{"id":94,"date":"2026-11-01T09:00:00","date_gmt":"2026-11-01T01:00:00","guid":{"rendered":"https:\/\/panovacuum.cn\/blog\/helium-leak-test-vs-pressure-rise-en\/"},"modified":"2026-11-05T16:29:33","modified_gmt":"2026-11-05T08:29:33","slug":"helium-leak-test-vs-pressure-rise-en","status":"publish","type":"post","link":"https:\/\/panovacuum.cn\/blog\/helium-leak-test-vs-pressure-rise-en\/","title":{"rendered":"Helium leak testing and pressure-rise testing differ by five orders of magnitude"},"content":{"rendered":"<p>A common question is whether pressure-rise testing is acceptable. It answers whether a chamber leaks; helium mass spectrometry answers how much and where. The gap is five orders of magnitude \u2014 a limit of the method, not of the instrument price.<\/p>\n<h2>1. Leak rate turns tightness into a number<\/h2>\n<p>Q = \u0394p\u00b7V\/\u0394t. A 1 m\u00b3 vessel changing 1 Pa in 1 s carries 1 Pa\u00b7m\u00b3\/s. For scale: a 4 L bicycle inner tube losing 1 bar over 30 days is 1.5\u00d710\u207b\u2074 Pa\u00b7m\u00b3\/s; a refrigerator leaking 10 g of R134a over ten years is 7.1\u00d710\u207b\u2077. The refrigerator is two orders tighter than the tube and still far from a semiconductor chamber.<\/p>\n<h2>2. Pressure rise measures more than leakage<\/h2>\n<p>With the valve closed, the rising pressure contains real leakage plus wall outgassing. Water outgassing decays as 1\/t, approximately 3\u00d710\u207b\u2079\/t (hours) in mbar\u00b7L\/(s\u00b7cm\u00b2). A freshly cleaned chamber can outgas several orders above its true leak for hours, so the reading is outgassing, not leakage, unless the background is measured and subtracted first.<\/p>\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\"  src=\"https:\/\/panovacuum.cn\/blog\/wp-content\/uploads\/2026\/11\/helium-leak-test-ul1000-vacuum-chamber-720w.webp\" alt=\"Final helium leak test on a vacuum chamber, performed unloaded\" width=\"720\" height=\"480\" loading=\"lazy\" decoding=\"async\" \/><figcaption>Final leak test: helium spray performed unloaded, with readings and instrument model written into the record.<\/figcaption><\/figure>\n<h2>3. Units differ by a factor of ten<\/h2>\n<p>1 mbar\u00b7L\/s = 0.1 Pa\u00b7m\u00b3\/s. Reading 1.5\u00d710\u207b\u2074 Pa\u00b7m\u00b3\/s as 1.5\u00d710\u207b\u2074 mbar\u00b7L\/s relaxes the requirement tenfold. Units in a contract matter more than the instrument model.<\/p>\n<h2>4. Temperature is not in the formula<\/h2>\n<p>Q = \u0394p\u00b7V\/\u0394t has three quantities and no temperature term; the source material neither discusses temperature effects on pressure rise nor provides a correction (not covered). Any claim of temperature compensation should come with the formula.<\/p>\n<h2>5. Why helium testing reaches 10\u207b\u00b9\u00b3<\/h2>\n<p>The mass spectrometer must operate below 10\u207b\u2074 hPa, maintained by the instrument&#8217;s own pumps. The turbopump compresses air far more than light gases, so air is held back while helium passes \u2014 it acts as a selective filter rather than a pump. Counterflow covers 1 to 10\u207b\u2079 Pa\u00b7m\u00b3\/s and dominates production use; main flow is more sensitive but needs 10\u207b\u00b2 hPa on both specimen and instrument. A quartz-window variant uses a 7 \u00b5m SiO\u2082 membrane with a 5\u00d710\u207b\u2079 detection limit.<\/p>\n<h2>6. What each method can reach<\/h2>\n<p>Spray helium outside an evacuated specimen: < 5\u00d710\u207b\u00b9\u00b3 Pa\u00b7m\u00b3\/s at a 1000 hPa differential. Sniffing a pressurised specimen: < 1\u00d710\u207b\u2078, specimen must withstand overpressure. Accumulation: mainly above 1\u00d710\u207b\u2075, and slow. For a 10\u207b\u2079 verdict only vacuum-mode mass spectrometry qualifies; sniffing is floored by the 5 ppm helium naturally present in air.<\/p>\n<h2>7. Large chambers test slowly<\/h2>\n<p>In molecular flow (< 10\u207b\u00b3 hPa) speed is set by specimen volume and effective helium pumping speed; above 1 hPa, laminar flow puts the backing pump in charge and everything slows. Longer waits on large chambers are geometry, not operator error \u2014 plan the response time into the schedule.<\/p>\n<h2>8. Three sources of misreading<\/h2>\n<p>5 ppm atmospheric helium; helium dissolved in oil-sealed backing-pump oil diffusing back into the high-vacuum side (open the gas ballast after a large leak); and no purge after a strong signal.<\/p>\n<h2>9. How we do it<\/h2>\n<p>Helium mass spectrometry against the criterion agreed on the project drawing. The capability we publish is the 1\u00d710\u207b\u2079 Pa\u00b7m\u00b3\/s range, with every unit tested rather than sampled. The method references GB\/T 36176-2018 and GB\/T 32218-2015, and the report is dispatched with the chamber. Pressure-rise testing is not used as an acceptance criterion here for one reason: it cannot separate leakage from outgassing, nor account for temperature error. For process judgement and rough localisation it remains entirely adequate; the sheet that gets signed calls for helium.<\/p>\n<p>Leak testing is a verdict, not a step. A verdict that cannot be stated precisely makes the report meaningless. The same verdict applies to your project once a drawing is submitted.<\/p>\n<h2>Frequently asked questions<\/h2>\n<h3>Can pressure-rise testing replace helium leak testing?<\/h3>\n<p>For process judgement, yes; as an acceptance criterion, no. The pressure-rise method cannot separate leakage from outgassing and carries no temperature correction. The document you sign has to rest on helium testing.<\/p>\n<h3>What magnitude can helium leak testing reach?<\/h3>\n<p>External helium spray in vacuum mode reaches the 5\u00d710\u207b\u00b9\u00b3 Pa\u00b7m\u00b3\/s range. Our factory acceptance testing follows the criterion on the project drawing; the capability we disclose externally is the 1\u00d710\u207b\u2079 Pa\u00b7m\u00b3\/s range.<\/p>\n<h3>Why does a large chamber take so long to test?<\/h3>\n<p>In the molecular-flow regime (below 10\u207b\u00b3 hPa) the response time is governed by chamber volume and effective helium pumping speed (V\/S). Above roughly 1 hPa, in the viscous regime, it is governed by the backing pump \u2014 the larger the chamber, the slower the response.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A common question is whether pressure-rise testing is acceptable. It answers whether a chamber leaks; helium mass spectrometry answers how much and where. The gap is five orders of magnitude \u2014 a limit of the method, not of the instrument price.<\/p>\n","protected":false},"author":1,"featured_media":115,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8,4],"tags":[],"class_list":["post-94","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-en","category-leak-testing"],"_links":{"self":[{"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/posts\/94","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/comments?post=94"}],"version-history":[{"count":3,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/posts\/94\/revisions"}],"predecessor-version":[{"id":149,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/posts\/94\/revisions\/149"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/media\/115"}],"wp:attachment":[{"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/media?parent=94"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/categories?post=94"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/panovacuum.cn\/blog\/wp-json\/wp\/v2\/tags?post=94"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}