碳酸氢钠浸提测定土壤有效磷研究

本文根据碳酸氢钠浸提-钼锑抗分光光度法测定土壤中有效磷的分析过程,对土壤中有效磷的测定进行了检出限、精密度和准确度的验证,证实该方法不仅操作简单、仪器普及率高,且检出限较低、精密度和准确度良好,具有普遍适用性。     

Na_2CO_3/H_2O_2“稳定”的CO_2的型体研究(Ⅱ)——“稳定性二氧化氯”溶液的UV吸收光谱、纸层析特性、微观结构和离子色谱分析

本文对以稳定剂H_2O_2和Na_2CO_3与ClO_2制备的所谓"稳定性二氧化氯"溶液的UV吸收光谱、纸层析特性、微观结构及离子色谱进行了分析,并与纯NaClO_2及ClO_2溶液做了对比.结果表明,“稳定性二氧化氯” 与NaClO_2在UV吸收光谱、层析比移值、微观结构、离子色谱这几方面都具有很好或极其相似的一致性 表明“稳定性二氧化氮’与NaClO_2溶液中氯氧化物存在型体的一致性.因此,认为“稳定性二氧化氯“溶液中ClO_2是以亚氯酸盐ClO_2~-的型体存在的.     

碳酸氢钠及其固态分解产物对玉米淀粉爆炸抑制实验研究*

为研究NaHCO3对玉米淀粉爆炸的抑制效果,采用20 L球形爆炸装置测试玉米淀粉在添加不同抑制比NaHCO3及其固态分解产物Na2CO3后爆炸参数变化规律,并分析NaHCO3抑制淀粉爆炸过程。结果表明:NaHCO3及Na2CO3对玉米淀粉爆炸均有抑制作用,NaHCO3抑制效果优于Na2CO3;混合粉尘的最大爆炸压力、最大爆炸压力上升速率与爆炸指数随抑制比增大而逐渐减小,爆炸时间随抑制比增大而逐渐延长。随着NaHCO3浓度增加,物理抑制效果逐渐增加,化学抑制效果基本保持不变。NaHCO3浓度不同时,其抑制主导过程不同,当抑制比为0.1~0.5时,NaHCO3抑制效果以化学抑制为主,物理抑制为辅;抑制比为0.8和1.2时,NaHCO3抑制效果以物理抑制为主,化学抑制为辅;当抑制比为1.2时,玉米淀粉爆炸完全被NaHCO3抑制,此时物理抑制起主导作用。     

嘉兴农村不同土地利用方式下沟渠底泥中的氮磷形态分布特征

沟渠是农田氮、磷营养物质排入地表水体的通道. 对嘉兴大田、集约化菜地、集约化果园、集约化养殖场4种土地利用方式下的农村沟渠0～5 cm表层底泥氮、磷的形态分布特征进行了研究. 结果表明:67个沟渠底泥样品的w(全氮)为1 560～7 480 mg/kg,其中w(交换态氮)为31.15～704.38 mg/kg,占w(全氮)的1.29%～10.01%;交换态氮中以铵态氮为主,占w(交换态氮)的62.15%～100%. 沟渠底泥样品的w(全磷)为580～6 420 mg/kg,w(碳酸氢钠溶解磷)为19.53～359.72 mg/kg,占w(全磷)的2.05%～18.96%;w(水溶性磷)为0.29～18.88 mg/kg,占w(碳酸氢钠溶解磷)的1.11%～14.63%. 土地利用方式对沟渠底泥氮、磷的形态分布有显著影响(P<0.01),集约化养殖场沟渠底泥中的w(全氮), w(交换态氮),w(铵态氮), w(硝态氮), w(交换态氮)/w(全氮), w(全磷), w(水溶性磷), w(碳酸氢钠溶解磷)均显著高于其他土地利用方式. 底泥w(全氮), w(交换态氮), w(铵态氮)和w(硝态氮)两两间以及w(全磷), w(水溶性磷), w(碳酸氢钠溶解磷)两两间均在α0.01时显著相关,w(全磷)与w(碳酸氢钠溶解磷)的相关性(r0.81,P<0.01)好于与w(水溶性磷)的相关性(r0.51,P<0.01).      

一种草甘膦合成中间体双甘膦制备过程中废水处理的新工艺

该发明涉及草甘膦合成中间体双甘膦制备过程中废水处理的新方法。该方法主要是在双甘膦制备过程中，过滤去除双甘膦晶体后，往剩下滤液或浓缩后滤液中加入一定量碳酸氢铵，充分反应，过滤，得碳酸氢钠和含有氯化铵的滤液。碳酸氢钠能回收利用于双甘膦的制备，滤液经浓缩可得到氯化铵副产。     

Reaction kinetic model for a recent co-produced water treatment technology

With the increasing demand for fossil based energy and implementation of progressively strict environmental pollution control standards, treatment of a large amount of co-produced waters (CPWs) from fossil based energy production has become increasingly important. Removal of bicarbonate with H2SO4 has been recently studied as a simple and cost-e ective method to decrease the alkalinity of CPWs. The present work investigates the kinetics of the reaction between H2SO4 and NaHCO3, which could provide the base for scaling-up the CPW treatment technology. Based on the measured quantity change of the CO2 gas generated from the reaction between H2SO4 and NaHCO3 with time under specified initial reaction conditions, the reaction orders with respect to H2SO4 and NaHCO3 were determined. Experiments were also conducted within the temperature of 15–30°C to find various global rate coe cients of the reaction to calculate the activation energy and the pre-exponential factor of the empirical Arrhenius form of the bicarbonate removal reaction, which are 197.7 kJ/mol and 3.13 1034 (mol??3:7 L3:7 sec??1), respectively.     

Effects of bicarbonate and cathode potential on hydrogen production in a biocathode electrolysis cell

A biocathode with microbial catalyst in place of a noble metal was successfully developed for hydrogen evolution in a microbial electrolysis cell （MEC）. The strategy for fast biocathode cultivation was demonstrated. An exoelectrogenic reaction was initially extended with an H2-full atmosphere to enrich Ha-utilizing bacteria in a MEC bioanode. This bioanode was then inversely polarized with an applied voltage in a half-cell to enrich the hydrogen-evolving biocathode. The electrocatalytic hydrogen evolution reaction （HER） kinetics of the biocathode MEC could be enhanced by increasing the bicarbonate buffer concentration from 0.05 mol·L-1 to 0.5 mol· L-1 and/or by decreasing the cathode potential from -0.9 V to - 1.3 V vs. a saturated calomel electrode （SCE）. Within the tested potential region in this study, the HER rate of the biocathode MEC was primarily influenced by the microbial catalytic capability. In addition, increasing bicarbonate concentration enhances the electric migration rate of proton carriers. As a consequence, more mass H＋ can be released to accelerate the biocathode-catalyzed HER rate. A hydrogen production rate of 8.44 m3. m 3. d1 with a current density of 951.6 A. m-3 was obtained using the biocathode MEC under a cathode potential of - 1.3 V vs. SCE and 0.4 mol· L-1 bicarbonate. This study provided information on the optimization of hydrogen production in biocathode MEC and expanded the practical applications thereof.     

苏打水是一种什么水

“苏打水”,一个名字几种内涵。“苏打水”这个名词来源于英文“soda water”。在英文中,它也被称为“碳酸水(carbonated water)”或者“起泡水(sparkling water或者seltzer water)”。“起泡水”可以简单地理解为“倒在杯子中能看到气泡的水”。之所以能够起泡,是因为水中的二氧化碳超过了自然压力下的饱和浓度,所以会聚集成气泡逸出。有一些矿泉水天然满足这样的要求,被称为“含气天然矿泉水”。可以通过人为地在加压的情况下充入二氧化碳而得到的,叫作“充气天然矿泉水”。二氧化碳在水中形成碳酸,可以离解出氢离子,所以这样的“起泡水”有可能是弱酸性的。在这个意义上的苏打水,并不一定含有碳酸氢钠,更不一定是弱碱性的。     

活化赤泥除氟剂的制备及除氟性能试验研究

分别采用(NH4)2HPO4,NH4HCO3,NaHCO3等对赤泥进行活化处理,并制备成球形颗粒,同时研究了活化剂浓度、焙烧温度、焙烧时间等对赤泥除氟剂吸附性能的影响。结果表明：在活化剂质量浓度为10%左右、焙烧温度500℃,焙烧时间2 h时制备的除氟剂具有较好的除氟效果,且采用(NH4)2HPO4,NH4HCO3,NaHCO3对赤泥进行活化处理制备的除氟剂能分别使溶液中氟离子的质量浓度从19 mg/L分别降低到0.085,0.13及0.19 mg/L,相应地除氟剂的吸附容量均达0.94 mg/g以上。     

干法碳酸氢钠脱硫过程及影响因素分析

通过固定床反应装置模拟了NaHCO_3粉末与SO_2反应,考察了NaHCO_3粒径和反应温度对脱硫过程的影响,设计了经热解处理后的NaHCO_3与SO_2反应,推导出NaHCO_3热激活脱硫机制。研究发现:150～360℃内,温度越高SO_2脱除率越高; NaHCO_3粒径越小脱硫效果越好;当NaHCO_3粒径为1500目、反应温度为360℃时,SO_2脱除率高达99. 1%。反应温度为240～390℃时,脱硫反应可分为2个阶段:第1阶段主要为SO_2在NaHCO_3颗粒表面与之直接反应;第2阶段为高温下NaHCO_3分解生成Na_2CO_3和CO_2,CO_2从体相逸出后可提供大量微孔结构,有利于提高反应比表面积和反应速率。