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"ion pair chromatography"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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¿µ¹® pH, hydrogen ion concentration ÇÑ±Û ¼ö¼ÒÀ̿³óµµÁö¼ö
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  Ç÷¾×À̳ª ¼Òº¯¿¡¼­ ½Ç½ÃÇϴ °Ë»çÇ׸ñ. pH°Ë»ç´Â ÀÎüÀǠü¾×ÀÇ »ê¼º, ¾ËÄ®¸®¼ºÀ» ¾Ë¾Æº¸´Â Áß¿äÇÑ °Ë»çÀÌ´Ù. ÀÎü´Â ¾à¾ËÄ®¸®¼º¿¡ ¼ÓÇϳª, À̺¸´Ù pHÀÇ Áõ°¡³ª °¨¼Ò°¡ ³ªÅ¸³¯ °æ¿ì, »ý¸í¿¡ À§ÇèÀÌ ¹ß»ýÇÑ´Ù. ÀÎü³»¿¡´Â ÀÌ·± »êµµÀÇ Áõ°¨À» ¸·±âÀ§ÇØ, À̸¥¹Ù ¿ÏÃæÁ¦µéÀÌ ¸¹ÀÌ Á¸ÀçÇϸç, Æ¯È÷ ÇãÆÄ¿Í ÄáÆÏÀÌ ¿ÏÃæÀÛ¿ëÀ» ¼öÇàÇϴ ÁÖ¿ä±â°üÀÌ´Ù.
  
  ÄáÆÏÀº »êµµ°¡ ³ôÀ» °æ¿ì, ¼Òº¯¿¡¼­ »êµµ¸¦ Áõ°¡½ÃÄÑ ¹èÃâÇÔÀ¸·Î½á Ç÷¾×³»ÀÇ ¾ËÄ®¸®¼º ³óµµ°¡ Áõ°¡Çϵµ·Ï ÇÑ´Ù. ¶ÇÇÑ ÇãÆÄ¿¡¼­µµ, Ç÷¾×³»¿¡ »êµµ°¡ Áõ°¡½Ã È£ÈíÀ» Áõ°¡ÇÔÀ¸·Î½á ¹ÛÀ¸·Î »êÀÇ ¹èÃâÀ» Áõ°¡½ÃŲ´Ù. ÀÌ·± ÇãÆÄ¿Í ÄáÆÏÀÇ ±ÕÇüÀº ¾ÆÁÖ ÀûÀýÈ÷ ÀÌ·ç¾îÁö°í ÀÖÀ¸¸ç, ¾î´À ÇÑ ±â°üÀÇ ÀÌ»óÀÌ ¹ß»ýÇϸé, ÀÌ·± ±ÕÇüÀº ±ú¾îÁö±â ½±´Ù.
¿µ¹® ion ÇÑ±Û ÀÌ¿Â
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  ºÐÀÚ¸¦ Àü±âºÐÇØÇÒ ¶§ ºÐ¸®µÇ´Â, Àü±â¸¦ ¶í ¹Ì¸³Àڷμ­ ¾çÀü±â¸¦ ¶í ¾çÀ̿°ú À½Àü±â¸¦ ¶í À½ÀÌ¿ÂÀÌ ÀÖ´Ù.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • base pair
    ¿°±â½Ö
  • base pair substitution
    ¿°±â½Öġȯ
  • complementary pair
    º¸Ã¼Â¦
  • mating pair
    ¦Áþ±â½Ö, ±³¹è½Ö
  • pair
    ¦, ½Ö
  • sib-pair method
    ÇüÁ¦½Ö¿¬±¸¹ý
  • affinity chromatography
    ģȭũ·Î¸¶Åä±×·¡ÇÇ
  • column chromatography
    ¿øÅëÅ©·Î¸¶Åä±×·¡ÇÇ
  • chromatography
    Å©·Î¸¶Åä±×·¡ÇÇ
  • gas-liquid chromatography
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
    °í¼º´É¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • high-pressure liquid chromatography
    °í¾Ð¾×üũ·Î¸¶Åä±×·¡ÇÇ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • chromatography
    Å©·Î¸¶Åä±×·¡ÇÇ
  • pair
    ¦, ½Ö
  • base pair
    ¿°±â½Ö
  • ion
    ÀÌ¿Â
  • positive ion
    ¾çÀÌ¿Â
  • ion trapping
    ÀÌ¿ÂÆ÷Âø
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • base pair
    ¿°±â½Ö
  • base pair substitution
    ¿°±â½Ö´ëÄ¡
  • complementary pair
    º¸ÇÕ¦
  • mating pair
    ¦Áþ±â½Ö, ±³¹è½Ö
  • sib-pair method
    ÇüÁ¦½Ö¿¬±¸¹ý
  • pair
    ¦, ½Ö
  • affinity chromatography
    ģȭũ·Î¸¶Åä±×·¡ÇÇ
  • chromatography
    Å©·Î¸¶Åä±×·¡ÇÇ
  • column chromatography
    ¿øÅëÅ©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
    °íÀÛÀ§¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • high-pressure liquid chromatography
    °í¾Ð·Â¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • hydrophobic chromatography
    ¼Ò¼ö¼ºÅ©·Î¸¶Åä±×·¡ÇÇ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • GLC= gas liquid chromatography
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • affinity chromatography
    ģȭ(öÑûú) Å©·Î¸¶Åä±×¶óÇÇ.
  • affinity chromatography
    ģȭ¼º Å©·Î¸¶Åä±×·¡ÇÇ
  • anion exchange chromatography
    À½À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • gas liquid chromatography =GLC
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
    °íÀÛÀ§(íÂêÓ)¾×üũ·Î¸¶Åä±×¶óÇÇ
  • high-pressure liquid chromatography
    °í¾Ð·Â¾×ü Å©·Î¸¶Åä±×¶óÇÇ
  • hydrophobic chromatography
    ¼Ò¼ö¼º Å©·Î¸¶Åä±×·¡ÇÇ
  • H+ (Hydrogen ion)
    ¼ö¼ÒÀÌ¿Â
  • Hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • Hydroxyl ion
    ÇÏÀ̵å·Ï½ÇÀÌ¿Â
  • Ion gradient
    À̿°æ»ç(ÌËÞØ)
  • air ion
    °ø±âÀÌ¿Â.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion exchange chromatography
    À̿±³È¯Å© ·Î¸¶Åä±×·¡ÇÇ.
  • ion-exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • base pair
    ¿°±â½Ö
  • base pair substitution
    ¿°±â½Ö´ëü
  • base pair, complementary
    »óº¸¼º ¿°±â½Ö
  • buffer pair
    ¿ÏÃæ½Ö.
  • complementary pair
    º¸ÇÕ¦.
  • electron pair
    ÀüÀÚ½Ö(ï³í­äª).
  • electron pair bond
    ÀüÀÚ½Ö°áÇÕ(¡­Ì¿ùê).
  • electron pair creation
    ÀüÀÚ½Öâ»ý(¡­óÜßæ).
  • line pair/mm
    mm´ç ¼±ÀÇ ¼ö
  • mating pair
    ¦Áþ±â½Ö, ±³¹è½Ö
  • pair, mating
    ±³¹è¦, ±³¹è½Ö
  • sib-pair methods
    ÇüÁ¦½Ö ¿¬±¸¹ý
  • affinity chromatography
    ģȭ(öÑûú) Å©·Î¸¶Åä±×¶óÇÇ.
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion pair chromatography
    À̿¦ Å©·Î¸¶Åä±×·¡ÇÇ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion pair
    À̿ ½Ö(äª)
  • zwitterion-pair chromatography
    ¾ç»ó(Õ×àõ)À̿½Ö(äª) Å©·Î¸¶Åä±×·¡ÇÇ
  • ion-ion interaction
    ÀÌ¿Â-À̿ »óÈ£ÀÛ¿ë(ßÓû»íÂéÄ)
  • ion chromatography
    À̿ ũ·Î¸¶Åä±×·¡ÇÇ
  • ion-exchange chromatography
    À̿±³È¯(Îßüµ) Å©·Î¸¶Åä±×·¡ÇÇ
  • ion filtration chromatography
    À̿¿©°ú(ÕëΦ) Å©·Î¸¶Åä±×·¡ÇÇ
  • paired-ion chromatography
    ½Ö(äª)À̿ ũ·Î¸¶Åä±×·¡ÇÇ
  • AT pair
    AT ½Ö(äª)
  • base pair
    1. ¿°±â ¦ 2. ¿°±â ½Ö(äª)
  • base pair
    (Ó¤êÈ) base pair
  • base-pair ratio
    ¿°±â¦ ºñ(Ýï)
  • base-pair substitution
    ¿°±â¦ ġȯ(öÇüµ)
  • conjugate acid-base pair
    ¦ÁöÀº »ê¿°±â½Ö(ß«ç¤Ðñäª)
  • "d,l pair"
    "d,l ¦ (ÔÒ) a pair of enantiomers"
  • electron pair bond
    ÀüÀÚ½Ö °áÇÕ(ï³í­äªÌ¿ùê)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • ion pair
    À̿½Ö
  • electron pair
    ÀüÀÚ½Ö
  • line pair/mm
    mm´ç ¼±ÀǼö
  • ion
    ÀÌ¿Â
  • ion chamber
    Àü¸®ÇÔ
  • paramagnetic ion
    »óÀÚ¼ºÀÌ¿Â
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
IPC intermittent pneumatic compression; International Poliomyelitis Congress; ion pair chromatography; i...
HPLC high-performance liquid chromatography; high-power liquid chromatography; high-pressure liquid chrom...
RPIPP reverse phase ion-pair partition
g-ion gram-ion
ISS idiopathic short stature; injury severity score; International Society of Surgery; ion-scattering sp...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
GC-NICI-MS gas chromatography-negative ion chemical ionisation mass spectrometry
IMAC Immobilised metal ion affinity chromatography
IC Ion Chromatography
IEC Ion-exchange chromatography
GC--MS--SIM gas chromatography--mass spectrometry--selected ion monitoring
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • ion pair
    À̿½Ö
  • affinity chromatography
    ģȭ¼º Å©·Î¸¶Åä±×·¡ÇÇ
    ģȭ¼ºÀ» ÀÌ¿ëÇÏ¿© ƯÁ¤ ¹°ÁúÀ» ¿ë¾× ¼Ó¿¡¼­ ºÐ¸®ÇÏ´Â Å©·Î¸¶Åä±×·¡ÇÇ. Ç׿ø-Ç×ü, ±âÁú-È¿¼Ò, µ¶¼Ò-µ¶¼Ò°¡ °áÇÕÇÏ´Â ¼ö¿ëü, lectin-lectin °áÇÕ¼ö¿ëü µîÀÇ ÇÑÆíÀ» ºÒ¿ë¼ºÀÇ ´ãü¿¡ °øÀ¯°áÇÕ½Ã۰í À̰Ͱú ºÐ¸®ÇÏ°í ½ÍÀº ¿ë¾×À» ¹ÝÀÀ½ÃÄÑ Àß ¼¼Á¤Çϸé ģȭ¼ºÀÌ ³ôÀº ¹°Áú¸¸ÀÌ °áÇÕÇϹǷΠ½Å¼ÓÇÏ°Ô ¿øÇÏ´Â ¹°ÁúÀ» È¿À²ÀûÀ¸·Î ²ø¾î³¾ ¼ö ÀÖ´Ù.
  • anion exchange chromatography
    À½À̿ ±³È¯ Å©·Î¸¶Åä±×·¡ÇÇ
  • base pair
    ¿°±â½Ö
  • chromatography
    Âø»ö Á¶¿µ¼ú, Å©·Î¸¶Åä±×·¡ÇÇ
    È­ÇÐ ºÐ¼®ÀÇ ÇÑ ¹æ¹ý. ºÐ¼®µÇ´Â ¿ë¾×À» ÈíÂøÁ¦¸¦ ³Ö¾î ¼¼¿î À¯¸®°ü¿¡ ºÎÀ¸¸é °¢°¢ÀÇ ¿ë¾×Àº °íÁ¤»ó¿¡ ´ëÇÑ ÈíÂøµµ¿¡ µû¶ó¼­ ´Ù¸¥ ¼Óµµ·Î Åë°ú À̵¿ÇÏ¿©, ÈíÂø Ä®·³ÀÇ ´Ù¸¥ ³ôÀÌÀÇ »ö´ë¸¦ »ý¼ºÇÑ´Ù. ÀÌ ¸»Àº Ä®·³¿¡ »öÃþÀ» »ý¼ºÇÏÁö ¾Ê´Â °æ¿ì¿¡µµ, °°Àº ¿ø¸®¸¦ ÀÌ¿ëÇÏ´Â ´Ù¸¥ ¹æ¹ýµµ Æ÷ÇÔÇÏ¿© È®´ëÇØ¼­ »ç¿ëµÈ´Ù. Ä«¿Ã¸°, ¾Ë·ç¹Ì³ª, ½Ç¸®Ä«, Ȱ¼ºÅºÀÌ ÈíÂøÁ¦·Î¼­ »ç¿ëµÇ°í ÀÖ´Ù. Å©·Î¸¶Åä±×·¡ÇÇ´Â »ç¿ëµÇ´Â ÈíÂøÁ¦ÀÇ ¼ºÁú, °íÁ¤»óÀÇ ¹°¸®ÇÐÀû Ư¼º ȤÀº »ç¿ëµÇ´Â ¹æ¹ý µî¿¡ µû¶ó¼­ ºÐ·ùµÈ´Ù.
  • co-chromatography
    º¸Á¶ »öÃþ ºÐ¼®
  • column chromatography
    Ä®·³ Å©·Î¸¶Åä±×¶óÇÇ
  • complementary base pair
    »óº¸¼º ¿°±â½Ö
  • electron pair
    ÀüÀÚ ½Ö
  • electron pair creation
    ÀüÀÚ½Ö Ã¢»ý
  • pair bond
    ½Ö°áÇÕ
    »ýŰ迡 À־ ¾ÏÄÆ°ú ¼öÄÆÀÌ ±³¹Ì³ª ÀÚ½ÄÀ» ±â¸£´Â °ÍÀ» ¸ñÀûÀ¸·Î ÇÑ ¹Ý¿µ±¸Àû °ü°è.
  • paper chromatography
    ÆäÀÌÆÛ Å©·Î¸¶Åä±×·¡ÇÇ
    ÈíÂø Ä®·³´ë½Å ÈíÃëÁö³ª º¸ÅëÀÇ ¿©°úÁö¸¦ »ç¿ëÇÏ´Â Å©·Î¸¶Åä±×·¡ÇÇ. °¢ ¼ººÐÀÌ °¢°¢ ´Ù¸¥ À̵¿ ¼Óµµ¿¡ ÀÇÇØ¼­ ºÐ¸®µÈ ÈÄ °¡½Ã Å©·Î¸¶Åä±×·¥ÀÌ ¸¸µé¾îÁø´Ù.
  • hydrogen ion
    ¼ö¼Ò ÀÌ¿Â
    ¼ö¼Ò ¿øÀÚÀÇ ÇÙ ¶Ç´Â ÀüÀÚ¸¦ »ó½ÇÇÑ ¼ö¼Ò ¿øÀÚ. À̰ÍÀº ÀüÀÚÀÇ À½ ÀüÇÏ¿Í µ¿·®ÀÇ ¾ç ÀüÇϸ¦ °¡Áø´Ù.
  • hydrogen ion exchange
    ¼ö¼Ò À̿ ±³È¯
  • hydronium ion
    ¿Á¼Ò´½ ÀÌ¿Â
    ÇÏÀ̵å·Î´½.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
chromatography, ion exchange Separation technique in which the stationary phase consists of ion exchange resins. The resins contain loosely held small ions that easily exchange places with other small ions of like charge present in solutions washed over the resins.
(12 Dec 1998)
ion exchange chromatography <procedure> Separation of molecules by absorption and desorption from charged polymers. An important technique for protein purification.
For small molecules the support is usually polystyrene, but for macromolecules, cellulose, acrylamide or agarose supports give less non-specific absorption and denaturation. Typical charged residues are CM carboxymethyl) or DEAE (diethylaminoethyl).
(27 Oct 1998)
absorption chromatography <investigation> Techniques for separating molecules based on differential absorption and elution. Term for separation methods involving flow of a fluid carrier over a nonmobile absorbing phase.
(18 Nov 1997)
adsorption chromatography Chromatography in which separation of substances is achieved by the difference in degree of adsorption of the compounds to a stationary phase.
(05 Mar 2000)
affinity chromatography <investigation> A technique of analytical chemistry used to separate and purify a biological molecule from a mixture, based on the attraction of the molecule of interest to a particular ligand which has been previously attached to a solid, inert substance.
The mixture is passed through a column containing the ligand attached to the stationary substance, so that the molecule of interest stays within the column while the rest of the mixture continues through to the end. Then, a different chemical is flushed through the column to detach the molecule from the ligand and bring it out separately from the rest of the mixture.
(09 Feb 1998)
gas chromatography <technique> A chromatographic technique (a type of column chromatography) in which the stationary phase is solid while the mobile phase is gaseous samples.
The gaseous samples are separated based on their different adsorption ability to the solid phase.
(09 Oct 1997)
gas-liquid chromatography <technique> A chemistry lab technique, a type of column chromatography, used to separate the components of a mixed substance.
The substance is held stationary by an inert solid coated with an inert liquid which is not likely to evaporate (i.e. Is nonvolatile), while a gas (called an eluant) flows past it bringing out the components one at a time.
(09 Oct 1997)
paper chromatography <technique> Separation method in which filter paper is used as the support.
A type of chromatography in which the stationary phase is a sheet of special-grade filter paper. It is in all other aspects similar to thin-layer chromatography.
Not a very sensitive method, but historically important as one of the first methods available for separating natural compounds.
(07 Mar 2000)
gel exclusion chromatography <investigation> A lab technique, a type of column chromatography, used to separate the components of a mixture by molecular size and to collect the molecules which are larger than a certain size. It is similar to gel filtration, small molecules are slowed or trapped by the pores in the gel beads filling the column, while large molecules, too large to fit into the pores, slide past the beads and get to the bottom of the column first. at this point, the large molecules are collected. Gel exclusion refers to the maximum size of molecule which will fit into the gel bead pores, and this lab technique is used to collect the molecules in the mixture which are larger than, or excluded from, the pores.
(09 Oct 1997)
gel filtration chromatography See: gel filtration.
(05 Mar 2000)
partition chromatography The separation of similar substances by repeated divisions between two immiscible liquids, so that the substances, in effect, cross the partition between the liquids in opposite directions; where one of the liquids is bound as a film on filter paper, the process is termed paper partition chromatography or paper chromatography.
(05 Mar 2000)
reversed phase chromatography A form of partitionary chromatography in which the stationary phase is more polar than the mobile phase.
(05 Mar 2000)
chromatography <investigation> Techniques for separating molecules based on differential absorption and elution. Term for separation methods involving flow of a fluid carrier over a nonmobile absorbing phase.
(18 Nov 1997)
chromatography, affinity A chromatographic technique that utilises the ability of biological molecules to bind to certain ligands specifically and reversibly. It is used in protein biochemistry.
(12 Dec 1998)
chromatography, agarose A method of gel filtration chromatography using agarose, the non-ionic component of agar, for the separation of compounds with molecular weights up to several million.
(12 Dec 1998)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • chromatography
    »öÃþºÐ¼®
  • gas chromatography
    °¡½º Å©·Î¸¶Åä±×·¡ÇÁ¹ý(À¯±âÈ­ÇÕ¹° È¥ÇÕü ºÐ¼®¹ý) ?,
  • gas liquid chromatography
    =GAS CHROMATOGRATOGRAPHY
  • -ion
    ¶óƾ¾î°èµ¿»ç ¾î¹Ì¿¡ ºÙ¾î¼­ (»óÅÂ,µ¿ÀÛ)À» ³ªÅ¸³»´Â ¸í»ç ¾î¹Ì
  • field ion microscope
    À̿ ¹æ»ç Çö¹Ì°æ;Àü°è À̿ Çö¹Ì°æ
  • hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • ion
    (È­)ÀÌ¿Â;¾çÀÌ¿Â(cation);À½ÀÌ¿Â(anion)
  • ion engine
    (°ø)À̿¿£Áø(ion rocket)
  • ion etching
    (¹°)À̿¿¡Äª(±Ý¼Óµî¿¡ °í¿¡³ÊÁö ÀÌ¿ÂÀ» ÂØ¾î ºÎ½Ä½Ã۱â)
  • ion exchange
    (¹°,È­)À̿±³È¯
  • ion implantation
    (¹°)À̿ ÁÖÀÔ(¹ý)(¹ÝµµÃ¼¸¦ ¾ò´Â ¹æ¹ýÀÇ Çϳª)
  • ion milling
    ION ETCHING
  • ion propulsion
    (¿ìÁÖ¼± µîÀÇ)À̿ ÃßÁø
  • ion rocket
    ION ENGINE
  • positive ion
    ¾çÀÌ¿Â
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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