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研究生:林嘉猷
論文名稱:台灣酸性土壤之交換酸度特性
論文名稱(外文):The Characteristics of Exchangeable Acidity in Taiwan Acidic Soils
指導教授:洪崑煌洪崑煌引用關係
學位類別:碩士
校院名稱:國立臺灣大學
系所名稱:農業化學研究所
學門:農業科學學門
學類:農業化學類
論文種類:學術論文
論文出版年:1996
畢業學年度:84
語文別:中文
論文頁數:85
中文關鍵詞:酸性土壤交換酸度特性
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  酸性土壤本質上,在不考慮腐值酸以及其他各種可溶性酸存在對酸性土壤酸度的貢獻情形下,其土壤溶液和交換體上都是以鋁離子和氫離子為主,亦即為氫鋁混合黏土;對於強酸性土壤而言,土壤酸的來源包含氫和鋁離子。鋁離子對酸度的貢獻,則是藉由鋁離子的水解所產生的。因此為了探討鋁離子與氫離子對交換酸度的貢獻,本文採用台灣五種酸性土壤,並以不同離子強度抽出液,仿照大工原氏連續抽出法,以土水比為1:2.5之條件,將混合液振盪2小時、靜置22小時後,取出其上清液一半之量後,再行添加同量之新鮮抽出液,採該步驟連續反覆進行十次;藉由抽出過程中所測得pH、滴定酸度、滴定鋁量、及由原子吸光儀分析所測得鋁、鈣、鎂之量,來探討台灣酸性土壤之交換酸度特性。除此之外,亦採用四種測定土壤CEC值之方法,對供試土壤進行測定,以期對台灣酸性土壤做更進一步的了解。
  將有效酸度量與本實驗所得之十次酸度總量進行比較,發現1MKC1所抽得總量與有效酸度量相當(94%~109%),但隨著抽出液濃度降低、所抽得之酸度總量亦跟著減少;仿照大工原氏連續抽出法之理論式,即當抽出次數達到無限次時,其土壤酸度總量到用S =2*(Y1+a1/(1-K))公式表示。利用該公式所求得之總酸度量與採用土水比1:10之批次法所抽得之總酸度相比較,則可發現1M KC1部份所得之總量佔批次法所得之總量的82%~92%、而0.1M KC1則能表現出總量50%~70%、至於0.01M KC1則只能反映出20%~30%。此表示土壤的交換酸度總量明顯受到抽出液濃度的影響。而計算中所採用的K值則多落於0.8~0.9之間,其結果與大工原氏的結果相近;而鈣、鎂離子的交換總量,1M與0.1M KC1所抽得總量值則相同。
  就滴定鋁量佔滴定酸度的百分比來看,1M KC1所抽出之滴定鋁量所佔百分比為平鎮系、老埤系為80%,而淇武蘭系、淡水系則分別佔71%與76%,至於坡堵部份則僅佔53%,其原因應是其pH值較高所導致。而0.1M KCl部份除了淇武蘭系所佔百分比減少為45%,其餘土則皆維持於1M濃度水準,當抽出液濃度降至0.01M時,所有土系之滴定鋁量佔滴定酸度百分比皆大幅下降。
  這五種酸性土壤平衡溶液中pH與鋁離子活性關係,若以A1(OH)3形式進行離子積計算時,無論是何種濃度的抽出液,其值皆介於-34.5~-33之間,所得值與Gibbsite之-33.96相近,此顯示含鋁礦物的溶解沈澱可能會控制溶液中鋁離子活性。
  由實驗結果推測,土壤與抽出液發生反應時,溶液中鈣、鎂離子平衡的達成僅藉由離子交換所完成,而鋁離子平衡的達成則是由離子交換與含鋁礦物溶解沈澱所共同完成。
  Aluminum and hydrogen ions comprise the main parts of the soil solution and exchange cations of an acid soil, disregarding those derived from organic matter, i.e. an acid soil is a mixed Al-H clay system. In an strongly acid soil, the acidity is made up of exchangeable Al and H ions. Aluminum ion contributes to the acidity by its hydrolysis. In order to understand the contribution of aluminum ion to the soil acidity, five acid soils were selected, their soil acidity were determined by Daikuhara''s procedure, using various concentration of KC1 solutions and a soil: solution ratio of 1:2.5. The soil suspension was shaken for 2 hours, and after being left standing for 22 hours, a half volume of the supernatant solution was withdrawn for analyses of extracted H, Al, Ca, and Mg ions. To the remaining soil solution mixture a fresh original extracting solution was replenished to the original volume, and the extraction procedure repeated 10 times altogether. The amounts of H and Al in each extract were determined by titration with a standard NaOH solution, those of Ca and Mg were determined by atomic absorption spectrometry. The cation exchange capacities of the soils were determined by four different methods, the results were compared to understand the acid characteristics of the acid soils of Taiwan.
  By comparing the effective acidity and those extacted in the 10 successive extractions, it is found that the total acidity extracted by 1M KC1 solution corresponded to the effective acidity (94-109%), but the acidity extracted decreased with the decrease in the concentration of the extracting solution. According to Daikuhara''s, the total acidity present in the soil (S) should equal to S+2{y1+a1/(1-K)}, in which y1 is a half of the acidity determined in the first extract, a1=y2-y1/2, and K=a2/a1=a3/a2=…and it should not be dependent on the concentration of the extracting solution. If the soil: solution ratio was 1:10, the total acidity obtained was 82-92% of the value which was obtained with a soil: solution ratio of 1:2.5. When the extracting solution was 0.1M KC1, the total acidity determined was 50-70% of that obtained with 1M KC1. When the extracting solution was 0.01M KC1, the total acidity obtained d was even less, being 20-30% of that obtained with 1M KC1. The K values were in the range of 0.8 to 0.9, which were close to those obtained by Daikuhara''s. The total Ca and Mg extracted with 1M KC1and 0.1M KC1 were the same with the total exchangeable Ca and Mg, respectively.
  The results show that extractable Al comprised about 80% of total soil acidity of Pingchen and Laopi series, while for Chiwulan and Tanshui series, the extractable Al comprised 71 and 76%, respectively. For the Potu series, the total extractable Al comprised only 53% of the total acidity ,probably due to its relatively higher pH. With 0.1M KC1, the proportions of extractable Al to the total acidity were nearly the same with those extracted by 1M KC1, except that of Chiwulan series, in which the proportion reduced to 45%. With 0.01M KC1, the proportion of extractable Al reduced markedly for all soils studied. The amounts of Al extracted into the solution were remarkably affected by the concentration of the extracting solution.
  The logarithms of the ionic product, log[(Al3+)(OH)3], of all solutions were in the range of -34.5 to -33.0, which were quite close to the value of gibbsite, -33.96. It indicates that the presence of aluminum hydroxide mineral is controlling the aluminum ion activities of the equilibrium solutions.
  From the experimental result we may deduce when acid soils reacted with extraction solution, which Ca, Mg ionic equilibrium only by ion exchange but that the aluminum ionic equilibrium included the ion exchange reaction and the dissolution of a form of aluminum hydroxide mineral present in the acid soil.
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