生产现况及对比3国的售价,提出中国钙镁磷肥应与世界熔成磷肥的标准与价格接轨,有利于我国磷资源的合理利用。     

氢氧化镁中微量元素硼硅铝的测定

以盐湖高镁卤水为原料生产的氢氧化镁产品纯度不高,含有部分无机杂质离子,为提高产品质量,改进产品性能,通过实验确定了氢氧化镁中微量元素硼、硅、铝的分光光度测定方法。此方法准确度与精密度较高,测定样品中的硼、硅、铝加标回收率分别为98.3%-101.5%,96.0%-99.3%,96.5%-97.3%,相对标准偏差（n=6）分别为2.06%,2.27%,2.39%,快速、简便、成本低,可作为企业生产的常规检测方法使用。     

氯化镁处理方式对负载钛催化剂催化活性的影响

采用研磨方式制备了氯化镁负载钛催化剂,比较了氯化镁处理方式及球磨方式和球磨时间对催化活性的影响。结果表明,氯化镁结晶水的存在降低了催化剂活性,在制备过程中应避免氯化镁潮解形成结晶水。高温及使用异丁基铝预处理氯化镁均不利于提高催化活性,振动球磨较滚动球磨有利于提高催化活性,高活性催化剂的制备时间应大于15h。     

白云石中钙镁含量的测定研究

经典测定白云石中钙、镁含量的方法是先用EDTA标准溶液测定钙镁总量再测定钙含量，然后运用差减法计算出镁的含量。采用在指示剂中加入表面活性剂的方法，使其在滴定过程中生成三元络合物，提高了显色反应的灵敏度，增加有色化合物的稳定性。实验中确定了十二烷基硫酸钠作为加入指示剂的表面活性剂。在测定钙的过程中，苦味酸的加入消除了终点时微红色的干扰，终点易于观察和判断。与普通法相比，新方法终点变色敏锐，准确度、精密度均较高，结果令人满意。     

PE-LLD／EVA／Mg（OH）2／复合阻燃剂高效无卤阻燃体系的研究

采用线形低密度聚乙烯/乙烯-醋酸乙烯共聚物作为复合材料主体,表面处理过的氢氧化镁(Mg(OH)2)为主阻燃剂,以微胶囊化红磷和自制硅类阻燃剂为核心的复合阻燃剂为阻燃增效剂,重点探讨了Mg(OH)2和复合阻燃剂的阻燃效果。结果表明,Mg(OH)2与复合阻燃剂并用具有良好的协同效应,当Mg(OH)2用量40份,复合阻燃剂5～7份时,可获得较高的氧指数,垂直燃烧试验通过FV0级,且材料抗静电能力提高,力学性能、加工性能较好。     

绿色水处理剂氢氧化镁应用的研究进展

氢氧化镁(氧化镁)被称为绿色安全的废水处理剂,本文评述了氢氧化镁在环境保护方面的研究与应用进展,包括工业废水中铅、铬、镍等重金属离子的去除和酸性废水的中和处理,并列举了氢氧化镁对一些实际废水的良好处理效果,包括其对一些特殊废水如含硼废水和放射性废水的处理效果,最后展望了其在生产和应用方面的发展前景。