Catalogue family for medium-pressure compressed air. The table includes fixed-speed and permanent-magnet variable-frequency model codes from CM75G through CM320GPV, with printed working-pressure ranges up to 4.0 MPa.
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| Model | Pressure MPa | Pressure psi | FAD m³/min | FAD cfm | Power kW | Power HP | Noise dB(A) | Weight kg | Dimensions L×W×H mm | Source note |
|---|---|---|---|---|---|---|---|---|---|---|
| CM75G | 2.0-4.0 | 290-580 | 6.3 | 222 | 75 | 100 | 70 | 2100 | 2750×1250×1480 | fixed-speed |
| CM75GPV | 2.0-4.0 | 290-580 | 2.5-6.3 | 88-222 | 37 / 37 | 50 / 50 | 70 | 2250 | 2000×1900×1480 | catalogue repeats the power line |
| CM90G | 2.0-4.0 | 290-580 | 8.2 | 290 | 90 | 123 | 72 | 2580 | 3000×1350×1540 | fixed-speed |
| CM110GPV | 2.0-4.0 | 290-580 | 3.3-8.2 | 117-290 | 55 / 55 | 75 / 75 | 72 | 2450 | 2500×2000×1550 | catalogue repeats the power line |
| CM110G | 2.0-4.0 | 290-580 | 10.2 | 360 | 110 | 150 | 72 | 2630 | 3000×1350×1540 | fixed-speed |
| CM130GPV | 2.0-3.0 | 290-435 | 5.4-13.5 | 191-477 | 55 / 75 | 75 / 100 | 75 | 3000 | 2500×2000×1550 | two power alternatives printed |
| CM150GPV | 2.0-4.0 | 290-580 | 5.4-13.5 | 191-477 | 75 / 75 | 100 / 100 | 75 | 3100 | 2500×2000×1550 | catalogue repeats the power line |
| CM200GPV | 2.0-4.0 | 290-580 | 7.1-17.8 | 251-629 | 90 / 110 | 120 / 150 | 75 | 3850 | 2760×2250×1670 | two power alternatives printed |
| CM242GPV | 2.0-4.0 | 290-580 | 9.6-24.0 | 339-847 | 110 / 132 | 150 / 180 | 75 | 3950 | 2760×2250×1670 | two power alternatives printed |
| CM320GPV | 2.0-4.0 | 290-580 | 12.6-31.5 | 445-1113 | 160 / 160 | 220 / 220 | 85 | 5100 | 3800×2100×2250 | catalogue repeats the power line |
How to read the table: select a pressure row first, then compare FAD, motor power, cooling form, noise, weight and outline dimensions. FAD is catalogue data; verify reference inlet conditions and permitted tolerances in the quotation.
Catalogue family for medium-pressure compressed air. The table includes fixed-speed and permanent-magnet variable-frequency model codes from CM75G through CM320GPV, with printed working-pressure ranges up to 4.0 MPa.
The medium-pressure family is presented in the catalogue for 2.0–4.0 MPa service, with one model limited in the printed table to 2.0–3.0 MPa. Several GPV rows show two power entries or repeat a power line. Those values are reproduced exactly because the source uses merged cells and alternative entries; they must be resolved on the approved quotation and drawing. Medium-pressure air can support PET bottle blowing and other high-pressure air duties. It must not be interpreted as permission to compress oxygen-rich gas: oxygen service requires a separate, explicitly engineered compressor and oxygen-compatible risk assessment.
The intended application scope includes medium-pressure oil-free air for PET bottle blowing and other high-pressure air systems, subject to project-specific treatment, receiver and pressure-equipment review. The compressor is a source of compressed air. For a medical oxygen plant it normally sits upstream of the oxygen generator, air treatment and buffer vessels. It is not a compressor for oxygen gas and it should never be connected to oxygen-enriched gas unless a separate design explicitly approves that service.
State normal, minimum and peak FAD; required pressure at the process inlet; operating hours; start-stop limitations; and whether a single unit, duty/standby pair or sequenced station is required. Use actual plant measurements when replacing an existing machine. Do not add an arbitrary safety factor without documenting why it is needed.
The model table gives compressor working pressure. The process receives less after pressure losses through the aftercooler, separator, dryers, filters, check valves, receiver, distribution header and oxygen-generation skid. Calculate the worst credible pressure loss at peak flow and dirty-filter condition.
Write the required ISO 8573-1 class notation for particles, water and oil at the stated measurement point. The catalogue presents an oil-free/Class 0 marketing claim, but a purchase specification should request the exact class triplet, test method, sampling point and evidence for the offered configuration.
In a pressure-swing adsorption system, clean compressed air is the feedstock from which nitrogen is preferentially adsorbed. Compressor selection therefore affects oxygen-plant throughput, cycle stability, adsorbent protection and total energy use. The site must coordinate compressor FAD and pressure with the oxygen generator's validated inlet window rather than choosing both packages independently. A feed-air receiver can reduce short-cycle demand, while correctly sized filtration and drainage protect the downstream process from condensate and particulates.
The health-facility oxygen system is wider than the compressor. It may include inlet filtration, air treatment, oxygen generator, analyzer, product receiver, booster or filling system where permitted, alarms, reserve supply, pipeline distribution and documented commissioning. The compressor page therefore does not claim that the machine alone creates medical oxygen or that it is a certified medical device. Local regulations, pharmacopoeial requirements, risk management and the oxygen-system supplier's validation control the final project.
For medical-air service, the required quality and monitoring regime can be different from feed air for an oxygen generator. The buyer should identify whether the air will contact patients, drive instruments, feed a PSA plant, or serve a general industrial utility. Never merge these duties under a generic “medical compressor” label without a piping and hazard review.
The catalogue distinguishes air-cooled values with an “F” suffix and orange data in the standard-pressure tables, while models without “F” are described as water-cooled. This distinction changes package dimensions and weight, and it changes the buyer's utility checklist. For air cooling, confirm maximum ambient temperature, altitude, ventilation path, recirculation risk, inlet cleanliness and the heat rejected to the compressor room. For water cooling, specify inlet temperature, allowable temperature rise, water quality, pressure, flow, fouling allowance, corrosion control and whether the circuit is once-through, tower water or closed loop.
Water-lubricated compression also requires attention to water quality and separator performance. The supplied catalogue illustrates a lubricating-water filtration system, water cooler and water/air separation barrel. The order specification should identify consumables, drainage, water make-up, winterization and the consequences of a utility-water interruption. These details are not fully defined in the catalogue and remain engineering-review items.
Electrical data must include site voltage, phase, frequency, permitted voltage variation, earthing, short-circuit level, motor starting constraints, VFD harmonic requirements where relevant, and the control interface. Catalogue kW and HP values are model-table fields, not a complete electrical schedule.
Commissioning should not be reduced to “machine starts and makes pressure.” A medical oxygen project needs a traceable handover showing that the compressor, treatment train and oxygen system operate together through normal, peak, standby and fault scenarios.
Use the supplied operation manual and serial-number-specific parts list. A useful maintenance plan separates daily condition checks from calendar tasks, running-hour tasks and condition-based interventions. Daily checks can include pressure, temperature, drain function, abnormal sound, water level or quality indicators, cooling performance and alarm history. Planned work may include intake and process filtration, cooling surfaces, water filtration, separator inspection, electrical connections, safety devices and calibration of critical instruments.
Low pressure at the process can result from excessive demand, a dirty intake, downstream pressure loss, a control set point, a leaking valve or a compressor problem. High temperature can result from ventilation recirculation, inadequate cooling water, fouled heat exchange surfaces, incorrect water flow or high ambient conditions. Frequent starts often indicate insufficient receiver volume, an unsuitable control band, leakage or a machine that is oversized for the minimum demand. Diagnose the system before replacing major parts.
For oxygen-generation duty, trend oxygen purity and production together with compressor pressure and FAD. A falling oxygen result may come from air supply, air treatment, valve timing, adsorbent condition, analyzer issues or downstream leakage. The compressor should not be blamed—or cleared—without correlated data.
Final manufacture and shipment must follow the approved quotation, model schedule, wiring diagram, P&ID and general arrangement drawing. The website table is a selection aid and evidence transcription; it does not replace the signed project documents.
No. The catalogue supports oil-free compressed-air packages. In a medical oxygen plant the machine normally supplies air to the PSA/VPSA generator. Oxygen-gas compression requires a separate oxygen-service design.
Use it for shortlist and RFQ preparation. The approved quotation and drawing must resolve cooling form, voltage, options, exact interfaces, ambiguous merged cells and project compliance.
The catalogue footnote states that CM-F indicates an air-cooled model and orange data are air-cooled parameters. Models without F are water-cooled.
No. Oil-free compression addresses one contamination route. Medical oxygen or medical air quality depends on the complete system, treatment, monitoring, commissioning and applicable regulation.
Compare the measured demand profile, minimum demand, pressure stability, control method, sequencing plan, lifecycle energy and maintenance—not only motor power or maximum FAD.
We will map the requirement to catalogue-supported configurations and identify the information that still needs an approved engineering drawing.
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