竹炭对生物油模型组分的吸附特性试验   总被引：1，自引：0，他引：1  

李允超  王贤华  隋海清  杨海平  胡海涛  陈汉平 《农业机械学报》2013,44(11):154-159,149

以竹子为前躯体热解制得竹炭,选取糠醛、乙酸、苯酚、葡萄糖为生物油模型化合物,研究竹炭对生物油模型组成各单组分的静态吸附特性及双、四组分混合下的竞争吸附行为。结果表明：竹炭对不同组分的吸附特性存在较大差异;单组分吸附24h,竹炭对糠醛的吸附量最大,乙酸次之,对葡萄糖的吸附量最小;吸附平衡时,竹炭对苯酚的吸附量将超过乙酸;糠醛-葡萄糖双组分竞争下,竹炭对糠醛显示出强烈的选择性吸附特征;4种组分竞争下,各组分吸附量相对单组分均有所下降,其中乙酸降幅最大,且乙酸等物质在吸附过程中出现浓度突变现象,这可能是因为吸附性能较好的糠醛将已经吸附的乙酸从竹炭上置换下来;在选用的所有试验工况下,竹炭对葡萄糖均表现出低的吸附态势。  相似文献   

黄土性土壤在连续液流条件下吸附、解吸磷酸根的动力学研究   总被引：9，自引：2，他引：9  

薛泉宏  尉庆丰  薛喜乐 《土壤学报》1995,32(2):142-150

采用连续液流法研究了黄土性土壤吸附,解吸磷酸根的动力学性质。结果表明：（１）供试土壤对磷酸根的吸附,解吸扫速率可分为快,中,慢三种反应类型;（２）描述吸附,解吸反应的最优模型均为Ｅｌｏｖｉｃｈ方程,最差模型分别为一级反应方程及双常数方程,拟合差的模型对反应速率变化“敏感”,可用于反应类型划分和机理研究;（３）粘粒含量及代换量对吸附速率有著影响,游离铁对吸附速率,ＣａＣＯ３对较低温度下的吸附及较高温  相似文献   

硫酸盐对锌和镉在可变电荷土壤上吸附的影响   总被引：8，自引：1，他引：8  

ZHANG Gang-Y  G. W. BRMMER  ZHANG Xiao-Nian 《土壤圈》1998,8(3):245-250

SO4^2- and Zn^2 or Cd^2 were added to three variable charge soils in different sequences.In one sequence sulfate was added first ,and in the other,Zn^2 or Cd^2 first.The addition of sulfate to the system invariably caused an increase in adsorption of the heavy metal added,with the effect more remarkable whn the soil reacted with the sulfate prior to the metal.the shift in pH50 for both Zn and Cd adsorption was aslo comparatively larger in the first sequence of reactions .It was suggested that the increase in negative charge density and the resultant negative potential of the soil were the primary cause of the pronounced effect of sulfate on adsorption of Zn or Cd,and the formaiton of the ternary surface complex-S-SO4-M might also play a role in the effect.  相似文献   

The effect of soil flooding on the transformation of Fe oxides and the adsorption/desorption behavior of phosphate     

Yongsong Zhang  Xianyong Lin  Wilfried Werner 《植物养料与土壤学杂志》2003,166(1):68-75

As repeatedly reported, soil flooding improves the availability of P to rice. This is in contrast with an increased P sorption in paddy soils. The effects of soil flooding on the transformation of Fe oxides and the adsorption/desorption of P of two paddy soils of Zhejiang Province in Southeast‐China were studied in anaerobic incubation experiments (submerging with water in N₂ atmosphere). Soil flooding significantly increased oxalate‐extractable Fe (Fe_ox), mainly at the expense of dithionite‐soluble Fe (Fe_DCB), as well as oxalate‐extractable P (P_ox), but decreased the ratio of P_ox/Fe_ox. Flooding largely increased both, P adsorption and the maximum P adsorption capacity. The majority of newly sorbed P in the soils was P_ox, but also more newly retained P was found to be not extractable by oxalate. Flooding also changed the characteristics of P desorption in the soils. Due to a decrease of the saturation index of the P sorption capacity, P adsorbed by flooded soils was much less desorbable than that from non‐flooded soils. There are obviously significant differences in the nature of both, the Fe_ox and P_ox fractions under non‐flooded and flooded conditions. The degree of the changes in Fe_ox, P_ox, P adsorption and P desorption by flooding depended on the contents of amorphous and total Fe oxides in non‐flooded soils. Our results confirm that the adsorption and desorption behavior of P in paddy soils is largely controlled by the transformation of the Fe oxides. The reasons of the often‐reported improved P availability to rice induced by flooding, in spite of the unfavorable effect on P desorbability, are discussed.  相似文献   

有机肥非水溶性分解产物对 铜 、镉吸附及解吸的影响   总被引：9，自引：0，他引：9  

谷勋刚  王果  方玲 《植物营养与肥料学报》2001,7(1):93-102

研究了稻草、紫云英和猪粪淹水培养的非水溶性分解产物、两种土壤( 红壤、潮土) 与这 3 种有机肥共同淹水培养后的非水溶性产物( 水溶性物质被除去) 对铜、镉的沉淀、吸附及解吸作 用的影响。 结果表明, 当铜初始浓度为 10-4mol/ L, pH <6 时有机残渣促进铜的沉淀;当 pH >6 时则抑制了铜的沉淀。 当铜初始浓度降为 10-5mol/ L 时, 有机残渣对铜沉淀的促进作用加强。 3 种有机残渣均促进镉的沉淀, 但促进程度比铜低。 与有机肥共同培养的红壤, 在相同的 pH 条 件下, 提高对铜、镉的吸附;在不调节 pH 条件下, 由于有机肥料有提高 pH 的作用, 进一步提高 对铜 、镉的吸附。 与有机肥共同培养的潮土, 在相同的 pH 条件下, 对铜、镉吸附的影响很小;在 不调节 pH 时, 提高了潮土对铜的吸附, 但对镉吸附的影响则较复杂。 上述结果表明, 有机肥的 非水溶性分解产物主要通过提高体系的 pH 值、与铜、镉形成不溶性的络合物而影响铜、镉的吸 附。 与有机物料共同培养的红壤所吸附的铜、镉的解吸率均不同程度降低。  相似文献   

Occurrence of Polycyclic Musks in Sewage Sludge and their Behaviour in Soils and Plants. Part 1: Behaviour of Polycyclic Musks in Sewage Sludge of Different Treatment Plants in Summer and Winter (5 pp)     

Josef Müller  Walter Böhmer 《Journal of Soils and Sediments》2006,6(4):231-235

Background, Aim and Scope   Part 1: Behaviour of Polycyclic Musks in Sewage Sludge of Different Treatment Plants in Summer and Winter Part 2: Investigation of Polycyclic Musks in Soils and Plants -  Preamble. In Part 1 of the study, screening tests were performed to investigate the occurrence of PCMs in sewage sludges. For a preliminary risk assessment, further information is needed about their behaviour in the terrestrial environment. Hence, Part 2 examined the adsorption of PCMs to soil, their dissipation and leaching in soil and their uptake by plants. Background, Aim and Scope   Polycyclic Musks (PCMs) enter the environment via the waste water system. Because of their persistence, they can accumulate in different matrices like sewage sludge or biota. By the use of sewage sludge as a fertilizer, PCMs are transferred to agricultural soils. Therefore, in Part 1 of the study, screening tests were performed to investigate the occurrence of PCMs in sewage sludge. For a preliminary risk assessment, further information is needed about their behaviour in the terrestrial environment. Hence, Part 2 of the study examined the adsorption of PCMs to soil, their dissipation and leaching in soil, and their uptake by plants. Materials and Methods: In the screening study, samples of activated sewage sludge were taken both in summer and in winter at 21 treatment plants. In order to get an overview of the contamination situation, sampling covered different types of treatment plants (in rural, urban, industrial areas). Analytical methods for the determination of HHCB, AHTN, ADBI, ATTN, AHDI and ATII in the sludge samples were developed and applied. Results: The analytical screening of PCMs showed their presence in activated and dried sewage sludge samples. HHCB and AHTN represented about 95% of the PCMs investigated. Their concentrations in the activated sludge samples varied between 2.9 and 10.4 mg/kg dry mass (dm) and 1.1 to 4.2 mg/kg dm, respectively. Although different types of sewage treatment plants were investigated, similar PCM levels were found, showing the widespread input of these compounds into domestic waste water. Discussion: PCM concentrations in activated sludge varied widely. The variation drops substantially when concentrations are related to the varying dry mass. In dehydrated sludge, PCM concentrations were up to 24 mg/kg dm for HHCB and up to 6.9 mg/kg dm for AHTN. These high values are comparable to those obtained in other investigations analysing PCMs. If the degradation of organic mass during anaerobic decomposition is included in the evaluation, the figures obtained are comparable to those for activated sludge. Elimination in sewage sludge was higher in summer than in winter. Therefore, the contamination of the sludges in winter reached higher levels compared to the summer. Conclusions: The results show that PCMs are widespread contaminants in sewage sludge. Recommendations and Perspectives: PCM should be considered in a risk assessment as potential contaminants of sewage sludge destined for agricultural use. Due to the high PCM levels in sewage sludge, further investigations into the degradation and elimination behaviour in sewage sludge have to be carried out, including that involving PCM metabolites such as lactone derivatives.  相似文献   

pH对砖红壤和黄棕壤Cu~(2+)吸附与解吸的影响   总被引：3，自引：0，他引：3  

徐明岗  曾希柏  李菊梅 《土壤通报》2005,36(3):349-351

对砖红壤和黄棕壤在不同浓度、不同pH下吸附和解吸Cu2+进行了测定。结果表明, 2种土壤Cu2+吸附量均随平衡液中Cu2+浓度增加而增大,两者关系较好地符合Langmuir吸附方程。Cu2+吸附量随pH升高而增加,Cu2+分配系数的对数与pH呈极显著的线性正相关,吸附一个Cu2+所释放H+的平均数砖红壤(1. 19)大于黄棕壤(1. 01)。可解吸Cu2+的数量随pH升高和吸附Cu2+的数量增加而增加,在pH4~6下,黄棕壤吸附Cu2+及可解吸Cu2+的比例(平均为10. 5% )大于砖红壤(平均为3. 1% )。由此认为, 2种土壤吸附Cu2+虽以专性吸附为主,但砖红壤的表面吸附点位较少,专性吸附点位的比例较高,对Cu2+的亲和性或专性吸附性大于黄棕壤。  相似文献   

不同液土比和温度条件下塿土铵离子吸附     

WANG Yu  ZHANG Yi-Ping 《土壤圈》2004,14(2):253-257

Effects of NH₄⁺ concentration, solution/soil ratio and temperature on NH₄⁺ adsorption were studied in a Eum-Orthic Anthrosol. The slopes of the soil NH₄⁺ adsorption isotherms and the fitted n, the coefficient for the adsorption intensity, and k, the coefficient related to adsorption capacity, of the Freundlich equation increased with increasing solution/soil ratio (SSR) and with decreasing temperature (T). For the range of experimental conditions, the value of ∂q/∂c, the rate of change of the amount of NH₄⁺ adsorbed in the soil solid phase (q) with respect to the equilibrium concentration of NH₄⁺ in soil solution (c), was 0.840, indicating that q increased with increasing c. From 2 to 45 ℃, ∂q/∂SSR, the rate of change of q with respect to SSR, decreased from 2.598 to 1.996, showing that q increased with increasing SSR, while its increasing rate decreased with temperature. From SSR 1:1 to 20:1, ∂q/∂T, the rate of change of q with respect to T, decreased from -0.095 to -0.361, indicating that q decreased with increasing temperature, and at the same time the negative effect of temperature became larger as SSR increased. Thus under the experimental conditions the order of importance in determining the amount of NH₄⁺ adsorbed in the soil solid phase was ∂q/∂SSR > ∂q/∂c > |∂q/∂T|, indicating that the greatest effect on the amount of NH₄⁺ adsorbed was with the solution/soil ratio; the equilibrium concentration of NH₄⁺ had a lesser effect; and temperature had the least effect.  相似文献   

几种有机酸对恒电荷和可变电荷土壤吸附Cu²⁺的影响   总被引：15，自引：3，他引：15       下载免费PDF全文

胡红青  刘华良  贺纪正 《土壤学报》2005,42(2):232-237

以恒电荷土壤(黄褐土和黄棕壤)和可变电荷土壤(红壤和砖红壤)为供试材料,研究了乙酸、草酸、酒石酸和柠檬酸对土壤吸附重金属铜离子(Cu2 )的影响。结果表明,在相同酒石酸浓度下,土壤对酒石酸的吸附量依次为黄棕壤(2 1 8mmolkg-1) >红壤(15 4mmolkg-1) >砖红壤(9 5mmolkg-1) ,土壤吸附有机酸后负电荷量增加,相同条件下增幅为砖红壤>红壤>黄棕壤;无有机酸配体时,供试土壤对Cu2 的吸附量为黄褐土>黄棕壤>砖红壤>红壤;加入有机酸时,随有机酸浓度增高,土壤对Cu2 的吸附一般表现为“峰”形曲线,峰所对应的有机酸浓度因有机酸类型而异,且随土壤可变电荷性质增强而增高;土壤吸附有机酸后对Cu2 的次级吸附不同于有机酸与铜共存时的竞争吸附,且因土壤性质表现迥异。这些结果意味着在存在有机酸配体的根际环境中,恒电荷土壤与可变电荷土壤对Cu2 的吸附明显不同,并将影响重金属离子在根际的转化与有效性  相似文献   

氟离子、磷酸根和铬酸根在可变电荷土壤表面吸附过程中羟基释放动力学     

姜军  徐仁扣  王永  赵安珍 《土壤》2008,40(6):949-953

用恒pH自动电位滴定装置研究了氟离子(F-)、磷酸根(H2PO4-)和铬酸根(CrO42-)在3种可变电荷土壤表面吸附过程中羟基(-OH)释放的动力学。研究结果表明,3种阴离子在可变电荷土壤表面吸附时-OH释放量的大小顺序为:F->>H2PO4->CrO42-,这与土壤对3种阴离子吸附量的大小顺序一致。pH对不同阴离子体系中-OH释放的影响不同,在F-体系中,pH5.0时-OH释放量最高,其次为pH6.0时,pH4.0时-OH释放量最小;CrO42-体系中-OH释放量随pH的增加而减小;pH对H2PO4-体系中-OH释放的影响较小。Elovich方程(Y=a kln(t))能够很好拟合2～60min之间的动力学数据,说明-OH释放的速率随时间增加而减小。比较速率常数k的大小可以发现,虽然F-体系中3种可变电荷土壤在前2min释放的-OH量有很大差异,但在2～60min内,-OH释放速率差别不大。在H2PO4-和CrO42-体系中,-OH释放速率的大小顺序是:昆明砖红壤>徐闻砖红壤>江西红壤,与土壤铁、铝氧化物含量一致。  相似文献