堿脫脂 的英文怎麼說
中文拼音 [jiǎntuōzhī]
堿脫脂
英文
alkali degreasing-
Sodium metasilicate has strong alkalinity and good buffering capacity. it can neutralize acidic dirt, emulsify grease and oil, and provide corrosion proofing to metals. it is a basic material for the detergent industry, widely used in domesticindustrial detergent, food cleaner, metal cleaner, washing carbonated drink bottles, printing aid for textile, deinking recycled paper, etc
偏硅酸鈉具有強堿性，去污力強，緩沖能力大，可中和酸性污物，使脂肪和油類乳化，對無機物有反絮凝作用，對金屬有防腐蝕作用，是洗滌業不可替代的原料，廣泛應用於家庭洗衣粉、工業洗滌劑、食品清洗劑、金屬清洗劑、酒瓶清洗劑、除油紡織印染助劑及紙張脫墨劑等。The main functions of the bleaching earth adsorption in the refining processing are to remove the rest phosphatides and soap stock in the degummed oi1 or in the neutralized oi1
摘要白土吸附在油脂精練過程中的主要作用是吸附脫膠油或堿煉油中的殘磷和殘皂。Br - i - 1a strong - base degreasing agent is a composite of cation surface activator, anion surface activator and other auxiliary agents
Br - 1a強堿脫脂劑，它用陰離子表面活性劑陽離子表面活性劑和其它助劑復配而成。Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells
方法：採用成年大鼠肺組織無血清培養，運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿（ pc ）合成量； rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶（ cct ） mrna含量；透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化；免疫組織化學染色檢測glu的受體nmdar1亞單位的表達；生化測定肺組織乳酸脫氫酶（ ldh ）釋放量和肺組織勻漿中一氧化氮合酶（ nos ）活性、一氧化氮（ no ）生成量、超氧化物歧化酶（ sod ）水平以及丙二醛（ mda ）含量。分享友人