suspension polymerization 中文意思是什麼

suspension polymerization 解釋
懸浮聚合
  • suspension : n 1 懸吊，懸掛；懸垂；懸架吊架。2 中止，停止；停止支付[宣判，處刑]；停職，停學，停權。3 懸置，保...
  • polymerization : 聚合酌
  1. Study on graft copolymer of natural rubber by suspension polymerization

    懸浮聚合法合成天然橡膠接枝共聚物的研究
  2. Syntheses of soluble starch graft copolymers by inverse suspension polymerization

    反相懸浮聚合法合成可溶性澱粉接枝共聚物
  3. And the adsorbability of this novel adso rbent for ldl was determined. in order to prepare the solid supports in accordance with with the request of adsorbent for ldl, paam beads were synthesized by inverse suspension polymerization. the composition of the polymerization system is shown as follows : the concentration of monomer and dispersant are 12 % and 0. 65 % respectively, the volume ratio of oil / water isl : 3, the mole ratio of aam and mba is 18 : 1

    本文用反相懸浮聚合法合成符合ldl吸附劑載體要求的聚丙烯酰胺微珠，經實驗篩選出反應體系所需的最佳單體濃度（ 12 ） 、最佳分散劑用量（ 0 . 65 ） 、最佳油水比值（ 1 ： 3 ） 、最佳單體（ aam ）與交聯劑（ mba ）的物質的量之比（ 18 ： 1 ） 。
  4. Some amino acids and drugs imprinted spheres ( mipm ) were prepared via seeds swelling and suspension polymerization, suspension polymerization and emulsion polymerization. the physical and chemical properties of the polymers were analyzed by scanning electron microscope, thermogravimetric analyzer, electron spectrum and solid phase extraction ( microextraction ) technology. the imprinting and recognizing principle of mipm in water was studied through bi - templates imprinting method as well

    分別採用種子溶脹懸浮聚合法、懸浮聚合法和乳液聚合法，在水相中體系制備得到了一系列氨基酸和藥物印跡的分子印跡聚合物微球（ mipm ） ；採用掃描電鏡、熱失重分析、電子能譜分析、固相（微）萃取等技術對制備所得的mipm進行了分析和表徵；採用雙模板印跡的方法對水相中mipm的印跡和識別機理進行了探討。
  5. Poly butyl acrylate ( pba ) / mmt composites were prepared by emulsion polymerization. then, pvc / ( pba - mmt ) nanocomposites were prepared by suspension polymerization of vinyl chloride in the presence of pba / mmt composites

    利用乳液聚合的方法制備了聚丙烯酸丁酯（ pba ）無機mmt復合膠乳，並在pba mmt復合膠乳存在下，採用懸浮聚合法制備了pvc （ pba - mmt ）納米復合材料。
  6. The inserting method and properties of the composite materials in consist of omt and poly ( styrene - butyl acrylate ) had been researched ; the ultra - fine organic rigid particles crosslinked polystyrene ( xps ) has been synthesized by emulsion polymerization, the effect of the synthesis process on the size of organic rigid particles was discussed. the cause of the increasing mechanical properties of pp composite materials, which were strengthened and toughened with organic rigid particles and elastomer, had been investigated. the results of studying viscosity and precipitate height of sio2 nano - particles suspension showed that the sio2 nano - particles are very good dispersed by dp270 or cat 639w dispersant

    通過粘度法和沉降法測定結果的一致性，說明分散劑dp270和cat639w對sio _ 2納米粒子有較好的分散性， dp270的最佳用量為0 . 2時懸浮液粘度從35 . 1mpa ? s降為23 . 3mpa ? s ， cat639w最佳用量為0 . 4時懸浮液的粘度從35 . 1mpa ? s降為23 . 1mpa ? s ；通過研究分散劑存在下納米粒子的苯丙乳液聚合動力學，發現納米粒子的存在對乳液聚合有一定的緩聚作用，並討論了乳化體系、溫度、引發劑、表面處理劑以及納米粒子用量對聚合的影響。
  7. White powdered homopolymer resin produced through suspension polymerization ( medium degree of polymerization )

    以懸浮聚合方式製造的單聚合物樹脂，是白色粉狀的中聚合度產品，消光效果優良。
  8. Preparation of steady porous polymer microespheres by suspension polymerization

    懸浮聚合法制備穩定的多孔高分子微球
  9. It is significant for reducing the product cost and improving the comprehensive property of the superabsorbent composite. using ammonium eerie nitrate and n, n ' - methylene - bis - acrylamide as an initiator and crosslink agent respectively, a superabsorbent composite is prepared by graft polymerization of acrylamide on starch at the presence of clay suspension, followed by hydrolyzing, washing, drying, grounding and filtering

    本文以硝酸鈰銨為引發劑， n ， n -亞甲基雙丙烯酰胺為交聯劑，使澱粉、粘土接枝共聚丙烯酰胺，經過水解，洗滌，乾燥，粉碎制得粘土-澱粉接枝共聚丙烯酰胺的超吸水性復合材料。
  10. Reversed phase suspension polymerization

    反相懸浮聚合
  11. Besides, pvc / organo - mmt ( ommt ) nanocomposites were synthesized with two types of ommt by suspension polymerization

    此外，利用兩種有機蒙脫土（ ommt ）通過懸浮聚合的方法合成了pvc ommt納米復合材料。
  12. Amino acid molecules imprinted polymeric composite microspheres with magnetic susceptibility ( ms - smips ) were prepared by suspension polymerization ( sp ) and inverse emulsion - suspension polymerization ( iesp ), respectively. protein molecules imprinted soft - wet gel composite microspheres with magnetic susceptibility ( ms - pigms ) were prepared by inverse suspension polymerization ( isp ) and seeded inverse suspension polymerization ( sisp ), respectively. the resulting ms - smips and ms - pigms were characterized by scanning electron microscope ( sem ), thermogravimetric analyzer ( tg ), vibrating sample magnetometer ( vsm ), infrared spectrum ( ftir ), high performance liquid chromatography ( hplc ), and so on

    分別採用懸浮聚合法和反相乳液?懸浮聚合法制備了氨基酸分子印跡聚合物磁性復合微球（ ms - smips ） ；分別採用反相懸浮聚合法和種子反相懸浮聚合法制備了蛋白質分子印跡磁性軟濕凝膠復合微球（ ms - pigms ） ；用掃描電子顯微鏡、熱重分析儀、振動樣品磁強計、紅外光譜、高效液相色譜等對所制備的ms - smips和ms - pigms進行了表徵。
  13. It was showed that mipm between 50 - 300 ? m with macro - pores could be prepared via both seeds swelling and suspension polymerization method and suspension polymerization method, the former method could prepared the mipm with narrower size distribution while the later one was easier to carry out and more time - saving. the morphology of the mipm was influenced by many factors including swelling solvent, stirring speed, dosage of seeds, dispersant, dilute and progenic solvent

    M的、具有大孔結構的mipm ，前者的產物具有相對較窄的粒徑分佈，但後者的制備工藝則較簡單、制備周期也較短；溶脹劑、攪拌速度、種球用量、分散劑、稀釋劑和致孔劑是影響產物微球形態的主要因素；乳液聚合法能夠制備得到0 . 16 - 0 . 56
  14. Then, by suspension, emulsion and bulk polymerization, pmma / mmt ( ommt ) nanocomposites is prepared

    然後分別通過懸浮、乳液及本體聚合法制備了pmma mmt （ ommt ）納米復合材料。
  15. Xrd and tem characterizations show that the spacings of ommt are expanded and exfoliated in pmma / ommt nanocomposites by suspension and emulsion methods, while pmma / mmt and pmma / ommt nanocomposites by bulk polymerization belong to intercalated and exfoliated type, respectively

    Xrd和tem測試表明，懸浮法pmma ommt復合材料中， ommt層間距增大，且大多以厚度小於20nm的片層聚集體均勻分散於pmma基體中；乳液法pmma ommt復合材料中， ommt基本已發生剝離；而本體法pmma mmt和pmma ommt復合材料分別屬插層型和剝離型。
  16. So far, although numerous synthetic routes, such as suspension polymerization, emulsion polymerization, dispersion polymerization, etc, have been developed to produce magnetic composite microspheres, there are still a lot of problems need to be resolved for preparing ideal and useful magnetic composite microspheres. these problems include low magnetic content, low efficiency of encapsulation, big size, polydispersity of particle size, the contamination of composite microspheres by some additives, etc. it is realized recently that the preparation of high quality magnetic composite microspheres relies on the breakthrough of synthesis approaches and the detail understanding of the polymerization mechanism in the presence of magnetic inorganic particles

    本文針對當前磁性復合微球磁含量低、潔凈度較差，且主要是微米級產品的研究現狀，以提高磁性復合微球磁含量、提高復合微球的潔凈度及在維持較高磁含量的基礎上有效減小復合微球的粒徑為主要目標，採用改進乳液聚合法、細乳液聚合法及活性游離基dpe法三種方法制備了不同粒徑及磁含量的磁性復合微球。
  17. Furthermore two suitable monomers were chosen to produce such kind of grin polymer micro - spheres by suspension diffusion co - polymerization method. next, the refractive index distribution curve and other optic parameters of the micro - lens were measured

    進而選擇兩種適當的聚合物單體，利用懸浮擴散共聚的方法加工制備獲得此類微球透鏡，並測量了所得透鏡的折射率分佈曲線和其它光學參數。
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