波谱学杂志
波譜學雜誌
파보학잡지
CHINESE JOURNAL OF MAGNETIC RESONANCE
2014年
3期
372-380
,共9页
邵朱伟%张明辉%李新宇
邵硃偉%張明輝%李新宇
소주위%장명휘%리신우
时域核磁共振(TD NMR)%固化%自旋-自旋弛豫时间(T2)%自旋-晶格弛豫时间(T1)%脲醛树脂
時域覈磁共振(TD NMR)%固化%自鏇-自鏇弛豫時間(T2)%自鏇-晶格弛豫時間(T1)%脲醛樹脂
시역핵자공진(TD NMR)%고화%자선-자선이예시간(T2)%자선-정격이예시간(T1)%뇨철수지
time-domain nuclear magnetic resonance%solidification%spin-spin relaxation time%spin-lattice relaxation time%urea-formaldehyde resin
利用时域核磁共振(TD NMR)技术对无固化剂的脲醛树脂在不同温度下固化过程进行了研究,实验结果表明:脲醛树脂在120℃左右时开始固化,在180℃左右时固化反应基本结束.随着温度的升高,自旋-自旋弛豫时间(T2)的总峰面积逐渐减少,当温度高于140℃时,总峰面积减少的程度较大.在30℃~140℃温度范围内,自旋-晶格弛豫时间T1(1)=0.014 ms时,随着温度的升高,峰面积先逐渐减少而后略微增加;T1(2)=327.455 ms时,随着温度的升高,峰面积逐渐减少.在30℃~180℃温度范围内,自旋-晶格弛豫时间(T1)分布的总峰面积随着温度的升高而逐渐减少.在固化过程中,随着温度的升高,脲醛树脂体系的质量逐渐减少,说明脲醛树脂胶黏剂体系发生了缩聚交联反应,同时生成了甲醛和水.
利用時域覈磁共振(TD NMR)技術對無固化劑的脲醛樹脂在不同溫度下固化過程進行瞭研究,實驗結果錶明:脲醛樹脂在120℃左右時開始固化,在180℃左右時固化反應基本結束.隨著溫度的升高,自鏇-自鏇弛豫時間(T2)的總峰麵積逐漸減少,噹溫度高于140℃時,總峰麵積減少的程度較大.在30℃~140℃溫度範圍內,自鏇-晶格弛豫時間T1(1)=0.014 ms時,隨著溫度的升高,峰麵積先逐漸減少而後略微增加;T1(2)=327.455 ms時,隨著溫度的升高,峰麵積逐漸減少.在30℃~180℃溫度範圍內,自鏇-晶格弛豫時間(T1)分佈的總峰麵積隨著溫度的升高而逐漸減少.在固化過程中,隨著溫度的升高,脲醛樹脂體繫的質量逐漸減少,說明脲醛樹脂膠黏劑體繫髮生瞭縮聚交聯反應,同時生成瞭甲醛和水.
이용시역핵자공진(TD NMR)기술대무고화제적뇨철수지재불동온도하고화과정진행료연구,실험결과표명:뇨철수지재120℃좌우시개시고화,재180℃좌우시고화반응기본결속.수착온도적승고,자선-자선이예시간(T2)적총봉면적축점감소,당온도고우140℃시,총봉면적감소적정도교대.재30℃~140℃온도범위내,자선-정격이예시간T1(1)=0.014 ms시,수착온도적승고,봉면적선축점감소이후략미증가;T1(2)=327.455 ms시,수착온도적승고,봉면적축점감소.재30℃~180℃온도범위내,자선-정격이예시간(T1)분포적총봉면적수착온도적승고이축점감소.재고화과정중,수착온도적승고,뇨철수지체계적질량축점감소,설명뇨철수지효점제체계발생료축취교련반응,동시생성료갑철화수.
The curing process urea-formaldehyde resin without the use of hardeners was studied by time-domain nuclear magnetic resonance (TD NMR) at different temperatures. The results showed that urea-formaldehyde resin started curing at about 120℃and ended around 180℃. The total peak area for T2 decrease gradually with increasing temperature;and larger changes were observed when the temperature was above 140℃. At temperature range between 30 ℃ to 140 ℃, the peak areas decreased gradually and then increased slightly with increasing temperature at T1 (1)=0.014 ms;the peak areas decreased gradually with increasing temperature at T1 (2)= 327.455 ms. The total peak area for T1 decrease gradually with increasing temperature between 30℃and 180 ℃. The urea-formaldehyde resin system weight decreased gradually with increasing temperature in the solidification process, confirming that cross-linking condensation reaction may occur, giving off formaldehyde and water.