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Galaigh go mbeidh sé tirim agus corraigh ó am go chéile le slat ghloine.
Evaporate to dryness, occasionally stirring with a glass rod.
Galaigh go mbeidh sé tirim agus corraigh ó am go chéile le slat ghloine.
Evaporate to dryness, occasionally stirring with a glass rod.
Galaigh go dtí tirimeacht é, á chorraí go hócáideach le slat ghloine.
Evaporate to dryness, occasionally stirring with a glass rod.
Galaigh an tuaslagán go dtí thart ar 0,5 ml i sruth nítrigine.
Evaporate the solution to ca. 0,5 ml in a stream of nitrogen.
Lig dó fuarú, cuir leis cúpla braon uisce agus ansin idir 10 agus 15 ml d'aigéad hidreafluarach (3.4) agus galaigh go mbeidh sé tirim ag 150°C tuairim. Má bhíonn aon silice fágtha san iarmhar déan é a atuaslagadh i gcúpla millilíotar d'aigéad hidreafluarach (3.4) agus galaigh go mbeidh sé tirim.
Allow to cool, add a few drops of water followed by 10 to 15 ml of hydrofluoric acid (3.4) and evaporate to dryness at about 150°C. If any silica remains in the residue, redissolve it in a few millilitres of hydrofluoric acid (3.4) and evaporate to dryness.
Lig dó fuarú, cuir roinnt braonta uisce agus 10 go 15 ml d’aigéad hidreafluarach (pointe 3.4) ina dhiaidh sin leis agus galaigh go dtí tirimeacht ag thart ar 150 °C é. Má tá aon silice fágtha san iarmhar, atuaslaig i roinnt millilítear d’aigéad hidreafluarach (pointe 3.4) agus galaigh go dtí tirimeacht í.
Allow to cool, add a few drops of water followed by 10 to 15 ml of hydrofluoric acid (point 3.4) and evaporate to dryness at about 150 °C.
Tuaslaig an t-iarmhar le 2 ml tuairim d'aigéad hidreaclórach (3.1), galaigh go mbeidh sé tirim agus cuir leis 5 ml d'aigéad hidreaclórach 6N (3.2).
Dissolve the residue with about 2 ml of hydrochloric acid (3.1), evaporate to dryness and add 5 ml of 6 N hydrochloric acid (3.2).
Lig dó fuarú, cuir leis cúpla braon uisce agus ansin idir 10 agus 15 ml d'aigéad hidreafluarach (3.4) agus galaigh go mbeidh sé tirim ag 150°C tuairim.
Allow to cool, add a few drops of water followed by 10 to 15 ml of hydrofluoric acid (3.4) and evaporate to dryness at about 150°C.
Má bhíonn aon silice fágtha san iarmhar, déan é a atuaslagadh i gcúpla millilíotar d'aigéad hidreafluarach (3.4) agus galaigh go mbeidh sé tirim.
If any silica remains in the residue, redissolve it in a few millilitres of hydrofluoric acid (3.4) and evaporate to dryness.
Galaigh an scagáit go dtriomóidh sí i mias galúcháin platanaim agus téigh go mbíonn dath murtallach dearg uirthi agus go mbíonn meáchan an iarmhair tairiseach.
Evaporate the filtrate to dryness in a platinum evaporating dish and heat to a dull red until the weight of the residue is constant.
Gálú: galaigh agus cuir an táirge neamhchaolaithe chun ábhar pacáistithe a ghlanadh de réir treoracha oibriúcháin an mheasín pacáistithe.
Vaporization: vaporize and apply undiluted product to clean packaging material according to packaging machine operating instructions.
Bain 200 ml den scagáit agus galaigh é go dtí go mbeidh thart ar leith a toirte ann chun an chuid is mó den eatánól a dhíchur.
Remove 200 ml of the filtrate and evaporate to approximately half volume in order to eliminate most of the ethanol.
Cuir an scagáit sa bhreogán fuaraithe, galaigh í go dtí go mbeidh sí tirim, luaithrigh agus meáigh í.
Place the filtrate in the cooled crucible, evaporate until dry, ash and weigh.
Cuir an t-eascra ar dhabhach ghainimh agus galaigh é go dtí go mbeidh sé tirim chun an tsilice a dhéanamh dothuaslagtha.
Place the beaker on a sand bath and evaporate until dry to make the silica insoluble.
Galaigh an tuaslagóir go dtí tirimeacht, nach mór, ar an ngalaitheoir rothlach (pointe 4.1) agus brú laghdaithe ann ag teocht nach mó ná 40 °C.
Evaporate the solvent nearly to dryness on the rotary evaporator (point 4.1) with reduced pressure at a bath temperature not exceeding 40 °C.
Déan an t-iarmhar a thuaslagadh le thart ar 2 ml d’aigéad hidreaclórach (pointe 3.1), galaigh go dtí tirimeacht agus cuir 5 ml d’aigéad hidreaclórach 6 mhol/lítear leis (pointe 3.2).
Dissolve the residue with about 2 ml of hydrochloric acid (point 3.1), evaporate to dryness and add 5 ml of 6 mol/litre hydrochloric acid (point 3.2).
Galaigh an meatánól ar an sceoghalaitheoir rothlach (pointe 4.2), ní mór gan teocht na daibhche uisce a bheith níos mó ná 40 °C.
Evaporate the methanol on the rotary film evaporator (point 4.2), the temperature of the water bath must not exceed 40 °C.
Galaigh an codán sin go dtí go mbeidh tirimeacht díreach bainte amach aige trí bhíthin an sceoghalaitheora rothlaigh (pointe 4.3) ag 60 °C.
Evaporate this fraction until it has just reached dryness by means of the rotary evaporator (point 4.3) at 60 °C.
Galaigh é go dtí go mbeidh tirimeacht díreach bainte amach aige, faoi bhrú laghdaithe ag 60 °C trí bhíthin an ghalaitheora rothlaigh (pointe 4.3).
Evaporate until it has just reached dryness, under reduced pressure at 60 °C by means of the rotary evaporator (point 4.3).
Galaigh go dtí thart ar 4 ml i ngalaitheoir rothlach ag teocht nach mó ná 35°C. Caolaigh an t-iarmhar le huisce chun cion tuartha bhaiceatraicín since de 0.42 a.i./ml (=U8) a fháil.
Evaporate to about 4 m1 in a rotary evaporator at a temperature not exceeding 35°C. Dilute the residue with water to obtain an expected zinc bacitracin content of 0.42 i.u./ml (= U8).
Galaigh 100 ml den eastóscán sin ar an ngalaitheoir rothlach (féach pointe 5.4) go dtí go mbeidh sé nach mór tirim, déan an tuaslagóir atá fágtha a bhaint le sruth nítrigine (pointe 3.10) agus atuaslaig an t-iarmhar in 10,0 ml de mheatánól (pointe 3.3).
Evaporate 100 ml of this extract on the rotary evaporator (see point 5.4) nearly to dryness, remove the remaining solvent with a stream of nitrogen (point 3.10) and redissolve the residue in 10,0 ml of methanol (point 3.3).
Galaigh 25 ml den eastóscán sin ar an ngalaitheoir rothlach (féach pointe 5.4) go dtí go mbeidh sé nach mór tirim, déan an tuaslagóir atá fágtha a bhaint le sruth nítrigine (pointe 3.9) agus atuaslaig an t-iarmhar in 25,0 ml de mheatánól (pointe 3.3).
Evaporate 25 ml of this extract on the rotary evaporator (see point 5.4) nearly to dryness, remove the remaining solvent with a stream of nitrogen (point 3.9) and redissolve the residue in 25,0 ml of methanol (point 3.3).
Chun é a threisiú ag leibhéal 100 mg/kg, aistrigh 10,0 ml den bhuntuaslagán caighdeánach (pointe 3.10.1) chuig fleascán cónúil 250 ml agus galaigh an tuaslagán go dtí thart ar 0,5 ml.
To fortify at a level of 100 mg/kg, transfer 10,0 ml of the stock standard (point 3.10.1) to a 250 ml conical flask and evaporate the solution to approximately 0,5 ml.
Chun é a threisiú ag leibhéal 100 mg/kg, aistrigh 10,0 ml den bhuntuaslagán caighdeánach (pointe 3.7.1) chuig fleascán cónúil 250 ml agus galaigh an tuaslagán go dtí thart ar 0,5 ml.
To fortify at a level of 100 mg/kg, transfer 10,0 ml of the stock standard solution (point 3.7.1) to a 250 ml conical flask and evaporate the solution to approximately 0,5 ml.